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Sample records for bromine 81 reactions

  1. Complex Kinetics in the Reaction of Taurine with Aqueous Bromine ...

    African Journals Online (AJOL)

    Complex Kinetics in the Reaction of Taurine with Aqueous. Bromine and Acidic Bromate: A Possible Cytoprotective. Role against Hypobromous Acid. Reuben H. Simoyi1*, Kevin Streete2, Claudius Mundoma2 and Rotimi Olojo2. 1Department of Chemistry, University of Cape Town, Rondebosch, 7700 South Africa.

  2. Vibrationally Driven Hydrogen Abstraction Reaction by Bromine Radical in Solution

    Science.gov (United States)

    Shin, Jae Yoon; Shalowski, Michael A.; Crim, F. Fleming

    2013-06-01

    Previously, we have shown that preparing reactants in specific vibrational states can affect the product state distribution and branching ratios in gas phase reactions. In the solution phase, however, no vibrational mediation study has been reported to date. In this work, we present our first attempt of vibrationally mediated bimolecular reaction in solution. Hydrogen abstraction from a solvent by a bromine radical can be a good candidate to test the effect of vibrational excitation on reaction dynamics because this reaction is highly endothermic and thus we can suppress any thermally initiated reaction in our experiment. Br radical quickly forms CT (charge transfer) complex with solvent molecule once it is generated from photolysis of a bromine source. The CT complex strongly absorbs visible light, which allows us to use electronic transient absorption for tracking Br radical population. For this experiment, we photolyze bromoform solution in dimethyl sulfoxide (DMSO) solvent with 267 nm to generate Br radical and excite the C-H stretch overtone of DMSO with 1700 nm a few hundred femtoseconds after the photolysis. Then, we monitor the population of Br-DMSO complex with 400 nm as a function of delay time between two pump beams and probe beam. As a preliminary result, we observed the enhancement of loss of Br-DMSO complex population due to the vibrational excitation. We think that increased loss of Br-DMSO complex is attributed to more loss of Br radical that abstracts hydrogen from DMSO and it is the vibrational excitation that promotes the reaction. To make a clear conclusion, we will next utilize infrared probing to directly detect HBr product formation.

  3. Utilization of bromination reactions for the determination of carbamazepine using bromate–bromide mixture as a green brominating agent

    Directory of Open Access Journals (Sweden)

    Kanakapura Basavaiah

    2014-07-01

    Full Text Available One titrimetric and two spectrophotometric procedures have been developed for the assay of carbamazepine (CBZ in bulk drug, formulations and spiked human urine. The methods are based on the bromination of CBZ by the bromine generated in situ by the action of the acid on the bromate–bromide mixture. The twin advantages of avoiding liquid bromine and analysis in a cost-effective manner are realized. In titrimetry, the drug was treated with a known excess of bromate–bromide mixture in hydrochloric acid medium followed by the determination of unreacted bromine iodometrically. Spectrophotometry involves the addition of a measured excess of bromate–bromide reagent in acid medium to CBZ, and after the reaction is ensured to be complete, the residual bromine was determined by reacting with a fixed amount of either methyl orange and measuring the absorbance at 510 nm (method A or indigo carmine and measuring the absorbance at 610 nm (method B. Titrimetric procedure is applicable over the range of 1.00–7.50 mg CBZ, and the calculations are based on a 1:1 reaction stoichiometry (CBZ:KBrO3. In spectrophotometric methods, Beer’s law is valid within concentration ranges of 0.25–1.50 and 0.50–6.00 μg ml−1 CBZ for methods A and B, respectively. The proposed methods were successfully applied to the determination of CBZ in tablets and syrup, in addition to spiked human urine by the spectrophotometric methods, with mean recoveries of 95.50–104.0% and the results were statistically compared with those of an official method by applying Student’s t-test and F-test.

  4. Utilization of oxidation reactions for the spectrophotometric determination of captopril using brominating agents

    Science.gov (United States)

    El-Didamony, Akram M.; Erfan, Eman A. H.

    2010-03-01

    Three simple, accurate and sensitive methods (A-C) for the spectrophotometric assay of captopril (CPL) in bulk drug, in dosage forms and in the presence of its oxidative degradates have been described. The methods are based on the bromination of captopril with a solution of excess brominating mixture in hydrochloric acid medium. After bromination, the excess brominating mixture is followed by the estimation of surplus bromine by three different reaction schemes. In the first method (A), the determination of the residual bromine is based on its ability to bleach the indigo carmine dye and measuring the absorbance at 610 nm. Method B, involves treating the unreacted bromine with a measured excess of iron(II) and the remaining iron(II) is complexed with 1,10-phenanthroline and the increase in absorbance is measured at 510 nm. In method (C), the surplus bromine is treated with excess of iron(II) and the resulting iron(III) is complexed with thiocyanate and the absorbance is measured at 478 nm. In all the methods, the amount of bromine reacted corresponds to the drug content. The different experimental parameters affecting the development and stability of the color are carefully studied and optimized. Beer's law is valid within a concentration range of 0.4-6.0, 0.4-2.8 and 1.2-4.8 μg mL -1 for methods A, B and C, respectively. The calculated apparent molar absorptivity was found to be 5.16 × 10 4, 9.95 × 10 4 and 1.74 × 10 5 L mol -1 cm -1, for methods A, B and C, respectively. Sandell's sensitivity, correlation coefficients, detection and quantification limits are also reported. No interference was observed from common additives found in pharmaceutical preparations. The proposed methods are successfully applied to the determination of CPL in the tablet formulations with mean recoveries of 99.94-100.11% and the results were statistically compared with those of a reference method by applying Student's t- and F-test.

  5. The Reaction between Bromine and the Water Dimer and the Highly Exothermic Reverse Reaction.

    Science.gov (United States)

    Li, Guoliang; Wang, Hui; Li, Qian-Shu; Xie, Yaoming; Schaefer, Henry F

    2016-01-15

    The entrance complex, transition state, and exit complex for the bromine atom plus water dimer reaction Br + (H2O)2 → HBr + (H2O)OH and its reverse reaction have been investigated using the CCSD(T) method with correlation consistent basis sets up to cc-pVQZ-PP. Based on the CCSD(T)/cc-pVQZ-PP results, the reaction is endothermic by 31.7 kcal/mol. The entrance complex Br⋯(H2O)2 is found to lie 6.5 kcal/mol below the separated reactants. The classical barrier lies 28.3 kcal/mol above the reactants. The exit complex HBr⋯(H2O)OH is bound by 6.0 kcal/mol relative to the separated products. Compared with the corresponding water monomer reaction Br + H2 O → HBr + OH, the second water molecule lowers the relative energies of the entrance complex, transition state, and exit complex by 3.0, 3.8, and 3.7 kcal/mol, respectively. Both zero-point vibrational energies and spin-orbit coupling effects make significant changes to the above classical energetics. Including both effects, the predicted energies relation to separated Br + (H2O)2 are -3.0 kcal/mol [Br···(H2O)2 ], 28.2 kcal/mol [transition state], 26.4 kcal/mol [HBr···(H2O)OH], and 30.5 kcal/mol [separated HBr + (H2O)OH]. The potential energy surface for the Br + (H2O)2 reaction is related to that for the valence isoelectronic Cl + (H2O)2 system but radically different from the F + (H2O)2 system. © 2015 Wiley Periodicals, Inc.

  6. Solid-state NMR spectroscopy of the quadrupolar halogens: chlorine-35/37, bromine-79/81, and iodine-127.

    Science.gov (United States)

    Bryce, David L; Sward, Gregory D

    2006-04-01

    A thorough review of 35/37Cl, 79/81Br, and 127I solid-state nuclear magnetic resonance (SSNMR) data is presented. Isotropic chemical shifts (CS), quadrupolar coupling constants, and other available information on the magnitude and orientation of the CS and electric field gradient (EFG) tensors for chlorine, bromine, and iodine in diverse chemical compounds is tabulated on the basis of over 200 references. Our coverage is through July 2005. Special emphasis is placed on the information available from the study of powdered diamagnetic solids in high magnetic fields. Our survey indicates a recent notable increase in the number of applications of solid-state quadrupolar halogen NMR, particularly 35Cl NMR, as high magnetic fields have become more widely available to solid-state NMR spectroscopists. We conclude with an assessment of possible future directions for research involving 35/37Cl, 79/81Br, and 127I solid-state NMR spectroscopy. 2006 John Wiley & Sons, Ltd.

  7. UV Spectrometric Indirect Analysis of Brominated MWCNTs with UV Active Thiols and an Alkene—Reaction Kinetics, Quantification and Differentiation of Adsorbed Bromine and Oxygen

    Directory of Open Access Journals (Sweden)

    Sven Hanelt

    2013-07-01

    Full Text Available Indirect UV-absorption spectrometry was shown to be a valuable tool for chemical characterization of functionalized carbon nanotubes (CNTs. It complements data from X-ray photoelectron spectroscopy (XPS or FTIR analysis since it helps to clarify the type and concentration of functional groups. The principles of indirect application of UV-spectrometry and its mathematical interpretation are discussed. Their facile application, together with their adequate sensitivity and high flexibility, make UV-absorption-based approaches a valuable alternative to fluorescence spectrometry. Here, the approach was applied to the chemical analysis of oxidizing substances on CNTs. For this, pristine CNTs of low but finite oxygen content as well as brominated CNTs were analyzed by reaction in suspension with UV-active thiol reagents and a styrene derivative. It was shown that carefully selected reagents allow differentiation and quantification of bromine and generally oxidizing entities like oxygen. For brominated CNTs, it was shown that physisorbed bromine may dominate the overall bromine content.

  8. Complex Kinetics in the Reaction of Taurine with Aqueous Bromine ...

    African Journals Online (AJOL)

    molecule is the only one that can engage in reactions.10 The range of taurine implication ... H2O2 and Cl–, some studies have shown that EPO is less active than MPO with .... taurine shows a strong absorption peak at 240 nm with an ab- sorptivity of 2713 ... Applying the Beer-Lambert law for monobromo- taurine at 288 nm ...

  9. Production of hydrogen bromide by bromine-methane reactions at elevated temperature.

    Energy Technology Data Exchange (ETDEWEB)

    Bradshaw, Robert W.; Larson, Richard S.

    2003-05-01

    Hydrogen bromide is a potentially useful intermediate for hydrogen production by electrolysis because it has a low cell potential and is extremely soluble in water. Processes have been proposed to exploit these properties, but among the important issues to be resolved is the efficiency of HBr production from hydrocarbon precursors. This investigation evaluated a fundamental facet of such a technology by studying the reaction of methane and bromine at elevated temperature to determine the yield and kinetics of HBr formation. Laboratory experimentation and computational chemistry were combined to provide a description of this reaction for possible application to reactor design at a larger scale. Experimental studies with a tubular flow reactor were used to survey a range of reactant ratios and reactor residence times at temperatures between 500 C and 800 C. At temperatures near 800 C with excess methane, conversions of bromine to HBr exceeded 90% and reaction products included solid carbon (soot) in stoichiometric amounts. At lower temperatures, HBr conversion was significantly reduced, the products included much less soot, and the formation of bromocarbon compounds was indicated qualitatively. Calculations of chemical equilibrium behavior and reaction kinetics for the experimental conditions were performed using the Sandia CHEMKIN package. An elementary multistep mechanism for the gas-phase chemistry was used together with a surface mechanism that assumed facile deposition of radical species at the reactor walls. Simulations with the laminar-flow boundary-layer code of the CHEMKIN package gave reasonable agreement with experimental data.

  10. Theoretical study of the reaction kinetics of atomic bromine with tetrahydropyran

    KAUST Repository

    Giri, Binod

    2015-02-12

    A detailed theoretical analysis of the reaction of atomic bromine with tetrahydropyran (THP, C5H10O) was performed using several ab initio methods and statistical rate theory calculations. Initial geometries of all species involved in the potential energy surface of the title reaction were obtained at the B3LYP/cc-pVTZ level of theory. These molecular geometries were reoptimized using three different meta-generalized gradient approximation (meta-GGA) functionals. Single-point energies of the stationary points were obtained by employing the coupled-cluster with single and double excitations (CCSD) and fourth-order Møller-Plesset (MP4 SDQ) levels of theory. The computed CCSD and MP4(SDQ) energies for optimized structures at various DFT functionals were found to be consistent within 2 kJ mol-1. For a more accurate energetic description, single-point calculations at the CCSD(T)/CBS level of theory were performed for the minimum structures and transition states optimized at the B3LYP/cc-pVTZ level of theory. Similar to other ether + Br reactions, it was found that the tetrahydropyran + Br reaction proceeds in an overall endothermic addition-elimination mechanism via a number of intermediates. However, the reactivity of various ethers with atomic bromine was found to vary substantially. In contrast with the 1,4-dioxane + Br reaction, the chair form of the addition complex (c-C5H10O-Br) for THP + Br does not need to undergo ring inversion to form a boat conformer (b-C4H8O2-Br) before the intramolecular H-shift can occur to eventually release HBr. Instead, a direct, yet more favorable route was mapped out on the potential energy surface of the THP + Br reaction. The rate coefficients for all relevant steps involved in the reaction mechanism were computed using the energetics of coupled cluster calculations. On the basis of the results of the CCSD(T)/CBS//B3LYP/cc-pVTZ level of theory, the calculated overall rate coefficients can be expressed as kov.,calc.(T) = 4.60 × 10

  11. Reaction of bromine and chlorine with phenolic compounds and natural organic matter extracts--Electrophilic aromatic substitution and oxidation.

    Science.gov (United States)

    Criquet, Justine; Rodriguez, Eva M; Allard, Sebastien; Wellauer, Sven; Salhi, Elisabeth; Joll, Cynthia A; von Gunten, Urs

    2015-11-15

    Phenolic compounds are known structural moieties of natural organic matter (NOM), and their reactivity is a key parameter for understanding the reactivity of NOM and the disinfection by-product formation during oxidative water treatment. In this study, species-specific and/or apparent second order rate constants and mechanisms for the reactions of bromine and chlorine have been determined for various phenolic compounds (phenol, resorcinol, catechol, hydroquinone, phloroglucinol, bisphenol A, p-hydroxybenzoic acid, gallic acid, hesperetin and tannic acid) and flavone. The reactivity of bromine with phenolic compounds is very high, with apparent second order rate constants at pH 7 in the range of 10(4) to 10(7) M(-1) s(-1). The highest value was recorded for the reaction between HOBr and the fully deprotonated resorcinol (k = 2.1 × 10(9) M(-1) s(-1)). The reactivity of phenolic compounds is enhanced by the activating character of the phenolic substituents, e.g. further hydroxyl groups. With the data set from this study, the ratio between the species-specific rate constants for the reactions of chlorine versus bromine with phenolic compounds was confirmed to be about 3000. Phenolic compounds react with bromine or chlorine either by oxidation (electron transfer, ET) or electrophilic aromatic substitution (EAS) processes. The dominant process mainly depends on the relative position of the hydroxyl substituents and the possibility of quinone formation. While phenol, p-hydroxybenzoic acid and bisphenol A undergo EAS, hydroquinone, catechol, gallic acid and tannic acid, with hydroxyl substituents in ortho or para positions, react with bromine by ET leading to quantitative formation of the corresponding quinones. Some compounds (e.g. phloroglucinol) show both partial oxidation and partial electrophilic aromatic substitution and the ratio observed for the pathways depends on the pH. For the reaction of six NOM extracts with bromine, electrophilic aromatic substitution

  12. Cobalt catalyzed peroxymonosulfate oxidation of tetrabromobisphenol A: Kinetics, reaction pathways, and formation of brominated by-products

    Energy Technology Data Exchange (ETDEWEB)

    Ji, Yuefei [Department of Environmental Science and Engineering, Nanjing Agricultural University, Nanjing 210095 (China); Kong, Deyang [Nanjing Institute of Environmental Science, Ministry of Environmental Protection of PRC, Nanjing 210042 (China); Lu, Junhe, E-mail: jhlu@njau.edu.cn [Department of Environmental Science and Engineering, Nanjing Agricultural University, Nanjing 210095 (China); Jin, Hao; Kang, Fuxing; Yin, Xiaoming; Zhou, Quansuo [Department of Environmental Science and Engineering, Nanjing Agricultural University, Nanjing 210095 (China)

    2016-08-05

    Highlights: • Cobalt catalyzed peroxymonosulfate oxidation of tetrabromobisphenol A. • Phenolic moiety was the reactive site for sulfate radical attack. • Pathways include β-scission, oxidation, debromination and coupling reactions. • Brominated disinfection by-products were found during TBBPA degradation. • Humic acid inhibited TBBPA degradation but promoted DBPs formation. - Abstract: Degradation of tetrabromobisphenol A (TBBPA), a flame retardant widely spread in the environment, in Co(II) catalyzed peroxymonosulfate (PMS) oxidation process was systematically explored. The second-order-rate constant for reaction of sulfate radical (SO{sub 4}{sup ·−}) with TBBPA was determined to be 5.27 × 10{sup 10} M{sup −1} s{sup −1}. Apparently, degradation of TBBPA showed first-order kinetics to the concentrations of both Co(II) and PMS. The presence of humic acid (HA) and bicarbonate inhibited TBBPA degradation, most likely due to their competition for SO{sub 4}{sup ·−}. Degradation of TBBPA was initiated by an electron abstraction from one of the phenolic rings. Detailed transformation pathways were proposed, including β-scission of isopropyl bridge, phenolic ring oxidation, debromination and coupling reactions. Further oxidative degradation of intermediates in Co(II)/PMS process yielded brominated disinfection by-products (Br-DBPs) such as bromoform and brominated acetic acids. Evolution profile of Br-DBPs showed an initially increasing and then decreasing pattern with maximum concentrations occurring around 6–10 h. The presence of HA enhanced the formation of Br-DBPs significantly. These findings reveal potentially important, but previously unrecognized, formation of Br-DBPs during sulfate radical-based oxidation of bromide-containing organic compounds that may pose toxicological risks to human health.

  13. Reaction of atomic bromine with acetylene and loss rate of atmospheric acetylene due to reaction with OH, Cl, O, and Br

    Science.gov (United States)

    Payne, W. A.; Nava, D. F.; Brunning, J.; Stief, L. J.

    1986-01-01

    The first-order, diffusion, and bimolecular rate constants for the reaction Br + C2H2 yields C2H3Br are evaluated. The rate constants are measured at 210, 248, 298, and 393 K and at pressures between 15-100 torr Ar using flash photolysis combined with time-resolved detection of atomic bromine via Br resonance radiation. It is observed that the reaction is not affected by pressure or temperature and the bimolecular constant = (4.0 + or - 0.8) x 10 to the -15th cu cm/sec with an error of two standard deviations. The C2H2 + Br reaction rates are compared with reactions of C2H2 with Cl, OH, NH2, and H. The loss rates for atmospheric C2H2 for reactions with OH, Cl, O, and Br are calculated as a function of altitude.

  14. The chemistry of bromine in the stratosphere: Influence of a new rate constant for the reaction BrO + HO2

    Science.gov (United States)

    Pirre, Michel; Marceau, Francois J.; Lebras, Georges; Maguin, Francoise; Poulet, Gille; Ramaroson, Radiela

    1994-01-01

    The impact of new laboratory data for the reaction BrO + HO2 yields HOBr + O2 in the depletion of global stratospheric ozone has been estimated using a one-dimensional photochemical model taking into account the heterogeneous reaction on sulphate aerosols which converts N2O5 into HNO3. Assuring an aerosol loading 2 times as large as the 'background' and a reaction probability of 0.1 for the above heterogeneous reaction, the 6 fold increase in the measured rate constant for the reaction of BrO with HO2 increases the computed depletion of global ozone produced by 20 ppt of total bromine from 2.01 percent to 2.36 percent. The use of the higher rate constant increases the HOBr mixing ratio and makes the bromine partitioning and the ozone depletion very sensitive to the branching ratio of the potential channel forming HBr in the BrO + HO2 reaction.

  15. Oxidative treatment of bromide-containing waters: formation of bromine and its reactions with inorganic and organic compounds--a critical review.

    Science.gov (United States)

    Heeb, Michèle B; Criquet, Justine; Zimmermann-Steffens, Saskia G; von Gunten, Urs

    2014-01-01

    Bromide (Br(-)) is present in all water sources at concentrations ranging from ≈ 10 to >1000 μg L(-1) in fresh waters and about 67 mg L(-1) in seawater. During oxidative water treatment bromide is oxidized to hypobromous acid/hypobromite (HOBr/OBr(-)) and other bromine species. A systematic and critical literature review has been conducted on the reactivity of HOBr/OBr(-) and other bromine species with inorganic and organic compounds, including micropollutants. The speciation of bromine in the absence and presence of chloride and chlorine has been calculated and it could be shown that HOBr/OBr(-) are the dominant species in fresh waters. In ocean waters, other bromine species such as Br2, BrCl, and Br2O gain importance and may have to be considered under certain conditions. HOBr reacts fast with many inorganic compounds such as ammonia, iodide, sulfite, nitrite, cyanide and thiocyanide with apparent second-order rate constants in the order of 10(4)-10(9)M(-1)s(-1) at pH 7. No rate constants for the reactions with Fe(II) and As(III) are available. Mn(II) oxidation by bromine is controlled by a Mn(III,IV) oxide-catalyzed process involving Br2O and BrCl. Bromine shows a very high reactivity toward phenolic groups (apparent second-order rate constants kapp ≈ 10(3)-10(5)M(-1)s(-1) at pH 7), amines and sulfamides (kapp ≈ 10(5)-10(6)M(-1)s(-1) at pH 7) and S-containing compounds (kapp ≈ 10(5)-10(7)M(-1)s(-1) at pH 7). For phenolic moieties, it is possible to derive second-order rate constants with a Hammett-σ-based QSAR approach with [Formula in text]. A negative slope is typical for electrophilic substitution reactions. In general, kapp of bromine reactions at pH 7 are up to three orders of magnitude greater than for chlorine. In the case of amines, these rate constants are even higher than for ozone. Model calculations show that depending on the bromide concentration and the pH, the high reactivity of bromine may outweigh the reactions of chlorine during

  16. UTILIZATION OF BROMINATION REACTION FOR THE SPECTROPHOTOMETRIC ASSAY OF DOMPERIDONE IN PHARMACEUTICALS

    Directory of Open Access Journals (Sweden)

    O. ZENITA DEVI

    2011-03-01

    Full Text Available Three simple and sensitive spectrophotometric methods are described for the determination of domperidone (DOM in bulk drug and in dosage forms using bromate-bromide mixture as brominating agent in acid medium and three dyes, meta-cresol purple (MCP, amaranth (AMR and erioglaucine (EGC. The methods involve the addition of a known excess of bromate-bromide mixture to an acidified solution of DOM followed by the determination of the residual bromine by reacting with a fixed amount of either MCP dye and measuring the absorbance at 530 nm (method A or AMR dye and measuring the absorbance at 520 nm (method B or EGC dye and measuring the absorbance at 630 nm (method C. Beer’s law is obeyed over the concentration ranges, 0.63–10.0, 0.25-4.0 and 0.13-2.0 µg mL-1 for method A, B and C, respectively. The ap¬parent molar absorptivities are calculated to be 3.751x104, 6.604x104 and 1.987x105 L mol-1cm-1 for method A, B and C, respectively, and the corresponding sandell sensitivity values are 0.011, 0.006 and 0.002 μg cm-2. The limit of detection and the limit of quantification are also reported for all the three methods. No interference was observed from common additives found in pharmaceutical preparations. Statistical comparisons of the results with those of the reference method showed excellent agreement, and indicated no significant difference in accuracy and precision. The accuracy and reliability of the methods were further ascertained by performing recovery tests via standardaddition technique.

  17. Theoretical Investigation of Electrophilic Transannular Addition Reactions of Bromine to Face-to-Face (Juxtaposed) Double Bonds in Strained Polycyclic Hydrocarbons.

    Science.gov (United States)

    Abbasoglu, Rza

    2017-06-01

    Transannular electrophilic addition reaction of halogens to face-to-face(juxtaposed) double bonded strained alkenes were theoretically investigated. General rules that allow us to stipulate the factors that direct the main steps of the energy hypersurface of reactions as well as the products were established. Direction of the reaction flow is determined by direction of intramolecular skeletal isomerisation of cyclic-bridged halogenium cation and isomerisation takes place to create a more stable skeletal structure. Stability of resultant skeletal structure is determined by the number of σ bonds between isolated double bonds of the alkene and bonding-type of double bonds (N- and U-type). When the number of σ bonds between double bonds of the alkene is three (m = 3), the reaction takes place to predominantly give an N-type product, and when four (m = 4), N- and U-type products are formed. Structure and stability of cation intermediates (bridged, N- and U-type cations) of electrophilic addition reaction of homohipostrofen molecule, whose double bonds were linked by three σ bonds, with bromine were investigated by DFT methods in detail. Also the addition reaction of endo,endo-tetracyclo[6.2.2.23,6.02,7]tetradeca-4,9-dien molecule, whose double bonds were linked by four σ bonds, with bromine were investigated by quantum chemistry.

  18. Production of medically useful bromine isotopes via alpha-particle induced nuclear reactions

    Science.gov (United States)

    Breunig, Katharina; Scholten, Bernhard; Spahn, Ingo; Hermanne, Alex; Spellerberg, Stefan; Coenen, Heinz H.; Neumaier, Bernd

    2017-09-01

    The cross sections of α-particle induced reactions on arsenic leading to the formation of 76,77,78Br were measured from their respective thresholds up to 37 MeV. Thin sediments of elemental arsenic powder were irradiated together with Al degrader and Cu monitor foils using the established stacked-foil technique. For determination of the effective α-particle energies and of the effective beam current through the stacks the cross-section ratios of the monitor nuclides 67Ga/66Ga were used. This should help resolve discrepancies in existing literature data. Comparison of the data with the available excitation functions shows some slight energy shifts as well as some differences in curve shapes. The calculated thick target yields indicate, that 77Br can be produced in the energy range Eα = 25 → 17 MeV free of isotopic impurities in quantities sufficient for medical application.

  19. Production of medically useful bromine isotopes via alpha-particle induced nuclear reactions

    Directory of Open Access Journals (Sweden)

    Breunig Katharina

    2017-01-01

    Full Text Available The cross sections of α-particle induced reactions on arsenic leading to the formation of 76,77,78Br were measured from their respective thresholds up to 37 MeV. Thin sediments of elemental arsenic powder were irradiated together with Al degrader and Cu monitor foils using the established stacked-foil technique. For determination of the effective α-particle energies and of the effective beam current through the stacks the cross-section ratios of the monitor nuclides 67Ga/66Ga were used. This should help resolve discrepancies in existing literature data. Comparison of the data with the available excitation functions shows some slight energy shifts as well as some differences in curve shapes. The calculated thick target yields indicate, that 77Br can be produced in the energy range Eα = 25 → 17 MeV free of isotopic impurities in quantities sufficient for medical application.

  20. The zinc bromine battery

    Energy Technology Data Exchange (ETDEWEB)

    Jonshagen, B. [ZBB (Australia) Ltd., West Perth, WA (Australia)

    1996-12-31

    The Zinc Bromine Battery electrolyte is essentially zinc bromide salt dissolved in water. Unlike the lead acid and most other batteries, the Zinc Bromine Battery uses electrodes that cannot and do not take part in the reactions but merely serve as substrates for the reactions. There is therefore no loss of performance, as in most re-chargeable batteries, from repeated cycling which causes electrode material deterioration. When the Zinc Bromine Battery is completely discharged all the metal zinc plated on the negative electrodes is dissolved in the electrolyte and again produced the next time the batter is charged. In the discharged state the battery can be shorted and left that way indefinitely. This paper presents an overview of large scale Zinc Bromine battery systems that are currently being commercialized as an economically attractive alternative to utility upgrades. Also outlined is how the battery can improve the viability of renewable energy and reduce diesel use in isolated grids and remote power installations. (author). 11 figs., 2 refs.

  1. Brominated graphitized carbon fibers

    Science.gov (United States)

    Hung, Ching-Cheh (Inventor)

    1991-01-01

    Low cost, high break elongation graphitized carbon fibers having low degree of graphitization are inert to bromine at room or higher temperatures, but are brominated at -7 to 20 C, and then debrominated at ambient. Repetition of this bromination-debromination process can bring the bromine content to 18 percent. Electrical conductivity of the brominated fibers is three times of the before-bromination value.

  2. Application of dual carbon-bromine isotope analysis for investigating abiotic transformations of tribromoneopentyl alcohol (TBNPA).

    Science.gov (United States)

    Kozell, Anna; Yecheskel, Yinon; Balaban, Noa; Dror, Ishai; Halicz, Ludwik; Ronen, Zeev; Gelman, Faina

    2015-04-07

    Many of polybrominated organic compounds, used as flame retardant additives, belong to the group of persistent organic pollutants. Compound-specific isotope analysis is one of the potential analytical tools for investigating their fate in the environment. However, the isotope effects associated with transformations of brominated organic compounds are still poorly explored. In the present study, we investigated carbon and bromine isotope fractionation during degradation of tribromoneopentyl alcohol (TBNPA), one of the widely used flame retardant additives, in three different chemical processes: transformation in aqueous alkaline solution (pH 8); reductive dehalogenation by zero-valent iron nanoparticles (nZVI) in anoxic conditions; oxidative degradation by H2O2 in the presence of CuO nanoparticles (nCuO). Two-dimensional carbon-bromine isotope plots (δ(13)C/Δ(81)Br) for each reaction gave different process-dependent isotope slopes (Λ(C/Br)): 25.2 ± 2.5 for alkaline hydrolysis (pH 8); 3.8 ± 0.5 for debromination in the presence of nZVI in anoxic conditions; ∞ in the case of catalytic oxidation by H2O2 with nCuO. The obtained isotope effects for both elements were generally in agreement with the values expected for the suggested reaction mechanisms. The results of the present study support further applications of dual carbon-bromine isotope analysis as a tool for identification of reaction pathway during transformations of brominated organic compounds in the environment.

  3. Bromination of olefins with HBr and DMSO.

    Science.gov (United States)

    Karki, Megha; Magolan, Jakob

    2015-04-03

    A simple and inexpensive methodology is reported for the conversion of alkenes to 1,2-dibromo alkanes via oxidative bromination using HBr paired with dimethyl sulfoxide, which serves as the oxidant as well as cosolvent. The substrate scope includes 21 olefins brominated in good to excellent yields. Three of six styrene derivatives yielded bromohydrins under the reaction conditions.

  4. Bromine Safety

    Energy Technology Data Exchange (ETDEWEB)

    Meyers, B

    2001-04-09

    The production and handling in 1999 of about 200 million kilograms of bromine plus substantial derivatives thereof by Great Lakes Chemical Corp. and Albemarle Corporation in their southern Arkansas refineries gave OSHA Occupational Injury/Illness Rates (OIIR) in the range of 0.74 to 1.60 reportable OIIRs per 200,000 man hours. OIIRs for similar industries and a wide selection of other U.S. industries range from 1.6 to 23.9 in the most recent OSHA report. Occupational fatalities for the two companies in 1999 were zero compared to a range in the U.S.of zero for all computer manufacturing to 0.0445 percent for all of agriculture, forestry and fishing in the most recent OSHA report. These results show that bromine and its compounds can be considered as safe chemicals as a result of the bromine safety standards and practices at the two companies. The use of hydrobromic acid as an electrical energy storage medium in reversible PEM fuel cells is discussed. A study in 1979 of 20 megawatt halogen working fluid power plants by Oronzio de Nora Group found such energy to cost 2 to 2.5 times the prevailing base rate at that time. New conditions may reduce this relative cost. The energy storage aspect allows energy delivery at maximum demand times where the energy commands premium rates. The study also found marginal cost and performance advantages for hydrobromic acid over hydrochloric acid working fluid. Separate studies in the late 70s by General Electric also showed marginal performance advantages for hydrobromic acid.

  5. Bromine and carbon isotope effects during photolysis of brominated phenols.

    Science.gov (United States)

    Zakon, Yevgeni; Halicz, Ludwik; Gelman, Faina

    2013-12-17

    In the present study, carbon and bromine isotope effects during UV-photodegradation of bromophenols in aqueous and ethanolic solutions were determined. An anomalous relatively high inverse bromine isotope fractionation (εreactive position up to +5.1‰) along with normal carbon isotope effect (εreactive position of -12.6‰ to -23.4‰) observed in our study may be attributed to coexistence of both mass-dependent and mass-independent isotope fractionation of C-Br bond cleavage. Isotope effects of a similar scale were observed for all the studied reactions in ethanol, and for 4-bromophenol in aqueous solution. This may point out related radical mechanism for these processes. The lack of any carbon and bromine isotope effects during photodegradation of 2-bromophenol in aqueous solution possibly indicates that C-Br bond cleavage is not a rate-limiting step in the reaction. The bromine isotope fractionation, without any detectable carbon isotope effect, that was observed for 3-bromophenol photolysis in aqueous solution probably originates from mass-independent fractionation.

  6. Abiotic Bromination of Soil Organic Matter

    Energy Technology Data Exchange (ETDEWEB)

    Leri, Alessandra C.; Ravel, Bruce

    2015-11-17

    Biogeochemical transformations of plant-derived soil organic matter (SOM) involve complex abiotic and microbially mediated reactions. One such reaction is halogenation, which occurs naturally in the soil environment and has been associated with enzymatic activity of decomposer organisms. Building on a recent finding that naturally produced organobromine is ubiquitous in SOM, we hypothesized that inorganic bromide could be subject to abiotic oxidations resulting in bromination of SOM. Through lab-based degradation treatments of plant material and soil humus, we have shown that abiotic bromination of particulate organic matter occurs in the presence of a range of inorganic oxidants, including hydrogen peroxide and assorted forms of ferric iron, producing both aliphatic and aromatic forms of organobromine. Bromination of oak and pine litter is limited primarily by bromide concentration. Fresh plant material is more susceptible to bromination than decayed litter and soil humus, due to a labile pool of mainly aliphatic compounds that break down during early stages of SOM formation. As the first evidence of abiotic bromination of particulate SOM, this study identifies a mechanistic source of the natural organobromine in humic substances and the soil organic horizon. Formation of organobromine through oxidative treatments of plant material also provides insights into the relative stability of aromatic and aliphatic components of SOM.

  7. Bromination of selected pharmaceuticals in water matrices.

    Science.gov (United States)

    Benitez, F Javier; Acero, Juan L; Real, Francisco J; Roldan, Gloria; Casas, Francisco

    2011-11-01

    The bromination of five selected pharmaceuticals (metoprolol, naproxen, amoxicillin, phenacetin, and hydrochlorothiazide) was studied with these compounds individually dissolved in ultra-pure water. The apparent rate constants for the bromination reaction were determined as a function of the pH, obtaining the sequence amoxicillin>naproxen>hydrochlorothiazide≈phenacetin≈metoprolol. A kinetic mechanism specifying the dissociation reactions and the species formed for each compound according to its pK(a) value and the pH allowed the intrinsic rate constants to be determined for each elementary reaction. There was fairly good agreement between the experimental and calculated values of the apparent rate constants, confirming the goodness of the proposed reaction mechanism. In a second stage, the bromination of the selected pharmaceuticals simultaneously dissolved in three water matrices (a groundwater, a surface water from a public reservoir, and a secondary effluent from a WWTP) was investigated. The pharmaceutical elimination trend agreed with the previously determined rate constants. The influence of the main operating conditions (pH, initial bromine dose, and characteristics of the water matrix) on the degradation of the pharmaceuticals was established. An elimination concentration profile for each pharmaceutical in the water matrices was proposed based on the use of the previously evaluated apparent rate constants, and the theoretical results agreed satisfactorily with experiment. Finally, chlorination experiments performed in the presence of bromide showed that low bromide concentrations slightly accelerate the oxidation of the selected pharmaceuticals during chlorine disinfection. Copyright © 2011 Elsevier Ltd. All rights reserved.

  8. Vanadium haloperoxidase-catalyzed bromination and cyclization of terpenes.

    Science.gov (United States)

    Carter-Franklin, Jayme N; Parrish, Jon D; Tschirret-Guth, Richard A; Little, R Daniel; Butler, Alison

    2003-04-02

    Marine red algae (Rhodophyta) are a rich source of bioactive halogenated natural products, including cyclic terpenes. The biogenesis of certain cyclic halogenated marine natural products is thought to involve marine haloperoxidase enzymes. Evidence is presented that vanadium bromoperoxidase (V-BrPO) isolated and cloned from marine red algae that produce halogenated compounds (e.g., Plocamium cartilagineum, Laurencia pacifica, Corallina officinalis) can catalyze the bromination and cyclization of terpenes and terpene analogues. The V-BrPO-catalyzed reaction with the monoterpene nerol in the presence of bromide ion and hydrogen peroxide produces a monobromo eight-membered cyclic ether similar to laurencin, a brominated C15 acetogenin, from Laurencia glandulifera, along with noncyclic bromohydrin, epoxide, and dibromoproducts; however, reaction of aqueous bromine with nerol produced only noncyclic bromohydrin, epoxide, and dibromoproducts. The V-BrPO-catalyzed reaction with geraniol in the presence of bromide ion and hydrogen peroxide produces two singly brominated six-membered cyclic products, analogous to the ring structures of alpha and beta snyderols, brominated sesquiterpenes from Laurencia, spp., along with noncyclic bromohydrin, epoxide, and dibromoproducts; again, reaction of geraniol with aqueous bromine produces only noncyclic bromohydrin, epoxide, and dibromoproducts. Thus, V-BrPO can direct the electrophilic bromination and cyclization of terpenes.

  9. The metabolism and de-bromination of bromotyrosine in vivo

    NARCIS (Netherlands)

    A.R. Mani (Ali); J.C. Moreno (José C.); T.J. Visser (Theo); K.P. Moore (Kevin P.)

    2016-01-01

    textabstractDuring inflammation, leukocyte-derived eosinophil peroxidase catalyses the formation of hypobromous acid, which can brominate tyrosine residues in proteins to form bromotyrosine. Since eosinophils are involved in the pathogenesis of allergic reactions, such as asthma, urinary

  10. Bromine intercalated graphite for lightweight composite conductors

    KAUST Repository

    Amassian, Aram

    2017-07-20

    A method of fabricating a bromine-graphite/metal composite includes intercalating bromine within layers of graphite via liquid-phase bromination to create brominated-graphite and consolidating the brominated-graphite with a metal nanopowder via a mechanical pressing operation to generate a bromine-graphite/metal composite material.

  11. Effect of solvent on the lithium-bromine exchange of aryl bromides: reactions of n-butyllithium and tert-butyllithium with 1-bromo-4-tert-butylbenzene at 0 degrees C.

    Science.gov (United States)

    Bailey, William F; Luderer, Mark R; Jordan, Kevin P

    2006-03-31

    The outcome of reactions of 1-bromo-4-tert-butylbenzene (1), a representative aryl bromide, with n-BuLi or t-BuLi at 0 degrees C in a variety of solvent systems has been investigated. The products of reactions of 1 with n-BuLi vary significantly with changes in solvent composition: 1 does not react with n-BuLi in pure heptane; the exchange reaction to give (4-tert-butylphenyl)lithium, which is slow in pure diethyl ether, is virtually quantitative in heptane containing a small quantity of THF; and the reaction of 1 with n-BuLi in THF leads to considerable coupling. Lithium-bromine exchange is the virtually exclusive outcome of reactions of 1 with t-BuLi in every solvent studied except pure heptane: the presence of a small quantity of any of a variety of structurally diverse ethers (Et(2)O, THF, THP, MTBE) in the predominantly hydrocarbon medium affords (4-tert-butylphenyl)lithium, assayed as tert-butylbenzene, in yields exceeding 97%. The only side products observed from reactions of 1 with t-BuLi are small amounts of benzyne-derived hydrocarbons.

  12. Spectroscopy of low-lying single-particle states in $^{81}$Zn populated in the $^{80}$Zn(d,p) reaction

    CERN Multimedia

    The aim of this proposal is the study of single-particle states of $^{81}$Zn via the $^{80}$Zn(d,p) reaction in inverse kinematics. $^{81}$Zn will be produced by means of a laser-ionized, 5.5 MeV/u HIE-Isolde $^{80}$Zn beam impinging on a deuterated-polyethylene target. The protons and $\\gamma$-rays emitted in the reaction will be studied using the Miniball + T-REX setup. This experiment will constitute the first spectroscopic study of $^{81}$Zn, which is critically important to determine the energy and ordering of neutron single-particle orbits above the N=50 gap and the properties of $^{78}$Ni.

  13. Bromine-Chlorine Coupling in the Antarctic Ozone Hole

    Science.gov (United States)

    Danilin, Michael Y.; Sze, Nien-Dak; Ko, Malcolm K. W.; Rodriquez, Jose M.; Prather, Michael J.

    1996-01-01

    The contribution from the chlorine and bromine species in the formation of the Antarctic ozone hole is evaluated. Since chlorine and bromine compounds are of different industrial origin, it is desirable, from a policy point of view, to be able to attribute chlorine-catalyzed loss of ozone with those reactions directly involving chlorine species, and likewise for bromine-catalyzed loss. In the stratosphere, however, most of the chemical families are highly coupled, and, for example, changes in the chlorine abundance will alter the partitioninig in other families and thus the rate of ozone loss. This modeling study examines formation of the Antarctic ozone hole for a wide range of bromine concentrations (5 - 25 pptv) and for chlorine concentrations typical of the last two decades (1.5, 2.5 and 3.5 ppbv). We follow the photochemical evolution of a single parcel of air, typical of the inner Antarctic vortex (50 mbar, 70 deg. S, NO(sub y) = 2 ppbv, with Polar Stratospheric Clouds(PSC)) from August 1 to November 1. For all of these ranges of chlorine and bromine loading, we would predict a substantial ozone hole (local depletion greater than 90%) within the de-nitrified, PSC- perturbed vortex. The contributions of the different catalytic cycles responsible for ozone loss are tabulated. The deep minimum in ozone is driven primarily by the chlorine abundance. As bromine levels decrease, the magnitude of the chlorine-catalyzed ozone loss increases to take up the slack. This is because bromine suppresses ClO by accelerating the conversion of ClO an Cl2O2 back to HCI. For this range of conditions, the local relative efficiency of ozone destruction per bromine atom to that per chlorine atom (alpha-factor) ranges from 33 to 55, decreasing with increase of bromine.

  14. Horizontal and vertical structure of reactive bromine events probed by bromine monoxide MAX-DOAS

    Directory of Open Access Journals (Sweden)

    W. R. Simpson

    2017-08-01

    Full Text Available Heterogeneous photochemistry converts bromide (Br− to reactive bromine species (Br atoms and bromine monoxide, BrO that dominate Arctic springtime chemistry. This phenomenon has many impacts such as boundary-layer ozone depletion, mercury oxidation and deposition, and modification of the fate of hydrocarbon species. To study environmental controls on reactive bromine events, the BRomine, Ozone, and Mercury EXperiment (BROMEX was carried out from early March to mid-April 2012 near Barrow (Utqiaġvik, Alaska. We measured horizontal and vertical gradients in BrO with multiple-axis differential optical absorption spectroscopy (MAX-DOAS instrumentation at three sites, two mobile and one fixed. During the campaign, a large crack in the sea ice (an open lead formed pushing one instrument package ∼ 250 km downwind from Barrow (Utqiaġvik. Convection associated with the open lead converted the BrO vertical structure from a surface-based event to a lofted event downwind of the lead influence. The column abundance of BrO downwind of the re-freezing lead was comparable to upwind amounts, indicating direct reactions on frost flowers or open seawater was not a major reactive bromine source. When these three sites were separated by ∼ 30 km length scales of unbroken sea ice, the BrO amount and vertical distributions were highly correlated for most of the time, indicating the horizontal length scales of BrO events were typically larger than ∼ 30 km in the absence of sea ice features. Although BrO amount and vertical distribution were similar between sites most of the time, rapid changes in BrO with edges significantly smaller than this ∼ 30 km length scale episodically transported between the sites, indicating BrO events were large but with sharp edge contrasts. BrO was often found in shallow layers that recycled reactive bromine via heterogeneous reactions on snowpack. Episodically, these surface-based events propagated aloft when

  15. Snowmelt onset hinders bromine monoxide heterogeneous recycling in the Arctic

    Science.gov (United States)

    Burd, Justine A.; Peterson, Peter K.; Nghiem, Son V.; Perovich, Don K.; Simpson, William R.

    2017-08-01

    Reactive bromine radicals (bromine atoms, Br, and bromine monoxide, BrO) deplete ozone and alter tropospheric oxidation chemistry during the Arctic springtime (February-June). As spring transitions to summer (May-June) and snow begins to melt, reactive bromine events cease and BrO becomes low in summer. In this study, we explore the relationship between the end of the reactive bromine season and snowmelt timing. BrO was measured by Multi-AXis Differential Optical Absorption Spectrometer at Utqiaġvik (Barrow), AK, from 2012 to 2016 and on drifting buoys deployed in Arctic sea ice from 2011 to 2016, a total of 13 site and year combinations. The BrO seasonal end date (SED) was objectively determined and was compared to surface-air-temperature-derived melt onset date (MOD). The SED was highly correlated with the MOD (N = 13, R2 = 0.983, RMS = 1.9 days), and BrO is only observed at subfreezing temperatures. In subsets of these sites and years where ancillary data were available, we observed that snowpack depth reduced and rain precipitation occurred within a few days of the SED. These data are consistent with snowpack melting hindering BrO recycling, which is necessary to maintain enhanced BrO concentrations. With a projected warmer Arctic, a shift to earlier snowmelt seasons could alter the timing and role of halogen chemical reactions in the Arctic with impacts on ozone depletion and mercury deposition.Plain Language SummaryReactive bromine events in the Arctic are common in spring and deplete ozone and cause mercury deposition. These events are affected by snow and ice, which are changing in the Arctic; therefore, we need to understand how environmental conditions affect reactive bromine chemistry. We find that the reactive bromine season ends when snowpack begins to melt. Through these full seasonal observations, we find that reactive bromine events occur to warmer temperatures than previously reported, with 0°C being the observed threshold above which reactive

  16. Temperature dependence of bromine activation due to reaction of bromide with ozone in a proxy for organic aerosols and its importance for chemistry in surface snow.

    Science.gov (United States)

    Edebeli, Jacinta; Ammann, Markus; Gilgen, Anina; Trachsel, Jürg; Avak, Sven; Eichler, Anja; Schneebeli, Martin; Bartels-Rausch, Thorsten

    2017-04-01

    Tropospheric ozone depletion events (ODEs) via halogen activation are observed in both cold and warm climates [1-3]. Very recently, it was suggested that this multiphase halogen activation chemistry dominates in the tropical and subtropical upper troposphere [4]. These occurrences beg the question of temperature dependence of halogen activation in sea-salt aerosol, which are often mixtures of sea-salt and organic molecules [3, 5]. With the application of flow-tubes, the aim of this study is to investigate the temperature dependence of bromine activation via ozone interaction in a bromide containing film as a proxy for mixed organic - sea-salt aersol. Citric acid is used in this study as a hygroscopically characterized matrix and a proxy for oxidized organics, which is of relevance to atmospheric chemistry. Here, we present reactive ozone uptake measured between 258 and 289 K. The data show high reproducibility. With available knowledge, we have reproduced the measured uptake with modelled bulk uptake while accounting for temperature dependence of the substrate's properties as diffusivity, viscosity, and gas solubility. This work is part of a cross-disciplinary project with the aim to investigate the impact of metamorphism on impurity location in aging snow and its consequences for chemical reactivity. Metamorphism drastically shapes the structure and physical properties of snow, which has impacts on heat transfer, albedo, and avalanche formation. Such changes can be driven by water vapour fluxes in dry metamorphism with a mass turnover of as much as 60% per day - much greater than previously thought [6]. The consequences for atmospheric science are a current question of research [7]. Here, we show first results of a joint experiment to probe the re-distribution of impurities during snow metamorphism in artificial snow combined with an investigation of the samples structural changes. Future work is planned with the goal to investigate to which extend the observed re

  17. Very-short-lived brominated substances (VSLBr) and inorganic bromine (Bry) in the Pacific tropical tropopause layer

    Science.gov (United States)

    Navarro, Maria A.; Atlas, Elliot L.; Saiz-Lopez, Alfonso; Cuevas, Carlos A.; Kinnison, Douglas; Lamarque, Jean-Francois; Tilmes, Simone; Rodriguez-Lloveras, Xavier; Filus, Michal; Harris, Neil R. P.; Meneguz, Elena; Ashfold, Matthew J.; Manning, Alistair J.; Fernandez, Rafael P.; Schauffler, Sue; Donets, Valeria; Thornberry, Troy; Rollins, Andrew; Elkins, James W.; Hintsa, Eric J.

    2017-04-01

    Organic very-short-lived brominated substances (VSLBr) and inorganic bromine species (Bry) play an important role in the chemistry of upper troposphere/lower stratosphere (UT/LS) region. Their distribution, vertical structure, and variability provide information about sources and transport. In addition, an accurate quantification of the reactive and reservoirs species defines the halogen budget and assists in the assessment of the ozone depletion potential for brominated trace gases. In the last decade, there have been efforts to better understand the chemical and physical processes that occur in the Tropical Tropopause Layer (TTL), including convection, dehydration, and heterogeneous recycling reactions, which influence the partitioning of the trace gas species that enter the stratosphere. However, uncertainties in the estimation of the organic and inorganic partitioning of bromine and the input to the stratosphere still persist. Based on the measurements of samples collected by the Global Hawk Whole Air Sampler (GWAS) during the NASA-Airborne Tropical Tropopause Experiment (ATTREX), and chemistry climate simulations (using CAM-Chem along ATTREX flight tracks), we will examine the vertical distribution of selected organic species in the UT/LS of the Eastern and Western Pacific. We also will describe the budget and partitioning of bromine at the tropical tropopause and evaluate the contribution of bromine to ozone destruction in the lower stratosphere.

  18. Effect of solvent and temperature on the lithium-bromine exchange of vinyl bromides: reactions of n-butyllithium and t-butyllithium with (E)-5-bromo-5-decene.

    Science.gov (United States)

    Bailey, William F; Luderer, Mark R; Uccello, Daniel P; Bartelson, Ashley L

    2010-04-16

    The outcome of reactions of (E)-5-bromo-5-decene (1), a representative vinyl bromide, with t-BuLi or n-BuLi at 0 degrees C and room temperature, respectively, in a variety of solvent systems has been investigated. Vinyl bromide 1 does not react with t-BuLi in pure heptane; however, the presence of even small quantities of an ether in a predominantly heptane medium resulted in virtually complete consumption of 1 at 0 degrees C, resulting in nearly the same distribution of products, including 60-80% of (Z)-5-decenyllithium, regardless of the solvent composition. Vinyl bromide 1 reacts slowly with n-BuLi at room temperature in a variety of ether and heptane-ether mixtures to afford a mixture of products including significant quantities of recovered starting material. The results of these experiments demonstrate that lithium-bromine exchange between a vinyl bromide and either t-BuLi or n-BuLi at temperatures significantly above -78 degrees C is not an efficient method for the generation of a vinyllithium.

  19. A rotating disk study of gold dissolution by bromine

    Science.gov (United States)

    Pesic, Batric; Sergent, Rodney H.

    1991-12-01

    Gold dissolution with bromine was studied using the rotating disk technique with Geobrom™ 3400 as a source of bromine. The parameters studied were speed of rotation, lixiviant concentration, pH, temperature, sulfuric acid and hydrochloric acid concentrations, and the concentrations of various cations (i.e., copper, iron, zinc, aluminum, manganese, potassium, and sodium) and anions (i.e., chloride, bromide, sulfate, nitrate, and iodide). According to the Lavich plot and activation energy, gold dissolution is controlled by a chemical reaction rate. Copper, iron, and manganese in their highest oxidation states, as well as aluminum, zinc, sodium, and potassium, have no effect on the rate of gold dissolution. The presence of manganous ion substantially decreases the gold dissolution rate. The kinetic performance of bromine was found to be dramatically better than the performance of cyanide and thiourea.

  20. Formation of brominated disinfection by-products and bromate in cobalt catalyzed peroxymonosulfate oxidation of phenol.

    Science.gov (United States)

    Liu, Kuo; Lu, Junhe; Ji, Yuefei

    2015-11-01

    Formation of halogenated disinfection by-products (DBPs) in sulfate radical [Formula: see text] based oxidation processes attracted considerable attention recently. However, the underlying reaction pathways have not been well explored. This study focused on the transformation of Br(-) in cobalt activated peroxymonosulfate (Co(2+)/PMS) oxidation process. Phenol was added as a model compound to mimic the reactivity of natural organic matter (NOM). It was revealed that Br(-) was efficiently transformed to reactive bromine species (RBS) including free bromine and bromine radicals (Br, [Formula: see text] , etc.) in Co(2+)/PMS system. [Formula: see text] played a principal role during this process. RBS thus generated resulted in the bromination of phenol and formation brominated DBPs (Br-DBPs) including bromoform and bromoacetic acids, during which brominated phenols were detected as the intermediates. Br-DBPs were further degraded by excessive [Formula: see text] and transformed to bromate ultimately. Free bromine was also formed in the absence of Co(2+), suggesting Br(-) could be oxidized by PMS per se. Free bromine was incorporated to phenol sequentially leading to Br-DBPs as well. However, Br-DBPs could not be further transformed in the absence of [Formula: see text] . This is the first study that elucidated the comprehensive transformation map of Br(-) in PMS oxidation systems, which should be taken into consideration when PMS was applied to eliminate contamination in real practice. Copyright © 2015 Elsevier Ltd. All rights reserved.

  1. Nuclear transparency from quasielastic A(e,e[prime]p) reactions up to Q2 = 8.1 (GeV/c)2

    Energy Technology Data Exchange (ETDEWEB)

    K. Garrow; D. McKee; A. Ahmidouch; C. S. Armstrong; J. Arrington; R. Asaturyan; S. Avery; O. K. Baker; D. H. Beck; H. P. Blok; C. W. Bochna; W. Boeglin; P. Bosted; M. Bouwhuis; H. Breuer; D. S. Brown; A. Bruell; R. D. Carlini; N. S. Chant; A. Cochran; L. Cole; S. Danagoulian; D. B. Day; J. Dunne; D. Dutta; R. Ent; H. C. Fenker; B. Fox; L. Gan; D. Gaskell; A. Gasparian; H. Gao; D. F. Geesaman; R. Gilman; P. L. J. Gueye; M. Harvey; R. J. Holt; X. Jiang; C. E. Keppel; E. Kinney; Y. Liang; W. Lorenzon; A. Lung; D. J. Mack; P. Markowitz; J. W. Martin; K. McIlhany; D. Meekins; M. A. Miller; R. G. Milner; J. H. Mitchell; H. Mkrtchyan; B. A. Mueller; A. Nathan; G. Niculescu; I. Niculescu; T. G. O' Neill; V. Papavassiliou; S. Pate; R. B. Piercey; D. Potterveld; R. D. Ransome; J. Reinhold; E. Rollinde; P. Roos; A. J. Sarty; R. Sawafta; E. C. Schulte; E. Segbefia; C. Smith; S. Stepanyan; S. Strauch; V. Tadevosyan; L. Tang; R. Tieulent; A. Uzzle; W. F. Vulcan; S. A. Wood; F. Xiong; L. Yuan; M. Zeier; B. Zihlmann; V. Ziskin

    2002-10-01

    The quasielastic (e,e[prime]p) reaction was studied on targets of deuterium, carbon, and iron up to a value of momentum transfer Q2 of 8.1 (GeV/c)2. A nuclear transparency was determined by comparing the data to calculations in the plane-wave impulse approximation. The dependence of the nuclear transparency on Q2 and the mass number A was investigated in a search for the onset of the color transparency phenomenon. We find no evidence for the onset of color transparency within our range of Q2. A fit to the world's nuclear transparency data reflects the energy dependence of the free-proton-nucleon cross section.

  2. On the bromination of the dihydroazulene/vinylheptafulvene photo-/thermoswitch

    DEFF Research Database (Denmark)

    Mazzanti, Virginia; Cacciarini, Martina; Broman, Søren Lindbæk

    2012-01-01

    Background: The dihydroazulene (DHA)/vinylheptafulvene (VHF) system (with two cyano groups at C1) functions as a photo-/thermoswitch. Direct ionic bromination of DHA has previously furnished a regioselective route to a 7,8-dibromide, which by elimination was converted to a 7-bromo-substituted DHA....... This compound has served as a central building block for functionalization of the DHA by palladium-catalyzed cross-coupling reactions. The current work explores another bromination protocol for achieving the isomeric 3-bromo-DHA and also explores the outcome of additional bromination of this compound as well...... as of the known 7-bromo-DHA.Results: Radical bromination on two different VHFs by using N-bromosuccinimide/benzoyl peroxide and light, followed by a ring-closure reaction generated the corresponding 3-bromo-DHAs, as confirmed in one case by X-ray crystallography. According to a (1)H NMR spectroscopic study...

  3. Snow-sourced bromine and its implications for polar tropospheric ozone

    Directory of Open Access Journals (Sweden)

    X. Yang

    2010-08-01

    Full Text Available In the last two decades, significant depletion of boundary layer ozone (ozone depletion events, ODEs has been observed in both Arctic and Antarctic spring. ODEs are attributed to catalytic destruction by bromine radicals (Br plus BrO, especially during bromine explosion events (BEs, when high concentrations of BrO periodically occur. However, neither the exact source of bromine nor the mechanism for sustaining the observed high BrO concentrations is completely understood. Here, by considering the production of sea salt aerosol from snow lying on sea ice during blowing snow events and the subsequent release of bromine, we successfully simulate the BEs using a global chemistry transport model. We find that heterogeneous reactions play an important role in sustaining a high fraction of the total inorganic bromine as BrO. We also find that emissions of bromine associated with blowing snow contribute significantly to BrO at mid-latitudes. Modeled tropospheric BrO columns generally compare well with the tropospheric BrO columns retrieved from the GOME satellite instrument (Global Ozone Monitoring Experiment. The additional blowing snow bromine source, identified here, reduces modeled high latitude lower tropospheric ozone amounts by up to an average 8% in polar spring.

  4. Electronic properties of bromine-doped carbon nanotubes

    CERN Document Server

    Jhi, S H; Cohen, M L

    2002-01-01

    Intercalation of bromine molecules (Br2) into single-wall carbon nanotube (SWNT) ropes is studied using the ab initio pseudopotential density functional method. Electronic and vibrational properties of the SWNT and Br2 are studied for various bromine concentrations. A drastic change in the charge transfer, bromine stretching-mode, and bromine bond-length is observed when the bromine-bromine distance decreases. Calculated electronic structures show that, at high bromine concentrations, the bromine ppsigma level broadens due to the interbromine interaction. These states overlap with the electronic bands of the SWNT near the Fermi level which results in a substantial charge transfer from carbon to bromine.

  5. The contribution of anthropogenic bromine emissions to past stratospheric ozone trends: a modelling study

    Directory of Open Access Journals (Sweden)

    B.-M. Sinnhuber

    2009-04-01

    Full Text Available Bromine compounds play an important role in the depletion of stratospheric ozone. We have calculated the changes in stratospheric ozone in response to changes in the halogen loading over the past decades, using a two-dimensional (latitude/height model constrained by source gas mixing ratios at the surface. Model calculations of the decrease of total column ozone since 1980 agree reasonably well with observed ozone trends, in particular when the contribution from very short-lived bromine compounds is included. Model calculations with bromine source gas mixing ratios fixed at 1959 levels, corresponding approximately to a situation with no anthropogenic bromine emissions, show an ozone column reduction between 1980 and 2005 at Northern Hemisphere mid-latitudes of only ≈55% compared to a model run including all halogen source gases. In this sense anthropogenic bromine emissions are responsible for ≈45% of the model estimated column ozone loss at Northern Hemisphere mid-latitudes. However, since a large fraction of the bromine induced ozone loss is due to the combined BrO/ClO catalytic cycle, the effect of bromine would have been smaller in the absence of anthropogenic chlorine emissions. The chemical efficiency of bromine relative to chlorine for global total ozone depletion from our model calculations, expressed by the so called α-factor, is 64 on an annual average. This value is much higher than previously published results. Updates in reaction rate constants can explain only part of the differences in α. The inclusion of bromine from very short-lived source gases has only a minor effect on the global mean α-factor.

  6. Global Inorganic Source of Atmospheric Bromine

    OpenAIRE

    Enami, S.; Vecitis, C. D.; Cheng, J.; Hoffmann, M.R.; Colussi, A.J.

    2007-01-01

    A few bromine molecules per trillion (ppt) causes the complete destruction of ozone in the lower troposphere during polar spring and about half of the losses associated with the “ozone hole” in the stratosphere. Recent field and aerial measurements of the proxy BrO in the free troposphere suggest an even more pervasive global role for bromine. Models, which quantify ozone trends by assuming atmospheric inorganic bromine (Br_y) stems exclusively from long-lived bromoalkane gases, significantly...

  7. Chlorine and bromine ions in the D-region

    Science.gov (United States)

    Kopp, Ernest; Fritzenwallner, Johnny

    1997-01-01

    In the first D-region negative ion measurements of March 7, 1970 above Wallops Island by Narcisi's group at the Geophysical Laboratory in Bedford no chlorine ions were reported. However, already in the second measurement from the Andoya rocket range on March 23, 1970, by Arnold's group at Heidelberg the presence of the two chlorine ion isotopes 35 and 37 amu/q were found as minor ions of the D-region. Since then the negative chlorine ion was observed regularly in the D-region negative ion population, but its chemistry is still not fully understood. In a solar eclipse campaign in February 1979 the ion composition was measured with a new mass spectrometer by the Bern group. In this measurement Cl^- was the most abundant ion below about 70 km. In addition, good evidence was found for the presence of both bromine isotopes 79 and 81 amu/q and also of clustered chlorine ions. Since the source of chlorine and bromine ions is the stratosphere, time-dependant changes of these compounds will also contribute to a change of chlorine and bromine negative ions in the D-region. Both ions play an important role in the ion population of the D-region, a fact which is not taken into account by today's standard models.

  8. New insight into photo-bromination processes in saline surface waters: The case of salicylic acid

    Energy Technology Data Exchange (ETDEWEB)

    Tamtam, Fatima; Chiron, Serge, E-mail: serge.chiron@msem.univ-montp2.fr

    2012-10-01

    It was shown, through a combination of field and laboratory observations, that salicylic acid can undergo photo-bromination reactions in sunlit saline surface waters. Laboratory-scale experiments revealed that the photochemical yields of 5-bromosalicylic acid and 3,5-dibromosalicylic acid from salicylic acid were always low (in the 4% range at most). However, this might be of concern since these compounds are potential inhibitors of the 20{alpha}-hydroxysteroid dehydrogenase enzyme, with potential implications in endocrine disruption processes. At least two mechanisms were involved simultaneously to account for the photo-generation of brominated substances. The first one might involve the formation of reactive brominated radical species (Br{center_dot}, Br{sub 2}{center_dot}{sup -}) through hydroxyl radical mediated oxidation of bromide ions. These ions reacted more selectively than hydroxyl radicals with electron-rich organic pollutants such as salicylic acid. The second one might involve the formation of hypobromous acid, through a two electron oxidation of bromine ions by peroxynitrite. This reaction was catalyzed by nitrite, since these ions play a crucial role in the formation of nitric oxide upon photolysis. This nitric oxide further reacts with superoxide radical anions to yield peroxynitrite and by ammonium through the formation of N-bromoamines, probably due to the ability of N-bromoamines to promote the aromatic bromination of phenolic compounds. Field measurements revealed the presence of salicylic acid together with 5-bromosalicylic and 3,5-dibromosalicylic acid in a brackish coastal lagoon, thus confirming the environmental significance of the proposed photochemically induced bromination pathways. -- Highlights: Black-Right-Pointing-Pointer Brominated derivatives of salicylic acid were detected in a brackish lagoon. Black-Right-Pointing-Pointer A photochemical pathway was hypothesized to account for bromination of salicylic acid. Black

  9. New Methods for Labeling RGD Peptides with Bromine-76.

    Science.gov (United States)

    Lang, Lixin; Li, Weihua; Jia, Hong-Mei; Fang, De-Cai; Zhang, Shushu; Sun, Xilin; Zhu, Lei; Ma, Ying; Shen, Baozhong; Kiesewetter, Dale O; Niu, Gang; Chen, Xiaoyuan

    2011-01-01

    Direct bromination of the tyrosine residues of peptides and antibodies with bromine-76, to create probes for PET imaging, has been reported. For peptides that do not contain tyrosine residues, however, a prosthetic group is required to achieve labeling via conjugation to other functional groups such as terminal α-amines or lysine ε-amines. The goal of this study was to develop new strategies for labeling small peptides with Br-76 using either a direct labeling method or a prosthetic group, depending on the available functional group on the peptides. A new labeling agent, N-succinimidyl-3-[(76)Br]bromo-2,6-dimethoxybenzoate ([(76)Br]SBDMB) was prepared for cyclic RGD peptide labeling. N-succinimidyl-2, 6-dimethoxybenzoate was also used to pre-attach a 2, 6-dimethoxybenzoyl (DMB) moiety to the peptide, which could then be labeled with Br-76. A competitive cell binding assay was performed to determine the binding affinity of the brominated peptides. PET imaging of U87MG human glioblastoma xenografted mice was performed using [(76)Br]-BrE[c(RGDyK)](2) and [(76)Br]-BrDMB-E[c(RGDyK)](2). An ex vivo biodistribution assay was performed to confirm PET quantification. The mechanisms of bromination reaction between DMB-c(RGDyK) and the brominating agent CH(3)COOBr were investigated with the SCRF-B3LYP/6-31G* method with the Gaussian 09 program package. The yield for direct labeling of c(RGDyK) and E[c(RGDyK)](2) using chloramine-T and peracetic acid at ambient temperature was greater than 50%. The yield for [(76)Br]SBDMB was over 60% using peracetic acid. The conjugation yields for labeling c(RGDfK) and c(RGDyK) were over 70% using the prosthetic group at room temperature. Labeling yield for pre-conjugated peptides was over 60%. SDMB conjugation and bromination did not affect the binding affinity of the peptides with integrin receptors. Both [(76)Br]Br-E[c(RGDyK)](2) and [(76)Br]BrDMB-E[c(RGDyK)](2) showed high tumor uptake in U87MG tumor bearing mice. The specificity of

  10. Search for HBr and bromine photochemistry on Venus

    Science.gov (United States)

    Krasnopolsky, Vladimir A.; Belyaev, Denis A.

    2017-09-01

    HBr (1-0) R2 2605.8/6.2 cm-1, the strongest line of the strongest band of HBr, was observed when searching for this species on Venus. The observation was conducted using the NASA IRTF and a high-resolution long-slit spectrograph CSHELL with resolving power of 4 × 104. 101 spectra of Venus were analyzed, and the retrieved HBr abundances varied from -8 to + 5 ppb. Their mean value is -1.2 ppb, standard deviation is 2.5 ppb, and uncertainty of the mean is 0.25 ppb. The negative value presumes a systematic error, and the estimated upper limit of the HBr mixing ratio at the cloud tops of Venus is ∼1 ppb. From the simultaneously retrieved CO2 abundances, this corresponds to an altitude of 78 km for the uniform distribution of HBr. A simplified version of the bromine photochemistry is included into the photochemical model (Krasnopolsky 2012, Icarus 218, 230-246). Photolysis of HBr and its reactions with O and H deplete the HBr mixing ratio at 70-80 km relative to that below 60 km by a factor of ≈300. Reanalysis of the observational data with the calculated profile of HBr gives an upper limit of 20-70 ppb for HBr below 60 km and the aerosol optical depth of 0.7 at 70 km and 3.84 μm. The bromine chemistry may be effective on Venus even under the observed upper limit. However, if a Cl/Br ratio in the Venus atmosphere is similar to that in the Solar System, then HBr is ≈1 ppb in the lower atmosphere and the bromine chemistry is insignificant. Thermodynamic calculations based on the chemical kinetic model (Krasnopolsky 2013, Icarus 225, 570-580) predict HBr as a major bromine species in the lower atmosphere.

