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Sample records for vanadium oxide bronzes

  1. Sol-gel synthesis and XPS study of vanadium-hydroquinone oxide bronze films

    Energy Technology Data Exchange (ETDEWEB)

    Bondarenka, V. [Semiconductor Physics Institute, A. Gostauto 11, 01108 Vilnius (Lithuania); Vilnius Pedagogical University, Studentu 39, 08106 Vilnius (Lithuania); Tvardauskas, H.; Grebinskij, S.; Senulis, M.; Pasiskevicius, A. [Semiconductor Physics Institute, A. Gostauto 11, 01108 Vilnius (Lithuania); Volkov, V.; Zakharova, G. [Institute of Solid State Chemistry, Pervomaiskaia 91, 620219 Yekaterinburg (Russian Federation)

    2009-12-15

    A vanadium - hydroquinone oxide bronze has been synthesized by using a sol gel technology. The V{sub 2}O{sub 5} powder, hydrogen peroxide, and hydroquinone C{sub 6}H{sub 4}(OH){sub 2} were used as the starting materials to produce the bronze. At first the vanadium gel was made by the dissolving of vanadium pentoxide powder in hydrogen peroxide at 273 K. Then the solution was heated up to 350 K for the dissociation of peroxide complexes. An aqueous solution of hydroquinone was mixed with the formed gel in molar ratio 0.33:1. In this way the V{sub 2}O{sub 5{+-}}{sub {delta}}.nH{sub 2}O/HQ (HQ-hydroquinone) gel was synthesized. These gels are applied on the Ni pad and dried in an air (wet gel synthesis) or heated up to 580 K in air for 1 h for the water removal from gel (bronze production). The wet gel, as well as a bronze, was investigated by means of XPS method. Analysis of V-O region of XPS spectra shows that vanadium in both cases (wet gel and bronze) is in stable V{sup 5+} state. Oxygen in wet gel can be associated with V ions, hydroxide group and water. In bronze oxygen is connected with V and hydrogen (hydroxide). (copyright 2009 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  2. Highly Stable Aqueous Zinc-ion Storage Using Layered Calcium Vanadium Oxide Bronze Cathode

    KAUST Repository

    Xia, Chuan

    2018-02-12

    Cost-effective aqueous rechargeable batteries are attractive alternatives to non-aqueous cells for stationary grid energy storage. Among different aqueous cells, zinc-ion batteries (ZIBs), based on Zn2+ intercalation chemistry, stand out as they can employ high-capacity Zn metal as anode material. Herein, we report a layered calcium vanadium oxide bronze as cathode material for aqueous Zn batteries. For the storage of Zn2+ ions in aqueous electrolyte, we demonstrate that calcium based bronze structure can deliver a high capacity of 340 mAh g-1 at 0.2 C, good rate capability and very long cycling life (96% retention after 3000 cycles at 80 C). Further, we investigate the Zn2+ storage mechanism, and the corresponding electrochemical kinetics in this bronze cathode. Finally, we show that our Zn cell delivers an energy density of 267 Wh kg-1 at a power density of 53.4 W kg-1.

  3. Catalytic oxidations by vanadium complexes

    NARCIS (Netherlands)

    Ligtenbarg, A.G J; Hage, R.; Feringa, B.L.

    Vanadium haloperoxidases catalyse the oxidation of halides leading to halogenation of substrates or, in the absence of suitable substrates, to oxidation of hydrogen peroxide into singlet oxygen and water. Furthermore, V-haloperoxidases are capable to give enantioselective sulfoxidation under the

  4. Vanadium

    OpenAIRE

    Pourret, Olivier; Dia, Aline

    2017-01-01

    International audience; Vanadium (chemical symbol, V) is a d-block transition metal,silver in color, appearing in the first long period of the peri-odic table between titanium and chromium. Vanadium hastwo stable isotopes: 50V and 51V, with atomic abundance of0.25 % and 99.75 %, respectively. Vanadium has several oxidation forms (between 2+ and 5+). In the lithosphere, Voccurs as reducing V(III) form, whereas in oxidizing con- ditions V prevails under V(IV) form. Vanadium(II) is partic- ularl...

  5. Crystal structure determination of a new sodium vanadium bronze electrochemically formed

    Science.gov (United States)

    Safrany Renard, Marianne; Emery, Nicolas; Roginskii, Evgenii M.; Baddour-Hadjean, Rita; Pereira-Ramos, Jean-Pierre

    2017-10-01

    γ-Na0.97V2O5 is synthesized by electrochemical reduction at constant current of γ'-V2O5 in a 1 M NaClO4 propylene carbonate electrolyte. This sodium vanadium pentoxide bronze has not heretofore been prepared. The structure of this new sodium insertion compound was solved by Rietveld refinement of the X-ray diffraction data and Raman spectroscopy. It exhibits an orthorhombic layered structure type (Pnma space group) with Na ions located in the large octahedral sites of the interlayer space. The structural features of γ-Na0.97V2O5 at the long range and atomic scale are provided and compared to those of γ'-V2O5 and the lithiated analogue γ-LiV2O5. Reliable 'structure-Raman spectrum' correlations are proposed and Raman peaks characteristics of the different structural units are identified. Preliminary electrochemical experiments show a strong interest of γ-Na0.97V2O5 as rechargeable high voltage cathode for Na batteries (specific capacity of 80-125 mAh g-1 at c. a. 3.3 V vs Na+/Na).

  6. Lithium insertion in sputtered vanadium oxide film

    DEFF Research Database (Denmark)

    West, K.; Zachau-Christiansen, B.; Skaarup, S.V.

    1992-01-01

    were oxygen deficient compared to V2O5. Films prepared in pure argon were reduced to V(4) or lower. The vanadium oxide films were tested in solid-state lithium cells. Films sputtered in oxygen showed electrochemical properties similar to crystalline V2O5. The main differences are a decreased capacity...

  7. Vanadium

    Science.gov (United States)

    Kelley, Karen D.; Scott, Clinton T.; Polyak, Désirée E.; Kimball, Bryn E.; Schulz, Klaus J.; DeYoung, John H.; Seal, Robert R.; Bradley, Dwight C.

    2017-12-19

    sands, and oil shales may be important future sources.Vanadium occurs in one of four oxidation states in nature: +2, +3, +4, and +5. The V3+ ion has an octahedral radius that is almost identical to that of (Fe3+) and (Al3+) and, therefore, it substitutes in ferromagnesian minerals. During weathering, much of the vanadium may partition into newly formed clay minerals, and it either remains in the +3 valence state or oxidizes to the +4 valence state, both of which are relatively insoluble. If erosion is insignificant but chemical leaching is intense, the residual material may be enriched in vanadium, as are some bauxites and laterites. During the weathering of igneous, residual, or sedimentary rocks, some vanadium oxidizes to the +5 valence state, especially in the intensive oxidizing conditions that are characteristic of arid climates.The average contents of vanadium in the environment are as follows: soils [10 to 500 parts per million (ppm)]; streams and rivers [0.2 to 2.9 parts per billion (ppb)]; and coastal seawater (0.3 to 2.8 ppb). Concentrations of vanadium in soils (548 to 7,160 ppm) collected near vanadium mines in China, the Czech Republic, and South Africa are many times greater than natural concentrations in soils. Additionally, if deposits contain sulfide minerals such as chalcocite, pyrite, and sphalerite, high levels of acidity may be present if sulfide dissolution is not balanced by the presence of acid-neutralizing carbonate minerals. Some of the vanadium-bearing deposit types, particularly some SSV and black-shale deposits, contain appreciable amounts of carbonate minerals, which lowers the acid-generation potential.Vanadium is a micronutrient with a postulated requirement for humans of less than 10 micrograms per day, which can be met through dietary intake. Primary and secondary drinking water regulations for vanadium are not currently in place in the United States. Vanadium toxicity is thought to result from an intake of more than 10 to 20 milligrams

  8. Partial Oxidation of n-Pentane over Vanadium Phosphorus Oxide ...

    African Journals Online (AJOL)

    The selective oxidation of n-pentane to value-added products, maleic anhydride or phthallic anhydride by vanadium phosphorus oxide loaded on hydroxyapatites as catalysts and oxygen as oxidant was investigated. Hydroxyapatite (HAp) and cobalthydroxyapatite (Co-HAp) were prepared by the co-precipitation method ...

  9. Modified lithium vanadium oxide electrode materials products and methods

    Science.gov (United States)

    Thackeray, Michael M.; Kahaian, Arthur J.; Visser, Donald R.; Dees, Dennis W.; Benedek, Roy

    1999-12-21

    A method of improving certain vanadium oxide formulations is presented. The method concerns fluorine doping formulations having a nominal formula of LiV.sub.3 O.sub.8. Preferred average formulations are provided wherein the average oxidation state of the vanadium is at least 4.6. Herein preferred fluorine doped vanadium oxide materials, electrodes using such materials, and batteries including at least one electrode therein comprising such materials are provided.

  10. Vanadium Oxidation State Determination by X-Ray Absorption Spectroscopy

    Science.gov (United States)

    Duchesne, Marc A.; Nakano, Jinichiro; Hu, Yongfeng; MacLennan, Aimee; Hughes, Robin W.; Bennett, James; Nakano, Anna

    Vanadium is found in slags produced during metal refinement and fossil fuel combustion/gasification. The oxidation state of vanadium in slag has technological and environmental implications. For example, it may affect slag flow and refractory wear inside reactors, as well as leachability and toxicity of industrial by-products. Determination of vanadium's oxidation state in crystalline phases can be achieved via the widely adopted X-ray diffraction (XRD) technique. However, this technique does not provide information on vanadium in amorphous phases. The objective of this research is to determine the oxidation state of vanadium in petroleum coke gasification samples and laboratory samples using X-ray absorption spectroscopy (XAS) with Canadian Light Source's soft X-ray micro-characterization beamline (SXRMB). Linear combination fitting of XAS spectra with reference samples allowed quantitative determination of vanadium speciation.

  11. Hydrothermal Synthesis of Nanostructured Vanadium Oxides

    Directory of Open Access Journals (Sweden)

    Jacques Livage

    2010-08-01

    Full Text Available A wide range of vanadium oxides have been obtained via the hydrothermal treatment of aqueous V(V solutions. They exhibit a large variety of nanostructures ranging from molecular clusters to 1D and 2D layered compounds. Nanotubes are obtained via a self-rolling process while amazing morphologies such as nano-spheres, nano-flowers and even nano-urchins are formed via the self-assembling of nano-particles. This paper provides some correlation between the molecular structure of precursors in the solution and the nanostructure of the solid phases obtained by hydrothermal treatment.

  12. Comparative analysis of niobium and vanadium carbide efficiency in the high energy mechanical milling of aluminum bronze alloy

    Directory of Open Access Journals (Sweden)

    Alexandre Nogueira Ottoboni Dias

    Full Text Available Abstract This study aims to analyze the efficiency of niobium and vanadium carbides in the high energy mechanical milling of aluminum bronze alloy. Two series of experiments were made following the same steps for both niobium carbide (NbC and vanadium carbide (VC additions: 30 g of chips were weighed and placed in a stainless steel jar with 3 % of carbide and 1 % of stearic acid for a mass/sphere relationship of 1:10. The milling was realized using a planetary ball mill for 10, 30 and 50 hours in an inert argon atmosphere at 300 rpm. Results shown in laser diffraction indicate a great reduction in the particle sizes of powders when VC is used. For 30 hours milling, D50 values ranged from 1580 µm with NbC to 182.3 µm with VC addition. The D50 values ranged from 251.5 µm with NbC to 52.26 µm with VC addition, for 50 hours milling. The scanning electron microscopy showed that in 10 hours of milling, the energy was not sufficient to achieve the shear of chips in both cases. For 30 hours, it's possible to observe particles with sizes between 100 µm and 800 µm with NbC addition while for the same milling time, with VC it's possible to see particles with different sizes, but with many shapes of fine particulates. For 50 hours milling, particles achieved the smaller sizes between 50 and 200 µm with NbC and ranging from 5 until 50 µm with VC addition.

  13. Platinum-Vanadium Oxide Nanotube Hybrids

    Science.gov (United States)

    Mello, Filipe L. S.; Costa, Lídia O. O.; Hernández, Eduardo Padrón; de Farias, Andréa M. Duarte; Fraga, Marco A.

    2010-06-01

    The present contribution reports on the features of platinum-based systems supported on vanadium oxide nanotubes. The synthesis of nanotubes was carried out using a commercial vanadium pentoxide via hydrothermal route. The nanostructured hybrid materials were prepared by wet impregnation using two different platinum precursors. The formation of platinum nanoparticles was evaluated by applying distinct reduction procedures. All nanostructured samples were essentially analysed by X-ray diffraction and transmission electron microscopy. After reduction, transmission electron microscopy also made it possible to estimate particle size distribution and mean diameter calculations. It could be seen that all reduction procedures did not affect the nanostructure of the supports and that the formation of metallic nanoparticles is quite efficient with an indistinct distribution along the nanotubes. Nevertheless, the reduction procedure determined the diameter, dispersion and shape of the metallic particles. It could be concluded that the use of H2PtCl6 is more suitable and that the use of hydrogen as reducing agent leads to a nanomaterial with unagglomerated round-shaped metallic particles with mean size of 6-7 nm.

  14. Platinum–Vanadium Oxide Nanotube Hybrids

    Directory of Open Access Journals (Sweden)

    Hernández EduardoPadrón

    2010-01-01

    Full Text Available Abstract The present contribution reports on the features of platinum-based systems supported on vanadium oxide nanotubes. The synthesis of nanotubes was carried out using a commercial vanadium pentoxide via hydrothermal route. The nanostructured hybrid materials were prepared by wet impregnation using two different platinum precursors. The formation of platinum nanoparticles was evaluated by applying distinct reduction procedures. All nanostructured samples were essentially analysed by X-ray diffraction and transmission electron microscopy. After reduction, transmission electron microscopy also made it possible to estimate particle size distribution and mean diameter calculations. It could be seen that all reduction procedures did not affect the nanostructure of the supports and that the formation of metallic nanoparticles is quite efficient with an indistinct distribution along the nanotubes. Nevertheless, the reduction procedure determined the diameter, dispersion and shape of the metallic particles. It could be concluded that the use of H2PtCl6 is more suitable and that the use of hydrogen as reducing agent leads to a nanomaterial with unagglomerated round-shaped metallic particles with mean size of 6–7 nm.

  15. Extraction of vanadium from vanadium slag by high pressure oxidative acid leaching

    Science.gov (United States)

    Zhang, Guo-quan; Zhang, Ting-an; Lü, Guo-zhi; Zhang, Ying; Liu, Yan; Liu, Zhuo-lin

    2015-01-01

    To extract vanadium in an environment friendly manner, this study focuses on the process of leaching vanadium from vanadium slag by high pressure oxidative acid leaching. Characterizations of the raw slag, mineralogy transformation, and the form of leach residues were made by X-ray diffraction, scanning electron microscopy, and energy dispersive X-ray spectroscopy. The result shows that the vanadium slag is composed of major phases of fayalite, titanomagnetite, and spinel. During the high pressure oxidative acid leaching process, the fayalite and spinel phases are gradually decomposed by sulfuric acid, causing the release of vanadium and iron in the solution. Meanwhile, unreacted silicon and titanium are enriched in the leach residues. With the initial concentration of sulfuric acid at 250 g·L-1, a leaching temperature of 140°C, a leaching time of 50 min, a liquid-solid ratio of 10:1 mL·g-1, and oxygen pressure at 0.2 MPa, the leaching rate of vanadium reaches 97.69%.

  16. High Performance Pillared Vanadium Oxide Cathode for Lithium Ion Batteries

    Science.gov (United States)

    2015-04-24

    Performance Pillared Vanadium Oxide Cathode for Lithium Ion Batteries Siu on Tung, Krista L. Hawthorne, Yi Ding, James Mainero, and Levi T. Thompson...Automotive Research Development and Engineering Center, Warren, MI 48387, USA Keywords: nanostructured materials, lithium ion batteries , cathode...2014 to 00-00-2015 4. TITLE AND SUBTITLE High Performance Pillared Vanadium Oxide Cathode for Lithium Ion Batteries 5a. CONTRACT NUMBER 5b. GRANT

  17. Novel vanadium phosphate phases as catalysts for selective oxidation

    Indian Academy of Sciences (India)

    Unknown

    important vanadium phosphate phases used as selective oxidation catalysts, it has been observed that ... molybdenum oxides are the most widely used ones for the selective oxidation of alkanes. Amongst these the ... pentane to maleic and pthalic anhydride, and in the oxidative dehydrogenation of ethane, propane etc 4.

  18. Conceptual chemistry approach towards the support effect in supported vanadium oxides: valence bond calculations on the ionicity of vanadium catalysts

    NARCIS (Netherlands)

    Fievez, T.; De Proft, F.; Geerlings, P.; Weckhuysen, B.M.; Havenith, R.W.A.

    2011-01-01

    The concept of bond ionicity, obtained via a valence bond analysis, is invoked in the interpretation of the catalytic activity of supported vanadium oxides, in analogy with previous work conducted within the framework of conceptual DFT. For a set of model clusters representing the vanadium oxide

  19. Conceptual chemistry approach towards the support effect in supported vanadium oxides : Valence bond calculations on the ionicity of vanadium catalysts

    NARCIS (Netherlands)

    Fievez, Tim; De Proft, Frank; Geerlings, Paul; Weckhuysen, Bert M.; Havenith, Remco W. A.

    2011-01-01

    The concept of bond ionicity, obtained via a valence bond analysis, is invoked in the interpretation of the catalytic activity of supported vanadium oxides, in analogy with previous work conducted within the framework of conceptual DFT. For a set of model clusters representing the vanadium oxide

  20. Vanadium Doped Tungsten Oxide Material - Electrical Physical and Sensing Properties

    Directory of Open Access Journals (Sweden)

    Shishkin N. Y.

    2008-05-01

    Full Text Available The electrical physical and sensing (to VOCs and inorganic gases properties of vanadium doped tungsten oxide in the regions of phase transition temperature were investigated. Vanadium oxide (II dimerization was observed in the doped material, corresponding to new phase transition. The extreme sensitivity and selectivity to chemically active gases and vapors in small concentrations: CO, NOx, NH3 acetone, ethanol near phase transitions temperature was found. Sensor elements were manufactured for the quantitative detection (close to 1 ppm of alcohol and ammonia.

  1. THE INFLUENCE OF NIOBIUM ON THE ACIDITY AND STRUCTURE OF GAMMA-ALUMINA-SUPPORTED VANADIUM OXIDES

    Directory of Open Access Journals (Sweden)

    Sathler M.N.B.

    1998-01-01

    Full Text Available Gamma-alumina-supported niobium oxide was used as a support for vanadium oxides. The influence of the addition of niobium oxide was studied by looking for changes in the structure and acid-base character of superficial species. Vanadium oxide was deposited using the continuous adsorption method; niobium oxide was impregnated using the incipient wetness method. The catalysts were characterized by XPS, UV-visible and IR spectroscopy. Catalytic tests were performed using propane oxidation reaction at 400oC. For coverage below the monolayer, both vanadium and niobium oxides were observed in slightly condensed superficial species. The presence of vanadium oxide on the support was found to increase the Lewis acidity and create some Bronsted acidity. Higher catalytic activity and selectivity for propene were associated with vanadium oxides. The presence of niobium did not contribute to the modification of the chemical properties of superficial vanadium but did decrease the adsorption of vanadium on the alumina.

  2. Novel hybrid materials based on the vanadium oxide nanobelts

    Energy Technology Data Exchange (ETDEWEB)

    Zabrodina, G.S., E-mail: kudgs@mail.ru [G.A. Razuvaev Institute of Organometallic Chemistry of Russian Academy of Sciences, Nizhny Novgorod 603950 (Russian Federation); Lobachevsky State University, Nizhny Novgorod 603950 (Russian Federation); Makarov, S.G.; Kremlev, K.V. [G.A. Razuvaev Institute of Organometallic Chemistry of Russian Academy of Sciences, Nizhny Novgorod 603950 (Russian Federation); Lobachevsky State University, Nizhny Novgorod 603950 (Russian Federation); Yunin, P.A.; Gusev, S.A. [Institute for Physics of Microstructures Russian Academy of Sciences, Nizhny Novgorod 603087 (Russian Federation); Kaverin, B.S.; Kaverina, L.B. [G.A. Razuvaev Institute of Organometallic Chemistry of Russian Academy of Sciences, Nizhny Novgorod 603950 (Russian Federation); Ketkov, S.Yu. [G.A. Razuvaev Institute of Organometallic Chemistry of Russian Academy of Sciences, Nizhny Novgorod 603950 (Russian Federation); Lobachevsky State University, Nizhny Novgorod 603950 (Russian Federation)

    2016-04-15

    Graphical abstract: - Highlights: • Flat and curved vanadium oxide nanobelts have been synthesized. • Hybrid material was prepared via decoration of flexible nanobelts with zinc phthalocyanine. • Investigations of the thermal stability, morphologies and structures were carried out. - Abstract: Novel hybrid materials based on zinc phthalocyanine and nanostructured vanadium oxides have attracted extensive attention for the development of academic research and innovative industrial applications such as flexible electronics, optical sensors and heterogeneous catalysts. Vanadium oxides nanobelts were synthesized via a hydrothermal treatment V{sub 2}O{sub 5}·nH{sub 2}O gel with surfactants (TBAB, CTAB) used as structure-directing agents, where CTAB – cetyltrimethylammonium bromide, TBAB – tetrabutylammonium bromide. Hybrid materials were prepared decoration of (CTA){sub 0.33}V{sub 2}O{sub 5} flexible nanobelts with cationic zinc phthalocyanine by the ion-exchange route. Investigations of the thermal stability, morphologies and structures of the (CTA){sub 0.33}V{sub 2}O{sub 5}, (TBA){sub 0.16}V{sub 2}O{sub 5} nanobelts and zinc phthalocyanine exchange product were carried out. The hybrid materials based on the nanostructured vanadium oxide and zinc phthalocyanine were tested as photocatalysts for oxidation of citronellol and 2-mercaptoethanol by dioxygen.

  3. Chemistry, spectroscopy and the role of supported vanadium oxides in heterogeneous catalysis

    NARCIS (Netherlands)

    Weckhuysen, B.M.; Keller, D.E.

    2003-01-01

    Supported vanadium oxide catalysts are active in a wide range of applications. In this review, an overview is given of the current knowledge available about vanadium oxide-based catalysts. The review starts with the importance of vanadium in heterogeneous catalysis, a discussion of the molecular

  4. Vanadium oxide/polypyrrole aerogel nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Dave, B.C.; Dunn, B.S.; Wong, H.P. [Univ. of California, Los Angeles, CA (United States). Dept. of Materials Science and Engineering; Leroux, F.; Nazar, L.F. [Univ. of Waterloo, Ontario (Canada). Dept. of Chemistry

    1996-12-31

    Vanadium pentoxide/polypyrrole aerogel (ARG) nanocomposites were prepared by hydrolysis of VO(OC{sub 3}H{sub 7}){sub 3} using pyrrole/water/acetone mixtures. Monolithic green-black gels with polypyrrole/V ratios ranging from 0.15 to 1.0 resulted from simultaneously polymerization of the pyrrole and vanadium alkoxide precursors. Supercritical drying yielded high surface (150--200 m{sup 2}/g) aerogels, of sufficient mechanical integrity to allow them to be cut without fracturing. TEM studies of the aerogels show that they are comprised of fibers similar to that of V{sub 2}O{sub 5} ARG`s, but with a much shorter chain length. Evidence from IR that the inorganic and organic components strongly interact leads them to propose that this impedes the vanadium condensation process. The result is ARG`s that exhibit decreased electronic conductivity with increasing polymer content. Despite the unexpected deleterious effect of the conductive polymer on the bulk conductivity, at low polymer content, the nanocomposite materials show enhanced electrochemical properties for Li insertion compared to the pristine aerogel.

  5. Rechargeable lithium cells with modified vanadium oxide cathodes

    Science.gov (United States)

    Chung, S. K.; Chmilenko, N. A.; Borovykov, A. Ya; Lee, S. H.

