WorldWideScience

Sample records for bromine chlorides

  1. Bromine

    Science.gov (United States)

    Ober, J.A.

    2013-01-01

    The element bromine is found principally as a dissolved species in seawater, evaporitic (salt) lakes and underground brines associated with petroleum deposits. Seawater contains about 65 parts per million of bromine or an estimated 907 Gt (100 trillion st). In the Middle East, the highly saline waters of the Dead Sea are estimated to contain 907 Mt (1 billion st) of bromine. Bromine also may be recovered from seawater as a coproduct during evaporation to produce salt.

  2. Effect of Brominated Furanones on the Formation of Biofilm by Escherichia coli on Polyvinyl Chloride Materials

    OpenAIRE

    Lianhua, Ye; Yunchao, Huang; Geng, Xu; Youquang, Zhou; Guangqiang, Zhao; Yujie, Lei

    2013-01-01

    To study the influence of brominated furanones on the biofilm (BF) formation by Escherichia coli (E. coli) on polyvinyl chloride (PVC) material, and to provide new ways of surface modification of materials to clinically prevent biomaterial centered infection. Three brominated furanones, dissolved in ethanol, furanone-1(3,4-dibromo-5-hydroxyl-furanone), furanone-2(4-bromo-5-(4-methoxypheny)-3-(methylamino)-furanone), and furanone-3(3,4-dibromo-5,5-dimethoxypheny-2(5H)-furanone) with representa...

  3. 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 ...

  4. Effect of brominated furanones on the formation of biofilm by Escherichia coli on polyvinyl chloride materials.

    Science.gov (United States)

    Lianhua, Ye; Yunchao, Huang; Geng, Xu; Youquang, Zhou; Guangqiang, Zhao; Yujie, Lei

    2013-01-01

    To study the influence of brominated furanones on the biofilm (BF) formation by Escherichia coli (E. coli) on polyvinyl chloride (PVC) material, and to provide new ways of surface modification of materials to clinically prevent biomaterial centered infection. Three brominated furanones, dissolved in ethanol, furanone-1(3,4-dibromo-5-hydroxyl-furanone), furanone-2(4-bromo-5-(4-methoxypheny)-3-(methylamino)-furanone), and furanone-3(3,4-dibromo-5,5-dimethoxypheny-2(5H)-furanone) with representative chemical structure, were coated on the surfaces of separate PVC materials (1 × 1 cm), respectively. The surface-modified PVC materials were incubated with E. coli and for controls, 75 % ethanol-treated PVC materials were used. This treatment played as control group. The cultivation incubations were for 6, 12, 18, and 24 h. The thickness of bacterial BF and bacterial community quantity unit area on the PVC materials was determined by confocal laser scanning microscopy (CLSM), and the surface structure of bacterial BF formation was examined by scanning electron microscopy (SEM). The results of CLSM indicated the thickness of bacterial BF and bacterial community quantity unit area on PVC materials treated with furanone-3 were significantly lower than that of control at all time points (P 0.05). The results of SEM indicated that after 6 h incubation, the quantity of bacterial attachment to the surface of PVC material treated with furanone-3 was lower than the control group. By 18 h incubation there was completely formed BF structure on the surface of control PVC material. However, there was no significant BF formation on the surface of PVC material treated with furanone-3. The impact of different brominated furanones on SA biofilm formation on the surface of PVC materials are different, furanone-3 can inhibit E. coli biofilm formation on the surface of PVC material.

  5. Resistivity features in intercalated graphite compounds with bromine and iodine chloride in the region of structural phase transitions in the layer of intercalate

    International Nuclear Information System (INIS)

    In the paper anomalous changes of resistivity in graphite intercalated compounds with iodine chloride and bromine are investigated in the phase transition temperature interval. It is shown that these anomalies are caused by the change of carriers mobility in the phase transitional interval as well as by the origin of ''mobile ions liquids''

  6. 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...

  7. 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.

  8. Bromination of Phenol

    Science.gov (United States)

    Talbot, Christopher

    2013-01-01

    This "Science note" examines the bromination of phenol, a reaction that is commonly taught at A-level and IB (International Baccalaureate) as an example of electrophilic substitution. Phenol undergoes bromination with bromine or bromine water at room temperature. A white precipitate of 2,4,6-tribromophenol is rapidly formed. This…

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

    Energy Technology Data Exchange (ETDEWEB)

    Vainikka, P.

    2011-12-15

    estimated by thermodynamic equilibrium modelling. A positive correlation was observed between the halogen (Br, Cl) and the metal (Cu, Pb, and Zn) concentrations in the lower furnace vapours when measured next to the waterwalls. Further, bromine was observed both in the wall deposits and in the corrosion front of the waterwall tubes. This was found to take place even if the bromine content in the SRF was less than 60 mg kg-1 in SRF. Laboratory scale oven tests with commercial boiler steels showed that a bromine containing salt induced a higher corrosion rate than the corresponding chloride. (orig.)

  10. Synthesis of 1-Bromo-3-methoxy-4-propoxy-5-iodobenzene-A Novel Efficient Process for the Synthesis of Brominated Aromatic Compound

    Institute of Scientific and Technical Information of China (English)

    Hong Xin SHI; Hui LIN; Gérard MANDVILLE

    2004-01-01

    The reaction of aromatic carboxylic acid with oxalyl chloride gives rise to the corres- ponding acid chloride which without purification is treated with the sodium salt of mercapto- pyridine oxide in the presence of 2,2-azo-bisisobutyronitrile (AIBN), radical initiator to give a brominated aromatic compound. After etherification and oxidation, 5-iodovaniline was converted to trisubstituted benzene carboxylic acid which give 1-bromo-3-methoxy-4-propoxy-5-iodo- benzene by this new brominating process with a yield of 74 %.

  11. Two new brominated diterpenes from Laurencia decumbens

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Two new brominated diterpenes, namely, laurendecumtriol and 11-deacetylpinnaterpene C, were isolated and identified from the marine red alga Laurencia decumbens. Their structures were established on the basis of various NMR spectroscopic techniques and HR-ESI-MS analyses.

  12. Stability and metastability of bromine clathrate polymorphs.

    Science.gov (United States)

    Nguyen, Andrew H; Molinero, Valeria

    2013-05-23

    Clathrate hydrates are crystals in which water forms a network of fully hydrogen-bonded polyhedral cages that contain small guests. Clathrate hydrates occur mostly in two cubic crystal polymorphs, sI and sII. Bromine is one of two guests that yield a hydrate with the tetragonal structure (TS), the topological dual of the Frank-Kasper σ phase. There has been a long-standing disagreement on whether bromine hydrate also forms metastable sI and sII crystals. To date there are no data on the thermodynamic range of stability (e.g., the melting temperatures) of the metastable polymorphs. Here we use molecular dynamics simulations with the coarse-grained model of water mW to (i) investigate the thermodynamic stability of the empty and guest-filled the sI, sII, TS, and HS-I hydrate polymorphs, (ii) develop a coarse-grained model of bromine compatible with mW water, and (iii) evaluate the stability of the bromine hydrate polymorphs. The mW model predicts the same relative energy of the empty clathrate polymorphs and the same phase diagram as a function of water-guest interaction than the fully atomistic TIP4P water model. There is a narrow region in water-guest parameter space for which TS is marginally more stable than sI or sII. We parametrize a coarse-grained model of bromine compatible with mW water and use it to determine the order of stability of the bromine hydrate polymorphs. The melting temperatures of the bromine hydrate polymorphs predicted by the coarse-grained model are 281 ± 1 K for TS, 279 ± 1 K for sII, and 276 ± 1 K for sI. The closeness of the melting temperatures supports the plausibility of formation of metastable sII and sI bromine hydrates.

  13. 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.

  14. Abiotic Bromination of Soil Organic Matter.

    Science.gov (United States)

    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.

  15. 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...

  16. 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...

  17. Nitrogenous disinfection byproducts in English drinking water supply systems: Occurrence, bromine substitution and correlation analysis.

    Science.gov (United States)

    Bond, Tom; Templeton, Michael R; Mokhtar Kamal, Nurul Hana; Graham, Nigel; Kanda, Rakesh

    2015-11-15

    Despite the recent focus on nitrogenous disinfection byproducts in drinking water, there is limited occurrence data available for many species. This paper analyses the occurrence of seven haloacetonitriles, three haloacetamides, eight halonitromethanes and cyanogen chloride in 20 English drinking water supply systems. It is the first survey of its type to compare bromine substitution factors (BSFs) between the haloacetamides and haloacetonitriles. Concentrations of the dihalogenated haloacetonitriles and haloacetamides were well correlated. Although median concentrations of these two groups were lower in chloraminated than chlorinated surface waters, median BSFs for both in chloraminated samples were approximately double those in chlorinated samples, which is significant because of the higher reported toxicity of the brominated species. Furthermore, median BSFs were moderately higher for the dihalogenated haloacetamides than for the haloacetonitriles. This indicates that, while the dihalogenated haloacetamides were primarily generated from hydrolysis of the corresponding haloacetonitriles, secondary formation pathways also contributed. Median halonitromethane concentrations were remarkably unchanging for the different types of disinfectants and source waters: 0.1 μg · mgTOC(-1) in all cases. Cyanogen chloride only occurred in a limited number of samples, yet when present its concentrations were higher than the other N-DBPs. Concentrations of cyanogen chloride and the sum of the halonitromethanes were not correlated with any other DBPs.

  18. PHONONS IN GRAPHITE INTERCALATED WITH BROMINE

    OpenAIRE

    Batallan, F.; Rosenman, I.; Simon, C; Furdin, G.; Lauter, H.

    1981-01-01

    We have investigated the phonon spectrum in stage 2 graphite intercalate with bromine by using inelastic neutron scattering. We have observed longitudinal and transverse phonons along the c direction as well as in the layer plane. Results are presented for energies up to 15 THz at 300 K. A linear chain model explains most of our results.

  19. Brominated flame retardants and endocrine disruption

    NARCIS (Netherlands)

    Vos, J.G.; Becher, G.; Berg, van den M.; Boer, de J.; Leonards, P.E.G.

    2003-01-01

    From an environmental point of view, an increasing important group of organohalogen compounds are the brominated flame retardants (BFRs), which are widely used in polymers and textiles and applied in construction materials, furniture, and electronic equipment. BFRs with the highest production volume

  20. 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.

  1. Symproportionation versus Disproportionation in Bromine Redox Systems

    International Nuclear Information System (INIS)

    Graphical abstract: Display Omitted -- Highlights: • The disproportionation and symproportionation of bromine in different media is presented. • All the redox systems are elaborated according to the principles of the generalized approach to electrolytic redox systems (GATES/GEB). • All physicochemical knowledge is involved in the algorithm applied for this purpose. • The graphical representation of the systems is the basis of gaining the detailed physicochemical knowledge on the systems in question. -- Abstract: The paper refers to dynamic (titration) redox systems where symproportionation or disproportionation of bromine species occur. The related systems are modeled according to principles assumed in the Generalized Approach to Electrolytic Redox Systems (GATES), with Generalized Electron Balance (GEB) concept involved in the GATES/GEB software. The results obtained from calculations made with use of iterative computer programs prepared according to MATLAB computational software, are presented graphically, as 2D and 3D graphs

  2. Membrane-less hydrogen bromine flow battery

    CERN Document Server

    Braff, W A; Buie, C R

    2014-01-01

    In order for the widely discussed benefits of flow batteries for electrochemical energy storage to be applied at large scale, the cost of the electrochemical stack must come down substantially. One promising avenue for reducing stack cost is to increase the system power density while maintaining efficiency, enabling smaller stacks. Here we report on a membrane-less, hydrogen bromine laminar flow battery as a potential high power density solution. The membrane-less design enables power densities of 0.795 W cm$^{-2}$ at room temperature and atmospheric pressure, with a round-trip voltage efficiency of 92\\% at 25\\% of peak power. Theoretical solutions are also presented to guide the design of future laminar flow batteries. The high power density achieved by the hydrogen bromine laminar flow battery, along with the potential for rechargeable operation, will translate into smaller, inexpensive systems that could revolutionize the fields of large-scale energy storage and portable power systems.

  3. Surface Snowpack Key to Bromine Activation in a Changing Arctic Environment

    Science.gov (United States)

    Pratt, Kerri; Custard, Kyle; Shepson, Paul; Douglas, Thomas; Pöhler, Denis; Stephan, General; Zielcke, Johannes; Simpson, William; Platt, Ulrich; von Glasow, Roland; Tanner, David; Huey, L. Gregory; Carlsen, Mark; Stirm, Brian

    2013-04-01

    Arctic sea ice is rapidly declining and transforming from a multiyear ice pack to thinner, more saline, seasonal ice, which has important implications for Arctic atmospheric composition. Following springtime polar sunrise, "ozone depletion events", attributed to bromine chemistry, lead to episodic decreases in lower tropospheric ozone concentrations to near zero, concurrent with mercury depletion and deposition. Despite our increasing understanding of the spatial variability of BrO and possible reaction pathways based on laboratory studies, important questions remain regarding the most efficient sources of and mechanisms for Arctic halogen activation. During the March-April 2012 BRomine, Ozone, and Mercury EXperiment (BROMEX) in Barrow, Alaska, outdoor chamber experiments with snow and ice samples were conducted. Ozone was added as the precursor oxidant, and the samples were investigated with and without ambient sunlight. Samples included first-year sea ice, brine icicles, several layers of snow above first-year sea ice, and seasonal snow above the tundra. Chemical ionization mass spectrometry was utilized to monitor Br2 production. Tundra snow and surface snow above sea ice produced the most Br2, with no production resulting from sea ice and basal snow directly above sea ice. Overall, the most efficient Br2 production was observed from snow samples characterized by lower pH and higher bromide/chloride ratios. Br2 was only observed in the presence of sunlight, indicating the role of snowpack photochemical reactions and the hydroxyl radical in its production. Br2 production via the surface snowpack explains previously-observed BrO enhancements above sea ice, as well as observations of inland tundra hotspots in measured BrO by aircraft-based nadir MAX-DOAS (Multi Axis-Differential Optical Absorption Spectroscopy) measurements, conducted during BROMEX. The findings indicate that atmospherically processed snow is likely a major source of Arctic bromine release, which

  4. Brominated thiophenes as precursors in the preparation of brominated and arylated anthraquinones.

    Science.gov (United States)

    Thiemann, Thies; Tanaka, Yasuko; Iniesta, Jesus

    2009-01-01

    Brominated anthraquinones can be synthesized directly from bromothiophenes when these are reacted with 1,4-naphthoquinones in the presence of meta-chloroperoxybenzoic acid. The bromoanthraquinones are versatile building blocks in the preparation of arylated anthraquinones and of extended pi-systems with interspersed anthraquinone units. PMID:19305356

  5. Brominated Thiophenes as Precursors in the Preparation of Brominated and Arylated Anthraquinones

    Directory of Open Access Journals (Sweden)

    Thies Thiemann

    2009-03-01

    Full Text Available Brominated anthraquinones can be synthesized directly from bromothiophenes when these are reacted with 1,4-naphthoquinones in the presence of meta-chloroperoxybenzoic acid. The bromoanthraquinones are versatile building blocks in the preparation of arylated anthraquinones and of extended π-systems with interspersed anthraquinone units.

  6. Brominated Thiophenes as Precursors in the Preparation of Brominated and Arylated Anthraquinones

    OpenAIRE

    Thies Thiemann; Jesus Iniesta; Yasuko Tanaka

    2009-01-01

    Brominated anthraquinones can be synthesized directly from bromothiophenes when these are reacted with 1,4-naphthoquinones in the presence of meta-chloroperoxybenzoic acid. The bromoanthraquinones are versatile building blocks in the preparation of arylated anthraquinones and of extended π-systems with interspersed anthraquinone units.

  7. Polyvinylpolypyrrolidone-bromine complex: Mild and efficient polymeric reagent for bromination of activated aromatic compounds

    Institute of Scientific and Technical Information of China (English)

    Masoud Mokhtary; Moslem M. Lakouraj

    2011-01-01

    Mild and efficient method for bromination of electron-rich aromatic compounds is described using polyvinylpolypyrrolidonebromine complex (PVPP-Br2). The reaction proceeded smoothly with phenols and N,N-alkylated amines to afford the corresponding monobrominated product in good yields at ambient temperature.

  8. Fire-retardant coatings based on organic bromine/phenoxy or brominated epoxy systems

    Energy Technology Data Exchange (ETDEWEB)

    Hoffman, D.M.; Chiu, Ing L.

    1989-06-01

    Thin phenoxy and brominated epoxy/curing agent films were prepared by solvent casting on Mylar and Kapton. Thicknesses were approximated assuming volume additivity. Important parameters were uniformity of thickness, distribution of the bromine-containing fire retardant, adhesion to carrier substrate (either Mylar or Kapton), and uniformity of the coating, i.e., absence of pinholes, blush, blistering, etc. Wetting behavior was modified using fluoro, silicone or polyurea surfactants. Several solvent systems were examined and a ternary solvent system was ultimately used. Distribution of fire-retardant bromine was analyzed using electron microprobe, x-ray fluorescence and wet chemical methods. Significant discrepancies in the /mu/m-scale analyses of the microprobe measurements have not been resolved. Some of the brominated fire retardants were insoluble in the resin systems and the phase separation was immediately obvious. Similarly, some of the crystallizable epoxies could not be cast easily into homogeneous, amorphous films. Castings were made on a standard 8'' /times/ 10'' aluminum vacuum plate polished with jeweler's rouge prior to every casting. Solvent was removed in a forced air or vacuum oven. Removal and/or curing was accelerated with temperature. The fire-retardant bromine was required to be stable in alcohol/salt solutions. Final formulation used after a significant amount of testing was phenoxy resin PKHC in a ternary solvent system composed of methylethyl ketone, cellosolve acetate and toluene. Tetrabromobisphenol A was used as the flame retardant with FC-430 as surfactant. The dying schedule was 30 minutes at 150/degree/C. 4 refs., 6 figs., 3 tabs.

  9. Formation of THMs and HANs during bromination of Microcystis aeruginosa

    Institute of Scientific and Technical Information of China (English)

    Yunzhu Pu; Lingzhao Kong; Xin Huang; Guoji Ding; Naiyun Gao

    2013-01-01

    Bromine-contained disinfectants and biocides are widely used in swimming pools,recreational waters and cooling towers.The objective of this study was to evaluate the formation of thrihalomethanes (THMs) and haloacetonitriles (HANs) and their cytotoxicity in algae solutions during free bromine disinfection.Disinfection by-products formation potential experiments were conducted using modelsolutions containing 7mg/L (as total organic carbon) Microcystis aeruginosa cells.Effects of free bromine dosage,pH and ammonia were investigated.The results showed that brominated disinfection by-products were the major products when free bromine was applied.The total THMs formed during bromination was much as that formed during chlorination,whereas HANs were elevated by using bromination instead of chlorination.Dibromoacetonitrice (C2H2NBr2) and bromoform (CHBr3) were the only detected species during free bromine disinfection.The production of C2H2NBr2 and CHBr3 increased with disinfectant dosage but decreased with dosing ammonia.CHBr3 increased with the pH changing from 5 to 9.However,C2H2NBr2 achieved the highest production at neutral pH,which was due to a joint effect of variation in hydrolysis rate and free bromine reactivity.The hydrolysis of C2H2NBr2 was basecatalytic and nearly unaffected by disinfectant.Finally,estimation of cytotoxicity of the disinfected algae solutions showed that HANs formation was responsible for the majority of toxicity.Considering its highest toxicity among the measured disinfection by-products,the elevated C2H2NBr2 should be considered when using bromine-related algaecide.

  10. New infrared spectroscopic database for bromine nitrate

    Science.gov (United States)

    Wagner, Georg; Birk, Manfred

    2016-08-01

    Fourier transform infrared measurements of bromine nitrate have been performed in the spectral region 675-1400 cm-1 at 0.014 cm-1 spectral resolution. Absorption cross sections were derived from 38 spectra covering the temperature range from 203 to 296 K and air pressure range from 0 to 190 mbar. For line-by-line analysis, further spectra were recorded at 0.00094 cm-1 spectral resolution at 223 and 293 K. The sample was synthesized from ClONO2 and Br2. Band strengths of the bands ν3 around 803 cm-1 and ν2 around 1286 cm-1 were determined from three pure BrONO2 measurements at different temperatures and pressures. Number densities in the absorption cell were derived from pressure measurements of the purified sample taking into account small amounts of impurities determined spectroscopically. Resulting band strengths are Sν3 = 2.872(52) × 10-17 cm2 molec-1 cm-1 and Sν2 = 3.63(15) × 10-17 cm2 molec-1 cm-1. Absorption cross sections of all measurements were scaled to these band strengths. Further data reduction was achieved with an interpolation scheme based on two-dimensional polynomials in ln(pressure) and temperature. The database is well-suited for remote-sensing application and should reduce the atmospheric bromine nitrate error budget substantially.

  11. Use of Bromine and Bromo-Organic Compounds in Organic Synthesis.

    Science.gov (United States)

    Saikia, Indranirekha; Borah, Arun Jyoti; Phukan, Prodeep

    2016-06-22

    Bromination is one of the most important transformations in organic synthesis and can be carried out using bromine and many other bromo compounds. Use of molecular bromine in organic synthesis is well-known. However, due to the hazardous nature of bromine, enormous growth has been witnessed in the past several decades for the development of solid bromine carriers. This review outlines the use of bromine and different bromo-organic compounds in organic synthesis. The applications of bromine, a total of 107 bromo-organic compounds, 11 other brominating agents, and a few natural bromine sources were incorporated. The scope of these reagents for various organic transformations such as bromination, cohalogenation, oxidation, cyclization, ring-opening reactions, substitution, rearrangement, hydrolysis, catalysis, etc. has been described briefly to highlight important aspects of the bromo-organic compounds in organic synthesis.

  12. Determination of total chlorine and bromine in solid wastes by sintering and inductively coupled plasma-sector field mass spectrometry.

    Science.gov (United States)

    Osterlund, Heléne; Rodushkin, Ilia; Ylinenjärvi, Karin; Baxter, Douglas C

    2009-04-01

    A sample preparation method based on sintering, followed by analysis by inductively coupled plasma-sector field mass spectrometry (ICP-SFMS) for the simultaneous determination of chloride and bromide in diverse and mixed solid wastes, has been evaluated. Samples and reference materials of known composition were mixed with a sintering agent containing Na(2)CO(3) and ZnO and placed in an oven at 560 degrees C for 1h. After cooling, the residues were leached with water prior to a cation-exchange assisted clean-up. Alternatively, a simple microwave-assisted digestion using only nitric acid was applied for comparison. Thereafter the samples were prepared for quantitative analysis by ICP-SFMS. The sintering method was evaluated by analysis of certified reference materials (CRMs) and by comparison with US EPA Method 5050 and ion chromatography with good agreement. Median RSDs for the sintering method were determined to 10% for both chlorine and bromine, and median recovery to 96% and 97%, respectively. Limits of detection (LODs) were 200mg/kg for chlorine and 20mg/kg for bromine. It was concluded that the sintering method is suitable for chlorine and bromine determination in several matrices like sewage sludge, plastics, and edible waste, as well as for waste mixtures. The sintering method was also applied for determination of other elements present in anionic forms, such as sulfur, arsenic, selenium and iodine. PMID:19091539

  13. Bromine content and brominated flame retardants in food and animal feed from the UK.

    Science.gov (United States)

    Fernandes, A R; Mortimer, D; Rose, M; Smith, F; Panton, S; Garcia-Lopez, M

    2016-05-01

    Current occurrence data for polybrominated diphenyl ethers (PBDE) and hexa-bromocyclododecane (HBCD) measured in most commonly consumed foods (n = 156) and animal feeds (n = 51) sampled in the UK, demonstrates an ongoing ubiquity of these contaminants in human and animal diets. PBDE concentrations for the sum of 17 measured congeners ranged from 0.02 ng/g to 8.91 ng/g whole weight for food, and 0.11 ng/g to 9.63 ng/g whole weight for animal feeds. The highest concentration ranges, and mean values were detected in fish, processed foods and fish feeds. HBCD diastereomers (alpha-HBCD was the most commonly detected) generally occurred at lower concentrations (from animal feed) and less frequently than PBDEs, but tetrabromobisphenol A which was also measured, was rarely detected. The total bromine content of the samples was also determined in an attempt to use a mass balance approach to investigate some of these samples for the occurrence of novel and emerging BFRs. Although the approach was further refined by measuring organic bromine content, the concentrations of bromine were too high (in most cases by orders of magnitude) to allow use of the approach. A selected sub-set of samples was screened by GC-MS, for the presence of novel/emerging brominated flame retardants (PBT, TBX, PBEB, DBHCTD, HCTBPH and OBTMPI) but these were not detected at the higher limits of detection that result from full scan (GC-MS) screening. This data will contribute to the EU wide risk assessment on these contaminants.

  14. Ruthenium-Catalyzed meta-Selective C—H Bromination

    Science.gov (United States)

    Teskey, Christopher J; Lui, Andrew Y W; Greaney, Michael F

    2015-01-01

    The first example of a transition-metal-catalyzed, meta-selective C–H bromination procedure is reported. In the presence of catalytic [{Ru(p-cymene)Cl2}2], tetrabutylammonium tribromide can be used to functionalize the meta C–H bond of 2-phenylpyridine derivatives, thus affording difficult to access products which are highly predisposed to further derivatization. We demonstrate this utility with one-pot bromination/arylation and bromination/alkenylation procedures to deliver meta-arylated and meta-alkenylated products, respectively, in a single step. PMID:26288217

  15. Ruthenium-Catalyzed meta-Selective C—H Bromination

    OpenAIRE

    Teskey, Christopher J; Lui, Andrew Y W; Greaney, Michael F.

    2015-01-01

    The first example of a transition-metal-catalyzed, meta-selective C–H bromination procedure is reported. In the presence of catalytic [{Ru(p-cymene)Cl2}2], tetrabutylammonium tribromide can be used to functionalize the meta C–H bond of 2-phenylpyridine derivatives, thus affording difficult to access products which are highly predisposed to further derivatization. We demonstrate this utility with one-pot bromination/arylation and bromination/alkenylation procedures to deliver meta-arylated and...

  16. Magnetic Trapping of Cold Bromine Atoms

    CERN Document Server

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

    2014-01-01

    Magnetic trapping of bromine atoms at temperatures in the milliKelvin regime is demonstrated for the first time. The atoms are produced by photodissociation of Br$_2$ 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 only lost 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...

  17. Bromine and bromide in rainfall, cloud, stream and groundwater in the Plynlimon area of mid-Wales

    Directory of Open Access Journals (Sweden)

    2007-01-01

    Full Text Available Bromine in rainfall, cloud water, stream water and groundwater were measured in the upper River Severn catchments at Plynlimon in mid-Wales using two analytical procedures for bromide determination: a colorimetric method and, later, ion chromatography. Discrepancies between the methods indicated that the colorimetric method was measuring more than just bromide so it was "dissolved labile bromine" (DLBr (Neal et al., 2007. This paper reports the variation in DLBr and bromide across the Plynlimon region and assesses the differences between these two measures. The average DLBr concentration in the streams ranges between 18.3 and 27.8 µg l−1 compared with a rainfall average concentration of 15.6 µg l−1. The corresponding bromide concentrations in the streams are 13.8–18.6 µg l−1 and 13.2 µg l−1 in rainfall. For cloud water, throughfall and stemflow, DLBr concentrations are an order of magnitude higher than in rainfall and the concentrations are strongly correlated with chloride. Average values of bromide in rainfall and cloud water are similar to those of DLBr and are strongly correlated with chloride: unfortunately, no bromide measurements were taken in throughfall and stemflow. These results indicate that marine aerosol inputs are high and that the DLBr in these inputs is dominated by bromide. For cloud water, DLBr was correlated with dissolved organic carbon (DOC as well as with chloride; hence, there may well be an organic-associated component. Within the streams draining the forested areas, DLBr increases with time as DOC increases. DLBr concentrations in the streams are correlated with DOC in most cases and, to a lesser degree, with chloride. However, for bromide there is no correlation with DOC, but a weak correlation with chloride remains and the gradient is higher than for the DLBr case. Increasing concentrations of both DLBr and DOC may well reflect the wetting up of the catchments as transpiration diminshes as the trees age

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

    NARCIS (Netherlands)

    A.R. Mani (Ali); J.C. Moreno (José C.); T.J. Visser (Theo J.); 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 bromotyrosi

  19. 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

  20. Chloride ingress prediction

    DEFF Research Database (Denmark)

    Frederiksen, Jens Mejer; Geiker, Mette Rica

    2008-01-01

    Prediction of chloride ingress into concrete is an important part of durability design of reinforced concrete structures exposed to chloride containing environment. This paper presents experimentally based design parameters for Portland cement concretes with and without silica fume and fly ash in...

  1. Probing the tropical tropopause layer for organic and inorganic bromine

    Science.gov (United States)

    Werner, Bodo; Pfeilsticker, Klaus; Atlas, Elliot; Cheung, Ross; Chipperfield, Martyn; Colosimo, Fedele; Deutschmann, Tim; Elkins, Jim; Fahey, David; Feng, Wu; Festa, James; Gao, Ru-Shan; Hossaini, Ryan; Navarro, Maria; Raecke, Rasmus; Scalone, Lisa; Spolaor, Max; Thornberry, Troy; Tsai, Catalina; Stutz, Jochen

    2016-04-01

    Bromine chemistry impacts the levels of ozone in the upper troposphere and the stratosphere. An accurate quantitative understanding of the sources, sinks, and chemical transformation of bromine species is thus important to understand the photochemistry and budget of bromine in the tropical upper troposphere, tropopause layer and lowermost stratosphere (UT/TTL/LS). These regions are also known to serve as a gateway for delivery of ozone depleting gases to the stratosphere. CH3Br, halons, short-lived organic bromine precursors (VSLS), such as CHBr3, CH2Br2, and possibly inorganic product gases have been identified as the main bromine gases delivered to the stratosphere. However, many important details of the transport and delivery of VSLS and inorganic bromine compounds through the TTL are still uncertain. Moreover, a number of chemical processes, including the transformation of the source gases and cycling of inorganic bromine species at low ambient temperature and on ice particles are also poorly understood. The presentation reports measurements of CH4, O3, NO2, and BrO performed by different instruments and techniques during the 2013 NASA-ATTREX flights in the TTL and LS. The interpretation of our measurements is supported by chemical transport model (SLIMCAT) simulations. SLIMCAT results, in conjunction with extensive radiative transfer calculations using the Monte Carlo model McArtim, also are used to improve retrieval of O3, NO2, and BrO concentrations from limb scattered sunlight measurements made with the Differential Optical Absorption Spectroscopy (DOAS) technique during ATTREX. The chemical transport model also allows us to attribute observed concentration variations to transport and to photochemical processes. When properly accounting for the transport-related concentration variations in methane and ozone, we find that measured BrO mostly agrees with model simulations. An exception are regions where the contribution of the short-lived CH2Br2 or the

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

    Indian Academy of Sciences (India)

    Rajendra Dongre; Minakshi Thakur; Dinesh Ghugal; Jostna Meshram

    2012-10-01

    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 pretreatment alters porosity and specific surface area of chitosan by means of physicochemical interaction with cationic sites of chitosan skeleton, besides imparting anionic alteration at amino linkages of chitosan, to remove lead (II) by chemical interactions on superfluous active sites as characterized by FTIR, SEM, DTA and elemental analysis. Lead adsorptions were studied in batch mode by varying parameters viz. pH, bromine loading, sorbent dosage, initial lead concentration, contact time and temperature. The adsorption equilibrium data was well fitted to Freundlich isotherm and maximum sorption capacity of 30% bromine pretreated chitosan sorbent was 1.755 g/kg with 85–90% lead removal efficiency. Though cost and applicability of sorbent is unproven, yet contrast to raw chitosan derivatives, activated carbons and some resins, 30% bromine pretreated chitosan endow benign and efficient lead abatement technique.

  3. 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, sedime

  4. Environmental monitoring of brominated flame retardants

    Science.gov (United States)

    Vagula, Mary C.; Kubeldis, Nathan; Nelatury, Charles F.

    2011-06-01

    Brominated flame retardants (BFRs) are synthetic organobromide compounds which inhibit ignition and combustion processes. Because of their immense ability to retard fire and save life and property, they have been extensively used in many products such as TVs, computers, foam, plastics etc. The five major classes of BFRs are tetrabromobisphenol-A (TBBPA), hexabromocyclododecane (HBCD), pentabromodiphenyl ether, octabromodiphenyl ether, and decabromodiphenyl ether. The last three are also commonly called PBDEs. BDE-85 and BDE-209 are the two prominent congeners of PBDEs and this study reports the adverse effects of these congeners in rodents. Exposure of rat sciatic nerves to 5 μg/mL and 20 μg/mL of BDE-85 and BDE-209 respectively lead to significant, concentration dependent reduction in nerve conduction function. Glucose absorption in the rat intestinal segments exposed to 5 μg/mL of BDE-85 and BDE-209 was significantly reduced for both the compounds tested. Lastly, mice when exposed to 0.25 mg/kg body weight for four days showed a disruption in oxidant and antioxidant equilibrium. The tissues namely liver and brain have shown increase in the levels of lipid hydroperoxides indicating oxidative stress. Moreover, all the protective enzymes namely superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase, and glutathione S transferase (GST) have shown tissue specific alterations indicating the induction of damaging oxidative stress and setting in of lipid peroxidation in exposed animals. The results indicate monitoring of PBDEs in the environment is essential because levels as low as 5 μg/mL and 0.25 mg/kg body weight were able to cause damage to the functions of rodents.

  5. The geochemistry of stable chlorine and bromine isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Eggenkamp, Hans [Onderzock and Beleving, Bussum (Netherlands)

    2014-11-01

    First book solely dedicated to the geochemistry of chlorine and bromine isotopes. Detailed description of analytical techniques, including their advantages and disadvantages. Indication of research fields where measurement of these isotopes is especially useful. This book provides detailed information on the history, analysis and applications of chlorine and bromine isotope geochemistry. Chlorine and bromine are geochemically unique as they prefer to exist as single charged negative ions. For this reason isotope fractionation reflects mostly processes that are not related to changes in the redox state and this fractionation is generally modest. The book will describe the processes that are most easily detected using these isotopes. Also isotope variations, and processes that cause them, measured in oxidised species such as perchlorates and in organic molecules will be described in this book.

  6. 40 CFR 180.519 - Bromide ion and residual bromine; tolerances for residues.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Bromide ion and residual bromine... Tolerances § 180.519 Bromide ion and residual bromine; tolerances for residues. (a) General. The food additives, bromide ion and residual bromine, may be present in water, potable in accordance with...

  7. Chloride ingress prediction

    DEFF Research Database (Denmark)

    Frederiksen, Jens Mejer; Geiker, Mette Rica

    2008-01-01

    makes physical sense for the design engineer, i.e. the achieved chloride diffusion coefficients at 1 year and 100 years, D1 and D100 respectively, and the corresponding achieved chloride concentrations at the exposed concrete surface, C1 and C100. Data from field exposure supports the assumption of time...... dependent surface chloride concentrations and the diffusion coefficients. Model parameters for Portland cement concretes with and without silica fume and fly ash in marine atmospheric and submerged South Scandinavian environment are suggested in a companion paper based on 10 years field exposure data....

  8. Discovery of zinc, selenium, bromine, and neodymium isotopes

    International Nuclear Information System (INIS)

    Currently, thirty-two zinc, thirty-two selenium, twenty-nine bromine, and thirty-one neodymium isotopes have been observed and the discovery of these isotopes is described here. For each isotope a brief synopsis of the first refereed publication, including the production and identification method, is presented.

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

    NARCIS (Netherlands)

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

    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

  10. Bromine provides new weapons to combat mercury emissions

    Energy Technology Data Exchange (ETDEWEB)

    Hardtke, W. [Albermarle Europe (Germany)

    2011-04-15

    Brominated powdered activated carbon has been demonstrated to capture over 90% of mercury emissions from coal fired plants, operating at high temperatures and capturing the metal in concrete-friendly, non-leaching forms to help tackle a rising global health threat. 6 refs., 5 figs.

  11. 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.

  12. Discovery of Zinc, Selenium, Bromine, and Neodymium Isotopes

    OpenAIRE

    J.L. Gross; Claes, J.; Kathawa, J.; Thoennessen, M

    2010-01-01

    Currently, thirty-two zinc, thirty-two selenium, twenty-nine bromine and thirty-one neodymium isotopes have been observed and the discovery of these isotopes is discussed here. For each isotope a brief synopsis of the first refereed publication, including the production and identification method, is presented.

  13. 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. PMID:26504212

  14. 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.

  15. Chloride removal from vitrification offgas

    International Nuclear Information System (INIS)

    This study identified and investigated techniques of selectively purging chlorides from the low-level waste (LLW) vitrification process with the purge stream acceptable for burial on the Hanford Site. Chlorides will be present in high concentration in several individual feeds to the LLW Vitrification Plant. The chlorides are highly volatile in combustion type melters and are readily absorbed by wet scrubbing of the melter offgas. The Tank Waste Remediation System (TWRS) process flow sheets show that the resulting chloride rich scrub solution is recycled back to the melter. The chlorides must be purged from the recycle loop to prevent the buildup of excessively high chloride concentrations

  16. A chemical probe technique for the determination of reactive halogen species in aqueous solution: Part 2 – chloride solutions and mixed bromide/chloride solutions

    Directory of Open Access Journals (Sweden)

    C. Anastasio

    2006-02-01

    Full Text Available Although reactive halogen species (X*=X●, ●X2−, X2 and HOX, where X=Br, Cl, or I are important environmental oxidants, relatively little is known about their kinetics in condensed phases such as seawater and sea-salt particles. Here we describe a new technique to determine reactive chlorine and bromine species in aqueous solutions by using allyl alcohol (CH2=CHCH2OH as a chemical probe. This probe is combined with competition kinetics in order to determine steady state concentrations of X*(aq. In some cases the technique also can be used to determine the rates of formation and lifetimes of X* in aqueous solution. In a companion paper we reported the results of our method development for aqueous solutions containing only bromide (Br−. In this paper, we discuss method development for solutions containing chloride (Cl− alone, and for solutions containing both bromide and chloride.

  17. Bromination of hydrocarbons with CBr4, initiated by light-emitting diode irradiation

    Directory of Open Access Journals (Sweden)

    Yuta Nishina

    2013-08-01

    Full Text Available The bromination of hydrocarbons with CBr4 as a bromine source, induced by light-emitting diode (LED irradiation, has been developed. Monobromides were synthesized with high efficiency without the need for any additives, catalysts, heating, or inert conditions. Action and absorption spectra suggest that CBr4 absorbs light to give active species for the bromination. The generation of CHBr3 was confirmed by NMR spectroscopy and GC–MS spectrometry analysis, indicating that the present bromination involves the homolytic cleavage of a C–Br bond in CBr4 followed by radical abstraction of a hydrogen atom from a hydrocarbon.

  18. High selectively oxidative bromination of toluene derivatives by the H2O2-HBr system

    Institute of Scientific and Technical Information of China (English)

    Jie Ju; Yu Jin Li; Jian Rong Gao; Jian Hong Jia; Liang Han; Wei Jian Sheng; Yi Xia Jia

    2011-01-01

    An aqueous solution of hydrogen peroxide and hydrogen bromide illuminated by a 60 W incandescent light bulb serves as a source of bromine radicals. Various substituted toluenes (NO2,Cl, Br, H, CH3) were high selectively brominated at the benzyl position for monobromination in CH2C12 at ice water with catalyst free. This simple but effective bromination of toluene derivatives with an aqueous H2O2-HBr system is characterized with the use of inexpensive reagents and a lower impact on the environment, which make it a good alternative to the existing bromination methods.

  19. Elemental Bromine Production by TiO2 Photocatalysis and/or Ozonation.

    Science.gov (United States)

    Parrino, Francesco; Camera Roda, Giovanni; Loddo, Vittorio; Palmisano, Leonardo

    2016-08-22

    Significant production of elemental bromine (Br2 ) was observed for the first time when treating bromide containing solutions at acidic pH, with TiO2 photocatalyst, ozone, or a combination thereof. Br2 selectivities up to approximately 85 % were obtained and the corresponding bromine mass balance values satisfied. The process is general and may be applied at a laboratory scale for green bromination reactions, or industrially as a cheap, safe, and environmentally sustainable alternative to the currently applied bromine production methods.

  20. 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.

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

    OpenAIRE

    Tas, E.; Peleg, M.; D. U. Pedersen; Matveev, V; Pour Biazar, A.; Luria, M.

    2006-01-01

    International audience 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. ...

  2. Inorganic bromine in the marine boundary layer: a critical review

    Directory of Open Access Journals (Sweden)

    R. Sander

    2003-06-01

    Full Text Available The cycling of inorganic bromine in the marine boundary layer (mbl has received increased attention in recent years. Bromide, a constituent of sea water, is injected into the atmosphere in association with sea-salt aerosol by breaking waves on the ocean surface. Measurements reveal that supermicrometer sea-salt aerosol is depleted in bromine by about 50% relative to conservative tracers, whereas marine submicrometer aerosol is often enriched in bromine. Model calculations, laboratory studies, and field observations strongly suggest that these depletions reflect the chemical transformation of particulate bromide to reactive inorganic gases that influence the processing of ozone and other important constituents of marine air. However, currently available techniques cannot reliably quantify many chem{Br}-containing compounds at ambient concentrations and, consequently, our understanding of inorganic Br cycling over the oceans and its global significance are uncertain. To provide a more coherent framework for future research, we have reviewed measurements in marine aerosol, the gas phase, and in rain. We also summarize sources and sinks, as well as model and laboratory studies of chemical transformations. The focus is on inorganic bromine over the open oceans, excluding the polar regions. The generation of sea-salt aerosol at the ocean surface is the major tropospheric source producing about 6.2 Tg/a of bromide. The transport of  Br from continents (as mineral aerosol, and as products from biomass-burning and fossil-fuel combustion can be of local importance. Transport of degradation products of long-lived Br-containing compounds from the stratosphere and other sources contribute lesser amounts. Available evidence suggests that, following aerosol acidification, sea-salt bromide reacts to form Br2 and BrCl that volatilize to the gas phase and photolyze in daylight to produce atomic Br and Cl. Subsequent transformations can destroy

  3. [Degradation of succinylcholine chloride].

    Science.gov (United States)

    Németh, G; Török, I; Paál, T

    1993-05-01

    Quantitative thin-layer chormatographic method has been developed for the investigation of the degradation of injection formulations containing succinylcholinium chloride. The method is based on the denistometric determination of the main degradation product, choline at 430 nm after visualization with iodine vapour. The stability of the injection was investigated under various storage conditions and it has been stated that considerable decomposition takes place during as short a period as one week. PMID:8362654

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

    International Nuclear Information System (INIS)

    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 20α-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·, Br2·−) 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: ► Brominated derivatives of salicylic acid were detected in a brackish lagoon. ► A photochemical pathway was hypothesized to account for bromination of salicylic acid. ► Radical bromine species are partly responsible for the bromination process. ► Hypobromous acid might

  5. 40 CFR 721.775 - Brominated aromatic com-pound (generic name).

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Brominated aromatic com-pound (generic name). 721.775 Section 721.775 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.775 Brominated aromatic com-pound (generic name). (a)...

  6. Visible-light photoredox catalysis enabled bromination of phenols and alkenes

    Directory of Open Access Journals (Sweden)

    Yating Zhao

    2014-03-01

    Full Text Available A mild and efficient methodology for the bromination of phenols and alkenes has been developed utilizing visible light-induced photoredox catalysis. The bromine was generated in situ from the oxidation of Br− by Ru(bpy33+, both of which resulted from the oxidative quenching process.

  7. The Evolution of a Green Chemistry Laboratory Experiment: Greener Brominations of Stilbene

    Science.gov (United States)

    McKenzie, Lallie C.; Huffman, Lauren M.; Hutchison, James E.

    2005-01-01

    The use of green metrics to compare three bromination laboratory procedures demonstrates the effectiveness of an incremental greening process for chemistry curricula. Due to this process, the bromination of alkenes can be introduced to students through the use of a safe, effective, modern practice.

  8. Accurate measurement of bromine contents in plastic samples by instrumental neutron activation analysis.

    Science.gov (United States)

    Kim, I J; Lee, K S; Hwang, E; Min, H S; Yim, Y H

    2013-03-26

    Accurate measurements of bromine contents in plastic samples were made by the direct comparator instrumental neutron activation analysis (INAA). Individual factors affecting the measurements were comprehensively evaluated and compensated, including the volatility loss of bromine from standard comparators, the background bromine level in the filter papers used for preparation of the standard comparators, nuclear interference, γ-ray spectral interference and the variance among replicates of the samples. Uncertainty contributions from those factors were thoroughly evaluated and included in the uncertainty budgeting of the INAA measurement. (81)Br was chosen as the target isotope, and the INAA measurements for bromine were experimentally confirmed to exhibit good linearity within a bromine content range of 10-170 μg. The established method has been applied to the analysis of eight plastic samples: four commercially available certified reference materials (CRMs) of polyethylene and polystyrene and four acrylonitrile butadiene styrene (ABS) samples prepared as the candidate reference materials (KRISS CRM 113-01-012, -013, -014 and -015). The bromine contents of the samples were calculated at three different γ-ray energies and compared, showing good agreement. The results of the four CRMs also showed good consistency with their certified values within the stated uncertainties. Finally, the bromine contents of the ABS samples were determined with expanded uncertainties (at a 95% level of confidence) between 2.5% and 5% in a bromine content range of 25-900 mg kg(-1). PMID:23498117

  9. The Cyclotron Production and Nuclear Imaging of BROMINE-77.

    Science.gov (United States)

    Galiano, Eduardo

    In this investigation, bromine-77 was produced with a medical cyclotron and imaged with gamma cameras. Br -77 emits a 240 kev photon with a half life of 56 hours. The C-Br bond is stronger than the C-I bond and bromine is not collected in the thyroid. Bromine can be used to label many organic molecules by methods analogous to radioiodination. The only North American source of Br-77 in the 70's and 80's was Los Alamos National Laboratory, but it discontinued production in 1989. In this method, a p,3n reaction on Br-77 produces Kr-77 which decays with a 1.2 hour half life to Br-77. A cyclotron generated 40 MeV proton beam is incident on a nearly saturated NaBr or LiBr solution contained in a copper or titanium target. A cooling chamber through which helium gas is flowed separates the solution from the cyclotron beam line. Helium gas is also flowed through the solution to extract Kr-77 gas. The mixture flows through a nitrogen trap where Kr-77 freezes and is allowed to decay to Br-77. Eight production runs were performed, three with a copper target and five with a titanium target with yields of 40, 104, 180, 679, 1080, 685, 762 and 118 uCi respectively. Gamma ray spectroscopy has shown the product to be very pure, however corrosion has been a major obstacle, causing the premature retirement of the copper target. Phantom and in-vivo rat nuclear images, and an autoradiograph in a rat are presented. The quality of the nuclear scans is reasonable and the autoradiograph reveals high isotope uptake in the renal parenchyma, a more moderate but uniform uptake in pulmonary and hepatic tissue, and low soft tissue uptake. There is no isotope uptake in the brain or the gastric mucosa.

  10. Preparation of bromine-77 labeled proteins using bromoperoxidase

    Energy Technology Data Exchange (ETDEWEB)

    Lambert, F.; Slegers, G. (Ghent Univ. (Belgium). Lab. of Radiopharmacy)

    1994-01-01

    The halogenating enzyme bromoperoxidase, isolated from the brown algae Ascophyllum nodosum, was used to catalyze the radiobromination of an anti-hPLAP monoclonal antibody. Radiobromination of bovine serum albumin was also performed and used as control method. The proteins are labeled with bromine-77, produced by the [sup 75]As ([alpha], 2n) [sup 77]Br reaction. The essential reaction parameters, such as concentration of protein and hydrogen peroxide, the amount of bromoperoxidase, the pH of the reaction mixture, the reaction time and temperature were optimized. The immunoreactivity of the radiolabeled monoclonal antibody was checked with a ''Sandwich'' ELISA. (author).

  11. 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.

  12. Labeling of receptor ligands with bromine radionuclides. Progress report, March 1, 1981-February 28, 1982

    International Nuclear Information System (INIS)

    In recent years there has been an interest in the use of various radioisotopes of bromine as labels for radiopharmaceuticals. Although radioisotopes of iodine have been used extensively as radiopharmaceutical labels, there are several advantages associated with the use of radiobromine as a label, due primarily to increased stability of bonds to the radiohalide and smaller steric perturbation resulting from substitution of the radiohalide. Methods of attaching radiobromine to receptor ligands with the potential of mapping estrogen receptors in mammary tumors and uteri were studied. Two ligands were studied extensively in vitro and in animal models; preliminary studies were also carried out in humans. To date, the only radioisotope of bromine used was bromine-77. In addition, a series of model compounds were labeled with bromine-77 using a recently described method for rapid bromination; the scope and limitations of this new rapid radiobromination technique were evaluated

  13. Effect of bromine substituents in the formation of PXDD from poly halogenated phenols

    Energy Technology Data Exchange (ETDEWEB)

    Sakurai, T.; Ohono, T.; Weber, R.

    2002-07-01

    The condensation of chlorophenols has been studied extensively in the last two decades and was discussed as one mechanism in particular for the formation of PCDD in thermal processes. Brominated flame retardants and brominated and brominated-chlorinated dibenzodioxins and dibenzofurans have received increased attention recently due to the growing use of brominated flame retardants during the last decade. This is resulting than increase of brominated compounds in waste (e.g. Electric and electronic shredder waste), containing a considerable amount of bromine, in the form of brominated flame retardants. Many studies reported on the formation of PBDD/PBDF from brominated diphenylethers, or bromophenosl. However with the exception of Sodhu et al, a comparison of the condensation behaviour of bromophenols and chlorophenols was not done. The condensation of brominated phenols is interesting from several aspects. Bromophenols are used as flame retardants and might be a source of PBDD/F during thermal stress. Bromophenols can also be generated during the combustion/pyrolysis of bromodiphenylether or tetrabromobisphenol A containing material, serving as potential precursors for the formation of PBDD/PBDF. Further, in municipal waste incinerators with sufficient secondary combustion, the largest amount of chlorinated aromatic compounds (PCDD, PCDF, PCBs, PCNs, and chlorophenols) are formed in the cooling section (boiler, duct, dust filtration). Therefore in combustion processes involving high concentrations of brominated flame retardants, mixed PXDD/PXDF might be formed by condensation reactions of precursors or de novo synthesis in the cooling zone. Therefore we investigated the condensation of abrominated phenol in more detail and compare it to the condensation reaction of the analogous chlorophenol. (Author)

  14. 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.

  15. Comparative environmental analysis of waste brominated plastic thermal treatments

    International Nuclear Information System (INIS)

    The aim of this research activity is to investigate the environmental impact of different thermal treatments of waste electric and electronic equipment (WEEE), applying a life cycle assessment methodology. Two scenarios were assessed, which both allow the recovery of bromine: (A) the co-combustion of WEEE and green waste in a municipal solid waste combustion plant, and (B) the staged-gasification of WEEE and combustion of produced syngas in gas turbines. Mass and energy balances on the two scenarios were set and the analysis of the life cycle inventory and the life cycle impact assessment were conducted. Two impact assessment methods (Ecoindicator 99 and Impact 2002+) were slightly modified and then used with both scenarios. The results showed that scenario B (staged-gasification) had a potentially smaller environmental impact than scenario A (co-combustion). In particular, the thermal treatment of staged-gasification was more energy efficient than co-combustion, and therefore scenario B performed better than scenario A, mainly in the impact categories of 'fossil fuels' and 'climate change'. Moreover, the results showed that scenario B allows a higher recovery of bromine than scenario A; however, Br recovery leads to environmental benefits for both the scenarios. Finally the study demonstrates that WEEE thermal treatment for energy and matter recovery is an eco-efficient way to dispose of this kind of waste

  16. 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 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.