  11. Dissociation rate of bromine diatomics in an argon heat bath

    Science.gov (United States)

    Razner, R.; Hopkins, D.

    1973-01-01

    The evolution of a collection of 300 K bromine diatomics embedded in a heat bath of argon atoms at 1800 K was studied by computer, and a dissociation-rate constant for the reaction Br2 + BR + Ar yields Br + Ar was determined. Previously published probability distributions for energy and angular momentum transfers in classical three-dimensional Br2-Ar collisions were used in conjunction with a newly developed Monte Carlo scheme for this purpose. Results are compared with experimental shock-tube data and the predictions of several other theoretical models. A departure from equilibrium is obtained which is significantly greater than that predicted by any of these other theories.

  12. Observations of bromine monoxide transport in the Arctic sustained on aerosol particles

    Science.gov (United States)

    Peterson, Peter K.; Pöhler, Denis; Sihler, Holger; Zielcke, Johannes; General, Stephan; Frieß, Udo; Platt, Ulrich; Simpson, William R.; Nghiem, Son V.; Shepson, Paul B.; Stirm, Brian H.; Dhaniyala, Suresh; Wagner, Thomas; Caulton, Dana R.; Fuentes, Jose D.; Pratt, Kerri A.

    2017-06-01

    The return of sunlight in the polar spring leads to the production of reactive halogen species from the surface snowpack, significantly altering the chemical composition of the Arctic near-surface atmosphere and the fate of long-range transported pollutants, including mercury. Recent work has shown the initial production of reactive bromine at the Arctic surface snowpack; however, we have limited knowledge of the vertical extent of this chemistry, as well as the lifetime and possible transport of reactive bromine aloft. Here, we present bromine monoxide (BrO) and aerosol particle measurements obtained during the March 2012 BRomine Ozone Mercury EXperiment (BROMEX) near Utqiaġvik (Barrow), AK. The airborne differential optical absorption spectroscopy (DOAS) measurements provided an unprecedented level of spatial resolution, over 2 orders of magnitude greater than satellite observations and with vertical resolution unable to be achieved by satellite methods, for BrO in the Arctic. This novel method provided quantitative identification of a BrO plume, between 500 m and 1 km aloft, moving at the speed of the air mass. Concurrent aerosol particle measurements suggest that this lofted reactive bromine plume was transported and maintained at elevated levels through heterogeneous reactions on colocated supermicron aerosol particles, independent of surface snowpack bromine chemistry. This chemical transport mechanism explains the large spatial extents often observed for reactive bromine chemistry, which impacts atmospheric composition and pollutant fate across the Arctic region, beyond areas of initial snowpack halogen production. The possibility of BrO enhancements disconnected from the surface potentially contributes to sustaining BrO in the free troposphere and must also be considered in the interpretation of satellite BrO column observations, particularly in the context of the rapidly changing Arctic sea ice and snowpack.

  13. An exemplary case of a bromine explosion event linked to cyclone development in the Arctic

    Science.gov (United States)

    Blechschmidt, A.-M.; Richter, A.; Burrows, J. P.; Kaleschke, L.; Strong, K.; Theys, N.; Weber, M.; Zhao, X.; Zien, A.

    2016-02-01

    Intense, cyclone-like shaped plumes of tropospheric bromine monoxide (BrO) are regularly observed by GOME-2 on board the MetOp-A satellite over Arctic sea ice in polar spring. These plumes are often transported by high-latitude cyclones, sometimes over several days despite the short atmospheric lifetime of BrO. However, only few studies have focused on the role of polar weather systems in the development, duration and transport of tropospheric BrO plumes during bromine explosion events. The latter are caused by an autocatalytic chemical chain reaction associated with tropospheric ozone depletion and initiated by the release of bromine from cold brine-covered ice or snow to the atmosphere. In this manuscript, a case study investigating a comma-shaped BrO plume which developed over the Beaufort Sea and was observed by GOME-2 for several days is presented. By making combined use of satellite data and numerical models, it is shown that the occurrence of the plume was closely linked to frontal lifting in a polar cyclone and that it most likely resided in the lowest 3 km of the troposphere. In contrast to previous case studies, we demonstrate that the dry conveyor belt, a potentially bromine-rich stratospheric air stream which can complicate interpretation of satellite retrieved tropospheric BrO, is spatially separated from the observed BrO plume. It is concluded that weather conditions associated with the polar cyclone favoured the bromine activation cycle and blowing snow production, which may have acted as a bromine source during the bromine explosion event.

  14. An exemplary case of a bromine explosion event linked to cyclone development in the Arctic

    Directory of Open Access Journals (Sweden)

    A.-M. Blechschmidt

    2016-02-01

    Full Text Available Intense, cyclone-like shaped plumes of tropospheric bromine monoxide (BrO are regularly observed by GOME-2 on board the MetOp-A satellite over Arctic sea ice in polar spring. These plumes are often transported by high-latitude cyclones, sometimes over several days despite the short atmospheric lifetime of BrO. However, only few studies have focused on the role of polar weather systems in the development, duration and transport of tropospheric BrO plumes during bromine explosion events. The latter are caused by an autocatalytic chemical chain reaction associated with tropospheric ozone depletion and initiated by the release of bromine from cold brine-covered ice or snow to the atmosphere. In this manuscript, a case study investigating a comma-shaped BrO plume which developed over the Beaufort Sea and was observed by GOME-2 for several days is presented. By making combined use of satellite data and numerical models, it is shown that the occurrence of the plume was closely linked to frontal lifting in a polar cyclone and that it most likely resided in the lowest 3 km of the troposphere. In contrast to previous case studies, we demonstrate that the dry conveyor belt, a potentially bromine-rich stratospheric air stream which can complicate interpretation of satellite retrieved tropospheric BrO, is spatially separated from the observed BrO plume. It is concluded that weather conditions associated with the polar cyclone favoured the bromine activation cycle and blowing snow production, which may have acted as a bromine source during the bromine explosion event.

  15. Observations of bromine monoxide transport in the Arctic sustained on aerosol particles

    Directory of Open Access Journals (Sweden)

    P. K. Peterson

    2017-06-01

    Full Text Available The return of sunlight in the polar spring leads to the production of reactive halogen species from the surface snowpack, significantly altering the chemical composition of the Arctic near-surface atmosphere and the fate of long-range transported pollutants, including mercury. Recent work has shown the initial production of reactive bromine at the Arctic surface snowpack; however, we have limited knowledge of the vertical extent of this chemistry, as well as the lifetime and possible transport of reactive bromine aloft. Here, we present bromine monoxide (BrO and aerosol particle measurements obtained during the March 2012 BRomine Ozone Mercury EXperiment (BROMEX near Utqiaġvik (Barrow, AK. The airborne differential optical absorption spectroscopy (DOAS measurements provided an unprecedented level of spatial resolution, over 2 orders of magnitude greater than satellite observations and with vertical resolution unable to be achieved by satellite methods, for BrO in the Arctic. This novel method provided quantitative identification of a BrO plume, between 500 m and 1 km aloft, moving at the speed of the air mass. Concurrent aerosol particle measurements suggest that this lofted reactive bromine plume was transported and maintained at elevated levels through heterogeneous reactions on colocated supermicron aerosol particles, independent of surface snowpack bromine chemistry. This chemical transport mechanism explains the large spatial extents often observed for reactive bromine chemistry, which impacts atmospheric composition and pollutant fate across the Arctic region, beyond areas of initial snowpack halogen production. The possibility of BrO enhancements disconnected from the surface potentially contributes to sustaining BrO in the free troposphere and must also be considered in the interpretation of satellite BrO column observations, particularly in the context of the rapidly changing Arctic sea ice and snowpack.

  16. Brominated Flame Retardants and Perfluorinated Chemicals

    Science.gov (United States)

    Brominated flame retardants (BFRs) and perfluorinated chemicals (PFCs) belong to a large class of chemicals known as organohalogens. It is believed that both BFRs and PFCs saved lives by reducing flammability of materials commonly used and bactericidal (biocidal) properties. Thes...

  17. Ultrasound-assisted green bromination of N-cinnamoyl amino acid amides - Structural characterization and antimicrobial evaluation

    Science.gov (United States)

    Stoykova, Boyka; Chochkova, Maya; Ivanova, Galya; Markova, Nadezhda; Enchev, Venelin; Tsvetkova, Iva; Najdenski, Hristo; Štícha, Martin; Milkova, Tsenka

    2017-05-01

    N-phenylpropenoyl amino acid amides have been brominated using two alternative sonochemically activated green chemistry procedures. The first synthetic procedure has involved an ultrasound assisted bromination in an aqueous medium using ionic liquid as a catalyst of the reaction, whereas in the second one an in situ formation of Br2 via oxidation of HBr by H2O2 has been used. For comparison, the conventional bromination procedure was also used. The newly brominated compounds were characterized by appropriate analytical techniques. A detailed NMR spectroscopic analysis and quantum chemical calculations using Density Functional Theory (DFT) methods have been used to define the stereochemistry of the products. The results confirmed the physicochemical identity and similar yields of the products obtained by the three synthetic procedures employed, and reveal the co-existence of two diastereoisomeric forms of the newly synthesized products. The antibacterial and antifungal activities of the dibrominated amides were evaluated.

  18. Sources of reactive bromine in polar regions and its implications for ozone in the troposphere

    Science.gov (United States)

    Griffiths, Paul; Archibald, Alex; Yang, Xin; Pyle, John

    2014-05-01

    In the last two decades, significant depletion of boundary layer ozone (ozone depletion events, ODEs) has been observed in both Arctic and Antarctic spring. ODEs are attributed to catalytic destruction by bromine radicals (Br plus BrO), especially during bromine explosion events, when high concentrations of BrO periodically occur. The source of bromine and the mechanism that sustains the high BrO levels are still the subject of study, and there remains scope for improving our understanding of reactive bromine budgets in polar regions. Yang et al. (2008) suggested snow could provide a source of (depleted) sea-salt aerosol if blown from the surface of ice, while recent work by Pratt et al. (2013) posits Br2 production within saline snow and sea ice. In this poster, we consider the production of sea-salt aerosol from a mixture of snow and sea ice during periods of strong wind. We use a combination of box models and the United Kingdom Chemistry and Aerosols scheme, run as a component of the UK Met Office Unified Model, to quantify the effect of bromine release in the boundary layer and its effect on ozone at the regional scale. The importance of heterogeneous reactions is quantified and new data from the recent Polarstern cruise by members of the British Antarctic Survey as part of the NERC-funded BLOWSEA project will be considered.

  19. Selective and Efficient Generation of ortho-Brominated para-Substituted Phenols in ACS-Grade Methanol.

    Science.gov (United States)

    Georgiev, David; Saes, Bartholomeus W H; Johnston, Heather J; Boys, Sarah K; Healy, Alan; Hulme, Alison N

    2016-01-13

    The mono ortho-bromination of phenolic building blocks by NBS has been achieved in short reaction times (15-20 min) using ACS-grade methanol as a solvent. The reactions can be conducted on phenol, naphthol and biphenol substrates, giving yields of >86% on gram scale. Excellent selectivity for the desired mono ortho-brominated products is achieved in the presence of 10 mol % para-TsOH, and the reaction is shown to be tolerant of a range of substituents, including CH3, F, and NHBoc.

  20. Selective and Efficient Generation of ortho-Brominated para-Substituted Phenols in ACS-Grade Methanol

    Directory of Open Access Journals (Sweden)

    David Georgiev

    2016-01-01

    Full Text Available The mono ortho-bromination of phenolic building blocks by NBS has been achieved in short reaction times (15–20 min using ACS-grade methanol as a solvent. The reactions can be conducted on phenol, naphthol and biphenol substrates, giving yields of >86% on gram scale. Excellent selectivity for the desired mono ortho-brominated products is achieved in the presence of 10 mol % para-TsOH, and the reaction is shown to be tolerant of a range of substituents, including CH3, F, and NHBoc.

  1. Bromide oxidation by ferrate(VI): The formation of active bromine and bromate.

    Science.gov (United States)

    Jiang, Yanjun; Goodwill, Joseph E; Tobiason, John E; Reckhow, David A

    2016-06-01

    Ferrate (VI) (abbreviated as Fe(VI)) has long been considered as a green oxidant that does not produce any known hazardous byproducts. However, this work shows that Fe(VI) can slowly oxidize bromide forming active bromine (HOBr/OBr(-)) and bromate, and in natural waters total organic bromine (TOBr) can also be detected. Results showed that the highest levels of active bromine and bromate were formed at lower pHs and in the absence of phosphate. Hydrogen peroxide, which forms from the reaction of Fe(VI) and water, plays an essential role in suppressing bromate formation by reducing active bromine back to bromide. Fe(VI) decomposition products (assumed to be particulate phase Fe(III)) can catalyze the decomposition of hydrogen peroxide by Fe(VI). Phosphate had a substantial inhibiting effect on the formation of active bromine, but less so on bromate formation. The presence of the raw water matrix in natural water suppressed bromate formation. For a natural water spiked with 0.1 mg/L of bromide, the bromate and TOBr concentrations after Fe(VI) oxidation were below 3.0 and 15 μg/L, respectively. No consistent trend regarding the effect of pH or buffer ions on TOBr formation was observed due to the competition between Fe(VI), hydrogen peroxide, and natural organic matter (NOM) for reaction with active bromine. Under environmentally relevant conditions, the formation of bromate and TOBr would not be a problem for Fe(VI) application as their concentration levels are quite low. Copyright © 2016 Elsevier Ltd. All rights reserved.

  2. A, a Brominated Flame Retardant

    Directory of Open Access Journals (Sweden)

    Tomomi Takeshita

    2013-01-01

    Full Text Available Tetrabromobisphenol A (TBBPA, a brominated flame retardant, has been found to exacerbate pneumonia in respiratory syncytial virus- (RSV- infected mice. We examined the effect of Brazilian propolis (AF-08 on the exacerbation of RSV infection by TBBPA exposure in mice. Mice were fed a powdered diet mixed with 1% TBBPA alone, 0.02% AF-08 alone, or 1% TBBPA and 0.02% AF-08 for four weeks and then intranasally infected with RSV. TBBPA exposure increased the pulmonary virus titer and level of IFN-γ, a representative marker of pneumonia due to RSV infection, in the lungs of infected mice without toxicity. AF-08 was significantly effective in reducing the virus titers and IFN-γ level increased by TBBPA exposure. Also, AF-08 significantly reduced proinflammatory cytokine (TNF-α and IL-6 levels in the lungs of RSV-infected mice with TBBPA exposure, but Th2 cytokine (IL-4 and IL-10 levels were not evidently increased. Neither TBBPA exposure nor AF-08 treatment affected the anti-RSV antibody production in RSV-infected mice. In flow cytometry analysis, AF-08 seemed to be effective in reducing the ratio of pulmonary CD8a+ cells in RSV-infected mice with TBBPA exposure. TBBPA and AF-08 did not exhibit anti-RSV activity in vitro. Thus, AF-08 probably ameliorated pneumonia exacerbated by TBBPA exposure in RSV-infected mice by limiting excess cellular immune responses.

  3. Catalytic degradation of brominated flame retardants by copper oxide nanoparticles

    Science.gov (United States)

    Dror, I.; Yecheskel, Y.; Berkowitz, B.

    2013-12-01

    Brominated flame retardants (BFRs) have been added to various products like plastic, textile, electronics and synthetic polymers at growing rates. In spite of the clear advantages of reducing fire damages, many of these BFRs may be released to the environment after their beneficial use which may lead to contamination of water resources. In this work we present the catalytic degradation of two brominated flame retardants (BFRs), tribromoneopentyl alcohol (TBNPA) and 2,4 dibromophenol (2,4-DBP) by copper oxide nanoparticles (nCuO) in aqueous solution. The degradation kinetics, the debromination, and the formation of intermediates by nCuO catalysis are compared to Fenton oxidation and to reduction by nano zero-valent iron (nZVI). The two studied BFRs are shown to degrade fully by the nCuO system within hours to days. Shorter reaction times showed differences in reaction pathways and kinetics for the two compounds. The 2,4-DBP showed faster degradation than TBNPA, by nCuO catalysis. Relatively high resistance to degradation was recorded for 2,4-DBP with nZVI, yielding 20% degradation after 24 h, while the TBNPA was degraded by 85% within 12 hours. A catalytic mechanism for radical generation and BFR degradation by nCuO is proposed. It is further suggested that H2O2 plays an essential role in the activation of the catalyst.

  4. 21 CFR 180.30 - Brominated vegetable oil.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Brominated vegetable oil. 180.30 Section 180.30... Brominated vegetable oil. The food additive brominated vegetable oil may be safely used in accordance with... used on an interim basis as a stabilizer for flavoring oils used in fruit-flavored beverages, for which...

  5. 40 CFR 721.3420 - Brominated arylalkyl ether.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Brominated arylalkyl ether. 721.3420... Substances § 721.3420 Brominated arylalkyl ether. (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substance identified generically as brominated arylalkyl ether (P-83-906) is...

  6. Tetrameric DABCO™-Bromine: an Efficient and Versatile Reagent ...

    African Journals Online (AJOL)

    Tetrameric DABCO™-bromine is a powerful brominating agent but shows reasonable selectivity with certain substrates. The selective bromination for activated aromatic compounds and alkenes is reported. Synthesis of -bromo ketones and nitriles has also been achieved by using this reagent and the results are also ...

  7. 40 CFR 721.9740 - Brominated triazine derivative.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Brominated triazine derivative. 721... Substances § 721.9740 Brominated triazine derivative. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a brominated triazine derivative...

  8. Numerical simulation of bromine crossover behavior in flow battery

    Science.gov (United States)

    Jia, Yaobin; Cheng, Shijian; Chu, Dandan; Li, Xin

    2017-03-01

    Br2 and HBr has its own series of advantages as the positive electrolyte solution, so some batteries select the Br2/Br- as the positive electrolyte solution, such as sodium polysulfide/bromine flow battery, zinc/bromine flow battery, vanadium/ bromine flow batteries and hydrogen/bromine flow batteries. But the crossover benavior of bromine occurs in these batteries too, resulting in cross-contamination, capacity loss and affecting battery's performance. In this work, we build numerical models to study the influence of bromine crossover phenomenon on the three forms of bromine crossover, the concentration of electrolyte on the cathode side and the flow rate of the negative side in the quinone bromine flow battery, to find the main models affecting the bromine crossover and the impact of bromine crossover on battery performance. It was found that the three ways of crossover through the membranes was mainly by diffusion. By reducing the concentration of positive electrolyte solution, the bromine crossover can be reduced and Coulomb Efficiency can be improved. Rising the flow rate of the electrolyte solution on the negative side and reducing the differential between positive side's pressure and negative side's pressure can also reduce the amount of bromine crossover to improve Coulomb efficiency in the battery.

  9. Sulfate production by reactive bromine: Implications for the global sulfur and reactive bromine budgets

    Science.gov (United States)

    Chen, Q.; Schmidt, J. A.; Shah, V.; Jaeglé, L.; Sherwen, T.; Alexander, B.

    2017-07-01

    Sulfur and reactive bromine (Bry) play important roles in tropospheric chemistry and the global radiation budget. The oxidation of dissolved SO2 (S(IV)) by HOBr increases sulfate aerosol abundance and may also impact the Bry budget, but is generally not included in global climate and chemistry models. In this study, we implement HOBr + S(IV) reactions into the GEOS-Chem global chemical transport model and evaluate the global impacts on both sulfur and Bry budgets. Modeled HOBr mixing ratios on the order of 0.1-1.0 parts per trillion (ppt) lead to HOBr + S(IV) contributing to 8% of global sulfate production and up to 45% over some tropical ocean regions with high HOBr mixing ratios (0.6-0.9 ppt). Inclusion of HOBr + S(IV) in the model leads to a global Bry decrease of 50%, initiated by the decrease in bromide recycling in cloud droplets. Observations of HOBr are necessary to better understand the role of HOBr + S(IV) in tropospheric sulfur and Bry cycles.

  10. Boiling of simulated tap water: effect on polar brominated disinfection byproducts, halogen speciation, and cytotoxicity.

    Science.gov (United States)

    Pan, Yang; Zhang, Xiangru; Wagner, Elizabeth D; Osiol, Jennifer; Plewa, Michael J

    2014-01-01

    Tap water typically contains numerous halogenated disinfection byproducts (DBPs) as a result of disinfection, especially of chlorination. Among halogenated DBPs, brominated ones are generally significantly more toxic than their chlorinated analogues. In this study, with the aid of ultra performance liquid chromatography/electrospray ionization-triple quadrupole mass spectrometry by setting precursor ion scans of m/z 79/81, whole spectra of polar brominated DBPs in simulated tap water samples without and with boiling were revealed. Most polar brominated DBPs were thermally unstable and their levels were substantially reduced after boiling via decarboxylation or hydrolysis; the levels of a few aromatic brominated DBPs increased after boiling through decarboxylation of their precursors. A novel adsorption unit for volatile total organic halogen was designed, which enabled the evaluation of halogen speciation and mass balances in the simulated tap water samples during boiling. After boiling for 5 min, the overall level of brominated DBPs was reduced by 62.8%, of which 39.8% was volatilized and 23.0% was converted to bromide; the overall level of chlorinated DBPs was reduced by 61.1%, of which 44.4% was volatilized and 16.7% was converted to chloride; the overall level of halogenated DBPs was reduced by 62.3%. The simulated tap water sample without boiling was cytotoxic in a chronic (72 h) exposure to mammalian cells; this cytotoxicity was reduced by 76.9% after boiling for 5 min. The reduction in cytotoxicity corresponded with the reduction in overall halogenated DBPs. Thus, boiling of tap water can be regarded as a "detoxification" process and may reduce human exposure to halogenated DBPs through tap water ingestion.

  11. Contribution of very short-lived substances to stratospheric bromine loading: uncertainties and constraints

    Directory of Open Access Journals (Sweden)

    J. Aschmann

    2013-02-01

    shifted away from HBr, according to our current state of knowledge the only member of the Bry family which is efficiently adsorbed on ice particles. This effect is caused by very efficient heterogeneous reactions on ice surfaces which reduce the HBr/Bry fraction below 15% at the tropical tropopause. Under these circumstances there is no significant loss of Bry due to dehydration in the model, VSLS contribute fully to stratospheric bromine. In addition, we conduct several sensitivity calculations to test the robustness of this result. If heterogeneous chemistry is ignored, the HBr/Bry fraction exceeds 50% and about 10% of bromine from VSLS is scavenged. Dehydration plays a minor role for Bry removal under the assumption that HOBr is efficiently adsorbed on ice as well since the heterogeneous reactions alter the partitioning equilibrium of Bry in favor of HOBr. In this case, up to 12% of bromine from VSLS is removed. Even in the extreme and unrealistic case that adsorbed species on ice particles are instantaneously removed the maximum loss of bromine does not exceed 25%. Assuming 6 parts per trillion by volume (pptv of bromine short-lived source gases in convective updrafts, a value that is supported by observational data, we find a most likely contribution of VSLS to stratospheric bromine in the range of 4.5–6 pptv.

  12. Biodegradation of brominated and organophosphorus flame retardants

    NARCIS (Netherlands)

    Waaijers, S.L.; Parsons, J.R.

    2016-01-01

    Brominated flame retardants account for about 21% of the total production of flame retardants and many of these have been identified as persistent, bioaccumulative and toxic. Nevertheless, debromination of these chemicals under anaerobic conditions is well established, although this can increase

  13. Bromocontryphan: post-translational bromination of tryptophan.

    Science.gov (United States)

    Jimenez, E C; Craig, A G; Watkins, M; Hillyard, D R; Gray, W R; Gulyas, J; Rivier, J E; Cruz, L J; Olivera, B M

    1997-02-04

    We demonstrate that post-translational bromination of a tryptophan residue occurs in the biologically active octapeptide bromocontryphan, purified and characterized from Conus radiatus venom. Clones encoding bromocontryphan were identified from a cDNA library made from C. radiatus venom ducts. The mRNA sequence obtained predicts a prepropeptide which has the mature peptide sequence at the C-terminal end, with the L-6-bromotryptophan residue encoded by UGG, the Trp codon. These data provide the first direct evidence for post-translational bromination of a polypeptide which is translated through the normal cellular machinery. In addition to bromination, the peptide, which induces a "stiff tail" syndrome in mice, has several other modifications as shown by the sequence [Formula: See Text] in which Hyp = hydroxyproline. Asterisks indicate post-translational modifications (left to right): proteolytic cleavage at the N-terminus; hydroxylation of Pro3; epimerization of Trp4; bromination of Trp7, and C-terminal amidation. Bromocontryphan appears to have the highest density of post-translational modifications known among gene-encoded polypeptides. The overall result is a molecule which closely resembles marine natural products produced through specialized biosynthetic pathways comprising many enzyme-catalyzed steps.

  14. Structure and functionality of bromine doped graphite.

    Science.gov (United States)

    Hamdan, Rashid; Kemper, A F; Cao, Chao; Cheng, H P

    2013-04-28

    First-principles calculations are used to study the enhanced in-plane conductivity observed experimentally in Br-doped graphite, and to study the effect of external stress on the structure and functionality of such systems. The model used in the numerical calculations is that of stage two doped graphite. The band structure near the Fermi surface of the doped systems with different bromine concentrations is compared to that of pure graphite, and the charge transfer between carbon and bromine atoms is analyzed to understand the conductivity change along different high symmetry directions. Our calculations show that, for large interlayer separation between doped graphite layers, bromine is stable in the molecular form (Br2). However, with increased compression (decreased layer-layer separation) Br2 molecules tend to dissociate. While in both forms, bromine is an electron acceptor. The charge exchange between the graphite layers and Br atoms is higher than that with Br2 molecules. Electron transfer to the Br atoms increases the number of hole carriers in the graphite sheets, resulting in an increase of conductivity.

  15. Distribution of copper, silver and gold during thermal treatment with brominated flame retardants

    Energy Technology Data Exchange (ETDEWEB)

    Oleszek, Sylwia, E-mail: sylwia_oleszek@yahoo.com [Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 1,1 Katahira, 2-Chome, Sendai 980-8577 (Japan); Institute of Environmental Engineering of the Polish Academy of Sciences, 34 M. Sklodowska-Curie St., 41-819 Zabrze (Poland); Grabda, Mariusz, E-mail: mariusz@mail.tagen.tohoku.ac.jp [Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 1,1 Katahira, 2-Chome, Sendai 980-8577 (Japan); Institute of Environmental Engineering of the Polish Academy of Sciences, 34 M. Sklodowska-Curie St., 41-819 Zabrze (Poland); Shibata, Etsuro, E-mail: etsuro@tagen.tohoku.ac.jp [Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 1,1 Katahira, 2-Chome, Sendai 980-8577 (Japan); Nakamura, Takashi, E-mail: ntakashi@tagen.tohoku.ac.jp [Institute of Multidisciplinary Research for Advanced Materials (IMRAM), Tohoku University, 1,1 Katahira, 2-Chome, Sendai 980-8577 (Japan)

    2013-09-15

    Highlights: • Copper, silver and gold during thermal treatment with brominated flame retardants. • Distribution of copper, silver and gold during thermal processing. • Thermodynamic considerations of the bromination reactions. - Abstract: The growing consumption of electric and electronic equipment results in creating an increasing amount of electronic waste. The most economically and environmentally advantageous methods for the treatment and recycling of waste electric and electronic equipment (WEEE) are the thermal techniques such as direct combustion, co-combustion with plastic wastes, pyrolysis and gasification. Nowadays, this kind of waste is mainly thermally treated in incinerators (e.g. rotary kilns) to decompose the plastics present, and to concentrate metals in bottom ash. The concentrated metals (e.g. copper, precious metals) can be supplied as a secondary raw material to metal smelters, while the pyrolysis of plastics allows the recovery of fuel gases, volatilising agents and, eventually, energy. Indeed, WEEE, such as a printed circuit boards (PCBs) usually contains brominated flame retardants (BFRs). From these materials, hydrobromic acid (HBr) is formed as a product of their thermal decomposition. In the present work, the bromination was studied of copper, silver and gold by HBr, originating from BFRs, such as Tetrabromobisphenol A (TBBPA) and Tetrabromobisphenol A-Tetrabromobisophenol A diglycidyl ether (TTDE) polymer; possible volatilization of the bromides formed was monitored using a thermo-gravimetric analyzer (TGA) and a laboratory-scale furnace for treating samples of metals and BFRs under an inert atmosphere and at a wide range of temperatures. The results obtained indicate that up to about 50% of copper and silver can evolve from sample residues in the form of volatile CuBr and AgBr above 600 and 1000 °C, respectively. The reactions occur in the molten resin phase simultaneously with the decomposition of the brominated resin. Gold is

  16. Vapor pressures, aqueous solubilities, and Henry's law constants of some brominated flame retardants.

    Science.gov (United States)

    Tittlemier, Sheryl A; Halldorson, Thor; Stern, Gary A; Tomy, Gregg T

    2002-09-01

    The subcooled liquid vapor pressures (P0(L),25S) and aqueous solubilities (Sw,25s) were determined and Henry's law constants (H25s) were estimated for a number of brominated flame retardants (BFRs) at 25 degrees C. The established methods of the gas chromatography-retention time and generator column techniques were used to experimentally determine P0(L),25 and Sw,25 for hexabromobenzene and a series of brominated diphenyl ether (BDE) congeners. The H25 was estimated as the ratio of P0(L)25 to the subcooled liquid aqueous solubility. Values of PL0(L),25 obtained ranged from 0.000000282 Pa (BDE-190) to 0.259 Pa (BDE-3); Sw,25 ranged from 0.00000087 g/L (BDE-153 and BDE-154) to 0.00013 g/L (BDE-15); and H25 ranged from 0.0074 Pa m3/mol (BDE-183) to 21 Pa m3/mol (BDE-15). An increase in the bromine content of polybrominated diphenyl ether congeners resulted in significant decreases Of P0(L),25, Sw25, and H25. A simple four-compartment equilibrium distribution model suggested that the majority of BFRs being released into the environment would reside in soil and sediment and have localized distributions. The model also suggested that lower brominated congeners tend to be somewhat more mobile. Degradative debromination reactions that yield these congeners would mobilize them environmentally, and ultimately affect the fate and distribution of BFRs.

  17. The role of vanadium haloperoxidases in the formation of volatile brominated compounds and their impact on the environment.

    Science.gov (United States)

    Wever, Ron; van der Horst, Michael A

    2013-09-07

    Vanadium haloperoxidases differ strongly from heme peroxidases in substrate specificity and stability and in contrast to a heme group they contain the bare metal oxide vanadate as a prosthetic group. These enzymes specifically oxidize halides in the presence of hydrogen peroxide into hypohalous acids. These reactive halogen intermediates will react rapidly and aspecifically with many organic molecules. Marine algae and diatoms containing these iodo- and bromoperoxidases produce short-lived brominated methanes (bromoform, CHBr3 and dibromomethane CH2Br2) or iodinated compounds. Some seas and oceans are supersaturated with these compounds and they form an important source of bromine to the troposphere and lower stratosphere and contribute significantly to the global budget of halogenated hydrocarbons. This perspective focuses, in particular, on the biosynthesis of these volatile compounds and the direct or indirect involvement of vanadium haloperoxidases in the production of huge amounts of bromoform and dibromomethane. Some of the global sources are discussed and from the literature a picture emerges in which oxidized brominated species generated by phytoplankton, seaweeds and cyanobacteria react with dissolved organic matter in seawater, resulting in the formation of intermediate brominated compounds. These compounds are unstable and decay via a haloform reaction to form an array of volatile brominated compounds of which bromoform is the major component followed by dibromomethane.

  18. Hydrogen-bromine fuel cell advance component development

    Science.gov (United States)

    Charleston, Joann; Reed, James

    1988-01-01

    Advanced cell component development is performed by NASA Lewis to achieve improved performance and longer life for the hydrogen-bromine fuel cells system. The state-of-the-art hydrogen-bromine system utilizes the solid polymer electrolyte (SPE) technology, similar to the SPE technology developed for the hydrogen-oxygen fuel cell system. These studies are directed at exploring the potential for this system by assessing and evaluating various types of materials for cell parts and electrode materials for Bromine-hydrogen bromine environment and fabricating experimental membrane/electrode-catalysts by chemical deposition.

  19. Formation and speciation characteristics of brominated trihalomethanes in seawater chlorination.

    Science.gov (United States)

    Padhi, R K; Sowmya, M; Mohanty, A K; Bramha, S N; Satpathy, K K

    2012-11-01

    Formation character of brominated-trihalomethanes (Br-THMs) in chlorinated seawater and its dependence on applied chlorine dose, reaction time, and temperature were investigated in the laboratory. Seawater was collected from the east coast of India and a chlorine dose of 1, 3, 5, and 10 ppm was each applied at a temperature of 20, 30, and 40 degrees C to investigate the yield and kinetics of Br-THMs formation. Qualitative and quantitative estimation of THM formation at various intervals of time ranging from 5 min to 168 h was determined by a gas chromatograph equipped with an electron capture detector (GC-ECD). Chlorine dose, chlorine contact time, and reaction temperature positively affected the load of THMs. The ratio of chlorine dose to halogen incorporation decreased from 12% to 5% with increasing applied chlorine dose from 1 to 10 ppm. Significant levels of THMs were found to be formed within 0.5 h of reaction, followed by a very slow rate of formation. Elevated temperature favored both increased rate of formation and overall THM yield. The formation order of different trihalomethane species at all studied temperatures was observed to be bromodichloromethane (CHCl2Br) < dibromochloromethane (CHClBr2) < bromoform (CHBr3). Formation of chloroform was not observed, and bromoform was the dominant (96% to 98%) among the three THM species formed.

  20. Alkaline hydrothermal treatment of brominated high impact polystyrene (HIPS-Br) for bromine and bromine-free plastic recovery

    OpenAIRE

    Brebu, Mihai; Bhaskar, Thallada; Muto, Akinori; Sakata, Yusaku

    2006-01-01

    A method to recover both Br and Br-free plastic from brominated flame retardant high impact polystyrene (HIPS-Br) was proposed. HIPS-Br containing 15% Br was treated in autoclave at 280℃ using water or KOH solution of various amounts and concentrations. Hydrothermal treatment (30 ml water) leads to 90% debromination of 1 g HIPS-Br but plastic is strongly degraded and could not be recovered. previous termAlkalinenext term hydrothermal treatment (45 ml or 60 ml KOH 1 M) showed similar debromina...

  1. Brominated flame retardants: occurrence, dietary intake and risk assessment

    NARCIS (Netherlands)

    Winter-Sorkina R de; Bakker MI; Wolterink G; Zeijlmaker MJ; SIR

    2006-01-01

    Brominated flame retardants have entered the human food chain. For the time being the occurrence of these chemicals in Dutch food does not pose a human health risk. However, this might easily change at increasing contents of flame retardants in Dutch food. The monitoring of brominated flame

  2. Bromine pretreated chitosan for adsorption of lead (II) from water

    Indian Academy of Sciences (India)

    Pollution by heavy metals like lead (II) is responsible for health hazards and environmental degradation. Adsorption is a prevalent method applied for removal of heavy metal pollutants from water. This study explored adsorption performances of 30% bromine pretreated chitosan for lead (II) abatement from water. Bromine ...

  3. Modeling the inorganic bromine partitioning in the tropical tropopause layer over the eastern and western Pacific Ocean

    Directory of Open Access Journals (Sweden)

    M. A. Navarro

    2017-08-01

    Full Text Available The stratospheric inorganic bromine (Bry burden arising from the degradation of brominated very short-lived organic substances (VSLorg and its partitioning between reactive and reservoir species is needed for a comprehensive assessment of the ozone depletion potential of brominated trace gases. Here we present modeled inorganic bromine abundances over the Pacific tropical tropopause based on aircraft observations of VSLorg from two campaigns of the Airborne Tropical TRopopause EXperiment (ATTREX 2013, carried out over the eastern Pacific, and ATTREX 2014, carried out over the western Pacific and chemistry-climate simulations (along ATTREX flight tracks using the specific meteorology prevailing. Using the Community Atmosphere Model with Chemistry (CAM-Chem we model that BrO and Br are the daytime dominant species. Integrated across all ATTREX flights, BrO represents ∼ 43 and 48 % of daytime Bry abundance at 17 km over the western and eastern Pacific, respectively. The results also show zones where Br / BrO > 1 depending on the solar zenith angle (SZA, ozone concentration, and temperature. On the other hand, BrCl and BrONO2 were found to be the dominant nighttime species with ∼  61 and 56 % of abundance at 17 km over the western and eastern Pacific, respectively. The western-to-eastern differences in the partitioning of inorganic bromine are explained by different abundances of ozone (O3, nitrogen dioxide (NO2, total inorganic chlorine (Cly, and the efficiency of heterogeneous reactions of bromine reservoirs (mostly BrONO2 and HBr occurring on ice crystals.

  4. Modeling the inorganic bromine partitioning in the tropical tropopause layer over the eastern and western Pacific Ocean

    Science.gov (United States)

    Navarro, Maria A.; Saiz-Lopez, Alfonso; Cuevas, Carlos A.; Fernandez, Rafael P.; Atlas, Elliot; Rodriguez-Lloveras, Xavier; Kinnison, Douglas; Lamarque, Jean-Francois; Tilmes, Simone; Thornberry, Troy; Rollins, Andrew; Elkins, James W.; Hintsa, Eric J.; Moore, Fred L.

    2017-08-01

    The stratospheric inorganic bromine (Bry) burden arising from the degradation of brominated very short-lived organic substances (VSLorg) and its partitioning between reactive and reservoir species is needed for a comprehensive assessment of the ozone depletion potential of brominated trace gases. Here we present modeled inorganic bromine abundances over the Pacific tropical tropopause based on aircraft observations of VSLorg from two campaigns of the Airborne Tropical TRopopause EXperiment (ATTREX 2013, carried out over the eastern Pacific, and ATTREX 2014, carried out over the western Pacific) and chemistry-climate simulations (along ATTREX flight tracks) using the specific meteorology prevailing. Using the Community Atmosphere Model with Chemistry (CAM-Chem) we model that BrO and Br are the daytime dominant species. Integrated across all ATTREX flights, BrO represents ˜ 43 and 48 % of daytime Bry abundance at 17 km over the western and eastern Pacific, respectively. The results also show zones where Br / BrO > 1 depending on the solar zenith angle (SZA), ozone concentration, and temperature. On the other hand, BrCl and BrONO2 were found to be the dominant nighttime species with ˜ 61 and 56 % of abundance at 17 km over the western and eastern Pacific, respectively. The western-to-eastern differences in the partitioning of inorganic bromine are explained by different abundances of ozone (O3), nitrogen dioxide (NO2), total inorganic chlorine (Cly), and the efficiency of heterogeneous reactions of bromine reservoirs (mostly BrONO2 and HBr) occurring on ice crystals.

  5. the aluminum and bromine reaction revisited: on the hazard during ...

    African Journals Online (AJOL)

    unesco

    Institute of Chemistry, Faculty of Natural Sciences and Mathematics, Ss Cyril &. Methodius University, PO Box ... of Sciences and. Arts and a leader of the structural chemistry in Macedonia, on the occasion of his 65th birthday. .... P. Atkins, J. de Paula, Atkins' Physical Chemistry, Eighth Ed., Oxford University. Press, New York ...

  6. Production of HBR from bromine and steam for off-peak electrolytic hydrogen generation

    Energy Technology Data Exchange (ETDEWEB)

    Schlief, R.E.; Hanrahan, R.J.; Stoy, M.A. [Univ. of Florida, Gainesville, FL (United States)] [and others

    1995-09-01

    Progress is reported on the development of a renewable energy source based solar-electrolytic system for production of hydrogen and oxygen. It employs water, bromine, solar energy and supplemental electrical power. The concept is being developed by Solar Reactor Technologies, Inc., (SRT), with the U.S. Department of Energy (DOE). An overview of the nature and objectives of this program is provided here, and technical progress made during the first (three-month) performance period of the Phase I work effort is reported. The SRT concept entails (1) absorption of concentrated solar radiation by bromine vapor Br{sub 2(g)} in a high-temperature reactor producing Br{sub (g)} atoms, (2) reaction of Br{sub (g)} with water yielding hydrogen bromide (HBr), and (3) electrolysis of stored hydrogen bromide for production of H{sub 2(g)} and recovery of Br{sub 2(I)}. Incorporation of solar radiation in the primary photochemical step (1) reduces by 50 - 70% the electrical power required to split water. The SRT concept is very attractive from an economic viewpoint as well. The reversible fuel cell, employed in the SRT electrolysis concept is capitalized via its use in load leveling by the utility. A 1 kW solar reactor was designed and constructed during the first three-month performance period by SRT personnel at the University of Florida, Gainesville. It was employed in taking survey data of the reaction between bromine and steam at temperatures between 900 and 1300 K. This reaction was run under purely thermal conditions, i.e. in the absence of solar photons. The experimental data are reported and interpreted employing concomitant thermodynamic calculations. The anticipated improvement is discussed briefly as well as the effect of a photochemical boost to the reaction. The amount of this enhancement will be studied in the next three month performance period.

  7. Tropospheric bromine chemistry: implications for present and pre-industrial ozone and mercury

    Directory of Open Access Journals (Sweden)

    J. P. Parrella

    2012-08-01

    Full Text Available We present a new model for the global tropospheric chemistry of inorganic bromine (Bry coupled to oxidant-aerosol chemistry in the GEOS-Chem chemical transport model (CTM. Sources of tropospheric Bry include debromination of sea-salt aerosol, photolysis and oxidation of short-lived bromocarbons, and transport from the stratosphere. Comparison to a GOME-2 satellite climatology of tropospheric BrO columns shows that the model can reproduce the observed increase of BrO with latitude, the northern mid-latitudes maximum in winter, and the Arctic maximum in spring. This successful simulation is contingent on the HOBr + HBr reaction taking place in aqueous aerosols and ice clouds. Bromine chemistry in the model decreases tropospheric ozone mixing ratios by <1–8 nmol mol−1 (6.5% globally, with the largest effects in the northern extratropics in spring. The global mean tropospheric OH concentration decreases by 4%. Inclusion of bromine chemistry improves the ability of global models (GEOS-Chem and p-TOMCAT to simulate observed 19th-century ozone and its seasonality. Bromine effects on tropospheric ozone are comparable in the present-day and pre-industrial atmospheres so that estimates of anthropogenic radiative forcing are minimally affected. Br atom concentrations are 40% higher in the pre-industrial atmosphere due to lower ozone, which would decrease by a factor of 2 the atmospheric lifetime of elemental mercury against oxidation by Br. This suggests that historical anthropogenic mercury emissions may have mostly deposited to northern mid-latitudes, enriching the corresponding surface reservoirs. The persistent rise in background surface ozone at northern mid-latitudes during the past decades could possibly contribute to the observations of elevated mercury in subsurface waters of the North Atlantic.

  8. WEEE plastic sorting for bromine essential to enforce EU regulation.

    Science.gov (United States)

    Hennebert, Pierre; Filella, Montserrat

    2018-01-01

    The plastics of waste of electric and electronic equipment (WEEE) are improved for fire safety by flame retardants, and particularly brominated flame retardants (BFR). As waste, the management of these plastic fractions must comply with the update of the regulation of waste hazard classification (2014, 2017), the publication of a technical standard on management of WEEE (2015), and a restriction of use for decabromodiphenylether in the product regulation (2017). Data of bromine (n=4283) and BFR concentrations (n=98) in plastics from electric and electronic equipment (EEE), and from WEEE processing facilities before and after sorting for bromine in four sites in France have been studied for chemical composition and for regulatory classification. The WEEE was analysed by handheld X-ray fluorescence, and the waste was sorted after shredding, by on-line X-ray transmission for total bromine content ( 2000 mg/kg) in small household appliances (SHA), cathode ray tubes (CRT) and flat screens plastics. In equipment (n=347), 15% of the equipment items have no bromine, while 46% have at least one part with bromine, and 39% have all parts brominated. The bromine concentration in plastics is very heterogeneous, found in high concentrations in large household appliance (LHA) plastics, and also found in unexpected product categories, as observed by other authors. Clearly, an unwanted global loop of brominated substances occurs via the international recycling of plastic scrap. In waste (n=65), polybromobiphenyls, polybromodiphenylethers (PBDE), tetrabromobisphenol A (TBBPA) and hexabromocyclododecane were analysed. The most concentrated BFRs are decaBDE (3000 mg/kg) and TBBPA (8000 mg/kg). The bromine concentration of regulated brominated substances was identified in 2014 and 2015 to be up to 86% of total bromine in "old" waste (SHA, CRT), 30-50% in "younger" waste (Flat screens), and a mean of only 8% in recent products (2009-2013). Regulated substances are a minority of

  9. Analysis of reactive bromine production and ozone depletion in the Arctic boundary layer using 3-D simulations with GEM-AQ: inference from synoptic-scale patterns

    Science.gov (United States)

    Toyota, K.; McConnell, J. C.; Lupu, A.; Neary, L.; McLinden, C. A.; Richter, A.; Kwok, R.; Semeniuk, K.; Kaminski, J. W.; Gong, S.-L.; Jarosz, J.; Chipperfield, M. P.; Sioris, C. E.

    2011-04-01

    Episodes of high bromine levels and surface ozone depletion in the springtime Arctic are simulated by an online air-quality model, GEM-AQ, with gas-phase and heterogeneous reactions of inorganic bromine species and a simple scheme of air-snowpack chemical interactions implemented for this study. Snowpack on sea ice is assumed to be the only source of bromine to the atmosphere and to be capable of converting relatively stable bromine species to photolabile Br2 via air-snowpack interactions. A set of sensitivity model runs are performed for April 2001 at a horizontal resolution of approximately 100 km×100 km in the Arctic, to provide insights into the effects of temperature and the age (first-year, FY, versus multi-year, MY) of sea ice on the release of reactive bromine to the atmosphere. The model simulations capture much of the temporal variations in surface ozone mixing ratios as observed at stations in the high Arctic and the synoptic-scale evolution of areas with enhanced BrO column amount ("BrO clouds") as estimated from satellite observations. The simulated "BrO clouds" are in modestly better agreement with the satellite measurements when the FY sea ice is assumed to be more efficient at releasing reactive bromine to the atmosphere than on the MY sea ice. Surface ozone data from coastal stations used in this study are not sufficient to evaluate unambiguously the difference between the FY sea ice and the MY sea ice as a source of bromine. The results strongly suggest that reactive bromine is released ubiquitously from the snow on the sea ice during the Arctic spring while the timing and location of the bromine release are largely controlled by meteorological factors. It appears that a rapid advection and an enhanced turbulent diffusion associated with strong boundary-layer winds drive transport and dispersion of ozone to the near-surface air over the sea ice, increasing the oxidation rate of bromide (Br-) in the surface snow. Also, if indeed the surface

  10. Analysis of reactive bromine production and ozone depletion in the Arctic boundary layer using 3-D simulations with GEM-AQ: inference from synoptic-scale patterns

    Directory of Open Access Journals (Sweden)

    K. Toyota

    2011-04-01

    Full Text Available Episodes of high bromine levels and surface ozone depletion in the springtime Arctic are simulated by an online air-quality model, GEM-AQ, with gas-phase and heterogeneous reactions of inorganic bromine species and a simple scheme of air-snowpack chemical interactions implemented for this study. Snowpack on sea ice is assumed to be the only source of bromine to the atmosphere and to be capable of converting relatively stable bromine species to photolabile Br2 via air-snowpack interactions. A set of sensitivity model runs are performed for April 2001 at a horizontal resolution of approximately 100 km×100 km in the Arctic, to provide insights into the effects of temperature and the age (first-year, FY, versus multi-year, MY of sea ice on the release of reactive bromine to the atmosphere. The model simulations capture much of the temporal variations in surface ozone mixing ratios as observed at stations in the high Arctic and the synoptic-scale evolution of areas with enhanced BrO column amount ("BrO clouds" as estimated from satellite observations. The simulated "BrO clouds" are in modestly better agreement with the satellite measurements when the FY sea ice is assumed to be more efficient at releasing reactive bromine to the atmosphere than on the MY sea ice. Surface ozone data from coastal stations used in this study are not sufficient to evaluate unambiguously the difference between the FY sea ice and the MY sea ice as a source of bromine. The results strongly suggest that reactive bromine is released ubiquitously from the snow on the sea ice during the Arctic spring while the timing and location of the bromine release are largely controlled by meteorological factors. It appears that a rapid advection and an enhanced turbulent diffusion associated with strong boundary-layer winds drive transport and dispersion of ozone to the near-surface air over the sea ice, increasing the oxidation rate of bromide (Br in the surface

  11. On-line orientation of bromine isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Barham, C.G.; Alghamdi, S.S.; Grant, I.S. (Schuster Lab., Manchester Univ. (United Kingdom)); Bhagwat, A.; Singleton, B.D.D.; Walker, P.M. (Dept. of Physics, Univ. of Surrey, Guildford (United Kingdom)); Booth, M.; Lindroos, M.; Rikovska, J.; Stone, N.J. (Clarendon Lab., Oxford Univ. (United Kingdom))

    1992-11-01

    Assignments for the principal Nilsson configuration in light [beta][sup +]-decaying bromine isotopes were proposed in a contribution to the OLNO-1 conference. These assignments were made on the basis of magnetic moments derived from the temperature dependence of anisotropies in daughter Se isotopes observed in the DOLIS-COLD facility at Daresbury. Anisotropy measurements have since been extended to a lower base temperature in [sup 74m]Br and [sup 72g]Br decay, leading to more stringent limits on the ground state moment of [sup 72]Br. The proposed [pi][312]3/2 configuration for [sup 75]Br has also now been confirmed by a measurement of the sign of its magnetic moment. This was done by observing the [beta]-asymmetry in [sup 75]Br decay using high purity Si detectors mounted within the dilution refrigerator. (orig.).

  12. Magnetic trapping of cold bromine atoms.

    Science.gov (United States)

    Rennick, C J; Lam, J; Doherty, W G; Softley, T P

    2014-01-17

    Magnetic trapping of bromine atoms at temperatures in the millikelvin regime is demonstrated for the first time. The atoms are produced by photodissociation of Br2 molecules in a molecular beam. The lab-frame velocity of Br atoms is controlled by the wavelength and polarization of the photodissociation laser. Careful selection of the wavelength results in one of the pair of atoms having sufficient velocity to exactly cancel that of the parent molecule, and it remains stationary in the lab frame. A trap is formed at the null point between two opposing neodymium permanent magnets. Dissociation of molecules at the field minimum results in the slowest fraction of photofragments remaining trapped. After the ballistic escape of the fastest atoms, the trapped slow atoms are lost only by elastic collisions with the chamber background gas. The measured loss rate is consistent with estimates of the total cross section for only those collisions transferring sufficient kinetic energy to overcome the trapping potential.

  13. Synthesis and Reactions of Acenaphthenequinones-Part-2. The Reactions of Acenaphthenequinones

    Directory of Open Access Journals (Sweden)

    Mahmoud Shoukry

    2002-02-01

    Full Text Available The reactions of acenaphthenequinone and its derivatives with different nucleophiles, organic and inorganic reagents are reviewed. This survey also covers their oxidation and reduction reactions, in addition to many known reactions such as Friedel Crafts, Diels-Alder, bromination and thiolation.

  14. Cadmium, lead and bromine in beached microplastics.

    Science.gov (United States)

    Massos, Angelo; Turner, Andrew

    2017-08-01

    Samples of microplastic (n = 924) from two beaches in south west England have been analysed by field-portable-x-ray fluorescence (FP-XRF) spectrometry, configured in a low-density mode and with a small-spot facility, for the heavy metals, Cd and Pb, and the halogen, Br. Primary plastics in the form of pre-production pellets were the principal type of microplastic (>70%) on both beaches, with secondary, irregularly-shaped fragments representing the remainder of samples. Cadmium and Pb were detected in 6.9% and 7.5% of all microplastics, respectively, with concentrations of either metal that exceeded 103 μg g-1 usually encountered in red and yellow pellets or fragments. Respective correlations of Cd and Pb with Se and Cr were attributed to the presence of the coloured, inorganic pigments, cadmium sulphoselenide and lead chromate. Bromine, detected in 10.4% of microplastics and up to concentrations of about 13,000 μg g-1, was mainly encountered in neutrally-coloured pellets. Its strong correlation with Sb, whose oxides are effective fire suppressant synergists, suggests the presence of a variety of brominated flame retardants arising from the recycling of plastics originally used in casings for heat-generating electrical equipment. The maximum bioaccessible concentrations of Cd and Pb, evaluated using a physiological extraction based on the chemical characteristics of the proventriculus-gizzard of the northern fulmar, were about 50 μg g-1 and 8 μg g-1, respectively. These concentrations exceed those estimated for the diet of local seabirds by factors of about 50 and 4, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

  15. C-6 regioselective bromination of methyl indolyl-3-acetate.

    Science.gov (United States)

    Suárez-Castillo, Oscar R; Meléndez-Rodríguez, Myriam; Beiza-Granados, Lidia; Cano-Escudero, Indira C; Morales-Ríos, Martha S; Joseph-Nathan, Pedro

    2011-04-01

    An efficient route to natural occurring methyl 6-bromoindolyl-3-acetate 1c from methyl indolyl-3-acetate 3 was achieved in 3 steps and 68% overall yield. Thus, in order to regioselectively brominate 3 at the C6-position, introduction of electron withdrawing substituents at N1 and C8 was affected to give intermediate 4 in 82% yield. Bromination of 4 with 8 equiv of bromine in CCl4 and washings with aqueous Na2SO3 gave 5 in 86% yield, which was N- and C-decarbomethoxylated by treatment with NaCN in DMSO, affording 1c in 97% yield. The regioselectivity of bromination was evidenced by NMR spectroscopy and X- ray diffraction analysis.

  16. Spectrophotometric determination of lansoprazole in pharmaceuticals using bromate-bromide mixture based on redox and complexation reactions

    OpenAIRE

    Basavaiah, K.; Ramakrishna, V.; U. R. Anil Kumar; Somashekar, B. C.

    2007-01-01

    Two sensitive spectrophotometric methods are described for the determination of lansoprazole (LPZ) in bulk drug and in capsule formulation. The methods are based on the oxidation of lansoprazole by insitu generated bromine followed by determination of unreacted bromine by two different reaction schemes. In one procedure (method A), the residual bromine is treated with excess of iron (II), and the resulting iron (III) is complexed with thiocyanate and measured at 470 nm. The second approach (m...

  17. New Methods for Labeling RGD Peptides with Bromine-76

    OpenAIRE

    Lixin Lang, Weihua Li, Hong-Mei Jia, De-Cai Fang, Shushu Zhang, Xilin Sun, Lei Zhu, Ying Ma, Baozhong Shen, Dale O. Kiesewetter, Gang Niu, Xiaoyuan Chen

    2011-01-01

    Direct bromination of the tyrosine residues of peptides and antibodies with bromine-76, to create probes for PET imaging, has been reported. For peptides that do not contain tyrosine residues, however, a prosthetic group is required to achieve labeling via conjugation to other functional groups such as terminal α-amines or lysine ε-amines. The goal of this study was to develop new strategies for labeling small peptides with Br-76 using either a direct labeling method or a prosthetic...

  18. Development of Bromine-77 from the LAMPF facility

    Energy Technology Data Exchange (ETDEWEB)

    Mettler, F.A. Jr.

    1982-01-01

    The objective of the work is to conduct the necessary studies required to evaluate the efficacy, potential benefit and role of bromine-77 labelled steroids in the detection and evaluation of treatment for hormone-dependent tumors. The synthetic goals of the project are to prepose estradiol derivatives which are labelled with bromine-77 at specific positions in the steroid nucleus. In addition, animal studies imaging studies, and cooperative studies are being conducted. (KJD)

  19. Oxyhalogen-sulfur chemistry: kinetics and mechanism of oxidation of N-acetyl homocysteine thiolactone by acidified bromate and aqueous bromine.

    Science.gov (United States)

    Mbiya, Wilbes; Choi, Boyoung; Martincigh, Bice S; Morakinyo, Moshood K; Simoyi, Reuben H

    2013-12-12

    N-acetyl homocysteine thiolactone (NAHT), medically known as citiolone, can be used as a mucolytic agent and for the treatment of certain hepatic disorders. We have studied the kinetics and mechanisms of its oxidation by acidic bromate and aqueous bromine. In acidic bromate conditions the reaction is characterized by a very short induction period followed by a sudden and rapid formation of bromine and N-acetyl homocysteine sulfonic acid. The stoichiometry of the bromate-NAHT reaction was deduced to be: BrO3(-) + H2O + CH3CONHCHCH2CH2SCO → CH3CONHCHCH2CH2(SO3H)COOH + Br(-) (S1) while in excess bromate it was deduced to be: 6BrO3(-) + 5CH3CONHCHCH2CH2SCO + 6H(+) → 3Br2 + 5CH3CONHCHCH2CH2(SO3H)COOH + 2H2O (S2). For the reaction of NAHT with bromine, a 3:1 stoichiometric ratio of bromine to NAHT was obtained: 3Br2 + CH3CONHCHCH2CH2SCO + 4H2O → 6Br(-) + CH3CONHCHCH2CH2(SO3H)COOH + 6H(+) (S3). Oxidation occurred only on the sulfur center where it was oxidized to the sulfonic acid. No sulfate formation was observed. The mechanism involved an initial oxidation to a relatively stable sulfoxide without ring-opening. Further oxidation of the sulfoxide involved two pathways: one which involved intermediate formation of an unstable sulfone and the other involves ring-opening coupled with oxidation through to the sulfonic acid. There was oligooscillatory production of aqueous bromine. Bromide produced in S1 reacts with excess bromate to produce aqueous bromine. The special stability associated with the sulfoxide allowed it to coexist with aqueous bromine since its further oxidation to the sulfone was not as facile. The direct reaction of aqueous bromine with NAHT was fast with an estimated lower limit bimolecular rate constant of 2.94 ± 0.03 × 10(2) M(-1) s(-1).

  20. Alkaline hydrothermal treatment of brominated high impact polystyrene (HIPS-Br) for bromine and bromine-free plastic recovery.

    Science.gov (United States)

    Brebu, Mihai; Bhaskar, Thallada; Muto, Akinori; Sakata, Yusaku

    2006-08-01

    A method to recover both Br and Br-free plastic from brominated flame retardant high impact polystyrene (HIPS-Br) was proposed. HIPS-Br containing 15% Br was treated in autoclave at 280 degrees C using water or KOH solution of various amounts and concentrations. Hydrothermal treatment (30 ml water) leads to 90% debromination of 1g HIPS-Br but plastic is strongly degraded and could not be recovered. Alkaline hydrothermal treatment (45 ml or 60 ml KOH 1M) showed similar debromination for up to 12 g HIPS-Br and plastic was recovered as pellets with molecular weight distribution close to that of the initial material. Debromination occurs at melt plastic/KOH solution interface when liquid/vapour equilibrium is attained inside autoclave (280 degrees C and 7 MPa in our experimental conditions) and depends on the plastic amount/KOH volume ratio. The antimony oxide synergist from HIPS-Br remains in recovered plastic during treatment. A pictorial imagination of the proposed debromination process is presented.

  1. TSCA Work Plan Chemical Technical Supplement – Physicochemical Properties and Environmental Fate of the Brominated Phthalates Cluster (BPC) Chemicals

    Science.gov (United States)

    TSCA Work Plan Chemical Technical Supplement – Physicochemical Properties and Environmental Fate of the Brominated Phthalates Cluster (BPC) Chemicals -- Brominated Phthalates Cluster Flame Retardants.

  2. [Alkene bromination used for detailed hydrocarbon and bulk hydrocarbon group-type analysis of gasolines containing alkenes].

    Science.gov (United States)

    Liu, Ying-Rong; Yang, Hai-Ying; Li, Chang-Xiu

    2002-07-01

    The optimized reaction conditions of selective alkene bromination for gasolines containing aromatics and saturated hydrocarbons are presented. By this way, the interfering problem in alkene determination from coeluting saturated hydrocarbons has been solved. So the detailed hydrocarbon analysis can be improved by a simple system containing polar and non-polar columns or by a gas chromatograph coupled with an atomic emission detector (GC-AED). Under the optimized conditions, it was found that the alkene compounds were selectively and completely brominated but the aromatics and alkane compounds were remained unaffected. A simple treatment, 90 s-120 s for reaction and 10 s-20 s for removing the excess bromine, can be easily realized. The treatment is applied for the different types of gasoline containing 0-100% alkene. Besides, one of the most important applications of this treatment is to analyse the hydrocarbons in detail from the fluid catalytic cracking (FCC) gasoline. The samples in these cases may not be accurately analyzed when using the traditional method of hydrocarbon analysis because of the presence of coeluted interfering olefins above C7.

  3. Application of bromate-bromide mixture as a green brominating agent for the spectrophotometric determination of atenolol in pharmaceuticals

    Directory of Open Access Journals (Sweden)

    Prashanth Nagaraj Kudige

    2012-01-01

    Full Text Available Two highly sensitive spectrophotometric methods are proposed for the quantification of atenolol (ATN in pure drug as well as in pharmaceutical formulations. The methods are based on the bromination reaction of ATN with a known excess of bromate-bromide mixture in acid medium followed by the determination of unreacted bromine. The residual bromine is determined by its reaction with excess iodide and the liberated iodine (I3□ is either measured at 360 nm (method A or reacted with starch followed by the measurement of the starch-iodine chromogen at 570 nm (method B. Under the optimum conditions, ATN could be assayed in the concentration ranges of 0.5-9.0 and 0.3-6.0μg mL-1 for method A and method B, respectively, with corresponding molar absorptivity values of 2.36×104 and 2.89×104 L/mol.cm. Sandell’s sensitivity values are found to be 0.0113 and 0.0092 μg/cm2 for method A and method B, respectively. The proposed methods were successfully applied to the analysis of different commercial brands of pharmaceutical formulations and the results obtained by the proposed methods were in good agreement with those obtained using the reference method. The reliability of the methods was further ascertained by recovery studies using standard- addition method.

  4. Levels and trends of brominated flame retardants in the European environment

    NARCIS (Netherlands)

    Law, R.J.; Allchin, C.R.; Boer, de J.; Covaci, A.; Herzke, D.; Lepom, P.; Morris, S.; Tronczynski, J.; Wit, de C.A.

    2006-01-01

    In this paper, we review those data which have recently become available for brominated flame retardants (particularly the brominated diphenyl ethers (BDEs) and hexabromocyclododecane (HBCD)) in samples from the European environment. Environmental compartments studied comprise the atmosphere,

  5. A standardized method for assessment of oxidative transformations of brominated phenols in water.

    Science.gov (United States)

    Bastos, Patricia Moreira; Eriksson, Johan; Green, Nicholas; Bergman, Ake

    2008-01-01

    The term persistence has been used to confusion since it is used as a conceptual parameter without a uniform definition. Work is therefore being done in order to unite ideas and describe persistence based on the chemical reactivity and chemico-physical properties of compounds via investigation of the main degradation pathways in the environment; photolysis, hydrolysis-substitution-elimination (hse), oxidation, reduction and radical reactions. The present work is focused on developing a method to determine oxidative degradation rates of chemicals and thereby measurement of their susceptibility to undergo oxidation reactions. The method based on potassium permanganate works well for water soluble compounds and is easy, robust, inexpensive and reproducible. By using the method and varying the analysed substances, the degradation rates for brominated phenols, two chlorinated phenols and high volume production compounds such as tetrabromobisphenol A (TBBPA), tetrachlorobisphenol A (TCBPA) and bisphenol A (BPA) have been determined at pH 7.6+/-0.2. The reaction rates of the two halogenated BPA's are particularly fast, giving half-lives in seconds. The other test compounds have slower reaction rates but easily measured under the reaction conditions applied. The reactions are temperature dependent. There is evidence that pK(a) and the substitution pattern of the halogens affects the rate of the reactions. The method is robust and applicable for reaction rate constant measurements of present and potential future environmental contaminants.

  6. Distribution of copper, silver and gold during thermal treatment with brominated flame retardants.

    Science.gov (United States)

    Oleszek, Sylwia; Grabda, Mariusz; Shibata, Etsuro; Nakamura, Takashi

    2013-09-01

    The growing consumption of electric and electronic equipment results in creating an increasing amount of electronic waste. The most economically and environmentally advantageous methods for the treatment and recycling of waste electric and electronic equipment (WEEE) are the thermal techniques such as direct combustion, co-combustion with plastic wastes, pyrolysis and gasification. Nowadays, this kind of waste is mainly thermally treated in incinerators (e.g. rotary kilns) to decompose the plastics present, and to concentrate metals in bottom ash. The concentrated metals (e.g. copper, precious metals) can be supplied as a secondary raw material to metal smelters, while the pyrolysis of plastics allows the recovery of fuel gases, volatilising agents and, eventually, energy. Indeed, WEEE, such as a printed circuit boards (PCBs) usually contains brominated flame retardants (BFRs). From these materials, hydrobromic acid (HBr) is formed as a product of their thermal decomposition. In the present work, the bromination was studied of copper, silver and gold by HBr, originating from BFRs, such as Tetrabromobisphenol A (TBBPA) and Tetrabromobisphenol A-Tetrabromobisophenol A diglycidyl ether (TTDE) polymer; possible volatilization of the bromides formed was monitored using a thermo-gravimetric analyzer (TGA) and a laboratory-scale furnace for treating samples of metals and BFRs under an inert atmosphere and at a wide range of temperatures. The results obtained indicate that up to about 50% of copper and silver can evolve from sample residues in the form of volatile CuBr and AgBr above 600 and 1000°C, respectively. The reactions occur in the molten resin phase simultaneously with the decomposition of the brominated resin. Gold is resistant to HBr and remains unchanged in the residue. Copyright © 2013 Elsevier Ltd. All rights reserved.

  7. A closer look at the bromine-lithium exchange with tert-butyllithium in an aryl sulfonamide synthesis.

    Science.gov (United States)

    Waldmann, Christopher; Schober, Otmar; Haufe, Günter; Kopka, Klaus

    2013-06-21

    A practical protocol for the one-pot synthesis of various aryl sulfonamides, notably of pyridine-core-substituted 7-azaindolyl sulfonamides, is described. A key step is the well-known bromine-lithium exchange reaction of an aryl bromide with tert-butyllithium (t-BuLi). Differing from the common practice to use 2 or more equiv of organolithium, the exact amount of t-BuLi needed for a sufficient exchange reaction is determined for each aryl bromide in a GC-MS-assisted experiment.

  8. Nuclear Transparency and Single Particle Spectral Functions from Quasielastic A(e,e'p) Reactions up to Q2=8.1 GeV2

    Energy Technology Data Exchange (ETDEWEB)

    McKee, David Wayne [New Mexico State Univ., Las Cruces, NM (United States)

    2003-05-01

    High statistics elastic and quasielastic scattering measurements were performed on hydrogen, deuterium, carbon, and iron at squared momentum transfers up to 8.1 GeV2. Both the nuclear transparency and the single particle spectral functions were extracted by means of comparison with a Plane- Wave Impulse Approximation calculation. Our data provide no evidence of the onset of color transparency within our kinematic range.

  9. Brominated flame retardant: environmental and exposed individuals' health impact.

    Science.gov (United States)

    Dufour, Patrice; Charlier, Corinne

    2017-04-01

    Since Antiquity, men have used chemicals to protect their goods against fire. Effective and easy to use, brominated flame retardants are used since decades massively in plastic industry. Such like other organohalogenated compounds, brominated flame retardants are very persistent in the environment and able to accumulate along the food chain. Many authors highlight their presence in the environment, in many animal species and in the human serum. Worryingly, man is exposed as soon as the pregnancy and then by the breastfeeding. This exposition may have consequence on our health. Many studies (in vitro, in vivo or epidemiologic) highlight brominated flame retardant negative effects on the endocrine system, mainly on the thyroid function but also on the reproduction, the neurodevelopment in the children and on the metabolism with increasing diabetes risk. If authorities and some big enterprises are aware about the problematic, new studies are needed to confirm previous results, elucidate endocrine disrupting mechanisms and highlight hypothetical synergies with other pollutants such like PCBs.