    Modified vanadium oxide has been prepared by melting V 2O 5 with additives of 3-3.5% of sodium orthosilicate at 690°C for 3 h followed by fast cooling to an ambient temperature. Charge-discharge characteristics of this oxide were studied as an active cathode material for lithium secondary batteries. The oxide undergoes irreversible transition to become essentially amorphous after first discharge to cut-off voltage of 2 V vs. Li, and then exhibits excellent rechargeability in the 1.5 to 3.9 V potential range. The coin type 2325 size secondary cells have been manufactured and tested with the modified vanadium oxide cathodes and Li-Al alloy anodes. Preliminary shallow cycling modifies the cells' performance and allows to obtain rating capacity 50 mA h in the voltage diapason of 2.0-3.9 V with draining current 0.5 mA.

  6. Low-temperature solution-processed hydrogen molybdenum and vanadium bronzes for an efficient hole-transport layer in organic electronics.

    Science.gov (United States)

    Xie, Fengxian; Choy, Wallace C H; Wang, Chuandao; Li, Xinchen; Zhang, Shaoqing; Hou, Jianhui

    2013-04-11

    A simple one-step method is reported to synthesize low-temperature solution-processed transition metal oxides (TMOs) of molybdenum oxide and vanadium oxide with oxygen vacancies for a good hole-transport layer (HTL). The oxygen vacancy plays an essential role for TMOs when they are employed as HTLs: TMO films with excess oxygen are highly undesirable for their application in organic electronics. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Crossing points in the electronic band structure of vanadium oxide

    Directory of Open Access Journals (Sweden)

    Keshav N. Shrivastava

    2010-03-01

    Full Text Available The electronic band structures of several models of vanadium oxide are calculated. In the models 1-3, every vanadium atom is connected to 4 oxygen atoms and every oxygen atom is connected to 4 vanadium atoms. In model 1, a=b=c 2.3574 Å; in model 2, a= 4.7148 Å, b= 2.3574 Å and c= 2.3574 Å; and in model 3, a= 4.7148 Å, b= 2.3574 Å and c= 4.7148 Å. In the models 4-6, every vanadium atom is connected to 4 oxygen atoms and every oxygen atom is connected to 2 vanadium atoms. In model 4, a=b= 4.551 Å and c= 2.851 Å; in model 5, a=b=c= 3.468 Å; and in model 6, a=b=c= 3.171 Å. We have searched for a crossing point in the band structure of all the models. In model 1 there is a point at which five bands appear to meet but the gap is 7.3 meV. In model 2 there is a crossing point between G and F points and there is a point between F and Q with the gap ≈ 3.6608 meV. In model 3, the gap is very small, ~ 10-5 eV. In model 4, the gap is 5.25 meV. In model 5, the gap between Z and G points is 2.035 meV, and in model 6 the gap at Z point is 4.3175 meV. The crossing point in model 2 looks like one line is bent so that the supersymmetry is broken. When pseudopotentials are replaced by a full band calculation, the crossing point changes into a gap of 2.72 x 10-4 eV.

  8. Study of propane partial oxidation on vanadium-containing catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Komashko, G.A.; Khalamejda, S.V.; Zazhigalov, V.A. [AN Ukrainskoj SSR, Kiev (Ukraine). Inst. Fizicheskoj Khimii

    1998-12-31

    The present results indicate that maximum selectivity to acrylic acid can be reached over V-P-Zr-O catalysts. When the hydrocarbon concentration is 5.1 vol.% the selectivity is about 30% at quite high paraffin conversion. Conclusively, some explanations to the observed facts can be given. The V-P-O catalyst promotion with lanthanum by means of mechanochemical treatment is distinguished by the additive uniform spreading all over the matrix surface. Such twophase system is highly active in propane conversion (lanthanum oxide) and further oxidation of the desired products. The similar properties are attributed to V-P-Bi-La-O catalyst. Bismuth, tellurium and zirconium additives having clearly defined acidic properties provoke the surface acidity strengthening and make easier desorption of the acidic product (acrylic acid) from the surface lowering its further oxidation. Additionally, since bismuth and zirconium are able to form phosphates and, according to, to create space limitations for the paraffin molecule movement out of the active group boundaries, this can be one more support in favour of the selectivity increase. With this point of view very interesting results were obtained. It has been shown that the more limited the size of the vanadium unit, the higher the selectivity is. Monoclinic phase AV{sub 2}P{sub 2}O{sub 10} which consists in clusters of four vanadium atoms is sensibly more reactive than the orthorhombic phase consists in V{sub {infinity}} infinite chains. (orig.)

  9. Preparation, characterization, and electrochemical properties of lithium vanadium oxide nanoribbons

    Energy Technology Data Exchange (ETDEWEB)

    Zhuo Shujuan [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, Jiangsu 215123 (China); Anhui Key Laboratory of Functional Molecular Solids, College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241000 (China); Shao Mingwang, E-mail: mwshao@suda.edu.cn [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, Jiangsu 215123 (China); Zhou Qing; Liao Fan [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou, Jiangsu 215123 (China)

    2011-07-15

    Graphical abstract: Display Omitted Highlights: > The lithium ions can easily move between the layers of lithium vanadium oxide. > It can highly increase the electron transfer between the electrode and dopamine. > The reversibility of electrochemical process was significantly improved. - Abstract: Highly uniform lithium vanadium oxide nanoribbons were successfully prepared in large quantities using a facile hydrothermal approach without employing any surfactants or templates. The as-prepared products were up to hundreds of micrometers in length, about 200 nm in width, and 20 nm in thickness. These nanoribbons and nafion composite were employed to modify glassy carbon electrode, which displayed excellent electrochemical sensitivity and rapid response in detecting dopamine in phosphate buffer solution. Lithium ions can greatly increase the electron transfer between the electrode and biological materials, and significantly increase the reversibility of electrochemical process. A linear relationship between the concentrations of dopamine and its oxidation peak currents was obtained. The linear range for the detection of dopamine was 2.0 x 10{sup -6} to 1.0 x 10{sup -4} M with a detection limit of 1.0 x 10{sup -7} M. In addition, the good reproducibility and long-term stability of the sensor make it valuable for further application.

  10. High-pressure synthesis of fully occupied tetragonal and cubic tungsten bronze oxides

    Energy Technology Data Exchange (ETDEWEB)

    Ikeuchi, Yuya; Takatsu, Hiroshi; Tassel, Cedric; Goto, Yoshihiro; Murakami, Taito; Kageyama, Hiroshi [Graduate School of Engineering, Kyoto University (Japan)

    2017-05-15

    A high-pressure reaction yielded the fully occupied tetragonal tungsten bronze K{sub 3}W{sub 5}O{sub 15} (K{sub 0.6}WO{sub 3}). The terminal phase shows an unusual transport property featuring slightly negative temperature-dependence in resistivity (dρ/dT<0) and a large Wilson ratio of R{sub W}=3.2. Such anomalous metallic behavior possibly arises from the low-dimensional electronic structure with a van Hove singularity at the Fermi level and/or from enhanced magnetic fluctuations by geometrical frustration of the tungsten sublattice. The asymmetric nature of the tetragonal tungsten bronze K{sub x}WO{sub 3}-K{sub 0.6-y}Ba{sub y}WO{sub 3} phase diagram implies that superconductivity for x≤0.45 originates from the lattice instability because of potassium deficiency. A cubic perovskite KWO{sub 3} phase was also identified as a line phase - in marked contrast to Na{sub x}WO{sub 3} and Li{sub x}WO{sub 3} with varying quantities of x (<1). This study presents a versatile method by which the solubility limit of tungsten bronze oxides can be extended. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  11. Sulfur-vanadium oxide gel composites as thin film cathodes for rechargeable lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Mukherjee, S.P.; Gavrilov, A.B.; Skotheim, T.A.

    1998-07-01

    A class of novel electroactive cathode materials based on composites produced from elemental sulfur and vanadium oxide xerogels or aerogels has been developed as models for lithium battery applications. The use of elemental sulfur in rechargeable lithium batteries has been hindered due to certain limitations such as, very low electronic conductivity and the out-diffusion of polysulfides during the cycling process which reduces the cycling efficiency. Vanadium oxide xerogels and aerogels have certain desirable characteristic physico-chemical properties, such as, high surface areas with nono-scale interconnecting porosity, high electronic conductivity, non- or nanocrystallinity, and oxidation reduction catalytic activity. Since these properties may improve the performance of sulfur based rechargeable batteries, a family of composite cathodes containing elemental sulfur and vanadium oxide gels were produced. The performance of the composites cathodes, in thin film form, were evaluated in coin cells and AA cells with metallic lithium anodes and liquid electrolytes. The multifunctional role of vanadium oxide gels on the cell performance of the cells having composite cathodes has been qualitatively explored. Results indicate that the cathodes having xerogel composites based on vanadium oxide sol from vanadium oxide isopropoxide can be made with high sulfur content (80 wt %) and with low carbon content (5 wt %) and without any polymer binder. This shows the contribution of adhesive properties and electronic conductivity of vanadium oxide xerogels. A significant suppression of polysulfide out-diffusion is observed with appropriate processing of the composite cathodes. It is anticipated that the nanoscale interconnecting porosity of gels plays an important role in this behavior. An excellent rate capability is observed with the vanadium-oxide sulfur composite cathodes indicating the contribution of intrinsic electrochemical properties of the vanadium oxide.

  12. Directed synthesis of bio-inorganic vanadium oxide composites using genetically modified filamentous phage

    Science.gov (United States)

    Mueller, Michael; Baik, Seungyun; Jeon, Hojeong; Kim, Yuchan; Kim, Jungtae; Kim, Young Jun

    2015-05-01

    The growth of crystalline vanadium oxide using a filamentous bacteriophage template was investigated using sequential incubation in a V2O5 precursor. Using the genetic modification of the bacteriophage, we displayed two cysteines that constrained the RSTB-1 peptide on the major coat protein P8, resulting in vanadium oxide crystallization. The phage-driven vanadium oxide crystals with different topologies, microstructures, photodegradation and vanadium oxide composites were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), quartz microbalance and dissipation (QCM-D) and X-ray photoelectron spectroscopy (XPS). Non-specific electrostatic attraction between a wild-type phage (wt-phage) and vanadium cations in the V2O5 precursor caused phage agglomeration and fiber formation along the length of the viral scaffold. As a result, the addition of recombinant phage (re-phage) in V2O5 precursors formed heterogeneous structures, which led to efficient condensation of vanadium oxide crystal formation in lines, shown by QCM-D analysis. Furthermore, re-phage/VxOx composites showed significantly enhanced photodegradation activities compared with the synthesized wt-phage-V2O5 composite under illumination. This study demonstrates that peptide-mediated vanadium oxide mineralization is governed by a complicated interplay of peptide sequence, local structure, kinetics and the presence of a mineralizing aid, such as the two cysteine-constrained peptides on the phage surface, and has potential for use in nanotechnology applications.

  13. Partial Oxidation of n-Butane over a Sol-Gel Prepared Vanadium Phosphorous Oxide

    Directory of Open Access Journals (Sweden)

    Juan M. Salazar

    2013-01-01

    Full Text Available Vanadium phosphorous oxide (VPO is traditionally manufactured from solid vanadium oxides by synthesizing VOHPO4∙0.5H2O (the precursor followed by in situ activation to produce (VO2P2O7 (the active phase. This paper discusses an alternative synthesis method based on sol-gel techniques. Vanadium (V triisopropoxide oxide was reacted with ortho-phosphoric acid in an aprotic solvent. The products were dried at high pressure in an autoclave with a controlled excess of solvent. This procedure produced a gel of VOPO4 with interlayer entrapped molecules. The surface area of the obtained materials was between 50 and 120 m2/g. Alcohol produced by the alkoxide hydrolysis reduced the vanadium during the drying step, thus VOPO4 was converted to the precursor. This procedure yielded non-agglomerated platelets, which were dehydrated and evaluated in a butane-air mixture. Catalysts were significantly more selective than the traditionally prepared materials with similar intrinsic activity. It is suggested that the small crystallite size obtained increased their selectivity towards maleic anhydride.

  14. Processing, characterization, and bactericidal activity of undoped and silver-doped vanadium oxides

    Energy Technology Data Exchange (ETDEWEB)

    Tousley, M.E.; Wren, A.W.; Towler, M.R. [Inamori School of Engineering, Alfred University, Alfred, NY 14803 (United States); Mellott, N.P., E-mail: mellott@alfred.edu [Inamori School of Engineering, Alfred University, Alfred, NY 14803 (United States)

    2012-12-14

    Vanadium oxide (V) and silver-doped vanadium oxide (Ag-V) powders were prepared via sol-gel processing. Structural evolution and bactericidal activity was examined as a function of temperature ranging from 250, 350, 450 and 550 Degree-Sign C. Powders were characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and Raman spectroscopy. Results from all techniques showed vanadium pentoxide (V{sub 2}O{sub 5}) is the predominant phase regardless of heat treatment temperature or the addition of silver (Ag). XRD analysis suggests Ag is present as AgCl in samples heat treated to 250, 350, and 450 Degree-Sign C and as AgV{sub 6}O{sub 15} at 550 Degree-Sign C. Bactericidal activity was evaluated against Escherichia coli using the agar disk diffusion method considering both Ag-V and undoped, V powders. While the addition of Ag significantly increased bactericidal properties, the specific Ag valency, or crystal structure and morphology formed at higher temperatures, had little effect on functionality. -- Highlights: Black-Right-Pointing-Pointer Vanadium and silver-doped vanadium oxide powders were prepared via sol-gel. Black-Right-Pointing-Pointer Powders were characterized using advanced, complementary structural techniques. Black-Right-Pointing-Pointer Bactericidal activity was evaluated against E. coli. Black-Right-Pointing-Pointer Both vanadium and silver doped vanadium oxide show bactericidal activity.

  15. On oxygen chemisorption for characterization of silica-supported vanadium oxide catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Faraldos, M.; Banares, M.A.; Fierro, J.L.G. [Instituto de Catalysis y Petroleoquimica, Madrid (Spain)] [and others

    1997-05-01

    Oxygen chemisorption experiments on prereduced silica- supported vanadia catalysts have been performed in order to determine the optimum conditions for measuring the relative dispersion of vanadium oxide on the silica substrate. By following the extent of vanadia reduction microgravimetrically, it is shown that an appropriate prereduction of the catalyst at 823 K under hydrogen is fundamental in obtaining a reproducible well-defined stoichiometrically reduced vanadium oxide system (V{sup 3+}). AT 643 K the reduction process is very much slower and requires very long times in order to approach a plateau. Measurement of the binding energies of the V{sub 2}p{sub 3/2} core level spectra indicates that high-temperature oxygen chemisorption (643 K) results in a reoxidation of the prereduced vanadium oxide species within crystallites leading to an overestimation of the number of exposed vanadium sites. Chemisorption at low temperatures (298 or 195 K) does not affect the stoichiometrically reduced vanadium oxide species within crystallites, thus allowing the number of exposed surface vanadium sites to be measured. 25 refs., 5 figs., 1 tab.

  16. Influence of vanadium oxidation states on the performance of V-Mg-Al mixed-oxide catalysts for the oxidative dehydrogenation of propane

    Energy Technology Data Exchange (ETDEWEB)

    Schacht, L. [IPN, Escuela Superior de Fisica y Matematicas, Departamento de Ciencia de Materiales, Av. IPN s/n, Edificio 9, Col. Lindavista, 07738 Mexico D. F. (Mexico); Navarrete, J.; Schacht, P.; Ramirez, M. A., E-mail: pschacha@imp.m [Instituto Mexicano del Petroleo, Programa de Ingenieria Molecular, Eje Central Lazaro Cardenas No. 152, 07730 Mexico D. F. (Mexico)

    2010-07-01

    V-Mg-Al mixed-oxide catalysts for oxidative dehydrogenation of propane were prepared by thermal decomposition of Mg-Al-layered double hydroxides with vanadium interlayer doping. The obtained catalysts were tested for the oxidative dehydrogenation of propane, obtaining good results in catalytic activity (conversion 16.55 % and selectivity 99.97 %) Results indicated that catalytic performance of these materials depends on how vanadium is integrated in the layered structure, which is determined by the Mg/Al ratio. Vanadium interlayer doping modifies the oxidation state of vanadium and consequently catalytic properties. Surface properties were studied by X-ray photoelectron spectroscopic and diffuse reflectance, UV-visible spectroscopy, and temperature programmed reduction. The analyses provided information about the oxidation state, before and after the reaction. From these results, it is suggested that selectivity to propylene and catalytic activity depend mainly of vanadium oxidation state. (Author)

  17. Sputter-deposited low reflectance vanadium oxide-molybdenum oxide thin films on silicon

    Science.gov (United States)

    Nayak, Manish Kumar; Esther, A. Carmel Mary; Bera, Parthasarathi; Dey, Arjun

    2017-09-01

    A single layer antireflective, smart, crystalline and nanocolumnar pulsed RF magnetron sputtered vanadium oxide-molybdenum oxide thin film on silicon is proposed for the alternate antireflective material for silicon based futuristic solar cell application. The VO-MO film with 130 nm thickness grown at 200 W shows significant low reflectance (1% within the 500-600 nm region). The VO-MO film with lowest reflectance shows a phase transition at around 55 °C which is beneficial due to film inherent variable IR emittance behaviour which may be helpful for eliminating excess heat load generated during in-service of silicon solar cell.

  18. Study of the kinetic behavior of mandelic acid oxidation by vanadium(V in sulfuric acid medium: effect of CTAB presence

    Directory of Open Access Journals (Sweden)

    Rômulo Augusto Ando

    2006-02-01

    Full Text Available The mandelic acid oxidation by vanadium (V in sulfuric acid medium was studied at 303 K. The reaction rate was determined spectrophotometrically by means of the formation of vanadium (IV at 760 nm. The oxidation reaction showed first order dependence in terms of vanadium (VThe mandelic acid oxidation by vanadium (V in sulfuric acid medium was studied at 303 K. The reaction rate was determined spectrophotometrically by means of the formation of vanadium (IV at 760 nm. The oxidation reaction showed first order dependence in terms of vanadium (V.

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

    Science.gov (United States)

    Ngamsai, Kittima; Arpornwichanop, Amornchai

    2015-11-01

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

  20. Vanadium oxide nanotubes as cathode material for Mg-ion batteries

    DEFF Research Database (Denmark)

    Christensen, Christian Kolle; Sørensen, Daniel Risskov; Bøjesen, Espen Drath

    Vanadium oxide compounds as cathode material for secondary Li-ion batteries gained interest in the 1970’s due to high specific capacity (>250mAh/g), but showed substantial capacity fading.1 Developments in the control of nanostructured morphologies have led to more advanced materials, and recently...... vanadium oxide nanotubes (VOx-NT) were shown to perform well as a cathode material for Mg-ion batteries.2 The VOx-NTs are easily prepared via a hydrothermal process to form multiwalled scrolls of VO layer with primary amines interlayer spacer molecules.3 The tunable and relative large layer spacing 1-3 nm...... synchrotron powder X-ray diffraction measured during battery operation. These results indicate Mg-intercalation in the multiwalled VOx-NTs occurs within the space between the individual vanadium oxide layers while the underlying VOx frameworks constructing the walls are affected only to a minor degree...

  1. ESR study of deoxygenated and oxidated forms of vanadium(4) porphyrins

    Energy Technology Data Exchange (ETDEWEB)

    Selyutin, G.E.; Shklyaev, A.A. (AN SSSR, Krasnoyarsk. Inst. Khimii i Khimicheskoj Tekhnologii)

    1982-01-01

    Halogenated and oxidated forms of porphyrins of oxovanadium VOP (ethioporphyrin-EP and tetraphenylporphyrin) with different halides are studied using the ESR method. In reactions of vanadylporphyrins with metal halides deoxygenation of vanadyl ion is realized and octahedral complex of dihalogenovanadium (4) of porphyrin (P) are formed and at the intermediate stage bimetal complex of vanadiumporphyrin with halide is formed, in which halide cation is bonded by means of the bridge oxygen atom with vanadium ion. In dihalide complexes VX/sub 2//sup -/P for vanadium (4) ion a regular octahedral surrounding is realized and the axis of tetragonal distortion can be oriented both in perpendicular and lay in porphyrin plane. The oxidated forms, formed during oxidation in the presence of halides, present dihalide vanadium (4) complexes with mono- and dication of porphyrin ligand.

  2. Vanadium oxide thin films deposited on silicon dioxide buffer layers by magnetron sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Chen Sihai [Department of Optoelectronic Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China) and Wuhan National laboratory for Optoelectronics, Wuhan 430074 (China)]. E-mail: cshai99@yahoo.com; Ma Hong [Department of Electronics and Information Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Wang Shuangbao [Department of Optoelectronic Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Shen Nan [Department of Optoelectronic Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Xiao Jing [Department of Optoelectronic Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Zhou Hao [Department of Optoelectronic Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Zhao Xiaomei [Department of Optoelectronic Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Wuhan National laboratory for Optoelectronics, Wuhan 430074 (China); Li Yi [Department of Optoelectronic Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); State Key Laboratory for Imaging Recognization and Intelligence Control, Huazhong University of Science and Technology, Wuhan 430074 (China); Yi Xinjian [State Key Laboratory for Imaging Recognization and Intelligence Control, Huazhong University of Science and Technology, Wuhan 430074 (China)

    2006-02-21

    Thin films made by vanadium oxide have been obtained by direct current magnetron sputtering method on SiO{sub 2} buffer layers. A detailed electrical and structural characterization has been performed on the deposited films by four-point probe method and scanning electron microscopy (SEM). At room temperature, the four-point probe measurement result presents the resistance of the film to be 25 kU/sheet. The temperature coefficient of resistance is - 2.0%/K. SEM image indicates that the vanadium oxide exhibits a submicrostructure with lamella size ranging from 60 nm to 300 nm. A 32 x 32-element test microbolometer was fabricated based on the deposited thin film. The infrared response testing showed that the response was 200 mV. The obtained results allow us to conclude that the vanadium oxide thin films on SiO{sub 2} buffer layers is suitable for uncooled focal plane arrays applications.

  3. Theoretical study of vanadium oxides interaction with Y-zeolite.

    Science.gov (United States)

    Arroyo, M; Sansores, L E; Salcedo, R; Montoya, J A

    2008-12-01

    A current problem about oils and feedstock in fluid catalytic cracking (FCC) is the continuous cumulative deposition of metal contaminants on the catalyst, resulting in important modifications of its properties. Vanadium plays a detrimental role on the catalyst components because enhances the destruction of the Y-zeolite structure during regeneration stage when it is exposed by steam and oxygen at high temperatures. Knowledge of the mechanism interaction of vanadium with the catalyst is important to improve FCC performance. Quantum Molecular Dynamics calculations were done introducing the VO, V2O3, VO2 or V2O5 molecules at the center of a Y-zeolite ring simulating regeneration conditions. The results indicate that the principal reaction is carried out among the zeolite and the vanadium atoms of molecules. This happens, when interaction is presented, since the loss of a hydrogen atom of the active place causes high degree of oxygen reactivity.

  4. Nature of active vanadium nanospecies in MCM-41 type catalysts for olefins oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Chanquía, Corina M., E-mail: cchanquia@cab.cnea.gov.ar [Centro Atómico Bariloche, Comisión Nacional de Energía Atómica (CAB-CNEA). Av. Bustillo 9500, R8402AGP, San Carlos de Bariloche, Río Negro (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Avenida Rivadavia 1917, C1033AAJ, Ciudad Autónoma de Buenos Aires (Argentina); Cánepa, Analía L. [Centro de Investigación y Tecnología Química (CITeQ), Universidad Tecnológica Nacional, Facultad Regional Córdoba (UTN-FRC), Maestro López esq. Cruz Roja Argentina, Ciudad Universitaria, 5016, Córdoba Capital (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Avenida Rivadavia 1917, C1033AAJ, Ciudad Autónoma de Buenos Aires (Argentina); Winkler, Elin L. [Centro Atómico Bariloche, Comisión Nacional de Energía Atómica (CAB-CNEA). Av. Bustillo 9500, R8402AGP, San Carlos de Bariloche, Río Negro (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Avenida Rivadavia 1917, C1033AAJ, Ciudad Autónoma de Buenos Aires (Argentina); and others

    2016-06-01

    A multi-technique physicochemical investigation including UV–Vis-DRS, Raman spectroscopy, XPS, ESR and FTIRS with pyridine adsorption was performed to analyze the nature of different vanadium nanospecies present on MCM-41 type catalysts. By employing a direct hydrothermal synthesis, vanadium species were incorporated into siliceous structure mainly as tetrahedrally coordinated isolated V{sup δ+} ions, which would be located inside the wall and on the wall surface of the mesoporous channels. The coexistence of both vanadium oxidation states V{sup 4+} and V{sup 5+} was also revealed. Acidity measurements permitted to infer about the majority presence of Lewis acid sites, which increase with vanadium content. The catalytic performance of these materials was evaluated in the reaction of α-pinene oxidation with H{sub 2}O{sub 2}. The highest intrinsic activity of the sample with lower V loading was attributed to the high dispersion and efficiency of the isolated V{sup δ+} species that actuate as active sites. A mixture of reaction products arising from competitive processes of epoxidation and allylic oxidation was found. - Highlights: • Nature of vanadium nanospecies in mesoporous silicates was investigated. • From hydrothermal sol–gel synthesis, isolated V{sup δ+} sites were mainly generated. • The coexistence of both vanadium oxidation states V{sup 4+} and V{sup 5+} was revealed. • The catalytic performance was evaluated in α-pinene oxidation with H{sub 2}O{sub 2}. • The high catalytic activity is attributed to high dispersion of isolated V{sup δ+} ions.

