Sample records for metal sulfides exceptionally

  1. Sulfidation kinetics of silver nanoparticles reacted with metal sulfides. (United States)

    Thalmann, Basilius; Voegelin, Andreas; Sinnet, Brian; Morgenroth, Eberhard; Kaegi, Ralf


    Recent studies have documented that the sulfidation of silver nanoparticles (Ag-NP), possibly released to the environment from consumer products, occurs in anoxic zones of urban wastewater systems and that sulfidized Ag-NP exhibit dramatically reduced toxic effects. However, whether Ag-NP sulfidation also occurs under oxic conditions in the absence of bisulfide has not been addressed, yet. In this study we, therefore, investigated whether metal sulfides that are more resistant toward oxidation than free sulfide, could enable the sulfidation of Ag-NP under oxic conditions. We reacted citrate-stabilized Ag-NP of different sizes (10-100 nm) with freshly precipitated and crystalline CuS and ZnS in oxygenated aqueous suspensions at pH 7.5. The extent of Ag-NP sulfidation was derived from the increase in dissolved Cu(2+) or Zn(2+) over time and linked with results from X-ray absorption spectroscopy (XAS) analysis of selected samples. The sulfidation of Ag-NP followed pseudo first-order kinetics, with rate coefficients increasing with decreasing Ag-NP diameter and increasing metal sulfide concentration and depending on the type (CuS and ZnS) and crystallinity of the reacting metal sulfide. Results from analytical electron microscopy revealed the formation of complex sulfidation patterns that seemed to follow preexisting subgrain boundaries in the pristine Ag-NP. The kinetics of Ag-NP sulfidation observed in this study in combination with reported ZnS and CuS concentrations and predicted Ag-NP concentrations in wastewater and urban surface waters indicate that even under oxic conditions and in the absence of free sulfide, Ag-NP can be transformed into Ag2S within a few hours to days by reaction with metal sulfides.

  2. Layered metal sulfides capture uranium from seawater. (United States)

    Manos, Manolis J; Kanatzidis, Mercouri G


    Uranium is the main source for nuclear energy but also one of the most toxic heavy metals. The current methods for uranium removal from water present limitations, such as narrow pH operating range, limited tolerance to high salt concentrations, or/and high cost. We show here that a layered sulfide ion exchanger K(2)MnSn(2)S(6) (KMS-1) overcomes these limitations and is exceptionally capable in selectively and rapidly sequestering high (ppm) as well as trace (ppb) quantities of UO(2)(2+) under a variety of conditions, including seawater. KMS-1 can efficiently absorb the naturally occurring U traces in seawater samples. The results presented here reveal the exceptional potential of sulfide-based ion-exchangers for remediating of uranium-containing wastes and groundwater and for extracting uranium from the sea.

  3. Nanostructured metal sulfides for energy storage. (United States)

    Rui, Xianhong; Tan, Huiteng; Yan, Qingyu


    Advanced electrodes with a high energy density at high power are urgently needed for high-performance energy storage devices, including lithium-ion batteries (LIBs) and supercapacitors (SCs), to fulfil the requirements of future electrochemical power sources for applications such as in hybrid electric/plug-in-hybrid (HEV/PHEV) vehicles. Metal sulfides with unique physical and chemical properties, as well as high specific capacity/capacitance, which are typically multiple times higher than that of the carbon/graphite-based materials, are currently studied as promising electrode materials. However, the implementation of these sulfide electrodes in practical applications is hindered by their inferior rate performance and cycling stability. Nanostructures offering the advantages of high surface-to-volume ratios, favourable transport properties, and high freedom for the volume change upon ion insertion/extraction and other reactions, present an opportunity to build next-generation LIBs and SCs. Thus, the development of novel concepts in material research to achieve new nanostructures paves the way for improved electrochemical performance. Herein, we summarize recent advances in nanostructured metal sulfides, such as iron sulfides, copper sulfides, cobalt sulfides, nickel sulfides, manganese sulfides, molybdenum sulfides, tin sulfides, with zero-, one-, two-, and three-dimensional morphologies for LIB and SC applications. In addition, the recently emerged concept of incorporating conductive matrices, especially graphene, with metal sulfide nanomaterials will also be highlighted. Finally, some remarks are made on the challenges and perspectives for the future development of metal sulfide-based LIB and SC devices.

  4. Single-layer transition metal sulfide catalysts (United States)

    Thoma, Steven G [Albuquerque, NM


    Transition Metal Sulfides (TMS), such as molybdenum disulfide (MoS.sub.2), are the petroleum industry's "workhorse" catalysts for upgrading heavy petroleum feedstocks and removing sulfur, nitrogen and other pollutants from fuels. We have developed an improved synthesis technique to produce SLTMS catalysts, such as molybdenum disulfide, with potentially greater activity and specificity than those currently available. Applications for this technology include heavy feed upgrading, in-situ catalysis, bio-fuel conversion and coal liquefaction.

  5. Synthesis of arsenic transition metal sulfides and metal arsenides

    Energy Technology Data Exchange (ETDEWEB)

    Singhal, G.H.; Brown, L.D.; Ryan, D.F. [Exxon Research & Development Labs, Baton Rouge, LA (United States)


    One of the chief problems in upgrading shale oil is the presence of inherent arsenic which is known to poison downstream catalysts. Highly dispersed transition metal sulfides formed in situ from the decomposition of dithiocarbamate (DTC) complexes of transition metals show excellent potential as dearsenation agents. The authors have studied the reaction of these sulfides with various arsenic compositions and characterized the metal arsenides and arsenic metal sulfides formed as well as the ease of their formation. Thus, the reaction of bis(butyldithiocarbamato)Ni, (NiBuDTC) with model compounds was very facile and gave NiAs, NiAsS, and NiAs2=xSx. In general the effectiveness of the sulfides for dearsenation followed the sequence Ni>Mo{much_gt}Co, while iron sulfides were totally ineffective. Based upon these results, tests were run in autoclaves (as well as a fixed-bed flow-through unit) with NiBuDTC and shale oil having 73 ppm inherent As. Under optimum conditions, dearsenation down to les than 1 ppm was obtained.

  6. Synthesis and characterization of metal sulfide clusters for toxicological studies. (United States)

    Bowles, L C; Bell, Russell A; Ernste, Michael J; Kramer, James R; Manolopoulos, Helen; Ogden, Nancy


    Zinc sulfide clusters were synthesized and characterized at low micromolar concentrations to assess the effect of metal-sulfide ligands on metal toxicity to aquatic organisms in oxic environments. Recommended preparation times are greater than 2 h initial reaction of equimolar sodium sulfide and zinc nitrate, followed by oxic aeration for 3 d. Ionic strength, pH, and anoxic stabilization time were found to be relatively unimportant in controlling the final yield. Adsorptive losses of zinc sulfide (ZnS) clusters to surfaces, however, were significant for a variety of vessel materials and membrane filters. Ionic strength and pH were found to be important factors controlling the extent of adsorptive losses with minimal loss for pHs greater than 9 and for soft waters. The Ag(I), Cu(II), and Hg(II) as metal sulfides completely suppress the analysis of sulfide, whereas Pb(II), Mn(II), and Co(II) partially suppress the analysis of sulfide by the methylene blue technique. Ultraviolet and fluorescence spectra are shown for synthesized ZnS clusters.

  7. Platinum Metals in Magmatic Sulfide Ores (United States)

    Naldrett, A. J.; Duke, J. M.


    Platinum-group elements (PGE) are mined predominantly from deposits that have formed by the segregation of molten iron-nickel-copper sulfides from silicate magmas. The absolute concentrations of PGE in sulfides from different deposits vary over a range of five orders of magnitude, whereas those of other chalcophile elements vary by factors of only 2 to 100. However, the relative proportions of the different PGE in a given deposit are systematically related to the nature of the parent magma. The absolute and relative concentrations of PGE in magmatic sulfides are explained in terms of the degree of partial melting of mantle peridotite required to produce the parent magma and the processes of batch equilibration and fractional segregation of sulfides. The Republic of South Africa and the U.S.S.R. together possess more than 97 percent of the world PGE reserves, but significant undeveloped resources occur in North America. The Stillwater complex in Montana is perhaps the most important example.

  8. Metal sulfide electrodes and energy storage devices thereof

    Energy Technology Data Exchange (ETDEWEB)

    Chiang, Yet-Ming; Woodford, William Henry; Li, Zheng; Carter, W. Craig


    The present invention generally relates to energy storage devices, and to metal sulfide energy storage devices in particular. Some aspects of the invention relate to energy storage devices comprising at least one flowable electrode, wherein the flowable electrode comprises an electroactive metal sulfide material suspended and/or dissolved in a carrier fluid. In some embodiments, the flowable electrode further comprises a plurality of electronically conductive particles suspended and/or dissolved in the carrier fluid, wherein the electronically conductive particles form a percolating conductive network. An energy storage device comprising a flowable electrode comprising a metal sulfide electroactive material and a percolating conductive network may advantageously exhibit, upon reversible cycling, higher energy densities and specific capacities than conventional energy storage devices.

  9. Separation of platinum metals by theirs extraction as sulfides

    International Nuclear Information System (INIS)

    Pilipenko, A.T.; Ryabushko, O.P.; Ty Van Mak


    Separation of platinum metals by means of their sediment in the form of sulfides with subsequent extraction is studied. The optimum conditions of metal sulfide extraction are determined, the metal output dependence from acidness and aqueous phase composition and also the organic solvent nature are investigated. Ruthenium concentration was determined photometrically. Ruthenium sulfide is extracted by butyl spirit from 1-4 normal hydrochloric acid. The maximum extraction grade of 63% is reached in 3.2-normal acid. When the mixture of acetic and hydrochloric acids (2:1) is used for decomposition of ruthenium tiosalts, the grade of ruthenium extraction by amyl spirit or the mixture of anyl and butyl spirits (1:1) constitutes 100%

  10. Magnetite-sulfide-metal complexes in the Allende meteorite (United States)

    Haggerty, S. E.; Mcmahon, B. M.


    A model of liquid immiscibility is presented that seemingly accounts for the sulfide-oxide-metal complexes that are present in olivine-rich chondrules in the Allende meteorite. The four major assemblages that are identified are: (1) magnetite + Ni-Fe metal; (2) magnetite + troilite + Ni-Fe metal; (3) magnetite + troilite + pentlandite + Ni-Fe metal; and (4) troilite + or - pentlandite. Specific attention is focused on oxide-metal associations and experimental data confirm earlier suggestions that magnetite results from the oxidation of an initially high-Fe-content metal alloy. Oxidation decreases the modal abundance of the Fe metal and this is accompanied by substantial increases in Ni contents which reach a maximum of approximately 70 wt % Ni. The proposed oxidation mechanism is entirely consistent with condensation of Fe-metal + olivine (Fa5) that subsequently reequilibrated at lower temperatures. Although the sulfide constituents could also have formed by the reaction of Fe-Ni metal + gaseous H2S, sulfide immiscibility under increased conditions of partial O2 pressure is the preferred process.

  11. Transition Metal Sulfide Hydrogen Evolution Catalysts for Hydrobromic Acid Electrolysis

    NARCIS (Netherlands)

    Ivanovskaya, Anna; Singh, Nirala; Liu, Ru-Fen; Kreutzer, Haley; Baltrusaitis, Jonas; Nguyen, Trung Van; Metiu, Horia; McFarland, Eric


    Mixed metal sulfides containing combinations of W, Fe, Mo, Ni, and Ru were synthesized and screened for activity and stability for the hydrogen evolution reaction (HER) in aqueous hydrobromic acid (HBr). Co- and Ni-substituted RuS2 were identified as potentially active HER electrocatalysts by

  12. Preparation of transition metal sulfide nanoparticles via hydrothermal route

    International Nuclear Information System (INIS)

    Fei-Ling, P.; Chin-Hua, C.; Sarani Zakaria; Tze-Khong, L.; Mohd Ambar Yarmo; Nay-Ming, H.


    Nano sized copper sulfide, iron sulfide and molybdenum sulfide were successfully synthesised via a simple hydrothermal method. Sodium thiosulfate pentahydrate (Na 2 S 2 O 3 ·5H 2 O) and hydroxylamine sulfate ((H 3 NO) 2 ·H 2 SO 4 ) were used as the starting materials and reacted with the transition metal source at 200 degree Celsius for 90 min. The products were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX) and Fourier transform infrared spectroscopy (FTIR). Spherical shape CuS and FeS 2 nanoparticles with high crystallinity were successfully produced. The transmission electron micrographs revealed the well-dispersibility of the produced nanoparticles. Scanning electron micrograph showed the MoS 2 nanoparticles possessed a spherical shape with sheet-like structure covering on the outer surface of the particles. (author)

  13. Metal sulfide and rare-earth phosphate nanostructures and methods of making same (United States)

    Wong, Stanislaus; Zhang, Fen


    The present invention provides a method of producing a crystalline metal sulfide nanostructure. The metal is a transitional metal or a Group IV metal. In the method, a porous membrane is placed between a metal precursor solution and a sulfur precursor solution. The metal cations of the metal precursor solution and sulfur ions of the sulfur precursor solution react, thereby producing a crystalline metal sulfide nanostructure.

  14. Volcanic sulfur degassing and the role of sulfides in controlling volcanic metal emissions (United States)

    Edmonds, M.; Liu, E.


    Volcanoes emit prodigious quantities of sulfur and metals, their behaviour inextricably linked through pre-eruptive sulfide systematics and through degassing and speciation in the volcanic plume. Fundamental differences exist in the metal output of ocean island versus arc volcanoes, with volcanoes in Hawaii and Iceland outgassing large fluxes of gaseous and particulate chalcophiles; and arc volcanoes' plumes, in contrast, enriched in Zn, Cu, Tl and Pb. Metals and metalloids partition into a magmatic vapor phase from silicate melt at crustal pressures. Their abundance in magmatic vapor is influenced strongly by sulfide saturation and by the composition of the magmatic vapor phase, particularly with respect to chloride. These factors are highly dependent on tectonic setting. Metal outgassing is controlled by magma water content and redox: deep saturation in vapor and minimal sulfide in arc basalts yields metal-rich vapor; shallow degassing and resorption of sulfides feeds the metal content of volcanic gas in ocean islands. We present a detailed study of the sulfide systematics of the products of the 2014-2015 Holuhraun basaltic fissure eruption (Bárðarbunga volcanic system, Iceland) to illustrate the interplay between late water and sulfur outgassing; sulfide saturation and breakdown; and metal partitioning into a vapor phase. Sulfide globules, representing quenched droplets of an immiscible sulfide liquid, are preserved within erupted tephra. Sulfide globules in rapidly quenched tephra are preserved within both matrix glass and as inclusions in crystals. The stereologically-corrected 3D size distribution of sulfide globules ranges from eruption and co-existed with an immiscible sulfide liquid throughout much of ol-cpx-plag crystallisation. Individual globules are associated with locally elevated dissolved sulfur concentrations, with concentration gradients away from sulfides preserved over distances of 10-40 µm from the melt-sulfide interfaces. We discuss the

  15. Some problems of synthesis of coordination compounds - the molecular predecessors of metal sulfides

    International Nuclear Information System (INIS)

    Larionov, S.V.


    Processes of metal sulfide preparations which require preliminary synthesis of coordination compounds o the metals (Cd, In, etc.) with organic sulfur-containing ligands have been considered. The promising trends in the synthesis are as follows: synthesis of chelate compounds and salts with rationally selected anions; synthesis of different-ligand compounds; synthesis of precursors for complex sulfides preparation. 14 refs

  16. Remediation of Cd-contaminated soil around metal sulfide mines (United States)

    Lu, Xinzhe; Hu, Xuefeng; Kang, Zhanjun; Luo, Fan


    The mines of metal sulfides are widely distributed in the southwestern part of Zhejiang Province, Southeast China. The activities of mining, however, often lead to the severe pollution of heavy metals in soils, especially Cd contamination. According to our field investigations, the spatial distribution of Cd-contaminated soils is highly consistent with the presence of metal sulfide mines in the areas, further proving that the mining activities are responsible for Cd accumulation in the soils. To study the remediation of Cd-contaminated soils, a paddy field nearby large sulfide mines, with soil pH 6 and Cd more than 1.56 mg kg-1, five times higher than the national recommended threshold, was selected. Plastic boards were deeply inserted into soil to separate the field and make experimental plots, with each plot being 4 m×4 m. Six treatments, TK01˜TK06, were designed to study the effects of different experimental materials on remediating Cd-contaminated soils. The treatment of TK01 was the addition of 100 kg zeolites to the plot; TK02, 100 kg apatites; TK03, 100 kg humid manure; TK04, 50 kg zeolites + 50 kg apatites; TK05, 50 kg zeolites + 50 kg humid manure; TK06 was blank control (CK). One month after the treatments, soil samples at the plots were collected to study the possible change of chemical forms of Cd in the soils. The results indicated that these treatments reduced the content of available Cd in the soils effectively, by a decreasing sequence of TK04 (33%) > TK02 (25%) > TK01 (23%) > TK05 (22%) > TK03 (15%), on the basis of CK. Correspondingly, the treatments also reduced the content of Cd in rice grains significantly, by a similar decreasing sequence of TK04 (83%) > TK02 (77%) > TK05 (63%) > TK01 (47%) > TK03 (27%). The content of Cd in the rice grains was 0.071 mg kg-1, 0.094 mg kg-1, 0.159 mg kg-1, 0.22 mg kg-1 and 0.306 mg kg-1, respectively, compared with CK, 0.418 mg kg-1. This experiment suggested that the reduction of available Cd in the soils is

  17. Ceramic/metal seals. [refractory materials for hermetic seals for lighium-metal sulfide batteries (United States)

    Bredbenner, A. M.


    Design criteria are discussed for a hermetic seal capable of withstanding the 450 C operating temperature of a lithium-metal sulfide battery system. A mechanical seal consisting of two high strength alloy metal sleeves welded or brazed to a conductor assembly and pressed onto a ceramic is described. The conductor center passes through the ceramic but is not sealed to it. The seal is effected on the outside of the taper where the tubular part is pressed down over and makes contact.

  18. The metal-rich sulfides and phosphides of the early transition metals

    Energy Technology Data Exchange (ETDEWEB)

    Franzen, H.F. [Ames Lab., IA (United States)]|[Iowa State Univ., Ames, IA (United States). Dept. of Chemistry


    Early work on the preparation of refractory metal-rich compounds of the early transition metals resulted in the understanding that metal-metal bonding results in a structural variety that plays an important role in the high-temperature chemistry of these systems. The binary metal-rich systems have been thoroughly studied at high temperatures, and the structures of most, if not all, of the refractory sulfides and phosphides are known. More recently new ternary phases have been discovered, and these have been shown to result from distributed fractional site occupation of metal atom sites in complex structures. The extent of metal-metal bonding has been quantified by Extended-Hueckel Tight-Bonding calculations using Mullikan Overlap Populations. Correlations of site occupancy with MOP based upon the DFSO model have been observed. 44 refs.

  19. Precipitation of heavy metals from coal ash leachate using biogenic hydrogen sulfide generated from FGD gypsum. (United States)

    Jayaranjan, Madawala Liyanage Duminda; Annachhatre, Ajit P


    Investigations were undertaken to utilize flue gas desulfurization (FGD) gypsum for the treatment of leachate from the coal ash (CA) dump sites. Bench-scale investigations consisted of three main steps namely hydrogen sulfide (H(2)S) production by sulfate reducing bacteria (SRB) using sulfate from solubilized FGD gypsum as the electron acceptor, followed by leaching of heavy metals (HMs) from coal bottom ash (CBA) and subsequent precipitation of HMs using biologically produced sulfide. Leaching tests of CBA carried out at acidic pH revealed the existence of several HMs such as Cd, Cr, Hg, Pb, Mn, Cu, Ni and Zn. Molasses was used as the electron donor for the biological sulfate reduction (BSR) process which produced sulfide rich effluent with concentration up to 150 mg/L. Sulfide rich effluent from the sulfate reduction process was used to precipitate HMs as metal sulfides from CBA leachate. HM removal in the range from 40 to 100% was obtained through sulfide precipitation.

  20. Superconductivity and magnetism in iron sulfides intercalated by metal hydroxides. (United States)

    Zhou, Xiuquan; Eckberg, Christopher; Wilfong, Brandon; Liou, Sz-Chian; Vivanco, Hector K; Paglione, Johnpierre; Rodriguez, Efrain E


    Inspired by naturally occurring sulfide minerals, we present a new family of iron-based superconductors. A metastable form of FeS known as the mineral mackinawite forms two-dimensional sheets that can be readily intercalated by various cationic guest species. Under hydrothermal conditions using alkali metal hydroxides, we prepare three different cation and metal hydroxide-intercalated FeS phases including (Li 1- x Fe x OH)FeS, [(Na 1- x Fe x )(OH) 2 ]FeS, and K x Fe 2- y S 2 . Upon successful intercalation of the FeS layer, the superconducting critical temperature T c of mackinawite is enhanced from 5 K to 8 K for the (Li 1- x Fe x OH) δ + intercalate. Layered heterostructures of [(Na 1- x Fe x )(OH) 2 ]FeS resemble the natural mineral tochilinite, which contains an iron square lattice interleaved with a hexagonal hydroxide lattice. Whilst heterostructured [(Na 1- x Fe x )(OH) 2 ]FeS displays long-range magnetic ordering near 15 K, K x Fe 2- y S 2 displays short range antiferromagnetism.

  1. Sythesis of metal sulfide nanomaerials via thermal decomposition of single-source percursors

    Energy Technology Data Exchange (ETDEWEB)

    Jen-La Plante, Ilan; Zeid, Tahani W.; Yang, Peidong; Mokari, Taleb


    In this report, we present a synthetic method for the formation of cuprous sulfide (Cu2S) and lead sulfide (PbS) nanomaterials directly on substrates from the thermolysis of single-source precursors. We find that the final morphology and arrangement of the nanomaterials may be controlled through the concentration of the dissolved precursors and choice of solvent. One-dimensional (1-D) morphologies may also be grown onto substrates with the addition of a metal catalyst layer through solution-liquid-solid (SLS) growth. These synthetic techniques may be expanded to other metal sulfide materials.

  2. Spatial variation of metals and acid volatile sulfide in floodplain lake sediment

    NARCIS (Netherlands)

    Griethuysen, van C.; Meijboom, E.W.; Koelmans, A.A.


    In risk assessment of aquatic sediments, much attention is paid to the immobilizing effect of acid volatile sulfide (AVS) on trace metals. The difference of AVS and simultaneously extracted metals (SEM) gives an indication of metal availability. In floodplain sediments, where changing redox

  3. Metal-organic frameworks for the storage and delivery of biologically active hydrogen sulfide

    Energy Technology Data Exchange (ETDEWEB)

    Allan, Phoebe K; Wheatley, Paul S; Aldous, David; Mohideen, M Infas; Tang, Chiu; Hriljac, Joseph A; Megson, Ian L; Chapman, Karena W; De Weireld, Guy; Vaesen, Sebastian; Morris, Russell E [St Andrews


    Hydrogen sulfide is an extremely toxic gas that is also of great interest for biological applications when delivered in the correct amount and at the desired rate. Here we show that the highly porous metal-organic frameworks with the CPO-27 structure can bind the hydrogen sulfide relatively strongly, allowing the storage of the gas for at least several months. Delivered gas is biologically active in preliminary vasodilation studies of porcine arteries, and the structure of the hydrogen sulfide molecules inside the framework has been elucidated using a combination of powder X-ray diffraction and pair distribution function analysis.

  4. Production of aluminum metal by electrolysis of aluminum sulfide (United States)

    Minh, N.Q.; Loutfy, R.O.; Yao, N.P.


    Metallic aluminum may be produced by the electrolysis of Al/sub 2/S/sub 3/ at 700 to 800/sup 0/C in a chloride melt composed of one or more alkali metal chlorides, and one or more alkaline earth metal chlorides and/or aluminum chloride to provide improved operating characteristics of the process.

  5. Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions

    Directory of Open Access Journals (Sweden)

    Hua Zhang


    Full Text Available A highly efficient transition-metal-free catalytic system Br2/NaNO2/H2O has been developed for a robust and economic acid-free aerobic oxidation of sulfides. It is noteworthy that the sulfide function reacts under mild conditions without over-oxidation to sulfone. The role of NaNO2as an efficient NO equivalent for the activation of molecular oxygen was identified. Under the optimal conditions, a broad range of sulfide substrates were converted into their corresponding sulfoxides in high yields by molecular oxygen. The present catalytic system utilizes cheap and readily available agents as the catalysts, exhibits high selectivity for sulfoxide products and releases only innocuous water as the by-products.

  6. From Metal Thiobenzoates to Metal Sulfide Nanocrystals: An Experimental and Theoretical Investigation

    Directory of Open Access Journals (Sweden)

    Fenfang Yin


    Full Text Available A simple preparation of metal sulfide nanoparticles via the decomposition of thiobenzoate precursors at room temperature is presented and discussed. Long chain alkylamines were found to mediate the breakdown of metal thiobenzoates, such as those containing Ag, Cu, In and Cd, to produce uniform Ag2S, Cu2−xS, In2S3 and CdS nanoparticles respectively. The long chain amines are assumed to play dual roles as the nucleophilic reagent and the capping agent. It was found that sizes of the nanoparticles can be controlled by changing the type of amine used, as well as the molar ratio between amine and the precursor. We performed DFT calculations on a proposed mechanism involving an initial nucleophilic addition of amine molecule onto the thiocarboxylates. The proposed reaction was also confirmed through the analysis of by-products via infrared spectroscopy. On the basis of this understanding, we propose to manipulate the stability of the precursors by coordination with suitable stabilizing groups, such that the reaction kinetics can be modified to generate different nanostructures of interest.

  7. From Metal Thiobenzoates to Metal Sulfide Nanocrystals: An Experimental and Theoretical Investigation (United States)

    Zhang, Zhihua; Lim, Wen Pei; Wong, Chiong Teck; Xu, Hairuo; Yin, Fenfang; Chin, Wee Shong


    A simple preparation of metal sulfide nanoparticles via the decomposition of thiobenzoate precursors at room temperature is presented and discussed. Long chain alkylamines were found to mediate the breakdown of metal thiobenzoates, such as those containing Ag, Cu, In and Cd, to produce uniform Ag2S, Cu2−xS, In2S3 and CdS nanoparticles respectively. The long chain amines are assumed to play dual roles as the nucleophilic reagent and the capping agent. It was found that sizes of the nanoparticles can be controlled by changing the type of amine used, as well as the molar ratio between amine and the precursor. We performed DFT calculations on a proposed mechanism involving an initial nucleophilic addition of amine molecule onto the thiocarboxylates. The proposed reaction was also confirmed through the analysis of by-products via infrared spectroscopy. On the basis of this understanding, we propose to manipulate the stability of the precursors by coordination with suitable stabilizing groups, such that the reaction kinetics can be modified to generate different nanostructures of interest. PMID:28348299

  8. A General Route for Growing Metal Sulfides onto Graphene Oxide and Exfoliated Graphite Oxide. (United States)

    Lopes, Joana L; Estrada, Ana C; Fateixa, Sara; Ferro, Marta; Trindade, Tito


    Graphene-based materials are elective materials for a number of technologies due to their unique properties. Also, semiconductor nanocrystals have been extensively explored due to their size-dependent properties that make them useful for several applications. By coupling both types of materials, new applications are envisaged that explore the synergistic properties in such hybrid nanostructures. This research reports a general wet chemistry method to prepare graphene oxide (GO) sheets decorated with nanophases of semiconductor metal sulfides. This method allows the in situ growth of metal sulfides onto GO by using metal dialkyldithiocarbamate complexes as single-molecule precursors. In particular, the role of GO as heterogeneous substrate for the growth of semiconductor nanocrystals was investigated by using Raman spectroscopic and imaging methods. The method was further extended to other graphene-based materials, which are easily prepared in a larger scale, such as exfoliated graphite oxide (EGO).

  9. Ternary metal-rich sulfide with a layered structure (United States)

    Franzen, Hugo F.; Yao, Xiaoqiang


    A ternary Nb-Ta-S compound is provided having the atomic formula, Nb.sub.1.72 Ta.sub.3.28 S.sub.2, and exhibiting a layered structure in the sequence S-M3-M2-M1-M2-M3-S wherein S represents sulfur layers and M1, M2, and M3 represent Nb/Ta mixed metal layers. This sequence generates seven sheets stacked along the [001] direction of an approximate body centered cubic crystal structure with relatively weak sulfur-to-sulfur van der Waals type interactions between adjacent sulfur sheets and metal-to-metal bonding within and between adjacent mixed metal sheets.

  10. Functional metal sulfides and selenides for the removal of hazardous dyes from Water. (United States)

    Shamraiz, Umair; Hussain, Raja Azadar; Badshah, Amin; Raza, Bareera; Saba, Sonia


    Water contamination by organic dyes, is among the most alarming threats to healthy green environment. Complete removal of organic dyes is necessary to make water healthy for drinking, cooking, and for other useful aspects. Recently use of nanotechnology for removing organic dyes, became fruitful because of high surface to volume ratio and adsorption properties. Among these materials, metal chalcogenides emerge as new class of active materials for water purification. In this review article, we gathered information related to sulfide and selenide based nanomaterials which include metal sulfides and selenides, their binary composites, and use of different capping agents and dopants for enhancing photocatalysis. We have discussed in detail, about adsorption power of different dyes, relative percentage degradation, reaction time and concentration. Copyright © 2016 Elsevier B.V. All rights reserved.

  11. Metal sulfide nanoparticles synthesized via enzyme treatment of biopolymer stabilized nanosuspensions (United States)

    Kim, Yi-Yeoun; Walsh, Dominic


    Nanoparticles of CuS, CuxS, Ag2S and CdS were successfully prepared using a novel general and green synthetic process to give dextran biopolymer stabilised metal sulfifde nanosuspensions. Following preparation, dextranase enzyme was used to remove the bulk of the bound dextran to give pure stable metal sulfide nanocrystals for application in for example aspects of medicine, photonics and solar cells. Particles of good homogeneity were obtained and the CuS nanoparticle size was controlled to 9-27 nm by adjusting the reaction conditions. Cu2S nanoparticles were 14 nm, Ag2S nanoparticles were 20-50 nm and CdS nanoparticles were 9 nm is size. The complexing mechanism of nanoparticle sulfides to dextrans was further studied using carboxylmethyl dextran as a complexing agent and crosslinked Sephadex (dextran) `beads as substrate. Particles were characterized by TEM, XRD, TGA, FT-IR and zeta-potential measurement, and their UV-vis spectroscopic absorption properties were determined. Stabilization of the sulfide nanoparticles with soluble hydroxylated biopolymers such as dextran is previously unreported and is here interpreted in terms of viscosity, pH of the system and weak polar S-H or S(metal)OH2+ interactions with dextran depending on the material. Notably, the complexing mechanism appears to differ significantly from that taking place in known dextran-metal oxide systems. The process shown here has good potential for scale-up as a biosynthetic route for a range of functional sulfide nanoparticles.Nanoparticles of CuS, CuxS, Ag2S and CdS were successfully prepared using a novel general and green synthetic process to give dextran biopolymer stabilised metal sulfifde nanosuspensions. Following preparation, dextranase enzyme was used to remove the bulk of the bound dextran to give pure stable metal sulfide nanocrystals for application in for example aspects of medicine, photonics and solar cells. Particles of good homogeneity were obtained and the CuS nanoparticle size

  12. Hydrogen evolution on nano-particulate transition metal sulfides

    DEFF Research Database (Denmark)

    Bonde, Jacob Lindner; Moses, Poul Georg; Jaramillo, Thomas F.


    The hydrogen evolution reaction (HER) on carbon supported MoS2 nanoparticles is investigated and compared to findings with previously published work on Au(111) supported MoS2. An investigation into MoS2 oxidation is presented and used to quantify the surface concentration of MoS2. Other metal...

  13. A computational study of adhesion between rubber and metal sulfides at rubber–brass interface

    International Nuclear Information System (INIS)

    Ling, Chian Ye; Hirvi, Janne T.; Suvanto, Mika; Bazhenov, Andrey S.; Ajoviita, Tommi; Markkula, Katriina; Pakkanen, Tapani A.


    Highlights: • An atomic level model for brass–rubber interactions has been presented. • The main adhesion force has been tracked to the rubber sulfur–brass zinc or brass copper interaction. • The model gives new understanding of the adhesion and can be used for further developments of the system. - Abstract: Computational study at level of density functional theory has been carried out in order to investigate the adhesion between rubber and brass plated steel cord, which has high importance in tire manufacturing. Adsorption of natural rubber based adsorbate models has been studied on zinc sulfide, ZnS(1 1 0), and copper sulfide, Cu 2 S(1 1 1) and CuS(0 0 1), surfaces as the corresponding phases are formed in adhesive interlayer during rubber vulcanization. Saturated hydrocarbons exhibited weak interactions, whereas unsaturated hydrocarbons and sulfur-containing adsorbates interacted with the metal atoms of sulfide surfaces more strongly. Sulfur-containing adsorbates interacted with ZnS(1 1 0) surface stronger than unsaturated hydrocarbons, whereras both Cu 2 S(1 1 1) and CuS(0 0 1) surfaces showed opposite adsorption preference as unsaturated hydrocarbons adsorbed stronger than sulfur-containing adsorbates. The different interaction strength order can play role in rubber–brass adhesion with different relative sulfide concentrations. Moreover, Cu 2 S(1 1 1) surface exhibits higher adsorption energies than CuS(0 0 1) surface, possibly indicating dominant role of Cu 2 S in the adhesion between rubber and brass

  14. The Formation and Chronology of the PAT 91501 Impact-Melt L-Chondrite with Vesicle-Metal-Sulfide Assemblages (United States)

    Benedix, G. K.; Ketcham, R. A.; Wilson, L.; McCoy, T. J.; Bogard, D. D.; Garrison, D. H.; Herzog, G. F.; Xue, S.; Klein, J.; Middleton, R.


    The L chondrite Patuxent Range (PAT) 41 91501 is an 8.5-kg unshocked, homogeneous, igneous-textured impact melt that cooled slowly compared to other meteoritic impact melts in a crater floor melt sheet or sub-crater dike. We conducted mineralogical and tomographic studies of previously unstudied mm- to cm-sized metal-sulfide-vesicle assemblages and chronologic studies of the silicate host. Metal-sulfide clasts constitute about 1 vol.%, comprise zoned taenite, troilite and pentlandite, and exhibit a consistent orientation between metal and sulfide and of metal-sulfide contacts. Vesicles make up approximately 2 vol.% and exhibit a similar orientation of long axes. Ar-39-Ar-40 measurements date the time of impact at 4.461 +/- 0.008 Gyr B.P. Cosmogenic noble gases and Be-10 and Al-2l activities suggest a pre-atmospheric radius of 40-60 cm and a cosmic ray exposure age of 25-29 Myr, similar to ages of a cluster of L chondrites. PAT 91501 dates the oldest known impact on the L chondrite parent body. The dominant vesicle-forming gas was S2 (approximately 15-20 ppm), which formed in equilibrium with impact-melted sulfides. The meteorite formed in an impact melt dike beneath a crater, as did other impact melted L chondrites, such as Chico. Cooling and solidification occurred over approximately 2 hours. During this time, approximately 90% of metal and sulfide segregated from the local melt. Remaining metal and sulfide grains oriented themselves in the local gravitational field, a feature nearly unique among meteorites. Many of these metal sulfide grains adhered to vesicles to form aggregates that may have been close to neutrally buoyant. These aggregates would have been carried upward with the residual melt, inhibiting further buoyancy-driven segregation. Although similar processes operated individually in other chondritic impact melts, their interaction produced the unique assemblage observed in PAT 91501.

  15. A kinetic approach to evaluate the association of acid volatile sulfide and simultaneously extracted metals in aquatic sediments

    NARCIS (Netherlands)

    Poot, A.; Meerman, E.; Gillissen, F.; Koelmans, A.A.


    The acid volatile sulfide (AVS) and simultaneously extracted metals (¿SEM) method is widely used for evaluating potential bioavailability of heavy metals in soil and sediment. It is also criticized, because the requirement that AVS and SEM metals (i.e., Cd, Cu, Ni, Pb, and Zn) are associated in the

  16. Synthesis of free-standing metal sulfide nanoarrays via anion exchange reaction and their electrochemical energy storage application. (United States)

    Xia, Xinhui; Zhu, Changrong; Luo, Jingshan; Zeng, Zhiyuan; Guan, Cao; Ng, Chin Fan; Zhang, Hua; Fan, Hong Jin


    Metal sulfides are an emerging class of high-performance electrode materials for solar cells and electrochemical energy storage devices. Here, a facile and powerful method based on anion exchange reactions is reported to achieve metal sulfide nanoarrays through a topotactical transformation from their metal oxide and hydroxide preforms. Demonstrations are made to CoS and NiS nanowires, nanowalls, and core-branch nanotrees on carbon cloth and nickel foam substrates. The sulfide nanoarrays exhibit superior redox reactivity for electrochemical energy storage. The self-supported CoS nanowire arrays are tested as the pseudo-capacitor cathode, which demonstrate enhanced high-rate specific capacities and better cycle life as compared to the powder counterparts. The outstanding electrochemical properties of the sulfide nanoarrays are a consequence of the preservation of the nanoarray architecture and rigid connection with the current collector after the anion exchange reactions.

  17. Hydrogen Sulfide Induced Carbon Dioxide Activation by Metal-Free Dual Catalysis. (United States)

    Kumar, Manoj; Francisco, Joseph S


    The role of metal free dual catalysis in the hydrogen sulfide (H2S)-induced activation of carbon dioxide (CO2) and subsequent decomposition of resulting monothiolcarbonic acid in the gas phase has been explored. The results suggest that substituted amines and monocarboxylic type organic or inorganic acids via dual activation mechanisms promote both activation and decomposition reactions, implying that the judicious selection of a dual catalyst is crucial to the efficient C-S bond formation via CO2 activation. Considering that our results also suggest a new mechanism for the formation of carbonyl sulfide from CO2 and H2S, these new insights may help in better understanding the coupling between the carbon and sulfur cycles in the atmospheres of Earth and Venus. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Electronic structures and water reactivity of mixed metal sulfide cluster anions. (United States)

    Saha, Arjun; Raghavachari, Krishnan


    The electronic structures and chemical reactivity of the mixed metal sulfide cluster anion (MoWS4(-)) have been investigated with density functional theory. Our study reveals the presence of two almost isoenergetic structural isomers, both containing two bridging sulfur atoms in a quartet state. However, the arrangement of the terminal sulfur atoms is different in the two isomers. In one isomer, the two metals are in the same oxidation state (each attached to one terminal S). In the second isomer, the two metals are in different oxidation states (with W in the higher oxidation state attached to both terminal S). The reactivity of water with the two lowest energy isomers has also been studied, with an emphasis on pathways leading to H2 release. The reactive behavior of the two isomers is different though the overall barriers in both systems are small. The origin of the differences are analyzed and discussed. The reaction pathways and barriers are compared with the corresponding behavior of monometallic sulfides (Mo2S4(-) and W2S4(-)) as well as mixed metal oxides (MoWO4(-)).

  19. Selectivity of layered double hydroxides and their derivative mixed metal oxides as sorbents of hydrogen sulfide. (United States)

    Othman, Mohamed A; Zahid, Waleed M; Abasaeed, Ahmed E


    In the context of finding high efficient sorbent materials for removing hydrogen sulfide (H2S) from air stream, a screening study was performed to find the best combination of metals for the synthesis of layered double hydroxides (LDHs) and their derivative mixed metal oxides. Based on selectivity of 998 natural mineral species of sulfur-containing compounds, Cu(2+), Ni(2+) and Zn(2+) were selected as divalent metals, and Fe(3+), Al(3+) and Cr(3+) as trivalent metals to synthesis the LDHs sorbents. 10 LDHs materials and their calcined mixed metal oxides, Ni(0.66)Al(0.34), Cu(0.35)Ni(0.32)Al(0.33), Zn(0.66)Al(0.34), Cu(0.36)Zn(0.32)Al(0.32), Ni(0.64)Fe(0.36), Cu(0.35)Ni(0.31)Fe(0.34), Ni(0.66)Cr(0.34), Cu(0.35)Ni(0.31)Cr(0.34), Zn(0.66)Cr(0.34), Cu(0.33)Zn(0.32)Cr(0.35) were synthesized, characterized chemically and physically, and then tested using breakthrough test to determine their sulfur uptake. Ni(0.64)Fe(0.36) mixed metal oxides was found to have the best uptake of hydrogen sulfide (136 mg H₂S/g). Regeneration of spent Ni(0.64)Fe(0.36) mixed metal oxides was studied using two different mixture solutions, NaCl/NaOH and acetate-buffer/NaCl/NaOH. The latter mixture successfully desorbed the sulfur from the Ni0.64Fe0.36 sorbent for 2 cycles of regeneration/sorption. Copyright © 2013 Elsevier B.V. All rights reserved.

  20. Lithium/metal sulfide cells and battery development progress at Eagle-Picher Industries (United States)

    Cupp, E. B.

    A program aimed at the design, development, and fabrication of lithium/metal sulfide secondary batteries with a molten-salt electrolyte that has been under way since 1975 is reviewed. The goals of the program are to develop a long-life, high-power, high-energy-density battery for electric-vehicle applications. The tasks accomplished so far are discussed with particular attention given to the development of current collectors for both FeS and FeS2 cells, separator improvements, sealing techniques, and active-material balances. The present state-of-the-art Li/MS(x) molten-salt batteries are characterized.

  1. Sahara 03505 sulfide-rich iron meteorite: Evidence for efficient segregation of sulfide-rich metallic melt during high-degree impact melting of an ordinary chondrite (United States)

    Orazio, M. D.; Folco, L.; Chaussidon, M.; Rochette, P.


    The Sahara 03505 meteorite is a 65 g sulfide-rich iron found in an undisclosed locality of the Sahara. It consists of roughly equal volumetric proportion of polycrystalline troilite (crystal size 1.5-7.5 mm) enclosing cellular/dendritic metallic Fe-Ni (width of the dendrite arms, ~100 µm). The mineral assemblage is completed by sparse skeletal crystals of chromite, abundant droplets, 5- 100 µm in size, of anhydrous Fe-, Fe-Na-, and Fe-Mn-Mg-Ca-Na-K-phosphates, tiny crystals of schreibersite, and particles of metallic Cu. The medium- to fine-grained quench texture, and cooling modeling suggest that Sahara 03505 formed through crystallization of a sulfur-rich metallic melt under rapid cooling conditions (1- 4 °C s-1). The low troilite/metallic Fe-Ni ratio (~0.6 by weight) shows that this liquid was generated at much higher temperatures (>1300 °C) with respect to the FeS-Fe,Ni cotectic liquids. Based on bulk chemistry and oxygen isotope composition of chromite, we propose that Sahara 03505 formed by extensive impact melting of an ordinary chondrite lithology, followed by the efficient segregation of the immiscible silicate and metallic liquids. The sulfur-rich metallic liquid rapidly cooled either by radiation into space as a small lump, or by conduction to a chondrite country rock as a vein intruded into the walls of an impact crater. Sahara 03505 belongs to a small group of sulfide-rich iron meteorites which are characterized by medium- to fine-grained quench textures and by bulk chemistry that is different from the other iron meteorite groups. We propose here to use the descriptive term “sulfide-irons” for this meteorite group, by analogy with the stony-irons.

  2. Fractionation of rhenium from osmium during noble metal alloy formation in association with sulfides: Implications for the interpretation of model ages in alloy-bearing magmatic rocks (United States)

    Fonseca, Raúl O. C.; Brückel, Karoline; Bragagni, Alessandro; Leitzke, Felipe P.; Speelmanns, Iris M.; Wainwright, Ashlea N.


    Although Earth's continental crust is thought to derive from melting of the Earth's mantle, how the crust has formed and the timing of its formation are not well understood. The main difficulty in understanding how the crust was extracted from the Earth's mantle is that most isotope systems recorded in mantle rocks have been disturbed by crustal recycling, metasomatic activity and dilution of the signal by mantle convection. In this regard, important age constraints can be obtained from Re-Os model ages in platinum group minerals (PGM), as Re-poor and Os-rich PGM show evidence of melting events up to 4.1 Ga. To constrain the origin of the Re-Os fractionation and Os isotope systematics of natural PGM, we have investigated the linkage between sulfide and PGM grains of variable composition via a series of high-temperature experiments carried out at 1 bar. We show that with the exception of laurite, all experimentally-produced PGM, in particular Pt3Fe (isoferroplatinum) and Pt-Ir metal grains, are systematically richer in Re than their sulfide precursors and will develop radiogenic 187Os /188Os signatures over time relative to their host base metal sulfides. Cooling of an PGM-saturated sulfide assemblage shows a tendency to amplify the extent of Re-Os fractionation between PGM and the different sulfide phases present during cooling. Conversely, laurite grains (RuS2) are shown to accept little to no Re in them and their Os isotope composition changes little over time as a result. Laurite is therefore the PGM that provides the most robust Re-depletion ages in mantle lithologies. Our results are broadly consistent with observations made on natural PGM, where laurites are systematically less radiogenic than Pt-rich PGM. These experimental results highlight the need for the acquisition of large datasets for both mantle materials and ophiolite-derived detrital grains that include measurements of the Os isotope composition of minerals rich in highly siderophile elements at

  3. Novel Metal Sulfides to Achieve Effective Capture and Durable Consolidation of Radionuclides

    Energy Technology Data Exchange (ETDEWEB)

    Kanatzidis, Mercouri [Northwestern Univ., Evanston, IL (United States); Riley, Brian [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Chun, Jaehun [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)


    This report documents the work done under NEUP grant to examine the capability of novel chalcogels and some binary metal chalcogenides as a host matrix for the capture of gaseous iodine and the feasibility of their iodine-laden materials to be converted into a permanent waste form. The presented work was conducted over last two years. A number of novel chalcogels Zn2Sn2S6, Sb4Sn4S12, NiMoS4, CoMoS4, antimony sulfide (SbSx) chalcogels, silver functionalized chalcogels and binary metal sulfides (Sb2S3) were developed and studies for their iodine absorption efficacies. A new and simple route was devised for the large scale preparation of antimony sulfide chalcogel. The chalcogel was obtained by treating Sb2S3 with Na2S in the presence of water followed by addition of formamide. The obtained gels have a low-density sponge like network of meso porous nature having BET surface area of 125 m2/g. The chalcogels, silver functionalized chalcogel and the binary metal sulfides were exposed to iodine vapors in a closed container. Silver-functionalized chalcogels and Sb2S3 powders showed iodine uptake up to 100 wt%, the highest iodine uptake of 200 wt% was observed for the SbS-III chalcogel. The PXRD patterns of iodine-laden specimens revealed that iodine shows spontaneous chemisorption to the matrix used. The iodine loaded chalcogels and the binary chalcogenides were sealed under vacuum in fused silica ampoules and heated in a temperature controlled furnace. The consolidated products were analyzed by PXRD, energy dispersive spectroscopy (EDS), UV-Vis and Raman spectroscopy. The final products were found to be amorphous in most of the cases with high amount (~4-35 wt%) of iodine and aapproximately ~60- 90 % of the absorbed iodine could be consolidated into the final waste form. Alginate

  4. Aerobic transformation of cadmium through metal sulfide biosynthesis in photosynthetic microorganisms. (United States)

    Edwards, Chad D; Beatty, Joseph C; Loiselle, Jacqueline B R; Vlassov, Katya A; Lefebvre, Daniel D


    Cadmium is a non-essential metal that is toxic because of its interference with essential metals such as iron, calcium and zinc causing numerous detrimental metabolic and cellular effects. The amount of this metal in the environment has increased dramatically since the advent of the industrial age as a result of mining activities, the use of fertilizers and sewage sludge in farming, and discharges from manufacturing activities. The metal bioremediation utility of phototrophic microbes has been demonstrated through their ability to detoxify Hg(II) into HgS under aerobic conditions. Metal sulfides are generally very insoluble and therefore, biologically unavailable. When Cd(II) was exposed to cells it was bioconverted into CdS by the green alga Chlamydomonas reinhardtii, the red alga Cyanidioschyzon merolae, and the cyanobacterium, Synechoccocus leopoliensis. Supplementation of the two eukaryotic algae with extra sulfate, but not sulfite or cysteine, increased their cadmium tolerances as well as their abilities to produce CdS, indicating an involvement of sulfate assimilation in the detoxification process. However, the combined activities of extracted serine acetyl-transferase (SAT) and O-acetylserine(thiol)lyase (OASTL) used to monitor sulfate assimilation, was not significantly elevated during cell treatments that favored sulfide biosynthesis. It is possible that the prolonged incubation of the experiments occurring over two days could have compensated for the low rates of sulfate assimilation. This was also the case for S. leopoliensis where sulfite and cysteine as well as sulfate supplementation enhanced CdS synthesis. In general, conditions that increased cadmium sulfide production also resulted in elevated cysteine desulfhydrase activities, strongly suggesting that cysteine is the direct source of sulfur for CdS synthesis. Cadmium(II) tolerance and CdS formation were significantly enhanced by sulfate supplementation, thus indicating that algae and cyanobacteria

  5. Geochemical, metagenomic and metaproteomic insights into trace metal utilization by methane-oxidizing microbial consortia in sulfidic marine sediments

    Energy Technology Data Exchange (ETDEWEB)

    Glass, DR. Jennifer [California Institute of Technology, Pasadena; Yu, DR. Hang [California Institute of Technology, Pasadena; Steele, Joshua [California Institute of Technology, Pasadena; Dawson, Katherine [California Institute of Technology, Pasadena; Sun, S [University of California, San Diego; Chourey, Karuna [ORNL; Hettich, Robert {Bob} L [ORNL; Orphan, V [California Institute of Technology, Pasadena


    Microbes have obligate requirements for trace metals in metalloenzymes that catalyze important biogeochemical reactions. In anoxic methane- and sulfide-rich environments, microbes may have unique adaptations for metal acquisition and utilization due to decreased bioavailability as a result of metal sulfide precipitation. However, micronutrient cycling is largely unexplored in cold ( 10 C) and sulfidic (>1 mM H2S) deep-sea methane seep ecosystems. We investigated trace metal geochemistry and microbial metal utilization in methane seeps offshore Oregon and California, USA, and report dissolved concentrations of nickel (0.5-270 nM), cobalt (0.5-6 nM), molybdenum (10-5,600 nM) and tungsten (0.3-8 nM) in Hydrate Ridge sediment porewaters. Despite low levels of cobalt and tungsten, metagenomic and metaproteomic data suggest that microbial consortia catalyzing anaerobic oxidation of methane utilize both scarce micronutrients in addition to nickel and molybdenum. Genetic machinery for cobalt-containing vitamin B12 biosynthesis was present in both anaerobic methanotrophic archaea (ANME) and sulfate-reducing bacteria (SRB). Proteins affiliated with the tungsten-containing form of formylmethanofuran dehydrogenase were expressed in ANME from two seep ecosystems, the first evidence for expression of a tungstoenzyme in psychrotolerant microorganisms. Finally, our data suggest that chemical speciation of metals in highly sulfidic porewaters may exert a stronger influence on microbial bioavailability than total concentration

  6. Metal Nanoparticle-Decorated Two-Dimensional Molybdenum Sulfide for Plasmonic-Enhanced Polymer Photovoltaic Devices

    Directory of Open Access Journals (Sweden)

    Ming-Kai Chuang


    Full Text Available Atomically thin two-dimensional (2D transition metal dichalcogenides have also attracted immense interest because they exhibit appealing electronic, optical and mechanical properties. In this work, we prepared gold nanoparticle-decorated molybdenum sulfide (AuNP@MoS2 through a simple spontaneous redox reaction. Transmission electron microscopy, UV-Vis spectroscopy, and Raman spectroscopy were used to characterize the properties of the AuNP@MoS2 nanomaterials. Then we employed such nanocomposites as the cathode buffer layers of organic photovoltaic devices (OPVs to trigger surface plasmonic resonance, leading to noticeable enhancements in overall device efficiencies. We attribute the primary origin of the improvement in device performance to local field enhancement induced by the effects of localized surface plasmonic resonance. Our results suggest that the metal nanoparticle-decorated two-dimensional materials appear to have great potential for use in high-performance OPVs.

  7. Damage of Metal Structures Under the Action of Hydrogen Sulfide Containing Environments (United States)

    Kushnarenko, V. M.; Uzyakov, R. N.; Repyakh, V. S.


    The effect of hydrogen sulfide containing environments, stress-strain states, stress concentration and external actions on the hydrogen sulfide cracking of steels is considered. Examples of typical and atypical action of hydrogen sulfide containing environments on carbon and stainless steels are presented. The factors responsible for hydrogen sulfide cracking are determined. Recommendations are given on design and production of equipment contacting hydrogen sulfide environments.

  8. Complex sulfides and thiosalts

    International Nuclear Information System (INIS)

    Uehlls, A.


    Different types of the structures of complex sulfides, thiosalts of alkali, alkaline earth, rare earth, transition and actinide metals are considered in the review of the papers published before 1980 and devoted to the crystal structure of complex sulfides

  9. Origin of kamacite, schreibersite, and perryite in metal-sulfide nodules of the enstatite chondrite Sahara 97072 (EH3) (United States)

    Lehner, Stephen W.; Buseck, Peter R.; McDonough, William F.


    Perryite [(Fe,Ni)x(Si,P)y], schreibersite [(Fe,Ni)3P], and kamacite (αFeNi) are constituent minerals of the metal-sulfide nodules in the Sahara 97072 (EH3) enstatite chondrite meteorite. We have measured concentrations of Ni, Cu, Ga, Au, Ir, Ru, and Pd in these minerals with laser ablation, inductively coupled plasma mass spectrometry (ICP-MS). We also measured their Fe, Ni, P, Si, and Co concentrations with electron microprobe. In kamacite, ratios of Ru/Ir, Pd/Ir, and Pd/Ru cluster around their respective CI values and all elements analyzed plot near the intersection of the equilibrium condensation trajectory versus Ni and the respective CI ratios. In schreibersite, the Pd/Ru ratio is near the CI value and perryite contains significant Cu, Ga, and Pd. We propose that schreibersite and perryite formed separately near the condensation temperatures of P and Si in a reduced gas and were incorporated into Fe-Ni alloy. Upon further cooling, sulfidation of Fe in kamacite resulted in the formation of additional perryite at the sulfide interface. Still later, transient heating re-melted this perryite near the Fe-FeS eutectic temperature during partial melting of the metal-sulfide nodules. The metal-sulfide nodules are pre-accretionary objects that retain CI ratios of most siderophile elements, although they have experienced transient heating events.

  10. Na, Rb and Cs partitioning between metal, silicate and sulfide: Implications for volatile depletion in terrestrial planets (United States)

    Boujibar, A.; Fei, Y.; Du, Z.; Righter, K.; Bullock, E. S.


    Inner Solar System materials are known for their depletion in volatile elements, including the moderately volatile alkalis: Na, K, Rb, and Cs. The origin of this depletion is still uncertain, as several processes could have been involved, during the nebular condensation or planetary accretion. Volatile depletion is commonly estimated through comparison of alkali concentrations relatively to those of chondrites, assuming they remain in planetary mantles during core segregation. However, experimental studies show that substantial K can partition into metals that are enriched in sulfur and oxygen. Several models have also suggested that sulfides may have played an important role during episodes of sulfide segregation from a crystallizing magma ocean (sulfide matte) or accretion of S-rich planetary embryos. For Mercury, a sulfide layer could be present between core and mantle, due to immiscibility between Si-rich and S-rich metals. Therefore, here we investigate whether alkali elements (Na, Cs and Rb) could be partly sequestered in planetary cores during their differentiation. We conducted experiments at high pressure and temperature (1 to 5 GPa and up to 1900 °C) to determine partition coefficients of Na, Rb and Cs between metal and silicate. Our results show that pressure, temperature, sulfur and oxygen in metals enhance the partitioning of Na, Rb and Cs into metals, as previously found for K. For all three investigated alkalis (Na, Rb and Cs), we found a maximum partition coefficient of 1 between sulfides containing 13 wt% O and silicate melt. Therefore, S-rich cores or sulfide layers formed due to immiscibility in Fe-S-O systems could have acted as important geochemical reservoirs for alkali elements. Using our experimental data and different assumptions on initial bulk abundances, we evaluate volatile depletion in terrestrial planets, by comparing resulting mantle alkali concentrations after core segregation, with actual concentrations in the Earth's mantle.

  11. Acid-volatile sulfide and simultaneously extracted metals in surface sediments of the southwestern coastal Laizhou Bay, Bohai Sea: concentrations, spatial distributions and the indication of heavy metal pollution status. (United States)

    Zhuang, Wen; Gao, Xuelu


    Surface sediments were collected from the coastal waters of southwestern Laizhou Bay and the rivers it connects with during summer and autumn 2012. The acid-volatile sulfide (AVS) and simultaneously extracted metals (SEM) were measured to assess the sediment quality. The results showed that not all sediments with [SEM]-[AVS]>0 were capable of causing toxicity because the organic carbon is also an important metal-binding phase in sediments. Suppose the sediments had not been disturbed and the criteria of US Environmental Protection Agency had been followed, heavy metals in this area had no adverse biological effects in both seasons except for few riverine samples. The major ingredient of SEM was Zn, whereas the contribution of Cd - the most toxic metal studied - to SEM was marine sediments. Copyright © 2013 Elsevier Ltd. All rights reserved.

  12. Growth and characterization of semiconducting nickel sulfide nanocrystals from air-stable single-source metal organic precursors

    Directory of Open Access Journals (Sweden)

    Sohail Saeed


    Full Text Available Three symmetrical and unsymmetrical nickel(II complexes [cis-(C3H72NC(SNC(OC6H3(3,5-NO22]2Ni(II, [cis-(C4H92NC(SNC(OC6H3(3,5-NO22]2Ni(II, and [cis-(Hex(Me2NC(SNC(O C6H3(3,5-NO22]2Ni(II were synthesized and characterized by FTIR spectroscopy, elemental analysis, and mass spectrometry. These metal complexes have been used as single-source precursors for the preparation of semiconducting nickel sulfide nanocrystals. Rapid injection of metal complexes into oleylamine at 230°C, followed by immediate cooling, led to the formation of irregular-shaped 20–170-nm nickel sulfide nanocrystals. The deposited nickel sulfide nanocrystals were characterized by X-ray powder diffraction and transmission electron microscopy.

  13. Studies of high temperature ternary phases in mixed-metal-rich early transition metal sulfide and phosphide systems

    Energy Technology Data Exchange (ETDEWEB)

    Marking, Gregory Allen [Iowa State Univ., Ames, IA (United States)


    Investigations of ternary mixed early transition metal-rich sulfide and phosphide systems resulted in the discovery of new structures and new phases. A new series of Zr and Hf - group V transition metal - sulfur K-phases was synthesized and crystallographically characterized. When the group V transition metal was Nb or Ta, the unit cell volume was larger than any previously reported K-phase. The presence of adventitious oxygen was determined in two K-phases through a combination of neutron scattering and X-ray diffraction experiments. A compound Hf10Ta3S3 was found to crystallize in a new-structure type similar to the known gamma brasses. This structure is unique in that it is the only reported "stuffed" gamma-brass type structure. The metal components, Hf and Ta, are larger in size and more electropositive than the metals found in normal gamma brasses (e.g. Cu and Zn) and because of the larger metallic radii, sulfur can be incorporated into the structure where it plays an integral role in stabilizing this phase relative to others. X-ray single-crystal, X-ray powder and neutron powder refinements were performed on this structure. A new structure was found in the ternary Nb-Zr-P system which has characteristics in common with many known early transition metal-rich sulfides, selenides, and phosphides. This structure has the simplest known interconnection of the basic building blocks known for this structural class. Anomalous scattering was a powerful tool for differentiating between Zr and Nb when using Mo Kα X-radiation. The compounds ZrNbP and HfNbP formed in the space group Prima with the simple Co2Si structure which is among the most common structures found for crystalline solid materials. Solid solution compounds in the Ta-Nb-P, Ta-Zr-P, Nb-Zr-P, Hf-Nb-P, and Hf-Zr-S systems were crystallographically characterized. The structural information corroborated ideas about bonding in metal-rich compounds.

  14. Assessing pollution in a Mediterranean lagoon using acid volatile sulfides and estimations of simultaneously extracted metals. (United States)

    Zaaboub, Noureddine; Helali, Mohamed Amine; Martins, Maria Virgínia Alves; Ennouri, Rym; Béjaoui, Béchir; da Silva, Eduardo Ferreira; El Bour, Monia; Aleya, Lotfi


    Bizerte Lagoon is a southern Mediterranean semi-enclosed lagoon with a maximum depth of 12 m. After assessing sediment quality, the authors report on the physicochemical characteristics of the lagoon's surface sediment using SEM (simultaneously extracted metals) and AVS (acid volatile sulfides) as proxies. Biogeochemical tools are used to investigate the environmental disturbance at the water-sediment interface by means of SEM and AVS to seek conclusions concerning the study area's pollution status. Results confirm accumulation of trace elements in sediment. The use of the SEM-AVS model with organic matter in sediment (ƒOC) confirms possible bioavailability of accumulated trace elements, especially Zn, in the southern part of the lagoon, with organic matter playing an important role in SEM excess correction to affirm a nontoxic total metal sediment state. Individual trace element toxicity is dependent on the bioavailable fraction of SEM Metal on sediment, as is the influence of lagoon inflow from southern water sources on element bioavailability. Appropriate management strategies are highly recommended to mitigate any potential harmful effects on health from this heavy-metal-based pollution.

  15. Multiplexed electrochemical immunoassay of biomarkers using metal sulfide quantum dot nanolabels and trifunctionalized magnetic beads. (United States)

    Tang, Dianping; Hou, Li; Niessner, Reinhard; Xu, Mingdi; Gao, Zhuangqiang; Knopp, Dietmar


    A novel multiplexed stripping voltammetric immunoassay protocol was designed for the simultaneous detection of multiple biomarkers (CA 125, CA 15-3, and CA 19-9 used as models) using PAMAM dendrimer-metal sulfide quantum dot (QD) nanolabels as distinguishable signal tags and trifunctionalized magnetic beads as an immunosensing probe. The probe was prepared by means of co-immobilization of primary monoclonal anti-CA 125, anti-CA 15-3 and anti-CA 19-9 antibodies on a single magnetic bead. The PAMAM dendrimer-metal sulfide QD nanolabels containing CdS, ZnS and PbS were synthesized by using in situ synthesis method, which were utilized for the labeling of polyclonal rabbit anti-CA 125, anti-CA 15-3 and anti-CA 19-9 detection antibodies, respectively. A sandwich-type immunoassay format was adopted for the simultaneous determination of target biomarkers in a low-binding microtiter plate. The subsequent anodic stripping voltammetric analysis of cadmium, zinc, and lead components released by acid from the corresponding QD nanolabels was conducted at an in situ prepared mercury film electrode based on the difference of peak potentials. Experimental results indicated that the multiplexed immunoassay enabled the simultaneous detection of three cancer biomarkers in a single run with wide dynamic ranges of 0.01-50 U mL(-1) and detection limits (LODs) of 0.005 U mL(-1). Intra-assay and inter-assay coefficients of variation (CVs) were less than 7.2% and 10.4%, respectively. No significant differences at the 0.05 significance level were encountered in the analysis of 10 clinical serum specimens between the multiplexed immunoassay and a commercially available enzyme-linked immunosorbent assay (ELISA). Copyright © 2013 Elsevier B.V. All rights reserved.

  16. Solvent-Free Synthesis of Quaternary Metal Sulfide Nanoparticles Derived from Thiourea

    KAUST Repository

    Bhunia, Manas Kumar


    The synthesis of metal sulfide (MS) materials with sizes in the sub-10 nm regime often requires capping agents with long hydrocarbon chains that affect their structures and properties. Herein, this study presents a molten-state synthesis method for a series of transition-MS nanoparticles using thiourea as a reactive precursor without capping agents. This study also reports the synthesis of MS with single metals (Fe, Co, Ni, Cu, and Zn) and quaternary CuGa2In3S8 using the same synthesis protocol. Thiourea first melts to form a molten-state condition to serve as the reaction medium at a relatively low temperature (<200 °C), followed by its thermal decomposition to induce a reaction with the metal precursor to form different MS. This synthesis protocol, owing to its dynamic characteristics, involves the formation of a variety of organic carbon nitride polymeric complexes around the MS particles. Dynamic nuclear polarization surface-enhanced nuclear magnetic resonance spectroscopy is effective to identify the polymeric compositions and structures as well as their interactions with the MS. These results provided thorough structural descriptions of the MS nanoparticles surrounded by the carbon nitride species derived from thiourea, which may find various applications, including photocatalytic water splitting.

  17. Metal-adeninate vertices for the construction of an exceptionally porous metal-organic framework. (United States)

    An, Jihyun; Farha, Omar K; Hupp, Joseph T; Pohl, Ehmke; Yeh, Joanne I; Rosi, Nathaniel L


    Metal-organic frameworks comprising metal-carboxylate cluster vertices and long, branched organic linkers are the most porous materials known, and therefore have attracted tremendous attention for many applications, including gas storage, separations, catalysis and drug delivery. To increase metal-organic framework porosity, the size and complexity of linkers has increased. Here we present a promising alternative strategy for constructing mesoporous metal-organic frameworks that addresses the size of the vertex rather than the length of the organic linker. This approach uses large metal-biomolecule clusters, in particular zinc-adeninate building units, as vertices to construct bio-MOF-100, an exclusively mesoporous metal-organic framework. Bio-MOF-100 exhibits a high surface area (4,300 m(2) g(-1)), one of the lowest crystal densities (0.302 g cm(-3)) and the largest metal-organic framework pore volume reported to date (4.3 cm(3) g(-1)).

  18. Exceptional function of nanoporous metal organic framework particles in emulsion stabilisation. (United States)

    Xiao, Bo; Yuan, Qingchun; Williams, Richard A


    A new concept of nanoporous metal organic framework particles stabilising emulsions was investigated. The copper benzenetricarboxylate MOF particles adsorbed at the oil/water interface play an exceptional role in stabilising both oil-in-water and water-in-oil emulsions.