  17. Valyl benzyl ester chloride

    Directory of Open Access Journals (Sweden)

    Grzegorz Dutkiewicz

    2010-02-01

    Full Text Available In the title compound (systematic name: 1-benzyloxy-3-methyl-1-oxobutan-2-aminium chloride, C12H18NO2+·Cl−, the ester group is approximately planar, with a maximum deviation of 0.040 (2 Å from the least-squares plane, and makes a dihedral angle of 28.92 (16° with the phenyl ring. The crystal structure is organized by N—H...Cl hydrogen bonds which join the two components into a chain along the b axis. Pairs of chains arranged antiparallel are interconnected by further N—H...Cl hydrogen bonds, forming eight-membered rings. Similar packing modes have been observed in a number of amino acid ester halides with a short unit-cell parameter of ca 5.5 Å along the direction in which the chains run.

  18. Pulse radiolysis studies of the reactions of bromine atoms and dimethyl sulfoxide-bromine atom complexes with alcohols

    International Nuclear Information System (INIS)

    Dimethylsulfoxide (DMSO)-Br complexes were generated by pulse radiolysis of DMSO/bromomethane mixtures and the formation mechanism and spectral characteristics of the formed complexes were investigated in detail. The rate constant for the reaction of bromine atoms with DMSO and the extinction coefficient of the complex were obtained to be 4.6x109 M-1 s-1 and 6300 M-1 cm-1 at the absorption maximum of 430 nm. Rate constants for the reaction of bromine atoms with a series of alcohols were determined in CBrCl3 solutions applying a competitive kinetic method using the DMSO-Br complex as the reference system. The obtained rate constants were ∼108 M-1 s-1, one or two orders larger than those reported for highly polar solvents. Rate constants of DMSO-Br complexes with alcohols were determined to be ∼ 107 M-1 s-1. A comparison of the reactivities of Br atoms and DMSO-Br complexes with those of chlorine atoms and chlorine atom complexes which are ascribed to hydrogen abstracting reactants strongly indicates that hydrogen abstraction from alcohols is not the rate determining step in the case of Br atoms and DMSO-Br complexes

  19. 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.

  20. 40 CFR 61.65 - Emission standard for ethylene dichloride, vinyl chloride and polyvinyl chloride plants.

    Science.gov (United States)

    2010-07-01

    ... dichloride, vinyl chloride and polyvinyl chloride plants. 61.65 Section 61.65 Protection of Environment... dichloride, vinyl chloride and polyvinyl chloride plants. An owner or operator of an ethylene dichloride, vinyl chloride, and/or polyvinyl chloride plant shall comply with the requirements of this section....

  1. Brominated lipids identify lipid binding sites on the surface of the reaction center from Rhodobacter sphaeroides.

    Science.gov (United States)

    Roszak, Aleksander W; Gardiner, Alastair T; Isaacs, Neil W; Cogdell, Richard J

    2007-03-20

    This study describes the use of brominated phospholipids to distinguish between lipid and detergent binding sites on the surface of a typical alpha-helical membrane protein. Reaction centers isolated from Rhodobacter sphaeroides were cocrystallized with added brominated phospholipids. X-ray structural analysis of these crystals has revealed the presence of two lipid binding sites from the characteristic strong X-ray scattering from the bromine atoms. These results demonstrate the usefulness of this approach to mapping lipid binding sites at the surface of membrane proteins.

  2. Enhancement of the carbon electrode capacitance by brominated hydroquinones

    Science.gov (United States)

    Gastol, Dominika; Walkowiak, Jedrzej; Fic, Krzysztof; Frackowiak, Elzbieta

    2016-09-01

    This paper presents supercapacitors utilizing new redox-active electrolytes with bromine species. Two sources of Br specimen were investigated, i.e. dibromodihydroxybenzene dissolved in KOH and potassium bromide dissolved in KOH with hydroxybenzene additive. KOH-activated carbon, exhibiting a well-developed porosity, was incorporated as an electrode material. The tested systems revealed a capacitance enhancement explained by Br- and partial BrO3- redox activity. The optimisation of the electrolyte concentration resulted in a capacitance value of 314 F g-1 achieved at 1.1 V voltage range. Good cyclability performance (11% capacitance loss) combined with a high capacitance value (244 F g-1) were obtained for the system operating in 0.2 mol L- 1 C6H4Br2O2 in 2 mol L-1 KOH electrolytic solution.

  3. Selective nitration and bromination of surprisingly ruffled phosphorus corroles.

    Science.gov (United States)

    Pomarico, Giuseppe; Tortora, Luca; Fronczek, Frank R; Smith, Kevin M; Paolesse, Roberto

    2016-05-01

    Phosphorus complexes of corrole have recently attracted increasing interest since these compounds can be easily prepared in good yields, are stable, and show unusual optical properties. For these reasons, phosphorus corroles represent a class of interesting compounds to be exploited in the field of material science or for biomedical investigations and the definition of synthetic pathways for their functionalization is an important step to optimize their properties for various applications. We report here the reactivity of the phosphorus complex of 5,10,15-tritolylcorrole in the nitration or bromination reaction. Both these attempts were successful, allowing the preparation of substituted phosphorus corroles, which can be used as intermediates of more complex architectures endowed with useful properties. Furthermore, the crystallographic characterization of both complexes shows that they have an unusual ruffled geometry of the corrole core, a conformation that has not been considered possible for such a macrocycle.

  4. The third international interlaboratory study on brominated flame retardants

    Energy Technology Data Exchange (ETDEWEB)

    Boer, J. de [Netherlands Institute for Fisheries Research, IJmuiden (Netherlands); Wells, D. [FRS Marine Laboratory, Aberdeen (United Kingdom)

    2004-09-15

    Polybrominated diphenyl ethers (PBDEs) have been produced as brominated flame retardants (BFRs) since the early 1970s and have been found in the aquatic environment since the late 1970s. However, as a result of their detection in sperm whales from deeper Atlantic waters and in human milk, many laboratories are now measuring PBDEs in environmental samples. A first international interlaboratory study (ILS) on the analysis of PBDEs, organised by the Bromine Science and Environmental Forum (BSEF), Brussels, Belgium, in collaboration with the Netherlands Institute for Fisheries Research (RIVO) was conducted in 1999-2000. The results showed that the 18 participating laboratories produced comparable results for BDE 47 in various matrices but had analytical difficulties for other BDEs, in particular for the BDEs 99 and 209. A second study was organised in 2001-2002 by BSEF, QUASIMEME and RIVO. That study showed improvement in comparability of the participating laboratories for BDE99 and some other BDEs. However, there was no improvement for BDE209. Hexabromocyclododecane (HBCD), tetrabromobisphenol-A (TBBP-A) and the dimethyl derivative of TBBP-A (dimethyl TBBP-A) were included in the second study. However, it appeared that only two or three laboratories were able to analyse these determinands. Others laboratories were still in the development phase with their methods for these BFRs. This third study was organised as a development exercise by QUASIMEME, in collaboration with RIVO between September and December 2003. The BFRs selected were the same as in the second study. Two biota test materials, a harbor sediment, a sewage sludge, and two standard solutions were dispatched to the participants.

  5. Sodium chloride, potassium chloride, and virulence in Listeria monocytogenes.

    OpenAIRE

    MYERS, E. R.; Dallmier, A W; Martin, S E

    1993-01-01

    Virulence, as determined in a mouse model, and the virulence factor activities of catalase, superoxide dismutase, and listeriolysin O were examined in a parental strain (10403S) and in a nonhemolytic mutant strain (DP-L224) of Listeria monocytogenes. The cells were propagated in media containing various concentrations of sodium chloride or potassium chloride. Strains 10403S and DP-L224 exhibited significant increases in catalase activity and listeriolysin O activity when grown in medium conta...

  6. Dynamic dielectric properties and the γ transition of bromine doped polyacrylonitrile

    Directory of Open Access Journals (Sweden)

    2007-10-01

    Full Text Available Based on monitoring the γ process (the lowest temperature-relaxation in polyacrylonitrile (PAN by dynamic dielectric spectroscopy, new evidence for the formation of a charge transfer complex between bromine dopants and nitrile groups is presented. The experimental work is carried out on PAN and nitrile polymerized PAN with and without bromine doping and the effects of these factors on the γ process are measured. Nitrile polymerization results in diminishing of the γ process and in a 15% increase in its activation energy, whereas bromine doping produces splitting of the original γ process in PAN – coupled with a significant activation energy increase – and its complete disappearance in nitrile polymerized PAN. Both the splitting of the γ process and the higher activation energy reflect bromine-nitrile adduct formation..

  7. Potent competitive interactions of some brominated flame retardants and related compounds with human transthyretin in vitro

    NARCIS (Netherlands)

    Meerts, I.A.T.M.; Zanden, van J.J.; Luijks, E.A.C.; Leeuwen-Bol, van I.; Marsh, G.; Jakobsson, E.; Bergman, A.; Brouwer, A.

    2000-01-01

    Brominated flame retardants such as polybrominated diphenyl ethers (PBDEs), pentabromophenol (PBP), and tetrabromobisphenol A (TBBPA) are produced in large quantities for use in electronic equipment, plastics, and building materials. Because these compounds have some structural resemblance to the th

  8. A Novel Protocol for the Regioselective Bromination of Primary Alcohols in Unprotected Carbohydrates or Glycosides

    Institute of Scientific and Technical Information of China (English)

    薛伟华; 张立芬

    2012-01-01

    The regioselective and efficient bromination of primary hydroxyl groups in unprotected carbohydrates or glycosides is successfully achieved by using (chloro-phenylthio-methylene)dimethylammoniumchloride (CPMA) in the presence of tetrabutylammonium bromide (TBAB) in dry DMF.

  9. Bromine determination by neutron activation analysis and its distribution in the atmosphere

    International Nuclear Information System (INIS)

    Bromine, one of the main participants in ozone layer destruction, is 10 to 100 times more effective than chlorine. There are two principal sources of methyl bromide emissions: the oceans and some pesticides that are used in farming. Bromine was detected in 'premium' and 'magna sin' gasolines (2.86±0.96 and 1.54±0.38 ppm, respectively) as well as in condensed water found in exhaust pipes of vehicles. In addition, samples of rainwater were also analyzed to determine atmospheric bromine concentration. In water samples Br concentrations ranging from 2.09 to 0.06 ppm were found. The techniques utilised were neutron activation analysis and high voltage electrophoresis, the latter to determine the chemical form of bromine in condensed water samples. Finally, suspended particles from rainwater were also analysed by scanning electron microscopy (SEM). (author)

  10. 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

  11. METHOD OF SEPARATING URANIUM, PLUTONIUM AND FISSION PRODUCTS BY BROMINATION AND DISTILLATION

    Science.gov (United States)

    Jaffey, A.H.; Seaborg, G.T.

    1958-12-23

    The method for separation of plutonium from uranium and radioactive fission products obtained by neutron irradiation of uranlum consists of reacting the lrradiated material with either bromine, hydrogen bromide, alumlnum bromide, or sulfur and bromine at an elevated temperature to form the bromides of all the elements, then recovering substantlally pure plutonium bromide by dlstillatlon in combinatlon with selective condensatlon at prescribed temperature and pressure.

  12. Bromine-lithium exchange: An efficient tool in the modular construction of biaryl ligands.

    Science.gov (United States)

    Bonnafoux, Laurence; Leroux, Frédéric R; Colobert, Françoise

    2011-01-01

    Regioselective bromine-lithium exchange reactions on polybrominated biaryls enable the modular synthesis of various polysubstituted biphenyls such as bis(dialkylphosphino)-, bis(diarylphosphino)- and dialkyl(diaryl)phosphinobiphenyls. All permutations of substituents at the ortho positions of the biphenyls are possible. In a similar manner, one can gain access to monophosphine analogues. So far, such a process, based on the effective discrimination between bromine atoms as a function of their chemical environment, has been observed only sporadically.

  13. Bromine atom production and chain propagation during springtime Arctic ozone depletion events in Barrow, Alaska

    OpenAIRE

    Thompson, Chelsea R.; Shepson, Paul B.; Liao, Jin; Huey, L. Greg; Cantrell, Chris; Flocke, Frank; Orlando, John

    2016-01-01

    Ozone depletion events (ODEs) in the Arctic are primarily controlled by a bromine radical-catalyzed destruction mechanism that depends on the efficient production and recycling of Br atoms. Numerous laboratory and modeling studies have suggested the importance of heterogeneous recycling of Br through HOBr reaction with bromide on saline surfaces. However, the gas-phase regeneration of bromine atoms through BrO-BrO radical reactions has been assumed to be an efficient, if not dominant, pa...

  14. Gaia Paradigm: A Biotic Origin Of The Polar Sunrise Arctic Bromine Explosion

    OpenAIRE

    Iudin, M.

    2008-01-01

    The main attention is given to discussion of the natural causes and regularities of the Arctic bromine pollution. We make notice of marine microbial organisms and their metabolism as a prime driving force for the elemental biogeochemical cycles. One of the important conclusions of this study is on similarity between ocean bromine concentrating as by-product of the marine microbial activities and nitrogen fixation by soil bacteria. In both cases, microbial organisms and their food webs maintai...

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

    OpenAIRE

    Bai, Peng; Bazant, Martin Z.

    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, wh...

  16. Chloride channels in stroke

    Institute of Scientific and Technical Information of China (English)

    Ya-ping ZHANG; Hao ZHANG; Dayue Darrel DUAN

    2013-01-01

    Vascular remodeling of cerebral arterioles,including proliferation,migration,and apoptosis of vascular smooth muscle cells (VSMCs),is the major cause of changes in the cross-sectional area and diameter of the arteries and sudden interruption of blood flow or hemorrhage in the brain,ie,stroke.Accumulating evidence strongly supports an important role for chloride (Clˉ) channels in vascular remodeling and stroke.At least three Clˉ channel genes are expressed in VSMCs:1) the TMEM16A (or Ano1),which may encode the calcium-activated Clˉ channels (CACCs); 2) the CLC-3 Clˉ channel and Clˉ/H+ antiporter,which is closely related to the volume-regulated Clˉ channels (VRCCs); and 3) the cystic fibrosis transmembrane conductance regulator (CFTR),which encodes the PKA-and PKC-activated Clˉ channels.Activation of the CACCs by agonist-induced increase in intracellular Ca2+ causes membrane depolarization,vasoconstriction,and inhibition of VSMC proliferation.Activation of VRCCs by cell volume increase or membrane stretch promotes the production of reactive oxygen species,induces proliferation and inhibits apoptosis of VSMCs.Activation of CFTR inhibits oxidative stress and may prevent the development of hypertension.In addition,Clˉ current mediated by gammaaminobutyric acid (GABA) receptor has also been implicated a role in ischemic neuron death.This review focuses on the functional roles of Clˉ channels in the development of stroke and provides a perspective on the future directions for research and the potential to develop Clˉ channels as new targets for the prevention and treatment of stroke.

  17. Vanadate-dependent bromoperoxidases from Ascophyllum nodosum in the synthesis of brominated phenols and pyrroles.

    Science.gov (United States)

    Wischang, Diana; Radlow, Madlen; Hartung, Jens

    2013-09-01

    Bromoperoxidases from the brown alga Ascophyllum nodosum, abbreviated as V(Br)PO(AnI) and V(Br)PO(AnII), show 41% sequence homology and differ by a factor of two in the percentage of α-helical secondary structures. Protein monomers organize into homodimers for V(Br)PO(AnI) and hexamers for V(Br)PO(AnII). Bromoperoxidase II binds hydrogen peroxide and bromide by approximately one order of magnitude stronger than V(Br)PO(AnI). In oxidation catalysis, bromoperoxidases I and II turn over hydrogen peroxide and bromide similarly fast, yielding in morpholine-4-ethanesulfonic acid (MES)-buffered aqueous tert-butanol (pH 6.2) molecular bromine as reagent for electrophilic hydrocarbon bromination. Alternative compounds, such as tribromide and hypobromous acid are not sufficiently electrophilic for being directly involved in carbon-bromine bond formation. A decrease in electrophilicity from bromine via hypobromous acid to tribromide correlates in a frontier molecular orbital (FMO) analysis with larger energy gaps between the π-type HOMO of, for example, an alkene and the σ*(Br,X)-type LUMO of the bromination reagent. By using this approach, the reactivity of substrates and selectivity for carbon-bromine bond formation in reactions mediated by vanadate-dependent bromoperoxidases become predictable, as exemplified by the synthesis of bromopyrroles occurring naturally in marine sponges of the genera Agelas, Acanthella, and Axinella. PMID:23881071

  18. Photothermally induced bromination of carbon/polymer bipolar plate materials for fuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Schade, Martin; Franzka, Steffen [Fakultät für Chemie, Universität Duisburg-Essen, 45117 Essen (Germany); Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Carl-Benz-Straße 199, 47057 Duisburg (Germany); Cappuccio, Franco; Peinecke, Volker; Heinzel, Angelika [Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Carl-Benz-Straße 199, 47057 Duisburg (Germany); Zentrum für BrennstoffzellenTechnik (ZBT), Carl-Benz-Straße 201, 47057 Duisburg (Germany); Hartmann, Nils, E-mail: nils.hartmann@uni-due.de [Fakultät für Chemie, Universität Duisburg-Essen, 45117 Essen (Germany); Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Carl-Benz-Straße 199, 47057 Duisburg (Germany)

    2015-05-01

    Graphical abstract: - Highlights: • Photothermal laser bromination of carbon/polymer materials is demonstrated. • Using a microfocused laser functionalized domains with diameters of 5 μm and 100 μm and more can be fabricated. • Bromine groups can be transformed in a variety of other chemical functionalities, i.e. amine groups. • Depending on the chemical functionality, the local chemical affinity and wettability is changed. • The routine can be applied to standard bipolar plate materials used for fuel cell applications. - Abstract: A facile photothermal procedure for direct functionalization of carbon/polymer bipolar plate materials is demonstrated. Through irradiation with a microfocused beam of an Ar{sup +}-laser at λ = 514 nm in gaseous bromine and distinct laser powers and pulse lengths local bromination of the carbon/polymer material takes place. At a 1/e spot diameter of 2.1 μm, functionalized surface areas with diameters down to 5 μm are fabricated. In complementary experiments large-area bromination is investigated using an ordinary tungsten lamp. For characterization contact angle goniometry, X-ray photoelectron spectroscopy and electron microscopy in conjunction with labeling techniques are employed. After irradiation bromine groups can easily be substituted by other chemical functionalities, e.g. azide and amine groups. This provides a facile approach in order to fabricate surface patterns and gradient structures with varying wetting characteristics. Mechanistic aspects and prospects of photothermal routines in micropatterning of carbon/polymer materials are discussed.

  19. Springtime surface ozone fluctuations at high Arctic latitudes and their possible relationship to atmospheric bromine

    Science.gov (United States)

    Oltmans, Samuel J.; Sheridan, Patrick J.; Schnell, Russell C.; Winchester, John W.

    1988-01-01

    At high Arctic stations such as Barrow, Alaska, springtime near-surface ozone amounts fluctuate between the highest and lowest values seen during the course of the year. Episodes when the surface ozone concentration is essentially zero last up to several days during this time of year. In the Arctic Gas and Aerosol Sampling Program (AGASP-I and AGASP-II) in 1983 and 1986, it was found that ozone concentrations often showed a very steep gradient in altitude with very low values near the surface. The cold temperatures, and snow-covered ground make it unlikely that the surface itself would rapidly destroy significant amounts of ozone. The AGASP aircraft measurements that found low ozone concentrations in the lowest layers of the troposphere also found that filterable excess bromine (the amount of bromine in excess of the sea salt component) in samples collected wholly or partially beneath the temperature inversion had higher bromine concentrations than other tropospheric samples. Of the four lowest ozone minimum concentrations, three of them were associated with the highest bromine enrichments. Surface measurements of excess filterable bromine at Barrow show a strong seasonal dependence with values rising dramatically early in March, then declining in May. The concentration of organic bromine gases such as bromoform rise sharply during the winter and then begin to decline after March with winter and early spring values at least three times greater than the summer minimum.

  20. Addition of bromine as a diagnostic gas to inertial confinement fusion target microspheres

    International Nuclear Information System (INIS)

    Currently, direct fuel rho r measurements on Inertial Confinement Fusion (ICF) targets by neutron activation of the argon tracer gas mixed with the DT fuel would require a 100 fold increase in neutron yield. Bromine, on the other hand, has excellent properties for neutron activation analysis at neutron yields of 10two' to 108, when present at an internal pressure of from 0.1 to 0.2 atmospheres. Bromine addition is accomplished in a 2 furnace system using the dried-gel method of microsphere production. An upper furnace operated at 15000C is separated from a lower furnace by a cooled zone. The lower furnace is filled with bromine gas and operated at approximately 12500C. The upper furnace is the glass production furnace. The cooled zone in between the upper and lower furnace is to prevent the hot bromine gas from rising into the upper furnace. The microspheres pass through the cooled zone and immediately into the 12500C bromine furnace where the bromine permeates into the spheres

  1. XPS STUDIES ON SURFACE MODIFIED POLY[1-(TRIMETHYLSILYL)-1-PROPYNE] MEMBRANES Ⅱ SURFACE MODIFICATION BY BROMINE VAPOR

    Institute of Scientific and Technical Information of China (English)

    XU Guanfan; SUN Xiaoguang; QIU Xuepeng; ZHANG Jinlan; ZHENG Guodong

    1994-01-01

    Surface modification of poly [ 1-(trimethylsilyl )-1-propyne ] ( PTMSP ) membranes by bromine vapor has been studied. It is shown that Br/C atomic ratio at the surfacesincreased with the time of bromination until about 60 min, then it reached a plateau. The results of XPS and IR studies indicated that the addition of bromine to double bonds and the replacement of H on CH3 by bromine had taken place so that a new peak at 286.0 eV (C-Br)in C1sspectra and some new bands, e. g. at 1220 and 580cm-1,in IR spectra were formed. The fact, Po2, permeability of oxygen, decreased and αO2/N2, separation factor of oxygen relative to nitrogen, increased with bromination time, shows that surface modification of PTMSP by bromine may be an efficient approachto prepare PTMSP membranes used for practical gas separations.

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

    OpenAIRE

    Ayman A. Gouda

    2013-01-01

    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 ...

  3. Bromine partitioning between olivine and melt at OIB source conditions: Indication for volatile recycling

    Science.gov (United States)

    Joachim, Bastian; Ruzié, Lorraine; Burgess, Ray; Pawley, Alison; Clay, Patricia L.; Ballentine, Christopher J.

    2016-04-01

    Halogens play a key role in our understanding of volatile transport processes in the Earth's mantle. Their moderate (fluorine) to highly (iodine) incompatible and volatile behavior implies that their distribution is influenced by partial melting, fractionation and degassing processes as well as fluid mobilities. The heavy halogens, particularly bromine and iodine, are far more depleted in the Earth's mantle than expected from their condensation temperature (Palme and O'Neill 2014), so that their very low abundances in basalts and peridotites (ppb-range) make it analytically challenging to investigate their concentrations in Earth's mantle reservoirs and their behavior during transport processes (Pyle and Mather, 2009). We used a new experimental technique, which combines the irradiation technique (Johnson et al. 2000), laser ablation and conventional mass spectrometry. This enables us to present the first experimentally derived bromine partition coefficient between olivine and melt. Partitioning experiments were performed at 1500° C and 2.3 GPa, a P-T condition that is representative for partial melting processes in the OIB source region (Davis et al. 2011). The bromine partition coefficient between olivine and silicate melt at this condition has been determined to DBrol/melt = 4.37•10-4± 1.96•10-4. Results show that bromine is significantly more incompatible than chlorine (˜1.5 orders of magnitude) and fluorine (˜2 orders of magnitude) due to its larger ionic radius. We have used our bromine partitioning data to estimate minimum bromine abundances in EM1 and EM2 source regions. We used minimum bromine bulk rock concentrations determined in an EM1 (Pitcairn: 1066 ppb) and EM2 (Society: 2063 ppb) basalt (Kendrick et al. 2012), together with an estimated minimum melt fraction of 0.01 in OIB source regions (Dasgupta et al. 2007). The almost perfect bromine incompatibility results in minimum bromine abundances in EM1 and EM2 OIB source regions of 11 ppb and 20

  4. Non-polar halogenated natural products bioaccumulated in marine samples. II. Brominated and mixed halogenated compounds.

    Science.gov (United States)

    Vetter, Walter; Jun, Wu

    2003-07-01

    Several identified and potential natural brominated bioaccumulative compounds were studied in this work. 4,6-dibromo-2-(2('),4(')-dibromo)phenoxyanisole (BC-2) previously detected in Australian marine mammals and isolated from sponges, was synthesized. Two byproducts (a tetrabromo isomer and a tribromo congener) were investigated as well. The byproducts of the synthesis were not identified in the environmental samples investigated. Previously described natural brominated compounds (BC-1, BC-2, BC-3, BC-10, BC-11, MHC-1) and anthropogenic brominated diphenyl ethers (BDE-47, BDE-99, BDE-100, BDE-154) were detected in a sample of human milk. The sample was from a woman from the Faeroe Islands who frequently consumed fish as well as whale blubber and meat. The most abundant compound originated from the natural tetrabromo phenoxyanisole BC-3 which may have a 3:1 distribution of bromine on the two phenyl units. This sample also accumulated a dibromochloroanisole, as well as a previously unknown mixed halogenated compound (MHC-X) and an unknown, most likely aromatic brominated compound. Co-elutions on a DB-5 column were found for BDE-99 and BC-11 as well as BDE-154 and the unknown brominated compound. This suggests that quantification of these two compounds has to be carried out carefully.Two samples of lower trophic level, namely Baltic cod liver and Mexican mussel tissue, were investigated as well. The cod liver samples contained BDE congeners but also abundant signals for the natural 2,3,3('),4,4('),5,5(')-heptachloro-1(')-methyl-1,2(')-bipyrrole Q1 and tribromoanisole (TBA). The mussel sample contained Q1, TBA, another halogenated anisole, BC-1, BC-2, and BC-3, as well as additional, potential natural brominated compounds in the elution range of tribromophenoxyanisoles. PMID:12738265

  5. 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.

  6. Excited atomic bromine energy transfer and quenching mechanisms

    Science.gov (United States)

    Johnson, Ray O.

    1993-08-01

    Pulsed and steady-state photolysis experiments have been conducted to determine the rate coefficients for collisional deactivation of the spin-orbit excited state of atomic bromine, Br((sup 2)P(sub 1/2)). Pulsed lifetime studies for quenching by Br2 and CO2 established absolute rate coefficients at room temperature of k(sub Br2) = 1.2 +/- 0.1 x 10(exp-12) and k(sub CO2) = 1.5 +/0.2 x 10(exp-11) cu cm/molecule-s. Steady-state photolysis methods were used to determine the quenching rates for the rare gases, N2, 02, H2, D2, NO, NO2, N2O, SF6, CF4, CH4, CO, CO2, COS, SO2, H2S, HBr, HC1, and HI relative to that for Br2. Quenching rate temperature dependence was examined for Br2, CO2, N2O, HCl, COS, NO, and NO2 for temperatures from 300 to 420 K. Diffusion and three body effects were examined in order to determine the slowest relative quenching rate measurable by this experimental technique.

  7. Untypical bromine corrosion in boilers co-firing biomass

    Directory of Open Access Journals (Sweden)

    A. Hernas

    2012-09-01

    Full Text Available Purpose: The aim of this study was to determine the untypical corrosion resistance of rotary air preheaters in a biomass co-fired power plant.Design/methodology/approach: The selected results of some components of regenerative rotary air preheaters in a biomass co-fired power plant are presented. The macro and microstructure of corroded components of a LUVO preheater after 3 years of service are presented. The chemical composition of corrosion products was determined by X-ray microanalysis.Findings: Data concerning toxicity and identification of PBDEs (Polibrominated diphenyl ethers in the biomass is very limited. The presented research provides information and the proposed corrosion reaction mechanism in environments containing biomass with aggressive compounds like Cl, Si, H and Br.Research limitations/implications: An extended research on PBDEs in power plant fuels is necessary to give a full assessment of the corrosion mechanism in the presented environment; obligatory classification of the co-fired biomass.Originality/value: Firstly, an assessment of the danger for boiler materials co-firing biomass containing brominated organic flame and presentation of the reaction during the corrosion process and degradation of power boiler components in the presented environment. Secondly, the highlighting of the problem that there is a need to properly select and determine the chemical composition of the biomass used.

  8. Brominated flame retardants in Belgian little owl (Athene noctua) eggs

    Energy Technology Data Exchange (ETDEWEB)

    Jaspers, V.; Covaci, A.; Maervoet, J.; Dauwe, T.; Schepens, P.; Eens, M. [Antwerp Univ. (Belgium)

    2004-09-15

    Since the 1960s, polybrominated diphenylethers (PBDEs), a class of brominated flame retardants (BFRs), are widely used in textiles, plastics, electronic equipment and other materials. Their massive use has led to the ubiquitous presence of PBDEs in the environment and in biota in which the PBDE levels seem to increase rapidly. High concentrations of some congeners may cause adverse effects in both wildlife and in human populations1 and this has led to the growing concern of scientists over the last decade and to the need for more data on environmental levels of PBDEs. The little owl (Athene noctua) is a small sedentary predator, which makes it a very suitable biomonitoring species. This owl species feeds on a variety of preys, including small mammals and birds, reptiles, amphibians, earthworms and beetles, depending on the season and the local circumstances. Because very limited information is available about contamination levels in the little owl, a study was conducted to determine the concentrations of PBDEs, polybrominated biphenyls (PBBs), polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) in deserted or addled eggs of little owls in Belgium. Eggs have been used successfully as a monitoring tool for persistent organic pollutants (POPs) in several studies. Although the analysis of POPs in deserted or addled eggs has clear limitations, these can be partially avoided by analysing only highly persistent components, for which the original composition will not change due to 'posthatching' microbiological degradation.

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

    Directory of Open Access Journals (Sweden)

    A. Pour Biazar

    2006-06-01

    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 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. Further, 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 positive correlation observed between BrO and O3 at low O3 concentrations, and for the jagged diurnal pattern of BrO observed in the Dead Sea area. The present study has shown that the heterogeneous decomposition of BrONO2 has the potential to greatly affect the RBS activity in areas under anthropogenic influence, 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.

  11. Stability of succinylcholine chloride injection.

    Science.gov (United States)

    Schmutz, C W; Mühlebach, S F

    1991-03-01

    The stability of succinylcholine chloride injection prepared by a hospital pharmacy was studied under a wide variety of conditions. Batches of succinylcholine chloride injection 10 mg/mL containing sodium chloride, methyl-4-hydroxybenzoate, hydrochloric acid, and water were prepared. Samples were tested for the effect of initial pH (3.0 and 4.2) and sterilization (steam treatment at 100 degrees C for 30 minutes and 121 degrees C for 20 minutes) on stability after three weeks; long-term stability under refrigeration (12, 17, and 23 months of storage at 4 degrees C); and the effect of storage temperature (4-6 degrees C, 20-26 degrees C, 35 degrees C, and 70 degrees C) and light exposure at various intervals up to 12 months. Samples were analyzed by thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC). Unlike heating at 121 degrees C, heating at 100 degrees C produced no significant loss of succinylcholine chloride, independent of the initial pH. Succinylcholine chloride was hydrolyzed only minimally over 23 months if the solution was stored at 4-6 degrees C. A 10% loss of drug content occurred if solutions were kept at 20-26 degrees C for five months, at 35 degrees C for one month, or at 70 degrees C for one day. Initial degradation was slowed if the solution was protected from light. The assessments by TLC proved to be more sensitive than the HPLC measurements. Succinylcholine chloride injection sterilized at 100 degrees C for 30 minutes can be stored for up to five months at room temperature if protected from light. The preparation is stable for at least two years under refrigeration. PMID:2028996

  12. Chloride in vesicular trafficking and function.

    Science.gov (United States)

    Stauber, Tobias; Jentsch, Thomas J

    2013-01-01

    Luminal acidification is of pivotal importance for the physiology of the secretory and endocytic pathways and its diverse trafficking events. Acidification by the proton-pumping V-ATPase requires charge compensation by counterion currents that are commonly attributed to chloride. The molecular identification of intracellular chloride transporters and the improvement of methodologies for measuring intraorganellar pH and chloride have facilitated the investigation of the physiology of vesicular chloride transport. New data question the requirement of chloride for pH regulation of various organelles and furthermore ascribe functions to chloride that are beyond merely electrically shunting the proton pump. This review surveys the currently established and proposed intracellular chloride transporters and gives an overview of membrane-trafficking steps that are affected by the perturbation of chloride transport. Finally, potential mechanisms of membrane-trafficking modulation by chloride are discussed and put into the context of organellar ion homeostasis in general. PMID:23092411

  13. Electrochemical Chloride extraction using external electrodes?

    DEFF Research Database (Denmark)

    Ottosen, Lisbeth M.; Pedersen, Anne Juul

    2006-01-01

    Electrochemical methods for the removal of chloride from concrete have been developed and the methods are primarily designed for situations where corrosion has started due to an increased chloride concentration in the vicinity of the reinforcement. In these methods the reinforcement is used...... as the cathode. However, some unwanted side effects can occur, including alkali-silica reaction and in some cases hydrogen embrittlement. It is also suggested also to use electrochemical chloride extraction in a preventive way in constructions where chloride induced corrosion is likely to be a problem after...... a period of time, i.e. remove the chlorides before the chloride front reaches the reinforcement. If the chlorides are removed from outer few centimetres from the surface, the chloride will not reach the reinforcement and cause damage. By using the electrochemical chloride removal in this preventive way...

  14. 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).

  15. Chloride binding of cement-based materials subjected to external chloride environment - A review

    OpenAIRE

    Yuan, Q.; Shi, C; Schutter, G. de; Audenaert, K.; Deng, D.

    2009-01-01

    This paper reviews the chloride binding of cement-based materials subjected to external chloride environments. Chloride ion exist either in the pore solution, chemically bound to the hydration products, or physically held to the surface of the hydration products. Chloride binding of cement-based material is very complicated and influenced by many factors, such as chloride concentration, cement composition, hydroxyl concentration, cation of chloride salt, temperature, supplementary cementing m...

  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. GAS SORPTION AND TRANSPORT IN POLY (PHENYLENE OXIDE )(PPO)AND ARYL-BROMINATED PPO MEMBRANES

    Institute of Scientific and Technical Information of China (English)

    JIA Lianda; F.R.SHEU, R.T. CHERN; H.B. HOPFENBERG

    1989-01-01

    The apparent solubility (S), concentration- average diffusivity (D), and permeability (P), for CO2,CH4 and N2 through PPO and aryl- brominated PPO at 35 ℃ for pressure ranging from 1 to 26 atm are reported. It is found that P,D, and Sof the membranes to all the three gases vary with the extent of bromination. S increases with the increase of the perecnt of bromine in each case, but D to CO2 increases remarkably only at higher degree of bromination, and therefore, P to CO2 is increased by more than 100% over a wide range of pressure in the case .The solubility data are well described by the dual mode sorption model. It is found that the gas molecules sorbed by the Langmuir mode are relatively more immobilized and the contribution of the nonequilibrium character of the polymer to gas permeation increases obviously for CO2 and is hardly changed for CH4 with increasing bromine content. These observations are interpreted in terms of changes in specific free volume (SFV)and the cohesive energy density (CED) of the polymers.

  18. 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.

  19. 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.

  20. Bromine and bromide content in soils: Analytical approach from total reflection X-ray fluorescence spectrometry.

    Science.gov (United States)

    Gallardo, Helena; Queralt, Ignasi; Tapias, Josefina; Candela, Lucila; Margui, Eva

    2016-08-01

    Monitoring total bromine and bromide concentrations in soils is significant in many environmental studies. Thus fast analytical methodologies that entail simple sample preparation and low-cost analyses are desired. In the present work, the possibilities and drawbacks of low-power total reflection X-ray fluorescence spectrometry (TXRF) for the determination of total bromine and bromide contents in soils were evaluated. The direct analysis of a solid suspension using 20 mg of fine ground soil (soils (Br content range in soils = 5-40 mg kg(-1)). Information about bromide determination in soils is also possible by analyzing the Br content in water soil extracts. In this case, the TXRF analysis can be directly performed by depositing 10 μL of the internal standardized soil extract sample on a quartz glass reflector in a measuring time of 1500 s. The bromide limit of detection by this approach was 10 μg L(-1). Good agreement was obtained between the TXRF results for the total bromine and bromide determinations in soils and those obtained by other popular analytical techniques, e.g. energy dispersive X-ray fluorescence spectrometry (total bromine) and ionic chromatography (bromide). As a study case, the TXRF method was applied to study bromine accumulation in two agricultural soils fumigated with a methyl bromide pesticide and irrigated with regenerated waste water. PMID:27179429

  1. 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.

  2. Characterization of unknown brominated disinfection byproducts during chlorination using ultrahigh resolution mass spectrometry.

    Science.gov (United States)

    Zhang, Haifeng; Zhang, Yahe; Shi, Quan; Zheng, Hongdie; Yang, Min

    2014-03-18

    Brominated disinfection byproducts (Br-DBPs), formed from the reaction of disinfectant(s) with natural organic matter in the presence of bromide in raw water, are generally more cytotoxic and genotoxic than their chlorinated analogues. To date, only a few Br-DBPs in drinking water have been identified, while a significant portion of Br-DBPs in drinking water is still unknown. In this study, negative ion electrospray ionization ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR MS) was used to characterize unknown Br-DBPs in artificial drinking water. In total, 441 formulas for one-bromine-containing products and 37 formulas for two-bromine-containing products, most of which had not been previously reported, were detected in the chlorinated sample. Most Br-DBPs have corresponding chlorine-containing analogues with identical CHO composition. In addition, on-resonance collision-induced dissociation (CID) of single ultrahigh resolved bromine containing mass peaks was performed in the ICR cell to isolate single bromine-containing components in a very complex natural organic matter spectrum and provide structure information. Relatively abundant neutral loss of CO2 was observed in MS-MS spectra, indicating that the unknown Br-DBPs are rich in carboxyl groups. The results demonstrate that the ESI FT-ICR MS method could provide valuable molecular composition and structure information on unknown Br-DBPs.

  3. 1,5-Diaminotetrazolium chloride

    Directory of Open Access Journals (Sweden)

    Ling-Qiao Meng

    2010-04-01

    Full Text Available The title compound, CH5N6+·Cl−, crystallized with two indepedent 1,5-diaminotetrazolium cations and two independent chloride anions in the asymmetric unit. In the crystal, there are a number of N—H...Cl hydrogen-bonding interactions, which generate a three-dimensional network.

  4. Chloride : The queen of electrolytes?

    NARCIS (Netherlands)

    Berend, Kenrick; van Hulsteijn, Leonard Hendrik; Gans, Rijk O. B.

    2012-01-01

    Background: Channelopathies, defined as diseases that are caused by mutations in genes encoding ion channels, are associated with a wide variety of symptoms and have been documented extensively over the past decade. In contrast, despite the important role of chloride in serum, textbooks in general d

  5. The NBS Reaction: A Simple Explanation for the Predominance of Allylic Substitution over Olefin Addition by Bromine at Low Concentrations.

    Science.gov (United States)

    Wamser, Carl C.; Scott, Lawrence T.

    1985-01-01

    Examines mechanisms related to use of N-bromosuccinimide (NBS) for bromination at an allylic position. Also presents derived rate laws for three possible reactions of molecular bromine with an alkene: (1) free radical substitution; (2) free radical addition; and (3) electrophilic addition. (JN)

  6. Determination of bromine contents in blood and hair of workers exposed to methyl by radioactivation analysis method bromide

    International Nuclear Information System (INIS)

    The bromine contained in blood and hair samples obtained from workers exposed to methyl bromide was analyzed by nondestructive activation analysis. The samples were irradiated for 1 min in pneumatic irradiation facility of Kyoto University research reactor with an estimated thermal neutron flux density at 2 x 1013 n.cm-2.sec-1. The irradiation was counted with Ge(Li) detector. The duration of measurement of radionuclide bromine in blood and hair was 200 sec within 2 - 10 min after irradiation. The bromine content of serum sample obtained from a worker suspected of methyl bromide poisoning was found to be 412 μg/g on 13 days apart from exposure to methyl bromide. The biological half-life of bromine in this case was found to be about 16 days. Then bromine contents in serum and hair samples obtained from workers exposed to methyl bromide were found to be 1.7 and 2.6 times higher respectively than those of nonexposed workers. Any correlations of bromine contents were not observed between serum and hair samples obtained from workers exposed to methyl bromide, nor between bromine amount in the serum of workers exposed to methyl bromide and the terms exposed to it, but statistically significant positive correlation was observed between bromine amount in the hair of workers exposed to methyl bromide and the terms exposed to it. (author)

  7. Bromination of Marine Dissolved Organic Matter following Full Scale Electrochemical Ballast Water Disinfection.

    Science.gov (United States)

    Gonsior, Michael; Mitchelmore, Carys; Heyes, Andrew; Harir, Mourad; Richardson, Susan D; Petty, William Tyler; Wright, David A; Schmitt-Kopplin, Philippe

    2015-08-01

    An extensively diverse array of brominated disinfection byproducts (DBPs) were generated following electrochemical disinfection of natural coastal/estuarine water, which is one of the main treatment methods currently under consideration for ballast water treatment. Ultra-high-resolution mass spectrometry revealed 462 distinct brominated DBPs at a relative abundance in the mass spectra of more than 1%. A brominated DBP with a relative abundance of almost 22% was identified as 2,2,4-tribromo-5-hydroxy-4-cyclopentene-1,3-dione, which is an analogue to several previously described 2,2,4-trihalo-5-hydroxy-4-cyclopentene-1,3-diones in drinking water. Several other brominated molecular formulas matched those of other known brominated DBPs, such as dibromomethane, which could be generated by decarboxylation of dibromoacetic acid during ionization, dibromophenol, dibromopropanoic acid, dibromobutanoic acid, bromohydroxybenzoic acid, bromophenylacetic acid, bromooxopentenoic acid, and dibromopentenedioic acid. Via comparison to previously described chlorine-containing analogues, bromophenylacetic acid, dibromooxopentenoic acid, and dibromopentenedioic acid were also identified. A novel compound at a 4% relative abundance was identified as tribromoethenesulfonate. This compound has not been previously described as a DBP, and its core structure of tribromoethene has been demonstrated to show toxicological implications. Here we show that electrochemical disinfection, suggested as a candidate for successful ballast water treatment, caused considerable production of some previously characterized DBPs in addition to novel brominated DBPs, although several hundred compounds remain structurally uncharacterized. Our results clearly demonstrate that electrochemical and potentially direct chlorination of ballast water in estuarine and marine systems should be approached with caution and the concentrations, fate, and toxicity of DBP need to be further characterized.

  8. Microbial reductive dehalogenation of vinyl chloride

    Energy Technology Data Exchange (ETDEWEB)

    Spormann, Alfred M [Stanford, CA; Muller, Jochen A [Baltimore, MD; Rosner, Bettina M [Berlin, DE; Von Abendroth, Gregory [Mannheim, DE; Meshulam-Simon, Galit [Los Angeles, CA; McCarty, Perry L [Stanford, CA

    2014-02-11

    Compositions and methods are provided that relate to the bioremediation of chlorinated ethenes, particularly the bioremediation of vinyl chloride by Dehalococcoides-like organisms. An isolated strain of bacteria, Dehalococcoides sp. strain VS, that metabolizes vinyl chloride is provided; the genetic sequence of the enzyme responsible for vinyl chloride dehalogenation; methods of assessing the capability of endogenous organisms at an environmental site to metabolize vinyl chloride; and a method of using the strains of the invention for bioremediation.

  9. Progress of Carbonation in Chloride Contaminated Concretes

    OpenAIRE

    Wang, Yaocheng; Basheer, P.A.M.; Nanukuttan, S; Bai, Y.

    2016-01-01

    Concretes used in marine environment are generally under the cyclic effect of CO2 and chloride ions (Cl-). To date, the influence of carbonation on ingress of chloride ions in concretes has been widely studied; in comparison, study on the influence of Cl- on the progress of carbonation is limited. During the study, concretes were exposed to independent and combined mechanisms of carbonation and chloride ingress regimes. Profiles of apparent pH and chloride concentration were used to indicate ...

  10. Photochemical bromination of substituted indan-1-one derivatives: synthesis of new polybromoindan-1-one derivatives

    OpenAIRE

    KUŞ, Nermin Şimşek

    2009-01-01

    The photobromination of substituted indan derivatives was studied. Four products, 2,3-dibromo-inden-1-one (5), trans-2,3-dibromoindan-1-one (6), 2,2-dibromoindan-1,3-dione (7) and 2,2-dibromoindan-1-one (8), were obtained by the bromination of indan-1-one (4). The bromination of 2-methyl indanone (9) and 3-methyl-indanone (13) gave the corresponding monobromo, dibromo, and tribromo compounds in high yield. 4-Nitro indan (16) was tribrominated under same condition reaction. The stru...

  11. Chloride sublimation of gold-arsenic concentrates

    International Nuclear Information System (INIS)

    Present article is devoted to chloride sublimation of gold-arsenic concentrates. The results of studies of chloride sublimation of gold-arsenic comprising concentrates of Chore deposit of Tajikistan are considered. It is found that by application sodium chloride for gold-arsenic comprising concentrates it is possible to extract gold and silver from flotation concentrates.

  12. 21 CFR 172.180 - Stannous chloride.

    Science.gov (United States)

    2010-04-01

    ... Preservatives § 172.180 Stannous chloride. The food additive stannous chloride may be safely used for color... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Stannous chloride. 172.180 Section 172.180 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR...

  13. Shock compression of polyvinyl chloride

    Science.gov (United States)

    Neogi, Anupam; Mitra, Nilanjan

    2016-04-01

    This study presents shock compression simulation of atactic polyvinyl chloride (PVC) using ab-initio and classical molecular dynamics. The manuscript also identifies the limits of applicability of classical molecular dynamics based shock compression simulation for PVC. The mechanism of bond dissociation under shock loading and its progression is demonstrated in this manuscript using the density functional theory based molecular dynamics simulations. The rate of dissociation of different bonds at different shock velocities is also presented in this manuscript.

  14. 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...

  15. Bromine partitioning in the tropical tropopause layer: implications for stratospheric injection

    Directory of Open Access Journals (Sweden)

    R. P. Fernandez

    2014-07-01

    Full Text Available Very short-lived (VSL bromocarbons are produced at a prodigious rate by ocean biology and these source compounds (SGVSL, together with their degradation inorganic products (PGVSL, are lofted by vigorous convection to the tropical tropopause layer (TTL. Using a state-of-the-art photochemical mechanism within a global model, we calculate annual average stratospheric injection of total bromine due to VSL sources to be 5 pptv, with ~3 pptv entering the stratosphere as PGVSL and ~2 pptv as SGVSL. The geographic distribution and partitioning of VSL bromine within the TTL, and its consequent stratospheric injection, is highly dependent on the oceanic flux, the strength of convection and the occurrence of heterogeneous recycling reactions. Our calculations indicate atomic Br should be the dominant inorganic species in large regions of the TTL during daytime, due to the low ozone and cold conditions of this region. We propose the existence of a "tropical ring of atomic bromine" located approximately between 15 and 19 km and 30° N to 30° S. Daytime Br / BrO ratios of up to ~4 are predicted within the Br ring in regions of highly convective transport, such as the tropical Western Pacific. Then, we suggest experimental programs designed to quantify the bromine budget of the TTL and the stratospheric injection of VSL biogenic bromocarbons should include a strategy for the measurement of atomic Br during daytime and HOBr or BrCl during nighttime.

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

    OpenAIRE

    Han Wang; Kun Wen; Nurbiya Nurahmat; Yan Shao; He Zhang; Chao Wei; Ya Li; Yongjia Shen; Zhihua Sun

    2012-01-01

    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.

  17. 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.

  18. Microbial degradation of the brominated flame retardant TBNPA by groundwater bacteria: laboratory and field study.

    Science.gov (United States)

    Balaban, Noa; Bernstein, Anat; Gelman, Faina; Ronen, Zeev

    2016-08-01

    In the present study, the biodegradation of the brominated flame retardant tribromoneopentylalcohol (TBNPA) by a groundwater enrichment culture was investigated using a dual carbon ((13)C/(12)C)- bromine ((81)Br/(79)Br) stable isotope analysis. An indigenous aerobic bacterial consortium was enriched from the polluted groundwater underlying an industrial site in the northern Negev Desert, Israel, where TBNPA is an abundant pollutant. Aerobic biodegradation was shown to be rapid, with complete debromination within a few days, whereas anaerobic biodegradation was not observed. Biodegradation under aerobic conditions was accompanied by a significant carbon isotope effect with an isotopic enrichment factor of ɛCbulk = -8.8‰ ± 1.5‰, without any detectable bromine isotope fractionation. It was found that molecular oxygen is necessary for biodegradation to occur, suggesting an initial oxidative step. Based on these results, it was proposed that H abstraction from the C-H bond is the first step of TBNPA biodegradation under aerobic conditions, and that the C-H bond cleavage results in the formation of unstable intermediates, which are rapidly debrominated. A preliminary isotopic analysis of TBNPA in the groundwater underlying the industrial area revealed that there are no changes in the carbon and bromine isotope ratio values downstream of the contamination source. Considering that anoxic conditions prevail in the groundwater of the contaminated site, the lack of isotope shifts in TBNPA indicates the lack of TBNPA biodegradation in the groundwater, in accordance with our findings. PMID:27183339

  19. METABOLISM OF BROMINATED FLAME RETARDANTS IN HUMAN ASTROCYTES AND EFFECTS ON THYROID HORMONE HOMEOSTASIS

    Science.gov (United States)

    In this proposed study, hydroxylated PBDEs and brominated phenols likely will be formed in astrocytes as a result of cytochrome p450-mediated metabolism. Previous studies have shown that polychlorinated biphenyls (PCBs) affect the regulation of thyroid hormones at the bloo...

  20. Photothermally induced bromination of carbon/polymer bipolar plate materials for fuel cell applications

    Science.gov (United States)

    Schade, Martin; Franzka, Steffen; Cappuccio, Franco; Peinecke, Volker; Heinzel, Angelika; Hartmann, Nils

    2015-05-01

    A facile photothermal procedure for direct functionalization of carbon/polymer bipolar plate materials is demonstrated. Through irradiation with a microfocused beam of an Ar+-laser at λ = 514 nm in gaseous bromine and distinct laser powers and pulse lengths local bromination of the carbon/polymer material takes place. At a 1/e spot diameter of 2.1 μm, functionalized surface areas with diameters down to 5 μm are fabricated. In complementary experiments large-area bromination is investigated using an ordinary tungsten lamp. For characterization contact angle goniometry, X-ray photoelectron spectroscopy and electron microscopy in conjunction with labeling techniques are employed. After irradiation bromine groups can easily be substituted by other chemical functionalities, e.g. azide and amine groups. This provides a facile approach in order to fabricate surface patterns and gradient structures with varying wetting characteristics. Mechanistic aspects and prospects of photothermal routines in micropatterning of carbon/polymer materials are discussed.

  1. XAS AND XPS CHARACTERIZATION OF MERCURY BINDING ON BROMINATED ACTIVATED CARBON

    Science.gov (United States)

    Brominated powdered activated carbon sorbents have been shown to e quite effective for mercury capture when injected into the flue gas duct at coal-fired power plants and are especially useful when buring Western low-chlorine subbituminous coals. X-ray absorption spectroscopy (X...

  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...

  3. Canadian Arctic sea ice reconstructed from bromine in the Greenland NEEM ice core.

    Science.gov (United States)

    Spolaor, Andrea; Vallelonga, Paul; Turetta, Clara; Maffezzoli, Niccolò; Cozzi, Giulio; Gabrieli, Jacopo; Barbante, Carlo; Goto-Azuma, Kumiko; Saiz-Lopez, Alfonso; Cuevas, Carlos A; Dahl-Jensen, Dorthe

    2016-09-21

    Reconstructing the past variability of Arctic sea ice provides an essential context for recent multi-year sea ice decline, although few quantitative reconstructions cover the Holocene period prior to the earliest historical records 1,200 years ago. Photochemical recycling of bromine is observed over first-year, or seasonal, sea ice in so-called "bromine explosions" and we employ a 1-D chemistry transport model to quantify processes of bromine enrichment over first-year sea ice and depositional transport over multi-year sea ice and land ice. We report bromine enrichment in the Northwest Greenland Eemian NEEM ice core since the end of the Eemian interglacial 120,000 years ago, finding the maximum extension of first-year sea ice occurred approximately 9,000 years ago during the Holocene climate optimum, when Greenland temperatures were 2 to 3 °C above present values. First-year sea ice extent was lowest during the glacial stadials suggesting complete coverage of the Arctic Ocean by multi-year sea ice. These findings demonstrate a clear relationship between temperature and first-year sea ice extent in the Arctic and suggest multi-year sea ice will continue to decline as polar amplification drives Arctic temperatures beyond the 2 °C global average warming target of the recent COP21 Paris climate agreement.