  5. Geochemical behaviour of vanadium in iron—titanium oxides

    NARCIS (Netherlands)

    Schuiling, R.D.; Feenstra, A.

    The following geochemical rules-of-thumb seem to hold for vanadium: 1. (1) Magnetites as a group have higher V contents than either hematites or ilmenites. 2. (2) In magnetite—hematite pairs, however, the hematite has the higher V content. 3. (3) In magnetite—ilmenite pairs, the magnetite

  6. Infrared study of the selective oxidation of toluene and o-xylene on vanadium oxide/TiO2

    NARCIS (Netherlands)

    van Hengstum, A.J.; Pranger, J.; Hengstum-Nijhuis, S.M.; van Ommen, J.G.; Gellings, P.J.

    1986-01-01

    Infrared spectroscopy was used to obtain information on the mechanism of the selective oxidation of toluene and o-xylene over vanadium oxide catalysts. The interaction of these aromatic hydrocarbons and the products benzaldehyde and o-tolualdehyde with the surface of a V2O5/TiO2 monolayer catalyst

  7. Structural, optical and electrochemical properties of F-doped vanadium oxide transparent semiconducting thin films

    Science.gov (United States)

    Mousavi, M.; Khorrami, Gh. H.; Kompany, A.; Yazdi, Sh. Tabatabai

    2017-12-01

    In this study, F-doped vanadium oxide thin films with doping levels up to 60 at % were prepared by spray pyrolysis method on glass substrates. To measure the electrochemical properties, some films were deposited on fluorine-tin oxide coated glass substrates. The effect of F-doping on the structural, electrical, optical and electrochemical properties of vanadium oxide samples was investigated. The X-ray diffractographs analysis has shown that all the samples grow in tetragonal β-V2O5 phase structure with the preferred orientation of [200]. The intensity of (200) peak belonging to β-V2O5 phase was strongest in the undoped vanadium oxide film. The scanning electron microscopy images show that the samples have nanorod- and nanobelt-shaped structure. The size of the nanobelts in the F-doped vanadium oxide films is smaller than that in the pure sample and the width of the nanobelts increases from 30 to 70 nm with F concentration. With increasing F-doping level from 10 to 60 at %, the resistivity, the transparency and the optical band gap decrease from 111 to 20 Ω cm, 70 to 50% and 2.4 to 2.36 eV, respectively. The cyclic voltammogram (CV) results show that the undoped sample has the most extensive CV and by increasing F-doping level from 20 to 60 at %, the area of the CV is expanded. The anodic and cathodic peaks in F-doped samples are stronger.

  8. Bipolar resistive switching in room temperature grown disordered vanadium oxide thin-film devices

    Science.gov (United States)

    Wong, Franklin J.; Sriram, Tirunelveli S.; Smith, Brian R.; Ramanathan, Shriram

    2013-09-01

    We demonstrate bipolar switching with high OFF/ON resistance ratios (>104) in Pt/vanadium oxide/Cu structures deposited entirely at room temperature. The SET (RESET) process occurs when negative (positive) bias is applied to the top Cu electrode. The vanadium oxide (VOx) films are amorphous and close to the vanadium pentoxide stoichiometry. We also investigated Cu/VOx/W structures, reversing the position of the Cu electrode, and found the same polarity dependence with respect to the top and bottom electrodes, which suggests that the bipolar nature is linked to the VOx layer itself. Bipolar switching can be observed at 100 °C, indicating that it not due to a temperature-induced metal-insulator transition of a vanadium dioxide second phase. We discuss how ionic drift can lead to the bipolar electrical behavior of our junctions, similar to those observed in devices based on several other defective oxides. Such low-temperature processed oxide switches could be of relevance to back-end or package integration processing schemes.

  9. Investigation of the interaction of benzene with vanadium-molybdenum oxide catalysts by programmed thermal desorption

    Energy Technology Data Exchange (ETDEWEB)

    Belokopytov, Yu.V.; Pyatnitskii, Yu.I.; Grebennikov, Yu.N.

    1985-09-01

    Programmed thermal desorption was used to investigate the interaction of benzene with vanadium-molybdenum oxide catalysts. It was established that the amount of maleic anhydride desorbed from the catalyst surface depends on the catalyst composition and that it varies with its activity and selectivity.

  10. A comprehensive model for the supported vanadium oxide catalyst: The umbrella model

    NARCIS (Netherlands)

    Lingen, J.N.J. van

    2006-01-01

    Supported vanadium oxide catalysts are widely used in industry. However, the molecular structure of the active species, responsible for the actual catalysis, is for a large part still unknown. This thesis describes four years study on the elucidation of this molecular structure. It mainly focuses on

  11. Raman and XPS characterization of vanadium oxide thin films with temperature

    Energy Technology Data Exchange (ETDEWEB)

    Ureña-Begara, Ferran, E-mail: ferran.urena@uclouvain.be [Université catholique de Louvain, Institute of Information and Communication Technologies, Electronics and Applied Mathematics (ICTEAM), Louvain-la-Neuve (Belgium); Crunteanu, Aurelian [XLIM Research Institute, UMR 7252, CNRS/Université de Limoges, Limoges (France); Raskin, Jean-Pierre [Université catholique de Louvain, Institute of Information and Communication Technologies, Electronics and Applied Mathematics (ICTEAM), Louvain-la-Neuve (Belgium)

    2017-05-01

    Highlights: • Comprehensive study of the oxidation of VO{sub 2} thin films from R.T. up to 550 °C. • Phase changes and mixed-valence vanadium oxides formed during the oxidation process. • Reported Raman and XPS signatures for each vanadium oxide. • Monitoring of the current and resistance evolution at the surface of the films. • Oxidation model describing the evolution of the vanadium oxides and phase changes. - Abstract: The oxidation mechanisms and the numerous phase transitions undergone by VO{sub 2} thin films deposited on SiO{sub 2}/Si and Al{sub 2}O{sub 3} substrates when heated from room temperature (R.T.) up to 550 °C in air are investigated by Raman and X-ray photoelectron spectroscopy. The results show that the films undergo several intermediate phase transitions between the initial VO{sub 2} monoclinic phase at R.T. and the final V{sub 2}O{sub 5} phase at 550 °C. The information about these intermediate phase transitions is scarce and their identification is important since they are often found during the synthesis of vanadium dioxide films. Significant changes in the film conductivity have also been observed to occur associated to the phase transitions. In this work, current and resistance measurements performed on the surface of the films are implemented in parallel with the Raman measurements to correlate the different phases with the conductivity of the films. A model to explain the oxidation mechanisms and phenomena occurring during the oxidation of the films is proposed. Peak frequencies, full-width half-maxima, binding energies and oxidation states from the Raman and X-ray photoelectron spectroscopy experiments are reported and analyzed for all the phases encountered in VO{sub 2} films prepared on SiO{sub 2}/Si and Al{sub 2}O{sub 3} substrates.

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

    DEFF Research Database (Denmark)

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

    2016-01-01

    Low-speed marine diesel engines are mostly operated on heavy fuel oils, which have a high content of sulfur andash, including trace amounts of vanadium, nickel, and aluminum. In particular, vanadium oxides could catalyze in-cylinderoxidation of SO2 to SO3, promoting the formation of sulfuric acid...... and enhancing problems of corrosion. In the present work, thekinetics of the catalyzed oxidation was studied in a fixed-bed reactor at atmospheric pressure. Vanadium oxide nanoparticles weresynthesized by spray flame pyrolysis, i.e., by a mechanism similar to the mechanism leading to the formation...

  13. Electrical and Infrared Optical Properties of Vanadium Oxide Semiconducting Thin-Film Thermometers

    Science.gov (United States)

    Zia, Muhammad Fakhar; Abdel-Rahman, Mohamed; Alduraibi, Mohammad; Ilahi, Bouraoui; Awad, Ehab; Majzoub, Sohaib

    2017-10-01

    A synthesis method has been developed for preparation of vanadium oxide thermometer thin film for microbolometer application. The structure presented is a 95-nm thin film prepared by sputter-depositing nine alternating multilayer thin films of vanadium pentoxide (V2O5) with thickness of 15 nm and vanadium with thickness of 5 nm followed by postdeposition annealing at 300°C in nitrogen (N2) and oxygen (O2) atmospheres. The resulting vanadium oxide (V x O y ) thermometer thin films exhibited temperature coefficient of resistance (TCR) of -3.55%/°C with room-temperature resistivity of 2.68 Ω cm for structures annealed in N2 atmosphere, and TCR of -3.06%/°C with room-temperature resistivity of 0.84 Ω cm for structures annealed in O2 atmosphere. Furthermore, optical measurements of N2- and O2-annealed samples were performed by Fourier-transform infrared ellipsometry to determine their dispersion curves, refractive index ( n), and extinction coefficient ( k) at wavelength from 7000 nm to 14,000 nm. The results indicate the possibility of applying the developed materials in thermometers for microbolometers.

  14. X-Ray Absorption Studies of Vanadium-Containing Metal Oxide Nanocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Hohn, Keith, L.

    2006-01-09

    Metal oxide nanocrystals offer significant potential for use as catalysts or catalyst supports due to their high surface areas and unique chemical properties that result from the high number of exposed corners and edges. However, little is known about the catalytic activity of these materials, especially as oxidation catalysts. This research focused on the preparation, characterization and use of vanadium-containing nanocrystals as selective oxidation catalysts. Three vanadium-containing nanocrystals were prepared using a modified sol-gel procedure: V/MgO, V/SiO2, and vanadium phosphate (VPO). These represent active oxidation catalysts for a number of industrially relevant reactions. The catalysts were characterized by x-ray diffraction and Raman, UV-VIS, infrared and x-ray absorption spectroscopies with the goal of determining the primary structural and chemical differences between nanocrystals and microcrystals. The catalytic activity of these catalysts was also studied in oxidative dehydrogenation of butane and methanol oxidation to formaldehyde. V/MgO nanocrystals were investigated for activity in oxidative dehydrogenation of butane and compared to conventional V/MgO catalysts. Characterization of V/MgO catalysts using Raman spectroscopy and x-ray absorption spectroscopy showed that both types of catalysts contained magnesium orthovanadate at vanadium loadings below 15 weight%, but above that loading, magnesium pyrovanadate may have been present. In general, MgO nanocrystals had roughly half the crystal size and double the surface area of the conventional MgO. In oxidative dehydrogenation of butane, nanocrystalline V/MgO gave higher selectivity to butene than conventional V/MgO at the same conversion. This difference was attributed to differences in vanadium domain size resulting from the higher surface areas of the nanocrystalline support, since characterization suggested that similar vanadium phases were present on both types of catalysts. Experiments in

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

    DEFF Research Database (Denmark)

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

    2016-01-01

    Low-speed marine diesel engines are mostly operated on heavy fuel oils, which have a high content of sulfur andash, including trace amounts of vanadium, nickel, and aluminum. In particular, vanadium oxides could catalyze in-cylinderoxidation of SO2 to SO3, promoting the formation of sulfuric acid...... and enhancing problems of corrosion. In the present work, thekinetics of the catalyzed oxidation was studied in a fixed-bed reactor at atmospheric pressure. Vanadium oxide nanoparticles weresynthesized by spray flame pyrolysis, i.e., by a mechanism similar to the mechanism leading to the formation...... of the catalyticspecies within the engine. Experiments with different particle compositions (vanadium/sodium ratio) and temperatures (300−800 °C) show that both the temperature and sodium content have a major impact on the oxidation rate. Kinetic parameters forthe catalyzed reaction are determined, and the proposed...

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

    Science.gov (United States)

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

    2003-12-01

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

  17. Diagnosis of deactivation sources for vanadium catalysts used in SO{sub 2} oxidation reaction and optimization of vanadium extraction from deactivated catalysts

    Energy Technology Data Exchange (ETDEWEB)

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

    2003-12-30

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

  18. Multisensor system for determination of polyoxometalates containing vanadium at its different oxidation states.

    Science.gov (United States)

    Rudnitskaya, Alisa; Evtuguin, Dmitry V; Gamelas, Jose A F; Legin, Andrey

    2007-04-30

    The electronic tongue (ET) multisensor system has been employed for the detection of metal-oxygen cluster anions (polyoxometalates) containing vanadium (IV/V) atoms. Sensitivity of a variety of potentiometric chemical sensors with plasticized polyvinyl chloride and chalcogenide glass membranes was evaluated with respect to vanadyl/vanadate ions, decavanadate and a series of Keggin-type polyoxometalates (POM) such as alpha-[SiW(11)V(IV)O(40)](6-), alpha-[SiW(11)V(V)O(40)](5-), alpha-[BW(11)V(IV)O(40)](7-), alpha-[BW(11)V(V)O(40)](6-), alpha-[PW(11)V(IV)O(40)](5-) and alpha-[PW(12-n)V(n)(V)O(40)]((3+n)-) (n=1, 2, 3). Sensor's responses to vanadium complexes were evaluated in the pH range of 2.4-6.5 and a set of sensors appropriate for detecting a variety of vanadium species was selected. Such sensor array was able to distinguish different vanadium complexes allowing their simultaneous quantification in binary (V(IV)/V(V)) mixtures. The vanillyl alcohol oxidation with alpha-[SiW(11)V(V)O(40)](5-) was monitored using ET to evaluate the capacity of proposed analytic system to detect simultaneously V(IV)/V(V) in POM under dynamic equilibrium. ET was demonstrated to be a promising tool for the discrimination and quantification of vanadium-containing POMs at different oxidation states. In particular, such a system could represent a significant interest for the mechanistic studies of redox reactions with POMs.

  19. A new hybrid electrochromic material: vanadium oxide/ eriochrome black T

    Science.gov (United States)

    Junior, L. F. R.; de Oliveira, R. S.; Ponzio, E. A.

    2015-03-01

    In this work, we describe the synthesis of a new hybrid material, which is consists of the eriochrome black T (sodium 1-[(1-hydroxynaphthcalen-2-yl-hydrazinylidene]-6-nitro-2- naphthol-4-sulfonate) and vanadium pentoxide xerogel using a melting sonoquenching technique. This hybrid material was apply in electrochromic electrodes. The hybrid material was characterized by X-ray difraction, FT-IR, AFM and spectroelectrochemically. The hybrid presented good reversibility and cyclability during 50 cycles studied, electrochromic efficiencies were about 50 cm2 C-1 (375 nm and 400 nm) and the ΔOD at 375 nm and 400 nm were 0.236 and 0.159 respectively wavelenghts. The response times were 0.7 to 3.3 s for 375 nm and 0.7 to 2.0 s for 400 nm. The hybrid is a potential material to be used in electrochromic applications.

  20. Structure-property relationships in NOx sensor materials composed of arrays of vanadium oxide nanoclusters

    Science.gov (United States)

    Putrevu, Naga Ravikanth; Darling, Seth B.; Segre, Carlo U.; Ganegoda, Hasitha; Khan, M. Ishaque

    2017-12-01

    The mixed-valent vanadium oxide based three-dimensional framework structure species [Cd3(H2O)12V16IVV2VO36(OH)6 (AO4)]·24H2O, (A = V,S) (Cd3(VO)o) represents a rare example of an interesting sensor material which exhibits NOx {NO + NO2} semiconducting gas sensor properties under ambient conditions. The electrical resistance of the sensor material Cd3(VO)o decreases in air. Combined characterization studies revealed that the building block, {V18O42(AO4)} cluster, of 3-D framework undergoes oxidation and remains intact for at least 2 months. The decrease in resistance is attributable to the reactivity of molecular oxygen towards vanadium which results in an increase in the oxidation state as well as the coordination number of vanadium center and decrease in band gap of Cd3(VO)o. Based on these results we propose that the changes in semiconducting properties of Cd3(VO)o under ambient conditions are due to the greater overlap between the O 2p and V 3d orbitals occurring during the oxidation.

  1. High-Performance Silver Window Electrodes for Top-Illuminated Organic Photovoltaics Using an Organo-molybdenum Oxide Bronze Interlayer.

    Science.gov (United States)

    Tyler, Martin S; Walker, Marc; Hatton, Ross A

    2016-05-18

    We report an organo-molybdenumn oxide bronze that enables the fabrication of high-performance silver window electrodes for top-illuminated solution processed organic photovoltaics without complicating the process of device fabrication. This hybrid material combines the function of wide-band-gap interlayer for efficient hole extraction with the role of metal electrode seed layer, enabling the fabrication of highly transparent, low-sheet-resistance silver window electrodes. Additionally it is also processed from ethanol, which ensures orthogonality with a large range of solution processed organic semiconductors. The key organic component is the low cost small molecule 3-mercaptopropionic acid, which (i) promotes metal film formation and imparts robustness at low metal thickness, (ii) reduces the contact resistance at the Ag/molybdenumn oxide bronze interface, (iii) and greatly improves the film forming properties. Silver electrodes with a thickness of 8 nm deposited by simple vacuum evaporation onto this hybrid interlayer have a sheet resistance as low as 9.7 Ohms per square and mean transparency ∼80% over the wavelength range 400-900 nm without the aid of an antireflecting layer, which makes them well-matched to the needs of organic photovoltaics and applicable to perovskite photovoltaics. The application of this hybrid material is demonstrated in two types of top-illuminated organic photovoltaic devices.

  2. Lattice Breathing Inhibited Layered Vanadium Oxide Ultrathin Nanobelts for Enhanced Sodium Storage.

    Science.gov (United States)

    Wei, Qiulong; Jiang, Zhouyang; Tan, Shuangshuang; Li, Qidong; Huang, Lei; Yan, Mengyu; Zhou, Liang; An, Qinyou; Mai, Liqiang

    2015-08-26

    Operating as the "rocking-chair" battery, sodium ion battery (SIB) with acceptable high capacity is a very promising energy storage technology. Layered vanadium oxide xerogel exhibits high sodium storage capacity. But it undergoes large lattice breathing during sodiation/desodiation, resulting in fast capacity fading. Herein, we develop a facile hydrothermal method to synthesize iron preintercalated vanadium oxide ultrathin nanobelts (Fe-VOx) with constricted interlayer spacing. Using the Fe-VOx as cathode for SIB, the lattice breathing during sodiation/desodiation is largely inhibited and the interlayer spacing is stabilized for reversible and rapid Na(+) insertion/extraction, displaying enhanced cycling and rate performance. This work presents a new strategy to reduce the lattice breathing of layered materials for enhanced sodium storage through interlayer spacing engineering.

  3. Morphology-dependent vanadium oxide nanostructures grown on Ti foil for Li-ion battery.

    Science.gov (United States)

    Wei, Lunzhen; Wang, Yuhang; Wang, Yanli; Xu, Ming; Zheng, Gengfeng

    2014-10-15

    Vanadium oxide is considered as a potential cathode material for lithium-ion batteries, while its performance is significantly restricted by its poor Li(+) ion diffusion rate and low electric conductivity. These ion and charge transport rates, however, are also well correlated with the 3-dimensional (3D) morphologies/structures of the electroactive materials. Herein, we synthesized three different nanostructured vanadium oxides on Ti foils. The comparison of electrochemical properties of these materials shows that the structures of electrodes have great influences on their performances. Among these structures, the nanoribbons are most beneficial for fast charge transfer and reduced contact resistance. In addition, the spaces between each nanoribbon provide efficient ion transport pathways and sufficient electrolyte penetration. The initial discharge and charge capacities of vanadium oxide nanoribbon reach to 322 and 310mAhg(-)(1), with a reversible discharge/charge capacity of 200mAhg(-)(1) at the current rate of 1C (1C=300mAg(-)(1)). Copyright © 2014 Elsevier Inc. All rights reserved.

  4. In situ laser Raman spectroscopy during sequential oxidizing and reducing conditions for a vanadium-phosphorous-oxide catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Soejarto, A. D.; Schrader, G. L. [Iowa State Univ. of Science and Technology, Ames, IA (United States). Dept. of Chemical Engineering; Coulston, G. W. [Dupont Central Research and Development, Wilmington, DE (United States)

    1996-10-01

    A vanadium-phosphorous-oxide (VPO) catalyst was studied by in situ laser Raman spectroscopy for n-butane oxidation to maleic anhydride. Raman characterization during steady-state flow revealed the presence of (VO){sub 2}P{sub 2}O{sub 7}. Sequential oxidizing and reducing conditions were explored at 350 degrees C and 400 degrees C. These unsteady-state operations showed that the formation of V(5+) phases was enhanced during oxidizing conditions, while Raman bands increased during reducing conditions, the latter due to the presence of (VO){sub 2}P{sub 2}O{sub 7}. 16 refs., 2 tabs. 6 figs.

  5. Effects of Vanadium Ions in Different Oxidation States on Myosin ATPase Extracted from the Solitary Ascidian, Halocynthia roretzi (Drasche) : Biochemistry

    OpenAIRE

    Hitoshi, Michibata; YUTAKA, ZENKO; Kenji, YAMADA; Masato, HASEGAWA; TATSURO, TERADA; TAKAHARU, NUMAKUANI; Biological Institute, Faculty of Science, University of Kanazawa; Department of Chemistry, Toyama College of Technology; Marine Biological Station,Tohoku University

    1989-01-01

    Some ascidians are known to accumulate vanadium ion within their tissues by 10^6-fold as that in sea water and store the metal ion in its reduced tetravalent and/or trivalent states. It is also well known that phosphoenzymes are inhibited by pentavalent vanadium ion over a range of 10nM to 1mM. In the present experiment we have therefore examined the effects of vanadium ions in different oxidation states on the activity of myosin ATPase extracted from the mantle of the ascidian, Halocynthia r...

  6. Oxidative dehydration of glycerol to acrylic acid over vanadium-impregnated zeolite beta

    Energy Technology Data Exchange (ETDEWEB)

    Pestana, Carolina F.M.; Guerra, Antonio C.O.; Turci, Cassia C. [Universidade Federal do Rio de Janeiro, RJ (Brazil). Inst. de Quimica; Ferreira, Glaucio B. [Universidade Federal Fluminense, Niteroi, RJ (Brazil). Inst. de Quimica; Mota, Claudio J.A., E-mail: cmota@iq.ufrj.br [INCT Energia e Ambiente, Universidade Federal do Rio de Janeiro, RJ (Brazil)

    2013-01-15

    The oxidative dehydration of glycerol to acrylic acid was studied over vanadium-impregnated zeolite Beta. Catalysts were prepared by wet impregnation of ammonium metavanadate over ammonium-exchanged zeolite Beta, followed by air calcination at 823 K. Impregnation reduced the specific surface area, but did not significantly affected the acidity (Bronsted and Lewis) of the zeolites. The catalytic evaluation was carried out in a fixed bed flow reactor using air as the carrier and injecting glycerol by means of a syringe pump. Acrolein was the main product, with acetaldehyde and hydroxy-acetone (acetol) being also formed. Acrylic acid was formed with approximately 25% selectivity at 548 K over the impregnated zeolites. The result can be explained by XPS (X-ray photoelectron spectroscopy) measurements, which indicated a good dispersion of the vanadium inside the pores. (author)

  7. A high-performance catalyst support for methanol oxidation with graphene and vanadium carbonitride.

    Science.gov (United States)

    Huang, Taizhong; Mao, Shun; Zhou, Guihua; Zhang, Zhaoliang; Wen, Zhenhai; Huang, Xingkang; Ci, Suqin; Chen, Junhong

    2015-01-28

    In this study, a graphene-vanadium carbonitride (G-V(C, N)) hybrid is reported as a novel support for the Pt catalyst in methanol oxidation. The catalytic activity of the Pt/G-V(C, N) hybrid for methanol oxidation is greatly enhanced compared with that of a commercial Pt/C catalyst with carbon black as the catalyst support. The outstanding catalytic activity of the Pt/G-V(C, N) catalyst suggests the potential of using graphene-metal carbonitride as the catalyst support in fuel cells.