  19. Photocatalytic properties of zinc sulfide nanocrystals biofabricated by metal-reducing bacterium Shewanella oneidensis MR-1

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Xiang [School of The Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013 (China); State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Ma, Xiao-Bo [School of The Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013 (China); Yuan, Hang [Key Laboratory of Ion Beam Bioengineering, Institute of Technical Biology & Agriculture Engineering, Chinese Academy of Sciences, Hefei 230031 (China); Liu, Peng-Cheng; Lei, Yu-Bin; Xu, Hui [School of The Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013 (China); Du, Dao-Lin, E-mail: [School of The Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013 (China); State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China); Sun, Jian-Fan [School of The Environment and Safety Engineering, Jiangsu University, Zhenjiang 212013 (China); Feng, Yu-Jie, E-mail: [State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150090 (China)


    Highlights: • S. oneidensis MR-1 biofabricated ZnS nanocrystals using artificial wastewater. • ZnS nanocrystals were 5 nm in diameter and aggregated extracellularly. • ZnS had good catalytic activity in the degradation of RHB under UV irradiation. • Photogenerated holes mainly contributed to the degradation of RhB. - Abstract: Accumulation and utilization of heavy metals from wastewater by biological treatment system has aroused great interest. In the present study, a metal-reducing bacterium Shewanella oneidensis MR-1 was used to explore the biofabrication of ZnS nanocrystals from the artificial wastewater. The biogenic H{sub 2}S produced via the reduction of thiosulfate precipitated the Zn(II) as sulfide extracellularly. Characterization by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), and field emission scanning electron microscope (FESEM) confirmed the precipitates as ZnS nanocrystals. The biogenic ZnS nanocrystals appeared spherical in shape with an average diameter of 5 nm and mainly aggregated in the medium and cell surface of S. oneidensis MR-1. UV–vis DRS spectra showed ZnS nanoparticles appeared a strong absorption below 360 nm. Thus, the photocatalytic activity of ZnS was evaluated by the photodegradation of rhodamine B (RhB) under UV irradiation. The biogenic ZnS nanocrystals showed a high level of photodegradation efficiency to RhB coupled with a significant blue-shift of maximum adsorption peak. A detailed analysis indicated the photogenerated holes, rather than hydroxyl radicals, contributed to the photocatalytic decolorization of RhB. This approach of coupling biosynthesis of nanoparticles with heavy metal removal may offer a potential avenue for efficient bioremediation of heavy metal wastewater.

  20. Photocatalytic properties of zinc sulfide nanocrystals biofabricated by metal-reducing bacterium Shewanella oneidensis MR-1

    International Nuclear Information System (INIS)

    Xiao, Xiang; Ma, Xiao-Bo; Yuan, Hang; Liu, Peng-Cheng; Lei, Yu-Bin; Xu, Hui; Du, Dao-Lin; Sun, Jian-Fan; Feng, Yu-Jie


    Highlights: • S. oneidensis MR-1 biofabricated ZnS nanocrystals using artificial wastewater. • ZnS nanocrystals were 5 nm in diameter and aggregated extracellularly. • ZnS had good catalytic activity in the degradation of RHB under UV irradiation. • Photogenerated holes mainly contributed to the degradation of RhB. - Abstract: Accumulation and utilization of heavy metals from wastewater by biological treatment system has aroused great interest. In the present study, a metal-reducing bacterium Shewanella oneidensis MR-1 was used to explore the biofabrication of ZnS nanocrystals from the artificial wastewater. The biogenic H 2 S produced via the reduction of thiosulfate precipitated the Zn(II) as sulfide extracellularly. Characterization by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), and field emission scanning electron microscope (FESEM) confirmed the precipitates as ZnS nanocrystals. The biogenic ZnS nanocrystals appeared spherical in shape with an average diameter of 5 nm and mainly aggregated in the medium and cell surface of S. oneidensis MR-1. UV–vis DRS spectra showed ZnS nanoparticles appeared a strong absorption below 360 nm. Thus, the photocatalytic activity of ZnS was evaluated by the photodegradation of rhodamine B (RhB) under UV irradiation. The biogenic ZnS nanocrystals showed a high level of photodegradation efficiency to RhB coupled with a significant blue-shift of maximum adsorption peak. A detailed analysis indicated the photogenerated holes, rather than hydroxyl radicals, contributed to the photocatalytic decolorization of RhB. This approach of coupling biosynthesis of nanoparticles with heavy metal removal may offer a potential avenue for efficient bioremediation of heavy metal wastewater

  1. The removal of hydrogen sulfide from gas streams using an aqueous metal sulfate absorbent : Part I. the absorption of hydrogen sulfide in metal sulfate solutions

    NARCIS (Netherlands)

    Ter Maat, H.; Hogendoorn, J. A.; Versteeg, G. F.


    The desulfurization of gas streams using aqueous iron(II)sulfate (Fe(II)SO4), zinc sulfate (ZnSO4) and copper sulfate (CuSO4) solutions as washing liquor is studied theoretically and experimentally. The desulfurization is accomplished by a precipitation reaction that occurs when sulfide ions and

  2. Synthesis and Characterization of Metal Sulfides Nanoparticles/Poly(methyl methacrylate Nanocomposites

    Directory of Open Access Journals (Sweden)

    Peter A. Ajibade


    Full Text Available Metal sulfides nanoparticles in poly(methyl methacrylate matrices were prepared and characterized by infrared spectroscopy, thermogravimetric analysis, powder X-ray diffraction, scanning electron microscope (SEM, and transmission electron microscope (TEM. The FTIR confirms the dispersion of the nanoparticles in PMMA matrices with the C=O and C–O–C bonds of the PMMA shifting slightly which may be attributed to the interactions between the nanoparticles and PMMA. The ZnS nanoparticles in PMMA have average crystallite sizes of 4–7 nm while the CdS has particle size of 10 nm and HgS has crystallite sizes of 8–20 nm. The increasing order of particle sizes as calculated from the XRD is ZnS/PMMA

  3. Rapid microwave-assisted preparation of binary and ternary transition metal sulfide compounds

    Energy Technology Data Exchange (ETDEWEB)

    Butala, Megan M.; Perez, Minue A.; Arnon, Shiri; Göbel, Claudia; Preefer, Molleigh B.; Seshadri, Ram


    Transition metal chalcogenides are of interest for energy applications, including energy generation in photoelectrochemical cells and as electrodes for next-generation electrochemical energy storage. Synthetic routes for such chalcogenides typically involve extended heating at elevated temperatures for multiple weeks. We demonstrate here the feasibility of rapidly preparing select sulfide compounds in a matter of minutes, rather than weeks, using microwave-assisted heating in domestic microwaves. We report the preparations of phase pure FeS2, CoS2, and solid solutions thereof from the elements with only 40 min of heating. Conventional furnace and rapid microwave preparations of CuTi2S4 both result in a majority of the targeted phase, even with the significantly shorter heating time of 40 min for microwave methods relative to 12 days using a conventional furnace. The preparations we describe for these compounds can be extended to related structures and chemistries and thus enable rapid screening of the properties and performance of various compositions of interest for electronic, optical, and electrochemical applications.


    Directory of Open Access Journals (Sweden)

    Khoirina Dwi Nugrahaningtyas


    Full Text Available The two-new catalysts had been prepared by using the impregnation method according to Nugrahaningtyas [6] and Li [4]. One catalyst is of Nickel (Ni, supported on Ultra Stable Zeolite Y (USY, whereas the other one is NiMo supported on same supporting agent. These new catalysts are expected to be more effective when applied on the hydrotreatment reaction in standpoint of its capabilities on removing the unwanted-heteroatom. Characterization those two types of catalysts then carried out by using the criteria of acidity, porosity and, metal content. The result shows that these non-sulfide catalysts have several good characters that supporting their usefulness in hydrotreatment-catalytic reaction. In addition, catalyst NiMo/USY - 1 performs many ideal criteria as the best functional catalyst.   Keywords: Non-sulfided Catalyst, hydro-treating, preparation, characterization

  5. Diffused vs. Focused Flow - Metaproteogenomic Insights into Effects of Hydrothermal Fluid Flow on Metal-Sulfide Chimney Colonizing Biofilms (United States)

    Pjevac, P.; Markert, S.; Richter, M.; Gruber-Vodicka, H.; Schweder, T.; Amann, R.; Meyerdierks, A.


    At many sites of hydrothermal discharge in the deep-sea, the deposition of metal sulfides from hydrothermal fluids leads to the formation of geological structures known as hydrothermal chimneys. The mixing of reduced hydrothermal fluids with oxygenated seawater leads to the formation of steep redox gradients within the chimney walls. These gradients facilitate the co-existence of metabolically diverse microorganisms in the narrow habitable zone of hydrothermal chimney walls. However, the overall composition of chimney-associated microbial community is usually of low complexity and represents an environment suitable for metaomic-based studies. We used metagenomic and metaproteomic tools to compare microbial communities colonizing two metal-sulfide chimneys from the Manus Basin back-arc spreading center in the Bismarck Sea off Papua New Guinea. These chimneys were supplied by the same source hydrothermal fluids, but exhibited different fluid flow regimes. One chimney (RMR5) had a focused venting edifice, while the other (RMR-D) displayed diffuse fluid efflux on its entire outer surface. Although the microbial diversity of both chimneys is similar and dominated by mesophilic Epsilonproteobacteria, our results indicate a strong structuring effect of hydrothermal fluid flow regime on chimney-associated biofilms. The microbial community composition indicates a homogeneous colonization of the diffuse chimney walls. In contrast, the walls of the focused venting chimney appear to be colonized in layers reflecting different temperature tolerances of the dominant microorganisms. Sulfide-oxidation is likely the key metabolism in both chimneys, which is in line with the high sulfide content of the source hydrothermal fluid. However, preliminary metaproteome analysis indicates high activity of low-abundant methanotrophic Bacteria in the diffuser chimney walls. This finding is particularly interesting in light of the very low methane content of the source hydrothermal fluid

  6. Metal-free catalytic oxidation of sulfides to sulfoxides with ammonium nitrate, ammonium hydrogen sulfate and ammonium bromide as catalyst


    Ghorbani-Choghamarani, Arash; Zolfigol, Mohammad Ali; Ayazi-Nasrabadi, Roia


    A general and metal-free catalytic oxidation of aliphatic and aromatic sulfides to their corresponding sulfoxides via combination of ammonium nitrate (NH4NO3), supported ammonium hydrogen sulfate on silica gel (NH4HSO4-SiO2) and a catalytic amount of ammonium bromide (NH4Br) in the presence of wet SiO2 (50%, w/w) has been investigated. The reactions were carried out heterogeneously and selectively in short reaction times in CH2Cl2 at room temperature. This protocol is mild and efficient compa...

  7. Exceptional CO2 working capacity in a heterodiamine-grafted metal-organic framework. (United States)

    Lee, Woo Ram; Jo, Hyuna; Yang, Li-Ming; Lee, Hanyeong; Ryu, Dae Won; Lim, Kwang Soo; Song, Jeong Hwa; Min, Da Young; Han, Sang Soo; Seo, Jeong Gil; Park, Yong Ki; Moon, Dohyun; Hong, Chang Seop


    An amine-functionalized metal-organic framework (MOF), dmen-Mg 2 (dobpdc) (dmen = N , N -dimethylethylenediamine), which contains a heterodiamine with both primary and tertiary amines, was prepared via a post-synthetic method. This material exhibits a significant selectivity factor for CO 2 over N 2 that is commensurate with top-performing MOFs. It is remarkable that the solid is fully regenerated under vacuum or flowing Ar at low desorption temperatures, and following this can take up CO 2 at more than 13 wt%. An exceptionally high working capacity is achieved at low regeneration temperatures and after exposure to humid conditions, which are important parameters for a real post-combustion CO 2 capture process.

  8. Risk assessment of heavy metals in Vembanad Lake sediments (south-west coast of India), based on acid-volatile sulfide (AVS)-simultaneously extracted metal (SEM) approach. (United States)

    Shyleshchandran, Mohanachandran Nair; Mohan, Mahesh; Ramasamy, Eswara Venkatesaperumal


    Contamination of estuarine system due to heavy metals is a severe issue in tropical countries, especially in India. For the evaluation of the risk due to heavy metals, the current study assessed spatial and temporal variation of acid-volatile sulfide (AVS), simultaneously extracted metal (SEM), and total metal concentration as toxicity indicator of aquatic sediments in Vembanad Lake System (VLS), India. Surface sediment samples collected from 12 locations from the northern portion of VLS for 4 years during different seasons. The results suggest, in post-monsoon season, 91% of the sampling locations possessed high bioavailability of metals and results in toxicity to aquatic biota. The average seasonal distribution of SEM during the period of observations was in the order post-monsoon > pre-monsoon > monsoon (1.76 ± 2.00 > 1.35 ± 0.60 > 0.80 ± 0.54 μmol/g). The concentration of individual metals on ∑SEM are in the order SEM Zn > SEM Cu> SEM Cd ≈ SEM Pb > SEM Hg. Considering annual ΣSEM/AVS ratio, 83% of the sites cross the critical value of 'One,' reveals that active sulfide phase of the sediment for fixing the metals is saturated. The molar ratio (differences between SEM and AVS) and its normalized organic carbon ratio reveals that in the post-monsoon season, about 42% of the sites are in the category of adverse effects are possible. The study suggests the toxicity and mobility of the metals largely depend on the available AVS, and the current situation may pose harm to benthic organisms.

  9. Clean thermal decomposition of tertiary-alkyl metal thiolates to metal sulfides: environmentally-benign, non-polar inks for solution-processed chalcopyrite solar cells (United States)

    Heo, Jungwoo; Kim, Gi-Hwan; Jeong, Jaeki; Yoon, Yung Jin; Seo, Jung Hwa; Walker, Bright; Kim, Jin Young


    We report the preparation of Cu2S, In2S3, CuInS2 and Cu(In,Ga)S2 semiconducting films via the spin coating and annealing of soluble tertiary-alkyl thiolate complexes. The thiolate compounds are readily prepared via the reaction of metal bases and tertiary-alkyl thiols. The thiolate complexes are soluble in common organic solvents and can be solution processed by spin coating to yield thin films. Upon thermal annealing in the range of 200-400 °C, the tertiary-alkyl thiolates decompose cleanly to yield volatile dialkyl sulfides and metal sulfide films which are free of organic residue. Analysis of the reaction byproducts strongly suggests that the decomposition proceeds via an SN1 mechanism. The composition of the films can be controlled by adjusting the amount of each metal thiolate used in the precursor solution yielding bandgaps in the range of 1.2 to 3.3 eV. The films form functioning p-n junctions when deposited in contact with CdS films prepared by the same method. Functioning solar cells are observed when such p-n junctions are prepared on transparent conducting substrates and finished by depositing electrodes with appropriate work functions. This method enables the fabrication of metal chalcogenide films on a large scale via a simple and chemically clear process.

  10. Composition Directed Generation of Reactive Oxygen Species in Irradiated Mixed Metal Sulfides Correlated with Their Photocatalytic Activities. (United States)

    He, Weiwei; Jia, Huimin; Yang, Dongfang; Xiao, Pin; Fan, Xiaoli; Zheng, Zhi; Kim, Hyun-Kyung; Wamer, Wayne G; Yin, Jun-Jie


    The ability of nanostructures to facilitate the generation of reactive oxygen species and charge carriers underlies many of their chemical and biological activities. Elucidating which factors are essential and how these influence the production of various active intermediates is fundamental to understanding potential applications of these nanostructures, as well as potential risks. Using electron spin resonance spectroscopy coupled with spin trapping and spin labeling techniques, we assessed 3 mixed metal sulfides of varying compositions for their abilities to generate reactive oxygen species, photogenerate electrons, and consume oxygen during photoirradiation. We found these irradiated mixed metal sulfides exhibited composition dependent generation of ROS: ZnIn2S4 can generate (•)OH, O2(-•) and (1)O2; CdIn2S4 can produce O2(-•) and (1)O2, while AgInS2 only produces O2(-•). Our characterizations of the reactivity of the photogenerated electrons and consumption of dissolved oxygen, performed using spin labeling, showed the same trend in activity: ZnIn2S4 > CdIn2S4 > AgInS2. These intrinsic abilities to generate ROS and the reactivity of charge carriers correlated closely with the photocatalytic degradation and photoassisted antibacterial activities of these nanomaterials.

  11. Dual Roles of Protein as a Template and a Sulfur Provider: A General Approach to Metal Sulfides for Efficient Photothermal Therapy of Cancer. (United States)

    Sheng, Jianping; Wang, Liqiang; Han, Yajing; Chen, Wansong; Liu, Hong; Zhang, Min; Deng, Liu; Liu, You-Nian


    Fabrication of clinically translatable nanoparticles (NPs) as photothermal therapy (PTT) agents against cancer is becoming increasingly desirable, but still challenging, especially in facile and controllable synthesis of biocompatible NPs with high photothermal efficiency. A new strategy which uses protein as both a template and a sulfur provider is proposed for facile, cost-effective, and large-scale construction of biocompatible metal sulfide NPs with controlled structure and high photothermal efficiency. Upon mixing proteins and metal ions under alkaline conditions, the metal ions can be rapidly coordinated via a biuret-reaction like process. In the presence of alkali, the inert disulfide bonds of S-rich proteins can be activated to react with metal ions and generate metal sulfide NPs under gentle conditions. As a template, the protein can confine and regulate the nucleation and growth of the metal sulfide NPs within the protein formed cavities. Thus, the obtained metal sulfides such as Ag 2 S, Bi 2 S 3 , CdS, and CuS NPs are all with small size and coated with proteins, affording them biocompatible surfaces. As a model material, CuS NPs are evaluated as a PTT agent for cancer treatment. They exhibit high photothermal efficiency, high stability, water solubility, and good biocompatibility, making them an excellent PTT agent against tumors. This work paves a new avenue toward the synthesis of structure-controlled and biocompatible metal sulfide NPs, which can find wide applications in biomedical fields. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Bioavailability assessment of toxic metals using the technique "acid-volatile sulfide (AVS)-simultaneously extracted metals (SEM)" in marine sediments collected in Todos os Santos Bay, Brazil. (United States)

    Silva, Jucelino B; Nascimento, Rodrigo A; de Oliva, Sergio T; de Oliveira, Olívia M C; Ferreira, Sergio L C


    This paper reports the bioavailability of the metals (cadmium, copper, zinc, lead, and nickel) in sediment samples collected in seven stations from the São Paulo Estuary, Todos os Santos Bay, Brazil. The bioavailability was determined by employing the technique "acid-volatile sulfide (AVS) and simultaneously extracted metal (SEM)". The elements cadmium, copper, lead, and zinc were determined using differential pulse anodic stripping voltammetry (DPASV), while nickel was quantified utilizing electrothermal atomic absorption spectrometry (ET AAS). The accuracy of these methods was confirmed using a certified reference material of estuarine sediment (NIST 1646). The sulfide was quantified using potentiometry with selective electrode and the organic matter determination employing an indirect volumetric method using potassium dichromate and iron(II) sulfate solutions. The bioavailability of the metals was estimated by relationship between the concentration of AVS and the sum of the concentrations of the simultaneously extracted metals (ΣSEM), considering a significant toxicity when (ΣSEM)/(AVS) is higher than 1. The bioavailability values in the seven stations studied varied from 0.93 to 1.31 (June, 2014) and from 0.34 to 0.58 (September, 2014). These results demonstrated a critical condition of toxicity (bioavailability >1) in six of the seven sediment samples collected during the rainy season (June, 2014). In the other period (September, 2014), the bioavailability was always lower than 1 for all sediment samples collected in the seven stations. The individual values of the concentrations of the five metals were compared with the parameters PEL (probable effects level) and TEL (threshold effects level), which are commonly employed for characterization of ecological risk in environmental systems. This comparison revealed that all metals have concentrations lower than the PEL and only zinc and lead in some stations have contents higher than the TEL. The

  13. Mesoporous Metal-Organic Frameworks with Exceptionally High Working Capacities for Adsorption Heat Transformation. (United States)

    Mo, Zong-Wen; Zhou, Hao-Long; Zhou, Dong-Dong; Lin, Rui-Biao; Liao, Pei-Qin; He, Chun-Ting; Zhang, Wei-Xiong; Chen, Xiao-Ming; Zhang, Jie-Peng


    Pore size is one of the most important parameters of adsorbents, and mesoporous materials have received intense attention for large guests. Here, a series of mesoporous coordination polymers underlying a new framework prototype for fast expansion of pore size is reported and the profound effect of pore size on adsorption heat transformation is demonstrated. Three isostructural honeycomb-like frameworks are designed and synthesized by combining ditopic linear metal oxalate chains and triangular tris-pyridine ligands. Changing the ligand bridging length from 5.5 to 8.6 and 9.9 Å gives rise to effective pore diameter from 20 to 33 and 37 Å, surface area from 2096 to 2630 and 2749 m 2 g -1 , and pore volume from 1.19 to 1.93 and 2.36 cm 3 g -1 , respectively. By virtue of the unique and tunable isotherm shape of mesopores, exceptionally large working capacity up to 1.19 g g -1 or 0.38 g cm -3 for adsorption heat transformation can be achieved using R-134a (1,1,1,2-tetrafluroethane) as a working fluid. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. Integrated process using non-stoichiometric sulfides or oxides of potassium for making less active metals and hydrocarbons

    International Nuclear Information System (INIS)

    Swanson, R.


    Disclosed is a combinative integrated chemical process using inorganic reactants and yielding, if desired, organic products. The process involves first the production of elemental potassium by the thermal or thermal-reduced pressure decomposition of potassium oxide or potassium sulfide and distillation of the potassium. This elemental potassium is then used to reduce ores or ore concentrates of copper, zinc, lead, magnesium, cadmium, iron, arsenic, antimony or silver to yield one or more of these less active metals in elemental form. Process potassium can also be used to produce hydrogen by reaction with water or potassium hydroxide. This hydrogen is reacted with potassium to produce potassium hydride. Heating the latter with carbon produces potassium acetylide which forms acetylene when treated with water. Acetylene is hydrogenated to ethene or ethane with process hydrogen. Using Wurtz-Fittig reaction conditions, the ethane can be upgraded to a mixture of hydrocarbons boiling in the fuel range

  15. The dynamics of the laser-induced metal-semiconductor phase transition of samarium sulfide (SmS)

    International Nuclear Information System (INIS)

    Kaempfer, Tino


    The present thesis is dedicated to the experimental study of the metal-semiconductor phase transition of samarium sulfide (SmS): Temperature- and time-resolved experiments on the characterization of the phase transition of mixed-valence SmS samples (M-SmS) are presented. The measurement of the dynamics of the laser-induced phase transition pursues via time-resolved ultrashort-time microscopy and by X-ray diffraction with sub-picosecond time resolution. The electronic and structural processes, which follow an excitation of M-SmS with infrared femtosecond laser pulses, are physically interpreted on the base of the results obtained in this thesis and model imaginations. [de

  16. Metallic Iron-Nickel Sulfide Ultrathin Nanosheets As a Highly Active Electrocatalyst for Hydrogen Evolution Reaction in Acidic Media. (United States)

    Long, Xia; Li, Guixia; Wang, Zilong; Zhu, HouYu; Zhang, Teng; Xiao, Shuang; Guo, Wenyue; Yang, Shihe


    We report on the synthesis of iron-nickel sulfide (INS) ultrathin nanosheets by topotactic conversion from a hydroxide precursor. The INS nanosheets exhibit excellent activity and stability in strong acidic solutions as a hydrogen evolution reaction (HER) catalyst, lending an attractive alternative to the Pt catalyst. The metallic α-INS nanosheets show an even lower overpotential of 105 mV at 10 mA/cm(2) and a smaller Tafel slope of 40 mV/dec. With the help of DFT calculations, the high specific surface area, facile ion transport and charge transfer, abundant electrochemical active sites, suitable H(+) adsorption, and H2 formation kinetics and energetics are proposed to contribute to the high activity of the INS ultrathin nanosheets toward HER.

  17. Microkinetic interpretation of HDS/HYDO selectivity of the transformation of a model FCC gasoline over transition metal sulfides

    Energy Technology Data Exchange (ETDEWEB)

    Daudin, A. [UMR CNRS 6503, Catalyse en Chimie Organique, Universite de Poitiers, Faculte des Sciences Fondamentales et Appliquees, 40 Avenue du Recteur Pineau, 86022 Poitiers Cedex (France); IFP-Lyon, Direction Catalyse et Separation, BP 3, 69390 Vernaison (France); Lamic, A.F.; Perot, G.; Brunet, S. [UMR CNRS 6503, Catalyse en Chimie Organique, Universite de Poitiers, Faculte des Sciences Fondamentales et Appliquees, 40 Avenue du Recteur Pineau, 86022 Poitiers Cedex (France); Raybaud, P. [IFP, Direction Chimie et Physico-Chimie Appliquees, 1-4 Av. de Bois Preau, 92858 Rueil Malmaison (France); IFP-Lyon, Direction Catalyse et Separation, BP 3, 69390 Vernaison (France); Bouchy, C. [IFP-Lyon, Direction Catalyse et Separation, BP 3, 69390 Vernaison (France)


    The conversion of a model FCC gasoline (composed of 2-methylthiophene (2MT), 2,3-dimethylbut-2-ene (23DMDB2N) and orthoxylene in n-heptane) under realistic hydrodesulfurization (HDS) conditions was investigated over a series of transition monometallic sulfides (Ni{sub 3}S{sub 2}, PdS, Co{sub 9}S{sub 8}, Rh{sub 2}S{sub 3}, RuS{sub 2}, PtS and MoS{sub 2}) and unsupported transition bimetallic sulfide catalysts (NiMoS and CoMoS). The results reveal for the first time that a volcano curve relationship exists between the ab initio calculated sulfur-metal bond energy, E(MS), descriptor of bulk TMS and their activities in olefin hydrogenation and in alkylthiophene desulfurization measured simultaneously. In particular, Rh{sub 2}S{sub 3} with an intermediate sulfur-metal bond energy of 119 kJ/mol is the most active catalyst in both case hydrogenation of the olefin and in HDS of a sulfur compound. Furthermore, the HDS/HYDO selectivity which is the most important parameter in the deep HDS of gasoline, presents a maximum for the NiMoS catalyst with E(MS) of 128 kJ/mol. A microkinetic model based on Broensted-Evans-Polanyi relationships and the competitive adsorption of the sulfur molecule and alkene on the catalytic site is proposed to give a rational interpretation of the experimental catalytic results. (author)

  18. Magmatic Hydrothermal Fluids: Experimental Constraints on the Role of Magmatic Sulfide Crystallization and Other Early Magmatic Processes in Moderating the Metal Content of Ore-Forming Fluids (United States)

    Piccoli, P. M.; Candela, P. A.


    It has been recognized for some time that sulfide phases, although common in intermediate-felsic volcanic rocks, are not as common in their plutonic equivalents. That sulfide crystallization, or the lack thereof, is important in the protracted magmatic history of porphyry Cu and related systems is supported by the work of e.g., Rowins (2000). Candela and Holland (1986) suggested that sulfide crystallization could moderate the ore metal concentrations in porphyry environments. Experiments show clearly that Au and Cu can partition into Cl-bearing vapor and brine. This effect can be enhanced by S (Simon, this session). However, in some instances enhances this effect. That is, the partitioning of Au and Cu into vapor+brine is highly efficient (e.g. Simon et al. 2003; Frank et al 2003). This suggests that if sulfides do not sequester ore metals early during the history of a magma body from the melt, they will partition strongly into the volatile phases. Whether volatile release occurs in the porphyry ore environment, or at deeper levels upon magma rise, is a yet unsolved question. Little is known about deep release of volatiles (during magma transport at lower- to mid-crustal levels). Saturation of melts with a CO2-bearing fluid could happen at levels much deeper than those typical of ore formation. CO2 is released preferentially, so a high CO2 concentration in fluids in the porphyry ore environment argues against deep fluid release. Of course, this depends upon the specific processes of crystallization and fluid release, which may be complex. Our experiments on sulfides have concentrated on pyrrhotite and Iss. Our partitioning data for Po/melt exhibit wide variations from metal to metal: Cu (2600); Co (170); Au (140); Ni (100); Bi, Zn and Mn (2). These results suggest that crystallization of Po can contribute to variable ore metal ratios (e.g. Cu/Au). Other sulfides behave differently. If a melt is Iss (Cpy) saturated, then Cu will be buffered at a high value, and Au

  19. Electrosprayed Metal Oxide Semiconductor Films for Sensitive and Selective Detection of Hydrogen Sulfide

    NARCIS (Netherlands)

    Ghimbeu, C.M.; Lumbreras, M.; Schoonman, J.; Siadat, M.


    Semiconductor metal oxide films of copper-doped tin oxide (Cu-SnO2), tungsten oxide (WO3) and indium oxide (In2O3) were deposited on a platinum coated alumina substrate employing the electrostatic spray deposition technique (ESD). The morphology studied with scanning electron microscopy (SEM) and

  20. Metal recovery by bioleaching of sulfidic mining wastes — Application to a European case study (United States)

    Guézennec, A. G.; Jacob, J.; Joulian, C.; Dupraz, S.; Menard, Y.; d'Hugues, P.

    The non-energy extractive industry (NEEI) of the EU-25 generated a direct turnover of about €40 billion, and provided employment to about 250000 people in 16629 companies in 2004. The use of primary raw materials in the production of other branches of EU industry means they have a central role in guaranteeing industrial and economic sustainability. Nevertheless current demand exceeds production, and so the EU is heavily dependent on minerals and metals imports. In this context of securing access to metals, turning mining wastes into new resources of currently unexploited valuable metals is an important challenge. The mining wastes can contain base and precious metals, but also metalloids and rare earth elements that are nowadays considered as highly critical for the industrial development of the European Union. Nevertheless, the development of alternative routes to conventional processing is still required in order to decrease the cost associated to the treatment of these unconventional resources which are more complex in composition and with lower grades.

  1. Structural study of high temperature metal-rich titanium sulfide phases

    Energy Technology Data Exchange (ETDEWEB)

    Owens, J.P.


    Ti/sub 2/S and Ti/sub 8/S/sub 3/ have been prepared by high temperature annealing techniques. The crystal structures of these two phases have been determined from single crystal x-ray diffraction data. Both structures were refined using a full-matrix least-squares treatment of positional parameters and isotropic temperature factor coefficients. Ti/sub 2/S crystallizes with orthorhombic symmetry, space group Pnnm, having unit cell dimensions a = 11.367A, b= 14.060A, and c = 3.326A. Ti/sub 2/S is isostructural with Ta/sub 2/P. Ti/sub 8/S/sub 3/ crystallizes with monoclinic symmetry, space group C2/m, a = 32.69A, b = 3.327A, c = 19.35A, ..beta.. = 139.9/sup 0/ (b - unique). Ti/sub 2/S and Ti/sub 8/S/sub 3/ have structural features similar to the features of a large number of metal-rich transition-metal chalcogenides and pnictides. These various structure types have been characterized in terms of nonmetal trigonal prismatic coordination polyhedra, eight different metal partial coordination polyhedra, a short (approximately equal to 3.4A) crystallographic axis, two unique layers of atoms containing both metal and nonmetal atom positions, and mirror planes coincident with the two layers of atom positions. The existence of a variety of structures with these structural features has led to their consideration as a unique structural class. The structural similarities and differences between the structure types of this class have been discussed in detail. Comparison of different structure types emphasized the importance of the metal bonding contribution in understanding the structural features and suggested limitations on qualitative bonding models used to understand the structural-chemical principles underlying structure stability.

  2. Comprehensive recovery of gold and base-metal sulfide minerals from a low-grade refractory ore (United States)

    Li, Wen-juan; Liu, Shuang; Song, Yong-sheng; Wen, Jian-kang; Zhou, Gui-ying; Chen, Yong


    The comprehensive recovery of small amounts of valuable minerals such as gold and base-metal sulfide minerals from a low-grade refractory ore was investigated. The following treatment strategy was applied to a sample of this ore: gold flotation-gold concentrate leaching-lead and zinc flotation from the gold concentrate leaching residue. Closed-circuit trials of gold flotation yielded a gold concentrate that assayed at 40.23 g·t-1 Au with a recovery of 86.25%. The gold concentrate leaching rate was 98.76%. Two variants of lead-zinc flotation from the residue—preferential flotation of lead and zinc and bulk flotation of lead and zinc—were tested using the middling processing method. Foam from the reflotation was returned to the lead rougher flotation or lead-zinc bulk flotation, whereas middlings from reflotation were discarded. Sulfur concentrate was a byproduct. The combined strategy of flotation, leaching, and flotation is recommended for the treatment of this kind of ore.

  3. A nanoscale Zr-based fluorescent metal-organic framework for selective and sensitive detection of hydrogen sulfide (United States)

    Li, Yanping; Zhang, Xin; Zhang, Ling; Jiang, Ke; Cui, Yuanjing; Yang, Yu; Qian, Guodong


    Hydrogen sulfide (H2S) has been commonly viewed as a gas signaling molecule in various physiological and pathological processes. However, the highly efficient H2S detection still remains challenging. Herein, we designed a new robust nano metal-organic framework (MOF) UiO-66-CH=CH2 as a fluorescent probe for rapid, sensitive and selective detection of biological H2S. UiO-66-CH=CH2 was prepared by heating ZrCl4 and 2-vinylterephthalic acid via a simple method. UiO-66-CH=CH2 displayed fluorescence quenching to H2S and kept excellent selectivity in the presence of biological relevant analytes especially the cysteine and glutathione. This MOF-based probe also exhibited fast response (10 s) and high sensitivity with a detection limit of 6.46 μM which was within the concentration range of biological H2S in living system. Moreover, this constructed MOF featured water-stability, nanoscale (20-30 nm) and low toxicity, which made it a promising candidate for biological H2S sensing.

  4. Band gap tuning and fluorescence properties of lead sulfide Pb0.9A0.1S (A: Fe, Co, and Ni) nanoparticles by transition metal doping (United States)

    Parveen, Azra; Agrawal, Shraddha; Azam, Ameer


    Transition metal-doped lead sulfide nanoparticles (PbS-NPs) were synthesized by co-precipitation method. The crystallite phase and morphological studies were carried out by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Optical studies were performed by UV-Visible absorption, fluorescence emission spectroscopy and Fourier transforms infrared spectroscopy (FTIR). XRD analysis reveals that the pure and transition metal-doped PbS- NPs have a single crystalline phase with cubic structure devoided of any other secondary phase. The notable effect on optical absorbance and band gap was observed with transition metal doping in lead sulphide. The optical energy band gap values were found to increase with the doping of transition metal. UV-Visible absorption and fluorescence emission spectra display a blue shift with subsequent transition metal doping which may arise due to quantum confinement effect making it worth for having applications in optoelectronic devices.

  5. Metal-hydrogen systems with an exceptionally large and tunable thermodynamic destabilization

    NARCIS (Netherlands)

    Ngene, Peter; Longo, Alessandro; Mooij, L.P.A.; Bras, Wim; Dam, B.


    Hydrogen is a key element in the energy transition. Hydrogen-metal systems have been studied for various energy-related applications, e.g., for their use in reversible hydrogen storage, catalysis, hydrogen sensing, and rechargeable batteries. These applications depend strongly on the

  6. Exceptional Hydrophobicity of a Large-Pore Metal-Organic Zeolite

    NARCIS (Netherlands)

    He, C.T.; Jiang, L.; Ye, Z.M.; Krishna, R.; Zhong, Z.S.; Liao, P.Q.; Xu, J.; Ouyang, G.; Zhang, J.P.; Chen, X.M.


    Porous materials combining high hydrophobicity, large surface area, as well as large and uniform pore size are very useful but rare. The nanoporous zeolitic metal azolate framework, RHO-[Zn(eim)(2)] (MAF-6, Heim = 2-ethylimidazole), is an attractive candidate but thought to be unobtainable/unstable.

  7. Metals impact into the Paranaguá Estuarine Complex (Brazil during the exceptional flood of 2011

    Directory of Open Access Journals (Sweden)

    Marilia Lopes da Rocha

    Full Text Available Abstract Particulate and dissolved metal concentrations were determined after the largest flood in the last 30 years on the east-west axis of the Paranaguá Estuarine Complex (PEC and compared to the those of the dry period at two stations. Results confirmed that the flood greatly affected riverine outflows and the behavior of metals in the PEC. In particular, a sharp decrease in salinity was followed by extremely high SPM concentrations leading to a decrease in DO concentrations at both stations. For the dissolved phase, ANOSIM analysis showed a significant dissimilarity at each station between the sampled periods, whereas for the particulate phase this dissimilarity was found only for the samplings taken at the Antonina Station. KD values suggested dissolved Cu behavior was related to the presence of organic complexes and dissolved Mn had sediment resuspension of redox sediments and or/pore water injection as sources. Metal concentrations were lower than in polluted estuaries, though high enrichment factors found after the flood pointed to the influence of anthropogenic sources. In conclusion, the flood's influence was more evident at the Antonina Station, due to its location in the upper estuary, whereas in Paranaguá a high SPM content with low metal concentration was found, following the common pattern generally found in other marine systems subject to heavy rainfall events.

  8. Chalcophile element (Ni, Cu, PGE, and Au) variations in the Tamarack magmatic sulfide deposit in the Midcontinent Rift System: implications for dynamic ore-forming processes (United States)

    Taranovic, Valentina; Ripley, Edward M.; Li, Chusi; Rossell, Dean


    The Tamarack magmatic sulfide deposit is hosted by the Tamarack Intrusive Complex (1105.6 ± 1.2 Ma) in the Midcontinent Rift System. The most important sulfide mineralization in the Complex occurs in the northern part, which consists of two separate intrusive units: an early funnel-shaped layered peridotite body containing relatively fine-grained olivine (referred to as the FGO Intrusion) at the top, and a late gabbro-troctolite-peridotite dike-like body containing relatively coarse-grained olivine (referred to as the CGO Intrusion) at the bottom. Disseminated, net-textured, and massive sulfides occur in the base of the FGO Intrusion as well as in the upper part of the CGO Intrusion. The widest part of the CGO Intrusion also hosts a large semi-massive (net-textured) sulfide ore body locally surrounded by disseminated sulfide mineralization. Small massive sulfide veins occur in the footwall of the FGO Intrusion and in the wall rocks of the CGO dike. The sulfide mineralization is predominantly composed of pyrrhotite, pentlandite, and chalcopyrite, plus minor magnetite. Pyrrhotite containing the highest Ni and Co contents occurs in the FGO disseminated sulfides and in the CGO semi-massive sulfide ores, respectively. The most important platinum-group minerals associated with the base metal sulfides are sperrylite (PtAs2), sudburyite (PdSb), and michenerite (PdBiTe). Nickel shows a strong positive correlation with S in all types of sulfide mineralization, and Cu shows a strong positive correlation with S in the disseminated sulfide mineralization. At a given S content, the concentrations of Pt, Pd, and Au in the CGO disseminated sulfides are significantly higher than those in the FGO disseminated sulfides. The semi-massive sulfide ores are characterized by significantly higher IPGE (Ir, Os, Ru, and Rh) concentrations than most of the massive sulfide ores. With few exceptions, all of the various textural types of sulfide mineralization collectively show a good positive

  9. Bad-metal-layered sulfide oxide CsV{sub 2}S{sub 2}O

    Energy Technology Data Exchange (ETDEWEB)

    Valldor, Martin; Merz, Patrick; Prots, Yurii; Schnelle, Walter [Max Planck Institute for Chemical Physics of Solids, Dresden (Germany)


    Through a solid-state reaction between stoichiometric amounts of a mixed cesium oxide Cs{sub 2}O{sub 1.3}, VS, S, and V{sub 2}O{sub 5}, a polycrystalline powder of CsV{sub 2}S{sub 2}O was obtained. Small single crystals could be grown in a CsCl melt by allowing Cs{sub 2}SO{sub 4}, V metal and S powders to react. The crystals have a plate-like morphology, consistent with the tetragonal crystal-structure symmetry [P4/mmm, a = 3.9455(1), c = 7.4785(1) Aa]. Magnetic measurements suggest that CsV{sub 2}S{sub 2}O is a temperature-independent paramagnet, and resistivity data concur with a bad metal. The mixed oxidation state of V on one crystallographic site offers a tentative explanation of the electronic properties of the title compound. (Abstract Copyright, Wiley Periodicals, Inc.)

  10. SHI irradiation of metal doped zinc sulfide polymer nanocomposites synthesized using micro emulsion method

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Satyendra [Department of Applied Physics, School of Physical Sciences, Babasaheb Bhimrao Ambedkar University, Lucknow 226025 (India); Singh, Paramjit [University School of Basics and Applied Sciences, Guru Gobind Singh Indraprastha University, New Delhi 110078 (India); Sonkawade, R.G. [Inter University Aceelerator Centre, New Delhi 110067 (India); Awasthi, Kamlendra [Department of Physics, Malaviya National Institute of Technology, Jaipur 302017 (India); Kumar, Rajesh, E-mail: [University School of Basics and Applied Sciences, Guru Gobind Singh Indraprastha University, New Delhi 110078 (India)


    The metal doped ZnS nanoparticles dispersed in polystyrene were synthesized using micro emulsion method. The synthesized free standing nanocomposites films of 18 μm thickness were irradiated with 60 MeV nickel ions at two different fluences for the modification of structural, optical and chemical properties. The pristine and irradiated samples were characterized by X-ray diffraction, UV–visible and FTIR spectrophotometer. The SEM and XRD results confirmed the synthesis of nanoparticles. The ion irradiation shifted the optical absorption towards higher wavelength and decreased the band gap energy to significant levels. The infrared band at 465 cm{sup −1} confirmed the Zn–S bonding. The intensity of other absorption bands was modified after ion irradiation.

  11. Mesoporous Fluorinated Metal-Organic Frameworks with Exceptional Adsorption of Fluorocarbons and CFCs. (United States)

    Chen, Teng-Hao; Popov, Ilya; Kaveevivitchai, Watchareeya; Chuang, Yu-Chun; Chen, Yu-Sheng; Jacobson, Allan J; Miljanić, Ognjen Š


    Two mesoporous fluorinated metal-organic frameworks (MOFs) were synthesized from extensively fluorinated tritopic carboxylate- and tetrazolate-based ligands. The tetrazolate-based framework MOFF-5 has an accessible surface area of 2445 m(2) g(-1), the highest among fluorinated MOFs. Crystals of MOFF-5 adsorb hydrocarbons, fluorocarbons, and chlorofluorocarbons (CFCs)-the latter two being ozone-depleting substances and potent greenhouse species-with weight capacities of up to 225%. The material exhibits an apparent preference for the adsorption of non-spherical molecules, binding unusually low amounts of both tetrafluoromethane and sulfur hexafluoride. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Effects of sediment resuspension on the oxidation of acid-volatile sulfides and release of metals (iron, manganese, zinc) in Pescadero estuary (CA, USA). (United States)

    Richards, Chandra M; van Puffelen, Jasper L; Pallud, Céline


    Bar-built estuaries are unique ecosystems characterized by the presence of a sandbar barrier, which separates the estuary from the ocean for extended periods and can naturally reopen to the ocean with heavy rainfall and freshwater inflows. The physical effects associated with the transition from closed to open state, specifically water mixing and sediment resuspension, often indirectly worsen water quality conditions and are suspected to drive near-annual fish kills at the Pescadero estuary in northern California. The effects of sediment acid-volatile sulfide (AVS) oxidation, specifically oxygen depletion, acidification, and metal release, are believed to aggravate water conditions for fish but remain poorly understood. We performed slurry incubations containing sediment from 4 sites in the Pescadero estuary, representing a gradient from the Pacific Ocean to freshwater tributaries. We measured near-maximum rates of aqueous hydrogen sulfide oxidation, sediment AVS oxidation, sulfate production, and acidification, as well as near-maximum release rates of iron (Fe), manganese (Mn), and zinc (Zn) to the water column. We estimated AVS oxidation rates of 8 to 21 mmol S kg -1  d -1 , which were 3 orders of magnitude higher than aqueous hydrogen sulfide oxidation rates, 6 to 26 μmol S kg -1  d -1 . We suggest that aqueous hydrogen sulfide cannot be responsible for the observed kills because of low concentrations and minimal oxidative effects on pH and metal concentrations. However, the oxidative effects of AVS are potentially severe, decreasing pH to strongly acidic levels and releasing aqueous Fe, Mn, and Zn concentrations up to 11.2 mM, 0.46 mM, and 88 μM, respectively, indicating a potential role in worsening water conditions for fish in the Pescadero estuary. Environ Toxicol Chem 2018;9999:1-14. © 2017 SETAC. © 2017 SETAC.

  13. Partitioning of U, Th and K Between Metal, Sulfide and Silicate, Insights into the Volatile-Content of Mercury (United States)

    Habermann, M.; Boujibar, A.; Righter, K.; Danielson, L.; Rapp, J.; Righter, M.; Pando, K.; Ross, D. K.; Andreasen, R.; Chidester, B.


    During the early stages of the Solar System formation, especially during the T-Tauri phase, the Sun emitted strong solar winds, which are thought to have expelled a portion of the volatile elements from the inner solar system. It is therefore usually believed that the volatile depletion of a planet is correlated with its proximity to the Sun. This trend was supported by the K/Th and K/U ratios of Venus, the Earth, and Mars. Prior to the MESSENGER mission, it was expected that Mercury is the most volatile-depleted planet. However, the Gamma Ray Spectrometer of MESSENGER spacecraft revealed elevated K/U and K/Th ratios for the surface of Mercury, much higher than previous expectations. It is possible that the K/Th and K/U ratios on the surface are not a reliable gauge of the bulk volatile content of Mercury. Mercury is enriched in sulfur and is the most reduced of the terrestrial planets, with oxygen fugacity (fO2) between IW-6.3 and IW-2.6 log units. At these particular compositions, U, Th and K behave differently and can become more siderophile or chalcophile. If significant amounts of U and Th are sequestered in the core, the apparent K/U and K/Th ratios measured on the surface may not represent the volatile budget of the whole planet. An accurate determination of the partitioning of these elements between silicate, metal, and sulfide phases under Mercurian conditions is therefore essential to better constrain Mercury's volatile content and assess planetary formation models.

  14. Electrosprayed metal oxide semiconductor films for sensitive and selective detection of hydrogen sulfide. (United States)

    Ghimbeu, Camelia Matei; Lumbreras, Martine; Schoonman, Joop; Siadat, Maryam


    Semiconductor metal oxide films of copper-doped tin oxide (Cu-SnO(2)), tungsten oxide (WO(3)) and indium oxide (In(2)O(3)) were deposited on a platinum coated alumina substrate employing the electrostatic spray deposition technique (ESD). The morphology studied with scanning electron microscopy (SEM) and atomic force microscopy (AFM) shows porous homogeneous films comprising uniformly distributed aggregates of nano particles. The X-ray diffraction technique (XRD) proves the formation of crystalline phases with no impurities. Besides, the Raman cartographies provided information about the structural homogeneity. Some of the films are highly sensitive to low concentrations of H(2)S (10 ppm) at low operating temperatures (100 and 200 °C) and the best response in terms of R(air)/R(gas) is given by Cu-SnO(2) films (2500) followed by WO(3) (1200) and In(2)O(3) (75). Moreover, all the films exhibit no cross-sensitivity to other reducing (SO(2)) or oxidizing (NO(2)) gases.

  15. Intermediate sulfidation type base metal mineralization at Aliabad-Khanchy, Tarom-Hashtjin metallogenic belt, NW Iran (United States)

    Kouhestani, Hossein; Mokhtari, Mir Ali Asghar; Chang, Zhaoshan; Johnson, Craig A.


    The Aliabad-Khanchy epithermal base metal deposit is located in the Tarom-Hashtjin metallogenic belt (THMB) of northwest Iran. The mineralization occurs as Cu-bearing brecciated quartz veins hosted by Eocene volcanic and volcaniclastic rocks of the Karaj Formation. Ore formation can be divided into five stages, with most ore minerals, such as pyrite and chalcopyrite being formed in the early stages. The main wall-rock alteration is silicification, and chlorite, argillic and propylitic alteration. Microthermometric measurements of fluid inclusion assemblages show that the ore-forming fluids have eutectic temperatures between −30 and −52 °C, trapping temperatures of 150–290 °C, and salinities of 6.6–12.4 wt% NaCl equiv. These data demonstrate that the ore-forming fluids were medium- to high-temperature, medium- to low-salinity, and low-density H2O–NaCl–CaCl2 fluids. Calculated δ18O values indicate that ore-forming hydrothermal fluids had δ18Owater ranging from +3.6‰ to +0.8‰, confirming that the ore–fluid system evolved from dominantly magmatic to dominantly meteoric. The calculated 34SH2S values range from −8.1‰ to −5.0‰, consistent with derivation of the sulfur from either magma or possibly from local volcanic wall-rock. Combined, the fluid inclusion and stable isotope data indicate that the Aliabad-Khanchy deposit formed from magmatic-hydrothermal fluids. After rising to a depth of between 790 and 500 m, the fluid boiled and subsequent hydraulic fracturing may have led to inflow and/or mixing of early magmatic fluids with circulating groundwater causing deposition of base metals due to dilution and/or cooling. The Aliabad-Khanchy deposit is interpreted as an intermediate-sulfidation style of epithermal mineralization. Our data suggest that the mineralization at Aliabad-Khanchy and other epithermal deposits of the THMB formed by hydrothermal activity related to shallow late Eocene magmatism. The altered Eocene volcanic and

  16. Deposition of very thin uniform indium sulfide layers over metallic nano-rods by the Spray-Ion Layer Gas Reaction method

    Energy Technology Data Exchange (ETDEWEB)

    Genduso, G. [Dipartimento di Ingegneria Chimica, Gestionale, Informatica, Meccanica, Università di Palermo, Viale delle Scienze, 90100 Palermo (Italy); Institut for Heterogeneous Material Systems, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Hahn-Meitner-Platz 1, D-14109 Berlin (Germany); Inguanta, R.; Sunseri, C.; Piazza, S. [Dipartimento di Ingegneria Chimica, Gestionale, Informatica, Meccanica, Università di Palermo, Viale delle Scienze, 90100 Palermo (Italy); Kelch, C.; Sáez-Araoz, R. [Institut for Heterogeneous Material Systems, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Hahn-Meitner-Platz 1, D-14109 Berlin (Germany); Zykov, A. [Institut for Heterogeneous Material Systems, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Hahn-Meitner-Platz 1, D-14109 Berlin (Germany); present address: Institut für Physik, Humboldt-Universität zu Berlin, Newtonstr. 15,12489 Berlin (Germany); Fischer, Ch.-H., E-mail: [Institut for Heterogeneous Material Systems, Helmholtz-Zentrum Berlin für Materialien und Energie GmbH, Hahn-Meitner-Platz 1, D-14109 Berlin (Germany); second affiliation: Free University Berlin, Chemistry Institute, Takustr. 3, D-14195 Berlin (Germany)


    Very thin and uniform layers of indium sulfide were deposited on nickel nano-rods using the sequential and cyclical Spray-ILGAR® (Ion Layer Gas Reaction) technique. Substrates were fabricated by electrodeposition of Ni within the pores of polycarbonate membranes and subsequent chemical dissolution of the template. With respect to the depositions on flat substrates, experimental conditions were modified and optimized for the present geometry. Our results show that nano-rods up to a length of 10 μm were covered uniformly along their full length and with an almost constant film growth rate, thus allowing a good control of the coating thickness; the effect of the deposition temperature was also investigated. However, for high numbers of process steps, i.e. thickness, the films became uneven and crusty, especially at higher temperature, mainly owing to the simultaneous side reaction of the metallic Ni forming nickel sulfide at the surface of the rods. However, such a problem occurs only in the case of reactive nano-rod materials, such as less noble metals. It could be strongly reduced by doubling the spray step duration and thereby sealing the metallic surface before the process step of the sulfurization. Thus, quite smooth, about 100 nm thick coatings could be obtained. - Highlights: • Ni nano-rod substrates were grown within polycarbonate membranes. • We can coat nano-rods uniformly by the Ion Layer Gas Reaction method. • As a model we deposited up to about 100 nm In{sub 2}S{sub 3} on Ni nanorods (250 nm × 10 μm). • Element mapping at insulated rods showed homogenous coating over the full length. • Parameter optimization reduced effectively the Ni sulfide formation.

  17. Platinum-group elements and gold in base metal sulfides, platinum-group minerals, and Re-Os isotope compositions of the Uitkomst complex, South Africa

    Czech Academy of Sciences Publication Activity Database

    Trubač, Jakub; Ackerman, Lukáš; Gauert, Ch.; Ďurišová, Jana; Hrstka, Tomáš


    Roč. 113, č. 2 (2018), s. 439-461 ISSN 0361-0128 R&D Projects: GA ČR GA13-15390S Institutional support: RVO:67985831 Keywords : binary alloys * copper compounds * economic geology * gold * iridium * isotopes * ore deposits * osmium * palladium * platinum * platinum metals * pyrites * Rhenium * rhenium alloys * ruthenium * solid solutions * sulfur compounds * crustal materials * mass-balance calculations * massive sulfides * mineralized zone * monosulfide solid solutions * platinum group elements * platinum group elements (PGEs) * platinum group minerals Subject RIV: DB - Geology ; Mineralogy; AC - Archeology, Anthropology, Ethnology (ARUB-Q) OBOR OECD: Geology; Archaeology (ARUB-Q) Impact factor: 2.519, year: 2016

  18. Metal endowment reflected in chemical composition of silicates and sulfides of mineralized porphyry copper systems, Urumieh-Dokhtar magmatic arc, Iran (United States)

    Zarasvandi, Alireza; Rezaei, Mohsen; Raith, Johann G.; Pourkaseb, Houshang; Asadi, Sina; Saed, Madineh; Lentz, David R.


    The present work attempts to discriminate between the geochemical features of magmatic-hydrothermal systems involved in the early stages of mineralization in high grade versus low grade porphyry copper systems, using chemical compositions of silicate and sulfide minerals (i.e., plagioclase, biotite, pyrite and chalcopyrite). The data indicate that magmatic plagioclase in all of the porphyry copper systems studied here has high An% and Al content with a significant trend of evolution toward AlAl3SiO8 and □Si4O8 endmembers, providing insight into the high melt water contents of the parental magmas. Comparably, excess Al and An% in the high grade deposits appears to be higher than that of selected low grade deposits, representing a direct link between the amounts of exsolving hydrothermal fluids and the potential of metal endowment in porphyry copper deposits (PCDs). Also, higher Al contents accompanied by elevated An% are linked to the increasing intensity of disruptive alteration (phyllic) in feldspars from the high grade deposits. As calculated from biotite compositions, chloride contents are higher in the exsolving hydrothermal fluids that contributed to the early mineralization stages of highly mineralized porphyry systems. However, as evidenced by scattered and elevated log (fH2O)/(fHF) and log (fH2O)/(fHCl) values, chloride contents recorded in biotite could be influenced by post potassic fluids. Geothermometry of biotite associated with the onset of sulfide mineralization indicates that there is a trend of increasing temperature from high grade to low grade porphyry systems. Significantly, this is coupled with a sharp change in copper content of pyrite assemblages precipitated at the early stages of mineralization such that Cu decreased with increasing temperature. Based on EMPA and detailed WDS elemental mapping, trace elements do not exhibit complex compositional zoning or solid solution in the sulfide structure. Nevertheless, significant amounts of Cu and

  19. Results of LA-ICP-MS sulfide mapping from Algoma-type BIF gold systems with implications for the nature of mineralizing fluids, metal sources, and deposit models (United States)

    Gourcerol, B.; Kontak, D. J.; Thurston, P. C.; Petrus, J. A.


    Quantitative laser ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS) element distribution maps combined with traverse mode analyses have been acquired on various sulfides (pyrite, pyrrhotite, arsenopyrite) from three Canadian Algoma-type BIF-hosted gold deposits ( 4 Moz Au Meadowbank, ≥ 2.8 Moz Au Meliadine district, 6 Moz Au Musselwhite). These data, in conjunction with detailed petrographic and SEM-EDS observations, provide insight into the nature and relative timing of gold events, the presence and implication of trace element zoning regarding crystallization processes, and elemental associations that fingerprint gold events. Furthermore, the use of an innovative method of processing the LA-ICP-MS data in map and traverse modes, whereby the results are fragmented into time-slice data, to generate various binary plots (Ag versus Ni) provides a means to identify elemental associations (Te, Bi) not otherwise apparent. This integrated means of treating geochemical data, along with petrography, allows multiple gold events and remobilization processes to be recognized and their elemental associations determined. The main gold event in each of these deposits is characterized by the coupling of an As-Se-Te-Ag element association coincident with intense stratabound sulfide-replacement of the Fe-rich host rock. Additionally, the data indicate presence of a later remobilization event, which upgraded the Au tenor, as either non-refractory or refractory type, along fracture networks due to the ingress of subsequent base metal-bearing metamorphic fluids (mainly a Pb-Bi association). Furthermore, the data reveal a stratigraphic influence, as reflected in the elemental associations and the elemental enrichments observed and the nature of the sulfide phase hosting the gold mineralization (arsenopyrite versus pyrite).

  20. Siderophile element distribution in metal-sulfide nodules of EH3 Sahara 97072: A relict condensation signature overprinted by transient melting events (United States)

    Lehner, S. W.; Buseck, P.; McDonough, W. F.; Ash, R.


    Evidence of a condensation signature has been detected in the textures and compositions of metal-sulfide nodules (MSN) from the unequilibrated enstatite chondrite Sahara 97072 (EH3). There are two end-member models, both of which can reproduce the siderophile element relations and distribution among the kamacite (αFeNi), schreibersite (FeNiP3), and perryite [(FeNi)x(SiP)y] observed in the MSN. These minerals may have condensed as a single metal alloy that subsequently decomposed in transient melting events or they could have condensed as separate phases. Most likely the minerals were produced from some combination of both processes. Kamacite, schreibersite, and perryite compositions in MSN can reasonably be recombined to produce a metallic phase with Co/Ni and P/Ni ratios similar to those in primitive CI meteorites. The recombined metal has siderophile element (Ir, Ru, Co, Pd, Au, Ga,) ratios closer to CI values than kamacite alone, suggesting it could have been a condensing metal that remained in equilibrium with a cooling reduced gas of near solar composition until Au and Ga condensed. Alternatively, nearly CI chondritic Pd/Ru ratios in schreibersite suggest it could be an early condensate. Perryite may have initially formed as a condensate, as a product of metal sulfurization, or both, but, if so, it appears to also have re-crystallized from a liquid rich in Ni and Si during partial melting of the MSN. Fe, Ni, and P distributions in kamacite near perryite and schreibersite suggest they are primitive minerals in disequilibrium with the metal, indicating they formed in transient melting events as opposed to slow metamorphic heating. The siderophile element distribution in Sahara 97072 MSN is consistent with early condensing material that was later reprocessed by transient melting events.

  1. The geological record of base metal sulfides in the cratonic mantle: A microscale 187Os/188Os study of peridotite xenoliths from Somerset Island, Rae Craton (Canada) (United States)

    Bragagni, A.; Luguet, A.; Fonseca, R. O. C.; Pearson, D. G.; Lorand, J.-P.; Nowell, G. M.; Kjarsgaard, B. A.


    We report detailed petrographic investigations along with 187Os/188Os data in Base Metal Sulfide (BMS) on four cratonic mantle xenoliths from Somerset Island (Rae Craton, Canada). The results shed light on the processes affecting the Re-Os systematics and provide time constraints on the formation and evolution of the cratonic lithospheric mantle beneath the Rae craton. When devoid of alteration, BMS grains mainly consist of pentlandite + pyrrhotite ± chalcopyrite. The relatively high BMS modal abundance of the four investigated xenoliths cannot be reconciled with the residual nature of these peridotites, but requires addition of metasomatic BMS. This is especially evident in the two peridotites with the highest bulk Pd/Ir and Pd/Pt. Metasomatic BMS likely formed during melt/fluid percolation in the Sub Continental Lithospheric Mantle (SCLM) as well as during infiltration of the host kimberlite magma, when djerfisherite crystallized around older Fe-Ni-sulfides. On the whole-rock scale, kimberlite metasomatism is visible in a subset of bulk xenoliths, which defines a Re-Os errorchron that dates the host magma emplacement. The 187Os/188Os measured in the twenty analysed BMS grains vary from 0.1084 to >0.17 and it shows no systematic variation depending on the sulfide mineralogical assemblage. The largest range in 187Os/188Os is observed in BMS grains from the two xenoliths with the highest Pd/Ir, Pd/Pt, and sulfide modal abundance. The whole-rock TRD ages of these two samples underestimate the melting age obtained from BMS, demonstrating that bulk Re-Os model ages from peridotites with clear evidence of metasomatism should be treated with caution. The TRD ages determined in BMS grains are clustered around 2.8-2.7, ∼2.2 and ∼1.9 Ga. The 2.8-2.7 Ga TRD ages document the main SCLM building event in the Rae craton, which is likely related to the formation of the local greenstone belts in a continental rift setting. The Paleoproterozoic TRD ages can be explained by

  2. Sulfide silver architectonics of rat, cat, and guinea pig spinal cord. A light microscopic study with Timm's method for demonstration of heavy metals

    DEFF Research Database (Denmark)

    Schroder, H D


    The distribution of heavy metals in the spinal cord of the cat, rat, and guinea pig has been studied histochemically with Timm's sulfide silver method. There was considerable variation in the degree of staining of the neuropil. The dorsal horn showed a laminar staining pattern corresponding......, characterized by heterogeneous staining, also appeared dark, although less obvious in the guinea pig. In the ventral horn the coarser stained particles in lamina IX contrasted with the surrounding lamina. Cell staining varied between different cell groups, and within single cell populations. In the cat thoracic...... cord the cells in nucleus intermedio-lateralis (IL) and nucleus intercalatus (IC) stained very weakly. In Clarke's column and in the motoneuron area cells, uniform in Nissl preparations, could be seen different after Timm staining. The results are discussed in relation to other histochemical patterns...

  3. Prevention of sulfide oxidation in sulfide-rich waste rock (United States)

    Nyström, Elsa; Alakangas, Lena


    The ability to reduce sulfide oxidation in waste rock after mine closure is a widely researched area, but to reduce and/or inhibit the oxidation during operation is less common. Sulfide-rich (ca 30 % sulfur) waste rock, partially oxidized, was leached during unsaturated laboratory condition. Trace elements such as As and Sb were relatively high in the waste rock while other sulfide-associated elements such as Cu, Pb and Zn were low compared to common sulfide-rich waste rock. Leaching of unsaturated waste rock lowered the pH, from around six down to two, resulting in continuously increasing element concentrations during the leaching period of 272 days. The concentrations of As (65 mg/L), Cu (6.9 mg/L), Sb (1.2 mg/L), Zn (149 mg/L) and S (43 g/L) were strongly elevated at the end of the leaching period. Different alkaline industrial residues such as slag, lime kiln dust and cement kiln dust were added as solid or as liquid to the waste rock in an attempt to inhibit sulfide oxidation through neo-formed phases on sulfide surfaces in order to decrease the mobility of metals and metalloids over longer time scale. This will result in a lower cost and efforts of measures after mine closure. Results from the experiments will be presented.

  4. Membrane for hydrogen recovery from streams containing hydrogen sulfide (United States)

    Agarwal, Pradeep K.


    A membrane for hydrogen recovery from streams containing hydrogen sulfide is provided. The membrane comprises a substrate, a hydrogen permeable first membrane layer deposited on the substrate, and a second membrane layer deposited on the first layer. The second layer contains sulfides of transition metals and positioned on the on a feed side of the hydrogen sulfide stream. The present invention also includes a method for the direct decomposition of hydrogen sulfide to hydrogen and sulfur.

  5. Oxidation and Precipitation of Sulfide in Sewer Networks

    DEFF Research Database (Denmark)

    Nielsen, A. H.

    (Fe(II)) and precipitated subsequently with dissolved sulfide as ferrous sulfide (FeS). The ferrous sulfide precipitation was relatively fast, but not immediate. Despite the very low solubility of ferrous sulfide, initially present iron did not react completely with sulfide. This observation...... were studied in both wastewater and biofilms. Particular emphasis was on the importance of iron in the sulfur cycle. Iron is typically among the dominant metals in wastewater. The experiments showed that, ferric iron (Fe(III)) that was added to anaerobic wastewater was rapidly reduced to ferrous iron...... was probably explained by the presence of ligands in the wastewater, which reacted with the iron. The biofilm experiments showed that sulfide accumulated along with several metals in anaerobic biofilms as the result of metal sulfide precipitation. Particularly, zinc and cupper were important...

  6. Periodic Trends Transition Metal Sulfide Catalysis: Intuition and Theory; Evolution des proprietes catalytiques en hydrodesulfurisation en fonction de la position du metal de transition dans la classification periodique: intuition et theorie

    Energy Technology Data Exchange (ETDEWEB)

    Chianelli, R.R. [Texas at El Paso Univ., Materials Research Technology Institute, TX (United States)


    The use of Transition Metal Sulfide (TMS) catalysts came about as the need to hydrogenate coal to liquid fuels became urgent in the 1920's. Sabatier won the Nobel Prize in 1912 for describing the phenomenon of hydrogenation by transition metals. However, when the transition metals were used to hydrogenate coal, the TMS emerged as the stable catalytic states due to high sulfur content in the coal liquids. From 1920-1930 I.G. Farbenindustrie A.G. tested over 6000 catalysts. It was from these origins that modern Co (Ni)/Mo/Al{sub 2}O{sub 3} arose. Since that time scientists have developed an understanding of the fundamental properties that lead to both the activity of the simple binary sulfides and the mechanism by which two metals (Co+Mo) acted together to enhance activity (promotion). Initial efforts focused on supported commercial catalysts with limited success. In the early 1980's the periodic trends of TMS catalysts on unsupported catalysts were discovered and these results formed the foundation for further basic understanding of the key properties that led to catalytic activity. These results have been extended over the years to include supported catalysts and many petroleum based substrates. Early results related catalytic activity to the heats of formation of the sulfides and Pauling % d-character of the transition metals. These correlations both pointed to the importance of the 4d an 5d electrons and also to the well established catalytic principle that the metal sulfur bonds needed to be 'just right', not too strong nor too weak thus allowing facile turnover of the adsorbing and de-sorbing molecules. Averaging of the heat of formation of Co{sub 9}S{sub 8} and MoS{sub 2} suggested that promotion operated through sulfur vacancies formed by atoms that shared both a Co atom and a Mo atom on the surface. Theoretical studies also began in this period that further supported the idea that d-electrons in the frontier orbitals of the catalysts were

  7. U-Pb age for some base-metal sulfide deposits in Ireland: genetic implications for Mississippi Valley-type mineralization

    International Nuclear Information System (INIS)

    Duane, M.J.; Welke, H.J.; Allsopp, H.L.