  10. Dichlorinated and Brominated Rugulovasines, Ergot Alkaloids Produced by Talaromyces wortmannii

    Directory of Open Access Journals (Sweden)

    Lívia Soman de Medeiros

    2015-09-01

    Full Text Available UHPLC-DAD-HRMS based dereplication guided the detection of new halogenated alkaloids co-produced by Talaromyces wortmannii. From the fungal growth in large scale, the epimers 2,8-dichlororugulovasines A and B were purified and further identified by means of a HPLC-SPE/NMR hyphenated system. Brominated rugulovasines were also detected when the microbial incubation medium was supplemented with bromine sources. Studies from 1D/2D NMR and HRMS spectroscopy data allowed the structural elucidation of the dichlorinated compounds, while tandem MS/HRMS data analysis supported the rationalization of brominated congeners. Preliminary genetic studies revealed evidence that FADH2 dependent halogenase can be involved in the biosynthesis of the produced halocompounds.

  11. New Methods for Labeling RGD Peptides with Bromine-76

    OpenAIRE

    Lang, Lixin; Li, Weihua; Jia, Hong-Mei; Fang, De-Cai; Zhang, Shushu; Sun, Xilin; Zhu, Lei; Ma, Ying; Shen, Baozhong; Kiesewetter, Dale O.; Niu, Gang; Chen, Xiaoyuan

    2011-01-01

    Direct bromination of the tyrosine residues of peptides and antibodies with bromine-76, to create probes for PET imaging, has been reported. For peptides that do not contain tyrosine residues, however, a prosthetic group is required to achieve labeling via conjugation to other functional groups such as terminal α-amines or lysine ε-amines. The goal of this study was to develop new strategies for labeling small peptides with Br-76 using either a direct labeling method or a prosthetic group, de...

  12. Pyrolysis of brominated feedstock plastic in a fluidised bed reactor

    OpenAIRE

    Hall, W.J.; Williams, P.T.

    2006-01-01

    Fire retarded high impact polystyrene has been pyrolysed using a fluidised bed reactor with a sand bed. The yield and composition of the products have been investigated in relation to fluidised bed temperature. The bromine distribution between the products and a detailed analysis of the oils using GC-FID/ECD, GC-MS, FT-ir, and size exclusion chromatography has been carried out. It was found that the majority of the bromine transfers to the pyrolysis oil and the antimony was detected in both t...

  13. Cyclic Performance Analysis of Hydrogen/Bromine Flow Batteries for Grid-Scale Energy Storage

    Energy Technology Data Exchange (ETDEWEB)

    Cho, KT; Tucker, MC; Ding, M; Ridgway, P; Battaglia, VS; Srinivasan, V; Weber, AZ

    2014-06-03

    This paper explores the critical factors dominating the cycle performance of the hydrogen/bromine redox flow battery (RFB). Carbon electrode oxidation to CO2 was seen as the dominant side reaction, which can be prevented by operating the cell below 1.4 V. Crossover of bromide species from the positive to the negative electrode, especially during charge, dominates the coulombic efficiency, and can result in dissolution of the Pt catalyst if an adequate hydrogen supply is not maintained. This paper also describes the tradeoffs in voltaic, energy, and coulombic efficiencies during cycling, including the determination of the peak energy efficiency with respect to the HBr concentration and current density. Long-term cycling demonstrates negligible cell-component degradation over 600 cycles (approximate to 3 months), with capacity loss caused by the bromine from the system, which can be mitigated by proper system design. The data and methodologies provided in this paper can be used to understand better the operation of this and other RFBs.

  14. Tropospheric Bromine Chemistry: Implications for Present and Pre-industrial Ozone and Mercury

    Science.gov (United States)

    Parella, J. P.; Jacob, D. J.; Liang, Q.; Zhang, Y.; Mickley, L. J.; Miller, B.; Evans, M. J.; Yang, X.; Pyle, J. A.; Theys, N.; hide

    2012-01-01

    We present a new model for the global tropospheric chemistry of inorganic bromine (Bry) coupled to oxidant-aerosol chemistry in the GEOS-Chem chemical transport model (CTM). Sources of tropospheric Bry include debromination of sea-salt aerosol, photolysis and oxidation of short-lived bromocarbons, and transport from the stratosphere. Comparison to a GOME-2 satellite climatology of tropospheric BrO columns shows that the model can reproduce the observed increase of BrO with latitude, the northern mid-latitudes maximum in winter, and the Arctic maximum in spring. This successful simulation is contingent on the HOBr + HBr reaction taking place in aqueous aerosols and ice clouds. Bromine chemistry in the model decreases tropospheric ozone mixing ratios by mercury against oxidation by Br. This suggests that historical anthropogenic mercury emissions may have mostly deposited to northern mid-latitudes, enriching the corresponding surface reservoirs. The persistent rise in background surface ozone at northern mid-latitudes during the past decades could possibly contribute to the observations of elevated mercury in subsurface waters of the North Atlantic.

  15. Possible role of electric forces in bromine activation during polar boundary layer ozone depletion and aerosol formation events

    Science.gov (United States)

    Tkachenko, Ekaterina

    2017-11-01

    This work presents a hypothesis about the mechanism of bromine activation during polar boundary layer ozone depletion events (ODEs) as well as the mechanism of aerosol formation from the frost flowers. The author suggests that ODEs may be initiated by the electric-field gradients created at the sharp tips of ice formations as a result of the combined effect of various environmental conditions. According to the author's estimates, these electric-field gradients may be sufficient for the onset of point or corona discharges followed by generation of high local concentrations of the reactive oxygen species and initiation of free-radical and redox reactions. This process may be responsible for the formation of seed bromine which then undergoes further amplification by HOBr-driven bromine explosion. The proposed hypothesis may explain a variety of environmental conditions and substrates as well as poor reproducibility of ODE initiation observed by researchers in the field. According to the author's estimates, high wind can generate sufficient conditions for overcoming the Rayleigh limit and thus can initiate ;spraying; of charged aerosol nanoparticles. These charged aerosol nanoparticles can provoke formation of free radicals, turning the ODE on. One can also envision a possible emission of halogen ion as a result of the ;electrospray; process analogous to that of electrospray ionization mass-spectrometry.

  16. Utilization of a Green Brominating Agent for the Spectrophotometric Determination of Pipazethate HCl in Pure Form and Pharmaceutical Preparations

    Directory of Open Access Journals (Sweden)

    Ayman A. Gouda

    2013-01-01

    Full Text Available Five simple, accurate, and sensitive spectrophotometric methods (A–E have been described for the indirect assay of pipazethate HCl (PZT either in pure form or in pharmaceutical preparations. The proposed methods are based on the bromination of pipazethate HCl with a solution of excess bromate-bromide mixture in hydrochloric acid medium and subsequent estimation of the residual bromine by different reaction schemes. In the first three methods (A–C, the determination of the residual bromine is based on its ability to bleach the color of methyl orange, indigo carmine, or thymol blue dyes and measuring the absorbance at 520, 610, and 550 nm for methods A, B, and C, respectively. Methods D and E involves treating the unreacted bromine with a measured excess of iron(II, and the remaining iron(II is complexed with 1,10-phenanthroline, and the increase in absorbance is measured at 510 nm for method D and the resulting iron(III is complexed with thiocyanate and the absorbance is measured at 480 nm for method E. The different experimental parameters affecting the development and stability of the color are carefully studied and optimized. Regression analysis of the Beer-Lambert plots showed good correlation in the concentration ranges of 0.5–8.0 μg . The apparent molar absorptivity, Sandell's sensitivity, detection and quantitation limits were evaluated. The proposed methods have been applied and validated successfully for the analysis of the drug in its pure form and pharmaceutical formulations with mean recoveries of 99.94%–100.15% and relative standard deviation ≤1.53. No interference was observed from a common pharmaceutical adjuvant. Statistical comparison of the results with the reference method shows excellent agreement and indicates no significant difference in accuracy and precision.

  17. Airborne measurements of organic bromine compounds in the Pacific tropical tropopause layer.

    Science.gov (United States)

    Navarro, Maria A; Atlas, Elliot L; Saiz-Lopez, Alfonso; Rodriguez-Lloveras, Xavier; Kinnison, Douglas E; Lamarque, Jean-Francois; Tilmes, Simone; Filus, Michal; Harris, Neil R P; Meneguz, Elena; Ashfold, Matthew J; Manning, Alistair J; Cuevas, Carlos A; Schauffler, Sue M; Donets, Valeria

    2015-11-10

    Very short-lived brominated substances (VSLBr) are an important source of stratospheric bromine, an effective ozone destruction catalyst. However, the accurate estimation of the organic and inorganic partitioning of bromine and the input to the stratosphere remains uncertain. Here, we report near-tropopause measurements of organic brominated substances found over the tropical Pacific during the NASA Airborne Tropical Tropopause Experiment campaigns. We combine aircraft observations and a chemistry-climate model to quantify the total bromine loading injected to the stratosphere. Surprisingly, despite differences in vertical transport between the Eastern and Western Pacific, VSLBr (organic + inorganic) contribute approximately similar amounts of bromine [∼6 (4-9) parts per trillion] [corrected] to the stratospheric input at the tropical tropopause. These levels of bromine cause substantial ozone depletion in the lower stratosphere, and any increases in future abundances (e.g., as a result of aquaculture) will lead to larger depletions.

  18. Brominated flame retardants in Dutch North Sea surface sediments

    NARCIS (Netherlands)

    Klamers, H.J.C.; Villerius, L.A.; Leonards, P.E.G.; Bakker, J.F.

    2001-01-01

    Brominated flame retardants (BFR) concentrations were determined in the fine fraction (<63?m) of 10 surface sediments located in the southern part of the Dutch section of the North Sea Continental Shelf. Concentrations generally decreased with increasing distance from the Dutch shore. Highest

  19. Brominated Dioxins: Little-Known New Health Hazards - A Review

    Directory of Open Access Journals (Sweden)

    Piskorska-Pliszczyńska Jadwiga

    2014-10-01

    Full Text Available This article reviews the present state of the science concerning the polybrominated dibenzo-p-dioxins (PBDDs and dibenzofurans (PBDFs. Everywhere in the world people are exposed to anthropogenic origin chemicals. Some of them are long-lived organic compounds, which persist over the years in the environment. Persistent organic pollutants, such as organohalogen compounds, accumulate in environmental and biological compartments and have adverse effects on the health of humans and animals. Little is known about the brominated and mixed chloro/bromo dioxin and furans. Existing literature suggests that brominated dioxins and furans have similar toxicity profiles to their chlorinated analogues. The exposure data are extremely limited, showing a major data gap in estimating the potential environmental and health risk of these chemicals. The rapid increase in the use of brominated flame retardants (the main source of these pollutants has raised the level of concern over environmental and health damage from brominated dioxins and furans. It is likely that human as well as wildlife exposure to these contaminants will increase with their greater use. The findings reported here present strong evidence of the PBDDs and PBDFs as an emerging new class of contaminants.

  20. Thymol bromination: a comparison between enzymatic and chemical catalysis

    NARCIS (Netherlands)

    Sabuzi, F.; Churakova, E.; Galloni, P.; Wever, R.; Hollmann, F.; Floris, B.; Conte, V.

    2015-01-01

    The catalytic activity of the vanadium-dependent bromoperoxidase isolated from the brown alga Ascophyllum nodosum is compared with the activity of a cheap, commercially available V-catalyst precursor in the bromination of thymol. Organic solvents have been avoided to make the system appealing from a

  1. Bromine pretreated chitosan for adsorption of lead (II) from water

    Indian Academy of Sciences (India)

    Abstract. Pollution by heavy metals like lead (II) is responsible for health hazards and environmental degradation. Adsorption is a prevalent method applied for removal of heavy metal pollutants from water. This study explored adsorption performances of 30% bromine pretreated chitosan for lead (II) abatement from water.

  2. Oxyhalogen-sulfur chemistry: kinetics and mechanism of oxidation of captopril by acidified bromate and aqueous bromine.

    Science.gov (United States)

    Kapungu, G P; Rukweza, G; Tran, Thai; Mbiya, Wilbes; Adigun, Risikat; Ndungu, Patrick; Martincigh, Bice; Simoyi, Reuben H

    2013-04-04

    By nature of their nucleophilicity, all thiol-based drugs are oxidatively metabolized in the physiological environment. The key to understanding the physiological role of a hypertension drug, (2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolidine-2-carboxylic acid, medically known as captopril is through studying its oxidation pathway: its reactive intermediates and oxidation products. The oxidation of captopril by aqueous bromine and acidified bromate has been studied by spectrophotometric and electrospray ionization techniques. The stoichiometry for the reaction of acidic bromate with captopril is 1:1, BrO3(-) + (C4H6N)(COOH)(COCHCH3CH2)-SH → (C4H6N)(COOH)(COCHCH3CH2)-SO3H + Br(-), with reaction occurring only at the thiol center. For the direct reaction of bromine with captopril, the ratio is 3:1; 3Br2 + (C4H6N)(COOH)(COCHCH3CH2)-SH + 3H2O → (C4H6N)(COOH)(COCHCH3CH2)-SO3H + 6HBr. In excess acidic bromate conditions the reaction displays an initial induction period followed by a sharp rise in absorbance at 390 nm due to rapid formation of bromine. The direct reaction of aqueous bromine with captopril was much faster than oxidation of the thiol by acidified bromate, with a bimolecular rate constant of (1.046 (±0.08) × 10(5) M(-1) s(-1). The detection of thiyl radicals confirms the involvement of radicals as intermediates in the oxidation of Captopril by acidified BrO3(-). The involvement of thiyl radicals in oxidation of captopril competes with a nonradical pathway involving 2-electron oxidations of the sulfur center. The oxidation product of captopril under these strong oxidizing conditions is a sulfonic acid as confirmed by electrospray ionization mass spectrometry (ESI-MS), iodometric titrations, and proton nuclear magnetic resonance ((1)H NMR) results. There was no evidence from ESI-MS for the formation of the sulfenic and sulfinic acids in the oxidation pathway as the thiol group is rapidly oxidized to the sulfonic acid. A computer simulation analysis of

  3. Bromine measurements in ozone depleted air over the Arctic Ocean

    Directory of Open Access Journals (Sweden)

    J. A. Neuman

    2010-07-01

    Full Text Available In situ measurements of ozone, photochemically active bromine compounds, and other trace gases over the Arctic Ocean in April 2008 are used to examine the chemistry and geographical extent of ozone depletion in the arctic marine boundary layer (MBL. Data were obtained from the NOAA WP-3D aircraft during the Aerosol, Radiation, and Cloud Processes affecting Arctic Climate (ARCPAC study and the NASA DC-8 aircraft during the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS study. Fast (1 s and sensitive (detection limits at the low pptv level measurements of BrCl and BrO were obtained from three different chemical ionization mass spectrometer (CIMS instruments, and soluble bromide was measured with a mist chamber. The CIMS instruments also detected Br2. Subsequent laboratory studies showed that HOBr rapidly converts to Br2 on the Teflon instrument inlets. This detected Br2 is identified as active bromine and represents a lower limit of the sum HOBr + Br2. The measured active bromine is shown to likely be HOBr during daytime flights in the arctic. In the MBL over the Arctic Ocean, soluble bromide and active bromine were consistently elevated and ozone was depleted. Ozone depletion and active bromine enhancement were confined to the MBL that was capped by a temperature inversion at 200–500 m altitude. In ozone-depleted air, BrO rarely exceeded 10 pptv and was always substantially lower than soluble bromide that was as high as 40 pptv. BrCl was rarely enhanced above the 2 pptv detection limit, either in the MBL, over Alaska, or in the arctic free troposphere.

  4. Occurrence of bromine in fluidised bed combustion of solid recovered fuel

    Energy Technology Data Exchange (ETDEWEB)

    Vainikka, P.

    2011-12-15

    Corrosive ash species are the single most important factor limiting the electric efficiency of steam boiler plants fired with waste or biomass. Chlorine has been found to have a central role in the chemistry involved as it reduces the melting temperature of ash, forms corrosive vapour and gas species in the furnace and halogenated deposits on boiler heat transfer surfaces. In this context chlorine has been extensively researched. At the time of writing this thesis there was hardly any published data available on the occurrence of bromine (Br) in the aforementioned context. The objective of this work was to review the occurrence of bromine in solid fuels and characterise the behaviour of bromine in full-scale fluidised bed combustion. The review on the occurrence of bromine in solid fuels revealed that in anthropogenic wastes bromine is mainly found in connection to flame retarded substances. Several weight percentages of bromine can be found in plastics treated with brominated flame retardants (BFRs). Bromine is typically found some 100-200 mg kg-1 in mixed municipal solid wastes (MSW). Bromine may be enriched in fuels with high share of plastics, such as solid recovered fuel (SRF) or refuse derived fuel (RDF). Up to 2000 mg kg-1 was found as a monthly average in SRF, typical levels being 20-200 mg kg-1. Wastewater sludge from paper mills may contain bromine 20-100 mg kg-1 due the use of bromine based biocides. In other fuels bromine may be found in significant amounts in marine influenced coal deposits and peat as well as in biomass treated with brominated pesticides. In the experimental part SRF, spruce bark and wastewater sludge from a paper mill were co-fired in a full- scale bubbling fluidised bed (BFB) boiler, and the collected fuels, aerosols and waterwall deposits were analysed with the focus on the fate of bromine. Bromine was mainly found to form water soluble high vapour pressure alkali metal halides in the furnace - in the form of KBr(g) and NaBr(g) as

  5. Rapid identification of polystyrene foam wastes containing hexabromocyclododecane or its alternative polymeric brominated flame retardant by X-ray fluorescence spectroscopy.

    Science.gov (United States)

    Schlummer, Martin; Vogelsang, Jörg; Fiedler, Dominik; Gruber, Ludwig; Wolz, Gerd

    2015-07-01

    The brominated flame retardant hexabromocyclododecane (HBCDD) was added to Annex A of the list of persistent organic pollutants (POPs) of the Stockholm Convention. Thus, production and use of HBCDD will be banned, and the recycling of HBCDD-containing foam waste will be restricted. In reaction a special polymeric brominated flame retardant (PolyFR) was developed to replace HBCDD in expanded and extruded polystyrene foams for building and construction applications. A decision has to be made at some future time whether expanded and extruded polystyrene foam waste is to be subjected to incineration (with HBCDD) or to recycling (without HBCDD). Therefore, an appropriate and rapid field method is required to distinguish between foams containing HBCDD and foams free from HBCDD. Here we present a screening method for identifying HBCDD containing expanded and extruded polystyrene foams. The test principle is based on the fact that PolyFR (a brominated polymeric macromolecule) is not extractable whereas HBCDD (a low molecular weight substance) is extractable. Following rapid extraction of HBCDD the brominated flame retardant is identified and quantified via bromine analysis using a handheld X-ray fluorescence instrument. The method was applied successfully to 27 expanded and extruded polystyrene foam samples (foams and extruded polystyrene foam raw materials), which were provided without any information about the applied flame retardant. The presence of HBCDD was confirmed for all HBCDD-positive samples in the test. A robustness test revealed a high degree of correctness and a high repeatability for the test system: samples containing HBCDD and HBCDD-free samples were identified correctly with relative standard deviations of quantitative results below 14%. Moreover, X-ray fluorescence spectroscopy test results agree well with HBCDD determinations performed in a laboratory with a gas chromatograph coupled to a flame ionisation detector. © The Author(s) 2015.

  6. Windows 8.1 bible

    CERN Document Server

    Boyce, Jim; Tidrow, Rob

    2014-01-01

    Windows 8.1 coverage that goes above and beyond all competitors? Serving as an evolutionary update to Windows 8, Windows 8.1 provides critical changes to parts of Windows 8, such as greater customization of the interface and boot operations, return of a 'start button' that reveals apps, greater integration between the two interfaces, and updates to apps. Weighing in at nearly 1000 pages, Windows 8.1 Bible provides deeper Windows insight than any other book on the market. It's valuable for both professionals needing a guide to the nooks and crannies of Windows and regular users wanting a wide

  7. Sodium, Iodine and Bromine in Polar Ice Cores

    DEFF Research Database (Denmark)

    Maffezzoli, Niccolo

    back trajectory analyses of the past 17 years. The results identify the aerosol source area influencing the Renland ice cap, a result necessary for the interpretation of impurity records obtained from the ice core. Chapter 6 reviews the published ice/snow measurements of bromine and iodine at polar......Abstract: This research focuses on sodium, bromine and iodine in polar ice cores, with the aim of reviewing and advancing their current understanding with additional measurements and records, and investigating the connections of these tracers with sea ice and their feasibility as sea ice indicators....... Modern Arctic sea ice decline clearly yields further motivation in this direction, as the reconstruction of past sea ice conditions could provide clues to the mechanisms in play nowadays and in the future projections. Inductively Coupled Plasma Mass Spectroscopy (ICP-MS) has been applied...

  8. Specific heat of pristine and brominated graphite fibers, composites and HOPG. [Highly Oriented Pyrolytic Graphite

    Science.gov (United States)

    Hung, Ching-Chen; Maciag, Carolyn

    1987-01-01

    Differential scanning calorimetry was used to obtain specific heat values of pristine and brominated P-100 graphite fibers and brominated P-100/epoxy composite as well as pristine and brominated highly oriented pyrolytic graphite (HOPG) for comparison. Based on the experimental results obtained, specific heat values are calculated for several different temperatures, with a standard deviation estimated at 1.4 percent of the average values. The data presented here are useful in designing heat transfer devices (such as airplane de-icing heaters) from bromine fibers.

  9. Sonogashira–Hagihara reactions of halogenated glycals

    Directory of Open Access Journals (Sweden)

    Dennis C. Koester

    2012-05-01

    Full Text Available Herein, we report on our findings of the Sonogashira–Hagihara reaction with 1-iodinated and 2-brominated glycals using several aromatic and aliphatic alkynes. This Pd-catalyzed cross-coupling reaction presents a facile access to alkynyl C-glycosides and sets the stage for a reductive/oxidative refunctionalization of the enyne moiety to regenerate either C-glycosidic structures or pyran derivatives with a substituent in position 2.

  10. Robust flow-batch coulometric/biamperometric titration system: determination of bromine index and bromine number of petrochemicals.

    Science.gov (United States)

    Pasquini, Celio; de Aquino, Emerson Vidal; das Virgens Reboucas, Marcio; Gonzaga, Fabiano Barbieri

    2007-09-26

    A flow-batch system was constructed and evaluated to perform coulometric titrations with biamperometric end point detection. The flow section of the system is employed for sampling by injecting a sample volume (50-300 microL) in a flow injection-like system. About 1.5 mL of a suitable carrier solution is delivered by a peristaltic pump in order to quantitatively transfer the sample to the system titration cell (2.0 mL total inner volume). The carrier contains the coulometric precursor for the titrant species. The cell contains two pairs of platinum electrodes used for coulometric generation of reagent and biamperometric detection and is actively stirred. The titrant species is generated and the titration is performed by the usual batch procedure with the excess of titrant being detected by biamperometry following the analysis of the titration curve. System operation is computer controlled and all operations are automated, including titration curve analysis and cell cleaning after the titration is ended. The system is characterized by its robustness because its operation does not depend on flow rates, and the work using coulometric methods which generate gases at the counter-electrode is not troublesome. The flow-batch system has been evaluated for determination of bromine index and bromine number (relative to the total reactive olefin content) in petrochemicals according to an ASTM procedure. Typical precision (R.S.D.) is between 0.5 and 6% for different petrochemicals whose bromine number/index vary from 1000 to 10mg of bromine per 100g of sample, respectively. Recoveries for standard additions are between 92 and 123% for 10mg of Br(2) per 100g increments and 98 to 101% for 100mg per 100g increments. Accuracy of the proposed system was evaluated against results obtained by the standard ASTM with no significant difference detected at 95% confidence level.

  11. Global atmospheric model for mercury including oxidation by bromine atoms

    Directory of Open Access Journals (Sweden)

    C. D. Holmes

    2010-12-01

    Full Text Available Global models of atmospheric mercury generally assume that gas-phase OH and ozone are the main oxidants converting Hg0 to HgII and thus driving mercury deposition to ecosystems. However, thermodynamic considerations argue against the importance of these reactions. We demonstrate here the viability of atomic bromine (Br as an alternative Hg0 oxidant. We conduct a global 3-D simulation with the GEOS-Chem model assuming gas-phase Br to be the sole Hg0 oxidant (Hg + Br model and compare to the previous version of the model with OH and ozone as the sole oxidants (Hg + OH/O3 model. We specify global 3-D Br concentration fields based on our best understanding of tropospheric and stratospheric Br chemistry. In both the Hg + Br and Hg + OH/O3 models, we add an aqueous photochemical reduction of HgII in cloud to impose a tropospheric lifetime for mercury of 6.5 months against deposition, as needed to reconcile observed total gaseous mercury (TGM concentrations with current estimates of anthropogenic emissions. This added reduction would not be necessary in the Hg + Br model if we adjusted the Br oxidation kinetics downward within their range of uncertainty. We find that the Hg + Br and Hg + OH/O3 models are equally capable of reproducing the spatial distribution of TGM and its seasonal cycle at northern mid-latitudes. The Hg + Br model shows a steeper decline of TGM concentrations from the tropics to southern mid-latitudes. Only the Hg + Br model can reproduce the springtime depletion and summer rebound of TGM observed at polar sites; the snowpack component of GEOS-Chem suggests that 40% of HgII deposited to snow in the Arctic is transferred to the ocean and land reservoirs, amounting to a net deposition flux to the Arctic of 60 Mg a−1. Summertime events of depleted Hg0 at Antarctic sites due to subsidence are much better simulated by

  12. Beginning Windows 8.1

    CERN Document Server

    Halsey, Mike

    2013-01-01

    Windows 8 has been described by Microsoft as its 'boldest' Windows release ever and the 8.1 update enhances the paradigm further. Beginning Windows 8.1 takes you through the new features and helps you get more out of the familiar to reveal the fullest possibilities for this amazing new operating system. You will learn, with non-technical language used throughout, how to get up and running in the new Windows interface, minimize downtime, maximize productivity, and harness the features you never knew existed to take control of your computer and enjoy the peace of mind and excitement that comes w

  13. Formation of brominated phenolic contaminants from natural manganese oxides-catalyzed oxidation of phenol in the presence of Br(.).

    Science.gov (United States)

    Lin, Kunde; Song, Lianghui; Zhou, Shiyang; Chen, Da; Gan, Jay

    2016-07-01

    Brominated phenolic compounds (BPCs) are a class of persistent and potentially toxic compounds ubiquitously present in the aquatic environment. However, the origin of BPCs is not clearly understood. In this study, we investigated the formation of BPCs from natural manganese oxides (MnOx)-catalyzed oxidation of phenol in the presence of Br(-). Experiments at ambient temperature clearly demonstrated that BPCs were readily produced via the oxidation of phenol by MnOx in the presence of Br(-). In the reaction of MnOx sand with 0.213 μmol/L phenol and 0.34 mmol/L Br(-) for 10 min, more than 60% of phenol and 56% of Br(-) were consumed to form BPCs. The yield of BPCs increased with increasing concentrations of phenol and Br(-). Overall, a total of 14 BPCs including simple bromophenols (4-bromophenol, 2,4-dibromophenol, and 2,4,6-tribromophenol), hydroxylated polybrominated diphenyl ethers (OH-PBDEs), and hydroxylated polybrominated biphenyls (OH-PBBs) were identified. The production of BPCs increased with increasing concentrations of Br(-) or phenol. It was deduced that Br(-) was first oxidized to form active bromine, leading to the subsequent bromination of phenol to form bromophenols. The further oxidation of bromophenols by MnOx resulted in the formation of OH-PBDEs and OH-PBBs. In view of the ubiquity of phenol, Br(-), and MnOx in the environment, MnOx-mediated oxidation may play a role on the natural production of BPCs. Copyright © 2016 Elsevier Ltd. All rights reserved.

  14. High-performance zinc bromine flow battery via improved design of electrolyte and electrode

    Science.gov (United States)

    Wu, M. C.; Zhao, T. S.; Jiang, H. R.; Zeng, Y. K.; Ren, Y. X.

    2017-07-01

    The zinc bromine flow battery (ZBFB) is regarded as one of the most promising candidates for large-scale energy storage attributed to its high energy density and low cost. However, it suffers from low power density, primarily due to large internal resistances caused by the low conductivity of electrolyte and high polarization in the positive electrode. In this work, chloride based salts including KCl and NH4Cl are investigated as supporting electrolyte to enhance electrolyte conductivity, while graphite-felt electrodes are thermally treated to improve electrocatalytic activity. It is found that the use of 4 M NH4Cl as a supporting electrolyte enables the battery to be operated at a current density of 40 mA cm-2 with an energy efficiency of 74.3%, whereas without the addition of a supporting electrolyte the battery only outputs an energy efficiency of 60.4%. In combination with a thermally treated graphite-felt electrode, efficiency further reaches up to 81.8% at the same current density. More impressively, we demonstrate that even at a high current density of up to 80 mA cm-2, the battery is capable of delivering an energy efficiency of 70%, representing one of the highest performances of ZBFBs in the open literature.

  15. Mercury oxidation from bromine chemistry in the free troposphere over the southeastern US

    Directory of Open Access Journals (Sweden)

    S. Coburn

    2016-03-01

    Breeze. The column integral oxidation rates are about 3.6  × 105 molec cm−2 s−1 for bromine, while the contribution from ozone (O3 is 0.8  ×  105 molec cm−2 s−1. Chlorine-induced oxidation is estimated to add  <  5 % to these mercury oxidation rates. The GOM formation rate is sensitive to recently proposed atmospheric scavenging reactions of the HgBr adduct by nitrogen dioxide (NO2, and to a lesser extent also HO2 radicals. Using a 3-D CTM, we find that surface GOM variations are also typical of other days, and are mainly derived from the FT. Bromine chemistry is active in the FT over Gulf Breeze, where it forms water-soluble GOM that is subsequently available for wet scavenging by thunderstorms or transport to the boundary layer.

  16. Distribution of bromine in mixed iodide-bromide organolead perovskites and its impact on photovoltaic performance

    NARCIS (Netherlands)

    Zhou, Yang; Wang, Feng; Fang, Hong-Hua; Loi, Maria Antonietta; Xie, Fang-Yan; Zhao, Ni; Wong, Ching-Ping

    2016-01-01

    Mixed iodide-bromide (I-Br) organolead perovskites are of great interest for both single junction and tandem solar cells since the optical bandgap of the materials can be tuned by varying the bromine to iodine ratio. Yet, it remains unclear how bromine incorporation modifies the properties of the

  17. Bromination of Benzonorbornadiene Using a Mixture of Sodium Bromide and Sodium Perborate at High Temperatures

    OpenAIRE

    Şenocak, Erdal; Yavuz TAŞKESENLİGİL

    2014-01-01

    Bromination of benzonorbornadiene (1) with sodium bromide in the presence of sodium perborate at room temperature gave only one product, the dibromide 2 produced via Wagner-Meerwein rearrangement. However, at high temperatures, bromination resulted predominantly in the formation of rearranged solvolytic products whose formation mechanisms are discussed.

  18. DOAS measurements of tropospheric bromine oxide in mid-latitudes

    Science.gov (United States)

    Hebestreit; Stutz; Rosen; Matveiv; Peleg; Luria; Platt

    1999-01-01

    Episodes of elevated bromine oxide (BrO) concentration are known to occur at high latitudes in the Arctic boundary layer and to lead to catalytic destruction of ozone at those latitudes; these events have not been observed at lower latitudes. With the use of differential optical absorption spectroscopy (DOAS), locally high BrO concentrations were observed at mid-latitudes at the Dead Sea, Israel, during spring 1997. Mixing ratios peaked daily at around 80 parts per trillion around noon and were correlated with low boundary-layer ozone mixing ratios.

  19. Highly brominated antimicrobial metabolites from a marine Pseudoalteromonas sp.

    Science.gov (United States)

    Fehér, Domonkos; Barlow, Russell; McAtee, Jesse; Hemscheidt, Thomas K

    2010-11-29

    Extracts of a marine Pseudoalteromonas sp. (CMMED 290) isolated from the surface of a nudibranch collected in Kaneohe Bay, Oahu, displayed significant antimicrobial activity against methicillin-resistant Staphylococcus aureus. Bioassay-guided fractionation of the lipophilic extract led to the isolation and structure elucidation of two new highly brominated compounds, 2,3,5,7-tetrabromobenzofuro[3,2-b]pyrrole (1) and 4,4',6-tribromo-2,2'-biphenol (2). In addition, we have identified the known compounds pentabromopseudilin and bromophene. We describe the isolation and structure elucidation of the compounds 1 and 2 together with their antimicrobial activities against methicillin-resistant Staphylococcus aureus.

  20. Theoretical performance of hydrogen-bromine rechargeable SPE fuel cell

    Science.gov (United States)

    Savinell, Robert F.; Fritts, S. D.

    1987-01-01

    A mathematical model was formulated to describe the performance of a hydrogen-bromine fuel cell. Porous electrode theory was applied to the carbon felt flow-by electrode and was coupled to theory describing the solid polymer electrolyte (SPE) system. Parametric studies using the numerical solution to this model were performed to determine the effect of kinetic, mass transfer, and design parameters on the performance of the fuel cell. The results indicate that the cell performance is most sensitive to the transport properties of the SPE membrane. The model was also shown to be a useful tool for scale-up studies.

  1. Pollution of Lake Mjoesa by brominated flame retardants

    Energy Technology Data Exchange (ETDEWEB)

    Schlabach, M.; Gundersen, H.; Mariussen, E. [NILU, Kjeller (Norway); Fjeld, E.; Breivik, E. [NIVA, Oslo (Norway); Kjellberg, G. [NIVA, Hamar (Norway)

    2004-09-15

    The worldwide use of brominated flame retardants (BFRs) is extensive and there are significant release of these components to the environment. The last twenty years the levels of the polybrominated diphenyl ethers (PBDE) in biota have increased, and in some areas the levels are comparable or even higher to what is reported for the polychlorinated biphenyls (PCB). This study was focused on the pollution of PBDEs in Lake Mjoesa, where unusually high concentrations have been found in fish. The objective of this part of the survey was to make a broader documentation of the PBDE levels in sediments and fish, and to localize areas with point sources of PBDEs.

  2. Future chlorine-bromine loading and ozone depletion

    Science.gov (United States)

    Prather, Michael J.; Ibrahim, Abdel Moneim; Sasaki, Toru; Stordal, Frode; Visconti, Guido

    1991-01-01

    The prediction of future ozone requires three elements: (1) a scenario for the net emissions of chemically and radiatively active trace gases from the land and oceans; (2) a global atmospheric model that projects the accumulation of these gases; and (3) a chemical transport model that describes the distribution of ozone for a prescribed atmospheric composition and climate. This chapter, of necessity, presents models for all three elements and focuses on the following: (1) atmospheric abundance of chlorine and bromine in the form of halocarbons; and (2) the associated perturbations to stratospheric ozone.

  3. Impact of reactive bromine chemistry in the troposphere

    Directory of Open Access Journals (Sweden)

    R. von Glasow

    2004-01-01

    Full Text Available Recently several field campaigns and satellite observations have found strong indications for the presence of bromine oxide (BrO in the free troposphere. Using a global atmospheric chemistry transport model we show that BrO mixing ratios of a few tenths to 2 pmol mol-1 lead to a reduction in the zonal mean O3 mixing ratio of up to 18% in widespread areas and regionally up to 40% compared to a model run without bromine chemistry. A lower limit approach for the marine boundary layer, that does not explicitly include the release of halogens from sea salt aerosol, shows that for dimethyl sulfide (DMS the effect is even larger, with up to 60% reduction of its tropospheric column. This is accompanied by dramatic changes in DMS oxidation pathways, reducing its cooling effect on climate. In addition there are changes in the HO2:OH ratio that also affect NOx and PAN. These results imply that potentially significant strong sinks for O3 and DMS have so far been ignored in many studies of the chemistry of the troposphere.

  4. Algae form brominated organic compounds in surface waters

    Energy Technology Data Exchange (ETDEWEB)

    Huetteroth, A.; Putschew, A.; Jekel, M. [Tech. Univ. Berlin (Germany)

    2004-09-15

    Monitoring of organic halogen compounds, measured as adsorbable organic bromine (AOBr) revealed seasonal high concentrations of organic bromine compounds in a surface water (Lake Tegel, Berlin, Germany). Usually, in late summer, concentrations are up to five times higher than during the rest of the year. The AOBr of the lake inflows (throughout the year less then 6 {mu}g/L) were always lower then those in the lake, which indicates a production of AOBr in the lake. A correlation of the AOBr and chlorophyll-a concentration (1) in the lake provides first evidence for the influence of phototrophic organisms. The knowledge of the natural production of organohalogens is relatively recent. Up to now there are more then 3800 identified natural organohalogen compounds that have been detected in marine plants, animals, and bacteria and also in terrestrial plants, fungi, lichen, bacteria, insects, some higher animals, and humans. Halogenated organic compounds are commonly considered to be of anthropogenic origin; derived from e.g. pharmaceuticals, herbicides, fungicides, insecticides, flame retardants, intermediates in organic synthesis and solvents. Additionally they are also produced as by-products during industrial processes and by waste water and drinking water disinfection. Organohalogen compounds may be toxic, persistent and/or carcinogenic. In order to understand the source and environmental relevance of naturally produced organobromine compounds in surface waters, the mechanism of the formation was investigated using batch tests with lake water and algae cultures.

  5. On the DFT ground state of crystalline bromine and iodine.

    Science.gov (United States)

    George, Janine; Reimann, Christoph; Deringer, Volker L; Bredow, Thomas; Dronskowski, Richard

    2015-03-16

    We report on an erroneous ground state within common density functional theory (DFT) methods for the solid elements bromine and iodine. Phonon computations at the GGA level for both molecular crystals yield imaginary vibrational modes, erroneously indicating dynamic instability-that fact alone could easily pass as a computational artefact, but these imaginary modes lead to energetically more favorable and dynamically stable structures, made up of infinite monoatomic chains. In contrast, meta-GGA and hybrid functionals yield the correct energetic order for bromine, while for iodine, most global hybrids do not improve the GGA result significantly. The qualitatively correct answer, in both cases, is given by the long-range corrected hybrid LC-ωPBE, the Minnesota functionals M06L and M06, and by periodic Hartree-Fock and MP2 theory. This poor performance of economic DFT functionals should be kept in mind, for example, during global structure optimizations of systems with significant contributions from halogen bonds. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Characterization of vanadium bromoperoxidase from Macrocystis and Fucus: reactivity of vanadium bromoperoxidase toward acyl and alkyl peroxides and bromination of amines.

    Science.gov (United States)

    Soedjak, H S; Butler, A

    1990-08-28

    Vanadium bromoperoxidase (V-BrPO) has been isolated and purified from the marine brown algae Fucus distichus and Macrocystis pyrifera. V-BrPO catalyzes the oxidation of bromide by hydrogen peroxide, resulting in the bromination of certain organic acceptors or the formation of dioxygen. V-BrPO from F. distichus and M. pyrifera have subunit molecular weights of 65,000 and 74,000, respectively, and specific activities of 1580 units/mg (pH 6.5) and 1730 units/mg (pH 6) for the bromination of monochlorodimedone, respectively. As isolated, the enzymes contain a substoichiometric vanadium/subunit ratio; the vanadium content and specific activity are increased by addition of vanadate. V-BrPO (F. distichus, M. pyrifera, and Ascophyllum nodosum) also catalyzes the oxidation of bromide using peracetic acid. In the absence of an organic acceptor, a mixture of oxidized bromine species (e.g., hypobromous acid, bromine, and tribromide) is formed. Bromamine derivatives are formed from the corresponding amines, while 5-bromocytosine is formed from cytosine. In all cases, the rate of the V-BrPO-catalyzed reaction is much faster than that of the uncatalyzed oxidation of bromide by peracetic acid, at pH 8.5, 1 mM bromide, and 2 mM peracetic acid. In contrast to hydrogen peroxide, V-BrPO does not catalyze formation of dioxygen from peracetic acid in either the presence or absence of bromide. V-BrPO also uses phenylperacetic acid, m-chloroperoxybenzoic acid, and p-nitroperoxybenzoic acid to catalyze the oxidation of bromide; dioxygen is not formed with these peracids. V-BrPO does not catalyze bromide oxidation or dioxygen formation with the alkyl peroxides ethyl hydroperoxide, tert-butyl hydroperoxide, and cuminyl hydroperoxide.

  7. 40 CFR 81.336 - Ohio.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Ohio. 81.336 Section 81.336 Protection... AREAS FOR AIR QUALITY PLANNING PURPOSES Section 107 Attainment Status Designations § 81.336 Ohio. Ohio... affecting § 81.336, see the List of CFR Sections Affected, which appears in the Finding Aids section of the...

  8. Brominated VSLS and their influence on ozone under a changing climate

    Directory of Open Access Journals (Sweden)

    S. Falk

    2017-09-01

    Full Text Available Very short-lived substances (VSLS contribute as source gases significantly to the tropospheric and stratospheric bromine loading. At present, an estimated 25 % of stratospheric bromine is of oceanic origin. In this study, we investigate how climate change may impact the ocean–atmosphere flux of brominated VSLS, their atmospheric transport, and chemical transformations and evaluate how these changes will affect stratospheric ozone over the 21st century. Under the assumption of fixed ocean water concentrations and RCP6.0 scenario, we find an increase of the ocean–atmosphere flux of brominated VSLS of about 8–10 % by the end of the 21st century compared to present day. A decrease in the tropospheric mixing ratios of VSLS and an increase in the lower stratosphere are attributed to changes in atmospheric chemistry and transport. Our model simulations reveal that this increase is counteracted by a corresponding reduction of inorganic bromine. Therefore the total amount of bromine from VSLS in the stratosphere will not be changed by an increase in upwelling. Part of the increase of VSLS in the tropical lower stratosphere results from an increase in the corresponding tropopause height. As the depletion of stratospheric ozone due to bromine depends also on the availability of chlorine, we find the impact of bromine on stratospheric ozone at the end of the 21st century reduced compared to present day. Thus, these studies highlight the different factors influencing the role of brominated VSLS in a future climate.

  9. STS-81 Flight Day 6

    Science.gov (United States)

    1997-01-01

    On this sixth day of the STS-81 mission, the flight crew, Cmdr. Michael A. Baker, Pilot Brent W. Jett, Mission Specialists, John M. Grunsfeld, Marsha S. Ivins, Peter J.K. Wisoff, and John Blaha, and the cosmonauts of the Mir Space Station continue to transfer hundreds of pounds of food, water and supplies between each other's spacecraft for a third day. Jerry M. Linenger spent several hours continuing to familiarize himself with his new orbital home, unpacking experiment hardware and helping astronaut John Blaha transfer biomedical samples back to Atlantis for Blaha's trip back to Earth. Blaha is wrapping up his four-month tour of duty in space.

  10. Chlorine and Bromine Isotope Fractionation of Halogenated Organic Compounds in Electron Ionization Mass Spectrometry

    OpenAIRE

    Tang, Caiming; Tan, Jianhua; Shi, Zhiqiang; Tang, Caixing; Xiong, Songsong; Liu, Jun; Fan, Yujuan; Peng, Xianzhi

    2017-01-01

    Revelation of chlorine and bromine isotope fractionation of halogenated organic compounds (HOCs) in electron ionization mass spectrometry (EI-MS) is crucial for compound-specific chlorine/bromine isotope analysis (CSIA-Cl/Br) using gas chromatography EI-MS (GC-EI-MS). This study systematically investigated chlorine/bromine isotope fractionation in EI-MS of HOCs including 12 organochlorines and 5 organobromines using GC-double focus magnetic-sector high resolution MS (GC-DFS-HRMS). Chlorine/br...

  11. STS-81 Flight Day 4

    Science.gov (United States)

    1997-01-01

    On this fourth day of the STS-81 mission, the flight crew, Cmdr. Michael A. Baker, Pilot Brent W. Jett, Mission Specialists, John M. Grunsfeld, Marsha S. Ivins, Peter J.K. Wisoff, and Jerry M. Linenger, prepare for the fifth linkup of the Space Shuttle and the Mir Space Station. The Atlantis docks with Mir at a point 210 nautical miles above the Earth southeast of Moscow, culminating a three-day rendezvous. Two hours after docking, the hatches between Atlantis and Mir are opened and Baker and Mir 22 Commander Valery Korzun share a hug to mark the start of five days of joint operations between the two crews. After an informal welcoming ceremony in the Mir's core module, the STS-81 crewmembers receive a station safety briefing. Linenger becomes the fourth American to occupy a position on the Russian Space Station following the docking of Atlantis to the outpost. During the docked phase of the mission, the two crews transfer nearly three tons of food, water and supplies to Mir.

  12. A Practical Recycle of a Ligand-Free Palladium Catalyst for Heck Reactions

    NARCIS (Netherlands)

    Vries, André H.M. de; Parlevliet, Floris J.; Schmieder-van de Vondervoort, Lizette; Mommers, John H.M.; Henderickx, Huub J.W.; Walet, Monique A.M.; Vries, Johannes G. de

    2002-01-01

    Ligand-free palladium can be recovered almost quantitatively from Heck reaction mixtures by filtration after its deposition on a carrier such as silica or celite. Subsequently, it is re-activated to its original activity by adding a small amount of iodine or bromine prior to the next reaction cycle.

  13. Indium(III)-catalyzed reductive bromination and iodination of carboxylic acids to alkyl bromides and iodides: scope, mechanism, and one-pot transformation to alkyl halides and amine derivatives.

    Science.gov (United States)

    Moriya, Toshimitsu; Yoneda, Shinichiro; Kawana, Keita; Ikeda, Reiko; Konakahara, Takeo; Sakai, Norio

    2013-11-01

    Highly effective indium(III)-catalyzed reductive bromination or iodination of a variety of carboxylic acids with 1,1,3,3-tetramethyldisiloxane (TMDS) and a source of bromine or iodine is described. This functional group interconversion has high tolerance for several functional groups, such as halogens, a hydroxy group, a nitro group, an olefin part, and a sulfide moiety. This indium catalytic system is also applicable to the reductive iodination of aldehyded, acyl chlorides, and esters. Furthermore, this reducing system can be applied to the one-pot synthesis of alkyl halides and amine derivatives via the addition of nucleophiles. Insight into the reaction mechanism was gained via the time course of (1)H and (13)C NMR monitoring experiments and the corresponding stepwise reactions.

  14. One-electron reduction of N-chlorinated and N-brominated species is a source of radicals and bromine atom formation.

    Science.gov (United States)

    Pattison, David I; O'Reilly, Robert J; Skaff, Ojia; Radom, Leo; Anderson, Robert F; Davies, Michael J

    2011-03-21

    Hypochlorous (HOCl) and hypobromous (HOBr) acids are strong bactericidal oxidants that are generated by the human immune system but are implicated in the development of many human inflammatory diseases (e.g., atherosclerosis, asthma). These oxidants react readily with sulfur- and nitrogen-containing nucleophiles, with the latter generating N-halogenated species (e.g., chloramines/bromamines (RR'NX; X = Cl, Br)) as initial products. Redox-active metal ions and superoxide radicals (O(2)(•-)) can reduce N-halogenated species to nitrogen- and carbon-centered radicals. N-Halogenated species and O(2)(•-) are generated simultaneously at sites of inflammation, but the significance of their interactions remains unclear. In the present study, rate constants for the reduction of N-halogenated amines, amides, and imides to model potential biological substrates have been determined. Hydrated electrons reduce these species with k(2) > 10(9) M(-1) s(-1), whereas O(2)(•-) reduced only N-halogenated imides with complex kinetics indicative of chain reactions. For N-bromoimides, heterolytic cleavage of the N-Br bond yielded bromine atoms (Br(•)), whereas for other substrates, N-centered radicals and Cl(-)/Br(-) were produced. High-level quantum chemical procedures have been used to calculate gas-phase electron affinities and aqueous solution reduction potentials. The effects of substituents on the electron affinities of aminyl, amidyl, and imidyl radicals are rationalized on the basis of differential effects on the stabilities of the radicals and anions. The calculated reduction potentials are consistent with the experimental observations, with Br(•) production predicted for N-bromosuccinimide, while halide ion formation is predicted in all other cases. These data suggest that interaction of N-halogenated species with O(2)(•-) may produce deleterious N-centered radicals and Br(•).

  15. Nuclear Data Sheets for A = 81

    Science.gov (United States)

    Baglin, Coral M.

    2008-10-01

    Nuclear structure data pertaining to all nuclei with mass number A = 81 (Zn, Ga, Ge, As, Se, Br, Kr, Rb, Sr, Y, Zr, Nb) have been compiled and evaluated and incorporated into the ENSDF data file. This publication for A = 81 supersedes the previous publication (Coral M. Baglin, Nuclear Data Sheets79, 447 (1996), literature cutoff 1 November 1996) and the subsequent updates by C. Baglin for 81Y (literature cutoff 8 October 1998) and 81Zr (literature cutoff 24 March 2000). All literature available prior to 15 August 2008 has been considered. Subsequent to previous A = 81 evaluations, excited states have been reported for the first time in 81Ga, and knowledge of excited state properties for 81Y and 81Zr has been significantly expanded. However, the expected ɛ+β decay of 81Zr has yet to be studied.

  16. Exposure to brominated trihalomethanes in drinking water and reproductive outcomes.

    Science.gov (United States)

    Patelarou, Evridiki; Kargaki, Sophia; Stephanou, Euripides G; Nieuwenhuijsen, Mark; Sourtzi, Panayota; Gracia, Esther; Chatzi, Leda; Koutis, Anthonis; Kogevinas, Manolis

    2011-06-01

    Exposure to disinfection by-products (DBPs) during pregnancy has been associated with adverse birth outcomes. We evaluated exposure to DBPs through ingestion, inhalation and dermal absorption among pregnant women in Crete, in relation to birth weight and gestational age. The mother-child birth cohort in Crete ('Rhea' study) enrolled 1359 pregnant women at the third month of pregnancy (2007-2008), residents in the prefecture of Heraklion. Exposures were assessed through three questionnaires administered during pregnancy requesting extensive information on personal water-related habits. Tap water samples were collected in representative mother homes on the basis of detailed water distribution patterns, and were analysed for major DBPs including trihalomethanes (THMs). Logistic and linear regression models were applied. Pregnant women reported a high consumption of bottled water at home (76%) and work (96%). More than half the women (59%) washed dishes by hand, nearly all women (94%) took showers rather than baths (1%), and only 2% attended a swimming pool. THM levels were low (<20 μg/l) with a high proportion of brominated compounds. When using quantitative estimates of residential exposure, we found no association with low birth weight (LBW, OR 0.7, 95% CI 0.4 to 1.4), small for gestational age for weight (SGAweight, OR 1.1, 95% CI 0.6 to 2.2) and preterm delivery (OR 0.8, 95% CI 0.5 to 1.3). Similar results were observed when taking into account uptake of THMs through all exposure routes. We found no evidence for an increased risk of LBW, SGA and preterm delivery at the relatively low level exposure to THMs and particularly brominated THMs in Cretan drinking water.

  17. Maternal exposure to brominated flame retardants and infant Apgar scores.

    Science.gov (United States)

    Terrell, Metrecia L; Hartnett, Kathleen P; Lim, Hyeyeun; Wirth, Julie; Marcus, Michele

    2015-01-01

    Brominated flame retardants (BFRs) and other persistent organic pollutants have been associated with adverse health outcomes in humans and may be particularly toxic to the developing fetus. We investigated the association between in utero polybrominated biphenyl (PBB) and polychlorinated biphenyl (PCB) exposures and infant Apgar scores in a cohort of Michigan residents exposed to PBB through contaminated food after an industrial accident. PBB and PCB concentrations were measured in serum at the time the women were enrolled in the cohort. PBB concentrations were also estimated at the time of conception for each pregnancy using a validated elimination model. Apgar scores, a universal measure of infant health at birth, measured at 1 and 5min, were taken from birth certificates for 613 offspring born to 330 women. Maternal PCB concentrations at enrollment were not associated with below-median Apgar scores in this cohort. However, maternal PBB exposure was associated with a dose-related increase in the odds of a below-median Apgar score at 1min and 5min. Among infants whose mothers had an estimated PBB at conception above the limit of detection of 1 part per billion (ppb) to <2.5ppb, the odds ratio=2.32 (95% CI: 1.22-4.40); for those with PBB⩾2.5ppb the OR=2.62 (95% CI: 1.38-4.96; test for trend p<0.01). Likewise, the odds of a below-median 5min Apgar score increased with higher maternal PBB at conception. It remains critical that future studies examine possible relationships between in utero exposures to brominated compounds and adverse health outcomes. Copyright © 2014 Elsevier Ltd. All rights reserved.

  18. Recycling of plastic waste: Screening for brominated flame retardants (BFRs).

    Science.gov (United States)

    Pivnenko, K; Granby, K; Eriksson, E; Astrup, T F

    2017-11-01

    Flame retardants are chemicals vital for reducing risks of fire and preventing human casualties and property losses. Due to the abundance, low cost and high performance of bromine, brominated flame retardants (BFRs) have had a significant share of the market for years. Physical stability on the other hand, has resulted in dispersion and accumulation of selected BFRs in the environment and receiving biota. A wide range of plastic products may contain BFRs. This affects the quality of waste plastics as secondary resource: material recycling may potentially reintroduce the BFRs into new plastic product cycles and lead to increased exposure levels, e.g. through use of plastic packaging materials. To provide quantitative and qualitative data on presence of BFRs in plastics, we analysed bromophenols (tetrabromobisphenol A (TBBPA), dibromophenols (2,4- and 2,6-DBP) and 2,4,6-tribromophenol (2,4,6-TBP)), hexabromocyclododecane stereoisomers (α-, β-, and γ-HBCD), as well as selected polybrominated diphenyl ethers (PBDEs) in samples of household waste plastics, virgin and recycled plastics. A considerable number of samples contained BFRs, with highest concentrations associated with acrylonitrile butadiene styrene (ABS, up to 26,000,000ngTBBPA/g) and polystyrene (PS, up to 330,000ng∑HBCD/g). Abundancy in low concentrations of some BFRs in plastic samples suggested either unintended addition in plastic products or degradation of higher molecular weight BFRs. The presence of currently restricted flame retardants (PBDEs and HBCD) identified in the plastic samples illustrates that circular material flows may be contaminated for extended periods. The screening clearly showed a need for improved documentation and monitoring of the presence of BFRs in plastic waste routed to recycling. Copyright © 2017 Elsevier Ltd. All rights reserved.

  19. STS-81 Flight Day 5

    Science.gov (United States)

    1997-01-01

    On this fifth day of the STS-81 mission, the flight crew, Cmdr. Michael A. Baker, Pilot Brent W. Jett, Mission Specialists, John M. Grunsfeld, Marsha S. Ivins, Peter J.K. Wisoff, and John Blaha, and the Mir cosmonauts including astronaut Jerry M. Linenger continue with the transfer of food, water and supplies between the two spacecrafts for a second day of joint operations. With both spacecraft in excellent shape, the nine crewmembers float back and forth between Atlantis and the Mir, hauling bags of water, satchels of logistical supplies and experiment hardware. The supplies and hardware will be used by cosmonauts and Linenger during his four months of scientific research aboard the Mir. Linenger, who officially became a Mir crewmember earlier, spends time with his precedessor; John Blaha to get familiar with his new home.

  20. Some aspects of bromine determination by ICP-OES in salinated waters

    Energy Technology Data Exchange (ETDEWEB)

    Mitko, K.; Bebek, M. [General Mining Inst., Katowice (Poland). Dept. of Environmental Monitoring

    2004-04-01

    An alternative to the manual iodometric titration method for the analysis of sum bromide and free bromine in water is presented. It uses continuous-flow on-line oxidation of bromide in a mixed acid medium and an ICP-OES instrument, equipped with an axial view of the argon plasma as the detector. Some problems and practical aspects of this method are discussed. Due to the availability of only one weak spectral line of bromine (700.52 nm) in the instrument used in this study, the detection limit obtained is relatively high (2 mg/L) but suitable for the analysis of salinated waters originating in the Silesian coal mines. Accuracy and precision is in the range of 10% when the bromine concentration is about 5 times higher than the detection limit. The power of this method can be easily and to a large degree improved using the 163-nm bromine spectral line.

  1. MLS/Aura Level 2 Bromine Monoxide (BrO) Mixing Ratio V004

    Data.gov (United States)

    National Aeronautics and Space Administration — ML2BRO is the EOS Aura Microwave Limb Sounder (MLS) standard product for bromine monoxide derived from radiances measured by the 640 GHz radiometer. The current...

  2. MLS/Aura L2 Bromine Monoxide (BRO) Mixing Ratio V002

    Data.gov (United States)

    National Aeronautics and Space Administration — ML2BRO is the EOS Aura Microwave Limb Sounder (MLS) standard product for bromine monoxide derived from radiances measured by the 640 GHz radiometer. The current...

  3. MLS/Aura L2 Bromine Monoxide (BRO) Mixing Ratio V003

    Data.gov (United States)

    National Aeronautics and Space Administration — ML2BRO is the EOS Aura Microwave Limb Sounder (MLS) standard product for bromine monoxide derived from radiances measured by the 640 GHz radiometer. The current...

  4. Evaluation of carbon cryogels used as cathodes for non-flowing zinc-bromine storage cells

    Energy Technology Data Exchange (ETDEWEB)

    Ayme-Perrot, David; Walter, Serge; Gabelica, Zelimir [Groupe Securite et Ecologie Chimiques (GSEC), ENSCMu, 3 rue Alfred Werner, F-68093 Mulhouse Cedex (France); Valange, Sabine [Laboratoire de Catalyse en Chimie Organique (LACCO), ESIP, 40 Avenue du Recteur Pineau, F-86022 Poitiers Cedex (France)

    2008-01-03

    Monolithic megaloporous carbon cryogels were examined for their potential applications as cathodic electrodes in secondary zinc-bromine cells. This work investigates the possibility of using their particular macroporous texture as microscopic bromine tanks in a zinc/bromine battery. The electrochemical behaviour of a cell based upon such a Br{sub 2} electrode was studied and discussed in terms of energy yields, energy storage capability and cycle life. Good storages (over 20 Wh kg{sup -1}) could be obtained during the first 2 h of cell charging for currents between 10 and 20 mA g{sup -1}. The energy yield remains almost constant during a fairly large number of cycles, basically for weak charges (e.g. 25 C g{sup -1}). Our findings show that the good cyclability of the cathodic electrode is a consequence of the liquid state of the active bromine phase. (author)

  5. Molecular dynamics simulations and thermochemistry of reactive ion etching of silicon by chlorine, chlorine dimer, bromine, and bromine dimer cations

    Energy Technology Data Exchange (ETDEWEB)

    Valone, S.M.; Hanson, D.E.; Kress, J.D.

    1998-05-08

    Simulations of Cl plasma etch of Si surfaces with MD techniques agree reasonably well with the available experimental information on yields and surface morphologies. This information has been supplied to a Monte Carlo etch profile resulting in substantial agreement with comparable inputs provided through controlled experiments. To the extent that more recent measurements of etch rates are more reliable than older ones, preliminary MD simulations using bond-order corrections to the atomic interactions between neighboring Si atoms on the surface improves agreement with experiment through an increase in etch rate and improved agreement with XPS measurements of surface stoichiometry. Thermochemical and geometric analysis of small Si-Br molecules is consistent with the current notions of the effects of including brominated species in etchant gases.

  6. Surface Response of Brominated Carbon Media on Laser and Thermal Excitation: Optical and Thermal Analysis Study

    OpenAIRE

    Volodymyr V. Multian; Kinzerskyi, Fillip E.; Anna V. Vakaliuk; Grishchenko, Liudmyla M.; Diyuk, Vitaliy E.; Boldyrieva, Olga Yu; Kozhanov, Vadim O.; Oleksandr V. Mischanchuk; Vladyslav V. Lisnyak; Gayvoronsky, Volodymyr Ya.

    2017-01-01

    The present study is objected to develop an analytical remote optical diagnostics of the functionalized carbons surface. Carbon composites with up to 1 mmol g?1 of irreversibly adsorbed bromine were produced by the room temperature plasma treatment of an activated carbon fabric (ACF) derived from polyacrylonitrile textile. The brominated ACF (BrACF) was studied by elastic optical scattering indicatrix analysis at wavelength 532 nm. The obtained data were interpreted within results of the ther...

  7. Chlorine and Bromine Isotope Fractionation of Halogenated Organic Pollutants on Gas Chromatography Columns

    OpenAIRE

    Tang, Caiming; Tan, Jianhua; Xiong, Songsong; Liu, Jun; Fan, Yujuan; Peng, Xianzhi

    2017-01-01

    Compound-specific chlorine/bromine isotope analysis (CSIA-Cl/Br) has become a useful approach for degradation pathway investigation and source appointment of halogenated organic pollutants (HOPs). CSIA-Cl/Br is usually conducted by gas chromatography-mass spectrometry (GC-MS), which could be negatively impacted by chlorine and bromine isotope fractionation of HOPs on GC columns. In this study, 31 organochlorines and 4 organobromines were systematically investigated in terms of Cl/Br isotope f...

  8. Surface Response of Brominated Carbon Media on Laser and Thermal Excitation: Optical and Thermal Analysis Study.

    Science.gov (United States)

    Multian, Volodymyr V; Kinzerskyi, Fillip E; Vakaliuk, Anna V; Grishchenko, Liudmyla M; Diyuk, Vitaliy E; Boldyrieva, Olga Yu; Kozhanov, Vadim O; Mischanchuk, Oleksandr V; Lisnyak, Vladyslav V; Gayvoronsky, Volodymyr Ya

    2017-12-01

    The present study is objected to develop an analytical remote optical diagnostics of the functionalized carbons surface. Carbon composites with up to 1 mmol g-1 of irreversibly adsorbed bromine were produced by the room temperature plasma treatment of an activated carbon fabric (ACF) derived from polyacrylonitrile textile. The brominated ACF (BrACF) was studied by elastic optical scattering indicatrix analysis at wavelength 532 nm. The obtained data were interpreted within results of the thermogravimetric analysis, X-ray photoelectron spectroscopy and temperature programmed desorption mass spectrometry. The bromination dramatically reduces the microporosity producing practically non-porous material, while the incorporated into the micropores bromine induces the dielectric and structural impact on surface polarizability and conductivity due to the charging effect. We have found that the elastic optical scattering in proper solid angles in the forward and the backward hemispheres is sensitive to the kind of the bromine bonding, e.g., physical adsorption or chemisorption, and the bromination level, respectively, that can be utilized for the express remote fabrication control of the nanoscale carbons with given interfaces.

  9. 45 CFR 81.41 - Computation.

    Science.gov (United States)

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Computation. 81.41 Section 81.41 Public Welfare... 80 OF THIS TITLE Time § 81.41 Computation. In computing any period of time under the rules in this... holidays shall be excluded from the computation. ...

  10. 45 CFR 1356.81 - Reporting population.

    Science.gov (United States)

    2010-10-01

    ... 45 Public Welfare 4 2010-10-01 2010-10-01 false Reporting population. 1356.81 Section 1356.81... § 1356.81 Reporting population. The reporting population is comprised of all youth in the following categories: (a) Served population. Each youth who receives an independent living service paid for or provided...

  11. 38 CFR 61.81 - Outreach activities.

    Science.gov (United States)

    2010-07-01

    ... 38 Pensions, Bonuses, and Veterans' Relief 2 2010-07-01 2010-07-01 false Outreach activities. 61.81 Section 61.81 Pensions, Bonuses, and Veterans' Relief DEPARTMENT OF VETERANS AFFAIRS (CONTINUED) VA HOMELESS PROVIDERS GRANT AND PER DIEM PROGRAM § 61.81 Outreach activities. Recipients of capital...

  12. 24 CFR 81.62 - Mortgage reports.

    Science.gov (United States)

    2010-04-01

    ... 24 Housing and Urban Development 1 2010-04-01 2010-04-01 false Mortgage reports. 81.62 Section 81... THE SECRETARY OF HUD'S REGULATION OF THE FEDERAL NATIONAL MORTGAGE ASSOCIATION (FANNIE MAE) AND THE FEDERAL HOME LOAN MORTGAGE CORPORATION (FREDDIE MAC) Reporting Requirements § 81.62 Mortgage reports. (a...

  13. 32 CFR 1605.81 - Interpreters.

    Science.gov (United States)

    2010-07-01

    ... 32 National Defense 6 2010-07-01 2010-07-01 false Interpreters. 1605.81 Section 1605.81 National... ORGANIZATION Interpreters § 1605.81 Interpreters. (a) The local board, district appeal board and the National Selective Service Appeal Board are authorized to use interpreters when necessary. (b) The following oath...

  14. 25 CFR 81.16 - Interpreters.

    Science.gov (United States)

    2010-04-01

    ... 25 Indians 1 2010-04-01 2010-04-01 false Interpreters. 81.16 Section 81.16 Indians BUREAU OF... STATUTE § 81.16 Interpreters. Interpreters, where needed, may be provided to explain the manner of voting... that the interpreter does not influence the voter in casting the ballot. The interpreter may accompany...

  15. 21 CFR 600.81 - Distribution reports.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 7 2010-04-01 2010-04-01 false Distribution reports. 600.81 Section 600.81 Food... BIOLOGICAL PRODUCTS: GENERAL Reporting of Adverse Experiences § 600.81 Distribution reports. The licensed... between distribution reports shall be 6 months. Upon written notice, FDA may require that the licensed...

  16. 45 CFR 81.11 - Appearance.

    Science.gov (United States)

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Appearance. 81.11 Section 81.11 Public Welfare DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL ADMINISTRATION PRACTICE AND PROCEDURE FOR HEARINGS UNDER PART 80 OF THIS TITLE Appearance and Practice § 81.11 Appearance. A party may appear in person or by...

  17. 40 CFR 81.355 - Puerto Rico.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Puerto Rico. 81.355 Section 81.355... AREAS FOR AIR QUALITY PLANNING PURPOSES Section 107 Attainment Status Designations § 81.355 Puerto Rico. Puerto Rico—SO2 Designated area Does not meet primary standards Does not meet secondary standards Cannot...

  18. 34 CFR 81.8 - Representation.

    Science.gov (United States)

    2010-07-01

    ... 34 Education 1 2010-07-01 2010-07-01 false Representation. 81.8 Section 81.8 Education Office of the Secretary, Department of Education GENERAL EDUCATION PROVISIONS ACT-ENFORCEMENT General Provisions § 81.8 Representation. A party to, or other participant in, a case may be represented by counsel...

  19. 42 CFR 81.0 - Background.

    Science.gov (United States)

    2010-10-01

    ... 42 Public Health 1 2010-10-01 2010-10-01 false Background. 81.0 Section 81.0 Public Health PUBLIC HEALTH SERVICE, DEPARTMENT OF HEALTH AND HUMAN SERVICES OCCUPATIONAL SAFETY AND HEALTH RESEARCH AND... OCCUPATIONAL ILLNESS COMPENSATION PROGRAM ACT OF 2000 Introduction § 81.0 Background. The Energy Employees...

  20. 28 CFR 551.81 - Manuscript preparation.

    Science.gov (United States)

    2010-07-01

    ... 28 Judicial Administration 2 2010-07-01 2010-07-01 false Manuscript preparation. 551.81 Section 551.81 Judicial Administration BUREAU OF PRISONS, DEPARTMENT OF JUSTICE INSTITUTIONAL MANAGEMENT MISCELLANEOUS Inmate Manuscripts § 551.81 Manuscript preparation. An inmate may prepare a manuscript for private...