  8. System Assessment of Carbon Dioxide Used as Gas Oxidant and Coolant in Vanadium-Extraction Converter

    Science.gov (United States)

    Du, Wei Tong; Wang, Yu; Liang, Xiao Ping

    2017-10-01

    With the aim of reducing carbon dioxide (CO2) emissions and of using waste resources in steel plants, the use of CO2 as a gas oxidant and coolant in the converter to increase productivity and energy efficiency was investigated in this study. Experiments were performed in combination with thermodynamic theory on vanadium-extraction with CO2 and oxygen (O2) mixed injections. The results indicate that the temperature of the hot metal bath decreased as the amount of CO2 introduced into O2 increased. At an injection of 85 vol.% O2 and 15 vol.% CO2, approximately 12% of additional carbon was retained in the hot metal. Moreover, the content of vanadium trioxide in the slag was higher. In addition, the O2 consumption per ton of hot metal was reduced by 8.5% and additional chemical energy was recovered by the controlled injection of CO2 into the converter. Therefore, using CO2 as a gas coolant was conducive to vanadium extraction, and O2 consumption was reduced.

  9. Oxydehydrogenation of Propane over Vanadium Oxide Supported on Kieselguhr or MCM-41

    Directory of Open Access Journals (Sweden)

    BY Jibril

    2012-06-01

    Full Text Available Supported vanadium oxide (5 wt% on either Kieselguhr or mesoporous MCM-41 was prepared using impregnation method and tested as a catalyst in propane oxidative dehydrogenation (POD. The catalyst samples were characterized using X-ray elemental analysis, Brunauer-Emmett-Teller (BET physisorption, and Z-ray Photoelectron Spectroscopy (XPS. After impregnation, the catalyst surface area decreased compared with that of the support. More drastic decrease was observed in the case of MCM-41 (77% than the Kieselguhr supported sample (48%. There are also different degrees of vanadium oxide-support interaction as reflected by the XPS result. Si-O binding energy of 531.5 eV was observed on MCM-41-supported sample compared with 529.5 eV for the Kieselguhr-supported sample. The catalyst tests were conducted at atmospheric pressure, with a propane to oxygen ratio of 0.7 - 3.6 and a reaction temperature of 400 - 700 °C. Oxidative dehydrogenation and combustion products were observed. Minor cracking reaction products (methane, ethane, and ethene were also produced above 550 °C. The highest propene yield of 14% was obtained from the Kieselguhr-supported sample at 700 °C and with a C3 H8 /O2  ratio of 1.5.

  10. Hysteresis Phenomena in Sulfur Dioxide Oxidation over Supported Vanadium Catalysts

    DEFF Research Database (Denmark)

    Masters, Stephen G.; Eriksen, Kim Michael; Fehrmann, Rasmus

    1997-01-01

    Catalyst deactivation and hysteresis behavior in industrial SO2-oxidation catalysts have been studied in the temperature region 350-480 C by combined in situ EPR spectroscopy and catalytic activity measurements. The feed gas composition simulated sulfuric acid synthesis gas and wet/dry de...

  11. Influence of phosphorus and potassium impurities on the properties of vanadium oxide supported on TiO2

    NARCIS (Netherlands)

    van Hengstum, A.J.; Pranger, J.; van Ommen, J.G.; Gellings, P.J.

    1984-01-01

    The catalytic properties of vanadium oxide catalysts supported on TiO2 from Tioxide were strongly affected by phosphorus and potassium, present as impurities in the TiO2 support. The effects observed were stronaly dependent on the type of hydrocarbon oxidised. In the oxidation of toluene to benzoic

  12. The oxidation of organic additives in the positive vanadium electrolyte and its effect on the performance of vanadium redox flow battery

    Science.gov (United States)

    Nguyen, Tam D.; Whitehead, Adam; Scherer, Günther G.; Wai, Nyunt; Oo, Moe O.; Bhattarai, Arjun; Chandra, Ghimire P.; Xu, Zhichuan J.

    2016-12-01

    Despite many desirable properties, the vanadium redox flow battery is limited, in the maximum operation temperature that can be continuously endured, before precipitation begins in the positive electrolyte. Many additives have been proposed to improve the thermal stability of the charged positive electrolyte. However, we have found that the apparent stability, revealed in laboratory testing, is often simply an artifact of the test method and arises from the oxidation of the additive, with corresponding partial reduction of V(V) to V(IV). This does not improve the stability of the electrolyte in an operating system. Here, we examined the oxidation of some typical organic additives with carboxyl, alcohol, and multi-functional groups, in sulfuric acid solutions containing V(V). The UV-vis measurements and titration results showed that many compounds reduced the state-of-charge (SOC) of vanadium electrolyte, for example, by 27.8, 88.5, and 81.9% with the addition of 1%wt of EDTA disodium salt, pyrogallol, and ascorbic acid, respectively. The cell cycling also indicated the effect of organic additives on the cell performance, with significant reduction in the usable charge capacity. In addition, a standard screening method for thermally stable additives was introduced, to quickly screen suitable additives for the positive vanadium electrolyte.

  13. Synthesis and characterization of alumina-supported vanadium oxide catalysts prepared by the molecular designed dispersion of VO(acac)2 complexes

    NARCIS (Netherlands)

    Weckhuysen, B.M.; Baltes, M.; Voort, P. van der; Ramachandra Rao, R.; Catana, Gabriela; Schoonheydt, R.A.; Vansant, E.F.

    2000-01-01

    Alumina-supported vanadium oxide catalysts have been prepared by the molecular designed dispersion method, using the vanadyl acetylacetonate complex (VO(acac)2). The complex has been adsorbed on the support from solution, followed by thermal conversion into the corresponding supported vanadium oxide

  14. FT-IR Study of Adsorption and Oxidation of Toluene on Vanadium Oxide layered on ZrO_2

    OpenAIRE

    Ohno, Takashi; Hatayama, Fumikazu; Yoshida, Tsukasa; Miyata, Hisashi

    1994-01-01

    The adsorption and oxdation of toluene on mono- and multi-layer V-Zr oxides prepared by the gas-phase method and the surface structure of the catalysts under reaction conditions have been studied by Fourier-transform infrared spectroscopy as well as the microcatalytic method. From the adsorption of toluene on the V-Zr oxides, it is found that Lewis-acidic sites (vanadium ion) play an important role to form a π-complex of toluene. The methyl group of the π-complex is dehydrogenated by the V=O ...

  15. Oxidation of lactic acid by Vanadium(V) in sulphuric acid medium: a kinetic and mechanistic study

    OpenAIRE

    Clementin, Rosilene Maria; Takashima, Keiko

    1993-01-01

    The rate of lactic acid, HL, oxidation by vanadium(V), V(V), in sulphuric acid solution has been measured by monitoring, spectrophotometrically, the absorbance change of vanadium(IV), V(IV) in 760 nm at 30°C. This oxidation is a acid-catalysed, its dependence on acidity being complex. The rate constant or not the ionic strength. This reaction exhibited first order dependence on the V(V) and HL concentrations respectively and minimal dependence on sulphuric acid at lower concentrations (0.25 -...

  16. Development of Vanadium Phosphaate Catalysts for Methanol Production by Selective Oxidation of Methane.

    Energy Technology Data Exchange (ETDEWEB)

    McCormick, R.L.

    1997-10-01

    This DOE sponsored study of methane partial oxidation was initiated at Amax Research and Development in Golden, CO in October of 1993. Shortly thereafter the management of Amax closed this R&D facility and the PI moved to the Colorado School of Mines. The project was begun again after contract transfer via a novation agreement. Experimental work began with testing of vandyl pyrophosphate (VPO), a well known alkane selective oxidation catalyst. It was found that VPO was not a selective catalyst for methane conversion yielding primarily CO. However, promotion of VPO with Fe, Cr, and other first row transition metals led to measurable yields for formaldehyde, as noted in the summary table. Catalyst characterization studies indicated that the role of promoters was to stabilize some of the vanadium in the V{sup 5+} oxidation state rather than the V{sup 4+} state formally expected for (VO){sub 2}P{sub 2}O{sub 7}.

  17. Ameliorative effect of vanadium on oxidative stress in stomach tissue of diabetic rats

    Science.gov (United States)

    Yilmaz-Ozden, Tugba; Kurt-Sirin, Ozlem; Tunali, Sevim; Akev, Nuriye; Can, Ayse; Yanardag, Refiye

    2014-01-01

    Between their broad spectrum of action, vanadium compounds are shown to have insulin mimetic/enhancing effects. Increasing evidence in experimental and clinical studies suggests that oxidative stress plays a major role in the pathogenesis of diabetes and on the onset of diabetic complications. Thus, preventive therapy can alleviate the possible side effects of the disease. The aim of the present study was to investigate the effect of vanadyl sulfate supplementation on the antioxidant system in the stomach tissue of diabetic rats. Male Swiss albino rats were randomly divided into 4 groups: control; control+vanadyl sulfate; diabetic; diabetic+vanadyl sulfate. Diabetes was induced by intraperitoneal injection of streptozotocin (STZ; 65 mg/kg body weight). Vanadyl sulfate (100 mg/kg body weight) was given daily by gavage for 60 days. At the last day of the experiment, stomach tissues were taken and homogenized to make a 10% (w/v) homogenate. Catalase (CAT), superoxide dismutase (SOD), glutathione reductase (GR), glutathione peroxidase (GPx), glutathione-S-transferase (GST), myeloperoxidase (MPO), carbonic anhydrase (CA), glucose-6-phosphate dehydrogenase (G6PD) and lactate dehydrogenase (LDH) activities were determined in the stomach tissue. CAT, SOD, GR, GPx, GST, CA, G6PD and LDH activities were increased in diabetic rats when compared to normal rats. Vanadium treatment significantly reduced the elevated activities of GR, GPx, GST compared with the diabetic group whereas the decreases in CAT, SOD, CA, G6PD and LDH activities were insignificant. No significant change was seen for MPO activity between the groups. It was concluded that vanadium could be used for its ameliorative effect against oxidative stress in diabetes. PMID:24856383

  18. A family of rare earth molybdenum bronzes: Oxides consisting of periodic arrays of interacting magnetic units

    Energy Technology Data Exchange (ETDEWEB)

    Schneemeyer, L.F. [Department of Chemistry, Montclair State University, Montclair, NJ 07043 (United States); Siegrist, T., E-mail: tsiegrist@fsu.edu [Department of Chemical and Biomedical Engineering, FAMU-FSU College of Engineering, Tallahassee, FL 32310 (United States); National High Magnetic Field Laboratory, Tallahassee, FL 32310 (United States); Besara, T. [National High Magnetic Field Laboratory, Tallahassee, FL 32310 (United States); Lundberg, M. [Department of Chemical and Biomedical Engineering, FAMU-FSU College of Engineering, Tallahassee, FL 32310 (United States); National High Magnetic Field Laboratory, Tallahassee, FL 32310 (United States); Sun, J. [Department of Chemical and Biomedical Engineering, FAMU-FSU College of Engineering, Tallahassee, FL 32310 (United States); Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6056 (United States); Singh, D.J. [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6056 (United States)

    2015-07-15

    The family of rare earth molybdenum bronzes, reduced ternary molybdates of composition LnMo{sub 16}O{sub 44,} was synthesized and a detailed structural study carried out. Bond valence sum (BVS) calculations clearly show that the molybdenum ions in tetrahedral coordination are hexavalent while the electron count in the primitive unit cell is odd. Yet, measurements show that the phases are semiconductors. The temperature dependence of the magnetic susceptibility of samples containing several different rare earth elements was measured. These measurements verified the presence of a 6.5 K magnetic phase transition not arising from the rare earth constituent, but likely associated with the unique isolated ReO{sub 3}-type Mo{sub 8}O{sub 36} structural subunits in this phase. To better understand the behavior of these materials, electronic structure calculations were performed within density functional theory. Results suggest a magnetic state in which these structural moieties have an internal ferromagnetic arrangement, with small ~1/8 μ{sub B} moments on each Mo. We suggest that the Mo{sub 8}O{sub 36} units behave like pseudoatoms with spin 1/2 derived from a single hole distributed over the eight Mo atoms that are strongly hybridized with the O atoms of the subunit. Interestingly, while the compound is antiferromagnetic, our calculations suggest that a field-stabilized ferromagnetic state, if achievable, will be a narrow band half-metal. - Graphical abstract: LnMo{sub 16}O{sub 44} phases comprise corner sharing tetrahedral and octahedral molybdenum ions. The MoO{sub 6} octahedra form Mo{sub 8}O{sub 36} units that are well separated and act like pseudo-atoms, accommodating 11 electrons each. - Highlights: • Single crystal X-ray diffraction refinements of LnMo{sub 16}O{sub 44} single crystals for Ln=Ce, Pr, Nd, Tb, Dy and Ho. • DFT calculations based on LaMo{sub 16}O{sub 44}. • [Mo{sub 8}O{sub 36}] units behaving as superatoms with a net magnetic moment of 1 µ

  19. Preparation of silicon carbide-supported vanadium oxide and its application of removing NO by ammonia

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Zi-Bo; Xu, Xu [Yangzhou University, College of Environmental Science and Engineering, Yangzhou, Jiangsu (China); Bai, Shu-Li [Wuyi University, College of Chemical and Environmental Engineering, Jiangmen, Guangdong (China); Guan, Yu-Jiang; Jiang, Sheng-Tao [Taizhou University, Environmental Engineering, Taizhou, Zhejiang (China)

    2017-03-15

    The aim of this work was to study the preparation of SiC-supported V{sub 2}O{sub 5} catalysts and the kinetics on selective catalytic reduction for NO with NH{sub 3} on the catalysts. Using incipient wetness impregnation methods, vanadium oxide was applied to silicon carbide to prepare a SiC-supported vanadium oxide. X-ray photoelectron spectroscopy analysis confirmed that V{sub 2}O{sub 5} existed in the prepared materials. Using the prepared materials as catalysts, selective catalytic reduction for NO by NH{sub 3} has been analyzed, and reaction kinetics on the catalysts was studied at 150-300 C. The obtained results showed that the reduction reaction on the catalysts is close to zero-order kinetics with respect to NH{sub 3}, first-order with respect to NO, and half-order to O{sub 2}. Apparent activation energy for the reduction reaction was found to be 38 kJ mol{sup -1}. The prepared materials are stable and reusable. (orig.)

  20. A family of rare earth molybdenum bronzes: Oxides consisting of periodic arrays of interacting magnetic units

    Science.gov (United States)

    Schneemeyer, L. F.; Siegrist, T.; Besara, T.; Lundberg, M.; Sun, J.; Singh, D. J.

    2015-07-01

    The family of rare earth molybdenum bronzes, reduced ternary molybdates of composition LnMo16O44, was synthesized and a detailed structural study carried out. Bond valence sum (BVS) calculations clearly show that the molybdenum ions in tetrahedral coordination are hexavalent while the electron count in the primitive unit cell is odd. Yet, measurements show that the phases are semiconductors. The temperature dependence of the magnetic susceptibility of samples containing several different rare earth elements was measured. These measurements verified the presence of a 6.5 K magnetic phase transition not arising from the rare earth constituent, but likely associated with the unique isolated ReO3-type Mo8O36 structural subunits in this phase. To better understand the behavior of these materials, electronic structure calculations were performed within density functional theory. Results suggest a magnetic state in which these structural moieties have an internal ferromagnetic arrangement, with small ~1/8 μB moments on each Mo. We suggest that the Mo8O36 units behave like pseudoatoms with spin 1/2 derived from a single hole distributed over the eight Mo atoms that are strongly hybridized with the O atoms of the subunit. Interestingly, while the compound is antiferromagnetic, our calculations suggest that a field-stabilized ferromagnetic state, if achievable, will be a narrow band half-metal.

  1. Vanadium and cadmium in vivo effects in teleost cardiac muscle: metal accumulation and oxidative stress markers.

    Science.gov (United States)

    Soares, S S; Martins, H; Gutiérrez-Merino, C; Aureliano, M

    2008-03-01

    Several biological studies associate vanadium and cadmium with the production of reactive oxygen species (ROS), leading to lipid peroxidation and antioxidant enzymes alterations. The present study aims to analyse and compare the oxidative stress responses induced by an acute intravenous exposure (1 and 7 days) to a sub-lethal concentration (5 mM) of two vanadium solutions, containing different vanadate n-oligomers (n=1-5 or n=10), and a cadmium solution on the cardiac muscle of the marine teleost Halobatrachus didactylus (Lusitanian toadfish). It was observed that vanadium is mainly accumulated in mitochondria (1.33+/-0.26 microM), primarily when this element was administrated as decameric vanadate, than when administrated as metavanadate (432+/-294 nM), while the highest content of cadmium was found in cytosol (365+/-231 nM). Indeed, decavanadate solution promotes stronger increases in mitochondrial antioxidant enzymes activities (catalase: +120%; superoxide dismutase: +140%) than metavanadate solution. On contrary, cadmium increases cytosolic catalase (+111%) and glutathione peroxidases (+50%) activities. It is also observed that vanadate oligomers induce in vitro prooxidant effects in toadfish heart, with stronger effects induced by metavanadate solution. In summary, vanadate and cadmium are differently accumulated in blood and cardiac subcellular fractions and induced different responses in enzymatic antioxidant defence mechanisms. In the present study, it is described for the first time the effects of equal doses of two different metals intravenously injected in the same fish species and upon the same exposure period allowing to understand the mechanisms of vanadate and cadmium toxicity in fish cardiac muscle.

  2. Structure, activity and kinetics of supported molybdenum oxide and mixed molybdenum-vanadium oxide catalysts prepared by flame spray pyrolysis for propane OHD

    DEFF Research Database (Denmark)

    Høj, Martin; Kessler, Thomas; Beato, Pablo

    2013-01-01

    . The catalytic experiments showed that the most selective molybdenum oxide catalysts for the ODH reaction were those with high Mo loadings of 7 to 15 wt% Mo, while the most selective mixed molybdenum-vanadium oxide catalyst were at 4 wt% Mo, where separate surface species of molybdenum and vanadium oxide were...... observed by Raman spectroscopy. A simple kinetic model based on the propane ODH reaction, parallel combustion of propane and sequential combustion of propene described the experimental results well and could be used to determine the optimal reaction conditions. © 2013 Elsevier B.V....

  3. Facile Synthesis of Vanadium Oxide/Reduced Graphene Oxide Composite Catalysts for Enhanced Hydroxylation of Benzene to Phenol

    Directory of Open Access Journals (Sweden)

    Yongli Dong

    2016-05-01

    Full Text Available The vanadium oxide/reduced graphene oxide (VOx/RGO composites have been prepared by a simple solvothermal method with the assistance of cationic surfactant cetyltrimethylammonium bromide (CTAB. The microstructure and morphology of the resultant VOx/RGO composites have been well characterized. The VOx nanoparticles are highly dispersed on the RGO sheets with a particle size of about 25 nm. When used as hydroxylation catalysts, the VOx/RGO composites are more efficient than individual RGO and vanadium oxide catalysts. The enhanced catalytic performance may be related to not only the well dispersed VOx active species, but also the hydrophobic surface and huge π-electron system of RGO for the adsorption and activation of benzene. In addition, the effects of calcination conditions on the microstructure and catalytic properties of VOx/RGO composites have also been investigated. The uniform VOx nanoparticles on the separated RGO sheets show highly efficient catalytic performance, while the formation of aggregated HxV2O5 and bulk V2O5 species along with the destruction of RGO sheets are poor for the hydroxylation of benzene. Up to 17.4% yield of phenol is achieved under the optimized catalytic reaction conditions.

  4. Three-terminal field effect devices utilizing thin film vanadium oxide as the channel layer

    Science.gov (United States)

    Ruzmetov, Dmitry; Gopalakrishnan, Gokul; Ko, Changhyun; Narayanamurti, Venkatesh; Ramanathan, Shriram

    2010-06-01

    Electrostatic control of the metal-insulator transition (MIT) in an oxide semiconductor could potentially impact the emerging field of oxide electronics. Vanadium dioxide (VO2) is of particular interest due to the fact that the MIT happens in the vicinity of room temperature and it is considered to exhibit the Mott transition. We present a detailed account of our experimental investigation into three-terminal field effect transistor-like devices using thin film VO2 as the channel layer. The gate is separated from the channel through an insulating gate oxide layer, enabling true probing of the field effect with minimal or no interference from large leakage currents flowing directly from the electrode. The influence of the fabrication of multiple components of the device, including the gate oxide deposition, on the VO2 film characteristics is discussed. Further, we discuss the effect of the gate voltage on the device response, point out some of the unusual characteristics including temporal dependence. A reversible unipolar modulation of the channel resistance upon the gate voltage is demonstrated for the first time in optimally engineered devices. The results presented in this work are of relevance toward interpreting gate voltage response in such oxides as well as addressing challenges in advancing gate stack processing for oxide semiconductors.

  5. Graphene Oxide Wrapped Amorphous Copper Vanadium Oxide with Enhanced Capacitive Behavior for High-Rate and Long-Life Lithium-Ion Battery Anodes.

    Science.gov (United States)

    Zhao, Kangning; Liu, Fengning; Niu, Chaojiang; Xu, Wangwang; Dong, Yifan; Zhang, Lei; Xie, Shaomei; Yan, Mengyu; Wei, Qiulong; Zhao, Dongyuan; Mai, Liqiang

    2015-12-01

    Graphene oxide-wrapped amorphous copper vanadium oxide is fabricated through a template-engaged redox reaction followed by vacuum dehydration. This material exhibits high reversible capacity, excellent rate capability, and out standing high-rate cyclability. The outstanding performance is attributed to the fast capacitive charge storage and the in situ formed copper with enhanced electrical conductivity.

  6. Application of vanadium incorporated phosphomolybdate supported on the modified kaolinin synthesis of diphenyl carbonate by oxidative carbonylation with phenol

    Directory of Open Access Journals (Sweden)

    Peng Meng

    2017-01-01

    Full Text Available Keggin-type molybdophosphoric acid, molybdophosphoric salt and vanadium incorporated molybdophosphoric salt supported on the modified kaolin (MK were investigated as redox co-catalysts for the oxidative carbonylation of phenol to diphenyl carbonate (DPC in the absence of solvent. The 20 wt.% of MnAMPV5 (one kind of vanadium incorporated molybdophosphoric salt loaded on MK showed the highest catalytic activity with the yield of 24.68% and a TON of 306, while the selectivity amounts to nearly 100% in all the carbonylation reactions. The catalysts were characterized by XRD, BET, XPS and H2-TPR. The reusability study showed that the catalysts were stable and active.

  7. Vanadium carbide and graphite promoted Pd electrocatalyst for ethanol oxidation in alkaline media

    Science.gov (United States)

    Yan, Zaoxue; Zhang, Mingmei; Xie, Jimin; Shen, Pei Kang

    2013-12-01

    The vanadium carbide particles with the diameter of 1-3 nm on graphitized resin (GC-V8C7) are synthesized through ionic exchange process. The materials are characterized by XRD, Raman, TEM, SEM and EDS measurements. The results prove that the ion-exchange resin as both carbon source and dispersion media favors the formation of very uniform and small (1-3 nm) V8C7 particles, and protect the V8C7 from conglomeration even at the temperature of 1500 °C. Meanwhile, the vanadium compound is found efficient catalytic effect on graphitization of ion-exchange resin, leading to high graphitization degree of GC-V8C7. Pd particles are loaded on the GC-V8C7 materials as electrocatalyst (Pd/GC-V8C7) for ethanol oxidation in alkaline media. The cyclic voltammograms measurements show that both V8C7 and GC (graphitized ion-exchange resin) give Pd electrocatalyst improved catalytic performance in activity, stability and overpotential, compared with that of Pd supporting on Vulcan XC-72 carbon (Pd/C). The present synthesizing method of GC-V8C7 is simple and effective, which can be readily scaled up for mass production of other nanomaterials.