  4. Bromine-82 Labelling of Human Serum Albumin, Insulin and Fibrinogen by Electrochemical Means

    International Nuclear Information System (INIS)

    The authors describe results obtained with a method using bromine-82 to label human serum albumin, fibrinogen and insulin, three organic substances of special importance in diagnostics and biological research. The method involves electrolytic bromination in an aqueous solution; this is performed in an electrolysis cell, whose anodic zone containing the substance to be labelled is partitioned from the cathodic zone by a dialysis membrane. For each of the three substances mentioned, the degree of bromination produced by a direct current (200, 200, 300 x 10-6 Å) was studied as a function of anode potential in 10-3 and 10-4 M solutions of NH4Br, the amount of bromine-labelled substance formed being checked by radio electrophoresis for various anodic potential values differing from each other by 50 mV. By immuno- electrophoresis it was ascertained that denaturation of albumin and fibrinogen only starts at anodic potential values for which the degree of labelling is already very high as compared with that yielded by chemical methods of labelling. The method here described has the advantage of rapid execution and is well suited to remote handling in a shielded zone. (author)

  5. In vitro profiling of the endocrine-disrupting potency of brominated flame retardants

    NARCIS (Netherlands)

    Hamers, T.H.M.; Kamstra, J.H.; Sonneveld, E.; Murk, A.J.; Kester, M.H.A.; Andersson, P.L.; Legler, J.; Brouwer, A.

    2006-01-01

    Over the last years, increasing evidence has become available that some brominated flame retardants (BFRs) may have endocrine disrupting (ED) potencies. The goal of the current study was to perform a systematic in vitro screening of the ED potencies of BFRs (1) to elucidate possible modes of action

  6. Molecular characterization of brominated persistent pollutants using extended X-ray absorption fine structure (EXAFS) spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Bergknut, Magnus; Skyllberg, Ulf [Swedish University of Agricultural Sciences (SLU), Department of Forest Ecology and Management, Umeaa (Sweden); Persson, Per [Umeaa University, Department of Chemistry, Umeaa (Sweden)

    2008-02-15

    X-ray absorption fine structure (EXAFS) spectroscopy spectra were collected for three brominated persistent pollutants: 6-bromo-2,4,5-trichlorophenol (BrTriClP), pentabromophenol (PentaBrP) and 3,3',5,5'-tetrabromobisphenol A (TBBA). The substances were selected to be symmetrical (BrTriClP and TBBA) or asymmetrical (PentaBrP) with respect to the atomic Br positions and to differ in the number of bromine and other halide atoms, as well as their relative positions. The asymmetrical PentaBrP was modelled with special detail as not all bromine atoms have identical coordination environments. The studied substances displayed unique EXAFS spectra, which could be used to determine the molecular structure in fair detail. We conclude that EXAFS spectroscopy is a suitable technique for molecular characterization of the comparatively complex molecules within the class of compounds of brominated organic persistent pollutants. A detailed understanding of the EXAFS spectra of the pure compounds opens up possibilities to study the interactions with soil and sediment matrices by means of EXAFS spectroscopy. (orig.)

  7. Deposition history of brominated flame retardant compounds in an ice core from Holtedahlfonna, Svalbard, Norway

    NARCIS (Netherlands)

    Hermanson, M.H.; Isaksson, E.; Forsström, S.; Teixeira, C.; Muir, D.C.G.; Pohjola, V.A.; van de Wal, R.S.W.

    2010-01-01

    Brominated flame retardants (BFRs) have been found in Arctic wildlife, lake sediment, and air. To identify the atmospheric BFR deposition history on Svalbard, Norway, we analyzed 19 BFRs, including hexabromocyclododecane (HBCD), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), decabromodiphenyl ethane

  8. Kinetics of aerobic cometabolic biodegradation of chlorinated and brominated aliphatic hydrocarbons: A review.

    Science.gov (United States)

    Jesus, João; Frascari, Dario; Pozdniakova, Tatiana; Danko, Anthony S

    2016-05-15

    This review analyses kinetic studies of aerobic cometabolism (AC) of halogenated aliphatic hydrocarbons (HAHs) from 2001-2015 in order to (i) compare the different kinetic models proposed, (ii) analyse the estimated model parameters with a focus on novel HAHs and the identification of general trends, and (iii) identify further research needs. The results of this analysis show that aerobic cometabolism can degrade a wide range of HAHs, including HAHs that were not previously tested such as chlorinated propanes, highly chlorinated ethanes and brominated methanes and ethanes. The degree of chlorine mineralization was very high for the chlorinated HAHs. Bromine mineralization was not determined for studies with brominated aliphatics. The examined research period led to the identification of novel growth substrates of potentially high interest. Decreasing performance of aerobic cometabolism were found with increasing chlorination, indicating the high potential of aerobic cometabolism in the presence of medium- and low-halogenated HAHs. Further research is needed for the AC of brominated aliphatic hydrocarbons, the potential for biofilm aerobic cometabolism processes, HAH-HAH mutual inhibition and the identification of the enzymes responsible for each aerobic cometabolism process. Lastly, some indications for a possible standardization of future kinetic studies of HAH aerobic cometabolism are provided. PMID:26874310

  9. 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

  10. 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 t

  11. Brominated Flame Retardants and their metabolites: Novel insights into endocrine disruptive properties.

    NARCIS (Netherlands)

    Fernández Cantón, R.

    2008-01-01

    Brominated flame retardants (BFRs) are chemicals that are added to materials to inhibit or suppress ignition and are incorporated during the manufacture of e.g. electronic equipment, furniture, construction materials and textiles. BFRs have become an increasingly important group of organohalogen com

  12. Canadian Arctic sea ice reconstructed from bromine in the Greenland NEEM ice core

    Science.gov (United States)

    Spolaor, Andrea; Vallelonga, Paul; Turetta, Clara; Maffezzoli, Niccolò; Cozzi, Giulio; Gabrieli, Jacopo; Barbante, Carlo; Goto-Azuma, Kumiko; Saiz-Lopez, Alfonso; Cuevas, Carlos A.; Dahl-Jensen, Dorthe

    2016-01-01

    Reconstructing the past variability of Arctic sea ice provides an essential context for recent multi-year sea ice decline, although few quantitative reconstructions cover the Holocene period prior to the earliest historical records 1,200 years ago. Photochemical recycling of bromine is observed over first-year, or seasonal, sea ice in so-called “bromine explosions” and we employ a 1-D chemistry transport model to quantify processes of bromine enrichment over first-year sea ice and depositional transport over multi-year sea ice and land ice. We report bromine enrichment in the Northwest Greenland Eemian NEEM ice core since the end of the Eemian interglacial 120,000 years ago, finding the maximum extension of first-year sea ice occurred approximately 9,000 years ago during the Holocene climate optimum, when Greenland temperatures were 2 to 3 °C above present values. First-year sea ice extent was lowest during the glacial stadials suggesting complete coverage of the Arctic Ocean by multi-year sea ice. These findings demonstrate a clear relationship between temperature and first-year sea ice extent in the Arctic and suggest multi-year sea ice will continue to decline as polar amplification drives Arctic temperatures beyond the 2 °C global average warming target of the recent COP21 Paris climate agreement. PMID:27650478

  13. Thermoelectric properties of bromine filled CoSb3 skutterudite

    Energy Technology Data Exchange (ETDEWEB)

    Ortiz, Brenden R.; Crawford, Caitlin M.; McKinney, Robert W.; Parilla, Philip A.; Toberer, Eric S.

    2016-01-01

    Historically, the improved thermoelectric performance of skutterudite compounds has largely been driven by the incorporation of electropositive donors on interstitial sites. These 'rattlers' serve to optimize both electronic and thermal properties by tuning the carrier concentration and scattering phonons. In this work, we show that interstitial bromine can be incorporated into CoSb3 and assess the impact on electronic and thermal transport. In contrast to prior high pressure syntheses with iodine, interstitial bromine incorporation is achieved at ambient pressure. Transport properties are stable up to at least 375 degrees C. Bromine serves as an electronegative acceptor and can induce degenerate (>5 x 1019 cm-3) hole densities. In contrast to other p-type skutterudite compositions, bromine preserves the intrinsically high hole mobility of CoSb3 while significantly reducing the lattice thermal conductivity. The development of a stable p-type dopant for the interstitial filler site enables the development of skutterudites with both donor and acceptor interstitials to maximize phonon scattering while maintaining the high mobility of CoSb3.

  14. The Effects of Bromination Methods on the Microstructure of Brominated Natural Rubbers from Latex%溴化方式对胶乳法溴化天然橡胶结构的影响

    Institute of Scientific and Technical Information of China (English)

    赵法敏; 薛行华; 张子琦; 张利伟; 李光

    2013-01-01

    为改善溴化天然橡胶(BNR)的溶解性能,在胶乳法的基础上改变溴化方式,以常规溴化方式和分步溴化方式分别制备了BNR.通过实验发现,体系溴浓度相同时分步溴化方式的溴含量比常规溴化方式高,而凝胶含量较低,所以分步溴化方式在甲苯中的溶解性能较好.通过傅里叶红外光谱对样品进行表征,并使用核磁共振对其微观结构进行了定性定量分析.红外光谱分析表明,2种溴化方式制备的BNR产物均发生了一定程度的溴加成反应和溴取代反应;核磁共振的分析证实了在体系溴浓度较低的情况下,与胶乳法常规溴化相反,胶乳法分步溴化的溴化过程主要以溴加成反应为主,少量发生溴取代反应.%In order to improve the solubility property of the brominated natural rubbers (BNR)from latex, BNR were prepared by changing the bromination ways from conventional bromination to step bromination. Through the experiment, it was discovered that the bromine content of the latter was higher than the former, but the gel content was less under the same bromine concentration. The latter showed much better solubility in the solvent of toluene. The structure of the procured sample was characterized by Fourier transform infrared spectroscopy (FTIR), and the microstructures of brominated nature rubber were qualitatively and quantitatively analyzed by nuclear magnetic resonance (NMR). FTIR showed that there were both a degree of brominated addition reaction and brominated substitution reaction in the obtained BNR by two different methods; Contrary to the conventional bromination from latex, the analysis of NMR proved that the bromination process of step bromination from latex was mainly in the form of addition reaction, and only a small amount of the substitution reaction did occur.

  15. 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

  16. Preparation of hydrophilic vinyl chloride copolymer hollow fiber membranes with antifouling properties

    Science.gov (United States)

    Rajabzadeh, Saeid; Sano, Rie; Ishigami, Toru; Kakihana, Yuriko; Ohmukai, Yoshikage; Matsuyama, Hideto

    2015-01-01

    Hydrophilic vinyl chloride copolymer hollow fiber membranes with antifouling properties were prepared from brominated vinyl chloride-hydroxyethyl methacrylate copolymer (poly(VC-co-HEMA-Br)). The base membrane was grafted with two different zwitterionic monomers, (2-methacryloyloxyethylphosphorylcholine) (MPC) and [2-(methacryloyloxy) ethyl] dimethyl (3-sulfopropyl) ammonium hydroxide) (MEDSAH), and poly(ethylene glycol) methyl ether methacrylate (PEGMA). The effect of the grafting on the base membrane hydrophilicity and antifouling properties was investigated. For comparison of the results, the pure water permeabilities and pore sizes at the outer surfaces of the grafted hollow fiber membranes were controlled to be similar. A poly(VC-co-HEMA-Br) hollow fiber membrane with similar pure water permeability and pore size was also prepared as a control membrane. A BSA solution was used as a model fouling solution for evaluation of the antifouling properties. Grafting with zwitterionic monomers and PEGMA improved the antifouling properties compared with the control membrane. The PEGMA grafted membrane showed the best antifouling properties among the grafted membranes

  17. Interactions of bromine, chlorine, and iodine photochemistry during ozone depletions in Barrow, Alaska

    Directory of Open Access Journals (Sweden)

    C. R. Thompson

    2014-11-01

    Full Text Available The springtime depletion of tropospheric ozone in the Arctic is known to be caused by active halogen photochemistry resulting from halogen atom precursors emitted from snow, ice, or aerosol surfaces. The role of bromine in driving ozone depletion events (ODEs has been generally accepted, but much less is known about the role of chlorine radicals in ozone depletion chemistry. While the potential impact of iodine in the High Arctic is more uncertain, there have been indications of active iodine chemistry through observed enhancements in filterable iodide, probable detection of tropospheric IO, and recently, detection of atmospheric I2. Despite decades of research, significant uncertainty remains regarding the chemical mechanisms associated with the bromine-catalyzed depletion of ozone, as well as the complex interactions that occur in the polar boundary layer due to halogen chemistry. To investigate this, we developed a zero-dimensional photochemical model, constrained with measurements from the 2009 OASIS field campaign in Barrow, Alaska. We simulated a 7 day period during late March that included a full ozone depletion event lasting 3 days and subsequent ozone recovery to study the interactions of halogen radicals under these different conditions. In addition, the effects of iodine added to our base model were investigated. While bromine atoms were primarily responsible for ODEs, chlorine and iodine were found to enhance the depletion rates and iodine was found to be more efficient per atom at depleting ozone than Br. The interaction between chlorine and bromine is complex, as the presence of chlorine can increase the recycling and production of Br atoms, while also increasing reactive bromine sinks under certain conditions. Chlorine chemistry was also found to have significant impacts on both HO2 and RO2. The results of this work highlight the need for future studies on the production mechanisms of Br2 and Cl2, as well as on the potential

  18. 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.

  19. 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

  20. A case study of a transported bromine explosion event in the Canadian high arctic

    Science.gov (United States)

    Zhao, X.; Strong, K.; Adams, C.; Schofield, R.; Yang, X.; Richter, A.; Friess, U.; Blechschmidt, A.-M.; Koo, J.-H.

    2016-01-01

    Ozone depletion events in the polar troposphere have been linked to extremely high concentrations of bromine, known as bromine explosion events (BEE). However, the optimum meteorological conditions for the occurrence of these events remain uncertain. On 4-5 April 2011, a combination of both blowing snow and a stable shallow boundary layer was observed during a BEE at Eureka, Canada (86.4°W, 80.1°N). Measurements made by a Multi-Axis Differential Optical Absorption Spectroscopy spectrometer were used to retrieve BrO profiles and partial columns. During this event, the near-surface BrO volume mixing ratio increased to ~20 parts per trillion by volume, while ozone was depleted to ~1 ppbv from the surface to 700 m. Back trajectories and Global Ozone Monitoring Experiment-2 satellite tropospheric BrO columns confirmed that this event originated from a bromine explosion over the Beaufort Sea. From 30 to 31 March, meteorological data showed high wind speeds (24 m/s) and elevated boundary layer heights (~800 m) over the Beaufort Sea. Long-distance transportation (~1800 km over 5 days) to Eureka indicated strong recycling of BrO within the bromine plume. This event was generally captured by a global chemistry-climate model when a sea-salt bromine source from blowing snow was included. A model sensitivity study indicated that the surface BrO at Eureka was controlled by both local photochemistry and boundary layer dynamics. Comparison of the model results with both ground-based and satellite measurements confirmed that the BEE observed at Eureka was triggered by transport of enhanced BrO from the Beaufort Sea followed by local production/recycling under stable atmospheric shallow boundary layer conditions.

  1. Interactions of bromine, chlorine, and iodine photochemistry during ozone depletions in Barrow, Alaska

    Science.gov (United States)

    Thompson, C. R.; Shepson, P. B.; Liao, J.; Huey, L. G.; Apel, E. C.; Cantrell, C. A.; Flocke, F.; Orlando, J.; Fried, A.; Hall, S. R.; Hornbrook, R. S.; Knapp, D. J.; Mauldin, R. L., III; Montzka, D. D.; Sive, B. C.; Ullmann, K.; Weibring, P.; Weinheimer, A.

    2015-08-01

    The springtime depletion of tropospheric ozone in the Arctic is known to be caused by active halogen photochemistry resulting from halogen atom precursors emitted from snow, ice, or aerosol surfaces. The role of bromine in driving ozone depletion events (ODEs) has been generally accepted, but much less is known about the role of chlorine radicals in ozone depletion chemistry. While the potential impact of iodine in the High Arctic is more uncertain, there have been indications of active iodine chemistry through observed enhancements in filterable iodide, probable detection of tropospheric IO, and recently, observation of snowpack photochemical production of I2. Despite decades of research, significant uncertainty remains regarding the chemical mechanisms associated with the bromine-catalyzed depletion of ozone, as well as the complex interactions that occur in the polar boundary layer due to halogen chemistry. To investigate this, we developed a zero-dimensional photochemical model, constrained with measurements from the 2009 OASIS field campaign in Barrow, Alaska. We simulated a 7-day period during late March that included a full ozone depletion event lasting 3 days and subsequent ozone recovery to study the interactions of halogen radicals under these different conditions. In addition, the effects of iodine added to our Base Model were investigated. While bromine atoms were primarily responsible for ODEs, chlorine and iodine were found to enhance the depletion rates and iodine was found to be more efficient per atom at depleting ozone than Br. The interaction between chlorine and bromine is complex, as the presence of chlorine can increase the recycling and production of Br atoms, while also increasing reactive bromine sinks under certain conditions. Chlorine chemistry was also found to have significant impacts on both HO2 and RO2, with organic compounds serving as the primary reaction partner for Cl atoms. The results of this work highlight the need for future

  2. Iodine and bromine speciation in snow and the effect of orographically induced precipitation

    Directory of Open Access Journals (Sweden)

    H. Biester

    2007-05-01

    Full Text Available Iodine is an essential trace element for all mammals and may also influence climate through new aerosol formation. Atmospheric bromine cycling is also important due to its well-known ozone depletion capabilities. Despite precipitation being the ultimate source of iodine in the terrestrial environment, the processes effecting its distribution, speciation and transport are relatively unknown. The aim of this study was to determine the effect of orographically induced precipitation on iodine concentrations in snow and also to quantify the inorganic and organic iodine and bromine species. Snow samples were collected over an altitude profile (~840 m from the northern Black Forest and were analysed by ion-chromatography - inductively coupled plasma mass spectrometry (IC-ICP-MS for iodine and bromine species and trace metals (ICP-MS. All elements and species concentrations in snow showed significant (r2>0.65 exponential decrease relationships with altitude despite the short (5 km horizontal distance of the transect. In fact, total iodine more than halved (38 to 13 nmol/l over the 840 m height change. The results suggest that orographic lifting and subsequent precipitation has a major influence on iodine concentrations in snow. This orographically induced removal effect may be more important than lateral distance from the ocean in determining iodine concentrations in terrestrial precipitation. The microphysical removal process was common to all elements indicating that the iodine and bromine are internally mixed within the snow crystals. We also show that organically bound iodine is the dominant iodine species in snow (61–75%, followed by iodide. Iodate was only found in two samples despite a detection limit of 0.3 nmol/l. Two unknown but most likely anionic organo-I species were also identified in IC-ICP-MS chromatograms and comprised 2–10% of the total iodine. The majority of the bromine was inorganic bromide with a max. of 32% organo-Br.

  3. Amines and ammonium compounds. CXCVIII. Reaction of ammonium salts containing a 2-alkynyl group with bromine and iodine

    Energy Technology Data Exchange (ETDEWEB)

    Gyul' nazaryan, A.K.; Khachatryan, N.G.; Saakyan, T.A.; Kinoyan, F.S.; Panosyan, G.A.; Babayan, A.T.

    1988-08-10

    The reactions of monoammonium, 1,4-and 1,5-bistertiaryammonium, and bisquaternary ammonium salts containing a 2-alkynyl group with bromine and iodine were studied. It was shown that these salts form molecular complexes with iodine and that addition of iodine at the triple bond does not occur. In reaction with bromine in all cases except 1,4-bistrimethylammonio-2-butyne dihalides one molecule of the halogen adds at the triple bond with the formation of salts containing the 2,3-dibromo-2-alkenyl group, which then form a 1:1 complex with bromine.

  4. The effect of bromination of carbon fibers on the coefficient of thermal expansion of graphite fiber-epoxy composites

    Science.gov (United States)

    Jaworske, D. A.; Maciag, C.

    1987-01-01

    To examine the effect of bromination of carbon fibers on the coefficient of thermal expansion (CTE) of carbon fiber epoxy composites, several pristine and brominated carbon fiber-epoxy composite samples were subjected to thermomechanical analysis. The CTE's of these samples were measured in the uniaxial and transverse directions. The CTE was dominated by the fibers in the uniaxial direction, while it was dominated by the matrix in the transverse directions. Bromination had no effect on the CTE of any of the composites. In addition, the CTE of fiber tow was measured in the absence of a polymer matrix, using an extension probe. The results from this technique were inconclusive.

  5. Smog Chamber Investigation on the Iron-Catalyzed Activation of Chloride from Modeled Saltpans

    Science.gov (United States)

    Wittmer, Julian; Bleicher, Sergej; Oeste <, Franz Dietrich; Zetzsch, Cornelius

    2014-05-01

    Halogen activation on sea spray aerosols and other halide surfaces and thus the formation of reactive halogen species (RHS), influencing trace and greenhouse gases, has become an important topic of research in recent years. In this context the chloride and bromide activation, in particular the formation of RHS by photochemically induced halogen release from (sea) salt surface and reactions with ozone (O3) and nitrogen oxides (NOx), came into focus [1,2]. Our studies concentrate on the quantification of atomic chlorine (Cl), bromine (Br) and hydroxyl (OH) radicals in the gas phase above lab-models of salt pans, enriched in iron(III) chloride (FeCl3), that are exposed to simulated sunlight in a smog chamber. The applied radical clock method [3] results in time profiles and source strengths for Cl, Br and OH, which are combined with the various compositions of humidified salts. In particular, the influence of bromine, sulfate, oxalate, and catechol on the FeCl3 enriched salt is investigated. Comparable investigations only exist for the aqueous phase chemistry of FeCl3 (e.g. [4]). Driven by the photolytic reduction from Fe(III) to Fe(II), an enormous amount of chlorine atoms (>107 cm-3) could be detected for sodium chloride (NaCl) salt pans with low addition of FeCl3 (0.5 - 2 wt%), even in an O3 and NOx free environment. The Cl2 source strength reaches a maximum of 8×1011 Cl2 molecules per cm3 within the first hour of the experiment, corresponding to a Cl2 mixing ratio of 30 ppbv at standard pressure. These concentrations exceeded the release above pure NaCl samples by a factor of 1000. A crucial factor for the Cl2 release is the pH and thus the formation of iron(III) complexes on the salt crystals that differ in their sensitivity for photolysis. Whereas the presence of sodium bromide normally strengthens the chlorine release, a suppression accompanied by strong bromine activation (>1010 cm-3) could be observed for iron enriched samples. Furthermore, the addition of

  6. 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

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

    Directory of Open Access Journals (Sweden)

    C. D. Holmes

    2010-08-01

    Full Text Available Global models of atmospheric mercury generally assume that 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 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 of 60 Mg a−1. Summertime events of depleted Hg0 at Antarctic sites due to subsidence are much better simulated by the Hg + Br model. Model

  8. Simple chloride sensors for continuous groundwater monitoring

    DEFF Research Database (Denmark)

    Thorn, Paul; Mortensen, John

    2012-01-01

    The development of chloride sensors which can be used for continuous, on-line monitoring of groundwater could be very valuable in the management of our coastal water resources. However, sensor stability, drift, and durability all need to be addressed in order for the sensors to be used...... in continuous application. This study looks at the development of a simple, inexpensive chloride electrode, and evaluates its performance under continuous use, both in the laboratory and in a field test in a monitoring well. The results from the study showed a consistent response to changing chloride...... sensor remained responsive even at low chloride concentrations, where the conductivity electrode was no longer responding to changing chloride levels. With the results, it is believed that the simple chloride sensor could be used for continuous monitoring of groundwater quality....

  9. Combustion and inorganic bromine emission of waste printed circuit boards in a high temperature furnace

    International Nuclear Information System (INIS)

    Highlights: ► The combustion efficiency of waste printed circuit boards (PCBs) depends on temperature, excess air factor, and high temperature zone residence time. Temperature has the most significant impact. Under the proposed condition, combustion of waste PCBs alone is quite complete within the furnace. ► High temperature prompts a more complete bromine release and conversion. When temperature is high enough, 99.9% organobrominated compounds, the potential precursors for brominated dixoins formation, are destroyed efficiently and convert to inorganic bromine in flue gas, as HBr and Br2. ► Temperature has crucial influence over the inhibition of HBr conversion to Br2, while the oxygen partial pressure plays a reverse role in the conversion to a very small extent. Increasing temperature will decrease the volume percentage ratio of Br2/HBr in flue gas greatly. ► The thermodynamic equilibrium approach of bromine conversion was investigated. The two forms of inorganic bromine in flue gas substantially reach thermodynamic equilibrium within 0.25 s. Under the proposed operating condition, the reaction of Br transfer and conversion finish. - Abstract: High temperature combustion experiments of waste printed circuit boards (PCBs) were conducted using a lab-scale system featuring a continuously-fed drop tube furnace. Combustion efficiency and the occurrence of inorganic bromine (HBr and Br2) were systematically studied by monitoring the main combustion products continuously. The influence of furnace temperature (T) was studied from 800 to 1400 °C, the excess air factor (EAF) was varied from 1.2 to 1.9 and the residence time in the high temperature zone (RTHT) was set at 0.25, 0.5, or 0.75 s. Combustion efficiency depends on temperature, EAF and RTHT; temperature has the most significant effect. Conversion of organic bromine from flame retardants into HBr and Br2 depends on temperature and EAF. Temperature has crucial influence over the ratio of HBr to Br2

  10. ENVIRONMENTAL EXPOSURE TO VINYL CHLORIDE

    Directory of Open Access Journals (Sweden)

    Henryka Langauer-Lewowicka

    2010-09-01

    Full Text Available Vinyl chloride (VC monomer is a wellknown carcinogenic and mutagenic substance causes liver damages, angiosarcoma of the liver, acro – osteolysis, sclerodermalike changes in workers chronically exposed to this gas. There are following VC emitors to the environment: VC production plants, polymerization facilities and planes where polyvinyl products are fabricated. Because of that, the general population is coming into VC contact through polluted air, food and water. VC concentration in all mentioned sites is very low, often not detectable. There was found any health risk for the general population. The VC air concentration in the vicinity to antropogenic emitors is always higher. Such a situation may causes undesirable health effect for residents living in the neighbourhood. Epidemiological studies are performed to detect the adverse VC effect in selected cohorts. Non of the study did not confirmed cases of angiosarcoma among residents living near a vinyl chloride sites. VC production is growing permanently, so VC emission will be higher. Because of that health monitoring of general population and especially of selected groups seems to be necessary in the future.

  11. Green process to recover magnesium chloride from residue solution of potassium chloride production plant

    Institute of Scientific and Technical Information of China (English)

    Lin WANG; Yunliang HE; Yanfei WANG; Ying BAO; Jingkang WANG

    2008-01-01

    The green process to recover magnesium chlor-ide from the residue solution of a potassium chloride pro-duction plant, which comes from the leach solution of a potash mine in Laos, is designed and optimized. The res-idue solution contains magnesium chloride above 25 wt-%, potassium chloride and sodium chloride together below 5 wt-% and a few other ions such as Br-, SO2-4and Ca2+. The recovery process contains two steps: the previous impurity removal operation and the two-stage evapora-tion-cooling crystallization procedure to produce magnes-ium chloride. The crystallized impurity carnallite obtained from the first step is recycled to the potassium chloride plant to recover the potassium salt. The developed process is a zero discharge one and thus fulfills the requirements for green chemical industrial production. The produced magnesium chloride is up to industrial criteria.

  12. Hydroxylated polybrominated diphenyl ethers exhibit different activities on thyroid hormone receptors depending on their degree of bromination

    Energy Technology Data Exchange (ETDEWEB)

    Ren, Xiao-Min, E-mail: rxm200318@gmail.com; Guo, Liang-Hong, E-mail: LHGuo@rcees.ac.cn; Gao, Yu, E-mail: francesscototti@gmail.com; Zhang, Bin-Tian, E-mail: nktianster@gmail.com; Wan, Bin, E-mail: binwan@rcees.ac.cn

    2013-05-01

    Polybrominated diphenyl ethers (PBDEs) have been shown to disrupt thyroid hormone (TH) functions in experimental animals, and one of the proposed disruption mechanisms is direct binding of hydroxylated PBDE (OH-PBDE) to TH receptors (TRs). However, previous data on TH receptor binding and TH activity of OH-PBDEs were very limited and sometimes inconsistent. In the present paper, we examined the binding potency of ten OH-PBDEs with different degrees of bromination to TR using a fluorescence competitive binding assay. The results showed that the ten OH-PBDEs bound to TR with potency that correlated to their bromination level. We further examined their effect on TR using a coactivator binding assay and GH3 cell proliferation assay. Different TR activities of OH-PBDEs were observed depending on their degree of bromination. Four low-brominated OH-PBDEs (2′-OH-BDE-28, 3′-OH-BDE-28, 5-OH-BDE-47, 6-OH-BDE-47) were found to be TR agonists, which recruited the coactivator peptide and enhanced GH3 cell proliferation. However, three high-brominated OH-PBDEs (3-OH-BDE-100, 3′-OH-BDE-154, 4-OH-BDE-188) were tested to be antagonists. Molecular docking was employed to simulate the interactions of OH-PBDEs with TR and identify the structural determinants for TR binding and activity. According to the docking results, low-brominated OH-PBDEs, which are weak binders but TR agonists, bind with TR at the inner side of its binding pocket, whereas high-brominated compounds, which are potent binders but TR antagonists, reside at the outer region. These results indicate that OH-PBDEs have different activities on TR (agonistic or antagonistic), possibly due to their different binding geometries with the receptor. - Highlights: ► Thyroid hormone (TH) activity of OH-PBDEs with different Br number was evaluated. ► Four different experimental approaches were employed to investigate the mechanism. ► Low-brominated OH-PBDEs were agonists, but high-brominated ones were antagonists.

  13. Influence of Chloride-Ion Adsorption Agent on Chloride Ions in Concrete and Mortar

    OpenAIRE

    Gai-Fei Peng; Nai-Qian Feng; Qi-Ming Song

    2014-01-01

    The influence of a chloride-ion adsorption agent (Cl agent in short), composed of zeolite, calcium aluminate hydrate and calcium nitrite, on the ingress of chloride ions into concrete and mortar has been experimentally studied. The permeability of concrete was measured, and the chloride ion content in mortar was tested. The experimental results reveal that the Cl agent could adsorb chloride ions effectively, which had penetrated into concrete and mortar. When the Cl agent was used at a dosage...

  14. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    OpenAIRE

    H. Guan; Love, A. J.; C. T. Simmons; Makhnin, O.; A. S. Kayaalp

    2010-01-01

    Chloride is commonly used as an environmental tracer for studying water flow and solute transport in the environment. It is especially useful for estimating groundwater recharge based on the commonly used chloride mass balance (CMB) method. Strong spatial variability in chloride deposition in coastal areas is one difficulty encountered in appropriately applying the method. A high-resolution bulk chloride deposition map in the coastal region is thus needed. The aim of this study is to construc...

  15. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    OpenAIRE

    H. Guan; Love, A. J.; C. T. Simmons; Makhnin, O.; A. S. Kayaalp

    2010-01-01

    Chloride is commonly used as an environmental tracer for studying water flow and solute transport in the environment. It is especially useful for estimating groundwater recharge based on the commonly used chloride mass balance (CMB) method. Strong spatial variability in chloride deposition in coastal areas is one difficulty encountered in appropriately applying the method. A high-resolution bulk chloride deposition map in the coastal region is thus needed. The aim of this st...

  16. The effect of representing bromine from VSLS on the simulation and evolution of Antarctic ozone

    Science.gov (United States)

    Oman, Luke D.; Douglass, Anne R.; Salawitch, Ross J.; Canty, Timothy P.; Ziemke, Jerald R.; Manyin, Michael

    2016-09-01

    We use the Goddard Earth Observing System Chemistry-Climate Model, a contributor to both the 2010 and 2014 World Meteorological Organization Ozone Assessment Reports, to show that inclusion of 5 parts per trillion (ppt) of stratospheric bromine (Bry) from very short lived substances (VSLS) is responsible for about a decade delay in ozone hole recovery. These results partially explain the significantly later recovery of Antarctic ozone noted in the 2014 report, as bromine from VSLS was not included in the 2010 Assessment. We show multiple lines of evidence that simulations that account for VSLS Bry are in better agreement with both total column BrO and the seasonal evolution of Antarctic ozone reported by the Ozone Monitoring Instrument on NASA's Aura satellite. In addition, the near-zero ozone levels observed in the deep Antarctic lower stratospheric polar vortex are only reproduced in a simulation that includes this Bry source from VSLS.

  17. 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.

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

    Institute of Scientific and Technical Information of China (English)

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

    2014-01-01

    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 ehmination 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.

  19. Co-doping of Potassium and Bromine in Carbon Nanotubes: A Density Functional Theory Study

    Institute of Scientific and Technical Information of China (English)

    XIAO Yong; YAN xiao-Hong; DING Jian-Wen

    2007-01-01

    We investigate the co-doping of potassium and bromine in singlewalled carbon nanotubes (SWCNTs)and doublewalled carbon nanotubes(DWCNTs)based on density functional theory.In the co-doped(6,O)SWCNTs,the 4s electron of potassium is transferred to nanotube and Br,leading to the n-type feature of SWCNTs.When potassium is intercalated into inner tube and bromine is put on outer tube,the positive and negative charges reside on the outer and inner tubes of the(7.0)@(16,0)DWCNT,respectively.It is expected that DWCNTs would be an ideal candidate for p-n junction and diode applications.

  20. Chloride ingress in cement paste and mortar

    DEFF Research Database (Denmark)

    Jensen, Ole Mejlhede; Hansen, Per Freiesleben; Coats, Alison M.;

    1999-01-01

    modelled on Fick's law modified by a term for chloride binding. Inclusion of chloride binding significantly improves the profile shape of the modelled ingress profiles. The presence of fine aggregate and formation of interfacial transition zones at paste-aggregate boundaries does not significantly affect...

  1. Chloride ingress in cement paste and mortar

    DEFF Research Database (Denmark)

    Jensen, Ole Mejlhede; Hansen, Per Freiesleben; Coats, Alison M.;

    1999-01-01

    In this paper chloride ingress in cement paste and mortar is followed by electron probe microanalysis. The influence of several paste and exposure parameters on chloride ingress are examined (e.g., water-cement ratio, silica fume addition, exposure time, and temperature), The measurements...

  2. 75 FR 19657 - Barium Chloride From China

    Science.gov (United States)

    2010-04-15

    ... Commission found that the domestic interested party group response to its notice of institution (74 FR 31757... COMMISSION Barium Chloride From China AGENCY: United States International Trade Commission. ACTION: Notice of... chloride from China. SUMMARY: The Commission hereby gives notice that it will proceed with a full...

  3. Chloride binding site of neurotransmitter sodium symporters

    DEFF Research Database (Denmark)

    Kantcheva, Adriana Krassimirova; Quick, Matthias; Shi, Lei;

    2013-01-01

    Neurotransmitter:sodium symporters (NSSs) play a critical role in signaling by reuptake of neurotransmitters. Eukaryotic NSSs are chloride-dependent, whereas prokaryotic NSS homologs like LeuT are chloride-independent but contain an acidic residue (Glu290 in LeuT) at a site where eukaryotic NSSs...

  4. Chronopotentiometric chloride sensing using transition time measurement

    NARCIS (Netherlands)

    Abbas, Y.; Graaf, de D.B.; Olthuis, W.; Berg, van den A.

    2013-01-01

    Detection of chloride ions is crucial to accurately access the concrete structure durability[1]. The existing electrochemical method of chloride ions detection in concrete, potentiometry[1], is not suitable for in-situ measurement due to the long term stability issue of conventional reference electr

  5. Chemische contaminanten in diervoeder additief Choline Chloride

    NARCIS (Netherlands)

    Traag, W.A.; Hoogenboom, L.A.P.; Jong, de J.; Egmond, van H.J.; Dam, ten G.

    2010-01-01

    Dit briefrapport beschrijft de resultaten van een onderzoek naar chemische contaminanten in Choline Chloride. De doelstellingen waren: 1) Inzicht te verkrijgen in het voorkomen van (gebromeerde) vlamvertragers en broomdioxines in het diervoederadditief Choline Chloride en het, op basis van de result

  6. Occupational exposure to brominated flame retardants : With emphasis on polybrominated diphenyl ethers

    OpenAIRE

    Thuresson, Kaj

    2004-01-01

    Brominated flame retardants (BFRs) are a diverse group of chemicals, which are used to slow down or inhibit the development of fires. BFRs are incorporated into a wide range of consumer products that are considered as potential fire hazards, such as TV-sets, household appliances, computers, and textiles. The production and use of BFRs is extensive and consists of mainly tetrabromobisphenol A (TBBPA), polybrominated diphenyl ethers (PBDEs) and hexabromocyclododecan (HBCD). BFRs in general, but...

  7. Ship-source pollution by polychlorinated biphenyls and brominated flame retardants

    OpenAIRE

    ČULIN, Jelena; Bielić, Toni

    2015-01-01

    Polychlorinated biphenyls (PCBs) and brominated flame retardants (BFRs) are groups of anthropogenic contaminants that have been routinely used in many applications for several decades. Prior to the discovery of their detrimental health effects and subsequent implementation of regulatory measures they were widely applied in shipbuilding. They are still found onboard active and inactive ships and pose a risk to human and environment. Therefore, it is important to continue to carry out preven...

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

    OpenAIRE

    N. Bobrowski; Giuffrida, G

    2012-01-01

    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 ...

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

    OpenAIRE

    S. Coburn; Dix, B.; Edgerton, E.; Holmes, C. D; Kinnison, D.; Liang, Q; A. ter Schure; Wang, S.; R. Volkamer

    2015-01-01

    The elevated deposition of atmospheric mercury over the Southeastern United States is currently not well understood. Here we measure partial columns and vertical profiles of bromine monoxide (BrO) radicals, a key component of mercury oxidation chemistry, to better understand the processes and altitudes at which mercury is being oxidized in the atmosphere. We use the data from a ground-based MAX-DOAS instrument located at a coastal site ~ 1 km from the Gulf o...

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

    Directory of Open Access Journals (Sweden)

    J. P. Parrella

    2012-04-01

    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 concentrations 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.

  11. 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.

  12. Toxicity of brominated flame retardants with focus on retinoid system disturbances

    OpenAIRE

    Litens Karlsson, Sabina

    2015-01-01

    Background: Brominated flame retardants (BFR) are detected in the environment and biota all over the world. They contribute to the human body burden of industrial chemicals and exposure is mainly via food. Indoor dust contributes substantially in some exposure situations, which involve small children. Regulatory restrictions and bans have been introduced as some BFRs can impact proper development, potentially via the endocrine system. Objectives: The study aim was to clarify the role of...

  13. Bromine-catalyzed conversion of CO2 and epoxides to cyclic carbonates under continuous flow conditions.

    Science.gov (United States)

    Kozak, Jennifer A; Wu, Jie; Su, Xiao; Simeon, Fritz; Hatton, T Alan; Jamison, Timothy F

    2013-12-11

    A continuous method for the formation of cyclic carbonates from epoxides and carbon dioxide (CO2) is described. The catalysts used are inexpensive and effective in converting the reagents to the products in a residence time (t(R)) of 30 min. The cyclic carbonate products are obtained in good to excellent yield (51-92%). On the basis of a series of kinetics experiments, we propose a reaction mechanism involving epoxide activation by electrophilic bromine and CO2 activation by an amide.

  14. Detailed modeling of the atmospheric degradation mechanism of very-short lived brominated species

    OpenAIRE

    G. Krysztofiak; Catoire, Valéry; Poulet, G.; Marécal, V.; Pirre, Michel; Louis, F.; Canneaux, S.; B. Josse

    2012-01-01

    International audience Detailed chemical reaction schemes for the atmospheric degradations of the very short-lived species (VSLS) bromoform (CHBr3) and dibromomethane (CH2Br2) have been established. These degradation schemes have been implemented in the meteorological/tracer transport model CATT-BRAMS used in the present case as pseudo one-dimensional model with chemistry of CH4, CO, HOx, NOx, NOy and Ox. They include the main possible reactions of the intermediate brominated peroxy radica...

  15. 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.

  16. Reactive airways dysfunction and systemic complaints after mass exposure to bromine.

    OpenAIRE

    Woolf, A; Shannon, M.

    1999-01-01

    Occasionally children are the victims of mass poisoning from an environmental contaminant that occurs due to an unexpected common point source of exposure. In many cases the contaminant is a widely used chemical generally considered to be safe. In the following case, members of a sports team visiting a community for an athletic event were exposed to chemicals while staying at a local motel. Bromine-based sanitizing agents and other chemicals such as hydrochloric acid, which were used in exces...

  17. Interactions of bromine, chlorine, and iodine photochemistry during ozone depletions in Barrow, Alaska

    OpenAIRE

    Thompson, C. R.; P. B. Shepson; Liao, J.; Huey, L.G.; E. C. Apel; Cantrell, C. A.; Flocke, F.; Orlando, J.; Fried, A.; Hall, S. R; R. S. Hornbrook; D. J. Knapp; Mauldin III, R. L; Montzka, D. D.; B. C. Sive

    2014-01-01

    The springtime depletion of tropospheric ozone in the Arctic is known to be caused by active halogen photochemistry resulting from halogen atom precursors emitted from snow, ice, or aerosol surfaces. The role of bromine in driving ozone depletion events (ODEs) has been generally accepted, but much less is known about the role of chlorine radicals in ozone depletion chemistry. While the potential impact of iodine in the High Arctic is more uncertain, there ha...

  18. Interactions of bromine, chlorine, and iodine photochemistry during ozone depletions in Barrow, Alaska

    OpenAIRE

    Thompson, C. R.; P. B. Shepson; Liao, J.; Huey, L.G.; E. C. Apel; Cantrell, C. A.; Flocke, F.; Orlando, J.; Fried, A.; Hall, S. R; R. S. Hornbrook; D. J. Knapp; Mauldin III, R. L; Montzka, D. D.; B. C. Sive

    2015-01-01

    The springtime depletion of tropospheric ozone in the Arctic is known to be caused by active halogen photochemistry resulting from halogen atom precursors emitted from snow, ice, or aerosol surfaces. The role of bromine in driving ozone depletion events (ODEs) has been generally accepted, but much less is known about the role of chlorine radicals in ozone depletion chemistry. While the potential impact of iodine in the High Arctic is more uncertain, there have been indicatio...

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

    International Nuclear Information System (INIS)

    Highlights: → We examined the flame retardants in electronics, curtains, wallpaper and insulator. → Use of alternative brominated and organophosphate flame retardants was suggested. → All the products investigated also contained PBDEs, TBBPA and polybromophenols. → 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.

  20. On bromine, nitrogen oxides and ozone depletion in the tropospheric plume of Erebus volcano (Antarctica)

    OpenAIRE

    Boichu, Marie; Oppenheimer, Clive; Roberts, Tjarda J.; V. I. Tsanev; Kyle, Philip R

    2011-01-01

    International audience Since the discovery of bromine oxide (BrO) in volcanic emissions, there has been speculation concerning its role in chemical evolution and notably ozone depletion in volcanic plumes. We report the first measurements using Differential Optical Absorption Spectroscopy (DOAS) of BrO in the tropospheric plume of the persistently degassing Erebus volcano (Antarctica). These are the first observations pertaining to emissions from an alkaline phonolitic magma. The observed ...

  1. Iodine and Bromine speciation in snow and the effect of elevation

    Directory of Open Access Journals (Sweden)

    B. S. Gilfedder

    2007-01-01

    Full Text Available Iodine is an essential trace element for all mammals and may also influence climate through new aerosol formation. Atmospheric bromine cycling is also important due to its well-known ozone depletion capabilities. Despite precipitation being the ultimate source of iodine in the terrestrial environment, the processes effecting the distribution, speciation and transport of these elements are relatively unknown. The aim of this study was to determine the effect of orographic lifting on iodine concentrations and also quantify inorganic and organic iodine and bromine species. Snow samples were collected over an altitude profile (~800 m from the northern Black Forest and were analysed (IC-ICP-MS for iodine and bromine species and trace metals (ICP-MS. All elements and species showed a significant (r2>0.65 inverse relationship with altitude despite the short (5 km horizontal distance of the transect. In fact, total iodine more than halved (38 to 13 nmol/l over the 800 m height change. The results suggest that orographic lifting of cloud masses has a major influence on iodine levels in precipitation and is perhaps more important than lateral distances in determining iodine concentrations in terrestrial precipitation. The microphysical removal process was common to all elements. We also show that organically bound iodine is the dominant iodine species in snow (61–75%, followed by iodide. Iodate was only found in two samples despite a detection limit of 0.3 nmol/l. Two unknown but most likely anionic organo-I species were also identified in IC-ICP-MS chromatograms and comprised 2–10% of the total iodine. The majority of the bromine was inorganic bromide with a max.~of 32% organo-Br.

  2. Thermal Recycling of Brominated Flame Retardants with Fe2O3.

    Science.gov (United States)

    Altarawneh, Mohammednoor; Ahmed, Oday H; Jiang, Zhong-Tao; Dlugogorski, Bogdan Z

    2016-08-01

    Plastics containing brominated flame retardants (BFRs) constitute the major fraction of nonmetallic content in e-waste. Co-pyrolysis of BFRs with hematite (Fe2O3) represents a viable option for the thermal recycling of BFRs. Consensus of experimental findings confirms the excellent bromine fixation ability of Fe2O3 and the subsequent formation of iron bromides. This contribution provides a comprehensive mechanistic account of the primary reactions between a cluster model of Fe2O3 and major bromine-bearing products from the decomposition of tetrabromobisphenol A (TBBA), the most commonly deployed BFR. We estimate the thermo-kinetic parameters for interactions of Fe2O3 with HBr, brominated alkanes and alkenes, bromobenzene, and bromophenol. Dissociative addition of HBr at a Fe-O bond proceeds through a trivial barrier of 8.2 kcal/mol with fitted parameters in the Arrhenius equation of k(T) = 7.96 × 10(11) exp(-6400/RT) s(-1). The facile and irreversible nature for HBr addition to Fe2O3 accords with the experimentally reported 90% reduction in HBr emission when Fe2O3 interacts with TBBA pyrolysates. A detailed kinetic analysis indicates that, transformation of Fe2O3 into iron bromides and oxybromides occurs via successive addition of HBr to Fe(Br)-O(H) entities. Elimination of a water molecule proceeds through an intramolecular H transfer. A direct elimination one-step mechanism operates in the dehydrohalogenation of bromoethane into ethene over Fe2O3. Dissociative decomposition and direct elimination channels assume comparable reaction rates in formation of acetylene from vinyl bromide. Results from this study provide an atomic-based insight into a promising thermal recycling route of e-waste. PMID:27366936

  3. Diffusion behavior of chloride ions in concrete

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, T.; Gjoerv, O.E. [Norwegian Univ. of Science and Technology, Trondheim (Norway). Div. of Building Materials

    1996-06-01

    In the present paper, an analysis of the diffusion behavior of chloride ions in concrete is presented. In concentrated electrolytic aqueous solutions such as seawater or that typically used in laboratory experiments, the effect of ionic interaction may significantly reduce the chemical potential and thus the driving force of the diffusing species. Because of different drift velocities of the cations and chloride ions in the solution, the lagging motion of the cations will also retard the drift velocity of the chlorides. In addition, both the electrical double layer forming on the solid surface and the chemical binding may significantly interfere with the transport of the chloride ions. As a result, the diffusion behavior of the chloride ions in concrete is a more complex and complicated transport process than what can be described by Fick`s law of diffusion.

  4. Brominating activity of the seaweed Ascophyllum nodosum: Impact on the biosphere

    Energy Technology Data Exchange (ETDEWEB)

    Wever, R.; Tromp, M.G.M.; Krenn, B.E.; Marjani, A.; Van Tol, M. (Univ. of Amsterdam (Netherlands))

    1991-03-01

    Macroalgae are an important source of volatile halogenated organic compounds, such as bromoform and dibromomethane. The mechanism by which these compounds are formed is still elusive. The authors report that the brown seaweeds Laminaria saccharina, Laminaria digitata, Fucus vesiculosis, Pelvetia canaliculata, and Ascophyllum nodosum and the red seaweeds Chondrus crispus and Plocamium hamatum contain bromoperoxidases. The intact plants are able to brominate exogeneous organic compounds when H{sub 2}O{sub 2} and Br{sup {minus}} are added to seawater. Further, the authors show that the brominating activity of the brown macroalga A. nodosum, which contains a vanadium bromoperoxidase located on the thallus surface, occurs when the plant is exposed to light and not in the dark. The rate of bromination of exogenous organic compounds in seawater by this plant is 68 nmol (g of wet alga){sup {minus}1} h{sup {minus}1}. HOBr is a strong biocidal agent and the authors propose that the formation of HOBr by this seaweed is part of a host defense system.

  5. Discrimination of hexabromocyclododecane from new polymeric brominated flame retardant in polystyrene foam by nuclear magnetic resonance.

    Science.gov (United States)

    Jeannerat, Damien; Pupier, Marion; Schweizer, Sébastien; Mitrev, Yavor Nikolaev; Favreau, Philippe; Kohler, Marcel

    2016-02-01

    Hexabromocyclododecane (HBCDD) is a brominated flame retardant (BFR) and major additive to polystyrene foam thermal insulation that has recently been listed as a persistent organic pollutant by the Stockholm Convention. During a 2013/2014 field analytical survey, we measured HBCDD content ranging from 0.2 to 2.4% by weight in 98 polystyrene samples. Liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) analyses indicated that expandable (EPS) and extruded (XPS) polystyrene foams significantly differed in the α/γ HBCDD isomer ratio, with a majority of α and γ isomers in XPS and EPS, respectively. Interestingly, this technique indicated that some recent materials did not contain HBCDD, but demonstrated bromine content when analysed with X-ray fluorescence (XRF). Further investigation by Nuclear Magnetic Resonance (NMR) was able to discriminate between the BFRs present. In addition to confirming the absence or presence of HBCDD in polystyrene samples, high-field NMR spectroscopy provided evidence of the use of brominated butadiene styrene (BBS) as copolymer in the production of polystyrene. Use of this alternative flame retardant is expected to cause fewer health and environmental concerns. Our results highlight a trend towards the use of copolymerized BFRs as an alternative to HBCDD in polystyrene foam boards. In addition to providing a rapid NMR method to identify polymeric BFR, our analytical approach is a simple method to discriminate between flame-retardants in polystyrene foam insulating materials.

  6. Heterogeneous processing of bromine compounds by atmospheric aerosols: Relation to the ozone budget

    Energy Technology Data Exchange (ETDEWEB)

    Robinson, J.M.; Henson, B.F.; Dubey, M.K.; Casson, J.L.; Johal, M.S. [Los Alamos National Lab., NM (US); Wilson, K.R. [Univ. of California, Berkeley, CA (US)

    1998-11-01

    This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) project at Los Alamos National Laboratory (LANL). The depletion of ozone, particularly above Antarctica, has been investigated extensively to formulate public policy on the use of halocarbons. While it has been shown that heterogeneous reactions of chlorine compounds on stratospheric particulates cause the ozone hole, little is known of the analogous bromine mechanisms, even though it has been recognized for two decades that catalytic destruction of ozone by bromine could be more efficient than chlorine. Furthermore, field measurements and modeling calculations suggest that these heterogeneous (gas/surface) reactions are not restricted to the Antarctic regions but occur globally. The authors have performed laboratory measurements of the uptake of bromine compounds and other halogens on simulated stratospheric aerosols to help elucidate their role in catalytic ozone destruction cycles. Their studies contribute to the data base required to make assessments of the effects of human activities on global change, including the Montreal Protocol.