    Evidence is presented that links the timing of vein-type (Cu-Ag(U)) to stratiform Mississippi Valley-type (MVT, Pb-Zn) ore events in Ireland. The rare occurrence of pitchblende, coffinite(?), and brannerite mineralization, which is regarded as a precursor component to the sulfide mineralization in the Gortdrum deposit (Ireland), provides the first direct radiometric dating tool for these carbonate-hosted deposits. The U-Pb (340 +25/-20 Ma) and Pb-Pb (359 +/- 26 Ma) whole-rock ages constrain the uranium and base-metal mineralizing events to the Early Carboniferous. The data support a model according to which MVT and earlier uranium mineralization stages of some major ore bodies resulted from fracturing coincident with large basin-dewatering events. The Pb-Pb and concordia data are consistent with an Early Carboniferous age for the mineralization at Gortdrum and agree closely with a previously published Rb-Sr age of 359 +/- 22 Ma, obtained for Missouri glauconites. Furthermore, other comparative geologic data from Ireland and from North American MVT mineral provinces support a model of Pb-Zn-Cu(U) mobilization on a regional scale that implicates the later closing stages of the proto-Atlantic. 40 references, 3 figures, 1 table

  8. Gum Arabic Microgels As Template for In Situ Metal-Sulfide Based Quantum Dots Preparation and Their Thermal, Spectroscopic, Optical, and Magnetic Characterization (United States)

    Farooq, Muhammad; Sagbas, Selin; Yildiz, Mustafa; Meral, Kadem; Siddiq, Mohammad; Aktas, Nahit; Sahiner, Nurettin


    Here, gum arabic (GA) microgel in 5-50 μm size range was used as a template for in situ quantum dot (QD) preparation. The in situ synthesis of metal sulfide quantum dots (QDs) such as CdS, PbS, CuS, ZnS, CoS, and MnS was accomplished by the absorption of the corresponding metal ions from aqueous solutions and then in situ precipitation with S2- treatments within GA microgels. Transmission electron microscopy (TEM) confirmed the existence of the evenly distributed QDs within GA microgel matrices for each of the prepared QDs. All the fabricated GA-QD composites have shown excellent semiconducting behaviors with relatively larger band gap values of 4.87 eV, 4.60 eV, 6.71 eV, 4.81 eV, 3.68 eV, 5.2 eV, and 4.0 eV for CdS, PbS, ZnS, CuS, CoS, MoS, and MnS, respectively. The results revealed that CdS and ZnS are found to be the most efficient florescence materials amongst the all QDs with 630 and 70 cd/cm2 fluorescence intensities, respectively. Moreover, the magnetic susceptibility study suggests that Mn(IV), Co(III), and Mo(IV), have mononuclear octahedral geometries whereas Zn(II), Cd(II), and Pb(II) show binuclear geometries.

  9. The Hydrolysis of Carbonyl Sulfide at Low Temperature: A Review (United States)

    Zhao, Shunzheng; Yi, Honghong; Tang, Xiaolong; Jiang, Shanxue; Gao, Fengyu; Zhang, Bowen; Zuo, Yanran; Wang, Zhixiang


    Catalytic hydrolysis technology of carbonyl sulfide (COS) at low temperature was reviewed, including the development of catalysts, reaction kinetics, and reaction mechanism of COS hydrolysis. It was indicated that the catalysts are mainly involved metal oxide and activated carbon. The active ingredients which can load on COS hydrolysis catalyst include alkali metal, alkaline earth metal, transition metal oxides, rare earth metal oxides, mixed metal oxides, and nanometal oxides. The catalytic hydrolysis of COS is a first-order reaction with respect to carbonyl sulfide, while the reaction order of water changes as the reaction conditions change. The controlling steps are also different because the reaction conditions such as concentration of carbonyl sulfide, reaction temperature, water-air ratio, and reaction atmosphere are different. The hydrolysis of carbonyl sulfide is base-catalyzed reaction, and the force of the base site has an important effect on the hydrolysis of carbonyl sulfide. PMID:23956697

  10. Exceptional phenomenology

    DEFF Research Database (Denmark)

    Aggerholm, Kenneth; Moltke Martiny, Kristian

    Phenomenological research is in traditional terms a matter of going 'back to the things themselves', as Husserl famously stated. But if phenomenology is to renew itself in creative ways and reveal new aspects of human experience it is of value to look for a certain kind of phenomena: exceptions....... Through exceptional cases we can gain a deeper understanding of the ordinary. This was already a guiding thread in Merleau-Ponty’s phenomenological investigations, but this paper will take the idea further by grounding the methodology in ‘hands on’ research in elite sport (football) and pathological cases...... (cerebral palsy). Within this method exceptional phenomena serve as exemplary cases, which can challenge and expand our conception of ”normal” experience. Thus, we will focus on two central aspects of exceptional phenomenology: a) it is grounded in exceptional practice and b) it lets this practical...

  11. Sulfide chemiluminescence detection (United States)

    Spurlin, S.R.; Yeung, E.S.


    A method is described for chemiluminescently determining a sulfide which is either hydrogen sulfide or methyl mercaptan by reacting the sulfide with chlorine dioxide at low pressure and under conditions which allow a longer reaction time in emission of a single photon for every two sulfide containing species, and thereafter, chemiluminescently detecting and determining the sulfide. The invention also relates not only to the detection method, but the novel chemical reaction and a specifically designed chemiluminescence detection cell for the reaction. 4 figs.

  12. Sulfidation behavior of Fe20Cr alloys

    International Nuclear Information System (INIS)

    Pillis, Marina Fuser


    Alloys for use in high temperature environments rely on the formation of an oxide layer for their protection. Normally, these protective oxides are Cr 2 O 3 , Al 2 O 3 and, some times, SiO 2 . Many industrial gaseous environments contain sulfur. Sulfides, formed in the presence of sulfur are thermodynamically less stable, have lower melting points and deviate much more stoichiometrically, compared to the corresponding oxides. The mechanism of sulfidation of various metals is as yet not clear, in spite of the concerted efforts during the last decade. To help address this situation, the sulfidation behavior of Fe20Cr has been studied as a function of compositional modifications and surface state of the alloy. The alloys Fe20Cr, Fe20Cr0.7Y, Fe20Cr5Al and Fe20Cr5Al0.6Y were prepared and three sets of sulfidation tests were carried out. In the first set, the alloys were sulfidized at 700 deg C and 800 deg C for 10h. In the second set, the alloys were pre-oxidized at 1000 deg C and then sulfidized at 800 deg C for up to 45h. In the third set of tests, the initial stages of sulfidation of the alloys was studied. All the tests were carried out in a thermobalance, in flowing H 2 /2%H 2 S, and the sulfidation behavior determined as mass change per unit area. Scanning electron microscopy coupled to energy dispersive spectroscopy and X-ray diffraction analysis were used to characterize the reaction products. The addition of Y and Al increased sulfidation resistance of Fe20Cr. The addition of Y altered the species that diffused predominantly during sulfide growth. It changed from predominant cationic diffusion to predominant anionic diffusion. The addition of Al caused an even greater increase in sulfidation resistance of Fe20Cr, with the parabolic rate constant decreasing by three orders of magnitude. Y addition to the FeCrAl alloy did not cause any appreciable alteration in sulfidation resistance. Pre-oxidation of the FeCrAl and FeCrAlY alloys resulted in an extended

  13. Petroleum sulfides, sulfoxides, and sulfones used as extragents

    International Nuclear Information System (INIS)

    Nikitin, Yu.E.; Lyapina, N.K.; Murinov, Yu.I.


    Possibilities of using petroleum sulfides, sulfoxides and sulfones for extraction and separation of wide range of elements are considered. It is shown that petroleum sulfides appear to be effective and selective extractants in extraction and separation of noble metals (Ru, Au, Pt, etc.). Petroleum sulfoxides are promising for solvent extraction of transition metals, actinides, rare earths etc

  14. Effect of metal sulfide pulp density on gene expression of electron transporters in Acidithiobacillus sp. FJ2. (United States)

    Fatemi, Faezeh; Miri, Saba; Jahani, Samaneh


    In Acidithiobacillus ferrooxidans, one of the most important bioleaching bacterial species, the proteins encoded by the rus operon are involved in the electron transfer from Fe 2+ to O 2 . To obtain further knowledge about the mechanism(s) involved in the adaptive responses of the bacteria to growth on the different uranium ore pulp densities, we analyzed the expression of the four genes from the rus operon by real-time PCR, when Acidithiobacillus sp. FJ2 was grown in the presence of different uranium concentrations. The uranium bioleaching results showed the inhibitory effects of the metal pulp densities on the oxidation activity of the bacteria which can affect Eh, pH, Fe oxidation and uranium extractions. Gene expression analysis indicated that Acidithiobacillus sp. FJ2 tries to survive in the stress with increasing in the expression levels of cyc2, cyc1, rus and coxB, but the metal toxicity has a negative effect on the gene expression in different pulp densities. These results indicated that Acidithiobacillus sp. FJ2 could leach the uranium even in high pulp density (50%) by modulation in rus operon gene responses.

  15. Metal-Silicate-Sulfide Partitioning of U, Th, and K: Implications for the Budget of Volatile Elements in Mercury (United States)

    Habermann, M.; Boujibar, A.; Righter, K.; Danielson, L.; Rapp, J.; Righter, M.; Pando, K.; Ross, D. K.; Andreasen, R.


    During formation of the solar system, the Sun produced strong solar winds, which stripped away a portion of the volatile elements from the forming planets. Hence, it was expected that planets closest to the sun, such as Mercury, are more depleted in volatile elements in comparison to other terrestrial planets. However, the MESSENGER mission detected higher than expected K/U and K/Th ratios on Mercury's surface, indicating a volatile content between that of Mars and Earth. Our experiments aim to resolve this discrepancy by experimentally determining the partition coefficients (D(sup met/sil)) of K, U, and Th between metal and silicate at varying pressure (1 to 5 GPa), temperature (1500 to 1900 C), oxygen fugacity (IW-2.5 to IW-6.5) and sulfur-content in the metal (0 to 33 wt%). Our data show that U, Th, and K become more siderophile with decreasing fO2 and increasing sulfur-content, with a stronger effect for U and Th in comparison to K. Using these results, the concentrations of U, Th, and K in the bulk planet were calculated for different scenarios, where the planet equilibrated at a fO2 between IW-4 and IW-7, assuming the existence of a FeS layer, between the core and mantle, with variable thickness. These models show that significant amounts of U and Th are partitioned into Mercury's core. The elevated superficial K/U and K/Th values are therefore only a consequence of the sequestration of U and Th into the core, not evidence of the overall volatile content of Mercury.

  16. Robust silver-mediated imidazolo-dC base pairs in metal DNA: dinuclear silver bridges with exceptional stability in double helices with parallel and antiparallel strand orientation. (United States)

    Jana, Sunit Kumar; Guo, Xiurong; Mei, Hui; Seela, Frank


    A new unprecedented metal-mediated base pair was designed that stabilizes reverse Watson-Crick DNA (parallel strand orientation, ps) as well as canonical Watson-Crick DNA (antiparallel strand orientation, aps). This base pair contains two imidazolo-dC units decorated with furan residues. Tm measurements and spectroscopic studies reveal that each silver-mediated furano-imidazolo-dC forms exceptionally stable duplexes with ps and aps chain orientation. This stability increase by a silver-mediated base pair is the highest reported so far for ps and aps DNA helices.

  17. The dynamics of the laser-induced metal-semiconductor phase transition of samarium sulfide (SmS); Die Dynamik des laserinduzierten Metall-Halbleiter-Phasenuebergangs von Samariumsulfid (SmS)

    Energy Technology Data Exchange (ETDEWEB)

    Kaempfer, Tino


    The present thesis is dedicated to the experimental study of the metal-semiconductor phase transition of samarium sulfide (SmS): Temperature- and time-resolved experiments on the characterization of the phase transition of mixed-valence SmS samples (M-SmS) are presented. The measurement of the dynamics of the laser-induced phase transition pursues via time-resolved ultrashort-time microscopy and by X-ray diffraction with sub-picosecond time resolution. The electronic and structural processes, which follow an excitation of M-SmS with infrared femtosecond laser pulses, are physically interpreted on the base of the results obtained in this thesis and model imaginations. [German] Die vorliegende Arbeit ist der experimentellen Untersuchung des Metall-Halbleiter-Phasenuebergangs von Samariumsulfid (SmS) gewidmet. Es werden temperatur- und zeitaufgeloeste Experimente zur Charakterisierung des Phasenuebergangs gemischt-valenter SmS Proben (M-SmS) vorgestellt. Die Messung der Dynamik des laserinduzierten Phasenuebergangs erfolgt ueber zeitaufgeloeste Ultrakurzzeit-Mikroskopie und durch Roentgenbeugung mit subpikosekunden Zeitaufloesung. Die elektronischen und strukturellen Prozesse, welche einer Anregung von M-SmS mit infraroten Femtosekunden-Laserpulsen folgen, werden auf der Basis der in dieser Arbeit gewonnenen Ergebnisse und Modellvorstellungen physikalisch interpretiert. (orig.)

  18. Robust and conductive two-dimensional metal-organic frameworks with exceptionally high volumetric and areal capacitance (United States)

    Feng, Dawei; Lei, Ting; Lukatskaya, Maria R.; Park, Jihye; Huang, Zhehao; Lee, Minah; Shaw, Leo; Chen, Shucheng; Yakovenko, Andrey A.; Kulkarni, Ambarish; Xiao, Jianping; Fredrickson, Kurt; Tok, Jeffrey B.; Zou, Xiaodong; Cui, Yi; Bao, Zhenan


    For miniaturized capacitive energy storage, volumetric and areal capacitances are more important metrics than gravimetric ones because of the constraints imposed by device volume and chip area. Typically used in commercial supercapacitors, porous carbons, although they provide a stable and reliable performance, lack volumetric performance because of their inherently low density and moderate capacitances. Here we report a high-performing electrode based on conductive hexaaminobenzene (HAB)-derived two-dimensional metal-organic frameworks (MOFs). In addition to possessing a high packing density and hierarchical porous structure, these MOFs also exhibit excellent chemical stability in both acidic and basic aqueous solutions, which is in sharp contrast to conventional MOFs. Submillimetre-thick pellets of HAB MOFs showed high volumetric capacitances up to 760 F cm-3 and high areal capacitances over 20 F cm-2. Furthermore, the HAB MOF electrodes exhibited highly reversible redox behaviours and good cycling stability with a capacitance retention of 90% after 12,000 cycles. These promising results demonstrate the potential of using redox-active conductive MOFs in energy-storage applications.

  19. Kelvin probe imaging of photo-injected electrons in metal oxide nanosheets from metal sulfide quantum dots under remote photochromic coloration (United States)

    Kondo, A.; Yin, G.; Srinivasan, N.; Atarashi, D.; Sakai, E.; Miyauchi, M.


    Metal oxide and quantum dot (QD) heterostructures have attracted considerable recent attention as materials for developing efficient solar cells, photocatalysts, and display devices, thus nanoscale imaging of trapped electrons in these heterostructures provides important insight for developing efficient devices. In the present study, Kelvin probe force microscopy (KPFM) of CdS quantum dot (QD)-grafted Cs4W11O362- nanosheets was performed before and after visible-light irradiation. After visible-light excitation of the CdS QDs, the Cs4W11O362- nanosheet surface exhibited a decreased work function in the vicinity of the junction with CdS QDs, even though the Cs4W11O362- nanosheet did not absorb visible light. X-ray photoelectron spectroscopy revealed that W5+ species were formed in the nanosheet after visible-light irradiation. These results demonstrated that excited electrons in the CdS QDs were injected and trapped in the Cs4W11O362- nanosheet to form color centers. Further, the CdS QDs and Cs4W11O362- nanosheet composite films exhibited efficient remote photochromic coloration, which was attributed to the quantum nanostructure of the film. Notably, the responsive wavelength of the material is tunable by adjusting the size of QDs, and the decoloration rate is highly efficient, as the required length for trapped electrons to diffuse into the nanosheet surface is very short owing to its nanoscale thickness. The unique properties of this photochromic device make it suitable for display or memory applications. In addition, the methodology described in the present study for nanoscale imaging is expected to aid in the understanding of electron transport and trapping processes in metal oxide and metal chalcogenide heterostructure, which are crucial phenomena in QD-based solar cells and/or photocatalytic water-splitting systems.Metal oxide and quantum dot (QD) heterostructures have attracted considerable recent attention as materials for developing efficient solar cells

  20. Platinum and Palladium Exsolution Textures in Quenched Sulfide Melts (United States)

    Reo, G.; Frank, M. R.; Loocke, M. P.; Macey, C. J.


    Magmatic sulfide ore deposits account for over 80% of the world's platinum group element (PGE) reserves. Layered mafic intrusions (LMIs), a type of magmatic sulfide ore deposit, contain alternating layers of silicate and sulfide mineralization that are thought to have coexisted as an immiscible silicate + sulfide melt pair. Platinum and palladium, the most common PGEs found in LMIs, heavily favor the sulfide melt. Nernst partition coefficients for Pt (D = wt% of Pt in sulfide/wt% of Pt in silicate) range from 102 to 109. This study examined the Pt- and Pd-bearing phases that formed from the quenched sulfide melts to better constrain the PGE-rich sulfide layers of LMIs system. Experiments were conducted with a basalt melt, sulfide melt, and Pt-Pd metal in a vertical tube furnace at 1100°C and 1 atm and with oxygen fugacity buffered to QFM (quartz-fayalite-magnetite). Following the experiments, run products containing both sulfide and silicate glasses (quenched melts) were analyzed by a Shimadzu EPMA-1720HT Electron Probe Microanalyzer. The focus here is on the quenched Fe-rich sulfides whereas data on the partitioning of Pt and Pd between the coexisting silicate and sulfide melts will be presented in the future. The sulfide samples were imaged in back-scattering mode and major and trace element concentrations of separate metal-rich phases in the sulfide matrix were ascertained through wavelength-dispersive x-ray spectroscopy. Three discernable PGE-rich phases were found to have exsolved from the sulfide matrix upon quenching of the sulfide melt. All of these phases had Fe and S of 21-24 and 16-22 wt.%, respectively. An irregularly shaped Pd- and Cu-rich sulfide phase ( 36 and 14 wt.%, respectively) makes up the majority of the exsolution product. A separate Pd- and Ni-rich phase ( 22 and 14 wt%, respectively) can be found as grains or rims adjacent to the exsolved Pd- and Cu-rich phase. A third Pd- and Pt-rich phase ( 26 and 18 wt.%, respectively) exhibits a

  1. Sulfur K-edge XANES and acid volatile sulfide analyses of changes in chemical speciation of S and Fe during sequential extraction of trace metals in anoxic sludge from biogas reactors. (United States)

    Shakeri Yekta, Sepehr; Gustavsson, Jenny; Svensson, Bo H; Skyllberg, Ulf


    The effect of sequential extraction of trace metals on sulfur (S) speciation in anoxic sludge samples from two lab-scale biogas reactors augmented with Fe was investigated. Analyses of sulfur K-edge X-ray absorption near edge structure (S XANES) spectroscopy and acid volatile sulfide (AVS) were conducted on the residues from each step of the sequential extraction. The S speciation in sludge samples after AVS analysis was also determined by S XANES. Sulfur was mainly present as FeS (≈ 60% of total S) and reduced organic S (≈ 30% of total S), such as organic sulfide and thiol groups, in the anoxic solid phase. Sulfur XANES and AVS analyses showed that during first step of the extraction procedure (the removal of exchangeable cations), a part of the FeS fraction corresponding to 20% of total S was transformed to zero-valent S, whereas Fe was not released into the solution during this transformation. After the last extraction step (organic/sulfide fraction) a secondary Fe phase was formed. The change in chemical speciation of S and Fe occurring during sequential extraction procedure suggests indirect effects on trace metals associated to the FeS fraction that may lead to incorrect results. Furthermore, by S XANES it was verified that the AVS analysis effectively removed the FeS fraction. The present results identified critical limitations for the application of sequential extraction for trace metal speciation analysis outside the framework for which the methods were developed. Copyright © 2011 Elsevier B.V. All rights reserved.

  2. Platinum-group element, Gold, Silver and Base Metal distribution in compositionally zoned sulfide droplets from the Medvezky Creek Mine, Noril'sk, Russia (United States)

    Barnes, S.-J.; Cox, R.A.; Zientek, M.L.


    Concentrations of Ag, Au, Cd, Co, Re, Zn and Platinum-group elements (PGE) have been determined in sulfide minerals from zoned sulfide droplets of the Noril'sk 1 Medvezky Creek Mine. The aims of the study were; to establish whether these elements are located in the major sulfide minerals (pentlandite, pyrrhotite, chalcopyrite and cubanite), to establish whether the elements show a preference for a particular sulfide mineral and to investigate the model, which suggests that the zonation in the droplets is caused by the crystal fractionation of monosulfide solid solution (mss). Nickel, Cu, Ag, Re, Os, Ir, Ru, Rh and Pd, were found to be largely located in the major sulfide minerals. In contrast, less than 25% of the Au, Cd, Pt and Zn in the rock was found to be present in these sulfides. Osmium, Ir, Ru, Rh and Re were found to be concentrated in pyrrhotite and pentlandite. Palladium and Co was found to be concentrated in pentlandite. Silver, Cd and Zn concentrations are highest in chalcopyrite and cubanite. Gold and platinum showed no preference for any of the major sulfide minerals. The enrichment of Os, Ir, Ru, Rh and Re in pyrrhotite and pentlandite (exsolution products of mss) and the low levels of these elements in the cubanite and chalcopyrite (exsolution products of intermediate solid solution, iss) support the mss crystal fractionation model, because Os, Ir, Ru, Rh and Re are compatible with mss. The enrichment of Ag, Cd and Zn in chalcopyrite and cubanite also supports the mss fractionation model these minerals are derived from the fractionated liquid and these elements are incompatible with mss and thus should be enriched in the fractionated liquid. Gold and Pt do not partition into either iss or mss and become sufficiently enriched in the final fractionated liquid to crystallize among the iss and mss grains as tellurides, bismithides and alloys. During pentlandite exsolution Pd appears to have diffused from the Cu-rich portion of the droplet into

  3. Sulfidogenic biotreatment of synthetic acid mine drainage and sulfide oxidation in anaerobic baffled reactor. (United States)

    Bekmezci, Ozan K; Ucar, Deniz; Kaksonen, Anna H; Sahinkaya, Erkan


    The treatment of synthetic acid mine drainage (AMD) water (pH 3.0-6.5) containing sulfate (3.0-3.5 g L(-1)) and various metals (Co, Cu, Fe, Mn, Ni, and Zn) was studied in an ethanol-fed sulfate-reducing 4-compartment anaerobic baffled reactor (ABR) at 32°C. The reactor was operated for 160 days at different chemical oxygen demand (COD)/sulfate ratios, hydraulic retention times (HRT), pH, and metal concentrations to study the robustness of the process. The last compartment of the reactor was aerated at different rates to study the bio-oxidation of sulfide to elemental sulfur. The highest sulfate reduction efficiency (88%) was obtained with a feed sulfate concentration of 3.5 g L(-1), COD/sulfate mass ratio of 0.737, feed pH of 3.0 and HRT of 2 days without aeration in the 4th compartment. The corresponding COD removal efficiency was about 92%. The alkalinity produced in the sulfidogenic ethanol oxidation neutralized the acidic mine water from pH 3.0-4.5 to pH 7.0-8.0. Effluent soluble and total heavy metal concentrations were substantially reduced with removal efficiencies generally higher than 99%, except for Mn (25-77%). Limited aeration in the 4th compartment of ABR promoted incomplete oxidation of sulfide to elemental sulfur rather than complete oxidation to sulfate. Depending on the aeration rate and HRT, 32-74% of produced sulfide was oxidized to elemental sulfur. This study demonstrates that by optimizing operating conditions, sulfate reduction, metal removal, alkalinity generation, and excess sulfide oxidation can be achieved in a single ABR treating AMD. Copyright © 2011 Elsevier B.V. All rights reserved.


    Directory of Open Access Journals (Sweden)

    Oana-Andreea Pirnuta


    Full Text Available In an interconnected world where foreign relations matter not only for resources or military alliances but also for cultural relationships, it is highly important to have a better understanding of the power relations among nations. The information carries certain meanings that have important outcomes thus defining the power of a given nation. Foreign policy is the channel through which global politics is exercised. International politics is a hierarchy of power being determined by important cultural, economic as well as geographical aspects. The reasons and strategies that are used in order to reach the outcomes in global politics represent the focus of the present paper. The United States has been the leader in international politics since the early 20th century due to its vast resources and wealth as well as its cultural output. America’s interest in preserving a democratic and free world has its foundation in the beliefs and values it stands for the aim of this paper is to question whether or not there is a concrete premise for the idea of American exceptionalism.

  5. Efficient and selective heavy metal sequestration from water by using layered sulfide K 2x Sn 4-x S 8-x (x = 0.65–1; KTS-3)

    Energy Technology Data Exchange (ETDEWEB)

    Sarma, Debajit; Islam, Saiful M.; Subrahmanyam, K. S.; Kanatzidis, Mercouri G.


    Heavy metal ions (Cd2+, Hg2+, As3+ and Pb2+) are an important contributor to the contamination of groundwater and other water bodies in and around industrial areas. Herein, we demonstrate the rapid and efficient capacity of a layered metal sulfide material, K2xSn4-xS8-x (x = 0.65-1, KTS-3) for heavy metal ion removal from water. The effect of concentration, pH, kinetics, and competitive ions such as Na+/Ca2+ on the heavy metal ion removal capacity of KTS-3 was systematically investigated. X-ray photoelectron spectroscopy (XPS), elemental analyses, and powder X-ray diffraction studies revealed that the heavy metal ion-exchange of KTS-3 is complete (quantitative replacement of all potassium ions) and topotactic. The heavy metal ion-exchange by using KTS-3 follows the Langmuir-Freundlich model with high exchange capacities, q(m) 205(17) mg g-1 for Cd2+, 372(21) mg g-1 for Hg2+ and 391(89) mg g-1 for Pb2+. KTS-3 retains excellent heavy metal ion-exchange capacity even in very high concentration (1 M) of competing ions (Na+/Ca2+) and also over a broad pH range (2-12). KTS-3 also exhibits very good ion-exchange capacity for precious Ag+ and toxic As3+ ions. The kinetics of heavy metal ion adsorption by KTS-3 are rapid (absorbs all ions within a few minutes). These properties and the environmentally friendly character of KTS-3 make it a promising candidate for sequestration of heavy metal ions from water.

  6. Aerobic sulfide production and cadmium precipitation by Escherichia coli expressing the Treponema denticola cysteine desulfhydrase gene. (United States)

    Wang, C L; Lum, A M; Ozuna, S C; Clark, D S; Keasling, J D


    The cysteine desulfhydrase gene of Treponema denticola was over-expressed in Escherichia coli to produce sulfide under aerobic conditions and to precipitate metal sulfide complexes on the cell wall. When grown in a defined salts medium supplemented with cadmium and cysteine, E. coli producing cysteine desulfhydrase secreted sulfide and removed nearly all of the cadmium from solution after 48 h. A control strain produced significantly less sulfide and removed significantly less cadmium. Measurement of acid-labile sulfide and energy dispersive X-ray spectroscopy indicated that cadmium was precipitated as cadmium sulfide. Without supplemental cysteine, both the E. coli producing cysteine desulfhydrase and the control E. coli demonstrated minimal cadmium removal.

  7. Hydrogen sulfide removal in water-based drilling fluid by metal oxide nanoparticle and ZnO/TiO2 nanocomposite (United States)

    Salehi Morgani, M.; Saboori, R.; Sabbaghi, S.


    Advanced approaches to the application of nanomaterials for environmental studies, such as waste-water treatment and pollution removal/adsorption, have been considered in recent decades. In this research, hydrogen sulfide removal from water-based drilling fluid by ZnO and TiO2 nanoparticles and a ZnO/TiO2 nanocomposite was studied experimentally. The ZnO and TiO2 nanoparticles were synthesized by sedimentation and the sol-gel method. A sol-chemical was employed to synthesize the ZnO/TiO2 nanocomposite. X-ray diffraction, scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) surface analysis, inductively coupled plasma mass spectrometry (ICP), dynamic light scattering (DLS) and Fourier transform infrared spectroscopy were used to characterize the produced ZnO and TiO2 nanoparticles, and the ZnO/TiO2 nanocomposite. The results showed that the concentration of hydrogen sulfide decreased from 800 ppm to about 250 ppm (about 70% removal) and less than 150 ppm (more than 80% removal) using the TiO2 and ZnO nanoparticles with a 0.67 wt% concentration, respectively. Hydrogen sulfide removal using the ZnO/TiO2 nanocomposite with a 0.67 wt% showed the highest value of removal in comparison with the TiO2 and ZnO nanoparticles. The hydrogen sulfide level was lowered from 800 ppm to less than 5 ppm (99% removal) by the nanocomposite.

  8. Antitumor Allium Sulfides. (United States)

    Nohara, Toshihiro; Fujiwara, Yukio; El-Aasr, Mona; Ikeda, Tsuyoshi; Ono, Masateru; Nakano, Daisuke; Kinjo, Junei


    We examined the sulfides in onion (Allium cepa L.), Welsh onion (A. fistulosum L.), and garlic (A. sativum L.), and obtained three new thiolane-type sulfides (onionins A 1 -A 3 ) from onion; two new thiabicyclic-type sulfides (welsonins A 1 , A 2 ), together with onionins A 1 -A 3 , from Welsh onion; and six new acyclic-type sulfides (garlicnins L-1-L-4, E, and F), ten new thiolane-type sulfides (garlicnins A, B 1 -B 4 , C 1 -C 3 , K 1 , and K 2 ), and three new atypical cyclic-type sulfides (garlicnins G, I, and J) from garlic. Acetone extracts showed the potential of these sulfides in inhibiting the polarization of M2 activated macrophages that are capable of suppressing tumor-cell proliferation. The effect of the thiolane-type sulfide of a major component, onionin A 1 , on tumor progression and metastasis in both osteosarcoma and ovarian cancer-bearing mouse models was then examined. Tumor proliferation was depressed, and tumor metastasis was controlled by regulating macrophage activation. These results showed that onionin A 1 is an effective agent for controlling tumors in both in vitro and in vivo models, and that the antitumor effects observed in vivo are likely caused by reversing the antitumor immune system. Activation of the antitumor immune system by onionin A 1 might be an effective adjuvant therapy for patients with osteosarcoma, ovarian cancer and other malignant tumors. Based on these findings, pharmacological investigations will be conducted in the future to develop natural and healthy foods and anti-cancer agents that can prevent or combat disease.

  9. Sulfidation behavior of rhenium and cobalt-rhenium alloys

    International Nuclear Information System (INIS)

    Shiring, R.; Douglass, D.L.


    The sulfidation behavior of Re and three Co-Re alloys, 15, 30, and 45 w/o, was studied over the temperature range 700--800 C at sulfur pressures of 10 -4 and 10 -2 atm. The kinetics of sulfidation followed the parabolic rate law and the activation energies for all alloys were similar to that of pure cobalt. A positive rate dependency on sulfur pressure was observed and Pt markers were located at the metal-scale interface, both observations clearly suggesting that outward cation diffusion through a P-type sulfide scale occurred. Two dominant sulfides, Co 9 S 8 and ReS 2 , formed. Weight gains decreased for a given set of conditions with increasing rhenium content. An order of magnitude decrease in the sulfidation rate occurred as the rhenium content increased from 15 to 45 w/o. Preferential sulfidation of cobalt initially occurred, causing a rhenium-enriched zone to form in the substrate beneath the cobalt-sulfide scale. The initial sulfide to form was Co 3 S 4 , but, subsequently, Co 9 S 8 became the dominant sulfide, forming beneath the outer Co 3 S 4 layer. ReS 2 formed at lower cobalt levels. Pure Re was also studied, the sulfidation rate being about 10 4 times slower than that of cobalt. The decreasing rate of sulfidation with increasing Re content is attributed primarily to slower cobalt diffusion outward through the Re-enriched substrate, a phenomenon similar to that observed by C. Wagner for the oxidation of Ni-Pt alloys

  10. Sulfide treatment to inhibit mercury adsorption onto activated carbon in carbon-in-pulp gold recovery circuits

    Energy Technology Data Exchange (ETDEWEB)

    Touro, F.J.; Lipps, D.A.


    A process for treating a mercury-contaminated, precious metal-containing ore slurry is described comprising: (a) reacting sulfide anions in an aqueous ore slurry of a mercury and precious metal-containing carbonaceous ore, and (b) conducting a simultaneous cyanide leach and carbon-in-pulp adsorption of the precious metal from the carbonaceous ore in the sulfide-containing ore slurry.

  11. Geology of volcanogenic massive sulfide deposit near Meli ...

    African Journals Online (AJOL)


    Chloritization is the dominant alteration among others, and the ore body is associated with mafic to intermediate ... attracted both national and international mineral exploration companies to search for the metallic ... metal sulfides are attracting the attention of many exploration companies like, National Mining. Company ...

  12. Titanocene sulfide chemistry

    Czech Academy of Sciences Publication Activity Database

    Horáček, Michal


    Roč. 314, MAY 2016 (2016), s. 83-102 ISSN 0010-8545 R&D Projects: GA ČR(CZ) GAP207/12/2368 Institutional support: RVO:61388955 Keywords : titanocene sulfide chemistry * photolysis * titanocene hydrosulfides Ti-(SH)n Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 13.324, year: 2016

  13. Promotion of Mo/Al2O3 Sulfide Catalyst by Noble Metals in Simultaneous Hydrodesulfurization of Thiophene and Hydrodenitrogenation of Pyridine: A Comparative Study

    Czech Academy of Sciences Publication Activity Database

    Vít, Zdeněk; Cinibulk, Josef; Gulková, Daniela


    Roč. 272, 1-2 (2004), s. 99-107 ISSN 0926-860X R&D Projects: GA AV ČR IAA4072103 Institutional research plan: CEZ:AV0Z4072921 Keywords : Mo catalyst * noble metal * HDS Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor : 2.378, year: 2004

  14. Sulfidation behavior and mechanism of zinc silicate roasted with pyrite (United States)

    Ke, Yong; Peng, Ning; Xue, Ke; Min, Xiaobo; Chai, Liyuan; Pan, Qinglin; Liang, Yanjie; Xiao, Ruiyang; Wang, Yunyan; Tang, Chongjian; Liu, Hui


    Sulfidation roasting followed by flotation is widely known as a possible generic technology for enriching valuable metals in low-grade Zn-Pb oxide ores. Zn2SiO4 is the primary Zn phase in willemite. Zn4Si2O7(OH)2(H2O), the main Zn phase in hemimorphite, transforms into Zn2SiO4 at temperatures above 600 °C. To enrich the Zn in willemite and hemimorphite, the Zn species should first be converted to ZnS. Therefore, a thorough understanding of the sulfidation reaction of Zn2SiO4 during roasting with pyrite is of vital important. In this study, the sulfidation behavior and reaction mechanisms of a Zn2SiO4-pyrite roasting system were determined using HSC 5.0 software, TG-FTIR spectroscopy, XRD, XPS and SEM-EDS. The results indicate that the sulfidation process can be divided into three steps: the decomposition of pyrite and formation of a sulfur-rich environment, the sulfur-induced migration of O2- and transformation of sulfur vapor, and the sulfidation reaction via oxygen-sulfur exchange. During the sulfidation roasting process, pyrite was converted to loose and porous Fe3O4, whereas Zn2SiO4 was transformed into ZnS and SiO2 in situ. These findings provide theoretical support for controlling the sulfidation roasting process of willemite and hemimorphite.

  15. Synthesis and Crystal Structure of the New Mixed-metal Bismuth Indium Sulfide, Bi{sub 0.76}In{sub 1.24}S{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Woojin; Kim, Kyounghee; Yun, Hoseop [Ajou University, Suwon (Korea, Republic of)


    In these compounds, In atoms are usually coordinated by six S atoms in distorted octahedral fashions but both octahedral and tetrahedral In atoms are found in Bi{sub 2}In{sub 4}S{sub 9}. Compared with In, Bi atoms adopt much more complicated coordinations. In our laboratory, reactive halide fluxes have been exploited to prepare numerous chalcogenophosphates as single crystals and this synthetic technique should be of general utility in finding new metal chalcogenides. In an attempt to search for new phases in the Bi-n-S system using halide-flux techniques, we have found a new nonstoichiometric ternary sulfide. The tube was evacuated to 0.133 Pa, sealed, and heated gradually (20 K/h) to 923 K, where it was kept for 72 h. The tube was cooled to 473 K at the rate 3 K/h and then was quenched to room temperature. The excess halide was removed with distilled water and black needle-shaped crystals were obtained. The crystals are stable in air and water. A qualitative X-ray fluorescence analysis of the crystal indicated the presence of Bi, In, and S. Optical diffuse reflectance spectra of the powdered sample were measured at room temperature using a Shimadzu UV-2400 PC spectrophotometer (Kyoto, Japan) operating in the range of 200-800 nm. Barium sulfate powder was used as reference material. The absorption data were calculated from the diffuse reflectance data with the use of the Kubelka-Munk relation.

  16. Synthesis and evaluation of novel biochar-based and metal oxide-based catalysts for removal of model tar (toluene), ammonia, and hydrogen sulfide from simulated producer gas (United States)

    Bhandari, Pushpak

    Gasification is a thermochemical conversion process in which carbonaceous feedstock is gasified in a controlled atmosphere to generate producer gas. The producer gas is used for production of heat, power, fuels and chemicals. Various contaminants such as tars, NH3, and H2S in producer gas possess many problems due to their corrosive nature and their ability to clog and deactivate catalysts. In this study, several catalysts were synthesized, characterized, and tested for removal of three contaminants (toluene (model tar), NH3, and H2S) from the biomass-generated producer gas. Biochar, a catalyst, was generated from gasification of switchgrass. Activated carbon and acidic surface activated carbon were synthesized using ultrasonication method from biochar. Acidic surface was synthesized by coating activated carbon with dilute acid. Mixed metal oxide catalysts were synthesized from hydrotalcite precursors using novel synthesis technique using microwave and ultrasonication. Surface area of activated carbon (˜900 m2/g) was significantly higher than that of its precursor biochar (˜60 m2/g). Surface area of metal oxide catalyst was approximately 180 m2/g after calcination. Biochar, activated carbon, and acidic surface activated carbon showed toluene removal efficiencies of approximately 78, 88, and 88 %, respectively, when the catalysts were tested individually with toluene in the presence of producer gas at 800 °C. The toluene removal efficiencies increased to 86, 91, and 97 % using biochar, activated carbon and acidic surface activated carbon, respectively in the presence of NH3 and H2S in the producer gas. Increase in toluene removal efficiencies in presence of NH3 and H2S indicates that NH3 and H 2S play a role in toluene reforming reactions during simultaneous removal of contaminants. Toluene removal efficiency for mixed metal oxide was approximately 83%. Ammonia adsorption capacities were 0.008 g NH3/g catalyst for biochar and 0.03g NH3/g catalyst for activated

  17. 40Ar/39Ar dating of exceptional concentration of metals by weathering of Precambrian rocks at the Precambrian–Cambrian boundary

    DEFF Research Database (Denmark)

    Parnell, John; Mark, Darren F.; Frei, Robert


    The sub-Cambrian surface, including diverse metalliferous deposits, shows evidence of intense weathering of Precambrian rocks to form supergene-enriched ores and metalliferous placers, followed by widespread peneplanation. Much of the metal would have been flushed to the Cambrian ocean during...

  18. Trace metals partitioning among different sedimentary mineral phases and the deposit-feeding polychaete Armandia brevis

    Energy Technology Data Exchange (ETDEWEB)

    Díaz-de-Alba, Margarita [Department of Analytical Chemistry, Institute of Biomolecules (INBIO), Faculty of Sciences, CEI-MAR, University of Cadiz, Campus Rio S. Pedro, E-11510, Puerto Real, Cadiz (Spain); Huerta-Diaz, Miguel Angel, E-mail: [Instituto de Investigaciones Oceanológicas, Universidad Autónoma de Baja California, Campus Ensenada, Km. 103 Carr. Tijuana-Ensenada, Ensenada 22800, Baja California (Mexico); Delgadillo-Hinojosa, Francisco [Instituto de Investigaciones Oceanológicas, Universidad Autónoma de Baja California, Campus Ensenada, Km. 103 Carr. Tijuana-Ensenada, Ensenada 22800, Baja California (Mexico); Hare, Landis [Centre Eau Terre Environnement, 490, rue de la Couronne, Québec, Québec G1K 9A9 (Canada); Galindo-Riaño, M. Dolores [Department of Analytical Chemistry, Institute of Biomolecules (INBIO), Faculty of Sciences, CEI-MAR, University of Cadiz, Campus Rio S. Pedro, E-11510, Puerto Real, Cadiz (Spain); Siqueiros-Valencia, Arturo [Instituto de Investigaciones Oceanológicas, Universidad Autónoma de Baja California, Campus Ensenada, Km. 103 Carr. Tijuana-Ensenada, Ensenada 22800, Baja California (Mexico)


    Trace metals (Cd, Co, Cu, Fe, Mn, Ni, Pb, Zn) were determined in two operationally defined fractions (HCl and pyrite) in sediments from Ensenada and El Sauzal harbors (Mexico). The HCl fraction had significantly higher metal concentrations relative to the pyrite fraction in both harbors, underlining the weak tendency of most trace metals to associate with pyrite. Exceptionally, Cu was highly pyritized, with degrees of trace metal pyritization (DTMP) > 80% in both harbors. Dissolved Fe flux measurements combined with solid phase Fe sulfide data indicated that 98 mt of Fe are precipitated as iron sulfides every year in Ensenada Harbor. These Fe sulfides (and associated trace metals) will remain preserved in the sediments, unless they are perturbed by dredging or sediment resuspension. Calculations indicate that dredging activities could export to the open ocean 0.20 ± 0.13 to (0.30 ± 0.56) × 10{sup 3} mt of Cd and Cu, respectively, creating a potential threat to marine benthic organisms. Degrees of pyritization (DOP) values in Ensenada and El Sauzal harbors were relatively low (< 25%) while degrees of sulfidization (DOS) were high (~ 50%) because of the contribution of acid volatile sulfide. DOP values correlated with DTMP values (p ≤ 0.001), indicating that metals are gradually incorporated into pyrite as this mineral is formed. Significant correlations were also found between DTMP values and − log(K{sub sp(MeS)}/K{sub sp(pyr)}) for both harbors, indicating that incorporation of trace metals into the pyrite phase is a function of the solubility product of the corresponding metal sulfide. The order in which elements were pyritized in both harbors was Zn ≈ Mn < Fe < Cd ≈ Pb < Ni ≈ Co < < Cu. Lastly, a strong correlation (r{sup 2} = 0.87, p < 0.01) was found between average reactive trace metal concentrations and metal concentrations measured in Armandia brevis (a deposit-feeding Opheliid polychaete), suggesting that these labile sedimentary metals are

  19. Exceptional gravimetric and volumetric CO2 uptake in a palladated NbO-type MOF utilizing cooperative acidic and basic, metal-CO2 interactions. (United States)

    Spanopoulos, I; Bratsos, I; Tampaxis, C; Vourloumis, D; Klontzas, E; Froudakis, G E; Charalambopoulou, G; Steriotis, T A; Trikalitis, P N


    A novel NbO-type MOF is reported based on a palladated organic linker, showing a remarkable gravimetric and volumetric CO2 uptake, reaching 201.8 cm(3) g(-1) (9.0 mmol g(-1), 39.7 wt%) and 187.8 cm(3) cm(-3) at 273 K and 1 bar, respectively. Accurate theoretical calculations revealed that the exceptional CO2 uptake is due to the combination of Lewis base Pd(ii)-CO2 (24.3 kJ mol(-1)) and Lewis acid Cu(ii)-CO2 (30.3 kJ mol(-1)) interactions, as well as synergistic pore size effects.

  20. Suicide with hydrogen sulfide. (United States)

    Sams, Ralph Newton; Carver, H Wayne; Catanese, Charles; Gilson, Thomas


    This presentation will address the recent rise of suicide deaths resulting from the asphyxiation by hydrogen sulfide (H2S) gas.Hydrogen sulfide poisoning has been an infrequently encountered cause of death in medical examiner practice. Most H2S deaths that have been reported occurred in association with industrial exposure.More recently, H2S has been seen in the commission of suicide, particularly in Japan. Scattered reports of this phenomenon have also appeared in the United States.We have recently observed 2 intentional asphyxial deaths in association with H2S. In both cases, the decedents committed suicide in their automobiles. They generated H2S by combining a sulfide-containing tree spray with toilet bowl cleaner (with an active ingredient of hydrogen chloride acid). Both death scenes prompted hazardous materials team responses because of notes attached to the victims' car windows indicating the presence of toxic gas. Autopsy findings included discoloration of lividity and an accentuation of the gray matter of the brain. Toxicology testing confirmed H2S exposure with the demonstration of high levels of thiosulfate in blood.In summary, suicide with H2S appears to be increasing in the United States.

  1. Micro-aeration for hydrogen sulfide removal from biogas (United States)

    Duangmanee, Thanapong

    The presence of sulfur compounds (e.g. protein, sulfate, thiosulfate, sulfite, etc.) in the feed stream generates highly corrosive and odorous hydrogen sulfide during anaerobic digestion. The high sulfide level in the biogas stream is not only poisonous to many novel metal catalysts employed in thermo-catalytic processes but also reduces the quality of methane to produce renewable energy. This study used an innovative, low-maintenance, low-cost biological sulfide removal technology to remove sulfides simultaneously from both gas and liquid phase. ORP (Oxidation-Reduction-Potential) was used as the controlling parameter to precisely regulate air injection to the sulfide oxidizing unit (SOU). The microaeration technique provided just enough oxygen to partially oxidize sulfides to elemental sulfur without inhibiting methanogenesis. The SOU was equipped with a diffuser at the bottom for the dispersion of sulfide-laden biogas and injected air throughout the column. The SOU can be operated as a standalone unit or coupled with an anaerobic digester to simultaneously remove sulfide from the biogas and effluent. The integrated system was capable of reducing hydrogen sulfide in biogas from 2,450 to less than 2 ppmV with minimal sulfate production at the highest available sulfide loading rate of 0.24 kg/m3-day. More than 98% of sulfide removed was recovered as elemental sulfur. However, the standalone SOU was able to operate at high hydrogen sulfide loading of 1.46 kg/m 3-day at inlet sulfide concentration of 3000 ppmV and reduce the off-gas hydrogen sulfide concentrations to less than 10 ppmV. The experiment also revealed that the ORP controlled aeration was sensitive enough to prevent oxygen overdosing (dampening effect) during unexpected surges of aeration. Using generalized linear regression, a model predicting output H2S concentration based on input H2S concentrations, SOU medium heights, and biogas flow rates, was derived. With 95% confidence, output H2S concentration

  2. Sulfide oxidation in a biofilter

    DEFF Research Database (Denmark)

    Pedersen, Claus Lunde; Dezhao, Liu; Hansen, Michael Jørgen

    oxidizing bacteria but several fungal families including Trichocomaceae. A positive correlation was found between the presence of mold and sulfide uptake. However there have been no reports on fungi metabolizing hydrogen sulfide. We hypothesize that the mold increases the air exposed surface, enabling...... higher hydrogen sulfide uptake followed by oxidation catalyzed by iron-containing enzymes such as cytochrome c oxidase in a process uncoupled from energy conservation....

  3. Sulfide oxidation in a biofilter

    DEFF Research Database (Denmark)

    Pedersen, Claus Lunde; Liu, Dezhao; Hansen, Michael Jørgen


    oxidizing bacteria but several fungal families including Trichocomaceae. A positive correlation was found between the presence of mold and sulfide uptake. However there have been no reports on fungi metabolizing hydrogen sulfide. We hypothesize that the mold increases the air exposed surface, enabling...... higher hydrogen sulfide uptake followed by oxidation catalyzed by iron-containing enzymes such as cytochrome c oxidase in a process uncoupled from energy conservation....

  4. Catalysts for the selective oxidation of hydrogen sulfide to sulfur (United States)

    Srinivas, Girish; Bai, Chuansheng


    This invention provides catalysts for the oxidation of hydrogen sulfide. In particular, the invention provides catalysts for the partial oxidation of hydrogen sulfide to elemental sulfur and water. The catalytically active component of the catalyst comprises a mixture of metal oxides containing titanium oxide and one or more metal oxides which can be selected from the group of metal oxides or mixtures of metal oxides of transition metals or lanthanide metals. Preferred metal oxides for combination with TiO.sub.2 in the catalysts of this invention include oxides of V, Cr, Mn, Fe, Co, Ni, Cu, Nb, Mo, Tc, Ru, Rh, Hf, Ta, W, Au, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu. Catalysts which comprise a homogeneous mixture of titanium oxide and niobium (Nb) oxide are also provided. A preferred method for preparing the precursor homogenous mixture of metal hydroxides is by coprecipitation of titanium hydroxide with one or more other selected metal hydroxides. Catalysts of this invention have improved activity and/or selectivity for elemental sulfur production. Further improvements of activity and/or selectivity can be obtained by introducing relatively low amounts (up to about 5 mol %)of a promoter metal oxide (preferably of metals other than titanium and that of the selected second metal oxide) into the homogeneous metal/titanium oxide catalysts of this invention.

  5. Extraction of Nanosized Cobalt Sulfide from Spent Hydrocracking Catalyst

    Directory of Open Access Journals (Sweden)

    Samia A. Kosa


    Full Text Available The processes used for the extraction of metals (Co, Mo, and Al from spent hydrotreating catalysts were investigated in this study. A detailed mechanism of the metal extraction process is described. Additionally, a simulation study was performed to understand the sulfidizing mechanism. The suggested separation procedure was effective and achieved an extraction of approximately 80–90%. In addition, the sulfidization mechanism was identified. This sulfidizing process for Co was found to involve an intermediate, the structure of which was proposed. This proposed intermediate was confirmed through simulations. Moreover, the activities of the spent and the regenerated catalyst were examined in the cracking of toluene. The modification of the spent catalyst through the use of different iron oxide loadings improved the catalytic activity.

  6. Co-settling of Chromite and Sulfide Melt Droplets and Trace Element Partitioning between Sulfide and Silicate Melts (United States)

    Manoochehri, S.; Schmidt, M. W.; Guenther, D.


    Gravitational settling of immiscible, dense sulfide melt droplets together with other cumulate phases such as chromite, combined with downward percolation of these droplets through a cumulate pile, is thought to be one of the possible processes leading to the formation of PGE rich sulfide deposits in layered mafic intrusions. Furthermore some chromitite seams in the Merensky Reef (Bushveld Complex) are considered to be acting as a filter or barrier for further downward percolation of sulfide melts into footwall layers. To investigate the feasibility of such mechanical processes and to study the partitioning behavior of 50 elements including transition metals and REEs (but not PGEs) between a silicate and a sulfide melt, two separate series of high temperature (1250-1380 °C) centrifuge-assisted experiments at 1000 g, 0.4-0.6 GPa were conducted. A synthetic silicate glass with a composition representative of the parental magma of the Bushveld Complex (~ 55 wt% SiO2) was mixed with pure FeS powder. For the first series of experiments, 15 or 25 wt% natural chromite with average grain sizes of ~ 5 or 31 μm were added to a mixture of silicate glass and FeS (10 wt%) adding 1 wt% water. For the second series, a mixture of the same glass and FeS was doped with 50 trace elements. These mixtures were first statically equilibrated and then centrifuged. In the first experimental series, sulfide melt droplets settled together with, but did not segregate from chromite grains even after centrifugation at 1000 g for 12 hours. A change in initial chromite grain size and proportions didn't have any effect on segregation. Without chromite, the starting mixture resulted in the formation of large sulfide melt pools together with finer droplets still disseminated through the silicate glass and both at the bottom of the capsule. The incomplete segregation of sulfide melt is interpreted as being due to high interfacial energies between sulfide and silicate melts/crystals which hinder

  7. Measurements of corrosion rates of carbon steels exposed to alkaline sulfide environments

    International Nuclear Information System (INIS)

    Yeske, R.A.


    Corrosion of carbon steel by alkaline sulfide liquors is a serious problem for pulp mills using kraft pulping processes. Studies have been conducted to characterize corrosion rates for carbon steels exposed to simulated liquors with various concentrations of major and minor species known to be present in kraft liquors. Corrosion rate measurements made by linear polarization methods have been compared with results of concurrent weight loss tests. With the exception of solutions containing high concentrations of polysulfides, linear polarization tests are in good qualitative agreement with weight loss measurements. Oxidation of species in the liquor apparently masquerades as metal dissolution in solutions where the rest potential is raised by oxidizing polysulfides. Some uncertainties remain regarding the origins of the Tafel slope constants and oxidation numbers required for agreement between the linear polarization and weight loss results

  8. Platinum-group elements and gold in sulfide melts from modern arc basalt (Tolbachik volcano, Kamchatka) (United States)

    Zelenski, M.; Kamenetsky, V. S.; Mavrogenes, J. A.; Danyushevsky, L. V.; Matveev, D.; Gurenko, A. A.


    Sulfide melt inclusions entrapped in primitive olivine phenocrysts can be used to understand the compositions of early sulfide melts that may ultimately contribute to magmatic sulfide ore deposits. Sulfide globules hosted in olivine (86-92 mol% Fo) from the Tolbachik basalt (the 1941 eruption) are characterized in terms of their major and trace element abundances using electron microscopy and LA-ICP-MS analysis. Distribution of major elements within individual sulfide globules varies from homogeneous to heterogeneous. Phases include monosulfide solid solution (MSS) and intermediate solid solution (ISS) intergrowths and exsolved low-temperature minerals such as pyrrhotite, pentlandite, chalcopyrite and cubanite. Trace elements (platinum-group elements - PGE, Ag, Te, Au, Pb and Bi) are also present in solid solution in sulfide phases and as micron-sized particles ("nuggets"). Such nuggets of dominantly Au, Pt, Au-Pd and Pd-Te are contained randomly within sulfide matrices or, more commonly, at phase boundaries. Nuggets are also attached to outer surfaces of sulfide globules. Concentrations of PGE in sulfides follow a log normal distribution over four orders of magnitude. The highest measured noble metal concentrations in the analyzed globules (436 ppm Au + PGE) are 13.3 ppm Au, 115 ppm Pt and 299 ppm Pd, whereas 40% of globules have < 15 ppm of noble metals. Gold and PGE concentrations correlate, suggesting these elements were concentrated by the same process(es). We propose that a number of anomalous concentrations of one or several noble metals in the analyzed globules can be best explained by entrapment of Au-PGE-rich particles (solid or liquid) from the silicate melt. Although the individual Tolbachik sulfide globules have variable PGE abundances, their mean composition resembles those of major PGE-sulfide ore deposits (e.g., Norilsk, Sudbury, Platreef and Merensky Reef).

  9. Development of sulfide calibration standards for the laser ablation inductively-coupled plasma mass spectrometry technique (United States)

    Wilson, S.A.; Ridley, W.I.; Koenig, A.E.


    The requirements of standard materials for LA-ICP-MS analysis have been difficult to meet for the determination of trace elements in sulfides. We describe a method for the production of synthetic sulfides by precipitation from solution. The method is detailed by the production of approximately 200 g of a material, PS-1, with a suite of chalcophilic trace elements in an Fe-Zn-Cu-S matrix. Preliminary composition data, together with an evaluation of the homogeneity for individual elements, suggests that this type of material meets the requirements for a sulfide calibration standard that allows for quantitative analysis. Contamination of the standard with Na suggests that H2S gas may prove a better sulfur source for future experiments. We recommend that calibration data be collected in whatever mode is closest to that employed for the analysis of the unknown material, because of variable fractionation effects as a function of analytical mode. For instance, if individual spot analyses are attempted on unknown sample, then a raster of several individual spot analyses, not a continuous scan, should be collected and averaged for the standard. Hg and Au are exceptions to the above and calibration data should always be collected in a scanning mode. Au is more heterogeneously distributed than other trace metals and large-area scans are required to provide an average value for calibration purposes. We emphasize that the values given in Table 1 are preliminary values. Further chemical characterization of this standard, through a round-robin analysis program, will allow the USGS to provide both certified and recommended values for individual elements. The USGS has developed PS-1 as a potential new LA-ICP-MS standard for use by the analytical community, and requests for this material should be addressed to S. Wilson. However, it is stressed that an important aspect of the method described here is the flexibility for individual investigators to produce sulfides with a wide range

  10. Experimental constraints on gold and silver solubility in iron sulfides

    International Nuclear Information System (INIS)

    Pal'yanova, Galina; Mikhlin, Yuri; Kokh, Konstantin; Karmanov, Nick; Seryotkin, Yurii


    Experiments were performed to determine crystallization of Fe,S-melts (pyriti≿ and troilitic with molar ratio S/Fe ratios of 2 and 1, respectively) containing traces of gold and silver at (Ag/Au) wt ratios varying from 10 to 0.1. The solid products were studied by optical microscopy, scanning electron microscopy, X-ray powder diffraction (XRD), microprobe analysis, and X-ray photoelectron spectroscopy (XPS) in order to reveal the concentration limits of “invisible” gold and silver in magmatic iron sulfides, and to determine the influence of sulfur on forms of precious metals in the Fe–S system with different Ag/Au ratios. Au–Ag phases do not form inclusions but instead concentrate on the grain boundaries in the synthetic pyrrhotite and troilite, while pyrite comprises micro- (1–5 μm) and macroinclusions of Au–Ag alloys and Au–Ag sulfides. In “pyriti≿” systems, the fineness of alloys increases from 650 to 970‰ and the composition of sulfides changes from acanthite (Ag 2 S) to uytenbogaardtite (Ag 3 AuS 2 ) and petrovskaite (AgAuS) as the Ag/Au ratio decreases. The concentrations of “invisible” precious metals revealed in troilite were 0.040 ± 0.013 wt.% Au and 0.079 ± 0.016 wt.% Ag. Measured concentrations in pyrite and pyrrhotite were <0.024 wt.% Au and <0.030 wt.% Ag. The surface layers of iron sulfides probed with XPS were enriched in the precious metals, and in silver relative to gold, especially in the systems with Fe/S = 1, probably, due to depletion of the metallic alloy surfaces with gold. Au- and Ag-bearing iron sulfides crystallized primarily from melts may be the source of redeposited phases in hydrothermal and hypergene processes. - Highlights: • The samples of Fe–S–Au–Ag system were synthesized. • Coupled solubility of gold and silver in iron sulfides was specified. • Ag–Au inclusions on surfaces of iron sulfides are likely to be enriched in silver. • Au–Ag sulfides can exist along with native gold in

  11. Spectral induced polarization and electrodic potential monitoring of microbially mediated iron sulfide transformations

    Energy Technology Data Exchange (ETDEWEB)

    Hubbard, Susan; Personna, Y.R.; Ntarlagiannis, D.; Slater, L.; Yee, N.; O' Brien, M.; Hubbard, S.


    Stimulated sulfate-reduction is a bioremediation technique utilized for the sequestration of heavy metals in the subsurface.We performed laboratory column experiments to investigate the geoelectrical response of iron sulfide transformations by Desulfo vibriovulgaris. Two geoelectrical methods, (1) spectral induced polarization (SIP), and (2) electrodic potential measurements, were investigated. Aqueous geochemistry (sulfate, lactate, sulfide, and acetate), observations of precipitates (identified from electron microscopy as iron sulfide), and electrodic potentials on bisulfide ion (HS) sensitive silver-silver chloride (Ag-AgCl) electrodes (630 mV) were diagnostic of induced transitions between an aerobic iron sulfide forming conditions and aerobic conditions promoting iron sulfide dissolution. The SIP data showed 10m rad anomalies during iron sulfide mineralization accompanying microbial activity under an anaerobic transition. These anomalies disappeared during iron sulfide dissolution under the subsequent aerobic transition. SIP model parameters based on a Cole-Cole relaxation model of the polarization at the mineral-fluid interface were converted to (1) estimated biomineral surface area to pore volume (Sp), and (2) an equivalent polarizable sphere diameter (d) controlling the relaxation time. The temporal variation in these model parameters is consistent with filling and emptying of pores by iron sulfide biofilms, as the system transitions between anaerobic (pore filling) and aerobic (pore emptying) conditions. The results suggest that combined SIP and electrodic potential measurements might be used to monitor spatiotemporal variability in microbial iron sulfide transformations in the field.

  12. Phototrophic sulfide oxidation: environmental insights and a method for kinetic analysis

    Directory of Open Access Journals (Sweden)

    Thomas E Hanson


    Full Text Available Previously, we presented data that indicated microbial sulfide oxidation would out-compete strictly chemical, abiotic sulfide oxidation reactions under nearly all conditions relevant to extant ecosystems (Luther et al., 2011. In particular, we showed how anaerobic microbial sulfide oxidation rates were several orders of magnitude higher than even metal catalyzed aerobic sulfide oxidation processes. The fact that biotic anaerobic sulfide oxidation is kinetically superior to abiotic reactions implies that nearly all anaerobic and sulfidic environments should host microbial populations that oxidize sulfide at appreciable rates. This was likely an important biogeochemical process during long stretches of euxinia in the oceans suggested by the geologic record. In particular, phototrophic sulfide oxidation allows the utilization of carbon dioxide as the electron acceptor suggesting that this process should be particularly widespread rather than relying on the presence of other chemical oxidants. Using the Chesapeake Bay as an example, we argue that phototrophic sulfide oxidation may be more important in many environments than is currently appreciated. Finally, we present methodological considerations to assist other groups that wish to study this process.

  13. Origin of Ni-Cu Sulfide Deposits: Questioning 'High-Flux' Models' (United States)

    Arndt, N. T.


    Magmatic sulfide ore bodies contain large amounts of sulfide with high concentrations of metals such as Ni, Cu and PGE. Their presence in relatively small intrusions commonly is attributed to the segregation and accumulation of sulfide droplets from magmas that flow rapidly through conduits. This 'high-flux' model is at odds with the following observations. Many ores appear to have been emplaced as magmatic breccias (Norilsk-Talnakh, Aguablanca) or crystal mushes (Jinchuan) containing a high proportion of sulfide. Such mixtures are very dense and could not have risen up through the crust from a deeper staging chamber. At Uitkomst and Platreef, screens of sedimentary rock maintaining the same orientation as adjacent sedimentary strata separate layers of ultramafic cumulates, some containing abundant sulfide ore. This geometry suggests that ultramafic mush and ore sulfides oozed into the sedimentary sequence, replacing less resistant strata. A mechanism explaining these observations is as follows: mafic-ultramafic intrusions both large and small do not differentiate in place but grow through the injection of magmas of differing compositions and crystallinity. Highly mafic magmas, particularly those charged with ferromagnesian crystals and sulfide, have high densities and they are injected into the lower parts of growing intrusions while less-dense, more evolved and/or plagioclase-rich magmas are injected at higher levels. Accumulation of sulfides probably occurs higher in the magma conduits and sulfide-rich mushes migrate or slump downwards in the conduit to form the ore bodies.

  14. Micelle Mediated Trace Level Sulfide Quantification through Cloud Point Extraction

    Directory of Open Access Journals (Sweden)

    Samrat Devaramani


    Full Text Available A simple cloud point extraction protocol has been proposed for the quantification of sulfide at trace level. The method is based on the reduction of iron (III to iron (II by the sulfide and the subsequent complexation of metal ion with nitroso-R salt in alkaline medium. The resulting green-colored complex was extracted through cloud point formation using cationic surfactant, that is, cetylpyridinium chloride, and the obtained surfactant phase was homogenized by ethanol before its absorbance measurement at 710 nm. The reaction variables like metal ion, ligand, surfactant concentration, and medium pH on the cloud point extraction of the metal-ligand complex have been optimized. The interference effect of the common anions and cations was studied. The proposed method has been successfully applied to quantify the trace level sulfide in the leachate samples of the landfill and water samples from bore wells and ponds. The validity of the proposed method has been studied by spiking the samples with known quantities of sulfide as well as comparing with the results obtained by the standard method.

  15. Influences of species of metals and supports on the hydrogenation activity of carbon-supported metal sulfides catalysts; Tanso biryushi tanji shokubai no suisoka kassei ni taisuru kassei kinzoku oyobi tantaishu no eikyo

    Energy Technology Data Exchange (ETDEWEB)

    Sakanishi, K.; Hasuo, H.; Taniguchi, H.; Nagamatsu, T.; Mochida, I. [Kyushu University, Fukuoka (Japan). Institute of Advanced Material Study


    In order to design catalysts suitable for primary liquefaction stage and secondary upgrading stage respectively in the multi-stage liquefaction process, various carbon-supported catalysts were prepared. Catalytic activities of them were investigated for the hydrogenation of 1-methylnaphthalene, to discuss the influences of metals and carbon species on the catalytic activity. Various water soluble and oil soluble Mo and Ni salts were used for NiMo supported catalysts. Among various carbon supports, Ketjen Black (KB) was effective for preparing the catalyst showing the most excellent hydrogenation activity. The KB and Black Pearl 2000 (BP2000) showing high hydrogenation activity were fine particles having high specific surface area more than 1000 m{sup 2}/g and primary particle diameter around 30 nm. This was inferred to contribute to the high dispersion support of active metals. Since such fine particles of carbon exhibited hydrophobic surface, they were suitable for preparing catalysts from the methanol-soluble metals. Although Ni and Mo added iron-based catalysts provided lower aromatic hydrogenation activity, they exhibited liquefaction activity competing with the NiMo/KB catalyst. 3 refs., 1 fig., 3 tabs.

  16. Sulfide intrusion and detoxification in Zostera marina

    DEFF Research Database (Denmark)

    Hasler-Sheetal, Harald; Holmer, Marianne


    Sulfide intrusion in seagrasses represents a global threat to seagrasses. In contrast seegrasses grow in hostile sediments, where they are constantly exposed to sulfide intrusion. Little is known about the strategies to survive sulfide intrusion, if there are detoxification mechanisms and sulfur...... indicating a possible role of sulfide in the sulfur nutrition beside the detoxification function. Our results suggest different adaptations of Z. marina to reduced sediments and sulfide intrusion ranging from bacterial and chemical reoxidation of sulfide to sulfate to incorporation of sulfide into organic...

  17. MFTF exception handling system

    International Nuclear Information System (INIS)

    Nowell, D.M.; Bridgeman, G.D.


    In the design of large experimental control systems, a major concern is ensuring that operators are quickly alerted to emergency or other exceptional conditions and that they are provided with sufficient information to respond adequately. This paper describes how the MFTF exception handling system satisfies these requirements. Conceptually exceptions are divided into one of two classes. Those which affect command status by producing an abort or suspend condition and those which fall into a softer notification category of report only or operator acknowledgement requirement. Additionally, an operator may choose to accept an exception condition as operational, or turn off monitoring for sensors determined to be malfunctioning. Control panels and displays used in operator response to exceptions are described

  18. Apparatus for use in sulfide chemiluminescence detection (United States)

    Spurlin, S.R.; Yeung, E.S.


    A method is described for chemiluminescently determining a sulfide which is either hydrogen sulfide or methyl mercaptan by reacting the sulfide with chlorine dioxide at low pressure and under conditions which allow a longer reaction time in emission of a single photon for every two sulfide containing species, and thereafter, chemiluminescently detecting and determining the sulfide. The invention also relates not only to the detection method, but the novel chemical reaction and a specifically designed chemiluminescence detection cell for the reaction. 4 figs.

  19. Mechanochemical reduction of copper sulfide

    DEFF Research Database (Denmark)

    Balaz, P.; Takacs, L.; Jiang, Jianzhong


    The mechanochemical reduction of copper sulfide with iron was induced in a Fritsch P-6 planetary mill, using WC vial filled with argon and WC balls. Samples milled for specific intervals were analyzed by XRD and Mossbauer spectroscopy. Most of the reaction takes place during the first 10 min...... of milling and only FeS and Cu are found after 60 min. The main chemical process is accompanied by phase transformations of the sulfide phases as a result of milling. Djurleite partially transformed to chalcocite and a tetragonal copper sulfide phase before reduction. The cubic modification of FeS was formed...... first, transforming to hexagonal during the later stages of the process. The formation of off-stoichiometric phases and the release of some elemental sulfur by copper sulfide are also probable....