  8. Influence of doping on the properties of vanadium oxide gel films

    Energy Technology Data Exchange (ETDEWEB)

    Pergament, A L; Velichko, A A; Berezina, O Ya; Kazakova, E L; Kuldin, N A; Artyukhin, D V [Physics and Technology Department, Petrozavodsk State University, Petrozavodsk 185910 (Russian Federation)], E-mail: aperg@psu.karelia.ru

    2008-10-22

    The effect of doping with H and W on the properties of V{sub 2}O{sub 5} and VO{sub 2} derived from V{sub 2}O{sub 5} gel has been studied. It is shown that the treatment of V{sub 2}O{sub 5} in low-temperature RF hydrogen plasma for 1-10 min leads to either hydration of vanadium pentoxide or its reduction (depending on the treatment conditions) to lower vanadium oxides. For some samples, which are subject to plasma treatment in the discharge active zone, a non-ordinary temperature dependence of resistance, with a maximum at T{approx}100 K, is observed. For W-doped VO{sub 2} films, it is shown that substitution of V{sup 4+} with W{sup 6+} results in a decrease of the temperature of the metal-insulator transition. Also, it has been shown that the doping of initial films with {approx}3 at.% of W reduces the statistical scatter in the threshold parameters of the switching devices with S-shaped I-V characteristics on the basis of V{sub 2}O{sub 5} gel films. (fast track communication)

  9. Oxidation States of Grim Glasses in EET79001 Based on Vanadium Valence

    Science.gov (United States)

    Sutton, S. R.; Rao, M. N.; Nyquist, L. E.

    2010-01-01

    Gas-rich impact-melt (GRIM) glasses in SNC meteorites are very rich in Martian atmospheric noble gases and sulfur suggesting a possible occurrence of regolith-derived secondary mineral assemblages in these samples. Previously, we have studied two GRIM glasses, 506 and 507, from EET79001 Lith A and Lith B, respectively, for elemental abundances and spatial distribution of sulfur using EMPA (WDS) and FE-SEM (EDS) techniques and for sulfur-speciation using K-edge XANES techniques. These elemental and FE-SEM micro-graph data at several locations in the GRIM glasses from Shergotty (DBS), Zagami 994 and EET79001, Lith B showed that FeO and SO3 are positively correlated (SO3 represents a mixture of sulfide and sulfate). FE-SEM (EDS) study revealed that the sulfur-rich pockets in these glasses contain numerous micron-sized iron-sulfide (Fe-S) globules sequestered throughout the volume. However, in some areas (though less frequently), we detected significant Fe-S-O signals suggesting the occurrence of iron sulfate. These GRIM glasses were studied by K-edge microXANES techniques for sulfur speciation in association with iron in sulfur-rich areas. In both samples, we found the sulfur speciation dominated by sulfide with minor oxidized sulfur mixed in with various proportions. The abundance of oxidized sulfur was greater in 506 than in 507. Based on these results, we hypothesize that sulfur initially existed as sulfate in the glass precursor materials and, on shock-impact melting of the precursor materials producing these glasses, the oxidized sulfur was reduced to predominately sulfide. In order to further test this hypothesis, we have used microXANES to measure the valence states of vanadium in GRIM glasses from Lith A and Lith B to complement and compare with previous analogous measurements on Lith C (note: 506 and 507 contain the largest amounts of martian atmospheric gases but the gas-contents in Lith C measured by are unknown). Vanadium is ideal for addressing this re

  10. Properties of electrochromic nickel-vanadium oxide films sputter-deposited from nonmagnetic alloy target

    Science.gov (United States)

    Avendano, Esteban; Azens, Andris; Niklasson, Gunnar A.

    2001-11-01

    In this study we investigate the structure, composition, diffusion coefficient, and electrochromic properties of nickel-vanadium oxide films as a function of deposition conditions. Polycrystalline films have been deposited by DC magnetron sputtering from a nonmagnetic target of Ni0.93V0.07 in an atmosphere of O2/Ar and Ar/O2/H2, with the gas flow ratios varied systematically to cover the range from nearly-metallic to overoxidized films. The results contradict the usual view that films deposited in O2/Ar are dark brown in their as-deposited state. While such films can easily be deposited, the optimum electrochromic properties have been observed at O2/Ar ratios giving nearly transparent films. Addition of hydrogen to the sputtering atmosphere improved cycling stability of the films. The diffusion coefficient has been determined by the Galvanostatic Intermittent Titration Technique (GITT).

  11. Induced dipole in vanadium-doped zinc oxide nanosheets and its effects on photoelectrochemical water splitting

    Science.gov (United States)

    Lee, Song Mi; Shin, Sung-Ho; Nah, Junghyo; Lee, Min Hyung

    2017-09-01

    Appropriate control of energy band bending at the interface between semiconductors and electrolytes are closely related to performance of photoelectrochemical (PEC) water splitting. Dipoles formed near the surface of semiconductors induces energy band bending at the interface. Energy band bending control has been demonstrated by employing charged molecules and piezoelectric materials. However, chemical and piezoelectric approaches have demerit of chemical instability and inducement of instantaneous dipole, respectively. To overcome these problems, we adopted the ferroelectric material for PEC water splitting, where spontaneous dipoles in the material can be oriented by applying external electric field. In this work, we hydrothermally synthesized vanadium (V)-doped ferroelectric ZnO nanosheets and employed to systematically investigate the dipole effect on performance of V-doped ZnO PEC for water oxidation. Consequently, positively polarized V-doped ZnO photoanode exhibits 125% enhanced water splitting efficiency compared to negatively polarized ones due to favorable band bending for carrier transport from semiconductor to water.

  12. Switching adhesion forces by crossing the metal–insulator transition in Magnéli-type vanadium oxide crystals

    Directory of Open Access Journals (Sweden)

    Bert Stegemann

    2011-01-01

    Full Text Available Magnéli-type vanadium oxides form the homologous series VnO2n-1 and exhibit a temperature-induced, reversible metal–insulator first order phase transition (MIT. We studied the change of the adhesion force across the transition temperature between the cleavage planes of various vanadium oxide Magnéli phases (n = 3 … 7 and spherical titanium atomic force microscope (AFM tips by systematic force–distance measurements with a variable-temperature AFM under ultrahigh vacuum conditions (UHV. The results show, for all investigated samples, that crossing the transition temperatures leads to a distinct change of the adhesion force. Low adhesion corresponds consistently to the metallic state. Accordingly, the ability to modify the electronic structure of the vanadium Magnéli phases while maintaining composition, stoichiometry and crystallographic integrity, allows for relating frictional and electronic material properties at the nano scale. This behavior makes the vanadium Magnéli phases interesting candidates for technology, e.g., as intelligent devices or coatings where switching of adhesion or friction is desired.

  13. Vanadium sulfides interwoven nanoflowers based on in-situ sulfurization of vanadium oxides octahedron on nickel foam for efficient hydrogen evolution

    Science.gov (United States)

    Rao, Yi; Zhang, Li-Ming; Shang, Xiao; Dong, Bin; Liu, Yan-Ru; Lu, Shan-Shan; Chi, Jing-Qi; Chai, Yong-Ming; Liu, Chen-Guang

    2017-11-01

    Novel vanadium sulfides interwoven nanoflowers supported on nickel foam (VO-S/NF) has been synthesized through a facile two-step access. Firstly, octahedron-structured vanadium oxides as precursor were anchored on the surface of NF (VO/NF) by a hydrothermal process. Secondly, in-situ sulfurization in H2S gas has been applied to prepare VO-S/NF. XRD shows that VO-S/NF sample is composed of mixture phases including VS and Ni3S2, implying the interface effect between VS and Ni3S2. SEM images demonstrate that octahedron-structured VO from VO/NF changed to VO-S interwoven nanoflowers on VO-S/NF, which are composed of vertical interwoven nanosheets. It can enlarge surface area to expose abundant active sites and facilitate mass and charge transportation. The electrochemical measurements display the enhanced HER activity of VO-S/NF requiring an overpotential of 165 mV to deliver 10 mA cm-2, which may be ascribed to the novel structure of VS interwoven nanosheets and the synergistic effect between VS and Ni3S2. Furthermore, VO-S/NF remains high HER activity for at least 10 h with excellent structural stability confirmed by post-HER characterization such as XRD, SEM and XPS. Therefore, it may provide a new way to design multiple transition metal sulfides-based electrocatalysts with unique nanostructure as well as interface effect for HER in alkaline.

  14. Visible light photooxidative performance of a high-nuclearity molecular bismuth vanadium oxide cluster

    Directory of Open Access Journals (Sweden)

    Johannes Tucher

    2014-05-01

    Full Text Available The visible light photooxidative performance of a new high-nuclearity molecular bismuth vanadium oxide cluster, H3[{Bi(dmso3}4V13O40], is reported. Photocatalytic activity studies show faster reaction kinetics under anaerobic conditions, suggesting an oxygen-dependent quenching of the photoexcited cluster species. Further mechanistic analysis shows that the reaction proceeds via the intermediate formation of hydroxyl radicals which act as oxidant. Trapping experiments using ethanol as a hydroxyl radical scavenger show significantly decreased photocatalytic substrate oxidation in the presence of EtOH. Photocatalytic performance analyses using monochromatic visible light irradiation show that the quantum efficiency Φ for indigo photooxidation is strongly dependent on the irradiation wavelength, with higher quantum efficiencies being observed at shorter wavelengths (Φ395nm ca. 15%. Recycling tests show that the compound can be employed as homogeneous photooxidation catalyst multiple times without loss of catalytic activity. High turnover numbers (TON ca. 1200 and turnover frequencies up to TOF ca. 3.44 min−1 are observed, illustrating the practical applicability of the cluster species.

  15. Hydration effects on the molecular structure of silica-supported vanadium oxide catalysts: A combined IR, Raman, UV–vis and EXAFS study

    OpenAIRE

    Keller, D.E.; Visser, T; Soulimani, F.; Koningsberger, D. C.; Weckhuysen, B.M.

    2007-01-01

    The effect of hydration on the molecular structure of silica-supported vanadium oxide catalysts with loadings of 1–16 wt.% V has been systematically investigated by infrared, Raman, UV–vis and EXAFS spectroscopy. IR and Raman spectra recorded during hydration revealed the formation of V–OH groups, characterized by a band at 3660 cm−1. Hydroxylation was found to start instantaneously upon exposure to traces of water, reflecting a very high sensitivity of the supported vanadium oxide catalysts ...

  16. Molecular manipulation of solid state structure: influences of organic components on vanadium oxide architectures

    Science.gov (United States)

    Hagrman, Pamela J.; Finn, Robert C.; Zubieta, Jon

    2001-11-01

    /organic composites. In the past decade, this general strategy has been exploited in the evolution of a family of vanadium oxides incorporating structure-directing organic or secondary-metal organic subunits, which are the topic of this review. The synthetic approach to novel vanadium oxide solids occupies the interface between materials science and coordination chemistry. The emerging theme focuses on the association of an organic component, acting as a ligand, tether, or structure directing moiety, with the inorganic framework of the solid to provide unique composites. While some organic components may limit the size of inorganic cluster subunits of a solid by passivating the surface of an aggregate through capping, such ligands may also serve to link inorganic subunits into complex networks. In other cases, the organic subunit, rather than participating as a covalently bound unit of the framework, acts in a structure directing role, producing amphiphilic materials whose structures are determined by hydrophobic-hydrophilic interactions. This latter feature is reminiscent of the factors influencing biomineralization, a field which may prove relevant to the development of new strategies for the controlled synthesis of organized inorganic and organic/inorganic composite materials. These various approaches to the "design" of inorganic solids are discussed and assessed in terms of the new structural types recently observed in the vanadium oxide chemistry.

  17. Three-dimensional Nitrogen-Doped Reduced Graphene Oxide/Carbon Nanotube Composite Catalysts for Vanadium Flow Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Shaofang [School of Mechanical and Materials Engineering, Washington State University, WA, 99164 USA.; Zhu, Chengzhou [School of Mechanical and Materials Engineering, Washington State University, WA, 99164 USA.; Song, Junhua [School of Mechanical and Materials Engineering, Washington State University, WA, 99164 USA.; Engelhard, Mark H. [Environmental Molecular Science Laboratory, Pacific Northwest National Laboratory, Richland, WA 99354 USA.; Du, Dan [School of Mechanical and Materials Engineering, Washington State University, WA, 99164 USA.; Lin, Yuehe [School of Mechanical and Materials Engineering, Washington State University, WA, 99164 USA.; Environmental Molecular Science Laboratory, Pacific Northwest National Laboratory, Richland, WA 99354 USA.

    2017-02-22

    The development of vanadium redox flow battery is limited by the sluggish kinetics of the reaction, especially the cathodic VO2+/VO2+ redox couples. Therefore, it is vital to develop new electrocatalyst with enhanced activity to improve the battery performance. Herein, we first synthesized the hydrogel precursor by a facile hydrothermal method. After the following carbonization, nitrogen-doped reduced graphene oxide/carbon nanotube composite was obtained. By virtue of the large surface area and good conductivey, which are ensured by the unique hybrid structure, as well as the proper nitrogen doping, the as-prepared composite presents enhanced catalytic performance toward the VO2+/VO2+ redox reaction. We also demonstrated the composite with carbon nanotube loading of 2 mg/mL exhibits the highest activity and remarkable stability in aqueous solution due to the strong synergy between reduced graphene oxide and carbon nanotubes, indicating that this composite might show promising applications in vanadium redox flow battery.

  18. Amorphous Cobalt Vanadium Oxide as a Highly Active Electrocatalyst for Oxygen Evolution.

    Science.gov (United States)

    Liardet, Laurent; Hu, Xile

    2018-01-05

    The water-splitting reaction provides a promising mechanism to store renewable energies in the form of hydrogen fuel. The oxidation half-reaction, the oxygen evolution reaction (OER), is a complex four-electron process that constitutes an efficiency bottleneck in water splitting. Here we report a highly active OER catalyst, cobalt vanadium oxide. The catalyst is designed on the basis of a volcano plot of metal-OH bond strength and activity. The catalyst can be synthesized by a facile hydrothermal route. The most active pure-phase material ( a- CoVO x ) is X-ray amorphous and provides a 10 mA cm -2 current density at an overpotential of 347 mV in 1 M KOH electrolyte when immobilized on a flat substrate. The synthetic method can also be applied to coat a high-surface-area substrate such as nickel foam. On this three-dimensional substrate, the a- CoVO x catalyst is highly active, reaching 10 mA cm -2 at 254 mV overpotential, with a Tafel slope of only 35 mV dec -1 . This work demonstrates a- CoVO x as a promising electrocatalyst for oxygen evolution and validates M-OH bond strength as a practical descriptor in OER catalysis.

  19. Influence of Na diffusion on thermochromism of vanadium oxide films and suppression through mixed-alkali effect

    Energy Technology Data Exchange (ETDEWEB)

    Miller, Mark J.; Wang, Junlan, E-mail: junlan@u.washington.edu

    2015-10-15

    Highlights: • Vanadium oxide films were reactively sputtered on three types of glass substrates. • Na diffusion from soda-lime glass undesirably inhibited thermochromism. • Na diffusion was suppressed by replacing half of sodium in glass with potassium. • Mixed-alkali effect promotes thermochromic VO{sub 2} films on glass substrates. - Abstract: Vanadium(IV) oxide possesses a reversible first-order phase transformation near 68 °C. Potential applications of the material include advanced optical devices and thermochromic smart windows. In this study, vanadium oxide films were grown on three types of glass substrates using reactive DC magnetron sputtering and were then annealed in air. The substrates were characterized with energy-dispersive X-ray spectroscopy, and the films were characterized with X-ray photoelectron spectroscopy, X-ray diffraction, scanning electron microscopy, atomic force microscopy, transmission electron microscopy, and UV-Vis-NIR spectrophotometry. The results show that the composition of the substrate has a major impact on the microstructure and optical properties of the deposited films. Sodium (Na) in the glass can undesirably inhibit thermochromism; however, replacing half of the Na with potassium (K) suppresses the Na diffusion and promotes the nucleation of pure VO{sub 2} with superior thermochromic functionality. The improved performance is attributed to the mixed-alkali effect between Na and K. These findings are both scientifically and technologically important since soda (Na{sub 2}O) is an essential flux material in glass products such as windows.

  20. Release of vanadium from oxidized sediments: insights from different extraction and leaching procedures.

    Science.gov (United States)

    Cappuyns, V; Swennen, R

    2014-02-01

    Although the attention for vanadium (V) as a potentially harmful element is growing and some countries adopted threshold values for V in soils, sediments, groundwater, or surface water, V is generally of little importance in environmental legislation and the knowledge about the behavior of V in the environment is still limited. In the present study, the release of V from oxidized sediments, sediment-derived soils, and certified reference materials was investigated by means of several types of leaching tests and extractions that are frequently used for soil and sediment characterization. The pHstat leaching tests and single and sequential extractions applied in this study show that V generally displays a very limited actual and potential mobility in sediment. "Mobile" V concentrations, as estimated by the amount of V released by a single extraction with CaCl2 0.01 mol L(-1), were low, even in the most contaminated sediment samples. Only under strongly acidifying conditions (pH 2), such as in the case of ingestion of soil or sediment or in accidental spills, a substantial release of V can be expected.

  1. The microstructures and electrical properties of Y-doped amorphous vanadium oxide thin films

    Science.gov (United States)

    Gu, Deen; Zhou, Xin; Guo, Rui; Wang, Zhihui; Jiang, Yadong

    2017-03-01

    One of promising approaches for further improving the sensitivity of microbolometer arrays with greatly-reduced pixel size is using the thermal-sensitive materials with higher performance. In this paper, Y-doped vanadium oxide (VOx) thin films prepared by a reactively sputtering process exhibit enhanced performance for the microbolometer application compared with frequently-applied VOx thin films. Both undoped and Y-doped VOx thin films are amorphous due to the relatively low deposition temperature. Y-doped VOx thin films exhibit smoother surface morphology than VOx due to the restrained expansion of particles during depositions. Y-doping increases the temperature coefficient of resistivity by over 20% for the doping level of 1.30 at%. The change rate of resistivity, after aging for 72 h, of thin films was reduced from about 15% for undoped VOx to 2% due to the introduction of Y. Moreover, Y-doped VOx thin films have a low 1/f noise level as VOx ones. Y-doping provides an attractive approach for preparing VOx thermal-sensitive materials with enhanced performance for microbolometers.

  2. The mechanism of cysteine detection in biological media by means of vanadium oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Bezerra, A. G. [Universidade Tecnologica Federal do Parana, Departamento Academico de Fisica (Brazil); Barison, A. [Universidade Federal do Parana, Departamento de Quimica (Brazil); Oliveira, V. S. [Universidade Federal do Parana, Departamento de Fisica (Brazil); Foti, L.; Krieger, M. A. [Fundacao Oswaldo Cruz, Instituto de Biologia Molecular do Parana (Brazil); Dhalia, R.; Viana, I. F. T. [Fundacao Oswaldo Cruz, Centro de Pesquisas Aggeu Magalhaes (Brazil); Schreiner, W. H., E-mail: wido@fisica.ufpr.br [Universidade Federal do Parana, Departamento de Fisica (Brazil)

    2012-09-15

    We report on the interaction of vanadate nanoparticles, produced using the laser ablation in liquids synthesis, with cysteine in biological molecules. Cysteine is a very important amino acid present in most proteins, but also because cysteine and the tripeptide glutathione are the main antioxidant molecules in our body system. Detailed UV-Vis absorption spectra and dynamic light scattering measurements were done to investigate the detection of cysteine in large biological molecules. The intervalence band of the optical absorption spectra shows capability for quantitative cysteine sensing in the {mu}M range in biological macromolecules. Tests included cytoplasmic repetitive antigen and flagellar repetitive antigen proteins of the Trypanosoma cruzi protozoa, as well as the capsid p24 proteins from Human Immunodeficiency Virus type 1 and type 2. Detailed NMR measurements for hydrogen, carbon, and vanadium nuclei show that cysteine in contact with the vanadate looses hydrogen of the sulphydryl side chain, while the vanadate is reduced. The subsequent detachment of two deprotonated molecules to form cystine and the slow return to the vanadate complete the oxidation-reduction cycle. Therefore, the vanadate acts as a charge exchanging catalyst on cysteine to form cystine. The NMR results also indicate that the nanoparticles are not formed by the common orthorhombic V{sub 2}O{sub 5} form.

  3. Properties of Vanadium-Doped Indium Oxide Deposited at Room Temperature as Transparent Conductor for Inverted Polymer Solar Cells

    Science.gov (United States)

    Choi, Min-Jun; Lim, Keun Yong; Park, Hyun-Woo; Kim, Han-Ki; Hwang, Do Kyung; Lim, Sung-Jin; Shim, Jae Won; Chung, Kwun-Bum

    2017-10-01

    The properties of vanadium-doped indium oxide (IVO) deposited at room temperature as a transparent conductor for inverted polymer solar cells have been investigated as a function of the vanadium doping concentration. IVO film prepared with V doping concentration of 0.03% showed optimal properties for use as a transparent conductor with figure of merit of 4.35 × 10-3 Ohm-1, related to altered band alignment between the Fermi level and conduction-band minimum. In the optimal optoelectrical conditions for the IVO film, performance optimization of PTB7:PC70BM inverted polymer solar cells resulted in maximum power conversion efficiency of 4.7 ± 0.4% under simulated air mass 1.5 global illumination at 100 mW/cm2.

  4. A high-resolution electron microscopy investigation of TiO sub 2 (B)-supported vanadium oxide catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Wallenberg, L.R.; Sanati, M.; Andersson, A. (Lund Institute of Technology (Sweden))

    1990-11-01

    TiO{sub 2}(B) crystals were found to be isomorphic with those of its precursor, K{sub 2}TI{sub 4}O{sub 9}. The former crystals had a large number of facetted voids, 3-30 nm, formed as a result of the removal of potassium and water in preceding hydrolysis and calcination steps, respectively. TiO{sub 2}(B)-supported vanadium oxide catalysts with loadings in the range 0.25-10 theoretical layers were prepared by impregnation of the support with an oxalic acid solution of NH{sub 4}VO{sub 3} followed by calcination in air. HREM micrographs of catalysts with a low vanadium loading, recorded using a low electron-dose imaging technique, showed that the surfaces, in the initial stage, were without any anomalous surface structure. This observation may be due to a similar structure of the support and the deposited vanadia phase. At high vanadium loadings, both amorphous and crystalline particles were seen, in agreement with the features revealed by the use of IR spectroscopy. For catalysts with low vanadium loadings, the IR difference spectra showed the presence of tetrahedrally coordinated V{sup 4+} and V{sub 5+} species. In a fully converged electron beam, reduction of the support and the vanadia phases occurred, resulting in the formation of small crystallites. The catalysts were used for the oxidation of toluene to benzaldehyde. However, contrary to what has been observed for the ammoxidation producing benzonitrile, no enhanced catalytic properties, in comparison with those of crystalline V{sub 2}O{sub 5}, were obtained using TiO{sub 2}(B) as support.

  5. Investigation of Silica-Supported Vanadium Oxide Catalysts by High-Field 51 V Magic-Angle Spinning NMR

    Energy Technology Data Exchange (ETDEWEB)

    Jaegers, Nicholas R.; Wan, Chuan; Hu, Mary Y.; Vasiliu, Monica; Dixon, David A.; Walter, Eric; Wachs, Israel E.; Wang, Yong; Hu, Jian Zhi

    2017-03-14

    Supported V2O5/SiO2 catalysts were studied using solid state 51V MAS NMR at a sample spinning rate of 36 kHz and at a magnetic field of 19.975 T for a better understanding of the coordination of the vanadium oxide as a function of environmental conditions . Structural transformations of the supported vanadium oxide species between the catalyst in the dehydrated state and hydrated state under an ambient environment were revisited to examine the degree of oligomerization and the effect of water. The experimental results indicate the existence of a single dehydrated surface vanadium oxide species that resonates at -675 ppm and two vanadium oxide species under ambient conditions that resonate at -566 and -610 ppm, respectively. No detectable structural difference was found as a function of vanadium oxide loading on SiO2 (3% V2O5/SiO2 and 8% V2O5/SiO2). Quantum chemistry simulations of the 51V NMR chemical shifts on predicted surface structures were used as an aide in understanding potential surface vanadium oxide species on the silica support. The results suggest the formation of isolated surface VO4 units for the dehydrated catalysts with the possibility of dimer and cyclic trimer presence. The absence of bridging V-O-V vibrations (~200-300 cm-1) in the Raman spectra [Gao et al. J. Phys. Chem. B 1998, 102, 10842-10852], however, indicates that the isolated surface VO4 sites are the dominant dehydrated surface vanadia species on silica. Upon exposure to water, hydrolysis of the bridging V-O-Si bonds is most likely responsible for the decreased electron shielding experienced by vanadium. No indicators for the presence of hydrated decavanadate clusters or hydrated vanadia gels previously proposed in the literature were detected in this study.