  7. Effects of Assistant Solvents and Mixing Intensity on the Bromination Process of Butyl Rubber

    Institute of Scientific and Technical Information of China (English)

    王伟; 邹海魁; 初广文; 向阳; 彭晗; 陈建峰

    2014-01-01

    A slow bromination process of butyl rubber (IIR) suffers from low efficiency and low selectivity (S) of target-product. To obtain suitable approach to intensify the process, effects of assistant solvents and mixing inten-sity on the bromination process were systemically studied in this paper. The reaction process was found constantly accelerated with the increasing dosage and polarity of assistant solvent. Hexane with 30%(by volume) dichloro-methane was found as the suitable solvent component, where the stable conversion of 1,4-isoprene transferring to target product (xA1s) of 80.2%and the corresponding S of 91.2%were obtained in 5 min. The accelerated reaction process was demonstrated being remarkably affected by mixing intensity until the optimal stirring rate of 1100 r·min-1 in a stirred tank reactor. With better mixing condition, a further intensification of the process was achieved in a ro-tating packed bed (RPB) reactor, where xA1s of 82.6% and S of 91.9% were obtained in 2 min. The usage of the suitable solvent component and RPB has potential application in the industrial bromination process intensification.

  8. 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. PMID:25464945

  9. A satellite based study of tropospheric bromine explosion events and their linkages to polar cyclone development

    Science.gov (United States)

    Blechschmidt, Anne-Marlene; Richter, Andreas; Burrows, John P.; Kaleschke, Lars; Strong, Kimberly; Theys, Nicolas; Weber, Mark; Zhao, Xiaoyi; Zien, Achim; Hodges, Kevin I.

    2016-04-01

    Intense, cyclone-like shaped plumes of tropospheric bromine monoxide (BrO) are regularly observed by the UV-vis satellite instruments GOME-2/MetOp-A and SCIAMACHY/Envisat over Arctic and Antarctic sea ice in polar spring. The plumes are associated with an autocatalytic chemical chain reaction involving tropospheric ozone depletion and initiated by the release of bromine from cold brine-covered ice or snow to the atmosphere. This influences atmospheric chemistry as it affects the oxidising capacity of the troposphere through OH production and may also influence the local weather/temperature of the polar atmosphere, as ozone is a major greenhouse gas. Here, we make combined use of satellite retrievals and numerical model simulations to study individual BrO plume cases in the polar atmosphere. In agreement with previous studies, our analysis shows that the plumes are often transported by high latitude cyclones, sometimes over several days despite the short atmospheric lifetime of BrO. Moreover, general characteristics of bromine explosion events linked to transport by polar weather systems, such as frequency, spatial distribution and favourable weather conditions are derived based on a new detection method. Our results show that BrO cyclone transport events are by far more common in the Antarctic than in the Arctic.

  10. Effect of Bromine Substitution on Human Dermal Absorption of Polybrominated Diphenyl Ethers.

    Science.gov (United States)

    Abdallah, Mohamed Abou-Elwafa; Pawar, Gopal; Harrad, Stuart

    2015-09-15

    Human dermal absorption of eight mono- to deca-brominated diphenyl ethers (PBDEs) was investigated for the first time using EPISKIN human skin equivalent tissue. Using a standard in vitro protocol, EPISKIN tissues mounted in specially designed diffusion cells were exposed to the target PBDEs for 24 h. Estimated steady-state flux (Jss) and permeation coefficients (Papp) across the skin increased with decreasing bromine substitution from BDE-153 (Papp = 4.0 × 10(-4) cm/h) to BDE-1 (Papp = 1.1 × 10(-2) cm/h). This was accompanied by an increase in the time required to traverse the skin tissue into the receptor fluid (lag time) from 0.25 h for BDE-1 to 1.26 h for BDE-153. Papp values for the studied PBDEs were correlated significantly (P water solubility and log KOW. While less brominated congeners achieved faster dermal penetration, higher PBDEs displayed greater accumulation within the skin tissue. The PBDEs thus accumulated represent a contaminant depot from which they may be slowly released to the systemic circulation over a prolonged period. Maximal percutaneous penetration was observed for BDE-1 (∼ 30% of the applied 500 ng/cm(2) dose). Interestingly, BDE-183 and BDE-209 showed very low dermal absorption, exemplified by a failure to reach the steady state within the 24 h exposure period that was studied. PMID:26301594

  11. Bromine recovery in residual solutions generated in the 15 N isotopic determination methodology (Rittenberg, 1946)

    International Nuclear Information System (INIS)

    The isotopic determination of 15 N (Rittenberg, 1946) is a methodology used in the Laboratory of Isotope Stable (CENA/USP). In this procedure, in the oxidation of nitrogen species for N2, solution of Li Br O is used, generating as residue 50 L y-1 of solution contends Li Br and Li Br O. Seeking to recover the bromine contained in that residue, very toxic substance, a special line was built composed by reaction balloons (1 and 2 liters), addition funnel, gas flow regulator and connections in glass. In the system proposed, after the acidification (sulfuric acid) of the alkaline residual solution, the liberated bromine (Br2) it was then dragged by flow of nitrogen and reacted with solution of LiOH. That reaction facilitated the production of Li Br O in solution (Efficiency = 82±2%), that was reused later on same analytic procedure. The high cost of the liquid bromine is another attractiveness that corroborates the employment of the developed procedure. They took place isotopic determinations using the recovered solutions and prepared, and the observed values didn't show statistical difference (T test of Student). The presented procedure is part of the Management Program of Chemical Residues of CENA/USP, which seeks to destine the residues of responsibility of the institution appropriately, forming professionals to the practices of environmental management. (author)

  12. Discrimination of hexabromocyclododecane from new polymeric brominated flame retardant in polystyrene foam by nuclear magnetic resonance.

    Science.gov (United States)

    Jeannerat, Damien; Pupier, Marion; Schweizer, Sébastien; Mitrev, Yavor Nikolaev; Favreau, Philippe; Kohler, Marcel

    2016-02-01

    Hexabromocyclododecane (HBCDD) is a brominated flame retardant (BFR) and major additive to polystyrene foam thermal insulation that has recently been listed as a persistent organic pollutant by the Stockholm Convention. During a 2013/2014 field analytical survey, we measured HBCDD content ranging from 0.2 to 2.4% by weight in 98 polystyrene samples. Liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) analyses indicated that expandable (EPS) and extruded (XPS) polystyrene foams significantly differed in the α/γ HBCDD isomer ratio, with a majority of α and γ isomers in XPS and EPS, respectively. Interestingly, this technique indicated that some recent materials did not contain HBCDD, but demonstrated bromine content when analysed with X-ray fluorescence (XRF). Further investigation by Nuclear Magnetic Resonance (NMR) was able to discriminate between the BFRs present. In addition to confirming the absence or presence of HBCDD in polystyrene samples, high-field NMR spectroscopy provided evidence of the use of brominated butadiene styrene (BBS) as copolymer in the production of polystyrene. Use of this alternative flame retardant is expected to cause fewer health and environmental concerns. Our results highlight a trend towards the use of copolymerized BFRs as an alternative to HBCDD in polystyrene foam boards. In addition to providing a rapid NMR method to identify polymeric BFR, our analytical approach is a simple method to discriminate between flame-retardants in polystyrene foam insulating materials. PMID:26492426

  13. Computer simulation of the cluster destruction of stratospheric ozone by bromine

    Institute of Scientific and Technical Information of China (English)

    A.E.Galashev; O.R.Rakhmanova

    2012-01-01

    The interaction of (Br-)i(H2O)50-i,0≤i≤6 clusters with oxygen and ozone molecules is investigated by the method of molecular dynamics simulation.The ozone molecules as well as the bromine ions do not leave the cluster during the calculation of 25 ps.The ability of the cluster containing molecular oxygen to absorb the infrared (IR)radiation is reduced in the frequency range of 0 ≤ ω ≤ 3500 cm-1 when the number of the bromine ions in the cluster grows.The intensity of the Raman spectrum is not changed significantly when the Br-ions are added to the ozonecontaining system.The power of the emitted IR radiation is increased when the number of bromine ions grows in the oxygen-containing system.The data obtained in this study on the IR and the Raman spectra of the water clusters that contain ozone,oxygen,and Br-can be used to develop an investigation of the mechanisms of ozone depletion.

  14. Mechanochemical conversion of brominated POPs into useful oxybromides: a greener approach

    Science.gov (United States)

    Cagnetta, Giovanni; Liu, Han; Zhang, Kunlun; Huang, Jun; Wang, Bin; Deng, Shubo; Wang, Yujue; Yu, Gang

    2016-06-01

    Brominated organic pollutants are considered of great concern for their adverse effect on human health and the environment, so an increasing number of such compounds are being classified as persistent organic pollutants (POPs). Mechanochemical destruction is a promising technology for POPs safe disposal because it can achieve their complete carbonization by solvent-free high energy ball milling at room temperature. However, a large amount of co-milling reagent usually is necessary, so a considerable volume of residue is produced. In the present study a different approach to POPs mechanochemical destruction is proposed. Employing stoichiometric quantities of Bi2O3 or La2O3 as co-milling reagent, brominated POPs are selectively and completely converted into their corresponding oxybromides (i.e. BiOBr and LaOBr), which possess very peculiar properties and can be used for some actual and many more potential applications. In this way, bromine is beneficially reused in the final product, while POPs carbon skeleton is safely destroyed to amorphous carbon. Moreover, mechanochemical destruction is employed in a greener and more sustainable manner.

  15. Computer simulation of the cluster destruction of stratospheric ozone by bromine

    International Nuclear Information System (INIS)

    The interaction of (Br−)i(H2O)50−i, 0 ≤ i ≤ 6 clusters with oxygen and ozone molecules is investigated by the method of molecular dynamics simulation. The ozone molecules as well as the bromine ions do not leave the cluster during the calculation of 25 ps. The ability of the cluster containing molecular oxygen to absorb the infrared (IR) radiation is reduced in the frequency range of 0 ≤ ω ≤ 3500 cm−1 when the number of the bromine ions in the cluster grows. The intensity of the Raman spectrum is not changed significantly when the Br− ions are added to the ozone-containing system. The power of the emitted IR radiation is increased when the number of bromine ions grows in the oxygen-containing system. The data obtained in this study on the IR and the Raman spectra of the water clusters that contain ozone, oxygen, and Br− can be used to develop an investigation of the mechanisms of ozone depletion

  16. MISCIBILITY AND MORPHOLOGY OF THIN FILMS OF BLENDS OF POLYSTYRENE WITH BROMINATED POLYSTYRENES: EFFECTS OF VARYING THE MOLECULAR WEIGHT,BROMINATION DEGREE AND ANNEALING

    Institute of Scientific and Technical Information of China (English)

    Rui Song; De-bin Yang; Ling-hao He; Guang-tao Yao

    2006-01-01

    Thin films of incompatible polymer blends can form a variety of structures during preparation and subsequent annealing process. For the polymer blend system consisting of polystyrene and poly(styrene-co-p-bromo-styrene), I.e.,PS/PBrxS, its compatibility could be adjusted by varying the degree of bromination and the molecular weight of both components comprised. In this paper, surface chemical compositions of the cast and the annealing films were investigated by X-ray photoelectron spectroscopy (XPS) and contact angle measurement; meanwhile, surface topographical changes are followed by atomic force microscopy (AFM). In addition, substantial attention was paid to the effect of annealing on the morphologic variations induced by phase separation and/or dewetting of the thin film. Moreover, the influences of the molecular weight, Mw, as well as the brominated degree, x%, on the sample surface are explored systematically, and the corresponding observations are explained in virtue of the Flory-Huggins theory, along with the dewetting of the polymer thin film.

  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. Chloride Transport in Undersea Concrete Tunnel

    Directory of Open Access Journals (Sweden)

    Yuanzhu Zhang

    2016-01-01

    Full Text Available Based on water penetration in unsaturated concrete of underwater tunnel, a diffusion-advection theoretical model of chloride in undersea concrete tunnel was proposed. The basic parameters including porosity, saturated hydraulic conductivity, chloride diffusion coefficient, initial water saturation, and moisture retention function of concrete specimens with two water-binder ratios were determined through lab-scale experiments. The variation of chloride concentration with pressuring time, location, solution concentration, initial saturation, hydraulic pressure, and water-binder ratio was investigated through chloride transport tests under external water pressure. In addition, the change and distribution of chloride concentration of isothermal horizontal flow were numerically analyzed using TOUGH2 software. The results show that chloride transport in unsaturated concrete under external water pressure is a combined effect of diffusion and advection instead of diffusion. Chloride concentration increased with increasing solution concentration for diffusion and increased with an increase in water pressure and a decrease in initial saturation for advection. The dominant driving force converted with time and saturation. When predicting the service life of undersea concrete tunnel, it is suggested that advection is taken into consideration; otherwise the durability tends to be unsafe.

  20. Shelf life of unrefrigerated succinylcholine chloride injection.

    Science.gov (United States)

    Boehm, J J; Dutton, D M; Poust, R I

    1984-02-01

    The shelf life of succinylcholine chloride injection at several pH values when stored at room temperature was evaluated. Solutions containing 20 mg/ml of succinylcholine chloride were stored at 25 and 40 degrees C. The reaction was studied at pH values ranging from 3.0 to 4.5. At two-week intervals, the solutions were assayed by high-pressure liquid chromatography. The initial amount of succinylcholine chloride in all samples was 100.1 +/- 2.37% of label claim. Hydrolysis of succinylcholine chloride in unbuffered solutions followed apparent zero-order kinetics. The pH range of maximum stability was found to be from 3.75 to 4.50. Succinylcholine chloride decomposed at a considerably higher rate at 40 degrees C. Allowing for the effects of pH adjustment during manufacture and degradation during shipping, losses of 7.0% and 9.0% potency can be expected after storage at 25 degrees C for four and six weeks, respectively. Succinylcholine Chloride Injection, USP, should be stored in the refrigerator; if unbuffered succinylcholine chloride injection complying with USP pH limits must be stored at room temperature, it should not be kept for longer than four weeks. PMID:6702837

  1. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    Directory of Open Access Journals (Sweden)

    H. Guan

    2010-05-01

    Full Text Available Chloride is commonly used as an environmental tracer for studying water flow and solute transport in the environment. It is especially useful for estimating groundwater recharge based on the commonly used chloride mass balance (CMB method. Strong spatial variability in chloride deposition in coastal areas is one difficulty encountered in appropriately applying the method. A high-resolution bulk chloride deposition map in the coastal region is thus needed. The aim of this study is to construct a chloride deposition map in the Mount Lofty Ranges (MLR, a coastal hilly area of approximately 9000 km2 spatial extent in South Australia. We examined geographic (related to coastal distance, orographic, and atmospheric factors that may influence chloride deposition, using partial correlation and regression analyses. The results indicate that coastal distance, elevation, as well as terrain aspect and slope, appear to be significant factors controlling chloride deposition in the study area. Coastal distance accounts for 70% of spatial variability in bulk chloride deposition, with elevation, terrain aspect and slope an additional 15%. The results are incorporated into a de-trended residual kriging model (ASOADeK to produce a 1 km×1 km resolution bulk chloride deposition and concentration maps. The average uncertainty of the deposition map is about 20–30% in the western MLR, and 40–50% in the eastern MLR. The maps will form a useful basis for examining catchment chloride balance for the CMB application in the study area.

  2. Reliability-Based Planning of Chloride Measurements

    DEFF Research Database (Denmark)

    Sørensen, John Dalsgaard; Engelund, S.

    1996-01-01

    on measurements of the chloride content obtained from the given structure. In the present paper optimal planning of measurements of the chloride content in reinforced concrete structures is considered. It is shown how optimal experimental plans can be obtained using FORM-analysis. Bayesian statistics are used......In reinforced concrete structures corrosion is initiated when the chloride concentration around the reinforcement exceeds a threshold value. If corrosion starts then expensive repairs can be necessary. The estimation of the probability that corrosion has been initiated in a given structure is based...

  3. Binary Nucleation of Water and Sodium Chloride

    Energy Technology Data Exchange (ETDEWEB)

    Nemec, Thomas [Institute of Thermomechanics ASCR, Prague, Czech Republic; Marsik, Frantisek [Institute of Thermomechanics ASCR, Prague, Czech Republic; Palmer, Donald [ORNL

    2005-01-01

    Nucleation processes in the binary water-sodium chloride system are investigated in the sense of the classical nucleation theory (CNT). The CNT is modified to be able to handle the electrolytic nature of the system and is employed to investigate the acceleration of the nucleation process due to the presence of sodium chloride in the steam. This phenomenon, frequently observed in the Wilson zone of steam turbines, is called early condensation. Therefore, the nucleation rates of the water-sodium chloride mixture are of key importance in the power cycle industry.

  4. Surface adsorption in strontium chloride ammines

    DEFF Research Database (Denmark)

    Ammitzbøll, Andreas L.; Lysgaard, Steen; Klukowska, Agata;

    2013-01-01

    An adsorbed state and its implications on the ab- and desorption kinetics of ammonia in strontium chloride ammine is identified using a combination of ammonia absorption measurements, thermogravimetric analysis, and density functional theory calculations. During thermogravimetric analysis, ammoni...

  5. Catastrophic event modeling. [lithium thionyl chloride batteries

    Science.gov (United States)

    Frank, H. A.

    1981-01-01

    A mathematical model for the catastrophic failures (venting or explosion of the cell) in lithium thionyl chloride batteries is presented. The phenomenology of the various processes leading to cell failure is reviewed.

  6. Telomerization of Vinyl Chloride with Chloroform Initiated by Ferrous Chloride-Dimethylacetamide under Ultrasonic Conditions

    Directory of Open Access Journals (Sweden)

    Hua Qian

    2015-01-01

    Full Text Available Telomerization of vinyl chloride with chloroform was investigated using ferrous chloride-dimethylacetamide system, and 42.1% yield, more than four times the one reported before, was achieved. The addition of ultrasound further improved the reaction and yield was raised to 51.9% with trace byproducts at highly reduced reaction time and temperature. Ferrous chloride-dimethylacetamide under ultrasonic irradiation acts as a very efficient catalyst system for the 1 : 1 telomerization.

  7. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    OpenAIRE

    H. Guan; Love, A. J.; C. T. Simmons; A. S. Kayaalp

    2009-01-01

    Chloride is commonly used as an environmental tracer for studying water flow and solute transport in the environment. It is especially useful for estimating groundwater recharge based on the commonly used chloride mass balance (CMB) method. Strong spatial variability in chloride deposition in coastal areas is one difficulty encountered in appropriately applying the CMB approach. Furthermore, intensive vegetation clearance for agriculture, for example during the European settlement in many...

  8. Estimating the chloride transport in cement paste

    OpenAIRE

    Princigallo, A.

    2012-01-01

    A method was developed to measure the diffusion coefficient of chloride ions in cement paste based on an analytical solution to Fick’s 2nd law in a cylindrical coordinate system. This natural method yielded diffusivity results within as little as a month. Testing time was reduced by exploiting the three-dimensional inward flux in the specimen. In an attempt to determine the saturation concentration, dense portland cement pastes were exposed to a concentrated chloride solution. The method prov...

  9. Influence of Chloride-Ion Adsorption Agent on Chloride Ions in Concrete and Mortar

    Directory of Open Access Journals (Sweden)

    Gai-Fei Peng

    2014-04-01

    Full Text Available The influence of a chloride-ion adsorption agent (Cl agent in short, composed of zeolite, calcium aluminate hydrate and calcium nitrite, on the ingress of chloride ions into concrete and mortar has been experimentally studied. The permeability of concrete was measured, and the chloride ion content in mortar was tested. The experimental results reveal that the Cl agent could adsorb chloride ions effectively, which had penetrated into concrete and mortar. When the Cl agent was used at a dosage of 6% by mass of cementitious materials in mortar, the resistance to the penetration of chloride ions could be improved greatly, which was more pronounced when a combination of the Cl agent and fly ash or slag was employed. Such an effect is not the result of the low permeability of the mortar, but might be a result of the interaction between the Cl agent and the chloride ions penetrated into the mortar. There are two possible mechanisms for the interaction between the Cl agent and chloride ion ingress. One is the reaction between calcium aluminate hydrate in the Cl agent and chloride ions to form Friedel’s salt, and the other one is that calcium aluminate hydrate reacts with calcium nitrite to form AFm during the early-age hydration of mortar and later the NO2− in AFm is replaced by chloride ions, which then penetrate into the mortar, also forming Friedel’s salt. More research is needed to confirm the mechanisms.

  10. Effect of Chloride Type on Penetration of Chloride Ions in Concrete

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The influence of chloride type on the diffusivity of chloride ions in concrete was studied by experiment. The result shows that the glectric resistance of concrete and the chloride diffusion coefficient are influenced by chloride type. For the same water/cement ratio (W/C), the diffusion coefficient D in KCl solution is larger than that in NaCl solution; however, the concrete resistance in KCl solution is smaller than that in NaCl solution. The experimental result is analyzed with theory of diffusion.

  11. Assessment of PCDD/F and PBDD/F Emissions from Coal-fired Power Plants during Injection of Brominated Activated Carbon for Mercury Control

    Science.gov (United States)

    The effect of the injection of brominated powdered activated carbon (Br-PAC) on the emission of brominated and chlorinated dioxins and furans in coal combustion flue gas has been evaluated. The tests were performed at two U.S. Department of Energy (DOE) demonstration sites where ...

  12. Hyphenation of ultra performance liquid chromatography (UPLC) with inductively coupled plasma mass spectrometry (ICP-MS) for fast analysis of bromine containing preservatives

    DEFF Research Database (Denmark)

    Bendahl, Lars; Hansen, Steen Honoré; Gammelgaard, Bente;

    2006-01-01

    Ultra performance liquid chromatography (UPLC) was coupled to inductively coupled plasma mass spectrometry (ICP-MS) for fast analysis of three bromine-containing preservatives, monitoring the 79Br and 81Br isotopes simultaneously. Due to the efficiency of the 1.7 microm column packing material...... analysis of bromine-containing preservatives in commercially available cosmetic products....

  13. Molecular simulations and density functional theory calculations of bromine in clathrate hydrate phases

    International Nuclear Information System (INIS)

    Bromine forms a tetragonal clathrate hydrate structure (TS-I) very rarely observed in clathrate hydrates of other guest substances. The detailed structure, energetics, and dynamics of Br2 and Cl2 in TS-I and cubic structure I (CS-I) clathrate hydrates are studied in this work using molecular dynamics and quantum chemical calculations. X-ray diffraction studies show that the halogen-water–oxygen distances in the cages of these structures are shorter than the sum of the van der Waals radii of halogen and oxygen atoms. This suggests that the stabilizing effects of halogen bonding or other non-covalent interactions (NCIs) may contribute to the formation of the unique tetragonal bromine hydrate structure. We performed molecular dynamics simulations of Br2 and Cl2 clathrate hydrates using our previously developed five-site charge models for the dihalogen molecules [Dureckova et al. Can. J. Chem. 93, 864 (2015)] which reproduce the computed electrostatic potentials of the dihalogens and account for the electropositive σ-hole of the halogen bond donor (the dihalogen). Analysis of the radial distribution functions, enthalpies of encapsulation, velocity and orientation autocorrelation functions, and polar angle distributions are carried out for Br2 and Cl2 guests in various cages to contrast the properties of these guests in the TS-I and CS-I phases. Quantum chemical partial geometry optimizations of Br2 and Cl2 guests in the hydrate cages using the M06-2X functional give short halogen-water distances compatible with values observed in X-ray diffraction experiments. NCI plots of guest-cage structures are generated to qualitatively show the relative strength of the non-bonding interactions between dihalogens and water molecules. The differences between behaviors of Br2 and Cl2 guests in the hydrate cages may explain why bromine forms the unique TS-I phase

  14. 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.

  15. 21 CFR 178.3290 - Chromic chloride complexes.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Chromic chloride complexes. 178.3290 Section 178... SANITIZERS Certain Adjuvants and Production Aids § 178.3290 Chromic chloride complexes. Myristo chromic chloride complex and stearato chromic chloride complex may be safely used as release agents in the...

  16. 49 CFR 179.102-17 - Hydrogen chloride, refrigerated liquid.

    Science.gov (United States)

    2010-10-01

    ... 49 Transportation 2 2010-10-01 2010-10-01 false Hydrogen chloride, refrigerated liquid. 179.102-17...) § 179.102-17 Hydrogen chloride, refrigerated liquid. Each tank car used to transport hydrogen chloride... on or after March 16, 2009 used for the transportation of hydrogen chloride, refrigerated...

  17. Ways of reducing the bromine numbers of benzene for nitration with the use of the piperylene additive

    Energy Technology Data Exchange (ETDEWEB)

    Kolyandr, L.Ya.; Litvinenko, A.M.; Mastyukov, V.A.; Potapchenko, A.A.; Savikkova, M.T.; Shoherbakova, T.G.; Shuzhenko, E.A.; Titarenko, V.G.; Tkachenko, L.A.

    1981-01-01

    To study the diminution of the bromine numbers of benzene for nitration, an investigation has been made of the impurities according to the fractions of the tests of benzene production of three coke and chemical works: the works in Makeev-a, ka, Bagleisk and Yenakievo. It has been found that when the piperylene additive is used, the value of the bromine numbers of benzene for nitration is determined, in the main, not by the piperylenes removed during purification. When the intermediate BT fractions are not sufficiently clearly selected, the value of the bromine numbers of benzene is influenced also by the impurities which are concentrated in its terminal fractions. To radically remove piperylenes, it is necessary to improve the contact between the acid and the fraction being purified; this is attained by intensifying mixing and lengthening the purification process.

  18. Reaction modelling of Iron Oxide Bromination in the UT-3 thermochemical cycle for Hydrogen production from water

    International Nuclear Information System (INIS)

    Analysis modelling of the iron oxide bromination had been carried out using experiment data from the iron oxide bromination in the UT-3 thermochemical cycle. Iron oxide in the form of pellets were made of the calcination of the mixture of iron oxide, silica, graphite and cellulose at 1473 K. Thermobalance reactor was used to study the kinetic reactions of the iron oxide bromination at a temperature of 473 K for 2 - 6 hours. The data collected from the experiments were used as input for the common models. However, none of these models could not explain the result of the experiments. A new model, a combination of two kinetic reactions : exposed particle and coated particle was created and worked successfully

  19. SYNTHESIS AND GREEN BROMINATION OF SOME CHALCONES AND THEIR ANTIMICROBIAL SCREENING

    Directory of Open Access Journals (Sweden)

    Mayur R. Adokar

    2013-04-01

    Full Text Available Chalcones are the versatile molecules having the structural flexibility which permits structural transformations into flavonoids, flavanones, pyrazoles, oxazoles, pyrimidines etc. Changes in their structure have offered the development of new medicinal agents having improved pharmacological potency. Their derivatives have attracts increasing attention due to numerous pharmacological potential. In the present communication we report the synthesis of chalcones from various acetophenone derivatives with different aromatic aldehydes and green chemistry approach to their bromination with the help of Tetrabutylammonium Tribromide (TBATB. All the synthesized chalcone dibromides were screened for their antimicrobial activity against Aspergillus flavus, Rhizopus sp., Fusarium solani and Aspergillus niger.

  20. Brominated flame retardants in waste electrical and electronic equipment: substance flows in a recycling plant.

    Science.gov (United States)

    Morf, Leo S; Tremp, Josef; Gloor, Rolf; Huber, Yvonne; Stengele, Markus; Zennegg, Markus

    2005-11-15

    Brominated flame retardants (BFRs) are synthetic additives mainly used in electrical and electronic appliances and in construction materials. The properties of some BFRs are typical for persistent organic pollutants, and certain BFRs, in particular some polybrominated diphenyl ether (PBDE) congeners and hexabromocyclododecane (HBCD), are suspected to cause adverse health effects. Global consumption of the most demanded BFRs, i.e., penta-, octa-, and decaBDE, tetrabromobisphenol A (TBBPA), and HBCD, has doubled in the 1990s. Only limited and rather uncertain data are available regarding the occurrence of BFRs in consumer goods and waste fractions as well as regarding emissions during use and disposal. The knowledge of anthropogenic substance flows and stocks is essential for early recognition of environmental impacts and effective chemicals management. In this paper, actual levels of penta-, octa-, and decaBDE, TBBPA, and HBCD in waste electrical and electronic equipment (WEEE) as a major carrier of BFRs are presented. These BFRs have been determined in products of a modern Swiss recycling plant applying gas chromatography/electron capture detection and gas chromatography/mass spectrometry analysis. A substance flow analysis (SFA) technique has been used to characterize the flows of target substances in the recycling process from the bulk WEEE input into the output products. Average concentrations in small size WEEE, representing the relevant electric and electronic appliances in WEEE, sampled in 2003 amounted to 34 mg/kg for pentaBDE, 530 mg/kg for octaBDE, 510 mg/kg for decaBDE, 1420 mg/kg for TBBPA (as an additive), 17 mg/kg for HBCD, 5500 mg/kg for bromine, and 1700 mg/kg for antimony. In comparison to data that have been calculated by SFA for Switzerland from literature for the 1990s, these measured concentrations in small size WEEE were 7 times higher for pentaBDE, unexpectedly about 50% lower for decaBDE, and agreed fairly well for TBBPA (as an additive) and

  1. Antibacterial Activities of a New Brominated Diterpene from Borneon Laurencia spp

    Science.gov (United States)

    Vairappan, Charles Santhanaraju; Ishii, Takahiro; Lee, Tan Kai; Suzuki, Minoru; Zhaoqi, Zhan

    2010-01-01

    In our continuous interest to study the diversity of halogenated metabolites of Malaysian species of the red algal genus Laurencia, we examined the chemical composition of five populations of unrecorded Laurencia sp. A new brominated diterpene, 10-acetoxyangasiol (1), and four other known metabolites, aplysidiol (2), cupalaurenol (3), 1-methyl-2,3,5-tribromoindole (4), and chamigrane epoxide (5), were isolated and identified. Isolated metabolites exhibited potent antibacterial activities against clinical bacteria, Staphylococcus aureus, Staphylococcus sp., Streptococcus pyogenes, Salmonella sp. and Vibrio cholerae. PMID:20631866

  2. Antibacterial Activities of a New Brominated Diterpene from Borneon Laurencia spp.

    Directory of Open Access Journals (Sweden)

    Charles Santhanaraju Vairappan

    2010-05-01

    Full Text Available In our continuous interest to study the diversity of halogenated metabolites of Malaysian species of the red algal genus Laurencia, we examined the chemical composition of five populations of unrecorded Laurencia sp. A new brominated diterpene, 10-acetoxyangasiol (1, and four other known metabolites, aplysidiol (2, cupalaurenol (3, 1-methyl-2,3,5-tribromoindole (4, and chamigrane epoxide (5, were isolated and identified. Isolated metabolites exhibited potent antibacterial activities against clinical bacteria, Staphylococcus aureus, Staphylococcus sp., Streptococcus pyogenes, Salmonella sp. and Vibrio cholerae.

  3. Methyl chloride and methyl bromide emissions from baking: an unrecognized anthropogenic source.

    Science.gov (United States)

    Thornton, Brett F; Horst, Axel; Carrizo, Daniel; Holmstrand, Henry

    2016-05-01

    Methyl chloride and methyl bromide (CH3Cl and CH3Br) are the largest natural sources of chlorine and bromine, respectively, to the stratosphere, where they contribute to ozone depletion. We report the anthropogenic production of CH3Cl and CH3Br during breadbaking, and suggest this production is an abiotic process involving the methyl ester functional groups in pectin and lignin structural polymers of plant cells. Wide variations in baking styles allow only rough estimates of this flux of methyl halides on a global basis. A simple model suggests that CH3Br emissions from breadbaking likely peaked circa 1990 at approximately 200tonnes per year (about 0.3% of industrial production), prior to restrictions on the dough conditioner potassium bromate. In contrast, CH3Cl emissions from breadbaking may be of similar magnitude as acknowledged present-day CH3Cl industrial emissions. Because the mechanisms involve functional groups and compounds widely found in plant materials, this type of methyl halide production may occur in other cooking techniques as well. PMID:26878644

  4. The influence of nitrogen oxides on the activation of bromide and chloride in salt aerosol

    Science.gov (United States)

    Bleicher, S.; Buxmann, J. C.; Sander, R.; Riedel, T. P.; Thornton, J. A.; Platt, U.; Zetzsch, C.

    2014-04-01

    Experiments on salt aerosol with different salt contents were performed in a Teflon chamber under tropospheric light conditions with various initial contents of nitrogen oxides (NOx = NO + NO2). A strong activation of halogens was found at high NOx mixing ratios, even in samples with lower bromide contents such as road salts. The ozone depletion by reactive halogen species released from the aerosol, was found to be a function of the initial NOx mixing ratio. Besides bromine, large amounts of chlorine have been released in our smog chamber. Time profiles of the halogen species Cl2, Br2, ClNO2, BrNO2 and BrO, ClO, OClO and Cl atoms were simultaneously measured by various techniques (chemical ionization mass spectrometry, differential optical absorption spectrometry coupled with a multi-reflection cell and gas chromatography of hydrocarbon tracers for Cl and OH, employing cryogenic preconcentration and flame ionization detection). Measurements are compared to calculations by the CAABA/MECCA 0-D box model, which was adapted to the chamber conditions and took the aerosol liquid water content and composition into account. The model results agree reasonably with the observations and provide important information about the prerequisites for halogen release, such as the time profiles of the aerosol bromide and chloride contents as well as the aerosol pH.

  5. Factors influencing chloride deposition in a coastal hilly area and application to chloride deposition mapping

    Directory of Open Access Journals (Sweden)

    H. Guan

    2009-09-01

    Full Text Available Chloride is commonly used as an environmental tracer for studying water flow and solute transport in the environment. It is especially useful for estimating groundwater recharge based on the commonly used chloride mass balance (CMB method. Strong spatial variability in chloride deposition in coastal areas is one difficulty encountered in appropriately applying the CMB approach. Furthermore, intensive vegetation clearance for agriculture, for example during the European settlement in many coastal areas of Australia, may have perturbed catchment chloride balance conditions for appropriate use in CMB applications. In order to deal with these issues, a high resolution chloride deposition map in the coastal region is needed. In this study, we examined geographic, orographic, and atmospheric factors influencing chloride deposition in the Mount Lofty Ranges (MLR, a coastal hilly area of approximately 9000 km2 spatial extent in South Australia, using partial correlation and regression analyses. The results indicate that coastal distance, and terrain aspect and slope are two most significant factors controlling chloride deposition. Coastal distance accounts for 65% spatial variability in chloride deposition, with terrain aspect and slope for 8%. The deposition gradient is about 0.08 gm-2 year-1 km-1 as one progresses inland. The results are incorporated into a published de-trended residual kriging approach (ASOADeK to produce a 1 km×1 km resolution annual chloride deposition map and a bulk precipitation chloride concentration map. The average uncertainty of the deposition map is about 30% in the western MLR, and over 50% in the eastern MLR. The maps will form a very useful basis for examining catchment chloride balances for use in the CMB application in the study area.

  6. Price Wars and the Stability of Collusion: A Study of the Pre-World War I Bromine Industry

    OpenAIRE

    Margaret Levenstein

    1993-01-01

    Bromine producers colluded to raise prices and profits during most of the period between 1885 and 1914. Collusion was punctuated by price wars in which prices fell sharply. The characteristics of these price wars are compared with those in the Green-Porter and Abreu- Pearce-Stachetti models. Some of the bromine price wars resulted from the imperfect monitoring problems in these models. Those price wars were short and mild. More severe price wars were part of a bargaining process, in which fir...

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

    International Nuclear Information System (INIS)

    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

  8. Distribution and speciation of bromine in mammalian tissue and fluids by X-ray fluorescence imaging and X-ray absorption spectroscopy.

    Science.gov (United States)

    Ceko, Melanie J; Hummitzsch, Katja; Hatzirodos, Nicholas; Bonner, Wendy; James, Simon A; Kirby, Jason K; Rodgers, Raymond J; Harris, Hugh H

    2015-05-01

    Bromine is one of the most abundant and ubiquitous trace elements in the biosphere and until recently had not been shown to perform any essential biological function in animals. A recent study demonstrated that bromine is required as a cofactor for peroxidasin-catalysed formation of sulfilimine crosslinks in Drosophila. In addition, bromine dietary deficiency is lethal in Drosophila, whereas bromine replenishment restores viability. The aim of this study was to examine the distribution and speciation of bromine in mammalian tissues and fluids to provide further insights into the role and function of this element in biological systems. In this study we used X-ray fluorescence (XRF) imaging and inductively coupled plasma-mass spectrometry (ICP-MS) to examine the distribution of bromine in bovine ovarian tissue samples, follicular fluid and aortic serum, as well as human whole blood and serum and X-ray absorption spectroscopy (XAS) to identify the chemical species of bromine in a range of mammalian tissue (bovine, ovine, porcine and murine), whole blood and serum samples (bovine, ovine, porcine, murine and human), and marine samples (salmon (Salmo salar), kingfish (Seriola lalandi) and Scleractinian coral). Bromine was found to be widely distributed across all tissues and fluids examined. In the bovine ovary in particular it was more concentrated in the sub-endothelial regions of arterioles. Statistical comparison of the near-edge region of the X-ray absorption spectra with a library of bromine standards led to the conclusion that the major form of bromine in all samples analysed was bromide. PMID:25675086

  9. Inhibition of nitrite-induced toxicity in channel catfish by calcium chloride and sodium chloride

    Science.gov (United States)

    Tommasso J.R., Wright; Simco, B.A.; Davis, K.B.

    1980-01-01

    Environmental chloride has been shown to inhibit methemoglobin formation in fish, thereby offering a protective effect against nitrite toxicity. Channel catfish (Ictalurus punctatus) were simultaneously exposed to various environmental nitrite and chloride levels (as either CaCl2 or NaCl) in dechlorinated tap water (40 mg/L total hardness, 47 mg/L alkalinity, 4 mg/L chloride, pH = 6.9-7.1, and temperature 21-24°C). Methemoglobin levels in fish simultaneously exposed to 2.5 mg/L nitrite and up to 30 mg/L chloride as either CaCl2 or NaCl were similar but significantly lower than in unprotected fish. Exposure to 10 mg/L nitrite and 60 mg/L chloride resulted in methemoglobin levels similar to those of the controls; most unprotected fish died. Fish exposed to 10 mg/L nitrite had significantly lower methemoglobin levels when protected with 15.0 mg/L chloride as CaCl2 than with NaCl. Fish exposed to nitrite in the presence of 60 mg/L chloride (as either CaCl2 or NaCl) had similar 24-h LC50 values that were significantly elevated above those obtained in the absence of chloride. Calcium had little effect on tolerance to nitrite toxicity in channel catfish in contrast to its large effect reported in steelhead trout (Salmo gairdneri).

  10. Congenital Chloride Diarrhea: Diagnosis by Easy-Accessible Chloride Measurement in Feces

    Directory of Open Access Journals (Sweden)

    C. Gils

    2016-01-01

    Full Text Available Background. Congenital chloride diarrhea (CCD is an autosomal recessive disorder caused by mutations in the genes encoding the intestinal Cl−/HCO3- exchanger and is clinically characterized by watery, profound diarrhea, electrolyte disturbances, and metabolic alkalosis. The CCD diagnosis is based on the clinical symptoms and measurement of high chloride concentration in feces (>90 mmol/L and is confirmed by DNA testing. Untreated CCD is lethal, while long-term clinical outcome improves when treated correctly. Case Presentation. A 27-year-old woman had an emergency caesarian due to pain and discomfort in gestational week 36 + 4. The newborn boy had abdominal distension and yellow fluid per rectum. Therapy with intravenous glucose and sodium chloride decreased his stool frequency and improved his clinical condition. A suspicion of congenital chloride diarrhea was strongly supported using blood gas analyzer to measure an increased chloride concentration in the feces; the diagnosis was confirmed by DNA testing. Discussion. Measurement of chloride in feces using an ordinary blood gas analyzer can serve as a preliminary analysis when congenital chloride diarrhea is suspected. This measurement can be easily performed with a watery feces composition. An easy-accessible chloride measurement available will facilitate the diagnostics and support the initial treatment if CCD is suspected.

  11. Amine and Titanium (IV Chloride, Boron (III Chloride or Zirconium (IV Chloride-Promoted Baylis-Hillman Reactions

    Directory of Open Access Journals (Sweden)

    Shi-Cong Cui

    2001-10-01

    Full Text Available The Baylis-Hillman reactions of various aryl aldehydes with methyl vinyl ketone at temperatures below -20oC using Lewis acids such as titanium (IV chloride, boron (III chloride or zirconium (IV chloride in the presence of a catalytic amount of selected amines used as a Lewis bases afford the chlorinated compounds 1 as the major product in very high yields. Acrylonitrile can also undergo the same reaction to give the corresponding chlorinated product in moderate yield. A plausible reaction mechanism is proposed. However, if the reaction was carried out at room temperature (ca. 20oC, then the Z-configuration of the elimination product 3, derived from 1, was formed as the major product.

  12. Determination of bromide, chloride, fluoride, nitrate and sulphate by ion chromatography: comparisons of methodologies for rainfall, cloud water and river waters at the Plynlimon catchments of mid-Wales

    Directory of Open Access Journals (Sweden)

    2007-01-01

    Full Text Available The results of determination of bromide, chloride, fluoride, nitrate and sulphate using ion chromatography (IC are compared with those obtained by colorimetric and inductively coupled plasma optical emission spectroscopy (ICPOES for rainfall, cloud water and stream waters in the Plynlimon experimental catchments of mid-Wales. For bromide, the concentrations determined by IC are lower than those for the colorimetric method used; the colorimetric method probably determined bromide plus organo-bromine compounds. It is suggested that the values determined by the colorimetric method be termed dissolved labile bromine (DLBr. The study shows that sulphate is the overriding form of sulphur in the waters. For chloride and nitrate, measurements by both methods approach a 1:1 relationship that is barely statistically significantly different from unity. For fluoride, the IC method gives lower values than the colorimetric, especially for the stream waters. However, the colorimetric method determines total fluorine so that a difference is to be expected (for example, fluoride strongly complexes with aluminium that is present, especially in the streamwater.

  13. Chloride equilibrium potential in salamander cones

    Directory of Open Access Journals (Sweden)

    Bryson Eric J

    2004-12-01

    Full Text Available Abstract Background GABAergic inhibition and effects of intracellular chloride ions on calcium channel activity have been proposed to regulate neurotransmission from photoreceptors. To assess the impact of these and other chloride-dependent mechanisms on release from cones, the chloride equilibrium potential (ECl was determined in red-sensitive, large single cones from the tiger salamander retinal slice. Results Whole cell recordings were done using gramicidin perforated patch techniques to maintain endogenous Cl- levels. Membrane potentials were corrected for liquid junction potentials. Cone resting potentials were found to average -46 mV. To measure ECl, we applied long depolarizing steps to activate the calcium-activated chloride current (ICl(Ca and then determined the reversal potential for the current component that was inhibited by the Cl- channel blocker, niflumic acid. With this method, ECl was found to average -46 mV. In a complementary approach, we used a Cl-sensitive dye, MEQ, to measure the Cl- flux produced by depolarization with elevated concentrations of K+. The membrane potentials produced by the various high K+ solutions were measured in separate current clamp experiments. Consistent with electrophysiological experiments, MEQ fluorescence measurements indicated that ECl was below -36 mV. Conclusions The results of this study indicate that ECl is close to the dark resting potential. This will minimize the impact of chloride-dependent presynaptic mechanisms in cone terminals involving GABAa receptors, glutamate transporters and ICl(Ca.

  14. Dynamic Electrochemical Measurement of Chloride Ions.

    Science.gov (United States)

    Abbas, Yawar; de Graaf, Derk B; Olthuis, Wouter; van den Berg, Albert

    2016-02-05

    This protocol describes the dynamic measurement of chloride ions using the transition time of a silver silver chloride (Ag/AgCl) electrode. Silver silver chloride electrode is used extensively for potentiometric measurement of chloride ions concentration in electrolyte. In this measurement, long-term and continuous monitoring is limited due to the inherent drift and the requirement of a stable reference electrode. We utilized the chronopotentiometric approach to minimize drift and avoid the use of a conventional reference electrode. A galvanostatic pulse is applied to an Ag/AgCl electrode which initiates a faradic reaction depleting the Cl- ions near the electrode surface. The transition time, which is the time to completely deplete the ions near the electrode surface, is a function of the ion concentration, given by the Nernst equation. The square root of the transition time is in linear relation to the chloride ion concentration. Drift of the response over two weeks is negligible (59 µM/day) when measuring 1 mM [Cl-]using a current pulse of 10 Am(-2). This is a dynamic measurement where the moment of transition time determines the response and thus is independent of the absolute potential. Any metal wire can be used as a pseudo-reference electrode, making this approach feasible for long-term measurement inside concrete structures.

  15. Analytical approaches for determination of bromine in sediment core samples by X-ray fluorescence spectrometry.

    Science.gov (United States)

    Pashkova, Galina V; Aisueva, Tatyana S; Finkelshtein, Alexander L; Ivanov, Egor V; Shchetnikov, Alexander A

    2016-11-01

    Bromine has been recognized as a valuable indicator for paleoclimatic studies. Wavelength dispersive X-ray fluorescence (WDXRF) and total reflection X-ray fluorescence (TXRF) methods were applied to study the bromine distributions in lake sediment cores. Conventional WDXRF technique usually requires relatively large mass of a sediment sample and a set of calibration samples. Some analytical approaches were developed to apply WDXRF to small sediment core samples in the absence of adequate calibration samples with a known Br content. The mass of a sample to be analyzed was reduced up to 200-300mg and the internal standard method with correction using fundamental parameters was developed for Br quantification. TXRF technique based on the direct analysis of a solid suspension using 20mg of sediment sample by internal standard method was additionally tested. The accuracy of the WDXRF and TXRF techniques was assessed by the comparative analysis of reference materials of sediments, soil and biological samples. In general, good agreement was achieved between the reference values and the measured values. The detection limits of Br were 1mg/kg and 0.4mg/kg for WDXRF and TXRF respectively. The results of the Br determination obtained with different XRF techniques were comparable to each other and used for paleoclimatic reconstructions. PMID:27591627

  16. Synthesis of α-Bromine- Terminated Polystyrene Macroinitiator and Its Initiation of MMA Polymerization by ATRP

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    In the present paper the synthesis of block copolymers via the transformation from living anionic polymerization (LAP) to atom transfer radical polymerization (ATRP) was described. Α-Bromine-terminated polystyrenes(PStBr) in the LAP step was prepared by using n-BuLi as initiator, tetrahydrofuran (THF) as the activator, α-methylstyrene (α-MeSt) as the capping group and liquid bromine (Br2) as the bromating agent. The effects of reaction conditions such as the amounts of α-MeSt, THF, and Br2 as well as molecular weight of polystyrene on the bromating efficiency (BE) and coupling extent (CE) were examined. The present results show that the yield of PStBr obtained was more than 93.8% and the coupling reaction was substantially absent. PStBr was further used as the macroinitiator in the polymerization of methyl-methacrylate(MMA) in the presence of copper(Ⅰ) halogen and 2,2-bipyridine(bpy) complexes. It was found that the molecular weight of the resulted PSt-b-PMMA increased linearly with the increase of the conversion of MMA and the polydispersity was 1.2-1.6. The structures of PStBr and P(St-b-MMA) were characterized by 1H NMR spectra.

  17. Levelized cost of energy and sensitivity analysis for the hydrogen-bromine flow battery

    Science.gov (United States)

    Singh, Nirala; McFarland, Eric W.

    2015-08-01

    The technoeconomics of the hydrogen-bromine flow battery are investigated. Using existing performance data the operating conditions were optimized to minimize the levelized cost of electricity using individual component costs for the flow battery stack and other system units. Several different configurations were evaluated including use of a bromine complexing agent to reduce membrane requirements. Sensitivity analysis of cost is used to identify the system elements most strongly influencing the economics. The stack lifetime and round-trip efficiency of the cell are identified as major factors on the levelized cost of electricity, along with capital components related to hydrogen storage, the bipolar plate, and the membrane. Assuming that an electrocatalyst and membrane with a lifetime of 2000 cycles can be identified, the lowest cost market entry system capital is 220 kWh-1 for a 4 h discharge system and for a charging energy cost of 0.04 kWh-1 the levelized cost of the electricity delivered is 0.40 kWh-1. With systems manufactured at large scales these costs are expected to be lower.

  18. Hair as an indicator of endogenous tissue levels of brominated flame retardants in mammals.

    Science.gov (United States)

    D'Havé, Helga; Covaci, Adrian; Scheirs, Jan; Schepens, Paul; Verhagen, Ron; De Coen, Wim

    2005-08-15

    Few data are available on brominated flame retardants (BFRs) in terrestrial mammalian wildlife. Moreover, the use of hair in nondestructive monitoring of BFRs in mammals or humans has not been investigated. In the present study, concentrations of polybrominated diphenyl ethers (PBDEs) and brominated biphenyl 153 (BB 153) were analyzed in tissues of the European hedgehog Erinaceus europaeus. Road kills and carcasses from wildlife rescue centers were used to investigate relationships between concentrations of BFRs in hair and internal tissues, BFR tissue distribution (hair, liver, kidney, muscle, and adipose tissue), and PBDE congener tissue pattern dissimilarities. Liver concentrations of PBDEs and BB 153 were in the ranges 1-1178 and 0-2.5 ng/g of liver wet weight, respectively. PBDEs were predominant in adipose tissue and liver, while accumulation of BB 153 was tissue independent. The less persistent compound BDE 99 was more dominant in hair than in internal tissues. We observed positive relationships between BFR levels in hair and internal tissues for sum PBDEs and BDE 47 (0.37 terrestrial mammals which can be used in nondestructive monitoring schemes.

  19. 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. PMID:23398278

  20. 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.

  1. Novel Spectrophotometric Method for Determination of Macro-paracetamol via Reaction with Bromine

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    The reaction between Br2 and paracetamol(p-AAP) leads to the formation of a coloured product, which can be used for spectrophotometric determination of the p-AAP content in its pure form and in different pharmaceutical preparations with p-AAP. The stoichiometric composition of the reaction was found to be n(p-AAP)∶n(bromine)=1∶3. The effects of pH and time on the spectra of p-AAP-bromine redox reaction product were studied. The interference of different additives on the measured spectra of the obtained product was also studied. The results obtained by the present method were compared with those obtained by the standard method. The F- and t- test values were calculated for both of the applied procedures and they met a confidence level of 99%. The proposed procedure actually needs no separation of these drugs from their sources before analysis and was unaffected by interference of other phenolic compounds. The proposed method is simpler and faster than the repoeted ones.

  2. Selected chlorobornanes, polychlorinated naphthalenes and brominated flame retardants in Bjornoya (Bear Island) freshwater biota

    International Nuclear Information System (INIS)

    Levels of selected sparsely investigated persistent organic pollutants (POPs) have been measured in organisms from two Arctic lakes on Bjornoya (Bear Island). Elevated levels of chlorobornanes (CHBs) (up to 46.7 ng/g wet weight=ww), polybrominated diphenyl ethers (PBDEs) (up to 27.2 ng/g ww), polybrominated biphenyls (PBBs) (up to 1.1 ng/g ww) and polychlorinated naphthalenes (PCNs, only 4 congeners) (up to 62.7 pg/g ww), were measured in biota from Lake Ellasjoen. In Lake Oyangen, located only 5 km north of Ellasjoen, levels of these contaminants were significantly lower. δ15N-values were 7-10%o higher in organisms from Ellasjoen as compared to Oyangen. This is attributed to biological inputs related to seabird activities. The present study illustrates that contaminants such as CHBs, brominated flame retardants and PCNs accumulate in the Ellasjoen food web in a manner similar to PCBs and conventional organochlorine pesticides. Transport mechanisms that control PCB and DDT distributions, i.e. atmospheric long-range transport and biotransport by seabirds, are also relevant for the contaminants investigated in the present study. - Elevate levels of chlorobornanes, polychlorinated naphthalenes and brominated flame retardants have been measured in biota from a Norwegian Arctic lake

  3. 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.

  4. 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.; VanRoozendael, M.

    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.

  5. 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.