  1. 9 CFR 381.81 - Tuberculosis.

    Science.gov (United States)

    2010-01-01

    ... 9 Animals and Animal Products 2 2010-01-01 2010-01-01 false Tuberculosis. 381.81 Section 381.81 Animals and Animal Products FOOD SAFETY AND INSPECTION SERVICE, DEPARTMENT OF AGRICULTURE AGENCY... § 381.81 Tuberculosis. Carcasses of poultry affected with tuberculosis shall be condemned. ...

  2. 7 CFR 981.81 - Assessment.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Assessment. 981.81 Section 981.81 Agriculture... Regulating Handling Expenses and Assessments § 981.81 Assessment. (a) Requirement for payment. Each handler... own account (except as to receipts from other handlers on which assessments have been paid) as the...

  3. 45 CFR 81.78 - Evidence.

    Science.gov (United States)

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Evidence. 81.78 Section 81.78 Public Welfare... 80 OF THIS TITLE Hearing Procedures § 81.78 Evidence. Irrelevant, immaterial, unreliable, and unduly repetitious evidence will be excluded. ...

  4. 7 CFR 959.81 - Compliance.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Compliance. 959.81 Section 959.81 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Regulating Handling Compliance § 959.81 Compliance. Except as provided in this subpart, no handler shall...

  5. 7 CFR 947.81 - Compliance.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Compliance. 947.81 Section 947.81 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Miscellaneous Provisions § 947.81 Compliance. Except as provided in this subpart, no handler shall handle...

  6. 7 CFR 966.81 - Compliance.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Compliance. 966.81 Section 966.81 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Regulating Handling Miscellaneous Provisions § 966.81 Compliance. Except as provided in this subpart, no...

  7. 7 CFR 905.81 - Compliance.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Compliance. 905.81 Section 905.81 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... TANGELOS GROWN IN FLORIDA Order Regulating Handling Miscellaneous Provisions § 905.81 Compliance. Except as...

  8. 7 CFR 948.81 - Compliance.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Compliance. 948.81 Section 948.81 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Order Regulating Handling Compliance § 948.81 Compliance. Except as provided in this subpart, no handler...

  9. 40 CFR 81.312 - Hawaii.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Hawaii. 81.312 Section 81.312... AREAS FOR AIR QUALITY PLANNING PURPOSES Section 107 Attainment Status Designations § 81.312 Hawaii. Hawaii—TSP Designated area Does not meet primary standards Does not meet secondary standards Cannot be...

  10. 40 CFR 81.409 - Hawaii.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Hawaii. 81.409 Section 81.409... Visibility Is an Important Value § 81.409 Hawaii. Area name Acreage Public Law establishing Federal land manager Haleakala NP 27,208 87-744 USDI-NPS Hawaii Volcanoes 217,029 64-171 USDI-NPS ...

  11. 50 CFR 27.81 - Alcoholic beverages.

    Science.gov (United States)

    2010-10-01

    ... 50 Wildlife and Fisheries 6 2010-10-01 2010-10-01 false Alcoholic beverages. 27.81 Section 27.81... NATIONAL WILDLIFE REFUGE SYSTEM PROHIBITED ACTS Disturbing Violations: Personal Conduct § 27.81 Alcoholic beverages. Entering or remaining in any national wildlife refuge when under the influence of alcohol, to a...

  12. 45 CFR 81.114 - Expeditious treatment.

    Science.gov (United States)

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Expeditious treatment. 81.114 Section 81.114... HEARINGS UNDER PART 80 OF THIS TITLE Judicial Standards of Practice § 81.114 Expeditious treatment. Requests for expeditious treatment of matters pending before the responsible Department official or the...

  13. 7 CFR 52.81 - Plant survey.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 2 2010-01-01 2010-01-01 false Plant survey. 52.81 Section 52.81 Agriculture... Contract In-Plant Inspection Services 1 § 52.81 Plant survey. Prior to a plant being approved, or the..., the Administrator will make, or cause to be made, a survey and inspection of the plant where such...

  14. 7 CFR 989.81 - Accounting.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Accounting. 989.81 Section 989.81 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... CALIFORNIA Order Regulating Handling Expenses and Assessments § 989.81 Accounting. (a) If, at the end of the...

  15. 37 CFR 2.81 - Post publication.

    Science.gov (United States)

    2010-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2010-07-01 2010-07-01 false Post publication. 2.81 Section 2.81 Patents, Trademarks, and Copyrights UNITED STATES PATENT AND TRADEMARK OFFICE, DEPARTMENT OF COMMERCE RULES OF PRACTICE IN TRADEMARK CASES Publication and Post Publication § 2.81 Post publication. (a...

  16. 7 CFR 81.2 - Administration.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 3 2010-01-01 2010-01-01 false Administration. 81.2 Section 81.2 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Standards... PROGRAMS PRUNE/DRIED PLUM DIVERSION PROGRAM § 81.2 Administration. The program will be administered under...

  17. 4 CFR 81.2 - Administration.

    Science.gov (United States)

    2010-01-01

    ... 4 Accounts 1 2010-01-01 2010-01-01 false Administration. 81.2 Section 81.2 Accounts GOVERNMENT ACCOUNTABILITY OFFICE RECORDS PUBLIC AVAILABILITY OF GOVERNMENT ACCOUNTABILITY OFFICE RECORDS § 81.2 Administration. The Chief Quality Officer administers this part and may promulgate such supplemental rules or...

  18. 40 CFR 81.330 - New Hampshire.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false New Hampshire. 81.330 Section 81.330... AREAS FOR AIR QUALITY PLANNING PURPOSES Section 107 Attainment Status Designations § 81.330 New... days after November 13, 2009, unless otherwise noted. Editorial Note: For Federal Register citations...

  19. 40 CFR 81.340 - Rhode Island.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Rhode Island. 81.340 Section 81.340... AREAS FOR AIR QUALITY PLANNING PURPOSES Section 107 Attainment Status Designations § 81.340 Rhode Island. Rhode Island—TSP Designated area Does not meet primary standards Does not meet secondary standards...

  20. 21 CFR 640.81 - Processing.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 7 2010-04-01 2010-04-01 false Processing. 640.81 Section 640.81 Food and Drugs... STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS Albumin (Human) § 640.81 Processing. (a) Date of manufacture... solution. (b) Processing method. The processing method shall not affect the integrity of the product, and...

  1. 49 CFR 38.81 - Lighting.

    Science.gov (United States)

    2010-10-01

    ... 49 Transportation 1 2010-10-01 2010-10-01 false Lighting. 38.81 Section 38.81 Transportation Office of the Secretary of Transportation AMERICANS WITH DISABILITIES ACT (ADA) ACCESSIBILITY SPECIFICATIONS FOR TRANSPORTATION VEHICLES Light Rail Vehicles and Systems § 38.81 Lighting. (a) Any stepwell or...

  2. 43 CFR 12.81 - Financial reporting.

    Science.gov (United States)

    2010-10-01

    ... 43 Public Lands: Interior 1 2010-10-01 2010-10-01 false Financial reporting. 12.81 Section 12.81... Agreements to State and Local Governments Reports, Records Retention, and Enforcement § 12.81 Financial reporting. (a) General. (1) Except as provided in paragraphs (a) (2) and (5) of this section, grantees will...

  3. STS-81 Post Flight Presentation

    Science.gov (United States)

    1997-01-01

    The flight crew of the STS-81 mission, Commander Michael A. Baker, Pilot Brent W. Jett Jr, and Mission Specialists John M. Grunsfeld, Marsha S. Ivins, Peter J.K. Wisoff, and Jerry M. Linenger present a video mission over-view of their space flight. Images include prelaunch activities such as eating the traditional breakfast, crew suit-up, and the ride out to the launch pad. Also included are various panoramic views of the shuttle on the pad. The crew can be seen being readied in the "white room" for their mission. After the closing of the hatch and arm retraction, launch activities are shown including countdown, engine ignition, launch, and the separation of the Solid Rocket Boosters. During the presentation the astronauts take turns discussing aspects of the mission including: the SPACEHAB a double module that provides additional middeck locker space for secondary experiments. During the five days of docked operations with Mir, the crews is seen transferring water and supplies from one spacecraft to the other.

  4. STS-81 Flight Day 7

    Science.gov (United States)

    1997-01-01

    On this seventh first day of the STS-81 mission, the flight crew, Cmdr. Michael A. Baker, Pilot Brent W. Jett, Mission Specialists, John M. Grunsfeld, Marsha S. Ivins, Peter J.K. Wisoff, and John Blaha, and the cosmonauts of the Russian Space Station Mir continue to transfer hundreds of pounds of water, supplies, and logistical items to each other's spacecraft. More than 1,300 pounds of water have now been transferred from Atlantis to the Mir to resupply the Russian outpost, along with equipment that will be used by astronaut Jerry M. Linenger during his four-month research mission. A bioprocessing device and an experiment used to grow cartilage cells during astronaut John Blaha's four month stay on the Mir is also transferred to Atlantis for the trip back to Earth. Linenger spends most of the day collecting water samples from the Mir for analysis back on Earth and Blaha continues to exercise on a treadmill on the Mir to stay in shape for his return to Earth and a readaptation to gravity after four months of weightlessness.

  5. Excitation functions of 85Rb(p,xn)(85m,g,83,82,81)Sr reactions up to 100 MeV: integral tests of cross section data, comparison of production routes of 83Sr and thick target yield of 82Sr.

    Science.gov (United States)

    Kastleiner, S; Qaim, S M; Nortier, F M; Blessing, G; van der Walt, T N; Coenen, H H

    2002-05-01

    The beta+ emitter 83Sr (T(1/2) = 32.4 h, Ebeta+ = 1.23 MeV, Ibeta+ = 24%) is a potentially useful radionuclide for therapy planning prior to the use of the beta+ emitter 89Sr (T(1/2) = 50.5 d). In order to investigate its production possibility, cross section measurements on the 85Rb(p,xn)-reactions, leading to the formation of the isotopes (85m,g)Sr, 83Sr, 82Sr and 81Sr, were carried out using the stacked-foil technique. In a few cases, the products were separated via high-performance liquid chromatography. For 82Sr, both gamma-ray and X-ray spectrometry were applied; in other cases only gamma-ray spectrometry was used. From the measured excitation functions, the expected yields were calculated. For the energy range Ep = 37 --> 30 MeV the 83Sr yield amounts to 160 MBq/microA h and the level of the 85gSr (T(1,2) = 64.9 d) and 82Sr (T(1/2) = 25.5 d) impurities to 10 MeV the theoretical yield of 83Sr amounts to 5 MBq/microA h and the 82Sr impurity to about 0.2%. The method of choice for the production of 83Sr is thus the 85Rb(p,3n)-process, provided a 40 MeV cyclotron is available. During this study some supplementary information on the yield and purity of 82Sr was also obtained.

  6. Impact of deep convection and dehydration on bromine loading in the upper troposphere and lower stratosphere

    Directory of Open Access Journals (Sweden)

    J. Aschmann

    2011-03-01

    Full Text Available Stratospheric bromine loading due to very short-lived substances is investigated with a three-dimensional chemical transport model over a period of 21 years using meteorological input data from the European Centre for Medium-Range Weather Forecasts ERA-Interim reanalysis from 1989 to the end of 2009. Within this framework we analyze the impact of dehydration and deep convection on the amount of stratospheric bromine using an idealized and a detailed full chemistry approach. We model the two most important brominated short-lived substances, bromoform (CHBr3 and dibromomethane (CH2Br2, assuming a uniform convective detrainment mixing ratio of 1 part per trillion by volume (pptv for both species. The contribution of very short-lived substances to stratospheric bromine varies drastically with the applied dehydration mechanism and the associated scavenging of soluble species ranging from 3.4 pptv in the idealized setup up to 5 pptv using the full chemistry scheme. In the latter case virtually the entire amount of bromine originating from very short-lived source gases is able to reach the stratosphere thus rendering the impact of dehydration and scavenging on inorganic bromine in the tropopause insignificant. Furthermore, our long-term calculations show that the mixing ratios of very short-lived substances are strongly correlated to convective activity, i.e. intensified convection leads to higher amounts of very short-lived substances in the upper troposphere/lower stratosphere especially under extreme conditions like El Niño seasons. However, this does not apply to the inorganic brominated product gases whose concentrations are anti-correlated to convective activity mainly due to convective dilution and possible scavenging, depending on the applied approach.

  7. Modelling chemistry over the Dead Sea: bromine and ozone chemistry

    Directory of Open Access Journals (Sweden)

    R. von Glasow

    2009-07-01

    Full Text Available Measurements of O3 and BrO concentrations over the Dead Sea indicate that Ozone Depletion Events (ODEs, widely known to happen in polar regions, are also occuring over the Dead Sea due to the very high bromine content of the Dead Sea water. However, we show that BrO and O3 levels as they are detected cannot solely be explained by high Br levels in the Dead Sea water and the release of gas phase halogen species out of sea borne aerosol particles and their conversion to reactive halogen species. It is likely that other sources for reactive halogen compounds are needed to explain the observed concentrations for BrO and O3. To explain the chemical mechanism taking place over the Dead Sea leading to BrO levels of several pmol/mol we used the one-dimensional model MISTRA which calculates microphysics, meteorology, gas and aerosol phase chemistry. We performed pseudo Lagrangian studies by letting the model column first move over the desert which surrounds the Dead Sea region and then let it move over the Dead Sea itself. To include an additional source for gas phase halogen compounds, gas exchange between the Dead Sea water and the atmosphere is treated explicitly. Model calculations indicate that this process has to be included to explain the measurements.

  8. Structure/Reactivity Relationships in the Benzo[c]phenanthrene Skeleton: Stable Ion and Electrophilic Substitution (Nitration, Bromination) Study of Substituted Analogs; Novel Carbocations and Substituted Derivatives

    Science.gov (United States)

    Brulé, Cédric; Laali, Kenneth K.; Okazaki, Takao; Lakshman, Mahesh K.

    2008-01-01

    A series of novel carbocations were generated by low temperature protonation of substituted benzo[c]phenanthrenes B[c]Phs and their charge delocalization pathways were elucidated by NMR based on the magnitude of Δδ13C values. It has been shown that the protonation regioselectivity is strongly controlled by methoxy and hydroxyl substituents, whose directive effects override methyl substitution effects. Regiocontrol by –OMe and –OH substituents, and its stronger influence relative to methyl groups, was also observed in the nitration and bromination reactions. Charge distribution modes in the regioisomeric protonated carbocations via parent B[c]Ph as well as in the benzylic carbocation formed via fjord-region epoxide ring opening were deduced by GIAO-DFT, and from the NPA-derived changes in charges over CHs. These patterns were compared with those derived from NMR experiments in the substituted derivatives. NMR-based charge delocalization mapping provided insight into structure/activity relationships in the methylated and fluorinated B[c]Phs. Regioselectivities observed in the nitration and bromination reactions in representative cases are the same as those via protonations. Among a group of novel nitro and bromo derivatives synthesized in this study are examples where nitro group is introduced into the fjord-region, for which X-ray structure could be obtained in one case. PMID:17394355

  9. Measurement-based modeling of bromine chemistry in the boundary layer: 1. Bromine chemistry at the Dead Sea

    Directory of Open Access Journals (Sweden)

    E. Tas

    2006-01-01

    Full Text Available The Dead Sea is an excellent natural laboratory for the investigation of Reactive Bromine Species (RBS chemistry, due to the high RBS levels observed in this area, combined with anthropogenic air pollutants up to several ppb. The present study investigated the basic chemical mechanism of RBS at the Dead Sea using a numerical one-dimensional chemical model. Simulations were based on data obtained from comprehensive measurements performed at sites along the Dead Sea. The simulations showed that the high BrO levels measured frequently at the Dead Sea could only partially be attributed to the highly concentrated Br− present in the Dead Sea water. Furthermore, the RBS activity at the Dead Sea cannot solely be explained by a pure gas phase mechanism. This paper presents a chemical mechanism which can account for the observed chemical activity at the Dead Sea, with the addition of only two heterogeneous processes: the "Bromine Explosion" mechanism and the heterogeneous decomposition of BrONO2. Ozone frequently dropped below a threshold value of ~1 to 2 ppbv at the Dead Sea evaporation ponds, and in such cases, O3 became a limiting factor for the production of BrOx (BrO+Br. The entrainment of O3 fluxes into the evaporation ponds was found to be essential for the continuation of RBS activity, and to be the main reason for the jagged diurnal pattern of BrO observed in the Dead Sea area, and for the positive correlation observed between BrO and O3 at low O3 concentrations. The present study has shown that the heterogeneous decomposition of BrONO2 has a great potential to affect the RBS activity in areas influenced by anthropogenic emissions, mainly due to the positive correlation between the rate of this process and the levels of NO2. Further investigation of the influence of the decomposition of BrONO2 may be especially important in understanding the RBS activity at mid-latitudes.

  10. Theoretical Analysis of the Effect Provoked by Bromine-Addition on the Thermolysis and Chemiexcitation of a Model Dioxetanone

    Directory of Open Access Journals (Sweden)

    Luís Pinto da Silva

    2017-01-01

    Full Text Available Chemi-/bioluminescence are phenomena in which chemical energy is converted into electronically excited singlet states, which decay with light emission. Given this feature, along with high quantum yields and other beneficial characteristics, these systems have gained numerous applications in bioanalysis, in biomedicine, and in the pharmaceutical field. Singlet chemiexcitation is made possible by the formation of cyclic peroxides (as dioxetanones as thermolysis provides a route for a ground state reaction to produce singlet excited states. However, such thermolysis can also lead to the formation of triplet states. While triplet states are not desired in the typical applications of chemi-/bioluminescence, the efficient production of such states can open the door for the use of these systems as sensitizers in photocatalysis and triplet-triplet annihilation, among other fields. Thus, the goal of this study is to assess the effect of heavy atom addition on the thermolysis and triplet chemiexcitation of a model dioxetanone. Monobromination does not affect the thermolysis reaction but can improve the efficiency of intersystem crossing, depending on the position of monobromination. Addition of bromine atoms to the triplet state reaction product has little effect on its properties, except on its electron affinity, in which monobromination can increase between 3.1 and 8.8 kcal mol−1.

  11. Brominated flame retardants in end-of-life management not problematic regarding formation of brominated dioxins/furans (PBDD/F)

    Energy Technology Data Exchange (ETDEWEB)

    Drohmann, D. [Great Lakes Chemical, Bergisch Gladbach (Germany); Tange, L. [Eurobrom B.V., Rijswijk (Netherlands); Rothenbacher, K. [Bromine Science and Environmental Forum, Brussels (Belgium)

    2004-09-15

    Bromine is used as the building block for some of the most effective flame retarding agents available to the plastics industry today. They are used to protect against the risk of accidental fires in a wide range of products. Brominated flame retardants (BFRs), as all flame retardants, act to decrease the risk of fire by increasing the fire resistance of the materials in which they are applied. There is a perception that BFRs affect adversely the end-of-life management of plastics through formation of brominated dioxins and furans (PBDD/F). In fact, there exists a wide range of data and practical experience demonstrating that the end-of-life management of plastics containing BFRs are fully compliant with legislation setting the strictest limit values for PBDD/F and is fully compatible with an integrated waste management concept. Furthermore, all existing EU Risk Assessments on BFRs according to the European Existing Substance Regulations include an assessment of the potential formation of dioxins and furans. All assessments conclude that the risks along the life-cycle of the chemicals for human health and the environment associated with the potential formation of PBDD/F are negligible. Moreover, two recent Swedish studies found, that consumer products with BFRs emit less pollutants than the same products without any FRs. This paper summarises available studies and presents the latest results regarding potential formation of brominated dioxins and furans in end-of-life management of plastics containing brominated flame retardants. Additionally, before BFR products enter the market they are tested for PBDD/F according to the ''German Dioxin Ordinance''. Depending on the substitution pattern the limit values for PBDD/F are set at <1{mu}g/kg (ppb) respectively <5{mu}g/kg (ppb).

  12. Brominated Skeletal Components of the Marine Demosponges, Aplysina cavernicola and Ianthella basta: Analytical and Biochemical Investigations

    Directory of Open Access Journals (Sweden)

    Eike Brunner

    2013-04-01

    Full Text Available Demosponges possess a skeleton made of a composite material with various organic constituents and/or siliceous spicules. Chitin is an integral part of the skeleton of different sponges of the order Verongida. Moreover, sponges of the order Verongida, such as Aplysina cavernicola or Ianthella basta, are well-known for the biosynthesis of brominated tyrosine derivates, characteristic bioactive natural products. It has been unknown so far whether these compounds are exclusively present in the cellular matrix or whether they may also be incorporated into the chitin-based skeletons. In the present study, we therefore examined the skeletons of A. cavernicola and I. basta with respect to the presence of bromotyrosine metabolites. The chitin-based-skeletons isolated from these sponges indeed contain significant amounts of brominated compounds, which are not easily extractable from the skeletons by common solvents, such as MeOH, as shown by HPLC analyses in combination with NMR and IR spectroscopic measurements. Quantitative potentiometric analyses confirm that the skeleton-associated bromine mainly withstands the MeOH-based extraction. This observation suggests that the respective, but yet unidentified, brominated compounds are strongly bound to the sponge skeletons, possibly by covalent bonding. Moreover, gene fragments of halogenases suggested to be responsible for the incorporation of bromine into organic molecules could be amplified from DNA isolated from sponge samples enriched for sponge-associated bacteria.

  13. Removal of brominated flame retardant from electrical and electronic waste plastic by solvothermal technique

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Cong-Cong [Research Center For Eco-Environmental Sciences, Chinese Academy of Sciences, 18 Shuangqing Road, Beijing 100085 (China); Zhang, Fu-Shen, E-mail: fszhang@rcees.ac.cn [Research Center For Eco-Environmental Sciences, Chinese Academy of Sciences, 18 Shuangqing Road, Beijing 100085 (China)

    2012-06-30

    Highlights: Black-Right-Pointing-Pointer A process for brominated flame retardants (BFRs) removal in plastic was established. Black-Right-Pointing-Pointer The plastic became bromine-free with the structure maintained after this treatment. Black-Right-Pointing-Pointer BFRs transferred into alcohol solvent were easily debrominated by metallic copper. - Abstract: Brominated flame retardants (BFRs) in electrical and electronic (E and E) waste plastic are toxic, bioaccumulative and recalcitrant. In the present study, tetrabromobisphenol A (TBBPA) contained in this type of plastic was tentatively subjected to solvothermal treatment so as to obtain bromine-free plastic. Methanol, ethanol and isopropanol were examined as solvents for solvothermal treatment and it was found that methanol was the optimal solvent for TBBPA removal. The optimum temperature, time and liquid to solid ratio for solvothermal treatment to remove TBBPA were 90 Degree-Sign C, 2 h and 15:1, respectively. After the treatment with various alcohol solvents, it was found that TBBPA was finally transferred into the solvents and bromine in the extract was debrominated catalyzed by metallic copper. Bisphenol A and cuprous bromide were the main products after debromination. The morphology and FTIR properties of the plastic were generally unchanged after the solvothermal treatment indicating that the structure of the plastic maintained after the process. This work provides a clean and applicable process for BFRs-containing plastic disposal.

  14. Electrochemical performance and transport properties of a Nafion membrane in a hydrogen-bromine cell environment

    Science.gov (United States)

    Baldwin, Richard S.

    1987-01-01

    The overall energy conversion efficiency of a hydrogen-bromine energy storage system is highly dependent upon the characteristics and performance of the ion-exchange membrane utilized as a half-cell separator. The electrochemical performance and transport properties of a duPont Nafion membrane in an aqueous HBr-Br2 environment were investigated. Membrane conductivity data are presented as a function of HBr concentration and temperature for the determination of ohmic voltage losses across the membrane in an operational cell. Diffusion-controlled bromine permeation rates and permeabilities are presented as functions of solution composition and temperature. Relationships between the degree of membrane hydration and the membrane transport characteristics are discussed. The solution chemistry of an operational hydrogen-bromine cell undergoing charge from 45% HBr to 5% HBr is discussed, and, based upon the experimentally observed bromine permeation behavior, predicted cell coulombic losses due to bromine diffusion through the membrane are presented as a function of the cell state-of-charge.

  15. Effect of the Bromine-Based Flame Retardant Plastic Pyrolysis of Hydrotalcite

    Directory of Open Access Journals (Sweden)

    Morita N.

    2016-01-01

    Full Text Available In this study, a method is presented to decrease halogen compounds in the product oil from thermolysis of polystyrene and polypropylene mixed plastic spiked with tetrabromobisphenol A. A mixture of hydrotalcite and plastic was pyrolyzed in a glass reactor at 400 °C under a nitrogen atmosphere. Bromine compounds in the residual substances were measured. The yield of product oil increased using hydrotalcite as an additive. The bromine compounds that were the major ingredients in the oil after thermolysis at 400 °C from the mixed plastic, which also included toluene, ethyl benzene, styrene, and 1-methylethyl benzene, were 2-bromohexane, 3-bromo-1-propenyl benzene, 4,5-dibromodecane, 1-bromomethylbenzene, 3-bromophenol, and 4-bromo-2,6-dimethylbenzaniline. However, bromine compounds were not detected in the product oil, residue, or gas when hydrotalcite was added. After the thermolysis of the plastic, bromine compounds in the product oil may decrease because bromine was captured by the added hydrotalcite.

  16. Terminal elimination half-lives of the brominated flame retardants TBBPA, HBCD, and lower brominated PBDEs in humans

    Energy Technology Data Exchange (ETDEWEB)

    Geyer, H.J.; Schramm, K.W.; Feicht, E.A.; Fried, K.W.; Henkelmann, B.; Lenoir, D. [GSF-National Research Center, Institute of Ecological Chemistry, Neuherberg (Germany); Darnerud, P.O.; Aune, M. [Swedish National Food Administration, Uppsala (Sweden); Schmid, P. [Swiss Federal Laboratories for Materials Testing and Research, Laboratory of Organic Chemistry, EMPA Duebendorf (Switzerland); McDonald, T.A. [Office of Environmental Health Assessment, California EPA, Oakland, CA (United States)

    2004-09-15

    Brominated flame retardants (BFRs) are widely used in polymers and textiles and applied in electronic equipment, construction materials, and furniture for the purpose of fire prevention. BFRs with the highest production volume are tetrabromobisphenol A (TBBPA), 1,2,5,6,9,10- hexabromocyclododecanes (HBCDs: {alpha}-HBCD + {beta}-HBCD + {gamma}-HBCD), and polybrominated diphenyl ethers (PBDEs). Several BFRs are highly lipophilic persistent organic pollutants (POPs) which have been identified in the aquatic and terrestrial environment including wildlife and humans. In exposed organisms including humans toxic effects, bioaccumulation, metabolism, and pharmacokinetics (especially half-life t{sub 1/2}) are important criterions in the hazard assessment. The aim of the present study was to estimate the terminal elimination half-lives (t{sub 1/2H}) of the main BFRs from the whole body (also named body-burden half-life) and/or from the adipose tissue (fat) of adult humans. The t{sub 1/2H} data for the following BFRs were evaluated: TBBPA, HBCD, 2,2',4,4'- tetrabromodiphenyl ether (BDE-47), 2,2',4,4',5-pentaBDE (BDE-99), 2,2',4,4',6-pentaBDE (BDE- 100), 2,2',4,4',5,5'-hexaBDE (BDE-153), and 2,2',4,4',5,6-hexaBDE (BDE-154).

  17. Airborne particle-bound brominated flame retardants: Levels, size distribution and indoor-outdoor exchange.

    Science.gov (United States)

    Zhu, Yue-Shan; Yang, Wan-Dong; Li, Xiu-Wen; Ni, Hong-Gang; Zeng, Hui

    2017-10-12

    The quality of indoor environments has a significant impact on public health. Usually, an indoor environment is treated as a static box, in which physicochemical reactions of indoor air contaminants are negligible. This results in conservative estimates for primary indoor air pollutant concentrations, while also ignoring secondary pollutants. Thus, understanding the relationship between indoor and outdoor particles and particle-bound pollutants is of great significance. For this reason, we collected simultaneous indoor and outdoor measurements of the size distribution of airborne brominated flame retardant (BFR) congeners. The time-dependent concentrations of indoor particles and particle-bound BFRs were then estimated with the mass balance model, accounting for the outdoor concentration, indoor source strength, infiltration, penetration, deposition and indoor resuspension. Based on qualitative observation, the size distributions of ΣPBDE and ΣHBCD were characterized by bimodal peaks. According to our results, particle-bound BDE209 and γ-HBCD underwent degradation. Regardless of the surface adsorption capability of particles and the physicochemical properties of the target compounds, the concentration of BFRs in particles of different size fractions seemed to be governed by the particle distribution. Based on our estimations, for airborne particles and particle-bound BFRs, a window-open ventilated room only takes a quarter of the time to reach an equilibrium between the concentration of pollutants inside and outside compared to a closed room. Unfortunately, indoor pollutants and outdoor pollutants always exist simultaneously, which poses a window-open-or-closed dilemma to achieve proper ventilation. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Evaluation of Fenton Process in Removal of Direct Red 81

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Baghapour

    2016-01-01

    Full Text Available Background: Dyes are visible materials and are considered as one of the hazardous components that make up the industrial waste. Dye compounds in natural water, even in very low concentrations, will lead to environmental problems. Azo dyes are compounds with one or more –N=N– groups and are used in textile industry. Because of its low price, solubility, and stability, azo dyes are widely used in the textile industry. Direct Red 81 (DR81 is one of the azo dyes, which is removed from bodies of water, using various methods. This study aimed to assess DR81 dye removal by Fenton oxidation and the effects of various parameters on this process. Methods: Decolorization tests by Fenton oxidation were performed at dye concentrations of 50, 500, 100 and 1000 mg/L; hydrogen peroxide concentrations of 0, 10, 30, 60 and 120 mg/L; iron (II sulfate heptahydrate concentrations of 0, 3, 5, 20 and 50 mg/L; and pH levels of 3, 5, 7 and 10 for durations of 5, 10, 20, 30, 60 and 180 minutes. Results: The optimal condition occurred at a dye concentration of 20 mg/L, hydrogen peroxide concentration of 120 mg/L, bivalent iron concentration of 100 mg/L, pH of 3, and duration of 30 minutes. Under such conditions, the maximum dye removal rate was 88.98%. Conclusion: The results showed that DR81 could be decomposed and removed by Fenton oxidation. In addition, the removal of Direct Red 81 (DR81 depends on several factors such as dye concentration, reaction time, concentrations of hydrogen peroxide and iron, and pH

  19. Levels of Brominated Flame Retardants in Dutch fish and Shellfish including an estimation of the dietary intake

    NARCIS (Netherlands)

    Leeuwen, van S.P.J.; Pieters, H.; Mul, de A.; Boer, de J.

    2006-01-01

    Brominated flame retardants (BFRs) are used at relatively high concentrations in various materials and polymers.Their use has expanded considerably during the last three decades. The annual global demand was estimated to 200 000 tons in 1999. The most frequently used brominated flame retardants

  20. Neurotoxicity and risk assessment of brominated and alternative flame retardants.

    Science.gov (United States)

    Hendriks, Hester S; Westerink, Remco H S

    2015-01-01

    Brominated flame retardants (BFRs) are widely used chemicals that prevent or slow the onset and spreading of fire. Unfortunately, many of these compounds pose serious threats for human health and the environment, indicating an urgent need for safe(r) and less persistent alternative flame retardants (AFRs). As previous research identified the nervous system as a sensitive target organ, the neurotoxicity of past and present flame retardants is reviewed. First, an overview of the neurotoxicity of BFRs in humans and experimental animals is provided, and some common in vitro neurotoxic mechanisms of action are discussed. The combined epidemiological and toxicological studies clearly underline the need for replacing BFRs. Many potentially suitable AFRs are already in use, despite the absence of a full profile of their environmental behavior and toxicological properties. To prioritize the suitability of some selected halogenated and non-halogenated organophosphorous flame retardants and inorganic halogen-free flame retardants, the available neurotoxic data of these AFRs are discussed. The suitability of the AFRs is rank-ordered and combined with human exposure data (serum concentrations, breast milk concentrations and house dust concentrations) and physicochemical properties (useful to predict e.g. bioavailability and persistence in the environment) for a first semi-quantitative risk assessment of the AFRs. As can be concluded from the reviewed data, several BFRs and AFRs share some neurotoxic effects and modes of action. Moreover, the available neurotoxicity data indicate that some AFRs may be suitable substitutes for BFRs. However, proper risk assessment is hampered by an overall scarcity of data, particularly regarding environmental persistence, human exposure levels, and the formation of breakdown products and possible metabolites as well as their toxicity. Until these data gaps in environmental behavioral and toxicological profiles are filled, large scale use of

  1. Comparison between Two Bromine Containing Free Radical Initiators in PRESAGE®

    Energy Technology Data Exchange (ETDEWEB)

    Park, Hyeonsuk; Ryu, Dongmin; Ye, Sung-Joon [Seoul National University, Seoul (Korea, Republic of)

    2016-10-15

    PRESAGE® is an optically clear 3-D polyurethane dosimeter which contains a halogenated carbon as a free radical initiator and leucomalachite dye. The change of the optical density is known to be linear with respect to the absorbed dose and the sensitivity is related to the carbon–halogen bond dissociation energy of the free radical initiator. Although there are some studies regarding free radical initiators and dye materials, there’s a lack of reports about the effect of other elements like LMG solvent which can be added when there’s a difficulty mixing materials. Also, there are some studies about comparison between free radicals with different kind of halogen atoms but there’s a lack of studies of comparison between initiators with the same halogen atom. In this experiments, two kinds of halocarbon free radical initiator with the same halogen atom (bromine) as well as the effect of the LMG solvent were studied to use the dosimeter as a therapeutic purpose. Effective atomic numbers were also calculated. The initiators with the same halogen atom, CBr{sub 4} and C{sub 2}H{sub 2}Br{sub 4}, reacted totally differently. CBr{sub 4} was more sensitive to the radiation and emitted maximum 4 times more free radicals upon irradiation with no additional effective atomic number but the absorbance after irradiation was highly variable with time. For stable measurement, C{sub 2}H{sub 2}Br{sub 4} would be more appropriate as a free radical initiator.

  2. Crystallographic fragment-based drug discovery: use of a brominated fragment library targeting HIV protease.

    Science.gov (United States)

    Tiefenbrunn, Theresa; Forli, Stefano; Happer, Meaghan; Gonzalez, Ana; Tsai, Yingssu; Soltis, Michael; Elder, John H; Olson, Arthur J; Stout, Charles D

    2014-02-01

    A library of 68 brominated fragments was screened against a new crystal form of inhibited HIV-1 protease in order to probe surface sites in soaking experiments. Often, fragments are weak binders with partial occupancy, resulting in weak, difficult-to-fit electron density. The use of a brominated fragment library addresses this challenge, as bromine can be located unequivocally via anomalous scattering. Data collection was carried out in an automated fashion using AutoDrug at SSRL. Novel hits were identified in the known surface sites: 3-bromo-2,6-dimethoxybenzoic acid (Br6) in the flap site and 1-bromo-2-naphthoic acid (Br27) in the exosite, expanding the chemistry of known fragments for development of higher affinity potential allosteric inhibitors. At the same time, mapping the binding sites of a number of weaker binding Br-fragments provides further insight into the nature of these surface pockets. © 2013 John Wiley & Sons A/S.

  3. 18 CFR 367.81 - Maintenance.

    Science.gov (United States)

    2010-04-01

    ... 18 Conservation of Power and Water Resources 1 2010-04-01 2010-04-01 false Maintenance. 367.81... Expense Instructions § 367.81 Maintenance. (a) The cost of maintenance chargeable to the various operating... maintenance work. A list of work operations applicable generally to service company property is included in...

  4. 40 CFR 745.81 - Effective dates.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Effective dates. 745.81 Section 745.81... Effective dates. Link to an amendment published at 75 FR 24818, May 6, 2010. (a) Training, certification and... Right: Important Lead Hazard Information for Families, Child Care Providers and Schools. After that date...

  5. 9 CFR 201.81 - Suspended registrants.

    Science.gov (United States)

    2010-01-01

    ... 201.81 Animals and Animal Products GRAIN INSPECTION, PACKERS AND STOCKYARDS ADMINISTRATION (PACKERS AND STOCKYARDS PROGRAMS), DEPARTMENT OF AGRICULTURE REGULATIONS UNDER THE PACKERS AND STOCKYARDS ACT Services § 201.81 Suspended registrants. No stockyard owner, packer, market agency, or dealer shall employ...

  6. 33 CFR 211.81 - Reservoir areas.

    Science.gov (United States)

    2010-07-01

    ... 33 Navigation and Navigable Waters 3 2010-07-01 2010-07-01 false Reservoir areas. 211.81 Section... Lands in Reservoir Areas Under Jurisdiction of Department of the Army for Cottage Site Development and Use § 211.81 Reservoir areas. Delegations, rules and regulations in §§ 211.71 to 211.80 are applicable...

  7. 27 CFR 41.81 - Taxpayment.

    Science.gov (United States)

    2010-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 2 2010-04-01 2010-04-01 false Taxpayment. 41.81 Section 41.81 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT OF... each HTS item number; (ii) For large cigars with a sale price of not more than $235.294 per thousand...

  8. 27 CFR 6.81 - General.

    Science.gov (United States)

    2010-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2010-04-01 2010-04-01 false General. 6.81 Section 6.81 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT OF THE... manufacturer's invoice price); and (v) Charges to the retailer for any item. (2) Although no separate...

  9. 34 CFR 81.15 - Evidence.

    Science.gov (United States)

    2010-07-01

    ... 34 Education 1 2010-07-01 2010-07-01 false Evidence. 81.15 Section 81.15 Education Office of the... Evidence. (a) The Federal Rules of Evidence do not apply to proceedings under this part. However, the ALJ accepts only evidence that is— (1) Relevant; (2) Material; (3) Not unduly repetitious; and (4) Not...

  10. 7 CFR 958.81 - Compliance.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Compliance. 958.81 Section 958.81 Agriculture Regulations of the Department of Agriculture (Continued) AGRICULTURAL MARKETING SERVICE (Marketing Agreements... Compliance. No handler shall handle onions the handling of which has been prohibited or otherwise limited by...

  11. 40 CFR 81.339 - Pennsylvania.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Pennsylvania. 81.339 Section 81.339 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) DESIGNATION OF... Franklin Boro X East Taylor Twp X Middle Taylor Twp X West Taylor Twp X (B) Blair County: City of Altoona X...

  12. 40 CFR 81.348 - Washington.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false Washington. 81.348 Section 81.348 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) DESIGNATION OF... along a meander line following the middle of the Lake and Roesiger Creek to Woods Creek; thence...

  13. 40 CFR 600.502-81 - Definitions.

    Science.gov (United States)

    2010-07-01

    ... Automobiles)-Procedures for Determining Manufacturer's Average Fuel Economy § 600.502-81 Definitions. (a) The... 40 Protection of Environment 29 2010-07-01 2010-07-01 false Definitions. 600.502-81 Section 600... ECONOMY AND CARBON-RELATED EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy Regulations for Model Year...

  14. 24 CFR 84.81 - Definition.

    Science.gov (United States)

    2010-04-01

    ... 24 Housing and Urban Development 1 2010-04-01 2010-04-01 false Definition. 84.81 Section 84.81 Housing and Urban Development Office of the Secretary, Department of Housing and Urban Development UNIFORM ADMINISTRATIVE REQUIREMENTS FOR GRANTS AND AGREEMENTS WITH INSTITUTIONS OF HIGHER EDUCATION, HOSPITALS, AND OTHER...

  15. 31 CFR 103.81 - Submitting requests.

    Science.gov (United States)

    2010-07-01

    ... 31 Money and Finance: Treasury 1 2010-07-01 2010-07-01 false Submitting requests. 103.81 Section 103.81 Money and Finance: Treasury Regulations Relating to Money and Finance FINANCIAL RECORDKEEPING... which the request is made. (b) A request filed by a corporation shall be signed by a corporate officer...

  16. 40 CFR 152.81 - Applicability.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Applicability. 152.81 Section 152.81 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) PESTICIDE PROGRAMS PESTICIDE... the sole purpose of facilitating the marketing of a product in different geographic regions with...

  17. 28 CFR 81.1 - Purpose.

    Science.gov (United States)

    2010-07-01

    ... 28 Judicial Administration 2 2010-07-01 2010-07-01 false Purpose. 81.1 Section 81.1 Judicial Administration DEPARTMENT OF JUSTICE (CONTINUED) CHILD ABUSE AND CHILD PORNOGRAPHY REPORTING DESIGNATIONS AND... receive and investigate reports of child abuse under the provisions of section 226 of the Victims of Child...

  18. 12 CFR 34.81 - Definitions.

    Science.gov (United States)

    2010-01-01

    ... which banking use no longer is contemplated. This includes real estate originally acquired for future... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Definitions. 34.81 Section 34.81 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY REAL ESTATE LENDING AND APPRAISALS Other...

  19. 40 CFR 417.81 - Specialized definitions.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 28 2010-07-01 2010-07-01 true Specialized definitions. 417.81 Section 417.81 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS SOAP AND DETERGENT MANUFACTURING POINT SOURCE CATEGORY Manufacture of Liquid Soaps Subcategory...

  20. Recuperação de bromo em soluções aquosas residuais Bromine recovery from waste aqueous solutions

    Directory of Open Access Journals (Sweden)

    Glauco Arnold Tavares

    2004-04-01

    Full Text Available A laboratory procedure was devised to recover bromine from waste alkaline aqueous solutions used in the isotopic determination of N-15. The laboratory apparatus comprises two round bottom flasks (1 and 2 L, a dropping funnel, a gas bubbler, a gas regulator and glass fittings. The waste solution is acidified with sulfuric acid forming molecular bromine that is stripped out by a flow of nitrogen gas bubbled through the solution. This gas is then bubbled through a solution of lithium hydroxide generating lithium bromide and lithium hypobromite. The efficiency of bromine recovery was estimated to be 82±2%. This resulting solution was successfully reused in the isotopic determination of N-15. The procedure can recycle most of the bromine used in the laboratory saving resources and preserving the environment. The procedure can be adapted to recover bromine of other laboratory waste streams.

  1. Halogen-specific total organic halogen analysis: Assessment by recovery of total bromine.

    Science.gov (United States)

    Langsa, Markus; Allard, Sebastien; Kristiana, Ina; Heitz, Anna; Joll, Cynthia A

    2017-08-01

    Determination of halogen-specific total organic halogen (TOX) is vital for studies of disinfection of waters containing bromide, since total organic bromine (TOBr) is likely to be more problematic than total organic chlorine. Here, we present further halogen-specific TOX method optimisation and validation, focusing on measurement of TOBr. The optimised halogen-specific TOX method was validated based on the recovery of model compounds covering different classes of disinfection by-products (haloacetic acids, haloacetonitriles, halophenols and halogenated benzenes) and the recovery of total bromine (mass balance of TOBr and bromide concentrations) during disinfection of waters containing dissolved organic matter and bromide. The validation of a halogen-specific TOX method based on the mass balance of total bromine has not previously been reported. Very good recoveries of organic halogen from all model compounds were obtained, indicating high or complete conversion of all organic halogen in the model compound solution through to halide in the absorber solution for ion chromatography analysis. The method was also successfully applied to monitor conversion of bromide to TOBr in a groundwater treatment plant. An excellent recovery (101%) of total bromine was observed from the raw water to the post-chlorination stage. Excellent recoveries of total bromine (92%-95%) were also obtained from chlorination of a synthetic water containing dissolved organic matter and bromide, demonstrating the validity of the halogen-specific TOX method for TOBr measurement. The halogen-specific TOX method is an important tool to monitor and better understand the formation of halogenated organic compounds, in particular brominated organic compounds, in drinking water systems. Copyright © 2017. Published by Elsevier B.V.

  2. The application of a monolithic triphenylphosphine reagent for conducting Appel reactions in flow microreactors

    Directory of Open Access Journals (Sweden)

    Kimberley A. Roper

    2011-12-01

    Full Text Available Herein we describe the application of a monolithic triphenylphosphine reagent to the Appel reaction in flow-chemistry processing, to generate various brominated products with high purity and in excellent yields, and with no requirement for further off-line purification.

  3. Application of supercritical water to decompose brominated epoxy resin and environmental friendly recovery of metals from waste memory module.

    Science.gov (United States)

    Li, Kuo; Xu, Zhenming

    2015-02-03

    Waste Memory Modules (WMMs), a particular kind of waste printed circuit board (WPCB), contain a high amount of brominated epoxy resin (BER), which may bring a series of environmental and health problems. On the other hand, metals like gold and copper are very valuable and are important to recover from WMMs. In the present study, an effective and environmental friendly method using supercritical water (SCW) to decompose BER and recover metals from WMMs was developed instead of hydrometallurgy or pyrometallurgy simultaneously. Experiments were conducted under external-catalyst-free conditions with temperatures ranging from 350 to 550 °C, pressures from 25 to 40 MPa, and reaction times from 120 to 360 min in a semibatch-type reactor. The results showed that BER could be quickly and efficiently decomposed under SCW condition, and the mechanism was possibly free radical reaction. After the SCW treatments, the glass fibers and metal foils in the solid residue could be easily liberated and recovered, respectively. The metal recovery rate reached 99.80%. The optimal parameters were determined as 495 °C, 33 MPa, and 305 min on the basis of response surface methodology (RSM). This study provides an efficient and environmental friendly approach for WMMs recycling compared with electrolysis, pyrometallurgy, and hydrometallurgy.

  4. Red seaweed enzyme-catalyzed bromination of bromophenol red: An inquiry-based kinetics laboratory experiment for undergraduates.

    Science.gov (United States)

    Jittam, Piyachat; Boonsiri, Patcharee; Promptmas, Chamras; Sriwattanarothai, Namkang; Archavarungson, Nattinee; Ruenwongsa, Pintip; Panijpan, Bhinyo

    2009-03-01

    Haloperoxidase enzymes are of interest for basic and applied bioscientists because of their increasing importance in pharmaceutical industry and environmental cleanups. In a guided inquiry-based laboratory experiment for life-science, agricultural science, and health science undergraduates, the bromoperoxidase from a red seaweed was used to brominate bromophenol red, a novel starting substrate. Substrate and enzyme concentration dependence of this enzyme-catalyzed reaction as followed colorimetrically yielded initial rates of reaction that the students compared with those of their peers. The students worked as collaborative groups partially designing their own experiments and carrying them out. In performing the laboratory experiment, they were minimally guided by the instructor and teaching assistants. To engage the students before the laboratory, a short activity involving the enzyme-induced color change was carried out. At the end of the laboratory session, student groups discussed their results in front of the class and reached their own conclusions. Most students had better understanding of important concepts in enzyme kinetics and showed good attitude toward the overall student-centered laboratory exercise. Copyright © 2009 International Union of Biochemistry and Molecular Biology, Inc.

  5. BrO and inferred Bry profiles over the western Pacific: relevance of inorganic bromine sources and a Bry minimum in the aged tropical tropopause layer

    Science.gov (United States)

    Koenig, Theodore K.; Volkamer, Rainer; Baidar, Sunil; Dix, Barbara; Wang, Siyuan; Anderson, Daniel C.; Salawitch, Ross J.; Wales, Pamela A.; Cuevas, Carlos A.; Fernandez, Rafael P.; Saiz-Lopez, Alfonso; Evans, Mathew J.; Sherwen, Tomás; Jacob, Daniel J.; Schmidt, Johan; Kinnison, Douglas; Lamarque, Jean-François; Apel, Eric C.; Bresch, James C.; Campos, Teresa; Flocke, Frank M.; Hall, Samuel R.; Honomichl, Shawn B.; Hornbrook, Rebecca; Jensen, Jørgen B.; Lueb, Richard; Montzka, Denise D.; Pan, Laura L.; Reeves, J. Michael; Schauffler, Sue M.; Ullmann, Kirk; Weinheimer, Andrew J.; Atlas, Elliot L.; Donets, Valeria; Navarro, Maria A.; Riemer, Daniel; Blake, Nicola J.; Chen, Dexian; Huey, L. Gregory; Tanner, David J.; Hanisco, Thomas F.; Wolfe, Glenn M.

    2017-12-01

    corroborating evidence that inorganic bromine sources (e.g., SSA-derived gas-phase Bry) are needed to explain the gas-phase Bry budget in the upper free troposphere and TTL. They are also consistent with observations of significant bromide in Upper Troposphere-Lower Stratosphere aerosols. The total Bry budget in the TTL is currently not closed, because of the lack of concurrent quantitative measurements of gas-phase Bry species (i.e., BrO, HOBr, HBr, etc.) and aerosol bromide. Such simultaneous measurements are needed to (1) quantify SSA-derived Bry in the upper FT, (2) test Bry partitioning, and possibly explain the gas-phase Bry minimum in the aged TTL, (3) constrain heterogeneous reaction rates of bromine, and (4) account for all of the sources of Bry to the lower stratosphere.

  6. A small scale intercalibration study on organobromine compounds in Japan. Results on brominated dioxins, mixed halogenated dioxins and brominated flame retardants

    Energy Technology Data Exchange (ETDEWEB)

    Takahashi, S.; Sakai, Shin-ichi [National Institute for Environmental Studies, Tsukuba (Japan); Watanabe, I. [Osaka Prefectural Institute of Public Health, Osaka (Japan)

    2004-09-15

    Recently, environmental problems relating to brominated flame retardants (BFRs) have become a matter of great concern due to their potential toxic risk on human and wildlife and recent increase in levels of polybrominated diphenyl ethers (PBDEs). Many laboratories have started work on PBDEs and other BFRs such as tetrabromo-bisphenol A (TBBPA), tribromophenol (TBP) and hexabromocyclododecane (HBCD). International intercalibration studies on the analysis of PBDEs have been conducted. The results of intercalibration studies indicated that determination of some higher brominated diphenyl ethers such as BDEs 183 and 209 was not under the control in most laboratories although these compounds are major in commercial Octa- and Deca- BDE products. Moreover, results on BFRs other than PBDEs are very much limited. Another concern has been related to the thermal breakdown products of BFRs such as polybrominated and mixed brominated/chlorinated dibenzo-p-dioxins and dibenzofurans (PBDDs/DFs and mixed PXDDs/DFs). Considerable levels (ppm or even higher) of PBDDs/DFs were detected in waste television cabinets and other flame-retarded plastics. Based on 'the Law Concerning Special Measures against Dioxins (applied since January 2000)', the Ministry of the Environment, Japan is working to promote studies on brominated dioxins, and conducted a pilot survey in the environment8. PBDDs/DFs and monobromo-polychloro dibenzo-p-dioxins and dibenzofurans (MoBPCDDs/DFs) were found in various environmental media with BFRs. Although commercially available standards for these compounds are still limited, development of a good QA/QC system has become imperative. To evaluate the accuracy and reliability in the analysis for organobromine compounds, an intercalibration study in which 10 laboratories in Japan participated was initiated since April, 2003. In this presentation, the results on PBDD/DFs, MoBPCDDs/DFs and PBDEs, in 'Mixed Standard Solutions' and &apos

  7. Unilateral kidney blood flow measurement using the 81Rb/81mKr ratio.

    NARCIS (Netherlands)

    van Herk, G.; de Zeeuw, D.

    1978-01-01

    A new method has been developed for the continuous quantification of kidney blood flow, utilizing the unique physical and biological properties of the radioactive tracer couple: rubidium-81/krypton-81m. After intravenous injection, 81Rb concentrates primarily in the kidneys, where it continuously

  8. 50 CFR 81.1 - Definitions.

    Science.gov (United States)

    2010-10-01

    ... SPECIES OF FISH, WILDLIFE, AND PLANTS-COOPERATION WITH THE STATES § 81.1 Definitions. As used in this part..., reptile, mollusk, crustacean, arthropod or other invertebrate, and includes any part, product, egg, or...

  9. Critical review of the analysis of brominated flame retardants and their environmental levels in Africa

    NARCIS (Netherlands)

    Brits, M.; de Vos, J.; Weiss, J.M.; Rohwer, E.R.; de Boer, J.

    2016-01-01

    World-wide, the prevalence of brominated flame retardants (BFRs) is well documented for routine analysis of environmental and biological matrices. There is, however, limited information on these compounds in the African environment and insufficient information on the analytical approaches used to

  10. 75 FR 16104 - Bromine Registration Review Final Decision; Notice of Availability

    Science.gov (United States)

    2010-03-31

    ... each pesticide's registration is based on current scientific and other knowledge, including its effects... registration review decision for the pesticide Bromine, case 4015. Registration review is EPA's periodic review of pesticide registrations to ensure that each pesticide continues to satisfy the statutory standard...

  11. Preliminary study on the occurrence of brominated organic compounds in Dutch marine organisms.

    Science.gov (United States)

    Kotterman, Michiel; van der Veen, Ike; van Hesselingen, Judith; Leonards, Pim; Osinga, Ronald; de Boer, Jacob

    2003-07-01

    The extracts of three marine organisms; the ascidian Ciona intestinalis, the brown seaweed Sargassum muticum and the sponge Halichondria panicea, all elicited a number of brominated compounds, some of which were tentatively identified. Tribromophenol was observed in all species. This compound, also industrially produced as flame retardant and fungicide, was likely due to endogenous production.

  12. Toxicity of brominated flame retardants in fish, with emphasis on endocrine effects and reproduction

    NARCIS (Netherlands)

    Kuiper, R.V.

    2007-01-01

    Abstract The abundant use of brominated flame retardants (BFRs) in modern polymers has over the passed decades resulted in contamination of the environment, and BFRs are increasingly found in fish. Laboratory studies have shown that a number of BFRs and BFR-metabolites can interfere with thyroid and

  13. Bromine content in some seaweeds of Goa (Central West Coast of India)

    Digital Repository Service at National Institute of Oceanography (India)

    Naqvi, S.W.A.; Mittal, P.K.; Kamat, S.Y.; Solimabi; Reddy, C.V.G.

    in chloroform at 400 and 650 nm. The bromine content, on a dry dry weight basis, varied from 0.024 to 0.024% for the green algae, from 0.020 to 0.400% for the algae, and from 0.015 to 0.054% for the brown algae. Only two species @iChondria armata@@ and @i...

  14. Formation of brominated pollutants during the pyrolysis and combustion of tetrabromobisphenol A at different temperatures.

    Science.gov (United States)

    Ortuño, Nuria; Moltó, Julia; Conesa, Juan A; Font, Rafael

    2014-08-01

    Tetrabromobisphenol A (TBBPA) is the most widely used brominated flame retardant worldwide. A detailed examination of the degradation products emitted during thermal decomposition of TBBPA is presented in the study. Runs were performed in a laboratory furnace at different temperatures (650 and 800 °C) and in different atmospheres (nitrogen and air). More than one hundred semivolatile compounds have been identified by GC/MS, with special interest in brominated ones. Presence of HBr and brominated light hydrocarbons increased with temperature and in the presence of oxygen. Maximum formation of PAHs is observed at pyrolytic condition at the higher temperature. High levels of 2,4-, 2,6- and 2,4,6- bromophenols were found. The levels of polybrominated dibenzo-p-dioxins and furans have been detected in the ppm range. The most abundant isomers are 2,4,6,8-TeBDF in pyrolysis and 1,2,3,7,8-PeBDF in combustion. These results should be considered in the assessment of thermal treatment of materials containing brominated flame retardants. Copyright © 2014 Elsevier Ltd. All rights reserved.

  15. Exposure levels to brominated compounds in seawater swimming pools treated with chlorine.

    Science.gov (United States)

    Parinet, Julien; Tabaries, Sophie; Coulomb, Bruno; Vassalo, Laurent; Boudenne, Jean-Luc

    2012-03-01

    Despite evidence of formation of brominated compounds in seawater swimming pools treated with chlorine, no data about exposure levels to these compounds have been reported. To address this issue, a survey has been carried out in four establishments (representing 8 pools) fed with seawater and devoted to relaxing and cure treatments (thalassotherapy centres located in Southeast of France). Carcinogenic and mutagenic brominated disinfection byproducts (trihalomethanes -THM- and halogenated acetic acids -HAA-) were quantified at varying levels, statistically related to organic loadings brought by bathers, and not from marine organic matter, and also linked to activities carried out in the pools (watergym vs swimming). Bromoform and dibromoacetic acid, the most abundant THM and HAA detected, were measured at levels up to 18-fold greater than the maximum contaminant levels of 60 and 80 μg/L fixed by US.EPA in drinking waters. The correlations between these disinfection byproducts and other environmental factors such as nitrogen, pH, temperature, free residual chlorine, UV(254), chloride and bromide concentrations, and daily frequentation were examined. Because thalassotherapy and seawater swimming pools (hotels, cruise ships,…) are increasing in use around the world and because carcinogenic and mutagenic brominated byproducts may be produced in chlorinated seawater swimming pools, specific care should be taken to assure cleanliness of users (swimmers and patients taking the waters) and to increase water circulation through media filters to reduce levels of brominated byproducts. Copyright © 2011 Elsevier Ltd. All rights reserved.

  16. Raman study of bromine-doped single-walled carbon nanotubes under high pressure

    CERN Document Server

    Liu Bing Bing; Yu Miao; Zou Guang Tian; Carlsten, J; Wagberg, T; Sundqvist, B

    2002-01-01

    Raman results for different single-walled carbon nanotube bundles doped with Br sub 2 were studied both at ambient pressure and under high pressure up to 6 GPa. Our study indicates that bromine resides in the interstitial channel of nanotube bundles as a form of polymer.

  17. Degradation of brominated flame retardant in computer housing plastic by supercritical fluids.

    Science.gov (United States)

    Wang, Yanmin; Zhang, Fu-Shen

    2012-02-29

    The degradation process of brominated flame retardant (BFR) and BFR-containing waste computer housing plastic in various supercritical fluids (water, methanol, isopropanol and acetone) was investigated. The results showed that the debromination and degradation efficiencies, final products were greatly affected by the solvent type. Among the four tested solvents, isopropanol was the most suitable solvent for the recovery of oil from BFR-containing plastic for its (1) excellent debromination effectiveness (debromination efficiency 95.7%), (2) high oil production (60.0%) and (3) mild temperature and pressure requirements. However, in this case, the removed bromine mostly existed in the oil. Introduction of KOH into the sc-isopropanol could capture almost all the inorganic bromine from the oil thus bromine-free oil could be obtained. Furthermore, KOH could enhance the depolymerization of the plastic. The obtained oil mainly consisted of single- and duplicate-ringed aromatic compounds in a carbon range of C9-C17, which had alkyl substituents or aliphatic bridges, such as butyl-benzene, (3-methylbutyl)-benzene, 1,1'-(1,3-propanediyl)bis benzene. Phenol, alkyl phenols and esters were the major oxygen-containing compounds in the oil. This study provides an efficient approach for debromination and simultaneous recovering valuable chemicals from BFR-containing plastic in e-waste. Copyright © 2011 Elsevier B.V. All rights reserved.

  18. Brominated Flame Retardants in the Environment - The Price for our Convenience?

    NARCIS (Netherlands)

    Boer, de J.

    2004-01-01

    This paper reviews information on the occurrence of brominated flame retardants (BFRs) in various environmental compartments. The lack of information on BFRs other than pentabrominated diphenylethers (pentaBDEs) is emphasized, as well as the need for better analytical methods and the need for more

  19. Regioselective chlorination and bromination of unprotected anilines under mild conditions using copper halides in ionic liquids

    Directory of Open Access Journals (Sweden)

    Han Wang

    2012-05-01

    Full Text Available By using ionic liquids as solvents, the chlorination or bromination of unprotected anilines at the para-position can be achieved in high yields with copper halides under mild conditions, without the need for potentially hazardous operations such as supplementing oxygen or gaseous HCl.

  20. Performance and Degradation of A Lithium-Bromine Rechargeable Fuel Cell Using Highly Concentrated Catholytes

    CERN Document Server

    Bai, Peng

    2016-01-01

    Lithium-air batteries have been considered as ultimate solutions for the power source of long-range electrified transportation, but state-of-the-art prototypes still suffer from short cycle life, low efficiency and poor power output. Here, a lithium-bromine rechargeable fuel cell using highly concentrated bromine catholytes is demonstrated with comparable specific energy, improved power density, and higher efficiency. The cell is similar in structure to a hybrid-electrolyte Li-air battery, where a lithium metal anode in nonaqueous electrolyte is separated from aqueous bromine catholytes by a lithium-ion conducting ceramic plate. The cell with a flat graphite electrode can discharge at a peak power density around 9mW cm-2 and in principle could provide a specific energy of 791.8 Wh kg-1, superior to most existing cathode materials and catholytes. It can also run in regenerative mode to recover the lithium metal anode and free bromine with 80-90% voltage efficiency, without any catalysts. Degradation of the sol...

  1. 40 CFR 81.405 - California.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 17 2010-07-01 2010-07-01 false California. 81.405 Section 81.405 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) DESIGNATION OF...-58 USDA-FS Yolla-Bolly-Middle-Eel Wild 109,091 88-577 USDA-FS Yosemite NP 759,172 58-49 USDI-NPS 1 26...

  2. Bromine release from blowing snow and its impact on tropospheric chemistry

    Science.gov (United States)

    Griffiths, Paul; Yang, Xin; Abraham, N. Luke; Archibald, Alexander; Pyle, John

    2016-04-01

    In the last two decades, significant depletion of boundary layer ozone (ozone depletion events, ODEs) has been observed in both Arctic and Antarctic spring. ODEs are attributed to catalytic destruction by bromine radicals (Br plus BrO), especially during bromine explosion events (BEs), when high concentrations of BrO periodically occur. The source of bromine and the mechanism that sustains the high BrO levels are still the subject of study. Recent work by Pratt et al. (2013) posits Br2 production within saline snow and sea ice which leads to sudden ODEs. Previously, Yang et al. (2008) suggested snow could provide a source of (depleted) sea-salt aerosol if wicked from the surface of ice. They suggest that rapid depletion of bromide from the aerosol will constitute a source of photochemical Bry. Given the large sea ice extent in polar regions, this may constitute a significant source of sea salt and bromine in the polar lower atmosphere. While bromine release from blowing snow is perhaps less likely to trigger sudden ODEs, it may make a contribution to regional scale processes affecting ozone levels. Currently, the model parameterisations of Yang et al. assumes that rapid release of bromine occurs from fresh snow on sea ice during periods of strong wind. The parameterisation depends on an assumed sea-salt aerosol distribution generated via sublimation of the snow above the boundary layer, as well as taking into account the salinity of the snow. In this work, we draw on recent measurements by scientists from the British Antarctic Survey during a cruise aboard the Polarstern in the southern oceans. This has provided an extensive set of measurements of the chemical and physical characteristics of blowing snow over sea ice, and of the aerosol associated with it. Based on the observations, we have developed an improved parameterisation of the release of bromine from blowing snow. The paper presents results from the simulation performed using the United Kingdom Chemistry

  3. Peroxometal-mediated oxidation of bromine leading to ...

    Indian Academy of Sciences (India)

    Administrator

    Br + Bu4NBr + HBr. For instance: Versatility of this environmentally benign reaction protocol involving a variety of substrates has also been demonstrated by other collaborators. Implications of this investigation with reference to VBrPO activity ...

  4. Monitoring of WEEE plastics in regards to brominated flame retardants using handheld XRF

    Energy Technology Data Exchange (ETDEWEB)

    Aldrian, Alexia, E-mail: alexia.aldrian@unileoben.ac.at [Chair of Waste Processing Technology and Waste Management, Montanuniversitaet Leoben, Franz-Josef-Straße 18, 8700 Leoben (Austria); Ledersteger, Alfred, E-mail: a.ledersteger@saubermacher.at [Saubermacher Dienstleistungs AG, Hans-Roth-Straße 1, 8073 Feldkirchen bei Graz (Austria); Pomberger, Roland, E-mail: roland.pomberger@unileoben.ac.at [Chair of Waste Processing Technology and Waste Management, Montanuniversitaet Leoben, Franz-Josef-Straße 18, 8700 Leoben (Austria)

    2015-02-15

    Highlights: • Specification of an empirical factor for conversion from bromine to PBB and PBDE. • The handheld XRF device was validated for this particular application. • A very large number of over 4600 pieces of monitor housings was analysed. • The recyclable fraction mounts up to 85% for TV but only 53% of PC waste plastics. • A high percentage of pieces with bromine contents of over 50,000 ppm was obtained. - Abstract: This contribution is focused on the on-site determination of the bromine content in waste electrical and electronic equipment (WEEE), in particular waste plastics from television sets (TV) and personal computer monitors (PC) using a handheld X-ray fluorescence (XRF) device. The described approach allows the examination of samples in regards to the compliance with legal specifications for polybrominated biphenyls (PBBs) and polybrominated diphenyl ethers (PBDEs) directly after disassembling and facilitates the sorting out of plastics with high contents of brominated flame retardants (BFRs). In all, over 3000 pieces of black (TV) and 1600 pieces of grey (PC) plastic waste were analysed with handheld XRF technique for this study. Especially noticeable was the high percentage of pieces with a bromine content of over 50,000 ppm for TV (7%) and PC (39%) waste plastics. The applied method was validated by comparing the data of handheld XRF with results obtained by GC–MS. The results showed the expected and sufficiently accurate correlation between these two methods. It is shown that handheld XRF technique is an effective tool for fast monitoring of large volumes of WEEE plastics in regards to BFRs for on-site measurements.

  5. Brominated flame retardants and the formation of dioxins and furans in fires and combustion

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Mengmei [State key laboratory of clean energy utilisation, Institute for Thermal Power Engineering, Zhejiang University, Hangzhou (China); Buekens, Alfons [State key laboratory of clean energy utilisation, Institute for Thermal Power Engineering, Zhejiang University, Hangzhou (China); Formerly with Chemical Engineering department, Vrije Universiteit Brussel, Brussels (Belgium); Li, Xiaodong, E-mail: lixd@zju.edu.cn [State key laboratory of clean energy utilisation, Institute for Thermal Power Engineering, Zhejiang University, Hangzhou (China)

    2016-03-05

    Highlights: • BFRs (PBDEs, HBCD and TBBP-A) are the main sources of PBDD/Fs in combustion process. • Precursor formation is the most relevant pathway for PBDD/Fs formation. • Adding bromine into combustion system can enhance the formation of PCDD/Fs. • Primitive recycling of e-waste produces the largest amounts of PBDD/Fs. - Abstract: The widespread use and increasing inventory of brominated flame retardants (BFRs) have caused considerable concern, as a result of BFRs emissions to the environment and of the formation of both polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs) and mixed polybromochloro-dibenzo-p-dioxins and dibenzofurans (PBCDD/Fs or PXDD/Fs). Structural similarities between PBDD/Fs and polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) suggest the existence of comparable formation pathways of both PBDD/Fs and PCDD/Fs, yet BFRs also act as specific precursors to form additional PBDD/Fs. Moreover, elementary bromine (Br{sub 2}) seems to facilitate chlorination by bromination of organics, followed by Br/Cl-exchange based on displacement through the more reactive halogen. Overall, PBDD/Fs form through three possible pathways: precursor formation, de novo formation, and dispersion of parts containing BFRs as impurities and surviving a fire or other events. The present review summarises the formation mechanisms of both brominated (PBDD/Fs) and mixed dioxins (PXDD/Fs with X = Br or Cl) from BFRs, recaps available emissions data of PBDD/Fs and mixed PXDD/Fs from controlled waste incineration, uncontrolled combustion sources and accidental fires, and identifies and analyses the effects of several local factors of influence, affecting the formation of PBDD/Fs and mixed PXDD/Fs during BFRs combustion.

  6. Processing wastes and waste-derived fuels containing brominated flame retardants

    Energy Technology Data Exchange (ETDEWEB)

    Tohka, A.; Zevenhoven, R.