  6. Amorphous and Crystalline Vanadium Oxides as High-Energy and High-Power Cathodes for Three-Dimensional Thin-Film Lithium Ion Batteries.

    Science.gov (United States)

    Mattelaer, Felix; Geryl, Kobe; Rampelberg, Geert; Dendooven, Jolien; Detavernier, Christophe

    2017-04-19

    Flexible wearable electronics and on-chip energy storage for wireless sensors drive rechargeable batteries toward thin-film lithium ion batteries. To enable more charge storage on a given surface, higher energy density materials are required, while faster energy storage and release can be obtained by going to thinner films. Vanadium oxides have been examined as cathodes in classical and thin-film lithium ion batteries for decades, but amorphous vanadium oxide thin films have been mostly discarded. Here, we investigate the use of atomic layer deposition, which enables electrode deposition on complex three-dimensional (3D) battery architectures, to obtain both amorphous and crystalline VO2 and V2O5, and we evaluate their thin-film cathode performance. Very high volumetric capacities are found, alongside excellent kinetics and good cycling stability. Better kinetics and higher volumetric capacities were observed for the amorphous vanadium oxides compared to their crystalline counterparts. The conformal deposition of these vanadium oxides on silicon micropillar structures is demonstrated. This study shows the promising potential of these atomic layer deposited vanadium oxides as cathodes for 3D all-solid-state thin-film lithium ion batteries.

  7. Partial oxidation of n- and i-pentane over promoted vanadium-phosphorus oxide catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Zazhigalov, V.A.; Mikhajluk, B.D.; Komashko, G.A. [AN Ukrainskoj SSR, Kiev (Ukraine). Inst. Fizicheskoj Khimii

    1998-12-31

    It is known, that the cost of raw materials for catalytic oxidation processes is about 60% of the product price. Cheap initial compounds to produce variety of products and to replace olefins and aromatic hydrocarbons are paraffins. That is why catalytic systems which could be possibly rather efficient in selective oxidation of paraffin hydrocarbons are under very close investigation now. One of such processes in n-pentane oxidation. The obtained results on n-pentane oxidation over VPO catalysts were quite encouraging in respect of possible reach high selectivity and yield of phthalic anhydride. However, in our work it was shown that the main product of n-pentane oxidation in the presence of VPO catalytic system as well as VPMeO was maleic anhydride. Some later our results were confirmed in, where to grow the selectivity towards phthalic anhydride the Co-additive was introduced. On the basis of the proposal made before on the mechanism of paraffins conversion over the vanadyl pyrophosphate surface with their activation at the first and fourth carbon atoms, we assumed possible methylmaleic (citraconic) anhydride forming at n- and i-pentane oxidation. This assumption has been recently supported by both our and other researchers` experimental results. In it was also hypothized possible mechanistic features for phthalic anhydride forming from n-pentane. The present work deals with the results of n- and i-pentane oxidation over VPO catalysts promoted with Bi, Cs, Te, Zr. (orig.)

  8. Incorporation of Vanadium Oxide in Silica Nanofiber Mats via Electrospinning and Sol-Gel Synthesis

    Directory of Open Access Journals (Sweden)

    Jeanne E. Panels

    2006-01-01

    Full Text Available Submicron scale vanadia/silica hybrid nanofiber mats have been produced by electrospinning silica sol-gel precursor containing vanadium oxytriisopropoxide (VOTIP, followed by calcinations at high temperature. The properties of the resulting inorganic hybrid nanofiber mats are compared to those of electrospun pure silica nanofibers. SEM images show fibers are submicron in diameter and their morphology is maintained after calcination. Physisorption experiments reveal that silica nanofiber mats have a high specific surface area of 63 m2/g. FT-IR spectra exhibit Si—O vibrations and indicate the presence of V2O5 in the fibers. XPS studies reveal that the ratio of Si to O is close to 0.5 on the surface of fibers and the amount of vanadium on the surface of fibers increases with calcination. XRD diffraction patterns show that silica nanofibers are amorphous and orthorhombic V2O5 crystals have formed after calcination. EFTEM images demonstrate the growth of crystals on the surface of fibers containing vanadium after calcination. SEM images of fibers with high-vanadium content (50 mol% V: Si show that vanadia crystals are mostly aligned along the fiber axis. XPS shows an increase in vanadium contents at the surface, and XRD patterns exhibit an increase in the degree of crystallinity. A coaxial electrospinning scheme has successfully been employed to selectively place V2O5 in the skin layer.

  9. Silver Vanadium Phosphorous Oxide, Ag(2)VO(2)PO(4): Chimie Douce Preparation and Resulting Lithium Cell Electrochemistry.

    Science.gov (United States)

    Kim, Young Jin; Marschilok, Amy C; Takeuchi, Kenneth J; Takeuchi, Esther S

    2011-08-15

    Recently, we have shown silver vanadium phosphorous oxide (Ag(2)VO(2)PO(4), SVPO) to be a promising cathode material for lithium based batteries. Whereas the first reported preparation of SVPO employed an elevated pressure, hydrothermal approach, we report herein a novel ambient pressure synthesis method to prepare SVPO, where our chimie douce preparation is readily scalable and provides material with a smaller, more consistent particle size and higher surface area relative to SVPO prepared via the hydrothermal method. Lithium electrochemical cells utilizing SVPO cathodes made by our new process show improved power capability under constant current and pulse conditions over cells containing cathode from SVPO prepared via the hydrothermal method.

  10. Thermo-electrical properties of composite semiconductor thin films composed of nanocrystalline graphene-vanadium oxides.

    Science.gov (United States)

    Jung, Hye-Mi; Um, Sukkee

    2014-12-01

    This paper presents an experimental comparative study involving the characterization of the thermo-electrical and structural properties of graphene-based vanadium oxide (graphene-VOx) composite thin films on insulating and conducting surfaces (i.e., fused quartz and acrylic resin-impregnated graphite) produced by a sol-gel process via dipping-pyrolysis. A combination of FE-SEM and XPS analyses revealed that the graphene-VOx composite thin films (coated onto fused quartz) exhibiting the microstructure of 2-graded nanowire arrays with a diameter of 40-80 nm were composed of graphene, a few residual oxygen-containing functional groups (i.e., C-O and C=O), and the VO2 Magnéli phase. The temperature-dependent electrical resistance measured on the as-deposited thin films clearly demonstrated that the graphene-VOx composite nanowire arrays thermally grown on fused quartz act as a semiconductor switch, with a transition temperature of 64.7 degrees C in the temperature range of -20 degrees C to 140 degrees C, resulting from the contributions of graphene and graphene oxides. In contrast, the graphene-VOx composite thin films deposited onto acrylic resin-impregnated graphite exhibit a superlinear semiconducting property of extremely low electrical resistance with negative temperature coefficients (i.e., approximately four orders of magnitude lower than that of the fused quartz), despite the similar microstructural and morphological characteristics. This difference is attributed to the synergistic effects of the paramagnetic metal feature of the tightly stacked nanowire arrays consisting of hexagonal V2O3 on the intrinsic electrical properties of the acrylic resin-impregnated graphite substrate, as revealed by FE-SEM, EDX, AFM, and XRD measurements. Although the thermo-sensitive electrical properties of the graphene-VOx composite thin films are very substrate specific, the applicability of graphene sheets can be considerably effective in the formation of highly planar arrays

  11. Annealing effects on the structural and optical properties of vanadium oxide film obtained by the hot-filament metal oxide deposition technique (HFMOD)

    Energy Technology Data Exchange (ETDEWEB)

    Scarminio, Jair; Silva, Paulo Rogerio Catarini da, E-mail: scarmini@uel.br, E-mail: prcsilva@uel.br [Universidade Estadual de Londrina (UEL), PR (Brazil). Departamento de Fisica; Gelamo, Rogerio Valentim, E-mail: rogelamo@gmail.com [Universidade Federal do Triangulo Mineiro (UFTM), Uberaba, MG (Brazil); Moraes, Mario Antonio Bica de, E-mail: bmoraes@mailhost.ifi.unicamp.br [Universidade Estadual de Campinas (UNICAMP), SP (Brazil)

    2017-01-15

    Vanadium oxide films amorphous, nonstoichiometric and highly absorbing in the optical region were deposited on ITO-coated glass and on silicon substrates, by the hot-filament metal oxide deposition technique (HFMOD) and oxidized by ex-situ annealing in a furnace at 200, 300, 400 and 500 deg C, under an atmosphere of argon and rarefied oxygen. X-ray diffraction, Raman and Rutherford backscattering spectroscopy as well as optical transmission were employed to characterize the amorphous and annealed films. When annealed at 200 and 300 deg C the as-deposited opaque films become transparent but still amorphous. Under treatments at 400 and 500 deg C a crystalline nonstoichiometric V{sub 2}O{sub 5} structure is formed. All the annealed films became semiconducting, with their optical absorption coefficients changing with the annealing temperature. An optical gap of 2.25 eV was measured for the films annealed at 400 and 500 deg C. The annealing in rarefied oxygen atmosphere proved to be a useful and simple ex-situ method to modulate the structural and optical properties of vanadium oxide films deposited by HFMOD technique. This technique could be applied to other amorphous and non-absorbing oxide films, replacing the conventional and sometimes expensive method of modulate desirable film properties by controlling the film deposition parameters. Even more, the HFMOD technique can be an inexpensive alternative to deposit metal oxide films. (author)

  12. Electrodeposition of Vanadium Oxides at Room Temperature as Cathodes in Lithium-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Michalis Rasoulis

    2017-07-01

    Full Text Available Electrodeposition of vanadium pentoxide coatings was performed at room temperature and a short growth period of 15 min based on an alkaline solution of methanol and vanadyl (III acetyl acetonate. All samples were characterized by X-ray diffraction, Raman spectroscopy, field-emission scanning electron microscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. The current density and electrolyte concentration were found to affect the characteristics of the as-grown coatings presenting enhanced crystallinity and porous structure at the highest values employed in both cases. The as-grown vanadium pentoxide at current density of 1.3 mA·cm−2 and electrolyte concentration of 0.5 M indicated the easiest charge transfer of Li+ across the vanadium pentoxide/electrolyte interface presenting a specific discharge capacity of 417 mAh·g−1, excellent capacitance retention of 95%, and coulombic efficiency of 94% after 1000 continuous Li+ intercalation/deintercalation scans. One may then suggest that this route is promising to prepare large area vanadium pentoxide electrodes with excellent stability and efficiency at very mild conditions.

  13. Enzymatic halogenation and oxidation using an alcohol oxidase-vanadium chloroperoxidase cascade

    NARCIS (Netherlands)

    But, Andrada; Noord, Van Aster; Poletto, Francesca; Sanders, Johan P.M.; Franssen, Maurice C.R.; Scott, Elinor L.

    2017-01-01

    The chemo-enzymatic cascade which combines alcohol oxidase from Hansenula polymorpha (AOXHp) with vanadium chloroperoxidase (VCPO), for the production of biobased nitriles from amino acids was investigated. In the first reaction H2O2 (and acetaldehyde) are generated from ethanol and oxygen by AOXHp.

  14. Rf-sputtered vanadium oxide thin films: effect of oxygen partial pressure on structural and electrochemical properties

    CERN Document Server

    Park, Y J; Ryu, K S; Chang, S H; Park, S C; Yoon, S M; Kim, D K

    2001-01-01

    Vanadium oxide thin films with thickness of about 2000 A have been prepared by radio frequency sputter deposition using a V sub 2 O sub 5 target in a mixed argon and oxygen atmosphere with different Ar/O sub 2 ratio ranging from 99/1 to 90/10. X-ray diffraction and X-ray absorption near edge structure spectroscopic studies show that the oxygen content higher than 5% crystallizes a stoichiometric V sub O sub 5 phase, while oxygen deficient phase is formed in the lower oxygen content. The oxygen content in the mixed Ar + O sub 2 has a significant influence on electrochemical lithium insertion/deinsertion property. The discharge-charge capacity of vanadium oxide film increases with increasing the reactive oxygen content. The V sub O sub 5 film deposited at the Ar/O sub 2 ratio of 90/10 exhibits high discharge capacity of 100 mu Ah/cm sup 2 -mu m along with good cycle performance.

  15. Fabrication of polypyrrole/vanadium oxide nanotube composite with enhanced electrochemical performance as cathode in rechargeable batteries

    Science.gov (United States)

    Zhou, Xiaowei; Chen, Xu; He, Taoling; Bi, Qinsong; Sun, Li; Liu, Zhu

    2017-05-01

    Vanadium oxide nanotubes (VOxNTs) with hollow as well as multi-walled features were fabricated under hydrothermal condition by soft-template method. This novel VOxNTs can be used as cathode material for lithium ion batteries (LIBs), but displaying low specific capacity and poor cycling performance owing to the residual of a mass of soft-template (C12H27N) and intrinsic low conductivity of VOx. Cation exchange technique and oxidative polymerization process of pyrrole monomers were conducted to wipe off partial soft-template without electrochemical activity within VOxNTs and simultaneously form polypyrrole coating on VOxNTs, respectively. The resulting polypyrrole/VOxNTs nanocomposite delivers much improved capacity and cyclic stability. Further optimizations, such as complete elimination of organic template and enhancing the crystallinity, can make this unique nanostructure a promising cathode for LIBs.

  16. Vanadium oxide based cpd. useful as a cathode active material - is used in lithium or alkali metal batteries to prolong life cycles

    DEFF Research Database (Denmark)

    1997-01-01

    A mixt. of metallic iron particles and vanadium pentoxide contg. V in its pentavalent state in a liq. is reacted to convert at least some of the pentavalent V to its tetravalent state and form a gel. The liq. phase is then sepd. from the oxide based gel to obtain a solid material(I) comprising Fe...

  17. Hydration effects on the molecular structure of silica-supported vanadium oxide catalysts: A combined IR, Raman, UV–vis and EXAFS study

    NARCIS (Netherlands)

    Keller, D.E.; Visser, T.|info:eu-repo/dai/nl/110288327; Soulimani, F.|info:eu-repo/dai/nl/313889449; Koningsberger, D.C.|info:eu-repo/dai/nl/073704342; Weckhuysen, B.M.|info:eu-repo/dai/nl/285484397

    2007-01-01

    The effect of hydration on the molecular structure of silica-supported vanadium oxide catalysts with loadings of 1–16 wt.% V has been systematically investigated by infrared, Raman, UV–vis and EXAFS spectroscopy. IR and Raman spectra recorded during hydration revealed the formation of V–OH groups,

  18. Bronze Age Acrobats

    DEFF Research Database (Denmark)

    Iversen, Rune

    2014-01-01

    A Danish eighteenth-century find of some bronze figurines tells the story of the practising of similar ritual performances across Bronze Age Europe from Egypt to Scandinavia. The Danish figurines, as well as Swedish rock carvings, show backwards-bending female acrobats doing backward handsprings...... of the immaterial, ritual and cosmological exchange that characterized the second and early firstmillennium BC.Beliefs and ritual practices went hand in hand with the adoption of a series of elite items and an aristocratic lifestyle, thereby creating a unique and fascinating European Bronze Age....

  19. Vanadium oxide/polypyrrole aerogel nanocomposites. Technical report, 1 June 1995-31 May 1996

    Energy Technology Data Exchange (ETDEWEB)

    Dave, B.C.; Bunn, B.; Leroux, F.; Nazar, L.F.; Wong, H.P.

    1996-06-18

    Vanadium pentoxide/polypyrrole aerogel (ARG) nanocomposites were prepared by hydrolysis of VO(OC3H7)3 using pyrrole/water/acetone mixtures. Monolithic green-black gels with polypyrrole/V ratios ranging from 0.15 to 1.0 resulted from simultaneous polymerization of the pyrrole and vanadium alkoxide precursors. Supercritical drying yielded high surface (150-200 sq meters/g) aerogels, of sufficient mechanical integrity to allow them to be cut without fracturing. TEM studies of the aerogels show that they are comprised of fibers similar to that of V2O5 ARG`s, but with a much shorter chain length. Evidence from IR that the inorganic and organic components strongly interact leads us to propose that this impedes the vanadium condensation process. The result is ARG`s that exhibit decreased electronic conductivity with increasing polymer content. Despite the unexpected deleterious effect of the conductive polymer on the bulk conductivity, at low polymer content, the nanocomposite materials show enhanced electrochemical properties for Li insertion compared to the pristine aerogel.

  20. Studies of vanadium-phosphorus-oxygen selective oxidation catalysts by sup 31 P and sup 51 V NMR spin-echo and volume susceptibility measurements

    Energy Technology Data Exchange (ETDEWEB)

    Li, Juan.

    1991-10-01

    The purpose of this work is to characterize the vanadium-phosphorous oxide (V-P-O) catalysts for the selective oxidation of n-butane and 1-butene to maleic anhydride. The utility of solid state nuclear magnetic resonance as an analytical tool in this investigation lies in its sensitivity to the electronic environment surrounding the phosphorous and vanadium nuclei, and proximity of paramagnetic species. Spin-echo mapping NMR of {sup 31}p and {sup 51}v and volume magnetic susceptibility measurements were used as local microscopic probes of the presence of V{sup 5+}, V{sup 4+}, V{sup 3+} species in the model compounds: {beta}-VOPO{sub 4}, {beta}-VOPO{sub 4} treated with n-butane/1-butene, (VO){sub 2}P{sub 2}O{sub 7} treated with n-butane/1-butene; and industrial catalysts with P/V (phosphorus to vanadium) ratio of 0.9, 1.0 and 1.1, before and after treatment with n-butane and 1-butene. The NMR spectra provide a picture of how the oxidation states of vanadium are distributed in these catalysts. 73 refs., 32 figs., 8 tabs.

  1. Vanadyl precursors used to modify the properties of vanadium oxide thin films obtained by chemical vapor deposition

    Energy Technology Data Exchange (ETDEWEB)

    Barreca, D.; Franzato, E.; Rizzi, G.A.; Tondello, E.; Vettori, U. [Univ. di Padova (Italy); Depero, L.E.; Sangaletti, L. [Univ. di Brescia (Italy). Dipt. di Chimica e Fisica per i Materiali

    1999-02-01

    Vanadium oxide thin films were prepared by chemical vapor deposition using as precursors a series of vanadyl complexes of general formula VO(L){sub 2}(H), where L is a {beta}-diketonate ligand. The depositions were carried out on {alpha}-Al{sub 2}O{sub 3} substrates in O{sub 2}, N{sub 2}, and N{sub 2} + H{sub 2}O atmospheres. In order to elucidate the role played by different ligands and synthesis conditions on the properties of the obtained films, the chemical composition of the samples was investigated by X-ray photoelectron spectroscopy, while their microstructure and surface morphology were analyzed by X-ray diffraction, Raman and atomic force microscopy. The thermal decomposition of the precursors, with particular attention to their reactivity in the presence of water vapor, was studied by mass spectrometry and Fourier transform infrared spectroscopy.

  2. Structural and electrical properties of different vanadium oxide phases in thin film form synthesized using pulsed laser deposition

    Science.gov (United States)

    Majid, S. S.; Shukla, D. K.; Rahman, F.; Choudhary, R. J.; Phase, D. M.

    2015-06-01

    We present here the structural and electrical properties of the thin films of V2O3 (Vanadium sesquioxide) and V5O9. Both these oxide phases, V2O3 and V5O9, have beenachieved on (001) orientedSi substrate using the V2O5 target by optimizing the deposition parameters using pulsed laser deposition technique (PLD).Deposited films were characterized by X-ray diffraction(XRD)and four probe temperature dependent resistivity measurements. XRD studies reveal the V2O3 and V5O9 phases and the amount of strain present in both these films. The temperature dependency of electrical resistivity confirmed the characteristic metal-insulator transitions (MIT) for both the films, V2O3 and V5O9.

  3. Vanadium-substituted heteropolyacids immobilized on amine- functionalized mesoporous MCM-41: A recyclable catalyst for selective oxidation of alcohols with H{sub 2}O{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Dong, Xinbo [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, Department of Chemistry (Ministry of Education), Northwest University, Xi' an 710069 (China); Wang, Danjun [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, Department of Chemistry (Ministry of Education), Northwest University, Xi' an 710069 (China); College of Chemistry Chemical Engineering, Yanan University, Shaanxi Key Laboratory of Chemical Reaction Engineering, Yan' an 716000 (China); Li, Kebin [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, Department of Chemistry (Ministry of Education), Northwest University, Xi' an 710069 (China); Zhen, Yanzhong [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, Department of Chemistry (Ministry of Education), Northwest University, Xi' an 710069 (China); College of Chemistry Chemical Engineering, Yanan University, Shaanxi Key Laboratory of Chemical Reaction Engineering, Yan' an 716000 (China); Hu, Huaiming [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, Department of Chemistry (Ministry of Education), Northwest University, Xi' an 710069 (China); Xue, Ganglin, E-mail: xglin707@163.com [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, Department of Chemistry (Ministry of Education), Northwest University, Xi' an 710069 (China)

    2014-09-15

    Graphical abstract: Vanadium-substituted phosphotungstic acids are immobilized on amine- functionalized mesoporous MCM-41 and the hybrid catalyst is proved to be a highly efficient solid catalyst for the oxidation of aromatic alcohols to the corresponding carbonyl compounds with H{sub 2}O{sub 2}, featured by the high conversion and selectivity, easy recovery, and quite steady reuse. - Highlights: • Vanadium-substituted phosphotungstic acid immobilized on amine-functionalized mesoporous MCM-41 are prepared. • HPAs were fixed on the inner surface of mesoporous MCM-41 by chemical bonding to aminosilane groups. • The hybrid catalyst showed much higher catalytic activity than the pure HPAs. • The hybrid catalyst is a highly efficient recyclable solid catalyst for the selective oxidation of aromatic alcohols. - Abstract: New hybrid materials of vanadium-substituted phosphotungstic acids (VHPW) immobilized on amine-functionalized mesoporous MCM-41 (VHPW/MCM-41/NH{sub 2}) are prepared and characterized by FT-IR, XRD, N{sub 2} adsorption, elemental analysis, SEM and TEM for their structural integrity and physicochemical properties. It is found that the structure of the heteropolyacids is retained upon immobilization over mesoporous materials. The catalytic activities of these hybrid materials are tested in the selective oxidation of alcohols to the carbonyl products with 30% aqueous H{sub 2}O{sub 2} as oxidant in toluene. The catalytic activities of different number of vanadium-substituted phosphotungstic acid are investigated, and among the catalysts, H{sub 5}[PV{sub 2}W{sub 10}O{sub 40}] immobilized on amine-functionalized MCM-41 exhibits the highest activity with 97% conversion and 99% selectivity in the oxidation of benzyl alcohol to benzaldehyde. The hybrid catalyst is proved to be a highly efficient recyclable solid catalyst for the selective oxidation of aromatic alcohols to the corresponding aldehydes with H{sub 2}O{sub 2}.

  4. Bronze rainbow hologram mirrors

    Science.gov (United States)

    Dawson, P.

    2006-02-01

    This project draws on holographic embossing techniques, ancient artistic conventions of bronze mirror design and modelling and casting processes to accomplish portraiture of reflection. Laser scanning, 3D computer graphics and holographic imaging are employed to enable a permanent 3D static holographic image to appear integrated with the real-time moving reflection of a viewer's face in a polished bronze disc. The disc and the figure which holds it (caryatid) are cast in bronze from a lost wax model, a technique which has been used for millennia to make personal mirrors. The Caryatid form of bronze mirror which went through many permutations in ancient Egyptian, Greece and Rome shows a plethora of expressive figure poses ranging from sleek nudes to highly embellished multifigure arrangements. The prototype of this series was made for Australian choreographer Graeme Murphy, Artistic Director of the Sydney Dance Company. Each subsequent mirror will be unique in figure and holographic imagery as arranged between artist and subject. Conceptually this project references both the modern experience of viewing mirrors retrieved from ancient tombs, which due to deterioration of the surface no longer reflect, and the functioning of Chinese Magic mirrors, which have the ability to project a predetermined image. Inspired by the metaphorical potential of these mirrors, which do not reflect the immediate reality of the viewer, this bronze hologram mirror series enables each viewer to reflect upon himself or herself observing simultaneously the holographic image and their own partially obliterated reflection.