  6. Ultrafast optical limiting properties and transient dynamics of symmetrical phenoxazinium bromine salt

    Science.gov (United States)

    Xiao, Zhengguo; Ge, Jianfeng; Li, Zhongguo; Wu, Xingzhi; Fang, Yu; Shi, Guang; Zhang, Xueru; Wang, Yuxiao; Song, Yinglin

    2015-12-01

    A symmetrical phenoxazinium bromine salt with resonant D-π-D structure was prepared and spectroscopically characterized. The ultrafast nonlinear optical (NLO) response of the compound dissolved in DMF was investigated using open aperture Z-scan method with 190 fs laser pulses at 515 nm. And the photo-physical dynamics of the compound was studied using transient absorption spectra at femtosecond time regime. The titled sample showed strong reverse saturable absorption (RSA) at 515 nm. Transient absorption results demonstrated that the compound exhibited RSA signals at 478-580 nm and SA signals at 600-780 nm. A simplified three-energy-level model was used to determine the photo-physical parameters. And the excited-state lifetime was evaluated to be around one nanosecond. Our results show that the phenoxazinium bromine salt has a large ratio of singlet excited-state absorption cross-section to that of ground state cross-section (18.7), indicating it is a candidate material for future ultrafast optical limiters.

  7. Natural solar photolysis of total organic chlorine, bromine and iodine in water.

    Science.gov (United States)

    Abusallout, Ibrahim; Hua, Guanghui

    2016-04-01

    Municipal wastewater has been increasingly used to augment drinking water supplies due to the growing water scarcity. Wastewater-derived disinfection byproducts (DBPs) may negatively affect the aquatic ecosystems and human health of downstream communities during water reuse. The objective of this research was to determine the degradation kinetics of total organic chlorine (TOCl), bromine (TOBr) and iodine (TOI) in water by natural sunlight irradiation. Outdoor solar photolysis experiments were performed to investigate photolytic degradation of the total organic halogen (TOX) formed by fulvic acid and real water and wastewater samples. The results showed that TOX degradation by sunlight irradiation followed the first-order kinetics with half-lives in the range of 2.6-10.7 h for different TOX compounds produced by fulvic acid. The TOX degradation rates were generally in the order of TOI > TOBr ≅ TOCl(NH2Cl) > TOCl(Cl2). High molecular weight TOX was more susceptible to solar photolysis than corresponding low molecular weight halogenated compounds. The nitrate and sulfite induced indirect TOX photolysis rates were less than 50% of the direct photolysis rates under the conditions of this study. Fulvic acid and turbidity in water reduced TOX photodegradation. These results contribute to a better understanding of the fate of chlorinated, brominated and iodinated DBPs in surface waters.

  8. Selected chlorobornanes, polychlorinated naphthalenes and brominated flame retardants in Bjornoya (Bear Island) freshwater biota

    Energy Technology Data Exchange (ETDEWEB)

    Evenset, Anita [Akvaplan-niva, Polar Environmental Centre, N-9296 Tromso (Norway)]. E-mail: ae@akvaplan.niva.no; Christensen, Guttorm N. [Akvaplan-niva, Polar Environmental Centre, N-9296 Tromso (Norway); Kallenborn, Roland [Norwegian Institute for Air Research, P.O. Box 100, N-2027 Kjeller (Norway)

    2005-08-15

    Levels of selected sparsely investigated persistent organic pollutants (POPs) have been measured in organisms from two Arctic lakes on Bjornoya (Bear Island). Elevated levels of chlorobornanes (CHBs) (up to 46.7 ng/g wet weight=ww), polybrominated diphenyl ethers (PBDEs) (up to 27.2 ng/g ww), polybrominated biphenyls (PBBs) (up to 1.1 ng/g ww) and polychlorinated naphthalenes (PCNs, only 4 congeners) (up to 62.7 pg/g ww), were measured in biota from Lake Ellasjoen. In Lake Oyangen, located only 5 km north of Ellasjoen, levels of these contaminants were significantly lower. {delta}{sup 15}N-values were 7-10%o higher in organisms from Ellasjoen as compared to Oyangen. This is attributed to biological inputs related to seabird activities. The present study illustrates that contaminants such as CHBs, brominated flame retardants and PCNs accumulate in the Ellasjoen food web in a manner similar to PCBs and conventional organochlorine pesticides. Transport mechanisms that control PCB and DDT distributions, i.e. atmospheric long-range transport and biotransport by seabirds, are also relevant for the contaminants investigated in the present study. - Elevate levels of chlorobornanes, polychlorinated naphthalenes and brominated flame retardants have been measured in biota from a Norwegian Arctic lake.

  9. Levels and distribution of brominated flame retardants in the soil of Harbin in China

    Institute of Scientific and Technical Information of China (English)

    WANG Xu; REN Nanqi; QI Hong; MA Wanli; LI Yifan

    2009-01-01

    This study reports the presence of brominated flame retardants in the topsoil in and around Harbin,a city in northeastern China.Samples of soil were collected from 17 locations in 2006,and the levels of 9 polybrominated diphenylethers (PBDEs 17,28,47,66,99,100,153,154,and 183) ranged from 2.45 to 55.9 pg/g dry weight (dw) with a mean of 26.3 pg/g dw.These levels are very low compared with those for some cities in Europe and the USA.BDE 209 and hexabromocyclododecane were the two dominant congeners,with mean concentrations of 520 pg/g dw and 1750 pg/g dw,respectively.The concentrations of the total 9 PBDE congeners clearly decreased from urban areas to background,but the compositions of individual congeners differed.Proportions of heavier congeners decreased while those of lighter congeners increased,along urban-rural-background transect,providing evidence for an urban fractionation effect.Correlation analysis indicated similar sources for PBDEs,hexabromocyclododecane,and 1,2-bis(2,4,6-tribromophenoxy)-ethane from urban areas but pentabromoethylbenzene was probably present due to long-range atmospheric transport.Principal component analysis was used to determine the characteristics of the relationships among these brominated flame retardants in the field.

  10. 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. METHOD

  11. Different speciation for bromine in brown and red algae, revealed by in vivo X-ray absorption spectroscopic studies.

    Science.gov (United States)

    Küpper, Frithjof C; Leblanc, Catherine; Meyer-Klaucke, Wolfram; Potin, Philippe; Feiters, Martin C

    2014-08-01

    Members of various algal lineages are known to be strong producers of atmospherically relevant halogen emissions, that is a consequence of their capability to store and metabolize halogens. This study uses a noninvasive, synchrotron-based technique, X-ray absorption spectroscopy, for addressing in vivo bromine speciation in the brown algae Ectocarpus siliculosus, Ascophyllum nodosum, and Fucus serratus, the red algae Gracilaria dura, G. gracilis, Chondrus crispus, Osmundea pinnatifida, Asparagopsis armata, Polysiphonia elongata, and Corallina officinalis, the diatom Thalassiosira rotula, the dinoflagellate Lingulodinium polyedrum and a natural phytoplankton sample. The results highlight a diversity of fundamentally different bromine storage modes: while most of the stramenopile representatives and the dinoflagellate store mostly bromide, there is evidence for Br incorporated in nonaromatic hydrocarbons in Thalassiosira. Red algae operate various organic bromine stores - including a possible precursor (by the haloform reaction) for bromoform in Asparagopsis and aromatically bound Br in Polysiphonia and Corallina. Large fractions of the bromine in the red algae G. dura and C. crispus and the brown alga F. serratus are present as Br(-) defects in solid KCl, similar to what was reported earlier for Laminaria parts. These results are discussed according to different defensive strategies that are used within algal taxa to cope with biotic or abiotic stresses. PMID:26988449

  12. 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...

  13. Corrosion mechanism of 13Cr stainless steel in completion fluid of high temperature and high concentration bromine salt

    International Nuclear Information System (INIS)

    Highlights: • The corrosion behavior of 13Cr steel exposed to bromine salt completion fluid containing high concentration bromine ions was investigated. • There are passive circles around pits on the 13Cr steel surface after 7 d of exposure. • Macroscopic galvanic corrosion formed between the passive halo and the pit. • The mechanism of pitting corrosion on 13Cr stainless steel exposed to heavy bromine brine was established. - Abstract: A series of corrosion tests of 13Cr stainless steel were conducted in a simulated completion fluid environment of high temperature and high concentration bromine salt. Corrosion behavior of specimens and the component of corrosion products were investigated by means of scanning electron microscope (SEM), confocal laser scanning microscopy (CLSM) and X-ray photoelectron spectroscopy (XPS). The results indicate that 13Cr steel suffers from severe local corrosion and there is always a passive halo around every pit. The formation mechanism of the passive halo is established. OH− ligand generates and adsorbs in a certain scale because of abundant OH− on the surface around the pits. Passive film forms around each pit, which leads to the occurrence of passivation in a certain region. Finally, the dissimilarities in properties and morphologies of regions, namely the pit and its corresponding passive halo, can result in different corrosion sensitivities and may promote the formation of macroscopic galvanic pairs

  14. Exposure to brominated trihalomethanes in water during pregnancy and micronuclei frequency in maternal and cord blood lymphocytes

    DEFF Research Database (Denmark)

    Stayner, Leslie Thomas; Pedersen, Marie; Patelarou, Evridiki;

    2014-01-01

    BACKGROUND: Water disinfection by-products have been associated with an increased cancer risk. Micronuclei (MN) frequency in lymphocytes is a marker of genomic damage and can predict adult cancer risk. OBJECTIVE: We evaluated maternal exposure to drinking water brominated trihalomethanes (BTHM) i...

  15. Accumulation of organochlorines and brominated flame retardants in estuarine and marine food chains: Field measurements and model calculations

    NARCIS (Netherlands)

    Veltman, K.; Hendriks, J.; Huijbregts, M.; Leonards, P.E.G.; Heuvel-Greve, van den M.J.; Vethaak, D.

    2005-01-01

    Food chain accumulation of organochlorines and brominated flame retardants in estuarine and marine environments is compared to model estimations and fresh water field data. The food chain consists of herbivores, detritivores and primary and secondary carnivores i.e. fish, fish-eating birds and marin

  16. 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) leve

  17. Corrosion mechanism of 13Cr stainless steel in completion fluid of high temperature and high concentration bromine salt

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yan [Corrosion and Protection Center, Key Laboratory for Environmental Fracture (MOE), Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing 100083 (China); Xu, Lining, E-mail: xulining@ustb.edu.cn [Corrosion and Protection Center, Key Laboratory for Environmental Fracture (MOE), Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing 100083 (China); Lu, Minxu [Corrosion and Protection Center, Key Laboratory for Environmental Fracture (MOE), Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing 100083 (China); Meng, Yao [Beijing Institute of Aeronautical Materials, Beijing 100095 (China); Zhu, Jinyang; Zhang, Lei [Corrosion and Protection Center, Key Laboratory for Environmental Fracture (MOE), Institute for Advanced Materials and Technology, University of Science and Technology Beijing, Beijing 100083 (China)

    2014-09-30

    Highlights: • The corrosion behavior of 13Cr steel exposed to bromine salt completion fluid containing high concentration bromine ions was investigated. • There are passive circles around pits on the 13Cr steel surface after 7 d of exposure. • Macroscopic galvanic corrosion formed between the passive halo and the pit. • The mechanism of pitting corrosion on 13Cr stainless steel exposed to heavy bromine brine was established. - Abstract: A series of corrosion tests of 13Cr stainless steel were conducted in a simulated completion fluid environment of high temperature and high concentration bromine salt. Corrosion behavior of specimens and the component of corrosion products were investigated by means of scanning electron microscope (SEM), confocal laser scanning microscopy (CLSM) and X-ray photoelectron spectroscopy (XPS). The results indicate that 13Cr steel suffers from severe local corrosion and there is always a passive halo around every pit. The formation mechanism of the passive halo is established. OH{sup −} ligand generates and adsorbs in a certain scale because of abundant OH{sup −} on the surface around the pits. Passive film forms around each pit, which leads to the occurrence of passivation in a certain region. Finally, the dissimilarities in properties and morphologies of regions, namely the pit and its corresponding passive halo, can result in different corrosion sensitivities and may promote the formation of macroscopic galvanic pairs.

  18. Alkali metal and ammonium chlorides in water and heavy water (binary systems)

    CERN Document Server

    Cohen-Adad, R

    1991-01-01

    This volume surveys the data available in the literature for solid-fluid solubility equilibria plus selected solid-liquid-vapour equilibria, for binary systems containing alkali and ammonium chlorides in water or heavy water. Solubilities covered are lithium chloride, sodium chloride, potassium chloride, rubidium chloride, caesium chloride and ammonium chloride in water and heavy water.

  19. 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

  20. Method for preparation of melts of alkali metal chlorides with highly volatile polyvalent metal chlorides

    International Nuclear Information System (INIS)

    A method for production of alkali metal (Cs, Rb, K) chloride melts with highly volatile polyvalent metal chlorides is suggested. The method consists, in saturation of alkali metal chlorides, preheated to the melting point, by volatile component vapours (titanium tetrachloride, molybdenum or tantalum pentachloride) in proportion, corresponding to the composition reguired. The saturation is realized in an evacuated vessel with two heating areas for 1-1.5 h. After gradual levelling of temperature in both areas the product is rapidly cooled. 1 fig.; 1 tab

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

    Science.gov (United States)

    Abilama, Marc; Bates, Mike; Lohstroh, Annika

    2015-09-01

    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 5.7×1010 accumulated counts; another 32 detector samples were aged to 3.3×1010 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 chromium-plated samples

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

    Directory of Open Access Journals (Sweden)

    S. Coburn

    2015-10-01

    Full Text Available The elevated deposition of atmospheric mercury over the Southeastern United States is currently not well understood. Here we measure partial columns and vertical profiles of bromine monoxide (BrO radicals, a key component of mercury oxidation chemistry, to better understand the processes and altitudes at which mercury is being oxidized in the atmosphere. We use the data from a ground-based MAX-DOAS instrument located at a coastal site ~ 1 km from the Gulf of Mexico in Gulf Breeze, FL, where we had previously detected tropospheric BrO (Coburn et al., 2011. Our profile retrieval assimilates information about stratospheric BrO from the WACCM chemical transport model, and uses only measurements at moderately low solar zenith angles (SZA to estimate the BrO slant column density contained in the reference spectrum (SCDRef. The approach has 2.6 degrees of freedom, and avoids spectroscopic complications that arise at high SZA; knowledge about SCDRef helps to maximize sensitivity in the free troposphere (FT. A cloud-free case study day with low aerosol load (9 April 2010 provided optimal conditions for distinguishing marine boundary layer (MBL: 0–1 km and free tropospheric (FT: 1–15 km BrO from the ground. The average daytime tropospheric BrO vertical column density (VCD of ~ 2.3 × 1013 molec cm−2 (SZA 5 molec cm−2 s−1 for bromine, while contributions from ozone (O3 and chlorine (Cl were 0.9 × 105 and 0.2 × 105 molec cm−2 s−1, respectively. 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 chemical transport model, we find that surface GOM variations are typical also of other days, and are mainly derived from the free troposphere. 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

  3. 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

  4. Molecular simulations and density functional theory calculations of bromine in clathrate hydrate phases

    Energy Technology Data Exchange (ETDEWEB)

    Dureckova, Hana, E-mail: houci059@uottawa.ca; Woo, Tom K., E-mail: tom.woo@uottawa.ca [Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 5N6 (Canada); Alavi, Saman, E-mail: saman.alavi@nrc-cnrc.gc.ca [Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 5N6 (Canada); National Research Council of Canada, 100 Sussex Dr., Ottawa, Ontario K1N 6N5 (Canada); Department of Chemical and Biological Engineering, University of British Columbia, Vancouver, British Columbia V6T 1Z3 (Canada)

    2016-01-28

    Bromine forms a tetragonal clathrate hydrate structure (TS-I) very rarely observed in clathrate hydrates of other guest substances. The detailed structure, energetics, and dynamics of Br{sub 2} and Cl{sub 2} in TS-I and cubic structure I (CS-I) clathrate hydrates are studied in this work using molecular dynamics and quantum chemical calculations. X-ray diffraction studies show that the halogen-water–oxygen distances in the cages of these structures are shorter than the sum of the van der Waals radii of halogen and oxygen atoms. This suggests that the stabilizing effects of halogen bonding or other non-covalent interactions (NCIs) may contribute to the formation of the unique tetragonal bromine hydrate structure. We performed molecular dynamics simulations of Br{sub 2} and Cl{sub 2} clathrate hydrates using our previously developed five-site charge models for the dihalogen molecules [Dureckova et al. Can. J. Chem. 93, 864 (2015)] which reproduce the computed electrostatic potentials of the dihalogens and account for the electropositive σ-hole of the halogen bond donor (the dihalogen). Analysis of the radial distribution functions, enthalpies of encapsulation, velocity and orientation autocorrelation functions, and polar angle distributions are carried out for Br{sub 2} and Cl{sub 2} guests in various cages to contrast the properties of these guests in the TS-I and CS-I phases. Quantum chemical partial geometry optimizations of Br{sub 2} and Cl{sub 2} guests in the hydrate cages using the M06-2X functional give short halogen-water distances compatible with values observed in X-ray diffraction experiments. NCI plots of guest-cage structures are generated to qualitatively show the relative strength of the non-bonding interactions between dihalogens and water molecules. The differences between behaviors of Br{sub 2} and Cl{sub 2} guests in the hydrate cages may explain why bromine forms the unique TS-I phase.

  5. 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

  6. 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

  7. Liquid crystalline critical dynamics in decylammonium chloride

    CERN Document Server

    Lee, K W; Lee, C E; Kang, K H; Rhee, C; Kang, J K

    1999-01-01

    Collective chain dynamics and phase transitions in a model biomembrane, decylammonium chloride (C sub 1 sub 0 H sub 2 sub 1 NH sub 3 Cl), were studied by means of proton nuclear magnetic resonance. Our measurements sensitively reflect the critical dynamics associated with the smectic C to smectic A transition of the lipid bilayer.

  8. 75 FR 20625 - Barium Chloride From China

    Science.gov (United States)

    2010-04-20

    ... established a schedule for the conduct of this review (74 FR 62587, November 30, 2010). Subsequently, counsel... From the Federal Register Online via the Government Publishing Office INTERNATIONAL TRADE COMMISSION Barium Chloride From China AGENCY: United States International Trade Commission. ACTION:...

  9. Chloride migration in concrete with superabsorbent polymers

    DEFF Research Database (Denmark)

    Hasholt, Marianne Tange; Jensen, Ole Mejlhede

    2015-01-01

    Superabsorbent polymers (SAP) can be used as a means for internal curing of concrete. In the present study, the development of transport properties of concrete with SAP is investigated. The chloride migration coefficient according to NT BUILD 492 is used as a measure of this. Twenty concrete...

  10. Determination of chloride in uranium solutions

    Energy Technology Data Exchange (ETDEWEB)

    Danse, A.; Stoch, H.; Steele, T.W.

    1967-05-15

    Thiocyanate is first removed by precipitation with a small excess of a copper solution, and the cations are removed by passing the filtrate through a cation-exchange resin. The chloride is determined in the eluate by a potentiometric titration in which silver nitrate solution is used.

  11. Amperometric Sensor for Detection of Chloride Ions

    Directory of Open Access Journals (Sweden)

    Rene Kizek

    2008-09-01

    Full Text Available Chloride ion sensing is important in many fields such as clinical diagnosis, environmental monitoring and industrial applications. We have measured chloride ions at a carbon paste electrode (CPE and at a CPE modified with solid AgNO3, a solution of AgNO3 and/or solid silver particles. Detection limits (3 S/N for chloride ions were 100 μM, 100 μM and 10 μM for solid AgNO3, solution of AgNO3 and/or solid silver particles, respectively. The CPE modified with silver particles is the most sensitive to the presence chloride ions. After that we approached to the miniaturization of the whole electrochemical instrument. Measurements were carried out on miniaturized instrument consisting of a potentiostat with dimensions 35 × 166 × 125 mm, screen printed electrodes, a peristaltic pump and a PC with control software. Under the most suitable experimental conditions (Britton-Robinson buffer, pH 1.8 and working electrode potential 550 mV we estimated the limit of detection (3 S/N as 500 nM.

  12. Gebromeerde vlamvertragers en broomdioxines in Choline Chloride

    NARCIS (Netherlands)

    Egmond, van H.J.; Traag, W.A.; Hoogenboom, L.A.P.

    2008-01-01

    Sinds begin 2008 worden in het Nationaal Plan Diervoeder Choline Chloride monsters (= diervoeder additief) gevonden waarbij de DR CALUX screenings-assay een sterk verdacht signaal geeft, maar bij de GC-HRMS geen dioxines en dl-PCB's worden gevonden. Dit rapport beschrijft de resultaten van nader ond

  13. Regulated trafficking of the CFTR chloride channel

    NARCIS (Netherlands)

    Braakman, L.J.; Kleizen, B.; Jonge, H.R. de

    2000-01-01

    The cystic fibrosis transmembrane conductance regulator (CFTR), the ABC transporter encoded by the cystic fibrosis gene, is localized in the apical membrane of epithelial cells where it functions as a cyclic AMP-regulated chloride channel and as a regulator of other ion channels and transporters. Wh

  14. 21 CFR 582.3845 - Stannous chloride.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Stannous chloride. 582.3845 Section 582.3845 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS SUBSTANCES GENERALLY RECOGNIZED AS SAFE Chemical Preservatives §...

  15. Air-snowpack exchange of bromine, ozone and mercury in the springtime Arctic simulated by the 1-D model PHANTAS - Part 1: In-snow bromine activation and its impact on ozone

    Science.gov (United States)

    Toyota, K.; McConnell, J. C.; Staebler, R. M.; Dastoor, A. P.

    2014-04-01

    To provide a theoretical framework towards a better understanding of ozone depletion events (ODEs) and atmospheric mercury depletion events (AMDEs) in the polar boundary layer, we have developed a one-dimensional model that simulates multiphase chemistry and transport of trace constituents from porous snowpack and through the atmospheric boundary layer (ABL) as a unified system. This paper constitutes Part 1 of the study, describing a general configuration of the model and the results of simulations related to reactive bromine release from the snowpack and ODEs during the Arctic spring. A common set of aqueous-phase reactions describes chemistry both within the liquid-like layer (LLL) on the grain surface of the snowpack and within deliquesced "haze" aerosols mainly composed of sulfate in the atmosphere. Gas-phase reactions are also represented by the same mechanism in the atmosphere and in the snowpack interstitial air (SIA). Consequently, the model attains the capacity of simulating interactions between chemistry and mass transfer that become particularly intricate near the interface between the atmosphere and the snowpack. In the SIA, reactive uptake on LLL-coated snow grains and vertical mass transfer act simultaneously on gaseous HOBr, a fraction of which enters from the atmosphere while another fraction is formed via gas-phase chemistry in the SIA itself. A "bromine explosion", by which HOBr formed in the ambient air is deposited and then converted heterogeneously to Br2, is found to be a dominant process of reactive bromine formation in the top 1 mm layer of the snowpack. Deeper in the snowpack, HOBr formed within the SIA leads to an in-snow bromine explosion, but a significant fraction of Br2 is also produced via aqueous radical chemistry in the LLL on the surface of the snow grains. These top- and deeper-layer productions of Br2 both contribute to the release of Br2 to the atmosphere, but the deeper-layer production is found to be more important for the

  16. Air-snowpack exchange of bromine, ozone and mercury in the springtime Arctic simulated by the 1-D model PHANTAS – Part 1: In-snow bromine activation and its impact on ozone

    Directory of Open Access Journals (Sweden)

    K. Toyota

    2013-08-01

    Full Text Available To provide a theoretical framework towards better understanding of ozone depletion events (ODEs and atmospheric mercury depletion events (AMDEs in the polar boundary layer, we have developed a one-dimensional model that simulates multiphase chemistry and transport of trace constituents from porous snowpack and through the atmospheric boundary layer (ABL as a unified system. In this paper, we describe a general configuration of the model and the results of simulations related to reactive bromine release from the snowpack and ODEs during the Arctic spring. The model employs a chemical mechanism adapted from the one previously used for the simulation of multiphase halogen chemistry involving deliquesced sea-salt aerosols in the marine boundary layer. A common set of aqueous-phase reactions describe chemistry both in the liquid-like (or brine layer on the grain surface of the snowpack and in "haze" aerosols mainly composed of sulfate in the atmosphere. The process of highly soluble/reactive trace gases, whether entering the snowpack from the atmosphere or formed via gas-phase chemistry in the snowpack interstitial air (SIA, is simulated by the uptake on brine-covered snow grains and subsequent reactions in the aqueous phase while being traveled vertically within the SIA. A "bromine explosion", by which, in a conventional definition, HOBr formed in the ambient air is deposited and then converted heterogeneously to Br2, is a dominant process of reactive bromine formation in the top 1 mm (or less layer of the snowpack. Deeper in the snowpack, HOBr formed within the SIA leads to an in-snow bromine explosion, but a significant fraction of Br2 is also produced via aqueous radical chemistry in the brine on the surface of the snow grains. These top- and deeper-layer productions of Br2 both contribute to the Br2 release into the atmosphere, but the deeper-layer production is found to be more important for the net outflux of reactive bromine. Although ozone

  17. Investigation of factors influencing chloride extraction efficiency during electrochemical chloride extraction from reinforcing concrete

    Science.gov (United States)

    Sharp, Stephen R.

    2005-11-01

    Electrochemical chloride extraction (ECE) is an accelerated bridge restoration method similar to cathodic protection, but operates at higher current densities and utilizes a temporary installation. Both techniques prolong the life of a bridge by reducing the corrosion rate of the reinforcing bar when properly applied. ECE achieves this by moving chlorides away from the reinforcement and out of the concrete while simultaneously increasing the alkalinity of the electrolyte near the reinforcing steel. Despite the proven success, significant use of ECE has not resulted in part due to an incomplete understanding in the following areas: (1) An estimation of the additional service life that can be expected following treatment when the treated member is again subjected to chlorides; (2) The cause of the decrease in current flow and, therefore, chloride removal rate during treatment; (3) Influence of water-to-cement (w/c) ratio and cover depth on the time required for treatment. This dissertation covers the research that is connected to the last two areas listed above. To begin examining these issues, plain carbon steel reinforcing bars (rebar) were embedded in portland cement concrete slabs of varying water-to-cement (w/c) ratios and cover depths, and then exposed to chlorides. A fraction of these slabs had sodium chloride added as an admixture, with all of the slabs subjected to cyclical ponding with a saturated solution of sodium chloride. ECE was then used to remove the chlorides from these slabs while making electrical measurements in the different layers between the rebar (cathode) and the titanium mat (anode) to follow the progress of the ECE process. During this study, it was revealed that the resistance of the outer concrete surface layer increases during ECE, inevitably restricting current flow, while the resistance of the underlying concrete decreases or remains constant. During ECE treatment, a white residue formed on the surface of the concrete. Analyses of the

  18. Viscosity and density tables of sodium chloride solutions

    Energy Technology Data Exchange (ETDEWEB)

    Fair, J.A.; Ozbek, H. (comps.)

    1977-04-01

    A file is presented containing tabulated data extracted from the scientific literature on the density and viscosity of aqueous sodium chloride solutions. Also included is a bibliography of the properties of aqueous sodium chloride solutions. (MHR)

  19. Brominated flame retardants and organochlorine compounds in duplicate diet samples from a Portuguese academic community.

    Science.gov (United States)

    Coelho, Sónia D; Sousa, Ana C A; Isobe, Tomohiko; Kunisue, Tatsuya; Nogueira, António J A; Tanabe, Shinsuke

    2016-10-01

    Concentrations of persistent organic pollutants (POPs), including polybrominated diphenyl ethers (PBDEs), hexabromocyclododecanes (HBCDDs), polychlorinated biphenyls (PCBs), hexachlorocyclohexane isomers (HCHs), hexachlorobenzene (HCB), chlordane compounds (CHLs) and dichlorodiphenyltrichloroethane and its metabolites (DDTs), were measured in duplicate diet samples from 21 volunteers at a Portuguese academic community (University of Aveiro). Overall, the levels of the target compounds were low, with detection frequencies varying widely depending on the compounds and with brominated flame retardants (BFRs) registering the lowest detection frequencies. Among PCB congeners, nondioxin-like PCBs were predominant and detected in the majority of the samples. Organochlorine pesticides were also detected in the majority of the samples, with 100% detection for DDTs and HCHs. Estimated daily intakes (EDIs) were calculated using lower and upper bound estimations, and in both cases values were far below the currently established tolerable daily intakes for PCBs and OCs and the reference doses for PBDEs and HBCDDs. PMID:27367176

  20. Kinetics and mechanism of the oxidation of some -hydroxy acids by hexamethylenetetramine-bromine

    Indian Academy of Sciences (India)

    Dimple Garg; Seema Kothari

    2004-11-01

    The oxidation of lactic acid, mandelic acid and ten monosubstituted mandelic acids by hexamethylenetetramine-bromine (HABR) in glacial acetic acid, leads to the formation of the corresponding oxoacid. The reaction is first order with respect to each of the hydroxy acids and HABR. It is proposed that HABR itself is the reactive oxidizing species. The oxidation of -deuteriomandelic acid exhibits the presence of a substantial kinetic isotope effect (/ = 5.91 at 298 K). The rates of oxidation of the substituted mandelic acids show excellent correlation with Brown’s + values. The reaction constants are negative. The oxidation exhibits an extensive cross conjugation between the electron-donating substituent and the reaction centre in the transition state. A mechanism involving transfer of a hydride ion from the acid to the oxidant is postulated.

  1. Short-lived brominated hydrocarbons – observations in the source regions and the tropical tropopause layer

    Directory of Open Access Journals (Sweden)

    S. Brinckmann

    2012-02-01

    Full Text Available We conducted measurements of the five important short-lived organic bromine species in the marine boundary layer (MBL. Measurements were made in the Northern Hemisphere mid-latitudes (Sylt Island, North Sea in June 2009 and in the tropical Western Pacific during the TransBrom ship campaign in October 2009. For the one-week time series on Sylt Island, mean mixing ratios of CHBr3, CH2Br2, CHBr2Cl and CH2BrCl were 2.0, 1.1, 0.2, 0.1 ppt, respectively. We found maxima of 5.8 and 1.6 ppt for the two main components CHBr3 and CH2Br2. Along the cruise track in the Western Pacific (between 41° N and 13° S we measured mean mixing ratios of 0.9, 0.9, 0.2, 0.1 and 0.1 ppt for CHBr3, CH2Br2, CHBrCl2, CHBr2Cl and CH2BrCl. Air samples with coastal influence showed considerably higher mixing ratios than the samples with open ocean origin. Correlation analyses of the two data sets yielded strong linear relationships between the mixing ratios of four of the five species (except for CH2BrCl. Using a combined data set from the two campaigns and a comparison with the results from two former studies, rough estimates of the molar emission ratios between the correlated substances were: 9/1/0.35/0.35 for CHBr3/CH2Br2/CHBrCl2/CHBr2Cl. Additional measurements were made in the tropical tropopause layer (TTL above Teresina (Brazil, 5° S in June 2008, using balloon-borne cryogenic whole air sampling technique. Near the level of zero clear-sky net radiative heating (LZRH at 14.8 km about 2.25 ppt organic bromine was bound to the five short-lived species, making up 13% of total organic bromine (17.82 ppt. CH2Br2 (1.45 ppt and CHBr3 (0.56 ppt accounted for 90% of the budget of short-lived compounds in that region. Near the

  2. Responses of marine unicellular algae to brominated organic compounds in six growth media

    Energy Technology Data Exchange (ETDEWEB)

    Walsh, G.E.; Yoder, M.J.; McLaughlin, L.L.; Lores, E.M.

    1987-12-01

    Marine unicellular algae, Skeletonema costatum, Thalassiosira pseudonana, and Chlorella sp. were exposed to the industrial brominated compounds tetrabromobisphenol A, decabromobiphenyloxide (DBBO), hexabromocyclododecane (HBCD), pentabromomethylbenzene (PBMB), pentabromoethylbenzene (PBEB), and the herbicide bromoxynil (BROM), in six algal growth media. High concentrations of DBBO (1 mg liter-1), PBMB (1 mg liter-1), and PBEB (0.5 mg liter-1) reduced growth by less than 50%. EC50s of the other compounds varied with growth medium, with high EC50/low EC50 ratios between 1.3 and 9.9. Lowest EC50s, 9.3 to 12.0 micrograms liter-1, were obtained with S. costatum and HBCD. It is concluded that responses to toxicants in different media are the results of interactions among algae, growth medium, toxicant, and solvent carrier.

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

    Science.gov (United States)

    Coburn, Sean; Dix, Barbara; Edgerton, Eric; Holmes, Christopher D.; Kinnison, Douglas; Liang, Qing; ter Schure, Arnout; Wang, Siyuan; Volkamer, Rainer

    2016-03-01

    The elevated deposition of atmospheric mercury over the southeastern United States is currently not well understood. Here we measure partial columns and vertical profiles of bromine monoxide (BrO) radicals, a key component of mercury oxidation chemistry, to better understand the processes and altitudes at which mercury is being oxidized in the atmosphere. We use data from a ground-based MAX-DOAS instrument located at a coastal site ˜ 1 km from the Gulf of Mexico in Gulf Breeze, FL, where we had previously detected tropospheric BrO (Coburn et al., 2011). Our profile retrieval assimilates information about stratospheric BrO from the WACCM chemical transport model (CTM), and uses only measurements at moderately low solar zenith angles (SZAs) to estimate the BrO slant column density contained in the reference spectrum (SCDRef). The approach has 2.6 degrees of freedom, and avoids spectroscopic complications that arise at high SZA; knowledge about SCDRef further helps to maximize sensitivity in the free troposphere (FT). A cloud-free case study day with low aerosol load (9 April 2010) provided optimal conditions for distinguishing marine boundary layer (MBL: 0-1 km) and free-tropospheric (FT: 1-15 km) BrO from the ground. The average daytime tropospheric BrO vertical column density (VCD) of ˜ 2.3 × 1013 molec cm-2 (SZA < 70°) is consistent with our earlier reports on other days. The vertical profile locates essentially all tropospheric BrO above 4 km, and shows no evidence for BrO inside the MBL (detection limit < 0.5 pptv). BrO increases to ˜ 3.5 pptv at 10-15 km altitude, consistent with recent aircraft observations. Our case study day is consistent with recent aircraft studies, in that the oxidation of gaseous elemental mercury (GEM) by bromine radicals to form gaseous oxidized mercury (GOM) is the dominant pathway for GEM oxidation throughout the troposphere above Gulf Breeze. The column integral oxidation rates are about 3.6 × 105 molec cm-2 s-1 for bromine

  4. Bioactive brominated diterpenes from the marine red alga Jania Rubens (L.) Lamx.

    Science.gov (United States)

    Awad, Nagwa E

    2004-04-01

    Seven brominated diterpenes of the parguerene and isoparguerene series were isolated for the first time from the red alga Jania rubens (L.) Lamx., collected from the Red Sea coast at Hurghada, Egypt. The diterpenes were identified as isoparguerol (1), isoparguerol-16-acetate (2), isoparguerol-7,16-diacetate (3), parguerol-16-acetate (4), parguerol-7,16-diacetate (5), deoxyparguerol (6) and deoxyparguerol-7-acetate (7). The isolated diterpenes had a marked antitumour activity. Isoparguerol derivatives were slightly more effective than parguerol derivatives. Moreover, the data implied that the cytotoxicity of these compounds were dependent on the number of acetoxy groups. Also, anthelmintic activities of the isolated compounds on earthworms (Allolobophora caliginosa) were studied. PMID:15162360

  5. Thinning of CIGS solar cells: Part I: Chemical processing in acidic bromine solutions

    Energy Technology Data Exchange (ETDEWEB)

    Bouttemy, M.; Tran-Van, P. [Institut Lavoisier de Versailles (ILV-UMR 8180 CNRS/UVSQ), 45 av. des Etats Unis, 78035 Versailles (France); Gerard, I., E-mail: gerard@chimie.uvsq.fr [Institut Lavoisier de Versailles (ILV-UMR 8180 CNRS/UVSQ), 45 av. des Etats Unis, 78035 Versailles (France); Hildebrandt, T.; Causier, A. [Institut Lavoisier de Versailles (ILV-UMR 8180 CNRS/UVSQ), 45 av. des Etats Unis, 78035 Versailles (France); Pelouard, J.L.; Dagher, G. [Laboratoire de Photonique et de Nanostructures (LPN-CNRS), route de Nozay 91460 Marcoussis (France); Jehl, Z.; Naghavi, N. [Institut de Recherche et Developpement sur l' Energie Photovoltaique (IRDEP -UMR 7174 CNRS/EDF/Chimie-ParisTech), 6 quai Watier, 78401 Chatou (France); Voorwinden, G.; Dimmler, B. [Wuerth Elektronik Research GmbH, Industriestr. 4, 70565 Stuttgart (Germany); Powalla, M. [Zentrum fuer Sonnenenergie- und Wasserstoff-Forschung (ZSW), Industriestr. 6, 70565 Stuttgart (Germany); Guillemoles, J.F. [Institut de Recherche et Developpement sur l' Energie Photovoltaique (IRDEP -UMR 7174 CNRS/EDF/Chimie-ParisTech), 6 quai Watier, 78401 Chatou (France); Lincot, D. [Laboratoire de Photonique et de Nanostructures (LPN-CNRS), route de Nozay 91460 Marcoussis (France); Etcheberry, A. [Institut Lavoisier de Versailles (ILV-UMR 8180 CNRS/UVSQ), 45 av. des Etats Unis, 78035 Versailles (France)

    2011-08-31

    CIGSe absorber was etched in HBr/Br{sub 2}/H{sub 2}O to prepare defined thicknesses of CIGSe between 2.7 and 0.5 {mu}m. We established a reproducible method of reducing the absorber thickness via chemical etching. We determine the dissolution kinetics rate of CIGSe using trace analysis by graphite furnace atomic absorption spectrometry of Ga and Cu. The roughness of the etching surface decreases during the first 500 nm of the etching to a steady state value of the root-mean-square roughness near 50 nm. X-ray photoelectron spectroscopy analyses demonstrate an etching process occurring with a constant chemical composition of the treated surface acidic bromine solutions provide a controlled chemical thinning process resulting in an almost flat surface and a very low superficial Se{sup 0} enrichment.

  6. Surface-confined 2D polymerization of a brominated copper-tetraphenylporphyrin on Au(111)

    CERN Document Server

    Smykalla, Lars; Korb, Marcus; Lang, Heinrich; Hietschold, Michael

    2015-01-01

    A coupling-limited approach for the Ullmann reaction-like on-surface synthesis of a two-dimensional covalent organic network starting from a halogenated metallo-porphyrin is demonstrated. Copper-octabromo-tetraphenylporphyrin molecules can diffuse and self-assemble when adsorbed on the inert Au(111) surface. Splitting-off of bromine atoms bonded at the macrocyclic core of the porphyrin starts at room temperature after the deposition and is monitored by X-ray photoelectron spectroscopy for different annealing steps. Direct coupling between the reactive carbon sites of the molecules is, however, hindered by the molecular shape. This leads initially to an ordered non-covalently interconnected supramolecular structure. Further heating to 300{\\deg}C and an additional hydrogen dissociation step is required to link the molecular macrocycles via a phenyl group and form large ordered polymeric networks. This approach leads to a close-packed covalently bonded network of overall good quality. The structures are characte...

  7. 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.

  8. 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

  9. Determination of chlorine, fluorine, bromine, and iodine in coals with ICP-MS and IC

    Energy Technology Data Exchange (ETDEWEB)

    Bettinelli, M.; Spezia, S.; Minoia, C.; Ronchi, A. [Salvatore Maugeri Foundation, Pavia (Italy)

    2002-07-01

    The combustion process releases many organic and inorganic pollutants into the atmosphere, both in gaseous and solid form. During coal combustion in thermal power plants without pollution control equipment, chlorine, fluorine, bromine, and iodine present in coals are mainly volatilized as gaseous compounds. Limiting pollutant emissions is a precise requirement of the Italian legislation that fixes (in the case of power plants) 100 mg/Nm{sup 3} as the limit value for chlorine, and 5 mg/Nm{sup 3} for fluorine and bromine (expressed as hydrofluoric and hydrobromic acid respectively). No limit for iodine emissions has been established. From this point of view and in order to maintain control of emissions from combustion plants, it is important to monitor the concentration of halogens in fuels. Unfortunately, in literature there are very few data published with regard to the amount of halogens in fossil fuels, which emphasizes the analytical difficulties with regard to the determination of these analytes. In the present paper a, pyrohydrolysis of the sample at 1100{degree}C, followed by the absorption of volatilized compounds in Na{sub 2}CO{sub 3}/NaHCO{sub 3} solution and the final instrumental analysis of Cl, Br, and F with ion chromatography (IC) and Br and I with inductively coupled plasma mass spectrometry (ICP-MS) has been adopted. The accuracy of the method, evaluated by analyzing some certified reference materials, was better than 95% for all analytes and the detection limits adequate to the analytical requirements (0.1 mg/kg for Br and I, 1 mg/kg for F, and 10 mg/kg for C1).

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

    International Nuclear Information System (INIS)

    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

  11. Scientific Opinion on Emerging and Novel Brominated Flame Retardants (BFRs in Food

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Contaminants in the Food Chain (CONTAM

    2012-10-01

    Full Text Available EFSA was asked to deliver a scientific opinion on brominated flame retardants (BFRs other than PBDEs, PBBs, HBCDDs, TBBPA and brominated phenols and their derivatives. The BFRs that are the subject of the current opinion, were classified in groups termed ‘emerging’ and ‘novel’ BFRs. Information on 17 emerging and 10 novel BFRs was collected. The information varied widely for these BFRs. There is a lack of experimental data on physico-chemical characteristics, stability/reactivity and current use and production volume of all the emerging and novel BFRs. Due to the very limited information on occurrence, exposure and toxicity, the CONTAM Panel could not perform a risk characterisation for any of the BFRs considered. Instead, an attempt was made to identify those BFRs that could be a potential health concern and should be considered first for future investigations. For this purpose the Panel first evaluated the available experimental data on occurrence in food, behaviour in the environment and toxicity. Secondly, a modelling exercise was performed focussing on the potential of the emerging and novel BFRs for persistence in the environment and for their possible bioaccumulation potential. There is convincing evidence that tris(2,3-dibromopropyl phosphate (TDBPP and dibromoneopentyl glycol (DBNPG are genotoxic and carcinogenic, warranting further surveillance of their occurrence in the environment and in food. Based on the limited experimental data on environmental behaviour, 1,2-bis(2,4,6-tribromophenoxyethane (BTBPE and hexabromobenzene (HBB were identified as compounds that could raise a concern for bioaccumulation. For the modelling exercise, the CONTAM Panel selected two environmental characteristics, overall persistence and potential for bioaccumulation, as being most relevant to provide insight into the possibility that emerging or novel BFRs might accumulate in the food chain, and thus might appear in food intended for human

  12. Meteorological controls on the vertical distribution of bromine monoxide in the lower troposphere

    Directory of Open Access Journals (Sweden)

    P. K. Peterson

    2014-09-01

    Full Text Available Multiple axis differential absorption spectroscopy (MAX-DOAS measurements of bromine monoxide (BrO probed the vertical structure of halogen activation events during March–May 2012 at Barrow, Alaska. An analysis of the BrO averaging kernels and degrees of freedom obtained by optimal-estimation-based inversions from raw MAX-DOAS measurements reveals the information is best represented by reducing the retrieved BrO profile to two quantities, the integrated column from the surface through 200 m (VCD200 m, and the lower tropospheric vertical column density (LT-VCD which represents the integrated column of BrO from the surface through 2 km. The percentage of lower-tropospheric BrO in the lowest 200 m was found to be highly variable ranging from shallow layer events, where BrO is present primarily in the lowest 200 m to distributed column events where BrO is observed at higher altitudes. The highest observed LT-VCD events occurred when BrO was distributed throughout the lower troposphere, rather than concentrated near the surface. Atmospheric stability in the lowest 200 m influenced the percentage of LT-VCD that is in the lowest 200 m, with inverted temperature structures having a first-to-third quartile range (Q1–Q3 of VCD200 m/LT-VCD from 15–39% while near neutral temperature structures had a Q1–Q3 range of 7–13%. Data from this campaign show no clear influence of wind speed on either lower-tropospheric bromine activation (LT-VCD or the vertical distribution of BrO, while examination of seasonal trends and the temperature dependence of the vertical distribution supported the conclusion that the atmospheric stability affects the vertical distribution of BrO.

  13. Kinetics of Vinyl Chloride Polymerization with Mixture of Initiators

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Kinetic models for the rate constants of vinyl chloride polymerization in the presence of initiator mixtures were proposed. They may be used to design the initiator recipes for the vinyl chloride polymerization with uniform rate at different temperatures at which various grades of poly(vinyl chloride) will be prepared.

  14. Removal of iron contaminant from zirconium chloride solution

    International Nuclear Information System (INIS)

    This patent describes a process for eliminating iron contaminant from an aqueous zirconium chloride solution that has been contaminated with FeCl3 in a plant in which zirconium and hafnium chloride solutions are separated by a main MINK solvent extraction system and the FeCl3 is normally removed from the zirconium chloride solution by a secondary MINK solvent extraction system

  15. Revised Model of Chloride Diffusion in Concrete Bridge by Considering Complex Action of Load and Chloride Binding Capacity

    OpenAIRE

    Xiang, Yiqiang; Guo, DongMei

    2014-01-01

    Coastal concrete bridges will suffer from deterioration of RC structural performance and resistance attenuation because of the chloride penetration and other environment factors. This article discusses current different chloride diffusion models and puts forward the revised model of chloride diffusion in concrete bridge by considering the complex action of load influence and chloride-binding capacity. Comparison of numerical predicted values and relative experimental tests show the presented ...

  16. Synthesis of Trans-5-propyl-2-(4'-bromine-phenyl)-tetrahydropyran%反-5-丙基-2-(4'-溴-苯基)-四氢吡喃的合成

    Institute of Scientific and Technical Information of China (English)

    高丰琴; 何汉江; 郭强; 王小明; 李鹏; 张彦军

    2012-01-01

    以对溴苯甲酸为起始原料,经酰化后生成酰氯,酰氯与N,O-二甲基羟胺盐酸盐反应生成酰胺,再与氯乙烯基镁反应生成α,β不饱和酬. 同时,正戊醛与二正丙胺反应生成烯胺.α,β不饱和酬与烯胺经迈克尔加成反应生成分子内醛酮,分子内醛酮经关环反应、乙醇重结晶可得到色谱纯度99.5%以上的反-5-丙基-2-(4'-溴-苯基)-四氢吡喃.%The starting material of 4-bromobenzene carboxylic acid was aeylated to generate aeyl chloride. Then,acyl chloride reacted with N, O-dimethyl hydroxylamine hydrochloride to synthesize the amides, which then reacted with chlorovinylmagnesium to synthesize α, β unsaturated ketone. Meanwhile, allyl amine was synthesized from the reaction of pentanal with di-n-propylamine. By Michael addition reaction, α,β unsaturated ketone and allyl amine reacted to synthesize intramolecular aldehyde and ketone, which further reacted to synthesize trans-5-pmpyl-2-( 4'-bromine-phenyl ) -tetrahydropyran (3PyPBr) with a purity of more than 99.5% by closed loop reaction and recrystallization with ethanol.

  17. BARRIER PROPERTIES OF VINYLIDENE CHLORIDE COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    LI Yuesheng; WENG Zhixue; HUANG Zhiming; PAN Zuren

    1996-01-01

    The permeability coefficients of a series of copolymers of vinylidene chloride (VDC)with methyl acrylate (MA), butyl acrylate (BA) or vinyl chloride (VC) (as comonomer)to oxygen and carbon dioxide have been measured at 1.0 MPa and 30℃, while those to water vapor have been measured at 30℃ and 100% relative humidity. All the copolymers are semicrystalline. VDC/MA copolymers have lower melting temperature compared with VDC/BA copolymers, while that melting temperature of VDC/VC copolymer is higher than that of VDC/acrylate copolymers with the same VDC content. The barrier property of the copolymers is predominantly controlled by crystallite, free volume fraction, and cohesive energy. The permeability coefficients of VDC/MA copolymers to oxygen, carbon dioxide, and water vapor were successfully correlated with the ratio of free volume to cohesive energy.

  18. STABILISATION OF SILTY CLAY SOIL USING CHLORIDE

    Directory of Open Access Journals (Sweden)

    TAMADHER T. ABOOD

    2007-04-01

    Full Text Available The object of this paper is to investigate the effect of adding different chloride compounds including (NaCl, MgCl2, CaCl2 on the engineering properties of silty clay soil. Various amounts of salts (2%, 4%, and 8% were added to the soil to study the effect of salts on the compaction characteristics, consistency limits and compressive strength. The main findings of this study were that the increase in the percentage of each of the chloride compounds increased the maximum dry density and decrease the optimum moisture content. The liquid limit, plastic limit and plasticity index decreased with the increase in salt content. The unconfinedcompressive strength increased as the salt content increased.

  19. Chloride migration in concrete with superabsorbent polymers

    OpenAIRE

    Hasholt, Marianne Tange; Jensen, Ole Mejlhede

    2015-01-01

    Superabsorbent polymers (SAP) can be used as a means for internal curing of concrete. In the present study, the development of transport properties of concrete with SAP is investigated. The chloride migration coefficient according to NT BUILD 492 is used as a measure of this. Twenty concrete mixtures aretested 7, 14, and 28 days after casting. The development of degree of hydration is followed for 20 corresponding paste mixtures.Both when SAP is added with extra water to compensate the SAP wa...

  20. A Duplex Stainless Steel for Chloride Environments

    Science.gov (United States)

    Sridhar, N.; Kolts, J.; Flasche, L. H.

    1985-03-01

    This paper examines the effects of microstructural changes on the corrosion, stress corrosion cracking and corrosion fatigue resistance of a duplex stainless steel to chloride environments. The microstructural changes can be precipitation of phases such as sigma and carbides, or changes in the distribution of austenite and ferrite. The former can be important in hot forming operations while the latter is important in welding. The methods of minimizing these deleterious effects can sometimes be different from those used for austenitic stainless steel.

  1. Electrodeposition of Zinc from Chloride Solution

    OpenAIRE

    NAIK, Yanjerappa Arthoba; VENKATESHA, Thimmappa Venkatarangaiah

    2002-01-01

    The electroplating of zinc is carried out in the presence of 3,4,5-Trimethoxy benzaldehyde from a chloride bath. The bath constituents are optimized through Hull cell experiments. Operating parameters such as pH, temperature, and current density are also optimized. The current efficiency and throwing power are measured at different current densities. Polarization study is carried out under galvanostatic conditions. Corrosion resistance test indicated good protection of steel by the ...

  2. (tert-Butyl(2-hydroxyethylammonium chloride

    Directory of Open Access Journals (Sweden)

    Cintya Valerio-Cárdenas

    2014-07-01

    Full Text Available In the cation of the title molecular salt, C6H16NO+·Cl−, the N—C—C—O torsion angle is 176.5 (2°. In the crystal, the cations and chloride ions are linked by N—H...O and O—H...O hydrogen bonds, generating a two-dimensional network parallel to (100.