    2002-07-01

    Brominated flame retardants (BFRs) are widely used, often together with antimony-based flame retardants, in electronic and electric equipment, furniture and office equipment. While this increases the fire safety for these products, the BFRs are problematic when thermal processes are used during the treatment of waste streams from these products, such as waste from electrical and electronic equipment (WEEE). Not only do the BFRs negatively effect the incineration of old furniture, they interfere with thermal processes that aim at the recovery of, for example, valuable metals from WEEE. A flame retardant should inhibit or suppress a combustion process and that's why they are used in products which would otherwise have a high risk of fire. Including flame retardant into products is one way to improve their fire safety relatively cheap way. Depending on their nature, flame retardants can act chemically and/or physically in solid, liquid or gas phase. They interfere with combustion during a particular stage of this process, e.g. during heating, decomposition, ignition or flame spread. For BFRs the high molecular weight provides numerous advantages from manufacturers' point of view are such as low volatility, low migration rates at surface, ease of handling. This report gives an overview of which and how much BFRs are found in various products and waste streams and what problems this may bring to thermal processes for recovery and recycling or during incineration or waste-to-energy processing. Also the formation of brominated analogues of dioxins and furans, PBDD/Fs (poly brominated dibenzo -p- dioxins and - furans) is addressed, and analytical methods that allow for the identification and measurement of concentrations of brominated chemicals during thermal processing of BFR-containing waste streams. Bromine-related corrosion and the ozone depleting properties of methyl bromide (bromoform) are mentioned but not discussed.

  7. Comparative study of the formation of brominated disinfection byproducts in UV/persulfate and UV/H2O2 oxidation processes in the presence of bromide.

    Science.gov (United States)

    Wang, Lu; Ji, Yuefei; Lu, Junhe; Kong, Deyang; Yin, Xiaoming; Zhou, Quansuo

    2017-10-01

    The objective of this research was to compare the transformation of Br- and formation of brominated byproducts in UV/persulfate (PS) and UV/H2O2 processes. It was revealed that Br- was efficiently transformed to free bromine which reacted with humic acid (HA) or dihydroxybenzoic acid resulting in the formation of brominated byproducts such as bromoacetic acids (BAAs) in UV/PS system. In contrast, no free bromine and brominated byproducts could be detected in UV/H2O2 system, although the oxidization of Br- was evident. We presumed that the oxidation of Br- by hydroxyl radicals led to the formation of bromine radicals. However, the bromine radical species could be immediately reduced back to Br- by H2O2 before coupling to each other to form free bromine, which explains the undetection of free bromine and BAAs in UV/H2O2. In addition to free bromine, we found that the phenolic functionalities in HA molecules, which served as the principal reactive sites for free chlorine attack, could be in situ generated when HA was exposed to free radicals. This study demonstrates that UV/H2O2 is more suitable than UV/PS for the treatment of environmental matrices containing Br-. Graphical abstract Graphical abstract.

  8. Red seaweed enzyme-catalyzed bromination of bromophenol red: An inquiry-based kinetics laboratory experiment for undergraduates

    National Research Council Canada - National Science Library

    Jittam, Piyachat; Boonsiri, Patcharee; Promptmas, Chamras; Sriwattanarothai, Namkang; Archavarungson, Nattinee; Ruenwongsa, Pintip; Panijpan, Bhinyo

    2009-01-01

    .... In a guided inquiry-based laboratory experiment for life-science, agricultural science, and health science undergraduates, the bromoperoxidase from a red seaweed was used to brominate bromophenol red...

  9. MLS/Aura Level 3 Bromine Monoxide (BrO) Daily 10deg Lat Zonal Mean V003

    Data.gov (United States)

    National Aeronautics and Space Administration — ML3DZMBRO is the EOS Aura Microwave Limb Sounder (MLS) daily zonal mean product for bromine monoxide derived from radiances measured by the 640 GHz radiometer. The...

  10. MLS/Aura Level 2 Bromine Monoxide (BrO) Mixing Ratio V004 (ML2BRO) at GES DISC

    Data.gov (United States)

    National Aeronautics and Space Administration — ML2BRO is the EOS Aura Microwave Limb Sounder (MLS) standard product for bromine monoxide derived from radiances measured by the 640 GHz radiometer. The data version...

  11. Prenatal Exposure to Organohalogens, Including Brominated Flame Retardants, Influences Motor, Cognitive, and Behavioral Performance at School Age

    NARCIS (Netherlands)

    Roze, Elise; Meijer, Lisethe; Bakker, Attie; Van Braeckel, Koenraad N. J. A.; Sauer, Pieter J. J.; Bos, Arend F.

    2009-01-01

    BACKGROUND: Organohalogen compounds (OHCs) are known to have neurotoxic effects on the developing brain. OBJECTIVE: We investigated the influence of prenatal exposure to OHCs, including brominated flame retardants, on motor, cognitive, and behavioral outcome in healthy children of school age.

  12. Windows 8.1 for dummies

    CERN Document Server

    Rathbone, Andy

    2013-01-01

    The bestselling book on Windows, now updated for the new 8.1 features Microsoft has fine-tuned Windows 8 with some important new features, and veteran author Andy Rathbone explains every one in this all-new edition of a long-time bestseller. Whether you're using Windows for the first time, upgrading from an older version, or just moving from Windows 8 to 8.1, here's what you need to know. Learn about the dual interfaces, the new Start button, how to customize the interface and boot operations, and how to work with programs and files, use the web and social media, manage music and photos, and

  13. [Formation and Variation of Brominated Disinfection By-products in A Combined Ultrafiltration and Reverse Osmosis Process for Seawater Desalination].

    Science.gov (United States)

    Yang, Zhe; Sun, Ying-xue; Shi, Na; Hu, Hong-ying

    2015-10-01

    The characteristics of dissolved organic matter (DOM) and brominated disinfection by-products ( Br-DBPs ) during a seawater desalination ultrafiltration (UF) combined reverse osmosis (RO) process were studied. The seawater contained high level of bromide ion (45.6-50.9 mg x L(-1)) and aromatic compounds with specific ultraviolet absorbance ( SUVA) of 3.6-6.0 L x (mg x m)(-1). The tryptophan-like aromatic protein, fulvic acid-like and soluble microbial by-product-like were the main fluorescent DOM in the seawater. After pre-chlorination of the seawater, the concentrations of DBPs was significantly increased in the influent of UF, which was dominantly the Br-DBPs. Bromoform (CHBr3) accounted for 70.48% - 91.50% of total trihalomethanes (THMs), dibromoacetic acid (Br2CHCO2H) occupied 81.14% - 100% of total haloacetic acids (HAAs) and dibromoacetonitrile (C2HBr2N) occupied 83.77% - 87.45% of total haloacetonitriles ( HANs). The removal efficiency of THMs, HAAs and HANs by the UF membrane was 36.63% - 40.39%, 73.83% - 95.38% and 100%, respectively. The RO membrane could completely remove the HAAs, while a little of the THMs was penetrated. The antiestrogenic activity in the seawater was 0.35 - 0.44 mg x L(-1), which was increased 32% - 69% after the pre-chlorination. The DBPs and other bio-toxic organics which formed during the UF-RO process were finally concentrated in the UF concentrate and RO concentrate.

  14. Metal-catalysed organic transformations in water: From bromination ...

    Indian Academy of Sciences (India)

    Reaction of ,-unsaturated aromatic carboxylic acids with KBr and H2O2 in the presence of Na2MoO4 ⋅ H2O in aqueous medium affords -bromo alkenes in high yields. Metallocene dichlorides, Cp2MCl2 (M = Ti, Zr, or V) catalyse polymerisation of olefins in aqueous medium to afford high molecular weight polymers ...

  15. Oxyhalogen-sulfur chemistry: kinetics and mechanism of oxidation of chemoprotectant, sodium 2-mercaptoethanesulfonate, MESNA, by acidic bromate and aqueous bromine.

    Science.gov (United States)

    Adigun, Risikat Ajibola; Mhike, Morgen; Mbiya, Wilbes; Jonnalagadda, Sreekanth B; Simoyi, Reuben H

    2014-03-27

    The oxidation of a well-known chemoprotectant in anticancer therapies, sodium 2-mercaptoethanesulfonate, MESNA, by acidic bromate and aqueous bromine was studied in acidic medium. Stoichiometry of the reaction is: BrO3(-) + HSCH2CH2SO3H → Br(-) + HO3SCH2CH2SO3H. In excess bromate conditions the stoichiometry was deduced to be: 6BrO3(-) + 5HSCH2CH2SO3H + 6H(+) → 3Br2 + 5HO3SCH2CH2SO3H + 3H2O. The direct reaction of bromine and MESNA gave a stoichiometric ratio of 3:1: 3Br2 + HSCH2CH2SO3H + 3H2O → HO3SCH2CH2SO3H + 6Br(-) + 6H(+). This direct reaction is very fast; within limits of the mixing time of the stopped-flow spectrophotometer and with a bimolecular rate constant of 1.95 ± 0.05 × 10(4) M(-1) s(-1). Despite the strong oxidizing agents utilized, there is no cleavage of the C-S bond and no sulfate production was detected. The ESI-MS data show that the reaction proceeds via a predominantly nonradical pathway of three consecutive 2-electron transfers on the sulfur center to obtain the product 1,2-ethanedisulfonic acid, a well-known medium for the delivery of psychotic drugs. Thiyl radicals were detected but the absence of autocatalytic kinetics indicated that the radical pathway was a minor oxidation route. ESI-MS data showed that the S-oxide, contrary to known behavior of organosulfur compounds, is much more stable than the sulfinic acid. In conditions where the oxidizing equivalents are limited to a 4-electron transfer to only the sulfinic acid, the products obtained are a mixture of the S-oxide and the sulfonic acid with negligible amounts of the sulfinic acid. It appears the S-oxide is the preferred conformation over the sulfenic acid since no sulfenic acids have ever been stabilized without bulky substituent groups. The overall reaction scheme could be described and modeled by a minimal network of 18 reactions in which the major oxidants are HOBr and Br2(aq).

  16. Characterization of mercury binding onto a novel brominated biomass ash sorbent by X-ray absorption spectroscopy.

    Science.gov (United States)

    Bisson, Teresa M; MacLean, Lachlan C W; Hu, Yongfeng; Xu, Zhenghe

    2012-11-06

    Recent laboratory and field-scale experiments demonstrated the potential for brominated industrial solid waste from biomass combustion (Br-Ash) to be an efficient, cost-effective alternative to activated carbon for capturing mercury from coal-fired power plants. To develop this attractive alternative technology to a commercially sustainable level, a better understanding of mercury capture mechanisms by Br-Ash is required. For this purpose, X-ray absorption fine-structure (XAFS) spectra of Br-Ash were collected at the Hg L(III)-edge, Br K-edge and S K-edge, and analyzed to determine the local bonding environment of mercury atoms. The coordination environment of Hg was compared with that on a commercial brominated activated carbon. Our results indicate that the mercury was captured by chemisorption on both the commercial and biomass ash sorbents; however, the mercury binding environment was different for each sorbent. Mercury was found to bind to the reduced sulfur by the commercial brominated activated carbon, in contrast to mercury binding with carbon and bromine on the brominated biomass ash. Based on the results obtained, a mechanism of Hg capture involving oxidation of elemental Hg followed by binding of the oxidized mercury on the surface of the sorbent near Br was proposed for the brominated biomass ash.

  17. 21 CFR 113.81 - Product preparation.

    Science.gov (United States)

    2010-04-01

    ... Production and Process Controls § 113.81 Product preparation. (a) Before using raw materials and ingredients susceptible to microbiological contamination, the processor shall ensure that those materials and ingredients... and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR...

  18. 32 CFR 81.3 - Policy.

    Science.gov (United States)

    2010-07-01

    ... AND ADOPTION PROCEEDINGS INVOLVING MEMBERS AND FORMER MEMBERS OF THE ARMED FORCES § 81.3 Policy. (a... legal rights in the matter. See 42 U.S.C. 659. The member will be encouraged to render the necessary... availability of personnel to appear at an adoption hearing, where it is alleged that an active duty member is...

  19. 40 CFR 8.1 - Purpose.

    Science.gov (United States)

    2010-07-01

    ... provides for: (1) The environmental impact assessment of nongovernmental activities, including tourism, for... Environment ENVIRONMENTAL PROTECTION AGENCY GENERAL ENVIRONMENTAL IMPACT ASSESSMENT OF NONGOVERNMENTAL ACTIVITIES IN ANTARCTICA § 8.1 Purpose. (a) This part is issued pursuant to the Antarctic Science, Tourism...

  20. 28 CFR 81.5 - Definitions.

    Science.gov (United States)

    2010-07-01

    ... Administration DEPARTMENT OF JUSTICE (CONTINUED) CHILD ABUSE AND CHILD PORNOGRAPHY REPORTING DESIGNATIONS AND PROCEDURES § 81.5 Definitions. Local child protective services agency means that agency of the federal government, of a state, of a tribe or of a local government that has the primary responsibility for child...

  1. 28 CFR 81.11 - Purpose.

    Science.gov (United States)

    2010-07-01

    ... Administration DEPARTMENT OF JUSTICE (CONTINUED) CHILD ABUSE AND CHILD PORNOGRAPHY REPORTING DESIGNATIONS AND PROCEDURES Child Pornography Reporting Designations and Procedures § 81.11 Purpose. The regulations in this... pornography that are forwarded from the National Center for Missing and Exploited Children under the...

  2. 36 CFR 1192.81 - Lighting.

    Science.gov (United States)

    2010-07-01

    ... 1192.81 Parks, Forests, and Public Property ARCHITECTURAL AND TRANSPORTATION BARRIERS COMPLIANCE BOARD AMERICANS WITH DISABILITIES ACT (ADA) ACCESSIBILITY GUIDELINES FOR TRANSPORTATION VEHICLES Light Rail... lighted station platforms shall have outside lights which provide at least 1 footcandle of illumination on...

  3. Reinvestigation of bromination of 8-substituted quinolines and synthesis of novel phthalonitriles

    Directory of Open Access Journals (Sweden)

    Salih Ökten

    2016-12-01

    Full Text Available Bromination of a series of 8-substituted quinolines was reinvestigated and specified for optimum yields and isolation conditions. Mono bromination of 8-hydroxyquinoline ( 2a and 8-aminoquinoline ( 2c gave mixture of mono and dibromo derivatives 5,7-dibromo-8-hydroxyquinoline ( 3a ,5,7-dibromo-8-aminoquinoline (3c, 7-bromo-8-hydroxyquinoline (3d, 5-bromo-8-aminoquinoline (3ewhile 8-methoxy quinoline ( 2b furnished 5-bromo-8-methoxyquinoline ( 3f as sole product. N ovel phthalonitrile s, 4-(quinolin-8-yloxyphthalonitrile ( 6 and 4-chloro-5-(quinolin-8-yloxyphthalonitrile (8 of 8-hydroxyquinoline ( 2a were synthesized and converted into their respective bromo derivatives 4-(5-bromoquinolin-8-yloxyphthalonitrile ( 7 and4-((5-bromoquinolin-8-yloxy-5-chlorophthalonitrile (9 .

  4. Stratospheric ozone depletion and future levels of atmospheric chlorine and bromine

    Science.gov (United States)

    Prather, Michael J.; Watson, Robert T.

    1990-01-01

    The rise in atmospheric chlorine levels caused by the emission of chlorofluorocarbons and other halocarbons is thought to be the main cause of the appearance of the Antarctic ozone 'hole' in the late 1970s, and the more modest ozone depletion observed over parts of the Northern Hemisphere. Atmospheric bromine, also associated with halocarbon emissions, is believed to contribute to ozone depletion. Over the next decade, further increases in these compounds are inevitable. Model calculations show that by the end of the next century, atmospheric chlorine and bromine levels may return to those prevalent before the onset of the ozone hole, but only if more stringent regulations are applied to halocarbon production than those currently proposed.

  5. Development of rechargeable lithium-bromine batteries with lithium ion conducting solid electrolyte

    Science.gov (United States)

    Takemoto, Koshin; Yamada, Hirotoshi

    2015-05-01

    Electrochemical performances of a prototype lithium-bromine battery (LBB) employing a solid electrolyte is investigated. The discharge capacity decreases with repeating charge/discharge cycles. Electrochemical impedance analysis reveals that the capacity fading is mainly due to increase in the interfacial resistance between an aqueous active material solution and a solid electrolyte. Based on the results of symmetric cells and structural analysis of the surface of the solid electrolyte immersed in Br2 solutions, it is suggested that a Li+-depletion layer is formed on the surface of the solid electrolyte as a result of contact with bromine. Addition of tetraethylammonium bromide (TEABr) depresses the interfacial resistance, which results in improved cycleability. LBB with 1.0 M LiBr and 0.25 M TEABr shows discharge capacity of 139 mAh/g-LiBr and Coulombic efficiency of 99.6% at 5th cycle.

  6. Bromine number prediction for Colombian naphthas using near-infrared spectroscopy and chemometric methods

    Directory of Open Access Journals (Sweden)

    Carlos Aparicio

    2016-12-01

    Full Text Available Thirty-eight naphtha samples were used to develop a chemometric method to predict bromine number. All samples were characterized by Fourier transform near infrared spectroscopy (FT-NIR, and their spectra were correlated by similarity using principal component analysis (PCA. The models for bromine number determination (BN were established by Partial Least Squares regression (PLS and Multiple Polynomial Regression (MPR. PCA allowed classifying the samples into the light and heavy, determining the most significant spectral variables. These variables are located in the regions between 4000-4800 and 5200-6350cm-1. The results determined by combining FT-NIR spectroscopy and chemometrics were very close to those obtained by standardized methods. This approach may be an alternative for analysis of BN, which requires sample turnarounds lower than five minutes and lower cost compared to traditional methods.

  7. Formation pathways of brominated products from benzophenone-4 chlorination in the presence of bromide ions.

    Science.gov (United States)

    Xiao, Ming; Wei, Dongbin; Li, Liping; Liu, Qi; Zhao, Huimin; Du, Yuguo

    2014-12-01

    The brominated products, formed in chlorination treatment of benzophenone-4 in the presence of bromide ions, were identified, and the formation pathways were proposed. Under disinfection conditions, benzophenone-4 would undertake electrophilic substitution generating mono- or di-halogenated products, which would be oxidized to esters and further hydrolyzed to phenol derivatives. The generated catechol intermediate would be transformed into furan-like heterocyclic product. The product species were pH-dependent, while benzophenone-4 elimination was chlorine dose-dependent. When the chlorination treatment was performed on ambient water spiked with benzophenone-4 and bromide ions, most of brominated byproducts could be detected, and the acute toxicity significantly increased as well. Copyright © 2014. Published by Elsevier B.V.

  8. A comparison of the virucidal properties of chlorine, chlorine dioxide, bromine chloride and iodine.

    OpenAIRE

    Taylor, G R; Butler, M.

    1982-01-01

    Chlorine dioxide, bromine chloride and iodine were compared with chlorine as virucidal agents. Under optimal conditions all disinfectants were effective at low concentrations, but each disinfectant responded differently to acidity and alkalinity. Disinfection by chlorine was impaired by the presence of ammonia, but the other disinfectants retained much of their potency. Disinfection of poliovirus by iodine resulted in structural changes in the virions as seen by electron micrroscopy, but the ...

  9. Brominated and organophosphate flame retardants in selected consumer products on the Japanese market in 2008

    Energy Technology Data Exchange (ETDEWEB)

    Kajiwara, Natsuko, E-mail: kajiwara.natsuko@nies.go.jp [Research Center for Material Cycles and Waste Management, National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki 305-8506 (Japan); Noma, Yukio; Takigami, Hidetaka [Research Center for Material Cycles and Waste Management, National Institute for Environmental Studies, 16-2 Onogawa, Tsukuba, Ibaraki 305-8506 (Japan)

    2011-09-15

    Highlights: {yields} We examined the flame retardants in electronics, curtains, wallpaper and insulator. {yields} Use of alternative brominated and organophosphate flame retardants was suggested. {yields} All the products investigated also contained PBDEs, TBBPA and polybromophenols. {yields} Incorporation of recycled materials containing hazardous substance was suggested. - Abstract: The concentrations of traditional brominated flame retardants (BFRs) and organophosphate flame retardants (OPFRs) in new consumer products, including electronic equipment, curtains, wallpaper, and building materials, on the Japanese market in 2008 were investigated. Although some components of the electronic equipment contained bromine at concentrations on the order of percent by weight, as indicated by X-ray fluorescence analysis, the bromine content could not be fully accounted for by the BFRs analyzed in this study, which included polybrominated diphenylethers, decabromodiphenyl ethane, tetrabromobisphenol A, polybromophenols, and hexabromocyclododecanes. These results suggest the use of alternative BFRs such as newly developed formulations derived from tribromophenol, tetrabromobisphenol A, or both. Among the 11 OPFRs analyzed, triphenylphosphate was present at the highest concentrations in all the products investigated, which suggests the use of condensed-type OPFRs as alternative flame retardants, because they contain triphenylphosphate as an impurity. Tripropylphosphate was not detected in any samples; and trimethylphosphate, tributyl tris(2-butoxyethyl)phosphate, and tris(1,3-dichloro-2-propyl)phosphate were detected in only some components and at low concentrations. Note that all the consumer products evaluated in this study also contained traditional BFRs in amounts that were inadequate to impart flame retardancy, which implies the incorporation of recycled plastic materials containing BFRs that are of global concern.

  10. A dynamic system for delivering controlled bromine and chlorine vapor exposures to weanling swine skin.

    Science.gov (United States)

    Snider, Thomas H; Perry, Mark R; Richter, William R; Plahovinsak, Jennifer L; Rogers, James; Reid, Frances M; Graham, John S

    2014-06-01

    Assessing the hazards of accidental exposure to toxic industrial chemical (TIC) vapors and evaluating therapeutic compounds or treatment regimens require the development of appropriate animal models. The objective of this project was to develop an exposure system for delivering controlled vapor concentrations of TICs to the skin of anesthetized weanling pigs. Injury levels targeted for study were superficial dermal (SD) and deep dermal (DD) skin lesions as defined histopathologically. The exposure system was capable of simultaneously delivering chlorine or bromine vapor to four, 3-cm diameter exposure cups placed over skin between the axillary and inguinal areas of the ventral abdomen. Vapor concentrations were generated by mixing saturated bromine or chlorine vapor with either dried dilution air or nitrogen. Bromine exposure concentrations ranged from 6.5 × 10(-4) to 1.03 g/L, and exposure durations ranged from 1 to 45 min. A 7-min skin exposure to bromine vapors at 0.59 g/L was sufficient to produce SD injuries, while a 17-min exposure produced a DD injury. Chlorine exposure concentrations ranged from 1.0 to 2.9 g/L (saturated vapor concentration) for exposures ranging from 3 to 90 min. Saturated chlorine vapor challenges for up to 30 min did not induce significant dermal injuries, whereas saturated chlorine vapor with wetted material on the skin surface for 30-60 min induced SD injuries. DD chlorine injuries could not be induced with this system. The vapor exposure system described in this study provides a means for safely regulating, quantifying and delivering TIC vapors to the skin of weanling swine as a model to evaluate therapeutic treatments.

  11. Measurement and human exposure assessment of brominated flame retardants in household products from South China.

    Science.gov (United States)

    Chen, She-Jun; Ma, Yun-Juan; Wang, Jing; Tian, Mi; Luo, Xiao-Jun; Chen, Da; Mai, Bi-Xian

    2010-04-15

    Brominated flame retardants (BFRs), polybrominated diphenyl ethers (PBDEs), and decabromodiphenyl ethane (DBDPE) were examined in household products in the Pearl River Delta, South China, including electronic appliances, furniture and upholstery, car interiors, and raw materials for electronics. The concentrations of PBDEs derived from penta-BDE mixture were much lower (products. Our findings suggest the recycling of old electronic products and their reuse might be also a potential important source of discontinued PBDEs to the environment. DBDPE was found in 20.0% of all the samples, ranging from 311 to 268,230 ng/g. PBDE congener profiles in both the household products and raw materials suggest that some less brominated BDEs in the environment may be derived from the decomposition of higher brominated PBDEs in PBDE-containing products in process of the manufacturing, use and/or recycling. Human exposure to PBDEs from household products via inhalation ranged from 175 to 612 pg/kg bw day, accounting for a small proportion of the total daily exposure via indoor inhalation. Despite the low deleterious risk associated with household products with regard to PBDEs, they are of special concern because of the relatively higher exposures observed for young children and further work is required. 2009 Elsevier B.V. All rights reserved.

  12. The separation of waste printed circuit board by dissolving bromine epoxy resin using organic solvent.

    Science.gov (United States)

    Zhu, P; Chen, Y; Wang, L Y; Zhou, M; Zhou, J

    2013-02-01

    Separation of waste printed circuit boards (WPCBs) has been a bottleneck in WPCBs resource processing. In this study, the separation of WPCBs was performed using dimethyl sulfoxide (DMSO) as a solvent. Various parameters, which included solid to liquid ratio, temperature, WPCB sizes, and time, were studied to understand the separation of WPCBs by dissolving bromine epoxy resin using DMSO. Experimental results showed that the concentration of dissolving the bromine epoxy resin increased with increasing various parameters. The optimum condition of complete separation of WPCBs was solid to liquid ratio of 1:7 and WPCB sizes of 16 mm(2) at 145°C for 60 min. The used DMSO was vapored under the decompression, which obtained the regenerated DMSO and dissolved bromine epoxy resin. This clean and non-polluting technology offers a new way to separate valuable materials from WPCBs and prevent the environmental pollution of waste printed circuit boards effectively. Crown Copyright © 2012. Published by Elsevier Ltd. All rights reserved.

  13. Effects of sequential treatment with fluorine and bromine on graphite fibers

    Science.gov (United States)

    Hung, Ching-Cheh; Stahl, Mark; Maciag, Carolyn; Slabe, Melissa

    1987-01-01

    Three pitch based graphite fibers with different degrees of graphitization and one polyacryonitrile (PAN) based carbon fiber from Amoco Corporation were treated with 1 atm, room temperature fluorine gas for 90 hrs. Fluorination resulted in higher electrical conductivity for all pitch fibers. Further bromination after ambient condition defluorination resulted in further increases in electrical defluorination conductivity for less graphitized, less structurally ordered pitch fibers (P-55) which contain about 3% fluorine by weight before bromination. This product can be stable in 200 C air, or 100% humidity at 60 C. Due to its low cost, this less graphitized fiber may be useful for industrial application, such as airfoil deicer materials. The same bromination process, however, resulted in conductivity decreases for fluorine rich, more graphitized, structurally oriented pitch fibers (P-100 and P-75). Such decreases in electrical conductivity were partially reversed by heating the fibers at 185 C in air. Differential scanning calorimetric (DSC) data indicated that the more graphitized fibers (P-100) contained BrF3, whereas the less graphitized fibers (P-55) did not.

  14. Monitoring of WEEE plastics in regards to brominated flame retardants using handheld XRF.

    Science.gov (United States)

    Aldrian, Alexia; Ledersteger, Alfred; Pomberger, Roland

    2015-02-01

    This contribution is focused on the on-site determination of the bromine content in waste electrical and electronic equipment (WEEE), in particular waste plastics from television sets (TV) and personal computer monitors (PC) using a handheld X-ray fluorescence (XRF) device. The described approach allows the examination of samples in regards to the compliance with legal specifications for polybrominated biphenyls (PBBs) and polybrominated diphenyl ethers (PBDEs) directly after disassembling and facilitates the sorting out of plastics with high contents of brominated flame retardants (BFRs). In all, over 3000 pieces of black (TV) and 1600 pieces of grey (PC) plastic waste were analysed with handheld XRF technique for this study. Especially noticeable was the high percentage of pieces with a bromine content of over 50,000ppm for TV (7%) and PC (39%) waste plastics. The applied method was validated by comparing the data of handheld XRF with results obtained by GC-MS. The results showed the expected and sufficiently accurate correlation between these two methods. It is shown that handheld XRF technique is an effective tool for fast monitoring of large volumes of WEEE plastics in regards to BFRs for on-site measurements. Copyright © 2014 Elsevier Ltd. All rights reserved.

  15. Teach yourself visually Windows 8.1

    CERN Document Server

    McFedries, Paul

    2013-01-01

    A practical guide for visual learners eager to get started with Windows 8.1 If you learn more quickly when you can see how things are done, this Visual guide is the easiest way to get up and running on Windows 8.1. It covers more than 150 essential Windows tasks, using full-color screen shots and step-by-step instructions to show you just what to do. Learn your way around the interface and how to install programs, set up user accounts, play music and other media files, download photos from your digital camera, go online, set up and secure an e-mail account, and much more.The tried-and-true f

  16. STS-81 Crew Walkout for TCDT

    Science.gov (United States)

    1996-01-01

    The STS-81 mission flight crew walks out of the Operations and Checkout Building at KSC on their way to Launch Pad 39B during the final phase of the Terminal Countdown Demonstration Test (TCDT) exercises for that mission, a simulated final countdown until just before main engine ignition. They are (from right front): ): Mission Commander Michael A. Baker; Pilot Brent W. Jett, Jr.; and Mission Specialists J.M. 'Jerry' Linenger, Peter J. K. 'Jeff' Wisoff; John M. Grunsfeld and Marsha S. Ivins. STS- 81 is the fifth Shuttle-Mir docking mission and will feature the transfer of Linenger to Mir to replace astronaut John Blaha, who has been on the orbital laboratory since Sept. 19 after arrival there during the STS-79 mission. During STS-81, Shuttle and Mir crews will conduct risk mitigation, human life science, microgravity and materials processing experiments that will provide data for the design, development and operation of the International Space Station. The primary payload is the SPACEHAB- DM double module will provide space for more than 2,000 pounds of hardware, food and water that will be transferred into the Russian space station during five days of docking operations during the 10-day mission. The SPACEHAB will also be used to return experiment samples from the Mir to Earth for analysis and for microgravity experiments during the mission.

  17. Bromine monoxide / sulphur dioxide ratios in relation to volcanological observations at Mt. Etna 2006–2009

    Directory of Open Access Journals (Sweden)

    G. Giuffrida

    2012-12-01

    Full Text Available Over a 3-yr period, from 2006 to 2009, frequent scattered sunlight DOAS measurements were conducted at Mt. Etna at a distance of around 6 km downwind from the summit craters. During the same period and in addition to these measurements, volcanic observations were made by regularly visiting various parts of Mt. Etna. Here, results from these measurements and observations are presented and their relation is discussed. The focus of the investigation is the bromine monoxide/sulphur dioxide (BrO / SO2 ratio, and its variability in relation to volcanic processes. That the halogen/sulphur ratio can serve as a precursor or indicator for the onset of eruptive activity was already proposed by earlier works (e.g. Noguchi and Kamiya 1963; Menyailov, 1975; Pennisi and Cloarec, 1998; Aiuppa et al., 2002. However, there is still a limited understanding today because of the complexity with which halogens are released, depending on magma composition and degassing conditions. Our understanding of these processes is far from complete, for example of the rate and mechanism of bubble nucleation, growth and ascent in silicate melts (Carroll and Holloway, 1994, the halogen vapour-melt partitioning and the volatile diffusivity in the melt (Aiuppa et al., 2009. With this study we aim to add one more piece to the puzzle of what halogen/sulphur ratios might tell about volcanic activities. Our data set shows an increase of the BrO / SO2 ratio several weeks prior to an eruption, followed by a decline before and during the initial phase of eruptive activities. Towards the end of activity or shortly thereafter, the ratio increases to baseline values again and remains more or less constant during quiet phases. To explain the observed evolution of the BrO / SO2 ratio, a first empirical model is proposed. This model suggests that bromine, unlike chlorine and fluorine, is less soluble in the magmatic melt than sulphur. By using the DOAS method to determine SO2, we actually

  18. Brominated flame retardants and organochlorine pollutants in eggs of little owls (Athene noctua) from Belgium

    Energy Technology Data Exchange (ETDEWEB)

    Jaspers, Veerle [Department of Biology, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Wilrijk (Belgium); Covaci, Adrian [Toxicological Centre, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Wilrijk (Belgium)]. E-mail: adrian.covaci@ua.ac.be; Maervoet, Johan [Toxicological Centre, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Wilrijk (Belgium); Dauwe, Tom [Department of Biology, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Wilrijk (Belgium); Voorspoels, Stefan [Toxicological Centre, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Wilrijk (Belgium); Schepens, Paul [Toxicological Centre, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Wilrijk (Belgium); Eens, Marcel [Department of Biology, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Wilrijk (Belgium)

    2005-07-15

    Residues of brominated diphenylethers (PBDEs), organochlorinated pesticides (OCPs) and polychlorinated biphenyls (PCBs) were measured in 40 eggs of little owls (Athene noctua), a terrestrial top predator from Belgium. The major organohalogens detected were PCBs (median 2,600 ng/g lipid, range 790-23000 ng/g lipid). PCB 153,138/163, 170, 180 and 187 were the predominant congeners and constituted 71% of total sum PCBs. PBDEs were measurable in all samples, but their concentrations were much lower than for PCBs, with a range from 29-572 ng/g lipid (median 108 ng/g lipid). The most prevalent PBDE congeners in little owl egg samples were BDE 47, 99 and 153. This profile differs from the profile in marine bird species, for which BDE 47 was the dominant congener, indicating that terrestrial birds may be more exposed to higher brominated BDE congeners than marine birds. The fully brominated BDE 209 could be detected in one egg sample (17 ng/g lipid), suggesting that higher brominated BDEs may accumulate in terrestrial food chains. Brominated biphenyl (BB) 153 was determined in all egg samples, with levels ranging from 0.6 to 5.6 ng/g lipid (median 1.3 ng/g lipid). Additionally, hexabromocyclododecane (HBCD) could be identified and quantified in only two eggs at levels of 20 and 50 ng/g lipid. OCPs were present at low concentrations, suggesting a rather low contamination of the sampled environment with OCPs (median concentrations of sum DDTs: 826 ng/g lipid, sum chlordanes: 1,016 ng/g lipid, sum HCHs: 273 ng/g lipid). Hexachlorobenzene (HCB) and octachlorostyrene (OCS) were also found at low median levels of 134 and 3.4 ng/g lipid, respectively. Concentrations of most analytes were significantly higher in eggs collected from deserted nests in comparison to addled (unhatched) eggs, while eggshell thickness did not differ between deserted and addled eggs. No significant correlations were found between eggshell thickness and the analysed organohalogens. - PBDEs are measurable

  19. Bromine-80m-labeled estrogens: Auger-electron emitting, estrogen receptor-directed ligands with potential for therapy of estrogen receptor positive cancers

    Energy Technology Data Exchange (ETDEWEB)

    DeSombre, E.R.; Mease, R.C.; Hughes, A.; Harper, P.V.; DeJesus, O.T.; Friedman, A.M.

    1988-01-01

    A triphenylbromoethylene, 1,1-bis(p-hydroxyphenyl)-2-bromo-2-phenylethylene, Br-BHPE, and a bromosteroidal estrogen, 17..cap alpha..- bromovinylestradiol, BrVE/sub 2/, were labeled with the Auger electron emitting nuclide bromine-80m, prepared by the (p,n) reaction with /sup 80/Se. To assess their potential as estrogen receptor (ER) directed therapeutic substrates the bromine-80m labeled estrogens were injected into immature female rats and the tissue distribution studied at 0.5 and 2 hours. Both radiobromoestrogens showed substantial diethylstilbesterol (DES)-inhibitable localization in the ER rich tissues, uterus, pituitary, ovary and vagina at both time points. While the percent dose per gram tissue was higher for the Br-BHPE, the BrVE/sub 2/ showed higher tissue to blood ratios, especially at 2 hr, reflecting the lower blood concentrations of radiobromine following administration of the steroidal bromoestrogen. Comparing intraperitoneal, intravenous and subcutaneous routes of administration for the radiobromine labeled Br-BHPE, the intraperitoneal route was particularly advantageous to provide maximum, DES-inhibitable concentrations in the peritoneal, ER-rich target organs, the uterus, ovary and vagina. While uterine concentrations after BrBHPE were from 10--48% dose/g and after BrVE/sub 2/ were 15--25% dose/g, similar treatment with /sup 80m/Br as sodium bromide showed uniform low concentrations in all tissues at about the levels seen in blood. The effective specific activity of (/sup 80m/Br)BrBHPE, assayed by specific binding to ER in rat uterine cytosol, was 8700 Ci/mmole. 23 refs., 9 figs., 2 tabs.

  20. Hair keratin KRT81 is expressed in normal and breast cancer cells and contributes to their invasiveness.

    Science.gov (United States)

    Nanashima, Naoki; Horie, Kayo; Yamada, Toshiyuki; Shimizu, Takeshi; Tsuchida, Shigeki

    2017-05-01

    Keratins are fibrous proteins. Hair keratins constitute hard structures such as the hair and nails, and cytokeratins have been used as markers of breast carcinoma. However, the expression and function of full-size hair keratin genes have not been previously demonstrated in breast cancer. We investigated the expression of the hair keratin, KRT81, and its function in human breast cancer and normal mammary epithelial cells. Western blotting showed full size 55-kDa KRT81 expression in the human breast cancer cell lines, MCF7, SKBR3 and MDA-MB-231, normal human mammary epithelial cells (HMEC), and non-neoplastic cells (MCF10A). Reverse transcription-polymerase chain reaction revealed that the full size KRT81, including its 5' region is expressed in breast cells. Immunohistochemical and immunofluorescence analyses showed that KRT81 was located in the cytoplasm. To investigate the function of KRT81, we knocked down KRT81 by siRNA in MCF10A cells. Microarray analysis revealed that the expression of genes related to invasion such as matrix metallopeptidase (MMP)9 was decreased. In KRT81-knockdown MDA-MB231 cells, zymography revealed a decrease in MMP9 activity, while scratch and invasion assays revealed that KRT81-knockdown decreased cell migration and invasion abilities. This is the first study showing that full size KRT81 is expressed in normal breast epithelial cells and breast cancer cells. Moreover, our results indicate that KRT81 contributes to the migration and invasion of breast cancer cells.

  1. A quantitative analysis of the reactions involved in stratospheric ozone depletion in the polar vortex core

    Science.gov (United States)

    Wohltmann, Ingo; Lehmann, Ralph; Rex, Markus

    2017-09-01

    We present a quantitative analysis of the chemical reactions involved in polar ozone depletion in the stratosphere and of the relevant reaction pathways and cycles. While the reactions involved in polar ozone depletion are well known, quantitative estimates of the importance of individual reactions or reaction cycles are rare. In particular, there is no comprehensive and quantitative study of the reaction rates and cycles averaged over the polar vortex under conditions of heterogeneous chemistry so far. We show time series of reaction rates averaged over the core of the polar vortex in winter and spring for all relevant reactions and indicate which reaction pathways and cycles are responsible for the vortex-averaged net change of the key species involved in ozone depletion, i.e., ozone, chlorine species (ClOx, HCl, ClONO2), bromine species, nitrogen species (HNO3, NOx) and hydrogen species (HOx). For clarity, we focus on one Arctic winter (2004-2005) and one Antarctic winter (2006) in a layer in the lower stratosphere around 54 hPa and show results for additional pressure levels and winters in the Supplement. Mixing ratios and reaction rates are obtained from runs of the ATLAS Lagrangian chemistry and transport model (CTM) driven by the European Centre for Medium-Range Weather Forecasts (ECMWF) ERA-Interim reanalysis data. An emphasis is put on the partitioning of the relevant chemical families (nitrogen, hydrogen, chlorine, bromine and odd oxygen) and activation and deactivation of chlorine.

  2. A quantitative analysis of the reactions involved in stratospheric ozone depletion in the polar vortex core

    Directory of Open Access Journals (Sweden)

    I. Wohltmann

    2017-09-01

    Full Text Available We present a quantitative analysis of the chemical reactions involved in polar ozone depletion in the stratosphere and of the relevant reaction pathways and cycles. While the reactions involved in polar ozone depletion are well known, quantitative estimates of the importance of individual reactions or reaction cycles are rare. In particular, there is no comprehensive and quantitative study of the reaction rates and cycles averaged over the polar vortex under conditions of heterogeneous chemistry so far. We show time series of reaction rates averaged over the core of the polar vortex in winter and spring for all relevant reactions and indicate which reaction pathways and cycles are responsible for the vortex-averaged net change of the key species involved in ozone depletion, i.e., ozone, chlorine species (ClOx, HCl, ClONO2, bromine species, nitrogen species (HNO3, NOx and hydrogen species (HOx. For clarity, we focus on one Arctic winter (2004–2005 and one Antarctic winter (2006 in a layer in the lower stratosphere around 54 hPa and show results for additional pressure levels and winters in the Supplement. Mixing ratios and reaction rates are obtained from runs of the ATLAS Lagrangian chemistry and transport model (CTM driven by the European Centre for Medium-Range Weather Forecasts (ECMWF ERA-Interim reanalysis data. An emphasis is put on the partitioning of the relevant chemical families (nitrogen, hydrogen, chlorine, bromine and odd oxygen and activation and deactivation of chlorine.

  3. STS-81 Crew Arrival at SLF

    Science.gov (United States)

    1997-01-01

    The STS-81 flight crew conducts a press briefing on the runway of KSC Shuttle Landing Facility after they arrive at the space center for the final countdown preparations for the fifth Shuttle-Mir docking mission. They are (from left): Mission Commander Michael A. Baker; Pilot Brent W. Jett, Jr.; and Mission Specialists Peter J. K. 'Jeff' Wisoff; John M. Grunsfeld, Marsha S. Ivins, and J.M. 'Jerry' Linenger. The 10-day mission will feature the transfer of Linenger to Mir to replace astronaut John Blaha, who has been on the orbital laboratory since Sept. 19, 1996 after arrival there during the STS-79 mission. During STS- 81, Shuttle and Mir crews will conduct risk mitigation, human life science, microgravity and materials processing experiments that will provide data for the design, development and operation of the International Space Station. The primary payload is the SPACEHAB-DM double module will provide space for more than 2,000 pounds of hardware, food and water that will be transferred into the Russian space station during five days of docking operations. The SPACEHAB will also be used to return experiment samples from the Mir to Earth for analysis and for microgravity experiments during the mission.

  4. Reaction Automata

    OpenAIRE

    Okubo, Fumiya; Kobayashi, Satoshi; YOKOMORI, Takashi

    2011-01-01

    Reaction systems are a formal model that has been introduced to investigate the interactive behaviors of biochemical reactions. Based on the formal framework of reaction systems, we propose new computing models called reaction automata that feature (string) language acceptors with multiset manipulation as a computing mechanism, and show that reaction automata are computationally Turing universal. Further, some subclasses of reaction automata with space complexity are investigated and their la...

  5. New retrieval of BrO from SCIAMACHY limb: an estimate of the stratospheric bromine loading during April 2008

    Directory of Open Access Journals (Sweden)

    J. P. Parrella

    2013-10-01

    Full Text Available We present a new retrieval of stratospheric BrO (bromine monoxide from channel 2 SCIAMACHY (SCanning Imaging Absorption spectrometer for Atmospheric CHartographY limb observations. Retrievals are shown to agree with independent balloon observations to within one standard deviation of the retrieval noise. We retrieve BrO profiles for all of April 2008, and apply simulated [BrO]/[Bry] (bromine monoxide : stratospheric inorganic bromine ratios to estimate the stratospheric Bry loading. We find 23.5 ± 6 ppt Br, suggesting 7 ppt Br from short-lived bromocarbons to be at the high end of the current best estimate (3–8 ppt. The 6 ppt Br uncertainty estimate is dominated by the 21% uncertainty in the simulated [BrO] / [Bry] ratio due to propagation of errors from the underlying chemical kinetics.

  6. Trophic transfer of naturally produced brominated aromatic compounds in a Baltic Sea food chain.

    Science.gov (United States)

    Dahlgren, Elin; Lindqvist, Dennis; Dahlgren, Henrik; Asplund, Lillemor; Lehtilä, Kari

    2016-02-01

    Brominated aromatic compounds (BACs) are widely distributed in the marine environment. Some of these compounds are highly toxic, such as certain hydroxylated polybrominated diphenyl ethers (OH-PBDEs). In addition to anthropogenic emissions through use of BACs as e.g. flame retardants, BACs are natural products formed by marine organisms such as algae, sponges, and cyanobacteria. Little is known of the transfer of BACs from natural producers and further up in the trophic food chain. In this study it was observed that total sum of methoxylated polybrominated diphenyl ethers (MeO-PBDEs) and OH-PBDEs increased in concentration from the filamentous red alga Ceramium tenuicorne, via Gammarus sp. and three-spined stickleback (Gasterosteus aculeatus) to perch (Perca fluviatilis). The MeO-PBDEs, which were expected to bioaccumulate, increased in concentration accordingly up to perch, where the levels suddenly dropped dramatically. The opposite pattern was observed for OH-PBDEs, where the concentration exhibited a general trend of decline up the food web, but increased in perch, indicating metabolic demethylation of MeO-PBDEs. Debromination was also indicated to occur when progressing through the food chain resulting in high levels of tetra-brominated MeO-PBDE and OH-PBDE congeners in fish, while some penta- and hexa-brominated congeners were observed to be the dominant products in the alga. As it has been shown that OH-PBDEs are potent disruptors of oxidative phosphorylation and that mixtures of different congener may act synergistically in terms of this toxic mode of action, the high levels of OH-PBDEs detected in perch in this study warrants further investigation into potential effects of these compounds on Baltic wildlife, and monitoring of their levels. Copyright © 2015 Elsevier Ltd. All rights reserved.

  7. Seasonal variation of tropospheric bromine monoxide over the Rann of Kutch salt marsh seen from space

    Directory of Open Access Journals (Sweden)

    C. Hörmann

    2016-10-01

    Full Text Available The Rann of Kutch (India and Pakistan is one of the largest salt deserts in the world. Being a so-called "seasonal salt marsh", it is regularly flooded during the Indian summer monsoon. We present 10 years of bromine monoxide (BrO satellite observations by the Ozone Monitoring Instrument (OMI over the Great and Little Rann of Kutch. OMI spectra were analysed using Differential Optical Absorption Spectroscopy (DOAS and revealed recurring high BrO vertical column densities (VCDs of up to 1.4  ×  1014 molec cm−2 during April/May, but no significantly enhanced column densities during the monsoon season (June–September. In the following winter months, the BrO VCDs are again slightly enhanced while the salty surface dries up. We investigate a possible correlation of enhanced reactive bromine concentrations with different meteorological parameters and find a strong relationship between incident UV radiation and the total BrO abundance. In contrast, the second Global Ozone Monitoring Instrument (GOME-2 shows about 4 times lower BrO VCDs over the Rann of Kutch than found by OMI and no clear seasonal cycle is observed. One reason for this finding might be the earlier local overpass time of GOME-2 compared to OMI (around 09:30 vs. 13:30 LT, as the ambient conditions significantly differ for both satellite instruments at the time of the measurements. Further possible reasons are discussed and mainly attributed to instrumental issues. OMI additionally confirms the presence of enhanced BrO concentrations over the Dead Sea valley (Israel/Jordan, as suggested by former ground-based observations. The measurements indicate that the Rann of Kutch salt marsh is probably one of the strongest natural point sources of reactive bromine compounds outside the polar regions and is therefore supposed to have a significant impact on local and regional ozone chemistry.

  8. Structural Studies of ?-Turn-Containing Peptide Catalysts for Atroposelective Quinazolinone Bromination?

    OpenAIRE

    Metrano, A. J.; Abascal, N. C.; Mercado, B. Q.; Paulson, E. K.; Miller, S. J.

    2016-01-01

    We describe herein a crystallographic and NMR study of the secondary structural attributes of a ?-turn-containing tetra-peptide, Boc-Dmaa-D-Pro-Acpc-Leu-NMe2, which was recently reported as a highly effective catalyst in the atroposelective bromination of 3-arylquinazolin-4(3H)-ones. Inquiries pertaining to the functional consequences of residue substitutions led to the discovery of a more selective catalyst, Boc-Dmaa-D-Pro-Acpc-Leu-OMe, the structure of which was also explored. This new lead...

  9. In vivo speciation studies and antioxidant properties of bromine in Laminaria digitata reinforce the significance of iodine accumulation for kelps

    Science.gov (United States)

    Küpper, Frithjof C.; Carpenter, Lucy J.; Leblanc, Catherine; Toyama, Chiaki; Uchida, Yuka; Maskrey, Benjamin H.; Robinson, Joanne; Verhaeghe, Elodie F.; Malin, Gill; Luther, George W.; Kroneck, Peter M. H.; Kloareg, Bernard; Meyer-Klaucke, Wolfram; Muramatsu, Yasuyuki; Megson, Ian L.; Potin, Philippe; Feiters, Martin C.

    2013-01-01

    The metabolism of bromine in marine brown algae remains poorly understood. This contrasts with the recent finding that the accumulation of iodide in the brown alga Laminaria serves the provision of an inorganic antioxidant – the first case documented from a living system. The aim of this study was to use an interdisciplinary array of techniques to study the chemical speciation, transformation, and function of bromine in Laminaria and to investigate the link between bromine and iodine metabolism, in particular in the antioxidant context. First, bromine and iodine levels in different Laminaria tissues were compared by inductively coupled plasma MS. Using in vivo X-ray absorption spectroscopy, it was found that, similarly to iodine, bromine is predominantly present in this alga in the form of bromide, albeit at lower concentrations, and that it shows similar behaviour upon oxidative stress. However, from a thermodynamic and kinetic standpoint, supported by in vitro and reconstituted in vivo assays, bromide is less suitable than iodide as an antioxidant against most reactive oxygen species except superoxide, possibly explaining why kelps prefer to accumulate iodide. This constitutes the first-ever study exploring the potential antioxidant function of bromide in a living system and other potential physiological roles. Given the tissue-specific differences observed in the content and speciation of bromine, it is concluded that the bromide uptake mechanism is different from the vanadium iodoperoxidase-mediated uptake of iodide in L. digitata and that its function is likely to be complementary to the iodide antioxidant system for detoxifying superoxide. PMID:23606364

  10. Characterization of Some Real Mixed Plastics from WEEE: A Focus on Chlorine and Bromine Determination by Different Analytical Methods

    Directory of Open Access Journals (Sweden)

    Beatrice Beccagutti

    2016-10-01

    Full Text Available Bromine and chlorine are almost ubiquitous in waste of electrical and electronic equipment (WEEE and the knowledge of their content in the plastic fraction is an essential step for proper end of life management. The aim of this study is to compare the following analytical methods: energy dispersive X-ray fluorescence spectroscopy (ED-XRF, ion chromatography (IC, ion-selective electrodes (ISEs, and elemental analysis for the quantitative determination of chlorine and bromine in four real samples taken from different WEEE treatment plants, identifying the best analytical technique for waste management workers. Home-made plastic standard materials with known concentrations of chlorine or bromine have been used for calibration of ED-XRF and to test the techniques before the sample analysis. Results showed that IC and ISEs, based upon dissolution of the products of the sample combustion, have not always achieved a quantitative absorption of the analytes in the basic solutions and that bromine could be underestimated since several oxidation states occur after combustion. Elemental analysis designed for chlorine determination is subjected to strong interference from bromine and required frequent regeneration and recalibration of the measurement cell. The most reliable method seemed to be the non-destructive ED-XRF. Calibration with home-made standards, having a similar plastic matrix of the samples, enabled us to carry out quantitative determinations, which have been revealed to be satisfactorily accurate and precise. In all the analyzed samples a total concentration of chlorine and/or bromine between 0.6 and 4 w/w% was detected, compromising the feasibility of a mechanical recycling and suggesting the exploration of an alternative route for managing these plastic wastes.

  11. MUS81 promotes common fragile site expression

    DEFF Research Database (Denmark)

    Ying, Songmin; Minocherhomji, Sheroy; Chan, Kok Lung

    2013-01-01

    Fragile sites are chromosomal loci with a propensity to form gaps or breaks during early mitosis, and their instability is implicated as being causative in certain neurological disorders and cancers. Recent work has demonstrated that the so-called common fragile sites (CFSs) often impair the fait......Fragile sites are chromosomal loci with a propensity to form gaps or breaks during early mitosis, and their instability is implicated as being causative in certain neurological disorders and cancers. Recent work has demonstrated that the so-called common fragile sites (CFSs) often impair...... the faithful disjunction of sister chromatids in mitosis. However, the mechanisms by which CFSs express their fragility, and the cellular factors required to suppress CFS instability, remain largely undefined. Here, we report that the DNA structure-specific nuclease MUS81-EME1 localizes to CFS loci in early...

  12. Synchrotron X-ray fluorescence studies of a bromine-labelled cyclic RGD peptide interacting with individual tumor cells

    Energy Technology Data Exchange (ETDEWEB)

    Sheridan, Erin J.; Austin, Christopher J. D. [School of Chemistry, The University of Sydney, Sydney, NSW 2006 (Australia); Aitken, Jade B. [School of Chemistry, The University of Sydney, Sydney, NSW 2006 (Australia); Australian Synchrotron, Clayton, Victoria 3168 (Australia); Institute of Materials Structure Science, KEK, Tsukuba, Ibaraki 305-0801 (Japan); Vogt, Stefan [X-ray Science Division, Argonne National Laboratory, Argonne, IL 60439 (United States); Jolliffe, Katrina A. [School of Chemistry, The University of Sydney, Sydney, NSW 2006 (Australia); Harris, Hugh H. [School of Chemistry and Physics, The University of Adelaide, Adelaide, South Australia 5005 (Australia); Rendina, Louis M., E-mail: lou.rendina@sydney.edu.au [School of Chemistry, The University of Sydney, Sydney, NSW 2006 (Australia)

    2013-03-01

    The first example of synchrotron X-ray fluorescence imaging of cultured mammalian cells in cyclic peptide research is reported. The study reports the first quantitative analysis of the incorporation of a bromine-labelled cyclic RGD peptide and its effects on the biodistribution of endogenous elements (for example, K and Cl) within individual tumor cells. The first example of synchrotron X-ray fluorescence imaging of cultured mammalian cells in cyclic peptide research is reported. The study reports the first quantitative analysis of the incorporation of a bromine-labelled cyclic RGD peptide and its effects on the biodistribution of endogenous elements (for example, K and Cl) within individual tumor cells.

  13. Levels of persistent fluorinated, chlorinated and brominated compounds in human blood collected in Sweden in 1997-2000

    Energy Technology Data Exchange (ETDEWEB)

    Lindstroem, G.; Kaerrman, A.; Bavel, B. van [MTM Research Centre, Oerebro Univ. (Sweden); Hardell, L. [Dept. of Oncology, Univ. Hospital, Oerebro (Sweden); Hedlund, B. [Environmental Monitoring Section, Swedish EPA, Stockholm (Sweden)

    2004-09-15

    Levels of persistent fluorinated, chlorinated and brominated compounds in blood collected from the Swedish population have been determined in connection with several exposure and monitoring studies at the MTM Research Centre. A data base with 631 individual congener specific measurements on halogenated POPs such as dioxins, PCBs, HCB, DDE, chlordanes, PBDEs and PFAs including information on residency, age, BMI, diet, occupation, number of children, smoking habits, immunological status etc. has been compiled from samples collected between 1994 and 2004. A brief overview focusing on levels of some persistent chlorinated, brominated and fluorinated, compounds in blood collected in a background population group (n=83) in 1997-2000 is given here.

  14. Discovery of a Probable Nova in M81 and Photometry of Three M81 Novae

    Science.gov (United States)

    Hornoch, K.; Errmann, R.; Carlisle, Ch.; Vaduvescu, O.

    2015-02-01

    We report the discovery of a probable nova in M81 on a co-added 1600-s narrow-band H-alpha CCD image taken with the 2.5-m Isaac Newton Telescope (INT) + WFC at La Palma under ~1.6" seeing on 2015 Jan.

  15. Development of Zinc/Bromine Batteries for Load-Leveling Applications: Phase 2 Final Report

    Energy Technology Data Exchange (ETDEWEB)

    CLARK,NANCY H.; EIDLER,PHILLIP

    1999-10-01

    This report documents Phase 2 of a project to design, develop, and test a zinc/bromine battery technology for use in utility energy storage applications. The project was co-funded by the U.S. Department of Energy Office of Power Technologies through Sandia National Laboratories. The viability of the zinc/bromine technology was demonstrated in Phase 1. In Phase 2, the technology developed during Phase 1 was scaled up to a size appropriate for the application. Batteries were increased in size from 8-cell, 1170-cm{sup 2} cell stacks (Phase 1) to 8- and then 60-cell, 2500-cm{sup 2} cell stacks in this phase. The 2500-cm{sup 2} series battery stacks were developed as the building block for large utility battery systems. Core technology research on electrolyte and separator materials and on manufacturing techniques, which began in Phase 1, continued to be investigated during Phase 2. Finally, the end product of this project was a 100-kWh prototype battery system to be installed and tested at an electric utility.

  16. Electrospun Nafion(®)/Polyphenylsulfone Composite Membranes for Regenerative Hydrogen Bromine Fuel Cells.

    Science.gov (United States)

    Park, Jun Woo; Wycisk, Ryszard; Pintauro, Peter N; Yarlagadda, Venkata; Van Nguyen, Trung

    2016-02-29

    The regenerative H₂/Br₂-HBr fuel cell, utilizing an oxidant solution of Br₂ in aqueous HBr, shows a number of benefits for grid-scale electricity storage. The membrane-electrode assembly, a key component of a fuel cell, contains a proton-conducting membrane, typically based on the perfluorosulfonic acid (PFSA) ionomer. Unfortunately, the high cost of PFSA membranes and their relatively high bromine crossover are serious drawbacks. Nanofiber composite membranes can overcome these limitations. In this work, composite membranes were prepared from electrospun dual-fiber mats containing Nafion(®) PFSA ionomer for facile proton transport and an uncharged polymer, polyphenylsulfone (PPSU), for mechanical reinforcement, and swelling control. After electrospinning, Nafion/PPSU mats were converted into composite membranes by softening the PPSU fibers, through exposure to chloroform vapor, thus filling the voids between ionomer nanofibers. It was demonstrated that the relative membrane selectivity, referenced to Nafion(®) 115, increased with increasing PPSU content, e.g., a selectivity of 11 at 25 vol% of Nafion fibers. H₂-Br₂ fuel cell power output with a 65 μm thick membrane containing 55 vol% Nafion fibers was somewhat better than that of a 150 μm Nafion(®) 115 reference, but its cost advantage due to a four-fold decrease in PFSA content and a lower bromine species crossover make it an attractive candidate for use in H₂/Br₂-HBr systems.

  17. Biodegradation kinetics of selected brominated flame retardants in aerobic and anaerobic soil

    Energy Technology Data Exchange (ETDEWEB)

    Nyholm, Jenny Rattfelt, E-mail: jenny.rattfelt@chem.umu.s [Department of Chemistry, Umea University, SE-901 87 Umea (Sweden); Lundberg, Charlott; Andersson, Patrik L. [Department of Chemistry, Umea University, SE-901 87 Umea (Sweden)

    2010-06-15

    The purpose of the present study was to investigate the biodegradation kinetics in aerobic and anaerobic soil of the following brominated flame retardants: 2,4,4'-tribromodiphenyl ether (BDE 28), decabromodiphenyl ether (BDE 209), tetrabromobisphenol A (TBBPA), 1,2-dibromo-4-(1,2-dibromoethyl)cyclohexane (TBECH), 2,4,6-tribromophenol (246BrPh), and hexabromobenzene (HxBrBz). For comparison, the biodegradation of the chlorinated compounds 2,4,4'-trichlorodiphenyl ether (CDE 28), 2,4,6-trichlorophenol (246ClPh), hexachlorobenzene (HxClBz), and 2,2',4,4',5,5'-hexachlorobiphenyl (PCB 153) was also assessed. In aerobic soil, BDE 209 showed no significant degradation during the test period, but concentrations of the other BFRs declined, with half-lives decreasing in the following order: BDE 28 > TBBPA > TBECH > HxBrBz > 246BrPh. Declines in almost the same order were observed in anaerobic soil: BDE 28, BDE 209 > TBBPA > HxBrBz > TBECH >246BrPh. - Intra- and extrapolated half-lives in soil of tested brominated flame retardants ranged from 7 days for 2,4,6-tribromorophenol to >400 days for decabromodiphenyl ether.

  18. Trihalomethanes in chlorine and bromine disinfected swimming pools: air-water distributions and human exposure.

    Science.gov (United States)

    Lourencetti, Carolina; Grimalt, Joan O; Marco, Esther; Fernandez, Pilar; Font-Ribera, Laia; Villanueva, Cristina M; Kogevinas, Manolis

    2012-09-15

    This first study of trihalomethanes (THMs) in swimming pools using bromine agents for water disinfection under real conditions shows that the mixtures of these compounds are largely dominated by bromoform in a similar process as chloroform becomes the dominant THM in pools disinfected with chlorine agents. Bromoform largely predominates in air and water of the pool installations whose concentration changes are linearly correlated. However, the air concentrations of bromoform account for about 6-11% of the expected concentrations according to theoretical partitioning defined by the Henry law. Bromoform in exhaled air of swimmers is correlated with the air concentrations of this disinfectant by-product in the pool building. Comparison of the THM exhaled air concentrations between swimmers and volunteers bathing in the water without swimming or standing in the building outside the water suggest that physical activity enhance exposure to these disinfectant by-products. They also indicate that in swimming pools, besides inhalation, dermal absorption is a relevant route for the incorporation of THMs, particularly those with lower degree of bromination. Copyright © 2012 Elsevier Ltd. All rights reserved.

  19. Brominated diphenyl ethers in the sediments, porewater, and biota of the Chesapeake Bay, USA

    Energy Technology Data Exchange (ETDEWEB)

    Baker, K.; Klosterhaus, S.; Liebert, D.; Stapleton, H. [Maryland Univ., Solomons, MD (United States)

    2004-09-15

    Levels of brominated diphenyl ethers (BDEs) are rapidly increasing in the environment, and in a short time these chemicals have evolved from 'emerging contaminants' to globally-distributed organic pollutants. Recent research demonstrates BDEs are sufficiently stable to be transported long distances in the environment and to accumulate in higher trophic levels. Photolysis and metabolism appear to be dominant loss processes for the parent compounds, generating a variety of lower brominated diphenyl ethers, hydroxylated metabolites, and other products. BDEs are hydrophobic, and therefore their transport in aquatic systems is likely controlled by sorption to sediments and perhaps exchange across the air-water interface. To date, few studies have examined the geochemistry of BDEs in natural waters. In this paper, we review our recent measurements of BDEs in the Chesapeake Bay, a shallow, productive estuary in eastern North America. We focus on the distribution of BDE congeners sediment, porewater, and in faunal benthos along a contamination gradient downstream from a wastewater treatment plant and on the spatial distribution of BDEs in bottom-feeding and pelagic fish species.

  20. Electrospun Nafion®/Polyphenylsulfone Composite Membranes for Regenerative Hydrogen Bromine Fuel Cells

    Directory of Open Access Journals (Sweden)

    Jun Woo Park

    2016-02-01

    Full Text Available The regenerative H2/Br2-HBr fuel cell, utilizing an oxidant solution of Br2 in aqueous HBr, shows a number of benefits for grid-scale electricity storage. The membrane-electrode assembly, a key component of a fuel cell, contains a proton-conducting membrane, typically based on the perfluorosulfonic acid (PFSA ionomer. Unfortunately, the high cost of PFSA membranes and their relatively high bromine crossover are serious drawbacks. Nanofiber composite membranes can overcome these limitations. In this work, composite membranes were prepared from electrospun dual-fiber mats containing Nafion® PFSA ionomer for facile proton transport and an uncharged polymer, polyphenylsulfone (PPSU, for mechanical reinforcement, and swelling control. After electrospinning, Nafion/PPSU mats were converted into composite membranes by softening the PPSU fibers, through exposure to chloroform vapor, thus filling the voids between ionomer nanofibers. It was demonstrated that the relative membrane selectivity, referenced to Nafion® 115, increased with increasing PPSU content, e.g., a selectivity of 11 at 25 vol% of Nafion fibers. H2-Br2 fuel cell power output with a 65 μm thick membrane containing 55 vol% Nafion fibers was somewhat better than that of a 150 μm Nafion® 115 reference, but its cost advantage due to a four-fold decrease in PFSA content and a lower bromine species crossover make it an attractive candidate for use in H2/Br2-HBr systems.

  1. Dissolution of brominated epoxy resins by dimethyl sulfoxide to separate waste printed circuit boards.

    Science.gov (United States)

    Zhu, Ping; Chen, Yan; Wang, Liangyou; Qian, Guangren; Zhang, Wei Jie; Zhou, Ming; Zhou, Jin

    2013-03-19

    Improved methods are required for the recycling of waste printed circuit boards (WPCBs). In this study, WPCBs (1-1.5 cm(2)) were separated into their components using dimethyl sulfoxide (DMSO) at 60 °C for 45 min and a metallographic microscope was used to verify their delamination. An increased incubation time of 210 min yielded a complete separation of WPCBs into their components, and copper foils and glass fibers were obtained. The separation time decreased with increasing temperature. When the WPCB size was increased to 2-3 cm(2), the temperature required for complete separation increased to 90 °C. When the temperature was increased to 135 °C, liquid photo solder resists could be removed from the copper foil surfaces. The DMSO was regenerated by rotary decompression evaporation, and residues were obtained. Fourier transform infrared spectroscopy (FT-IR), thermal analysis, nuclear magnetic resonance, scanning electron microscopy, and energy-dispersive X-ray spectroscopy were used to verify that these residues were brominated epoxy resins. From FT-IR analysis after the dissolution of brominated epoxy resins in DMSO it was deduced that hydrogen bonding may play an important role in the dissolution mechanism. This novel technology offers a method for separating valuable materials and preventing environmental pollution from WPCBs.

  2. Development of the first certified reference materials for several brominated flame retardants in polymers.

    Science.gov (United States)

    Linsinger, Thomas P J; Birgersson-Liebich, Almuth; Lamberty, Andrée; Pellizzato, Francesca; Venelinov, Tony; Voorspoels, Stefan

    2009-05-15

    The first reference materials certified for several polybrominated flame retardants in polymers were developed. Commercially available polyethylene and polypropylene were fortified with technical mixtures of Pentabrominated diphenylether (Penta-BDE), Octa-BDE, Deca-BDE, and Decabrominated biphenyl (BB) (where the capitalized forms refer to the technical mixtures). Homogeneity was tested on 20 units of each material, and between-unit variation was confirmed to be below 4% for all congeners. Stability was assessed after storage of samples for 1 year at 4, 18, and 60 degrees C. Uncertainty of degradation during transport was found negligible for all congeners, whereas uncertainty of degradation for storage of 24 months at 4 degrees C was estimated between 2% and 11%. A characterization intercomparison involving 16 laboratories was organized. After exclusion of technically doubtful results, between-laboratory standard deviations ranged from 3% to 12%, making this intercomparison the best for this field of analysis so far. Statistical analysis revealed that the use of isotopically labeled internal standards did not improve analytical precision in this study. The good comparability, together with the independent confirmation of the assigned mass fractions via the total bromine content as well as by using non-GC/MS-based methods, allowed for the first time the certification of polymer materials for several brominated flame retardants.

  3. 12 CFR 222.80-222.81 - [Reserved

    Science.gov (United States)

    2010-01-01

    ... 12 Banks and Banking 3 2010-01-01 2010-01-01 false 222.80-222.81 Section 222.80-222.81 Banks and Banking FEDERAL RESERVE SYSTEM (CONTINUED) BOARD OF GOVERNORS OF THE FEDERAL RESERVE SYSTEM FAIR CREDIT REPORTING (REGULATION V) Duties of Users of Consumer Reports Regarding Identity Theft § 222.80-222.81 ...

  4. 27 CFR 71.81 - Suspension, revocation, or annulment.

    Science.gov (United States)

    2010-04-01

    ... annulment. 71.81 Section 71.81 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE... PROCEEDINGS Hearing Procedure Burden of Proof § 71.81 Suspension, revocation, or annulment. In hearings on the suspension, revocation, or annulment of a permit, the burden of proof is on the Government. General ...