  5. Preparation and characterization of graphene-based vanadium oxide composite semiconducting films with horizontally aligned nanowire arrays

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Hye-Mi; Um, Sukkee, E-mail: sukkeeum@hanyang.ac.kr

    2016-05-01

    Highly oriented crystalline hybrid thin films primarily consisting of Magnéli-phase VO{sub 2} and conductive graphene nanoplatelets are fabricated by a sol–gel process via dipping pyrolysis. A combination of chemical, microstructural, and electrical analyses reveals that graphene oxide (GO)-templated vanadium oxide (VO{sub x}) nanocomposite films exhibit a vertically stacked multi-lamellar nanostructure consisting of horizontally aligned vanadium oxide nanowire (VNW) arrays along the (hk0) set of planes on a GO template, with an average crystallite size of 41.4 Å and a crystallographic tensile strain of 0.83%. In addition, GO-derived VO{sub x} composite semiconducting films, which have an sp{sup 3}/sp{sup 2} bonding ratio of 0.862, display thermally induced electrical switching properties in the temperature range of − 20 °C to 140 °C, with a transition temperature of approximately 65 °C. We ascribe these results to the use of GO sheets, which serve as a morphological growth template as well as an electrochemically tunable platform for enhancing the charge-carrier mobility. Moreover, the experimental studies demonstrate that graphene-based Magnéli-phase VO{sub x} composite semiconducting films can be used in advanced thermo-sensitive smart sensing/switching applications because of their outstanding thermo-electrodynamic properties and high surface charge density induced by the planar-type VNWs. - Highlights: • VO{sub x}-graphene oxide composite (G/VO{sub x}) films were fabricated by sol–gel process. • The G/VO{sub x} films mainly consisted of Magnéli-phase VO{sub 2} and reduced graphene sheets. • The G/VO{sub x} films exhibited multi-lamellar textures with planar VO{sub x} nanowire arrays. • The G/VO{sub x} films showed the thermo-sensitive electrical switching properties. • Effects of GOs on the electrical characteristics of the G/VO{sub x} films were discussed.

  6. Melt quenched vanadium oxide embedded in graphene oxide sheets as composite electrodes for amperometric dopamine sensing and lithium ion battery applications

    Energy Technology Data Exchange (ETDEWEB)

    Sreejesh, M. [Materials Research Laboratory, Department of Physics, National Institute of Technology Karnataka, P.O. Srinivasnagar, Surathkal, Mangaluru 575 025 (India); Shenoy, Sulakshana [Functional Nanostructured Materials Research Laboratory, Department of Physics, National Institute of Technology Karnataka, P.O. Srinivasnagar, Surathkal, Mangaluru 575 025 (India); Sridharan, Kishore, E-mail: kishore@nitk.edu.in [Functional Nanostructured Materials Research Laboratory, Department of Physics, National Institute of Technology Karnataka, P.O. Srinivasnagar, Surathkal, Mangaluru 575 025 (India); Kufian, D.; Arof, A.K. [Centre for Ionics, Department of Physics, Faculty of Science, University of Malaya, 50603 Kuala Lumpur (Malaysia); Nagaraja, H.S., E-mail: nagaraja@nitk.edu.in [Materials Research Laboratory, Department of Physics, National Institute of Technology Karnataka, P.O. Srinivasnagar, Surathkal, Mangaluru 575 025 (India)

    2017-07-15

    Highlights: • Layered vanadium oxides (MVO) are prepared through melt quenching process. • MVO is hydrothermally treated with graphene oxide to form MVGO composites. • Dopamine detection capacity using MVGO is 0.07 μM with good selectivity. • Sensitivity of dopamine detection is 25.02 μA mM{sup −1} cm{sup −2}. • Discharge capacity of MVGO electrode is 200 mAhg{sup −1} after 10 cycles. - Abstract: Electrochemical sensors and lithium-ion batteries are two important topics in electrochemistry that have attracted much attention owing to their extensive applications in enzyme-free biosensors and portable electronic devices. Herein, we report a simple hydrothermal approach for synthesizing composites of melt quenched vanadium oxide embedded on graphene oxide of equal proportion (MVGO50) for the fabrication of electrodes for nonenzymatic amperometic dopamine sensor and lithium-ion battery applications. The sensing performance of MVGO50 electrodes through chronoamperometry studies in 0.1 M PBS solution (at pH 7) over a wide range of dopamine concentration exhibited a highest sensitivity of 25.02 μA mM{sup −1} cm{sup −2} with the lowest detection limit of 0.07 μM. In addition, the selective sensing capability of MVGO50 was also tested through chronoamperometry studies by the addition of a very small concentration of dopamine (10 μM) in the presence of a fairly higher concentration of uric acid (10 mM) as the interfering species. Furthermore, the reversible lithium cycling properties of MVGO50 are evaluated by galvanostatic charge-discharge cycling studies. MVGO50 electrodes exhibited enhanced rate capacity of up to 200 mAhg{sup −1} at a current of 0.1C rate and remained stable during cycling. These results indicate that MVGO composites are potential candidates for electrochemical device applications.

  7. Tunable Electrical Properties of Vanadium Oxide by Hydrogen-Plasma-Treated Atomic Layer Deposition

    Directory of Open Access Journals (Sweden)

    Helen Hejin Park

    2017-04-01

    Full Text Available In this study, a plasma-modified process was developed to control the electrical properties of atomic layer deposition (ALD-grown vanadium dioxide (VO2, which is potentially useful for applications such as resistive switching devices, bolometers, and plasmonic metamaterials. By inserting a plasma pulse with varying H2 gas flow into each ALD cycle, the insulator-to-metal transition (IMT temperature of postdeposition-annealed crystalline VO2 films was adjusted from 63 to 78 °C. Film analyses indicate that the tunability may arise from changes in grain boundaries, morphology, and compositional variation despite hydrogen not remaining in the annealed VO2 films. This growth method, which enables a systematic variation of the electronic behavior of VO2, provides capabilities beyond those of the conventional thermal ALD and plasma-enhanced ALD.

  8. Dehydrogenation of Isobutane with Carbon Dioxide over SBA-15-Supported Vanadium Oxide Catalysts

    Directory of Open Access Journals (Sweden)

    Chunling Wei

    2016-10-01

    Full Text Available A series of vanadia catalysts supported on SBA-15 (V/SBA with a vanadia (V content ranging from 1% to 11% were prepared by an incipient wetness method. Their catalytic behavior in the dehydrogenation of isobutane to isobutene with CO2 was examined. The catalysts were characterized by N2 adsorption, X-ray diffraction (XRD, scanning electron microscopy (SEM, Raman spectroscopy, and temperature-programmed reduction (TPR. It was found that these catalysts were effective for the dehydrogenation reaction, and the catalytic activity is correlated with the amount of dispersed vanadium species on the SBA-15 support. The 7% V/SBA catalyst shows the highest activity, which gives 40.8% isobutane conversion and 84.8% isobutene selectivity. The SBA-15-supported vanadia exhibits higher isobutane conversion and isobutene selectivity than the MCM-41-supported one.

  9. Synergistic effect of 3,5-dichlorophenol and trioctylphosphine oxide on the extraction of vanadium(V) with 2-methyl-8-quinolinol derivatives.

    Science.gov (United States)

    Tsuguchi, Akira; Ohashi, Akira; Choi, Sung-Yong; Imura, Hisanori; Ohashi, Kousaburo

    2002-11-01

    The extraction of vanadium(V) with 2-methyl-8-quinolinol derivatives (HA), such as 2-methyl-8-quinolinol (HMQ), 2-methyl-5-butyloxymethyl-8-quinolinol (HMO4Q), and 2-methyl-5-hexyloxymethyl-8-quinolinol (HMO6Q), from a weakly acidic solution into chloroform was studied in both the absence and presence of 3,5-dichlorophenol (Hdcp) and trioctylphosphine oxide (TOPO) as the synergists. Vanadium(V) was extracted with HA as VO(OH)(A)2 in the absence of synergists, and its extractability increased with an increase in the hydrophobicity of HA. Vanadium(V) was quantitatively extracted from the lower pH region upon the addition of Hdcp and TOPO as VO(OH)(A)2 x Hdcp and VO2(A)(TOPO), respectively. The enhancement of the synergistic effect of Hdcp on the extraction of vanadium(V) with HA increased in the following order: HMQ < HMO4Q < HMO6Q, as opposed to that of TOPO. This result was ascribable to the difference in the mechanisms of the occurrence of the synergistic effect by Hdcp and TOPO.

  10. VANADIUM ALLOYS

    Science.gov (United States)

    Smith, K.F.; Van Thyne, R.J.

    1959-05-12

    This patent deals with vanadium based ternary alloys useful as fuel element jackets. According to the invention the ternary vanadium alloys, prepared in an arc furnace, contain from 2.5 to 15% by weight titanium and from 0.5 to 10% by weight niobium. Characteristics of these alloys are good thermal conductivity, low neutron capture cross section, good corrosion resistance, good welding and fabricating properties, low expansion coefficient, and high strength.

  11. Roll-to-Roll Processing of Inverted Polymer Solar Cells using Hydrated Vanadium(V)Oxide as a PEDOT:PSS Replacement

    DEFF Research Database (Denmark)

    Martinez, Nieves Espinosa; Dam, Henrik Friis; Tanenbaum, David M.

    2011-01-01

    The use of hydrated vanadium(V)oxide as a replacement of the commonly employed hole transporting material PEDOT:PSS was explored in this work. Polymer solar cells were prepared by spin coating on glass. Polymer solar cells and modules comprising 16 serially connected cells were prepared using full...... roll-to-roll (R2R) processing of all layers. The devices were prepared on flexible polyethyleneterphthalate (PET) and had the structure PET/ITO/ZnO/P3HT:PCBM/V2O5·(H2O)n/Ag. The ITO and silver electrodes were processed and patterned by use of screen printing. The zinc oxide, P3HT:PCBM and vanadium...... to 0.18%, in contrast to single cells where efficiencies of 0.4% were achieved. Stability tests under indoor and outdoor conditions were accomplished over three weeks on a solar tracker....

  12. Electronic Excitations in Vanadium Oxide Phthalocyanine Studied via Resonant Soft X-ray Emission and Resonant Inelastic X-ray Scattering

    Energy Technology Data Exchange (ETDEWEB)

    Zhang,Y.; Wang, S.; Learmonth, T.; Plucinski, L.; Matsuura, A.; Bernardis, S.; ODonnell, C.; Downes, J.; Smith, K.

    2005-01-01

    The electronic structure of the organic semiconductor vanadium oxide phthalocyanine has been studied using resonant inelastic X-ray scattering and X-ray emission spectroscopy. The vanadyl species in the films is shown to be highly localized, and good agreement between the measurements and a density functional calculation is obtained. Both dipole forbidden V 3d to V 3d*, and O 2p to V 3d* charge transfer transitions are observed, and explained in a local molecular orbital model.

  13. Electro-optical evaluation of tungsten oxide and vanadium pentoxide thin films for modeling an electrochromic device

    Directory of Open Access Journals (Sweden)

    H Najafi Ashtiani

    2015-01-01

    Full Text Available In this study, tungsten oxide and vanadium oxide electrochromic thin films were placed in vacuum and in a thickness of 200 nm on a transparent conductive substrate of SnO2:F using the physical method of thermal evaporation. Then they were studied for the optical characteristics in the wavelength range from 400 to 700 nm and for their electrical potentials in the range form +1.5 to -1.5 volts. The films were post heated in order to assess changes in energy gap with temperature, at temperatures120 , 300 and 500°C. Refractive and extinction coefficients and the transition type of films in the visible light range and in the thickness of 200 nm were determined and measured. X-ray diffraction pattern and SEM images and cyclic Voltammetry of layers were also studied. The results of this study due to the deposition of layers, the layer thickness selected, the type of substrate, the range of annealing temperatures and selected electrolyte were in full compliance with the works of other researchers [1,2,3]. Therefore, these layers with features such as crystal structure, refractive and even extinction coefficients in the range of visible light, the appropriate response of chromic switch in the replication potential, good adhesion to the substrate, and the high amount of optical transmition and so on, prove useful to be used in an electrochromic device

  14. 51V Solid-state NMR and Density-Functional Theory Studies of Eight-Coordinate Non-Oxo Vanadium Complexes: Oxidized Amavadin

    Science.gov (United States)

    Ooms, Kristopher J.; Bolte, Stephanie E.; Baruah, Bharat; Choudhary, Muhammad Aziz; Crans, Debbie C.; Polenova, Tatyana

    2014-01-01

    SUMMARY Using 51V magic angle spinning solid-state NMR spectroscopy and Density Functional Theory calculations we have characterized the chemical shift and quadrupolar coupling parameters for two eight-coordinate vanadium complexes, [PPh4][V(V)(HIDPA)2] and [PPh4][V(V)(HIDA)2]; HIDPA = 2,2′-(hydroxyimino)dipropionate and HIDA = 2,2′-(hydroxyimino)diacetate. The coordination geometry under examination is the less common non-oxo eight coordinate distorted dodecahedral geometry that has not been previously investigated by solid-state NMR spectroscopy. Both complexes were isolated by oxidizing their reduced forms: [V(IV)(HIDPA)2]2- and [V(IV)(HIDA)2]2-. V(IV)(HIDPA)22- is also known as amavadin, a vanadium-containing natural product present in the Amanita muscaria mushroom and responsible for vanadium accumulation in nature. The quadrupolar coupling constants, CQ, are found to be moderate, 5.0 to 6.4 MHz while the chemical shift anisotropies are relatively small for vanadium complexes, −420 and 360 ppm. The isotropic chemical shifts in the solid state are −220 and −228 ppm for the two compounds, and near the chemical shifts observed in solution. Presumably this is a consequence of the combined effects of the increased coordination number and the absence of oxo groups. Density Functional Theory calculations of the electric field gradient parameters are in good agreement with the NMR results while the chemical shift parameters show some deviation from the experimental values. Future work on this unusual coordination geometry and a combined analysis by solid-state NMR and Density Functional Theory should provide a better understanding of the correlations between experimental NMR parameters and the local structure of the vanadium centers. PMID:19421628

  15. Organic ligand induced release of vanadium from the dissolution of stone coal oxide ore.

    Science.gov (United States)

    Hu, Xingyun; Yue, Yuyan; Peng, Xianjia

    2017-10-02

    The effects of low-molecular-weight dissolved organic matters (LMWDOMs) on the release of vanadium (V) under environmental conditions are part of a broader study on the environmental geochemistry behavior of V. Eight typical naturally occurring LMWDOMs with carboxyl, hydroxyl, and amidogen groups were chosen: citric acid, oxalic acid, EDTA, salicylic acid, catechol, glycine, cysteine, and glucose. The results showed that the release of V was largely promoted by LMWDOMs with carboxyl functional groups under acidic conditions and with catechol under basic conditions. In the presence of citric acid, oxalic acid, or EDTA at pH 4.0, the initial release rates of V were approximately 25-39 times greater than the rates in the control experiments; the steady release rates were 164, 95, and 49 times than the rates in the control experiments, respectively. For catechol, the release rate at pH 8.0 was approximately 20 times the rate at pH 4.0. Amino acids and alcohols had a minimal effect on the release of V. Ligand-promoted release rates of V were found primarily due to the faster detachment of surface complexes, the protonated sites from the mineral surface and the reduction of dissolved V (V) in the presence of citric acid, oxalic acid, EDTA, and catechol. This study helps understand the pollution risk of V in some mine areas and the fate of V in the environment.

  16. Selective nano alumina supported vanadium oxide catalysts for oxidative dehydrogenation of ethylbenzene to styrene using CO2 as soft oxidant

    Directory of Open Access Journals (Sweden)

    A.M. Elfadly

    2013-12-01

    Full Text Available Nano alumina-supported V2O5 catalysts with different loadings have been tested for the dehydrogenation of ethylbenzene with CO2 as an oxidant. High surface area nano-alumina was prepared and used as support for V2O5 as the catalyst. The catalysts were synthesized by impregnation techniques followed by calcinations and microwave treatment, denoted as V2O5/γ-Al2O3-C and V2O5/γ-Al2O3-MW, respectively. The V2O5 loading was varied on nano-alumina from 5 to 30 wt%. The support and catalysts were characterized by X-ray diffraction (XRD, Barett–Joyner–Halenda (BJH pore-size distribution, N2-adsorption isotherms, Fourier transform infrared (FT-IR, scanning electron microscopy (SEM, transmission electron microscopy (TEM and temperature programed desorption (TPD-NH3. The characterization results indicated that V2O5 is highly dispersed on alumina up to 30%-V2O5/γ-Al2O3-MW prepared by MW method. The TPD studies indicated that there are significant differences in acid amount and strength for V2O5/γ-Al2O3-C and V2O5/γ-Al2O3-MW-catalysts. The catalytic activity of the prepared catalysts was evaluated in the temperature range 450–600 °C in relation to the physicochemical properties and surface acidity. The results revealed that optimum catalytic activity and selectivity (∼100% toward styrene production were obtained using 10% V2O5/γ-Al2O3-MW catalyst treated with microwave.

  17. Study of the performance of vanadium based catalysts prepared by grafting in the oxidative dehydrogenation of propane

    Energy Technology Data Exchange (ETDEWEB)

    Santacesaria, E.; Carotenuto, G.; Tesser, R.; Di Serio, M. [Naples Univ. (Italy). Dept. of Chemistry

    2011-07-01

    The oxidative dehydrogenation (ODH) of propane has been investigated by using many different vanadia based catalysts, prepared by grafting technique and containing variable amounts of active phase supported on SiO{sub 2} previously coated, by grafting in three different steps, with multilayer of TiO{sub 2}. A depth catalytic screening, conducted in a temperature range of 400-600 C, at atmospheric pressure and in a range of residence time W/F=0.08-0.33 ghmol{sub -1}, has shown that the vanadium oxide catalysts on TiO{sub 2}-SiO{sub 2} support, prepared by grafting have good performances in the ODH of propane. In particular, a preliminary study has demonstrated that higher selectivities can be obtained employing catalysts having a well dispersed active phase that can be achieved with a V{sub 2}O{sub 5} content lower than 10%{sub w}t. It is well known that, in the case of redox catalysts, an increase of the selectivity can be achieved not only by using an adequate catalytic system but also via engineering routes like decoupling catalytic steps of reduction and re-oxidation. In fact it has been observed that by operating in dehydrogenating mode, on the same catalysts, a higher selectivity is obtained although the catalyst is poisoned by the formation of coke on the surface. As consequence of the results obtained in dehydrogenation, in this work has been explored the possibility to feed low amounts of oxygen, below the stoichiometric level with the aim to keep clean the surface from coke but maintaining high the selectivity, because, dehydrogenation reaction prevails. In this work, the behavior of catalysts containing different amounts of V2O5 has been studied in the propane-propene reaction by using different ratios C{sub 3}H{sub 8}/O{sub 2} included in the range 0-2. (orig.)

  18. Influence of oxygen flow rate on metal-insulator transition of vanadium oxide thin films grown by RF magnetron sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Xu; Liu, Xinkun; Li, Haizhu; Huang, Mingju [Henan University, Key Lab of Informational Opto-Electronical Materials and Apparatus, School of Physics and Electronics, Kaifeng (China); Zhang, Angran [South China Normal University, Institute of Electronic Paper Displays, South China Academy of Advanced Optoelectronics, Guangzhou (China)

    2017-03-15

    High-quality vanadium oxide (VO{sub 2}) films have been fabricated on Si (111) substrates by radio frequency (RF) magnetron sputtering deposition method. The sheet resistance of VO{sub 2} has a significant change (close to 5 orders of magnitude) in the process of the metal-insulator phase transition (MIT). The field emission-scanning electron microscope (FE-SEM) results show the grain size of VO{sub 2} thin films is larger with the increase of oxygen flow. The X-ray diffraction (XRD) results indicate the thin films fabricated at different oxygen flow rates grow along the (011) crystalline orientation. As the oxygen flow rate increases from 3 sccm to 6 sccm, the phase transition temperature of the films reduces from 341 to 320 K, the width of the thermal hysteresis loop decreases from 32 to 9 K. The thin films fabricated in the condition of 5 sccm have a high temperature coefficient of resistance (TCR) -3.455%/K with a small resistivity of 2.795 ρ/Ω cm. (orig.)

  19. Vanadium Oxide Supported on MSU-1 as a Highly Active Catalyst for Dehydrogenation of Isobutane with CO2

    Directory of Open Access Journals (Sweden)

    Guosong Sun

    2016-03-01

    Full Text Available Vanadium oxide supported on MSU-1, with VOx loading ranging from 2.5 to 17.5 wt. %, was developed as a highly active catalyst in dehydrogenation of isobutane with CO2. The obtained catalysts of VOx/MSU-1 were characterized by X-ray diffraction (XRD, N2 adsorption-desorption, and H2-temperature programmed reduction (H2-TPR methods and the results showed that the large surface area of MSU-1 was favorable for the dispersion of VOx species and the optimal loading of VOx was 12.0 wt. %. Meanwhile, the catalytic activity of VOx/MSU-1 was investigated, and VOx/MSU-1 with 12.0 wt. % VOx content was found to be the best one, with the conversion of isobutane (58.8% and the selectivity of isobutene (78.5% under the optimal reaction conditions. In contrast with the reaction in the absence of CO2, the presence of CO2 in the reaction stream could obviously enhance the isobutane dehydrogenation, which raised the conversion of reaction and the stability of VOx/MSU-1.

  20. Controlling interlayer interactions in vanadium pentoxide-poly(ethylene oxide) nanocomposites for enhanced magnesium-ion charge transport and storage

    Science.gov (United States)

    Perera, Sanjaya D.; Archer, Randall B.; Damin, Craig A.; Mendoza-Cruz, Rubén; Rhodes, Christopher P.

    2017-03-01

    Rechargeable magnesium batteries provide the potential for lower cost and improved safety compared with lithium-ion batteries, however obtaining cathode materials with highly reversible Mg-ion capacities is hindered by the high polarizability of divalent Mg-ions and slow solid-state Mg-ion diffusion. We report that incorporating poly(ethylene oxide) (PEO) between the layers of hydrated vanadium pentoxide (V2O5) xerogels results in significantly improved reversible Mg-ion capacities. X-ray diffraction and high resolution transmission electron microscopy show that the interlayer spacing between V2O5 layers was increased by PEO incorporation. Vibrational spectroscopy supports that the polymer interacts with the V2O5 lattice. The V2O5-PEO nanocomposite exhibited a 5-fold enhancement in Mg-ion capacity, improved stability, and improved rate capabilities compared with V2O5 xerogels. The Mg-ion diffusion coefficient of the nanocomposite was increased compared with that of V2O5 xerogels which is attributed to enhanced Mg-ion mobility due to the shielding interaction of PEO with the V2O5 lattice. This study shows that beyond only interlayer spacing, the nature of interlayer interactions of Mg-ions with V2O5, PEO, and H2O are key factors that affect Mg-ion charge transport and storage in layered materials. The design of layered materials with controlled interlayer interactions provides a new approach to develop improved cathodes for magnesium batteries.

  1. Interplay of electron-electron and electron-phonon interaction in the metal to insulator transition in vanadium oxides.

    Energy Technology Data Exchange (ETDEWEB)

    Baldassarre, Leonetta [CNR-INFM COHERENTIA, Roma (Italy); Experimentalphysik II, Universitaet Augsburg (Germany); Department of Physics, University of Rome ' La Sapienza' (Italy); Arcangeletti, Emanuele; Perucchi, Andrea; Nicoletti, Daniele; Di Castro, Daniele; Marini, Carlo; Postorino, Paolo; Lupi, Stefano [CNR-INFM COHERENTIA, Roma (Italy); Department of Physics, University of Rome ' La Sapienza' (Italy)

    2008-07-01

    Several families of vanadium oxides display metal to insulator transitions (MIT) often driven by both temperature (T) and pressure (P) with jumps of conductivity up to 7 orders of magnitude. While the transition in V{sub 2}O{sub 3} is considered as induced mainly by electronic correlation (Mott-Hubbard transition), the MIT mechanism that drives the electronic transition in VO{sub 2} is still unclear, probably determined by an interplay between electronic and lattice degrees of freedom. Here we present a complete investigation of MIT as a function of T and P of V{sub 2}O{sub 3} and VO{sub 2}. Infrared measurements have been performed in a wide range of T (10-600 K) and P (0-15 GPa) in order to cover the rich phase diagrams of those materials. P-dependent Raman measurements have also been performed on VO{sub 2} so to follow also the lattice dynamics. Moreover, the high temperature incoherent phase is discussed in V{sub 2}O{sub 3}, the ideal playground to study the correlation effects on the low-energy electrodynamics.