  20. Impact of the Prestige oil spill on marsh soils: Relationship between heavy metal, sulfide and total petroleum hydrocarbon contents at the Villarrube and Lires marshes (Galicia, Spain); Impacto de la marea negra del Prestige en suelos de marisma: relacion entre los contenidos de metales pesados, sulfuros e hidrocarburos en las marismas de Villarrube y Lires (Galicia, Espana)

    Energy Technology Data Exchange (ETDEWEB)

    Andrade, L.; Marcet, P.; Covelo, E.F.; Vega, F.A. [Department of Vegetable Biology and Soil Science, Vigo (Spain); Fernandez-Feal, L.; Fernandez-Feal, C. [Escuela Politecnica Superior, Universidad de la Coruna, Ferrol (Spain)


    The objectives of this study were to determine the effect of the Prestige oil spill on the total petroleum hydrocarbons and heavy metal contents of soils in two marshes (Lires and Villarrube, Galicia, Spain) and the relationship between their oxidation-reduction potential and the solubility of heavy metals with sulfide and sulfate contents. Soil samples were taken from polluted and unpolluted areas and their petroleum hydrocarbon contents, heavy metal contents and other chemical characteristics were measured. The soils affected by the oil spill show remarkable contents of Cr, Cu, Ni, Pb and V. The Lires marsh soils are more affected by fuel oil than Villarrube marsh. The effects of the contaminating agents on the soils reach distances of up to 500 m from the coastline. In the first 400 m, there are important spatial variations because the fuel oil penetrated into the soils through tidal action and not directly. The Cr, Cu, Ni, Pb and V contents of polluted soils were between 50 and 200 times higher than those of their unpolluted counterparts and the background concentrations in Galician coastal sediments. In the case of Cr, Cu, Ni, Pb and V, their origin through the fuel oil was corroborated by the high correlation (r > 0.90) between the concentrations of these metals and the total petroleum hydrocarbon content of the polluted soils, which shows the combined addition of these metals through the fuel oil. [Spanish] Los objetivos de este trabajo fueron determinar el efecto de la marea negra del buque tanque Prestige en el contenido total de hidrocarburos y de metales pesados en suelos de dos marismas (Lires y Villarrube, Galicia, Espana) y la relacion entre el potencial de oxidacion-reduccion y la solubilidad de los metales pesados con los contenidos de sulfuros y de sulfatos. Se tomaron muestras de suelos de las zonas contaminadas y no contaminadas y se determinaron diversas caracteristicas quimicas, el contenido total de hidrocarburos y de metales pesados. Los

  1. O papel dos sulfetos volatilizados por acidificação no controle do potencial de biodisponibilidade de metais em sedimentos contaminados de um estuário tropical, no sudeste do Brasil The role of acid volatile sulfide in the control of potential metal bioavailability in contaminated sediments from a tropical estuary, southeast Brazil

    Directory of Open Access Journals (Sweden)

    Érico Casare Nizoli


    Full Text Available Measurements of acid volatile sulfide (AVS and simultaneously extracted metals (SEM were combined in order to verify the ecological hazard of contaminated sediments from the Santos-Cubatão Estuarine System (SE Brazil, which is located in one of the most industrialized areas in the Latin America. Intertidal sediments from the Morrão River estuary were collected seasonally in short cores. The redox conditions, organic matter contents and grain-size were the main controlling factors on SEM distribution. However, clear relationships among these variables and AVS were not observed. The molar SEM/AVS ratios were frequently > 1 especially in the summer, suggesting major metal bioavailability hazard in this humid hot season.

  2. Why does the Conductivity of a Nickel Catalyst Increase during Sulfidation? An Exemplary Study Using an In Operando Sensor Device. (United States)

    Fremerey, Peter; Jess, Andreas; Moos, Ralf


    In order to study the sulfidation of a catalyst fixed bed, an in operando single pellet sensor was designed. A catalyst pellet from the fixed bed was electrically contacted and its electrical response was correlated with the catalyst behavior. For the sulfidation tests, a nickel catalyst was used and was sulfidized with H₂S. This catalyst had a very low conductivity in the reduced state. During sulfidation, the conductivity of the catalyst increased by decades. A reaction from nickel to nickel sulfide occurred. This conductivity increase by decades during sulfidation had not been expected since both nickel and nickel sulfides behave metallic. Only by assuming a percolation phenomenon that originates from a volume increase of the nickel contacts when reacting to nickel sulfides, this effect can be explained. This assumption was supported by sulfidation tests with differently nickel loaded catalysts and it was quantitatively estimated by a general effective media theory. The single pellet sensor device for in operando investigation of sulfidation can be considered as a valuable tool to get further insights into catalysts under reaction conditions.

  3. Infrared spectroscopy of solid hydrogen sulfide and deuterium sulfide. (United States)

    Fathe, Kristin; Holt, Jennifer S; Oxley, Susan P; Pursell, Christopher J


    The infrared spectra of solid hydrogen sulfide (H2S) and deuterium sulfide (D2S) were collected at very low temperatures. Vapor deposition of thin films at the lowest temperature of 10 K produced amorphous solids while deposition at 70 K yielded the crystalline phase III. Infrared interference fringe patterns produced by the films during deposition were used to determine the film thickness. Careful measurement of the integrated absorbance peaks, along with the film thickness, allowed determination of the integrated band intensities. This report represents the first complete presentation of the infrared spectra of the amorphous solids. Observations of peaks near 3.915 and 1.982 microm (ca. 2554 and 5045 cm(-1), respectively) may be helpful in the conclusive identification of solid hydrogen sulfide on the surface of Io, a moon of Jupiter.

  4. Silica-rich Chondrules in ALH 84170 and Sahara 97072 EH3 Meteorites: Evidence for Sulfidation of Silicates (United States)

    Lehner, S. W.; Buseck, P. R.


    Silica-rich chondrules in EH3 meteorites contain tridymite, niningerite, and troilite associated with enstatite and olivine and no Fe-Ni metal. We interpret these assemblages as evidence for the formation of niningerite by sulfidation of silicates.

  5. On exceptional instanton strings

    NARCIS (Netherlands)

    Del Zotto, M.; Lockhart, G.

    According to a recent classification of 6d (1, 0) theories within F-theory there are only six “pure” 6d gauge theories which have a UV superconformal fixed point. The corresponding gauge groups are SU(3), SO(8), F4, E6, E7, and E8. These exceptional models have BPS strings which are also instantons

  6. Nothing Exceptional: Against Agamben (United States)

    Colatrella, Steven


    Giorgio Agamben's work has become widely influential as a guide to explaining the extra-constitutional powers assumed by governments under the rubric of the War on Terror. His formulations, such as Homo Sacer and State of Exception, have been extended to apply to a wide variety of experiences of repression of liberties or social control, including…

  7. Oxidation process of cadmium sulfide

    International Nuclear Information System (INIS)

    Hashimoto, Koshiro; Toda, Yoshitomo; Sato, Takayori


    Complicated thermogravimetric curve was observed on oxidation process of cadmium sulfide precipitate in air. Phases of various oxidation stage were identified by X-ray diffraction method. Cadmium sulfide was first oxidized to cadmium oxide at 400 0 C, while the successive reaction with sulfur dioxide and oxygen gases gave rise to cadmium sulfate. The phases such as 2 CdS. CdSO 4 , Cd 3 SO 6 and β-CdSO 4 appeared during the oxidation process up to 1100 0 C, at which all the particles were converted into cadmium oxide at 1100 0 C. Cadmium sulfide kept in nitrogen gas above 700 0 C was directly converted into cadmium oxide when oxygen gas was introduced into the furnace. (auth.)

  8. The industrial separation of copper and arsenic as sulfides (United States)

    Gabb, P. J.; Davies, A. L.


    At the Kennecott Utah copper smelter in Magna, Utah, bleed streams from the refinery tankhouse and precious-metals plant are combined with smelter weak acid and electrostatic precipitator dust to produce leach solutions containing copper and impurities. Copper and arsenic are precipitated from the solutions as sulfides in a two-stage continuous process that enables excess arsenic to be removed from the circuit and routed to hazardous waste disposal as a highly concentrated material.

  9. Sulfidation treatment of molten incineration fly ashes with Na2S for zinc, lead and copper resource recovery. (United States)

    Kuchar, D; Fukuta, T; Onyango, M S; Matsuda, H


    The present study focuses on the conversion of heavy metals involved in molten incineration fly ashes to metal sulfides which could be thereafter separated by flotation. The sulfidation treatment was carried out for five molten incineration fly ashes (Fly ash-A to Fly ash-E) by contacting each fly ash with Na(2)S solution for a period of 10 min to 6h. The initial molar ratio of S(2-) to Me(2+) was adjusted to 1.20. The conversion of heavy metals to metal sulfides was evaluated by measuring the S(2-) residual concentrations using an ion selective electrode. The formation of metal sulfides was studied by XRD and SEM-EDS analyses. In the case of Fly ash-A to Fly ash-D, more than 79% of heavy metals of zinc, lead and copper was converted to metal sulfides within the contacting period of 0.5h owing to a fast conversion of metal chlorides to metal sulfides. By contrast, the conversion of about 35% was achieved for Fly ash-E within the same contacting period, which was attributed to a high content of metal oxides. Further, the S(2-) to Me(2+) molar ratio was reduced to 1.00 to minimize Na(2)S consumption and the conversions obtained within the contacting period of 0.5h varied from 76% for Fly ash-D to 91% for Fly ash-C. Finally, soluble salts such as NaCl and KCl were removed during the sulfidation treatment, which brought about a significant enrichment in metals content by a factor varying from 1.5 for Fly ash-D to 4.9 for Fly ash-A.

  10. 30 CFR 250.604 - Hydrogen sulfide. (United States)


    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false Hydrogen sulfide. 250.604 Section 250.604... OPERATIONS IN THE OUTER CONTINENTAL SHELF Oil and Gas Well-Workover Operations § 250.604 Hydrogen sulfide. When a well-workover operation is conducted in zones known to contain hydrogen sulfide (H2S) or in...

  11. 30 CFR 250.808 - Hydrogen sulfide. (United States)


    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false Hydrogen sulfide. 250.808 Section 250.808... OPERATIONS IN THE OUTER CONTINENTAL SHELF Oil and Gas Production Safety Systems § 250.808 Hydrogen sulfide. Production operations in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of H2S...

  12. 30 CFR 250.504 - Hydrogen sulfide. (United States)


    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false Hydrogen sulfide. 250.504 Section 250.504... OPERATIONS IN THE OUTER CONTINENTAL SHELF Oil and Gas Well-Completion Operations § 250.504 Hydrogen sulfide. When a well-completion operation is conducted in zones known to contain hydrogen sulfide (H2S) or in...

  13. Exceptionalism and globalism

    Directory of Open Access Journals (Sweden)

    John Cairns Jr


    Full Text Available ABSTRACT: Achieving sustainable use of the planet will require ethical judgments in both sciences and environmental politics. The purpose of this editorial is to discuss two paradigms, exceptionalism and globalism, that are important in this regard. Exceptionalism is the insistence that one set of rules or behaviors is acceptable for an individual or country but that a different set should be used for the rest of the world. For example, the disparity in per capita consumption of resources and economic status has increased dramatically in the last century, but the consumers of great amounts of resources do not feel a proportionate responsibility for addressing this issue. Globalism is defined as individual and societal willingness to diminish, postpone or forgo individual natural resource use to protect and enhance the integrity of the global ecological life support system. Increasing affluence and the still increasing human population, coupled with wide dissemination of information and an increasing awareness that humans occupy a finite planet, exacerbate this already difficult situation. Increased interest in sustainable use of the planet makes open discussion of these issues mandatory because individuals cannot function in isolation from the larger society of which they are a part. Similarly, no country can function in isolation from other countries, which collectively form an interactive mosaic. This discussion identifies some of the crucial issues related to exceptionalism and globalism, which must be addressed before sustainable use of the planet can be achieved.

  14. Exceptionality in vowel harmony (United States)

    Szeredi, Daniel

    Vowel harmony has been of great interest in phonological research. It has been widely accepted that vowel harmony is a phonetically natural phenomenon, which means that it is a common pattern because it provides advantages to the speaker in articulation and to the listener in perception. Exceptional patterns proved to be a challenge to the phonetically grounded analysis as they, by their nature, introduce phonetically disadvantageous sequences to the surface form, that consist of harmonically different vowels. Such forms are found, for example in the Finnish stem tuoli 'chair' or in the Hungarian suffixed form hi:d-hoz 'to the bridge', both word forms containing a mix of front and back vowels. There has recently been evidence shown that there might be a phonetic level explanation for some exceptional patterns, as the possibility that some vowels participating in irregular stems (like the vowel [i] in the Hungarian stem hi:d 'bridge' above) differ in some small phonetic detail from vowels in regular stems. The main question has not been raised, though: does this phonetic detail matter for speakers? Would they use these minor differences when they have to categorize a new word as regular or irregular? A different recent trend in explaining morphophonological exceptionality by looking at the phonotactic regularities characteristic of classes of stems based on their morphological behavior. Studies have shown that speakers are aware of these regularities, and use them as cues when they have to decide what class a novel stem belongs to. These sublexical phonotactic regularities have already been shown to be present in some exceptional patterns vowel harmony, but many questions remain open: how is learning the static generalization linked to learning the allomorph selection facet of vowel harmony? How much does the effect of consonants on vowel harmony matter, when compared to the effect of vowel-to-vowel correspondences? This dissertation aims to test these two ideas

  15. Sulfide intrusion and detoxification in seagrasses ecosystems

    DEFF Research Database (Denmark)

    Hasler-Sheetal, Harald; Holmer, Marianne

    is known about the strategies of seagrasses to survive sulfide intrusion, their potential detoxification mechanisms and sulfur nutrition in general. By a global review of sulfide intrusion, coupled with a series of field studies and in situ experiments we elucidate sulfide intrusion and different...... not present in terrestrial plants at that level. Sulfide is not necessarily toxic but used as sulfur nutrition, presupposing healthy seagrass ecosystems that can support detoxification mechanisms. Presence or absence of those mechanisms determines susceptibility of seagrass ecosystems to sediment sulfide...

  16. Use of bauxite residue (red mud) as a low cost sorbent for sulfide removal in polluted water remediation. (United States)

    Sheng, Yanqing; Sun, Qiyao; Sun, Ruichuan; Burke, Ian T; Mortimer, Robert J G

    Sulfide is an important pollutant in aqueous systems. Sulfide removal from polluted waters is required prior to discharge. Red mud (RM) is a solid waste of bauxite processing that is rich in reactive iron oxides and consequently has the potential to be used to remove sulfide from aqueous systems. A series of experiments was undertaken using raw and sintered RM to remove sulfide from waters. RM was highly efficient at sulfide removal (average 75% sulfide removal at initial concentration of ∼5 mg L(-1), with 500 mg L(-1) RM addition) due to both physical adsorption (high specific area) and chemical reaction (with amorphous Fe). Sintered RM, which has a lower surface area and lower mineral reactivity, was much less efficient at removing sulfide (∼20% removal under equivalent experimental conditions). Furthermore, concomitant metal release from raw RM was lower than for sintered RM during the sulfide removal process. The results showed that raw RM is a potentially suitable material for sulfide removal from polluted waters and consequently could be used as a low cost alternative treatment in certain engineering applications.

  17. Is India the Exception?

    DEFF Research Database (Denmark)

    Nielsen, Klaus; Storm, Rasmus K.


    in international sport events a similar impact of extraordinary growth rates has been almost totally absent in the case of India. Is India an exception? Several econometric studies have shown that income per capita is a significant variable explaining elite sport results such as results in the Olympic Games. From...... in the sports of the Olympic Summer Games. The findings show only a very weak correlation, if any at all. However, a detailed analysis of country evidence shows interesting trends and details. The paper concludes with tentative explanations for the findings including the contradictory country evidence....

  18. Is India the Exception?

    DEFF Research Database (Denmark)

    Nielsen, Klaus; Storm, Rasmus K.

    . Is India an exception? Several econometric studies have shown that income per capita is a significant variable explaining elite sport results such as results in the Olympic Games. From this stylized fact follows the hypothesis that 'above/below average' growth rates lead to relative improvements...... between growth in GNP per capita and growth in medal points (no. 1: five points, no. 2: three points, no.3: two points) in Olympic Summer Games. The findings show no correlation and in a few calculations a very weak correlation. Among the countries behaving in accordance with the hypothesis in the most...

  19. Role of biogenic sulfide in attenuating zinc oxide and copper nanoparticle toxicity to acetoclastic methanogenesis. (United States)

    Gonzalez-Estrella, Jorge; Puyol, Daniel; Sierra-Alvarez, Reyes; Field, Jim A


    Soluble ions released by zinc oxide (ZnO) and copper (Cu(0)) nanoparticles (NPs) have been associated with toxicity to methanogens. This study evaluated the role of biogenic sulfide in attenuating ZnO and Cu(0) NP toxicity to methanogens. Short- and long-term batch experiments were conducted to explore ZnO and Cu(0) NPs toxicity to acetoclastic methanogens in sulfate-containing (0.4mM) and sulfate-free conditions. ZnO and Cu(0) were respectively 14 and 7-fold less toxic in sulfate-containing than in sulfate-free assays as indicated by inhibitory constants (Ki). The Ki with respect to residual soluble metal indicated that soluble metal was well correlated with toxicity irrespective of the metal ion source or presence of biogenic sulfide. Long-term assays indicated that ZnO and Cu(0) NPs caused different effects on methanogens. ZnO NPs without protection of sulfide caused a chronic effect, whereas Cu(0) NPs caused an acute effect and recovered. This study confirms that biogenic sulfide effectively attenuates ZnO and Cu(0) NPs toxicity to methanogens by the formation of metal sulfides. Copyright © 2014 Elsevier B.V. All rights reserved.

  20. Replacive sulfide formation in anhydrite chimneys from the Pacmanus hydrothermal field, Papua New Guinea (United States)

    Los, Catharina; Bach, Wolfgang; Plümper, Oliver


    Hydrothermal flow within the oceanic crust is an important process for the exchange of energy and mass between the lithosphere, hydrosphere and biosphere. Infiltrated seawater heats up and interacts with wall rock, causing mineral replacement reactions. These play a large role in the formation of ore deposits; at the discharge zone, a hot, acidic and metal-rich potential ore fluid exits the crust. It mixes with seawater and forms chimneys, built up of sulfate minerals such as anhydrite (CaSO4), which are subsequently replaced by sulfide minerals. Sulfide formation is related to fluid pathways, defined by cracks and pores in the sulfate chimney. Over time, these systems might develop into massive sulfide deposits. The big question is then: how is sulfate-sulfide replacement related to the evolution of rock porosity? To address this question, sulfide-bearing anhydrite chimneys from the Pacmanus hydrothermal field (Manus Basin, Papua New Guinea) were studied using X-ray tomography, EMPA, FIB-SEM and -TEM. The apparently massive anhydrite turns out highly porous on the micro scale, with sulfide minerals in anhydrite cleavage planes and along grain boundaries. The size of the sulfide grains relates to the pores they grew into, suggesting a tight coupling between dissolution (porosity generation) and growth of replacive minerals. Some of the sulfide grains are hollow and apparently used the dissolving anhydrite as a substrate to start growth in a pore. Another mode of sulfide development is aggregates of euhedral pyrite cores surrounded by colloform chalcopyrite. This occurrence implies that fluid pathways have remained open for some time to allow several stages of precipitation during fluid evolution. To start the replacement and to keep it going, porosity generation is crucial. Our samples show that dissolution of anhydrite occurred along pathways where fluid could enter, such as cleavage planes and grain boundaries. It appears that fluids ascending within the inner

  1. Morphology and thermal studies of zinc sulfide and cadmium sulfide nanoparticles in polyvinyl alcohol matrix (United States)

    Osuntokun, Jejenija; Ajibade, Peter A.


    Zn(II) and Cd(II) metal complexes of 1-cyano-1-carboethoxyethylene-2,2-dithiolato-κS,S'-bis(N,N-dimethylthiourea-κS) have been synthesized and characterized with analytical and spectroscopic techniques. The complexes were thermolysed in hexadecylamine at 200 °C to prepare ZnS and CdS nanoparticles. The nanoparticles were characterized with scanning electron microscope (SEM), transmission electron microscope (TEM), and powder X-ray diffraction (p-XRD). TEM images showed spherically shaped nanoparticles, whose sizes are in the range 4.33-7.21 nm for ZnS and 4.95-7.7 nm CdS respectively and XRD confirmed cubic crystalline phases for the nanoparticles. The optical band gap energy evaluated from the absorption spectra are 2.88 eV (430 nm) and 2.81 eV (440 nm) for the ZnS and CdS nanoparticles respectively. The as-prepared metal sulfide nanoparticles were further incorporated into polyvinyl alcohol (PVA) to give ZnS/PVA and CdS/PVA composites. The polymer nanocomposites were studied to investigate their morphology and thermal properties relative to the pure PVA. XRD diffractions indicated that the crystalline phases of the nanoparticles and the sizes in PVA matrices remained unaltered. Infra-red spectra studies revealed interactions between the PVA and the metal sulfide nanoparticles and TGA studies show that the ZnS/PVA and CdS/PVA nanocomposites exhibit better thermal stability than the pure PVA.

  2. Morphology and thermal studies of zinc sulfide and cadmium sulfide nanoparticles in polyvinyl alcohol matrix

    Energy Technology Data Exchange (ETDEWEB)

    Osuntokun, Jejenija; Ajibade, Peter A., E-mail:


    Zn(II) and Cd(II) metal complexes of 1-cyano-1-carboethoxyethylene-2,2-dithiolato–κS,S’–bis (N,N-dimethylthiourea–κS) have been synthesized and characterized with analytical and spectroscopic techniques. The complexes were thermolysed in hexadecylamine at 200 °C to prepare ZnS and CdS nanoparticles. The nanoparticles were characterized with scanning electron microscope (SEM), transmission electron microscope (TEM), and powder X-ray diffraction (p-XRD). TEM images showed spherically shaped nanoparticles, whose sizes are in the range 4.33–7.21 nm for ZnS and 4.95–7.7 nm CdS respectively and XRD confirmed cubic crystalline phases for the nanoparticles. The optical band gap energy evaluated from the absorption spectra are 2.88 eV (430 nm) and 2.81 eV (440 nm) for the ZnS and CdS nanoparticles respectively. The as-prepared metal sulfide nanoparticles were further incorporated into polyvinyl alcohol (PVA) to give ZnS/PVA and CdS/PVA composites. The polymer nanocomposites were studied to investigate their morphology and thermal properties relative to the pure PVA. XRD diffractions indicated that the crystalline phases of the nanoparticles and the sizes in PVA matrices remained unaltered. Infra-red spectra studies revealed interactions between the PVA and the metal sulfide nanoparticles and TGA studies show that the ZnS/PVA and CdS/PVA nanocomposites exhibit better thermal stability than the pure PVA.

  3. Giftedness: an exceptionality examined. (United States)

    Robinson, A; Clinkenbeard, P R


    The study of giftedness has practical origins. High-level performance intrigues people. Theoretically, the study of giftedness is related to the psychology of individual differences and has focused on the constructs of intelligence, creativity, and motivation. At a practical level, the research is largely related to school and family contexts, which develop gifts and talents in children and youth. Although broadened definitions of giftedness have emerged, the most extensive body of research available for review concentrates on intellectual giftedness. The varying definitions of giftedness and the impact of social context and diversity on the development of talent pose significant challenges for the field. Finally, the study of exceptionally advanced performance provides insight into basic psychological processes and the school contexts that develop talents in children and youth.

  4. Amorphous molybdenum sulfides as hydrogen evolution catalysts. (United States)

    Morales-Guio, Carlos G; Hu, Xile


    Providing energy for a population projected to reach 9 billion people within the middle of this century is one of the most pressing societal issues. Burning fossil fuels at a rate and scale that satisfy our near-term demand will irreversibly damage the living environment. Among the various sources of alternative and CO2-emission-free energies, the sun is the only source that is capable of providing enough energy for the whole world. Sunlight energy, however, is intermittent and requires an efficient storage mechanism. Sunlight-driven water splitting to make hydrogen is widely considered as one of the most attractive methods for solar energy storage. Water splitting needs a hydrogen evolution catalyst to accelerate the rate of hydrogen production and to lower the energy loss in this process. Precious metals such as Pt are superior catalysts, but they are too expensive and scarce for large-scale applications. In this Account, we summarize our recent research on the preparation, characterization, and application of amorphous molybdenum sulfide catalysts for the hydrogen evolution reaction. The catalysts can be synthesized by electrochemical deposition under ambient conditions from readily available and inexpensive precursors. The catalytic activity is among the highest for nonprecious catalysts. For example, at a loading of 0.2 mg/cm(2), the optimal catalyst delivers a current density of 10 mA/cm(2) at an overpotential of 160 mV. The growth mechanism of the electrochemically deposited film catalysts was revealed by an electrochemical quartz microcrystal balance study. While different electrochemical deposition methods produce films with different initial compositions, the active catalysts are the same and are identified as a "MoS(2+x)" species. The activity of the film catalysts can be further promoted by divalent Fe, Co, and Ni ions, and the origins of the promotional effects have been probed. Highly active amorphous molybdenum sulfide particles can also be prepared

  5. Inhibition of Sulfide Mineral Oxidation by Surface Coating Agents: Batch (United States)

    Choi, J.; Ji, M. K.; Yun, H. S.; Park, Y. T.; Gee, E. D.; Lee, W. R.; Jeon, B.-H.


    Mining activities and mineral industries have impacted on rapid oxidation of sulfide minerals such as pyrite (FeS2) which leads to Acid Mine Drainage (AMD) formation. Some of the abandoned mines discharge polluted water without proper environmental remediation treatments, largely because of financial constraints in treating AMD. Magnitude of the problem is considerable, especially in countries with a long history of mining. As metal sulfides become oxidized during mining activities, the aqueous environment becomes acid and rich in many metals, including iron, lead, mercury, arsenic and many others. The toxic heavy metals are responsible for the environmental deterioration of stream, groundwater and soils. Several strategies to remediate AMD contaminated sites have been proposed. Among the source inhibition and prevention technologies, microencapsulation (coating) has been considered as a promising technology. The encapsulation is based on inhibition of O2 diffusion by surface coating agent and is expected to control the oxidation of pyrite for a long time. Potential of several surface coating agents for preventing oxidation of metal sulfide minerals from both Young-Dong coal mine and Il-Gwang gold mine were examined by conducting batch experiments and field tests. Powdered pyrite as a standard sulfide mineral and rock samples from two mine outcrops were mixed with six coating agents (KH2PO4, MgO and KMnO4 as chemical agents, and apatite, cement and manganite as mineral agents) and incubated with oxidizing agents (H2O2 or NaClO). Batch experiments with Young-Dong coal mine samples showed least SO42- production in presence of KMnO4 (16% sulfate production compared to no surface coating agents) or cement (4%) within 8 days. In the case of Il-Gwang mine samples, least SO42- production was observed in presence of KH2PO4 (8%) or cement (2%) within 8 days. Field-scale pilot tests at Il-Gwang site also showed that addition of KH2PO4 decreased sulfate production from 200 to

  6. Application of SnO2 nanoparticle as sulfide gas sensor using UV/VIS/NIR spectrophotometer (United States)

    Juliasih, N.; Buchari; Noviandri, I.


    Sulfide gas monitoring is required to protect organisms from its toxicity. Nanoparticles of metal oxides have characteristics that applicable as sensors for controlling environmental pollution like sulfide gas. Thin film of SnO2 as one part of the sulfide gas sensor was synthesized with the chemical liquid deposition method, and characterized by UV/VIS/NIR-Spectrophotometer before and after gas application, also using FTIR, SEM and XRD. Characterization studies showed nanoparticle sizes from the diameters range of 38-71 nm. Application of SnO2 thin film to sulfide gas detected by UV/VIS/NIR Spectrophotometer with diffuse reflectance showed chemical reaction by the shifting of maximum % R peak at wavelength of 1428 cm. The benefit of measurement of sulfide gas using this SnO2 nano thin film is that it could be done at the room temperature.

  7. Facile one-pot synthesis of spherical zinc sulfide-carbon nanocomposite powders with superior electrochemical properties as anode materials for Li-ion batteries. (United States)

    Jang, Yong Seung; Kang, Yun Chan


    A novel and simple one-pot method of systematically synthesizing spherical metal sulfide-carbon composite powders is reported for the first time. The zinc sulfide-carbon composite is selected as the first target material. The prepared composite powders show superior electrochemical properties as anode materials for lithium-ion batteries.

  8. Photovoltaic effect in individual asymmetrically contacted lead sulfide nanosheets (United States)

    Dogan, Sedat; Bielewicz, Thomas; Lebedeva, Vera; Klinke, Christian


    Solution-processable, two-dimensional semiconductors are promising optoelectronic materials which could find application in low-cost solar cells. Lead sulfide nanocrystals raised attention since the effective band gap can be adapted over a wide range by electronic confinement and observed multi-exciton generation promises higher efficiencies. We report on the influence of the contact metal work function on the properties of transistors based on individual two-dimensional lead sulfide nanosheets. Using palladium we observed mobilities of up to 31 cm2 V-1 s-1. Furthermore, we demonstrate that asymmetrically contacted nanosheets show photovoltaic effect and that the nanosheets' height has a decisive impact on the device performance. Nanosheets with a thickness of 5.4 nm contacted with platinum and titanium show a power conversion efficiency of up to 0.94% (EQE 75.70%). The results underline the high hopes put on such materials.Solution-processable, two-dimensional semiconductors are promising optoelectronic materials which could find application in low-cost solar cells. Lead sulfide nanocrystals raised attention since the effective band gap can be adapted over a wide range by electronic confinement and observed multi-exciton generation promises higher efficiencies. We report on the influence of the contact metal work function on the properties of transistors based on individual two-dimensional lead sulfide nanosheets. Using palladium we observed mobilities of up to 31 cm2 V-1 s-1. Furthermore, we demonstrate that asymmetrically contacted nanosheets show photovoltaic effect and that the nanosheets' height has a decisive impact on the device performance. Nanosheets with a thickness of 5.4 nm contacted with platinum and titanium show a power conversion efficiency of up to 0.94% (EQE 75.70%). The results underline the high hopes put on such materials. Electronic supplementary information (ESI) available. See DOI: 10.1039/c4nr06957a

  9. New Nordic Exceptionalism

    DEFF Research Database (Denmark)

    Danbolt, Mathias


    that have been central to the debates on the branding of Nordicity over the last decades: on the one hand, the discourse of “Nordic exceptionalism,” that since the 1960s has been central to the promotion of a Nordic political, socio-economic, and internationalist “third way” model, and, on the other hand......At the 2009 Nordic Culture Forum summit in Berlin that centered on the profiling and branding of the Nordic region in a globalized world, one presenter stood out from the crowd. The lobbyist Annika Sigurdardottir delivered a speech that called for the establishment of “The United Nations of Norden......, the discourse on the “New Nordic,” that emerged out of the New Nordic Food-movement in the early 2000s, and which has given art and culture a privileged role in the international re-fashioning of the Nordic brand. Through an analysis of Kim and Einhorn’s United Nations of Norden (UNN)-performance, the article...

  10. Exceptional composite dark matter

    Energy Technology Data Exchange (ETDEWEB)

    Ballesteros, Guillermo [Universite Paris Saclay, CEA, CNRS, Institut de Physique Theorique, Gif-sur-Yvette (France); Carmona, Adrian [CERN, Theoretical Physics Department, Geneva (Switzerland); Chala, Mikael [Universitat de Valencia y IFIC, Universitat de Valencia-CSIC, Departament de Fisica Teorica, Burjassot, Valencia (Spain)


    We study the dark matter phenomenology of non-minimal composite Higgs models with SO(7) broken to the exceptional group G{sub 2}. In addition to the Higgs, three pseudo-Nambu-Goldstone bosons arise, one of which is electrically neutral. A parity symmetry is enough to ensure this resonance is stable. In fact, if the breaking of the Goldstone symmetry is driven by the fermion sector, this Z{sub 2} symmetry is automatically unbroken in the electroweak phase. In this case, the relic density, as well as the expected indirect, direct and collider signals are then uniquely determined by the value of the compositeness scale, f. Current experimental bounds allow one to account for a large fraction of the dark matter of the Universe if the dark matter particle is part of an electroweak triplet. The totality of the relic abundance can be accommodated if instead this particle is a composite singlet. In both cases, the scale f and the dark matter mass are of the order of a few TeV. (orig.)

  11. On exceptional instanton strings (United States)

    Del Zotto, Michele; Lockhart, Guglielmo


    According to a recent classification of 6d (1 , 0) theories within F-theory there are only six "pure" 6d gauge theories which have a UV superconformal fixed point. The corresponding gauge groups are SU(3) , SO(8) , F 4 , E 6 , E 7, and E 8. These exceptional models have BPS strings which are also instantons for the corresponding gauge groups. For G simply-laced, we determine the 2d N=(0,4) worldsheet theories of such BPS instanton strings by a simple geometric engineering argument. These are given by a twisted S 2 compactification of the 4d N=2 theories of type H 2 , D 4 , E 6 , E 7 and E 8 (and their higher rank generalizations), where the 6d instanton number is mapped to the rank of the corresponding 4d SCFT. This determines their anomaly polynomials and, via topological strings, establishes an interesting relation among the corresponding T 2 × S 2 partition functions and the Hilbert series for moduli spaces of G instantons. Such relations allow to bootstrap the corresponding elliptic genera by modularity. As an example of such procedure, the elliptic genera for a single instanton string are determined. The same method also fixes the elliptic genus for case of one F 4 instanton. These results unveil a rather surprising relation with the Schur index of the corresponding 4d N=2 models.

  12. An experimental study of Fe-Ni exchange between sulfide melt and olivine at upper mantle conditions: implications for mantle sulfide compositions and phase equilibria (United States)

    Zhang, Zhou; von der Handt, Anette; Hirschmann, Marc M.


    attributable to differences in temperature and pressure between experimental studies. It may be related in part to the effects of metal/sulfur ratio in sulfide melt. Application of these results to the composition of molten sulfide in peridotite indicates that compositions are intermediate in composition (X_{{{Ni}}}^{{{sulfide}}} 0.4-0.6) in the shallow mantle at 50 km, becomes more Ni rich with depth as the O content of the melt diminishes, reaching a maximum (0.6-0.7) at depths near 80-120 km, and then becomes more Fe rich in the deeper mantle where conditions are more reduced, approaching (X_{{{Ni}}}^{{{sulfide}}} 0.28) > 140 km depth. Because Ni-rich sulfide in the shallow upper mantle melts at lower temperature than more Fe-rich compositions, mantle sulfide is likely molten in much of the deep continental lithosphere, including regions of diamond formation.

  13. Isotopic data from proterozoic sediment-hosted sulfide deposits of Brazil: Implications for their metallogenic evolution and for mineral exploration

    International Nuclear Information System (INIS)

    Misi, Aroldo; Coelho, Carlos E.S.; Franca Rocha, Washington J.S.; Gomez, Adriana S.R.; Cunha, Iona A.; Iyer, Sundaram S.; Tassinari, Colombo C.G.; Kyle, J. Richard


    Geological, petrographic, fluid inclusions studies and isotopic data of seven Proterozoic sediment-hosted Pb-Zn-Ag sulfide deposits of Brazil, permit the estimation of the age of the hosting sequence and the mineralization, the nature of the sulfur and metal sources, the temperature range of sulfide formation and the environment of deposition of the mineral deposits. The studies suggest that they were formed during periods of extensional tectonics: Growth faults or reactivated basement faults were responsible for localized circulation of metal-bearing fluids within the sedimentary sequences. In most cases, sulfides were formed by the reduction of sedimentary sulfates. Linear structures are important controls for sulfide concentration in these Proterozoic basins. (author)

  14. Formation of mercury sulfide from Hg(II)−thiolate complexes in natural organic matter (United States)

    Alain Manceau,; Cyprien Lemouchi,; Mironel Enescu,; Anne-Claire Gaillot,; Martine Lanson,; Valerie Magnin,; Pieter Glatzel,; Poulin, Brett; Ryan, Joseph N.; Aiken, George R.; Isabelle Gautier-Lunea,; Kathryn L. Nagy,


    Methylmercury is the environmental form of neurotoxic mercury that is biomagnified in the food chain. Methylation rates are reduced when the metal is sequestered in crystalline mercury sulfides or bound to thiol groups in macromolecular natural organic matter. Mercury sulfide minerals are known to nucleate in anoxic zones, by reaction of the thiol-bound mercury with biogenic sulfide, but not in oxic environments. We present experimental evidence that mercury sulfide forms from thiol-bound mercury alone in aqueous dark systems in contact with air. The maximum amount of nanoparticulate mercury sulfide relative to thiol-bound mercury obtained by reacting dissolved mercury and soil organic matter matches that detected in the organic horizon of a contaminated soil situated downstream from Oak Ridge, TN, in the United States. The nearly identical ratios of the two forms of mercury in field and experimental systems suggest a common reaction mechanism for nucleating the mineral. We identified a chemical reaction mechanism that is thermodynamically favorable in which thiol-bound mercury polymerizes to mercury–sulfur clusters. The clusters form by elimination of sulfur from the thiol complexes via breaking of mercury–sulfur bonds as in an alkylation reaction. Addition of sulfide is not required. This nucleation mechanism provides one explanation for how mercury may be immobilized, and eventually sequestered, in oxygenated surface environments.

  15. Soft chemical control of the crystal and magnetic structure of a layered mixed valent manganite oxide sulfide

    Directory of Open Access Journals (Sweden)

    Jack N. Blandy


    Full Text Available Oxidative deintercalation of copper ions from the sulfide layers of the layered mixed-valent manganite oxide sulfide Sr2MnO2Cu1.5S2 results in control of the copper-vacancy modulated superstructure and the ordered arrangement of magnetic moments carried by the manganese ions. This soft chemistry enables control of the structures and properties of these complex materials which complement mixed-valent perovskite and perovskite-related transition metal oxides.

  16. Sulfide mineralization in ultramafic rocks of the Faryab ophiolite complex, southern Kerman

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Rajabzadeh


    Full Text Available Introduction Worldwide, Ni-Cu and PGE magmatic sulfide deposits are confined to the lower parts of stratiform mafic and ultramafic complexes. However, ophiolite mafic and ultramafic complexes have been rarely explored for sulfide deposits despite the fact that they have been extensively explored and exploited for chromite. Sulfide saturation during magmatic evolution is necessary for sulfide mineralization, in which sulfide melts scavenge chalcophile metals from the parent magma and concentrate them in specific lithological zones. The lack of exploration for sulfides in this environment suggests that sulfide saturation is rarely attained in ophiolite-related magmas. Some ophiolites, however, contain sulfide deposits, such as at Acoje in Philippines, and Cliffs in Shetland, U.K. (Evans, 2000; Naldrett, 2004. The Faryab ophiolite complex in southern Kerman Province, the most important mining area for chromite deposits in Iran, is located in the southwest part of the Makran Zone. Evidence of sulfide mineralization has been reported there by some authors (e.g. Rajabzadeh and Moosavinasab, 2013. This paper discusses the genesis of sulfides in the Faryab ophiolite using mineral chemistry of the major mineral phases in different rocks of the ophiolite column in order to determine the possible lithological location of sulfide deposits. Materials and methods Seventy three rock samples from cumulate units were collected from surficial occurrences and drill core. The samples were studied using conventional microscopic methods and the mineralogy confirmed by x-ray diffraction. Electron microprobe analysis was carried out on different mineral phases in order to determine the chemistry of the minerals used in the interpretation of magma evolution in the Faryab ophiolite. Lithologically, the Faryab ophiolite complex is divided into two major parts: the northern part includes magmatic rocks and the southern part is comprised of rocks residual after partial

  17. Source and fate of inorganic soil contamination around the abandoned Phillips sulfide mine, hudson Highlands, New York (United States)

    Gilchrist, S.; Gates, A.; Elzinga, E.; Gorring, M.; Szabo, Z.


    The abandoned Phillips sulfide mine in the critical Highlands watershed in New York has been shown to produce strongly acidic mine drainage (AMD) with anomalous metal contaminants in first-order streams that exceeded local water standards by up to several orders of magnitude (Gilchrist et al., 2009). The metal-sulfide-rich tailings also produce contaminated soils with pH meter scale is self-similar to those in the bulk soil samples. Generally metals decreased, with some fluctuations, rapidly downslope through suspension of fines and dissolution in AMD leaving the area of substantial contamination << 0.5 km from the source.

  18. Students' Strategies for Exception Handling (United States)

    Rashkovits, Rami; Lavy, Ilana


    This study discusses and presents various strategies employed by novice programmers concerning exception handling. The main contributions of this paper are as follows: we provide an analysis tool to measure the level of assimilation of exception handling mechanism; we present and analyse strategies to handle exceptions; we present and analyse…

  19. Structural studies of copper sulfide films: effect of ambient atmosphere

    Directory of Open Access Journals (Sweden)

    Manisha Kundu et al


    Full Text Available We examined the structural properties of copper sulfide films as a function of the sulfurization time of 70-nm-thick Cu films. Copper sulfide films with various phases such as mixed metallic Cu-chalcocite, chalcocite, roxbyite, and covellite phases were formed with increasing sulfurization time. To evaluate the structural stability of various films, all the films were exposed to the ambient atmosphere for the same amount of time. Although the phase structure and stoichiometry of the films were maintained at a greater depth, the near-surface region of the films was oxidized and covered with overlayers of oxide, hydroxide, and/or sulfate species due to the exposure and reaction with the ambient atmosphere. The oxygen uptake and its reactivity with the copper sulfide film surfaces were enhanced with increasing sulfur content of the films. In addition, the type of divalent state of copper formed on the film surfaces depended on the phase structure, composition, and stoichiometry of the films.

  20. Nitrogen release from forest soils containing sulfide-bearing sediments (United States)

    Maileena Nieminen, Tiina; Merilä, Päivi; Ukonmaanaho, Liisa


    Soils containing sediments dominated by metal sulfides cause high acidity and release of heavy metals, when excavated or drained, as the aeration of these sediments causes formation of sulfuric acid. Consequent leaching of acidity and heavy metals can kill tree seedlings and animals such as fish, contaminate water, and corrode concrete and steel. These types of soils are called acid sulfate soils. Their metamorphic equivalents, such as sulfide rich black shales, pose a very similar risk of acidity and metal release to the environment. Until today the main focus in treatment of the acid sulfate soils has been to prevent acidification and metal toxicity to agricultural crop plants, and only limited attention has been paid to the environmental threat caused by the release of acidity and heavy metals to the surrounding water courses. Even less attention is paid on release of major nutrients, such as nitrogen, although these sediments are extremely rich in carbon and nitrogen and present a potentially high microbiological activity. In Europe, the largest cover of acid sulfate soils is found in coastal lowlands of Finland. Estimates of acid sulfate soils in agricultural use range from 1 300 to 3 000 km2, but the area in other land use classes, such as managed peatland forests, is presumably larger. In Finland, 49 500 km2 of peatlands have been drained for forestry, and most of these peatland forests will be at the regeneration stage within 10 to 30 years. As ditch network maintenance is often a prerequisite for a successful establishment of the following tree generation, the effects of maintenance operations on the quality of drainage water should be under special control in peatlands underlain by sulfide-bearing sediments. Therefore, identification of risk areas and effective prevention of acidity and metal release during drain maintenance related soil excavating are great challenges for forestry on coastal lowlands of Finland. The organic and inorganic nitrogen

  1. SIP response for volume content of sulfide mineral in artificial specimen (United States)

    Park, Mi Kyung; Park, Samgyu; Jong Yi, Myeong; Kim, Jung Ho


    Spectral Induced Polarization (SIP) method has recently been introduced to enhance mineral resource exploration techniques in metal ore deposit, South Korea. Because the valuable mineral ore contains various sulfide minerals such as pyrite (FeS), chalcopyrite (CuFeS2), and galena (PbS), which show IP (Induced Polarization) effect. The conventional IP method was not adequate to find these various sulfide minerals because of certain restrictions, including limited frequency. In order to solve this problem, the SIP (Spectral Induced Polarization) method was introduced, which measures responses like as amplitude (or resistivity) and phase for a wide frequency band. The application of the SIP method has been increasing as an exploration technology for mineral resources, because it can be used to acquire and analyze high quality IP data according to the spectral frequency. SIP responses are strong in the presence of the sulfide minerals; however, sufficient study on the characteristics of the SIP response for the various sulfide minerals is not available so far. In this study, in order to identify the SIP response characteristics of sulfide minerals, the SIP method was used in the laboratory; on artificial specimens filled with glass beads and sulfide minerals. The experiment was controlled by the changing volume content, and grain size, of three kinds of sulfide minerals (i.e., chalcopyrite, pyrite, and galena). The grain sizes of the sulfide minerals were varied in five steps: under 0.5 mm, 0.5 - 1.0 mm, 1.0 - 2.0 mm, 2.0 - 2.85 mm, and 2.85 - 4.0 mm, while the grain size of the glass beads was in the range of 0.75 - 1.0 mm. Variation of the volume content of the sulfide mineral was divided into eight grades. The sulfide minerals occupied 0.5, 1, 2, 3, 5, 7, 10, and 20 percent of the total volume 250 ml specimens. The volume content was converted from the weight using the density of a standard volume of 100 ml for each grain size. The results show that phase response

  2. Metal uptake by lolium perenne in contaminated soils using a four-steps approach

    NARCIS (Netherlands)

    Kalis, E.J.J.; Temminghoff, E.J.M.; Visser, A.; Riemsdijk, van W.H.


    Metal bioavailability and toxicity to aquatic organisms are greatly affected by variables such as pH, hardness, organic matter, and sediment acid-volatile sulfide (AVS). Sediment AVS, which reduces metal bioavailability and toxicity by binding and immobilizing metals as insoluble sulfides, has been

  3. Sulfide toxicity kinetics of a uasb reactor

    Directory of Open Access Journals (Sweden)

    D. R. Paula Jr.


    Full Text Available The effect of sulfide toxicity on kinetic parameters of anaerobic organic matter removal in a UASB (up-flow anaerobic sludge blanket reactor is presented. Two lab-scale UASB reactors (10.5 L were operated continuously during 12 months. The reactors were fed with synthetic wastes prepared daily using glucose, ammonium acetate, methanol and nutrient solution. One of the reactors also received increasing concentrations of sodium sulfide. For both reactors, the flow rate of 16 L.d-1 was held constant throughout the experiment, corresponding to a hydraulic retention time of 15.6 hours. The classic model for non-competitive sulfide inhibition was applied to the experimental data for determining the overall kinetic parameter of specific substrate utilization (q and the sulfide inhibition coefficient (Ki. The application of the kinetic parameters determined allows prediction of methanogenesis inhibition and thus the adoption of operating parameters to minimize sulfide toxicity in UASB reactors.

  4. Effect of hydraulic retention time on metal precipitation in sulfate reducing inverse fluidized bed reactors

    KAUST Repository

    Villa-Gómez, Denys Kristalia


    BACKGROUND: Metal sulfide recovery in sulfate reducing bioreactors is a challenge due to the formation of small precipitates with poor settling properties. The size of the metal sulfide precipitates with the change in operational parameters such as pH, sulfide concentration and reactor configuration has been previously studied. The effect of the hydraulic retention time (HRT) on the metal precipitate characteristics such as particle size for settling has not yet been addressed. RESULTS: The change in size of the metal (Cu, Zn, Pb and Cd) sulfide precipitates as a function of the HRT was studied in two sulfate reducing inversed fluidized bed (IFB) reactors operating at different chemical oxygen demand concentrations to produce high and low sulfide concentrations. The decrease of the HRT from 24 to 9h in both IFB reactors affected the contact time of the precipitates formed, thus making differences in aggregation and particle growth regardless of the differences in sulfide concentration. Further HRT decrease to 4.5h affected the sulfate reducing activity for sulfide production and hence, the supersaturation level and solid phase speciation. Metal sulfide precipitates affected the sulfate reducing activity and community in the biofilm, probably because of the stronger local supersaturation causing metal sulfides accumulation in the biofilm. CONCLUSIONS: This study shows that the HRT is an important factor determining the size and thus the settling rate of the metal sulfides formed in bioreactors.

  5. Reactive Precipitation of Anhydrous Alkali Sulfide Nanocrystals with Concomitant Abatement of Hydrogen Sulfide and Cogeneration of Hydrogen. (United States)

    Li, Xuemin; Zhao, Yangzhi; Brennan, Alice; McCeig, Miranda; Wolden, Colin A; Yang, Yongan


    Anhydrous alkali sulfide (M 2 S, M=Li or Na) nanocrystals (NCs) are important materials central to the development of next generation cathodes and solid-state electrolytes for advanced batteries, but not commercially available at present. This work reports an innovative method to directly synthesize M 2 S NCs through alcohol-mediated reactions between alkali metals and hydrogen sulfide (H 2 S). In the first step, the alkali metal is complexed with alcohol in solution, forming metal alkoxide (ROM) and releasing hydrogen (H 2 ). Next, H 2 S is bubbled through the ROM solution, where both chemicals are completely consumed to produce phase-pure M 2 S NC precipitates and regenerate alcohol that can be recycled. The M 2 S NCs morphology may be tuned through the choice of the alcohol and solvent. Both synthetic steps are thermodynamically favorable (ΔG m o <-100 kJ mol -1 ), proceeding rapidly to completion at ambient temperature with almost 100 % atom efficiency. The net result, H 2 S+2 m→M 2 S+H 2 , makes good use of a hazardous chemical (H 2 S) and delivers two value-added products that naturally phase separate for easy recovery. This scalable approach provides an energy-efficient and environmentally benign solution to the production of nanostructured materials required in emerging battery technologies. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Exploring the main function of reduced graphene oxide nano-flakes in a nickel cobalt sulfide counter electrode for dye-sensitized solar cell (United States)

    Lu, Man-Ning; Lin, Jeng-Yu; Wei, Tzu-Chien


    Addition of carbonaceous materials into transition metal sulfide counter electrode (CE) of a dye-sensitized solar cell (DSSC) is a common method to improve the performance of the CE and consequent photovoltaic performance. This improvement is almost without exception attributed to the improvement of overall conductivity after the carbonaceous material addition; however, the root function of these carbonaceous materials in promoting the solar cell efficiency is seldom discussed. In this study, highly crystallized nickel cobalt sulfide (NCS) micro-particles were mixed with a small portion of home-made reduced graphene oxide (rGO) nano-flakes. This NCS/rGO hybrid is subjected to extensive characterizations including X-ray diffraction, Raman spectroscopy, field emission scanning microscopy and electrochemical impedance spectroscopy. It is found that the rGO acts bi-functionally including a co-catalyst in accelerating the tri-iodide reduction for the main NCS catalysts, conductivity promotor to decrease the series resistance of the CE. Proved by electrochemical impedance spectroscopy, it is confirmed that the decrease in series resistance is less insignificant than that in charge transfer resistance, indicating rGO functions more profoundly as a co-catalyst than as a conductivity promotor. Moreover, an argument to highlight the requirement of a CE in a dim-light optimized DSSC is also proposed.

  7. The Exception Proves the Rule


    Holton, Richard


    Legal rules admit of exceptions; indeed, it has been a legal maxim that one can infer the existence of a rule from exceptions that are made to it. Hart claims that the exceptions do not admit of exhaustive statement (a form of legal particularism) but that nonetheless rules can bind. This paper develops a logical framework which accommodates this position, shows that it is available to a positivist, elucidates the role of rules within it, and concludes by discussing the relevan...

  8. Trends in Modern Exception Handling

    Directory of Open Access Journals (Sweden)

    Marcin Kuta


    Full Text Available Exception handling is nowadays a necessary component of error proof information systems. The paper presents overview of techniques and models of exception handling, problems connected with them and potential solutions. The aspects of implementation of propagation mechanisms and exception handling, their effect on semantics and general program efficiency are also taken into account. Presented mechanisms were adopted to modern programming languages. Considering design area, formal methods and formal verification of program properties we can notice exception handling mechanisms are weakly present what makes a field for future research.

  9. Metal fractionation in sludge from sewage UASB treatment. (United States)

    Braga, A F M; Zaiat, M; Silva, G H R; Fermoso, F G


    This study evaluates the trace metal composition and fractionation in sludge samples from anaerobic sewage treatment plants from six cities in Brazil. Ten metals were evaluated: Ni, Mn, Se, Co, Fe, Zn, K, Cu, Pb and Cr. Specific methanogenic activity of the sludge was also evaluated using acetic acid as the substrate. Among the essential trace metals for anaerobic digestion, Se, Zn, Ni and Fe were found at a high percentage in the organic matter/sulfide fraction in all sludge samples analyzed. These metals are less available for microorganisms than other metals, i.e., Co and K, which were present in significant amounts in the exchangeable and carbonate fractions. Cu is not typically reported as an essential metal but as a possible inhibitor. One of the samples showed a total Cu concentration close to the maximal amount allowed for reuse as fertilizer. Among the non-essential trace metals, Pb was present in all sludge samples at similar low concentrations and was primarily present in the residual fraction, demonstrating very low availability. Cr was found at low concentrations in all sludge samples, except for the sludge from STP5; interestingly, this sludge presented the lowest specific methanogenic activity, indicating possible Cr toxicity. Copyright © 2017 Elsevier Ltd. All rights reserved.

  10. Alternative waste residue materials for passive in situ prevention of sulfide-mine tailings oxidation: A field evaluation (United States)

    Nason, Peter; Johnson, Raymond H.; Neuschutz, Clara; Alakangas, Lena; Ohlander, Bjorn


    Novel solutions for sulfide-mine tailings remediation were evaluated in field-scale experiments on a former tailings repository in northern Sweden. Uncovered sulfide-tailings were compared to sewage-sludge biosolid amended tailings over 2 years. An application of a 0.2 m single-layer sewage-sludge amendment was unsuccessful at preventing oxygen ingress to underlying tailings. It merely slowed the sulfide-oxidation rate by 20%. In addition, sludge-derived metals (Cu, Ni, Fe, and Zn) migrated and precipitated at the tailings-to-sludge interface. By using an additional 0.6 m thick fly-ash sealing layer underlying the sewage sludge layer, a solution to mitigate oxygen transport to the underlying tailings and minimize sulfide-oxidation was found. The fly-ash acted as a hardened physical barrier that prevented oxygen diffusion and provided a trap for sludge-borne metals. Nevertheless, the biosolid application hampered the application, despite the advances in the effectiveness of the fly-ash layer, as sludge-borne nitrate leached through the cover system into the underlying tailings, oxidizing pyrite. This created a 0.3 m deep oxidized zone in 6-years. This study highlights that using sewage sludge in unconventional cover systems is not always a practical solution for the remediation of sulfide-bearing mine tailings to mitigate against sulfide weathering and acid rock drainage formation.

  11. Sulfide Intrusion and Detoxification in the Seagrass Zostera marina

    DEFF Research Database (Denmark)

    Hasler-Sheetal, Harald; Holmer, Marianne


    Gaseous sulfide intrusion into seagrasses growing in sulfidic sediments causes little or no harm to the plant, indicating the presence of an unknown sulfide tolerance or detoxification mechanism. We assessed such mechanism in the seagrass Zostera marina in the laboratory and in the field...... as sulfate throughout the plant. We conclude that avoidance of sulfide exposure by reoxidation of sulfide in the rhizosphere or aerenchyma and tolerance of sulfide intrusion by incorporation of sulfur in the plant are likely major survival strategies of seagrasses in sulfidic sediments....

  12. Electrochemical Synthesis and Characterization of Zinc Sulfide Nanoparticles


    M. Rahimi-Nasarabadi


    Electrosynthesis process has been used for preparation of zinc sulfide nanoparticles. Zinc sulfide nanoparticles in different size and shapes were electrodeposited by electrolysis of zinc plate as anode in sodium sulfide solution. Effects of several reaction variables, such as electrolysis voltage, sulfide ion concentration as reactant, stirring rate of electrolyte solution and temperature on particle size of prepared zinc sulfide were investigated. The significance of these parameters in tun...

  13. Dissolved organic matter enhances microbial mercury methylation under sulfidic conditions (United States)

    Graham, Andrew M.; Aiken, George R.; Gilmour, Cynthia


    Dissolved organic matter (DOM) is generally thought to lower metal bioavailability in aquatic systems due to the formation of metal–DOM complexes that reduce free metal ion concentrations. However, this model may not be pertinent for metal nanoparticles, which are now understood to be ubiquitous, sometimes dominant, metal species in the environment. The influence of DOM on Hg bioavailability to microorganisms was examined under conditions (0.5–5.0 nM Hg and 2–10 μM sulfide) that favor the formation of β-HgS(s) (metacinnabar) nanoparticles. We used the methylation of stable-isotope enriched 201HgCl2 by Desulfovibrio desulfuricans ND132 in short-term washed cell assays as a sensitive, environmentally significant proxy for Hg uptake. Suwannee River humic acid (SRHA) and Williams Lake hydrophobic acid (WLHPoA) substantially enhanced (2- to 38-fold) the bioavailability of Hg to ND132 over a wide range of Hg/DOM ratios (9.4 pmol/mg DOM to 9.4 nmol/mg DOM), including environmentally relevant ratios. Methylmercury (MeHg) production by ND132 increased linearly with either SRHA or WLHPoA concentration, but SRHA, a terrestrially derived DOM, was far more effective at enhancing Hg-methylation than WLHPoA, an aquatic DOM dominated by autochthonous sources. No DOM-dependent enhancement in Hg methylation was observed in Hg–DOM–sulfide solutions amended with sufficient l-cysteine to prevent β-HgS(s) formation. We hypothesize that small HgS particles, stabilized against aggregation by DOM, are bioavailable to Hg-methylating bacteria. Our laboratory experiments provide a mechanism for the positive correlations between DOC and MeHg production observed in many aquatic sediments and wetland soils.

  14. Crossett Hydrogen Sulfide Air Sampling Report (United States)

    This report summarizes the results of the EPA’s hydrogen sulfide air monitoring conducted along Georgia Pacific’s wastewater treatment system and in surrounding Crossett, AR, neighborhoods in 2017.

  15. Hydrogen peroxide oxidation of mustard-model sulfides catalyzed by iron and manganese tetraarylporphyrines. Oxygen transfer to sulfides versus H(2)O(2) dismutation and catalyst breakdown. (United States)

    Marques, A; Marin, M; Ruasse, M F


    Fe(III)- and Mn(III)-meso-tetraarylporphyrin catalysis of H(2)O(2) oxidation of dibenzyl and phenyl-2-chloroethyl sulfides, 1, is investigated in ethanol with the aim of designing catalytic systems for mustard decontamination. The sulfide conversion, the sulfoxide and sulfone yields, the oxygen transfer from H(2)O(2) to the sulfide, and the catalyst stability depend markedly on the metal, on the substituents of its ligand, and on the presence or the absence of a cocatalyst, imidazole or ammonium acetate. With Fe, sulfones, the only oxidation products, are readily obtained whatever the ligand (TPP, F(20)TPP, or TDCPP) and the cocatalyst; the oxygen transfer is fairly good, up to 95% when the catalyst concentration is small ([1]/[Cat] = 420); the catalyst breakdown is insignificant only in the absence of any cocatalyst. With Mn, the sulfide conversion is achieved completely when the ligand is TDCPP or TSO(3)PP, but not F(20)TPP or TPP; a mixture of sulfoxide, 2, and sulfone, 3, is always obtained with [2]/[3] = 3.5-0.85 depending on the ligand and the cocatalyst (electron withdrawing substituents favor 3 and NH(4)OAc, 2). The catalyst stability is very good, but the oxygen transfer is poor whatever the ligand and the cocatalyst. These results are discussed in terms of a scheme in which sulfide oxygenation, H(2)O(2) dismutation, and oxidative ligand breaking compete. It is shown that the efficiency of the oxygen transfer is related not only to the rate constant of the dismutation route but also to the concentration of the active metal-oxo intermediate, most likely a perferryl or permanganyl species, i.e., to the rate of its formation.

  16. Electrical properties of seafloor massive sulfides (United States)

    Spagnoli, Giovanni; Hannington, Mark; Bairlein, Katharina; Hördt, Andreas; Jegen, Marion; Petersen, Sven; Laurila, Tea


    Seafloor massive sulfide (SMS) deposits are increasingly seen as important marine metal resources for the future. A growing number of industrialized nations are involved in the surveying and sampling of such deposits by drilling. Drill ships are expensive and their availability can be limited; seabed drill rigs are a cost-effective alternative and more suitable for obtaining cores for resource evaluation. In order to achieve the objectives of resource evaluations, details are required of the geological, mineralogical, and physical properties of the polymetallic deposits and their host rocks. Electrical properties of the deposits and their ore minerals are distinct from their unmineralized host rocks. Therefore, the use of electrical methods to detect SMS while drilling and recovering drill cores could decrease the costs and accelerate offshore operations by limiting the amount of drilling in unmineralized material. This paper presents new data regarding the electrical properties of SMS cores that can be used in that assessment. Frequency-dependent complex electrical resistivity in the frequency range between 0.002 and 100 Hz was examined in order to potentially discriminate between different types of fresh rocks, alteration and mineralization. Forty mini-cores of SMS and unmineralized host rocks were tested in the laboratory, originating from different tectonic settings such as the intermediate-spreading ridges of the Galapagos and Axial Seamount, and the Pacmanus back-arc basin. The results indicate that there is a clear potential to distinguish between mineralized and non-mineralized samples, with some evidence that even different types of mineralization can be discriminated. This could be achieved using resistivity magnitude alone with appropriate rig-mounted electrical sensors. Exploiting the frequency-dependent behavior of resistivity might amplify the differences and further improve the rock characterization.

  17. Sulfide as a soil phytotoxin - A review

    Directory of Open Access Journals (Sweden)

    Leon P M Lamers


    Full Text Available In wetland soils and underwater sediments of marine, brackish and freshwater systems, the strong phytotoxin sulfide may accumulate as a result of microbial reduction of sulfate during anaerobiosis, its level depending on prevailing edaphic conditions. In this review, we compare an extensive body of literature on phytotoxic effects of this reduced sulfur compound in different ecosystem types, and review the effects of sulfide at multiple ecosystem levels: the ecophysiological functioning of individual plants, plant-microbe associations, and community effects including competition and facilitation interactions. Recent publications on multi-species interactions in the rhizosphere show even more complex mechanisms explaining sulfide resistance. It is concluded that sulfide is a potent phytotoxin, profoundly affecting plant fitness and ecosystem functioning in the full range of wetland types including coastal systems, and at several levels. Traditional toxicity testing including hydroponic approaches generally neglect rhizospheric effects, which makes it difficult to extrapolate results to real ecosystem processes. To explain the differential effects of sulfide at the different organizational levels, profound knowledge about the biogeochemical, plant physiological and ecological rhizosphere processes is vital. This information is even more important, as anthropogenic inputs of sulfur into freshwater ecosystems and organic loads into freshwater and marine systems are still much higher than natural levels, and are steeply increasing in Asia. In addition, higher temperatures as a result of global climate change may lead to higher sulfide production rates in shallow waters.

  18. Air-water transfer of hydrogen sulfide

    DEFF Research Database (Denmark)

    Yongsiri, C.; Vollertsen, J.; Rasmussen, M. R.


    The emissions process of hydrogen sulfide was studied to quantify air–water transfer of hydrogen sulfide in sewer networks. Hydrogen sulfide transfer across the air–water interface was investigated at different turbulence levels (expressed in terms of the Froude number) and pH using batch...... experiments. By means of the overall mass–transfer coefficient (KLa), the transfer coefficient of hydrogen sulfide (KLaH2S), referring to total sulfide, was correlated to that of oxygen (KLaO2) (i.e., the reaeration coefficient). Results demonstrate that both turbulence and pH in the water phase play...... a significant role for KLaH2S. An exponential expression is a suitable representation for the relationship between KLaH2S and the Froude number at all pH values studied (4.5 to 8.0). Because of the dissociation of hydrogen sulfide, KLaH2S increased with decreasing pH at a constant turbulence level. Relative...

  19. Mesostructured Metal Germanium Sulfide and Selenide Materials Based on the Tetrahedral [Ge 4S 10] 4- and [Ge 4Se 10] 4- Units: Surfactant Templated Three-Dimensional Disordered Frameworks Perforated with Worm Holes (United States)

    Wachhold, Michael; Kasthuri Rangan, K.; Lei, Ming; Thorpe, M. F.; Billinge, Simon J. L.; Petkov, Valeri; Heising, Joy; Kanatzidis, Mercouri G.


    The polymerization of [Ge4S10]4- and [Ge4Se10]4- unit clusters with the divalent metal ions Zn2+, Cd2+, Hg2+, Ni2+, and Co2+ in the presence of various surfactant cations leads to novel mesostructured phases. The surfactants are the quaternary ammonium salts C12H25NMe3Br, C14H29NMe3Br, C16H33NMe3Br, and C18H37NMe3Br, which play the role of templates, helping to assemble a three-dimensional mesostructured metal-germanium chalcogenide framework. These materials are stoichiometric in nature and have the formula of (R-NMe3)2[MGe4Q10] (Q=S, Se). The local atomic structure was probed by X-ray diffuse scattering and pair distribution function analysis methods and indicates that the adamantane clusters stay intact while the linking metal atoms possess a tetrahedral coordination environment. A model can be derived, from the comparison of measured and simulated X-ray powder diffraction patterns, describing the structure as an amorphous three-dimensional framework consisting of adamantane [Ge4Q10]4- units that are bridged by tetrahedral coordinated M2+ cations. The network structures used in the simulations were derived from corresponding disordered structures developed for amorphous silicon. The frameworks in (R-NMe3)2[MGe4Q10] are perforated with worm hole-like tunnels, occupied by the surfactant cations, which show no long-range order. This motif is supported by transmission electron microscopy images of these materials. The pore sizes of these channels were estimated to lie in the range of 20-30 Å, depending on the appointed surfactant cation length. The framework wall thickness of ca. 10 Å is thereby independent from the surfactant molecules used. Up to 80% of the surfactant molecules can be removed by thermal degradation under vacuum without loss of mesostructural integrity. Physical, chemical, and spectroscopic properties of these materials are discussed.

  20. Contributions to Exceptional Fossil Preservation


    Muscente, Anthony Drew


    Exceptionally preserved fossils—or fossils preserved with remains of originally non-biomineralized (i.e. soft) tissues—constitute a key resource for investigating the history of the biosphere. In comparison to fossils of biomineralized skeletal elements, which represent the majority of the fossil record but only a fraction of the total diversity that existed in the past, exceptionally preserved fossils are comparatively rare because soft tissues are rapidly destroyed in typical...

  1. Enhancement of metal bioleaching from contaminated sediment using silver ion. (United States)

    Chen, Shen-Yi; Lin, Jih-Gaw


    A silver-catalyzed bioleaching process was used to remove heavy metals from contaminated sediment in this study. The effects of silver concentration added on the performance of bioleaching process were investigated. High pH reduction rate was observed in the bioleaching process with silver ion. The silver ion added in the bioleaching process was incorporated into the lattice of the initial sulfide through a cationic interchange reaction. This resulted in the short lag phase and high metal solubilization in the bioleaching process. The maximum pH reduction rate and the ideal metal solubilization were obtained in the presence of 30 mg/L of silver ion. When the added silver ion was greater than 30 mg/L, the rates of pH reduction and metal solubilization gradually decreased. The solubilization efficiencies of heavy metals (Cu, Zn, Mn, Ni and Cr) were relatively high in the silver-enhanced bioleaching process, except Pb. No apparent effect of silver ion on the growth of sulfur-oxidizing bacteria was found in the bioleaching. These results indicate that the kinetics of metal solubilization can be enhanced by the addition of silver ion.