  5. 34 CFR 81.7 - Non-party participation.

    Science.gov (United States)

    2010-07-01

    ... 34 Education 1 2010-07-01 2010-07-01 false Non-party participation. 81.7 Section 81.7 Education... Provisions § 81.7 Non-party participation. (a) A person or organization, other than a party, that wishes to... application must— (1) Identify the case in which participation is sought; (2) State how the applicant's...

  6. 27 CFR 13.81 - Representation before TTB.

    Science.gov (United States)

    2010-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2010-04-01 2010-04-01 false Representation before TTB. 13.81 Section 13.81 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT OF THE TREASURY LIQUORS LABELING PROCEEDINGS Miscellaneous § 13.81 Representation before TTB. An...

  7. 45 CFR 81.12 - Authority for representation.

    Science.gov (United States)

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Authority for representation. 81.12 Section 81.12 Public Welfare DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL ADMINISTRATION PRACTICE AND PROCEDURE FOR HEARINGS UNDER PART 80 OF THIS TITLE Appearance and Practice § 81.12 Authority for representation. Any...

  8. 42 CFR 81.24 - Guidelines for leukemia.

    Science.gov (United States)

    2010-10-01

    ... 42 Public Health 1 2010-10-01 2010-10-01 false Guidelines for leukemia. 81.24 Section 81.24 Public... Causation § 81.24 Guidelines for leukemia. (a) For claims involving leukemia, DOL will calculate one or more probability of causation estimates from up to three of the four alternate leukemia risk models included in...

  9. 10 CFR 61.81 - Tests at land disposal facilities.

    Science.gov (United States)

    2010-01-01

    ... 10 Energy 2 2010-01-01 2010-01-01 false Tests at land disposal facilities. 61.81 Section 61.81 Energy NUCLEAR REGULATORY COMMISSION (CONTINUED) LICENSING REQUIREMENTS FOR LAND DISPOSAL OF RADIOACTIVE WASTE Records, Reports, Tests, and Inspections § 61.81 Tests at land disposal facilities. (a) Each...

  10. 10 CFR 781.81 - Transfer of custody.

    Science.gov (United States)

    2010-01-01

    ... 10 Energy 4 2010-01-01 2010-01-01 false Transfer of custody. 781.81 Section 781.81 Energy DEPARTMENT OF ENERGY DOE PATENT LICENSING REGULATIONS Special Provisions § 781.81 Transfer of custody. The Department may enter into an agreement to transfer custody of any patent to another Government agency for...

  11. 29 CFR 500.81 - Payment of wages when due.

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 3 2010-07-01 2010-07-01 false Payment of wages when due. 500.81 Section 500.81 Labor Regulations Relating to Labor (Continued) WAGE AND HOUR DIVISION, DEPARTMENT OF LABOR REGULATIONS MIGRANT AND SEASONAL AGRICULTURAL WORKER PROTECTION Worker Protections Wages and Payroll Standards § 500.81 Payment of...

  12. 45 CFR 81.42 - Extension of time or postponement.

    Science.gov (United States)

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Extension of time or postponement. 81.42 Section 81.42 Public Welfare DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL ADMINISTRATION PRACTICE AND PROCEDURE FOR HEARINGS UNDER PART 80 OF THIS TITLE Time § 81.42 Extension of time or postponement. Requests...

  13. 7 CFR 1230.81 - Books and records.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 10 2010-01-01 2010-01-01 false Books and records. 1230.81 Section 1230.81... CONSUMER INFORMATION Pork Promotion, Research, and Consumer Information Order Reports, Books, and Records § 1230.81 Books and records. Each person who is subject to this subpart shall maintain and, during normal...

  14. 7 CFR 301.81-2 - Regulated articles.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 5 2010-01-01 2010-01-01 false Regulated articles. 301.81-2 Section 301.81-2... Regulations § 301.81-2 Regulated articles. The following are regulated articles: (a) Imported fire ant queens... other articles, except potting soil that is shipped in original containers in which the soil was placed...

  15. 45 CFR 81.54 - Request for hearing.

    Science.gov (United States)

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Request for hearing. 81.54 Section 81.54 Public Welfare DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL ADMINISTRATION PRACTICE AND PROCEDURE FOR HEARINGS UNDER PART 80 OF THIS TITLE Proceedings Prior to Hearing § 81.54 Request for hearing. Within 20 days...

  16. 42 CFR 81.30 - Non-radiogenic cancers.

    Science.gov (United States)

    2010-10-01

    ... 42 Public Health 1 2010-10-01 2010-10-01 false Non-radiogenic cancers. 81.30 Section 81.30 Public... Causation § 81.30 Non-radiogenic cancers. The following cancers are considered non-radiogenic for the... cancers: (a) Chronic lymphocytic leukemia (ICD-9 code: 204.1) (b) ...

  17. 22 CFR 40.81 - Ineligible for citizenship.

    Science.gov (United States)

    2010-04-01

    ... 22 Foreign Relations 1 2010-04-01 2010-04-01 false Ineligible for citizenship. 40.81 Section 40.81... UNDER THE IMMIGRATION AND NATIONALITY ACT, AS AMENDED Ineligible for Citizenship. § 40.81 Ineligible for citizenship. An alien will be ineligible to receive an immigrant visa under INA 212(a)(8)(A) if the alien is...

  18. STS-81 Launch (side view across water)

    Science.gov (United States)

    1997-01-01

    The Space Shuttle Atlantis transforms the early morning at KSC into near-daylight as its more than 7 million pounds of rocket thrust propels it from Launch Pad 39B at 4:27:23 a.m. EST Jan. 12 on its way to dock with the Mir space station for the fifth time.The 10-day mission will feature the transfer of Mission Specialist Jerry Linenger to Mir to replace astronaut John Blaha, who has been on the orbital laboratory since Sept. 19, 1996. The other STS-81 crew members include Mission Commander Michael A. Baker; Pilot Brent W. Jett, Jr.; and Mission Specialists John M. Grunsfeld, Peter J. K. 'Jeff' Wisoff and Marsha S. Ivins. During the five-day docking operations, the Shuttle and Mir crews will conduct risk mitigation, human life science, microgravity and materials processing experiments that will provide data for the design, development and operation of the International Space Station. The primary payload is the SPACEHAB-DM double module that will provide space for more than 2,000 pounds of hardware, food and water that will be transferred into the Russian space station. The SPACEHAB will also be used to return experiment samples from the Mir to Earth for analysis and for microgravity experiments during the mission.

  19. STS-81 Shuttle Atlantis clears the tower

    Science.gov (United States)

    1997-01-01

    Like a rising sun lighting up the night, the Space Shuttle Atlantis soars from Launch Pad 39B at 4:27:23 a.m. EST Jan. 12 on its way to dock with the Mir space station for the fifth time. The 10-day mission will feature the transfer of Mission Specialist Jerry Linenger to Mir to replace astronaut John Blaha, who has been on the orbital laboratory since Sept. 19, 1996. The other STS-81 crew members include Mission Commander Michael A. Baker; Pilot Brent W. Jett, Jr.; and Mission Specialists John M. Grunsfeld, Peter J. K. 'Jeff' Wisoff and Marsha S. Ivins. During the five-day docking operations, the Shuttle and Mir crews will conduct risk mitigation, human life science, microgravity and materials processing experiments that will provide data for the design, development and operation of the International Space Station. The primary payload is the SPACEHAB-DM double module that will provide space for more than 2,000 pounds of hardware, food and water that will be transferred into the Russian space station.The SPACEHAB will also be used to return experiment samples from the Mir to Earth for analysis and for microgravity experiments during the mission.

  20. STS-81 Launch of Atlantis (side view)

    Science.gov (United States)

    1997-01-01

    The Space Shuttle Atlantis transforms the early morning at KSC into near-daylight as its more than 7 million pounds of rocket thrust propels it from Launch Pad 39B at 4:27:23 a.m. EST Jan. 12 on its way to dock with the Mir space station for the fifth time.The 10-day mission will feature the transfer of Mission Specialist Jerry Linenger to Mir to replace astronaut John Blaha, who has been on the orbital laboratory since Sept. 19, 1996. The other STS-81 crew members include Mission Commander Michael A. Baker; Pilot Brent W. Jett, Jr.; and Mission Specialists John M. Grunsfeld, Peter J. K. 'Jeff' Wisoff and Marsha S. Ivins. During the five-day docking operations, the Shuttle and Mir crews will conduct risk mitigation, human life science, microgravity and materials processing experiments that will provide data for the design, development and operation of the International Space Station. The primary payload is the SPACEHAB-DM double module that will provide space for more than 2,000 pounds of hardware, food and water that will be transferred into the Russian space station. The SPACEHAB will also be used to return experiment samples from the Mir to Earth for analysis and for microgravity experiments during the mission.

  1. STS-81 Launch (Landscape across water)

    Science.gov (United States)

    1997-01-01

    Like a rising sun lighting up the night, the Space Shuttle Atlantis soars from Launch Pad 39B at 4:27:23 a.m. EST Jan. 12 on its way to dock with the Mir space station for the fifth time. The 10-day mission will feature the transfer of Mission Specialist Jerry Linenger to Mir to replace astronaut John Blaha, who has been on the orbital laboratory since Sept. 19, 1996. The other STS-81 crew members include Mission Commander Michael A. Baker; Pilot Brent W. Jett, Jr.; and Mission Specialists John M. Grunsfeld, Peter J. K. 'Jeff' Wisoff and Marsha S. Ivins. During the five-day docking operations, the Shuttle and Mir crews will conduct risk mitigation, human life science, microgravity and materials processing experiments that will provide data for the design, development and operation of the International Space Station. The primary payload is the SPACEHAB-DM double module that will provide space for more than 2,000 pounds of hardware, food and water that will be transferred into the Russian space station.The SPACEHAB will also be used to return experiment samples from the Mir to Earth for analysis and for microgravity experiments during the mission.

  2. A rapid method for the determination of brominated flame retardant concentrations in plastics and textiles entering the waste stream.

    Science.gov (United States)

    Abdallah, Mohamed Abou-Elwafa; Drage, Daniel S; Sharkey, Martin; Berresheim, Harald; Harrad, Stuart

    2017-10-01

    Due to new European legislation, products going to waste are subject to 'low persistent organic pollutant concentration limits'. Concentrations of restricted brominated flame retardants in waste products must be determined. A rapid extraction and clean-up method was developed for determination of brominated flame retardants in various plastics and textiles. The optimised method used vortexing and ultrasonication in dichloromethane followed by sulfuric acid clean-up to determine target compounds. Poly-brominated diphenyl ethers were determined by gas chromatography with mass spectrometry and hexabromocyclododecane by liquid chromatography with tandem mass spectrometry. Good recoveries of target analytes were obtained after three extraction cycles. The method was validated using poly-propylene and poly-ethylene certified reference materials as well as previously characterised textiles, expanded and extruded poly-styrene samples. Measured concentrations of target compounds showed good agreement with the certified values indicating good accuracy and precision. Clean extracts provided low noise levels resulting in low limits of quantification (0.8-1.5 ng/g for poly-brominated diphenyl ethers and 0.3 ng/g for α-, β- and γ-hexabromocyclododecane). The developed method was applied successfully to real consumer products entering the waste stream and it provided various advantages over traditional methods, including reduced analysis time, solvent consumption, minimal sample contamination and high sample throughput, which is crucial to comply with the implemented legislation. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Application of ion-selective electrodes for the microdetermination of chlorine and bromine in volatile organic compounds

    NARCIS (Netherlands)

    Potman, W.; Dahmen, E.A.M.F.

    1972-01-01

    A method is described for the determination of chlorine and bromine in mg samples of highly halogenated volatile organic compounds. The samples are introduced into the combustion system by injection and burnt in a stream of oxygen at 1000° over platinum and quartz. The combustion gases are absorbed

  4. Bromination of Aromatic Compounds by Residual Bromide in Sodium Chloride Matrix Modifier Salt During Heated Headspace GC/MS Analysis

    Science.gov (United States)

    Analytical artifacts attributed to the bromination of toluene, xylenes, and trimethylbenzenes were found during the heated headspace gas chromatography/mass spectrometry (GC/MS) analysis of aqueous samples. The aqueous samples were produced from Fenton-like chemical oxidation rea...

  5. Subacute effects of the brominated flame retardants hexabromocyclododecane and tetrabromobisphenol A on hepatic cytochrome P450 levels in rats.

    NARCIS (Netherlands)

    Germer, Silke; Piersma, Aldert H; Ven, Leo T M van der; Kamyschnikow, Andreas; Fery, Yvonne; Schmitz, Hans-Joachim; Schrenk, Dieter

    2006-01-01

    The brominated flame retardants tetrabromobisphenol A (TBBPA) and hexabromocyclododecane (HBCD) are found in the environment, e.g., in sediments and organisms, in food items, human blood samples and mother's milk. In this study, the effects of both compounds on rat hepatic cytochrome P450 (CYP)

  6. Rapid Formation of Molecular Bromine from Deliquesced NaBr Aerosol in the Presence of Ozone and UV Light

    Science.gov (United States)

    The formation of gas-phase bromine from aqueous sodium bromide aerosols is investigated through a combination of chamber experiments and chemical kinetics modeling. Experiments show that Br2(g) is produced rapidly from deliquesced NaBr aerosols in the presence of OH radicals prod...

  7. Bromine in the tropical troposphere and stratosphere as derived from balloon-borne BrO observations

    Directory of Open Access Journals (Sweden)

    M. Dorf

    2008-12-01

    Full Text Available The first tropospheric and stratospheric (4 to 33 km BrO profile is presented for the inner tropics derived from balloon-borne DOAS (Differential Optical Absorption Spectroscopy measurements. In combination with photochemical modelling, total stratospheric inorganic bromine (Bry is deduced to be (21.5±2.5 ppt in 4.5-year-old air, probed in 2005. We derive a total contribution of (5.2±2.5 ppt from brominated very short-lived substances and inorganic product gases to stratospheric Bry Tropospheric BrO was found to be <1 ppt. Our results are compared to two 3-D CTM SLIMCAT model runs, which differ in the lifetime of the bromine source gases, affecting the vertical distribution of Bry in the lower stratosphere. Bromine source gas measurements performed 10 days earlier Laube et al., 2008, indicate a lower Bry of (17.5±0.4 ppt. Potential reasons for this discrepancy are discussed.

  8. A Novel Brominated Triazine-based Flame Retardant (TTBP-TAZ) in Plastic Consumer Products and Indoor Dust

    NARCIS (Netherlands)

    Ballesteros Gomez, A.M.; de Boer, J.; Leonards, P.E.G.

    2014-01-01

    The presence of a novel brominated flame retardant named 2,4,6-tris(2,4,6-tribromophenoxy)-1,3,5-triazine (TTBP-TAZ) is reported for the first time in plastic parts of consumer products and indoor dust samples. TTBP-TAZ was identified by untargeted screening and can be a replacement of the banned

  9. Drug Reactions

    Science.gov (United States)

    ... or diabetes. But medicines can also cause unwanted reactions. One problem is interactions, which may occur between ... more serious. Drug allergies are another type of reaction. They can be mild or life-threatening. Skin ...

  10. Peroxisome proliferator-activated receptor gamma regulates expression of the anti-lipolytic G-protein-coupled receptor 81 (GPR81/Gpr81)

    DEFF Research Database (Denmark)

    Jeninga, Ellen H; Bugge, Anne Skovsø; Nielsen, Ronni

    2009-01-01

    target genes that may contribute to the reduction of circulating free fatty acids after TZD treatment have been identified, the relevant PPARgamma target genes that may exert the anti-lipolytic effect of TZDs are unknown. Here we identified the anti-lipolytic human G-protein-coupled receptor 81 (GPR81......), GPR109A, and the (human-specific) GPR109B genes as well as the mouse Gpr81 and Gpr109A genes as novel TZD-induced genes in mature adipocytes. GPR81/Gpr81 is a direct PPARgamma target gene, because mRNA expression of GPR81/Gpr81 (and GPR109A/Gpr109A) increased in mature human and murine adipocytes...... as well as in vivo in epididymal fat pads of mice upon rosiglitazone stimulation, whereas small interfering RNA-mediated knockdown of PPARgamma in differentiated 3T3-L1 adipocytes showed a significant decrease in Gpr81 protein expression. In addition, chromatin immunoprecipitation sequencing analysis...

  11. Dbf4-dependent kinase and the Rtt107 scaffold promote Mus81-Mms4 resolvase activation during mitosis.

    Science.gov (United States)

    Princz, Lissa N; Wild, Philipp; Bittmann, Julia; Aguado, F Javier; Blanco, Miguel G; Matos, Joao; Pfander, Boris

    2017-03-01

    DNA repair by homologous recombination is under stringent cell cycle control. This includes the last step of the reaction, disentanglement of DNA joint molecules (JMs). Previous work has established that JM resolving nucleases are activated specifically at the onset of mitosis. In case of budding yeast Mus81-Mms4, this cell cycle stage-specific activation is known to depend on phosphorylation by CDK and Cdc5 kinases. Here, we show that a third cell cycle kinase, Cdc7-Dbf4 (DDK), targets Mus81-Mms4 in conjunction with Cdc5-both kinases bind to as well as phosphorylate Mus81-Mms4 in an interdependent manner. Moreover, DDK-mediated phosphorylation of Mms4 is strictly required for Mus81 activation in mitosis, establishing DDK as a novel regulator of homologous recombination. The scaffold protein Rtt107, which binds the Mus81-Mms4 complex, interacts with Cdc7 and thereby targets DDK and Cdc5 to the complex enabling full Mus81 activation. Therefore, Mus81 activation in mitosis involves at least three cell cycle kinases, CDK, Cdc5 and DDK Furthermore, tethering of the kinases in a stable complex with Mus81 is critical for efficient JM resolution. © 2017 The Authors. Published under the terms of the CC BY NC ND 4.0 license.

  12. Investigating the lifetime of bromine-quenched G.M. Counters with temperature

    Energy Technology Data Exchange (ETDEWEB)

    Abilama, Marc [Centronic Ltd., Croydon (United Kingdom); University of Surrey, Guildford (United Kingdom); Bates, Mike [Centronic Ltd., Croydon (United Kingdom); Lohstroh, Annika [University of Surrey, Guildford (United Kingdom)

    2015-09-21

    The amount of halogen quench gas as a percentage of the total fill gas contained within a gas-filled Geiger–Müller detector is directly linked to its operational characteristics. Preserving this halogen gas will help maintain the operating lifetime of the detectors. Such halogen gases are highly corrosive and the small quantities within a gas-filled detector can deplete rapidly via interactions with surrounding materials. The rate of interactions is thought to be proportional to not only temperature, but also to the current initiated by ionisation events associated with the formation of each signal pulse. As all pulses are of similar magnitudes, GM detector operational lifetimes are quantified in accumulated counts rather than a given operating time. We have studied three different types of corrosion-resistant mechanisms to protect the bromine halogen gas from any interactions with 446 stainless steel detector components of ZP1200 Geiger–Müller tubes at temperatures up to 125 °C. Three types of surface treatments for these detectors used were labelled as “raw” using only an oxygen-plasma-bombardment process, “passivated” using a combination of nitric acid passivation followed by an oxygen plasma-bombardment process, and thirdly plating with a few micron thickness of chromium followed by an oxygen plasma-bombardment process. 32 detector samples were irradiated at room temperature with a Caesium-137 source at dose rates of approximately 1.3 mSv/hr up to 5.7×10{sup 10} accumulated counts; another 32 detector samples were aged to 3.3×10{sup 10} counts at 125 °C. At room temperature, the chromium-plated samples exhibited an initial rise in their starting voltage readings. All other detector performance characteristics, for all detector types, did not change significantly during the ageing process, and the surface morphology of the detector cathodes was unaffected. At 125 °C, the chromium-based plating produced the most stable long-term response. These

  13. Bromine release during Plinian eruptions along the Central American Volcanic Arc

    Science.gov (United States)

    Hansteen, T. H.; Kutterolf, S.; Appel, K.; Freundt, A.; Perez-Fernandez, W.; Wehrmann, H.

    2010-12-01

    Volcanoes of the Central American Volcanic Arc (CAVA) have produced at least 72 highly explosive eruptions within the last 200 ka. The eruption columns of all these “Plinian” eruptions reached well into the stratosphere such that their released volatiles may have influenced atmospheric chemistry and climate. While previous research has focussed on the sulfur and chlorine emissions during such large eruptions, we here present measurements of the heavy halogen bromine by means of synchrotron radiation induced micro-XRF microanalysis (SR-XRF) with typical detection limits at 0.3 ppm (in Fe rich standard basalt ML3B glass). Spot analyses of pre-eruptive glass inclusions trapped in minerals formed in magma reservoirs were compared with those in matrix glasses of the tephras, which represent the post-eruptive, degassed concentrations. The concentration difference between inclusions and matrix glasses, multiplied by erupted magma mass determined by extensive field mapping, yields estimates of the degassed mass of bromine. Br is probably hundreds of times more effective in destroying ozone than Cl, and can accumulate in the stratosphere over significant time scales. Melt inclusions representing deposits of 22 large eruptions along the CAVA have Br contents between 0.5 and 13 ppm. Br concentrations in matrix glasses are nearly constant at 0.4 to 1.5 ppm. However, Br concentrations and Cl/Br ratios vary along the CAVA. The highest values of Br contents (>8 ppm) and lowest Cl/Br ratios (170 to 600) in melt inclusions occur across central Nicaragua and southern El Salvador, and correlate with bulk-rock compositions of high Ba/La > 85 as well as low La/Yb discharged 700 kilotons of Br. On average, each of the remaining 21 CAVA eruptions studied have discharged c.100 kilotons of bromine. During the past 200 ka, CAVA volcanoes have emitted a cumulative mass of 3.2 Mt of Br through highly explosive eruptions. There are six periods in the past (c. 2ka, 6ka, 25ka, 40ka, 60ka, 75

  14. Seasonal variation of bromine monoxide over the Rann of Kutch salt marsh seen from space

    Science.gov (United States)

    Hörmann, Christoph; Beirle, Steffen; Penning de Vries, Marloes; Sihler, Holger; Platt, Ulrich; Wagner, Thomas

    2015-04-01

    Bromine monoxide (BrO) is an important catalyst in the depletion of tropospheric and stratospheric ozone (O3). In the troposphere, reactive bromine can be released from sea ice, volcanoes, sea-salt aerosol or salt lakes. For all of these natural sources enhanced BrO vertical column densities (VCDs) have been successfully observed from ground using Differential Optical Absorption Spectroscopy (DOAS). Until now, satellite observations were only reported for polar regions during springtime and volcanic emissions (mostly for major eruptions). We present the first satellite observations of enhanced monthly mean BrO VCDs over a salt marsh, the Rann of Kutch (India/Pakistan), during 2004-2014 as seen by the Ozone Monitoring Instrument (OMI). The Rann of Kutch is a so-called 'seasonal' salt marsh. During India's summer monsoon (June/July - September/October), the flat desert of salty clay and mudflats, which average 15 meters above sea level, fills with standing rain and sea water. With more than 7500 km2 it is the largest salt desert in the world and additionally one of the hottest areas of India with summer temperatures around 50 ° C and winter temperatures decreasing below 0 ° C. Probably due to these rather extreme conditions, the Rann of Kutch has not been yet investigated for atmospheric composition measurements by ground-based instruments. Satellite observations, however, provide the unique possibility to investigate the entire area remotely over a long-time period. The OMI data reveals recurring maximum BrO VCDs during April/May, but no enhanced column densities during the monsoon season while the area is flooded. In the following months the signal only recovers slowly while the salty surface dries up. We discuss the possible effects of temperature, precipitation and relative humidity on the release of enhanced reactive bromine concentrations. In order to investigate a possible diurnal cycle of the BrO concentration, the OMI results (at a local overflight time

  15. Advanced degradation of brominated epoxy resin and simultaneous transformation of glass fiber from waste printed circuit boards by improved supercritical water oxidation processes.

    Science.gov (United States)

    Liu, Kang; Zhang, Zhiyuan; Zhang, Fu-Shen

    2016-10-01

    This work investigated various supercritical water oxidation (SCWO) systems, i.e. SCWO1 (only water), SCWO2 (water+H2O2) and SCWO3 (water+H2O2/NaOH), for waste printed circuit boards (PCBs) detoxification and recycling. Response surface methodology (RSM) was applied to optimize the operating conditions of the optimal SCWO3 systems. The optimal reaction conditions for debromination were found to be the NaOH of 0.21g, the H2O2 volume of 9.04mL, the time of 39.7min, maximum debromination efficiency of 95.14%. Variance analysis indicated that the factors influencing debromination efficiency was in the sequence of NaOH>H2O2>time. Mechanism studies indicated that the dissociated ions from NaOH in supercritical water promoted the debromination of brominated epoxy resins (BERs) through an elimination reaction and nucleophilic substitution. HO2, produced by H2O2 could induce the oxidation of phenol ring to open (intermediates of BERs), which were thoroughly degraded to form hydrocarbons, CO2, H2O and NaBr. In addition, the alkali-silica reaction between OH(-) and SiO2 induced the phase transformation of glass fibers, which were simultaneously converted into anorthite and albite. Waste PCBs in H2O2/NaOH improved SCWO system were fully degraded into useful products and simultaneously transformed into functional materials. These findings are helpful for efficient recycling of waste PCBs. Copyright © 2016 Elsevier Ltd. All rights reserved.

  16. Particle size distribution of brominated flame retardants in house dust from Japan

    Directory of Open Access Journals (Sweden)

    Natsuko Kajiwara

    2016-06-01

    Full Text Available The present study was conducted to examine the concentrations, profiles, and mass distributions of polybrominated diphenyl ethers (PBDEs, hexabromocyclododecanes (HBCDs, and polybrominated dibenzo-p-dioxins/furans (PBDD/Fs based on the particle sizes of house dust samples from five homes in Japan. After removal of impurities from house dust from vacuum cleaner bags, selected indoor dust samples were size fractionated (>2 mm, 1–2 mm, 0.5–1 mm, 250–500 μm, 106–250 μm, 53–106 μm, and 250 μm in size and fluffy dust were included. The conclusion is that particulate dust <250 μm in size without fluffy dust should be used to analyze dust for brominated flame retardants.

  17. Structural studies of β-turn-containing peptide catalysts for atroposelective quinazolinone bromination.

    Science.gov (United States)

    Metrano, A J; Abascal, N C; Mercado, B Q; Paulson, E K; Miller, S J

    2016-04-04

    We describe herein a crystallographic and NMR study of the secondary structural attributes of a β-turn-containing tetra-peptide, Boc-Dmaa-D-Pro-Acpc-Leu-NMe2, which was recently reported as a highly effective catalyst in the atroposelective bromination of 3-arylquinazolin-4(3H)-ones. Inquiries pertaining to the functional consequences of residue substitutions led to the discovery of a more selective catalyst, Boc-Dmaa-D-Pro-Acpc-Leu-OMe, the structure of which was also explored. This new lead catalyst was found to exhibit a type I'β-turn secondary structure both in the solid state and in solution, a structure that was shown to be an accessible conformation of the previously reported catalyst, as well.

  18. Bromination of deoxycytidine by eosinophil peroxidase: A mechanism for mutagenesis by oxidative damage of nucleotide precursors

    Science.gov (United States)

    Henderson, Jeffrey P.; Byun, Jaeman; Williams, Michelle V.; McCormick, Michael L.; Parks, William C.; Ridnour, Lisa A.; Heinecke, Jay W.

    2001-01-01

    Oxidants generated by eosinophils during chronic inflammation may lead to mutagenesis in adjacent epithelial cells. Eosinophil peroxidase, a heme enzyme released by eosinophils, generates hypobromous acid that damages tissue in inflammatory conditions. We show that human eosinophils use eosinophil peroxidase to produce 5-bromodeoxycytidine. Flow cytometric, immunohistochemical, and mass spectrometric analyses all demonstrated that 5-bromodeoxycytidine generated by eosinophil peroxidase was taken up by cultured cells and incorporated into genomic DNA as 5-bromodeoxyuridine. Although previous studies have focused on oxidation of chromosomal DNA, our observations suggest another mechanism for oxidative damage of DNA. In this scenario, peroxidase-catalyzed halogenation of nucleotide precursors yields products that subsequently can be incorporated into DNA. Because the thymine analog 5-BrUra mispairs with guanine in DNA, generation of brominated pyrimidines by eosinophils might constitute a mechanism for cytotoxicity and mutagenesis at sites of inflammation. PMID:11172002

  19. A global stratospheric bromine monoxide climatology based on the BASCOE chemical transport model

    Directory of Open Access Journals (Sweden)

    N. Theys

    2009-02-01

    Full Text Available A new climatology of stratospheric BrO profiles based on a parameterization using dynamical and chemical indicators has been developed, with the aim to apply it to the retrieval of tropospheric BrO columns from space nadir measurements. The adopted parameterization is based on three years of output data from the 3-D chemistry transport model BASCOE. The impact of the atmospheric dynamics on the stratospheric BrO distribution is treated by means of Bry/ozone correlations built from 3-D-CTM model results, while photochemical effects are taken into account using stratospheric NO2 columns as an indicator of the BrO/Bry ratio. The model simulations have been optimized for bromine chemistry and budget, and validated through comparisons using an extensive data set of ground-based, balloon-borne and satellite limb (SCIAMACHY stratospheric BrO observations.

  20. Evaluation of Common Use Brominated Flame Retardant (BFR) Toxicity Using a Zebrafish Embryo Model.

    Science.gov (United States)

    Usenko, Crystal Y; Abel, Erika L; Hopkins, Aaron; Martinez, Gerardo; Tijerina, Jonathan; Kudela, Molly; Norris, Nick; Joudeh, Lana; Bruce, Erica D

    2016-09-02

    Brominated flame retardants (BFRs) are used to reduce the flammability of plastics, textiles, and electronics. BFRs vary in their chemical properties and structures, and it is expected that these differences alter their biological interactions and toxicity. Zebrafish were used as the model organism for assessing the toxicity of nine structurally-diverse BFRs. In addition to monitoring for overt toxicity, the rate of spontaneous movement, and acetylcholinesterase and glutathione-S-transferase (GST) activities were assessed following exposure. The toxicities of BFRs tested can be ranked by LC50 as tetrabromobisphenol A (TBBPA) banned. These results suggest that zebrafish are sensitive to exposure to BFRs and can be used as a comparative screening model, as well as to determine alterations in behavior following exposure and probe mechanisms of action.

  1. Magnetic solid-phase extraction of brominated flame retardants from environmental waters with graphene-doped Fe3O4 nanocomposites.

    Science.gov (United States)

    Yang, Jing; Qiao, Jun-qin; Cui, Shi-hai; Li, Jia-yuan; Zhu, Jin-jin; Yin, He-xing; Zhan, Cheng-yan; Lian, Hong-zhen

    2015-06-01

    Graphene-doped Fe3O4 nanocomposites were prepared by a solvothermal reaction of an iron source with graphene. The nanocomposites were characterized by transmission electron microscopy, atomic force microscopy, X-ray diffraction, superconducting quantum interference, Raman spectroscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. This nanomaterial has been used as a magnetic solid-phase extraction sorbent to extract trace brominated flame retardants from environmental waters. Various extraction parameters were optimized including dosage and reusability of the nanocomposites, and pH of sample matrix. The reliability of the magnetic solid-phase extraction protocol based on graphene-doped Fe3O4 nanocomposites was evaluated by investigating the recoveries of 2,4,6-tribromophenol, tetrabromobisphenol A, 4-bromodiphenyl ether, and 4,4'-dibromodiphenyl ether in water samples. Good recoveries (85.0-105.0%) were achieved with the relative standard deviation ranging from 1.1-7.1%. Moreover, it is speculated from characterization and magnetic solid-phase extraction experiment that there is not only π-π stacking but also possible hydrophobic interaction between the graphene-doped Fe3O4 nanocomposites and analytes. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. Bromine in plastic consumer products - Evidence for the widespread recycling of electronic waste.

    Science.gov (United States)

    Turner, Andrew; Filella, Montserrat

    2017-12-01

    A range of plastic consumer products and components thereof have been analysed by x-ray fluorescence (XRF) spectrometry in a low density mode for Br as a surrogate for brominated flame retardant (BFR) content. Bromine was detected in about 42% of 267 analyses performed on electronic (and electrical) samples and 18% of 789 analyses performed on non-electronic samples, with respective concentrations ranging from 1.8 to 171,000μgg-1 and 2.6 to 28,500μgg-1. Amongst the electronic items, the highest concentrations of Br were encountered in relatively small appliances, many of which predated 2005 (e.g. a fan heater, boiler thermostat and smoke detector, and various rechargers, light bulb collars and printed circuit boards), and usually in association with Sb, a component of antimony oxide flame retardant synergists, and Pb, a heavy metal additive and contaminant. Amongst the non-electronic samples, Br concentrations were highest in items of jewellery, a coffee stirrer, a child's puzzle, a picture frame, and various clothes hangers, Christmas decorations and thermos cup lids, and were often associated with the presence of Sb and Pb. These observations, coupled with the presence of Br at concentrations below those required for flame-retardancy in a wider range of electronic and non-electronic items, are consistent with the widespread recycling of electronic plastic waste. That most Br-contaminated items were black suggests the current and recent demand for black plastics in particular is met, at least partially, through this route. Given many Br-contaminated items would evade the attention of the end-user and recycler, their disposal by conventional municipal means affords a course of BFR entry into the environment and, for food-contact items, a means of exposure to humans. Copyright © 2017 Elsevier B.V. All rights reserved.

  3. Associations between brominated flame retardants in house dust and hormone levels in men

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Paula I. [Department of Environmental Health Sciences, University of Michigan, 1415 Washington Heights, Ann Arbor, MI 48109 (United States); Stapleton, Heather M. [Nicholas School of the Environment, Box 90328, Duke University, Durham, NC 27708 (United States); Mukherjee, Bhramar [Department of Biostatistics, University of Michigan, 1415 Washington Heights, Ann Arbor, MI 48109 (United States); Hauser, Russ [Department of Environmental Health, Harvard School of Public Health, 677 Huntington Ave., Boston, MA 02115 (United States); Meeker, John D., E-mail: meekerj@umich.edu [Department of Environmental Health Sciences, University of Michigan, 1415 Washington Heights, Ann Arbor, MI 48109 (United States)

    2013-02-15

    Brominated flame retardants (BFRs) are used in the manufacture of a variety of materials and consumer products in order to meet fire safety standards. BFRs may persist in the environment and have been detected in wildlife, humans and indoor dust and air. Some BFRs have demonstrated endocrine and reproductive effects in animals, but human studies are limited. In this exploratory study, we measured serum hormone levels and flame retardant concentrations [31 polybrominated diphenyl ether (PBDE) congeners and 6 alternate flame retardants] in house dust from men recruited through a US infertility clinic. PBDE congeners in dust were grouped by commercial mixtures (i.e. penta-, octa- and deca-BDE). In multivariable linear regression models adjusted by age and body mass index (BMI), significant positive associations were found between house dust concentrations of pentaBDEs and serum levels of free T4, total T3, estradiol, and sex hormone binding globulin (SHBG), along with an inverse association with follicle stimulating hormone (FSH). There were also positive associations of octaBDE concentrations with serum free T4, thyroid stimulating hormone (TSH), luteinizing hormone (LH) and testosterone and an inverse association of decaBDE concentrations with testosterone. Hexabromocyclododecane (HBCD) was associated with decreased SHBG and increased free androgen index. Dust concentrations of bis-tribromophenoxyethane (BTBPE) and tetrabromo-diethylhexylphthalate (TBPH) were positively associated with total T3. These findings are consistent with our previous report of associations between PBDEs (BDE 47, 99 and 100) in house dust and hormone levels in men, and further suggest that exposure to contaminants in indoor dust may be leading to endocrine disruption in men. - Highlights: ► Brominated flame retardants (BFRs) including PBDEs and alternates were measured. ► Exposure to BFRs is characterized from concentrations in participant vacuum bag dust. ► Exposure to PBDEs and

  4. Detection of novel brominated flame retardants (NBFRs in the urban soils of Melbourne, Australia

    Directory of Open Access Journals (Sweden)

    Thomas J. McGrath

    2017-03-01

    Full Text Available A range of brominated flame retardants (BFRs have been incorporated into polymeric materials like plastics, electronic equipment, foams and textiles to prevent fires. The most common of these, polybrominated diphenyl ethers (PBDEs, have been subject to legislated bans and voluntary withdrawal by manufacturers in North America, Europe and Australia over the past decade due to long-range atmospheric transport, persistence in the environment, and toxicity. Evidence has shown that replacement novel brominated flame retardants (NBFRs are released to the environment by the same mechanisms as PBDEs and share similar hazardous properties. The objective of the current research was to characterize soil contamination by NBFRs in the urban soils of Melbourne, Australia. A variety of industrial and non-industrial land-uses were investigated with the secondary objective of determining likely point sources of pollution. Six NBFRs; pentabromotoluene (PBT, pentabromoethylbenzene (PBEB, hexabromobenzene (HBB, 2-ethylhexyl-2,3,4,5-tetrabromobenzoate (EH-TBB, 1,2-bis(2,4,6-tribromophenoxyethane (BTBPE and decabromodiphenyl ethane (DBDPE were measured in 30 soil samples using selective pressurized liquid extraction (S-PLE and gas chromatography coupled to triple quadrupole mass spectrometry (GC-MS/MS. NBFRs were detected in 24/30 soil samples with Σ5NBFR concentrations ranging from nd-385 ng/g dw. HBB was the most frequently detected compound (14/30, while the highest concentrations were observed for DBDPE, followed by BTBPE. Electronic waste recycling and polymer manufacturing appear to be key contributors to NBFR soil contamination in the city of Melbourne. A significant positive correlation between Σ8PBDEs and Σ5NBFR soil concentrations was observed at waste disposal sites to suggest that both BFR classes are present in Melbourne's waste streams, while no association was determined among manufacturing sites. This research provides the first account of NBFRs

  5. Catalytic-site mapping of pyruvate formate lyase. Hypophosphite reaction on the acetyl-enzyme intermediate affords carbon-phosphorus bond synthesis (1-hydroxyethylphosphonate).

    Science.gov (United States)

    Plaga, W; Frank, R; Knappe, J

    1988-12-15

    Pyruvate formate-lyase of Escherichia coli cells, a homodimeric protein of 2 x 85 kDa, is distinguished by the property of containing a stable organic free radical (g = 2.0037) in its resting state. The enzyme (E-SH) achieves pyruvate conversion to acetyl-CoA via two distinct half-reactions (E-SH + pyruvate in equilibrium E-S-acetyl + formate; E-S-acetyl + CoA in equilibrium E-SH + acetyl-CoA), the first of which has been proposed to involve reversible homolytic carbon-carbon bond cleavage [J. Knappe et al. (1984) Proc. Natl Acad. Sci. USA 81, 1332-1335]. Present studies identified Cys-419 as the covalent-catalytic cysteinyl residue via CNBr fragmentation of E-S-[14C]acetyl and radio-sequencing of the isolated peptide CB-Ac (amino acid residues 406-423). Reaction of the formate analogue hypophosphite with E-S-acetyl was investigated and found to produce 1-hydroxyethylphosphonate with a thioester linkage to the adjacent Cys-418. The structure was determined from the chymotryptic peptide CH-P (amino acid residues 415-425), using 31P-NMR spectroscopy (delta = 44 ppm) and by chemical characterisation through degradation into 1-hydroxyethylphosphonate with phosphodiesterase or bromine. This novel P-C-bond synthesis involves the enzyme-based free radical and is proposed to resemble the physiological C-C-bond synthesis (pyruvate production) from formate and E-S-acetyl. These findings are interpreted as proof of a radical mechanism for the action of pyruvate formate-lyase. The central Cys-418/Cys-419 pair of the active site shows a distinctive thiolate property even in the inactive (nonradical) form of the enzyme, as determined using an iodoacetate probe.

  6. Discovery of two nova candidates in M81

    Science.gov (United States)

    Williams, S. C.; Hornoch, K.; Kucakova, H.; Henze, M.; Darnley, M. J.; Meusinger, H.; Kaur, A.; Hartmann, D. H.; Sala, G.; Jose, J.; Figueira, J.; Hernanz, M.; Shafter, A. W.

    2017-05-01

    The M81 nova monitoring collaboration reports the discovery of two M81 nova candidates in H & alpha; imaging from the 2-m Liverpool Telescope (LT). The first, M81N 2017-05a, was discovered on 2017-05-03.89 UT at RA = 9h55m24.61s, Dec. = +69 & deg;06'59.1" (J2000, 1 & sigma; error 0.2").

  7. OMI/Aura Bromine Monoxide (BrO) Total Column 1-orbit L2 Swath 13x24 km V003 (OMBRO) at GES DISC

    Data.gov (United States)

    National Aeronautics and Space Administration — The Aura Ozone Monitoring Instrument (OMI) collection-3 Bromine Monoxide Product OMBRO from the Aura-OMI, is now available from the NASA Goddard Earth Sciences Data...

  8. OMI/Aura Bromine Monoxide (BrO) Total Column 1-orbit L2 Swath 13x24 km V003

    Data.gov (United States)

    National Aeronautics and Space Administration — The Collection-3 Bromine Monoxide Product OMBRO from the Aura-OMI, is now available http://disc.gsfc.nasa.gov/Aura/OMI/ombro_v003.shtml) from the NASA Goddard Earth...

  9. MLS/Aura Level 3 Bromine Monoxide (BrO) Daily 10degrees Lat Zonal Mean V004 (ML3DZMBRO) at GES DISC

    Data.gov (United States)

    National Aeronautics and Space Administration — ML3DZMBRO is the EOS Aura Microwave Limb Sounder (MLS) daily zonal mean product for bromine monoxide derived from radiances measured by the 640 GHz radiometer. The...

  10. The jet of the Low Luminosity AGN of M81

    Directory of Open Access Journals (Sweden)

    Alberdi A.

    2013-12-01

    Full Text Available In this contribution, we summarize our main results of a big campaign of global VLBI observations of the AGN in M81 (M81* phase-referenced to the radio supernova SN 1993J. Thanks to the precise multi-epoch and multi-frequency astrometry, we have determined the normalized core-shift of the relativistic jet of M81* and estimated both the magnetic field and the particle density at the jet base. We have also found evidence of jet precession in M81* coming from the systematic time evolution of the jet orientation correlated with changes in the overall flux density.

  11. 40 CFR 792.81 - Standard operating procedures.

    Science.gov (United States)

    2010-07-01

    ... CONTROL ACT (CONTINUED) GOOD LABORATORY PRACTICE STANDARDS Testing Facilities Operation § 792.81 Standard...) Test system room preparation. (2) Test system care. (3) Receipt, identification, storage, handling...

  12. Palladium-catalyzed cross coupling reactions of 4-bromo-6H-1,2-oxazines

    Directory of Open Access Journals (Sweden)

    Reinhold Zimmer

    2009-09-01

    Full Text Available A number of 4-aryl- and 4-alkynyl-substituted 6H-1,2-oxazines 8 and 9 have been prepared in good yields via cross coupling reactions of halogenated precursors 2, which in turn are easily accessible by bromination of 6H-1,2-oxazines 1. Lewis-acid promoted reaction of 1,2-oxazine 9c with 1-hexyne provided alkynyl-substituted pyridine derivative 12 thus demonstrating the potential of this approach for the synthesis of pyridines.

  13. Determination of soluble bromine in an extra-high-pressure mercury discharge lamp by sodium hydroxide decomposition-suppressed ion chromatography.

    Science.gov (United States)

    Mitsumata, Hiroshi; Mori, Toshio; Maeda, Tatsuo; Kita, Yoshiyuki; Kohatsu, Osamu

    2006-02-01

    We have established a simple method for assaying the quantity of soluble bromine in the discharge tubes of an extra-high-pressure mercury discharge lamp. Each discharge tube is destroyed in 5 ml of 10 mM sodium hydroxide, and the recovered sodium hydroxide solution is analyzed by suppressed-ion chromatography using gradient elution. We have clarified that this method can assay less than 1 microg of soluble bromine in a discharge tube.

  14. Central nervous system reactions during heliox and trimix dives to 51 ATA, DEEP EX 81.

    Science.gov (United States)

    Vaernes, R; Hammerborg, D; Ellertsen, B; Peterson, R; Tønjum, S

    1983-09-01

    Two groups of divers were compressed to 500 msw with heliox (n = 3) and trimix (n = 3). They were followed with repeated neuropsychological and neurological tests during compression, at stable intermediate depths, and at 500 msw. For the heliox group there was a marked increase in tremor and EEG slow waves and reduction in handgrip strength. For the trimix group the tremor increase did not occur, but the EEG changes were the same as in the heliox group. On motor tests only the trimix group showed impaired finger dexterity and manual dexterity. The same occurred for fine visuomotor coordination, but both groups had increased intentional tremor. On cognitive tests the same difference occurred. The trimix group was markedly impaired in reasoning and long-term memory, while only a mild impairment was found in the heliox group. Dizziness and other symptoms of high pressure nervous syndrome (HPNS) occurred in both groups. There were marked HPNS effects during compression for both groups. Only tremor was inhibited by the nitrogen. In addition, the trimix group was impaired because of nitrogen narcosis. These data indicated that 10% nitrogen did not inhibit HPNS effects during compression to 500 msw, but the considerable differences between subjects shows that susceptibility to compression must be an important area for future research.

  15. Determination of nuclear cross-section of 81Br (n,,,) Br82 reaction by ...

    African Journals Online (AJOL)

    ... flux of 4.2 x 1013 n cm-2 s-1. The BaBr2 was chemically processed and measured as Hydrogen Bromide (HBr82). The value of nuclear cross-section was determined to be 2.1 0.2 barns, which falls within the range of values as previously reported elsewhere. (Journal of Applied Science and Technology: 2001 6(1-2): 4-6) ...

  16. Targeting CD81 to Prevent Metastases in Breast Cancer

    Science.gov (United States)

    2015-10-01

    in tumor cells would curb the formation of CTCs. Briefly, 4T1 cells either WT or cells in which CD81 has been knocked down stably using CRISPR - Cas9 ...knocked down (CD81KO) using CRIPSR- Cas9 technology were added to whole blood from mouse and then processed to calculate detection efficiency. Note – The

  17. Limits on Ionized Gas in M81's Globular Clusters

    OpenAIRE

    Wrobel, J. M.; Johnson, K. E.

    2018-01-01

    We use NSF's Karl G. Jansky Very Large Array to constrain the mass of ionized gas in 206 globular star clusters (GCs) in M81, a nearby spiral galaxy. We detect none of the GCs and impose a typical gas-mass upper limit of 550 solar masses (3-sigma). These findings bear on GC evolution in M81.

  18. 44 CFR 5.81 - Statement of policy.

    Science.gov (United States)

    2010-10-01

    ... 44 Emergency Management and Assistance 1 2010-10-01 2010-10-01 false Statement of policy. 5.81 Section 5.81 Emergency Management and Assistance FEDERAL EMERGENCY MANAGEMENT AGENCY, DEPARTMENT OF... performance of the official functions of the Agency and to maintain strict impartiality with respect to...

  19. 50 CFR 216.81 - Visits to fur seal rookeries.

    Science.gov (United States)

    2010-10-01

    ... 50 Wildlife and Fisheries 7 2010-10-01 2010-10-01 false Visits to fur seal rookeries. 216.81... MAMMALS Pribilof Islands Administration § 216.81 Visits to fur seal rookeries. From June 1 to October 15... any fur seal rookery or hauling grounds nor pass beyond any posted sign forbidding passage. ...

  20. 18 CFR 4.81 - Contents of application.

    Science.gov (United States)

    2010-04-01

    ... hydraulic head for estimating capacity and energy output, and the estimated number, rated capacity, and.... 4.81 Section 4.81 Conservation of Power and Water Resources FEDERAL ENERGY REGULATORY COMMISSION, DEPARTMENT OF ENERGY REGULATIONS UNDER THE FEDERAL POWER ACT LICENSES, PERMITS, EXEMPTIONS, AND DETERMINATION...

  1. 29 CFR 452.81 - Rights in intermediate body elections.

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 2 2010-07-01 2010-07-01 false Rights in intermediate body elections. 452.81 Section 452... REPORTING AND DISCLOSURE ACT OF 1959 Campaign Safeguards § 452.81 Rights in intermediate body elections. While the literal language in section 401(c) relating to distribution of campaign literature and to...

  2. 24 CFR 81.83 - Civil money penalties.

    Science.gov (United States)

    2010-04-01

    ... 24 Housing and Urban Development 1 2010-04-01 2010-04-01 false Civil money penalties. 81.83... § 81.83 Civil money penalties. (a) Imposition. The Secretary may impose a civil money penalty on a GSE... writing of the Secretary's determination to impose a civil money penalty by issuing a Notice of Intent to...

  3. 10 CFR 76.81 - Authorized use of radioactive material.

    Science.gov (United States)

    2010-01-01

    ... 10 Energy 2 2010-01-01 2010-01-01 false Authorized use of radioactive material. 76.81 Section 76.81 Energy NUCLEAR REGULATORY COMMISSION (CONTINUED) CERTIFICATION OF GASEOUS DIFFUSION PLANTS Safety... the certificate and/or approved compliance plan. Except as otherwise provided, the certificate or...

  4. 27 CFR 24.81 - Filing of formulas.

    Science.gov (United States)

    2010-04-01

    ... Section 24.81 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT OF THE TREASURY LIQUORS WINE Administrative and Miscellaneous Provisions Formulas § 24.81 Filing of... each process used to produce the wine. The addition or elimination of ingredients, changes in...

  5. 27 CFR 479.81 - Scope of tax.

    Science.gov (United States)

    2010-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 3 2010-04-01 2010-04-01 false Scope of tax. 479.81... OTHER FIREARMS Transfer Tax § 479.81 Scope of tax. Except as otherwise provided in this part, each transfer of a firearm in the United States is subject to a tax to be represented by an adhesive stamp of...

  6. 7 CFR 81.17 - Death, incompetency, or disappearance.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 3 2010-01-01 2010-01-01 false Death, incompetency, or disappearance. 81.17 Section... DOMESTIC CONSUMPTION PROGRAMS PRUNE/DRIED PLUM DIVERSION PROGRAM § 81.17 Death, incompetency, or disappearance. In the case of death, incompetency, disappearance, or dissolution of a prune/plum producer that...

  7. 37 CFR 1.81 - Drawings required in patent application.

    Science.gov (United States)

    2010-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2010-07-01 2010-07-01 false Drawings required in patent application. 1.81 Section 1.81 Patents, Trademarks, and Copyrights UNITED STATES PATENT AND TRADEMARK OFFICE, DEPARTMENT OF COMMERCE GENERAL RULES OF PRACTICE IN PATENT CASES National Processing Provisions The Drawings...

  8. 37 CFR 3.81 - Issue of patent to assignee.

    Science.gov (United States)

    2010-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2010-07-01 2010-07-01 false Issue of patent to assignee. 3.81 Section 3.81 Patents, Trademarks, and Copyrights UNITED STATES PATENT AND TRADEMARK OFFICE... of patent to assignee. (a) With payment of the issue fee: An application may issue in the name of the...

  9. 28 CFR 345.81 - Pre-industrial training.

    Science.gov (United States)

    2010-07-01

    ... 28 Judicial Administration 2 2010-07-01 2010-07-01 false Pre-industrial training. 345.81 Section... INDUSTRIES (FPI) INMATE WORK PROGRAMS FPI Inmate Training and Scholarship Programs § 345.81 Pre-industrial training. FPI encourages the development and use of pre-industrial training programs. Such training...

  10. 33 CFR 52.81 - Reading room and index.

    Science.gov (United States)

    2010-07-01

    ... 33 Navigation and Navigable Waters 1 2010-07-01 2010-07-01 false Reading room and index. 52.81... FOR CORRECTION OF MILITARY RECORDS OF THE COAST GUARD Public Access to Decisions § 52.81 Reading room and index. After deleting only so much personal information as is necessary to prevent an unwarranted...

  11. Enhanced formation of bromate and brominated disinfection byproducts during chlorination of bromide-containing waters under catalysis of copper corrosion products.

    Science.gov (United States)

    Hu, Jun; Qiang, Zhimin; Dong, Huiyu; Qu, Jiuhui

    2016-07-01

    Copper corrosion products (CCPs) in water distribution pipes may catalyze the reactions among disinfectant, natural organic matter (NOM), and bromide (Br(-)). This study investigated the simultaneous formation of bromate (BrO3(-)) and brominated disinfection byproducts (Br-DBPs) during chlorination of Br(-)-containing waters in the presence of three CCPs (i.e., CuO, Cu2O, and Cu(2+)). In a synthetic water, both oxidant decay and BrO3(-) formation were enhanced by CCPs, whereas the presence of humic acid (HA) significantly inhibited BrO3(-) formation due to its competition for HOBr to form Br-DBPs. In the HOClBr(-)CuO system, the BrO3(-) yield increased obviously with increasing CuO dose and initial Br(-) concentration, while the catalytic formation of Br-DBPs was rather limited. A molar conversion (Br(-) to BrO3(-)) of 22.1% was observed under CuO catalysis, compared with little conversion in the absence of CuO. In the HOClBr(-)Cu2O/Cu(2+) systems, Cu2O or Cu(2+) mainly enhanced the formation of Br-DBPs, with enhancement ratios of 69.9% and 50.1%, respectively. The degree of enhancement on Br-DBPs formation became more apparent with increasing pH, while that on BrO3(-) formation reached maximal at pH 7.6. The catalytic formation of Br-DBPs and BrO3(-) by CCPs was also verified in three filtered real waters, although to a lesser extent because of the water matrix effect. In mechanism, the CCPs promoted the formation of BrO3(-) and Br-DBPs through catalyzing the HOBr disproportionation pathway and the reaction of HOBr toward HA, respectively. Copyright © 2016 Elsevier Ltd. All rights reserved.

  12. Iodine(III)-Catalyzed Cascade Reactions Enabling a Direct Access to β-Lactams and α-Hydroxy-β-amino Acids.

    Science.gov (United States)

    Patzelt, Christoph; Pöthig, Alexander; Gulder, Tanja

    2016-07-15

    In the presented method, a one-pot metal-free access to β-lactams is provided. The developed strategy employs a hypervalent iodine(III)-triggered bromination/rearrangement/cyclization cascade reaction that allows the straightforward synthesis of a broad range of structurally different lactams from cheap and easily available imides. This triple cascade reaction is furthermore extendable by an in situ ring-opening reaction, giving direct access to isoserine derivatives from simple imines in a four-step, one-pot reaction.

  13. Temporal development of brominated flame retardants in peregrine falcon (Falco peregrinus) eggs from South Greenland (1986-2003)

    DEFF Research Database (Denmark)

    Vorkamp, Katrin; Thomsen, Marianne; Falk, Knud

    2005-01-01

    A time trend between 1986 and 2003 was found for brominated flame retardants in peregrine falcon eggs from South Greenland, with significantly increasing concentrations of the polybrominated diphenyl ethers (PBDEs) 99, 100, 153, 154, and 209. For BDE-99 and -100, the concentration increased appro...... with increasing time trends exist for the BDEs 99, 100, 153, 154, and 209, while a decreasing contamination with the BDEs 183, 49, 47, 66 and 153 was indicated in a subset of eggs....

  14. Sensitive Spectrophotometric Determination of Atenolol in Pharmaceutical Formulations Using Bromate-Bromide Mixture as an Eco-Friendly Brominating Agent

    Directory of Open Access Journals (Sweden)

    Kudige N. Prashanth

    2012-01-01

    Full Text Available Three simple and sensitive spectrophotometric methods are proposed for the determination of atenolol (ATN in bulk drug and tablets. The methods are based on the bromination of ATN by the bromine generated in situ by the action of the acid on the bromate–bromide mixture followed by the determination of unreacted bromine by reacting with a fixed amount of either meta-cresol purple (MCP and measuring the absorbance at 540 nm (method A and 445 nm (method B or erioglaucine (EGC and measuring the absorbance at 630 nm (method C. Beer's law is valid within the concentration ranges of 1.0–20.0, 2.0–40.0 and 1.0–8.0 μg/mL for method A, method B and method C, respectively. The calculated molar absorptivities were found to be 1.20×104, 4.51×103 and 3.46×104  L/mol⋅cm for method A, method B and method C, respectively. Sandell’s sensitivity values, correlation coefficients, limits of detection and quantification are also reported. Recovery results were statistically compared with those of a reference method by applying Student’s t- and F-test. The novelty of the present study is the measurement of two different colors using MCP, that is, red-pink color of MCP in acid medium at 540 nm and yellowish-orange color of brominated MCP at 445 nm.

  15. An XPS study of bromine in methanol etching and hydrogen peroxide passivation treatments for cadmium zinc telluride radiation detectors

    OpenAIRE

    Babar, S.; Sellin, PJ; Watts, JF; Baker, MA

    2013-01-01

    The performance of single crystal CdZnTe radiation detectors is dependent on both the bulk and the surface properties of the material. After single crystal fabrication and mechanical polishing, modification of the surface to remove damage and reduce the surface leakage current is generally achieved through chemical etching followed by a passivation treatment. In this work, CdZnTe single crystals have been chemically etched using a bromine in methanol (BM) treatment. The BM concentrations empl...

  16. Prenatal Exposure to Organohalogens, Including Brominated Flame Retardants, Influences Motor, Cognitive, and Behavioral Performance at School Age

    OpenAIRE

    Roze, Elise; Meijer, Lisethe; Bakker, Attie; Van Braeckel, Koenraad N.J.A.; Sauer, Pieter J.J.; Bos, Arend F.

    2009-01-01

    Background Organohalogen compounds (OHCs) are known to have neurotoxic effects on the developing brain. Objective We investigated the influence of prenatal exposure to OHCs, including brominated flame retardants, on motor, cognitive, and behavioral outcome in healthy children of school age. Methods This study was part of the prospective Groningen infant COMPARE (Comparison of Exposure-Effect Pathways to Improve the Assessment of Human Health Risks of Complex Environmental Mixtures of Organoha...

  17. Bromination of Graphene: A New Route to Making High Performance Transparent Conducting Electrodes with Low Optical Losses

    KAUST Repository

    Mansour, Ahmed

    2015-07-22

    The unique optical and electrical properties of graphene have triggered great interest in its application as a transparent conducting electrode material and significant effort has been invested in achieving high conductivity while maintaining transparency. Doping of graphene has been a popular route for reducing its sheet resistance, but this has typically come at a significant cost in optical transmission. We demonstrate doping of few layers graphene with bromine as a means of enhancing the conductivity via intercalation without major optical losses. Our results demonstrate the encapsulation of bromine leads to air-stable transparent conducting electrodes with five-fold improvement of sheet resistance reaching at the cost of only 2-3% loss of optical transmission. The remarkably low tradeoff in optical transparency leads to the highest enhancements in the figure of merit reported thus far for FLG. Furthermore, we tune the workfunction by up to 0.3 eV by tuning the bromine content. These results should help pave the way for further development of graphene as a potential substitute to transparent conducting polymers and metal oxides used in optoelectronics, photovoltaics and beyond.

  18. Impact of biogenic very short-lived bromine on the Antarctic ozone hole during the 21st century

    Science.gov (United States)

    Fernandez, Rafael Pedro; Kinnison, Douglas E.; Lamarque, Jean-Francois; Tilmes, Simone; Saiz-Lopez, Alfonso

    2017-04-01

    Active bromine released from the photochemical decomposition of biogenic very short-lived bromocarbons (VSLBr) enhances stratospheric ozone depletion. Based on a dual set of 1960-2100 coupled chemistry-climate simulations (i.e. with and without VSLBr), we show that the maximum Antarctic ozone hole depletion increases by up to 14% when natural VSLBr are considered, in better agreement with ozone observations. The impact of the additional 5 pptv VSLBr on Antarctic ozone is most evident in the periphery of the ozone hole, producing an expansion of the ozone hole area of 5 million km2, which is equivalent in magnitude to the recently estimated Antarctic ozone healing due to the implementation of the Montreal Protocol. We find that the inclusion of VSLBr in CAM-Chem does not introduce a significant delay of the modelled ozone return date to 1980 October levels, but instead affect the depth and duration of the simulated ozone hole. Our analysis further shows that total bromine-catalysed ozone destruction in the lower stratosphere surpasses that of chlorine by year 2070, and indicates that natural VSLBr chemistry would dominate Antarctic ozone seasonality before the end of the 21st century. This work suggests a large influence of biogenic bromine on the future Antarctic ozone layer.

  19. Degradation of Polymeric Brominated Flame Retardants: Development of an Analytical Approach Using PolyFR and UV Irradiation.

    Science.gov (United States)

    Koch, Christoph; Dundua, Alexander; Aragon-Gomez, Jackelyn; Nachev, Milen; Stephan, Susanne; Willach, Sarah; Ulbricht, Mathias; Schmitz, Oliver J; Schmidt, Torsten C; Sures, Bernd

    2016-12-06

    Many well-established methods for studying the degradation of brominated flame retardants are not useful when working with polymeric and water insoluble species. An example for this specific class of flame retardants is PolyFR (polymeric flame retardant; CAS No 1195978-93-8), which is used as a substituent for hexabromocyclododecane. Although it has been on the market for two years now, almost no information is available about its long time behavior in the environment. Within this study, we focus on how to determine a possible degradation of both pure PolyFR as well as PolyFR in the final insulation product, expanded polystyrene foam. Therefore, we chose UV radiation followed by analyses of the total bromine content at different time points via ICP-MS and identified possible degradation products such as 2,4,6-tribromophenol through LC-MS. These results were then linked with measurements of the adsorbable organically bound bromine and total organic carbon in order to estimate their concentrations. With respect to the obtained (1)H NMR, GPC, and contact angle results, the possibility for further degradation was discussed, as UV irradiation can influence the decomposition of molecules in combination with other environmental factors like biodegradation.

  20. EFFECT OF BROMINE ATOMS NUMBER ON THE CYTOTOXICITY OF TWO 2-FURYLETHYLENE DERIVATIVE SUBSTANCES IN NORMAL AND TUMORAL CELL LINES.

    Directory of Open Access Journals (Sweden)

    Oscar Hernández

    2012-01-01

    Full Text Available The study was performed to investigate the effect of bromine atoms number present in two tested substances derivatives of 2-furylethylene on cell proliferation. The substances carrying one or two Br atoms were coded as MA and G1 respectively. The neutral red uptake (NRU assay and mitotic index (MI were used for this purpose. The presence of two bromine atoms on the molecule of G1 inhibited markedly the cytotoxicity of this composite. For CHO cell line, the IC50 values were 256.6 µM for G1 and 134.5 µM for MA; whereas in SK MEL-3 (human melanoma cell line, the IC50 were 413.4 µM and 264.1 µM for G1 and MA respectively. The IC50 values obtained in both cell lines were higher than 100 µM and showed no specificity for tumoral cells. The MI obtained with the G1 composite showed no significant differences with phytohaemoglutinine used as positive control. The anti-proliferative effect and MI were related with the number of bromine atoms on the molecules assayed. Another experiment was conducted with the MA product to obtain information about the acute oral toxicity class methods. The tested compound was classified in the 3th toxicity class with a fixed LD (50 cut-off value of 200 mg/kg of body weight.

  1. Characterization of Three Tetrabromobisphenol-S Derivatives in Mollusks from Chinese Bohai Sea: A Strategy for Novel Brominated Contaminants Identification.

    Science.gov (United States)

    Liu, Ai-feng; Tian, Yong; Yin, Nuo-ya; Yu, Miao; Qu, Guang-bo; Shi, Jian-bo; Du, Yu-guo; Jiang, Gui-bin

    2015-07-01

    Identification of novel brominated contaminants in the environment, especially the derivatives and byproducts of brominated flame retardants (BFRs), has become a wide concern because of their adverse effects on human health. Herein, we qualitatively and quantitatively identified three byproducts of tetrabromobisphenol-S bis(2,3-dibromopropyl ether) (TBBPS-BDBPE), including TBBPS mono(allyl ether) (TBBPS-MAE), TBBPS mono(2-bromoallyl ether) (TBBPS-MBAE) and TBBPS mono(2,3-dibromopropyl ether) (TBBPS-MDBPE) as novel brominated contaminants. Meanwhile, the mass spectra and analytical method for determination of TBBPS-BDBPE byproducts were presented for the first time. The detectable concentrations (dry weight) of TBBPS-MAE, TBBPS-MBAE and TBBPS-MDBPE were in the ranges 28-394 μg/g in technical TBBPS-BDBPE and 0.1-4.1 ng/g in mollusks collected from the Chinese Bohai Sea. The detection frequencies in mollusk samples were 5%, 39%, 95% for TBBPS-MAE, TBBPS-MBAE and TBBPS-MDBPE, respectively, indicating their prevailing in the environment. The results showed that they could be co-produced and leaked into the environment with production process, and might be more bioaccumulative and toxic than TBBPS-BDBPE. Therefore, the production and use of TBBPS derivatives lead to unexpected contamination to the surrounding environment. This study also provided an effective approach for identification of novel contaminants in the environment with synthesized standards and Orbitrap high resolution mass spectrometry.

  2. Occurrence of brominated flame retardants in black thermo cups and selected kitchen utensils purchased on the European market.

    Science.gov (United States)

    Samsonek, J; Puype, F

    2013-01-01

    In order to screen for the presence of a recycled polymer waste stream from waste electric and electronic equipment (WEEE), a market survey was conducted on black plastic food-contact articles (FCA). An analytical method was applied combining X-ray fluorescence spectrometry (XRF) with thermal desorption gas chromatography coupled with mass spectrometry (thermal desorption GC-MS). Firstly, XRF spectrometry was applied to distinguish bromine-positive samples. Secondly, bromine-positive samples were submitted for identification by thermal desorption GC-MS. Generally, the bromine-positive samples contained mainly technical decabromodiphenyl ether (decaBDE). Newer types of BFRs such as tetrabromobisphenol A (TBBPA), tetrabromobisphenol A bis(2,3-dibromopropyl), ether (TBBPA-BDBPE) and decabromodiphenylethane (DBDPE), replacing the polybrominated diphenyleters (PBDEs) and polybrominated diphenyls (PBBs), were also identified. In none of the tested samples were PBBs or hexabromocyclododecane (HBCD) found. Polymer identification was carried out using Fourier-transformed infrared spectroscopy measurement (FTIR) on all samples. The results indicate that polypropylene-polyethylene copolymers (PP-PE) and mainly styrene-based food-contact materials, such as acrylonitrile-butadiene-styrene (ABS) have the highest risk of containing BFRs.

  3. Properties of PTFE tape as a semipermeable membrane in fluorous reactions

    Directory of Open Access Journals (Sweden)

    Brendon A. Parsons

    2015-06-01

    Full Text Available In a PTFE tape phase-vanishing reaction (PV-PTFE, a delivery tube sealed with PTFE tape is inserted into a vessel which contains the substrate. The reagent diffuses across the PTFE tape barrier into the reaction vessel. PTFE co-polymer films have been found to exhibit selective permeability towards organic compounds, which was affected by the presence of solvents. In this study, we attempted to establish general trends of permeability of PTFE tape to different compounds and to better describe the process of solvent transport in PV-PTFE bromination reactions. Though PTFE tape has been reported as impermeable to some compounds, such as dimethyl phthalate, solvent adsorption to the tape altered its permeability and allowed diffusion through channels of solvent within the PTFE tape. In this case, the solvent-filled pores of the PTFE tape are chemically more akin to the adsorbed solvent rather than to the PTFE fluorous structure. The solvent uptake effect, which was frequently observed in the course of PV-PTFE reactions, can be related to the surface tension of the solvent and the polarity of the solvent relative to the reagent. The lack of pores in bulk PTFE prevents solvents from altering its permeability and, therefore, bulk PTFE is impermeable to most solvents and reagents. However, bromine, which is soluble in liquid fluorous media, diffused through the bulk PTFE. A better understanding of the PTFE phase barrier will make it possible to further optimize the PV-PTFE reaction design.