  3. Influence of chloride admixtures on cement matrix durability

    International Nuclear Information System (INIS)

    The influence of various inorganic salts, as chloride admixtures to Portland cement, on the mechanical properties and the durability of the matrix has been studied. The salts used in this study are chromium, nickel and cadmium chlorides. Improved compressive strength values are obtained which have been correlated to the stable metal hydroxide formation in high pH environment. Under static water conditions at 500C, hydrolyzed chloride ions exhibit adverse effects on the matrix durability through rapid release of calcium as calcium chloride in the initial period of leaching. On the contrary, enhanced matrix durability is obtained on long term leaching in the case of cement containing chromium chloride

  4. Boldine action against the stannous chloride effect.

    Science.gov (United States)

    Reiniger, I W; Ribeiro da Silva, C; Felzenszwalb, I; de Mattos, J C; de Oliveira, J F; da Silva Dantas, F J; Bezerra, R J; Caldeira-de-Araújo, A; Bernardo-Filho, M

    1999-12-15

    Peumus boldus extract has been used in popular medicine in the treatment of biliar litiase, hepatic insufficiency and liver congestion. Its effects are associated to the substance boldine that is present in its extract. In the present work, we evaluated the influence of boldine both in: (i) the structural conformation of a plasmid pUC 9.1 through gel electrophoresis analysis; and in (ii) the survival of the strain of Escherichia coli AB1157 submitted to reactive oxygen species (ROS), generated by a Fenton like reaction, induced by stannous chloride. Our results show a reduction of the lethal effect induced by stannous chloride on the survival of the E. coli culture in the presence of boldine. The supercoiled form of the plasmid is not modified by stannous chloride in the presence of boldine. We suggest that the protection induced by boldine could be explained by its anti-oxidant mechanism. In this way, the boldine could be reacting with stannous ions, protecting them against the oxidation and, consequently, avoiding the generation of ROS. PMID:10624900

  5. Potassium chloride production by microcline chlorination

    Energy Technology Data Exchange (ETDEWEB)

    Orosco, Pablo, E-mail: porosco@unsl.edu.ar [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina); Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis, Chacabuco y Pedernera, San Luis (Argentina); Ruiz, María del Carmen [Instituto de Investigaciones en Tecnología Química (INTEQUI), Chacabuco y Pedernera, San Luis (Argentina)

    2015-08-10

    Highlights: • Use of chlorination for the KCl production. • The reagents used were microcline, hydromagnesite and chlorine. • Isothermal and non-isothermal assays were performed in Cl{sub 2}–N{sub 2} mixture. • The chlorination generated KCl at 700 °C. • The chlorination products promote KCl formation. - Abstract: The potassium chloride is one of the most important fertilizers used in agriculture. The current demand of this salt makes interesting the study of potassium chloride production from unconventional potassium resources. In this work the potassium chloride production by chlorination of microcline was investigated. The starting reagents were microcline, hydromagnesite and chlorine. Non-isothermal and isothermal chlorination assays were carried out in a thermogravimetric device adapted to work in corrosive atmospheres. The temperature effect on potassium extraction and the phase transformations produced during chlorination of microcline were studied. The reagents and reaction products were analyzed by X-ray fluorescence (XRF) and X-ray diffraction (XRD). The experimental results indicated that by chlorination of microcline an important extraction of potassium in the temperature range from 800 to 900 °C was produced. Moreover, at 800 °C the forsterite, enstatite and magnesium aluminate spinel phases were generated.

  6. Understanding microwave vessel contamination by chloride species.

    Science.gov (United States)

    Recchia, Sandro; Spanu, Davide; Bianchi, Davide; Dossi, Carlo; Pozzi, Andrea; Monticelli, Damiano

    2016-10-01

    Microwaves are widely used to assist digestion, general sample treatment and synthesis. The use of aqua regia is extensively adopted for the closed vessel mineralization of samples prior to trace element detection, leading to the contamination of microwave vessels by chlorine containing species. The latter are entrapped in the polymeric matrix of the vessels, leading to memory effects that are difficult to remove, among which the risk of silver incomplete recoveries by removal of the sparingly soluble chloride is the predominant one. In the present paper, we determined by mass spectrometry that hydrogen chloride is the species entrapped in the polymeric matrix and responsible for vessel contamination. Moreover, several decontamination treatments were considered to assess their efficiency, demonstrating that several cleaning cycles with water, nitric acid or silver nitrate in nitric acid were inefficient in removing chloride contamination (contamination reduction around 90%). Better results (≈95% decrease) were achieved by a single decontamination step in alkaline environment (sodium hydroxide or ammonia). Finally, a thermal treatment in a common laboratory oven (i.e. without vacuum and ventilation) was tested: a one hour heating at 150°C leads to a 98.5% decontamination, a figure higher than the ones obtained by wet treatments which requires comparable time. The latter treatment is a major advancement with respect to existing treatments as it avoids the need of a vacuum oven for at least 17h as presently proposed in the literature.

  7. An autopsy case of zinc chloride poisoning.

    Science.gov (United States)

    Kondo, Takeshi; Takahashi, Motonori; Watanabe, Seiya; Ebina, Masatomo; Mizu, Daisuke; Ariyoshi, Koichi; Asano, Migiwa; Nagasaki, Yasushi; Ueno, Yasuhiro

    2016-07-01

    Ingestion of large amounts of zinc chloride causes corrosive gastroenteritis with vomiting, abdominal pain, and diarrhea. Some individuals experience shock after ingesting large amounts of zinc chloride, resulting in fatality. Here, we present the results of an administrative autopsy performed on a 70-year-old man who ingested zinc chloride solution and died. After drinking the solution, he developed vomiting, abdominal pain, and diarrhea, and called for an ambulance. Except for tachycardia, his vital signs were stable at presentation. However, he developed hypotension and severe metabolic acidosis and died. The patient's blood zinc concentration on arrival was high at 3030μg/dL. Liver cirrhosis with cloudy yellow ascites was observed, however, there were no clear findings of gastrointestinal perforation. The gastric mucosa was gray-brown, with sclerosis present in all gastric wall layers. Zinc staining was strongly positive in all layers. There was almost no postmortem degeneration of the gastric mucosal epithelium, and hypercontracture of the smooth muscle layer was observed. Measurement of the zinc concentration in the organs revealed the highest concentration in the gastric mucosa, followed by the pancreas and spleen. Clinically, corrosive gastroenteritis was the cause of death. However, although autopsy revealed solidification in the esophagus and gastric mucosa, there were no findings in the small or large intestine. Therefore, metabolic acidosis resulting from organ damage was the direct cause of death. PMID:27497327

  8. The Accelerated Test of Chloride Permeability of Concrete

    Institute of Scientific and Technical Information of China (English)

    TAN Ke-feng; ODD E Gjφrv

    2003-01-01

    The availability of accelerated chloride permeability test and the effect of w/c ratio, incorporation of silica fume, maximum aggregate size and aggregate type on the chloride permeability were studied. The mathematic analysis certifies that there is a linear relationship between accelerated test and natural diffusion. Test results show that the chloride permeability of concrete increases as w/c ratio increases whilst a limited amount of replacement of cement with silica fume, the chloride permeability decreases dramatically. The maximum aggregate size in the range of 8 to 25 mm seems also affect chloride permeability but with a much less significant level. The chloride permeability of silica fume lightweight aggregate concrete is very low, especially the concrete made with dry lightweight concrete. The chloride permeability can be evaluated by this accelerated test method.

  9. Chloride regulates afferent arteriolar contraction in response to depolarization

    DEFF Research Database (Denmark)

    Hansen, P B; Jensen, B L; Skott, O

    1998-01-01

    -Renal vascular reactivity is influenced by the level of dietary salt intake. Recent in vitro data suggest that afferent arteriolar contractility is modulated by extracellular chloride. In the present study, we assessed the influence of chloride on K+-induced contraction in isolated perfused rabbit...... afferent arterioles. In 70% of vessels examined, K+-induced contraction was abolished by acute substitution of bath chloride. Consecutive addition of Cl- (30, 60, 80, 100, 110, and 117 mmol/L) restored the sensitivity to K+, and half-maximal response was observed at 82 mmol/L chloride. The calcium channel...... antagonist diltiazem (10(-6) mol/L) abolished K+-induced contractions. Bicarbonate did not modify the sensitivity to chloride. Norepinephrine (10(-6) mol/L) induced full contraction in depolarized vessels even in the absence of chloride. Iodide and nitrate were substituted for chloride with no inhibitory...

  10. 40 CFR 61.64 - Emission standard for polyvinyl chloride plants.

    Science.gov (United States)

    2010-07-01

    ... Standard for Vinyl Chloride § 61.64 Emission standard for polyvinyl chloride plants. An owner or operator of a polyvinyl chloride plant shall comply with the requirements of this section and § 61.65. (a... is not to exceed 0.02 g vinyl chloride/kg (0.04 lb vinyl chloride/ton) of polyvinyl chloride...

  11. Chemistry of recoil atoms of bromine-82 in neutron-irradiated crystalline perbromates of the alkali metals and ammonium

    Energy Technology Data Exchange (ETDEWEB)

    Gavrilov, V.V.; Isupov, V.K.; Kirin, I.S.

    1975-01-01

    It was established by ion exchange chromatography that the recoil atoms of bromine-82 in perbromates with thermal neutrons are stabilized in the form of five valence forms: BrO/sub 4//sup -/, BrO/sub 3//sup -/, BrO/sub 2//sup -/, BrO/sup -/, Br/sup -/. The retention of bromine-82 of BrO/sub 4//sup -/ is 2.1 +- 0.4 percent for LiBrO/sub 4/, 2.1 +- 0.4 percent for NaBrO/sub 4/, 2.3 +- 0.4 percent for KBrO/sub 4/, 2.6 +- 0.4 percent for RbBrO/sub 4/, 2.2 +- 0.4 percent for CsBrO/sub 4/, and 1.6 +- 0.4 percent for NH/sub 4/BrO/sub 4/.

  12. 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...

  13. The mercury species and their association with carbonaceous compositions, bromine and iodine in PM2.5 in Shanghai.

    Science.gov (United States)

    Duan, Lian; Xiu, Guangli; Feng, Ling; Cheng, Na; Wang, Chenggang

    2016-03-01

    PM2.5 samples were collected in south Shanghai from November 2013 to October 2014. The species of particulate bounded mercury (PBM), including hydrochloric soluble particle-phase mercury (HPM), element soluble particle-phase mercury (EPM) and residual soluble particle-phase mercury (RPM), were determined in PM2.5. The chemical composition of PM2.5 including organic carbon (OC) and elemental carbon (EC), total bromine and iodine were also analyzed. The results showed that the annual average concentration of PBM was 0.30 ± 0.31 ng m(-3) and 0.34 ± 0.32 ng m(-3) in winter, 0.31 ± 0.19 ng m(-3) in spring, 0.30 ± 0.45 ng m(-3) in fall and 0.28 ± 0.17 ng m(-3) in summer. HPM took the highest fraction 51.2% in PBM, followed by RPM 27.7% and EPM 21.1%. EC positively correlated to particle mercury, especially in winter (r = 0.70), the same for OC in winter (r = 0.72), which indicated that the carbonaceous composition may affect the transformation of Hg in the atmosphere. Mercury species showed different correlations with bromine and iodine in the four seasons. The strongest correlation between bromine, iodine and mercury was found in spring and fall, respectively. Bromine showed the stronger correlation with total mercury and speciated particle mercury than iodine. In addition, the days were classified into haze and non-haze days based on the visibility and relative humidity, while the ratio of HPM in haze days was much higher than that in non-haze days. EC strongly correlated with PBM during haze and non-haze days while OC only positively correlated with PBM in non-haze days, this may indicate that the different carbonaceous part may affect PBM differently.

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

    OpenAIRE

    N. Bobrowski; Giuffrida, G

    2012-01-01

    Over a three year period, from 2006 to 2009, frequent scattered sun light DOAS measurements were conducted at Mt. Etna in a distance of around six kilometres 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.

    Results from these measurements and observations are presented and their relation is discussed. The focus of the investigation is the bromin...

  15. 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.

  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. An Empirical Approach to Determining the Boundary Layer Bromine Monoxide (BrO) Abundance from Satellite Total Column Measurements

    Science.gov (United States)

    Simpson, W. R.; Donohoue, D.; Carlson, D. A.

    2009-12-01

    Unique chemistry in the Arctic boundary layer during springtime liberates bromine from sea salt, producing reactive halogen gases (e.g. atomic bromine and bromine monoxide radicals) that then drastically alter atmospheric oxidation pathways. This phenomenon causes ozone depletion events and affects mercury deposition to the snowpack. Satellite remote sensing (e.g. OMI and GOME2 observations) techniques can detect the total column abundance of BrO, which is generally the primary species of the reactive bromine family. However, BrO is also present in the stratosphere, so it is necessary to partition the satellite-observed BrO column abundance into boundary layer and non-boundary layer (primarily stratospheric) partial columns to be able to infer boundary layer abundances and hence chemical affects near the Earth's surface (i.e. ozone and mercury impacts). In this presentation, we describe an empirical method for partitioning the BrO total column and apply it globally during spring 2008. The method indicates that some BrO total column enhancements ("hotspots") are not actually enhancements in the boundary layer BrO abundance but occur aloft. Movies and a statistical analysis of the inferred boundary layer BrO abundance are presented. The method has been tested and performs well at the Barrow field site. However, in areas that lack routine ground truth BrO measurements (e.g. Hudson Bay, Canada), large tropospheric BrO abundances are indicated. It is not clear if these inferred boundary layer BrO events are real or if the simple empirical method described here is failing in those locations. Verification of this method over large spatial regions of the Arctic is needed.

  18. Comparison of Nuclear Activation Methods for Bromine. Instrumental Analyses of Pesticides in Plant Materials Close to the Limit of Sensitivity

    International Nuclear Information System (INIS)

    There has been worldwide interest in pesticide residue analysis for control and ecological purposes. Although several agricultural research establishments have in the past developed suitable radioisotope tracer techniques to detect and remove organic pesticides from food, suitable micro-analytical techniques for the measurement of traces of toxic elements present in these materials have not been available. In cooperation with the United States Department of Agriculture, Plant Pest Control Laboratory, an investigation has been conducted on the use of neutron activation techniques for determining bromine, arsenic and mercury residues in soils, foliage, fruit, and vegetable materials. This paper discusses the various instrumental and data reduction techniques which were developed to measure traces of bromine by neutron activation methods, especially those employed in the limit of sensitivity range wherein special statistical methods are necessary. A large number of samples of soils, foliage, orange and vegetable materials, activated in the Texas A and M Research Reactor were counted at appropriate times after activation using three different counting systems: firstly, an automated system with an Nal (Tl) spectrometer; secondly, a 2 cm3 Ge(Li) solid-state detector connected to a Victoreen 3200-channel analyzer; and thirdly a slow γ-γ coincidence unit. The spectral data from the automated system were reduced by the AA-6 least squares method, and alternatively by means of computer spectrum stripping and peak area computation methods. The photopeak activities from the solid-state detector spectra were measured by the peak area method. The results obtained from the three counting systems using different data reduction techniques were compared to determine the best for the measurement of bromine concentration in the limit-of-sensitivity range. The γ-γ coincidence counting technique appears to have advantages in measuring the bromine content even in the ppm range in

  19. An investigation into the sensitivity of the atmospheric chlorine and bromine loading using a globally averaged mass balance model

    Science.gov (United States)

    Dowdell, David C.; Matthews, G. Peter; Wells, Ian

    Two globally averaged mass balance models have been developed to investigate the sensitivity and future level of atmospheric chlorine and bromine as a result of the emission of 14 chloro- and 3 bromo-carbons. The models use production, growth, lifetime and concentration data for each of the halocarbons and divide the production into one of eight uses, these being aerosol propellants, cleaning agents, blowing agents in open and closed cell foams, non-hermetic and hermetic refrigeration, fire retardants and a residual "other" category. Each use category has an associated emission profile which is built into the models to take into account the proportion of halocarbon retained in equipment for a characteristic period of time before its release. Under the Montreal Protocol 3 requirements, a peak chlorine loading of 3.8 ppb is attained in 1994, which does not reduce to 2.0 ppb (the approximate level of atmospheric chlorine when the ozone hole formed) until 2053. The peak bromine loading is 22 ppt, also in 1994, which decays to 12 ppt by the end of next century. The models have been used to (i) compare the effectiveness of Montreal Protocols 1, 2 and 3 in removing chlorine from the atmosphere, (ii) assess the influence of the delayed emission assumptions used in these models compared to immediate emission assumptions used in previous models, (iii) assess the relative effect on the chlorine loading of a tightening of the Montreal Protocol 3 restrictions, and (iv) calculate the influence of chlorine and bromine chemistry as well as the faster phase out of man-made methyl bromide on the bromine loading.

  20. [Formation of disinfection by-products by Microcystis aeruginosa intracellular organic matter: comparison between chlorination and bromination].

    Science.gov (United States)

    Tian, Chuan; Guo, Ting-Ting; Liu, Rui-Ping; Jefferson, William; Liu, Hui-Juan; Qu, Jiu-Hui

    2013-11-01

    In order to illustrate the effects of released algal organic matter in cyanobacteria blooms on raw water quality and water treatment process, intracellular organic matter (IOM) of Microcystis aeruginosa, which is the dominant species in cyanobacteria blooms, was chosen as a precursor and characterized. In addition, the transformation of IOM and the formation of disinfection byproducts were evaluated at different pH of 6.5, 7.1 and 8.4 after chlorination or bromination, with subsequent correlation analysis. The results indicated that IOM was primarily composed of macromolecular matter, i. e. , the species with relative molecular weight of > 30 x 10(3), constituting 68.8% of dissolved organic carbon (DOC). Fluorescence excitation-emission matrix indicated that IOM was mainly composed of aromatic protein-like matter with an intensity of 92.6 AU x L x mg(-1). After reaction with chlorine or bromine, the intensity of aromatic protein-like peaks decreased sharply by 76.6% - 93.3%, and its reduction correlated well with the formation of trihalomethane (THMs, R2 = 0.81) and haloacetic acid (HAAs, R2 = 0.77). The formation of THMs and HAAs increased with the increase in pH. Compared with chlorine, bromine formed more THMs and HAAs, and tended to form highly halogenated HAAs. However, with increasing pH, the reactivity with IOM between chlorine and bromine was closer, i.e, k(OBr-IOM)/k(OCl-(IOM) < k(HOBr-IOM/k(HOCl-IOM).

  1. Relation between chloride exchange diffusion and a conductive chloride pathway across the isolated skin of the toad (Bufo bufo)

    DEFF Research Database (Denmark)

    Kristensen, P; Larsen, Erik Hviid

    1978-01-01

    Substitution of chloride in the outside bathing medium of the toad skin with bromide, iodide, nitrate and sulphate leads to a reduction in the apparent exchange diffusion of chloride across this tissue, and also to a reduction of the chloride current recorded during hyperpolarization. A series...... of inhibitors (thiocyanate, furosemide, phloretin, and acetazolamide) also affects chloride exchange diffusion, hyperpolarization current as well as chloride influx during hyperpolarization. Although in some cases, effects on the short circuit current were also observed none of the effects on chloride transport....... On the basis of these findings, and the results reported in the previous paper (Hviid Larsen and Kristensen 1977) it is considered probable that the membrane molecules responsible to chloride exchange diffusion under short circuit conditions, are rearranged under the influence of a hyperpolarizing clamping...

  2. Anti-chloride permeability and anti-chloride corrodibility of a green high performance concrete admixture in concrete

    Institute of Scientific and Technical Information of China (English)

    ZHENG Yongbao; LIU Xinrong; LIU Dongyan; CHEN Jiangong; HUANG Xiongjun

    2003-01-01

    The effects of green high performance concrete (GHPC) admixture on the anti-chloride permeability and anti- chloride corrodibility of concrete are studied by a series of experiments designed on the basis of the diffusion principle and electrochemical principle. The GHPC admixture consists of fly ash, gangue, slag, red mud, etc., of which the mass fraction of industrial residues is over 96 %. The anti-permeabilities and anti-corrodibilities of the tested GHPC and normal concrete (NC) are evaluated by the Diffusion Coefficients of chloride which was obtained by measuring the concentration of chloride in the tested systems by the voltage difference method. It is found that the adoption of GHPC admixture greatly improves the anti-chloride permeability and anti-chloride corrodibility by modifying the inner structure and contracting the porosity of concrete to the reduce considerably the diffusion rate of chloride. The admixture is desirable regarding its engineering performances as well as economical and environmental interests.

  3. 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. PMID:24040839

  4. Bromination of Graphene: A New Route to Making High Performance Transparent Conducting Electrodes with Low Optical Losses

    KAUST Repository

    Mansour, Ahmed E.

    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.

  5. Occurrence of PBDEs and other alternative brominated flame retardants in sludge from wastewater treatment plants in Korea.

    Science.gov (United States)

    Lee, Sunggyu; Song, Geum-Ju; Kannan, Kurunthachalam; Moon, Hyo-Bang

    2014-02-01

    Studies on the occurrence of polybrominated diphenyl ethers (PBDEs) and other alternative brominated flame retardants in the environment are scarce. In this study, PBDEs and non-PBDE brominated flame retardants (NBFRs), including decabromodiphenyl ethane (DBDPE) and 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), were measured in sludge collected from three types of wastewater treatment plants (WWTPs) in Korea. Total concentrations of PBDEs (∑PBDE) in sludge ranged from 298 to 48,000 (mean: 3240) ng/g dry weight. Among 10 NBFRs analyzed, DBDPE and BTBPE were the only ones detected in sludge samples. Concentrations of DBDPE and BTBPE ranged from parametric multidimensional scaling ordination showed that congener profiles of PBDEs in sludge are dependent on the types of WWTPs. Almost all sludge samples contained a low ratio (mean: 0.18) of DBDPE/BDE 209, indicating an on-going contamination by PBDEs in Korea. However, the high ratios (>1) of DBDPE/BDE 209 were found in sludge from I-WWTPs, reflecting a shift in the usage pattern of BFRs by the Korean industry. The nationwide annual emission fluxes of ∑PBDE, DBDPE and BTBPE via WWTPs to the environment were estimated to be 7400, 480, and 3.7 kg/year, respectively. This is the first study on the occurrence of alternative brominated flame retardants in sludge from Korea. PMID:23993837

  6. Formation potentials of bromate and brominated disinfection by-products in bromide-containing water by ozonation.

    Science.gov (United States)

    Lin, Tao; Wu, Shouke; Chen, Wei

    2014-12-01

    The ozonation involved in drinking water treatment raises issues of water quality security when the raw water contains bromide (Br(-)). Br(-) ions may be converted to bromate (BrO3 (-)) during ozonation and some brominated disinfection by-products (Br-DBPs) in the following chlorination. In this study, the effects of ozone (O3) dosage, contact time, pH, and Br(-) and ammonia (NH3-N) concentrations on the formation of BrO3 (-) and Br-DBPs have been investigated. The results show that decreasing the initial Br(-) concentration is an effective means of controlling the formation of BrO3 (-). When the concentration of Br(-) was lower than 100 μg/L, by keeping the ratio of O3 dosage to dissolved organic carbon (DOC) concentration at less than 1, BrO3 (-) production was effectively suppressed. The concentration of BrO3 (-) steadily increased with increasing O3 dosage at high Br(-) concentration (>900 μg/L). Additionally, a longer ozonation time increased the concentrations of BrO3 (-) and total organic bromine (TOBr), while it had less impact on the formation potentials of brominated trihalomethanes (Br-THMFP) and haloacetic acids (Br-HAAFP). Higher pH value and the presence of ammonia may lead to an increase in the formation potential of BrO3 (-) and Br-DBPs.

  7. Brominated flame retardants in the surrounding soil of two manufacturing plants in China: Occurrence, composition profiles and spatial distribution.

    Science.gov (United States)

    Li, Wen-Long; Liu, Li-Yan; Zhang, Zi-Feng; Song, Wei-Wei; Huo, Chun-Yan; Qiao, Li-Na; Ma, Wan-Li; Li, Yi-Fan

    2016-06-01

    Surface soil samples were collected surrounding two brominated flame retardants (BFRs) manufacturing plants in China in August 2014 and analyzed for 23 polybrominated diphenyl ethers (PBDEs) and 8 novel brominated flame retardants (NBFRs). BDE209 and decabromodiphenylethane (DBDPE) were the predominant compounds in soil with the median levels of 1600 and 560 ng/g dw, respectively. The PBDEs profiles in soil samples were consistent with that of commercial product (comDecaBDE). The percentage contributions to total PBDEs decreased from higher to lower brominated homologues. Lower concentrations of NBFRs (excluding DBDPE) were detected in soil surrounding the two plants, suggesting they are byproducts or degradation products of the manufacturing activities. The concentrations of most BFRs dropped exponentially within 3-5 km of the manufacturing plants, suggesting recent deposition of these compounds to the soil. Directional distribution indicated that PBDEs and DBDPE concentrations were highest in the north direction of Plants 1. Three-day air parcel forward trajectories confirmed that the air parcel was responsible for the higher concentration of BFRs in the soil of north direction of the plant.

  8. Investigation of the Stratospheric Bromine Chemistry by Balloon-Borne Spectroscopic Observations and Photochemical Modelling: A Case Study of J(BrONO2) / k[BrO][NO2

    OpenAIRE

    Kreycy, Sebastian

    2013-01-01

    Besides chlorine, bromine is the second most important halogen when it comes to the destruction of ozone in the stratosphere. Although 150 times more chlorine than bromine is transported into the stratosphere, the higher ozone-depleting efficiency of bromine (by a factor of 45) makes it very important for catalytic cycles. In this study, balloon-borne DOAS (Differential Optical Absorption Spectroscopy) measurements of direct sunlight and limb measurements of scattered skylight, recorded...

  9. 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

  10. 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

  11. Modelling the impact of chlorine and bromine emissions from large Plinian eruptions on ozone

    Science.gov (United States)

    Brenna, Hans; Krüger, Kirstin; Kutterolf, Steffen

    2016-04-01

    Large Plinian volcanic eruptions inject large amounts of atmosphere-relevant gases (e.g. S, Cl, Br) and materials into the stratosphere. If the eruption occurs in the tropics, it can have a global impact due to the dispersal through the large scale meridional overturning circulation. Most climate model studies concentrate on the sulfate aerosol effects on climate. In contrast, ozone-depletion initiated by volcanic halogens from tropical eruptions was believed to play an insignificant role for the global atmosphere, based on observations from the recent El Chichon and Pinatubo eruptions. New results regarding the halogen release by Plinian eruptions, as well as recent volcanic plume observations and model simulations facilitate now our investigation into what effect the combined chlorine and bromine emissions from large tropical eruptions have on ozone and the atmosphere in general. A complete halogen data set for the last 200 ka (Kutterolf et al., 2015), derived by the petrological method from paleo-eruptions of the Central American Volcanic Arc (CAVA), are used to force simulations with the advanced chemistry climate model WACCM (Whole Atmosphere Community Climate Model). The goal is to quantify the impact of volcanic halogens on the preindustrial atmosphere when the background chlorine levels were low compared to the present day with the main focus on stratospheric ozone. We carried out 5 model simulations assuming that 10% of the Cl and Br (9.51e+6 kg Br and 2.93e+9 kg Cl) emitted from the average CAVA eruption is injected into the tropical stratosphere during January. The model response reveals a global impact on the ozone layer affecting via radiation also atmospheric dynamics for more than 5 years. Given the current decline in anthropogenic chlorine, the results will become relevant for future halogen-rich explosive eruptions in the tropics. References: Kutterolf, S., T. Hansteen, A. Freundt, H. Wehrmann, K. Appel, K. Krüger, and W. Pérez (2015), Bromine

  12. 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

  13. Temperature dependence of bromine activation due to reaction with ozone in a proxy for organic aerosols

    Science.gov (United States)

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

    2016-04-01

    The discovery of boundary layer ozone depletion events in the Polar Regions [1] and in the mid-latitudes [2], two areas of very different temperature regimes, begs the question of temperature dependence of reactions responsible for these observations [3]. These ODEs have been attributed to ozone reacting with halides leading to reactive halogens (halogen activation) of which bromide is extensively studied, R1 - R3 [4, 5] (R1 is a multiphase reaction). O3 + Br‑→ O2 + OBr‑ (R1) OBr‑ + H+ ↔ HOBr (R2) HOBr + H+ + Br‑→ Br2 + H2O (R3) Despite extensive studies of ozone-bromide interactions, the temperature dependence of bromine activation is not clear [3]. This limits parameterization of the involved reactions and factors in atmospheric models [3, 6]. Viscosity changes in the matrix (such as organic aerosols) due to temperature have been shown to influence heterogeneous reaction rates and products beyond pure temperature effect [7]. With the application of coated wall flow-tubes, the aim of this study is therefore to investigate the temperature dependence of bromine activation by ozone interaction while attempting to characterize the contributions of the bulk and surface reactions to observed ozone uptake. Citric acid is used in this study as a hygroscopically characterized matrix whose viscosity changes with temperature and humidity. Here, we present reactive ozone uptake measured between 258 and 289 K. The data show high reproducibility. Comparison of measured uptake with modelled bulk uptake at different matrix compositions (and viscosities) indicate that bulk reactive uptake dominates, but there are other factors which still need further consideration in the model. References 1. Barrie, L.A., et al., Nature, 1988. 334: p. 138 - 141. 2. Hebestreit, K., et al., Science, 1999. 283: p. 55-57. 3. Simpson, W.R., et al., Atmospheric Chemistry and Physics, 2007. 7: p. 4375 - 4418. 4. Haag, R.W. and J. Hoigné, Environ Sci Technol, 1983. 17: p. 261-267. 5. Oum

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

    Directory of Open Access Journals (Sweden)

    N. Bobrowski

    2012-03-01

    Full Text Available Over a three year period, from 2006 to 2009, frequent scattered sun light DOAS measurements were conducted at Mt. Etna in a distance of around six kilometres 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.

    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, 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 short afterwards, 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

  15. Chloride diffusion in partially saturated cementitious material

    DEFF Research Database (Denmark)

    Nielsen, Erik Pram; Geiker, Mette Rica

    2003-01-01

    The paper proposes a combined application of composite theory and Powers' model for microstructural development for the estimation of the diffusion coefficient as a function of the moisture content of a defect-free cementitious material. Measurements of chloride diffusion in mortar samples (440 kg....../m(3) rapid-hardening Portland cement, w/c = 0.5, maturity minimum 6 months) stored at 65% and 85% RH, as well as in vacuum-saturated mortar samples, illustrate the applicability of the method. (C) 2003 Elsevier Science Ltd. All rights reserved....

  16. Oral cadmium chloride intoxication in mice

    DEFF Research Database (Denmark)

    Andersen, O; Nielsen, J B; Svendsen, P

    1988-01-01

    Diethyldithiocarbamate (DDC) is known to alleviate acute toxicity due to injection of cadmium salts. However, when cadmium chloride was administered by the oral route, DDC enhanced rather than alleviated the acute toxicity; both oral and intraperitoneal (i.p.) administration of DDC had this effect....... Thus, orally administered DDC enhanced cadmium-induced duodenal and ileal tissue damage and inhibition of peristalsis, as indicated by an increased intestinal transit time. At low cadmium doses, the whole-body retention of cadmium was increased by oral DDC administration. Intraperitoneally administered...

  17. N-(2-Benzoylethylpropan-2-aminium chloride

    Directory of Open Access Journals (Sweden)

    Abdullah Aydın

    2012-09-01

    Full Text Available In the title salt, C12H18NO+·Cl−, N—H...Cl interactions between the free chloride anions and the organic cations connect the molecules into hydrogen-bond dimers, forming a R22(8 motif. The dimers are linked by C—H...O hydrogen bonds into chains extending along [301]. The carbonyl group is co-planar with the phenyl ring [C—C—C=O torsion angle = −3.3 (7°]. The side chain has an E conformation.

  18. Brominated flame retardants in Chinese air before and after the phase out of polybrominated diphenyl ethers

    Science.gov (United States)

    Li, Wen-Long; Qi, Hong; Ma, Wan-Li; Liu, Li-Yan; Zhang, Zhi; Mohammed, Mohammed O. A.; Song, Wei-Wei; Zhang, Zifeng; Li, Yi-Fan

    2015-09-01

    Brominated flame retardants (BFRs), including polybrominated diphenyl ethers (PBDEs) and novel non-BDE flame retardants (NBFRs), were analyzed in Chinese air during China's POPs Soil and Air Monitoring Program Phase I (SAMP-I) and Phase II (SAMP-II). The levels of Σ12PBDEs and Σ6NBFRs in urban sites were significantly higher than those in rural sites and background sites. The higher detection rate and concentrations of high molecular weight PBDEs and NBFRs in Phase II indicated the changing of the commercial pattern of BFRs after the phase out of PBDEs in China. Temperature was the major factor affecting the seasonal variations of molecular weight BFRs in atmosphere. A significant correlation between BFRs concentration and gross domestic product (GDP) was observed, with the GDP parameter explained 59.4% and 72.7% of the total variability for Octa-BDEs and low molecular weight NBFRs, respectively. Our findings indicated an evolving commercial usage of BFRs from SAMP-I to SAMP-II, i.e. shifting from lower molecular weight to higher molecular weight congeners in China.

  19. Formation of brominated trihalomethanes in chlorinated drinking-water from Lake Constance

    International Nuclear Information System (INIS)

    The formation of trihalomethanes (THMs) in raw water and drinking water from Lake Constance containing low amounts of DOC and bromide was studied with special emphasis on brominated trihalomethanes (Br-THMs). If the raw water was ozonated prior to chlorination, the formation of THMs was reduced by 37%, and if a rapid sandfiltration was interposed, the THM-formation was again slightly enhanced. The percentage of Br-THMs on total-THMs increased from 16% to 35% during the treatment process. In the drinking water distribution system of BWV the formation of Br-THMs and CHCl3 was studied with respect to residence time and post-chlorination. Unless the post-chlorination was performed, the THM-formation in the distribution system resembled that obtained from laboratory studies, except for small amounts of THMs being purged due to transport in the mains and residence in the reservoirs. Post-chlorination increased CHCl3- and the CHBrCl2-formation, but there was no effect on the formation of CHBr2Cl and CHBr3. However, the total THM-concentration in the drinking water never exceeded the German drinking water standard of 10 μg/L. (orig.)

  20. From Clothing to Laundry Water: Investigating the Fate of Phthalates, Brominated Flame Retardants, and Organophosphate Esters.

    Science.gov (United States)

    Saini, Amandeep; Thaysen, Clara; Jantunen, Liisa; McQueen, Rachel H; Diamond, Miriam L

    2016-09-01

    The accumulation of phthalate esters, brominated flame retardants (BFRs) and organophosphate esters (OPEs) by clothing from indoor air and transfer via laundering to outdoors were investigated. Over 30 days cotton and polyester fabrics accumulated 3475 and 1950 ng/dm(2) ∑5phthalates, 65 and 78 ng/dm(2) ∑10BFRs, and 1200 and 310 ng/dm(2) ∑8OPEs, respectively. Planar surface area concentrations of OPEs and low molecular weight phthalates were significantly greater in cotton than polyester and similar for BFRs and high molecular weight phthalates. This difference was significantly and inversely correlated with KOW, suggesting greater sorption of polar compounds to polar cotton. Chemical release from cotton and polyester to laundry water was >80% of aliphatic OPEs (log KOW 8) and BFRs (log KOW > 6). These results support the hypothesis that clothing acts an efficient conveyer of soluble semivolatile organic compounds (SVOCs) from indoors to outdoors through accumulation from air and then release during laundering. Clothes drying could as well contribute to the release of chemicals emitted by electric dryers. The results also have implications for dermal exposure. PMID:27507188

  1. [Optimization of determination of aflatoxins in foods with bromine postcolumn derivatization].

    Science.gov (United States)

    Czerwiecki, Ludwik; Wilczyńska, Grazyna

    2007-01-01

    The method for determination of aflatoxin B1, B2, G1 i G2 in nuts, culinary spices, cereals and cereal products was described. To optimize the analytical procedure in several products, condition of proper extraction, clean-up, HPLC and detection were selected. After extraction by means of methanol and water (80+20 v/v) or (70+30 v/v), clean-up on IAC columns, HPLC on C18 columns--Nucleosil and Nova Pak with mobile phase-methanol, acetonitrile, water (20+20+60 v/v) was performed. For fluorometric detection at 362/430 nm, post-column derivatization of aflatoxin B1 and G1 with bromine was carried out. The mean recovery of the method depending on matrix and aflatoxin, was 52-102% at RSD% 0.2-8.3. LOD and LOQ, respectively were: 0.01 and 0.02 microg/kg for nuts and 0.05 and 0.1 microg/kg for culinary spices and cereal products. The concentrations of aflatoxins in 86 samples of foods from market were below the permissible maximum levels legally binding. PMID:18246653

  2. Natural Oxidation of Bromide to Bromine in Evaporated Dead Sea Brines

    Science.gov (United States)

    Gavrieli, Ittai; Golan, Rotem; Lazar, Boaz; Baer, Gidi; Zakon, Yevgeni; Ganor, Jiwchar

    2016-04-01

    Highly evaporated Dead Sea brines are found in isolated sinkholes along the Dead Sea. Many of these brines reach densities of over 1.3 kg/L and pHacidic with a value of ~6.3. In comparison, seawater with the same alkalinity would have a pH value well above 8.3, meaning that H+ activity is 100 fold lower than that of Dead Sea brine. In the present work we assess the apparent dissociation constant value of boric acid (K`B) for the Dead Sea brine and use it to explain the brine's low pH value. We then show that pH decreases further as the brine evaporates and salinity increases. Finally we explain the reddish hue of the hypersaline brines in the sinkholes as due to the presence of dissolved bromine. The latter is the product of oxidation of dissolved bromide, a process that is enabled by the low pH of the hypersaline brines and their high bromide concentration.

  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. 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.

  5. Product oriented oxidative bromination of methane over Rh/SiO2 catalysts

    Institute of Scientific and Technical Information of China (English)

    Zhen Liu; Wensheng Li; Xiaoping Zhou

    2010-01-01

    Rh/SiO2 was prepared for the oxidative bromination of methane.The catalyst was prepared by calcination at different temperatures and for different times to obtain catalysts with different specific surface areas for the purposes of producing either CH3Br or CH3Br and CO.It was found that the catalyst having a low specific surface area(calcined at relatively high temperature)favors the selective oxidation of methane to prepare CH3Br,while the catalyst having a high specific surface area favors the deeper partial oxidation of methane,which is good for CH3Br and CO preparation.The 650 h on stream life-time test revealed that the catalytic performance of the 0.4Rh/SiO2-900-10 catalyst was excellent.Both methane conversion and CH3Br selectivity kept increasing trends during the life-time test.No matter how serious was the Rh leaching during the reaction,the 0.4Rh/SiO2-900-10 catalyst did not deactivate at all.

  6. Brominated flame retardants in the indoor environment - Comparative study of indoor contamination from three countries.

    Science.gov (United States)

    Venier, Marta; Audy, Ondřej; Vojta, Šimon; Bečanová, Jitka; Romanak, Kevin; Melymuk, Lisa; Krátká, Martina; Kukučka, Petr; Okeme, Joseph; Saini, Amandeep; Diamond, Miriam L; Klánová, Jana

    2016-09-01

    Concentrations of more than 20 brominated flame retardants (FRs), including polybrominated diphenyl ethers (PBDEs) and emerging FRs, were measured in air, dust and window wipes from 63 homes in Canada, the Czech Republic and the United States in the spring and summer of 2013. Among the PBDEs, the highest concentrations were generally BDE-209 in all three matrices, followed by Penta-BDEs. Among alternative FRs, EHTBB and BEHTBP were detected at the highest concentrations. DBDPE was also a major alternative FR detected in dust and air. Bromobenzenes were detected at lower levels than PBDEs and other alternative FRs; among the bromobenzenes, HBB and PBEB were the most abundant compounds. In general, FR levels were highest in the US and lowest in the Czech Republic - a geographic trend that reflects the flame retardants' market. No statistically significant differences were detected between bedroom and living room FR concentrations in the same house (n=10), suggesting that sources of FRs are widespread indoors and mixing between rooms. The concentrations of FRs in air, dust, and window film were significantly correlated, especially for PBDEs. We found a significant relationship between the concentrations in dust and window film and in the gas phase for FRs with log KOA values values >14. This hypothesis was confirmed by a large discrepancy between values predicted using a partitioning model and the measured values for FRs with log KOA values >14. PMID:27248661

  7. Simple and rapid quantification of brominated vegetable oil in commercial soft drinks by LC-MS.

    Science.gov (United States)

    Chitranshi, Priyanka; Gamboa da Costa, Gonçalo

    2016-12-15

    We report here a simple and rapid method for the quantification of brominated vegetable oil (BVO) in soft drinks based upon liquid chromatography-electrospray ionization mass spectrometry. Unlike previously reported methods, this novel method does not require hydrolysis, extraction or derivatization steps, but rather a simple "dilute and shoot" sample preparation. The quantification is conducted by mass spectrometry in selected ion recording mode and a single point standard addition procedure. The method was validated in the range of 5-25μg/mL BVO, encompassing the legal limit of 15μg/mL established by the US FDA for fruit-flavored beverages in the US market. The method was characterized by excellent intra- and inter-assay accuracy (97.3-103.4%) and very low imprecision [0.5-3.6% (RSD)]. The direct nature of the quantification, simplicity, and excellent statistical performance of this methodology constitute clear advantages in relation to previously published methods for the analysis of BVO in soft drinks. PMID:27451219

  8. From Clothing to Laundry Water: Investigating the Fate of Phthalates, Brominated Flame Retardants, and Organophosphate Esters.

    Science.gov (United States)

    Saini, Amandeep; Thaysen, Clara; Jantunen, Liisa; McQueen, Rachel H; Diamond, Miriam L

    2016-09-01

    The accumulation of phthalate esters, brominated flame retardants (BFRs) and organophosphate esters (OPEs) by clothing from indoor air and transfer via laundering to outdoors were investigated. Over 30 days cotton and polyester fabrics accumulated 3475 and 1950 ng/dm(2) ∑5phthalates, 65 and 78 ng/dm(2) ∑10BFRs, and 1200 and 310 ng/dm(2) ∑8OPEs, respectively. Planar surface area concentrations of OPEs and low molecular weight phthalates were significantly greater in cotton than polyester and similar for BFRs and high molecular weight phthalates. This difference was significantly and inversely correlated with KOW, suggesting greater sorption of polar compounds to polar cotton. Chemical release from cotton and polyester to laundry water was >80% of aliphatic OPEs (log KOW phthalates (log KOW 4-6), and phthalates (log KOW > 8) and BFRs (log KOW > 6). These results support the hypothesis that clothing acts an efficient conveyer of soluble semivolatile organic compounds (SVOCs) from indoors to outdoors through accumulation from air and then release during laundering. Clothes drying could as well contribute to the release of chemicals emitted by electric dryers. The results also have implications for dermal exposure.

  9. 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.

  10. Simple and rapid quantification of brominated vegetable oil in commercial soft drinks by LC-MS.

    Science.gov (United States)

    Chitranshi, Priyanka; Gamboa da Costa, Gonçalo

    2016-12-15

    We report here a simple and rapid method for the quantification of brominated vegetable oil (BVO) in soft drinks based upon liquid chromatography-electrospray ionization mass spectrometry. Unlike previously reported methods, this novel method does not require hydrolysis, extraction or derivatization steps, but rather a simple "dilute and shoot" sample preparation. The quantification is conducted by mass spectrometry in selected ion recording mode and a single point standard addition procedure. The method was validated in the range of 5-25μg/mL BVO, encompassing the legal limit of 15μg/mL established by the US FDA for fruit-flavored beverages in the US market. The method was characterized by excellent intra- and inter-assay accuracy (97.3-103.4%) and very low imprecision [0.5-3.6% (RSD)]. The direct nature of the quantification, simplicity, and excellent statistical performance of this methodology constitute clear advantages in relation to previously published methods for the analysis of BVO in soft drinks.

  11. Characterizing Variability in the Spatial Distribution of Bromine Explosion Events in the Vicinity of Barrow, Alaska

    Science.gov (United States)

    Peterson, P.; Pratt, K.; Simpson, W. R.; Shepson, P. B.; Pöhler, D.; Friess, U.; Zielcke, J.; Platt, U.; Nghiem, S. V.; Sihler, H.

    2015-12-01

    Reactive halogens (e.g. Br, BrO) are produced photochemically during springtime in the Arctic. Some dramatic effects of these halogen species are known (e.g. ozone depletion, mercury deposition), but changes in atmospheric composition related to this halogen chemistry, particularly those related to increasing sea ice loss and the transformation of Arctic sea ice cover, are unknown. In March 2012, the Bromine, Ozone, Mercury EXperiment (BROMEX) provided an opportunity to enhance our understanding of the spatial and temporal variability of halogen chemistry in the vicinity of Barrow, Alaska. During BROMEX, we used Multiple Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) to measure BrO lower tropospheric vertical column densities (LT-VCD) and near-surface mixing ratios at Barrow, as well as on land-fast ice 40 km north east of Barrow, and a drifting platform on seasonal sea ice west of Barrow. Concurrently, an aircraft equipped with the Heidelberg Airborne Imaging DOAS Instrument (HAIDI) collected airborne BrO data at altitudes up to 3 km. These measurements showed several instances of spatial gradients in BrO between measurement sites, as well as times when BrO was present up to 1km aloft. We explore explanations for these features using local and synoptic meteorology, back-trajectory modelling, MODIS and airborne imagery, as well as satellite-instrument-based maps of synoptic sea ice classes and tropospheric BrO.

  12. Photochemical transformation of five novel brominated flame retardants: Kinetics and photoproducts.

    Science.gov (United States)

    Zhang, Ya-Nan; Chen, Jingwen; Xie, Qing; Li, Yingjie; Zhou, Chengzhi

    2016-05-01

    Many novel brominated flame retardants (NBFRs) are used as substitutes of polybrominated diphenyl ethers (PBDEs) in recent years. However, little is known about their phototransformation behavior, which may influence the environmental fate of these chemicals. In this study, photochemical behavior of five NBFRs, allyl-2,4,6-tribromophenyl ether (ATE), 2-bromoallyl-2,4,6-tribromophenyl ether (BATE), 2,3-dibromopropyl-2,4,6-tribromophenyl ether (DPTE), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), and 2,4,6-tris(2,4,6-tribromophenoxy)-1,3,5-triazine (TTBP-TAZ) was investigated. Results show all the five NBFRs can undergo photochemical transformation under simulated sunlight irradiation. Quantum yields (Φ) of the five NBFRs varied from 0.012 of TTBP-TAZ in hexane to 0.091 of BTBPE in methanol. Half-lives (t1/2) relevant with solar irradiation of these NBFRs were estimated using the determined Φ, and the values are 1.5-12.0 d in summer and 17.1-165.0 d in winter. Debrominated and ether bond cleavage products were identified in the phototransformation of DPTE and BTBPE. Debromination on the phenyl is a main phototransformation pathway for DPTE, and both debromination and ether bond cleavage are main phototransformation pathways for BTBPE. This study is helpful to better understand the phototransformation behavior of the NBFRs. PMID:26796587

  13. Shuttle Environmental Assurance: Brominated Flame Retardants - Concerns, Drivers, Potential Impacts and Mitigation Strategies

    Science.gov (United States)

    Clark-Ingram, Marceia

    2010-01-01

    Brominated Flame Retardants (BFRs) are widely used in the manufacture of electrical and electronic components and as additives in formulations for foams, plastics and rubbers. The United States (US) and the European Union (EU)have increased regulation and monitoring of of targeted BFRs, such as Polybrominated Diphenyl Ethers (PBDEs) due to the bioaccumulative effects in humans and animals. In response, manufacturers and vendors of BFR-containing materials are changing flame-retardant additives, sometimes without notifying BFR users. In some instances, Deca-bromodiphenylether (Deca-BDE) and other families of flame retardants are being used as replacement flame retardants for penta-BDE and octa-BDE. The reformulation of the BFR-containing material typically results in the removal of the targeted PBDE and replacement with a non-PBDE chemical or non-targeted PBDE. Many users of PBDE -based materials are concerned that vendors will perform reformulation and not inform the end user. Materials performance such as flammability, adhesion , and tensile strength may be altered due to reformulation. The requalification of newly formulated materials may be required, or replacement materials may have to be identified and qualified. The Shuttle Enviornmental Assurance (SEA) team indentified a risk to the Space Shuttle Program associated with the possibility that targeted PBDEs may be replaced without notification. Resultant decreases in flame retardancy, Liquid Oxygen (LOX) compatibility, or material performance could have serious consequences.

  14. Identification of highly brominated analogues of Q1 in marine mammals

    International Nuclear Information System (INIS)

    Three novel halogenated organic compounds (HOCs) have been identified in the blubber of marine mammals from coastal New England with the molecular formulae C9H3N2Br6Cl, C9H3N2Br7, and C9H4N2Br5Cl. 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 μg/g (lipid weight). The regiospecificity of C9H3N2Br6Cl is suggestive of a biogenic origin. Debromination of C9H3N2Br6Cl may be significant in the formation of C9H4N2Br5Cl. - Three novel bioaccumulated compounds were identified as C9H3N2Br6Cl, C9H3N2Br7 and C9H4N2Br5Cl

  15. Brominated flame retardants (BFRs): A review on environmental contamination in China.

    Science.gov (United States)

    Yu, Gang; Bu, Qingwei; Cao, Zhiguo; Du, Xinming; Xia, Jing; Wu, Min; Huang, Jun

    2016-05-01

    Brominated flame retardants (BFRs) which were detected extensively in environmental and biota samples worldwide, have raised significant concerns during past decades for their persistence, bioaccumulation and potential toxicity to ecological environment and human health. In this paper, we have compiled and reviewed existing literature on the contamination status of BFRs in abiotic and biotic environments in China, including polybrominated diphenyl ethers (PBDEs), hexabromocyclododecane, tetrabromobisphenol A and new BFRs. Temporal trends were also summarized and evaluated. Based on this review, it has been concluded that (1) high concentrations of PBDEs were generally related to the e-waste disposal processing, while the spatial distribution pattern of other BFRs was not necessarily in accordance with this; (2) extremely high concentrations of BFRs in indoor dust emphasized the importance of indoor contamination to human body burdens, while more work need to be done to confirm its contribution; (3) PBDEs in electronics dismantling workers were higher compared to the general population, indicating the occupational exposure should be of particular concern; (4) more data are now becoming available for BFRs in aquatic and terrestrial organisms not previously studied, while studies that consider the occurrence of BFRs in organisms of different trophic levels are still of urgent need for evaluating the fate of BFRs in the food web; and (5) limited data showed a decreasing trend for PBDEs, while more data on time trends of BFR contamination in various matrices and locations are still needed before the impact of regulation of BFRs can be assessed.

  16. Interactions between chloride ingress and carbonation in cementitious materials

    OpenAIRE

    SAILLIO, Mickael; BARBERON, Fabien; BAROGHEL BOUNY, Véronique; GEGOUT, Philippe; PLATRET, Gérard; D'ESPINOSE DE LA CAILLERIE, JB

    2011-01-01

    Carbonation and chloride attacks are the major causes of reinforced concrete (RC) structure deterioration by initiation of steel rebar corrosion. These attacks are usually studied separately in the literature. Chloride-induced corrosion takes place mainly in marine environment or in the case of contact with deicing salts, while carbonation is systematically present in all RC structures at a variable degree. Since carbonation leads to significant microstructure changes, the effect of chloride ...

  17. Surface Chloride Concentration of Concrete under Shallow Immersion Conditions

    OpenAIRE

    Jun Liu; Kaifeng Tang; Dong Pan; Zongru Lei; Weilun Wang; Feng Xing

    2014-01-01

    Deposition of chloride ions in the surface layer of concrete is investigated in this study. In real concrete structure, chloride ions from the service environment can penetrate into concrete and deposit in the surface layer, to form the boundary condition for further diffusion towards the interior. The deposit amount of chloride ions in the surface layer is normally a function of time, rather than a constant. In the experimental investigation, concrete specimens with different mix proportions...

  18. N,N-Dimethyldehydroabietylammonium chloride ethanol monosolvate

    Directory of Open Access Journals (Sweden)

    Xiu-Zhi Huang

    2013-06-01

    Full Text Available The title compound {systematic name: 1-[(1R,4aS,10aR-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthren-1-yl]-N,N-dimethylmethanaminium chloride ethanol monosolvate}, C22H36N+·Cl−·C2H6O, was synthesized from dehydroabietylamine by N-methylation with formaldehyde/formic acid and transformation into the hydrochloride. The dehydroabietyl moiety exhibits the usual conformation with the two cyclohexane rings in chair and half-chair conformations and a trans-ring junction. The crystal structure is built up from columns of the dehydroabietyl moieties stacked along the a axis. These columns are held together by the chloride ions via N—H...Cl and C—H...Cl interactions, which establish a two-dimensional network parallel to (010. The ethanol solvent molecules are located between the columns and anchored via O—H...Cl hydrogen bonds.

  19. Open cycle lithium chloride cooling system

    Science.gov (United States)

    Lenz, T. G.; Loef, G. O. G.; Iyer, R.; Wenger, J.