  2. Sulfide response analysis for sulfide control using a pS electrode in sulfate reducing bioreactors

    NARCIS (Netherlands)

    Villa Gomez, D.K.; Cassidy, J.; Keesman, K.J.; Sampaio, R.M.; Lens, P.N.L.


    Step changes in the organic loading rate (OLR) through variations in the influent chemical oxygen demand (CODin) concentration or in the hydraulic retention time (HRT) at constant COD/SO4 2- ratio (0.67) were applied to create sulfide responses for the design of a sulfide control in sulfate reducing

  3. Heavy metal bioaccumulation in the organisms at hydrothermal fields of the Mid-Atlantic Ridge and East-Pacific Rise

    International Nuclear Information System (INIS)

    Demina, L.L.; Galkin, S.V.


    The influence of geochemical environment as well as biological parameters on the heavy metal bioaccumulation in the hydrothermal fauna at certain fields of the Mid-Atlantic ridge (MAR) and East Pacific Rise (EPR) are studied. The highest concentration of Fe, Zn, Cu, Mn, Ni, Cr, Co, Pb, Cd, Ag, Se, Sb, As, and Hg were detected in the tubes of the most thermophilic organism Alvinella caudata inhabited sulfide chimneys at 9 0 50 ' N EPR, i.e. at place where the influence of hydrothermal fluids was the maximal. Elevated heavy metals levels were typical for organs associated with the endo symbiotic bacteria activity, such as gills of specialized mussels Bathymodiolus, clams Archivestica gigas (Calyptogena magnifica), trophosome of vestimentifera Riftia, maxillipeds of shrimps Rimicaris exoculata. Inter-site (Broken Spur vs. Rainbow) comparison of the partitioning of metals within soft tissues has revealed that metal concentrations in the fauna habitats is an important albeit not the single factor that controls the metal content in the interior organs of the taxa. The external parts of mussels, such as shells, demonstrate patterns of bioaccumulation reflecting the metal concentrations in the micro-habitats. In spite of the minimal metal content was found in the mussel shells, they serve as a great reservoirs for heavy metal deposition and storage at the hydrothermal regions. For some elements a trend of heavy metal transferring through the food chains was revealed. There were no clear dependence between age of mussels and metal content (except Hg) in the soft tissues

  4. Physio-biochemical basis of iron-sulfide nanoparticle induced growth and seed yield enhancement in B. juncea. (United States)

    Rawat, Madhu; Nayan, Rajeev; Negi, Bhawana; Zaidi, M G H; Arora, Sandeep


    Metal nanoparticles have been reported to influence plant growth and productivity. However, the molecular mechanisms underlying the effects have not been completely understood yet. Current work describes the physio-biochemical basis of iron sulfide nanoparticle induced growth and yield enhancement in Brassica juncea. Iron sulfide nanoparticles (0, 2, 4, 6, 8 and 10 ppm) were used for foliar treatment of B. juncea at 30, 45 and 60 days after sowing, under field conditions. Foliar treatment of 4 ppm iron sulfide nanoparticle solution at 30 days after sowing brought maximal enhancement in agronomic attributes of the treated plants. Results of assays i.e. total chlorophyll, electrolyte leakage, Malondialdehyde (MDA), proline, H 2 O 2 and antioxidant enzyme activities indicated the benign effect of iron sulfide nanoparticles on plants. Consequently, improved redox status of the treated plants, enabled them to assimilate higher photosynthate. The augmentation in growth and seed yield in iron sulfide nanoparticle treated plants was amply supported by activation of RUBISCO small subunit (rubisco S), RUBISCO large subunit (rubisco L), glutamine synthetase (gs) and glutamate synthase (gogat) genes. Thus, iron sulfide nanoparticle induced growth and yield enhancement is proposed to be mediated through activation of carbon and nitrogen assimilatory pathways at specific growth stage. The iron content in the leaves and root tissues of the treated plants was also significantly improved. Copyright © 2017 Elsevier Masson SAS. All rights reserved.

  5. Synthesis of Copper Sulfide Nanoparticles Using Biogenic H2S Produced by a Low-pH Sulfidogenic Bioreactor

    Directory of Open Access Journals (Sweden)

    Camila Colipai


    Full Text Available The application of acidophilic sulfate-reducing bacteria (SRB for the treatment of acidic mine water has been recently developed to integrate mine water remediation and selective biomineralization. The use of biogenic hydrogen sulfide (H2S produced from the dissimilatory reduction of sulfate to fabricate valuable products such as metallic sulfide nanoparticles has potential applications in green chemistry. Here we report on the operation of a low-pH sulfidogenic bioreactor, inoculated with an anaerobic sediment obtained from an acid river in northern Chile, to recover copper via the production of copper sulfide nanoparticles using biogenic H2S. The laboratory-scale system was operated as a continuous flow mode for up to 100 days and the bioreactor pH was maintained by the automatic addition of a pH 2.2 influent liquor to compensate for protons consumed by biosulfidogenesis. The “clean” copper sulfide nanoparticles, produced in a two-step process using bacterially generated sulfide, were examined using transmission electron microscopy, dynamic light scattering, energy dispersive (X-ray spectroscopy and UV-Vis spectroscopy. The results demonstrated a uniform nanoparticle size distribution with an average diameter of less than 50 nm. Overall, we demonstrated the production of biogenic H2S using a system designed for the treatment of acid mine water that holds potential for large-scale abiotic synthesis of copper sulfide nanoparticles.

  6. Exceptional and Spinorial Conformal Windows

    DEFF Research Database (Denmark)

    Mojaza, Matin; Pica, Claudio; Ryttov, Thomas


    We study the conformal window of gauge theories containing fermionic matter fields, where the gauge group is any of the exceptional groups with the fermions transforming according to the fundamental and adjoint representations and the orthogonal groups where the fermions transform according...

  7. 78 FR 47021 - Excepted Service (United States)


    ...; E.O. 10577, 3 CFR, 1954-1958 Comp., p. 218. U.S. Office of Personnel Management. Elaine Kaplan... MANAGEMENT Excepted Service AGENCY: U.S. Office of Personnel Management (OPM). ACTION: Notice. SUMMARY: This... established or revoked from May 1, 2013, to May 31, 2013. FOR FURTHER INFORMATION CONTACT: Senior Executive...

  8. 75 FR 11206 - Excepted Service (United States)


    ... OFFICE OF PERSONNEL MANAGEMENT Excepted Service AGENCY: U.S. Office of Personnel Management (OPM... Activities. (1) Seven (7) positions to provide general administration, general art and information... following Schedule C appointments were approved during January 2010. Office of Science and Technology Policy...

  9. Metal removal efficiency and ecotoxicological assessment of field-scale passive treatment biochemical reactors (United States)

    Anaerobic biochemical reactors (BCRs) are useful for removing metals from mining-impacted water (MIW) at remote sites. Removal processes include sorption and precipitation of metal sulfides, carbonates and hydroxides. A question of interest is whether BCRs remove aquatic toxicit...

  10. Influence of temperature and the role of chromium on the kinetics of sulfidation of 310 stainless steel (United States)

    Rao, D. B.; Nelson, H. G.


    The sulfidation of 310 stainless steel was studied over the temperature range from 910 K to 1285 K. By adjusting the ratio of hydrogen sulfide, variations in sulfur potential were obtained. The effect of temperature on sulfidation was determined at three different sulfur potentials: 39/sqNm, 0.014/sqNm, and 0.00015/sqNm. All sulfide scales contained one or two surface layers in addition to a subscale. The second outer layer (OL-II), furthest from the alloy, contained primarily Fe-Ni-S. The first outer layer (OL-I), nearest the subscale, contained FE-Cr-S. The subscale consisted of sulfide inclusions in the metal matrix. At a given temperature and sulfur potential, the weight gain data obeyed the parabolic rate law after an initial transient period. The parabolic rate constants obtained at the sulfur potential of 39/sqNm did not show a break when the logarithm of the rate constant was plotted as a function of the inverse of absolute temperature. Sulfidation carried out at sulfur potentials below 0.02/sqNm, however, did show a break at 1145 K, which is termed as the transition temperature. This break was found to be associated with the changes which had occurred in the Fe:Cr ratio of OL-I. Below the transition temperature the activation energy was found to be approximately 125 kj/mole. Above the transition temperature the rate of sulfidation decreased with temperature but dependent on the Fe:Cr ratio in the iron-chromium-sulfide layers of the OL-I. A reaction mechanism consistent with the experimental results has been proposed.

  11. Reactivity of 4'-substituted 2,4-dinitrodiphenyl sulfides and sulfones during alkaline hydrolysis in aqueous dioxane

    Energy Technology Data Exchange (ETDEWEB)

    Ivanov, A.V.


    This paper studies the kinetics of alkaline hydrolysis of 4'-substituted 2,4-dinitrodiphenyl sulfides (I), 2,4-dinitrodiphenyl sulfones (II), and 1-substituted 2,4-dinitrobenzenes (III) in a 40% dioxane-water solution. Analysis of the results obtained are presented and it is shown that in its character, the influence of the substituents in carrying out the alkaline hydrolysis reaction in 40% dioxane for the reaction series (I) obeys the general patterns of activated nucleophilic substitution, with the exception of 2,4-dinitro-4'-methylthiodiphenyl sulfide.

  12. The new ret process for hydrogen sulfide

    Energy Technology Data Exchange (ETDEWEB)

    Nakamura, S.; Onishi, H.


    It was developed for gas streams from rayon production containing either 4500 ppM hydrogen sulfide and 5 ppM carbon disulfide or 900 ppM hydrogen sulfide and 16 ppM carbon disulfide (average values). The process consists of absorption towers, alkali scrubbers for the recovery of carbon disulfide, and an oxidation reactor. The process is catalyzed by an organic iron complex catalyst. For the removal of 1 kg hydrogen sulfide, the process uses 130 g sodium hydroxide, catalyst (20 yen), 2.5 kw-hr electricity, 15 kg steam (3 kg in winter), 2 cu m cooling water (1 cu m in winter), and 8 l. fresh water. The recovered sulfur (99%) is 99.9% pure. Eight litres of 0.03 kg COD wastewater are also produced. The process equipment is described. Flow diagrams, graph, and tables.

  13. Reactivity of non conventional supported mixed sulfides for hydro-treatment reactions; Reactivite de sulfures mixtes supportes non conventionnels pour les reactions d`hydrotraitement

    Energy Technology Data Exchange (ETDEWEB)

    Quartararo, J.


    The properties of non conventional NiM sulfides (M: Mn, Fe, Cu,Zn, Re, Ru) was evaluated for two hydro treating reactions: hydro desulfurization (HDS) of dibenzo thiophene and benzo thiophene and hydrogenation (HYD) of cyclohexyl. The reactions were t first studied on Ni, Mo and NiMo sulfide catalysts. The influence of the nature of the molecule on the magnitude of promoting effect was demonstrated. The non conventional mono-metallic and bimetallic catalysts studied in this work were characterized by XRD (X-ray diffraction), XPS (X-ray photoelectron spectroscopy) and TEM (transmission electron microscopy). Ni exhibits a negative effect on the activity of Mn, Cu, Zn and Re sulfide catalysts. This effect could be related to the formation of two separated sulfide phases: base metal sulfide and nickel sulfide. Nevertheless, a promoting effect was found in NiRu catalyst. In this catalyst, the Ru and the Ni are in a mixed phase. The results of this study demonstrate the importance of the type of metal associated to the nickel for the promoting effect and relate this effect to the formation of a mixed phase. (author)

  14. Refractory sulfides as IR window materials (United States)

    White, William B.


    The development of sulfide materials as infrared-transmitting optical ceramics is limited by intrinsic optical properties, thermomechanical properties, and considerations of chemical stability. Screening procedures with respect to band gap, electronic absorption, chemical stability, and refractory character reduced the set of all sulfides to about a dozen structural families. Systematic relationships were developed between crystal chemistry and phonon absorption edge, vibrational modes frequencies, and coefficient of thermal expansion which allow possible ranges of properties to be estimated. It is concluded that improved materials are possible but that radically improved new materials are unlikely.

  15. Iron-sulfide crystals in probe deposits

    DEFF Research Database (Denmark)

    Laursen, Karin; Frandsen, Flemming


    Iron-sulfides were observed in deposits collected on a probe inserted at the top of the furnace of a coal-fired power station in Denmark. The chemical composition of the iron-sulfides is equivalent to pyrrhotite (FeS). The pyrrhotites are present as crystals and, based on the shape of the crystals......, it was deduced that they were not deposited but instead grew within the deposit. The presence of unburned char particles within the deposits supports the concept that a reducing environment existed in the deposits. Two processes are proposed for explaining the existence of pyrrhotite crystals within a deposit...

  16. Acute inhalation toxicity of carbonyl sulfide

    Energy Technology Data Exchange (ETDEWEB)

    Benson, J.M.; Hahn, F.F.; Barr, E.B. [and others


    Carbonyl sulfide (COS), a colorless gas, is a side product of industrial procedures sure as coal hydrogenation and gasification. It is structurally related to and is a metabolite of carbon disulfide. COS is metabolized in the body by carbonic anhydrase to hydrogen sulfide (H{sub 2}S), which is thought to be responsible for COS toxicity. No threshold limit value for COS has been established. Results of these studies indicate COS (with an LC{sub 50} of 590 ppm) is slightly less acutely toxic than H{sub 2}S (LC{sub 50} of 440 ppm).

  17. What processes at mid-ocean ridges tell us about volcanogenic massive sulfide deposits (United States)

    Cathles, Lawrence M.


    Episodic seafloor spreading, ridge topography, and fault movement at ridges find (more extreme) analogs in the arc and back-arc setting where the volcanogenic massive sulfide (VMS) deposits that we mine today were formed. The factors affecting sulfide accumulation efficiency and the extent to which sulfides are concentrated spatially are the same in both settings, however. The processes occurring at mid-ocean ridges therefore provide a useful insight into those producing VMS deposits in arcs and back-arcs. The critical observation investigated here is that all the heat introduced by seafloor spreading at mid-ocean ridges is carried out of the crust within a few hundred meters of the ridge axis by ˜350°C hydrothermal fluids. The high-temperature ridge hydrothermal systems are tied to the presence of magma at the ridge axis and greatly reduce the size and control the shape of axial magma intrusions. The amount of heat introduced to each square kilometer of ocean crust during its formation can be calculated, and its removal by high-temperature convection allows calculation of the total base metal endowment of the ocean basins. Using reasonable metal deposition efficiencies, we conclude that the ocean floor is a giant VMS district with metal resources >600 times the total known VMS reserves on land and a copper resource which would last >6,000 years at current production rates.

  18. The Exceptional State in Africa

    DEFF Research Database (Denmark)

    Suzuki, Shogo


    China's relations with African states have undergone significant changes in recent years. China has projected its relationship with Africa as one of equality and ‘mutual help’. Such perceptions of foreign policy stem from the Five Principles of Peaceful Coexistence and the shared experience...... of imperialist domination and economic underdevelopment. Moreover, various public statements by China's elites suggest that China is expected to play a much more prominent, even exceptional role in Africa. This purportedly entails moving beyond the hegemonic West's interventionist aid or security policies......, and is also implicitly designed to highlight the West's shortcomings in promoting African economic growth or peace. Yet where does this perception of exceptionalism come from? Why does Beijing feel that it has to play a leading role in Africa's development? How can Beijing distinguish itself from the nations...

  19. Use of biogenic sulfide for ZnS precipitation

    NARCIS (Netherlands)

    Esposito, G.; Veeken, A.; Weijma, J.; Lens, P.N.L.


    A 600 ml continuously stirred tank reactor was used to assess the performance of a zinc sulfide precipitation process using a biogenic sulfide solution (the effluent of a sulfate-reducing bioreactor) as sulfide source. In all experiments, a proportional-integral (PI) control algorithm was used to

  20. A physiologically based kinetic model for bacterial sulfide oxidation

    NARCIS (Netherlands)

    Klok, J.B.M.; Graaff, de C.M.; Bosch, van den P.L.F.; Boelee, N.C.; Keesman, K.J.; Janssen, A.J.H.


    In the biotechnological process for hydrogen sulfide removal from gas streams, a variety of oxidation products can be formed. Under natron-alkaline conditions, sulfide is oxidized by haloalkaliphilic sulfide oxidizing bacteria via flavocytochrome c oxidoreductase. From previous studies, it was

  1. 40 CFR 425.03 - Sulfide analytical methods and applicability. (United States)


    ... § 425.03 Sulfide analytical methods and applicability. (a) The potassium ferricyanide titration method... ferricyanide titration method for the determination of sulfide in wastewaters discharged by plants operating in... 40 Protection of Environment 29 2010-07-01 2010-07-01 false Sulfide analytical methods and...

  2. Metal recovery via geobiotechnology

    International Nuclear Information System (INIS)

    Hedrich, Sabrina; Schippers, Axel


    Specialized acidophilic bacteria and archaea are able to extract valuable metals such as copper, gold, cobalt, nickel, zinc, and uranium from sulfide ores. This process is known as bioleaching and its application in the mining industry as biomining. Laboratory studies also demonstrated bioleaching of oxide ores such as laterites and of mining residues such as mine tailings as well as metal recycling from waste (secondary mining). Metals being leached have to be recovered from acidic polymetallic solutions (mine and process waters) which is possible via biosorption or biomineralisation.

  3. Sequential extraction of heavy metals during composting of sewage sludge. (United States)

    Amir, Soumia; Hafidi, Mohamed; Merlina, Georges; Revel, Jean-Claude


    The major limitation of soil application of sewage sludge compost is the total heavy metal contents and their bioavailability to the soil-plant system. This study was conducted to determine the heavy metal speciation and the influence of changing the physico-chemical properties of the medium in the course of composting on the concentrations, bioavailability or chemical forms of Cu, Zn, Pb and Ni in sewage sludge. Principal physical and chemical properties and FTIR spectroscopical characterization of sludge compost during treatment show the stability and maturity of end product. The total metal contents in the final compost were much lower than the limit values of composts to be used as good soil fertilizer. Furthermore, it was observed by using a sequential extraction procedure in sludge compost at different steps of treatment, that a large proportion of the heavy metals were associated to the residual fraction (70-80%) and more resistant fractions to extraction X-NaOH, X-EDTA, X-HNO3 (12-29%). Less than 2% of metals bound to bioavailable fractions X-(KNO3+H2O). Heavy metal distribution and bioavailability show some changes during composting depending on the metal itself and the physico-chemical properties of the medium. Bioavailable fractions of all elements tend to decrease except Ni-H2O. Zn and mainly Cu present more affinity to organic and carbonate fractions. In contrast, Pb is usually preferentially bound to sulfide forms X-HNO3. Nickel shows a significant decrease of organic form. Significant degrees of correlation were found between heavy metal fractions and changes of some selected variables (e.g. pH, ash, organic matter, humic substance) during the course of composting. Mobile fractions of metals are poorly predictable from the total content. The R2 value was significantly increased by the inclusion of other variables such as the amount of organic matter (OM) and pH.

  4. CMS : An exceptional load for an exceptional work site

    CERN Multimedia


    Components of the CMS vacuum tank have been delivered to the detector assembly site at Cessy. The complete inner shell was delivered to CERN by special convoy while the outer shell is being assembled in situ. The convoy transporting the inner shell of the CMS vacuum tank took a week to cover the distance between Lons-le-Saunier and Point 5 at Cessy. Left: the convoy making its way down from the Col de la Faucille. With lights flashing, flanked by police outriders and with roads temporarily closed, the exceptional load that passed through the Pays de Gex on Monday 20 May was accorded the same VIP treatment as a leading state dignitary. But this time it was not the identity of the passenger but the exceptional size of the object being transported that made such arrangements necessary. A convoy of two lorries was needed to transport the load, an enormous 13-metre long, 6 metre diameter cylinder weighing 120 tonnes. It took a week to cover the 120 kilometres between Lons-le-Saunier and the assembly site for...

  5. Microaeration reduces hydrogen sulfide in biogas (United States)

    Although there are a variety of biological and chemical treatments for removal of hydrogen sulfide (H2S) from biogas, all require some level of chemical or water inputs and maintenance. In practice, managing biogas H2S remains a significant challenge for agricultural digesters where labor and opera...


    The fate of arsenic in the environment is fundamentally linked to its speciation. Arsenic in aerobic environments is predominantly arsenate, however under reducing conditions arsenite species dominate. In anoxic or sulfidic environments thioarsenite ((As(OH)x(SH)yz-) species alon...

  7. Microbial Fuel Cells for Sulfide Removal

    NARCIS (Netherlands)

    Rabaey, K.; Sompel, van de S.; Maignien, L.; Boon, N.; Aelterman, P.; Clauwaert, P.; Schamphelaire, de L.; The Pham, H.; Vermeulen, J.; Verhaege, M.; Lens, P.N.L.; Verstraete, W.


    Thus far, microbial fuel cells (MFCs) have been used to convert carbon-based substrates to electricity. However, sulfur compounds are ubiquitously present in organic waste and wastewater. In this study, a MFC with a hexacyanoferrate cathodic electrolyte was used to convert dissolved sulfide to

  8. Support Effect in Hydrodesulfurization over Ruthenium Sulfide

    Czech Academy of Sciences Publication Activity Database

    Gulková, Daniela; Kaluža, Luděk; Vít, Zdeněk; Zdražil, Miroslav


    Roč. 51, č. 2 (2009), s. 146-149 ISSN 1337-7027 R&D Projects: GA ČR GA104/06/0705 Institutional research plan: CEZ:AV0Z40720504 Keywords : ruthenium sulfide * hydrodesulfurization * support effect Subject RIV: CC - Organic Chemistry

  9. Mitochondrial Sulfide Quinone Oxidoreductase Prevents Activation of the Unfolded Protein Response in Hydrogen Sulfide*


    Horsman, Joseph W.; Miller, Dana L.


    Hydrogen sulfide (H2S) is an endogenously produced gaseous molecule with important roles in cellular signaling. In mammals, exogenous H2S improves survival of ischemia/reperfusion. We have previously shown that exposure to H2S increases the lifespan and thermotolerance in Caenorhabditis elegans, and improves protein homeostasis in low oxygen. The mitochondrial SQRD-1 (sulfide quinone oxidoreductase) protein is a highly conserved enzyme involved in H2S metabolism. SQRD-1 is generally considere...

  10. Exceptional field theory: SL(5)

    International Nuclear Information System (INIS)

    Musaev, Edvard T.


    In this work the exceptional field theory formulation of supergravity with SL(5) gauge group is considered. This group appears as a U-duality group of D=7 maximal supergravity. In the formalism presented the hidden global duality group is promoted into a gauge group of a theory in dimensions 7+number of extended directions. This work is a continuation of the series of works for E 8,7,6 ,SO(5,5) and SL(3)×SL(2) duality groups.

  11. Exceptional circles of radial potentials

    International Nuclear Information System (INIS)

    Music, M; Perry, P; Siltanen, S


    A nonlinear scattering transform is studied for the two-dimensional Schrödinger equation at zero energy with a radial potential. Explicit examples are presented, both theoretically and computationally, of potentials with nontrivial singularities in the scattering transform. The singularities arise from non-uniqueness of the complex geometric optics solutions that define the scattering transform. The values of the complex spectral parameter at which the singularities appear are called exceptional points. The singularity formation is closely related to the fact that potentials of conductivity type are ‘critical’ in the sense of Murata. (paper)

  12. Hydrogen Sulfide Corrosion of Weld Regions in API X52 Steel

    Directory of Open Access Journals (Sweden)

    García-Cerecero G.


    Full Text Available The corrosion behavior of gas metal arc welding (GMAW regions has been studied using potentiodynamic polarization and polarization resistance (LPR techniques. Experiments were conducted in hydrogen sulfide (H2S-containing brine and in H2S-free brine. Welds were made on API 5L X52 steel. Due to differences in their microstructure, chemical composition and residual stress level, weld regions exhibited different responses under H2S corrosion. Base metal exhibited the highest corrosion rate (CR and the most cathodic corrosion potential.

  13. Fluorescent Lead(IV) Sulfide Nanoparticles Synthesized by Idiomarina sp. Strain PR58-8 for Bioimaging Applications. (United States)

    Srivastava, Pallavee; Kowshik, Meenal


    The fabrication of nanoparticles by microorganisms presents a "green" method for generating biocompatible nanomaterials. We discovered the intracellular biosynthesis of fluorescent lead(IV) sulfide nanoparticles by the moderate halophile, Idiomarina sp. strain PR58-8. The bacterium tolerated up to 8 mM Pb(NO 3 ) 2 during growth. Non-protein thiols dose-dependently increased in response to metal exposure, which suggests they are involved in the growth of PbS 2 crystals and lead detoxification. Using X-ray diffraction, transmission electron microscopy (TEM), high-resolution TEM, and energy dispersive analysis of X-rays, the nanoparticles were characterized as spherical β-PbS 2 nanoparticles (PbS 2 NPs) with a tetragonal crystal lattice, a crystallite domain size of 2.38 nm, and an interplanar distance of 0.318 nm. A narrow symmetric emission spectrum with a Gaussian distribution and an emission maximum at 386 nm was obtained when the particles were excited at 570 nm. The PbS 2 NPs exhibited a large Stokes' shift (8,362 cm -1 ) and a relatively high quantum yield (67%). These properties, along with fluorescence that was maintained in various microenvironments and their biocompatibility, make these nanoparticles excellent candidates for bioimaging. The particles were internalized by HeLa cells and evenly distributed within the cytoplasm, exhibiting their potential for in situ bioimaging applications. The "as-synthesized" lead(IV) sulfide nanoparticles may provide expanded opportunities for targeted bioimaging via modifying the surface of the particles. IMPORTANCE This article reports the intracellular synthesis of fluorescent lead(IV) sulfide nanoparticles (PbS 2 NPs) by a microorganism. All previous reports on the microbial synthesis of lead-based nanoparticles are on lead(II) sulfide that exhibits near-infrared fluorescence, requiring expensive instrumentation for bioimaging. Bioimaging using PbS 2 NPs can be achieved using routine epifluorescence microscopes, as it

  14. Electrochemical Synthesis and Characterization of Zinc Sulfide Nanoparticles

    Directory of Open Access Journals (Sweden)

    M. Rahimi-Nasarabadi


    Full Text Available Electrosynthesis process has been used for preparation of zinc sulfide nanoparticles. Zinc sulfide nanoparticles in different size and shapes were electrodeposited by electrolysis of zinc plate as anode in sodium sulfide solution. Effects of several reaction variables, such as electrolysis voltage, sulfide ion concentration as reactant, stirring rate of electrolyte solution and temperature on particle size of prepared zinc sulfide were investigated. The significance of these parameters in tuning the size of zinc sulfide particles was quantitatively evaluated by analysis of variance (ANOVA. Also, optimum conditions for synthesis of zinc sulfide nanoparticles via electrosynthesis reaction were proposed. The structure and composition of prepared nanoparticles under optimum condition was characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM, transmission electron microscopy (TEM, and UV-Vis spectrophotometry techniques.

  15. Quantifying heavy metals sequestration by sulfate-reducing bacteria in an acid mine drainage-contaminated wetland

    Directory of Open Access Journals (Sweden)

    John W Moreau


    Full Text Available Bioremediation strategies that depend on bacterial sulfate reduction for heavy metals remediation harness the reactivity of these metals with biogenic aqueous sulfide. Quantitative knowledge of the degree to which specific toxic metals are partitioned into various sulfide, oxide, or other phases is important for predicting the long-term mobility of these metals under environmental conditions. Here we report the quantitative partitioning into sedimentary biogenic sulfides of a suite of metals and metalloids associated with acid mine drainage contamination of a natural estuarine wetland for over a century.

  16. A major problem associated with removing metals sulfides as ...

    African Journals Online (AJOL)



    May 22, 2013 ... Laboratory scale bioreactors were used to investigate the treatment of arsenic species deliberately ... reverse osmosis (Geucke et al., 2009) have been used to treat ..... Figure 6 Changes in (a) redox potential and (b) pH as a function of initial percentage of As(III) in a total arsenic concentration of. 0.1 mg/l in ...

  17. Disorder and transport of silver in some layered metal sulfides

    NARCIS (Netherlands)

    Gerards, Anthonius Gijsbertus


    The chemical and physical properties of compounds with a layered structure are strongly determined by the two-dimensional nature of the bonding, viz. strong bonding within the layers and much weaker bonds between the layers; graphite is an example of such and anisotropic solid. the layered

  18. Understanding the mechanism of iron sulfide-induced fouling in upgrading

    Energy Technology Data Exchange (ETDEWEB)

    Panchal, C.B. [United States Dept. of Energy, Chicago, IL (United States). Argonne National Laboratory


    This presentation investigated the underlying mechanisms of iron sulfide-induced fouling and coking in upgrading processes. Experiments to determine the effects of dissolved metals on the rate of fouling were reviewed. It was noted that the presence of species such as active sulfur and diolefins can enhance the effect of dissolved metals. An investigation of a high temperature fouling unit was then conducted to investigate the effect of iron acetate and theiphenol additions to stable heavy gas oil. The deposition rate became strongly dependent on temperature in the presence of the dissolved metals. Fouling deposit analyses from various parts of the refining process consistently showed high concentrations of iron and sulfur. It was observed that the threshold tube-wall temperature corresponded to the decomposition temperature of iron salts. A review of current literature indicated that there is little information on the interactive effects of the thermal stability of dissolved organo-metallic compounds and the reactivity of organic species in generating fouling precursors. The creation of a predictive model of threshold fouling and coking conditions was recommended. It was suggested that the model should be used during the design phases of furnaces and heat exchangers. Other recommendations included the use of on-line sensors to detect iron sulfide formulation; and the monitoring of coking furnaces. Blending guidelines to minimize the interactive effects of dissolved metals and active sulfur compounds were also presented. refs., tabs., figs.

  19. Microvolume turbidimetry for rapid and sensitive determination of the acid labile sulfide fraction in waters after headspace single-drop microextraction with in situ generation of volatile hydrogen sulfide. (United States)

    Lavilla, I; Pena-Pereira, F; Gil, S; Costas, M; Bendicho, C


    In this work, we demonstrate the feasibility of applying headspace single-drop microextraction with in-drop precipitation for the quantitative determination of the acid labile sulfide fraction (H2S, HS-, and S2- (free sulfide), amorphous FeS and some metal sulfide complexes-clusters as ZnS) in aqueous samples by microvolume turbidimetry. The methodology lies in the in situ hydrogen sulfide generation and subsequent sequestration into an alkaline microdrop containing ZnO(2)(2-) and exposed to the headspace above the stirred aqueous sample. The ZnS formed in the drop was then determined by microvolume turbidimetry. The optimum experimental conditions of the proposed method were: 2 microL of a microdrop containing 750 mg L(-1) Zn(II) in 1 mol L(-1) NaOH exposed to the headspace of a 20-mL aqueous sample stirred at 1600 rpm during 80 s after derivatization with 1 mL of 6 mol L(-1) HCl. An enrichment factor of 1710 was achieved in only 80 s. The calibration graph was linear in the range of 5-100 microg L(-1) with a detection limit of 0.5 microg L(-1). The repeatability, expressed as relative standard deviation, was 5.8% (N = 9). Finally, the proposed methodology was successfully applied to the determination of the acid labile sulfide fraction in different natural water samples.

  20. The physics of exceptional points

    International Nuclear Information System (INIS)

    Heiss, W D


    A short résumé is given about the nature of exceptional points (EPs) followed by discussions about their ubiquitous occurrence in a great variety of physical problems. EPs feature in classical as well as in quantum mechanical problems. They are associated with symmetry breaking for PT-symmetric Hamiltonians, where a great number of experiments has been performed, in particular in optics, and to an increasing extent in atomic and molecular physics. EPs are involved in quantum phase transition and quantum chaos; they produce dramatic effects in multichannel scattering, specific time dependence and more. In nuclear physics, they are associated with instabilities and continuum problems. Being spectral singularities they also affect approximation schemes. This article is part of a special issue of Journal of Physics A: Mathematical and Theoretical devoted to ‘Quantum physics with non-Hermitian operators’. (paper)

  1. Exceptional plasticity of silicon nanobridges

    Energy Technology Data Exchange (ETDEWEB)

    Ishida, Tadashi; Sato, Takaaki; Toshiyoshi, Hiroshi; Collard, Dominique; Fujita, Hiroyuki [University of Tokyo, Institute of Industrial Science, 4-6-1 Komaba Meguro, Tokyo 153-8505 (Japan); Cleri, Fabrizio [Institut d' Electronique Microelectronique et Nanotechnologie (CNRS UMR 8520), Universite de Lille I, Avenue Poincare BP60069 59652 Villeneuve d' Ascq (France); Kakushima, Kuniyuki [Tokyo Institute of Technology, 4259, Nagatsuda, Midori, Yokohama, Kanagawa 226-8502 (Japan); Mita, Makoto [Department of Spacecraft Engineering, Japan Aerospace Exploration Agency, 3-1-1, Yoshinodai, Sagamihara, Kanagawa 229-8510 (Japan); Miyata, Masaki; Itamura, Noriaki; Sasaki, Naruo [Department of Materials and Life Sciences, Seikei University, 3-3-1, Kitamachi, Kichijoji, Musashino, Tokyo 180-8633 (Japan); Endo, Junji, E-mail: [FK Optical laboratory, 1-13-4 Nakano Niiza Saitama, 352-0005 (Japan)


    The plasticity of covalently bonded materials is a subject at the forefront of materials science, bearing on a wide range of technological and fundamental aspects. However, covalent materials fracture in a brittle manner when the deformation exceeds just a few per cent. It is predicted that a macroscopically brittle material like silicon can show nanoscale plasticity. Here we report the exceptional plasticity observed in silicon nanocontacts ('nanobridges') at room temperature using a special experimental setup combining a transmission electron microscope and a microelectromechanical system. When accounting for surface diffusion, we succeeded in elongating the nanocontact into a wire-like structure, with a fivefold increase in volume, up to more than twenty times the original length. Such a large plasticity was caused by the stress-assisted diffusion and the sliding of the intergranular, amorphous-like material among the nanocrystals.

  2. Formation of Zn- and Fe-sulfides near hydrothermal vents at the Eastern Lau Spreading Center: implications for sulfide bioavailability to chemoautotrophs

    Directory of Open Access Journals (Sweden)

    Yucel Mustafa


    Full Text Available Abstract Background The speciation of dissolved sulfide in the water immediately surrounding deep-ocean hydrothermal vents is critical to chemoautotrophic organisms that are the primary producers of these ecosystems. The objective of this research was to identify the role of Zn and Fe for controlling the speciation of sulfide in the hydrothermal vent fields at the Eastern Lau Spreading Center (ELSC in the southern Pacific Ocean. Compared to other well-studied hydrothermal systems in the Pacific, the ELSC is notable for unique ridge characteristics and gradients over short distances along the north-south ridge axis. Results In June 2005, diffuse-flow ( 250°C vent fluids were collected from four field sites along the ELSC ridge axis. Total and filtered Zn and Fe concentrations were quantified in the vent fluid samples using voltammetric and spectrometric analyses. The results indicated north-to-south variability in vent fluid composition. In the high temperature vent fluids, the ratio of total Fe to total Zn varied from 39 at Kilo Moana, the most northern site, to less than 7 at the other three sites. The concentrations of total Zn, Fe, and acid-volatile sulfide indicated that oversaturation and precipitation of sphalerite (ZnS(s and pyrite (FeS2(s were possible during cooling of the vent fluids as they mixed with the surrounding seawater. In contrast, most samples were undersaturated with respect to mackinawite (FeS(s. The reactivity of Zn(II in the filtered samples was tested by adding Cu(II to the samples to induce metal-exchange reactions. In a portion of the samples, the concentration of labile Zn2+ increased after the addition of Cu(II, indicating the presence of strongly-bound Zn(II species such as ZnS clusters and nanoparticles. Conclusion Results of this study suggest that Zn is important to sulfide speciation at ELSC vent habitats, particularly at the southern sites where Zn concentrations increase relative to Fe. As the hydrothermal

  3. Reduction of acid rock drainage using steel slag in cover systems over sulfide rock waste piles. (United States)

    de Almeida, Rodrigo Pereira; Leite, Adilson do Lago; Borghetti Soares, Anderson


    The extraction of gold, coal, nickel, uranium, copper and other earth-moving activities almost always leads to environmental damage. In metal and coal extraction, exposure of sulfide minerals to the atmosphere leads to generation of acid rock drainage (ARD) and in underground mining to acid mine drainage (AMD) due to contamination of infiltrating groundwater. This study proposes to develop a reactive cover system that inhibits infiltration of oxygen and also releases alkalinity to increase the pH of generated ARD and attenuate metal contaminants at the same time. The reactive cover system is constructed using steel slag, a waste product generated from steel industries. This study shows that this type of cover system has the potential to reduce some of the adverse effects of sulfide mine waste disposal on land. Geochemical and geotechnical characterization tests were carried out. Different proportions of sulfide mine waste and steel slag were studied in leachate extraction tests. The best proportion was 33% of steel slag in dry weight. Other tests were conducted as follows: soil consolidation, saturated permeability and soil water characteristic curve. The cover system was numerically modeled through unsaturated flux analysis using Vadose/w. The solution proposed is an oxygen transport barrier that allows rain water percolation to treat the ARD in the waste rock pile. The results showed that the waste pile slope is an important factor and the cover system must have 5 m thickness to achieve an acceptable effectiveness. © The Author(s) 2015.

  4. Effects of humic substances on precipitation and aggregation of zinc sulfide nanoparticles (United States)

    Deonarine, Amrika; Lau, Boris L.T.; Aiken, George R.; Ryan, Joseph N.; Hsu-Kim, Heileen


    Nanoparticulate metal sulfides such as ZnS can influence the transport and bioavailability of pollutant metals in anaerobic environments. The aim of this work was to investigate how the composition of dissolved natural organic matter (NOM) influences the stability of zinc sulfide nanoparticles as they nucleate and aggregate in water with dissolved NOM. We compared NOM fractions that were isolated from several surface waters and represented a range of characteristics including molecular weight, type of carbon, and ligand density. Dynamic light scattering was employed to monitor the growth and aggregation of Zn−S−NOM nanoparticles in supersaturated solutions containing dissolved aquatic humic substances. The NOM was observed to reduce particle growth rates, depending on solution variables such as type and concentration of NOM, monovalent electrolyte concentration, and pH. The rates of growth increased with increasing ionic strength, indicating that observed growth rates primarily represented aggregation of charged Zn−S−NOM particles. Furthermore, the observed rates decreased with increasing molecular weight and aromatic content of the NOM fractions, while carboxylate and reduced sulfur content had little effect. Differences between NOM were likely due to properties that increased electrosteric hindrances for aggregation. Overall, results of this study suggest that the composition and source of NOM are key factors that contribute to the stabilization and persistence of zinc sulfide nanoparticles in the aquatic environment.

  5. Global transcriptional responses of Acidithiobacillus ferrooxidans Wenelen under different sulfide minerals. (United States)

    Latorre, Mauricio; Ehrenfeld, Nicole; Cortés, María Paz; Travisany, Dante; Budinich, Marko; Aravena, Andrés; González, Mauricio; Bobadilla-Fazzini, Roberto A; Parada, Pilar; Maass, Alejandro


    In order to provide new information about the adaptation of Acidithiobacillus ferrooxidans during the bioleaching process, the current analysis presents the first report of the global transcriptional response of the native copper mine strain Wenelen (DSM 16786) oxidized under different sulfide minerals. Microarrays were used to measure the response of At. ferrooxidans Wenelen to shifts from iron supplemented liquid cultures (reference state) to the addition of solid substrates enriched in pyrite or chalcopyrite. Genes encoding for energy metabolism showed a similar transcriptional profile for the two sulfide minerals. Interestingly, four operons related to sulfur metabolism were over-expressed during growth on a reduced sulfur source. Genes associated with metal tolerance (RND and ATPases type P) were up-regulated in the presence of pyrite or chalcopyrite. These results suggest that At. ferrooxidans Wenelen presents an efficient transcriptional system developed to respond to environmental conditions, namely the ability to withstand high copper concentrations. Copyright © 2015 Elsevier Ltd. All rights reserved.

  6. Cobalt sulfide aerogel prepared by anion exchange method with enhanced pseudocapacitive and water oxidation performances (United States)

    Gao, Qiuyue; Shi, Zhenyu; Xue, Kaiming; Ye, Ziran; Hong, Zhanglian; Yu, Xinyao; Zhi, Mingjia


    This work introduces the anion exchange method into the sol-gel process for the first time to prepare a metal sulfide aerogel. A porous Co9S8 aerogel with a high surface area (274.2 m2 g‑1) and large pore volume (0.87 cm3 g‑1) has been successfully prepared by exchanging cobalt citrate wet gel in thioacetamide and subsequently drying in supercritical ethanol. Such a Co9S8 aerogel shows enhanced supercapacitive performance and catalytic activity toward oxygen evolution reaction (OER) compared to its oxide aerogel counterpart. High specific capacitance (950 F g‑1 at 1 A g‑1), good rate capability (74.3% capacitance retention from 1 to 20 A g‑1) and low onset overpotential for OER (220 mV) were observed. The results demonstrated here have implications in preparing various sulfide chalcogels.

  7. 42 CFR 423.578 - Exceptions process. (United States)


    ... 42 Public Health 3 2010-10-01 2010-10-01 false Exceptions process. 423.578 Section 423.578 Public..., Redeterminations, and Reconsiderations § 423.578 Exceptions process. (a) Requests for exceptions to a plan's tiered... sponsor may design its exception process so that very high cost or unique drugs are not eligible for a...

  8. As, Bi, Hg, S, Sb, Sn and Te geochemistry of the J-M Reef, Stillwater Complex, Montana: constraints on the origin of PGE-enriched sulfides in layered intrusions (United States)

    Zientek, M.L.; Fries, T.L.; Vian, R.W.


    The J-M Reef is an interval of disseminated sulfides in the Lower Banded series of the Stillwater Complex that is enriched in the platinum group elements (PGE). Palladium and Pt occur in solid solution in base-metal sulfides and as discrete PGE minerals. PGE minerals include sulfides, tellurides, arsenides, antimonides, bismuthides, and alloys with Fe, Sn, Hg, and Au. Several subpopulations can be delineated based on whole-rock chemical analyses for As, Bi, Cu, Hg, Pd, Pt, S, Sb and Te for samples collected from and adjacent to the J-M Reef. In general, samples from within the reef have higher Pt/Cu, Pd/Cu, Pd/Pt, Te/Bi and S/(Te+Bi) than those collected adjacent to the reef. Vertical compositional profiles through the reef suggest that Pd/Cu and Pt/Cu decrease systematically upsection from mineralized to barren rock. The majority of samples with elevated As, Sb and Hg occur adjacent to the reef, not within it, or in sulfide-poor rocks. Neither magma mixing nor fluid migration models readily explain why the minor quantities of sulfide minerals immediately adjacent to the sulfide-enriched layers that form the J-M Reef have different element ratios than the sulfide minerals that form the reef. If all the sulfides formed by exsolution during a magma mixing event and the modal proportion of sulfide now in the rocks are simply the result of mechanical processes that concentrated the sulfides into some layers and not others, then the composition of the sulfide would not be expected to be different. Models that rely upon ascending liquids or fluids are incompatible with the presence of sulfides that are not enriched in PGE immediately below or interlayered with the PGE-enriched sulfides layers. PGE-enriched postcumulus fluids should have reacted to the same extent with sulfides immediately outside the reef as within the reef. One explanation is that some of the sulfide minerals in the rocks outside the reef have a different origin than those that make up the reef. The

  9. Cadmium zinc sulfide by solution growth (United States)

    Chen, Wen S.


    A process for depositing thin layers of a II-VI compound cadmium zinc sulfide (CdZnS) by an aqueous solution growth technique with quality suitable for high efficiency photovoltaic or other devices which can benefit from the band edge shift resulting from the inclusion of Zn in the sulfide. A first solution comprising CdCl.sub.2 2.5H.sub.2 O, NH.sub.4 Cl, NH.sub.4 OH and ZnCl.sub.2, and a second solution comprising thiourea ((NH.sub.2).sub.2 CS) are combined and placed in a deposition cell, along with a substrate to form a thin i.e. 10 nm film of CdZnS on the substrate. This process can be sequentially repeated with to achieve deposition of independent multiple layers having different Zn concentrations.

  10. Iron-sulfide redox flow batteries (United States)

    Xia, Guan-Guang; Yang, Zhenguo; Li, Liyu; Kim, Soowhan; Liu, Jun; Graff, Gordon L


    Iron-sulfide redox flow battery (RFB) systems can be advantageous for energy storage, particularly when the electrolytes have pH values greater than 6. Such systems can exhibit excellent energy conversion efficiency and stability and can utilize low-cost materials that are relatively safer and more environmentally friendly. One example of an iron-sulfide RFB is characterized by a positive electrolyte that comprises Fe(III) and/or Fe(II) in a positive electrolyte supporting solution, a negative electrolyte that comprises S.sup.2- and/or S in a negative electrolyte supporting solution, and a membrane, or a separator, that separates the positive electrolyte and electrode from the negative electrolyte and electrode.

  11. Oxidation of Reduced Sulfur Species: Carbonyl Sulfide

    DEFF Research Database (Denmark)

    Glarborg, Peter; Marshall, Paul


    A detailed chemical kinetic model for oxidation of carbonyl sulfide (OCS) has been developed, based on a critical evaluation of data from the literature. The mechanism has been validated against experimental results from batch reactors, flow reactors, and shock tubes. The model predicts satisfact......A detailed chemical kinetic model for oxidation of carbonyl sulfide (OCS) has been developed, based on a critical evaluation of data from the literature. The mechanism has been validated against experimental results from batch reactors, flow reactors, and shock tubes. The model predicts...... satisfactorily oxidation of OCS over a wide range of stoichiometric air–fuel ratios (0.5 ≤λ≤7.3), temperatures (450–1700 K), and pressures (0.02–3.0 atm) under dry conditions. The governing reaction mechanisms are outlined based on calculations with the kinetic model. The oxidation rate of OCS is controlled...

  12. Ferrocene sulfonates as electrocatalysts for sulfide detection

    International Nuclear Information System (INIS)

    Lawrence, Nathan S.; Tustin, Gary J.; Faulkner, Michael; Jones, Timothy G.J.


    The electrochemical characterization of both the mono- and di-substituted forms of ferrocene sulfonate are given. The results show both species produce voltammograms consistent with quasi-irreversible diffusion controlled redox reactions. The FcSO 3 - species was found to be easier to oxidize than its Fc(SO 3 ) 2 2- counterpart, due to the electron withdrawing affect of the sulfonate group on the Fe centre. In the presence of sulfide, the voltammetric response of FcSO 3 - is shown to be consistent with the occurrence of an electrocatalytic EC' reaction. This analytical response was utilized as a means of determining sulfide and was found to be linear over the concentration 0.02-1 mM with a limit of detection of 14 μM

  13. Various communications concerning sulfigran (sodium sulfide)

    Energy Technology Data Exchange (ETDEWEB)

    Schmitt, H.; Montfort, F.; Wickert; Horn; Junkermann; Wissel, K.; Pier, M.


    Most of these communications concerned the problems experienced by Poelitz when its regular supplier of Sulfigran (sodium sulfide), the I.G. Farbenindustrie plant at Luverkusen, had to shut down for repairs and Poelitz had to get an impure form of Sulfigran mixture (a crude melt of ore) from other suppliers, including the I.G. Farbenindustrie plant at Wolfen (Bitterfeld). Various problems arose in the transition, including the fact that the mixture supplied was not ground finely enough for the coal-paste-preparing machinery at Poelitz to handle without damage. An analysis of one sample of the raw melt mixture gave 68.8% sodium sulfide, 12.0% carbon, 1.5% hydrogen, 1.6% silicon dioxide, 1.8% iron, 1.0% aluminum, 0.6% calcium, traces of magnesium and sulfate, and 15.4% water-insoluble. An analysis for another sample showed about 1.8% less sodium sulfide, 1.5% more silicon dioxide, 0.7% less iron, 0.5% less aluminum, 0.6% more calcium, etc., than the previous analysis. Finally one of the communications was a letter in which Ludwigshafen responded favorably to Poelitz's question about whether it would be advantageous to add Sulfigran directly to the first oven of a hydrogenation chamber instead of grinding it with the coal paste. Ludwigshafen said that in some experiments it had observed deposits at places where Sulfigran and coal paste encountered each other in preheater tubes. The deposits consisted of sodium sulfide and iron compounds. 3 tables.

  14. Hydrogen sulfide prodrugs—a review

    Directory of Open Access Journals (Sweden)

    Yueqin Zheng


    Full Text Available Hydrogen sulfide (H2S is recognized as one of three gasotransmitters together with nitric oxide (NO and carbon monoxide (CO. As a signaling molecule, H2S plays an important role in physiology and shows great potential in pharmaceutical applications. Along this line, there is a need for the development of H2S prodrugs for various reasons. In this review, we summarize different H2S prodrugs, their chemical properties, and some of their potential therapeutic applications.

  15. Sulfide Precipitation in Wastewater at Short Timescales

    DEFF Research Database (Denmark)

    Kiilerich, Bruno; van de Ven, Wilbert; Nielsen, Asbjørn Haaning


    that this is not the case for sulfide precipitation by ferric iron. Instead, the reaction time was found to be on a timescale where it must be considered when performing end-of-pipe treatment. For real wastewaters at pH 7, a stoichiometric ratio around 14 mol Fe(II) (mol S(−II))−1 was obtained after 1.5 s, while the ratio...

  16. Light Stops at Exceptional Points (United States)

    Goldzak, Tamar; Mailybaev, Alexei A.; Moiseyev, Nimrod


    Almost twenty years ago, light was slowed down to less than 10-7 of its vacuum speed in a cloud of ultracold atoms of sodium. Upon a sudden turn-off of the coupling laser, a slow light pulse can be imprinted on cold atoms such that it can be read out and converted into a photon again. In this process, the light is stopped by absorbing it and storing its shape within the atomic ensemble. Alternatively, the light can be stopped at the band edge in photonic-crystal waveguides, where the group speed vanishes. Here, we extend the phenomenon of stopped light to the new field of parity-time (P T ) symmetric systems. We show that zero group speed in P T symmetric optical waveguides can be achieved if the system is prepared at an exceptional point, where two optical modes coalesce. This effect can be tuned for optical pulses in a wide range of frequencies and bandwidths, as we demonstrate in a system of coupled waveguides with gain and loss.

  17. Microaeration for hydrogen sulfide removal in UASB reactor. (United States)

    Krayzelova, Lucie; Bartacek, Jan; Kolesarova, Nina; Jenicek, Pavel


    The removal of hydrogen sulfide from biogas by microaeration was studied in Up-flow Anaerobic Sludge Blanket (UASB) reactors treating synthetic brewery wastewater. A fully anaerobic UASB reactor served as a control while air was dosed into a microaerobic UASB reactor (UMSB). After a year of operation, sulfur balance was described in both reactors. In UASB, sulfur was mainly presented in the effluent as sulfide (49%) and in biogas as hydrogen sulfide (34%). In UMSB, 74% of sulfur was detected in the effluent (41% being sulfide and 33% being elemental sulfur), 10% accumulated in headspace as elemental sulfur and 9% escaped in biogas as hydrogen sulfide. The efficiency of hydrogen sulfide removal in UMSB was on average 73%. Microaeration did not cause any decrease in COD removal or methanogenic activity in UMSB and the elemental sulfur produced by microaeration did not accumulate in granular sludge. Copyright © 2014 Elsevier Ltd. All rights reserved.

  18. Platinum-group elements fractionation by selective complexing, the Os, Ir, Ru, Rh-arsenide-sulfide systems above 1020 °C (United States)

    Helmy, Hassan M.; Bragagni, Alessandro


    The platinum-group element (PGE) contents in magmatic ores and rocks are normally in the low μg/g (even in the ng/g) level, yet they form discrete platinum-group mineral (PGM) phases. IPGE (Os, Ir, Ru) + Rh form alloys, sulfides, and sulfarsenides while Pt and Pd form arsenides, tellurides, bismuthoids and antimonides. We experimentally investigate the behavior of Os, Ru, Ir and Rh in As-bearing sulfide system between 1300 and 1020 °C and show that the prominent mineralogical difference between IPGE (+Rh) and Pt and Pd reflects different chemical preference in the sulfide melt. At temperatures above 1200 °C, Os shows a tendency to form alloys. Ruthenium forms a sulfide (laurite RuS2) while Ir and Rh form sulfarsenides (irarsite IrAsS and hollingworthite RhAsS, respectively). The chemical preference of PGE is selective: IPGE + Rh form metal-metal, metal-S and metal-AsS complexes while Pt and Pd form semimetal complexes. Selective complexing followed by mechanical separation of IPGE (and Rh)-ligand from Pt- and Pd-ligand associations lead to PGE fractionation.

  19. Modeling Sulfides, pH and Hydrogen Sulfide Gas in the Sewers of San Francisco

    DEFF Research Database (Denmark)

    Vollertsen, Jes; Revilla, Nohemy; Hvitved-Jacobsen, Thorkild


    An extensive measuring campaign targeted on sewer odor problems was undertaken in San Francisco. It was assessed whether a conceptual sewer process model could reproduce the measured concentrations of total sulfide in the wastewater and H2S gas in the sewer atmosphere, and to which degree...... (WATS) sewer process concept, which never had been calibrated to such an extensive dataset. The study showed that the model was capable of reproducing the general levels of wastewater sulfide, wastewater pH, and sewer H2S gas. It could also reproduce the general variability of these parameters, albeit...

  20. One-Step Electrodeposited Nickel Cobalt Sulfide Nanosheet Arrays for High-Performance Asymmetric Supercapacitors

    KAUST Repository

    Chen, Wei


    A facile one-step electrodeposition method is developed to prepare ternary nickel cobalt sulfide interconnected nanosheet arrays on conductive carbon substrates as electrodes for supercapacitors, resulting in exceptional energy storage performance. Taking advantages of the highly conductive, mesoporous nature of the nanosheets and open framework of the three-dimensional nanoarchitectures, the ternary sulfide electrodes exhibit high specific capacitance (1418 F g(-1) at 5 A g(-1) and 1285 F g(-1) at 100 A g(-1)) with excellent rate capability. An asymmetric supercapacitor fabricated by the ternary sulfide nanosheet arrays as positive electrode and porous graphene film as negative electrode demonstrates outstanding electrochemical performance for practical energy storage applications. Our asymmetric supercapacitors show a high energy density of 60 Wh kg(-1) at a power density of 1.8 kW kg(-1). Even when charging the cell within 4.5 s, the energy density is still as high as 33 Wh kg(-1) at an outstanding power density of 28.8 kW kg(-1) with robust long-term cycling stability up to 50 000 cycles.

  1. Recent findings on sinks for sulfide in gravity sewer networks

    DEFF Research Database (Denmark)

    Nielsen, Asbjørn Haaning; Hvitved-Jacobsen, Thorkild; Vollertsen, Jes


    Sulfide buildup in sewer networks is associated with several problems, including health impacts, corrosion of sewer structures and odor nuisance. In recent years, significant advances in the knowledge of the major processes governing sulfide buildup in sewer networks have been made. This paper...... summarizes this newly obtained knowledge and emphasizes important implications of the findings. Model simulations of the in-sewer processes important for the sulfur cycle showed that sulfide oxidation in the wetted biofilm is typically the most important sink for dissolved sulfide in gravity sewers. However...

  2. Mechanisms of bacterial metals removal from solids

    International Nuclear Information System (INIS)

    Torma, A.E.; Pryfogle, P.A.


    The Great Lakes area sediments are contaminated with varying amounts of heavy metals and polychlorinated organic matter. With respect to the bioremediation of metallic contents of these sediments, it was shown that a number of microorganisms exist which can effectively solubilize heavy metals. The basic reaction mechanisms of bioleaching processes were discussed and the effects of semiconductor character of the sulfide substrate explained. A special emphasis was made to comment on INEL's bioremediation capability. 37 refs

  3. Mechanism of radiation and thermal decomposition of sulphide non-ferrous metals

    International Nuclear Information System (INIS)

    Mazhrenova, N.P.


    This paper deals with the non-ferrous metals sulfides in term of their radiative sensitivity, directed chances of their physical-chemical, and hence technological properties by radiation influence both on sulfide materials and on the processes with their participation. (author)

  4. Carbon steel protection in G.S. (Girlder sulfide) plants. Iron sulfide scales formation conditions. Pt. 1

    International Nuclear Information System (INIS)

    Bruzzoni, P.; Burkart, A.L.; Garavaglia, R.N.


    An ASTM A 516 degree 60 carbon steel superficial protection technique submitted to a hydrogen-water sulfide corrosive medium at 2 MPa of pressure and 40-125 deg C forming on itself an iron sulfide layer was tested. Studies on pH influence, temperature, passivating mean characteristics and exposure time as well as the mechanical resistance of sulfide layers to erosion are included. (Author) [es

  5. 76 FR 64022 - Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting (United States)


    ... Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting AGENCY: Environmental Protection Agency (EPA). ACTION: Lifting of Administrative Stay for Hydrogen Sulfide. SUMMARY: EPA is announcing... (EPCRA) section 313 toxic chemical release reporting requirements for hydrogen sulfide (Chemical...

  6. Microbial contributions to coupled arsenic and sulfur cycling in the acid-sulfide hot spring Champagne Pool, New Zealand. (United States)

    Hug, Katrin; Maher, William A; Stott, Matthew B; Krikowa, Frank; Foster, Simon; Moreau, John W


    Acid-sulfide hot springs are analogs of early Earth geothermal systems where microbial metal(loid) resistance likely first evolved. Arsenic is a metalloid enriched in the acid-sulfide hot spring Champagne Pool (Waiotapu, New Zealand). Arsenic speciation in Champagne Pool follows reaction paths not yet fully understood with respect to biotic contributions and coupling to biogeochemical sulfur cycling. Here we present quantitative arsenic speciation from Champagne Pool, finding arsenite dominant in the pool, rim and outflow channel (55-75% total arsenic), and dithio- and trithioarsenates ubiquitously present as 18-25% total arsenic. In the outflow channel, dimethylmonothioarsenate comprised ≤9% total arsenic, while on the outflow terrace thioarsenates were present at 55% total arsenic. We also quantified sulfide, thiosulfate, sulfate and elemental sulfur, finding sulfide and sulfate as major species in the pool and outflow terrace, respectively. Elemental sulfur concentration reached a maximum at the terrace. Phylogenetic analysis of 16S rRNA genes from metagenomic sequencing revealed the dominance of Sulfurihydrogenibium at all sites and an increased archaeal population at the rim and outflow channel. Several phylotypes were found closely related to known sulfur- and sulfide-oxidizers, as well as sulfur- and sulfate-reducers. Bioinformatic analysis revealed genes underpinning sulfur redox transformations, consistent with sulfur speciation data, and illustrating a microbial role in sulfur-dependent transformation of arsenite to thioarsenate. Metagenomic analysis also revealed genes encoding for arsenate reductase at all sites, reflecting the ubiquity of thioarsenate and a need for microbial arsenate resistance despite anoxic conditions. Absence of the arsenite oxidase gene, aio, at all sites suggests prioritization of arsenite detoxification over coupling to energy conservation. Finally, detection of methyl arsenic in the outflow channel, in conjunction with

  7. Stabilities of thiomolybdate complexes of iron; implications for retention of essential trace elements (Fe, Cu, Mo) in sulfidic waters. (United States)

    Helz, George R; Erickson, Britt E; Vorlicek, Trent P


    In aquatic ecosystems, availabilities of Fe, Mo and Cu potentially limit rates of critical biological processes, including nitrogen fixation, nitrate assimilation and N2O decomposition. During long periods in Earth's history when large parts of the ocean were sulfidic, what prevented these elements' quantitative loss from marine habitats as insoluble sulfide phases? They must have been retained by formation of soluble complexes. Identities of the key ligands are poorly known but probably include thioanions. Here, the first determinations of stability constants for Fe(2+)-[MoS4](2-) complexes in aqueous solution are reported based on measurements of pyrrhotite (hexagonal FeS) solubility under mildly alkaline conditions. Two linear complexes, [FeO(OH)MoS4](3-) and [(Fe2S2)(MoS4)2](4-), best explain the observed solubility variations. Complexes that would be consistent with cuboid cluster structures were less successful, implying that such clusters probably are minor or absent in aqueous solution under the conditions studied. The new data, together with prior data on stabilities of Cu(+)-[MoS4](2-) complexes, are used to explore computationally how competition of Fe(2+) and Cu(+) for [MoS4](2-), as well as competition of [MoS4](2-) and HS(-) for both metals would be resolved in solutions representative of sulfidic natural waters. Thiomolybdate complexes will be most important at sulfide concentrations near the [MoO4](2-)-[MoS4](2-) equivalence point. At lower sulfide concentrations, thiomolybdates are insufficiently stable to be competitive ligands in natural waters and at higher sulfide concentrations HS(-) ligands out-compete thiomolybdates.

  8. Inhibition of sulfate reduction by iron, cadmium and sulfide in granular sludge

    International Nuclear Information System (INIS)

    Gonzalez-Silva, Blanca M.; Briones-Gallardo, Roberto; Razo-Flores, Elias; Celis, Lourdes B.


    This study investigated the inhibition effect of iron, cadmium and sulfide on the substrate utilization rate of sulfate reducing granular sludge. A series of batch experiments in a UASB reactor were conducted with different concentrations of iron (Fe 2+ , 4.0-8.5 mM), cadmium (Cd 2+ , 0.53-3.0 mM) and sulfide (4.2-10.6 mM), the reactor was fed with ethanol at 1 g chemical oxygen demand (COD)/L and sulfate to yield a COD/SO 4 2- (g/g) ratio of 0.5. The addition of iron, up to a concentration of 8.1 mM, had a positive effect on the substrate utilization rate which increased 40% compared to the rate obtained without metal addition (0.25 g COD/g VSS-d). Nonetheless, iron concentration of 8.5 mM inhibited the specific substrate utilization rate by 57% compared to the substrate utilization rate obtained in the batch amended with 4.0 mM Fe 2+ (0.44 g COD/g VSS-d). Cadmium had a negative effect on the specific substrate utilization rate at the concentrations tested; at 3.0 mM Cd 2+ the substrate utilization rate was inhibited by 44% compared with the substrate utilization rate without metal addition. Cadmium precipitation with sulfide did not decrease the inhibition of cadmium on sulfate reduction. These results could have important practical implications mainly when considering the application of the sulfate reducing process to treat effluents with high concentrations of sulfate and dissolved metals such as iron and cadmium.

  9. Inhibition of sulfate reduction by iron, cadmium and sulfide in granular sludge

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez-Silva, Blanca M. [Division de Ciencias Ambientales, Instituto Potosino de Investigacion Cientifica y Tecnologica, Camino a la Presa San Jose 2055, Lomas 4a. Seccion, 78216, San Luis Potosi, S.L.P. (Mexico); Briones-Gallardo, Roberto [Facultad de Ingenieria-Instituto de Metalurgia, Universidad Autonoma de San Luis Potosi, Sierra Leona 550, Lomas 2a. Seccion, 78210, San Luis Potosi, S.L.P. (Mexico); Razo-Flores, Elias [Division de Ciencias Ambientales, Instituto Potosino de Investigacion Cientifica y Tecnologica, Camino a la Presa San Jose 2055, Lomas 4a. Seccion, 78216, San Luis Potosi, S.L.P. (Mexico); Celis, Lourdes B., E-mail: [Division de Ciencias Ambientales, Instituto Potosino de Investigacion Cientifica y Tecnologica, Camino a la Presa San Jose 2055, Lomas 4a. Seccion, 78216, San Luis Potosi, S.L.P. (Mexico)


    This study investigated the inhibition effect of iron, cadmium and sulfide on the substrate utilization rate of sulfate reducing granular sludge. A series of batch experiments in a UASB reactor were conducted with different concentrations of iron (Fe{sup 2+}, 4.0-8.5 mM), cadmium (Cd{sup 2+}, 0.53-3.0 mM) and sulfide (4.2-10.6 mM), the reactor was fed with ethanol at 1 g chemical oxygen demand (COD)/L and sulfate to yield a COD/SO{sub 4}{sup 2-} (g/g) ratio of 0.5. The addition of iron, up to a concentration of 8.1 mM, had a positive effect on the substrate utilization rate which increased 40% compared to the rate obtained without metal addition (0.25 g COD/g VSS-d). Nonetheless, iron concentration of 8.5 mM inhibited the specific substrate utilization rate by 57% compared to the substrate utilization rate obtained in the batch amended with 4.0 mM Fe{sup 2+} (0.44 g COD/g VSS-d). Cadmium had a negative effect on the specific substrate utilization rate at the concentrations tested; at 3.0 mM Cd{sup 2+} the substrate utilization rate was inhibited by 44% compared with the substrate utilization rate without metal addition. Cadmium precipitation with sulfide did not decrease the inhibition of cadmium on sulfate reduction. These results could have important practical implications mainly when considering the application of the sulfate reducing process to treat effluents with high concentrations of sulfate and dissolved metals such as iron and cadmium.

  10. Biofabrication of morphology improved cadmium sulfide nanoparticles using Shewanella oneidensis bacterial cells and ionic liquid: For toxicity against brain cancer cell lines. (United States)

    Wang, Li; Chen, Siyuan; Ding, Yiming; Zhu, Qiang; Zhang, Nijia; Yu, Shuqing


    The present work determines the anticancer activity of bio-mediated synthesized cadmium sulfide nanoparticles using the ionic liquid and bacterial cells (Shewanella oneidensis). Bacterial cells have been exposed to be important resources that hold huge potential as ecofriendly, cost-effective, evading toxic of dangerous chemicals and the alternative of conventional physiochemical synthesis. The Shewanella oneidensis is an important kind of metal reducing bacterium, known as its special anaerobic respiratory and sulfate reducing capacity. The crystalline nature, phase purity and surface morphology of biosynthesized cadmium sulfide nanoparticles were analyzed by Fourier transform infrared spectroscopy, X-ray diffraction, Field emission scanning electron microscopy, Energy dispersive spectroscopy and Transmission electron microscopy. The use of imidazolium based ionic liquids as soft templating agent for controlling self-assembly and crystal growth direction of metal sulfide nanoparticles has also advanced as an important method. The microscopic techniques showed that the nanoparticles are designed on the nano form and have an excellent spherical morphology, due to the self-assembled mechanism of ionic liquid assistance. The antitumor efficiency of the cadmium sulfide nanoparticles was investigated against brain cancer cell lines using rat glioma cell lines. The effectively improved nano-crystalline and morphological structure of CdS nanoparticles in the presence of IL exhibit excellent cytotoxicity and dispersion ability on the cell shape is completely spread out showing a nice toxic environment against cancer cells. The cytotoxicity effect of cadmium sulfide nanoparticles was discussed with a diagrammatic representation. Copyright © 2017. Published by Elsevier B.V.