  4. Sensitivity of the Reaction Mechanism of the Ozone Depletion Events during the Arctic Spring on the Initial Atmospheric Composition of the Troposphere

    Directory of Open Access Journals (Sweden)

    Le Cao

    2016-09-01

    Full Text Available Ozone depletion events (ODEs during the Arctic spring have been investigated since the 1980s. It was found that the depletion of ozone is highly associated with the release of halogens, especially bromine containing compounds. These compounds originate from various substrates such as the ice/snow-covered surfaces in Arctic. In the present study, the dependence of the mixing ratios of ozone and principal bromine species during ODEs on the initial composition of the Arctic atmospheric boundary layer was investigated by using a concentration sensitivity analysis. This analysis was performed by implementing a reaction mechanism representing the ozone depletion and halogen release in the box model KINAL (KInetic aNALysis of reaction mechanics. The ratios between the relative change of the mixing ratios of particular species such as ozone and the variation in the initial concentration of each atmospheric component were calculated, which indicate the relative importance of each initial species in the chemical kinetic system. The results of the computations show that the impact of various chemical species is different for ozone and bromine containing compounds during the depletion of ozone. It was found that CH3CHO critically controls the time scale of the complete removal of ozone. However, the rate of the ozone loss and the maximum values of bromine species are only slightly influenced by the initial value of CH3CHO. In addition, according to the concentration sensitivity analysis, the reduction of initial Br2 was found to cause a significant retardant of the ODE while the initial mixing ratio of HBr exerts minor influence on both ozone and bromine species. In addition, it is also interesting to note that the increase of C2H2 would significantly raise the amount of HOBr and Br in the atmosphere while the ozone depletion is hardly changed.

  5. Development of Zinc/Bromine Batteries for Load-Leveling Applications: Phase 1 Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Eidler, Phillip

    1999-07-01

    The Zinc/Bromine Load-Leveling Battery Development contract (No. 40-8965) was partitioned at the outset into two phases of equal length. Phase 1 started in September 1990 and continued through December 1991. In Phase 1, zinc/bromine battery technology was to be advanced to the point that it would be clear that the technology was viable and would be an appropriate choice for electric utilities wishing to establish stationary energy-storage facilities. Criteria were established that addressed most of the concerns that had been observed in the previous development efforts. The performances of 8-cell and 100-cell laboratory batteries demonstrated that the criteria were met or exceeded. In Phase 2, 100-kWh batteries will be built and demonstrated, and a conceptual design for a load-leveling plant will be presented. At the same time, work will continue to identify improved assembly techniques and operating conditions. This report details the results of the efforts carried out in Phase 1. The highlights are: (1) Four 1-kWh stacks achieved over 100 cycles, One l-kWh stack achieved over 200 cycles, One 1-kWh stack achieved over 300 cycles; (2) Less than 10% degradation in performance occurred in the four stacks that achieved over 100 cycles; (3) The battery used for the zinc loading investigation exhibited virtually no loss in performance for loadings up to 130 mAh/cm{sup 2}; (4) Charge-current densities of 50 ma/cm{sup 2} have been achieved in minicells; (5) Fourteen consecutive no-strip cycles have been conducted on the stack with 300+ cycles; (6) A mass and energy balance spreadsheet that describes battery operation was completed; (7) Materials research has continued to provide improvements in the electrode, activation layer, and separator; and (8) A battery made of two 50-cell stacks (15 kWh) was produced and delivered to Sandia National Laboratories (SNL) for testing. The most critical development was the ability to assemble a battery stack that remained leak free. The

  6. Brominated flame retardants in the Arctic. An overview of spatial and temporal trends

    Energy Technology Data Exchange (ETDEWEB)

    Wit, C. de [Institute of Applied Environmental Research, Stockholm (Sweden); Alaee, M.; Muir, D. [National Water Research Institute, Burlington, MA (United States)

    2004-09-15

    The Stockholm Convention on Persistent Organic Pollutants (POPs), which entered into force on May 17, 2004, includes wording that chemicals with the characteristics of POPs are those found in locations ''distant from sources'' and those for which ''monitoring data showing that long-range environmental transport of the chemical may have occurred''. Thus, the Arctic has become an important indicator region for assessment of persistence and bioaccumulation. The Arctic environment is well suited as a region in which to evaluate POPs. Some regions of thee Arctic, particularly the Barents Sea area north of Norway and western Russia are relatively close to source regions of POPs. Cold conditions favor persistence of POPs relative to temperate or tropical environments. The presence of fourth level carnivores (e.g. polar bears and seabirds), and storage of lipid as an energy source, make Arctic food webs vulnerable to bioaccumulative chemicals. Indigenous people in the Arctic utilizing a traditional diet, which is high in nutritionally beneficial fat, results in their elevated exposure to some POPs. The first indication that brominated flame retardants (BFRs) were reaching the Arctic was the detection by Jansson et al. of lower molecular weight polybrominated diphenyl ethers (PBDEs) in Svalbard Brunnichfs guillemots (130 ng/g lipid weight) and ringed seals (40 ng/g lw) collected in 1981. Whitefish collected from Lake Storvindeln in 1986, a pristine mountain lake in the Swedish mountains near Ammarnas, had {sigma}PBDE levels of 26 ng/g lw. Despite these early findings, only recently have the spatial and temporal trends of BFRs been studied in detail in the Arctic. The purpose of this paper is to review the new data on BFRs in the Arctic and assess whether this information supports the view that PBDEs and other BFRs of similar molecular weight are POPs and potential global pollutants. This review is based on a recent assessment of POPs

  7. Structures in solid state and solution of dimethoxy curcuminoids: regioselective bromination and chlorination

    Science.gov (United States)

    2013-01-01

    Background Several papers described the structure of curcumin and some other derivatives in solid and in solution. In the crystal structure of curcumin, the enol H atom is located symmetrically between both oxygen atoms of the enolone fragment with an O···O distance of 2.455 Å, which is characteristic for symmetrical H-bonds. In the solution, the geometry of the enolone fragment is attributed to the inherent disorder of the local environment, which solvates one of the basic sites better than the other, stabilizing one tautomer over the other. In this paper, how the position of methoxy groups in dimethoxy curcuminoids influence the conformation of molecules and how the halogen atoms change it when they are bonded at α-position in keto-enol part of molecules is described. Results Six isomers of dimethoxy curcuminoids were prepared. Conformations in solid state, which were determined by X-ray single crystallography and 1H MAS and 13C CPMAS NMR measurements, depend on the position of methoxy groups in curcuminoid molecules. In solution, a fast equilibrium between both keto-enol forms exists. A theoretical calculation finding shows that the position of methoxy groups changes the energy of HOMO and LUMO. An efficient protocol for the highly regioselective bromination and chlorination leading to α-halogenated product has been developed. All α-halogenated compounds are present mainly in cis keto-enol form. Conclusions The structures in solid state of dimethoxy curcuminoids depend on the position of methoxy groups. The NMR data of crystalline solid samples of 3,4-diOCH3 derivative, XRD measurements and X-ray structures lead us to the conclusion that polymorphism exists in solids. The same conclusion can be done for 3,5-diOCH3 derivative. In solution, dimethoxy curcuminoids are present in the forms that can be described as the coexistence of two equivalent tautomers being in fast equilibrium. The position of methoxy groups has a small influence on the enolic hydrogen

  8. Radionuclide venography using continuous Kr-81 m infusion: preliminary note

    Energy Technology Data Exchange (ETDEWEB)

    Ham, H.R.; Vandevivere, J.; Guillaume, M.; Niethammer, T.; Sergeysels, R.

    1981-10-01

    Continuous infusion of Kr-81m presents important advantages compared to the commonly used radionuclides for venography. High count rates can be accumulated, and a high resolution collimator can be employed to ensure good quality images. The study can be repeated immediately and multiple views can be performed until a satisfactory result is obtained. The production of radionuclide from a Rb-81--Kr-81m generator suitable for intravenous infusion is almost the same as that which is suitable for ventilation. The same generator can first be used for venography and then for ventilation imaging to complete the work-up patients suspected of having thromboembolic disease.

  9. What's new in Windows 8.1 for dummies

    CERN Document Server

    Underdahl, Brian

    2013-01-01

    What's New in Windows 8.1 For Dummies Pocket Edition provides a brief, inexpensive, and focused guide for Windows 8 users upgrading to 8.1. Chapters include:It's all about you: An exploration of the customization features, from flexible sizing on icons to shared wallpaper to boot options.We can build it better: Review of the updates to applications with special emphaisis on communications and media appsShiny new toys: Walkthroughs of the new features added to Windows 8.1, including the start button and search functionTen reasons you were smart to upgrade: In the spirit of the For Dummies Part

  10. Laboratory study on subgrade soil stabilization using RBI grade 81

    Science.gov (United States)

    Cynthia, J. Bernadette; Kamalambikai, B.; Prasanna Kumar, R.; Dharini, K.

    2017-07-01

    The present study investigates the effect of reinforcing the sub grade soils with RBI 81 material. A soil nearby was collected and preliminary tests were conducted to classify the soil and it was found from the results that the sample collected was a poorly graded clay. Subsequently Tests such as Proctor Compaction, CBR, and UCC were conducted to study the various engineering properties of the identified soil. In addition to the above tests were also conducted on the soil by reinforcing with varying percentages of RBI 81. From the analysis of test results it was found that this material (RBI 81) will significantly improve the CBR value of the soil.

  11. Eosinophil peroxidase-derived reactive brominating species target the vinyl ether bond of plasmalogens generating a novel chemoattractant, alpha-bromo fatty aldehyde.

    Science.gov (United States)

    Albert, Carolyn J; Thukkani, Arun K; Heuertz, Rita M; Slungaard, Arne; Hazen, Stanley L; Ford, David A

    2003-03-14

    Plasmalogens are a subclass of glycerophospholipids that are enriched in the plasma membrane of many mammalian cells. The vinyl ether bond of plasmalogens renders them susceptible to oxidation. Accordingly, it was hypothesized that reactive brominating species, a unique oxidant formed at the sites of eosinophil activation, such as in asthma, might selectively target plasmalogens for oxidation. Here we show that reactive brominating species produced by the eosinophil peroxidase system of activated eosinophils attack the vinyl ether bond of plasmalogens. Reactive brominating species produced by eosinophil peroxidase target the vinyl ether bond of plasmalogens resulting in the production of a neutral lipid and lysophosphatidylcholine. Chromatographic and mass spectrometric analyses of this neutral lipid demonstrated that it was 2-bromohexadecanal (2-BrHDA). Reactive brominating species produced by eosinophil peroxidase attacked the plasmalogen vinyl ether bond at acidic pH. Bromide was the preferred substrate for eosinophil peroxidase, and chloride was not appreciably used even at a 1000-fold molar excess. Furthermore, 2-BrHDA production elicited by eosinophil peroxidase-derived reactive brominating species in the presence of 100 microM NaBr doubled with the addition of 100 mM NaCl. The potential physiological significance of this pathway was suggested by the demonstration that 2-BrHDA was produced by phorbol myristate acetate-stimulated eosinophils and by the demonstration that 2-BrHDA is a phagocyte chemoattractant. Taken together, the present studies demonstrate the targeting of the vinyl ether bond of plasmalogens by the reactive brominating species produced by eosinophil peroxidase and by activated eosinophils, resulting in the production of brominated fatty aldehydes.

  12. Dissolved organic matter composition drives the marine production of brominated very short-lived substances.

    Science.gov (United States)

    Liu, Yina; Thornton, Daniel C O; Bianchi, Thomas S; Arnold, William A; Shields, Michael R; Chen, Jie; Yvon-Lewis, Shari A

    2015-03-17

    Brominated very short-lived substances (BrVSLS), such as bromoform, are important trace gases for stratospheric ozone chemistry. These naturally derived trace gases are formed via bromoperoxidase-mediated halogenation of dissolved organic matter (DOM) in seawater. Information on DOM type in relation to the observed BrVSLS concentrations in seawater, however, is scarce. We examined the sensitivity of BrVSLS production in relation to the presence of specific DOM moieties. A total of 28 model DOM compounds in artificial seawater were treated with vanadium bromoperoxidase (V-BrPO). Our results show a clear dependence of BrVSLS production on DOM type. In general, molecules that comprise a large fraction of the bulk DOM pool did not noticeably affect BrVSLS production. Only specific cell metabolites and humic acid appeared to significantly enhance BrVSLS production. Amino acids and lignin phenols suppressed enzyme-mediated BrVSLS production and may instead have formed halogenated nonvolatile molecules. Dibromomethane production was not observed in any experiments, suggesting it is not produced by the same pathway as the other BrVSLS. Our results suggest that regional differences in DOM composition may explain the observed BrVSLS concentration variability in the global ocean. Ultimately, BrVSLS production and concentrations are likely affected by DOM composition, reactivity, and cycling in the ocean.

  13. A study of the presence of brominated flame retardants in Australian fauna

    Energy Technology Data Exchange (ETDEWEB)

    Symons, R.; Burniston, D.; Piro, N.; Stevenson, G.; Yates, A. [Australian Government Analytical Laboratories, Sydney (Australia)

    2004-09-15

    Brominated flame retardants, in particular polybrominated diphenyl ethers (PBDEs) gained prominence in the late nineties when Noren et al. reported an exponential increase in PBDE levels found in Swedish mothers milk over a quarter of a century period with an associated decrease in levels of dioxin-like compounds. PBDEs have since become exceptionally widely studied being detected in most environmental compartments and food as well as human tissues. Only limited information on the distribution if PBDEs is available for the Southern Hemisphere, however, elevated levels of PBDEs in pork fat were detected during the routine screening for organochlorine pesticide residues. More recently an investigation of breast milk for PBDE levels also demonstrated that levels were comparable with those in the Northern Hemisphere. BFRs are not manufactured in Australia but it has been estimated that over 500 tonnes are imported yearly of which 340 tonnes are PBDEs. In addition, the amount of PBDEs that are contained in imported articles used both in domestic and industrial applications is unknown. In this paper, we report levels of PBDEs in a range of different Australian fauna that show that these POPs have indeed become widely distributed both in terms of the types of the fauna but also the levels determined.

  14. Effect of bromine-dopant on radiation-driven Rayleigh-Taylor instability in plastic foil

    Science.gov (United States)

    Xu, Binbin; Ma, Yanyun; Yang, Xiaohu; Tang, Wenhui; Ge, Zheyi; Zhao, Yuan; Ke, Yanzhao; Kawata, Shiego

    2017-10-01

    Effects of bromine (Br) dopant on the growth of radiation-driven ablative Rayleigh-Taylor instability (RTI) in plastic foils are studied by radiation hydrodynamics simulations and theoretical analysis. It is found that the Br-dopant in plastic foil reduces the seed of ablative RTI. The main reasons of the reduction are attributed to the smaller oscillation amplitude of ablative Richtmyer-Meshkov instability (RMI) induced by the smaller post-shock sound speed, and the smaller oscillation frequency of ablative RMI induced by the smaller ablation velocity and blow-off plasma velocity. The Br-dopant also decreases the linear growth rate of ablative RTI due to the smaller acceleration. Treating the perturbation growth as a function of foil’s displacement, the perturbation growth would increase in Br-doped foil at the phase of ablative RTI, which is attributed to the decrease of the ablation velocity and the density gradient scale length. The results are helpful for further understanding the influence of high-Z dopant on the radiation-driven ablative RTI.

  15. Soil contamination by brominated flame retardants in open waste dumping sites in Asian developing countries.

    Science.gov (United States)

    Eguchi, Akifimi; Isobe, Tomohiko; Ramu, Karri; Tue, Nguyen Minh; Sudaryanto, Agus; Devanathan, Gnanasekaran; Viet, Pham Hung; Tana, Rouch Seang; Takahashi, Shin; Subramanian, Annamalai; Tanabe, Shinsuke

    2013-03-01

    In Asian developing countries, large amounts of municipal wastes are dumped into open dumping sites each day without adequate management. This practice may cause several adverse environmental consequences and increase health risks to local communities. These dumping sites are contaminated with many chemicals including brominated flame retardants (BFRs) such as polybrominated diphenyl ethers (PBDEs) and hexabromocyclododecanes (HBCDs). BFRs may be released into the environment through production processes and through the disposal of plastics and electronic wastes that contain them. The purpose of this study was to elucidate the status of BFR pollution in municipal waste dumping sites in Asian developing countries. Soil samples were collected from six open waste dumping sites and five reference sites in Cambodia, India, Indonesia, Malaysia, and Vietnam from 1999 to 2007. The results suggest that PBDEs are the dominant contaminants in the dumping sites in Asian developing countries, whereas HBCD contamination remains low. Concentrations of PBDEs and HBCDs ranged from ND to 180 μg/kg dry wt and ND to 1.4 μg/kg dry wt, respectively, in the reference sites and from 0.20 to 430 μg/kg dry wt and ND to 2.5 μg/kg dry wt, respectively, in the dumping sites. Contamination levels of PBDEs in Asian municipal dumping sites were comparable with those reported from electronic waste dismantling areas in Pearl River delta, China. Copyright © 2012 Elsevier Ltd. All rights reserved.

  16. Chlorinated, brominated and fluorinated organic pollutants in African Penguin eggs: 30 years since the previous assessment.

    Science.gov (United States)

    Bouwman, Hindrik; Govender, Danny; Underhill, Les; Polder, Anuschka

    2015-05-01

    The African Penguin population has drastically declined over the last 100 years. Changes in food availability due to over-fishing and other oceanographic changes seem to be major causes. However, it has also been 30 years since organic pollutants as a potential factor have been assessed. We analysed penguin eggs collected in 2011 and 2012 from two breeding colonies 640 km apart: Robben Island near Cape Town on the Atlantic Ocean coast, and Bird Island near Port Elizabeth on the Indian Ocean coast of South Africa. We quantified organochlorine pesticides, brominated flame retardants, and perfluorinated compounds (PFCs). Compared to 30 years ago, concentrations of ΣDDT have remained about the same or slightly lower, while ΣPCBs declined almost four-fold. The use of DDT in malaria control is unlikely to have contributed. PFCs were detected in all eggs. Indications (non-significant) of eggshell thinning associated with ΣDDT and ΣPCB was found. It seems therefore that the concentrations of measured organic pollutants the African Penguin eggs are not contributing directly to its current demise, but concerns remain about thinner shells and desiccation. Effects of combinations of compounds and newer compounds cannot be excluded, as well as more subtle effects on reproduction, development, and behaviour. Copyright © 2014 Elsevier Ltd. All rights reserved.

  17. A Quorum Sensing-Disrupting Brominated Thiophenone with a Promising Therapeutic Potential to Treat Luminescent Vibriosis

    Science.gov (United States)

    Defoirdt, Tom; Benneche, Tore; Brackman, Gilles; Coenye, Tom; Sorgeloos, Patrick; Scheie, Anne Aamdal

    2012-01-01

    Vibrio harveyi is amongst the most important bacterial pathogens in aquaculture. Novel methods to control this pathogen are needed since many strains have acquired resistance to antibiotics. We previously showed that quorum sensing-disrupting furanones are able to protect brine shrimp larvae against vibriosis. However, a major problem of these compounds is that they are toxic toward higher organisms and therefore, they are not safe to be used in aquaculture. The synthesis of brominated thiophenones, sulphur analogues of the quorum sensing-disrupting furanones, has recently been reported. In the present study, we report that these compounds block quorum sensing in V. harveyi at concentrations in the low micromolar range. Bioluminescence experiments with V. harveyi quorum sensing mutants and a fluorescence anisotropy assay indicated that the compounds disrupt quorum sensing in this bacterium by decreasing the ability of the quorum sensing master regulator LuxR to bind to its target promoter DNA. In vivo challenge tests with gnotobiotic brine shrimp larvae showed that thiophenone compound TF310, (Z)-4-((5-(bromomethylene)-2-oxo-2,5-dihydrothiophen-3-yl)methoxy)-4-oxobutanoic acid, completely protected the larvae from V. harveyi BB120 when dosed to the culture water at 2.5 µM or more, whereas severe toxicity was only observed at 250 µM. This makes TF310 showing the highest therapeutic index of all quorum sensing-disrupting compounds tested thus far in our brine shrimp model system. PMID:22848604

  18. QSAR modeling and prediction of the endocrine-disrupting potencies of brominated flame retardants.

    Science.gov (United States)

    Papa, Ester; Kovarich, Simona; Gramatica, Paola

    2010-05-17

    In the European Union REACH regulation, the chemicals with particularly harmful behaviors, such as endocrine disruptors (EDs), are subject to authorization, and the identification of safer alternatives to these chemicals is required. In this context, the use of quantitative structure-activity relationships (QSAR) becomes particularly useful to fill the data gap due to the very small number of experimental data available to characterize the environmental and toxicological profiles of new and emerging pollutants with ED behavior such as brominated flame retardants (BFRs). In this study, different QSAR models were developed on different responses of endocrine disruption measured for several BFRs. The multiple linear regression approach was applied to a variety of theoretical molecular descriptors, and the best models, which were identified from all of the possible combinations of the structural variables, were internally validated for their performance using the leave-one-out (Q(LOO)(2) = 73-91%) procedure and scrambling of the responses. External validation was provided, when possible, by splitting the data sets in training and test sets (range of Q(EXT)(2) = 76-90%), which confirmed the predictive ability of the proposed equations. These models, which were developed according to the principles defined by the Organization for Economic Co-operation and Development to improve the regulatory acceptance of QSARs, represent a simple tool for the screening and characterization of BFRs.

  19. QSAR classification models for the prediction of endocrine disrupting activity of brominated flame retardants.

    Science.gov (United States)

    Kovarich, Simona; Papa, Ester; Gramatica, Paola

    2011-06-15

    The identification of potential endocrine disrupting (ED) chemicals is an important task for the scientific community due to their diffusion in the environment; the production and use of such compounds will be strictly regulated through the authorization process of the REACH regulation. To overcome the problem of insufficient experimental data, the quantitative structure-activity relationship (QSAR) approach is applied to predict the ED activity of new chemicals. In the present study QSAR classification models are developed, according to the OECD principles, to predict the ED potency for a class of emerging ubiquitary pollutants, viz. brominated flame retardants (BFRs). Different endpoints related to ED activity (i.e. aryl hydrocarbon receptor agonism and antagonism, estrogen receptor agonism and antagonism, androgen and progesterone receptor antagonism, T4-TTR competition, E2SULT inhibition) are modeled using the k-NN classification method. The best models are selected by maximizing the sensitivity and external predictive ability. We propose simple QSARs (based on few descriptors) characterized by internal stability, good predictive power and with a verified applicability domain. These models are simple tools that are applicable to screen BFRs in relation to their ED activity, and also to design safer alternatives, in agreement with the requirements of REACH regulation at the authorization step. Copyright © 2011 Elsevier B.V. All rights reserved.

  20. Crystal structure of a photobiologically active brominated angular pyranocoumarin: bromo-hydroxy-seselin

    Directory of Open Access Journals (Sweden)

    A. K. Bauri

    2017-03-01

    Full Text Available The title compound, C14H13BrO3 [systematic name: rac-(9S,10R-9-bromo-10-hydroxy-8,8-dimethyl-9,10-dihydro-2H,8H-pyrano[2,3-f]chromen-2-one], is a substituted pyranocoumarin, obtained by bromination of seselin [8,8-dimethyl-2H,8H-pyrano[2,3-f]chromen-2-one], which was isolated from the Indian herb Trachyspermum stictocarpum (Aajmod. The pyrano ring has a distorted half-chair conformation and its mean plane is inclined to the coumarin mean plane by 1.6 (2°. In the crystal, molecules are linked by pairs of O—H...O hydrogen bonds, forming inversion dimers with an R22(16 ring motif. The dimers stack along the a-axis direction and are linked by offset π–π interactions, forming columns [intercentroid distance = 3.514 (4 Å].

  1. Chlorine and bromine isotope fractionation of halogenated organic pollutants on gas chromatography columns.

    Science.gov (United States)

    Tang, Caiming; Tan, Jianhua; Xiong, Songsong; Liu, Jun; Fan, Yujuan; Peng, Xianzhi

    2017-09-08

    Compound-specific chlorine/bromine isotope analysis (CSIA-Cl/Br) has become a powerful approach to investigate degradation pathways and apportion sources of halogenated organic pollutants (HOPs) in the environment. CSIA-Cl/Br is usually conducted by gas chromatography-mass spectrometry (GC-MS), which could be negatively impacted by isotope fractionation on GC columns. In this study, on-column Cl/Br isotope fractionation of 31 organochlorines and 4 organobromines was explored using GC-double focus magnetic-sector high resolution MS (GC-DFS-HRMS). Twenty-nine HOPs exhibited inverse Cl/Br isotope fractionation for which the heavier isotopologues eluted faster than the lighter ones on GC columns, and two polychlorinated biphenyls (PCB-138 and PCB-153) showed normal isotope fractionation, whereas the rest four HOPs did not show observable isotope fractionation. The isotope fractionation extents varied from -13.0‰ to 73.1‰. Mechanisms of the on-column Cl/Br isotope fractionation were tentatively elucidated with a modified two-film model. The results demonstrate that integrating peak area as complete as possible for separable chromatographic peaks and integrating the middle retention-time segments for the inseparable peaks are helpful to improve precision and accuracy of the CSIA-Cl/Br data. The findings of this study will shed light on development of CSIA-Cl/Br methods with respect to improving precision and accuracy. Copyright © 2017 Elsevier B.V. All rights reserved.

  2. In vitro screening of the endocrine disrupting potency of brominated flame retardants and their metabolites

    Energy Technology Data Exchange (ETDEWEB)

    Hamers, T.; Kamstra, J.H. [Inst. for Environmental Studies (IVM), Amsterdam (Netherlands); Sonneveld, E. [BioDetection Systems (BDS), Amsterdam (Netherlands); Murk, A.J. [Wageningen Univ., Toxicology Group, Wageningen (Netherlands); Zegers, B.N.; Boon, J.P. [Royal Netherlands Inst. for Sea Research (NIOZ), Den Burg (Netherlands); Brouwer, A. [Umea Univ., Umea (Sweden)

    2004-09-15

    Substantial evidence is recently becoming available that brominated flame retardants (BFRs) are potential endocrine disruptors. The toxicological profile of BFRs, however, is too incomplete and insufficient to perform human and ecological risk assessment. To fill these gaps, the EU funded research program FIRE was started in December 2002. This program aims at the identification and toxicological characterization of the most potent and environmentally relevant BFRs and their possible risk for human and wildlife health. As part of a hazard identification approach, twenty seven BFRs have been selected within the framework of FIRE for pre-screening their endocrinedisrupting potencies. Selection of test compounds was based on a maximal variation in physicochemical characteristics of BFRs within the test set, allowing the establishment of quantitative structure-activity relationships (QSARs). In addition, environmental relevance (e.g. high production volumes and persistence) and availability for testing were used as selection criteria. BFRs were tested in seven different in vitro bioassays for their potency to interfere via estrogenic, thyroidal, androgenic, progestagenic, and Ah-receptor mediated pathways. Metabolisation rates of BFRs were determined using phenobarbital-induced rat liver microsomes. Finally, the endocrine disrupting potency of the metabolites was determined in the same in vitro bio-assays and compared to the potency of the parent compounds.

  3. Brominated diphenyl ether levels. A comparison of tributary sediments versus biosolid material

    Energy Technology Data Exchange (ETDEWEB)

    Kolic, T.M.; MacPherson, K.A.; Reiner, E.J. [Ontario Ministry of the Environment, Laboratory Services Branch, Toronto, ON (Canada); Ho, T.; Kleywegt, S. [Ontario Ministry of the Environment, Standards Development Branch, Toronto, ON (Canada); Dove, A.; Marvin, C. [Environment Canada, Burlington, ON (Canada)

    2004-09-15

    PBDEs are persistent in the environment, have low water solubility and are known to have a tendency to bioaccumulate in wildlife and humans. There are 209 possible PBDE congeners. There has been concern over the bioaccumulation of these compounds since they have been found in mother's milk. Some of the brominated diphenyl ethers are known to metabolize into hydroxylated compounds and these metabolites are known to compete with and reduce thyroxine (T4) from binding to the thyroxine binding protein, transthyretin. This disrupts the thyroid hormone system interaction that has recently been notable amongst women in the form of hypothyroidism that can affect the fetus development in the form of neurodevelopmental deficits. There have been reports of estrogenic activities regarding PBDEs and their hydroxylated counterparts. Information such as this is indicative that PBDEs are endocrine disruptors. Due to their lipophilic nature, PBDEs have a high binding affinity to particulates and accumulate in sediments. Various reports on sediments and sludge type matrices have been reported in Austria, Switzerland, Netherlands and Canada. The following paper is a presentation of levels of PBDEs found in Tributary sediments and their comparison of levels to nearby biosolid sampling locations along Lake Ontario.

  4. Kinetics of Brominated Flame Retardant (BFR) Releases from Granules of Waste Plastics.

    Science.gov (United States)

    Sun, Bingbing; Hu, Yuanan; Cheng, Hefa; Tao, Shu

    2016-12-20

    Plastic components of e-waste contain high levels of brominated flame retardants (BFRs), whose releases cause environmental and human health concerns. This study characterized the release kinetics of polybrominated diphenyl ethers (PBDEs) from millimeter-sized granules processed from the plastic exteriors of two scrap computer displays at environmentally relevant temperatures. The release rate of a substitute of PBDEs, 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), from the waste plastics, was reported for the first time. Deca-BDE was the most abundant PBDE congeners in both materials (87-89%), while BTBPE was also present at relatively high contents. The release kinetics of BFRs could be modeled as one-dimensional diffusion, while the temperature dependence of diffusion coefficients was well described by the Arrhenius equation. The diffusion coefficients of BFRs (at 30 °C) in the plastic matrices were estimated to be in the range of 10 -27.16 to 10 -19.96 m 2 ·s -1 , with apparent activation energies between 88.4 and 154.2 kJ·mol -1 . The half-lives of BFR releases (i.e., 50% depletion) from the plastic granules ranged from thousands to tens of billions of years at ambient temperatures. These findings suggest that BFRs are released very slowly from the matrices of waste plastics through molecular diffusion, while their emissions can be significantly enhanced with wear-and-tear and pulverization.

  5. 15 CFR 930.81 - Multiple permit review.

    Science.gov (United States)

    2010-01-01

    ... Shelf (OCS) Exploration, Development and Production Activities § 930.81 Multiple permit review. (a) A... consistency review (e.g., Corps of Engineer permits for the placement of structures on the OCS and for...

  6. 40 CFR 160.81 - Standard operating procedures.

    Science.gov (United States)

    2010-07-01

    ... GOOD LABORATORY PRACTICE STANDARDS Testing Facilities Operation § 160.81 Standard operating procedures... procedures shall be established for, but not limited to, the following: (1) Test system area preparation. (2...

  7. 49 CFR 174.81 - Segregation of hazardous materials.

    Science.gov (United States)

    2010-10-01

    ... 49 Transportation 2 2010-10-01 2010-10-01 false Segregation of hazardous materials. 174.81 Section... General Handling and Loading Requirements § 174.81 Segregation of hazardous materials. (a) This section... section: Segregation Table for Hazardous Materials Class or Division Notes 1.1, 1.2 1.3 1.4 1.5 1.6 2.1 2...

  8. The role of bromine and chlorine chemistry for arctic ozone depletion events in Ny-Ålesund and comparison with model calculations

    Directory of Open Access Journals (Sweden)

    M. Martinez

    1999-07-01

    Full Text Available During the Arctic Tropospheric Ozone Chemistry (ARCTOC campaigns at Ny-Ålesund, Spitsbergen, the role of halogens in the depletion of boundary layer ozone was investigated. In spring 1995 and 1996 up to 30 ppt bromine monoxide were found whenever ozone decreased from normal levels of about 40 ppb. Those main trace gases and others were specifically followed in the UV-VIS spectral region by differential optical absorption spectroscopy (DOAS along light paths running between 20 and 475 m a.s.l.. The daily variation of peroxy radicals closely followed the ozone photolysis rate J(O3(O1D in the absence of ozone depletion most of the time. However, during low ozone events this close correlation was no longer found because the measurement of radicals by chemical amplification (CA turned out to be sensitive to peroxy radicals and ClOx. Large CA signals at night can sometimes definitely be assigned to ClOx and reached up to 2 ppt. Total bromine and iodine were both stripped quantitatively from air by active charcoal traps and measured after neutron activation of the samples. Total bromine increased from background levels of about 15 ppt to a maximum of 90 ppt during an event of complete ozone depletion. For the spring season a strong source of bromine is identified in the pack ice region according to back trajectories. Though biogenic emission sources cannot be completely ruled out, a primary activation of halogenides by various oxidants seems to initiate an efficient autocatalytic process, mainly driven by ozone and light, on ice and perhaps on aerosols. Halogenides residing on pack ice surfaces are continuously oxidised by hypohalogenous acids releasing bromine and chlorine into the air. During transport and especially above open water this air mixes with upper layer pristine air. As large quantities of bromine, often in the form of BrO, have been observed at polar sunrise also around Antarctica, its release seems to be a natural phenomenon. The

  9. The role of bromine and chlorine chemistry for arctic ozone depletion events in Ny-Ålesund and comparison with model calculations

    Directory of Open Access Journals (Sweden)

    M. Martinez

    Full Text Available During the Arctic Tropospheric Ozone Chemistry (ARCTOC campaigns at Ny-Ålesund, Spitsbergen, the role of halogens in the depletion of boundary layer ozone was investigated. In spring 1995 and 1996 up to 30 ppt bromine monoxide were found whenever ozone decreased from normal levels of about 40 ppb. Those main trace gases and others were specifically followed in the UV-VIS spectral region by differential optical absorption spectroscopy (DOAS along light paths running between 20 and 475 m a.s.l.. The daily variation of peroxy radicals closely followed the ozone photolysis rate J(O3(O1D in the absence of ozone depletion most of the time. However, during low ozone events this close correlation was no longer found because the measurement of radicals by chemical amplification (CA turned out to be sensitive to peroxy radicals and ClOx. Large CA signals at night can sometimes definitely be assigned to ClOx and reached up to 2 ppt. Total bromine and iodine were both stripped quantitatively from air by active charcoal traps and measured after neutron activation of the samples. Total bromine increased from background levels of about 15 ppt to a maximum of 90 ppt during an event of complete ozone depletion. For the spring season a strong source of bromine is identified in the pack ice region according to back trajectories. Though biogenic emission sources cannot be completely ruled out, a primary activation of halogenides by various oxidants seems to initiate an efficient autocatalytic process, mainly driven by ozone and light, on ice and perhaps on aerosols. Halogenides residing on pack ice surfaces are continuously oxidised by hypohalogenous acids releasing bromine and chlorine into the air. During transport and especially above open water this air mixes with upper layer pristine air. As large quantities of bromine, often in the form of BrO, have been observed at polar sunrise also around Antarctica, its release

  10. Reactive brominating species produced by myeloperoxidase target the vinyl ether bond of plasmalogens: disparate utilization of sodium halides in the production of alpha-halo fatty aldehydes.

    Science.gov (United States)

    Albert, Carolyn J; Crowley, Jan R; Hsu, Fong-Fu; Thukkani, Arun K; Ford, David A

    2002-02-15

    Plasmalogens are a phospholipid molecular subclass that are enriched in the plasma membrane of many mammalian cells. The present study demonstrates that reactive brominating species produced by myeloperoxidase, as well as activated neutrophils, attack the vinyl ether bond of plasmalogens. Reactive brominating species produced by myeloperoxidase target the vinyl ether bond of plasmalogens, resulting in the production of a neutral lipid and lysophosphatidylcholine. Gas chromatography-mass spectrometry and proton NMR analyses of this neutral lipid demonstrated that it was 2-bromohexadecanal (2-BrHDA). In comparison to myeloperoxidase-generated reactive chlorinating species, reactive brominating species attacked the plasmalogen vinyl ether bond at neutral pH. In the presence of a 20-fold molar excess of NaCl compared with NaBr, myeloperoxidase-derived reactive halogenating species favored the production of 2-BrHDA over that of 2-chlorohexadecanal. Additionally, 2-BrHDA was preferentially produced from plasmalogen treated with hypochlorous acid in the presence of NaBr. The potential physiological significance of this pathway was suggested by the demonstration that both 2-BrHDA and 2-bromooctadecanal were produced by PMA-stimulated neutrophils. Taken together, the present studies demonstrate the targeting of the vinyl ether bond of plasmalogens by the reactive brominating species produced by myeloperoxidase and by activated neutrophils, resulting in the production of novel brominated fatty aldehydes.

  11. cycloaddition reactions

    Indian Academy of Sciences (India)

    Unknown

    models of regioselectivity in pericyclic reactions. In addition, local hard and soft acid base (HSAB) princi- ples have been also employed to predict the observed regioselectivity.2 In recent years, the conceptual density functional theory has been remarkably successful in explaining the reactivity and site selectivity.3 The.

  12. Prevalence of historical and replacement brominated flame retardant chemicals in New York City homes.

    Science.gov (United States)

    Cowell, Whitney J; Stapleton, Heather M; Holmes, Darrell; Calero, Lehyla; Tobon, Catherine; Perzanowski, Matthew; Herbstman, Julie B

    2017-03-01

    Until their phase-out between 2005 and 2013, polybrominated diphenyl ethers (PBDEs) were added to household products including furniture, rugs, and electronics to meet flammability standards. Replacement brominated flame retardant (BFR) chemicals, including 2-ethylhexyl-2,3,4,5 tetrabromobenzoate (TBB) and bis(2-ethylhexyl) 2,3,4,5-tetrabromophthalate (TBPH), which are components of the Firemaster 550® commercial mixture, are now being used to meet some flammability standards in furniture. The objective of this analysis was to evaluate the extent to which mothers and their children living in New York City are exposed to PBDEs, TBB, and TBPH. We measured PBDEs, TBB, and TBPH using gas chromatography mass spectrometry in dust (n = 25) and handwipe (n = 11) samples collected between 2012 and 2013 from mothers and children living in New York City. We defined dust as enriched if the proportional distribution for a given BFR exceeded two-thirds of the total BFR content. We detected PBDEs and TBPH in 100% of dust and handwipe samples and TBB in 100% of dust samples and 95% of handwipe samples. Dust from approximately two-thirds of households was enriched for either PBDEs (n = 9) or for TBB + TBPH (n = 8). Overall, the median house dust concentration of TBB + TBPH (1318 ng/g dust) was higher than that of ΣPentaBDE (802 ng/g dust) and BDE-209 (1171 ng/g dust). Children generally had higher BFR handwipe concentrations compared to mothers (ΣPentaBDE: 73%, BDE-209: 64%, TBB + TBPH: 55%) and within households, BFR concentrations from paired maternal-child handwipes were highly correlated. Among mothers, we found a significant positive relation between house dust and handwipe BDE-209 and TBB + TBPH concentrations. PBDEs, TBB and TBPH are ubiquitous in house dust and handwipes in a sample of mother-child pairs residing in New York City.

  13. Durability of carbon-plastic electrodes for zinc/bromine storage batteries

    Science.gov (United States)

    Arnold, C., Jr.

    1992-10-01

    In previous work, failure of early versions of the zinc/bromine battery was traced to degradation and warpage of the carbon-plastic electrode. These electrodes were fabricated from copolymers of ethylene and propylene (EP) containing structures that were found to be susceptible to degradation by the electrolyte. In this work, we evaluated two developmental electrodes from Johnson Controls Battery Group, Inc., in which the EP copolymer was replaced with a high-density polyethylene (HDPE) that contained glass-fiber reinforcing fillers. The glass fiber content of these two electrodes was different (19 vs. 31 percent). We determined the effect of electrolyte on sorption behavior, dimensional stability, chemical stability, and thermal, mechanical, and electrical properties under real-time and accelerated aging conditions. We also characterized unaged samples of both electrodes to determine their chemical composition and physical structure. We found that high glass content in the electrode minimizes sorption and increases dimensional stability. Both high and low glass content electrodes were found to be chemically and thermally stable toward the electrolyte. A slight decrease in the storage modulus (G') of both electrodes was attributed to sorption of non-ionic and hydrophobic ingredients in the electrolyte. The electrical conductivity of both electrodes appeared to improve (increase) upon exposure to the electrolyte. No time or temperature trends were observed for the chemical, thermal, or mechanical properties of electrodes made from HDPE. Since decreases in these properties were noted for electrodes made from EP copolymers under similar conditions, it appears that the HDPE-based electrodes have superior long-term stability in the ZnBr2 environment.

  14. Leaching characteristics of heavy metals and brominated flame retardants from waste printed circuit boards

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Xiaoyu [State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237 (China); Guo, Jie, E-mail: guojie@ecust.edu.cn [State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237 (China); Lin, Kuangfei [State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237 (China); Shanghai Key Laboratory of Functional Materials Chemistry, East China University of Science and Technology, Shanghai 200237 (China); Huang, Kai; Deng, Jingjing [State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, Shanghai 200237 (China)

    2013-02-15

    Highlights: ► Cu and Pb were the most leachable heavy metals in WPCBs according to TCLP and SPLP. ► Penta-BDE congeners were dominated in all extracts. ► High dissolved organic matter condition promoted the BFRs leaching rate. ► Leaching from WPCBs was a significant emission source of BFRs in landfill. -- Abstract: Leaching assessment on five heavy metals (copper, zinc, lead, nickel and cadmium) and two brominated flame retardants (BFRs), polybrominated diphenyl ethers (PBDEs) and tetrabromobisphenol A (TBBPA), from waste printed circuit boards (WPCBs) were conducted using various leaching methods. The mean leaching concentrations of copper were the highest in both toxicity characteristic leaching procedures (TCLP) and synthetic precipitation leaching procedures (SPLP) tests at 8.6 mg/L and 1.1 mg/L, while only lead (6.2 mg/L) exceeded the TCLP criteria and Chinese EPA regulatory limit (both 5.0 mg/L). However, PBDEs and TBBPA were not detected in TCLP and SPLP tests. Then the BFRs leaching trends and potential leachabilities were further investigated in actual landfill leachates using a modified method. Leaching characteristics that fast-leaching initially followed by slow-desorption over time were generally observed. In landfill leachate tests, the highest leaching concentrations of PBDEs and TBBPA were determined at 30.39 and 12.27 μg/L. Meanwhile, the highest leaching rates were estimated to reach 0.08% and 1.00%, respectively, which were significantly influenced by the dissolved organic carbon contents of extracts, the hydrophobicities of target BFRs and the specific surface areas of WPCBs materials. These results proved that leaching from WPCBs was a significant emission source of BFRs in landfill and electronic waste recycling dumpsite.

  15. Evaluation of Common Use Brominated Flame Retardant (BFR Toxicity Using a Zebrafish Embryo Model

    Directory of Open Access Journals (Sweden)

    Crystal Y. Usenko

    2016-09-01

    Full Text Available Brominated flame retardants (BFRs are used to reduce the flammability of plastics, textiles, and electronics. BFRs vary in their chemical properties and structures, and it is expected that these differences alter their biological interactions and toxicity. Zebrafish were used as the model organism for assessing the toxicity of nine structurally-diverse BFRs. In addition to monitoring for overt toxicity, the rate of spontaneous movement, and acetylcholinesterase and glutathione-S-transferase (GST activities were assessed following exposure. The toxicities of BFRs tested can be ranked by LC50 as tetrabromobisphenol A (TBBPA < 4,4′-isopropylidenebis[2-(2,6-dibromophenoxylethanol] (TBBPA-OHEE < Pentabromochlorocyclohexane (PBCH < 2-ethylhexyl 2,3,4,5-tetrabromobenzoate (TBB < hexabromocyclododecane (HBCD < hexabromobenzene (HBB < Tetrabromophthalic anhydride (PHT4. No adverse effect was observed in di(2-ethylhexyl tetrabromophthalate (TBPH or dibromoneopentyl glycol (DBNPG-treated embryos. The rate of spontaneous movement was decreased in a concentration-dependent manner following exposure to four of the nine compounds. GST activity was elevated following treatment with PBCH, TBBPA, HBCD, and HBB. The results indicate that exposure to several BFRs may activate an antioxidant response and alter behavior during early development. Some of the BFRs, such as TBBPA and TBBPA-OHEE, induced adverse effects at concentrations lower than chemicals that are currently banned. These results suggest that zebrafish are sensitive to exposure to BFRs and can be used as a comparative screening model, as well as to determine alterations in behavior following exposure and probe mechanisms of action.

  16. Characterization of brominated flame retardants from e-waste components in China.

    Science.gov (United States)

    Yu, Danfeng; Duan, Huabo; Song, Qingbin; Liu, Yicheng; Li, Ying; Li, Jinhui; Shen, Weijun; Luo, Jiahui; Wang, Jinben

    2017-10-01

    Many studies show that high levels of many toxic metals and persistent and bio-accumulative chemicals have been found in electronic waste (e-waste) dismantling sites and their surrounding environmental media. Both flame-retardant plastic housing materials and printed circuit boards (PCBs) could be the major contributors. However, relatively little work has focused on the use or content of toxic substances and their changing in scrap housing materials and PCBs from home appliances. This study evaluated the existence of brominated flame retardants (BFRs, including polybrominated diphenyl ethers (PBDEs) and Tetrabromobisphenol-A (TBBPA)) in housing plastics and PCBs from home appliances collected from various e-waste recyclers in China. These were then analyzed for the potential migration of BFRs from the e-waste components into their recycled products. The results show that both PBDEs and TBBPA were found with high level in most of e-waste samples, indicating that the widespread use of BFRs in home appliances are entering into the end-of-life stage. For the plastics samples, CRT TVs and LCD monitors should be given priority for the control of BFRs. Regarding PBDEs, the dominant congeners of BDE-209 in the plastics samples contributed 90.72-93.54% to the total concentrations of PBDEs, yet there are large variations for PCBs samples: BDE-28, -47, -99, and -153 were also important congeners compositions, except for BDE-209. Compared with previous studies, the BFRs concentrations in current Chinese e-waste are trending to decline. This study also found that BFRs in housing plastics and PCBs will be transferred into the recycled products with other purpose use, and the new products could have highly enriched capacities for BFRs. The obtained results could be helpful to manage e-waste and their components properly in order to minimize associated environmental and health risks of BFRs, particularly for their further reuse. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. Identification of highly brominated analogues of Q1 in marine mammals

    Energy Technology Data Exchange (ETDEWEB)

    Teuten, Emma L. [Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, 360 Woods Hole Road, Woods Hole, MA 02543 (United States)]. E-mail: emma.teuten@plymouth.ac.uk; Pedler, Byron E. [Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, 360 Woods Hole Road, Woods Hole, MA 02543 (United States)]. E-mail: bpedler@whoi.edu; Hangsterfer, Alexandra N. [Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, 360 Woods Hole Road, Woods Hole, MA 02543 (United States)]. E-mail: ahangsterfer@whoi.edu; Reddy, Christopher M. [Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, 360 Woods Hole Road, Woods Hole, MA 02543 (United States)]. E-mail: creddy@whoi.edu

    2006-11-15

    Three novel halogenated organic compounds (HOCs) have been identified in the blubber of marine mammals from coastal New England with the molecular formulae C{sub 9}H{sub 3}N{sub 2}Br{sub 6}Cl, C{sub 9}H{sub 3}N{sub 2}Br{sub 7}, and C{sub 9}H{sub 4}N{sub 2}Br{sub 5}Cl. They were identified using high and low resolution gas chromatography mass spectrometry (GCMS) and appear to be highly brominated analogues of Q1, a heptachlorinated HOC suspected to be naturally produced. These compounds were found in Atlantic white sided dolphin (Lagenorhynchus acutus), bottlenose dolphin (Tursiops truncatus), common dolphin (Delphinus delphis), Risso's dolphin (Grampus griseus), harbor porpoise (Phocoena phocoena), beluga whale (Delphinapterus leucas), fin whale (Balaenoptera physalus), grey seal (Halichoerus grypus), harp seal (Phoca groenlandica) and a potential food source (Loligo pealei) with concentrations as high as 2.7 {mu}g/g (lipid weight). The regiospecificity of C{sub 9}H{sub 3}N{sub 2}Br{sub 6}Cl is suggestive of a biogenic origin. Debromination of C{sub 9}H{sub 3}N{sub 2}Br{sub 6}Cl may be significant in the formation of C{sub 9}H{sub 4}N{sub 2}Br{sub 5}Cl. - Three novel bioaccumulated compounds were identified as C{sub 9}H{sub 3}N{sub 2}Br{sub 6}Cl, C{sub 9}H{sub 3}N{sub 2}Br{sub 7} and C{sub 9}H{sub 4}N{sub 2}Br{sub 5}Cl.

  18. Critical review of the analysis of brominated flame retardants and their environmental levels in Africa.

    Science.gov (United States)

    Brits, Martin; de Vos, Jayne; Weiss, Jana M; Rohwer, Egmont R; de Boer, Jacob

    2016-12-01

    World-wide, the prevalence of brominated flame retardants (BFRs) is well documented for routine analysis of environmental and biological matrices. There is, however, limited information on these compounds in the African environment and insufficient information on the analytical approaches used to obtain data. This paper presents a review on BFR levels in the African environment and the various analytical methodologies specifically applied in Africa for polybrominated diphenyl ethers (PBDEs), polybrominated biphenyls and alternative-BFRs. The analyses include liquid sample preparation using liquid-liquid and solid phase extraction and solid sample preparation involving Soxhlet extraction, with ultrasound-assisted extraction increasingly being applied. Instrumental detection techniques were limited to gas chromatography coupled with electron capture detector and electron impact ionisation with single quadrupole mass spectrometers. Information on congener profile prevalence in indoor dust, soil, aquatic environment (water, sediment, and aquatic organisms), eggs, wastewater treatment plant compartments, landfills (leachate and sediment) and breast milk are presented. Although PBDEs were inconsistently detected, contamination was reported for all investigated matrices in the African environment. The manifestation in remote regions indicates the ubiquitous prevalence and long-range transport of these compounds. Levels in sediment, and breast milk from some African countries were higher than reported for Asia and Europe. Due to limited data or non-detection of alternative-BFRs, it is unclear whether banned formulations were replaced in Africa. Most of the data reported for BFR levels in Africa were obtained in non-African laboratories or in South Africa and formed the basis for our discussion of reported contamination levels and related methodologies. Copyright © 2016 Elsevier Ltd. All rights reserved.

  19. Associations between brominated flame retardants in human milk and thyroid-stimulating hormone (TSH) in neonates.

    Science.gov (United States)

    Eggesbø, Merete; Thomsen, Cathrine; Jørgensen, Jens V; Becher, Georg; Odland, Jon Øyvind; Longnecker, Matthew P

    2011-08-01

    Brominated flame retardants (BFRs) have been in widespread use in a vast array of consumer products since the 1970s. The metabolites of some BFRs show a structural similarity to thyroid hormones and experimental animal studies have confirmed that they may interfere with thyroid hormone homeostasis. A major concern has been whether intrauterine exposure to BFRs may disturb thyroid homeostasis since the fetal brain is particularly susceptible to alterations in thyroid hormones. However, few reports on newborns have been published to date. To evaluate the association between BFRs and neonatal thyroid-stimulating hormone (TSH). We studied six polybrominated diphenyl ethers (PBDEs) measured in milk samples from 239 women who were part of the "Norwegian Human Milk Study" (HUMIS), 2003-2006. Hexabromocyclododecane (HBCD) and BDE-209 were measured in a subset of the women (193 and 46 milk samples, respectively). The milk was sampled at a median of 33 days after delivery. TSH was measured in babies three days after delivery as part of the routine national screening program for early detection of congenital hypothyroidism. Additional information was obtained through the Medical Birth Registry and questionnaires to the mothers. The PBDE concentrations in human milk in Norway were comparable to concentrations reported from other European countries and Asia, but not the US and Canada where levels are approximately one order of higher magnitude. We observed no statistically significant associations between BDE-47, 99, 153, 154, 209 and HBCD in human milk and TSH in models adjusted for possible confounders and other environmental toxicants including polychlorinated biphenyls (PCBs). We did not observe an association between TSH and exposure to HBCD and PBDEs within the exposure levels observed. Copyright © 2011 Elsevier Inc. All rights reserved.

  20. Occurrence of brominated disinfection byproducts in the air and water of chlorinated seawater swimming pools.

    Science.gov (United States)

    Manasfi, Tarek; Temime-Roussel, Brice; Coulomb, Bruno; Vassalo, Laurent; Boudenne, Jean-Luc

    2017-05-01

    An undesirable consequence of disinfection is the formation of chemical contaminants known as disinfection byproducts (DBPs). Chronic exposure to DBPs has been linked to adverse health effects. The occurrence of DBPs in chlorinated pools filled with seawater (such as thalassotherapy pools and pools in spas) has received little attention so far. The present study evaluated the speciation and levels of disinfection byproducts in indoor swimming pools filled with seawater and treated with chlorine. Water and air samples were collected from three indoor swimming pools located in Southern France. Several classes of DBPs including trihalomethanes, haloacetic acids, haloacetonitriles, and trihaloacetaldehydes were analyzed in water. Halogenated volatile organic compounds were analyzed in air. Extractable organic halides (EOX) contents were determined using combustion/micro-coulometry system. The speciation of DBPs identified in the three pools was predominantly brominated. The mean (arithmetic) concentration of bromoform, dibromoacetic acid, tribromoacetic acid, dibromoacetonitrile and bromal hydrate in the three pools was 79.2, 72.9, 59.9, 26.9 and 10.0μg/L, respectively. By weight, HAAs represented the most abundant chemical class followed by THMs. In air, bromoform was the most abundant THM occurring at a mean concentration of 133.2μg/m(3) in the three pools. The mean EOX level was 706μgCl(-)/L for the three pools. In average, the quantified DBPs accounted for only 14% of EOX, thus 86% of EOX remained unknown. Further research is warranted to identify the unknown DBPs. Copyright © 2017 Elsevier GmbH. All rights reserved.

  1. Chlorinated and brominated organic contaminants in fish from Shanghai markets: a case study of human exposure.

    Science.gov (United States)

    Qiu, Yanling; Strid, Anna; Bignert, Anders; Zhu, Zhiliang; Zhao, Jianfu; Athanasiadou, Maria; Athanassiadis, Ioannis; Bergman, Åke

    2012-10-01

    In the present study were two favorite edible fish species for local residents, i.e., mandarin fish and crawfish, collected from the Shanghai market and analyzed for selected organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), hexabromocyclododecane (HBCDD), polybrominated diphenyl ethers (PBDEs) and methoxylated PBDEs (MeO-PBDEs). Efforts were also made to identify the potential sources of these contaminants. Comparable concentrations of hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs) and HBCDD were found in muscle tissue of mandarin fish from Guangdong (GDF), the Pearl River Delta and from Taihu Lake (TLF), the Yangtze River Delta. Levels of chlordanes, PCBs and PBDEs were about one magnitude lower in TLF compared to GDF. The concentrations of OCPs in the butter-like gland of the crawfish (CFB) were 2-5 times of those in the crawfish muscle (CFM) while concentrations of PCBs, PBDEs and MeO-PBDEs were comparable. The different patterns and levels of chlorinated and brominated organohalogen contaminants seen in mandarin fish from GDF and TLF indicates that different types of chemicals might be used in the two delta regions. The present study also shows a good correlation between the concentrations of hexachlorobenzene (HCB) and pentachloroanisol (PCA) in fish for the first time. Fish consumption limits based on chemical contaminants with non-carcinogenic effects were calculated. The estimated maximum daily consumption limit for GDF, TLF, CFM and CFB were 1.5, 2.6, 3.7 and 0.08 kg, respectively, indicating no significant risk regarding the persistent organic pollutants measured in the present study. Copyright © 2012 Elsevier Ltd. All rights reserved.

  2. The first exposure assessment of legacy and unrestricted brominated flame retardants in predatory birds of Pakistan.

    Science.gov (United States)

    Abbasi, Naeem Akhtar; Eulaers, Igor; Jaspers, Veerle Leontina Bernard; Chaudhry, Muhammad Jamshed Iqbal; Frantz, Adrien; Ambus, Per Lennart; Covaci, Adrian; Malik, Riffat Naseem

    2017-01-01

    The exposure to legacy polybrominated diphenyl ethers (PBDEs), hexabromocyclododecanes (HBCDDs) and unrestricted 1,2-bis (2,4,6-tribromophenoxy) ethane (BTBPE), bis (2-ethylhexyl)-2,3,4,5-tetrabromophthalate (BEH-TEBP) and 2-ethylhexyl-2,3,4,5-tetrabromo-benzoate (EH-TBB) was examined in tail feathers of 76 birds belonging to ten predatory species inhabiting Pakistan. In addition, different feather types of six individuals of Black kite (Milvus migrans) were compared for their brominated flame retardant (BFR) levels. Black kite was found to be the most contaminated species with a median (minimum-maximum) tail feather concentration of 2.4 (0.70-7.5) ng g-1 dw for ∑PBDEs, 1.5 (0.5-8.1) ng g-1 dw for ∑HBCDDs and 0.10 (trophic guilds and between habitats, the latter for PBDEs only (P  0.05 for both). Similarly, no significant concentration differences were observed among different feather types (all P > 0.05) suggesting their similar exposure. While variables such as species, trophic guild and δ15N values were evaluated as major predictors for BFR accumulation in the studied species, we predict that combined effects of just mentioned factors may govern the intra- and interspecific differences in BFR contamination profiles. We urge for further investigation of BFR exposure and potential toxicological effects in predatory birds from Asia with a more extensive sample size per species and location. Copyright © 2016 Elsevier Ltd. All rights reserved.

  3. Occurrence of brominated dioxins in a study using various firefighting methods.

    Science.gov (United States)

    Bjurlid, Filip; Kärrman, Anna; Ricklund, Niklas; Hagberg, Jessika

    2017-12-01

    The use of different firefighting methods influences how fast a fire is extinguished and how fast the temperature drops in the area affected by the fire. These differences may also influence the formation of harmful pollutants during firefighting of an accidental fire. The aim was to study occurrence of brominated dibenzo-p-dioxins and furans (PBDD/Fs) in gas and soot during five fire scenarios resembling a small apartment fire and where different firefighting methods were used. Samples of gas and soot were taken both during the buildup of the fire and during the subsequent extinguishing of the fire while using different firefighting methods (nozzle, compressed air foam system, cutting extinguisher) and an extinguishing additive. New containers equipped with identical sets of combustible material were used for the five tests. The use of different firefighting methods and extinguishing additive induced variations in concentration and congener profiles of detected PBDD/Fs. The concentration range of ∑PBDD/Fs in gas was 4020-18,700pg/m3, and in soot 76-4092pg/m2. PBDFs were the predominant congeners and 1,2,3,4,6,7,8-HpBDF was the most abundant congener. Chlorinated dibenzo-p-dioxins and furans (PCDD/Fs) were also monitored. The PBDD/Fs contributed with in average 97% to the total (PCDD/Fs plus PBDD/Fs) toxic equivalents, in soot and gas. During extinguishing, the shorter time the temperature was around 300°C, the lower occurrence of PBDD/Fs. In the study the firefighting methods showed a difference in how effectively they induced a temperature decrease below 300°C in the fire zone during quenching, where cutting extinguishing using additive and the compressed air foam system showed the fastest drop in temperature. Copyright © 2017 Elsevier B.V. All rights reserved.

  4. The individual and cumulative effect of brominated flame retardant and polyvinylchloride (PVC) on thermal degradation of acrylonitrile-butadiene-styrene (ABS) copolymer.

    Science.gov (United States)

    Brebu, Mihai; Bhaskar, Thallada; Murai, Kazuya; Muto, Akinori; Sakata, Yusaku; Uddin, Md Azhar

    2004-08-01

    Acrylonitrile-butadiene-styrene (ABS) copolymers without and with a polybrominated epoxy type flame retardant were thermally degraded at 450 degrees C alone (10 g) and mixed with polyvinylchloride (PVC) (8 g/2 g). Gaseous and liquid products of degradation were analysed by various gas chromatographic methods (GC with TCD, FID, AED, MSD) in order to determine the individual and cumulative effect of bromine and chlorine on the quality and quantity of degradation compounds. It was found that nitrogen, chlorine, bromine and oxygen are present as organic compounds in liquid products, their quantity depends on the pyrolysed polymer or polymer mixture. Bromophenol and dibromophenols were the main brominated compounds that come from the flame retardant. 1-Chloroethylbenzene was the main chlorine compound observed in liquid products. It was also determined that interactions appear at high temperatures during decomposition between the flame retardant, PVC and the ABS copolymer.

  5. Field and Satellite Observations of the Formation and Distribution of Arctic Atmospheric Bromine Above a Rejuvenated Sea Ice Cover

    Science.gov (United States)

    Nghiem, Son V.; Rigor, Ignatius G.; Richter, Andreas; Burrows, John P.; Shepson, Paul B.; Bottenheim, Jan; Barber, David G.; Steffen, Alexandra; Latonas, Jeff; Wang, Feiyue; hide

    2012-01-01

    Recent drastic reduction of the older perennial sea ice in the Arctic Ocean has resulted in a vast expansion of younger and saltier seasonal sea ice. This increase in the salinity of the overall ice cover could impact tropospheric chemical processes. Springtime perennial ice extent in 2008 and 2009 broke the half-century record minimum in 2007 by about one million km2. In both years seasonal ice was dominant across the Beaufort Sea extending to the Amundsen Gulf, where significant field and satellite observations of sea ice, temperature, and atmospheric chemicals have been made. Measurements at the site of the Canadian Coast Guard Ship Amundsen ice breaker in the Amundsen Gulf showed events of increased bromine monoxide (BrO), coupled with decreases of ozone (O3) and gaseous elemental mercury (GEM), during cold periods in March 2008. The timing of the main event of BrO, O3, and GEM changes was found to be consistent with BrO observed by satellites over an extensive area around the site. Furthermore, satellite sensors detected a doubling of atmospheric BrO in a vortex associated with a spiral rising air pattern. In spring 2009, excessive and widespread bromine explosions occurred in the same region while the regional air temperature was low and the extent of perennial ice was significantly reduced compared to the case in 2008. Using satellite observations together with a Rising-Air-Parcel model, we discover a topographic control on BrO distribution such that the Alaskan North Slope and the Canadian Shield region were exposed to elevated BrO, whereas the surrounding mountains isolated the Alaskan interior from bromine intrusion.

  6. Synthesis and evaluation of a bromine-76-labeled PPAR{gamma} antagonist 2-bromo-5-nitro-N-phenylbenzamide

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Hsiaoju [Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110 (United States); Finck, Brian N. [Department of Internal Medicine, Division of Geriatrics and Nutritional Science, Washington University School of Medicine, St. Louis. MO 63110 (United States); Jones, Lynne A. [Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110 (United States); Welch, Michael J. [Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110 (United States); Mach, Robert H. [Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO 63110 (United States)]. E-mail: rhmach@mir.wustl.edu

    2006-10-15

    Peroxisome proliferator activated-receptor gamma (PPAR{gamma}) binds to peroxisome receptor response elements with its heterodimeric partner, retinoid X receptor, and regulates downstream gene expression. PPAR{gamma} transcriptionally modulates fat metabolism, and receptor agonists have been developed to treat type II diabetes. PPAR{gamma} is also overexpressed in some tumor cell lines and primary tumors, including breast and prostate tumors. Two PPAR{gamma} antagonists, 2-chloro-5-nitro-N-phenylbenzamide (GW9662) and 2-chloro-5-nitro-N-pyridin-4-yl-benzamide (T0070907), represent good lead compounds for radiotracer development. In the current study, four additional halogen substituted analogs were synthesized and evaluated in a whole cell screening assay for PPAR{gamma} binding activity. Two bromine-containing analogs having EC{sub 5} values <5 nM were chosen for bromine-76 radiolabeling. Bromine-76-labeled 2-bromo-5-nitro-N-phenyl-benzamide was selected for subsequent in vitro and in vivo studies due to its superior radiolabeling yield ({approx}70%) and the well-characterized pharmacological properties of its analog GW9662. An in vitro stability study showed that 40% of the compound remained intact in plasma and about 25% in whole blood after 30 min. Biodistribution studies in MDA-MB-435 human breast tumor-bearing nude mice were carried out at 5 min, 30 min, 2 h and 24 h post injection of the radiotracer. Although in vivo metabolite studies demonstrated rapid compound degradation, at least 10% of the parent compound was delivered to the tumor. We are currently exploring second generation analogs of these lead compounds for the development of radiolabeled antagonists of the PPAR{gamma} receptor.

  7. Accumulation of chlorinated and brominated persistent toxic substances (PTS) and their relationship to testosterone suppression in Norway rats from Japan

    Energy Technology Data Exchange (ETDEWEB)

    Takasuga, T.; Senthilkumar, K. [Shimadzu Techno-Research Inc. (Japan); Ishizuka, M.; Fujita, S. [Graduate School of Veterinary Medicine, Hokkaido Univ. (Japan); Tanikawa, R. [Inst. of Tech., Ikari Corp. (Japan)

    2004-09-15

    Contamination of chlorinated/brominated persistent toxic substances (PTS) such as polychlorinated, -dibenzo-p-dioxins (PCDDs), -dibenzofurans (PCDFs), -biphenyls (PCBs), - organochlorine pesticides (OCPs) {l_brace}e.g., aldrin, dieldrin, endrin, chlordane compounds [cis/transchlordane, cis/trans-nonachlor, oxychlordane, heptachlor, heptachlor epoxide], hexachlorobenzene (HCB), 2,2-bis(p-chlorophenyl)-1,1,1-trichloroethane (DDTs) and its metabolities [o,p/p,p'-DDD and DDE] and hexachlorocyclohexane (HCHs){r_brace} and -brominated diphenyl ethers (PBDEs) are considered to important class of chemicals due to persistence in nature, bioaccumulation potential and adverse health effects in wildlife and humans. Among South East Asian countries, Japan reported to contaminated with aforesaid chemicals with considerable amounts. There is no document reports contamination of PTS in wild animals, which in-habit near humans. Norway rat (NR) inhabits not only near human environment but also distributed worldwide. Especially, NR feeds on human waste and shelter in and around human environment and thus exposure of toxic contaminants in this animal considered to similar with those in humans. In addition, rats have unique physiology that match with humans (e.g., they have similar pathogens as humans have). Therefore, analysis of toxic contaminants in NR considered as indirect measure in humans. Considering those facts, in this study, we analyzed NR collected from urban area, rural area, waste dumping or land fill site and isolated remote island from Japan. Particularly several chlorinated and brominated organic contaminants such as PCDDs, PCDFs, PCBs, DDTs, HCHs, chlordane compounds, heptachlor, heptachlor epoxide, HCB, aldrin, dieldrin, endrin and PBDEs were analyzed in rat livers by isotope dilution technique using HRGC-HRMS. In addition, laboratory Wistar rats (WR) were used as control.