    1983-05-01

    A lithium chloride open cycle absorption chiller has been designed, built and tested. Solution reconcentration takes place in a small counter current packed column supplied with solar heated air. Removal of noncondensable gases that enter the chiller dissolved in the strong solution and the make-up refrigerant streams is accomplished by a liquid-jet ejector and a small vacuum pump. Cooling capacities approaching 1.4 tons and COP levels of 0.58 have been achieved at non-optimum operating conditions. Test results from preliminary system operation suggest that mass transfer processes in both the packed column reconcentrator and the absorber are controlled by concentration gradients in the lithium chloride solution. Liquid phase controlled mass transfer dictates an operating strategy different from the previously assumed gas phase controlled process to obtain maximum rates of evaporation in the packed column. Determination of optimal operating conditions leading to decreased electrical power consumption and improved cooling capacity and coefficient of performance will require further analysis and testing.

  20. Synthesis and structure characterization of diethyldiallylammonium chloride

    Institute of Scientific and Technical Information of China (English)

    刘立华; 龚竹青; 郑雅杰

    2003-01-01

    The unsaturated quaternary ammonium salt diethyldiallylammonium chloride(DEDAAC) was synthesized in a two-step synthetic method. The influences of the adding method of raw materials and temperature on the yields of diethylallylamine (DEAA), and drying and temperature on the synthesis of DEDAAC were investigated. The content of in-process product DEAA was determined by non-aqueous titration. The structure of product DEDAAC was identified with IR, 1 H NMR and elemental analysis. The results show that adding allyl chloride and sodium hydroxide alternately can increase the yield of DEAA and decrease by-products. In further synthesizing of DEDAAC from DEAA, the step of drying DEAA is very necessary. When DEAA is dried by solid sodium hydroxide, good columnar crystals with a high purity(mp 199.5-201.0 ℃) are obtained; when DEAA is undried or the content of water in DEAA is above 20%, only platelets with bad quality are obtained even without crystals. The suitable synthesis conditions for DEAA and DEDAAC are 35 ℃, 6 h and 40 ℃, 36 h, respectively, and their yields are 69.7% and 67.3%, respectively.

  1. Fault locator of an allyl chloride plant

    Directory of Open Access Journals (Sweden)

    Savković-Stevanović Jelenka B.

    2004-01-01

    Full Text Available Process safety analysis, which includes qualitative fault event identification, the relative frequency and event probability functions, as well as consequence analysis, was performed on an allye chloride plant. An event tree for fault diagnosis and cognitive reliability analysis, as well as a troubleshooting system, were developed. Fuzzy inductive reasoning illustrated the advantages compared to crisp inductive reasoning. A qualitative model forecast the future behavior of the system in the case of accident detection and then compared it with the actual measured data. A cognitive model including qualitative and quantitative information by fuzzy logic of the incident scenario was derived as a fault locator for an ally! chloride plant. The obtained results showed the successful application of cognitive dispersion modeling to process safety analysis. A fuzzy inductive reasoner illustrated good performance to discriminate between different types of malfunctions. This fault locator allowed risk analysis and the construction of a fault tolerant system. This study is the first report in the literature showing the cognitive reliability analysis method.

  2. Interpretation of postmortem vitreous concentrations of sodium and chloride.

    Science.gov (United States)

    Zilg, B; Alkass, K; Berg, S; Druid, H

    2016-06-01

    Vitreous fluid can be used to analyze sodium and chloride levels in deceased persons, but it remains unclear to what extent such results can be used to diagnose antemortem sodium or chloride imbalances. In this study we present vitreous sodium and chloride levels from more than 3000 cases. We show that vitreous sodium and chloride levels both decrease with approximately 2.2mmol/L per day after death. Since potassium is a well-established marker for postmortem interval (PMI) and easily can be analyzed along with sodium and chloride, we have correlated sodium and chloride levels with the potassium levels and present postmortem reference ranges relative the potassium levels. We found that virtually all cases outside the reference range show signs of antemortem hypo- or hypernatremia. Vitreous sodium or chloride levels can be the only means to diagnose cases of water or salt intoxication, beer potomania or dehydration. We further show that postmortem vitreous sodium and chloride strongly correlate and in practice can be used interchangeably if analysis of one of the ions fails. It has been suggested that vitreous sodium and chloride levels can be used to diagnose drowning or to distinguish saltwater from freshwater drowning. Our results show that in cases of freshwater drowning, vitreous sodium levels are decreased, but that this mainly is an effect of postmortem diffusion between the eye and surrounding water rather than due to the drowning process, since the decrease in sodium levels correlates with immersion time. PMID:27105154

  3. On Barium Oxide Solubility in Barium-Containing Chloride Melts

    Science.gov (United States)

    Nikolaeva, Elena V.; Zakiryanova, Irina D.; Bovet, Andrey L.; Korzun, Iraida V.

    2016-08-01

    Oxide solubility in chloride melts depends on temperature and composition of molten solvent. The solubility of barium oxide in the solvents with barium chloride content is essentially higher than that in molten alkali chlorides. Spectral data demonstrate the existence of oxychloride ionic groupings in such melts. This work presents the results of the BaO solubility in two molten BaCl2-NaCl systems with different barium chloride content. The received data together with earlier published results revealed the main regularities of BaO solubility in molten BaO-BaCl2-MCl systems.

  4. Catalytic Conversion of Cellulose to Levulinic Acid by Metal Chlorides

    Directory of Open Access Journals (Sweden)

    Beixiao Zhang

    2010-08-01

    Full Text Available The catalytic performance of various metal chlorides in the conversion of cellulose to levulinic acid in liquid water at high temperatures was investigated. The effects of reaction parameters on the yield of levulinic acid were also explored. The results showed that alkali and alkaline earth metal chlorides were not effective in conversion of cellulose, while transition metal chlorides, especially CrCl3, FeCl3 and CuCl2 and a group IIIA metal chloride (AlCl3, exhibited high catalytic activity. The catalytic performance was correlated with the acidity of the reaction system due to the addition of the metal chlorides, but more dependent on the type of metal chloride. Among those metal chlorides, chromium chloride was found to be exceptionally effective for the conversion of cellulose to levulinic acid, affording an optimum yield of 67 mol % after a reaction time of 180 min, at 200 °C, with a catalyst dosage of 0.02 M and substrate concentration of 50 wt %. Chromium metal, most of which was present in its oxide form in the solid sample and only a small part in solution as Cr3+ ion, can be easily separated from the resulting product mixture and recycled. Finally, a plausible reaction scheme for the chromium chloride catalyzed conversion of cellulose in water was proposed.

  5. Durability of cracked fibre reinforced concrete structures exposed to chlorides

    DEFF Research Database (Denmark)

    Hansen, Ernst Jan De Place; Ekman, Tom; Hansen, Kurt Kielsgaard

    1999-01-01

    is used as environmental load. The chloride penetration is characterized both qualitatively (UV-test) and quantitatively (chloride profile) and by microscopy. The test programme involves three different concrete qualities. Both steel fibres and polypropylene fibres are used in the concrete beams as well......Durability studies are carried out by subjecting FRC-beams to combined mechanical and environmental load. Mechanical load is obtained by exposing beams to 4-point bending until a predefined crack width is reached, using a newly developed test setup. Exposure to a concentrated chloride solution...... as main reinforcement. The effect of the cracks, the fibres and the concrete quality on the chloride penetration is studied....

  6. 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

  7. THE COMPATIBILITY OF BLENDS OF POLY(VINYL CHLORIDE) OR CHLORINATED POLY(VINYL CHLORIDE) WITH POLY(METHYL METHACRYLATE)

    Institute of Scientific and Technical Information of China (English)

    WANG Qingguo; CHENG Rongshi

    1988-01-01

    IR spectral shifts of carbonyl vibrational absorption for ethyl acetate, which acts analogically as the structural unit of poly(methyl methacrylate), in cyclohexane, chloroform, chlorinated paraffins, poly(vinyl chloride) and chlorinated poly(vinyl chloride) were measured. The results suggest that there are specific interactions between the carbonyl groups and the chlorinated hydrocarbons which could be responsible for the apparent compatibility of poly(vinyl chloride) -poly(methyl methacrylate) and chlorinated poly(vinyl chloride) -poly(methyl methacrylate) blends. Additionally, the effects of the preparation mode of blend films on phase separation and observed compatibility are discussed.

  8. Novel analytical approach for brominated flame retardants based on the use of gas chromatography-atmospheric pressure chemical ionization-tandem mass spectrometry with emphasis in highly brominated congeners.

    Science.gov (United States)

    Portolés, Tania; Sales, Carlos; Gómara, Belén; Sancho, Juan Vicente; Beltrán, Joaquim; Herrero, Laura; González, María José; Hernández, Félix

    2015-10-01

    The analysis of brominated flame retardants (BFRs) commonly relies on the use of gas chromatography coupled to mass spectrometry (GC-MS) operating in electron ionization (EI) and electron capture negative ionization (ECNI) modes using quadrupole, triple quadrupole, ion trap, and magnetic sector analyzers. However, these brominated contaminants are examples of compounds for which a soft and robust ionization technique might be favorable since they show high fragmentation in EI and low specificity in ECNI. In addition, the low limits of quantification (0.01 ng/g) required by European Commission Recommendation 2014/118/EU on the monitoring of traces of BFRs in food put stress on the use of highly sensitive techniques/methods. In this work, a new approach for the extremely sensitive determination of BFRs taking profit of the potential of atmospheric pressure chemical ionization (APCI) combined with GC and triple quadrupole (QqQ) mass analyzer is proposed. The objective was to explore the potential of this approach for the BFRs determination in samples at pg/g levels, taking marine samples and a cream sample as a model. Ionization and fragmentation behavior of 14 PBDEs (congeners 28, 47, 66, 85, 99, 100, 153, 154, 183, 184, 191, 196, 197, and 209) and two novel BFRs, decabromodiphenyl ethane (DBDPE) and 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), in the GC-APCI-MS system has been investigated. The formation of highly abundant (quasi) molecular ion was the main advantage observed in relation to EI. Thus, a notable improvement in sensitivity and specificity was observed when using it as precursor ion in tandem MS. The improved detectability (LODs < 10 fg) achieved when using APCI compared to EI has been demonstrated, which is especially relevant for highly brominated congeners. Analysis of samples from an intercomparison exercise and samples from the marine field showed the potential of this approach for the reliable identification and quantification at very low

  9. Emissions of Bromine and Iodine from the Marine Environment in New Zealand

    Science.gov (United States)

    Martinez-Aviles, M.; Kreher, K.; Johnston, P. V.; Hay, T.; Thomas, A.; Schofield, R.

    2009-12-01

    of determining coastal sites where high active halogen release could be observed. The selected sites had high biomass concentration of marine algae that would be exposed by low tides. Local macro algae type, tidal height, sunlight, temperature, and wind speed were recorded and correlated to the resulting data in order to better understand the environmental factors that modulate the emissions of halogen oxides from the marine environment to the troposphere. Results of this multi-disciplinary approach to studying brominated VSLS and their atmospheric implications are presented. As well, the chemical processes taking place and producing these halogen oxides are discussed in a thorough manner. This study contributes to a better understanding of the origin of bromine and iodine in the lowermost atmosphere (i.e. marine boundary layer). Particularly, the role that natural emissions of halogenated VSLS from the ocean may play in the halogen budget of the lower atmosphere is addressed by quantitatively understanding key links in this chain so that its potential future impacts on atmospheric chemistry, surface UV radiation, and the biosphere can be thoroughly assessed.

  10. Bromination vis-a-vis chlorination as a biocide feasibility study

    International Nuclear Information System (INIS)

    friendly. This paper highlights the brief details on the feasibility studies carried out on bromination. (author)

  11. Fabric phase sorptive extraction: Two practical sample pretreatment techniques for brominated flame retardants in water.

    Science.gov (United States)

    Huang, Guiqi; Dong, Sheying; Zhang, Mengfei; Zhang, Haihan; Huang, Tinglin

    2016-09-15

    Sample pretreatment is the critical section for residue monitoring of hazardous pollutants. In this paper, using the cellulose fabric as host matrix, three extraction sorbents such as poly (tetrahydrofuran) (PTHF), poly (ethylene glycol) (PEG) and poly (dimethyldiphenylsiloxane) (PDMDPS), were prepared on the surface of the cellulose fabric. Two practical extraction techniques including stir bar fabric phase sorptive extraction (stir bar-FPSE) and magnetic stir fabric phase sorptive extraction (magnetic stir-FPSE) have been designed, which allow stirring of fabric phase sorbent during the whole extraction process. In the meantime, three brominated flame retardants (BFRs) [tetrabromobisphenol A (TBBPA), tetrabromobisphenol A bisallylether (TBBPA-BAE), tetrabromobisphenol A bis(2,3-dibromopropyl)ether (TBBPA-BDBPE)] in the water sample were selected as model analytes for the practical evaluation of the proposed two techniques using high-performance liquid chromatography (HPLC). Moreover, various experimental conditions affecting extraction process such as the type of fabric phase, extraction time, the amount of salt and elution conditions were also investigated. Due to the large sorbent loading capacity and unique stirring performance, both techniques possessed high extraction capability and fast extraction equilibrium. Under the optimized conditions, high recoveries (90-99%) and low limits of detection (LODs) (0.01-0.05 μg L(-1)) were achieved. In addition, the reproducibility was obtained by evaluating the intraday and interday precisions with relative standard deviations (RSDs) less than 5.1% and 6.8%, respectively. The results indicated that two pretreatment techniques were promising and practical for monitoring of hazardous pollutants in the water sample. Due to low solvent consumption and high repeated use performance, proposed techniques also could meet green analytical criteria. PMID:27300591

  12. 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.

  13. 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.

  14. Characterization of bromine-76-labelled 5-bromo-6-nitroquipazine for PET studies of the serotonin transporter

    Energy Technology Data Exchange (ETDEWEB)

    Lundkvist, Camilla E-mail: Lundkvis@shfj.cea.fr; Loc' h, Christian; Halldin, Christer; Bottlaender, Michel; Ottaviani, Michele; Coulon, Christine; Fuseau, Chantal; Mathis, Chester; Farde, Lars; Maziere, Bernard

    1999-07-01

    The development of suitable radioligands for brain imaging of the serotonin transporter is of great importance for the study of depression and other affective disorders. The potent and selective serotonin transporter ligand, 5-iodo-6-nitro-2-piperazinylquinoline, has been labelled with iodine-123 and used as a radioligand for single photon emission computerized tomography. To evaluate the potential of the bromine-76-labelled analogue, 5-bromo-6-nitroquipazine, as a radioligand for positron emission tomography (PET), its brain distribution and binding characteristics were examined in rats. In vivo brain distribution and ex vivo autoradiography demonstrated that [{sup 76}Br]5-bromo-6-nitroquipazine enters the brain rapidly. The regional brain distribution of [{sup 76}Br]5-bromo-6-nitroquipazine was consistent with the known distribution of serotonin transporters in the midbrain, pons, thalamus, striatum, and neocortex. Specific binding was inhibited by the selective serotonin reuptake inhibitor citalopram. The peripheral metabolism in plasma was rapid, but more than 90% of the radioactivity in brain represented unchanged radioligand 2 h postinjection (p.i.). A preliminary PET study was also performed in a baboon. Following the intravenous injection of [{sup 76}Br]5-bromo-6-nitroquipazine in a baboon, there was a conspicuous accumulation of radioactivity in thalamus, striatum, and pons. The radioactivity in these brain regions was 1.5 times higher than in the cerebellum at 3 h and 2.5-4 times higher at 24 h. A rapid metabolism of the radioligand in plasma was observed (38% unchanged after 5 min). The results indicate that [{sup 76}Br]5-bromo-6-nitroquipazine has potential for PET imaging of the serotonin transporter.

  15. Response of wheat and pea seedlings on increase of bromine concentration in the growth medium.

    Science.gov (United States)

    Shtangeeva, Irina; Niemelä, Matti; Perämäki, Paavo; Timofeev, Sergey

    2015-12-01

    Biogeochemical cycles of bromine (Br) and its quantitative requirements for different plant species are still studied poorly. There is a need to examine Br pathways in plants and evaluate the factors important for Br accumulation in a plant. In the present work, the effects of different Br compounds on an uptake of Br by two plant species (wheat and pea) that tolerate Br differently (pea is more sensitive to Br compared with wheat) have been studied. The growth medium was spiked with either KBr or NaBr at concentrations 0, 10, 50 and 100 mg/L. Elemental analysis of the plants was performed using inductively coupled plasma optical emission spectrometry (ICP-OES) and ICP-MS analytical techniques after leaching of the samples with tetramethyl ammonium hydroxide at mild temperature (60 °C). The experimental results have shown that wheat and pea seedlings can accumulate rather large amounts of Br. An increase of Br concentration in a plant was not always directly proportional to the variations in the Br concentration in the growth medium. In wheat, the greater part of Br was accumulated during first 7 days. In pea, the uptake of Br lasted until the end of the experiment. Certain differences in the ability of plants to accumulate Br were observed when the plants were grown in a medium spiked with different Br compounds. In most cases, Br accumulation was higher in the leaves of the plants grown in the medium spiked with KBr. The same tendency was observed for another halogen, chlorine (Cl).

  16. Leaching characteristics of heavy metals and brominated flame retardants from waste printed circuit boards

    International Nuclear Information System (INIS)

    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

  17. Observations and modeling of bromine induced mercury oxidation in the tropical free troposphere during TORERO

    Science.gov (United States)

    Coburn, Sean; Wang, Siyuan; terSchure, Arnout; Evans, Matt; Volkamer, Rainer

    2013-04-01

    The Tropical Ocean tRoposphere Exchange experiment TORERO (Jan/Feb 2012) probed air-sea exchange of very short lived halogens and organic carbon species over the full tropospheric air column above the eastern tropical Pacific Ocean. It is well known that halogens influence the oxidative capacity in the marine boundary layer, but their distribution and abundance is less clear in the tropical free troposphere, where most of tropospheric ozone mass resides, and about 80% of the global methane destruction occurs. The oxidation of elemental mercury (GEM) by halogens (i.e., bromine) further forms gaseous oxidized mercury (GOM), and this oxidation is accelerated at the low temperatures in the free troposphere compared to the boundary layer. Free tropospheric halogen radical abundances are thus of particular importance to understand the entry pathways for GOM deposition from the free troposphere to ecosystem, and the subsequent bio-accumulation of this neurotoxin. This presentation summarizes new observational evidence for halogen vertical distributions over the full tropospheric air column, and their abundance in the tropical troposphere, at mid-latitudes in the Northern and Southern hemisphere. BrO and IO were measured simultaneously by the CU Airborne MAX-DOAS instrument, and organic halogen precursors were measured by online GC-MS (TOGA) during 22 research flights aboard the NSF/NCAR GV aircraft. We employ atmospheric box modeling constrained by observations of gas-phase hydrocarbons, aerosols, photolysis frequencies, and meterological parameters measured aboard the plane to test the observed BrO and IO abundances, and evaluate the rate of GEM oxidation in light of recent updates about the stability of the Hg-Br adduct, and it's fate (Goodsite et al., 2012; Dibble et al., 2012). Finally, we compare our measurements with output from the GEOS-Chem model for selected case studies.

  18. Formation of new brominated disinfection byproducts during chlorination of saline sewage effluents.

    Science.gov (United States)

    Ding, Guoyu; Zhang, Xiangru; Yang, Mengting; Pan, Yang

    2013-05-15

    Chlorination could be the most cost-effective method for disinfecting saline sewage effluents resulting from toilet flushing with seawater. Upon chlorination, the high levels of bromide ions in saline sewage effluents (up to 32 mg/L) can be oxidized to hypobromous acid/hypobromite, which could then react with organic matter in the sewage effluents to form brominated disinfection byproducts (Br-DBPs). In this study, primary and secondary saline sewage effluents were collected and chlorinated at different chlorine doses, and a powerful precursor ion scan method using ultra performance liquid chromatography/electrospray ionization-triple quadrupole mass spectrometry was adopted for detection and identification of polar Br-DBPs in these samples. With the new method, 54 major polar Br-DBPs were detected in the chlorinated saline effluents and six of them were newly identified as wastewater DBPs, including bromomaleic acid, 5-bromosalicylic acid, 3,5-dibromo-4-hydroxybenzaldehyde, 3,5-dibromo-4-hydroxybenzoic acid, 2,6-dibromo-4-nitrophenol, and 2,4,6-tribromophenol. The formation of polar Br-DBPs, especially those newly detected ones, during chlorination of the saline effluents was studied. For the secondary saline effluent, various polar Br-DBPs formed and reached their maximum levels at different chlorine doses, whereas for the primary saline effluent, the formation of polar Br-DBPs basically kept increasing with increasing chlorine dose. Compared with the secondary saline effluent, the primary saline effluent generated fewer and less Br-DBPs and rarely generated nitrogenous Br-DBPs.

  19. Fate and metabolism of the brominated flame retardant tetrabromobisphenol A (TBBPA) in rice cell suspension culture.

    Science.gov (United States)

    Wang, Songfeng; Cao, Siqi; Wang, Yongfeng; Jiang, Bingqi; Wang, Lianhong; Sun, Feifei; Ji, Rong

    2016-07-01

    Tetrabromobisphenol A (TBBPA) is the brominated flame retardant with the highest production volume and its bioaccumulation in environment has caused both human health and environmental concerns, however the fate and metabolism of TBBPA in plants is unknown. We studied the fate, metabolites, and transformation of (14)C-labeled TBBPA in rice cell suspension culture. During the incubation for 14 days, TBBPA degradation occurred continuously in the culture, accompanied by formation of one anisolic metabolite [2,6-dibromo-4-(2-(2-hydroxy)-propyl)-anisole] (DBHPA) (50% of the degraded TBBPA) and cellular debris-bound residues (46.4%) as well as mineralization (3.6%). The cells continuously accumulated TBBPA in the cytoplasm, while a small amount of DBHPA (2.1% of the initially applied TBBPA) was detectable inside the cells only at the end of incubation. The majority of the accumulated residues in the cells was attributed to the cellular debris-bound residues, accounting for 70-79% of the accumulation after the first incubation day. About 5.4% of the accumulation was associated with cell organelles, which contributed 7.5% to the cellular debris-bound residues. Based on the fate and metabolism of TBBPA in the rice cell suspension culture, a type II ipso-substitution pathway was proposed to describe the initial step for TBBPA degradation in the culture and balance the fate of TBBPA in the cells. To the best of our knowledge, our study provides for the first time the insights into the fate and metabolism of TBBPA in plants and points out the potential role of type II ipso-hydroxylation substitution in degradation of alkylphenols in plants. Further studies are required to reveal the mechanisms for the bound-residue formation (e.g., binding of residues to specific cell wall components), nature of the binding, and toxicological effects of the bound residues and DBHPA.

  20. Industry-sponsored research on the potential health and environmental effects of selected brominated flame retardants.

    Science.gov (United States)

    Hardy, M L; Biesemeier, J; Manor, O; Gentit, W

    2003-09-01

    Modern fire-fighting techniques, equipment and fire-resistant building design has lead to less destruction than in the previous centuries. However, a high fuel load in either a residence or a commercial building can overwhelm even the best firefighters or building construction, and factors affecting the fuel load have changed in recent decades. The fire load in a typical home has doubled over the last 50 years, furnishings typically include those made of petrochemicals that can behave as if containing built-in accelerant, and modern energy-efficient buildings are less able to disperse heat in the event of a fire. Flame retardant chemicals (FRs) are one means used to reduce the risk of fire. FRs are typically added or incorporated chemically into a polymer to slow or hinder the ignition or growth of a fire in low-to-moderate cost commodity polymers. One type of FR contains bromine atoms as the active moiety. The FR industry, either as individual companies or as consortia, has conducted a broad range of studies on the commercial deca-, octa- and pentabromodiphenyl oxide/ether, tetrabromobisphenol A and hexabromocyclododecane products. These five products have data in excess of the OECD Screening Informational Data Set (SIDS) and the U.S. High Production Volume (HPV) program, and sufficient data for the performance of formal EU risk assessments. The objective of this paper is to present the range of data developed by industry consortia and to provide sources for the information. We hope to facilitate further research by assembling references to industry consortia-sponsored research here. PMID:12850097

  1. [Survey of plasticizers in polyvinyl chloride toys].

    Science.gov (United States)

    Abe, Yutaka; Yamaguchi, Miku; Mutsuga, Motoh; Hirahara, Yoshichika; Kawamura, Yoko

    2012-01-01

    Plasticizers in 101 samples of polyvinyl chloride (PVC) toys on the Japanese market were surveyed. No phthalates were detected in designated toys, though bis(2-ethylhexyl)phthalate, diisononyl phthalate, diisobutyl phthalate, dibutyl phthalate, diisodecyl phthalate and benzyl butyl phthalate were detected in more than half of other toys. 2,2,4-Tributyl-1,3-pentanediol diisobutylate, o-acetyl tributyl citrate, adipates and diacetyl lauroyl glycerol, which are alternative plasticizers to phthalates, were detected. The results of structural analysis confirmed the presence of di(2-ethylhexyl)terephthalate, tributyl citrate, diisononyl 1,2-cyclohexanedicarboxylate and neopentyl glycol esters; these have not previonsly been reported in Japan. There appears to be a shift in plasticizers used for designated toys from phthalates to new plasticizers, and the number of different plasticizers is increasing.

  2. Estimating the chloride transport in cement paste

    Directory of Open Access Journals (Sweden)

    Princigallo, A.

    2012-06-01

    Full Text Available A method was developed to measure the diffusion coefficient of chloride ions in cement paste based on an analytical solution to Fick’s 2nd law in a cylindrical coordinate system. This natural method yielded diffusivity results within as little as a month. Testing time was reduced by exploiting the three-dimensional inward flux in the specimen. In an attempt to determine the saturation concentration, dense portland cement pastes were exposed to a concentrated chloride solution. The method proved to be useful for exploring cement hydration-induced changes in the diffusion coefficient of cement paste.

    Se ha desarrollado un método para medir el coeficiente de difusión de los iones cloruro en la pasta de cemento, partiendo de una aplicación analítica de la segunda ley de Fick en un sistema de coordinadas cilíndrico. Este método, que es natural, demostró ser capaz de producir resultados de difusividad en tan solo un mes. Se consiguió reducir el tiempo de ensayo mediante el aprovechamiento de la tridimensionalidad del flujo desde el exterior al interior de la probeta. A fin de determinar la concentración de saturación, se sometieron las pastas de cemento Portland a una disolución de cloruros concentrada. Este método resultó ser útil en el estudio de los cambios del coeficiente de difusión de la pasta de cemento provocados por las reacciones de hidratación que tienen lugar en esta.

  3. 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; Stern, Gary; Clemente-Colon, Pablo; Martin, Seelye; Hall, Dorothy K.; Kaleschke, Lars; Tackett, Philip; Neumann, Gregory; Asplin, Matthew G.

    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.

  4. 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.

  5. Experimental and numerical investigation of chloride ingress in cracked concrete

    NARCIS (Netherlands)

    Šavija, B.

    2014-01-01

    Chloride induced corrosion of reinforcing steel is recognized as the most common deterioration mechanism affecting reinforced concrete structures. As such, it has been in focus of research for more than thirty years. Numerous studies of chloride ingress, corrosion initiation, and corrosion propagati

  6. Hydrophobic treatment of concrete as protection against chloride penetration

    NARCIS (Netherlands)

    Vries, J. de; Polder, R.B.; Borsje, H.

    1996-01-01

    Hydrophobic treatment makes a concrete surface absorb less water and less chloride. Hydrophobic treatment was studied as a protection agninst chloride penetration from deicing salts. Test methods were designed. Nine hydrophobic products were tested, of which three complied to the requirements on fin

  7. Microwave Mapping Demonstration Using the Thermochromic Cobalt Chloride Equilibrium

    Science.gov (United States)

    Nguyen, Vu D.; Birdwhistell, Kurt R.

    2014-01-01

    An update to the thermochromic cobalt(II) chloride equilibrium demonstration is described. Filter paper that has been saturated with aqueous cobalt(II) chloride is heated for seconds in a microwave oven, producing a color change. The resulting pink and blue map is used to colorfully demonstrate Le Châtelier's principle and to illuminate the…

  8. Local impermeant anions establish the neuronal chloride concentration

    DEFF Research Database (Denmark)

    Glykys, J; Dzhala, V; Egawa, K;

    2014-01-01

    Neuronal intracellular chloride concentration [Cl(-)](i) is an important determinant of γ-aminobutyric acid type A (GABA(A)) receptor (GABA(A)R)-mediated inhibition and cytoplasmic volume regulation. Equilibrative cation-chloride cotransporters (CCCs) move Cl(-) across the membrane, but accumulat...

  9. Chlorides behavior in raw fly ash washing experiments

    International Nuclear Information System (INIS)

    Chloride in fly ash from municipal solid waste incinerators (MSWIs) is one of the obstructive substances in recycling fly ash as building materials. As a result, we have to understand the behavior of chlorides in recycling process, such as washing. In this study, we used X-ray absorption near edge structure (XANES) and X-ray diffraction (XRD) to study the chloride behavior in washed residue of raw fly ash (RFA). We found that a combination of XRD and XANES, which is to use XRD to identify the situation of some compounds first and then process XANES data, was an effective way to explain the chlorides behavior in washing process. Approximately 15% of the chlorine in RFA was in the form of NaCl, 10% was in the form of KCl, 51% was CaCl2, and the remainder was in the form of Friedel's salt. In washing experiments not only the mole percentage but also the amount of soluble chlorides including NaCl, KCl and CaCl2 decreases quickly with the increase of liquid to solid (L/S) ratio or washing frequency. However, those of insoluble chlorides decrease slower. Moreover, Friedel's salt and its related compound (11CaO.7Al2O3.CaCl2) were reliable standards for the insoluble chlorides in RFA, which are strongly related to CaCl2. Washing of RFA promoted the release of insoluble chlorides, most of which were in the form of CaCl2.

  10. Phosphatase inhibitors activate normal and defective CFTR chloride channels.

    OpenAIRE

    Becq, F; Jensen, T J; Chang, X B; Savoia, A.; Rommens, J M; Tsui, L C; Buchwald, M; Riordan, J R; Hanrahan, J W

    1994-01-01

    The cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel is regulated by phosphorylation and dephosphorylation at multiple sites. Although activation by protein kinases has been studied in some detail, the dephosphorylation step has received little attention. This report examines the mechanisms responsible for the dephosphorylation and spontaneous deactivation ("rundown") of CFTR chloride channels excised from transfected Chinese hamster ovary (CHO) and human airway epi...

  11. Monte Carlo calculation of chloride diffusion in concrete

    International Nuclear Information System (INIS)

    Coefficient of chloride diffusion is calculated by applying the Fick's second law of diffusion to a chloride concentration profile. Then from the signal strength for various chlorine gamma-ray energies was then calculated at the detector of the portable D-D neutron generator based PGNAA setup. (author)

  12. 21 CFR 172.165 - Quaternary ammonium chloride combination.

    Science.gov (United States)

    2010-04-01

    ... HUMAN CONSUMPTION Food Preservatives § 172.165 Quaternary ammonium chloride combination. The food... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Quaternary ammonium chloride combination. 172.165 Section 172.165 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN...

  13. Contribution on creep polygonization study in crystals. Creep of single crystalline silver chloride and sodium chloride

    International Nuclear Information System (INIS)

    Subgrain formation and their influence on plastic behavior of materials has been studied in the case of single crystals of silver chloride and sodium chloride crept at high temperature (T > 0.5 Tmelting). It is shown that the creep rate ε is a function of the mean subgrain diameter d. For secondary creep ε ∝ dk with k = 2 for NaCl and AgCl. During secondary creep, the substructure changes continuously: sub-boundaries migrate and sub-grains rotate. We find that sub-boundaries migration accounts for 35 pc of the total strain and that subgrain misorientation θ increases linearly with strain ε: θ ∝ 0.14 ε. The stability of permanent creep seems related to the power that the substructure is able to dissipate. The possible subgrain formation mechanisms are examined. It is shown that subgrain formation is closely related to the geometrical conditions of deformation and to the heterogeneities of this later. (author)

  14. Behavior and products of mechano-chemical dechlorination of polyvinyl chloride and poly (vinylidene chloride).

    Science.gov (United States)

    Xiao, Xiao; Zeng, Zigao; Xiao, Songwen

    2008-02-28

    The mechano-chemical (MC) dechlorination of polyvinyl chloride (PVC) and polyvinylidene chloride (PVDC) was performed by mechanical milling PVC/PVDC powder with zinc powder in a planetary ball mill, and the products of dechlorination were characterized by Infrared spectra (IR), X-ray diffraction (XRD), Raman spectroscopy, gas chromatography-mass spectrometry (GC-MS), and 13C solid-state nuclear magnetic resonance (NMR). The experimental results show that PVC/PVDC can be easily dechlorinated by milling with zinc powder, and formed various kinds of inorganic and organic products. Inorganic compounds included Zn2OCl(2).2H2O, Zn5(OH)8Cl2.H2O etc., and organic products involved diamond-like carbon, carbyne fragment, polyacetylene etc. Organic products formed following the paths of dechlorination, dehydrochlorination, crosslink, and oxidation. The mechano-chemical dechlorination process of PVC/PVDC may be an effective approach for carbyne synthesizing in the appropriate condition.

  15. PHASE EQUILIBRIUM FOR THE TERNARY SYSTEM VINYL CHLORIDE-CHLORINATED POLYETHYLENE-POLY (VINYL CHLORIDE)

    Institute of Scientific and Technical Information of China (English)

    LOU Jianfeng; WENG Zhixue; HUANG Zhiming; PAN Zuren

    1991-01-01

    Swelling capacity of vinyl chloride (VC) in chlorinated polyethylene (CPE) with 25- 40 wt% Cl at temperature 30- 57 ℃ was studied and their relationships were correlated with Langmuir and Freundlich adsorption equations. A ternary phase diagram for VC-CPE-PVC was also established.In-situ polymerization conditions of CPE-g -VC were proposed and CPE content control was analyzed for the manufacturing process of CPE-g-VC graft product based on results of phase equilibrium study.

  16. Highly brominated anthracenes as precursors for the convenient synthesis of 2,9,10-trisubstituted anthracene derivatives

    Directory of Open Access Journals (Sweden)

    2008-12-01

    Full Text Available When 9,10-dibromoanthracene was treated with bromine in CCl4 without a catalyst, 1,2,3,4,9,10-hexabromo-1,2,3,4-tetrahydroanthracene (3 was obtained in 95% yield in the absence of other stereoisomers or rearomatization products. We investigated the base-induced elimination reaction of hexabromide 3 under various conditions. Pyridine-induced elimination of hexabromide 3 afforded 2,9,10-tribromoanthracene (12 in 75% yield, and tribromide 12 was transformed to trimethoxy compound 13 and trinitrile 14 by copper-assisted nucleophilic substitution reactions.

  17. Detection of chlorine and bromine in free liquid from the sphenoid sinus as an indicator of seawater drowning.

    Science.gov (United States)

    Tanaka, Naoko; Kinoshita, Hiroshi; Jamal, Mostofa; Takakura, Ayaka; Kumihashi, Mitsuru; Miyatake, Nobuyuki; Tsutsui, Kunihiko; Ameno, Kiyoshi

    2015-09-01

    We have investigated the usefulness of elemental analysis by energy-dispersive X-ray spectroscopy (EDX) in the examination of free liquid from the sphenoid sinus of drowning victims. We detected both chlorine and bromine in liquid taken from the sphenoid sinus of seawater drowning victims. Because these elements were below the quantification limit in freshwater cases, we could easily distinguish seawater from freshwater drowning cases. Detection of these elements from the liquid in the sphenoid sinuses of drowning victims may be useful as a supportive measure for seawater drowning. PMID:26415653

  18. Experimental transition probabilities of intercombination transitions in Mg-like and Al-like ions of bromine

    International Nuclear Information System (INIS)

    Time-resolved extreme ultraviolet spectra of foil-excited 120-MeV Br ions have been recorded, using a spectrometer equipped with a position-sensitive detector. The spectra near λ=20--30 nm were measured at times after excitation of up to 6 ns. Prominent in the delayed spectra were the long-lived decays of the intercombination transitions in the Mg-like Br23+ and Al-like Br22+ ions. The present paper reports on lifetime measurements for intercombination transitions in highly charged bromine ions using such a position-sensitive detector

  19. Isoquinolinium bromochromate: An efficient and stable reagent for bromination of hydroxylated aromatic compounds and oxidation of alcohols

    Institute of Scientific and Technical Information of China (English)

    Sandeep V. Khansole; Shivaji B. Patwari; Archana Y. Vibhute; Yeshwant B. Vibhute

    2009-01-01

    The new chromium (VI) oxidizing reagent isoquinolinium bromochromate (IQBC) was prepared and characterized. The IQBC has been found to be stable and an efficient solid reagent which can be easily prepared in good yield. It act as an efficient brominating reagent for hydroxylated aromatic compounds as well as good oxidizing reagent for the conversion of alcohols to carbonyl compounds in good to excellent yield. The synthesized isoquinolinium bromochromate is more ideal reagent, with number of specification including: higher yield, mild conditions and easy preparation. The results obtained with isoquinolinium bromochromate are satisfactory and suggest that the reagent has few advantages over the existing chromium (VI) reagents.

  20. Analysis of Causes Leading to High Bromine Number of C8+Aromatics and Short Clay Service Life and Countermeasures Proposed

    Institute of Scientific and Technical Information of China (English)

    Li Yousong; Ni Xiaoliang; Yan Jun

    2007-01-01

    After comparing the operating status of other catalytic reforming units and evaluation of the side-cut stream tests,the refinery investigated the influence of the feedstock property,clay types,and operating regime of the clay tower and catalytic reforming unit on the service life of the clay.Test results had revealed that the low potential aromatic content of the reformer feed and high operating severity were the critical causes leading to high bromine number of the C8+ aromatics feed for the PX unit and the shortened service life of clay.This article also puts forward the corresponding remedial measures.

  1. 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

  2. OLGA experiments with {sup 261}104 under chlorinating and brominating conditions

    Energy Technology Data Exchange (ETDEWEB)

    Gaeggeler, H.W.; Eichler, B.; Jost, D.T.; Piguet, D.; Tuerler, A. [Paul Scherrer Inst. (PSI), Villigen (Switzerland); Buklanov, G.; Lebedev, V.; Timokhin, S.; Vedeev, M.V.; Yakushev, A.; Zvara, I. [FLNR, Dubna (Russian Federation); Huebener, S. [FZR (Germany)

    1997-09-01

    With the On-Line Gas chemistry Apparatus OLGA III the retention times of element 104 chloride and bromide was measured in a quartz column using the isotope {sup 261}104 with a half-life of 78 s. With HCl as chlorinating agent element 104 was found to quantitatively pass through the column at 150{sup o}C, whereas with HBr this temperature shifted to about 300{sup o}C. Under both halogenating conditions, the homologuous element Hf passed through the column at higher temperatures than element 104, in agreement with expectations. (author) 2 figs., 2 refs.

  3. Comparative effects of hydrogen chloride gas on tomato and chrysanthemum. I. Distribution and accumulation of chloride following exposure. II. Pathological anatomy of hydrogen chloride gas injury

    Energy Technology Data Exchange (ETDEWEB)

    Shriner, D.S.

    1969-01-01

    Hydrogen chloride (HCl) gas damage to plants has not been a historically important problem. However, recent practices in a number of industries, particularly glass manufacturing and pyrolysis of waste plastics, have increased the seriousness of the problem. Studies were carried out under carefully controlled exposure conditions to determine the effects of HCl gas on a relatively sensitive and a relatively resistant plant species. The macroscopic symptoms of most importance in acute damage to tomato and chrysanthemum are glazing of the lower surface, and a bifacial bronzing of interveinal and marginal areas of leaves. Microscopically, glazing was shown to be caused by a collapse of the lower epidermal cells and a partial disorganization of the spongy mesophyll of leaves. Bronzing was shown to be caused by the further collapse of the spongy mesophyll, and in some cases the palisade mesophyll and upper epidermis. Analysis of plant tissues for their free chloride content following an exposure to HCl gas was done with cell-free water extracts which were titrated on an automatic chloride titrator. On the basis of such studies, evidence suggest that the mechanism of accumulation of chlorides in plants is similar to that of fluorides, and that in subacute doses, chlorides are translocated toward the extremities of the foliar portions of the plant. In areas where a number of different types of pollution sources exist, and symptomotology is not definitive in pinpointing the source, chloride analysis of plant tissues should prove valuable as an aid to diagnosis if HCl gas was suspected.

  4. Spectroscopic UV/vis limb measurements from aboard the NASA Global Hawk: Implications for the photochemistry and budget of bromine in the tropical tropopause layer

    OpenAIRE

    Werner, Bodo

    2016-01-01

    The present thesis reports on the world's first measurements of the second most important ozone-depleting halogen bromine at the entrance to the stratosphere (14 - 18.5 km, theta = 330 - 400 K) over the East and Central Pacific in late winter 2013. The measurements were performed within the NASA-ATTREX project from aboard the unmanned aerial vehicle Global Hawk. For the interpretation of the remote-sensing DOAS measurements of O3, NO2 and BrO, use of complementary measurements of brominated s...

  5. Studies on Hypokalemia Induced by Trimethyltin Chloride

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    To determine the possible relationship between plasma potassium concentration and severity of acute trimethyltin chloride (TMT) poisoning and to assess the mechanism of TMT induced hypokalemia. Methods SD rats were treated with various dosages of TMT (ip). All the indices were measured and analysed for determing their possible relations with plasma K+. Results With increase of dosage, the plasma K+ level dropped rapidly, and deaths appeared more quickly. The LDs0 of TMT (ip) was 14.7 mg/kgbw. In the low dosage group (10 mg/kgbw), the plasma K+ level dropped slowly with the lowest dosage on day 6 (4.85 mmol/L). It rose again on day 11 (5.06 mmol/L), and recoverd on day 28. The poisoning signs corresponded with decline of the span of K+ level. The plasma Na+ level dropped half an hour after TMT treatment, but recovered 24 h later. In the high dosage group (46.4 mg/kgbw), the levels of plasma K+ and Na+ fell rapidly within half an hour (P<0.05), the intracellular potassium concentration of RBC did not decrerase obviously (P>0.05), the activities of Na+-K+-ATPase and Mg2+-ATPase in RBC membrane were depressed remarkably (P<0.01, P<0.05, respectively), the plasma aldosterone concentrations rose as high as tenfold (P<0.01), the arterial blood pH fell from 7.434 to 7.258 (P<0.01),pCO2 was raised from 29.62 to 45.33 mmHg (P<0.01). In the 24 h urine test, when rats were treated with TMT (21.5 mg/kgbw, ip), urine volume, urinary potassium, sodium and chloride increased significantly in comparison with those in the controls (P<0.01). Conclusion TMT could induce hypokalemia in SD rats. The available evidence suggests that TMT can induce acute renal leakage of potassium. At the same time, a significant rise of plasma aldosterone may play an important role in promoting potassium leakage from kidney to result in severe hypokalemia with inhaling acid-base abnormalities produced, which aggravate the poisoning symptoms. In the end the rats would die of respiratory

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

    Science.gov (United States)

    Ji, Yuefei; Kong, Deyang; Lu, Junhe; Jin, Hao; Kang, Fuxing; Yin, Xiaoming; Zhou, Quansuo

    2016-08-01

    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 (SO4(-)) with TBBPA was determined to be 5.27×10(10)M(-1)s(-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 SO4(-). 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 6-10h. 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. PMID:27107323

  7. Accumulation of organochlorines and brominated flame retardants in estuarine and marine food chains: field measurements and model calculations.

    Science.gov (United States)

    Veltman, Karin; Hendriks, Jan; Huijbregts, Mark; Leonards, Pim; van den Heuvel-Greve, Martine; Vethaak, Dick

    2005-10-01

    Food chain accumulation of organochlorines and brominated flame retardants in estuarine and marine environments is compared to model estimations and fresh water field data. The food chain consists of herbivores, detritivores and primary and secondary carnivores i.e. fish, fish-eating birds and marine mammals. Accumulation of polychlorinated biphenyls is predicted well by OMEGA for herbi-detritivores and primary and secondary carnivorous fish. Ratios are similar to those found for fresh water species. Accumulation ratios for fish-eating birds and mammals are overestimated by the model, which is attributed partly to biotransformation of meta-para unsubstituted congeners. Additionally, birds may feed in other less polluted areas. For brominated diphenylethers (BDE) accumulation patterns are highly species and congener specific. Accumulation depends on both K(ow) and metabolization capacities. BDE47 is the predominant congener in lower trophic levels. For marine birds and mammals accumulation ratios of BDE99 and 100 are similar to or higher than ratios of persistent PCBs. PMID:15893330

  8. 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.

  9. Tracing organophosphorus and brominated flame retardants and plasticizers in an estuarine food web.

    Science.gov (United States)

    Brandsma, Sicco H; Leonards, Pim E G; Leslie, Heather A; de Boer, Jacob

    2015-02-01

    Nine organophosphorus flame retardants (PFRs) were detected in a pelagic and benthic food web of the Western Scheldt estuary, The Netherlands. Concentrations of several PFRs were an order of magnitude higher than those of the brominated flame retardants (BFRs). However, the detection frequency of the PFRs (6-56%) was lower than that of the BFRs (50-97%). Tris(2-butoxyethyl) phosphate (TBOEP), tris(isobutyl) phosphate (TIBP) and tris(2-chloroisopropyl) phosphate (TCIPP) were the dominant PFRs in sediment with median concentrations of 7.0, 8.1 and 1.8 ng/g dry weight (dw), respectively. PFR levels in the suspended particular matter (SPM) were 2-12 times higher than that in sediment. TBOEP, TCIPP, TIBP, tris(2-chloroethyl) phosphate (TCEP) and tris(phenyl) phosphate (TPHP) were found in organisms higher in the estuarine food web. The highest PFR concentrations in the benthic food web were found in sculpin, goby and lugworm with median concentrations of 17, 7.4, 4.6 and 2.0 ng/g wet weight (ww) for TBOEP, TIBP, TCIPP and TPHP, respectively. Comparable levels were observed in the pelagic food web, BDE209 was the predominant PBDE in sediment and SPM with median concentrations up to 9.7 and 385 ng/g dw, respectively. BDE47 was predominant in the biotic compartment of the food web with highest median levels observed in sculpin and common tern eggs of 79 ng/g lipid weight (lw) (2.5 ng/g ww) and 80 ng/g lw (11 ng/g ww), respectively. Trophic magnification was observed for all PBDEs with the exception of BDE209. Indications of trophic magnification of PFRs were observed in the benthic food web for TBOEP, TCIPP and TCEP with tentative trophic magnification factors of 3.5, 2.2 and 2.6, respectively (pwebs. The relative high PFR levels in several fish species suggest high emissions and substantial exposure of organisms to PFRs in the Western Scheldt.

  10. Measurement-based modelling of bromine-induced oxidation of mercury above the Dead Sea

    Directory of Open Access Journals (Sweden)

    E. Tas

    2012-03-01

    Full Text Available Atmospheric mercury depletion events (AMDEs outside the polar region – driven by high levels of gaseous Br and BrO (i.e., BrOx – were observed recently in the warm Dead Sea boundary layer. The efficient oxidation of gaseous elemental mercury (GEM under temperate conditions by BrOx was unexpected considering that the thermal back dissociation reaction of HgBr is about 2.5 orders of magnitude higher under Dead Sea temperatures compared to polar temperatures, and hence was expected to significantly slow down GEM oxidation under warm temperatures. The goal of this modelling study was to improve understanding of the interaction of reactive bromine and mercury during Dead Sea AMDEs using numerical simulations based on a comprehensive measurement campaign in summer 2009.

    Our analysis is focused on daytime AMDE when chemical processes dominate concentration changes. Best agreements between simulations and observations were achieved using rate constants for kHg+Br and kHg+BrO of 2.7 × 10−13 cm3 molecule−1 s−1 and 1.5 × 10−13 cm3 molecule−1 s−1, respectively. Our model also predicted that a rate constant kHg+BrO of 5.0 × 10−14 cm3 molecule−1 s−1 may be considered as a minimum, which is higher than most reported values. These rate constants suggest that BrO could be a more efficient oxidant than Br in the troposphere as long as [Br]/[BrO] ratios are smaller than ~0.2 to 0.5. Under Dead Sea conditions, these kinetics demonstrate a high efficiency and central role of BrOx for AMDEs, with relative contributions to GEM depletion of more than ~90%. Unexpectedly, BrO was found to be the dominant oxidant with relative contributions above 80%. The strong contribution of BrO could explain why the efficiency of GEM

  11. Legacy and current-use brominated flame retardants in the Barn Owl.

    Science.gov (United States)

    Eulaers, Igor; Jaspers, Veerle L B; Pinxten, Rianne; Covaci, Adrian; Eens, Marcel

    2014-02-15

    The present study investigated the current-use brominated flame retardants (BFRs) tetrabromobisphenol A (TBBPA) and hexabromocyclododecane (HBCD), simultaneously with legacy polybrominated diphenyl ethers (PBDEs), in Barn Owls (Tyto alba) collected from two regions with a contrasting degree of urbanisation and vicinity to point sources (Flanders in Belgium versus Normandy in France). Both tissues (muscle, liver, adipose and preen gland) and feathers (primary, tail and body feathers) showed elevated HBCD concentrations in Flanders, close to Europe's sole HBCD production plant in the Netherlands, and identified Normandy as a historical source region for PBDEs. In sharp contrast, the reactive BFR TBBPA bioaccumulated poorly (2.3%) in tissue samples, but was present in 96% of all body feather samples (0.36-7.07ngg(-1)dw), equally in both regions. PBDE concentrations in tissues (7.46-903 ng g(-1)lw) were considerably lower in the investigated Flemish Barn Owls, collected in 2008/2009, compared to specimens collected in 2003/2004 (46-11,000 ng g(-1)lw), possibly suggesting the effectiveness of the 2004 European ban of Penta- and Octa-BDE mixtures. Feathers showed a similar trend and additionally exhibited HBCD concentrations (0.02-333 ng g(-1)dw) surpassing those of PBDEs (0.50-10.4 ng g(-1)dw). While body feathers were a reliable matrix to predict both internal PBDE (0.21 ≤ R(2)≤ 0.67) and HBCD body burdens (0.20 ≤ R(2) ≤ 0.37), the suitability of primary and tail feathers appeared to be confounded by external contamination and moult. In conclusion, the present study clearly showed that the reactive versus additive use of BFRs results in contrasting exposure scenarios in a species higher up the food chain, and therefore may have profound implications for environmental health. In addition, the presented results extend the promising use of feathers as a non-destructive sampling strategy for current-use BFRs, and show that birds of prey are valid early

  12. Redetermination of 1-carboxycyclohexan-1-aminium chloride

    Directory of Open Access Journals (Sweden)

    Teresa González

    2009-02-01

    Full Text Available The crystal structure of the title compound, C7H14NO2+·Cl−, was reported previously [Chacko, Srinivasan & Zand (1975. J. Cryst. Mol. Struct. 5, 353–357] from Weissenberg photographic data with R = 0.113. It has now been redetermined, providing a significant increase in the precision of the derived geometric parameters, viz. mean σ(C—C = 0.003 Å in the present work compared with 0.021 Å for the previous work. The complete cation is generated by crystallographic mirrror symmetry, with three C atoms, two O atoms and the N atom lying on the reflecting plane; the chloride anion also has m site symmetry. The crystal structure is established by a two-dimensional network of O—H...Cl and N—H...Cl hydrogen bonds, generating C12(4 and C12(7 chains, and R24(8 and R24(14 rings.

  13. Chloride, bromide and iodide scintillators with europium

    Energy Technology Data Exchange (ETDEWEB)

    Zhuravleva, Mariya; Yang, Kan

    2016-09-27

    A halide scintillator material is disclosed where the halide may comprise chloride, bromide or iodide. The material is single-crystalline and has a composition of the general formula ABX.sub.3 where A is an alkali, B is an alkali earth and X is a halide which general composition was investigated. In particular, crystals of the formula ACa.sub.1-yEu.sub.yI.sub.3 where A=K, Rb and Cs were formed as well as crystals of the formula CsA.sub.1-yEu.sub.yX.sub.3 (where A=Ca, Sr, Ba, or a combination thereof and X=Cl, Br or I or a combination thereof) with divalent Europium doping where 0.ltoreq.y.ltoreq.1, and more particularly Eu doping has been studied at one to ten mol %. The disclosed scintillator materials are suitable for making scintillation detectors used in applications such as medical imaging and homeland security.