  11. Hollow Cobalt-Based Bimetallic Sulfide Polyhedra for Efficient All-pH-Value Electrochemical and Photocatalytic Hydrogen Evolution. (United States)

    Huang, Zhen-Feng; Song, Jiajia; Li, Ke; Tahir, Muhammad; Wang, Yu-Tong; Pan, Lun; Wang, Li; Zhang, Xiangwen; Zou, Ji-Jun


    The development of highly active, universal, and stable inexpensive electrocatalysts/cocatalysts for hydrogen evolution reaction (HER) by morphology and structure modulations remains a great challenge. Herein, a simple self-template strategy was developed to synthesize hollow Co-based bimetallic sulfide (MxCo3-xS4, M = Zn, Ni, and Cu) polyhedra with superior HER activity and stability. Homogenous bimetallic metal-organic frameworks are transformed to hollow bimetallic sulfides by solvothermal sulfidation and thermal annealing. Electrochemical measurements and density functional theory computations show that the combination of hollow structure and homoincorporation of a second metal significantly enhances the HER activity of Co3S4. Specifically, the homogeneous doping in Co3S4 lattice optimizes the Gibbs free energy for H* adsorption and improves the electrical conductivity. Impressively, hollow Zn0.30Co2.70S4 exhibits electrocatalytic HER activity better than most of the reported nobel-metal-free electrocatalysts over a wide pH range, with overpotentials of 80, 90, and 85 mV at 10 mA cm(-2) and 129, 144, and 136 mV at 100 mA cm(-2) in 0.5 M H2SO4, 0.1 M phosphate buffer, and 1 M KOH, respectively. It also exhibits photocatalytic HER activity comparable to that of Pt cocatalyst when working with organic photosensitizer (Eosin Y) or semiconductors (TiO2 and C3N4). Furthermore, this catalyst shows excellent stability in the electrochemical and photocatalytic reactions. The strategy developed here, i.e., homogeneous doping and self-templated hollow structure, provides a way to synthesize transition metal sulfides for catalysis and energy conversion.

  12. Improvement of sulfide corrosion resistance of nickel heat resisting alloys by means alloying

    International Nuclear Information System (INIS)

    Oryshkin, I.V.


    Paper describes the effect of the alloying elements (chromium, aluminium, titanium, molybdenum, tungsten, niobium, cobalt) on sulfide corrosion (SC) resistance of nickel base heat-resisting alloys during 30 h in 75% Na 2 SO 4 +25% NaCl molten sat under 900 deg C temperature. The obtained patterns are compared with the effect of the mentioned metals on the long-term strength. SC high resistance and the adequate level of heat resistance are ensured by a certain doping of a nickel base [ru

  13. Technetium behavior in sulfide and ferrous iron solutions

    International Nuclear Information System (INIS)

    Lee, S.Y.; Bondietti, E.A.


    Pertechnetate oxyanion ( 99 TcO 4- ), a potentially mobile species in leachate from a breached radioactive waste repository, was removed from a brine solution by precipitation with sulfide, iron, and ferrous sulfide at environmental pH's. Maghemite (ν-Fe 2 O 3 ) and geothite (α-FeOOH) were the dominant minerals in the precipitate obtained from the TcO 4- -ferrous iron reaction. The observation of small particle size and poor crystallinity of the minerals formed in the presence of Tc suggested that the Tc was incorporated into the mineral structure after reduction to a lower valence state. Amorphous ferrous sulfide, an initial phase precipitating in the TcO 4- -ferrous iron-sulfide reaction, was transformed to goethite and hematite (α-Fe 2 O 3 ) on aging. The black precipitate obtained from the TcO 4- -sulfide reaction was poorly crystallized technetium sulfide (Tc 2 S 7 ) which was insoluble in both acid and alkaline solution in the absence of strong oxidents. The results suggested that ferrous- and/or sulfide-bearing groundwaters and minerals in host rocks or backfill barriers could reduce the mobility of Tc through the formation of less-soluble Tc-bearing iron and/or sulfide minerals

  14. Effect of Soluble Sulfide on the Activity of Luminescent Bacteria

    Directory of Open Access Journals (Sweden)

    Feng Wang


    Full Text Available Sulfide is an important water pollutant widely found in industrial waste water that has attracted much attention. S2−, as a weak acidic anion, is easy hydrolyzed to HS and H2S in aqueous solution. In this study, biological tests were performed to establish the toxicity of sulfide solutions on luminescent bacteria. Considering the sulfide solution was contained three substances—S2−, HS and H2S—the toxicity test was performed at different pH values to investigate which form of sulfide increased light emission and which reduced light emission. It was shown that the EC50 values were close at pH 7.4, 8.0 and 9.0 which were higher than pH 5 and 10. The light emission and sulfide concentrations displayed an inverse exponential dose-response relationship within a certain concentration range at pH 5, 6.5 and 10. The same phenomenon occurred for the high concentration of sulfide at pH 7.4, 8 and 9, in which the concentration of sulfide was HS >> H2S > S2−. An opposite hormesis-effect appeared at the low concentrations of sulfide.

  15. Sulfidation of zinc plating sludge with Na2S for zinc resource recovery

    International Nuclear Information System (INIS)

    Kuchar, D.; Fukuta, T.; Onyango, M.S.; Matsuda, H.


    A high amount of zinc disposed in the landfill sites as a mixed-metal plating sludge represents a valuable zinc source. To recover zinc from the plating sludge, a sulfidation treatment is proposed in this study, while it is assumed that ZnS formed could be separated by flotation. The sulfidation treatment was conducted by contacting simulated zinc plating sludge with Na 2 S solution at S 2- to Zn 2+ molar ratio of 1.5 for a period of 1-48 h, while changing the solid to liquid (S:L) ratio from 0.25:50 to 1.00:50. The conversion of zinc compounds to ZnS was determined based on the consumption of sulfide ions. The reaction products formed by the sulfidation of zinc were identified by X-ray diffraction (XRD). As a result, it was found that the conversion of zinc compounds to ZnS increased with an increase in S:L ratio. A maximum conversion of 0.809 was obtained at an S:L ratio of 1.00:50 after 48 h. However, when the zinc sludge treated at S:L ratio of 1.00:50 for 48 h was subjected to XRD analyses, only ZnS was identified in the treated zinc sludge. The result suggested that the rest of zinc sludge remained unreacted inside the agglomerates of ZnS. The formation behavior of ZnS was predicted by Elovich equation, which was found to describe the system satisfactorily indicating the heterogeneous nature of the sludge

  16. Hydrogen sulfide: from brain to gut. (United States)

    Kimura, Hideo


    Three hundred years have passed since the first description of the toxicity of hydrogen sulfide (H(2)S). Three papers in 1989 and 1990 described relatively high concentrations of sulfide in the brain. In 1996 we demonstrated that cystathionine beta-synthase (CBS) is a H(2)S producing enzyme in the brain and that H(2)S enhances the activity of NMDA receptors and facilitates the induction of hippocampal long-term potentiation (LTP), a synaptic model of memory. In the following year, we demonstrated that another H(2)S producing enzyme, cystathionine gamma-lyase is in the thoracic aorta, portal vein, and the ileum, and that H(2)S relaxes these tissues. Based on these observations we proposed H(2)S as a neuromodulator as well as a smooth muscle relaxant. We recently demonstrated that the third H(2)S-producing enzyme, 3-mercaptopyruvate sulfurtransferase (3MST) along with cysteine aminotransferase (CAT) produces H(2)S in the brain as well as in vascular endothelium. Various functions in many tissues have been proposed. H(2)S protects neurons and cardiac muscle from oxidative stress. H(2)S has pro- and anti-inflammatory effects, nociceptive effects, the regulatory function of insulin release, and is even involved in longevity. Recent progress in the studies of physiological functions of H(2)S in neurons and smooth muscle was described.

  17. Sulfurization of Dissolved Organic Matter Increases Hg-Sulfide-Dissolved Organic Matter Bioavailability to a Hg-Methylating Bacterium. (United States)

    Graham, Andrew M; Cameron-Burr, Keaton T; Hajic, Hayley A; Lee, Connie; Msekela, Deborah; Gilmour, Cynthia C


    Reactions of dissolved organic matter (DOM) with aqueous sulfide (termed sulfurization) in anoxic environments can substantially increase DOM's reduced sulfur functional group content. Sulfurization may affect DOM-trace metal interactions, including complexation and metal-containing particle precipitation, aggregation, and dissolution. Using a diverse suite of DOM samples, we found that susceptibility to additional sulfur incorporation via reaction with aqueous sulfide increased with increasing DOM aromatic-, carbonyl-, and carboxyl-C content. The role of DOM sulfurization in enhancing Hg bioavailability for microbial methylation was evaluated under conditions typical of Hg methylation environments (μM sulfide concentrations and low Hg-to-DOM molar ratios). Under the conditions of predicted metacinnabar supersaturation, microbial Hg methylation increased with increasing DOM sulfurization, likely reflecting either effective inhibition of metacinnabar growth and aggregation or the formation of Hg(II)-DOM thiol complexes with high bioavailability. Remarkably, Hg methylation efficiencies with the most sulfurized DOM samples were similar (>85% of total Hg methylated) to that observed in the presence of l-cysteine, a ligand facilitating rapid Hg(II) biouptake and methylation. This suggests that complexes of Hg(II) with DOM thiols have similar bioavailability to Hg(II) complexes with low-molecular-weight thiols. Overall, our results are a demonstration of the importance of DOM sulfurization to trace metal and metalloid (especially mercury) fate in the environment. DOM sulfurization likely represents another link between anthropogenic sulfate enrichment and MeHg production in the environment.

  18. Sulindac Sulfide, but Not Sulindac Sulfone, Inhibits Colorectal Cancer Growth

    Directory of Open Access Journals (Sweden)

    Christopher S. Williams


    Full Text Available Sulindac sulfide, a metabolite of the nonsteroidal antiinflammatory drug (NSAID sulindac sulfoxide, is effective at reducing tumor burden in both familial adenomatous polyposis patients and in animals with colorectal cancer. Another sulindac sulfoxide metabolite, sulindac sulfone, has been reported to have antitumor properties without inhibiting cyclooxygenase activity. Here we report the effect of sulindac sulfone treatment on the growth of colorectal carcinoma cells. We observed that sulindac sulfide or sulfone treatment of HCA-7 cells led to inhibition of prostaglandin E2 production. Both sulindac sulfide and sulfone inhibited HCA-7 and HCT-116 cell growth in vitro. Sulindac sulfone had no effect on the growth of either HCA-7 or HCT-116 xenografts, whereas the sulfide derivative inhibited HCA-7 growth in vivo. Both sulindac sulfide and sulfone inhibited colon carcinoma cell growth and prostaglandin production in vitro, but sulindac sulfone had no effect on the growth of colon cancer cell xenografts in nude mice.

  19. Hierarchical Architecturing for Layered Thermoelectric Sulfides and Chalcogenides (United States)

    Jood, Priyanka; Ohta, Michihiro


    Sulfides are promising candidates for environment-friendly and cost-effective thermoelectric materials. In this article, we review the recent progress in all-length-scale hierarchical architecturing for sulfides and chalcogenides, highlighting the key strategies used to enhance their thermoelectric performance. We primarily focus on TiS2-based layered sulfides, misfit layered sulfides, homologous chalcogenides, accordion-like layered Sn chalcogenides, and thermoelectric minerals. CS2 sulfurization is an appropriate method for preparing sulfide thermoelectric materials. At the atomic scale, the intercalation of guest atoms/layers into host crystal layers, crystal-structural evolution enabled by the homologous series, and low-energy atomic vibration effectively scatter phonons, resulting in a reduced lattice thermal conductivity. At the nanoscale, stacking faults further reduce the lattice thermal conductivity. At the microscale, the highly oriented microtexture allows high carrier mobility in the in-plane direction, leading to a high thermoelectric power factor. PMID:28787992

  20. Influence of Water Salinity on Air Purification from Hydrogen Sulfide

    Directory of Open Access Journals (Sweden)

    Leybovych L.I.


    Full Text Available Mathematical modeling of «sliding» water drop motion in the air flow was performed in software package FlowVision. The result of mathematical modeling of water motion in a droplet with diameter 100 microns at the «sliding» velocity of 15 m/s is shown. It is established that hydrogen sulfide oxidation occurs at the surface of phases contact. The schematic diagram of the experimental setup for studying air purification from hydrogen sulfide is shown. The results of the experimental research of hydrogen sulfide oxidation by tap and distilled water are presented. The dependence determining the share of hydrogen sulfide oxidized at the surface of phases contact from the dimensionless initial concentration of hydrogen sulfide in the air has been obtained.

  1. The selenium isotopic variations in chondrites are mass-dependent; Implications for sulfide formation in the early solar system (United States)

    Labidi, J.; König, S.; Kurzawa, T.; Yierpan, A.; Schoenberg, R.


    Element transfer from the solar nebular gas to solids occurred either through direct condensation or via heterogeneous reactions between gaseous molecules and previously condensed solid matter. The precursors of altered sulfides observed in chondrites are for example attributed to reactions between gaseous hydrogen sulfide and metallic iron grains. The transfer of selenium to solids likely occurred through a similar pathway, allowing the formation of iron selenides concomitantly with sulfides. The formation rate of sulfide however remains difficult to assess. Here we investigate whether the Se isotopic composition of meteorites contributes to constrain sulfide formation during condensation stages of our solar system. We present high precision Se concentration and δ 82 / 78 Se data for 23 chondrites as well as the first δ 74 / 78 Se , δ 76 / 78 Se and δ 77 / 78 Se data for a sub-set of seven chondrites. We combine our dataset with previously published sulfur isotopic data and discuss aspects of sulfide formation for various types of chondrites. Our Se concentration data are within uncertainty to literature values and are consistent with sulfides being the dominant selenium host in chondrites. Our overall average δ 82 / 78 Se value for chondrites is - 0.21 ± 0.43 ‰ (n = 23, 2 s.d.), or - 0.14 ± 0.21 ‰ after exclusion of three weathered chondrites (n = 20, 2 s.d.). These average values are within uncertainty indistinguishable from a previously published estimate. For the first time however, we resolve distinct δ 82 / 78 Se between ordinary (- 0.14 ± 0.07 ‰, n = 9, 2 s.d.), enstatite (- 0.27 ± 0.05 ‰, n = 3, 2 s.d.) and CI carbonaceous chondrites (- 0.01 ± 0.06 ‰, n = 2, 2 s.d.). We also resolve a Se isotopic variability among CM carbonaceous chondrites. In addition, we report on δ 74 / 78 Se , δ 76 / 78 Se and δ 77 / 78 Se values determined for 7 chondrites. Our data allow evaluating the mass dependency of the δ 82 / 78 Se variations. Mass

  2. Treatment of metal-contaminated water and vertical distribution of metal precipitates in an upflow anaerobic bioreactor. (United States)

    Quan, Z X; La, H J; Cho, Y G; Hwang, M H; Kim, L S; Lee, S T


    A lab-scale upflow anaerobic bioreactor filled with granular sludge and cow manure was operated for 140 days to determine the mechanism of metal removal and the vertical distribution of metal precipitates. Heavy metal ions were removed in the order of Cu2+, Cd2+, Zn2+, Fe2+ and Mn2+ with respect to the height in the reactor. The solid phase analysis showed that the heavy metals were mostly precipitated in the form of metal sulfides by sulfate reduction The contents of metal precipitates in the reactor were as follows: (i) Cd and Zn were highest in the bottom, (ii) Fe was highest at the low-middle layer, and (iii) Mn was increased with the height in the reactor. The vertical distribution of metal sulfides in the reactor was directly related to the solubility product (Ksp). Results obtained in this study suggest a feasibility of the application to separate precipitation metal-containing wastewater.


    Trace element solubility and availability in land-applied residuals is governed by fundamental chemical reactions between metal constituents, soil, and residual components. Iron, aluminum, and manganese oxides; organic matter; and phosphates, carbonates, and sulfides are importan...

  4. Reduced ternary molybdenum and tungsten sulfides and hydroprocessing catalysis therewith (United States)

    Hilsenbeck, S.J.; McCarley, R.E.; Schrader, G.L.; Xie, X.B.


    New amorphous molybdenum/tungsten sulfides with the general formula M{sup n+}{sub 2x/n}(L{sub 6}S{sub 8})S{sub x}, where L is molybdenum or tungsten and M is a ternary metal, has been developed. Characterization of these amorphous materials by chemical and spectroscopic methods (IR, Raman, PES) shows that the (M{sub 6}S{sub 8}){sup 0} cluster units are present. Vacuum thermolysis of the amorphous Na{sub 2x}(Mo{sub 6}S{sub 8})S{sub x}{hor_ellipsis}yMeOH first produces poorly crystalline NaMo{sub 6}S{sub 8} by disproportionation at 800 C and well-crystallized NaMo{sub 6}S{sub 8} at {>=} 900 C. Ion-exchange of the sodium material in methanol with soluble M{sup 2+} and M{sup 3+} salts (M=Sn, Co, Ni, Pb, La, Ho) produces the M{sup n+}{sub 2x/n}(Mo{sub 6}S{sub 8})S{sub x}{hor_ellipsis}yMeOH compounds. Additionally, the new reduced ternary molybdenum sulfides with the general formula M{sup n+}{sub 2x/n}Mo{sub 6}S{sub 8+x}(MeOH){sub y}[MMOS] (M=Sn, Co, Ni) is an effective hydrodesulfurization (HDS) catalyst both as-prepared and after a variety of pretreatment conditions. Under specified pretreatment conditions with flowing hydrogen gas, the SnMoS type catalyst can be stabilized, and while still amorphous, can be considered as ``Chevrel phase-like`` in that both contain Mo{sub 6}S{sub 8} cluster units. Furthermore, the small cation NiMoS and CoMoS type pretreated catalyst is shown to be very active HDS catalysts with rates that exceeded the model unpromoted and cobalt-promoted MoS{sub 2} catalysts. 9 figs.

  5. Carbon steel protection in G.S. (Girlder sulfide) plants. Pressure influence on iron sulfide scales formation. Pt. 5

    International Nuclear Information System (INIS)

    Delfino, C.A.; Lires, O.A.; Rojo, E.A.


    In order to protect carbon steel towers and piping of Girlder sulfide (G.S.) experimental heavy water plants against corrosion produced by the action of aqueous solutions of hydrogen sulfide, a method, previously published, was developed. Carbon steel, exposed to saturated aqueous solutions of hydrogen sulfide, forms iron sulfide scales. In oxygen free solutions evolution of corrosion follows the sequence: mackinawite → cubic ferrous sulfide → troilite → pyrrotite → pyrite. Scales formed by pyrrotite-pyrite or pyrite are the most protective layers (these are obtained at 130 deg C, 2MPa, for periods of 14 days). Experiments, at 125 deg C and periods of 10-25 days, were performed in two different ways: 1- constant pressure operations at 0.5 and 1.1 MPa. 2- variable pressure operation between 0.3-1 MPa. In all cases pyrrotite-pyrite scales were obtained. (Author) [es

  6. Charge space, exceptional observables and groups

    International Nuclear Information System (INIS)

    Guersey, F.


    It is shown that a class of exceptional quantum mechanical spaces represented by octonionic matrices and first introduced by Jordan, von Neumann and Wigner are suitable for representing the states of basic fermionic constituents (leptons and quarks) of elementary particles. In these exceptional spaces, the transformation groups that leave scalar products invariant are the exceptional groups. A gauge field theory based on E 7 is given as an example for the unification of weak, electromagnetic and strong interactions

  7. Sulfide gas effects on the power transmission lines; Efeito do gas sulfidrico nos componentes do sistema de transmissao de energia eletrica

    Energy Technology Data Exchange (ETDEWEB)

    Kajimoto, Zehbour Panossian; Almeida, Neusvaldo Lira de


    Copper and its alloys when exposed in atmosphere contaminated with sulphur compounds present stains due to sulfidation. This sulfidation is markedly influenced by temperature and air relative humidity. In this works, results from tests with three years of exposition in atmospheres containing H{sub 2}S and SO{sub 2} are related; such results show that the use of these materials in regions with these contaminants must be done with restriction. Besides the high copper corrosion rates, corrosion products which form on this metal can cause serious problems to the electric contact. (author) 8 refs., 4 figs., 4 tabs.

  8. Occupational exposure to hydrogen sulfide: management of hydrogen sulfide exposure victims (Preprint No. SA-5)

    International Nuclear Information System (INIS)

    Srivastava, P.P.


    National Institute of Occupational Safety and Health, U.S.A. has listed 73 industries with potential exposure to hydrogen sulphide. Though the toxicity of hydrogen sulfide is known to mankind since the beginning of seventeenth century the exact mode of its toxicity and effective therapeutic regimen remains unclear as yet. This paper presents current thoughts on the toxicity of this substance and a discussion on the role of various antidotes used in H 2 S poisoning. (autho r)

  9. Germanium sulfide-based solid electrolytes for non-volatile memory (United States)

    Balakrishnan, Muralikrishnan

    Programmable Metallization Cell (PMC) technology involves the storage of data as reduced metal ions in a solid electrolyte. Earlier work on Selenide-based (Ag-Ge-Se) PMC devices requires relatively low back-end-of-line processing (BEOL) since the electrolyte may undergo undesirable changes at process temperatures in excess of 200°C. This dissertation is focused on Sulfide-based (Ag/Cu-Ge-S) solid electrolytes which have better temperature stability and the PMC technology based on these materials is compatible with most BEOL process in CMOS Integrated Circuits. The devices fabricated using Ag-Ge-S and Cu-Ge-S solid electrolytes were tested after annealing at 300°C and 430°C. Extensive material analysis was performed on both the systems in an effort to understand the behavior of the devices at elevated temperatures. Electrical characterization testing involved standard memory characterization techniques such as quasi-static measurements tests, retention tests, speed tests, elevated temperature operation tests and endurance tests. The Ag-Ge-S PMC devices were made with different compositions to find out the optimum composition which would ensure reliable operation even after the high temperature anneal. The Sulfide-based PMC devices were also tested for reconfigurable logic applications with special test structures that would demonstrate the low resistance connections that can be achieved by programming the PMC elements using higher currents. Optimum composition of the starting glass was found from the material and data analysis, to ensure reliable operation of the Sulfide-based PMC devices with no degradation in the electrical characteristics even after the typical BEOL anneal.

  10. Photocatalytic degradation and sorption of methylene blue on the surface of metal oxides in aqueous solutions of the dye (United States)

    Kiselev, V. M.; Evstrop'ev, S. K.; Starodubtsev, A. M.


    The photocatalytic activity of some metal oxides and sulfides, as well of C60 fullerene, is compared using the method of photocatalytic degradation of methylene blue simultaneously with comparison of the efficiency of methylene blue adsorption on solid-phase powders of these oxides, sulfides, and fullerene in aqueous solution of the dye in the absence of irradiation.

  11. Trace metal speciation and bioavailability in anaerobic digestion: A review. (United States)

    Thanh, Pham Minh; Ketheesan, Balachandran; Yan, Zhou; Stuckey, David


    Trace metals are essential for the growth of anaerobic microorganisms, however, in practice they are often added to anaerobic digesters in excessive amounts, which can lead to inhibition. The concept of bioavailability of metals in anaerobic digestion has been poorly understood in the past, and a lack of deep understanding of the relationship between trace metal speciation and bioavailability can result in ineffective metal dosing strategies for anaerobic digesters. Sequential extraction schemes are useful for fractionating trace metals into their different forms, and metal sulfides can serve as a store and source for trace metals during anaerobic digestion, while natural/synthetic chelating agents (soluble microbial products-SMPs, extracellular polysaccharides-EPS, and EDTA/NTA) are capable of controlling trace metal bioavailability. Nevertheless, more work is needed to: investigate the speciation and bioavailability of Ca, Mg, Mn, W, and Se; compare the bioavailability of different forms of trace metals e.g. carbonates, sulfides, phosphates to different anaerobic trophic groups; determine what factors influence metal sulfide dissolution; investigate whether chelating agents can increase trace metal bioavailability; develop and adapt specialized analytical techniques, and; determine how trace metal dynamics change in an anaerobic membrane bioreactor (AnMBR). Copyright © 2015 Elsevier Inc. All rights reserved.

  12. Azo dye decolorization assisted by chemical and biogenic sulfide

    Energy Technology Data Exchange (ETDEWEB)

    Prato-Garcia, Dorian [Laboratory for Research on Advanced Processes for Water Treatment, Unidad Académica Juriquilla, Instituto de Ingeniería, Universidad Nacional Autónoma de México, Blvd. Juriquilla 3001, Querétaro 76230 (Mexico); Cervantes, Francisco J. [División de Ciencias Ambientales, Instituto Potosino de Investigación Científica y Tecnológica, Camino a la Presa de San José 2055, San Luis Potosí 78216 (Mexico); Buitrón, Germán, E-mail: [Laboratory for Research on Advanced Processes for Water Treatment, Unidad Académica Juriquilla, Instituto de Ingeniería, Universidad Nacional Autónoma de México, Blvd. Juriquilla 3001, Querétaro 76230 (Mexico)


    Highlights: ► Azo dyes were reduced efficiently by chemical and biogenic sulfide. ► Biogenic sulfide was more efficient than chemical sulfide. ► There was no competition between dyes and sulfate for reducing equivalents. ► Aromatic amines barely affected the sulfate-reducing process. -- Abstract: The effectiveness of chemical and biogenic sulfide in decolorizing three sulfonated azo dyes and the robustness of a sulfate-reducing process for simultaneous decolorization and sulfate removal were evaluated. The results demonstrated that decolorization of azo dyes assisted by chemical sulfide and anthraquinone-2,6-disulfonate (AQDS) was effective. In the absence of AQDS, biogenic sulfide was more efficient than chemical sulfide for decolorizing the azo dyes. The performance of sulfate-reducing bacteria in attached-growth sequencing batch reactors suggested the absence of competition between the studied azo dyes and the sulfate-reducing process for the reducing equivalents. Additionally, the presence of chemical reduction by-products had an almost negligible effect on the sulfate removal rate, which was nearly constant (94%) after azo dye injection.

  13. Sulfidic vapor phase catalysts, especially tungsten sulfide, in industrial coal hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Pier, M.


    The historical development of high-pressure processes of the I. G. Farbenindustrie, from ammonia through methanol and gasoline, and the special case of gasoline production with a fixed-bed catalyst (tungsten sulfide) were discussed. The preparation, properties, and uses of this versatile catalyst were discussed, but it was emphasized that with the sotrmy development of the process, a condition which still existed at the time of this report, and with a great number of practical problems to solve, no extensive study of basic facts had ben possible. This tungsten sulfide catalyst was an especially active vapor-phase catalyst which operated at lower temperatures than the molybdenum catalysts formerly used. It also permitted higher thruputs, even with the oils from bituminous coal that were difficult to split. For certain uses, such as the improvement of the antiknock properties or the saving in tungsten, it was strongly diluted. Studies on using up sulfur in the tungsten sulfide catalyst were in progress at this time and showed there was practically no reduction of it under the conditions of hydrogenation under pressure as long as the raw material contained sulfur.

  14. On the pelletizing of sulfide molybdenite concentrate

    International Nuclear Information System (INIS)

    Palant, A.A.


    Investigation results are discussed on the process of pelletizing with the use of various binders (water, syrup, sulfite-alcoholic residue and bentonite) for flotation sulfide molybdenite concentrate (∼84 % MoS 2 ) of the Mongolian deposit. It is established that with the use of syrup rather strong pellets (>300 g/p) of desired size (2-3 mm) can be obtained at a binder flowrate of 1 kg per 100 kg of concentrate. The main advantage of using syrup instead of bentonite lies in the fact that in this instance no depletion of a molybdenum calcine obtained by oxidizing roasting of raw ore takes place due to syrup complete burning out. This affects positively subsequent hydrometallurgical conversion because of decreasing molybdenum losses with waste cakes [ru

  15. Modulated structure calculated for superconducting hydrogen sulfide

    Energy Technology Data Exchange (ETDEWEB)

    Majumdar, Arnab; Tse, John S.; Yao, Yansun [Department of Physics and Engineering Physics, University of Saskatchewan, Saskatoon, SK (Canada)


    Compression of hydrogen sulfide using first principles metadynamics and molecular dynamics calculations revealed a modulated structure with high proton mobility which exhibits a diffraction pattern matching well with experiment. The structure consists of a sublattice of rectangular meandering SH{sup -} chains and molecular-like H{sub 3}S{sup +} stacked alternately in tetragonal and cubic slabs forming a long-period modulation. The novel structure offers a new perspective on the possible origin of the superconductivity at very high temperatures in which the conducting electrons in the SH chains are perturbed by the fluxional motions of the H{sub 3}S resulting in strong electron-phonon coupling. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  16. 48 CFR 39.204 - Exceptions. (United States)


    ... CONTRACTING ACQUISITION OF INFORMATION TECHNOLOGY Electronic and Information Technology 39.204 Exceptions. The... standards to the maximum extent practicable; (b) Is for a national security system; (c) Is acquired by a... 48 Federal Acquisition Regulations System 1 2010-10-01 2010-10-01 false Exceptions. 39.204 Section...

  17. 22 CFR 126.3 - Exceptions. (United States)


    ... 22 Foreign Relations 1 2010-04-01 2010-04-01 false Exceptions. 126.3 Section 126.3 Foreign Relations DEPARTMENT OF STATE INTERNATIONAL TRAFFIC IN ARMS REGULATIONS GENERAL POLICIES AND PROVISIONS... of the United States Government, the Director, Office of Defense Trade Controls may make an exception...

  18. Educating Exceptional Children: Current Issue for Educators (United States)

    Specht, Jacqueline


    The Oxford dictionary defines exceptionality as "forming an exception; very unusual; outstandingly good." A thesaurus provides the following synonyms: outstanding, excellent, brilliant, antonym of ordinary. In education and psychology textbooks and journals, however, it is often defined in ways that focus on limitations, with synonyms…

  19. 24 CFR 51.105 - Exceptions. (United States)


    ... 24 Housing and Urban Development 1 2010-04-01 2010-04-01 false Exceptions. 51.105 Section 51.105... ENVIRONMENTAL CRITERIA AND STANDARDS Noise Abatement and Control § 51.105 Exceptions. (a) Flexibility for non... acceptability standard of 65 decibels, the Acceptable Zone may be shifted to Ldn 70 on a case-by-case basis if...

  20. 7 CFR 4280.104 - Exception authority. (United States)


    ... 7 Agriculture 15 2010-01-01 2010-01-01 false Exception authority. 4280.104 Section 4280.104 Agriculture Regulations of the Department of Agriculture (Continued) RURAL BUSINESS-COOPERATIVE SERVICE AND... Efficiency Improvements Program § 4280.104 Exception authority. The Administrator may, on a case-by-case...

  1. 7 CFR 1779.17 - Exception authority. (United States)


    ... 7 Agriculture 12 2010-01-01 2010-01-01 false Exception authority. 1779.17 Section 1779.17 Agriculture Regulations of the Department of Agriculture (Continued) RURAL UTILITIES SERVICE, DEPARTMENT OF AGRICULTURE (CONTINUED) WATER AND WASTE DISPOSAL PROGRAMS GUARANTEED LOANS § 1779.17 Exception authority. The...

  2. 48 CFR 9.304 - Exceptions. (United States)


    ... 48 Federal Acquisition Regulations System 1 2010-10-01 2010-10-01 false Exceptions. 9.304 Section... CONTRACTOR QUALIFICATIONS First Article Testing and Approval 9.304 Exceptions. Normally, testing and approval is not required in contracts for— (a) Research or development; (b) Products requiring qualification...

  3. 75 FR 8889 - Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting (United States)


    ... Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting AGENCY: Environmental Protection... for hydrogen sulfide (Chemical Abstracts Service Number (CAS No.) 7783-06-4). Hydrogen sulfide was... requirements for hydrogen sulfide in order to evaluate issues brought to the Agency's attention after...

  4. Thermoelectric properties of non-stoichiometric lanthanum sulfides

    International Nuclear Information System (INIS)

    Shapiro, E.; Danielson, L.R.


    The lanthanum sulfides are promising candidate materials for high-efficiency thermoelectric applications at temperatures up to 1300 0 C. The nonstoichiometric lanthanum sulfides (LaS /SUB x/ , where 1.33 2 //rho/ can be chosen. The thermal conductivity remains approximately constant with stoichiometry, so a material with an optimum value of α 2 //rho/ should possess the optimum figure-of-merit. Data for the Seebeck coefficient and electrical resistivity of non-stoichiometric lanthanum sulfides is presented, together with structural properties of these materials

  5. Sulfide Oxidation in the Anoxic Black-Sea Chemocline

    DEFF Research Database (Denmark)



    per day, occurred in anoxic water at the top of the sulfide zone concurrent with the highest rates of dark CO2 assimilation. The main soluble oxidized products of sulfide were thiosulfate (68-82%) and sulfate. Indirect evidence was presented for the formation of elemental sulfur which accumulated...... that the measured H2S oxidation rates were 4-fold higher than could be explained by the downward flux of organic carbon and too high to balance the availability of electron acceptors such as oxidized iron or manganese. A nitrate maximum at the lower boundary of the O2 zone did not extend down to the sulfide zone....

  6. Iron sulfide corrosion in the 700 atm. liquid phase preheater

    Energy Technology Data Exchange (ETDEWEB)

    Donath, E.; Nonnenmacher, H.


    Equilibrium calculations gave lower bounds on partial pressure of hydrogen sulfide within a 500 atm. hydrogen gas stream, below which no corrosion of the steel tube walls would occur. AT 450/sup 0/C the lower bound was 0.5 atm., whereas at 500/sup 0/C the lower bound was 0.8 atm. However, in most plants, the hydrogen sulfide partial pressure exceeded values, so corrosion by formation of iron sulfide did usually occur. It was estimated that the corrosion reaction rate at 500/sup 0/C was about twice what it was at 450/sup 0/C.

  7. Conspicuous veils formed by vibrioid bacteria on sulfidic marine sediment

    DEFF Research Database (Denmark)

    Thar, Roland Matthias; Kühl, Michael


    We describe the morphology and behavior of a hitherto unknown bacterial species that forms conspicuous veils (typical dimensions, 30 by 30 mm) on sulfidic marine sediment. The new bacteria were enriched on complex sulfidic medium within a benthic gradient chamber in oxygen-sulfide countergradients......, but the bacteria have so far not been isolated in pure culture, and a detailed characterization of their metabolism is still lacking. The bacteria are colorless, gram-negative, and vibrioid-shaped (1.3- to 2.5- by 4- to 10-µm) cells that multiply by binary division and contain several spherical inclusions of poly...

  8. Use of sulfide-containing liquors for removing mercury from flue gases (United States)

    Nolan, Paul S.; Downs, William; Bailey, Ralph T.; Vecci, Stanley J.


    A method and apparatus for reducing and removing mercury in industrial gases, such as a flue gas, produced by the combustion of fossil fuels, such as coal, adds sulfide ions to the flue gas as it passes through a scrubber. Ideally, the source of these sulfide ions may include at least one of: sulfidic waste water, kraft caustic liquor, kraft carbonate liquor, potassium sulfide, sodium sulfide, and thioacetamide. The sulfide ion source is introduced into the scrubbing liquor as an aqueous sulfide species. The scrubber may be either a wet or dry scrubber for flue gas desulfurization systems.

  9. Source and Fate of Inorganic Soil Contamination Around the Abandoned Phillips Sulfide Mine Hudson Highlands New York

    Energy Technology Data Exchange (ETDEWEB)

    S Gilchrist; A Gates; E Elzinga; M Gorring; z Szabo


    The abandoned Phillips sulfide mine in the critical Highlands watershed in New York has been shown to produce strongly acidic mine drainage (AMD) with anomalous metal contaminants in first-order streams that exceeded local water standards by up to several orders of magnitude (Gilchrist et al., 2009). The metal-sulfide-rich tailings also produce contaminated soils with pH < 4, organic matter < 2.5% and trace metals sequestered in soil oxides. A geochemical transect to test worst-case soil contamination showed that Cr, Co and Ni correlated positively with Mn, (r = 0.72, r = 0.89, r = 0.80, respectively), suggesting Mn-oxide sequestration and that Cu and Pb correlated with Fe (r = 0.76, r = 0.83, respectively), suggesting sequestration in goethite. Ubiquitous, yellow coating on the mine wastes, including jarosite and goethite, is a carrier of the metals. Geochemical and {mu}-SXRF analyses determined Cu to be the major soil contaminant, {mu}-SXRF also demonstrated that the heterogeneous nature of the soil chemistry at the micro-meter scale is self-similar to those in the bulk soil samples. Generally metals decreased, with some fluctuations, rapidly downslope through suspension of fines and dissolution in AMD leaving the area of substantial contamination << 0.5 km from the source.

  10. Process for removing and detoxifying cadmium from scrap metal including mixed waste

    International Nuclear Information System (INIS)

    Kronberg, J.W.


    Cadmium-bearing scrap from nuclear applications, such as neutron shielding and reactor control and safety rods, must usually be handled as mixed waste since it is radioactive and the cadmium in it is both leachable and highly toxic. Removing the cadmium from this scrap, and converting it to a nonleachable and minimally radioactive form, would greatly simplify disposal or recycling. A process now under development will do this by shredding the scrap; leaching it with reagents which selectively dissolve out the cadmium; reprecipitating the cadmium as its highly insoluble sulfide; then fusing the sulfide into a glassy matrix to bring its leachability below EPA limits before disposal. Alternatively, the cadmium may be recovered for reuse. A particular advantage of the process is that all reagents (except the glass frit) can easily be recovered and reused in a nearly closed cycle, minimizing the risk of radioactive release. The process does not harm common metals such as aluminum, iron and stainless steel, and is also applicable to non-nuclear cadmium-bearing scrap such as nickel-cadmium batteries

  11. Geochemical features of sulfides from the Deyin-1 hydrothermal field at the southern Mid-Atlantic Ridge near 15°S (United States)

    Wang, Shujie; Li, Huaiming; Zhai, Shikui; Yu, Zenghui; Cai, Zongwei


    In this study, geochemical compositions of elements in sulfide samples collected from the Deyin-1 hydrothermal field near the 15°S southern Mid-Atlantic Ridge (SMAR) were analyzed by the X-ray fluorescence spectrometry (XRF) and inductively coupled plasma mass spectrometry (ICP-MS) to examine the enrichment regulations of ore-forming elements and hydrothermal mineralization. These sulfide precipitates can be classified macroscopically into three types: Fe-rich sulfide, Fe-Cu-rich sulfide and Fe-Zn-rich sulfide, and are characterized by the enrichment of base metal elements along with a sequence of Fe>Zn>Cu. Compared with sulfides from other hydrothermal fields on MAR, Zn concentrations of sulfides in the research area are significantly high, while Cu concentrations are relatively low. For all major, trace or rare-earth elements (REE), their concentrations and related characteristic parameters exhibit significant variations (up to one or two orders of magnitude), which indicates the sulfides from different hydrothermal vents or even a same station were formed at different stages of hydrothermal mineralization, and suggests the variations of chemical compositions of the hydrothermal fluid with respect to time. The hydrothermal temperatures of sulfides precipitation decreased gradually from station TVG10 (st.TVG10) to st.TVG12, and to st.TVG11, indicating that the precipitation of hydrothermal sulfides is subjected to conditions changed from high temperature to low temperature, and that the hydrothermal activity of study area was at the late stage of a general trend of evolution from strong to weak. The abnormally low concentrations of REE in sulfides and their similar chondrite-normalized REE patterns show that REEs in all sulfides were derived from a same source, but underwent different processes of migration or enrichment, or sulfides were formed at different stages of hydrothermal mineralization. The sulfides collected from the active hydrothermal vent were

  12. A study on the mechanism of stress corrosion cracking of duplex stainless steels in hot alkaline-sulfide solution (United States)

    Chasse, Kevin Robert

    . Environments having different ionic concentrations of inorganic salts, i.e. sodium hydroxide, sodium sulfide, and sodium chloride, were used to understand the effect of liquor alkalinity, percent sulfidity, and chloride content on the corrosion and SCC behavior. Hydrogen embrittlement of S32205 was studied to understand the electrochemical conditions and fracture features associated with this failure mode. The results showed that there is an appreciable increase in the susceptibility of DSS to SCC in the presence of sulfide and chloride in hot alkaline environments. Sulfide and chloride adsorption at active sites on the metal surface caused unstable passivity and defective film formation. Chloride and sulfide available at the electrolyte/film surface reduced the charge transfer resistance and shifted the response of the films to lower frequencies indicating the films became more defective. The surface films had an outer, discontinuous layer, and an inner, barrier layer. Fe, Mo, and Mn were selectively dissolved in hot alkaline environments. The onset of SCC was related to the extent of selective dissolution and was consistent with a slip-step dissolution mechanism. Selective corrosion of the austenite phase depended on percent sulfidity and liquor alkalinity. Chlorides enhanced crack initiation and coalescence along the austenite/ferrite boundaries. Crack initiation and transgranular growth strongly depended on the phase distribution in the banded microstructure of DSS. These findings will augment understanding of SCC in this alloy-environment combination and facilitate materials selection in hot alkaline-sulfide environments, particularly in the petrochemical, nuclear, chemical processing, and pulp and paper industries.

  13. Magmatic sulfide-rich nickel-copper deposits related to picrite and (or) tholeiitic basalt dike-sill complexes-A preliminary deposit model (United States)

    Schulz, Klaus J.; Chandler, Val W.; Nicholson, Suzanne W.; Piatak, Nadine M.; Seal, Robert R.; Woodruff, Laurel G.; Zientek, Michael L.


    Magmatic sulfide deposits containing nickel (Ni) and copper (Cu), with or without (?) platinum-group elements (PGEs), account for approximately 60 percent of the world's Ni production and are active exploration targets in the United States and elsewhere. On the basis of their principal metal production, magmatic sulfide deposits in mafic rocks can be divided into two major types: those that are sulfide-rich, typically with 10 to 90 percent sulfide minerals, and have economic value primarily because of their Ni and Cu contents; and those that are sulfide-poor, typically with 0.5 to 5 percent sulfide minerals, and are exploited principally for PGE. Because the purpose of this deposit model is to facilitate the assessment for undiscovered, potentially economic magmatic Ni-Cu?PGE sulfide deposits in the United States, it addresses only those deposits of economic significance that are likely to occur in the United States on the basis of known geology. Thus, this model focuses on deposits hosted by small- to medium-sized mafic and (or) ultramafic dikes and sills that are related to picrite and tholeiitic basalt magmatic systems generally emplaced in continental settings as a component of large igneous provinces (LIPs). World-class examples (those containing greater than 1 million tons Ni) of this deposit type include deposits at Noril'sk-Talnakh (Russia), Jinchuan (China), Pechenga (Russia), Voisey's Bay (Canada), and Kabanga (Tanzania). In the United States, this deposit type is represented by the Eagle deposit in northern Michigan, currently under development by Kennecott Minerals.

  14. Synthesis of sub-micron silver and silver sulfide particles via solvothermal silver azide decomposition

    International Nuclear Information System (INIS)

    Grocholl, Luke; Wang Jianjun; Gillan, Edward G.


    Many transition-metal azides are thermodynamically unstable with respect to the elements and thus, may serve as energetic precursor sources in nanoscale metal particle synthesis. This report describes the use of silver azide (AgN 3 ) in nonaqueous, solvothermal decomposition reactions to produce crystalline sub-micron silver particles and interconnected structures. The thermal decomposition of AgN 3 directly produces silver and N 2 and no secondary chemical reducing agent is required. This solvothermal conversion was examined in toluene, tetrahydrofuran (THF), and trioctylamine below 250 deg. C. The coordinating solvents produced the smallest particles (150-500 nm), while the toluene reaction products were near 1 μm in size. The addition of soluble elemental sulfur to the THF reaction results in the growth of silver sulfide particles near 1 μm in size. The silver and Ag 2 S products are crystalline by X-ray diffraction and show some faceting by scanning electron microscopy

  15. Microbial contributions to coupled arsenic and sulfur cycling in the acid-sulfide hot spring Champagne Pool, New Zealand

    Directory of Open Access Journals (Sweden)

    Katrin eHug


    Full Text Available Acid-sulfide hot springs are analogs of early Earth geothermal systems where microbial metal(loid resistance likely first evolved. Arsenic is a metalloid enriched in the acid-sulfide hot spring Champagne Pool (Waiotapu, New Zealand. Arsenic speciation in Champagne Pool follows reaction paths not yet fully understood with respect to biotic contributions and coupling to biogeochemical sulfur cycling. Here we present quantitative arsenic speciation from Champagne Pool, finding arsenite dominant in the pool, rim and outflow channel (55-75% total arsenic, and dithio- and trithioarsenates ubiquitously present as 18-25% total arsenic. In the outflow channel, dimethylmonothioarsenate comprised ≤9% total arsenic, while on the outflow terrace thioarsenates were present at 55% total arsenic. We also quantified sulfide, thiosulfate, sulfate and elemental sulfur, finding sulfide and sulfate as major species in the pool and outflow terrace, respectively. Elemental sulfur reached a maximum at the terrace. Phylogenetic analysis of 16S rRNA genes from metagenomic sequencing revealed the dominance of Sulfurihydrogenibium at all sites and an increased archaeal population at the rim and outflow channel. Several phylotypes were found closely related to known sulfur- and sulfide-oxidizers, as well as sulfur- and sulfate-reducers. Bioinformatic analysis revealed genes underpinning sulfur redox transformations, consistent with sulfur speciation data, and illustrating a microbial role in sulfur-dependent transformation of arsenite to thioarsenate. Metagenomic analysis also revealed genes encoding for arsenate reductase at all sites, reflecting the ubiquity of thioarsenate and a need for microbial arsenate resistance despite anoxic conditions. Absence of the arsenite oxidase gene, aio, at all sites suggests prioritization of arsenite detoxification over coupling to energy conservation. Finally, detection of methyl arsenic in the outflow channel, in conjunction with

  16. Audio magnetotelluric Investigation of Sulfide Mineralization in ...

    Indian Academy of Sciences (India)


    and Research (AMDER) for concealed uranium and rare-earth metals in SSZ. AMDER also carried out several airborne gamma-ray and radiometric surveys for uranium and rare earth metals over possible carbonatite-alkaline rock complexes (Krishnamurthy et al. 2004). Unfortunately, until today only geophysical survey i.e. ...

  17. Explanation for many of the unusual features of the massive sulfide deposits of the Iberian pyrite belt (United States)

    Solomon, M.; Tornos, F.; Gaspar, O. C.


    Newly published fluid-inclusion data from quartz in stockwork veins beneath seven massive sulfide lenses in the Iberian pyrite belt suggest that the lenses were formed from fluids that on reaching the sea reversed buoyancy and ponded in basins. Sulfides quenched in the resulting brine pool would have settled to form a sulfide mud. This process provides a relatively efficient trapping mechanism for metal in the fluids and effectively excludes ambient seawater, accounting for the deposits tending to have the characteristics of large size, sheet-like form, absence of relict chimney structures, and a mineral content characterized by pyrite-arsenopyrite, and absence or scarcity of barite, marcasite, and Fe oxides. If total S was less than total metals in the stockwork fluids, some or all of the more soluble Zn and Pb could have been swept from the basin at the overflow, accounting for the variable but generally low Zn and Pb contents of the ores. The lack of sedimentary source for the high salinities implicates magmatic intrusions, possibly similar to those related to Sn-W mineralization.

  18. Environmental geochemistry of a Kuroko-type massive sulfide deposit at the abandoned Valzinco mine, Virginia, USA (United States)

    Seal, R.R.; Hammarstrom, J.M.; Johnson, A.N.; Piatak, N.M.; Wandless, G.A.


    The abandoned Valzinco mine, which worked a steeply dipping Kuroko-type massive sulfide deposit in the Virginia Au-pyrite belt, contributed significant metal-laden acid-mine drainage to the Knight's Branch watershed. The host rocks were dominated by metamorphosed felsic volcanic rocks, which offered limited acid-neutralizing potential. The ores were dominated by pyrite, sphalerite, galena, and chalcopyrite, which represented significant acid-generating potential. Acid-base accounting and leaching studies of flotation tailings - the dominant mine waste at the site - indicated that they were acid generating and therefore, should have liberated significant quantities of metals to solution. Field studies of mine drainage from the site confirmed that mine drainage and the impacted stream waters had pH values from 1.1 to 6.4 and exceeded aquatic ecosystem toxicity limits for Fe, Al, Cd, Cu, Pb and Zn. Stable isotope studies of water, dissolved SO42 -, and primary and secondary sulfate and sulfide minerals indicated that two distinct sulfide oxidation pathways were operative at the site: one dominated by Fe(III) as the oxidant, and another by molecular O2 as the oxidant. Reaction-path modeling suggested that geochemical interactions between tailings and waters approached a steady state within about a year. Both leaching studies and geochemical reaction-path modeling provided reasonable predictions of the mine-drainage chemistry.

  19. Heavy metals in the spinal cord of normal rats and of animals treated with chelating agents

    DEFF Research Database (Denmark)

    Schrøder, H D; Fjerdingstad, E; Danscher, G


    of various levels along the cranio-caudal axis of the rat spinal cord revealed differences in the heavy metal content. The Timm sulfide silver staining method has demonstrated that metals in the spinal cord have a distinct regional distribution. To obtain a differentiation between the stainable metals...

  20. The effect of waste water treatment on river metal concentrations: removal or enrichment?

    NARCIS (Netherlands)

    Teuchies, J.; Bervoets, L.; Cox, T.J.S.; Meire, P.; de Deckere, E.


    Purpose Discharge of untreated domestic and industrial waste in many European rivers resulted in low oxygen concentrations and contamination with trace metals, often concentrated in sediments. Under these anoxic conditions, the formation of insoluble metal sulfides is known to reduce metal

  1. Instrument for Airborne Measurement of Carbonyl Sulfide, Phase I (United States)

    National Aeronautics and Space Administration — Southwest Sciences proposes to develop small, low power instrumentation for the real-time direct measurement of carbonyl sulfide (OCS) in the atmosphere, especially...

  2. Desulfurizing Difluorination Reaction of Benzyl Sulfides Using IF5


    Fukuhara, Tadahito; Hara, Shoji


    A desulfurizing difluorination reaction of benzyl sulfides having a functional group such as an ester, a ketone, a nitrile, or an amide was performed by a reaction with IF5. Consequently, gem-difluoro compounds could be obtained selectively.

  3. Synthesis of Black and Red Mercury Sulfide Nano-Powder by Traditional Indian Method for Biomedical Application

    International Nuclear Information System (INIS)

    Padhi, Payodhar; Sahoo, G.; Das, K.; Ghosh, Sudipto; Panigrahi, S. C.


    The use of metals and minerals in the traditional Indian system of medicine known as aired is very common and is practiced since seventh century B.C. Metals were reduced to calcined powder form for medicinal purpose. For detoxification, a further step of purification of the metals and minerals with different vegetable extracts was practiced. The people of East India were using mercury and its sulfide as medicine. Gradually this secret was leaked to Arabic physicians who used mercury in skin ointment. Subsequently Italian Physicians adopted Arabic prescriptions of mercurial ointments for skin diseases. In the olden days, metals and minerals were impregnated with decoction and juice of vegetables and animal products like milk and fat for purification. These were then reduced to fine particles by milling with a pestle and mortar. It was known by then that the fineness of the powder had a significant influence on the color, texture, and medicinal properties as is cited by Charak. Nagarjun studied in detail the processing of metals and minerals, particularly mercury and the influence of the processing parameters on the medicinal values. Mercury is unique in many aspects. Indian alchemy developed a wide variety a chemical processes for the ostensible transmutation of metals and preparation of elixir of life, in which mercury occupied a prime position .The present investigation attempts to use the traditional methods as prescribed in the ancient texts to prepare mercury sulfide in both red and black form for medicinal use. XRD, SEM and HRTEM investigations of the sulfides obtained shows that the ancient Indians were able to produce nano-sized powders. Possibly this may be taken as the earliest application of the production and use of nano powder. The study proves that even in ancient time the knowledge of nano particle synthesis was prevalent and used to enhance effectiveness of medicines. Further mercury in the free form is not acceptable in medicines. The ancient

  4. Processing of tenorite and galena with participation of material of steel mill solid to oxide-sulfide nano composites

    International Nuclear Information System (INIS)

    Urakaev, F.; Shevchenko, V.; Tyumentseva, O.; Aknazarov, C.; Ketegenov, T.


    New abrasive mechanic-chemical method was developed and used for reduction work up of tenorite and galena by its joint processing with amorphous quartz material in miller with steel furniture. Products of mechanical activation were investigated by X-ray phase analysis. Results of analysis show the proceeding of following processes: abrasive erase of steel miller solids; amorphization; reduction of copper from tenorite and lead from galena; crystalline phase absence both oxides and sulfides of iron - other products of reducing reactions, for example: CuO + Fe = Cu + FeO. Differences that take place at processing of tenorite and galena were discussed. So, processing of the natural minerals (tenorite, galena) in mixture with abrasive (melted quartz) in miller AGO-2 with steel furniture possesses to obtain nano composite metal-oxide-sulfide powder on the base of quartz matrix

  5. Reactions of Ti, Zr, and Hf atoms with hydrogen sulfide: argon matrix infrared spectra and theoretical calculations. (United States)

    Wang, Qiang; Zhao, Jie; Wang, Xuefeng


    Laser-ablated Ti, Zr, and Hf atoms have been codeposited at 4 K with hydrogen sulfide in excess argon. The metal atoms insert into the S-H bond of hydrogen sulfide to form the HMSH, H2MS, and H2M(SH)2 molecules (M = Ti, Zr, Hf), which were identified on the basis of the D2S and H2(34)S isotopic substitutions. The observed vibrational frequencies of these species were reproduced by B3LYP functional calculations. The reaction mechanisms have been proposed on the potential energy surface of the studied system to account for the formation of these molecules. We have made a theoretical prediction about the H2MS complexes dehydrogenation, which can provide a novel proposal for generating hydrogen from H2S.

  6. Determination of Hydrogen Sulfide in Fermentation Broths Containing SO21 (United States)

    Acree, T. E.; Sonoff, Elisabeth P.; Splittstoesser, D. F.


    A procedure for the determination of hydrogen sulfide in fermentation broths containing up to 100 μg of SO2 per ml is described. The method involves the sparging of H2S from the broth into a cadmium hydroxide absorption solution, the formation of methylene blue from the absorbed sulfide, and the measuring of this color spectrophotometrically. The use of cadmium hydroxide instead of zinc acetate, the common absorbent, substantially reduced the interference of SO2 with the analysis. PMID:5111300


    Directory of Open Access Journals (Sweden)

    Yu. P. Sedlukho


    Full Text Available The paper considers problems and features of biochemical removal of hydrogen sulfide from ground water. The analysis of existing methods for purification of ground water from hydrogen sulfide has been given in the paper. The paper has established shortcomings of physical and chemical purification of ground water. While using aeration methods for removal of hydrogen sulfide formation of colloidal sulfur that gives muddiness and opalescence to water occurs due to partial chemical air oxidation. In addition to this violation of sulfide-carbonate equilibrium taking place in the process of aeration due to desorption of H2S and CO2, often leads to clogging of degasifier nozzles with formed CaCO3 that causes serious operational problems. Chemical methods require relatively large flow of complex reagent facilities, storage facilities and transportation costs.In terms of hydrogen sulfide ground water purification the greatest interest is given to the biochemical method. Factors deterring widespread application of the biochemical method is its insufficient previous investigation and necessity to execute special research in order to determine optimal process parameters while purifying groundwater of a particular water supply source. Biochemical methods for oxidation of sulfur compounds are based on natural biological processes that ensure natural sulfur cycle. S. Vinogradsky has established a two-stage mechanism for oxidation of hydrogen sulfide with sulfur bacteria (Beggiatoa. The first stage presupposes oxidation of hydrogen sulphide to elemental sulfur which is accumulating in the cytoplasm in the form of globules. During the second stage sulfur bacteria begin to oxidize intracellular sulfur to sulfuric acid due to shortage of hydrogen sulfide.The paper provides the results of technological tests of large-scale pilot plants for biochemical purification of groundwater from hydrogen sulfide in semi-industrial conditions. Dependences of water quality

  8. Alternating current electroluminescent properties of zinc sulfide powders


    Salimian, Alireza


    In order to investigate the alternating current electroluminescent properties of zinc sulfide powders the following experiments were conducted: synthesis of zinc sulfide phosphors (comprised of zinc, sulfur and copper dopant); thermal shocking of phosphor materials (sudden cooling, using liquid nitrogen, of phosphor particles heated up to 500oC) and analysis of their alternating current electroluminescent properties as well as studies of particle crystal structures by synchrotron and conventi...

  9. Structural Properties of Zinc Sulfide Polymer Nanocomposite with Alginate


    A.M. Mieshkov; T.O. Berestok; L.F. Sukhodub; А.S. Оpanasyuk


    The comparison of structural and substructural characteristics of pure zinc sulfide and biopolymer based on ZnS composite with alginate was held by scanning electron microscopy, diffraction and X-ray fluorescence spectrometry. Films and nanostructures of zinc sulfide were obtained by chemical bath deposition from an aqueous solution of zinc nitrate, sodium alginate and tiaourea at 90 °C and synthesis time of 30-120 min. It is established that growth occurs through the formation of condensate ...

  10. 33 CFR 183.715 - Exception. (United States)


    ... SAFETY BOATS AND ASSOCIATED EQUIPMENT Start-in-Gear Protection § 183.715 Exception. Outboard motors... information must be displayed on the motor: “Warning—Ensure shift control is in neutral before starting motor...

  11. 7 CFR 1955.21 - Exception authority. (United States)


    ...) PROGRAM REGULATIONS (CONTINUED) PROPERTY MANAGEMENT Liquidation of Loans Secured by Real Estate and Acquisition of Real and Chattel Property § 1955.21 Exception authority. The Administrator may, in individual...

  12. 48 CFR 8.605 - Exceptions. (United States)


    ... REQUIRED SOURCES OF SUPPLIES AND SERVICES Acquisition From Federal Prison Industries, Inc. 8.605 Exceptions... determination that the FPI item of supply is not comparable to supplies available from the private sector that...

  13. From Ethical Exceptionalism to Ethical Exceptions: The Rule and exception Model and the Changing Meaning of Ethics In German Bioregulation. (United States)

    Braun, Kathrin


    Germany is an interesting case with respect to the governance of reprogenetics. It has a strong profile in the technosciences and high aims regarding the global bioeconomy, yet her regulation of human genetics, reproductive medicine and embryo research has for a long time been rather restrictive. German biopolitical exceptionalism has often been explained by reference to Catholicism and the legacy of the Nazi past. The Germans, so goes the common story, have learnt the lessons of history and translated them into unconditional respect for human dignity, which in turn translates into unconditional protection of human life, including the human embryo, and the firm repudiation of any eugenic distinction between 'life worth to live' and 'life not worth to live'. This, however, is not the whole story. Alongside deontological strictness we find another strand of governing body politics and reprogenetics in Germany, the rule-and-exception model, running from the mid-1970s abortion law via the 2002 Stem Cell Act to the 2011 regulation of pre-implantation genetic diagnosis. In contrast to the former, that strongly draws on Kant and his concept of human dignity, the latter bears resemblances to Carl Schmitt's concept of state of exception. The article will show that the rule-and-exception model builds the exception into the rule and transforms the meaning and mandate of ethics, namely from safeguarding ethical standards to deciding about the exception. Given that the exception has now tended to become the rule, the question is whether the lessons of history will govern German reprogenetics for much longer. © 2016 John Wiley & Sons Ltd.

  14. Sulfide oxidation in fluidized bed bioreactor using nylon support material. (United States)

    Midha, Varsha; Jha, M K; Dey, Apurba


    A continuous fluidized bed bioreactor (FBBR) with nylon support particles was used to treat synthetic sulfide wastewater at different hydraulic retention time of 25, 50 and 75 min and upflow velocity of 14, 17 and 20 m/hr. The effects of upflow velocity, hydraulic retention time and reactor operation time on sulfide oxidation rate were studied using statistical model. Mixed culture obtained from the activated sludge, taken from tannery effluent treatment plant, was used as a source for microorganisms. The diameter and density of the nylon particles were 2-3 mm and 1140 kg/m3, respectively. Experiments were carried out in the reactor at a temperature of (30 +/- 2) degrees C, at a fixed bed height of 16 cm after the formation of biofilm on the surface of support particles. Biofilm thickness reached (42 +/- 3) microm after 15 days from reactor start-up. The sulfide oxidation, sulfate and sulfur formation is examined at all hydraulic retention times and upflow velocities. The results indicated that almost 90%-92% sulfide oxidation was achieved at all hydraulic retention times. Statistical model could explain 94% of the variability and analysis of variance showed that upflow velocity and hydraulic retention time slightly affected the sulfide oxidation rate. The highest sulfide oxidation of 92% with 70% sulfur was obtained at hydraulic retention time of 75 min and upflow velocity of 14 m/hr.

  15. Simultaneous removal of sulfide, nitrate and acetate: Kinetic modeling. (United States)

    Wang, Aijie; Liu, Chunshuang; Ren, Nanqi; Han, Hongjun; Lee, Duujong


    Biological removal of sulfide, nitrate and chemical oxygen demand (COD) simultaneously from industrial wastewaters to elementary sulfur (S(0)), N(2), and CO(2), or named the denitrifying sulfide (DSR) process, is a cost effective and environmentally friendly treatment process for high strength sulfide and nitrate laden organic wastewater. Kinetic model for the DSR process was established for the first time on the basis of Activated Sludge Model No. 1 (ASM1). The DSR experiments were conducted at influent sulfide concentrations of 200-800 mg/L, whose results calibrate the model parameters. The model correlates well with the DSR process dynamics. By introducing the switch function and the inhibition function, the competition between autotrophic and heterotrophic denitrifiers is quantitatively described and the degree of inhibition of sulfide on heterotrophic denitrifiers is realized. The model output indicates that the DSR reactor can work well at 0.51000 mg/L influent sulfide, however, the DSR system will break down. Copyright 2010 Elsevier B.V. All rights reserved.

  16. Bioavailability and stability of mercury sulfide in Armuchee (USA) soil

    International Nuclear Information System (INIS)

    Han, Fengxiang; Shiyab, Safwan; Su, Yi; Monts, David L.; Waggoner, Charles A.; Matta, Frank B.


    Because of the adverse effects of elemental mercury and mercury compounds upon human health, the U.S. Department of Energy (DOE) is engaged in an on-going effort to monitor and remediate mercury-contaminated DOE sites. In order to more cost effectively implement those extensive remediation efforts, it is necessary to obtain an improved understanding of the role that mercury and mercury compounds play in the ecosystem. We have conducted pilot scale experiments to study the bioavailability of mercury sulfide in an Armuchee (eastern US ) soil. The effects of plants and incubation time on chemical stability and bioavailability of HgS under simulated conditions of the ecosystem have been examined, as has the dynamics of the dissolution of mercury sulfide by various extractants. The results show that mercury sulfide in contaminated Armuchee soil was still to some extent bioavailable to plants. After planting, soil mercury sulfide is more easily dissolved by both 4 M and 12 M nitric acid than pure mercury sulfide reagent. Dissolution kinetics of soil mercury sulfide and pure chemical reagent by nitric acid are different. Mercury release by EDTA from HgS-contaminated soil increased with time of reaction and soil mercury level. Chelating chemicals increase the solubility and bioavailability of mercury in HgS-contaminated soil. (authors)

  17. Laser cleaning of sulfide scale on compressor impeller blade

    International Nuclear Information System (INIS)

    Tang, Q.H.; Zhou, D.; Wang, Y.L.; Liu, G.F.


    Highlights: • The effects of sulfide layers and fluence values on the mechanism of laser cleaning were experimentally established. • The specimen surface with sulfide scale becomes slightly smoother than that before laser cleaning. • The mechanism of laser cleaning the sulfide scale of stainless steel is spallation without oxidization. • It would avoid chemical waste and dust pollution using a fiber laser instead of using nitric acids or sandblasting. - Abstract: Sulfide scale on the surface of a compressor impeller blade can considerably reduce the impeller performance and its service life. To prepare for subsequent remanufacturing, such as plasma spraying, it needs to be removed completely. In the corrosion process on an FV(520)B stainless steel, sulfide scale is divided into two layers because of different outward diffusion rates of Cr, Ni and Fe. In this paper, the cleaning threshold values of the upper and inner layers and the damage threshold value of the substrate were investigated using a pulsed fiber laser. To obtain experimental evidence, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and 3D surface profilometry were employed to investigate the two kinds of sulfide layers on specimens before, during, and after laser cleaning.

  18. Agamben, Hegel, and the State of Exception

    Directory of Open Access Journals (Sweden)

    Wendell Kisner


    Full Text Available span style="font-size: 10pt; font-family: Arial"In his account of the state of exception, Agamben repeatedly relies upon what Hegel would have called emWesenslogik/em or #39;transcendental thinking#39;. Because of this reliance, the state of exception appears in Agamben#39;s account as the hidden ground of modern liberal democracies. When conceived as such a ground, it appears to be a condition of possibility that inexorably persists in the modern state. Moreover, within the state of exception all juridical order is suspended, leaving no normative or juridical criteria on the basis of which to decide what the structure of any emergent political order should look like. This means that from the state of exception we can just as easily land in a totalitarian as we can in a liberal democratic or democratic socialist state. Without such criteria - lacking due to the total suspension characterizing the state of exception - Agamben#39;s own alignment with Benjaminian revolutionary messianism over Schmittian authoritarianism is arbitrary, and he leaves us with no basis for making any such decision ourselves. Drawing upon Hegel#39;s dialectic of freedom and his critique of transcendental thought, this paper argues that within the state of exception there is an implicit logic that points the way out of it. Furthermore, it does so in such a way that the state of exception is neither annexed by the structure of a predetermined juridical order along the lines proposed by Schmitt on the one hand nor posited it as a transcendental structure underlying or always preceding modern liberal democracies on the other. This alternative is overlooked by Agamben precisely because of his own insistence upon conceiving of the state of exception in a transcendent way./span

  19. 39 CFR 7.3 - Exceptions. (United States)


    ... 39 Postal Service 1 2010-07-01 2010-07-01 false Exceptions. 7.3 Section 7.3 Postal Service UNITED STATES POSTAL SERVICE THE BOARD OF GOVERNORS OF THE U.S. POSTAL SERVICE PUBLIC OBSERVATION (ARTICLE VII) § 7.3 Exceptions. Section 7.2 of these bylaws does not apply to a portion of a meeting, and §§ 7.4 and...