  8. Induction of Axial Chirality in 8-Arylquinolines through Halogenation Reactions Using Bifunctional Organocatalysts.

    Science.gov (United States)

    Miyaji, Ryota; Asano, Keisuke; Matsubara, Seijiro

    2017-07-26

    The enantioselective syntheses of axially chiral heterobiaryls were accomplished through the aromatic electrophilic halogenation of 3-(quinolin-8-yl)phenols with bifunctional organocatalysts that control the molecular conformations during successive halogenations. Axially chiral quinoline derivatives, which have rarely been synthesized in an enantioselective catalytic manner, were afforded in moderate-to-good enantioselectivities through bromination, and an analogous protocol also enabled enantioselective iodination. In addition, this catalytic reaction, which allows enantioselective control through the use of mono-ortho-substituted substrates, allowed the asymmetric synthesis of 8-arylquinoline derivatives bearing two different halogen groups in high enantioselectivities. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. Neurobehavioral function and low-level exposure to brominated flame retardants in adolescents: a cross-sectional study

    Directory of Open Access Journals (Sweden)

    Kiciński Michał

    2012-11-01

    Full Text Available Abstract Background Animal and in vitro studies demonstrated a neurotoxic potential of brominated flame retardants, a group of chemicals used in many household and commercial products to prevent fire. Although the first reports of detrimental neurobehavioral effects in rodents appeared more than ten years ago, human data are sparse. Methods As a part of a biomonitoring program for environmental health surveillance in Flanders, Belgium, we assessed the neurobehavioral function with the Neurobehavioral Evaluation System (NES-3, and collected blood samples in a group of high school students. Cross-sectional data on 515 adolescents (13.6-17 years of age was available for the analysis. Multiple regression models accounting for potential confounders were used to investigate the associations between biomarkers of internal exposure to brominated flame retardants [serum levels of polybrominated diphenyl ether (PBDE congeners 47, 99, 100, 153, 209, hexabromocyclododecane (HBCD, and tetrabromobisphenol A (TBBPA] and cognitive performance. In addition, we investigated the association between brominated flame retardants and serum levels of FT3, FT4, and TSH. Results A two-fold increase of the sum of serum PBDE’s was associated with a decrease of the number of taps with the preferred-hand in the Finger Tapping test by 5.31 (95% CI: 0.56 to 10.05, p = 0.029. The effects of the individual PBDE congeners on the motor speed were consistent. Serum levels above the level of quantification were associated with an average decrease of FT3 level by 0.18 pg/mL (95% CI: 0.03 to 0.34, p = 0.020 for PBDE-99 and by 0.15 pg/mL (95% CI: 0.004 to 0.29, p = 0.045 for PBDE-100, compared with concentrations below the level of quantification. PBDE-47 level above the level of quantification was associated with an average increase of TSH levels by 10.1% (95% CI: 0.8% to 20.2%, p = 0.033, compared with concentrations below the level of quantification. We did not

  10. Windows 8.1 for seniors for dummies

    CERN Document Server

    Weverka, Peter

    2013-01-01

    Seniors, here's what you need to get up and running on Windows 8.1 Microsoft, now a little older and wiser, is back with Windows 8.1, the revamped version that brings fresh changes and welcome improvements to the Windows 8 operating system. And now you savvy seniors can get the very most out of this easier-to-use Windows 8.1 with our friendly new guide. Using large print that makes the book easier to read plus magnified screen shots to help make Windows less intimidating, this book walks you through common tasks and show you how to get things done in fine style. Helps you get to know Windows

  11. Survivin S81A Enhanced TRAIL's Activity in Inducing Apoptosis

    Directory of Open Access Journals (Sweden)

    Ferry Sandra

    2010-12-01

    Full Text Available BACKGROUND: Survivin is rarely expressed in normal healthy adult tissues, however, it is upregulated in the majority of cancers. Survivin, which belongs to IAPs family, has been widely reported to protect cells from apoptosis by inhibiting caspases pathway. Survivin’s mitotic activity is modulated by many kinases, and its phosphor status can also influence its ability to inhibit apoptosis. There are several important survivin’s phosphorylation sites, such as S20 and T34. We have continued our investigation on other potential survivin’s phosphorylation sites that could be important site for regulating survivin’s cyto-protection. METHODS: By assuming that S81 could be a potential target to modify activity of survivin, wild-type survivin (Survivin, antisense survivin (Survivin-AS, mutated-survivin Thr34Ala (Survivin-T34A and mutated-survivin Ser81Ala (Survivin-S81A were constructed and inserted into pMSCV-IRES-GFP vector with cytomegalovirus (CMV promoter. Each retroviral product was produced in BOSC23 cells. LY294002 pretreatment and TRAIL treatment along with infection of retroviral products were performed in murine fibrosarcoma L929 cells. For analysis, flow cytometric apoptosis assay and western blot were performed. RESULTS: In our present study, survivin for providing cytoprotection was regulated by PI3K. The results showed that LY294002, an inhibitor of PI3K, effectively suppressed survivin-modulated cytoprotection in a TRAIL-induced apoptotic model. In addition, mutated survivin S81A showed marked suppression on survivin’s cytoprotection. Along with that, TRAIL’s apoptotic activity was enhanced for inducing apoptosis. CONCLUSIONS: We suggested that survivin could inhibit apoptosis through PI3K and S81A could be another potential target in order to inhibit Survivin-modulated cytoprotection as well as to sensitize efficacy of TRAIL or other related apoptotic inducers. KEYWORDS: apoptosis, survivin, TRAIL, S81A, L929, LY294002.

  12. Air-snowpack exchange of bromine, ozone and mercury in the springtime Arctic simulated by the 1-D model PHANTAS - Part 2: Mercury and its speciation

    Science.gov (United States)

    Toyota, K.; Dastoor, A. P.; Ryzhkov, A.

    2014-04-01

    Atmospheric mercury depletion events (AMDEs) refer to a recurring depletion of mercury occurring in the springtime Arctic (and Antarctic) boundary layer, in general, concurrently with ozone depletion events (ODEs). To close some of the knowledge gaps in the physical and chemical mechanisms of AMDEs and ODEs, we have developed a one-dimensional model that simulates multiphase chemistry and transport of trace constituents throughout porous snowpack and in the overlying atmospheric boundary layer (ABL). This paper constitutes Part 2 of the study, describing the mercury component of the model and its application to the simulation of AMDEs. Building on model components reported in Part 1 ("In-snow bromine activation and its impact on ozone"), we have developed a chemical mechanism for the redox reactions of mercury in the gas and aqueous phases with temperature dependent reaction rates and equilibrium constants accounted for wherever possible. Thus the model allows us to study the chemical and physical processes taking place during ODEs and AMDEs within a single framework where two-way interactions between the snowpack and the atmosphere are simulated in a detailed, process-oriented manner. Model runs are conducted for meteorological and chemical conditions that represent the springtime Arctic ABL characterized by the presence of "haze" (sulfate aerosols) and the saline snowpack on sea ice. The oxidation of gaseous elemental mercury (GEM) is initiated via reaction with Br-atom to form HgBr, followed by competitions between its thermal decomposition and further reactions to give thermally stable Hg(II) products. To shed light on uncertain kinetics and mechanisms of this multi-step oxidation process, we have tested different combinations of their rate constants based on published laboratory and quantum mechanical studies. For some combinations of the rate constants, the model simulates roughly linear relationships between the gaseous mercury and ozone concentrations as

  13. 24 CFR 200.81 - Disbursement of mortgage proceeds.

    Science.gov (United States)

    2010-04-01

    ... 24 Housing and Urban Development 2 2010-04-01 2010-04-01 false Disbursement of mortgage proceeds..., Commitment, and Endorsement Generally Applicable to Multifamily and Health Care Facility Mortgage Insurance Programs; and Continuing Eligibility Requirements for Existing Projects Mortgage Provisions § 200.81...

  14. East African Medical Journal - Vol 81, No 12 (2004)

    African Journals Online (AJOL)

    Coronary artery disease and symptoms of depression in a Kenyan population · EMAIL FREE FULL TEXT EMAIL FREE FULL TEXT · DOWNLOAD FULL TEXT DOWNLOAD FULL TEXT. FG Njenga, CG Kamotho, MD Joshi, DK Gikonyo, M Wanyoike, 611-615. http://dx.doi.org/10.4314/eamj.v81i12.9244 ...

  15. East African Medical Journal - Vol 81, No 5 (2004)

    African Journals Online (AJOL)

    Retinitis pigmentosa in Benin, Nigeria · EMAIL FREE FULL TEXT EMAIL FREE FULL TEXT · DOWNLOAD FULL TEXT DOWNLOAD FULL TEXT. CU Ukponmwan, A Atamah, 254-257. http://dx.doi.org/10.4314/eamj.v81i5.9169 ...

  16. Discovery of an Apparent Nova in M81

    Science.gov (United States)

    Hornoch, K.; Alfaro, M. Diaz; Ordonez-Etxeberria, I.; Vaduvescu, O.

    2015-01-01

    We report the discovery of an apparent nova in M81 on a co-added 1600-s narrow-band H-alpha CCD image taken with the 2.5-m Isaac Newton Telescope (INT) + WFC at La Palma under ~2.4" seeing on 2015 Jan. 15.126 UT.

  17. 45 CFR 74.81 - Prohibition against profit.

    Science.gov (United States)

    2010-10-01

    ... ORGANIZATIONS, AND COMMERCIAL ORGANIZATIONS Special Provisions for Awards to Commercial Organizations § 74.81 Prohibition against profit. Except for awards under the Small Business Innovation Research (SBIR) and Small... to any recipient even if the recipient is a commercial organization. Profit is any amount in excess...

  18. 19 CFR 181.81 - Applicability to NAFTA transactions.

    Science.gov (United States)

    2010-04-01

    ... 19 Customs Duties 2 2010-04-01 2010-04-01 false Applicability to NAFTA transactions. 181.81... to NAFTA transactions. Except as otherwise provided in § 181.82 of this part, all criminal, civil or... violations of the laws and regulations relating to the NAFTA. ...

  19. Information and Announcements Science Academies 81st Refresher ...

    Indian Academy of Sciences (India)

    IAS Admin

    2016-09-25

    Sep 25, 2016 ... ANN. RESONANCE | September 2016. Information and Announcements. Science Academies 81st Refresher Course on. Experimental Physics. 3–18, November 2016. Goa University, Goa. A Refresher Course in Experimental Physics will be held at Goa University, Goa from 03 to 18 November 2016 for.

  20. 9 CFR 81.4 - Issuance of certificates.

    Science.gov (United States)

    2010-01-01

    ... slaughter do not need to state that the animals are from a herd participating in the CWD Herd Certification... date the animals are being moved to slaughter. (b) Animal identification documents attached to... 9 Animals and Animal Products 1 2010-01-01 2010-01-01 false Issuance of certificates. 81.4 Section...

  1. 36 CFR 223.81 - Shorter advertising periods in emergencies.

    Science.gov (United States)

    2010-07-01

    ... 36 Parks, Forests, and Public Property 2 2010-07-01 2010-07-01 false Shorter advertising periods... OF AGRICULTURE SALE AND DISPOSAL OF NATIONAL FOREST SYSTEM TIMBER Timber Sale Contracts Advertisement and Bids § 223.81 Shorter advertising periods in emergencies. In emergency situations where prompt...

  2. I-81 in-place pavement recycling project.

    Science.gov (United States)

    2014-08-01

    During the 2011 construction season, the Virginia Department of Transportation (VDOT) completed an in-place pavement : recycling project to rehabilitate a section of pavement on I-81 near Staunton, Virginia. The project consisted of a 3.66-mile : sec...

  3. 20 CFR 631.81 - Availability of funds.

    Science.gov (United States)

    2010-04-01

    ... Employees' Benefits EMPLOYMENT AND TRAINING ADMINISTRATION, DEPARTMENT OF LABOR PROGRAMS UNDER TITLE III OF THE JOB TRAINING PARTNERSHIP ACT Disaster Relief Employment Assistance § 631.81 Availability of funds... within which is located an area that has suffered an emergency or a major disaster as defined in...

  4. Magnetic solid phase extraction of brominated flame retardants and pentachlorophenol from environmental waters with carbon doped Fe{sub 3}O{sub 4} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Jing [State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering and Center of Materials Analysis, Nanjing University, 22 Hankou Road, Nanjing 210093 (China); Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, Jiangsu Key Laboratory of Biomedical Materials, College of Chemistry and Materials Science, Nanjing Normal University, 1 Wenyuan Road, Nanjing 210023 (China); Li, Jia-yuan; Qiao, Jun-qin [State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering and Center of Materials Analysis, Nanjing University, 22 Hankou Road, Nanjing 210093 (China); Cui, Shi-hai [Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, Jiangsu Key Laboratory of Biomedical Materials, College of Chemistry and Materials Science, Nanjing Normal University, 1 Wenyuan Road, Nanjing 210023 (China); Lian, Hong-zhen, E-mail: hzlian@nju.edu.cn [State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering and Center of Materials Analysis, Nanjing University, 22 Hankou Road, Nanjing 210093 (China); Chen, Hong-yuan [State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering and Center of Materials Analysis, Nanjing University, 22 Hankou Road, Nanjing 210093 (China)

    2014-12-01

    Graphical abstract: - Highlights: • Magnetic Fe{sub 3}O{sub 4}/C nanospheres were used in MSPE of BFRs and PCP from water samples. • The method shows merits of simpleness, reliableness and environmental friendliness. • The bonding between Fe{sub 3}O{sub 4} and coated organic carbon has been demonstrated in Fe{sub 3}O{sub 4}/C. • The straight influences of synthesis conditions of Fe{sub 3}O{sub 4}/C on MSPE were investigated. • The extraction characteristics of Fe{sub 3}O{sub 4}/C nanoparticles were further elucidated. - Abstract: Carbon doped Fe{sub 3}O{sub 4} nanoparticles (Fe{sub 3}O{sub 4}/C) prepared by a facile hydrothermal reaction of glucose with iron resource have been applied as magnetic solid-phase extraction (MSPE) sorbent, for the first time, to extract trace brominated flame retardants (BFRs) and pentachlorophenol (PCP) from environmental waters. Various MSPE parameters were optimized including amount of Fe{sub 3}O{sub 4}/C nanoparticles, pH of sample solution, enrichment factor of analytes and reusability of Fe{sub 3}O{sub 4}/C sorbent. The reliability of the MSPE method was evaluated by the recoveries of BFRs and PCP in spiked water samples. Good recoveries (80.0–110.0%) were achieved with the relative standard deviations range from 0.3% to 6.8%. In this paper, the extraction characteristics of Fe{sub 3}O{sub 4}/C sorbent were further elucidated. It is found that the adsorption process of Fe{sub 3}O{sub 4}/C to analytes predominates the MSPE efficiency. There is hybrid hydrophobic interaction and hydrogen bonding or dipole–dipole attraction between Fe{sub 3}O{sub 4}/C and analytes. Notably, the chemical components of carbon layer on the surface of Fe{sub 3}O{sub 4} nanoparticles were identified by X-ray photoelectron spectroscopy and thermogravimetry-mass spectrometry, and in consequence the covalent bonds between Fe{sub 3}O{sub 4} and the coated carbon have been observed. In addition, the straight influence of synthesis condition of Fe

  5. An efficient and fast analytical procedure for the bromine determination in waste electrical and electronic equipment plastics.

    Science.gov (United States)

    Taurino, R; Cannio, M; Mafredini, T; Pozzi, P

    2014-01-01

    In this study, X-ray fluorescence (XRF) spectroscopy was used, in combination with micro-Raman spectroscopy, for a fast determination of bromine concentration and then of brominated flame retardants (BFRs) compounds in waste electrical and electronic equipments. Different samples from different recycling industries were characterized to evaluate the sorting performances of treatment companies. This investigation must be considered of prime research interest since the impact of BFRs on the environment and their potential risk on human health is an actual concern. Indeed, the new European Restriction of Hazardous Substances Directive (RoHS 2011/65/EU) demands that plastics with BFRs concentration above 0.1%, being potential health hazards, are identified and eliminated from the recycling process. Our results show the capability and the potential of Raman spectroscopy, together with XRF analysis, as effective tools for the rapid detection of BFRs in plastic materials. In particular, the use of these two techniques in combination can be considered as a promising method suitable for quality control applications in the recycling industry.

  6. BROMINATION OF 4-VINYLCYCLOHEXANE AND APPLYING THE RESULTING PRODUCT TO IMPROVE THE FLAME RETARDANT PROPERTIES OF WOOD

    Directory of Open Access Journals (Sweden)

    N. S. Nikulina

    2014-01-01

    Full Text Available Currently, the demand for timber is increasing. Wood and products on its basis are considered to be the most popular in the construction industry, furniture industry, as building materials and other However, along with the positive features of this material there are also negative factors, which include low resistance to biological degradation, high temperature, resistance. Wood and materials based on it are the most flammable, and fire safety is characterized by the velocity of propagation of fire on the wooden structure. He is able to destroy it in a matter of minutes. So the wooden house elements must be protected from fire. It was therefore necessary for the fire protection of wood. It is in the handling of wood with flame retardants. Basic fire fighting methods is the impregnation of wood antipyrene composition, painting fire paint and constructive ways - insulation of timber, non-combustible compositions which can resist the fire. In the work of brominated 4-vinylcyclohexane formed as a by-product in the petrochemical industry, in chloroform synthesized compound with bromine 62-64 % and the possibility of using this product to get antiferromag composition. It is established that the application for the protective treatment of wood synthesized flame retardant has shown that this product can be used for the protective treatment of natural wood to make it flame retardant properties. Use as antiperiodic compositions bromodomain based products 4-vinylcyclohexane allows to obtain images of wood first group of flame retardant efficiency.

  7. Direct spectral analysis and determination of high content of carcinogenic bromine in bread using UV pulsed laser induced breakdown spectroscopy.

    Science.gov (United States)

    Mehder, A O; Gondal, Mohammed A; Dastageer, Mohamed A; Habibullah, Yusuf B; Iqbal, Mohammed A; Oloore, Luqman E; Gondal, Bilal

    2016-01-01

    Laser induced breakdown spectroscopy (LIBS) was applied for the detection of carcinogenic elements like bromine in four representative brands of loaf bread samples and the measured bromine concentrations were 352, 157, 451, and 311 ppm, using Br I (827.2 nm) atomic transition line as the finger print atomic transition. Our LIBS system is equipped with a pulsed laser of wavelength 266 nm with energy 25 mJ pulse(-1), 8 ns pulse duration, 20 Hz repetition rate, and a gated ICCD camera. The LIBS system was calibrated with the standards of known concentrations in the sample (bread) matrix and such plot is linear in 20-500 ppm range. The capability of our system in terms of limit of detection and relative accuracy with respect to the standard inductively coupled plasma mass spectrometry (ICPMS) technique was evaluated and these values were 5.09 ppm and 0.01-0.05, respectively, which ensures the applicability of our system for Br trace level detection, and LIBS results are in excellent agreement with that of ICPMS results.

  8. On-line detection of heavy metals and brominated flame retardants in technical polymers with laser-induced breakdown spectrometry.

    Science.gov (United States)

    Stepputat, Michael; Noll, Reinhard

    2003-10-20

    The use of laser-induced breakdown spectrometry (LIBS) for the analysis of heavy metals and brominated flame retardants in end-of-life waste electric and electronic equipment (EOL-WEEE) pieces is investigated. Single- and double-pulse plasma excitation as well as the influence of detection parameters is studied to yield a parameter field with improved sensitivity and limits of detection. A LIBS analyzer was set up as an on-line measuring unit to detect heavy metals and brominated flame retardants in moving EOL-WEEE pieces in an automatic sorting line. An autofocusing unit with an adjustment range of 50 mm was incorporated to permit measurements of objects that pass by a LIBS analyzer with their surfaces at various distances from it. Tests with EOL-WEEE monitor housings on the conveyor belt of a pilot sorting system successfully demonstrated the capability of the LIBS analyzer to quantify the concentration of hazardous elements in real waste EOL-WEEE pieces.

  9. HPLC-ED of low-molecular weight brominated phenols and tetrabromobisphenol A using pretreated carbon fiber microelectrode.

    Science.gov (United States)

    Bartosova, Zdenka; Jirovsky, David; Riman, Daniel; Halouzka, Vladimir; Svidrnoch, Martin; Hrbac, Jan

    2014-05-01

    Electrochemically pretreated carbon fiber microelectrode was used to develop a simple, fast and sensitive HPLC-ECD method for the determination of brominated phenols. In addition to simple mono-, di- and tri-bromophenols (4-bromophenol, 2,4-dibromophenol, 2,6-dibromophenol, 2,4,6-tri-bromophenol) the possibility of electrochemical detection of 3,3',5,5'-tetrabromobisphenol A in oxidation mode is reported for the first time. The isocratic separation was achieved within 14 min using ternary mobile phase consisting of 50mM-phosphate buffer (pH 3.5), acetonitrile and methanol (35/15/50, v/v), and detection potential of E=+1450 mV (vs. Ag/AgCl). The carbon fiber microelectrode permitted to use high anodic potentials (up to +1800 mV vs. Ag/AgCl), the optimum analytical response was achieved at +1450 mV vs. Ag/AgCl. The limits of detection (LOD) for the studied analytes were within the range of 1.8-56.6 ng mL(-1). The developed method was applied to determination of brominated phenols in spiked water samples. Furthermore, after simple extraction with methyl tert-butyl ether, it was possible to quantify tetrabromobisphenol A (TBBA) in a piece of CRT monitor plastic casing. The found amount of TBBA was 10.22 mg kg(-1) (±0.43). Copyright © 2014 Elsevier B.V. All rights reserved.

  10. Bromination of graphene: a new route to making high performance transparent conducting electrodes with low optical losses

    KAUST Repository

    Mansour, Ahmed

    2015-09-03

    The high optical transmittance, electrical conductivity, flexibility and chemical stability of graphene have triggered great interest in its application as a transparent conducting electrode material and as a potential replacement for indium doped tin oxide. However, currently available large scale production methods such as chemical vapor deposition produce polycrystalline graphene, and require additional transfer process which further introduces defects and impurities resulting in a significant increase in its sheet resistance. Doping of graphene with foreign atoms has been a popular route for reducing its sheet resistance which typically comes at a significant loss in optical transmission. Herein, we report the successful bromine doping of graphene resulting in air-stable transparent conducting electrodes with up to 80% reduction of sheet resistance reaching ~180 Ω/ at the cost of 2-3% loss of optical transmission in case of few layer graphene and 0.8% in case of single layer graphene. The remarkably low tradeoff in optical transparency leads to the highest enhancements in figure of merit reported thus far. Furthermore, our results show a controlled increase in the workfunction up to 0.3 eV with the bromine content. These results should help pave the way for further development of graphene as potentially a highly transparent substitute to other transparent conducting electrodes in optoelectronic devices.

  11. Brominated flame retardants in black plastic kitchen utensils: Concentrations and human exposure implications.

    Science.gov (United States)

    Kuang, Jiangmeng; Abdallah, Mohamed Abou-Elwafa; Harrad, Stuart

    2018-01-01

    Concerns exist that restricted brominated flame retardants (BFRs) present in waste polymers may have, as a result of recycling, inadvertently contaminated items not required to meet flame retardancy regulations (e.g. plastic kitchen utensils). To investigate the extent to which kitchen utensils are contaminated with BFRs and the potential for resultant human exposure, we collected 96 plastic kitchen utensils and screened for Br content using a hand-held X-ray fluorescence (XRF) spectrometer. Only 3 out of 27 utensils purchased after 2011 contained detectable concentrations of Br (≥3μg/g). In contrast, Br was detected in 31 out of the 69 utensils purchased before 2011. Eighteen utensils with Br content higher than 100μg/g, and 12 new utensils were selected for GC-MS analysis of BFRs. BFRs targeted were polybrominated diphenyl ethers (PBDEs) BDE-28, 47, 99, 100, 153, 154, 183 and 209, and novel BFRs (NBFRs) pentabromoethylbenzene (PBEB), 2-ethylhexyl-2,3,4,5-tetrabromobenzoate (EH-TBB), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), bis(2-ethylhexyl)-3,4,5,6-tetrabromo-phthalate (BEH-TEBP) and decabromodiphenyl ethane (DBDPE). The ability of XRF to act as a surrogate metric of BFR concentration was indicated by a significant (Spearman coefficient=0.493; p=0.006) positive relationship between Br and ΣBFR concentration. Measurements of ΣBFRs were always exceeded by those of Br. This may be due partly to the presence of BFRs not targeted in our study and also to reduced extraction efficiency of BFRs from utensils. Of our target BFRs, BDE-209 was the most abundant one in most samples, but an extremely high concentration (1000μg/g) of BTBPE was found in one utensil. Simulated cooking experiments were conducted to investigate BFR transfer from selected utensils (n=10) to hot cooking oil, with considerable transfer (20% on average) observed. Estimated median exposure via cooking with BFR contaminated utensils was 60ng/day for total BFRs. In contrast, estimated

  12. Brominated flame retardants (BFRs) in air and dust from electronic waste storage facilities in Thailand.

    Science.gov (United States)

    Muenhor, Dudsadee; Harrad, Stuart; Ali, Nadeem; Covaci, Adrian

    2010-10-01

    This study reports concentrations of brominated flame retardants in dust samples (n=25) and in indoor (n=5) and outdoor air (n=10) (using PUF disk passive air samplers) from 5 electronic and electrical waste (e-waste) storage facilities in Thailand. Concentrations of Sigma(10)PBDEs (BDEs 17, 28, 47, 49, 66, 85, 99, 100, 153 and 154) in outdoor air in the vicinity of e-waste storage facilities ranged from 8 to 150 pg m(-3). Indoor air concentrations ranged from 46 to 350 pg m(-3), with highest concentrations found in a personal computer and printer waste storage room at an e-waste storage facility. These are lower than reported previously for electronic waste treatment facilities in China, Sweden, and the US. Concentrations of Sigma(21)PBDEs (Sigma(10)PBDEs+BDEs 181, 183, 184, 191, 196, 197, 203, 206, 207, 208 and 209), decabromodiphenylethane (DBDPE), decabromobiphenyl (BB-209) in dust were 320-290,000, 43-8700 and <20-2300 ng g(-1) respectively, with the highest concentrations of Sigma(21)PBDEs, BDE-209 and DBDPE in a room used to house discarded TVs, stereos and radios. PBDE concentrations in dust were slightly higher but within the range of those detected in workshop floor dust from an e-waste recycling centre in China. The highest concentration of BB-209 was detected in a room storing discarded personal computers and printers. Consistent with recent reports of elevated ratios of BDE-208:BDE-209 and BDE-183:BDE-209 in household electronics from South China, percentage ratios of BDE-208:BDE-209 (0.64-2.9%) and of BDE-208:BDE-183 (2.8-933%) in dust samples exceeded substantially those present in commercial deca-BDE and octa-BDE formulations. This suggests direct migration of BDE-208 and other nonabrominated BDEs from e-waste to the environment. Under realistic high-end scenarios of occupational exposure to BDE-99, workers in the facilities were exposed above a recently-published Health Based Limit Value for this congener. Reassuringly, estimated exposures to BDE

  13. Self-initiation of UV photopolymerization reactions using tetrahalogenated bisphenol A (meth)acrylates.

    Science.gov (United States)

    Pelras, Théophile; Knolle, Wolfgang; Naumov, Sergej; Heymann, Katja; Daikos, Olesya; Scherzer, Tom

    2017-05-17

    The potential of tetrachlorinated and tetrabrominated bisphenol A diacrylates and dimethacrylates for self-initiation of a radical photopolymerization was investigated. The kinetics of the photopolymerization of an acrylic model varnish containing halogenated monomers was studied by real-time FTIR spectroscopy, whereas the formation of reactive species and secondary products was elucidated by laser flash photolysis and product analysis by GC-MS after steady-state photolysis. The interpretation of the experimental data and the analysis of possible reaction pathways were assisted by quantum chemical calculations. It was shown that all halogenated monomers lead to a significant acceleration of the photopolymerization kinetics at a minimum concentration of 5 wt%. Steady-state and laser flash photolysis measurements as well as quantum chemical calculations showed that brominated and chlorinated samples do not follow the same pathway to generate radical species. Whereas chlorinated (meth)acrylates may cleave only at the C-O bonds of the carboxyl groups resulting in acrolein and oxyl radicals for initiation, brominated monomers may cleave either at the C-O bonds or at the C-Br bonds delivering aryl and bromine radicals. The quantum yields for the photolysis of the halogenated monomers were found to be in the order of 0.1 for acrylates and 0.2 for methacrylates (with an estimated error of 25%), independently of the attached Br and Cl halogens. Finally, the trihalogenated bisphenol A di(meth)acrylate radicals and the acrolein radicals were found to show the highest efficiencies for the reaction with another acrylic double bond leading to the formation of a polymer network.

  14. Spallation reactions; Reactions de spallation

    Energy Technology Data Exchange (ETDEWEB)

    Cugon, J.

    1996-12-31

    Spallation reactions dominate the interactions of hadrons with nuclei in the GeV range (from {approx} 0.1 to {approx} 10 GeV). They correspond to a sometimes important ejection of light particles leaving most of the time a residue of mass commensurate with the target mass. The main features of the experimental data are briefly reviewed. The most successful theoretical model, namely the intranuclear cascade + evaporation model, is presented. Its physical content, results and possible improvements are critically discussed. Alternative approaches are shortly reviewed. (author). 84 refs.

  15. Increased diversification of polyhydroxyalkanoates by modification reactions for industrial and medical applications.

    Science.gov (United States)

    Hazer, Baki; Steinbüchel, Alexander

    2007-02-01

    A wide range of diverse polyhydroxyalkanoates, PHAs, is currently available due to the low substrate specificity of PHA synthases and subsequent modifications by chemical reactions. These polymers are promising materials for a number of different applications due to their biocompatibility and biodegradability. This review summarizes the large variability of PHAs regarding chemical structure and material properties that can be currently produced. In the first part, in vivo and in vitro biosynthesis processes for production of a large variety of different PHAs will be summarized with regard to obtaining saturated and unsaturated copolyesters and side chain functionalized polyesters, including brominated, hydroxylated, methyl-branched polyesters, and phenyl derivatives of polyesters. In the second part, established chemical modifications of PHAs will be summarized as that by means of grafting reactions and graft/block copolymerizations, as well as by chlorination, cross-linking, epoxidation, hydroxylation, and carboxylation, reactions yield further functionalized PHAs.

  16. Effect of bromide in a surface water intake on the formation of brominated trihalomethanes at a public water system treatment plant

    Science.gov (United States)

    This project is a collaborative drinking water research study. EPA is evaluating water samples collected by PWS operators in order to investigate relationships between bromide in source water and the formation of brominated DBPs in finished drinking water. This study will includ...

  17. A comparison of the in vitro cyto- and neurotoxicity of brominated and halogen-free flame retardants : prioritization in search for safe(r) alternatives

    NARCIS (Netherlands)

    Hendriks, Hester S; Meijer, Marieke; Muilwijk, Mirthe; van den Berg, Martin; Westerink, Remco H S

    Brominated flame retardants (BFRs) are abundant persistent organic pollutants with well-studied toxicity. The toxicological and ecological concerns associated with BFRs argue for replacement by safe(r) alternatives. Though previous research identified the nervous system as a sensitive target organ

  18. Evaluation of a New Disinfection Approach: Efficacy of Chlorine and Bromine Halogenated Contact Disinfection for Reduction of Viruses and Microcystin Toxin

    Science.gov (United States)

    Coulliette, Angela D.; Peterson, Lauren A.; Mosberg, Joshua A. W.; Rose, Joan B.

    2010-01-01

    Contaminated drinking water is responsible for causing diarrheal diseases that kill millions of people a year. Additionally, toxin-producing blue-green algae associated with diarrhea and neurologic effects continues to be an issue for many drinking water supplies. Disinfection has been used to reduce these risks. A novel gravity-fed household drinking water system with canisters containing N-halamine bromine or chlorine media was challenged with MS2 bacteriophage and microcystin. Chlorine and bromine systems were effective against this virus, with an mean ± SE reduction of 2.98 ± 0.26 log10 and 5.02 ± 0.19 log10, respectively. Microcystin toxin was reduced by 27.5% and 88.5% to overall mean ± SE concentrations of 1,600 ± 98 ng/L and 259 ± 50 ng/L for the chlorine and bromine canisters, respectively. Only the bromine units consistently produced microcystin effluent < 1,000 ng/L (the World Health Organization recommended level) when challenged with 2,500 ng/L and consistently surpassed the U.S. Environmental Protection Agency virus reduction goal of 99.99%. PMID:20134006

  19. Determination of inorganic arsenic in algae using bromine halogenation and on-line nonpolar solid phase extraction followed by hydride generation atomic flourescence spectrometry

    Science.gov (United States)

    Accurate, stable and fast analysis of toxic inorganic arsenic (iAs) in complicated and arsenosugar-rich algae matrix is always a challenge. Herein, a novel analytical method for iAs in algae was reported, using bromine halogenation and on-line nonpolar solid phase extraction (SPE) followed by hydrid...

  20. Comparison of direct injection nebulizer and desolvating microconcentric nebulizer for analysis of chlorine-, bromine- and iodine-containing compounds by reversed phase HPLC with ICP-MS detection

    DEFF Research Database (Denmark)

    Jensen, B.P.; Gammelgaard, Bente; Hansen, S.H.

    2003-01-01

    the direct injection nebulizer at flow rates of 25 and 50 mul min(-1), the influence of 0-50% methanol and 0-25% acetonitrile on the sensitivity was studied. For chlorine and bromine, the relative sensitivity decreased with increasing amounts of organic solvent. For iodine, the relative sensitivity reached...

  1. Formation of brominated disinfection byproducts from natural organic matter isolates and model compounds in a sulfate radical-based oxidation process

    KAUST Repository

    Wang, Yuru

    2014-12-16

    A sulfate radical-based advanced oxidation process (SR-AOP) has received increasing application interest for the removal of water/wastewater contaminants. However, limited knowledge is available on its side effects. This study investigated the side effects in terms of the production of total organic bromine (TOBr) and brominated disinfection byproducts (Br-DBPs) in the presence of bromide ion and organic matter in water. Sulfate radical was generated by heterogeneous catalytic activation of peroxymonosulfate. Isolated natural organic matter (NOM) fractions as well as low molecular weight (LMW) compounds were used as model organic matter. Considerable amounts of TOBr were produced by SR-AOP, where bromoform (TBM) and dibromoacetic acid (DBAA) were identified as dominant Br-DBPs. In general, SR-AOP favored the formation of DBAA, which is quite distinct from bromination with HOBr/OBr- (more TBM production). SR-AOP experimental results indicate that bromine incorporation is distributed among both hydrophobic and hydrophilic NOM fractions. Studies on model precursors reveal that LMW acids are reactive TBM precursors (citric acid > succinic acid > pyruvic acid > maleic acid). High DBAA formation from citric acid, aspartic acid, and asparagine was observed; meanwhile aspartic acid and asparagine were the major precursors of dibromoacetonitrile and dibromoacetamide, respectively.

  2. Borehole completion data package for well 199-N-81

    Energy Technology Data Exchange (ETDEWEB)

    Hartman, M.J.

    1994-05-05

    Well 199-N-81 was drilled in 1993 as a RCRA groundwater monitoring for the 1324-N network. The well is completed at the top of the uppermost aquifer, in the Ringold Formation. This data package includes information on drilling, construction, development, and aquifer testing. Copies of forms, notes, and diagrams completed in the field comprise the bulk of this document. Few interpretations are included. Lithologic contacts were picked by the site geologist. An attempt was made to interpret aquifer test data.

  3. Discovery of a possible nova in M81

    Science.gov (United States)

    Williams, S. C.; Darnley, M. J.

    2016-10-01

    We report the discovery of a new nova candidate in M81 on 3 & times; 300s H & alpha; images taken using IO:O on the 2m Liverpool Telescope (Steele et al. 2004) on 2016 Oct 8.25 UT. The position of the new transient is RA = 9h55m17.035s, Dec. = +69 & deg;06'31.69" (J2000).

  4. STS-81 Crew Members in front of Atlantis

    Science.gov (United States)

    1996-01-01

    The STS-81 crew poses in front of the Space Shuttle Atlantis as it stands poised for liftoff from Launch Pad 39B to dock with the Mir space station. They are (from left): Mission Specialists Marsha S. Ivins, Mission Commander Michael A. Baker; Mission Specialists J.M. 'Jerry' Linenger and Peter J. K. 'Jeff' Wisoff; Pilot Brent W. Jett, Jr.; and Mission Specialist John M. Grunsfeld. STS81 is the fifth Shuttle-wazzu Mir docking mission and will feature the transfer of Linenger to Mir to replace astronaut John Blaha, who has been on the orbital laboratory since Sept. 19 after arrival there during the STS-79 mission. During STS-81, Shuttle and Mir crews will conduct risk mitigation, human life science, microgravity and materials processing experiments that will provide data for the design, development and operation of the International Space Station. The - primary payload is the SPACEHAB-DM double module will provide space for more than 2,000 pounds of hardware, food and water that will be transferred into the Russian space station during five days of docking operations during the 10-day mission. The SPACEHAB will also be used to return experiment samples from the Mir to Earth for analysis and for microgravity experiments during the mission.

  5. STS-81 Crew in white room for TCDT

    Science.gov (United States)

    1996-01-01

    The STS-81 flight crew poses in front of the Space Shuttle orbiter Atlantis' hatch in the White Room at Launch Pad 39B during Terminal Countdown Demonstration Test exercises for that mission. They are (foreground, seated): Mission Specialists Marsha S. Ivins and John M. Grunsfeld; (standing from left) Mission Commander Michael A. Baker; Missions Specialists J.M. 'Jerry' Linenger and Peter J. K. 'Jeff' Wisoff; and Pilot Brent W. Jett, Jr. STS-81 is the fifth Shuttle-Mir docking mission and will feature the transfer of Linenger to Mir to replace astronaut John Blaha, who has been on the orbital laboratory since Sept. 19 after arrival there during the STS-79 mission. During STS-81, Shuttle and Mir crews will conduct risk mitigation, human life science, microgravity and materials processing experiments that will provide data for the design, development and operation of the International Space StationThe primary payload is the SPACEHAB-DM . double module will provide space for more than 2,000 pounds of hardware, food and water that will be transferred into the Russian space station during five days of docking operations during the 10-day mission. The SPACEHAB will also be used to return experiment samples from the Mir to Earth for analysis and for microgravity experiments during the mission.

  6. Speciation of the bio-available iodine and bromine forms in edible seaweed by high performance liquid chromatography hyphenated with inductively coupled plasma-mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Romaris-Hortas, Vanessa; Bermejo-Barrera, Pilar [Department of Analytical Chemistry, Nutrition and Bromatology, Faculty of Chemistry, University of Santiago de Compostela, Avenida das Ciencias, s/n. 15782 - Santiago de Compostela (Spain); Moreda-Pineiro, Jorge [Department of Analytical Chemistry, Faculty of Sciences, University of A Coruna, Campus da Zapateira, s/n. 15071, A Coruna (Spain); Moreda-Pineiro, Antonio, E-mail: antonio.moreda@usc.es [Department of Analytical Chemistry, Nutrition and Bromatology, Faculty of Chemistry, University of Santiago de Compostela, Avenida das Ciencias, s/n. 15782 - Santiago de Compostela (Spain)

    2012-10-01

    Highlights: Black-Right-Pointing-Pointer Bioavailable iodine and bromine speciation in edible seaweed were developed. Black-Right-Pointing-Pointer In vitro dialyzability was used to assess the bioavailable fractions. Black-Right-Pointing-Pointer AEC hyphenated with inductively coupled plasma-mass spectrometry was used. Black-Right-Pointing-Pointer Iodide, MIT, DIT, bromide and bromate were found in dialyzates from edible seaweed. Black-Right-Pointing-Pointer Positive correlation between bioavailability and protein contents was found. - Abstract: A bioavailability study based on an in vitro dialyzability approach has been applied to assess the bio-available fractions of iodine and bromine species from edible seaweed. Iodide, iodate, 3-iodo-tyrosine (MIT), 3,5-diiodo-tyrosine (DIT), bromide and bromate were separated by anion exchange chromatography under a gradient elution mode (175 mM ammonium nitrate plus 15% (v/v) methanol, pH 3.8, as a mobile phase, and flow rates within the 0.5-1.5 mL min{sup -1} range). Inductively coupled plasma-mass spectrometry (ICP-MS) was used as a selective detector for iodine ({sup 127}I) and bromine ({sup 79}Br). Low dialyzability ratios (within the 2.0-18% range) were found for iodine species; whereas, moderate dialyzability percentages (from 9.0 to 40%) were obtained for bromine species. Iodide and bromide were the major species found in the dialyzates from seaweed, although MIT and bromate were also found in the dialyzates from most of the seaweed samples analysed. However, DIT was only found in dialyzates from Wakame, Kombu, and NIES 09 (Sargasso) certified reference material; whereas, iodate was not found in any dialyzate. Iodine dialyzability was found to be dependent on the protein content (negative correlation), and on the carbohydrate and dietary fibre levels (positive correlation). However, bromine dialyzability was only dependent on the protein amount in seaweed (negative correlation).

  7. Deriving an atmospheric budget of total organic bromine using airborne in situ measurements from the western Pacific area during SHIVA

    Science.gov (United States)

    Sala, S.; Bönisch, H.; Keber, T.; Oram, D. E.; Mills, G.; Engel, A.

    2014-07-01

    During the recent SHIVA (Stratospheric Ozone: Halogen Impacts in a Varying Atmosphere) project an extensive data set of all halogen species relevant for the atmospheric budget of total organic bromine was collected in the western Pacific region using the Falcon aircraft operated by the German Aerospace agency DLR (Deutsches Zentrum für Luft- und Raumfahrt) covering a vertical range from the planetary boundary layer up to the ceiling altitude of the aircraft of 13 km. In total, more than 700 measurements were performed with the newly developed fully automated in situ instrument GHOST-MS (Gas chromatograph for the Observation of Tracers - coupled with a Mass Spectrometer) by the Goethe University of Frankfurt (GUF) and with the onboard whole-air sampler WASP with subsequent ground-based state-of-the-art GC / MS analysis by the University of East Anglia (UEA). Both instruments yield good agreement for all major (CHBr3 and CH2Br2) and minor (CH2BrCl, CHBrCl2 and CHBr2Cl) VSLS (very short-lived substances), at least at the level of their 2σ measurement uncertainties. In contrast to the suggestion that the western Pacific could be a region of strongly increased atmospheric VSLS abundance (Pyle et al., 2011), we found only in the upper troposphere a slightly enhanced amount of total organic bromine from VSLS relative to the levels reported in Montzka and Reimann et al. (2011) for other tropical regions. From the SHIVA observations in the upper troposphere, a budget for total organic bromine, including four halons (H-1301, H-1211, H-1202, H-2402), CH3Br and the VSLS, is derived for the level of zero radiative heating (LZRH), the input region for the tropical tropopause layer (TTL) and thus also for the stratosphere. With the exception of the two minor VSLS CHBrCl2 and CHBr2Cl, excellent agreement with the values reported in Montzka and Reimann et al. (2011) is found, while being slightly higher than previous studies from our group based on balloon-borne measurements.

  8. Temperature dependent halogen activation by N2O5 reactions on halide-doped ice surfaces

    Directory of Open Access Journals (Sweden)

    J. A. Thornton

    2012-06-01

    Full Text Available We examined the reaction of N2O5 on frozen halide salt solutions as a function of temperature and composition using a coated wall flow tube technique coupled to a chemical ionization mass spectrometer (CIMS. The molar yield of photo-labile halogen compounds was near unity for almost all conditions studied, with the observed reaction products being nitryl chloride (ClNO2 and/or molecular bromine (Br2. The relative yield of ClNO2 and Br2 depended on the ratio of bromide to chloride ions in the solutions used to form the ice. At a bromide to chloride ion molar ratio greater than 1/30 in the starting solution, Br2 was the dominant product otherwise ClNO2 was primarily produced on these near pH-neutral brines. We demonstrate that the competition between chlorine and bromine activation is a function of the ice/brine temperature presumably due to the preferential precipitation of NaCl hydrates from the brine below 250 K. Our results provide new experimental confirmation that the chemical environment of the brine layer changes with temperature and that these changes can directly affect multiphase chemistry. These findings have implications for modeling air-snow-ice interactions in polar regions and likely in polluted mid-latitude regions during winter as well.

  9. Expression and intracellular localization of ACA and TRA-1-81 in smooth muscle cell tumors.

    Science.gov (United States)

    Sukhikh, G T; Becker-Kojić, Z; Kogan, E A; Demura, T A; Faizullina, N M; Nizyaeva, N V; Schott, A; Ureña-Peralta, J J; Askol'skaya, S I; Popov, Yu V

    2013-08-01

    We studied the expression and intracellular localization of ACA and TRA-1-81 in smooth muscle cell tumors. The study was performed on tissue specimens obtained during surgery from patients with uterine leiomyoma and leiomyosarcoma (mean age 34 and 51 years, respectively). ACA was present in leiomyoma, leiomyosarcoma, and control myometrium. Intracellular expression of ACA varied in different types of tumors and was minimum in normal myometrium and maximum in leiomyosarcoma. Membrane localization of the protein is typical of common and cellular leiomyoma, while in the growth zones of mitotically active leiomyoma and leiomyosarcoma the reaction product was primarily located in tumor cell cytoplasm. TRA was detected in some leiomyosarcoma cells. Thus, ACA dysregulation was revealed in the growth zones of leiomyomas and in leiomyosarcomas, which manifested in enhanced expression of this protein and its detachment from the plasma membrane, which leads ACA translocation into the cytoplasm and nucleus of tumor cells and potentiates their proliferative activity.

  10. Maternal transfer of emerging brominated and chlorinated flame retardants in European eels

    Energy Technology Data Exchange (ETDEWEB)

    Sühring, Roxana, E-mail: roxana.suehring@hzg.de [Helmholtz-Zentrum Geesthacht, Centre for Materials and Coastal Research, Institute of Coastal Research, Department for Environmental Chemistry, Max-Planck-Strasse 1, 21502 Geesthacht (Germany); Leuphana University Lüneburg, Institute of Sustainable and Environmental Chemistry, Scharnhorststraße 1, 21335 Lüneburg (Germany); Freese, Marko [Thünen Institute of Fisheries Ecology, Palmaille 9, 22767 Hamburg (Germany); Schneider, Mandy [Leuphana University Lüneburg, Institute of Sustainable and Environmental Chemistry, Scharnhorststraße 1, 21335 Lüneburg (Germany); Schubert, Sophia; Pohlmann, Jan-Dag [Thünen Institute of Fisheries Ecology, Palmaille 9, 22767 Hamburg (Germany); Alaee, Mehran [Water Science and Technology Directorate, Environment Canada, Burlington, Ontario, L7R4A6 Canada (Canada); Wolschke, Hendrik [Helmholtz-Zentrum Geesthacht, Centre for Materials and Coastal Research, Institute of Coastal Research, Department for Environmental Chemistry, Max-Planck-Strasse 1, 21502 Geesthacht (Germany); Leuphana University Lüneburg, Institute of Sustainable and Environmental Chemistry, Scharnhorststraße 1, 21335 Lüneburg (Germany); Hanel, Reinhold [Thünen Institute of Fisheries Ecology, Palmaille 9, 22767 Hamburg (Germany); Ebinghaus, Ralf [Helmholtz-Zentrum Geesthacht, Centre for Materials and Coastal Research, Institute of Coastal Research, Department for Environmental Chemistry, Max-Planck-Strasse 1, 21502 Geesthacht (Germany); Marohn, Lasse [Thünen Institute of Fisheries Ecology, Palmaille 9, 22767 Hamburg (Germany)

    2015-10-15

    The European eel (Anguilla anguilla) is regarded as a critically endangered species. Scientists are in agreement that the “quality of spawners” is a vital factor for the survival of the species. This quality can be impaired by parasites, disease and pollution. Especially endocrine disrupting organic chemicals pose a potential threat to reproduction and development of offspring. To our knowledge, the findings in this publication for the first time describe maternal transfer of contaminants in eels. We analysed the concentrations of in total 53 polybrominated diphenyl ethers (PBDEs) and their halogenated substitutes in muscle, gonads and eggs of artificially matured European eels and in muscle and gonads of untreated European eels that were used for comparison. We found evidence that persistent organic pollutants such as PBDEs, as well as their brominated and chlorinated substitutes are redistributed from muscle tissue to gonads and eggs. Concentrations ranged from 0.001 ng g{sup −1} ww for sum Dechlorane metabolites (DPMA, aCL{sub 10}DP, aCl{sub 11}DP) to 2.1 ng g{sup −1} ww for TBA in eggs, 0.001 ng g{sup −1} ww for Dechlorane metabolites to 9.4 ng g{sup −1} ww for TBA in gonads and 0.002 ng g{sup −1} ww for Dechlorane metabolites to 54 ng g{sup −1} ww for TBA in muscle tissue. Average egg muscle ratios (EMRs) for compounds detectable in artificially matured eels from both Schlei Fjord and Ems River ranged from 0.01 for Dechlorane 602 (DDC-DBF) to 10.4 for PBEB. Strong correlations were found between flame retardant concentrations and lipid content in the analysed tissue types, as well as transfer rates and octanol–water partitioning coefficient, indicating that these parameters were the driving factors for the observed maternal transfer. Furthermore, indications were found, that TBP-DBPE, TBP-AE, BATE and TBA have a significant uptake from the surrounding water, rather than just food and might additionally be formed by metabolism or

  11. Flash photolytic generation and study of p-quinone methide in aqueous solution. An estimate of rate and equilibrium constants for heterolysis of the carbon-bromine bond in p-hydroxybenzyl bromide.

    Science.gov (United States)

    Chiang, Y; Kresge, A J; Zhu, Y

    2002-06-05

    Flash photolysis of p-hydroxybenzyl acetate in aqueous perchloric acid solution and formic acid, acetic acid, biphosphate ion, and tris(hydroxymethyl)methylammonium ion buffers produced p-quinone methide as a short-lived species that underwent hydration to p-hydroxybenzyl alcohol in hydronium ion catalyzed (k(H(+)) = 5.28 x 10(4) M(-1) s(-1)) and uncatalyzed (k(uc) = 3.33 s(-1)) processes. The inverse nature of the solvent isotope effect on the hydronium ion-catalyzed reaction, k(H(+))/k(D(+)) = 0.41, indicates that this process occurs by rapid and reversible protonation of the quinone methide on its carbonyl carbon atom, followed by rate-determining capture of the p-hydroxybenzyl carbocation so produced by water, while the magnitude of the rate constant on the uncatalyzed process indicates that this reaction occurs by simple nucleophilic addition of water to the methylene group of the quinone methide. p-Quinone methide also underwent hydronium ion-catalyzed and uncatalyzed nucleophilic addition reactions with chloride ion, bromide ion, thiocyanate ion, and thiourea. The solvent isotope effects on the hydronium ion-catalyzed processes again indicate that these reactions occurred by preequilibrium mechanisms involving a p-hydroxybenzyl carbocation intermediate, and assignment of a diffusion-controlled value to the rate constant for reaction of this cation with thiocyanate ion led to K(SH) = 110 M as the acidity constant of oxygen-protonated p-quinone methide. In a certain perchloric acid concentration range, the bromide ion reaction became biphasic, and least-squares analysis of the kinetic data using a double-exponential function provided k(Br(-)) = 3.8 x 10(8) M(-1) s(-1) as the rate constant for nucleophilic capture of the p-hydroxybenzyl carbocation by bromide ion, k(ionz) = 8.5 x 10(2) s(-1) for ionization of the carbon-bromine bond of p-hydroxybenzyl bromide, and K = 4.5 x 10(5) M(-1) as the equilibrium constant for the carbocation-bromide ion combination

  12. Mercury oxidation via chlorine, bromine, and iodine under atmospheric conditions: thermochemistry and kinetics.

    Science.gov (United States)

    Auzmendi-Murua, Itsaso; Castillo, Álvaro; Bozzelli, Joseph W

    2014-04-24

    Emissions of gaseous mercury from combustion sources are the major source of Hg in the atmosphere and in environmental waters and soils. Reactions of Hg(o)(g) with halogens are of interest because they relate to mercury and ozone depletion events in the Antarctic and Arctic early spring ozone hole events, and the formation of Hg-halides (HgX2) is a method for removal of mercury from power generation systems. Thermochemistry and kinetics from published theoretical and experimental studies in the literature and from computational chemistry are utilized to compile a mechanism of the reactions considered as contributors to the formation of HgX2 (X = Cl, Br, I) to understand the reaction paths and mechanisms under atmospheric conditions. Elementary reaction mechanisms are assembled and evaluated using thermochemistry for all species and microscopic reversibility for all reactions. Temperature and pressure dependence is determined with quantum Rice Ramsperger Kassel (RRK) analysis for k(E) and master equation analysis for fall-off. We find that reactions of mercury with a small fraction of the reactor surface or initiation by low concentrations of halogen atoms is needed to explain the experimental conversion of Hg to HgX2 in the gas phase. The models do not replicate data from experiments that do not explicitly provide an atom source. The Hg insertion reaction into X2 (Hg + X2 → HgX2) that has been reported is further studied, and we find agreement with studies that report high barriers. The high barriers prevent this insertion path from explaining the experimental data on HgX2 formation and Hg conversion under atmospheric conditions. Mechanism studies with low initial concentrations of halogen radicals show significant conversion of Hg under the experimental conditions.

  13. HOBr in sulfuric acid solutions: Solubility and reaction with HCl as a function of temperature and concentration

    Energy Technology Data Exchange (ETDEWEB)

    Waschewsky, G.C.G.; Abbatt, J.P.D. [Univ. of Chicago, IL (United States). Dept. of the Geophysical Sciences

    1999-07-08

    Although the total atmospheric loading of inorganic bromine is relatively low, not exceeding a few tens of parts per trillion, there has been considerable interest in recent years in the heterogeneous interactions which brominated species undergo in the atmosphere. A detailed study of the interaction of HOBr and HCl in cold sulfuric acid solutions has been performed using a coated-wall flow tube coupled to an electron-impact mass spectrometer. The liquid-phase bimolecular rate constants, measured over a temperature range from 213 to 238 K and in solutions from 59.7 to 70.1 wt % composition, show a strong positive dependence on both acid composition and temperature. The solubility of HOBr has also been measured in these solutions by analyzing its time-dependent uptake. Henry`s Law constants (H) determined from the measured values of HD{sup 1/2} and the liquid-phase diffusion coefficient (D) are independent of acid composition over the above range of solution compositions. The values of H demonstrate a clear Clausius-Clapeyron temperature dependence, with a heat of solution of {minus}9 {+-} 1 kcal/mol. When the atmospheric importance of these data is assessed, two conclusions are reached. In the stratosphere, under aerosol conditions observed soon after the Mt. Pinatubo volcano eruption, the rates of HCl activation via the HOBr/HCl heterogeneous reaction are comparable with the rate of activation via gas-phase reaction with OH at relatively warm temperatures (205--220 K), where other HCl-activating heterogeneous reactions occur slowly. In the high Arctic boundary layer, it is possible that significant HCl activation could occur when elevated levels of photochemically active bromine are present.

  14. Determination of bromine and tin compounds in plastics using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS).

    Science.gov (United States)

    İzgi, Belgin; Kayar, Murat

    2015-07-01

    The polybrominated flame retardants and organotin compounds were screened in terms of bromine and tin content using laser ablation inductively coupled plasma mass spectrometry in plastics. The calibration standards were prepared using the fused-disk technique, and all samples were investigated under optimal conditions. Using a central composite experimental design, laser parameters, laser energy, pulse rate, scan rate and spot size were identified. The detection limits of the method were 1000 mgkg(-1) and 1600 mgkg(-1) for bromide and tin, whereas the relative standard deviation (%) values of the analysis were 9% and 6% (n=3) for ERM EC681k with 770 ± 70 mgkg(-1) Br and 86 ± 6 mgkg(-1) Sn respectively, and 106-115% of Br and 102-104% of Sn were observed for the tetrabromobisphenol A and butyltin trichloride spike plastics, respectively. Copyright © 2015 Elsevier B.V. All rights reserved.

  15. Meteorology and vertical structure of plumes of enhanced bromine monoxide as detected by satellite remote sensing during Arctic spring

    Science.gov (United States)

    Sihler, Holger; Dörner, Steffen; Pozzer, Andrea; Frieß, Udo; Platt, Ulrich; Wagner, Thomas

    2014-05-01

    Each year during spring, near-surface ozone in the polar troposphere is periodically depleted by catalytic processes involving reactive halogen species (RHS). The periods of decreased surface ozone mixing ratios are known as ozone depletion events (ODEs) lasting between hours and several days. One particular tracer for active halogen chemistry is bromine monoxide (BrO) which may be reliably detected using differential optical absorption spectroscopy (DOAS). Satellite observations show plumes of enhanced BrO up to several thousand square kilometres large. Additionally, ground-based measurements, reveal strong vertical BrO gradients controlled by boundary-layer meteorology. However, the processes leading to atmospheric bromine activation are not well understood yet. Furthermore, the influence of synoptic meteorology and the consequences for the tropospheric ozone budget need to be quantified. In this presentation, the evolution of BrO plumes observed from satellite is investigated based on case studies. Complementary information about the vertical structure of meteorology and tracers distribution are offered by ground-based measurements, also used in this study. The comparison between BrO distribution and ozone sonde as well as weather model data indicates that the distribution of BrO is mainly controlled by meteorology, and especially the evolution of the BrO plumes is strongly correlated to the dynamics of low-pressure weather systems Finally, most of the ozone destruction occurs in fronts; therefore, a modification in the Arctic dynamic caused by climate change will also produce a change in the strength of this important sink for tropospheric ozone.

  16. Polybrominated diphenyl ethers (PBDEs) and alternative brominated flame retardants in air and seawater of the European Arctic

    Energy Technology Data Exchange (ETDEWEB)

    Moeller, Axel, E-mail: axel.moeller@hzg.de [Helmholtz-Zentrum Geesthacht, Centre for Materials and Coastal Research, Institute of Coastal Research, Department for Environmental Chemistry, Max-Planck-Strasse 1, 21502 Geesthacht (Germany); Xie Zhiyong; Sturm, Renate; Ebinghaus, Ralf [Helmholtz-Zentrum Geesthacht, Centre for Materials and Coastal Research, Institute of Coastal Research, Department for Environmental Chemistry, Max-Planck-Strasse 1, 21502 Geesthacht (Germany)

    2011-06-15

    The spatial distribution of polybrominated diphenyl ethers (PBDEs) and several alternative non-PBDE, non-regulated brominated flame retardants (BFRs) in air and seawater and the air-seawater exchange was investigated in East Greenland Sea using high-volume air and water samples. Total PBDE concentrations (O{sub 10}PBDEs) ranged from 0.09 to 1.8 pg m{sup -3} in the atmosphere and from 0.03 to 0.64 pg L{sup -1} in seawater. Two alternative BFRs, Hexabromobenzene (HBB) and 2,3-dibromopropyl-2,4,6-tribromophenyl ether (DPTE), showed similar concentrations and spatial trends as PBDEs. The air-seawater gas exchange was dominated by deposition with fluxes up to -492 and -1044 pg m{sup -2} day{sup -1} for BDE-47 and DPTE, respectively. This study shows the first occurrence of HBB, DPTE and other alternative flame retardants (e.g., pentabromotoluene (PBT)) in the Arctic atmosphere and seawater indicating that they have a similar long-range atmospheric transport potential (LRAT) as the banned PBDEs. - Highlights: > Flame retardants undergo long-range atmospheric transport to East Greenland Sea. > Western Europe is a source of flame retardants in the European Arctic. > Alternative flame retardants HBB and DPTE show concentrations similar to PBDEs. > Air-sea exchange of brominated flame retardants is dominated by net deposition. - Alternative flame retardants hexabromobenzene (HBB) and 2,3-dibromopropyl-2,4,6-tribromophenyl ether (DPTE) undergo long-range atmospheric transport to the Arctic.

  17. Occurrence, profiles, and toxic equivalents of chlorinated and brominated polycyclic aromatic hydrocarbons in E-waste open burning soils.

    Science.gov (United States)

    Nishimura, Chiya; Horii, Yuichi; Tanaka, Shuhei; Asante, Kwadwo Ansong; Ballesteros, Florencio; Viet, Pham Hung; Itai, Takaaki; Takigami, Hidetaka; Tanabe, Shinsuke; Fujimori, Takashi

    2017-06-01

    We conducted this study to assess the occurrence, profiles, and toxicity of chlorinated polycyclic aromatic hydrocarbons (Cl-PAHs) and brominated polycyclic aromatic hydrocarbons (Br-PAHs) in e-waste open burning soils (EOBS). In this study, concentrations of 15 PAHs, 26 Cl-PAHs and 14 Br-PAHs were analyzed in EOBS samples. We found that e-waste open burning is an important emission source of Cl-PAHs and Br-PAHs as well as PAHs. Concentrations of total Cl-PAHs and Br-PAHs in e-waste open burning soil samples ranged from 21 to 2800 ng/g and from 5.8 to 520 ng/g, respectively. Compared with previous studies, the mean of total Cl-PAH concentrations of the EOBS samples in this study was higher than that of electronic shredder waste, that of bottom ash, and comparable to fly ash from waste incinerators in Korea and Japan. The mean of total Br-PAH concentrations of the EOBS samples was generally three to four orders of magnitude higher than those in incinerator bottom ash and comparable to incinerator fly ash, although the number of Br-PAH congeners measured differed among studies. We also found that the Cl-PAH and Br-PAH profiles were similar among all e-waste open burning soil samples but differed from those in waste incinerator fly ash. The profiles and principal component analysis results suggested a unique mechanism of Cl-PAH and Br-PAH formation in EOBS. In addition, the Cl-PAHs and Br-PAHs showed high toxicities equivalent to PCDD/Fs measured in same EOBS samples when calculated based on their relative potencies to benzo[a]pyrene. Along with chlorinated and brominated dioxins and PAHs, Cl-PAHs and Br-PAHs are important environmental pollutants to investigate in EOBS. Copyright © 2016 Elsevier Ltd. All rights reserved.

  18. Brominated flame retardants (BFRs) in indoor and outdoor air in a community in Guangzhou, a megacity of southern China.

    Science.gov (United States)

    Ding, Nan; Wang, Tao; Chen, She-Jun; Yu, Mei; Zhu, Zhi-Cheng; Tian, Mi; Luo, Xiao-Jun; Mai, Bi-Xian

    2016-05-01

    Indoor environments contribute a significant portion of human exposure to brominated flame retardants (BFRs) because of their extensive use in various household products. This study investigates the occurrence of a number of BFRs in the indoor and outdoor air in a megacity in southern China, in which little information on indoor BFRs contamination is available. The estimated total PBDE concentrations ranged from 1.43 to 57 pg/m(3) indoors and from 1.21 to 1522 pg/m(3) outdoors. The indoor concentrations of lower brominated PBDEs that are mainly derived from the technical penta- and octa-BDE mixtures were higher than or comparable to the outdoors, while the indoor levels of DecaBDEs and decabromodiphenyl ethane (DBDPE) were apparently lower than the outdoors. The seasonal variations of BFR concentrations indicated that evaporation from old indoor products is the primary source of Penta- and OctaBDEs in the air, whereas most DecaBDEs and DBDPE concentrations showing weak temperature-dependence are largely released from industrial activities. The PBDE congener profiles in the air were generally similar, which were dominated by BDE209, 28, and 47; whereas the appreciable indoor-outdoor differences in the compositions are possibly due to emission sources, photochemical degradation, or congener-specific transport of BFRs in the indoor and outdoor air. Significant correlations between the indoor and outdoor BFRs were observed suggesting the exchange of BFRs between the two compartments, which are more noticeable for PentaBDEs and DecaBDEs with strong indoor and outdoor emission sources, respectively. This study provides significant insights into the sources of BFRs in urban air in China. Copyright © 2016 Elsevier Ltd. All rights reserved.

  19. Levels of brominated flame retardants and other pesistent organic pollutants in breast milk samples from Limpopo province, South Africa

    Energy Technology Data Exchange (ETDEWEB)

    Darnerud, Per Ola, E-mail: poda@slv.se [Toxicology Division, National Food Administration, P.O. Box 622, SE-751 26 Uppsala (Sweden); Aune, Marie; Larsson, Lotta [Chemistry Division 2, National Food Administration, P.O. Box 622, SE-751 26 Uppsala (Sweden); Lignell, Sanna [Toxicology Division, National Food Administration, P.O. Box 622, SE-751 26 Uppsala (Sweden); Mutshatshi, Tshinanne; Okonkwo, Jonathan; Botha, Ben [Faculty of Science, Tshwane University of Technology, Pretoria (South Africa); Agyei, Nana [Department of Chemistry, Limpopo University, Medunsa (South Africa)

    2011-09-01

    The non-occupational exposure to brominated flame retardants, and other persistent organic pollutants (POPs) was studied by collecting human breast milk samples from mothers residing in Thohoyandou area, a rural district in the Limpopo Province, northern part of South Africa (SA). Of all collected samples to be analysed (n = 28), those with large enough milk volumes, (n = 14) were quantified for polybrominated diphenyl ethers (PBDEs) (9 congeners: BDE-28, 47, 66, 99, 100, 138, 153, 154, and 183) and hexabromocyclododecane (HBCD) on a GC equipped with dual capillary columns and dual electron-capture detectors (ECD). The levels of PBDE congeners (median sumBDE 1.3 ng/g of lipids) and of HBCD were not far from levels generally found in European studies, and this study may be the first report on the presence of PBDEs and HBCD in SA breast milk. On a congener basis, the finding of comparably high BDE-183 levels suggests a specific PBDE usage, or contamination situation in SA. Apart from BFRs, the high DDT levels found in the breast milk from this area (median and maximum sumDDT levels of about 4 600 and over 20 000 ng/g of lipids, respectively; n = 28) have earlier been reported. In addition, other POPs (PCBs, HCB and HCHs) were found in SA breast milk, at relatively low levels. To conclude, measurable levels of PBDEs and HBCD, and a specific BDE congener pattern, were found in breast milk from the Limpopo province, SA. A number of other POPs, including DDTs in high levels, were also present. - Highlights: {yields} Persistent organic pollutants (POPs) were analysed in South African breast milk. {yields} Focus of interest were brominated flame retardants (BRFs). {yields} Sampling area was the rural Limpopo Province, northern SA. {yields} Probably the first reported African data on BFRs (PBDEs, HBCD) in breast milk. {yields} Reported BFR data similar to European levels.

  20. OClO and BrO observations in the volcanic plume of Mt. Etna - implications on the chemistry of chlorine and bromine species in volcanic plumes

    Science.gov (United States)

    Gliß, J.; Bobrowski, N.; Vogel, L.; Platt, U.

    2014-10-01

    Spatial and temporal profiles of chlorine dioxide (OClO), bromine monoxide (BrO) and sulphur dioxide (SO2) were measured in the plume of Mt. Etna, Italy, in September 2012 using Multi-Axis-Differential-Optical-Absorption-Spectroscopy (MAX-DOAS). OClO (BrO) was detected in 119 (452) individual measurements covering plume ages up to 6 (23) minutes. The retrieved slant column densities (SCDs) reached values up to 2.0 × 1014 molecules cm-2 (OClO) and 1.1 × 1015 molecules cm-2 (BrO). In addition, the spectra were analysed for signatures of IO, OIO and OBrO, none of these species could be detected. The corresponding detection limits for IO / SO2, OIO / SO2 and OBrO / SO2 were 1.8 × 10-6, 2.0 × 10-5 and 1.1 × 10-5 respectively. The measurements were performed at plume ages (τ) from zero to 23 min downwind the emission source. The chemical variability of BrO and OClO in the plume was studied analysing the OClO / SO2 and BrO / SO2-ratio. A marked increase of both ratios was observed in the young plume (τ 3 min) with mean abundances of 3.17 × 10-5 (OClO / SO2), 1.55 × 10-4 (BrO / SO2) and 0.16 (OClO / BrO). Furthermore, enhanced BrO/SO2-ratios were found at the plume edges (by ~30-37%) and a strong indication of enhanced OClO / SO2-ratios as well (~10-250%). A measurement performed in the early morning (05:20-06:20 UTC, sunrise: 04:40 UTC) showed an BrO / SO2-ratio increasing with time until 05:35 UTC and a constant ratio afterwards. Observing this increase was only possible due to a correction for stratospheric BrO signals in the plume spectra. The corresponding OClO / SO2-ratio showed a similar trend stabilising around 06:13 UTC, approximately 40 min later than BrO. This is another strong indication for the photochemical nature of the reactions involved in the formation of oxidised halogens in volcanic plumes. In particular, these findings support the current understanding of the underlying chemistry, namely, that BrO is formed in an autocatalytic reaction