  14. NQR in tert-butyl chloride

    Science.gov (United States)

    Brunetti, Aldo H.

    2004-03-01

    Tert-butyl chloride has been broadly studied experimentally through various techniques such as X-ray crystallography, DTA, and NMR. It was also studied experimentally through nuclear quadrupole resonance (NQR), but this study was limited and incomplete. In this paper, we present a more detailed study of TBC through the NQR of 35Cl. Our results show that near 120 K, the onset of the CH 3 groups semirotations around symmetry axis C3 takes place with an activation energy U=16.1 kJ mol -1. This intramolecular movement produces a T1 minimum near 148 K and is the dominant mechanism of the nuclear spin-lattice relaxation in phase III of this compound. In phase II of TBC, we show that there are not only methyl groups semirotations, but also semirotations of the whole molecule around a different axis from the symmetry axis C' 3 (C-Cl bond) with an activation energy of E=10.4 kJ mol -1.

  15. Denitrification of fertilizer wastewater at high chloride concentration

    DEFF Research Database (Denmark)

    Ucisik, Ahmed Süheyl; Henze, Mogens

    Wastewater from fertilizer industry is characterized by high contents of chloride concentration, which normally vary between 60 and 76 g/l. Experiments with bilogical denitrification were performed in lab-scale "fill and draw" reactors with synthetic wastewater with chloride concentrations up to 77.......4 g/l. The results of the experiments showed that biological denitrification was feasible at the extreme environmental conditions prevailing in fertilizer wastewater. Stable continuous biological denitrfication of the synthetic high chloride wastewater was performed up to 77.4 g Cl/l at 37 degree C...

  16. Calcium chloride in stabilised soil roads and runways

    Directory of Open Access Journals (Sweden)

    Harsh Vardhan

    1952-09-01

    Full Text Available Mudless, dustless, hard and all weather driving surfaces is a serious requirement of the forces.  surfacing by mixtures of definite amounts of locally available stone, gravel, sand, clay and Silt to which calculated amount of calcium chloride is added quickly compact and ultimately harden like concrete. This provides an easy, quick and economic- means of meeting the requirement.  Necessity of such surfaces, use and action of calcium chloride and resulting effects are discussed. Different methods of construction and application of calcium chloride are briefly related.

  17. Durability Analysis of Subway Station in Chloride Environment

    Directory of Open Access Journals (Sweden)

    Yang LuFeng

    2013-02-01

    Full Text Available In this study, a finite element model for chloride ions transport in saturated concrete was proposed based on the Fick’s second law of diffusion. The governing partial differential equation was solved numerically in space as a boundary-value problem and in time as an initial-value problem by means of the finite element formulations. The maximum allowable value of chloride diffusion coefficient within different locations of subway station with service life of 100a was achieved and suggestions for durability analysis of subway station in chloride environment were also proposed.

  18. The ionic product of water in concentrated tetramethylammonium chloride solutions.

    Science.gov (United States)

    Sipos, P; Bódi, I; May, P M; Hefter, G T

    1997-04-01

    The ionic product of water, pK(w) = - log[H(+)][OH(-)] has been determined in aqueous solutions of tetramethylammonium chloride over the concentration range of 0.1-5.5 M at 25 degrees C using high-precision glass electrode potentiometric titrations. pK(w) data relating to aqueous potassium and sodium chlorides at ionic strengths up to 5 M are markedly lower than the tetramethylammonium chloride results. These differences are almost certainly due to weak associations between potassium and (especially) sodium and hydroxide ions.

  19. Ionometric determination of chloride ion in circulating and waste waters

    Energy Technology Data Exchange (ETDEWEB)

    Bebeshko, G.I.; Afanas' eva, V.I.; Danielova, I.I.; Dmitriev, M.A.; Radchenko, A.F.

    1986-09-01

    The authors attempt to develop selective ionometric methods to determine chloride ion in waste and circulating waters from technological ore processing, containing significant amounts of sulfide ion and various flotation reagents. These waters contain practically no cations that form hard to dissolve compounds with chloride ion such as Ag/sup +/, Cu/sup +/, Hg/sup +/ or Pb/sup 2 +/. The chloride ion concentration in water varies between 10 and 100 mg/liter. Information is shown on the concentration of the main anions and flotation reagents in waters that were analyzed.

  20. Stochastic Modeling of Reinforced Concrete Structures Exposed to Chloride Attack

    DEFF Research Database (Denmark)

    Sørensen, John Dalsgaard; Frier, Christian

    2003-01-01

    concentration and reinforcement cover depth are modeled by stochastic fields. The paper contains a description of the parameters to be included in a stochastic model and a proposal for the information needed to obtain values for the parameters in order to be ab le to perform reliability investigations...... the reinforcement exceeds a critical threshold value. In the present paper a stochastic model is described by which the chloride content in a reinforced concrete structure can be estimated. The chloride ingress is modeled by a 2-dimensional diffusion process and the diffusion coefficient, surface chloride...

  1. Applicability of boron-doped diamond electrode to the degradation of chloride-mediated and chloride-free wastewaters

    International Nuclear Information System (INIS)

    The electrochemical degradation of chloride-mediated and chloride-free dye wastewaters was investigated on a boron-doped diamond (BDD) electrode in comparison with that on a dimensionally stable anode (DSA), and the applicability of BDD electrode to the degradation of these two kinds of wastewaters was explored. In chloride-free wastewater, the electrochemical degradation efficiency of dye on BDD electrode was much higher than that on DSA, with a chemical oxygen demand (COD) removal of 100% and 26% for BDD and DSA, respectively. In chloride-mediated dye wastewater, COD removal was faster than that in chloride-free wastewater on both BDD and DSA electrodes with COD removal efficiencies higher than 95%, whereas the rate of COD removal on DSA was faster than that on BDD electrode. The investigation indicates that DSA is more suitable than BDD electrode in degradation of originally chloride contained dye wastewaters for the sake of energy and time saving. However, for chloride-free dye wastewaters, with the aim of environmental protection, BDD electrode is more appropriate to realize complete mineralization. At the same time, the secondary pollution can be avoided

  2. Adsorption of Tetradecylpyridinium Chloride on Aqueous Surfaces of Sodium Chloride Solutions

    OpenAIRE

    Fujio, Katsuhiko; Hayashi, Koji; Suzuki, Maki

    2014-01-01

    Surface tension of aqueous NaCl solutions of tetradecylpyridinium chloride (TPC) has been measured by the drop weight method at different NaCl concentrations from 0 to 1.000 mol dm−3 at 25◦C. Surface excess densities of tetradecylpyridinium ion (TP+), Cl− and Na+ have been obtained as functions of TPC concentration at different NaCl concentrations by applying the Gibbs adsorption isotherm to the surface tension data below the critical micelle concentration (CMC) of TPC. Surface excess densiti...

  3. Adsorption of Dodecylpyridinium Chloride on Aqueous Surfaces of Sodium Chloride Solutions

    OpenAIRE

    Fujio, Katsuhiko; TAKEUCHI, Kumiko; Suzuki, Maki

    2012-01-01

    Surface tension of aqueous NaCl solutions of dodecylpyridinium chloride (DPC) has been measured by the drop weight method at different NaCl concentrations from 0 to 1.000 mol dm-3 at 25℃. Applying the Gibbs adsorption isotherm to the surface tension data at DPC concentrations below the critical micelle concentration (CMC), surface excess densities of dodecylpyridinium ion (DP+), Cl- and Na+ have been obtained as functions of DPC concentration at different NaCl concentrations. Surface excess d...

  4. 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

    With the purpose of finding ways to combine micro-bore reversed phase HPLC with ICP-MS detection for analysis of drug substances containing chlorine, bromine and iodine, the suitability of a direct injection nebulizer and an Aridus desolvating microconcentric nebulizer was compared. Using the...

  5. 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.

  6. Brominated flame retardants in fish and shellfish - levels and contribution of fish consumption to dietary exposure of Dutch citizens to HBCD

    NARCIS (Netherlands)

    Leeuwen, van S.P.J.; Boer, de J.

    2008-01-01

    In order to determine the contamination with brominated flame retardants (BFR) in fish regularly consumed by Dutch citizens, 44 samples of freshwater fish, marine fish, and shellfish were analyzed for polybrominated diphenyl ethers (PBDE), tetrabromobisphenol-A (TBBP-A) and its methylated derivative

  7. 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

    2014-01-01

    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 f

  8. Brominated flame retardant levels in human milk and serum from MAMA study participants: Correlations over time, matrix, and with questionnaire results

    Science.gov (United States)

    Brominated flame retardants (BFRs) are synthetic, lipophilic, and bioaccumulative compounds used to prevent the combustion of a variety of items including electronics and furniture. There are 75 classes of BFRs, two of which are the polybrominated biphenyls (PBB) and the polybrom...

  9. Exposure to brominated flame retardants, perfluorinated compounds, phthalates and phenols in European birth cohorts: ENRIECO evaluation, first human biomonitoring results, and recommendations

    NARCIS (Netherlands)

    Casas, M.; Chevrier, C.; Hond, E.D.; Fernandez, M.F.; Pierik, F.; Philippat, C.; Slama, R.; Toft, G.; Vandentorren, S.; Wilhelm, M.; Vrijheid, M.

    2013-01-01

    There are emerging concerns about potential effects on child health and development of early-life exposure to substances such as brominated flame retardants (BFRs), perfluorinated compounds (PFCs), phthalates and phenols (including bisphenol A (BPA)); pregnancy and birth cohort studies are ideally d

  10. Simultaneous balloon-borne measurements of the key inorganic bromine species BrO and BrONO2 in the stratosphere: DOAS and MIPAS-B evaluation

    Science.gov (United States)

    Kazarski, Sebastian; Maucher, Guido; Ebersoldt, Andreas; Butz, André; Friedl-Vallon, Felix; Höpfner, Michael; Kleinert, Anne; Nordmeyer, Hans; Oelhaf, Hermann; Pfeilsticker, Klaus; Sinnhuber, Björn-Martin; Wetzel, Gerald; Orphal, Johannes

    2015-04-01

    Inorganic bromine contributes to a loss of stratospheric ozone of about 25 - 30%. Past studies have demonstrated several uncertainties in the photochemistry of stratospheric bromine, especially by considering the three body reaction (kBrONO2) BrO + NO2 + M → BrONO2 + M, and the photolysis frequencies of BrONO2 (jBrONO2). Hence, an improved knowledge of the ratio jBrONO2/kBrONO2 is crucial to better assess the bromine-related loss of ozone as well as the total amount of bromine in the stratosphere. Here, we report on the first simultaneous balloon-borne measurements of NO2, BrO, and BrONO2 in the stratosphere, performed over Timmins (Ontario, 49 °N, Canada) on Sept., 7th and 8th, 2014. During the flight the targeted species were monitored by remote sensing in the UV, visible and mid-IR spectral ranges by Differential Optical Absorption Spectroscopy (DOAS) and Michelson Interferometer for Passive Atmospheric Sounding (MIPAS-B), respectively. The analysis and interpretation of the measurements involves radiative transfer as well as photochemical modelling. Major features of the applied techniques are reported and first results of the DOAS as well as MIPAS-B evaluation are discussed. Further investigations address inter-comparisons of the retrieved NO2, BrO, and O3 concentrations and volume mixing ratios, to demonstrate validations of both evaluation methods.

  11. Nickel Chloride Promoted Glaser Coupling Reaction in Hot Water

    Institute of Scientific and Technical Information of China (English)

    Pin Hua LI; Lei WANG; Min WANG; Jin Can YAN

    2004-01-01

    A Glaser coupling reaction of terminal alkynes in the presence of nickel chloride without any organics and bases in hot water has been developed, which produces the corresponding homo-coupling products in good yields.

  12. Methyltrioctylammonium chloride catalysed sonochemical synthesis of acridine diones

    Indian Academy of Sciences (India)

    Bhupinder Kaur; Harish Kumar

    2013-09-01

    The greener, clean and efficient protocol for the synthesis of acridine diones derivatives has been achieved by reacting aromatic aldehyde, dimedone and amines using methyltrioctylammonium chloride (Aliquate 336) as a catalyst under ultrasonic irradiations.

  13. Use of saturated sodium chloride solution as a tissue fixative

    Directory of Open Access Journals (Sweden)

    A. Al-Saraj

    2010-01-01

    Full Text Available The present study was carried out to examine the capability of saturated sodium chloride solution as a fixative agent instead of formalin which is regarded as a carcinogenic material. For this purpose 3 rabbits were used and their livers, kidneys and spleens were exposed and removed. Neutral buffered formalin solution, saturated sodium chloride solution and distilled water were used as fixatives for specimens obtained from the first, second and third rabbits respectively. Routine histological technique was performed to prepare a stained histological sections for light microscopic examination. The result showed that the tissue sections which were obtained by using sodium chloride have the same histological features and without any artifacts when they compared with the results obtained using formalin fixation method. We conclude that the saturated sodium chloride solution can be used as a fixative agent in some circumstances when no any fixative agent is available.

  14. Thermodynamic calculation of self-diffusion in sodium chloride

    Science.gov (United States)

    Zhang, Baohua; Li, Chengbo; Shan, Shuangming

    2016-05-01

    Using the available pressure-volume-temperature equation of state of sodium chloride, we show that the self-diffusion coefficients of sodium and chloride in sodium chloride as a function of temperature and pressure can be successfully reproduced in terms of bulk elastic and expansivity data. We use a thermodynamic model that interconnects point-defect parameters with bulk properties. Our calculated diffusion coefficients and point-defect parameters, including activation enthalpy, activation entropy, and activation volume, well agree with reported experimental results when uncertainties are considered. Furthermore, the ionic conductivity of sodium chloride inferred from our predicted diffusivities of sodium through the Nernst-Einstein equation is compared with previous experimental data.

  15. Catalytic Decomposition of Methylene Chloride by Sulfated Titania Catalysts

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Catalytic decomposition of methylene chloride in air below 300℃ was studied.Sulfated titania was very effective in converting 959ppm methylene chloride selectively to CO,CO2 and HCl.Complete decomposition of methylene chloride was achieved at low temperature(275℃).It was found that the acidic property of catalyst was a determinant factor for the catalytic activity.The presence of water vapor in the feed stream remarkably reduced the catalytic activity,which could be due to the blockage of acidic sites on the surface of catalyst by water molecules.A bifunctional catalyst comprising copper oxide was developed to improve the selectivity of catalytic oxidation,which indicated that copper oxide can promote the deep oxidation of methylene chloride.The crystal form of TiO2 imposes an important influence upon the catalytic oxidation.

  16. Chloride supporting electrolytes for all-vanadium redox flow batteries.

    Science.gov (United States)

    Kim, Soowhan; Vijayakumar, M; Wang, Wei; Zhang, Jianlu; Chen, Baowei; Nie, Zimin; Chen, Feng; Hu, Jianzhi; Li, Liyu; Yang, Zhenguo

    2011-10-28

    This paper examines vanadium chloride solutions as electrolytes for an all-vanadium redox flow battery. The chloride solutions were capable of dissolving more than 2.3 M vanadium at varied valence states and remained stable at 0-50 °C. The improved stability appeared due to the formation of a vanadium dinuclear [V(2)O(3)·4H(2)O](4+) or a dinuclear-chloro complex [V(2)O(3)Cl·3H(2)O](3+) in the solutions over a wide temperature range. The all-vanadium redox flow batteries with the chloride electrolytes demonstrated excellent reversibility and fairly high efficiencies. Only negligible, if any, gas evolution was observed. The improved energy capacity and good performance, along with the ease in heat management, would lead to substantial reduction in capital cost and life-cycle cost, making the vanadium chloride redox flow battery a promising candidate for stationary applications. PMID:21922094

  17. Purification and reconstitution of chloride channels from kidney and trachea

    International Nuclear Information System (INIS)

    Chloride channels mediate absorption and secretion of fluid in epithelia, and the regulation of these channels is now known to be defective in cystic fibrosis. Indanyl-oxyacetic acid 94 (IAA-94) is a high-affinity ligand for the chloride channel, and an affinity resin based on that structure was developed. Solubilized proteins from kidney and trachea membranes were applied to the affinity matrix, and four proteins with apparent molecular masses of 97, 64, 40, and 27 kilodaltons were eluted from the column by excess IAA-94. A potential-dependent 36Cl- uptake was observed after reconstituting these proteins into liposomes. Three types of chloride channels with single-channel conductances of 26, 100, and 400 picosiemens were observed after fusion of these liposomes with planar lipid bilayers. Similar types of chloride channels have been observed in epithelia

  18. Stochastic modeling of reinforced concrete structures exposed to chloride attack

    DEFF Research Database (Denmark)

    Sørensen, John Dalsgaard; Frier, Christian

    2004-01-01

    For many reinforced concrete structures corrosion of reinforcement is an important problem since it can result in expensive maintenance and repair actions. Further, a significant reduction of the load-bearing capacity can occur. One mode of corrosion initiation is that the chloride content around...... the reinforcement exceeds a critical threshold value. In the present paper a stochastic model is described by which the chloride content in a reinforced concrete structure can be estimated. The chloride ingress is modeled by a 2-dimensional diffusion process and the diffusion coefficient, surface chloride...... concentration and reinforcement cover depth are modeled by stochastic fields. The paper contains a description of the parameters to be included in a stochastic model and a proposal for the information needed to obtain values for the parameters in order to be able to perform reliability investigations...

  19. Chloride supporting electrolytes for all-vanadium redox flow batteries.

    Science.gov (United States)

    Kim, Soowhan; Vijayakumar, M; Wang, Wei; Zhang, Jianlu; Chen, Baowei; Nie, Zimin; Chen, Feng; Hu, Jianzhi; Li, Liyu; Yang, Zhenguo

    2011-10-28

    This paper examines vanadium chloride solutions as electrolytes for an all-vanadium redox flow battery. The chloride solutions were capable of dissolving more than 2.3 M vanadium at varied valence states and remained stable at 0-50 °C. The improved stability appeared due to the formation of a vanadium dinuclear [V(2)O(3)·4H(2)O](4+) or a dinuclear-chloro complex [V(2)O(3)Cl·3H(2)O](3+) in the solutions over a wide temperature range. The all-vanadium redox flow batteries with the chloride electrolytes demonstrated excellent reversibility and fairly high efficiencies. Only negligible, if any, gas evolution was observed. The improved energy capacity and good performance, along with the ease in heat management, would lead to substantial reduction in capital cost and life-cycle cost, making the vanadium chloride redox flow battery a promising candidate for stationary applications.

  20. Solidification of spent TBP solvent with aluminium chloride compounds

    International Nuclear Information System (INIS)

    The new techniques for processing spent TBP was investigated. It was proved that treatment of TBP containing DBP with aluminium chloride resulted in the formation of aluminium phosphate suitable for long term storage and final disposal

  1. Reinforcement corrosion in alkaline chloride media with reduced oxygen concentrations

    International Nuclear Information System (INIS)

    It is commonly considered that the corrosion of steel in concrete is controlled by the oxygen content of the pore solution and there are service life models that relate the corrosion rate to the amount of oxygen. It is also commonly believed that in water saturated conditions the oxygen content in the pores is negligible and that underwater there is no risk of depassivation and the corrosion rate is very low. However, the available data on corrosion rates in immersed conditions do not indicate such performance; on the contrary corrosion develops when sufficient chloride reaches the reinforcement. In the present paper, results are presented for tests performed in alkaline chloride solutions that were purged with nitrogen to reduce the oxygen content. The results indicate that at very low oxygen concentrations, corrosion may develop in the presence of chlorides. The presence or absence of corrosion is influenced by the amount of chloride, the corrosion potential and the steel surface condition. (authors)

  2. Chlorides behavior in raw fly ash washing experiments

    Energy Technology Data Exchange (ETDEWEB)

    Zhu Fenfen, E-mail: zhu@hse.gcoe.kyoto-u.ac.jp [Department of Urban and Environmental Engineering, Graduate School of Engineering, Katsura Campus, Kyoto University, Nishikyo-ku, Kyoto 615-8540 (Japan); Takaoka, Masaki; Oshita, Kazuyuki [Department of Urban and Environmental Engineering, Graduate School of Engineering, Katsura Campus, Kyoto University, Nishikyo-ku, Kyoto 615-8540 (Japan); Kitajima, Yoshinori; Inada, Yasuhiro [High Energy Accelerator Research Organization (KEK), Institute of Material Structure Science (IMSS), Oho 1-1, Tsukuba, Ibaraki 305-0801 (Japan); Morisawa, Shinsuke; Tsuno, Hiroshi [Department of Urban and Environmental Engineering, Graduate School of Engineering, Katsura Campus, Kyoto University, Nishikyo-ku, Kyoto 615-8540 (Japan)

    2010-06-15

    Chloride in fly ash from municipal solid waste incinerators (MSWIs) is one of the obstructive substances in recycling fly ash as building materials. As a result, we have to understand the behavior of chlorides in recycling process, such as washing. In this study, we used X-ray absorption near edge structure (XANES) and X-ray diffraction (XRD) to study the chloride behavior in washed residue of raw fly ash (RFA). We found that a combination of XRD and XANES, which is to use XRD to identify the situation of some compounds first and then process XANES data, was an effective way to explain the chlorides behavior in washing process. Approximately 15% of the chlorine in RFA was in the form of NaCl, 10% was in the form of KCl, 51% was CaCl{sub 2}, and the remainder was in the form of Friedel's salt. In washing experiments not only the mole percentage but also the amount of soluble chlorides including NaCl, KCl and CaCl{sub 2} decreases quickly with the increase of liquid to solid (L/S) ratio or washing frequency. However, those of insoluble chlorides decrease slower. Moreover, Friedel's salt and its related compound (11CaO.7Al{sub 2}O{sub 3}.CaCl{sub 2}) were reliable standards for the insoluble chlorides in RFA, which are strongly related to CaCl{sub 2}. Washing of RFA promoted the release of insoluble chlorides, most of which were in the form of CaCl{sub 2}.

  3. Determination of chloride in geological samples by ion chromatography

    Science.gov (United States)

    Wilson, S.A.; Gent, C.A.

    1983-01-01

    Samples of silicate rocks are prepared by sodium carbonate fusion and then treated by ion chromatography. The method was tested for geological standards with chloride concentration between 0.003 and 3%. Observed chloride concentrations comparedd favorably with literature values. The relative standard deviation and detection limit for the method were 8% and 7 ppm, respectively. Up to 30 determination per 24-hour period were possible. ?? 1983.

  4. Optical Studies on Sol-Gel Derived Lead Chloride Crystals

    OpenAIRE

    Rejeena, I; Lillibai, B; Nithyaja, B; Nampoori, P.N V; P. Radhakrishnan

    2013-01-01

    Optical characterization of lead chloride crystals prepared by sol-gel method is reported. The relevant sol-gel technique is used for the preparation of PbCl2 samples with five different types. In this paper, we report the absorption and fluorescence behaviour of pure, UV& IR irradiated and electric & magnetic field applied lead chloride crystal samples in solution phase at two different concentrations. Optical bandgap and emission studies of these crystals are also done.

  5. Macrocycle Synthesis by Chloride-Templated Amide Bond Formation.

    Science.gov (United States)

    Martí-Centelles, Vicente; Burguete, M Isabel; Luis, Santiago V

    2016-03-01

    A new family of pseudopeptidic macrocyclic compounds has been prepared involving an anion-templated amide bond formation reaction at the macrocyclization step. Chloride anion was found to be the most efficient template in the macrocyclization process, producing improved macrocyclization yields with regard to the nontemplated reaction. The data suggest a kinetic effect of the chloride template, providing an appropriate folded conformation of the open-chain precursor and reducing the energy barrier for the formation of the macrocyclic product. PMID:26820908

  6. cis-Dichloridobis(1,10-phenanthrolinechromium(III chloride

    Directory of Open Access Journals (Sweden)

    Xiaoli Gao

    2011-02-01

    Full Text Available In the title complex, [CrCl2(C12H8N22]Cl, the CrIII ion is situated on a twofold rotation axis and displays a slightly distorted octahedral CrCl2N4 coordination geometry. The Cr environment is composed of a cis arrangement of two 1,10-phenanthroline and two chloride ligands. The chloride counter-anion exhibits half-occupation and is equally disordered over two positions.

  7. Recovering germanium from coal ash by chlorination with ammonium chloride

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A new process of enriching germanium from coal ash was developed. The process involves in mixing the coal ash and ammonium chloride and then roasting the mixture to produce germanium chloride that is then absorbed by dilute hydrochloric acid and hydrolyzed to germanium oxide. The germanium recovery reached to 80.2% at the optimum condition: mass ratio of NH4Cl/coal ash is 0.15, roasting temperature 400℃ and roasting time 90 min.

  8. Aqueous Chloride Operations Overview: Plutonium and Americium Purification/Recovery

    Energy Technology Data Exchange (ETDEWEB)

    Gardner, Kyle Shelton [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Kimball, David Bryan [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Skidmore, Bradley Evan [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-09-28

    These are a set of slides intended for an information session as part of recruiting activities at Brigham Young University. It gives an overview of aqueous chloride operations, specifically on plutonium and americium purification/recovery. This presentation details the steps taken perform these processes, from plutonium size reduction, dissolution, solvent extraction, oxalate precipitation, to calcination. For Americium recovery, it details the CLEAR (chloride extraction and actinide recovery) Line, oxalate precipitation and calcination.

  9. Effect of kaolin treatment temperature on mortar chloride permeability

    OpenAIRE

    Puertas, F.; Mejía de Gutiérrez, R.; J. Torres

    2007-01-01

    The present paper discusses the results of chloride resistance tests conducted on ordinary Portland cement (OPC) mortars containing a Colombian kaolin pre-treated at temperatures of from 600 to 800 ºC. The resulting metakaolin (MK) was added to OPC mortar mixes in proportions of 10 and 20% by cement weight. The mortars were compared for physical and chemical properties, including capillary absorption, chloride permeability and pore microstructure as assessed by mercury porosimetry....

  10. Extraction and immobilization of simulated pyrometallurgical chloride waste in Zeolite

    International Nuclear Information System (INIS)

    Zeolites are effective media for the removal and immobilization of fission products waste from pyrometallurgical reprocessing of nuclear fuels. In the present study, equilibration experiments between zeolite 4A and a simulated: pyrometallurgical chloride waste were carried out. Several batches of equilibration were carried out by varying the zeolite to salt (Z/S) ratio. The effects of Z/S on the extraction behaviour of the waste chloride salts were explored. (author)

  11. The effect of chloride and sulfate on Completely Recyclable Concrete

    OpenAIRE

    Arvaniti, E.; De Schepper, M.; De Belie, N.; De Buysser, K.; Van Driessche, I.

    2013-01-01

    Completely Recyclable Concrete (CRC) is intended to be recycled as raw material within the cement production from a predesign stage. However, concrete contributions that are exposed to aggressive environments (e.g. industrial and seaside buildings), could carry elements such as chlorides, sulfur and alkalis after demolition, which will end up in the recycled material. The aim of this study is to better understand the influence of chloride and sulfur in CRC on the final clinker properties. The...

  12. Hafnium extraction from acidic chloride solutions by Cyanex 923

    Energy Technology Data Exchange (ETDEWEB)

    El-Ammouri, E.; Distin, P.A. [McGill Univ., Montreal (Canada)

    1996-08-01

    Hafnium extraction from hydrochloric acid/lithium chloride solutions into Cyanex 923 in kerosene has been studied. Variables investigated were hydrochloric acid, total chloride and hafnium concentrations in the aqueous phase, and extractant/modifier (isodecanol) levels in the organic phase. Hafnium is considered to load as the tetrachloride complex forming a disolvate with Cyanex 923. Results are compared with equivalent data for zirconium extraction. 14 refs., 7 figs., 2 tabs.

  13. Intracellular chloride concentration of the mouse vomeronasal neuron

    OpenAIRE

    Kim, Sangseong; Ma, Limei; Unruh, Jay; McKinney, Sean; Yu, C. Ron

    2015-01-01

    Background The vomeronasal organ (VNO) is specialized in detecting pheromone and heterospecific cues in the environment. Recent studies demonstrate the involvement of multiple ion channels in VNO signal transduction, including the calcium-activated chloride channels (CACCs). Opening of CACCs appears to result in activation of VNO neuron through outflow of Cl− ions. However, the intracellular Cl− concentration remains undetermined. Results We used the chloride ion quenching dye, MQAE, to measu...

  14. Computational modelling of chloride ion transport in reinforced concrete

    OpenAIRE

    Meijers, S.J.H.; Bijen, J.M.J.M.; De Borst, R.; Fraaij, A.L.A.

    2001-01-01

    Exposure to a saline environment is a major threat with respect to the durability of reinforced concrete structures. The chloride ions, which are present in seawater and de-icing salts, are able to penetrate the concrete up to the depth of the reinforcement. They can eventually trigger a pitting corrosion process. The assessment of a corrosion-free service life of concrete structures is of paramount economic interest. However, the modelling of the ingress of chloride ions is complicated due t...

  15. Large Scale Synthesis of Carbon Nanofibres on Sodium Chloride Support

    OpenAIRE

    Ravindra Rajarao; Badekai Ramachandra Bhat

    2012-01-01

    Large scale synthesis of carbon nanofibres (CNFs) on a sodium chloride support has been achieved. CNFs have been synthesized using metal oxalate (Ni, Co and Fe) as catalyst precursors at 680 C by chemical vapour deposition method. Upon pyrolysis, this catalyst precursors yield catalyst nanoparticles directly. The sodium chloride was used as a catalyst support, it was chosen because of its non‐toxic and water soluble nature. Problems, such as the detrimental effect of CNFs, the detrimental ef...

  16. Durability Analysis of Subway Station in Chloride Environment

    OpenAIRE

    Yang LuFeng; Yu Bo; Hong Bin

    2013-01-01

    In this study, a finite element model for chloride ions transport in saturated concrete was proposed based on the Fick’s second law of diffusion. The governing partial differential equation was solved numerically in space as a boundary-value problem and in time as an initial-value problem by means of the finite element formulations. The maximum allowable value of chloride diffusion coefficient within different locations of subway station with service life of 100a was achieved and suggestions ...

  17. Influence of cracks on chloride penetration in concrete

    OpenAIRE

    Audenaert, K.; Schutter, G. de; MARSAVINA, L

    2009-01-01

    Chloride initiated reinforcement corrosion is the main durability problem for concrete structures in a marine environment. If the chlorides reach the reinforcement steel, it will depassivate and start to corrode in presence of air and water. Since the corrosion products have a larger volume than the initial products, concrete stresses are induced, leading to spalling and degradation of the concrete structures. If cracks, caused by early drying, thermal effects, shrinkage movements or overstre...

  18. 海水提溴技术的发展与研究现状%Research and development status of bromine extracting technique from sea water

    Institute of Scientific and Technical Information of China (English)

    林源; 王浩宇; 周亚蓉; 叶俊伟; 宁桂玲

    2012-01-01

    Bromine is one of the important chemical materials.lt has been widely used in the fields of flame retardants,oil exploration,fungicides,pesticides, photographic materials,and pharmaceutical etc..Bromine's preparation technology and potential value are highly attached by domestic and foreign scholars.The status of bromine production and extraction methods from sea water,including air stripping method,steam distillation method,ion exchange adsorption method,and membrane separation method at home and abroad were briefly introduced.The advantages and disadvantages of those methods were compared.Meanwhile, the preparation method of ultrapure bromine was briefly described.Finally, the future development direction of extracting bromine from sea water was suggested.%溴素是重要的化工原料之一,在阻燃剂、石油开采、杀菌剂、农药、感光材料及医药等领域广泛应用,其制备技术和应用价值受到国内外学者的高度重视.综述了国内外溴素生产现状和海水提溴的方法,介绍了空气吹出法、水蒸气蒸馏法、离子交换吸附法和膜分离法提溴技术的研究现状,分析了各种方法的优缺点.简述了超纯溴的制备方法.提出了海水提溴的未来发展方向.

  19. Speciation of the bio-available iodine and bromine forms in edible seaweed by high performance liquid chromatography hyphenated with inductively coupled plasma-mass spectrometry

    International Nuclear Information System (INIS)

    Highlights: ► Bioavailable iodine and bromine speciation in edible seaweed were developed. ► In vitro dialyzability was used to assess the bioavailable fractions. ► AEC hyphenated with inductively coupled plasma-mass spectrometry was used. ► Iodide, MIT, DIT, bromide and bromate were found in dialyzates from edible seaweed. ► 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−1 range). Inductively coupled plasma-mass spectrometry (ICP-MS) was used as a selective detector for iodine (127I) and bromine (79Br). 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).

  20. Chloride ion transport performance in slag mortar under fatigue loading

    Institute of Scientific and Technical Information of China (English)

    WANG CaiHui; SUN Wei; JIANG JinYang; HAN JianDe; YE BangTu

    2012-01-01

    The transport performance of chloride ion in slag cement mortar was investigated experimentally.In the self-designed experiment,fatigue loading was coupled simultaneously with ion transportation process,the diffusion law of chloride ion was obtained by titration and the AE (acoustic emission) technique was employed to detect the real-time damage distribution in the mortar specimen.The results for fatigue stress levels of 0.3,0.4 and 0.5 and slag contents of 0,10%,30% and 50% showed that fatigue loading accelerated the diffusion of chloride ion in mortar and the acceleration effect increased with the increase in stress levels.Slag addition was found to improve anti-chloride ion erosion performance effectively with the best substitution level at 30%,because the inhibition effect of slag on chloride ion diffusion diminished when the slag content exceeded 30%.The comparative experiments indicated that dynamic load has a significant effect on the transport performance of chloride ion in slag cement mortar.

  1. Removal of chloride from electric arc furnace dust.

    Science.gov (United States)

    Chen, Wei-Sheng; Shen, Yun-Hwei; Tsai, Min-Shing; Chang, Fang-Chih

    2011-06-15

    Electric arc furnace (EAF) dust with high chloride content increases the threat of dioxin emissions and the high chloride content reduces the value of recycled zinc oxide produced by EAF dust recycling plants. This study conducts a number of laboratory experiments to determine the technical feasibility of a new dechlorination method. These methods consist of a series of roasting processes and water washing processes. In the roasting process, EAF dust was heated in a tube furnace to evaluate the parameters of atmospheric conditions, roasting temperature, and roasting time. Results indicate that sulfation roasting is more efficient in reducing chloride content than other roasting processes. The water washing process can totally remove water-soluble chloride at a solid to liquid ratio of 1:10. However, the remaining water-insoluble substance is difficult to dechlorinate. For example, lead chloride forms a hydroxyl-halide (PbOHCl) and lead chloride carbonate (Pb(2)CO(3)Cl(2)) agglutinative matrix that is hard to wash away.

  2. Congenital chloride diarrhea: a review of twelve Arabian children

    Directory of Open Access Journals (Sweden)

    Elrefae F

    2013-06-01

    Full Text Available Fawaz Elrefae,1 Ahmed Farag Elhassanien,2 Hesham Abdel-Aziz Alghiaty3 1Pediatric Gastroenterology, Al-Adan Hospital, Kuwait; 2Faculty of Medicine, Elmansoura University, El Mansoura, El Dakahleya, Egypt; 3Faculty of Medicine, Benha University, Egypt Background: Congenital chloride diarrhea (CCD, a rare autosomal recessive disorder, is characterized by sustained watery diarrhea (due to defect of active Chloride/HCO3 exchange in the ileum and colon with high fecal chloride. Objective: To spotlight the common presentation of CCD for early management and prevention of complications. Subjects and methods: This is a retrospective case series study of patients diagnosed as CCD who were followed up in the pediatric department of Al-Adan Hospital, Kuwait. Results: Twelve patients diagnosed with CCD were born to consanguineous parents; had antenatal history of intrauterine growth retardation (IUGR; polyhydramnios; and distended hypoechoic fetal bowel; and presented with abdominal distension, hypotonia and muscle wasting. 90% of patients had maternal hypertension and 75% of patients had absence of normal meconium at birth. Our patients showed a decrease in serum sodium, potassium, chloride and urine chloride. Conclusion: A high level of suspicion for an early diagnosis of CCD should be considered for any infant presenting with chronic diarrhea, especially in the presence of consanguineous marriage, and the characteristic features in antenatal ultrasound. Thus, allowing for early investigations and appropriate management. Keywords: congenital chloride diarrhea, children, chronic diarrhea, metabolic alkalosis, prenatal diagnosis

  3. Stabilizing Plutonium oxide material containing Chloride salts at PFP

    International Nuclear Information System (INIS)

    PFP had over 900 items, weighing more than 1100 kg consisting of impure plutonium oxides referred to as high chloride content plutonium oxides. Tests were conducted to examine items for physical characteristics. After 17 years of storage, the inner food-pack cans maintained integrity with very little evidence of corrosion. Items were washed with water to remove chloride salts. Chloride was readily soluble with plutonium concentrations less than 0.05 g/L in wash solution from all but one of seven items. Washed material was calcined at 1000 C. The calcined material passed the storage test for less than 0.5% water. Unopened items were examined using gamma energy analysis to determine if a prompt gamma (n, x) interaction could be used to screen out items with low chloride concentrations. The prompt gamma was not measurable. A 2168 keV gamma from the (α, x) interaction with chloride correlated within 10% of the chloride concentration measured from washing the item with water

  4. DEVELOPMENTAL TOXICITY OF COPPER CHLORIDE, METHYLENE CHLORIDE,AND 6-AMINONICOTINAMIDE TO EMBRYOS OF THE GRASS SHRIMPPALAEMONETES PUGIO

    Science.gov (United States)

    Embryos of estuarine grass shrimp Palaemonetes pugio have demonstrated sensitivity to various solvents and petroleum products, indicating utility for evaluating estuarine contamination. Testing was performed to establish concentration-response curves for methylene chloride, cop...

  5. 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

  6. Maternal transfer of emerging brominated and chlorinated flame retardants in European eels

    International Nuclear Information System (INIS)

    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−1 ww for sum Dechlorane metabolites (DPMA, aCL10DP, aCl11DP) to 2.1 ng g−1 ww for TBA in eggs, 0.001 ng g−1 ww for Dechlorane metabolites to 9.4 ng g−1 ww for TBA in gonads and 0.002 ng g−1 ww for Dechlorane metabolites to 54 ng g−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 biotransformation processes. Dechloranes seem to be of

  7. A small synthetic molecule functions as a chloride-bicarbonate dual-transporter and induces chloride secretion in cells.

    Science.gov (United States)

    Liu, Peng-Yun; Li, Shing-To; Shen, Fang-Fang; Ko, Wing-Hung; Yao, Xiao-Qiang; Yang, Dan

    2016-05-31

    A C2 symmetric small molecule composed of l-phenylalanine and isophthalamide was found to function as a Cl(-)/HCO3(-) dual transporter and self-assemble into chloride channels. In Ussing-chamber based short-circuit current measurements, this molecule elicited chloride-dependent short-circuit current (Isc) increase in both Calu-3 cell and CFBE41o-cell (with F508del mutant CFTR) monolayers. PMID:27188496

  8. Ab initio Investigations of the Equilibria between Trichlorothioacetyl Chloride, Tetrachlorothiirane, and Trichloroethenesulfenyl Chloride, their Reactants and Decomposition Products

    DEFF Research Database (Denmark)

    Pedersen, Kim Vestergaard; Christensen, Henrik; Shim, Irene;

    2004-01-01

    Trichlorothioacetyl chloride 1, tetrachlorothiirane 2, and trichloroethenesulfenyl chloride 3 and the equilibria between them have been investigated by ab initio Hartree-Fock (HF), Møller-Plesset second order perturbation (MP2) calculations, and by Gaussian-3 theory, G3(MP2). The transition state...... of the isomerization reactions have been identified. Also investigated were possible reactions leading to the isomers and their possible decomposition products. The results show that the unobserved isomerization reactions are feasible....

  9. Technical note: Could benzalkonium chloride be a suitable alternative to mercuric chloride for preservation of seawater samples?

    OpenAIRE

    Gloël, J.; Robinson, C.; Tilstone, G. H.; Tarran, G.; J. Kaiser

    2015-01-01

    Instrumental equipment unsuitable or unavailable for fieldwork as well as lack of ship space can necessitate the preservation of seawater samples prior to analysis in a shore-based laboratory. Mercuric chloride (HgCl2) is routinely used for such preservation, but its handling and subsequent disposal incur environmental risks and significant expense. There is therefore a strong motivation to find less hazardous alternatives. Benzalkonium chloride (BAC) has been used previousl...

  10. Technical Note: Could benzalkonium chloride be a suitable alternative to mercuric chloride for preservation of seawater samples?

    OpenAIRE

    Gloël, J.; Robinson, C.; Tilstone, G. H.; Tarran, G.; J. Kaiser

    2015-01-01

    Instrumental equipment unsuitable or unavailable for fieldwork as well as lack of ship space can necessitate the preservation of seawater samples prior to analysis in a shore-based laboratory. Mercuric chloride (HgCl2) is routinely used for such preservation, but its handling and subsequent disposal incur significant risks and expense. Benzalkonium chloride (BAC) has been used previously for freshwater samples. Here, we assess BAC as a less hazardous alterna...

  11. 40 CFR 61.63 - Emission standard for vinyl chloride plants.

    Science.gov (United States)

    2010-07-01

    ... formation and purification: The concentration of vinyl chloride in each exhaust gas stream from any... 40 Protection of Environment 8 2010-07-01 2010-07-01 false Emission standard for vinyl chloride... for Vinyl Chloride § 61.63 Emission standard for vinyl chloride plants. An owner or operator of...

  12. Variation in concentrations of organochlorines and brominated flame retardants among eggs in abandoned clutches of a terrestrial raptor.

    Science.gov (United States)

    Bustnes, Jan O; Bangjord, Georg; Yoccoz, Nigel G

    2015-01-01

    Bird eggs are often used to measure various pollutants in monitoring programs. In protected species, however, it might only be possible to collect eggs abandoned by the parent birds. In order to assess the appropriateness of abandoned eggs for contaminant monitoring we examined intra-clutch variation in concentrations of 24 halogenated organic pollutants (16 organochlorines [OCs] and 8 brominated flame retardants) in six abandoned tawny owl (Strix aluco) clutches from central Norway. The variation among eggs within a clutch was low for nearly all compounds (intra-class correlation >0.9 both for lipid- and wet weight). This study suggests that abandoned eggs provide a relatively reliable measurement of lipophilic pollutants in clutches of terrestrial raptors such as the tawny owl. PMID:25463262

  13. Fission and nuclear fragmentation of silver and bromine nuclei by photons of 1-6 GeV

    International Nuclear Information System (INIS)

    The studies of fission and fragmentation of silver and bromine nuclei by Bremsstrahlung photons of 1.6 GeV energy range are presented. The Il ford-KO nuclear emulsion submitted to Bremsstrahlung beams in Deutsches Elektronen Synchrotron (DESY) with total doses of 10'' equivalent photons, was used for nuclear fragment detection. The discrimination of fission and fragmentation events was done analysing angular distribution, range and angles between fragments. The results of fragment range distributions, angular distributions, distributions of angles between fragments, distributions of ratio between range, velocity distributions forward/backward ratio, cross sections of fission and fragmentation, nuclear fissionability and ternary fission frequency are presented and discussed. (M.C.K.)

  14. Atmospheric bromine flux from the coastal Abu Dhabi sabkhat: A ground-water mass-balance investigation

    Science.gov (United States)

    Wood, W.W.; Sanford, W.E.

    2007-01-01

    A solute mass-balance study of ground water of the 3000 km2 coastal sabkhat (salt flats) of the Emirate of Abu Dhabi, United Arab Emirates, documents an annual bromide loss of approximately 255 metric tons (0.0032 Gmoles), or 85 kg/km2. This value is an order of magnitude greater than previously published direct measurements from the atmosphere over an evaporative environment of a salar in Bolivia. Laboratory evidence, consistent with published reports, suggests that this loss is by vapor transport to the atmosphere. If this bromine flux to the atmosphere is representative of the total earth area of active salt flats then it is a significant, and generally under recognized, input to the global atmospheric bromide flux.

  15. Determination of bromine, chlorine and iodine in environmental aqueous samples by epithermal neutron activation analysis and Compton suppression

    Science.gov (United States)

    Landsberger, S.; O'Kelly, D. J.; Braisted, J.; Panno, S.

    2006-01-01

    Halides, particularly Br- and Cl-, have been used as indicators of potential sources of Na+ and Cl- in surface water and groundwater with limited success. Contamination of groundwater and surface water by Na+ and Cl- is a common occurrence in growing urban areas and adversely affects municipal and private water supplies in Illinois and other states, as well as vegetation in environmentally sensitive areas. Neutron activation analysis (NAA) can be effectively used to determine these halogens, but often the elevated concentrations of sodium and chlorine in water samples can give rise to very high detection limits for bromine and iodine due to elevated backgrounds from the activation process. We present a detailed analytical scheme to determine Cl, Br and I in aqueous samples with widely varying Na and Cl concentrations using epithermal NAA in conjunction with Compton suppression. ?? 2006 Akade??miai Kiado??.

  16. Corrosion mechanism of 13Cr stainless steel in completion fluid of high temperature and high concentration bromine salt

    Science.gov (United States)

    Liu, Yan; Xu, Lining; Lu, Minxu; Meng, Yao; Zhu, Jinyang; Zhang, Lei

    2014-09-01

    A series of corrosion tests of 13Cr stainless steel were conducted in a simulated completion fluid environment of high temperature and high concentration bromine salt. Corrosion behavior of specimens and the component of corrosion products were investigated by means of scanning electron microscope (SEM), confocal laser scanning microscopy (CLSM) and X-ray photoelectron spectroscopy (XPS). The results indicate that 13Cr steel suffers from severe local corrosion and there is always a passive halo around every pit. The formation mechanism of the passive halo is established. OH- ligand generates and adsorbs in a certain scale because of abundant OH- on the surface around the pits. Passive film forms around each pit, which leads to the occurrence of passivation in a certain region. Finally, the dissimilarities in properties and morphologies of regions, namely the pit and its corresponding passive halo, can result in different corrosion sensitivities and may promote the formation of macroscopic galvanic pairs

  17. Characterization of the lanthanum chloride scintillation detector

    International Nuclear Information System (INIS)

    This paper reports about the investigations on the performance of the new earth-rare halide Scintillator, the LaCl3:10%Ce, which has been discovered with attractive scintillation properties: fast, efficient, and high-energy resolution. The combination of good brightness and linear response has naturally resulted in a very good energy resolution, whereas the fast decay time promoted counting applications at very high rate and very fast timing resolution. Energy resolutions of (2.99±0.02) %, (8.66±0.02) %, and (2.05±0.01) % have been achieved by exciting the detector with 662 keV 137Cs, 122 keV 152Eu, and 1332.5 keV 60Co sources respectively, at room temperature. The variations of the resolution as a function of both shaping time and high voltage have been studied and found to be relatively linear. The timing resolution was also studied. The value of 1.07 ns FWHM has been recorded with LaCl3:10%Ce and BaF2 detectors operating in coincidence mode, using 1333.5 keV γ-ray 60Co peak. Compared to similar studies, this timing resolution was worse than expected even if the exciting radioactive sources used in the two experiments were different. The efficiency values of (0.24±0.01)%, (0.01±0.01)% and (0.09±0.01)% were obtained with laboratory 137Cs, 152Eu, 60Co isotopes respectively. These detector efficiency values were very low, due to the smaller detector sizes used in these earlier crystals and to the large detector-source-distance used in this experiment. The Lanthanum Chloride Scintillator detector is hygroscopic and relatively expensive compared to established scintillators. In addition, it carries internal contamination in 138La and 227Ac for larger thicknesses. Nevertheless, the energy resolution figures achieved, twice as good as that of NaI(Tl), are in good agreement with those reported elsewhere. They credit the scintillation detectors as good challengers of semiconductor-based detectors, allowing their application fields to be extended. (author)

  18. [Pulmonary manifestations of polyvinyl chloride exposure].

    Science.gov (United States)

    Süyür, Hüseyin; Bayram, Nazan; Aydın, Neriman; Uyar, Meral; Gündoğdu, Nevhiz; Elbek, Osman

    2011-01-01

    There is currently no national data on the effects of polyvinyl chloride (PVC) exposure on pulmonary function. In this study we recruited workers and administrative staff from two PVC plants between July 2008 and July 2009. A questionnaire, pulmonary function tests, carbon monoxide diffusion capacity, and peak flows were recorded. Particulate matter analyses were performed by the Adana Central Laboratory of the Directorate of Occupational Health and Safety. Data were analyzed with SPSS 13.0 software. Nine of the 147 subjects were female. The incidence of a cough was more common in the administrative group. Of the study population, 59.1% were smokers. Tobacco addiction significantly increased cough and dyspnea [OR= 1.10 (1.00-1.20, 95% CI) p= 0.007 and OR= 1.08 (1.02-1.14, 95% CI), p= 0.008, respectively]. Dust exposure was correlated with the incidence of a cough [OR= 0.20 (0.04-0.80, 95% CI) p= 0.008]. The period of work correlated with sputum production [OR= 1.00 (1.00-1.02, 95% CI) p= 0.044]. The FVC% was significantly higher in the administrative group, and FEV1/FVC and DLCO were higher in the exposed group. Tobacco addiction increased the risk of airflow limitation, as evaluated by FEV1/FVC < 70% and FEF25-75 < 50% [OR= 1.15 (1.06-1.25, 95% CI) p= 0.001 and OR= 1.09 (1.02-1.17, 95% CI) p= 0.010, respectively]. Tobacco addiction and increasing duration of work had a negative influence on DLCO in the exposed group (r= -0.270, p= 0.025 and r= -0.210, p= 0.037). In the exposed group PEF variability was significantly greater on workdays, compared with rest days. This study shows that tobacco consumption has a greater affect on the airways than PVC dust exposure. A median of 36 months exposure to PVC dust had no significant impact on pulmonary function parameters, except for DLCO and PEF variability.

  19. 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. PMID:26952274

  20. Exposure to Brominated Trihalomethanes in Water During Pregnancy and Micronuclei Frequency in Maternal and Cord Blood Lymphocytes

    Science.gov (United States)

    Pedersen, Marie; Patelarou, Evridiki; Decordier, Ilse; Vande Loock, Kim; Chatzi, Leda; Espinosa, Ana; Fthenou, Eleni; Nieuwenhuijsen, Mark J.; Gracia-Lavedan, Esther; Stephanou, Euripides G.; Kirsch-Volders, Micheline; Kogevinas, Manolis

    2013-01-01

    Background: Water disinfection by-products have been associated with an increased cancer risk. Micronuclei (MN) frequency in lymphocytes is a marker of genomic damage and can predict adult cancer risk. Objective: We evaluated maternal exposure to drinking water brominated trihalomethanes (BTHM) in relation to MN frequency in maternal and cord blood lymphocytes. Methods: MN frequency was examined in 214 mothers and 223 newborns from the Rhea mother–child cohort in Crete, Greece, in 2007–2008. Residential BTHM water concentrations were estimated during pregnancy using tap water analyses and modeling. Questionnaires on water related habits were used to estimate BTHM exposure from all routes. Associations between BTHM and MN frequency were estimated using negative binomial regression. Results: BTHM concentrations in residential tap water during pregnancy ranged from 0.06 to 7.1 μg/L. MN frequency in maternal binucleated lymphocytes was found to increase with BTHM concentrations in residential water for exposure during the first [rate ratio (RR) for 1 μg/L = 1.05; 95% CI: 1.00, 1.11] and second trimesters (RR for 1 μg/L = 1.03; 95% CI: 1.00, 1.06), and through all routes of BTHM exposure during the first trimester (RR for 1 μg/week = 3.14; 95% CI: 1.16, 8.50). Conclusions: These findings suggest that exposure to BTHM may increase the frequency of MN in maternal binucleated lymphocytes. Citation: Stayner LT, Pedersen M, Patelarou E, Decordier I, Vande Loock K, Chatzi L, Espinosa A, Fthenou E, Nieuwenhuijsen MJ, Gracia-Lavedan E, Stephanou EG, Kirsch-Volders M, Kogevinas M. 2014. Exposure to brominated trihalomethanes in water during pregnancy and micronuclei frequency in maternal and cord blood lymphocytes. Environ Health Perspect 122:100–106; http://dx.doi.org/10.1289/ehp.1206434 PMID:24184846