  20. Cognitive function in families with exceptional survival

    DEFF Research Database (Denmark)

    Barral, Sandra; Cosentino, Stephanie; Costa, Rosann


    The authors investigated whether cognitive function may be used as an endophenotype for longevity by assessing the cognitive performance of a family-based cohort consisting of 1380 individuals from 283 families recruited for exceptional survival in field centers in Boston, New York, Pittsburgh...... members in the offspring generation demonstrate significantly better performance on multiple tasks requiring attention, working memory, and semantic processing when compared with individuals without a family history of exceptional survival, suggesting that cognitive performance may serve as an important...

  1. Understanding Cu release into environment from Kure massive sulfide ore deposits, Kastamonu, NW Turkey (United States)

    Demirel, Cansu; Sonmez, Seref; Balci, Nurgul


    Covering a wide range on the earth's crust, oxidation of metal sulfide minerals have vital environmental impacts on the aquatic environment, causing one of the major environmental problems known as acid mine drainage (AMD). Located in the Kastamonu province of the Western Black Sea region, Kure district is one of the major copper mining sites in Turkey. Mining activities in the area heads back to ancient times, such that operation is thought to be started with the Roman Empire. Currently, only the underground mining tunnels of Bakibaba and Asikoy are being operated. Thus, mining heaps and ores of those pyritic deposits have been exposed to the oxidative conditions for so long. As a result of weathering processes of past and recent heaps of the Kure volcanic massive sulfide deposits in addition to the main ore mineral (chalcopyrite), significant amount of metals, especially Cu, are being released into the environment creating undesirable environmental conditions. In order to elucidate Cu release mechanisms from Kure pyritic ore deposits and mining wastes, field and laboratory approaches were used. Surface water and sediment samples from the streams around the mining and waste sites were collected. Groundwater samples from the active underground mining site were also collected. Physical parameters (pH, Eh, T°C, and EC) of water samples were determined in situ and in the laboratory using probes (WTW pH 3110, WTW Multi 9310 and CRISON CM 35). Metal and ion concentrations of the water samples were analysed using ICP-MS and DR 2800 spectrophotometer, respectively. High Cu, Co, Zn and Fe concentrations were determined in the water samples with pH values ranging from 2.9- 4. Cu concentrions ranges from 345 ppm to 36 ppm in the water samples. Consistent with the water samples, high Cu, Fe, Zn and Co were also determined in the sediment samples. Laboratory chalcopyrite oxidation experiments under the conditions representing the field site were set up as biological and

  2. Influence of small additions of manganese, bismuth and zirconium on the reversible equilibrium US2-α - US2-β and on the electrical conductivity of these two sulfides between 900 and 10000C

    International Nuclear Information System (INIS)

    Rasneur, J.; Carton, D.; Dherbomez, N.


    The addition of manganese or bismuth ( 2 -α contrary to that of US 2 -β whereas the addition of zirconium is ineffectual. The electrical conductivity of the two sulfides is weakly modified except with the addition of bismuth increasing its values [fr

  3. Bio-orthogonal "click-and-release" donation of caged carbonyl sulfide (COS) and hydrogen sulfide (H2S). (United States)

    Steiger, Andrea K; Yang, Yang; Royzen, Maksim; Pluth, Michael D


    Hydrogen sulfide (H 2 S) is an important biomolecule with high therapeutic potential. Here we leverage the inverse-electron demand Diels-Alder (IEDDA) click reaction between a thiocarbamate-functionalized trans-cyclooctene and a tetrazine to deliver carbonyl sulfide (COS), which is quickly converted to H 2 S by the uniquitous enzyme carbonic anhydrase (CA), thus providing a new strategy for bio-orthogonal COS/H 2 S donation.

  4. Subnanometer Thin β-Indium Sulfide Nanosheets. (United States)

    Acharya, Shinjita; Sarkar, Suresh; Pradhan, Narayan


    Nanosheets are a peculiar kind of nanomaterials that are grown two-dimensionally over a micrometer in length and a few nanometers in thickness. Wide varieties of inorganic semiconductor nanosheets are already reported, but controlling the crystal growth and tuning their thickness within few atomic layers have not been yet explored. We investigate here the parameters that determine the thickness and the formation mechanism of subnanometer thin (two atomic layers) cubic indium sulfide (In2S3) nanosheets. Using appropriate reaction condition, the growth kinetics is monitored by controlling the decomposition rate of the single source precursor of In2S3 as a function of nucleation temperature. The variation in the thickness of the nanosheets along the polar [111] direction has been correlated with the rate of evolved H2S gas, which in turn depends on the rate of the precursor decomposition. In addition, it has been observed that the thickness of the In2S3 nanosheets is related to the nucleation temperature.

  5. Positive trends in Southern Hemisphere carbonyl sulfide (United States)

    Kremser, Stefanie; Jones, Nicholas B.; Palm, Mathias; Lejeune, Bernard; Wang, Yuting; Smale, Dan; Deutscher, Nicholas M.


    Transport of carbonyl sulfide (OCS) from the troposphere to the stratosphere contributes sulfur to the stratospheric aerosol layer, which reflects incoming short-wave solar radiation, cooling the climate system. Previous analyses of OCS observations have shown no significant trend, suggesting that OCS is unlikely to be a major contributor to the reported increases in stratospheric aerosol loading and indicating a balanced OCS budget. Here we present analyses of ground-based Fourier transform spectrometer measurements of OCS at three Southern Hemisphere sites spanning 34.45°S to 77.80°S. At all three sites statistically significant positive trends are seen from 2001 to 2014 with an observed overall trend in total column OCS at Wollongong of 0.73 ± 0.03%/yr, at Lauder of 0.43 ± 0.02%/yr, and at Arrival Heights of 0.45 ± 0.05%/yr. These observed trends in OCS imply that the OCS budget is not balanced and could contribute to constraints on current estimates of sources and sinks.

  6. Thiosulfate leaching of gold from sulfide wastes

    Energy Technology Data Exchange (ETDEWEB)

    Block-Bolten, A.; Torma, A.E.


    The kinetics of gold extraction from lead-zinc sulfide flotation tailings by thiosulfate leachants has been investigated. The order of reaction as well as the overall reaction rate constant were, with respect to thiosulfate concentration, calculated to be n=0.75 and k=1.05 x 10/sup -6/ mol/sup 1/4/ dm/sup 5/4/ min/sup -1/. The apparent activation energy was found to be a/=48.53 kJ and the frequency factor A=7.5 x 10/sup 2/ mol dm/sup -3/ min/sup -1/. This activation energy value suggests chemical control of the reaction mechanism. Optimum leach temperature of 50/sup 0/C was established. Gold extractions as high as 99% have been realized in two step countercurrent leachings. Change in pH throughout the leaching process was found to be an excellent indicator for the progress of the extraction. A preliminary economic evaluation of the process is given.

  7. Fluorescence sensing system for seafloor massive sulfides (United States)

    Yamazaki, T.; Okanishi, D.; Nagano, H.; Nakatani, N.; Arai, R.


    Seafloor Massive Sulfides (SMS) including Au, Ag, Cu, Zn, Pb and some rare earth elements exist in exclusive economic zones (EEZ) of Pacific island countries and the ones in Japan’s EEZ are the largest and very much attractive. However, there are many problems to be solved for the development. The most important point is the location of ore dressing. If SMS were dressed in the water, energy and cost of transport would drastically decrease. Therefore, fundamental ore dressing method which is an optical measurement, fluorescence sensing system in water is studied. It seems to be able to apply to exploration and mining. No sun light means that ideal optical measurements are possible under artificial one in deep water. However, quite less studies have been done for the optical measurements because general sensing methods at deep water are sound and supersonic waves. Using a light system, the light attenuation and fluorescence characteristics in water are studied. From this study, it is revealed that fluorescence sensing system is applicable and useful for the development of SMS.

  8. The role of hydrogen sulfide in stroke

    Directory of Open Access Journals (Sweden)

    Yang Dou


    Full Text Available Stroke is a kind of acute cerebrovascular disease characterized by the focal lack of neurological function, including ischemic stroke and hemorrhagic stroke. As society ages rapidly, stroke has become the second leading cause of disability and death, and also become the main threat to human health and life. In recent years, findings from increasing animal and clinical trials have supplied scientific evidences for the treatment of stroke. Hydrogen sulfide (H 2 S, which has always been seen as a toxic gas, now has been thought to be the third gaseous signaling molecule following nitric oxide and carbon monoxide. Accumulating evidences indicate that H 2 S plays an important role in stroke. Given that its neuroprotective effect is dose-dependent, only when its concentration is relatively low, H 2 S can yield the neuroprotection, while high dose may lead to neurotoxicity. All these study results suggest that H 2 S may offer a new promising application for the therapy of stroke. Here, our review will present the role of H 2 S in stroke from its mechanism to animal and clinical studies.

  9. Hydrogen Sulfide and Endothelium-Dependent Vasorelaxation

    Directory of Open Access Journals (Sweden)

    Jerzy Bełtowski


    Full Text Available In addition to nitric oxide and carbon monoxide, hydrogen sulfide (H2S, synthesized enzymatically from l-cysteine or l-homocysteine, is the third gasotransmitter in mammals. Endogenous H2S is involved in the regulation of many physiological processes, including vascular tone. Although initially it was suggested that in the vascular wall H2S is synthesized only by smooth muscle cells and relaxes them by activating ATP-sensitive potassium channels, more recent studies indicate that H2S is synthesized in endothelial cells as well. Endothelial H2S production is stimulated by many factors, including acetylcholine, shear stress, adipose tissue hormone leptin, estrogens and plant flavonoids. In some vascular preparations H2S plays a role of endothelium-derived hyperpolarizing factor by activating small and intermediate-conductance calcium-activated potassium channels. Endothelial H2S signaling is up-regulated in some pathologies, such as obesity and cerebral ischemia-reperfusion. In addition, H2S activates endothelial NO synthase and inhibits cGMP degradation by phosphodiesterase 5 thus potentiating the effect of NO-cGMP pathway. Moreover, H2S-derived polysulfides directly activate protein kinase G. Finally, H2S interacts with NO to form nitroxyl (HNO—a potent vasorelaxant. H2S appears to play an important and multidimensional role in endothelium-dependent vasorelaxation.

  10. Luminescent sulfides of monovalent and trivalent cations

    International Nuclear Information System (INIS)


    The invention discloses a family of luminescent materials or phosphors having a rhombohedral crystal structure and consisting essentially of a mixed host sulfide of at least one monovalent host cation and at least one trivalent host cation, and containing, for each mole of phosphor, 0.0005 to 0.05 mole of at least one activating cation. The monovalent host cations may be Na, K or Rb and Cs. The trivalent host cations may be Gd, La, Lu, Sc and Y. The activating cations may be one or more of trivalent As, Bi, Ce, Dy, Er, Pr, Sb, Sm, Tb and Tm; divalent Lu, Mn, Pb and Sn; and monovalent Ag, Cu and Tl. The novel phosphors may be used in devices to convert electron-beam, ultraviolet or x-ray energy to light in the visible spectrum. Such energy conversion can be employed for example in fluoroscopic screens, and in viewing screens of cathode-ray tubes and other electron tubes

  11. Hassle free synthesis of nanodimensional Ni, Cu and Zn sulfides for spectral sensing of Hg, Cd and Pb: A comparative study. (United States)

    Ansari, Zarina; Singha, Shib Shankar; Saha, Abhijit; Sen, Kamalika


    A simple room temperature synthesis method of Ni, Cu and Zn sulfide nanoparticles (NPs) in aqueous medium is reported here. The NPs stabilized in aqueous medium by the citrate ions were characterized by UV-vis, ζ potentials, TEM and Raman spectroscopic techniques. The solid NPs could be isolated from the aqueous medium when allowed to stand for a prolonged time (~20h). The solids were also characterized by IR and powder X-ray analysis. The nanoparticles were further used for the development of facile optical sensing and detection of heavy metal ions at trace scale. Alterations in the absorption spectra of the generated NPs were indicative of their interactions with heavy metal ions. Raman spectral measurements further validate the detection technique. It is found that out of the three synthesized nanoparticles, nickel sulfide NP is a specific sensor for mercury ions whereas zinc sulfide and copper sulfide NPs act as sensors for Hg 2+ , Cd 2+ and Pb 2+ . Copyright © 2017 Elsevier B.V. All rights reserved.

  12. Comparison of Carbon XANES Spectra from an Iron Sulfide from Comet Wild 2 with an Iron Sulfide Interplanetary Dust Particle (United States)

    Wirick, S.; Flynn, G. J.; Keller, L. P.; Sanford, S. A.; Zolensky, M. E.; Messenger, Nakamura K.; Jacobsen, C.


    Among one of the first particles removed from the aerogel collector from the Stardust sample return mission was an approx. 5 micron sized iron sulfide. The majority of the spectra from 5 different sections of this particle suggests the presence of aliphatic compounds. Due to the heat of capture in the aerogel we initially assumed these aliphatic compounds were not cometary but after comparing these results to a heated iron sulfide interplanetary dust particle (IDP) we believe our initial interpretation of these spectra was not correct. It has been suggested that ice coating on iron sulfides leads to aqueous alteration in IDP clusters which can then lead to the formation of complex organic compounds from unprocessed organics in the IDPs similar to unprocessed organics found in comets [1]. Iron sulfides have been demonstrated to not only transform halogenated aliphatic hydrocarbons but also enhance the bonding of rubber to steel [2,3]. Bromfield and Coville (1997) demonstrated using Xray photoelectron spectroscopy that "the surface enhancement of segregated sulfur to the surface of sulfided precipitated iron catalysts facilitates the formation of a low-dimensional structure of extraordinary properties" [4]. It may be that the iron sulfide acts in some way to protect aliphatic compounds from alteration due to heat.

  13. Method of winning aluminum metal from aluminous ore (United States)

    Loutfy, R.O.; Keller, R.; Yao, N.P.

    Aluminous ore such as bauxite containing alumina is blended with coke or other suitable form of carbon and reacted with sulfur gas at an elevated temperature. For handling, the ore and coke can be extruded into conveniently sized pellets. The reaction with sulfur gas produces molten aluminum sulfide which is separated from residual solid reactants and impurities. The aluminum sulfide is further increased in temperature to cause its decomposition or sublimation, yielding aluminum subsulfide liquid (A1S) and sulfur gas that is recycled. The aluminum monosulfide is then cooled to below its disproportionation temperature to again form molten aluminum sulfide and aluminum metal. A liquid-liquid or liquid-solid separation, depending on the separation temperature, provides product aluminum and aluminum sulfide for recycle to the disproportionation step.

  14. Process to separate alkali metal salts from alkali metal reacted hydrocarbons (United States)

    Gordon, John Howard; Alvare, Javier; Larsen, Dennis; Killpack, Jeff


    A process to facilitate gravimetric separation of alkali metal salts, such as alkali metal sulfides and polysulfides, from alkali metal reacted hydrocarbons. The disclosed process is part of a method of upgrading a hydrocarbon feedstock by removing heteroatoms and/or one or more heavy metals from the hydrocarbon feedstock composition. This method reacts the oil feedstock with an alkali metal and an upgradant hydrocarbon. The alkali metal reacts with a portion of the heteroatoms and/or one or more heavy metals to form an inorganic phase containing alkali metal salts and reduced heavy metals, and an upgraded hydrocarbon feedstock. The inorganic phase may be gravimetrically separated from the upgraded hydrocarbon feedstock after mixing at a temperature between about C. to C. for a time period between about 15 minutes and 2 hours.

  15. Can the hemoglobin characteristics of vesicomyid clam species influence their distribution in deep-sea sulfide-rich sediments? A case study in the Angola Basin (United States)

    Decker, C.; Zorn, N.; Le Bruchec, J.; Caprais, J. C.; Potier, N.; Leize-Wagner, E.; Lallier, F. H.; Olu, K.; Andersen, A. C.


    Vesicomyids live in endosymbiosis with sulfur-oxidizing bacteria and therefore need hydrogen sulfide to survive. They can nevertheless live in a wide range of sulfide and oxygen levels and depths, which may explain the exceptional diversity of this clam family in deep-sea habitats. In the Gulf of Guinea, nine species of vesicomyid clams are known to live in cold-seep areas with pockmarks from 600 to 3200 m deep, as well as in the organic-rich sediments of the Congo deep-sea fan at 5000 m deep. Our previous study showed that two species living in a giant pockmark have different oxygen carriers, suggesting different adaptations to hypoxia. Here, we studied the hemoglobin structure and oxygen affinity in three other species, Calyptogena valdiviae, Elenaconcha guiness and Abyssogena southwardae to determine whether the characteristics of their oxygen carriers contribute to their distribution in sulfide-rich sediments at a regional scale. Documenting pairwise species associations in various proportions, we give a semi-quantitative account of their local distribution and oxygen and sulfide measurements at seven sites. Mass spectrometry showed that each vesicomyid species has four intracellular monomeric hemoglobin molecules of 15-16 kDa, all differing in their molecular mass. As expected, the monomers showed no cooperativity in oxygen binding. Their oxygen affinities were very high (below 1 Torr), but differed significantly. C. valdiviae had the highest affinity and was dominant in the Harp pockmark, the site with the lowest oxygen content (half the value of fully oxygenated water). A. southwardae dominated in the Congo Lobe area, the site with the deepest sulfides. We discuss how hemoglobin may favor an active, vertical distribution of vesicomyids in sulfide-rich sediments.

  16. Mineralogy, geochemistry, and Sr-Pb isotopic geochemistry of hydrothermal massive sulfides from the 15.2°S hydrothermal field, Mid-Atlantic Ridge (United States)

    Wang, Hao; Li, Xiaohu; Chu, Fengyou; Li, Zhenggang; Wang, Jianqiang; Yu, Xing; Bi, Dongwei


    The 15.2°S hydrothermal field is located at 15.2°S, 13.4°W within the Mid-Atlantic Ridge (MAR) and was initially discovered during Cruise DY125-22 by the Chinese expedition during R/V Dayangyihao in 2011. Here, we provide detailed mineralogical, bulk geochemical, and Sr-Pb isotopic data for massive sulfides and basalts from the 15.2°S hydrothermal field to improve our understanding of the mineral compositions, geochemical characteristics, type of hydrothermal field, and the source of metals present at this vent site. The samples include 14 massive sulfides and a single basalt. The massive sulfides are dominated by pyrite with minor amounts of sphalerite and chalcopyrite, although a few samples also contain minor amounts of gordaite, a sulfate mineral. The sulfides have bulk compositions that contain low concentrations of Cu + Zn (mean 7.84 wt%), Co (mean 183 ppm), Ni (mean 3 ppm), and Ba (mean 16 ppm), similar to the Normal Mid-Ocean Ridge Basalt (N-MORB) type deposits along the MAR but different to the compositions of the Enriched-MORB (E-MORB) and ultramafic type deposits along this spreading ridge. Sulfides from the study area have Pb isotopic compositions (206Pb/204Pb = 18.4502-18.4538, 207Pb/204Pb = 15.4903-15.4936, 208Pb/204Pb = 37.8936-37.9176) that are similar to those of the basalt sample (206Pb/204Pb = 18.3381, 207Pb/204Pb = 15.5041, 208Pb/204Pb = 37.9411), indicating that the metals within the sulfides were derived from leaching of the surrounding basaltic rocks. The sulfides also have 87Sr/86Sr ratios (0.708200-0.709049) that are much higher than typical MAR hydrothermal fluids (0.7028-0.7046), suggesting that the hydrothermal fluids mixed with a significant amount of seawater during massive sulfide precipitation.

  17. Atmospheric measurements of carbonyl sulfide, dimethyl sulfide, and carbon disulfide using the electron capture sulfur detector (United States)

    Johnson, James E.; Bates, Timothy S.


    Measurements of atmospheric dimethyl sulfide (DMS), carbonyl sulfide (COS), and carbon disulfide (CS2) were conducted over the Atlantic Ocean on board the NASA Electra aircraft during the Chemical Instrumentation Test and Evaluation (CITE 3) project using the electron capture sulfur detector (ECD-S). The system employed cryogenic preconcentration of air samples, gas chromatographic separation, catalytic fluorination, and electron capture detection. Samples collected for DMS analysis were scrubbed of oxidants with NaOH impregnated glass fiber filters to preconcentration. The detection limits (DL) of the system for COS, DMS, and CS2 were 5, 5, and 2 ppt, respectively. COS concentrations ranged from 404 to 603 ppt with a mean of 489 ppt for measurements over the North Atlantic Ocean (31 deg N to 41 deg N), and from 395 to 437 ppt with a mean of 419 ppt for measurements over the Tropical Atlantic Ocean (11 deg S to 2 deg N). DMS concentrations in the lower marine boundary layer, below 600-m altitude, ranged from below DL to 150 ppt from flights over the North Atlantic, and from 9 to 104 ppt over the Tropical Atlantic. CS2 concentrations ranged from below DL to 29 ppt over the North Atlantic. Almost all CS2 measurements over the Tropical Atlantic were below DL.

  18. Silver sulfide nanoparticle assembly obtained by reacting an assembled silver nanoparticle template with hydrogen sulfide gas. (United States)

    Chen, Rui; Nuhfer, Noel T; Moussa, Laura; Morris, Hannah R; Whitmore, Paul M


    A fast, simple procedure is described for obtaining an assembly of silver sulfide nanoparticles (Ag(2)S NPs) on a glass substrate through reaction of a template of an assembled layer of silver nanoparticles (Ag NPs) with hydrogen sulfide (H(2)S) gas. The Ag NP template was prepared by assembling a monolayer of spherical Ag NPs (mean diameter of 7.4 nm) on a polyethylenimine-treated glass substrate. Exposure to pure H(2)S for 10 min converted the Ag NPs of the template to Ag(2)S NPs. The resulting Ag(2)S NP assembly, which retains the template nanostructure and particle distribution, was characterized by optical absorption spectroscopy, atomic force microscopy, transmission electron microscopy (TEM), scanning high resolution TEM, energy dispersive x-ray spectroscopy and x-ray photoelectron spectroscopy. The Ag(2)S NPs have a crystal structure of monoclinic acanthite, and while they retained the spherical shape of the original Ag NPs, their mean particle size increased to 8.4 nm due to changes to the crystal structure when the Ag NPs are converted into Ag(2)S NPs. The measured optical absorption edge of the Ag(2)S NP assembly indicated an indirect interband transition with a band gap energy of 1.71 eV. The Ag(2)S NP assembly absorbed light with wavelengths below 725 nm, and the absorbance increased monotonically toward the UV region.

  19. Hydrogen sulfide can inhibit and enhance oxygenic photosynthesis in a cyanobacterium from sulfidic springs. (United States)

    Klatt, Judith M; Haas, Sebastian; Yilmaz, Pelin; de Beer, Dirk; Polerecky, Lubos


    We used microsensors to investigate the combinatory effect of hydrogen sulfide (H2 S) and light on oxygenic photosynthesis in biofilms formed by a cyanobacterium from sulfidic springs. We found that photosynthesis was both positively and negatively affected by H2 S: (i) H2 S accelerated the recovery of photosynthesis after prolonged exposure to darkness and anoxia. We suggest that this is possibly due to regulatory effects of H2 S on photosystem I components and/or on the Calvin cycle. (ii) H2 S concentrations of up to 210 μM temporarily enhanced the photosynthetic rates at low irradiance. Modelling showed that this enhancement is plausibly based on changes in the light-harvesting efficiency. (iii) Above a certain light-dependent concentration threshold H2 S also acted as an inhibitor. Intriguingly, this inhibition was not instant but occurred only after a specific time interval that decreased with increasing light intensity. That photosynthesis is most sensitive to inhibition at high light intensities suggests that H2 S inactivates an intermediate of the oxygen evolving complex that accumulates with increasing light intensity. We discuss the implications of these three effects of H2 S in the context of cyanobacterial photosynthesis under conditions with diurnally fluctuating light and H2 S concentrations, such as those occurring in microbial mats and biofilms. © 2015 Society for Applied Microbiology and John Wiley & Sons Ltd.

  20. Chemical and colloidal aspects of collectorless flotation behavior of sulfide and non-sulfide minerals. (United States)

    Aghazadeh, Sajjad; Mousavinezhad, Seyed Kamal; Gharabaghi, Mahdi


    Flotation has been widely used for separation of valuable minerals from gangues based on their surface characterizations and differences in hydrophobicity on mineral surfaces. As hydrophobicity of minerals widely differs from each other, their separation by flotation will become easier. Collectors are chemical materials which are supposed to make selectively valuable minerals hydrophobic. In addition, there are some minerals which based on their surface and structural features are intrinsically hydrophobic. However, their hydrophobicities are not strong enough to be floatable in the flotation cell without collectors such as sulfide minerals, coal, stibnite, and so forth. To float these minerals in a flotation cell, their hydrophobicity should be increased in specific conditions. Various parameters including pH, Eh, size distribution, mill types, mineral types, ore characterization, and type of reaction in flotation cells affect the hydrophobicity of minerals. Surface analysis results show that when sulfide minerals experience specific flotation conditions, the reactions on the surface of these minerals increase the amount of sulfur on the surface. These phenomenons improve the hydrophobicity of these minerals due to strong hydrophobic feature of sulfurs. Collectorless flotation reduces chemical material consumption amount, increases flotation selectivity (grade increases), and affects the equipment quantities; however, it can also have negative effects. Some minerals with poor surface floatability can be increased by adding some ions to the flotation system. Depressing undesirable minerals in flotation is another application of collectorless flotation.

  1. Post-exceptionalism in public policy

    DEFF Research Database (Denmark)

    Daugbjerg, Carsten; Feindt, Peter H.


    Framing the special issue on the transformation of Food and Agricultural Policy, this article introduces the concept of post-exceptionalism in public policies. The analysis of change in agri-food policy serves as a generative example to conceptualize current transformations in sectoral policy...... arrangements in democratic welfare states. Often these arrangements have been characterized by an exceptionalist ideational framework that legitimizes a sector’s special treatment through compartmentalized, exclusive and producer-centered policies and politics. In times of internationalization of policy......-making, increasing interlinkage of policy areas and trends towards self-regulation, liberalization and performance-based policies, policy exceptionalism is under pressure to either transform or give way to (neo-)liberal policy arrangements. Post-exceptionalism denotes a partial transformation of exceptionalist ideas...

  2. Amendments to excepted benefits. Final rules. (United States)


    This document contains final regulations that amend the regulations regarding excepted benefits under the Employee Retirement Income Security Act of 1974, the Internal Revenue Code (the Code), and the Public Health Service Act. Excepted benefits are generally exempt from the health reform requirements that were added to those laws by the Health Insurance Portability and Accountability Act and the Patient Protection and Affordable Care Act. In addition, eligibility for excepted benefits does not preclude an individual from eligibility for a premium tax credit under section 36B of the Code if an individual chooses to enroll in coverage under a Qualified Health Plan through an Affordable Insurance Exchange. These regulations finalize some but not all of the proposed rules with minor modifications; additional guidance on limited wraparound coverage is forthcoming.

  3. Inhibition and Promotion of Pyrolysis by Hydrogen Sulfide (H2S) and Sulfanyl Radical (SH)

    DEFF Research Database (Denmark)

    Zeng, Zhe; Altarawneh, Mohammednoor; Oluwoye, Ibukun


    the weakest C–H sites in alkenes and alkynes, except for ethylene, appears noticeably exothermic. Furthermore, abstraction of H from propene, 1-butene, and iso-butene displays pronounced spontaneity (i.e., ΔrG° hydrogen bond. However......, an alkyl radical readily abstracts H atom from H2S, with H2S acting as a potent scavenger for alkyl radicals in combustion processes. That is, these reactions proceed in the opposite direction than those involving SH and alkene or alkyne species, exhibiting shallow barriers and strong spontaneity. Our...... findings demonstrate that the documented inhibition effect of hydrogen sulfide (H2S) on pyrolysis of alkanes does not apply to alkenes and alkynes. During interaction with hydrocarbons, the inhibitive effect of H2S and promoting interaction of SH radical depend on the reversibility of the H abstraction...

  4. The Potential Application of Raw Cadmium Sulfide Nanoparticles as CT Photographic Developer (United States)

    Wu, Qiang; Huang, Lingxin; Li, Zhan; An, Wenzhen; Liu, Dan; Lin, Jin; Tian, Longlong; Wang, Xinling; Liu, Bo; Qi, Wei; Wu, Wangsuo


    With the development of science and technology, new applications about nanoparticles should be explored to achieve full-scale knowledge. Therefore, in this work, the toxicity and potential application of raw cadmium sulfide nanoparticles (CdS) in vivo were further studied through ICP-OES and CTs. Surprisingly, CdS exhibited an excellent photographic property, except for finding the accumulation of CdS in the lungs, liver, spleen, and kidney with a strong dependence on time; it is also found that there were a significant uptake in the pancreas for an obvious CT imaging. And the following investigations showed that the raw CdS could damage the tissues accumulating nanoparticles. Through this work, it can be seen that the raw CdS being modified might be an excellent photographic developer for detecting cancers or other diseases.

  5. Chemical speciation of sulfur and metals in biogas reactors - Implications for cobalt and nickel bio-uptake processes. (United States)

    Yekta, Sepehr Shakeri; Skyllberg, Ulf; Danielsson, Åsa; Björn, Annika; Svensson, Bo H


    This article deals with the interrelationship between overall chemical speciation of S, Fe, Co, and Ni in relation to metals bio-uptake processes in continuous stirred tank biogas reactors (CSTBR). To address this topic, laboratory CSTBRs digesting sulfur(S)-rich stillage, as well as full-scale CSTBRs treating sewage sludge and various combinations of organic wastes, termed co-digestion, were targeted. Sulfur speciation was evaluated using acid volatile sulfide extraction and X-ray absorption spectroscopy. Metal speciation was evaluated by chemical fractionation, kinetic and thermodynamic analyses. Relative Fe to S content is identified as a critical factor for chemical speciation and bio-uptake of metals. In reactors treating sewage sludge, quantity of Fe exceeds that of S, inducing Fe-dominated conditions, while sulfide dominates in laboratory and co-digestion reactors due to an excess of S over Fe. Under sulfide-dominated conditions, metals availability for microorganisms is restricted due to formation of metal-sulfide precipitates. However, aqueous concentrations of different Co and Ni species were shown to be sufficient to support metal acquisition by microorganisms under sulfidic conditions. Concentrations of free metal ions and labile metal complexes in aqueous phase, which directly participate in bio-uptake processes, are higher under Fe-dominated conditions. This in turn enhances metal adsorption on cell surfaces and bio-uptake rates. Copyright © 2015 Elsevier B.V. All rights reserved.

  6. Session-based Choreography with Exceptions

    DEFF Research Database (Denmark)

    Carbone, Marco


    Choreography has recently emerged as a pragmatic and concise way of describing communication-based systems such as web services and financial protocols. Recent studies have investigated the transition from the design stage of a system to its implementation providing an automatic way of mapping...... a choreograhy into executable code. In this work, we focus on an extension of choreography with a communication-based (interactional) exception mechanism by giving its formal semantics. In particular, we discuss through some examples how interactional exceptions at choreography level can be implemented into end...

  7. Exception Handling in a Replicated Agent Environment


    Azmeh, Zeina; Dony, Christophe; Tibermacine, Chouki; Urtado, Christelle; Vauttier, Sylvain


    This document is the semestrial report of the Lirmm partner for the Facoma project. It concludes semester 2 - out of 6 - for the project. During this semester, partners from Lirmm and Lgi2p have worked on: i) defining an exception handling system for agents. This work is based on previous work that has been done by these partners on the Sage exception handling system that was adapted to the context of the Facoma pro ject; ii) refining their knowledge and understanding of the Dimax replicated ...

  8. A geometric formulation of exceptional field theory

    Energy Technology Data Exchange (ETDEWEB)

    Bosque, Pascal du [Arnold Sommerfeld Center for Theoretical Physics,Department für Physik, Ludwig-Maximilians-Universität München,Theresienstraße 37, 80333 München (Germany); Max-Planck-Institut für Physik, Werner-Heisenberg-Institut, Föhringer Ring 6, 80805 München (Germany); Hassler, Falk [Department of Physics and Astronomy, University of North Carolina, Phillips Hall, CB #3255, 120 E. Cameron Ave., Chapel Hill, NC 27599-3255 (United States); City University of New York, The Graduate Center, 365 Fifth Avenue, New York, NY 10016 (United States); Department of Physics, Columbia University, Pupin Hall, 550 West 120th St., New York, NY 10027 (United States); Lüst, Dieter [Arnold Sommerfeld Center for Theoretical Physics,Department für Physik, Ludwig-Maximilians-Universität München,Theresienstraße 37, 80333 München (Germany); Max-Planck-Institut für Physik, Werner-Heisenberg-Institut, Föhringer Ring 6, 80805 München (Germany); Malek, Emanuel [Arnold Sommerfeld Center for Theoretical Physics,Department für Physik, Ludwig-Maximilians-Universität München,Theresienstraße 37, 80333 München (Germany)


    We formulate the full bosonic SL(5) exceptional field theory in a coordinate-invariant manner. Thereby we interpret the 10-dimensional extended space as a manifold with SL(5)×ℝ{sup +}-structure. We show that the algebra of generalised diffeomorphisms closes subject to a set of closure constraints which are reminiscent of the quadratic and linear constraints of maximal seven-dimensional gauged supergravities, as well as the section condition. We construct an action for the full bosonic SL(5) exceptional field theory, even when the SL(5)×ℝ{sup +}-structure is not locally flat.

  9. Scalable production of microbially mediated zinc sulfide nanoparticles and application to functional thin films. (United States)

    Moon, Ji-Won; Ivanov, Ilia N; Joshi, Pooran C; Armstrong, Beth L; Wang, Wei; Jung, Hyunsung; Rondinone, Adam J; Jellison, Gerald E; Meyer, Harry M; Jang, Gyoung Gug; Meisner, Roberta A; Duty, Chad E; Phelps, Tommy J


    A series of semiconducting zinc sulfide (ZnS) nanoparticles were scalably, reproducibly, controllably and economically synthesized with anaerobic metal-reducing Thermoanaerobacter species. These bacteria reduced partially oxidized sulfur sources to sulfides that extracellularly and thermodynamically incorporated with zinc ions to produce sparingly soluble ZnS nanoparticles with ∼5nm crystallites at yields of ∼5gl(-1)month(-1). A predominant sphalerite formation was facilitated by rapid precipitation kinetics, a low cation/anion ratio and a higher zinc concentration compared to background to produce a naturally occurring hexagonal form at the low temperature, and/or water adsorption in aqueous conditions. The sphalerite ZnS nanoparticles exhibited narrow size distribution, high emission intensity and few native defects. Scale-up and emission tunability using copper doping were confirmed spectroscopically. Surface characterization was determined using Fourier transform infrared and X-ray photoelectron spectroscopies, which confirmed amino acid as proteins and bacterial fermentation end products not only maintaining a nano-dimensional average crystallite size, but also increasing aggregation. The application of ZnS nanoparticle ink to a functional thin film was successfully tested for potential future applications. Copyright © 2014 Acta Materialia Inc. All rights reserved.

  10. Corrosion Study of Super Ferritic Stainless Steel UNS S44660 (26Cr-3Ni-3Mo) and Several Other Stainless Steel Grades (UNS S31603, S32101, and S32205) in Caustic Solution Containing Sodium Sulfide (United States)

    Chasse, Kevin R.; Singh, Preet M.


    Electrochemical techniques, scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) were used in this study to show how the corrosion mechanism of several commercial grades of stainless steel in hot caustic solution is strongly influenced by the presence of sodium sulfide. Experimental results from super ferritic stainless steel UNS S44660 (26Cr-3Ni-3Mo) were compared to austenitic stainless steel UNS S31603, lean duplex stainless steel (DSS) UNS S32101, and standard DSS UNS S32205 in caustic solution, with and without sodium sulfide, at 443 K (170 °C). Weight loss measurements indicated that corrosion rates of UNS44660 were much lower than the other grades of stainless steel in the presence of the sodium sulfide. Potentiodynamic polarization and linear polarization resistance measurements showed that the electrochemical behavior was altered by the adhesion of sulfur species, which reduced the polarization resistances and increased the anodic current densities. SEM and XPS results imply that the surface films that formed in caustic solution containing sodium sulfide were defective due to the adsorption of sulfide, which destabilized the passive film and led to the formation of insoluble metal sulfide compounds.

  11. Solubility and permeation of hydrogen sulfide in lipid membranes.

    Directory of Open Access Journals (Sweden)

    Ernesto Cuevasanta

    Full Text Available Hydrogen sulfide (H(2S is mainly known for its toxicity but has recently been shown to be produced endogenously in mammalian tissues and to be associated with physiological regulatory functions. To better understand the role of biomembranes in modulating its biological distribution and effects; we measured the partition coefficient of H(2S in models of biological membranes. The partition coefficients were found to be 2.1±0.2, 1.9±0.5 and 2.0±0.6 in n-octanol, hexane and dilauroylphosphatidylcholine liposome membranes relative to water, respectively (25°C. This two-fold higher concentration of H(2S in the membrane translates into a rapid membrane permeability, P(m = 3 cm s(-1. We used a mathematical model in three dimensions to gain insight into the diffusion of total sulfide in tissues. This model shows that the sphere of action of sulfide produced by a single cell expands to involve more than 200 neighboring cells, and that the resistance imposed by lipid membranes has a significant effect on the diffusional spread of sulfide at pH 7.4, increasing local concentrations. These results support the role of hydrogen sulfide as a paracrine signaling molecule and reveal advantageous pharmacokinetic properties for its therapeutic applications.

  12. 49 CFR 374.505 - Exceptions. (United States)


    ... District (as defined in the Washington Metropolitan Area Transportation Regulation Compact, Pub. L. No. 86... 49 Transportation 5 2010-10-01 2010-10-01 false Exceptions. 374.505 Section 374.505 Transportation Other Regulations Relating to Transportation (Continued) FEDERAL MOTOR CARRIER SAFETY ADMINISTRATION...

  13. 40 CFR 170.103 - Exceptions. (United States)


    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Exceptions. 170.103 Section 170.103 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) PESTICIDE PROGRAMS WORKER PROTECTION... abatement, Mediterranean fruit fly eradication, or similar wide-area public pest control programs sponsored...

  14. 40 CFR 170.203 - Exceptions. (United States)


    ... 40 Protection of Environment 23 2010-07-01 2010-07-01 false Exceptions. 170.203 Section 170.203 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) PESTICIDE PROGRAMS WORKER PROTECTION...) For mosquito abatement, Mediterranean fruit fly eradication, or similar wide-area public pest control...

  15. 26 CFR 1.306-2 - Exception. (United States)


    ... 1036 (relating to exchanges of stock for stock in the same corporation) to the extent that gain or loss... TAXES Effects on Recipients § 1.306-2 Exception. (a) If a shareholder terminates his entire stock... payment for the stock sold or redeemed. In the case of a sale, only the stock interest need be terminated...

  16. 42 CFR 412.348 - Exception payments. (United States)


    ... period. Annual operating expenses are obtained from the Medicare cost report. Average age of fixed assets... may be made for up to 10 years beyond the end of the capital prospective payment system transition period. (1) Eligible hospitals. The following classes of hospitals are eligible to receive exceptions...

  17. Voices from the Classroom: Exceptional Teachers Speak. (United States)

    Maeroff, Gene I., Ed.

    The opinions and experiences reflected in this report are those of exceptional teachers chosen in a national competition, "Thanks to Teachers," sponsored by Apple Computer, Inc., the National Foundation for the Improvement of Education, the National Alliance of Business, and Group W Television. The report is divided into four sections: (1) the…

  18. 15 CFR 905.5 - Exceptions. (United States)


    ... the actual or attempted: (a) Assault, intimidation, or harassment (including sexual harassment) of any person; or (b) Impairment or interference with the duties of a voluntary fishery data collector. ... PROCEEDINGS OF INFORMATION COLLECTED BY VOLUNTARY FISHERY DATA COLLECTORS § 905.5 Exceptions. The provisions...

  19. Exceptional polynomials and SUSY quantum mechanics

    Indian Academy of Sciences (India)

    We show that for the quantum mechanical problem which admit classical Laguerre/Jacobi polynomials as solutions for the Schrödinger equations (SE), will also admit exceptional Laguerre/Jacobi polynomials as solutions having the same eigenvalues but with the ground state missing after a modification of the potential.

  20. 15 CFR 1180.7 - Exceptions. (United States)


    ... Commerce and Foreign Trade Regulations Relating to Commerce and Foreign Trade (Continued) TECHNOLOGY... INFORMATION TO THE NATIONAL TECHNICAL INFORMATION SERVICE § 1180.7 Exceptions. (a) An agency shall not be...) The product is an agency generated article that is published in a privately produced journal; or (5...

  1. 26 CFR 1.683-2 - Exceptions. (United States)


    ... receives after July 31, 1954, the distribution resulting from the trust's receipt of dividends, he is... resulting from the trust's receipt of dividends, he is deemed to have received the dividends ratably with... TAXES Miscellaneous § 1.683-2 Exceptions. (a) In the case of any beneficiary of an estate or trust...

  2. Exceptional polynomials and SUSY quantum mechanics

    Indian Academy of Sciences (India)

    Exceptional polynomials and SUSY quantum mechanics. K V S SHIV CHAITANYA1,∗, S SREE RANJANI2,. PRASANTA K PANIGRAHI3, R RADHAKRISHNAN4 and V SRINIVASAN4. 1BITS Pilani, Hyderabad Campus, Jawahar Nagar, Shameerpet Mandal, Hyderabad 500 078, India. 2Faculty of Science and Technology, ...

  3. Post-exceptionalism in public policy

    NARCIS (Netherlands)

    Daugbjerg, Carsten; Feindt, Peter H.


    Framing the special issue on the transformation of Food and Agricultural Policy, this article introduces the concept of post-exceptionalism in public policies. The analysis of change in agri-food policy serves as a generative example to conceptualize current transformations in sectoral policy

  4. 48 CFR 825.202 - Exceptions. (United States)


    ... 48 Federal Acquisition Regulations System 5 2010-10-01 2010-10-01 false Exceptions. 825.202... determination is required under FAR 25.202(a)(1), the contracting officer must submit the request for... the determination in the contract file. (2) Forward a copy of the determination, along with supporting...

  5. 48 CFR 825.103 - Exceptions. (United States)


    ... 48 Federal Acquisition Regulations System 5 2010-10-01 2010-10-01 false Exceptions. 825.103... contracting officer believes that a determination that domestic preference would be inconsistent with the public interest is necessary under FAR 25.103(a), the contracting officer must submit the request for...

  6. 48 CFR 225.7603 - Exceptions. (United States)


    ... 48 Federal Acquisition Regulations System 3 2010-10-01 2010-10-01 false Exceptions. 225.7603 Section 225.7603 Federal Acquisition Regulations System DEFENSE ACQUISITION REGULATIONS SYSTEM, DEPARTMENT OF DEFENSE SOCIOECONOMIC PROGRAMS FOREIGN ACQUISITION Secondary Arab Boycott of Israel 225.7603...

  7. Exceptional polynomials and SUSY quantum mechanics

    Indian Academy of Sciences (India)

    Abstract. We show that for the quantum mechanical problem which admit classical Laguerre/. Jacobi polynomials as solutions for the Schrödinger equations (SE), will also admit exceptional. Laguerre/Jacobi polynomials as solutions having the same eigenvalues but with the ground state missing after a modification of the ...

  8. Association between catastrophic paleovegetation changes during Devonian-Carboniferous boundary and the formation of giant massive sulfide deposits (United States)

    Menor-Salván, Cesar; Tornos, Fernando; Fernández-Remolar, David; Amils, Ricardo


    sulfide deposits formed where venting sulfur-poor but metal-rich hydrothermal brines flowed into a hydrogen sulfide-rich anoxic water column. The data presented strongly suggest that there was a temporal and causal relationship between the Devonian-Carboniferous geotectonic, climatic and biological crises and the formation of the giant volcano-sedimentary massive sulfide deposits of the southern Iberian Pyrite Belt.

  9. Organusulfur Catalysis With Reduced Molybdenum Sulfides Containing the Mo6S8 Cluster

    Energy Technology Data Exchange (ETDEWEB)

    Paskach, Thomas Jay [Iowa State Univ., Ames, IA (United States)


    Industrial synthesis of sulfur-containing organic chemicals basically focuses on the broad categories of mercaptans (thiols), alkylsulfides (thioethers), polysulfides, and thiophenes. Of the organo-sulfur compounds produced, by far the most important in terms of quantities produced is methyl mercaptan (methanethiol or MeSH), which is produced mainly for the downstream production of methionine and methanesulfonyl chloride. Higher thiols are also used in the manufacture of rubber and plastics as polymerization regulators, chain transfer agents, or initiators. Other important organosulfur chemicals are dimethyl sulfide (DMS) and dimethyl disulfide (DMDS), both of which are used extensively for presulfiding of industrial hydroprocessing catalysts, and substituted thiophenes which are used as intermediates for production of agrochemicals, dyes, and pharmaceuticals. Thiols are produced commercially at the rate of about 104 ton/yr from hydrogen sulfide (H2S) and alcohols or olefins, using homogeneous free-radical synthesis, or heterogeneous catalysts based on solid acids or supported metal oxides and/or sulfides. Despite this large production rate, and the industrial importance of the organosulfur compounds, only limited research has been devoted to the development of new catalytic materials for their synthesis. Additionally, for most organosulfur catalytic reactions, only limited information exists about reaction mechanisms, active sites, adsorbed surface species, and especially the nature of the catalysts under reaction conditions.

  10. Magmatic-vapor expansion and the formation of high-sulfidation gold deposits: Chemical controls on alteration and mineralization (United States)

    Henley, R.W.; Berger, B.R.


    Large bulk-tonnage high-sulfidation gold deposits, such as Yanacocha, Peru, are the surface expression of structurally-controlled lode gold deposits, such as El Indio, Chile. Both formed in active andesite-dacite volcanic terranes. Fluid inclusion, stable isotope and geologic data show that lode deposits formed within 1500. m of the paleo-surface as a consequence of the expansion of low-salinity, low-density magmatic vapor with very limited, if any, groundwater mixing. They are characterized by an initial 'Sulfate' Stage of advanced argillic wallrock alteration ?? alunite commonly with intense silicification followed by a 'Sulfide' Stage - a succession of discrete sulfide-sulfosalt veins that may be ore grade in gold and silver. Fluid inclusions in quartz formed during wallrock alteration have homogenization temperatures between 100 and over 500 ??C and preserve a record of a vapor-rich environment. Recent data for El Indio and similar deposits show that at the commencement of the Sulfide Stage, 'condensation' of Cu-As-S sulfosalt melts with trace concentrations of Sb, Te, Bi, Ag and Au occurred at > 600 ??C following pyrite deposition. Euhedral quartz crystals were simultaneously deposited from the vapor phase during crystallization of the vapor-saturated melt occurs to Fe-tennantite with progressive non-equilibrium fractionation of heavy metals between melt-vapor and solid. Vugs containing a range of sulfides, sulfosalts and gold record the changing composition of the vapor. Published fluid inclusion and mineralogical data are reviewed in the context of geological relationships to establish boundary conditions through which to trace the expansion of magmatic vapor from source to surface and consequent alteration and mineralization. Initially heat loss from the vapor is high resulting in the formation of acid condensate permeating through the wallrock. This Sulfate Stage alteration effectively isolates the expansion of magmatic vapor in subsurface fracture arrays

  11. High temperature corrosion of metals

    International Nuclear Information System (INIS)

    Quadakkers, W.J.; Schuster, H.; Ennis, P.J.


    This paper covers three main topics: 1. high temperature oxidation of metals and alloys, 2. corrosion in sulfur containing environments and 3. structural changes caused by corrosion. The following 21 subjects are discussed: Influence of implanted yttrium and lanthanum on the oxidation behaviour of beta-NiA1; influence of reactive elements on the adherence and protective properties of alumina scales; problems related to the application of very fine markers in studying the mechanism of thin scale formation; oxidation behaviour of chromia forming Co-Cr-Al alloys with or without reactive element additions; growth and properties of chromia-scales on high-temperature alloys; quantification of the depletion zone in high temperature alloys after oxidation in process gas; effects of HC1 and of N2 in the oxidation of Fe-20Cr; investigation under nuclear safety aspects of Zircaloy-4 oxidation kinetics at high temperatures in air; on the sulfide corrosion of metallic materials; high temperature sulfide corrosion of Mn, Nb and Nb-Si alloys; corrosion behaviour or NiCrAl-based alloys in air and air-SO2 gas mixtures; sulfidation of cobalt at high temperatures; preoxidation for sulfidation protection; fireside corrosion and application of additives in electric utility boilers; transport properties of scales with complex defect structures; observations of whiskers and pyramids during high temperature corrosion of iron in SO2; corrosion and creep of alloy 800H under simulated coal gasification conditions; microstructural changes of HK 40 cast alloy caused by exploitation in tubes in steam reformer installation; microstructural changes during exposure in corrosive environments and their effect on mechanical properties; coatings against carburization; mathematical modeling of carbon diffusion and carbide precipitation in Ni-Cr-based alloys. (MM)

  12. Sulfide Catalysts Supported on Porous Aromatic Frameworks for Naphthalene Hydroprocessing

    Directory of Open Access Journals (Sweden)

    Eduard Karakhanov


    Full Text Available This paper describes the first example of using porous aromatic frameworks as supports for sulfide catalysts for the hydrogenation of aromatic hydrocarbons. The synthesis of bimetallic Ni-W and Ni-Mo sulfides was performed by in situ decomposition of [(n-Bu4N]2[Ni(MeS42] (Me = W, Mo complexes, supported on mesoporous aromatic framework with a diamond-like structure. It is shown that the highest naphthalene conversions were achieved in the case of additional sulfidation with sulfur. After the reaction, catalysts were characterized by X-ray photoelectron spectroscopy and high-resolution transmission electron microscopy. The activity of synthesized catalysts has been studied using naphthalene as a model substrate. The materials used in this study were substantially active in hydrogenation and slightly in hydrocracking of naphthalene.

  13. Interaction of hydrogen sulfide with Zr0.92Y0.08O2-δ/40% Ni cermet

    International Nuclear Information System (INIS)

    Siriwardane, R.V.; Poston, J.A. Jr.; Fisher, E.P.


    The interaction of hydrogen sulfide with a cermet composed of zirconium oxide and yttrium oxide doped with metallic nickel (Ni) in the stoichiometric form Zr 0.92 Y 0.08 O 2-δ /40 vol% Ni and a pure nickel metal was studied at 500 and 650 deg. C utilizing high temperature X-ray photoelectron spectroscopy and high-temperature scanning electron microscopy. The hydrogen sulfide (H 2 S) did not appear to interact with the cermet at 500 deg. C with H 2 S exposures of 6 x 10 -5 Torr for 1 h, but interaction of H 2 S with the cermet was observed at 650 deg. C at similar H 2 S exposures. The amount and the rate of reaction of H 2 S were significantly lower with the cermet than with the pure nickel metal at 650 deg. C with similar H 2 S exposures. The dispersion of nickel in the zirconium and yttrium oxide matrix decreased the reaction of H 2 S with nickel in the cermet

  14. Oxidation of acid-volatile sulfide in surface sediments increases the release and toxicity of copper to the benthic amphipod Melita plumulosa. (United States)

    Simpson, Stuart L; Ward, Daniel; Strom, David; Jolley, Dianne F


    Acid-volatile sulfides (AVS) are an important metal-binding phase in sediments. For sediments that contain an excess of AVS over simultaneously extracted metal (SEM) concentrations, acute or chronic effects should not result from the metals Cd, Cu, Ni, Pb and Zn. While AVS phases may exist in surface sediments, the exposure to dissolved oxygen may oxidize the AVS and release metals to more bioavailable forms. We investigated the role of oxidation of AVS, and specifically copper sulfide phases, in surface sediments, in the toxicity to juveniles of the epibenthic amphipod, Melita plumulosa. Sediments containing known amounts of copper sulfide were prepared either in situ by reacting dissolved copper with AVS that had formed in field sediments or created in sediments within the laboratory, or by addition of synthesised CuS to sediments. Regardless of the form of the copper sulfide, considerable oxidation of AVS occurred during the 10-d tests. Sediments that had a molar excess of AVS compared to SEM at the start of the tests, did not always have an excess at the end of the tests. Consistent with the AVS-SEM model, no toxicity was observed for sediments with an excess of AVS throughout the tests. However, the study highlights the need to carefully consider the changes in AVS concentrations during tests, and that measurements of AVS and SEM concentrations should carefully target the materials to which the organisms are being exposed throughout tests, which in the case of juvenile M. plumulosa is the top few mm of the sediments. Crown Copyright © 2012. Published by Elsevier Ltd. All rights reserved.


    Carbon nanotube (CNT) modified glassy carbon electrodes exhibiting a strong and stable electrocatalytic response towards sulfide are described. A substantial (400 mV) decrease in the overvoltage of the sulfide oxidation reaction (compared to ordinary carbon electrodes) is...

  16. Becoming Exceptional: Exploring Selves and Assemblages in the National Exceptional Teaching in Disadvantaged Schools Program (United States)

    Ailwood, Jo; Ford, Margot


    This paper explores the work of "becoming exceptional" amongst a group of preservice teachers taking part in the National Exceptional Teaching for Disadvantaged Schools program (NETDS). The NETDS program is directed towards mentoring and supporting outstanding preservice teachers to transition into the schools where they can make a…

  17. Sulfide-Sulfate Equilibria in Subducted Lithosphere, Mantle Redox and the Deep Earth Sulfur Cycle in Space and Time (United States)

    Canil, D.


    The redox budget during subduction affects the deep-earth S cycle, and is tied to the evolution of oxygen and biogeochemical cycles on Earth's surface over time. One component in the deep S cycle and its redox is the sedimentary veneer that sits atop the subducted oceanic basalt crust. The conversion of subducted sulfide to sulfate (or vice versa) is an eight-electron change in redox state, with significant oxidation/ reduction capacity of mantle sources for magmas, and for controlling the mobility or extraction of chalcophile metals from the arc mantle. I calculate buffers on sulfate - sulfide stability in subducted oceanic crust within the eclogite facies, and their disposition relative to other redox couples in the mantle along both `hot' and `warm' P-T trajectories for subducted lithosphere. To a first order, sulfide stability in subducted crust passing through the eclogite facies beneath an arc is shifted 0.5-1 logfO2 units by variations in the bulk Ca/Fe of the subducting crust alone. Because sulfate is highly soluble, its liberation from subducted crust by either melting or fluid flow into the arc source region can vary in space or time, depending on bulk composition of subducted crust or on variations in subduction P-T trajectories. The released sulfate may be one cause of the increase in the fO2 of the arc mantle. Experimental data on melts of subducted sediment show the control of sulfide-sulfate stability on the solubility of chalcophile metals (Cu, As, Mo, Pb). By assuming the normalized abundances of Cu as a proxy for S, the effect of variable subducted sediment composition on sulfide-sulfate stability and release of chalcophiles beneath convergent margins can be recognized in arc basalts and andesites from several modern subduction zones. The release of S and chalcophiles in the convergent margin setting may have changed with time, however, simply due to changes in the nature of sedimentation in the oceans over the course of earth history.

  18. Development of mining technology and equipment for seafloor massive sulfide deposits (United States)

    Liu, Shaojun; Hu, Jianhua; Zhang, Ruiqiang; Dai, Yu; Yang, Hengling


    Seafloor massive sulfide(SMS) deposits which consist of Au, Ag, Cu, and other metal elements, have been a target of commercial mining in recent decades. The demand for established and reliable commercial mining system for SMS deposits is increasing within the marine mining industry. The current status and progress of mining technology and equipment for SMS deposits are introduced. First, the mining technology and other recent developments of SMS deposits are comprehensively explained and analyzed. The seafloor production tools manufactured by Nautilus Minerals and similar mining tools from Japan for SMS deposits are compared and discussed in turn. Second, SMS deposit mining technology research being conducted in China is described, and a new SMS deposits mining tool is designed according to the environmental requirement. Finally, some new trends of mining technology of SMS deposits are summarized and analyzed. All of these conclusions and results have reference value and guiding significance for the research of SMS deposit mining in China.

  19. Sulfide silver stainability of a type of bouton in spinal cord motoneuron neuropil

    DEFF Research Database (Denmark)

    Schrøder, H D


    Spinal cord motoneuron neuropil (cervical and lumbar enlargements) has been studied at the ultrastructural level after fixation with glutaraldehyde and staining with uranyl acetate and lead citrate. Based on the appearance of the synaptic specializations, different types of boutons were identified...... and correlated with the classification of bouton types based on osmicated tissue. The sulfide silver method for histochemical demonstration of heavy metals was applied to the same region. The localization of reaction products (silver grains) was predominantly in the terminals. Within the bouton, the grains were...... mainly in the specialized region of the synaptic contact, and the presynaptic network has also labelled, but to a lesser degree. All stained boutons had the same type of paramembranous synaptic specialization, but not all of the boutons with this type of specialization were stained. The stained boutons...

  20. Metal recovery via geobiotechnology; Metallgewinnung mittels Geobiotechnologie

    Energy Technology Data Exchange (ETDEWEB)

    Hedrich, Sabrina; Schippers, Axel [Bundesanstalt fuer Geowissenschaften und Rohstoffe (BGR), Hannover (Germany). Fachbereich Geochemie der Rohstoffe


    Specialized acidophilic bacteria and archaea are able to extract valuable metals such as copper, gold, cobalt, nickel, zinc, and uranium from sulfide ores. This process is known as bioleaching and its application in the mining industry as biomining. Laboratory studies also demonstrated bioleaching of oxide ores such as laterites and of mining residues such as mine tailings as well as metal recycling from waste (secondary mining). Metals being leached have to be recovered from acidic polymetallic solutions (mine and process waters) which is possible via biosorption or biomineralisation.

  1. Handbook of Phase Transition Sulfides, Selenides and Tellurides, (United States)


    Cinnabar) ........ A-108 In2S3 (Indium Sulfide or 01-Indium Trisulfide) ...... A-113 MnS (Manganese Monosulfide) ... .... .. .......... A-116 - MnS2...1n2S 3 Indium Sulfide or Di-Indium Trisulflde In2S3 exists as cubic a-In 2S3 and tetragonal 0-In 2S3. Until recently, no detailed studies on the...structure and the vibrational properties of In2S3 have been reported. 0-In 2S3 is the stable room temperature phase. At 420°C there is a transition to c

  2. High conducting oxide--sulfide composite lithium superionic conductor

    Energy Technology Data Exchange (ETDEWEB)

    Liang, Chengdu; Rangasamy, Ezhiylmurugan; Dudney, Nancy J.; Keum, Jong Kahk; Rondinone, Adam Justin


    A solid electrolyte for a lithium-sulfur battery includes particles of a lithium ion conducting oxide composition embedded within a lithium ion conducting sulfide composition. The lithium ion conducting oxide composition can be Li.sub.7La.sub.3Zr.sub.2O.sub.12 (LLZO). The lithium ion conducting sulfide composition can be .beta.-Li.sub.3PS.sub.4 (LPS). A lithium ion battery and a method of making a solid electrolyte for a lithium ion battery are also disclosed.

  3. Thermal stability of semiconductor sulfide phases in air

    International Nuclear Information System (INIS)

    Tsiulyanv, I.I.; Lyalikova, K.Y.; Zhitar, V.F.


    This paper investigates the semiconductor sulfide phases Zn 3 In 2 S 6 , Zn 3 Ga 2 S 6 , and Zn 3 GaInS 6 , produced by chemical transport reactions in a sealed space. A typical derivatogram is shown. Up to 873 K no weight changes appear in the TG curve. As indium atoms are replaced by gallium atoms the kinetic oxidation parameters of the sulfide phases change regularly, and they correlate with the calculated heat of atomization, which characterizes bond strength. The dependence of the temperature of the start of oxidation on composition shows that zinc thiogallate is the most stable when heated in air

  4. Global Trade issues and Cultural Exception

    Directory of Open Access Journals (Sweden)

    Vanessa MARSON


    Full Text Available Cultural exception has always been a key element in the French political and cultural field. It isbased on the principle that culture is not like any other merchandise because it goes beyond thecommercial. During the negotiations of the Uruguay Round (1986-1994 the United States offeredto liberalize cultural goods and services. Due to the sensitive nature of the cultural industries, theEuropean Union led by France refused to make an offer of liberalization on these fields. Afterheated debates between the United States and the European Union, cultural exception has finallybecome a global issue since 2005. On 20 October, the UNESCO convention on cultural diversitywas voted by 148 countries to two (The United States and Israel to legally and globally recognizethe specific nature of cultural goods and services in the liberalization process.

  5. The uncertain future of Slovenian exceptionalism

    DEFF Research Database (Denmark)

    Guardiancich, Igor


    The political-economy literature has so far almost unanimously regarded Slovenia as the social-democratic exception in Central and Eastern Europe, due to a combination of highly consensual democratic institutions, low party polarization, strong social partners, and developed social dialogue....... However, the situation, since the fall of the Liberal Democracy of Slovenia (LDS), which governed in 1992-2004, seems to be swiftly changing. Polarization has increased, union legitimacy declined, and social dialogue- especially in the aftermath of the 2007-2009 financial crisis-has all but collapsed....... The 2010 pension reform is an archetypical example of how Slovenia now much more resembles its quarrelsome Eastern neighbours than the idealized exception that political scientists usually point at....

  6. Electrocatalysis of the hydrogen evolution reaction by thermally formed sulfides on steels


    Kumar, Prem T; Sathyanarayana, S


    The electrocatalytic activity was studied of sulfides, formed by thermal sulfidization of various com. available steels, for the cathodic evolution of H from sodium chloride. The effects of certain surface active anions on the H evolution reaction on these sulfidized steels were also studied. Sulfidization of C steels and Si steels increases their electrocatalytic activity with respect to cathodic H evolution and thereby reduces the over potential in sodium chloride solns. (typically about ...

  7. Laws of Nature, Exceptions and Tropes


    Kistler, Max


    I propose a realist theory of laws formulated in terms of tropes (or property instances) that avoids both the problems of the "best-systems-analysis" and the "inference problem" of realism of universals. I analyze the concept of an exceptional situation, characterized as a situation in which a particular object satisfies the antecedent but not the consequent of the regularity associated with a law, without thereby falsifying that law. To take this possibility into account, the properties link...

  8. Weathering of PGE sulfides and Pt-Fe alloys in the Freetown Layered Complex, Sierra Leone (United States)

    Bowles, John F. W.; Suárez, Saioa; Prichard, Hazel M.; Fisher, Peter C.


    Fresh and weathered rocks and saprolite from Horizon B of the Freetown Layered Complex contain platinum-group minerals (PGM). The PGM in the fresh rocks are 1-7 μm across, including cooperite (PtS), isoferroplatinum (Pt3Fe), minor tetraferroplatinum (PtFe), tulameenite (Pt2FeCu), Os-bearing laurite (RuS2), and other base metal-sulfide (BMS)-bearing PGM. The weathered rocks contain fewer of those PGM but a high proportion of disordered Cu-(±Pd)-bearing Pt-Fe alloys. The saprolite hosts scarce, smaller (1-3 μm) ordered PtFe and disordered PtFe3. The Pt-Fe alloys became increasingly Fe rich as weathering proceeded. Pt-Fe oxides appeared during weathering. Copper sulfides associated with the primary PGM and cooperite (with <3% Pd) were destroyed to provide the minor Cu and Pd found in some of the disordered Pt-Fe alloys. Platinum- and Pd-bearing saprolites have retained the original rock fabric and, to a depth of about 2 m, surround residual rocks that show progressive weathering (corestones). Ground water passing through the saprolite has transported Pt and Pd (and probably Au) in solution down slope into saprolite over unmineralized rocks. Transport is marked by changes in the Pt/Pd ratio indicating that the metals have moved independently. Palladium is present in marginally higher concentrations in the deeper saprolite than in the corestones suggesting some retention of Pd in the deeper saprolite. Platinum and Pd are less concentrated in the upper saprolite than the deeper saprolite indicating surface leaching. Alteration occurred over a long period in an organic and microbial rich environment that may have contributed to the leaching and transport of PGE.

  9. Exceptional points in open quantum systems

    International Nuclear Information System (INIS)

    Mueller, Markus; Rotter, Ingrid


    Open quantum systems are embedded in the continuum of scattering wavefunctions and are naturally described by non-Hermitian Hamilton operators. In the complex energy plane, exceptional points appear at which two (or more) eigenvalues of the Hamilton operator coalesce. Although they are a countable set of single points in the complex energy plane and therefore of measure zero, they determine decisively the dynamics of open quantum systems. A powerful method for the description of open quantum systems is the Feshbach projection operator formalism. It is used in the present paper as a basic tool for the study of exceptional points and of the role they play for the dynamics of open quantum systems. Among others, the topological structure of the exceptional points, the rigidity of the phases of the eigenfunctions in their vicinity, the enhancement of observable values due to the reduced phase rigidity and the appearance of phase transitions are considered. The results are compared with existing experimental data on microwave cavities. In the last section, some questions being still unsolved, are considered

  10. The solubility of iron sulfides and their role in mass transport in Girdler-Sulfide heavy water plants

    International Nuclear Information System (INIS)

    Tewari, P.H.; Wallace, G.; Campbell, A.B.


    The solubilities of several iron sulfides, mackinawite FeSsub((1-x)), troilite FeS, pyrrhotite Fesub((1-x))S (monoclinic and hexagonal), and pyrite FeS 2 have been determined in aqueous H 2 S solution at 0.1 MPa and 1.8 MPa H 2 S pressures between 25 deg and 125 deg C. The dependence of solubility on the pH of the medium has also been studied. It is concluded that since mackinawite is the most soluble of the iron sulfides, and has the highest dissolution rate and the steepest decline in solubility with temperature, its prolonged formation during plant operation should be avoided to minimize iron transport from lower to higher temperature areas in Girdler-Sulfide (G.S.) heavy water plants. This can be achieved by a preconditioning of carbon steel surfaces to convert mackinawite to pyrrhotite and pyrite

  11. The weathering of a sulfide orebody: Speciation and fate of some potential contaminants (United States)

    Courtin-Nomade, A.; Grosbois, C.; Marcus, M.A.; Fakra, S.C.; Beny, J.-M.; Foster, A.L.


    Various potentially toxic trace elements such as As, Cu, Pb and Zn have been remobilized by the weathering of a sulfide orebody that was only partially mined at Leona Heights, California. As a result, this body has both natural and anthropogeni- cally modified weathering profiles only 500 m apart. The orebody is located in a heavily urbanized area in suburban Oakland, and directly affects water quality in at least one stream by producing acidic conditions and relatively high concentrations of dissolved elements (e.g., ??500 ??g/L Cu, ??3700 ??g/L Zn). Micrometric-scale mineralogical investigations were performed on the authigenic metal-bearing phases (less than 10 ??m in size) using electron-probe micro-analysis (EPMA), micro-Raman, micro X-ray absorption spectroscopy (??XAS), scanning X-ray diffraction ((??SXRD) and scanning X-ray fluorescence (??-SXRF) mapping techniques. Those measurements were coupled with classical mineralogical laboratory techniques, X-ray diffraction (XRD) and scanning electron microscopy (SEM). Authigenic metal-bearing phases identified are mainly sulfates (jarosite, epsomite, schwertmannite), Fe (oxy-)hydroxides (goethite, hematite and poorly crystalline Fe products) and poorly crystalline Mn (hydr-)oxides. Sulfates and Fe (oxy-)hydroxides are the two main secondary products at both sites, whereas Mn (hydr-) oxides were only observed in the samples from the non-mining site. In these samples, the various trace elements show different affinities for Fe or Mn compounds. Lead is preferentially associated with Mn (hydr-)oxides and As with Fe (oxy-)hydroxides or sulfates. Copper association with Mn and Fe phases is questionable, and the results obtained rather indicate that Cu is present as individual Cu-rich grains (Cu hydroxides). Some ochreous precipitates were found at both sites and correspond to a mixture of schwertmannite, goethite and jarosite containing some potentially toxic trace elements such as Cu, Pb and Zn. According to the trace


    Energy Technology Data Exchange (ETDEWEB)

    Courtin-Nomade, Alexandra; Grosbois, Cecile; Marcus, Matthew A.; Fakra, Sirine C.; Beny, Jean Michel; Foster, Andrea L.


    Various potentially toxic trace elements such as As, Cu, Pb and Zn have been remobilized by the weathering of a sulfide orebody that was only partially mined at Leona Heights, California. As a result, this body has both natural and anthropogenically modified weathering profiles only 500 m apart. The orebody is located in a heavily urbanized area in suburban Oakland, and directly affects water quality in at least one stream by producing acidic conditions and relatively high concentrations of dissolved elements (e.g., {approx}500 mg/L Cu, {approx}3700 mg/L Zn). Micrometric-scale mineralogical investigations were performed on the authigenic metal-bearing phases (less than 10 {mu}m in size) using electron-probe micro-analysis (EPMA), micro-Raman, micro X-ray absorption spectroscopy (mXAS), scanning X-ray diffraction (mSXRD) and scanning X-ray fluorescence (mSXRF) mapping techniques. Those measurements were coupled with classical mineralogical laboratory techniques, X-ray diffraction (XRD) and scanning electron microscopy (SEM). Authigenic metal-bearing phases identified are mainly sulfates (jarosite, epsomite, schwertmannite), Fe (oxy-)hydroxides (goethite, hematite and poorly crystalline Fe products) and poorly crystalline Mn (hydr-)oxides. Sulfates and Fe (oxy-)hydroxides are the two main secondary products at both sites, whereas Mn (hydr-) oxides were only observed in the samples from the non-mining site. In these samples, the various trace elements show different affinities for Fe or Mn compounds. Lead is preferentially associated with Mn (hydr-)oxides and As with Fe (oxy-)hydroxides or sulfates. Copper association with Mn and Fe phases is questionable, and the results obtained rather indicate that Cu is present as individual Cu-rich grains (Cu hydroxides). Some ochreous precipitates were found at both sites and correspond to a mixture of schwertmannite, goethite and jarosite containing some potentially toxic trace elements such as Cu, Pb and Zn. According to the


    NARCIS (Netherlands)



    The colorless sulfur bacterium Thiobacillus thioparus T5, isolated from a marine microbial mat, was grown in continuous culture under conditions ranging from sulfide limitation to oxygen limitation. Under sulfide-limiting conditions, sulfide was virtually completely oxidized to sulfate. Under

  14. Reliability of Electrochemical Techniques for Determining Corrosion Rates on Carbon Steel in Sulfide Media

    DEFF Research Database (Denmark)

    Hilbert, Lisbeth Rischel; Hemmingsen, T.; Nielsen, Lars Vendelbo


    Effects of film formation on carbon steel in hydrogen sulfide (H2S) media may corrupt corrosion rate monitoring by electrochemical techniques. Electrochemical data from H2S solutions, biological sulfide media, and natural sulfide containing geothermal water have been collected, and the process of...

  15. Sulfide-iron interactions in domestic wastewater from a gravity sewer

    NARCIS (Netherlands)

    Nielsen, A.H.; Lens, P.N.L.; Vollertsen, J.; Hvitved-Jacobsen, Th.


    Interactions between iron and sulfide in domestic wastewater from a gravity sewer were investigated with particular emphasis on redox cycling of iron and iron sulfide formation. The concentration ranges of iron and total sulfide in the experiments were 0.4-5.4 mg Fe L-1 and 0-5.1 mg S L-1,

  16. Is succession in wet calcareous dune slacks affected by free sulfide?

    NARCIS (Netherlands)

    Adema, EB; van Gemerden, H; Grootjans, AP; Adema, Erwin B.; Grootjans, Ab P.; Rapson, G.

    Consequences of sulfide toxicity on succession in wet calcareous dune slacks were investigated. Sulfide may exert an inhibitory effect on dune slack plants, but several pioneer species exhibit ROL (Radial Oxygen Loss) and thereby protect themselves against free sulfide. Under oxic conditions free

  17. Identifying the Prospective Area of Sulfide Groundwater within the Area of Palvantash Oil and Gas Deposit

    Directory of Open Access Journals (Sweden)

    M. R. Zhurayev


    Full Text Available This paper describes the methodology of prospecting for sulfide groundwater in the area of Palvantash oil fields. In result of study allowed determining the favorable conditions for the sulfide waters formation, and mapping the areas of different sulfide water concentration. The relatively permeable areas were established and the water borehole positions were recommended.

  18. 76 FR 69136 - Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting (United States)


    ... Hydrogen Sulfide; Community Right-to-Know Toxic Chemical Release Reporting AGENCY: Environmental Protection Agency (EPA). ACTION: Lifting of Administrative Stay for Hydrogen Sulfide; Correction. SUMMARY: The... Administrative Stay of the reporting requirements for hydrogen sulfide. The Office of the Federal Register...

  19. Trace hydrogen sulfide gas sensor based on tungsten sulfide membrane-coated thin-core fiber modal interferometer (United States)

    Deng, Dashen; Feng, Wenlin; Wei, Jianwei; Qin, Xiang; Chen, Rong


    A novel fiber-optic hydrogen sulfide sensor based on a thin-core Mach-Zehnder fiber modal interferometer (TMZFI) is demonstrated and fabricated. This in-line interferometer is composed of a short section of thin-core fiber sandwiched between two standard single mode fibers, and the fast response to hydrogen sulfide is achieved via the construction of tungsten sulfide film on the outside surface of the TMZFI using the dip-coating and calcination technique. The fabricated sensing nanofilm is characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS) spectrometer, Fourier transform infrared (FTIR) and spectroscopic analysis technology, etc. Experimental results showed that the WS2 sensing film has a hexagonal structure with a compact and porous morphology. The XPS and FTIR indicate that the existence of two elements (W and S) is demonstrated. With the increasing concentration of hydrogen sulfide, the interference spectra appear blue shift. In addition, a high sensitivity of 18.37 pm/ppm and a good linear relationship are obtained within a measurement range from 0 to 80 ppm. In addition, there is an excellent selectivity for H2S, which has also been proved by the surface adsorption energy results of tungsten sulfide with four gases (H2S, N2, O2 and CO2) by using the density functional theory calculations. This interferometer has the advantages of simple structure, high sensitivity and easy manufacture, and could be used in the safety monitoring field of hydrogen sulfide gas.

  20. Red coloration by heat treatment of the coprecipitate of cadmium sulfide and mercury(II) sulfide prepared from the nitrates

    International Nuclear Information System (INIS)

    Nakahara, Fujiya


    The effects of starting salts on the color, particle size and crystal structure of mercury-cadmium-sulfide pigments were investigated. The coprecipitate (N-S) of cadmium sulfide and mercury (II) sulfide was prepared by adding sodium sulfide solution to a mixed cadmium-mercury (II) nitrate solution. The coprecipitate (C-S) of cadmium sulfide and mercury (II) sulfide was also prepared from the mixed solution of their chlorides by the same method as described above. The coprecipitated products were heat-treated (calcination or hydrothermal treatment) at 350 0 C for 2 hours and subsequent changes in powder properties of both products were compared from each other. The powder properties of N-S, C-S and their heat-treated products were investigated by spectral reflectance, electron microscopy, X-ray diffraction and specific surface area measurements. Sample (N-C) obtained by the calcination of N-S was brown, indicating no red coloration, but the calcined product (C-C) of C-S developed a red color. Cl - and hot water were found to be effective for the red color development of the pigment. The effectiveness was confirmed by calcining N-S in the presence of NaCl or by treating it hydrothermally. It was found that halides other than NaCl, (e.g., NH 4 Cl, KCl, KBr and KI), were also effective for the color development of the pigment. The red samples are solid solutions with a basically hexagonal CdS structure, and it appears that CdS takes up HgS without any apparent structural changes. The particle size of the red samples are larger than those of the non red samples. (author)

  1. 49 CFR 173.426 - Excepted packages for articles containing natural uranium or thorium. (United States)


    ... outer surface of the uranium or thorium is enclosed in an inactive sheath made of metal or other durable... uranium or thorium. 173.426 Section 173.426 Transportation Other Regulations Relating to Transportation....426 Excepted packages for articles containing natural uranium or thorium. A manufactured article in...

  2. Stable Covalent Organic Frameworks for Exceptional Mercury Removal from Aqueous Solutions. (United States)

    Huang, Ning; Zhai, Lipeng; Xu, Hong; Jiang, Donglin


    The pre-designable porous structures found in covalent organic frameworks (COFs) render them attractive as a molecular platform for addressing environmental issues such as removal of toxic heavy metal ions from water. However, a rational structural design of COFs in this aspect has not been explored. Here we report the rational design of stable COFs for Hg(II) removal through elaborate structural design and control over skeleton, pore size, and pore walls. The resulting framework is stable under strong acid and base conditions, possesses high surface area, has large mesopores, and contains dense sulfide functional termini on the pore walls. These structural features work together in removing Hg(II) from water and achieve a benchmark system that combines capacity, efficiency, effectivity, applicability, selectivity, and reusability. These results suggest that COFs offer a powerful platform for tailor-made structural design to cope with various types of pollution.

  3. Development of an online sulfide analysis at the waste water treatment plant of a primary lead smelter; Entwicklung einer Online-Sulfidanalytik in der Abwasserbehandlungsanlage einer Primaerbleihuette

    Energy Technology Data Exchange (ETDEWEB)

    Steckenborn, Anja; Meurer, Urban [BERZELIUS Stolberg GmbH, Stolberg (Germany)


    In wastewater treatment of heavy metal containing fluids it is common practice to use soluble sulfides as precipitants. To run a stable system and ensure a complete reaction it is necessary to control the excess of sulfide continuously. There are diverse analytical methods to determine sulfide in aqueous solutions. Most of these techniques require a calibration or show a serious dependency on matrix effects. An argentometric precipitation titration is proved to be the best choice for the adverse ambience of high salts and solid containing fluids at an online analysis. The modular online System Metrohm ADI 2040 was tailored to the particular needs. The detection system is based on a combined platinum electrode with pH reference working in alkaline ammonia buffer. The system turns out to be unsusceptible to most matrix influences such as high concentrations of diverse anions and cat ions, flocking agents or up to a certain particle content. Below 3 mg/L the bigger part of results lies outside of {+-}20 % of the reference value. The accuracy enhances with increasing concentration. Solutions up to 10 mg/L sulfide show good reproducibility and analytical results. (orig.)

  4. Development of a low-cost alternative for metal removal from textile wastewater

    NARCIS (Netherlands)

    Sekomo Birame, C.


    Heavy metals (Cd, Cr, Cu, Pb and Zn) found in textile wastewater are removed by a combination of adsorption using volcanic rock as adsorbent, sulfide precipitation and phytoremediation techniques. The integrated system for metal removal combining anaerobic bioreactor as main treatment step and a

  5. Temporal variation of trace metal geochemistry in floodplain lake sediment subject to dynamic hydrological conditions

    NARCIS (Netherlands)

    Griethuysen, van C.; Luitwieler, M.; Joziasse, J.; Koelmans, A.A.


    Climate change and land use may significantly influence metal cycling in dynamic river systems. We studied temporal variation of sediment characteristics in a floodplain lake, including concentrations of dissolved organic carbon, acid volatile sulfide and trace metals. The sampling period included a

  6. Mineral potential for volcanogenic massive sulfide deposits in the Islamic Republic of Mauritania, (phase V, deliverable 77): Chapter L in Second projet de renforcement institutionnel du secteur minier de la République Islamique de Mauritanie (PRISM-II) (United States)

    Taylor, Cliff D.; Giles, Stuart A.


    Potential for base- and precious-metal-bearing volcanogenic massive sulfide deposits (VMS) exists in Mauritania in the greenstone belts of the southwestern Rgueïbat Shield and in the allochthonous portions of the central and southern Mauritanides. Additional potential exists for VMS deposits within the Tiris Complex of the central Rgueïbat Shield. Volcanosedimentary successions of Paleoproterozoic rocks of the northeastern portion of the Rgueïbat Shield are also permissive for volcanogenic massive sulfide deposits. These types of mineral occurrences are common features of marine volcanosedimentary successions worldwide and can be of almost any age, although Proterozoic examples are less abundant.

  7. 21 CFR 177.2490 - Polyphenylene sulfide resins. (United States)


    ... contact with food at temperatures up to and including normal baking and frying temperatures; provided that... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyphenylene sulfide resins. 177.2490 Section 177.2490 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED...

  8. An eco-friendly oxidation of sulfide compounds

    Indian Academy of Sciences (India)

    An improved green route has been developed for the oxidation of sulfide compounds. Albendazole is converted to ricobendazole or albendazole sulfone using H₂O₂ as an oxidant and H₂O as the solvent. High yields of the corresponding products were obtained by carrying out the reaction at room temperature.

  9. Hydrogen sulfide : role in vascular physiology and pathology

    NARCIS (Netherlands)

    Holwerda, Kim M.; Karumanchi, S. Ananth; Lely, A. Titia

    Purpose of reviewHydrogen sulfide (H2S), a colorless gas that is endogenously generated in mammals from cysteine, has important biological functions. Within the vasculature it regulates vessel tone and outgrowth of new vessels. This review summarizes recent literature on H2S signaling in the

  10. Diuretic action of exogenous hydrogen sulfide in spontaneously ...

    African Journals Online (AJOL)

    Diuretic action of exogenous hydrogen sulfide in spontaneously hypertensive diabetic rats. F ud Din Ahmad, MA Sattar, HA Rathore, S Akhter, O Hui Jin, EJ Johns. Abstract. Purpose: To examine the hypothesis that in hypertensive diabetic rats hydrogen sulphide (H2S) reduces blood pressure through diuretic action in ...

  11. Luminescence in Sulfides: A Rich History and a Bright Future

    Directory of Open Access Journals (Sweden)

    Philippe F. Smet


    Full Text Available Sulfide-based luminescent materials have attracted a lot of attention for a wide range of photo-, cathodo- and electroluminescent applications. Upon doping with Ce3+ and Eu2+, the luminescence can be varied over the entire visible region by appropriately choosing the composition of the sulfide host. Main application areas are flat panel displays based on thin film electroluminescence, field emission displays and ZnS-based powder electroluminescence for backlights. For these applications, special attention is given to BaAl2S4:Eu, ZnS:Mn and ZnS:Cu. Recently, sulfide materials have regained interest due to their ability (in contrast to oxide materials to provide a broad band, Eu2+-based red emission for use as a color conversion material in white-light emitting diodes (LEDs. The potential application of rare-earth doped binary alkaline-earth sulfides, like CaS and SrS, thiogallates, thioaluminates and thiosilicates as conversion phosphors is discussed. Finally, this review concludes with the size-dependent luminescence in intrinsic colloidal quantum dots like PbS and CdS, and with the luminescence in doped nanoparticles.


    Carbonyl sulfide (COS) is an intermediate in the production of pesticides and herbicides, and is a metabolite of the neurotoxicant carbon disulfide. The potential neurotoxicity of inhaled COS was investigated in F344 rats. Male rats were exposed to 0, 75, 150, 300, or 600 ppm COS...

  13. Carbon-supported iron and iron-molybdenum sulfide catalysts

    International Nuclear Information System (INIS)

    Ramselaar, W.L.T.M.


    The main objective was to describe the relations between the characteristics (composition and dispersion) of the actual sulfide phase and the catalytic activity. Attention was also paid to the influence of preparational aspects on these characteristics. The catalysts were characterized using in-situ Moessbauer spectroscopy down to 2.0 K. 254 refs.; 47 figs.; 22 tabs

  14. The Complex Resistivity Spectrum Characteristics About Stratabound Sulfide Deposits (United States)

    Dong, P.; Sun, B.; Wang, L.; Chen, Z.; Dong, Z.; Wu, Y.


    Complex resistivity method has become the key technique of deep prospecting, and widely applied in stratabound sulfide deposits which often form massive ores. However, the complex resistivity spectrum characteristics of stratabound sulfide deposits remains unknown. Through studying variation problem of two-dimensional polarization medium, deducing the differential equations and calculating formula,we applied Cole-Cole model to deduce the spectrum of complex resistivity based on the model of three-node and four-node finite element method, and programmed homologous procedure. We utilized the Earth Model of Geological Layers which has accurate analytical solution to test rationality and accuracy of our modeling. We applied the layer structure provided by drilling results in Chenmenshan copper mine,which is typical strata-bound sulfide deposits in Jiangxi province,China, and calculated the spectra of complex resistivity, then made comparison between modeled and measured values. We find good corellation between them. Our studies may have imporved the interpretation of complex resistivity data, which help apply complex resistivity methods of propecting on stratabound sulfide deposites.

  15. Support Effect in the Hydrodesulfurization of Thiophene over Rhodium Sulfide

    Czech Academy of Sciences Publication Activity Database

    Kaluža, Luděk; Vít, Zdeněk; Zdražil, Miroslav


    Roč. 101, č. 1 (2010), s. 63-72 ISSN 1878-5190 R&D Projects: GA ČR GA104/09/0751 Institutional research plan: CEZ:AV0Z40720504 Keywords : hydrodesulfurization * thiophene * rhodium sulfide Subject RIV: CI - Industrial Chemistry, Chemical Engineering

  16. Bio-reduction of sulfide minerals to recover invisible gold

    NARCIS (Netherlands)

    Hol, A.


      Sulfide minerals, like pyrite and arsenopyrite, are of economical interest due to the presence of invisible gold locked inside these minerals. As fine grinding is often not sufficient to liberate the gold from these minerals, additional destruction techniques, based on chemical and

  17. New Findings in Hydrogen Sulfide Related Corrosion of Concrete Sewers

    DEFF Research Database (Denmark)

    Nielsen, Asbjørn Haaning; Jensen, Henriette Stokbro; Hvitved-Jacobsen, Thorkild


    This paper summarizes major findings of a long-term study of hydrogen sulfide gas (H2S) adsorption and oxidation on concrete and plastic sewer pipe surfaces. The processes have been studied using a pilot-scale setup designed to replicate conditions in a gravity sewer located downstream of a force...

  18. Sulfide Concentration and Redox Potential Patterns in Mangrove ...

    African Journals Online (AJOL)

    The conclusion of these results is that spatial and temporal variation in the soil redox potential and sulfide concentrations, which are results of microbial activities in the sediment, influence mangrove seedling establishment. These soil factors are modified by the root systems, whereby sediments in areas with plenty of ...

  19. Luminescence in Sulfides: A Rich History and a Bright Future (United States)

    Smet, Philippe F.; Moreels, Iwan; Hens, Zeger; Poelman, Dirk


    Sulfide-based luminescent materials have attracted a lot of attention for a wide range of photo-, cathodo- and electroluminescent applications. Upon doping with Ce3+ and Eu2+, the luminescence can be varied over the entire visible region by appropriately choosing the composition of the sulfide host. Main application areas are flat panel displays based on thin film electroluminescence, field emission displays and ZnS-based powder electroluminescence for backlights. For these applications, special attention is given to BaAl2S4:Eu, ZnS:Mn and ZnS:Cu. Recently, sulfide materials have regained interest due to their ability (in contrast to oxide materials) to provide a broad band, Eu2+-based red emission for use as a color conversion material in white-light emitting diodes (LEDs). The potential application of rare-earth doped binary alkaline-earth sulfides, like CaS and SrS, thiogallates, thioaluminates and thiosilicates as conversion phosphors is discussed. Finally, this review concludes with the size-dependent luminescence in intrinsic colloidal quantum dots like PbS and CdS, and with the luminescence in doped nanoparticles.

  20. Rapid biosynthesis of cadmium sulfide (CdS) nanoparticles using ...

    African Journals Online (AJOL)

    Rapid biosynthesis of cadmium sulfide (CdS) nanoparticles using culture supernatants of Escherichia coli ATCC 8739, Bacillus subtilis ATCC 6633 and Lactobacillus ... The process of extracellular and fast biosynthesis may help in the development of an easy and eco-friendly route for the synthesis of CdS nanoparticles.

  1. Iridium Sulfide and Ir Promoted Mo Based Catalysts.

    Czech Academy of Sciences Publication Activity Database

    Vít, Zdeněk


    Roč. 322, - (2007), s. 142-151 ISSN 0926-860X R&D Projects: GA ČR(CZ) GA104/06/0870 Institutional research plan: CEZ:AV0Z40720504 Keywords : iridium sulfide * IrMo catalyst * hydrodesulfurization Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.166, year: 2007

  2. Estimation of bacterial hydrogen sulfide production in vitro

    Directory of Open Access Journals (Sweden)

    Amina Basic


    Full Text Available Oral bacterial hydrogen sulfide (H2S production was estimated comparing two different colorimetric methods in microtiter plate format. High H2S production was seen for Fusobacterium spp., Treponema denticola, and Prevotella tannerae, associated with periodontal disease. The production differed between the methods indicating that H2S production may follow different pathways.

  3. Exceptional Points and Dynamical Phase Transitions

    Directory of Open Access Journals (Sweden)

    I. Rotter


    Full Text Available In the framework of non-Hermitian quantum physics, the relation between exceptional points,dynamical phase transitions and the counter intuitive behavior of quantum systems at high level density is considered. The theoretical results obtained for open quantum systems and proven experimentally some years ago on a microwave cavity, may explain environmentally induce deffects (including dynamical phase transitions, which have been observed in various experimental studies. They also agree(qualitatively with the experimental results reported recently in PT symmetric optical lattices.

  4. Afterword: Intoxication as Zone of Exception

    Directory of Open Access Journals (Sweden)

    Joseph M. Gabriel


    Full Text Available In “Afterword: Intoxication as a Zone of Exception,” Joseph M. Gabriel turns our eye to what lies past intoxication: getting trashed or wasted. Even as he concedes that intoxication at its extreme marks the impossible boundary beyond the articles collected in this issue, he refuses to throw out the excess with the trash of its own terminology. Taken in the context of Michel Foucault and Giorgio Agamben’s theories, extreme intoxication represents a user’s resistance to the ways that enlightenment rationality comes up against and frames individual agency.

  5. Twistors and supertwistors for exceptional field theory

    Energy Technology Data Exchange (ETDEWEB)

    Cederwall, Martin [Dept. of Fundamental Physics, Chalmers University of Technology, Gothenburg, SE 412 96 (Sweden)


    As a means of examining the section condition and its possible solutions and relaxations, we perform twistor transforms related to versions of exceptional field theory with Minkowski signature. The spinor parametrisation of the momenta naturally solves simultaneously both the mass-shell condition and the (weak) section condition. It is shown that the incidence relations for multi-particle twistors force them to share a common section, but not to be orthogonal. The supersymmetric extension contains additional scalar fermionic variables shown to be kappa-symmetry invariants. We speculate on some implications, among them a possible relation to higher spin theory.

  6. Fate and transport of metals in H2S-rich waters at a treatment wetland

    Directory of Open Access Journals (Sweden)

    Frandsen Angela K


    Full Text Available The aqueous geochemistry of Zn, Cu, Cd, Fe, Mn and As is discussed within the context of an anaerobic treatment wetland in Butte, Montana. The water being treated had a circum-neutral pH with high concentrations of trace metals and sulfate. Reducing conditions in the wetland substrate promoted bacterial sulfate reduction (BSR and precipitation of dissolved metal as sulfide minerals. ZnS was the most common sulfide phase found, and consisted of framboidal clusters of individual spheres with diameters in the submicron range. Some of the ZnS particles passed through the subsurface flow, anaerobic cells in suspended form. The concentration of "dissolved" trace metals (passing through a 0.45 μm filter was monitored as a function of H2S concentration, and compared to predicted solubilities based on experimental studies of aqueous metal complexation with dissolved sulfide. Whereas the theoretical predictions produce "U-shaped" solubility curves as a function of H2S, the field data show a flat dependence of metal concentration on H2S. Observed metal concentrations for Zn, Cu and Cd were greater than the predicted values, particularly at low H2S concentration, whereas Mn and As were undersaturated with their respective metal sulfides. Results from this study show that water treatment facilities employing BSR have the potential to mobilize arsenic out of mineral substrates at levels that may exceed regulatory criteria. Dissolved iron was close to equilibrium saturation with amorphous FeS at the higher range of sulfide concentrations observed (>0.1 mmol H2S, but was more likely constrained by goethite at lower H2S levels. Inconsistencies between our field results and theoretical predictions may be due to several problems, including: (i a lack of understanding of the form, valence, and thermodynamic stability of poorly crystalline metal sulfide precipitates; (ii the possible influence of metal sulfide colloids imparting an erroneously high "dissolved

  7. Biogeographic congruency among bacterial communities from terrestrial sulfidic springs (United States)

    Headd, Brendan; Engel, Annette S.


    Terrestrial sulfidic springs support diverse microbial communities by serving as stable conduits for geochemically diverse and nutrient-rich subsurface waters. Microorganisms that colonize terrestrial springs likely originate from groundwater, but may also be sourced from the surface. As such, the biogeographic distribution of microbial communities inhabiting sulfidic springs should be controlled by a combination of spring geochemistry and surface and subsurface transport mechanisms, and not necessarily geographic proximity to other springs. We examined the bacterial diversity of seven springs to test the hypothesis that occurrence of taxonomically similar microbes, important to the sulfur cycle, at each spring is controlled by geochemistry. Complementary Sanger sequencing and 454 pyrosequencing of 16S rRNA genes retrieved five proteobacterial classes, and Bacteroidetes, Chlorobi, Chloroflexi, and Firmicutes phyla from all springs, which suggested the potential for a core sulfidic spring microbiome. Among the putative sulfide-oxidizing groups (Epsilonproteobacteria and Gammaproteobacteria), up to 83% of the sequences from geochemically similar springs clustered together. Abundant populations of Hydrogenimonas-like or Sulfurovum-like spp. (Epsilonproteobacteria) occurred with abundant Thiothrix and Thiofaba spp. (Gammaproteobacteria), but Arcobacter-like and Sulfurimonas spp. (Epsilonproteobacteria) occurred with less abundant gammaproteobacterial populations. These distribution patterns confirmed that geochemistry rather than biogeography regulates bacterial dominance at each spring. Potential biogeographic controls were related to paleogeologic sedimentation patterns that could control long-term microbial transport mechanisms that link surface and subsurface environments. Knowing the composition of a core sulfidic spring microbial community could provide a way to monitor diversity changes if a system is threatened by anthropogenic processes or climate change. PMID

  8. Hydrogen sulfide waste treatment by microwave plasma-chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Harkness, J.B.L.; Doctor, R.D.


    A waste-treatment process that recovers both hydrogen and sulfur from industrial acid-gas waste streams is being developed to replace the Claus technology, which recovers only sulfur. The proposed process is derived from research reported in the Soviet technical literature and uses microwave (or radio-frequency) energy to initiate plasma-chemical reactions that dissociate hydrogen sulfide into elemental hydrogen and sulfur. This process has several advantages over the current Claus-plus-tail-gas-cleanup technology, which burns the hydrogen to water. The primary advantage of the proposal process is its potential for recovering and recycling hydrogen more cheaply than the direct production of hydrogen. Since unconverted hydrogen sulfide is recycled to the plasma reactor, the plasma-chemical process has the potential for sulfur recoveries in excess of 99% without the additional complexity of the tail-gas-cleanup processes associated with the Claus technology. There may also be some environmental advantages to the plasma-chemical process, because the process purge stream would primarily be the carbon dioxide and water contained in the acid-gas waste stream. Laboratory experiments with pure hydrogen sulfide have demonstrated the ability of the process to operate at or above atmospheric pressure with an acceptable hydrogen sulfide dissociation energy. Experiments with a wide range of acid-gas compositions have demonstrated that carbon dioxide and water are compatible with the plasma-chemical dissociation process and that they do not appear to create new waste-treatment problems. However, carbon dioxide does have negative impacts on the overall process. First, it decreases the hydrogen production, and second, it increases the hydrogen sulfide dissociation energy.

  9. Biogeographic Congruency among Bacterial Communities from Terrestrial Sulfidic Springs

    Directory of Open Access Journals (Sweden)

    Brendan eHeadd


    Full Text Available Terrestrial sulfidic springs support diverse microbial communities by serving as stable conduits for geochemically diverse and nutrient-rich subsurface waters. Microorganisms that colonize terrestrial springs likely originate from groundwater, but may also be sourced from the surface. As such, the biogeographic distribution of microbial communities inhabiting sulfidic springs should be controlled by a combination of spring geochemistry and surface and subsurface transport mechanisms, and not necessarily geographic proximity to other springs. We examined the bacterial diversity of seven springs to test the hypothesis that occurrence of taxonomically similar microbes, important to the sulfur cycle, at each spring is controlled by geochemistry. Complementary Sanger sequencing and 454 pyrosequencing of 16S rRNA genes retrieved five proteobacterial classes, and Bacteroidetes, Chlorobi, Chloroflexi, and Firmicutes phyla from all springs, which suggested the potential for a core sulfidic spring microbiome. Among the putative sulfide-oxidizing groups (Epsilonproteobacteria and Gammaproteobacteria, up to 83% of the sequences from geochemically similar springs clustered together. Abundant populations of Hydrogenimonas-like or Sulfurovum-like spp. (Epsilonproteobacteria occurred with abundant Thiothrix and Thiofaba spp. (Gammaproteobacteria, but Arcobacter-like and Sulfurimonas spp. (Epsilonproteobacteria occurred with less abundant gammaproteobacterial populations. These distribution patterns confirmed that geochemistry rather than biogeography regulates bacterial dominance at each spring. Potential biogeographic controls were related to paleogeologic sedimentation patterns that could control long-term microbial transport mechanisms that link surface and subsurface environments. Knowing the composition of a core sulfidic spring microbial community could provide a way to monitor diversity changes if a system is threatened by anthropogenic processes or

  10. Metal transformation as a strategy for bacterial detoxification of heavy metals. (United States)

    Essa, Ashraf M M; Al Abboud, Mohamed A; Khatib, Sayeed I


    Microorganisms can modify the chemical and physical characters of metals leading to an alteration in their speciation, mobility, and toxicity. Aqueous heavy metals solutions (Hg, Cd, Pb, Ag, Cu, and Zn) were treated with the volatile metabolic products (VMPs) of Escherichia coli Z3 for 24 h using aerobic bioreactor. The effect of the metals treated with VMPs in comparison to the untreated metals on the growth of E. coli S1 and Staphylococcus aureus S2 (local isolates) was examined. Moreover, the toxic properties of the treated and untreated metals were monitored using minimum inhibitory concentration assay. A marked reduction of the treated metals toxicity was recorded in comparison to the untreated metals. Scanning electron microscopy and energy dispersive X-ray analysis revealed the formation of metal particles in the treated metal solutions. In addition to heavy metals at variable ratios, these particles consisted of carbon, oxygen, sulfur, nitrogen elements. The inhibition of metal toxicity was attributed to the existence of ammonia, hydrogen sulfide, and carbon dioxide in the VMPs of E. coli Z3 culture that might responsible for the transformation of soluble metal ions into metal complexes. This study clarified the capability of E. coli Z3 for indirect detoxification of heavy metals via the immobilization of metal ions into biologically unavailable species. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Exceptional quantum geometry and particle physics

    Directory of Open Access Journals (Sweden)

    Michel Dubois-Violette


    Full Text Available Based on an interpretation of the quark–lepton symmetry in terms of the unimodularity of the color group SU(3 and on the existence of 3 generations, we develop an argumentation suggesting that the “finite quantum space” corresponding to the exceptional real Jordan algebra of dimension 27 (the Euclidean Albert algebra is relevant for the description of internal spaces in the theory of particles. In particular, the triality which corresponds to the 3 off-diagonal octonionic elements of the exceptional algebra is associated to the 3 generations of the Standard Model while the representation of the octonions as a complex 4-dimensional space C⊕C3 is associated to the quark–lepton symmetry (one complex for the lepton and 3 for the corresponding quark. More generally it is suggested that the replacement of the algebra of real functions on spacetime by the algebra of functions on spacetime with values in a finite-dimensional Euclidean Jordan algebra which plays the role of “the algebra of real functions” on the corresponding almost classical quantum spacetime is relevant in particle physics. This leads us to study the theory of Jordan modules and to develop the differential calculus over Jordan algebras (i.e. to introduce the appropriate notion of differential forms. We formulate the corresponding definition of connections on Jordan modules.

  12. Pyrite formation and mineral transformation pathways upon sulfidation of ferric hydroxides depend on mineral type and sulfide concentration

    NARCIS (Netherlands)

    Peiffer, Stefan; Behrends, Thilo; Hellige, Katrin; Larese-Casanova, Philip; Wan, Moli; Pollok, Kilian


    The reaction of ferric (hydr)oxides with dissolved sulfide does not lead to the instantaneous production of thermodynamically stable products but can induce a variety of mineral transformations including the formation of metastable intermediates. The importance of the various transformation pathways

  13. The mechanism of the catalytic oxidation of hydrogen sulfide: II. Kinetics and mechanism of hydrogen sulfide oxidation catalyzed by sulfur

    NARCIS (Netherlands)

    Steijns, M.; Derks, F.; Verloop, A.; Mars, P.


    The kinetics of the catalytic oxidation of hydrogen sulfide by molecular oxygen have been studied in the temperature range 20–250 °C. The primary reaction product is sulfur which may undergo further oxidation to SO2 at temperatures above 200 °C. From the kinetics of this autocatalytic reaction we

  14. Reliability of Electrochemical Techniques for Determining Corrosion Rates on Carbon Steel in Sulfide Media

    DEFF Research Database (Denmark)

    Hilbert, Lisbeth Rischel; Hemmingsen, T.; Nielsen, Lars Vendelbo


    Effects of film formation on carbon steel in hydrogen sulfide (H2S) media may corrupt corrosion rate monitoring by electrochemical techniques. Electrochemical data from H2S solutions, biological sulfide media, and natural sulfide containing geothermal water have been collected, and the process of...... techniques like electrical resistance or mass loss should be used instead.......Effects of film formation on carbon steel in hydrogen sulfide (H2S) media may corrupt corrosion rate monitoring by electrochemical techniques. Electrochemical data from H2S solutions, biological sulfide media, and natural sulfide containing geothermal water have been collected, and the process...... if the biofilm in combination with ferrous sulfide corrosion products cover the steel surface. Corrosion rates can be overestimated by a factor of 10 to 100 with electrochemical techniques - both by linear polarization resistance (LPR) and electrochemicel impedance spectroscopy (EIS). Oxygen entering the system...

  15. Hydrogen sulfide and resolution of acute inflammation: A comparative study utilizing a novel fluorescent probe. (United States)

    Dufton, Neil; Natividad, Jane; Verdu, Elena F; Wallace, John L


    Hydrogen sulfide is an essential gasotransmitter associated with numerous pathologies. We assert that hydrogen sulfide plays an important role in regulating macrophage function in response to subsequent inflammatory stimuli, promoting clearance of leukocyte infiltrate and reducing TNF-α levels in vivo following zymosan-challenge. We describe two distinct methods of measuring leukocyte hydrogen sulfide synthesis; methylene blue formation following zinc acetate capture and a novel fluorescent sulfidefluor probe. Comparison of these methods, using pharmacological tools, revealed they were complimentary in vitro and in vivo. We demonstrate the application of sulfidefluor probe to spectrofluorimetry, flow cytometry and whole animal imaging, to monitor the regulation of hydrogen sulfide synthesis in vivo during dynamic inflammatory processes. Both methodologies revealed that granulocyte infiltration negatively affects hydrogen sulfide synthesis. Our report offers an insight into the profile of hydrogen sulfide synthesis during inflammation and highlight opportunities raised by the development of novel fluorescent hydrogen sulfide probes.

  16. Blood parameters and metabolites in the teleost fish Colossoma macropomum exposed to sulfide or hypoxia. (United States)

    Affonso, E G; Polez, V L P; Corrêa, C F; Mazon, A F; Araújo, M R R; Moraes, G; Rantin, F T


    Juvenile tambaqui, Colossoma macropomum, were exposed to sulfide and hypoxia for 12, 24, 48 and 96 h. Hemoglobin concentrations, red blood cell counts, and mean cell hemoglobin, were higher at 12 h in fish exposed to hypoxia. However, control fish and those exposed to sulfide and hypoxia had lower red blood cell count, hemoglobin concentration and hematocrit at 96 h. Methemoglobin was higher than in the controls, probably due to the hypoxemia induced by these stressors. Sulfhemoglobin was not detected in significant amounts in the blood of fish exposed to sulfide (in vivo), yet hemoglobin converted into sulfhemoglobin at 1-15 mM sulfide in vitro. Anaerobic metabolism seemed to be an important mechanism for adapting to sulfide exposure and blood pH returned to control values after 24 h of sulfide, preventing acidosis. The high sulfide tolerance in tambaqui is associated with its high tolerance to hypoxia.

  17. Photocatalytic degradation of 2-phenethyl-2-chloroethyl sulfide in liquid and gas phases. (United States)

    Vorontsov, Alexandre V; Panchenko, Alexander A; Savinov, Evgueni N; Lion, Claude; Smirniotis, Panagiotis G


    This work explores the ability of photocatalysis to decontaminate water and air from chemical warfare agent mustard using its simulant 2-phenethyl 2-chloroethyl sulfide (PECES). PECES like mustard slowly dissolves in water with hydrolysis, forming 2-phenethyl 2-hydroxyethyl sulfide (PEHES). Irradiation of TiO2 suspension containing PECES with the unfiltered light of a mercury lamp (lambda > or = 254 nm) decomposed all PECES mostly via photolysis. Reaction under filtered light (lambda > 300 nm) proceeds mainly photocatalytically and requires longer time. Sulfur from starting PECES is completely transformed into sulfuric acid at the end of the reaction. Detected volatile, nonvolatile, surface products, and the suggested scheme of degradation are reported. The main volatile products are styrene and benzaldehyde, nonvolatile--hydroxylated PEHES, surface--2-phenethyl disulfide. Photolysis of PECES produced the same set of volatile products as photocatalysis. Photocatalytic degradation of gaseous PECES in air results in its mineralization but is accompanied by TiO2 deactivation. The highest rate of mineralization with minimum deactivation was observed at about room temperature and a water concentration of 27,500 ppm. No gaseous products except CO2 were detected. The main extracted surface product was styrene. It was concluded that PECES photocatalytic degradation proceeds mainly via C-S bond cleavage and further oxidation of the products. Hydrolysis of the C-S bond was detected only in gas-phase photocatalytic degradation. The quantum efficiency of gas-phase degradation (0.28%) was much higher than that of liquid-phase degradation (0.008%). The results demonstrate the ability of photocatalysis to decontaminate an aqueous and especially an air environment

  18. Geochemical and mineralogical characterization of a neutral, low-sulfide/high-carbonate tailings impoundment, Markušovce, eastern Slovakia. (United States)

    Hiller, Edgar; Petrák, Marián; Tóth, Roman; Lalinská-Voleková, Bronislava; Jurkovič, L'ubomír; Kučerová, Gabriela; Radková, Anežka; Sottník, Peter; Vozár, Jaroslav


    Tailings deposits generated from mining activities represent a potential risk for the aquatic environment through the release of potentially toxic metals and metalloids occurring in a variety of minerals present in the tailings. Physicochemical and mineralogical characteristics of tailings such as total concentrations of chemical elements, pH, ratio of acid-producing to acid-neutralizing minerals, and primary and secondary mineral phases are very important factors that control the actual release of potentially toxic metals and metalloids from the tailings to the environment. The aims of this study are the determination of geochemical and mineralogical characteristics of tailings deposited in voluminous impoundment situated near the village of Markušovce (eastern Slovakia) and identification of the processes controlling the mobility of selected toxic metals (Cu, Hg) and metalloids (As, Sb). The studied tailings have unique features in comparison with the other tailings investigated previously because of the specific mineral assemblage primarily consisting of barite, siderite, quartz, and minor sulfides. To meet the aims, samples of the tailings were collected from 3 boreholes and 15 excavated pits and subjected to bulk geochemical analyses (i.e., determination of chemical composition, pH, Eh, acid generation, and neutralization potentials) combined with detailed mineralogical characterization using optical microscopy, X-ray diffraction (XRD), electron microprobe analysis (EMPA), and micro-X-ray diffraction (μ-XRD). Additionally, the geochemical and mineralogical factors controlling the transfer of potentially toxic elements from tailings to waters were also determined using short-term batch test (European norm EN 12457), sampling of drainage waters and speciation-equilibrium calculations performed with PHREEQC. The tailings mineral assemblage consists of siderite, barite, quartz, and dolomite. Sulfide minerals constitute only a minor proportion of the tailings

  19. Photocatalytic Activities of Copper Doped Cadmium Sulfide Microspheres Prepared by a Facile Ultrasonic Spray-Pyrolysis Method

    Directory of Open Access Journals (Sweden)

    Jinzhan Su


    Full Text Available Ultrasonic spray pyrolysis is a superior method for preparing and synthesizing spherical particles of metal oxide or sulfide semiconductors. Cadmium sulfide (CdS photocatalysts with different sizes and doped-CdS with different dopants and doping levels have been synthesized to study their properties of photocatalytic hydrogen production from water. The CdS photocatalysts were characterized with scanning electron microscopy (SEM, X-ray fluorescence-spectrometry (XRF, UV-Vis absorption spectra and X-ray diffraction (XRD to study their morphological and optical properties. The sizes of the prepared CdS particles were found to be proportional to the concentration of the metal nitrates in the solution. The CdS photocatalyst with smaller size showed a better photocatalytic activity. In addition, Cu doped CdS were also deposited and their photocatalytic activities were also investigated. Decreased bandgaps of CdS synthesized with this method were found and could be due to high density surface defects originated from Cd vacancies. Incorporating the Cu elements increased the bandgap by taking the position of Cd vacancies and reducing the surface defect states. The optimal Cu-doped level was found to be 0.5 mol % toward hydrogen evolution from aqueous media in the presence of sacrificial electron donors (Na2S and Na2SO3 at a pH of 13.2. This study demonstrated that ultrasonic spray pyrolysis is a feasible approach for large-scale photocatalyst synthesis and corresponding doping modification.

  20. The role of Zr and Nb in oxidation/sulfidation behavior of Fe-Cr-Ni alloys

    Energy Technology Data Exchange (ETDEWEB)

    Natesan, K. (Argonne National Lab., IL (USA)); Baxter, D.J. (Argonne National Lab., IL (USA) INCO Alloy Ltd., Hereford, England (UK))


    05Structural Fe-Cr-Ni alloys may undergo rapid degradation at elevated temperatures unless protective surface oxide scales are formed and maintained. The ability of alloys to resist rapid degradation strongly depends on their Cr content and the chemistry of the exposure environment. Normally, 20 wt % Cr is required for service at temperatures up to 1000{degree}C; the presence of sulfur, however, inhibits formation of a protective surface oxide scale. The oxidation and sulfidation behavior of Fe-Cr-Ni alloys is examined over a wide temperature range (650 to 1000{degree}C), with particular emphasis on the effects of alloy Cr content and the radiation of reactive elements such as Nb and Zr. Both Nb and Zr are shown to promote protective oxidation behavior on the 12 wt % Cr alloy in oxidizing environments and to suppress sulfidation in mixed oxygen/sulfur environments. Additions of Nb and Zr at 3 wt % level resulted in stabilization of Cr{sub 2}O{sub 3} scale and led to a barrier layer of Nb- or Zr-rich oxide at the scale/metal interface, which acted to minimize the transport of base metal cations across the scale. Oxide scales were preformed in sulfur-free environments and subsequently exposed to oxygen/sulfur mixed-gas atmospheres. Preformed scales were found to delay the onset of breakaway corrosion. Corrosions test results obtained under isothermal and thermal cycling conditions are presented. 58 refs., 55 figs., 8 tabs.

  1. Unidirectional reflectionless light propagation at exceptional points

    Directory of Open Access Journals (Sweden)

    Huang Yin


    Full Text Available In this paper, we provide a comprehensive review of unidirectional reflectionless light propagation in photonic devices at exceptional points (EPs. EPs, which are branch point singularities of the spectrum, associated with the coalescence of both eigenvalues and corresponding eigenstates, lead to interesting phenomena, such as level repulsion and crossing, bifurcation, chaos, and phase transitions in open quantum systems described by non-Hermitian Hamiltonians. Recently, it was shown that judiciously designed photonic synthetic matters could mimic the complex non-Hermitian Hamiltonians in quantum mechanics and realize unidirectional reflection at optical EPs. Unidirectional reflectionlessness is of great interest for optical invisibility. Achieving unidirectional reflectionless light propagation could also be potentially important for developing optical devices, such as optical network analyzers. Here, we discuss unidirectional reflectionlessness at EPs in both parity-time (PT-symmetric and non-PT-symmetric optical systems. We also provide an outlook on possible future directions in this field.

  2. Leibniz algebroids, twistings and exceptional generalized geometry (United States)

    Baraglia, D.


    We investigate a class of Leibniz algebroids which are invariant under diffeomorphisms and symmetries involving collections of closed forms. Under appropriate assumptions we arrive at a classification which in particular gives a construction starting from graded Lie algebras. In this case the Leibniz bracket is a derived bracket and there are higher derived brackets resulting in an L∞-structure. The algebroids can be twisted by a non-abelian cohomology class and we prove that the twisting class is described by a Maurer-Cartan equation. For compact manifolds we construct a Kuranishi moduli space of this equation which is shown to be affine algebraic. We explain how these results are related to exceptional generalized geometry.

  3. Is There Muslim Exceptionalism in Democracy Research?

    DEFF Research Database (Denmark)

    Hariri, Jacob Gerner

    to and between the 16th and 18th centuries are relatively less democratic today. The negative effect of early statehood on current levels of democracy is mediated by European colonization and settlement: Europeans were less likely to colonize and settle in territories with more developed state institutions......, also, to alternative theories of the causes and correlates of democracy. This paper presents evidence against the notion of Muslim exceptionalism in democracy research. Thus, outside the European continent, territories that were governed earlier and more consistently by state organizations up...... and were therefore less likely to bring nascent legalistic and representative institutions to these territories. When we remove the autocratic legacy of early statehood and the influence of European settlement, there is nothing signicantly negative about the degree of democracy in Muslim-majority countries....

  4. Projective Hilbert space structures at exceptional points (United States)

    Günther, Uwe; Rotter, Ingrid; Samsonov, Boris F.


    A non-Hermitian complex symmetric 2 × 2-matrix toy model is used to study projective Hilbert space structures in the vicinity of exceptional points (EPs). The bi-orthogonal eigenvectors of a diagonalizable matrix are Puiseux-expanded in terms of the root vectors at the EP. It is shown that the apparent contradiction between the two incompatible normalization conditions with finite and singular behaviour in the EP-limit can be resolved by projectively extending the original Hilbert space. The complementary normalization conditions correspond then to two different affine charts of this enlarged projective Hilbert space. Geometric phase and phase-jump behaviour are analysed, and the usefulness of the phase rigidity as measure for the distance to EP configurations is demonstrated. Finally, EP-related aspects of {\\cal P}{\\cal T} -symmetrically extended quantum mechanics are discussed and a conjecture concerning the quantum brachistochrone problem is formulated.

  5. Projective Hilbert space structures at exceptional points

    Energy Technology Data Exchange (ETDEWEB)

    Guenther, Uwe [Research Center Dresden-Rossendorf, PO 510119, D-01314 Dresden (Germany); Rotter, Ingrid [Max Planck Institute for the Physics of Complex Systems, D-01187 Dresden (Germany); Samsonov, Boris F [Physics Department, Tomsk State University, 36 Lenin Avenue, 634050 Tomsk (Russian Federation)


    A non-Hermitian complex symmetric 2 x 2-matrix toy model is used to study projective Hilbert space structures in the vicinity of exceptional points (EPs). The bi-orthogonal eigenvectors of a diagonalizable matrix are Puiseux-expanded in terms of the root vectors at the EP. It is shown that the apparent contradiction between the two incompatible normalization conditions with finite and singular behaviour in the EP-limit can be resolved by projectively extending the original Hilbert space. The complementary normalization conditions correspond then to two different affine charts of this enlarged projective Hilbert space. Geometric phase and phase-jump behaviour are analysed, and the usefulness of the phase rigidity as measure for the distance to EP configurations is demonstrated. Finally, EP-related aspects of PT-symmetrically extended quantum mechanics are discussed and a conjecture concerning the quantum brachistochrone problem is formulated.

  6. Transporting "exceptional cargo" on the CERN sites

    CERN Document Server

    EN Department


    When the Transport Service is managing "exceptional cargo", the driver and the escort are often in charge of an operation involving equipment worth many hundred thousand francs. Equipment that may well be irreplaceable for a facility or an experiment.   The members of the Transport Service who carry out these tasks are very professional and are – needless to say – highly concentrated on the job. They count on your understanding and support in the traffic on site. Their convoys are – for good reasons – moving slowly. Kindly do not overtake, do not cut in in front of them and do not drive too closely. Respect the escort and do not position yourself between the truck and the escort vehicles. The EN department counts on your courtesy on the road.  

  7. Metal dispersion resulting from mining activities in coastal environments: A pathways approach (United States)

    Koski, Randolph A.


    Acid rock drainage (ARD) and disposal of tailings that result from mining activities impact coastal areas in many countries. The dispersion of metals from mine sites that are both proximal and distal to the shoreline can be examined using a pathways approach in which physical and chemical processes guide metal transport in the continuum from sources (sulfide minerals) to bioreceptors (marine biota). Large amounts of metals can be physically transported to the coastal environment by intentional or accidental release of sulfide-bearing mine tailings. Oxidation of sulfide minerals results in elevated dissolved metal concentrations in surface waters on land (producing ARD) and in pore waters of submarine tailings. Changes in pH, adsorption by insoluble secondary minerals (e.g., Fe oxyhydroxides), and precipitation of soluble salts (e.g., sulfates) affect dissolved metal fluxes. Evidence for bioaccumulation includes anomalous metal concentrations in bivalves and reef corals, and overlapping Pb isotope ratios for sulfides, shellfish, and seaweed in contaminated environments. Although bioavailability and potential toxicity are, to a large extent, functions of metal speciation, specific uptake pathways, such as adsorption from solution and ingestion of particles, also play important roles. Recent emphasis on broader ecological impacts has led to complementary methodologies involving laboratory toxicity tests and field studies of species richness and diversity.

  8. Spatial and seasonal variation in heavy metals in interstitial water of salt marsh soils

    Energy Technology Data Exchange (ETDEWEB)

    Otero, X.L.; Macias, Felipe


    Soil colonization by plants affected spatial and seasonal variation in heavy metals. - The composition of interstitial water collected from a salt marsh in NW Spain showed clear seasonal and spatial variations associated with redox cycles of Fe and S. In the summer, salinity increased in all soils as a consequence of the increase in evapotranspiration. The pH and concentrations of heavy metals also differed with season, but not all environments showed the same variations. Soils not colonized by plants had the highest pH and lowest heavy metal concentrations in the summer. These results support the idea that higher temperatures lead to an increase in the activity of sulfate-reducing bacteria, which in turn leads to an increase in alkalinity and concentration of sulfides in the water. Trace metals tend to precipitate with sulfides under these conditions and are removed from the interstitial water. In contrast, in the soils colonized by Spartina maritima, the oxidation of metal sulfides during the summer led to a decrease in pH and an increase in the metal concentrations in the interstitial water. The results obtained concur with those found for seasonal variations in metal sulfides in soils from the same salt marsh.

  9. Mesoporous CuO–ZnO binary metal oxide nanocomposite for decontamination of sulfur mustard

    Energy Technology Data Exchange (ETDEWEB)

    Praveen Kumar, J.; Prasad, G.K., E-mail:; Ramacharyulu, P.V.R.K.; Garg, P.; Ganesan, K.


    Mesoporous CuO–ZnO binary metal oxide nanocomposites were studied as sorbent decontaminants against sulfur mustard, a well known chemical warfare agent. They were prepared by precipitation pyrolysis method and characterized by means of X-ray diffraction, transmission electron microscopy, nitrogen adsorption, Fourier transform infrared spectroscopy techniques. Obtained data indicated the presence of mesopores with diameter ranging from 2 to 80 nm and the materials exhibited relatively high surface area 86 m{sup 2} g{sup −1} when compared to the individual metal oxide nanoparticles. Reactive sites of mesoporous CuO–ZnO binary metal oxide nanocomposites were studied by infrared spectroscopy technique using pyridine as a probe molecule. These materials demonstrated superior decontamination properties against sulfur mustard when compared to single component metal oxides and decontaminated it to divinyl sulfide, chloroethyl vinyl sulfide, hemisulfur mustard, etc. - Graphical abstract: Mesoporous CuO–ZnO binary metal oxide nanocomposites were studied as sorbent decontaminants against sulfur mustard, a well known chemical warfare agent. These materials demonstrated superior decontamination properties against sulfur mustard and decontaminated it to divinyl sulfide, chloroethyl vinyl sulfide, hemisulfur mustard, etc. - Highlights: • Preparation of mesoporous CuO–ZnO binary metal oxide nanocomposite. • CuO–ZnO with better surface area was synthesized by precipitation pyrolysis. • Decontamination of HD using mesoporous CuO–ZnO binary metal oxide nanocomposite. • HD decontaminated by elimination and hydrolysis reactions.

  10. Mesoporous CuO–ZnO binary metal oxide nanocomposite for decontamination of sulfur mustard

    International Nuclear Information System (INIS)

    Praveen Kumar, J.; Prasad, G.K.; Ramacharyulu, P.V.R.K.; Garg, P.; Ganesan, K.


    Mesoporous CuO–ZnO binary metal oxide nanocomposites were studied as sorbent decontaminants against sulfur mustard, a well known chemical warfare agent. They were prepared by precipitation pyrolysis method and characterized by means of X-ray diffraction, transmission electron microscopy, nitrogen adsorption, Fourier transform infrared spectroscopy techniques. Obtained data indicated the presence of mesopores with diameter ranging from 2 to 80 nm and the materials exhibited relatively high surface area 86 m 2 g −1 when compared to the individual metal oxide nanoparticles. Reactive sites of mesoporous CuO–ZnO binary metal oxide nanocomposites were studied by infrared spectroscopy technique using pyridine as a probe molecule. These materials demonstrated superior decontamination properties against sulfur mustard when compared to single component metal oxides and decontaminated it to divinyl sulfide, chloroethyl vinyl sulfide, hemisulfur mustard, etc. - Graphical abstract: Mesoporous CuO–ZnO binary metal oxide nanocomposites were studied as sorbent decontaminants against sulfur mustard, a well known chemical warfare agent. These materials demonstrated superior decontamination properties against sulfur mustard and decontaminated it to divinyl sulfide, chloroethyl vinyl sulfide, hemisulfur mustard, etc. - Highlights: • Preparation of mesoporous CuO–ZnO binary metal oxide nanocomposite. • CuO–ZnO with better surface area was synthesized by precipitation pyrolysis. • Decontamination of HD using mesoporous CuO–ZnO binary metal oxide nanocomposite. • HD decontaminated by elimination and hydrolysis reactions

  11. Evaluation of protective effect of deposits formed by naphthenic corrosion and sulfidation on carbon steel and steel 5Cr-0.5Mo exposed in atmospheric distillation fractions

    Directory of Open Access Journals (Sweden)

    Gloria Duarte


    Full Text Available Refining of so-called opportunity crude oils with a high level of naphthenic acids and sulfur compounds has been increasing interest due to limited availability of light crude oils, however, considerable corrosive effects in the processing to high temperature on pipes and distillation towers mainly by the attack of naphthenic acids and sulfur compounds; sulfur compounds could be corrosive or can reduce the attack of naphthenic acids due to the formation of sulfides layers on the metal surface. In this work was evaluated the performance of deposits formed on the surface of carbon steel AISI SAE 1020 and 5% Cr-0.5% Mo steel exposed in crude oil fractions obtained from atmospheric distillation tower. For this, gravimetric tests were performed in dynamic autoclave using metal samples pre-treated in a crude oil fraction obtained from the atmospheric distillation tower of the Crude Distillation Unit (CDU # 1 in order to form layers of sulfides on the surface of the two materials and subsequently to expose pre-treated and non-pretreated samples in two different crude oil fractions obtained from atmospheric distillation tower of Crude Distillation Unit (CDU # 2. The evaluation showed that the samples pretreated decreased tendency to corrosion by naphthenic acids and sulfidation compared to untreated samples.

  12. Metal Nanoshells for Plasmonically Enhanced Solar to Fuel Photocatalytic Conversion (United States)


    facilitate charge separation of photo-excited carriers. Zinc indium sulfide (ZIS), a visible light- active photocatalyst, was used as the photocatalytic matrix...then coated with a thin layer of silica (SiO2), followed by a zinc indium sulfide (ZnIn2S4; ZIS) semiconductor shell. The blended-metal GS-NS cores...of pH values (ACS Appl. Mater. Interfaces 2013, 5, 2479). Such an improvement in stability not only offers alternative routes to the synthesis of

  13. A revised oxygen barometry in sulfide-saturated magmas and application to the Permian magmatic Ni-Cu deposits in the southern Central Asian Orogenic Belt (United States)

    Mao, Ya-Jing; Qin, Ke-Zhang; Barnes, Stephen J.; Ferraina, Clément; Iacono-Marziano, Giada; Verrall, Michael; Tang, Dongmei; Xue, Shengchao


    Oxygen fugacity is a key parameter in controlling the petrogenesis of mafic-ultramafic rocks and their associated sulfide mineralization, especially in convergent settings. This study uses new and previously published experimental data on olivine-sulfide pairs to reparameterize an expression for oxygen barometry using the distribution coefficient K D FeNi for Fe-Ni exchange between olivine and sulfide. We derive a new expression, ΔQFM = (9.775 + 0.416 • C Ni - K D FeNi)/4.308, where ΔQFM denotes divergence from the fayalite-magnetite-quartz buffer. The revised oxygen barometry has been applied to the Permian magmatic Ni-Cu deposits in the Central Asian Orogenic Belt, NW China. The Ni-Cu deposits in the East Tianshan—North Tianshan, Central Tianshan, and Beishan—are considered as a single mineral system, whereas the spatially separated deposits in the East Junggar are considered as a separate system. The deposit of the East Tianshan group exhibits a large range of oxygen fugacity (QFM - 2 to QFM + 1) and Ni tenor (metal concentration in pure sulfide, 5 to 16 wt%). The Poyi and Huangshannan deposits contain high-Ni tenor sulfides, varying from 12 to 16 wt%. The relatively high Fo values (> 85 mol%) and Ni contents (> 2000 ppm) in olivine of these deposits indicate that the high-Ni tenor sulfides were segregated from less differentiated high-Ni magmas that also had relatively high oxygen fugacity ( QFM + 1). The remaining Ni-Cu deposits in the East Tianshan—the Huangshandong, Huangshanxi, Hulu, Tulaergen, Tudun, and Xiangshanzhong deposits—have intermediate Ni tenors (5-8 wt%). These sulfides correspond to intermediate Fo values (80-84 mol%) and Ni contents (700-1400 ppm) in the coexisting olivine, illustrating that they were segregated from magmas with lower Ni contents thought to be the result of a large amount (15-20%) of olivine fractionation at depth. These magmas are more reduced (- 2 fugacity and Ni tenor in the Permian Ni-Cu deposits in the Central

  14. Tethered Transition Metals Promoted Photocatalytic System for Efficient Hydrogen Evolutions

    KAUST Repository

    Takanabe, Kazuhiro


    The present invention is directed, at least in part, to a process for improving the efficiency of a photocatalyst (a semiconductor photocatalyst) by tethering (depositing) a metal (e.g., metal ions of a late transition metal, such as nickel) to the semiconductor (photocatalyst) surface through the use of an organic ligand. More specifically, 1,2-ethanedithiol (EDT) functions as an excellent molecular linker (organic ligand) to attach a transition metal complex (e.g., nickel (Ni.sup.2+ ions)) to the semiconductor surface, which can be in the form of a cadmium sulfide surface. The photocatalyst has particular utility in generating hydrogen from H.sub.2S.

  15. Cadmium sulfide/copper ternary heterojunction cell research. Final report, April 1, 1980-August 25, 1982

    Energy Technology Data Exchange (ETDEWEB)

    Mickelsen, R. A.; Chen, W. S.


    The properties of polycrystalline, thin-film CuInSe/sub 2//CdS and CuInSe/sub 2//Zn/sub x/Cd/sub 1-x/S solar cells prepared by vacuum-evaporation techniques onto metallized-alumina substrates are described. An efficiency of 10.6% for a 1 cm/sup 2/ area cell and 8.3% for an 8 cm/sup 2/ cell when tested under simulated AM1 illumination is reported. The mixed-sulfide cells are described as exhibiting increased open-circuit voltages, slightly higher short-circuit currents, and improved efficiencies. Mixed-sulfide film preparation by evaporation of CdS and ZnS powders from a single source and from two sources is discussed with preference given to the later technique. Selenide-film preparation in a planetary or rotating substrate vacuum-deposition apparatus is described. A 1 cm/sup 2/ area cell without AR-coating produced by the planetary approach is reported to demonstrate a 7.5% efficiency. The results of cell heat-treatment studies showing a strong environmental dependence are presented and indicate the desirability of an oxygen-containing atmosphere. An automatic, computer-controlled, cell-measurement system for I-V, C-V, and spectral-response analysis is described. The results of the cell-analysis and cell-modeling studies on both the plain CdS and mixed Zn/sub x/Cd/sub 1-x/S thin-film devices are presented. Finally, data obtained from constant illumination and elevated temperature life-tests on the thin-film cells showing little degradation after 9300 hours is reported.

  16. 46 CFR 531.10 - Excepted and exempted commodities. (United States)


    ... 46 Shipping 9 2010-10-01 2010-10-01 false Excepted and exempted commodities. 531.10 Section 531.10... ARRANGEMENTS Exceptions and Implementation § 531.10 Excepted and exempted commodities. (a) Statutory exceptions... or paper waste. (b) Commission exemptions. The following commodities and/or services are not subject...

  17. A lithium-ion sulfur battery based on a carbon-coated lithium-sulfide cathode and an electrodeposited silicon-based anode. (United States)

    Agostini, Marco; Hassoun, Jusef; Liu, Jun; Jeong, Moongook; Nara, Hiroki; Momma, Toshiyuki; Osaka, Tetsuya; Sun, Yang-Kook; Scrosati, Bruno


    In this paper, we report a lithium-ion battery employing a lithium sulfide cathode and a silicon-based anode. The high capacity of the silicon anode and the high efficiency and cycling rate of the lithium sulfide cathode allowed optimal full cell balance. We show in fact that the battery operates with a very stable capacity of about 280 mAh g(-1) at an average voltage of 1.4 V. To the best of our knowledge, this battery is one of the rare examples of lithium-metal-free sulfur battery. Considering the high theoretical capacity of the employed electrodes, we believe that the battery here reported may be of potential interest as high-energy, safe, and low-cost power source for electric vehicles.

  18. The comparison of strata-bound massive sulfide deposits using the fuzzy-linguistic diagnosis of the Zlaté Hory deposits, Czechoslovakia, as an example (United States)

    Patočka, F.; Vrba, J.


    The Zlaté Hory ore deposits — as an example of volcanogenic, strata-bound, massive, base-metal sulfides occurring in the Devonian formations of the Jeseníky Mts. — are compared with distinctive Phanerozoic types representing this type of ore deposit, i.e., with Kuroko-type, Rosebery-type, Besshi-type and Cyprus-type deposits. The results of comparison performed with fuzzy-linguistic diagnosis indicate close resemblance of the Zlaté Hory deposits to Rosebery-type massive sulfides with regard to primary features; however, individual features point to certain original similarity with Kuroko-type deposits, too. The metamorphic history of the ore deposits studied was similar to that of the Rosebery and Besshi types.

  19. Influence of pipe material and surfaces on sulfide related odor and corrosion in sewers. (United States)

    Nielsen, Asbjørn Haaning; Vollertsen, Jes; Jensen, Henriette Stokbro; Wium-Andersen, Tove; Hvitved-Jacobsen, Thorkild


    Hydrogen sulfide oxidation on sewer pipe surfaces was investigated in a pilot scale experimental setup. The experiments were aimed at replicating conditions in a gravity sewer located immediately downstream of a force main where sulfide related concrete corrosion and odor is often observed. During the experiments, hydrogen sulfide gas was injected intermittently into the headspace of partially filled concrete and plastic (PVC and HDPE) sewer pipes in concentrations of approximately 1,000 ppm(v). Between each injection, the hydrogen sulfide concentration was monitored while it decreased because of adsorption and subsequent oxidation on the pipe surfaces. The experiments showed that the rate of hydrogen sulfide oxidation was approximately two orders of magnitude faster on the concrete pipe surfaces than on the plastic pipe surfaces. Removal of the layer of reaction (corrosion) products from the concrete pipes was found to reduce the rate of hydrogen sulfide oxidation significantly. However, the rate of sulfide oxidation was restored to its background level within 10-20 days. A similar treatment had no observable effect on hydrogen sulfide removal in the plastic pipe reactors. The experimental results were used to model hydrogen sulfide oxidation under field conditions. This showed that the gas-phase hydrogen sulfide concentration in concrete sewers would typically amount to a few percent of the equilibrium concentration calculated from Henry's law. In the plastic pipe sewers, significantly higher concentrations were predicted because of the slower adsorption and oxidation kinetics on such surfaces.

  20. NiMo-sulfide supported on activated carbon to produce renewable diesel

    Directory of Open Access Journals (Sweden)

    Nancy Y Acelas


    Full Text Available Due to their weak polarity and large surface area, activated carbon supports have the potential to enhance the dispersion of metal-sulfides. It is expected that the absence of a strong metal-support interaction can result in the formation of a very active and stable Ni-Mo-S phase. In this study, catalysts with different amounts of nickel and molybdenum supported on a commercial activated carbon were prepared by a co-impregnation method and characterized by BET, XRF, and SEM techniques. The catalytic activity for hydroprocessing of Jatropha oil was evaluated in a batch reactor, and the composition of the liquid and gaseous products were determined. Results showed that gaseous products are mainly composed of high amounts of propane and small amounts of other light hydrocarbons (C1 to C5. Liquid hydrocarbon products consisted of a mixture containing mainly n-paraffins of C15-C18 and some oxygenated compounds. The catalysts with a mass fraction of 3 % Ni, 15 % Mo (Ni3Mo15/AC presented the highest selectivity toward C17-C18 hydrocarbons, with a product distribution similar to a commercial alumina-supported Ni-Mo-S catalyst.