  2. Elucidation of the molecular structure of hydrated vanadium oxide species by X-ray absorption spectroscopy: correlation between the V--V coordination number and distance and the point of zero charge of the support oxide

    OpenAIRE

    Keller, D. E.; Koningsberger, D.C.; Weckhuysen, B. M.

    2006-01-01

    The effect of the point of zero charge (PZC) of the support oxide (Al(2)O(3), Nb(2)O(5), SiO(2) and ZrO(2)) on the molecular structure of hydrated vanadium oxide species has been investigated with EXAFS spectroscopy for low-loaded vanadium oxide catalysts. It was found that the degree of clustering (i.e., the V[dot dot dot]V coordination number) and the V...V distance increase with decreasing PZC of the support oxide; i.e., Al(2)O(3) (8.7) < ZrO(2) (7) < Nb(2)O(5) (3.3) < SiO(2) (2). Upon hyd...

  3. Effect of citric acid dosage and sintered temperature on the composition, morphology and electrochemical properties of lithium vanadium oxide prepared by a sol-gel method

    Science.gov (United States)

    Zhong, C. R.; Su, X. J.; Hou, G. L.; Liu, Z. H.; Yu, F. S.; Bi, S.; Li, H.

    2017-03-01

    A lithium vanadium oxide cathode material was synthesized via sol-gel processing using citric acid as the chelating agent. Different dosage of citric acid and sintered temperature were introduced to investigate their effects on the products composition, morphology and electrochemical properties. The results showed that the V2O3 yield was inhibited and the crystallization of grain was accelerated with the increasing dosage of citric acid. Furthermore, V2O3 was oxidized to LiV3O8 and Li0.3V2O5 with the increase of sintered temperature.

  4. Fabrication of polypyrrole/vanadium oxide nanotube composite with enhanced electrochemical performance as cathode in rechargeable batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Xiaowei, E-mail: zhouxiaowei@ynu.edu.cn [Department of Physics, School of Physics and Astronomy, Yunnan University, Kunming 650504, Yunnan (China); Chen, Xu; He, Taoling; Bi, Qinsong [Department of Physics, School of Physics and Astronomy, Yunnan University, Kunming 650504, Yunnan (China); Sun, Li [Department of Physics, School of Physics and Astronomy, Yunnan University, Kunming 650504, Yunnan (China); Department of Mechanical Engineering, University of Houston, Houston 77204, TX (United States); Liu, Zhu, E-mail: zhuliu@ynu.edu.cn [Department of Physics, School of Physics and Astronomy, Yunnan University, Kunming 650504, Yunnan (China); Yunnan Key Laboratory of Micro/Nano-Materials and Technology, Yunnan University, Kunming 650091, Yunnan (China)

    2017-05-31

    Highlights: • VO{sub x}NTs were hydrothermally prepared using C{sub 12}H{sub 27}N as soft template with scalability. • Polypyrrole/VO{sub x}NTs with less C{sub 12}H{sub 27}N template and higher conductivity were obtained. • Polypyrrole/VO{sub x}NTs exhibit better performance as cathode for LIBs compared to VO{sub x}NTs. • Further modification to VO{sub x}NTs with desired electrochemical property can be expected. - Abstract: Vanadium oxide nanotubes (VO{sub x}NTs) with hollow as well as multi-walled features were fabricated under hydrothermal condition by soft-template method. This novel VO{sub x}NTs can be used as cathode material for lithium ion batteries (LIBs), but displaying low specific capacity and poor cycling performance owing to the residual of a mass of soft-template (C{sub 12}H{sub 27}N) and intrinsic low conductivity of VO{sub x}. Cation exchange technique and oxidative polymerization process of pyrrole monomers were conducted to wipe off partial soft-template without electrochemical activity within VO{sub x}NTs and simultaneously form polypyrrole coating on VO{sub x}NTs, respectively. The resulting polypyrrole/VO{sub x}NTs nanocomposite delivers much improved capacity and cyclic stability. Further optimizations, such as complete elimination of organic template and enhancing the crystallinity, can make this unique nanostructure a promising cathode for LIBs.

  5. Solid solution formation between vanadium(V) and tungsten(V) oxide phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Roy, Subrata Chandra; Glaum, Robert [Institut fuer Anorganische Chemie, Rheinische Friedrich-Wilhelms-Universitaet Bonn (Germany); Abdullin, Dinar; Schiemann, Olav [Institut fuer Physikalische und Theoretische Chemie, Rheinische Friedrich-Wilhelms-Universitaet Bonn (Germany); Bac, Nguyen Quang; Lii, Kwang-Hwa [Department of Chemistry, National Central University, Jhongli, Taiwan (China)

    2014-08-15

    The solid solutions (V{sub 1-x}W{sub x})OPO{sub 4} with β-VOPO{sub 4} structure type (0.0 ≤ x ≤ 0.01) and α{sub II}-VOPO{sub 4} structure type (0.04 ≤ x ≤ 0.26) were obtained from mixtures of V{sup V}OPO{sub 4} and W{sup V}OPO{sub 4} by conventional solid state reactions and by solution combustion synthesis. Single crystals of up to 3 mm edge length were obtained by chemical vapor transport (CVT) (800 → 700 C, Cl{sub 2} as a transporting agent). Single crystal structure refinements of crystals at x = 0.10 [a = 6.0503(2) Aa, c = 4.3618(4) Aa, R{sub 1} = 0.021, wR{sub 2} = 0.058, 21 parameters, 344 independent reflections] and x = 0.26 [a = 6.0979(2) Aa, c = 4.2995(1) Aa, R{sub 1} = 0.030, wR{sub 2} = 0.081, 21 parameters, 346 independent reflections] confirm the α{sub II}-VOPO{sub 4} structure type (P4/n, Z = 2) with mixed occupancy V/W for the metal site. Due to the specific redox behavior of W{sup 5+} and V{sup 5+}, solid solutions (V{sub 1-x}W{sub x})OPO{sub 4} should be formulated as (V{sup IV}{sub x}V{sup V}{sub 1-2x}W{sup VI}{sub x})OPO{sub 4}. The valence states of vanadium and tungsten are confirmed by XPS measurements. V{sup 4+} with d{sup 1} configuration was identified by EPR spectroscopy and magnetic measurements. Electronic spectra of the solid solutions show the IVCT(V{sup 4+} → V{sup 5+}) and the LMCT(O{sup 2-} → V{sup 5+}). (V{sub 0.74}W{sub 0.26})OPO{sub 4} powders exhibit semi-conducting behavior (E{sub g} = 0.7 eV). (Copyright copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  6. Bronze amulet from Sidak

    OpenAIRE

    Smagulov Erbulat A.

    2014-01-01

    A bronze amulet in the shape of a horseman found on the citadel of the Sidak fortified settlement site in Turkestan district, Southern Kazakhstan oblast is described in the article. Similar findings are met on the vast Eurasian area ranging from Mongolia to the Urals. The published item may be referred to a series of similar finds from the handicraft centers located in the Syr Darya river basin, such as Khujand, Kanka, and, lately, Sidak. Handicraft centers of Sogdiana are traditionally regar...

  7. Vanadium(IV/V) speciation of pyridine-2,6-dicarboxylic acid and 4-hydroxy-pyridine-2,6-dicarboxylic acid complexes: potentiometry, EPR spectroscopy and comparison across oxidation states.

    Science.gov (United States)

    Jakusch, Tamás; Jin, Wenzheng; Yang, Luqin; Kiss, Tamás; Crans, Debbie C

    2003-05-01

    Evaluation of stability of vanadium(IV) and (V) complexes under similar conditions is critical for the interpretation and assessment of bioactivity of various vanadium species. Detailed understanding of the chemical properties of these complexes is necessary to explain differences observed their activity in biological systems. These studies are carried out to link the chemistry of both vanadium(IV) and (V) complexes of two ligands, 2,6-pyridinedicarboxylic acid (dipicolinic acid, H(2)dipic) and 4-hydroxy-2,6-pyridinedicarboxylic acid (H(2)dipic-OH). Solution speciation of the two 2,6-pyridinedicarboxylic acids with vanadium(IV) and vanadium(V) ions was determined by pH-potentiometry at I=0.2 M (KCl) ionic strength and at T=298 K. The stability and the metal affinities of the ligands were compared. Vanadium(V) complexes were found to form only tridentate coordinated 1:1 complexes, while vanadium(IV) formed complexes with both 1:1 and 1:2 stoichiometries. The formation constant reflects hindered coordination of a second ligand molecule, presumably because of the relatively small size of the metal ion. The most probable binding mode of the complexes was further explored using ambient and low temperature EPR spectroscopy for vanadium(IV) and 51V NMR spectroscopy for vanadium(V) systems. Upon complex formation the pyridinol-OH in position 4 deprotonates with pK approximately 3.7-4.1, which is approximately 6 orders of magnitude lower than that of the free ligand. The deprotonation enhances the ligand metal ion affinity compared to the parent ligand dipicolinic acid. In the light of the speciation and stability data of the metal complexes, the efficiency of the two ligands in transporting the metal ion in the two different oxidation states are assessed and discussed.

  8. Thermal oxidation of vanadium-free Ti alloys: An X-ray photoelectron spectroscopy study

    Energy Technology Data Exchange (ETDEWEB)

    Lopez, Maria Francisca, E-mail: mflopez@icmm.csic.es [Department of Surfaces and Coatings, ICMM-CSIC, Sor Juana Ines de la Cruz, 3, Cantoblanco, 28049 Madrid (Spain); Gutierrez, Alejandro [Departamento de Fisica Aplicada and Instituto Nicolas Cabrera, Universidad Autonoma de Madrid, Cantoblanco, E-28049 Madrid (Spain); Jimenez, Jose Antonio [Centro Nacional de Investigaciones Metalurgicas, CSIC, Avda. Gregorio del Amo 8, E-28040 Madrid (Spain); Martinesi, Maria; Stio, Maria; Treves, Cristina [Department of Biochemical Sciences of University of Florence, Viale Morgagni 50, 50134 Florence (Italy)

    2010-04-06

    In the present work, X-ray photoelectron spectroscopy (XPS) was used to study the surface chemical composition of three alloys for biomedical applications: Ti-7Nb-6Al, Ti-13Nb-13Zr and Ti-15Zr-4Nb. The surface of these alloys was modified by annealing in air at 750 deg. C for different times with the aim of developing an oxide thick layer on top. The evolution of surface composition with annealing time was studied by XPS, and compared with the composition of the native oxide layer present on the samples before annealing. Two different oxidation trends were observed depending on the alloying elements and their corresponding diffusion kinetics, which give rise to different chemical species at the topmost layers. These results were linked with an evaluation of the biological response of the alloys by bringing them in contact with human peripheral blood mononuclear cells (PBMC).

  9. Melt quenched vanadium oxide embedded in graphene oxide sheets as composite electrodes for amperometric dopamine sensing and lithium ion battery applications

    Science.gov (United States)

    Sreejesh, M.; Shenoy, Sulakshana; Sridharan, Kishore; Kufian, D.; Arof, A. K.; Nagaraja, H. S.

    2017-07-01

    Electrochemical sensors and lithium-ion batteries are two important topics in electrochemistry that have attracted much attention owing to their extensive applications in enzyme-free biosensors and portable electronic devices. Herein, we report a simple hydrothermal approach for synthesizing composites of melt quenched vanadium oxide embedded on graphene oxide of equal proportion (MVGO50) for the fabrication of electrodes for nonenzymatic amperometic dopamine sensor and lithium-ion battery applications. The sensing performance of MVGO50 electrodes through chronoamperometry studies in 0.1 M PBS solution (at pH 7) over a wide range of dopamine concentration exhibited a highest sensitivity of 25.02 μA mM-1 cm-2 with the lowest detection limit of 0.07 μM. In addition, the selective sensing capability of MVGO50 was also tested through chronoamperometry studies by the addition of a very small concentration of dopamine (10 μM) in the presence of a fairly higher concentration of uric acid (10 mM) as the interfering species. Furthermore, the reversible lithium cycling properties of MVGO50 are evaluated by galvanostatic charge-discharge cycling studies. MVGO50 electrodes exhibited enhanced rate capacity of up to 200 mAhg-1 at a current of 0.1C rate and remained stable during cycling. These results indicate that MVGO composites are potential candidates for electrochemical device applications.

  10. Performance enhancement of reduced graphene oxide-modified carbon electrodes for vanadium redox-flow systems

    NARCIS (Netherlands)

    Chakrabarti, B.; Nir, D.; Yufit, V; Tariq, F; Rubio-Garcia, J.; Maher, R.; Kucernak, A.; Purushothaman Vellayani, A.; Brandon, N.

    2017-01-01

    Reduced graphene oxide (rGO) suspended in an N,N′-dimethylformamide (DMF) solvent underwent electrophoretic deposition (EPD) on carbon paper (CP) electrodes. X-ray computed micro-tomography (XMT) indicates a 24 % increase in the specific surface area of CP modified with rGO in comparison to the

  11. Kinetics of oxidation of D-arabinose and D-xylose by vanadium (V in the presence of manganese II as homogeneous catalyst

    Directory of Open Access Journals (Sweden)

    Ezekiel O. Odebunmi

    2010-12-01

    Full Text Available Kinetics of oxidation of D-arabinose and D-xylose by acidic solution of vanadium (V ions in the presence of manganese (II has been reported. First-order dependence of the reaction rate was observed on [sugars] and [H+] at low concentrations throughout the oxidation reaction and a zero-order dependence on [sugar] and [H+] was observed at high concentrations. First-order kinetics with respect to [Mn (II] was also observed throughout the oxidation for both sugars. The results indicate the effect of Cl- concentration is negligible. The reaction rates increase with the ionic strength of the medium. Various activation parameters were evaluated and provide further support to the proposed mechanism. Formic acid was reported as one of the oxidation products of these sugars.

  12. Fundamental Studies of Butane Oxidation over Model-Supported Vanadium Oxide Catalysts: Molecular Structure-Reactivity Relationships

    NARCIS (Netherlands)

    Wachs, I.E.; Jehng, J.M.; Deo, G.; Weckhuysen, B.M.; Guliants, V.V.; Benziger, J.B.; Sundaresan, S.

    1997-01-01

    The oxidation of n-butane to maleic anhydride was investigated over a series of model-supported vanadia catalysts where the vanadia phase was present as a two-dimensional metal oxide overlayer on the different oxide supports (TiO2, ZrO2, CeO2, Nb2O5, Al2O3, and SiO2). No correlation was found

  13. Study of thermal degradation of vanadium and titanium acetylacetonate derivatives

    Energy Technology Data Exchange (ETDEWEB)

    Dyagileva, L.M.; Tsyganova, E.I.; Mar' in, V.P.; Aleksandrov, Yu.A. (Gor' kovskij Gosudarstvennyj Univ. (USSR). Nauchno-Issledovatel' skij Inst. Khimii)

    1982-09-01

    Kinetics and products of vanadium (+3), vanadyl (+3) and titanium (+3) acetylacetonates thermal degradation have been studied in vapor phase in the closed system at 300-470 deg C. Gaseous composition of pyrolysis has been determined at different levels of decomposition. It is supposed that vanadium and metal vanadium mixed oxides become vanadium (+3) pyrolysis products. It is shown that metal oxidation level does not affect the thermal degradation rate. Central atom substitution leads to the change in thermal stability. Titanium (+3) acetylacetate derivatives are less stable than vanadium (+3) ones.

  14. Etruscan and Italic bronze statuettes

    NARCIS (Netherlands)

    Galestin, Marianne Caroline

    1987-01-01

    In Central Italy, small bronze statuettes were made in thousands in antiquity and also the number which still remains is considerable. This amount is in shrill contrast to that of the life-size bronzes which amply decorated Etruscan cities, as the written sources tell us; very few of these larger

  15. The future of/for vanadium.

    Science.gov (United States)

    Rehder, Dieter

    2013-09-07

    Vanadium compounds are stored or employed by several groups of bacterial and eukaryotic organisms. Two types of vanadium-dependent enzymes have so far been characterised: vanadate-dependent haloperoxidases from fungi, lichens, marine macroalgae and Streptomyces bacteria, and vanadium nitrogenases in proteo- and cyanobacteria. Several bacterial strains can employ vanadate(V) as an external electron acceptor in respiration, reducing vanadate to VO(2+) and thus contributing to the mineralisation of vanadium and to the detoxification of vanadate-contaminated water. Amanita mushrooms and many sea squirts accumulate vanadium, without the importance of this practise being well understood. Further, the analogy between vanadate and phosphate implicates an interference of vanadate with metabolic processes involving phosphate, suggesting a regulatory role for vanadate in most if not all organisms, including humans, but also hinting at toxic effects at unphysiologically high vanadate concentrations. The antidiabetic effect of vanadium compounds is probably related to the phosphate-vanadate antagonism, as is the potentiality of vanadate in the amelioration of cardiovascular affliction. The anti-cancer action of vanadium compounds and their in vitro activity towards the protozoa causing amoebiasis, leishmaniasis and Chagas' disease again may be rooted in the intervention of vanadate with the activity of phosphatases and kinases. In addition, most likely the ability of vanadate(V) and oxidovanadium(IV) to regulate the cellular production of reactive oxygen species comes in, thus influencing cellular signalling. Future developments of vanadium chemistry are likely to emphasize topics related to biological, environmental and medicinal aspects. Condensation of monovanadate results in the formation of oligovanadates, polyvanadates and finally colloidal and solid vanadium oxides that, in part, convey bio-mimetic functions comparable to those of simple vanadate, including its catalytic

  16. Vanadium and molybdenum oxide thin films on Au(111). Growth and surface characterization

    Energy Technology Data Exchange (ETDEWEB)

    Guimond, Sebastien

    2009-06-04

    The growth and the surface structure of well-ordered V{sub 2}O{sub 3}, V{sub 2}O{sub 5} and MoO{sub 3} thin films have been investigated in this work. These films are seen as model systems for the study of elementary reaction steps occurring on vanadia and molybdena-based selective oxidation catalysts. It is shown that well-ordered V{sub 2}O{sub 3}(0001) thin films can be prepared on Au(111). The films are terminated by vanadyl groups which are not part of the V{sub 2}O{sub 3} bulk structure. Electron irradiation specifically removes the oxygen atoms of the vanadyl groups, resulting in a V-terminated surface. The fraction of removed vanadyl groups is controlled by the electron dose. Such surfaces constitute interesting models to probe the relative role of both the vanadyl groups and the undercoordinated V ions at the surface of vanadia catalysts. The growth of well-ordered V{sub 2}O{sub 5}(001) and MoO{sub 3}(010) thin films containing few point defects is reported here for the first time. These films were grown on Au(111) by oxidation under 50 mbar O{sub 2} in a dedicated high pressure cell. Contrary to some of the results found in the literature, the films are not easily reduced by annealing in UHV. This evidences the contribution of radiation and surface contamination in some of the reported thermal reduction experiments. The growth of ultrathin V{sub 2}O{sub 5} and MoO{sub 3} layers on Au(111) results in formation of interface-specific monolayer structures. These layers are coincidence lattices and they do not correspond to any known oxide bulk structure. They are assumed to be stabilized by electronic interaction with Au(111). Their formation illustrates the polymorphic character and the ease of coordination units rearrangement which are characteristic of both oxides. The formation of a second layer apparently precedes the growth of bulk-like crystallites for both oxides. This observation is at odds with a common assumption that crystals nucleate as soon as a

  17. Toward binder-free electrochemical capacitor electrodes of vanadium oxide-nanostructured carbon by supercritical fluid deposition: Precursor adsorption and conversion, and electrode performance

    Science.gov (United States)

    Do, Quyet H.; Smithyman, Jesse; Zeng, Changchun; Zhang, Chuck; Liang, Richard; Zheng, Jim P.

    2014-02-01

    Electrochemical capacitor electrodes were fabricated by depositing an ultra-thin layer of vanadium oxide on a high conducting, large specific surface area (SSA) materials (substrates) using a supercritical fluid adsorption-calcination method. The high SSA materials included binder free single walled carbon nanotube-activated carbon (SWCNT-AC) composites and the traditional electrode of activated carbon-carbon black-polymer binder (AC-CB-binder). The uptake of the organometallic precursor for the oxide (vanadium (III) acetylacetonate) on the substrates were investigated and related to their SSA. Precursor uptakes up to 54.7 wt% of the initial carbon substrate was achieved. Calcination conditions for converting the precursor to oxide and electrochemical properties of the electrodes were thoroughly investigated. The V2O5, which showed extremely high specific pseudo-capacitance (>1000 F g-1 at 100 mV s-1), greatly enhanced the overall electrode performances. Conversely, the V2O5 pseudo-capacitance was better utilized in the SWCNT-AC substrate, particularly at high working speeds, because of the significantly higher electrical conductivity. For example, the SWCNT-AC-V2O5 composite (weight ratio 40:60) had its volumetric capacitance doubled, comparing to the ∼50% increase in the AC-CB-binder sample at 100 mV s-1.

  18. Titanium–vanadium oxide nanocomposite thin films: Synthesis, characterization and antibacterial activity

    Energy Technology Data Exchange (ETDEWEB)

    Wren, A.W.; Adams, B.M.; Pradhan, D.; Towler, M.R.; Mellott, N.P., E-mail: mellott@alfred.edu

    2014-04-01

    A sol–gel based deposition method was successfully developed to produce a series of crack-free, spatially homogeneous undoped/silver doped titania–vanadia oxide nanocomposite thin films. Thin films were characterized using Glancing Incidence X-ray Diffraction (GIXRD), X-ray Photoelectron Spectroscopy (XPS), and Ultraviolet Visible Spectroscopy (UV–Vis). It was determined via both XRD and XPS that when calcined at 450 °C the nanocomposite crystallinity was a function of sol composition. Additionally, it was determined via GIXRD that upon silver doping, silver was incorporated into the vanadia structure or present in silver oxide form in crystalline films. A red shift within the UV–Vis spectra was observed with an increase of vanadia concentration from 0 to 100% respectively. Antibacterial analysis conducted on Escherichia coli and Staphylococcus epidermidis demonstrated that films exposed to light showed greater antibacterial properties. - Highlights: • Nanocomposite crystallinity was a function of sol composition. • Silver was incorporated into the vanadia structure. • A red shift was observed with an increase of vanadia concentration. • Antibacterial analysis conducted on Escherichia coli and Staphylococcus epidermidis.

  19. The Development of a New Kinetic Spectrophotometric Method for the Determination of Vanadium(V Based on its Catalytic Effect on the Oxidation of Malachite Green Oxalate by Bromate in Acidic and Micellar Medium

    Directory of Open Access Journals (Sweden)

    M. Keyvanfard

    2010-01-01

    Full Text Available A new, simple, sensitive and selective kinetic spectrophotometric method was developed for the determination of ultra trace amounts of vanadium(V. The method is based on the catalytic effect of vanadium(V on the oxidation of malachite green oxalate (MG by bromate in acidic and micellar medium. The reaction was monitored spectrophotometrically by measuring the decrease in the absorbance of malachite green oxalate (MG at 625 nm with a fixed-time method. The decrease in the absorbance of MG is proportional to the concentration of vanadium(V in the range of 1-100 ng/mL with a fixed time of 0.5-2 min from the initiation of the reaction. The limit of detection is 0.71 ng/mL of vanadium(V. The relative standard deviation for the determination of 5, 30, 50 ng/mL of vanadium(V was2.5% 2.6%, 2.4% and respectively. The method was applied to the determination of vanadium(V in water samples.

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

    Science.gov (United States)

    Hanson, Susan Kloek; Silks, Louis A; Wu, Ruilian

    2013-08-27

    The invention concerns processes for oxidizing an alcohol to produce a carbonyl compound. The processes comprise contacting the alcohol with (i) a gaseous mixture comprising oxygen; and (ii) an amine compound in the presence of a catalyst, having the formula: ##STR00001## where each of R.sup.1-R.sup.12 are independently H, alkyl, aryl, CF.sub.3, halogen, OR.sup.13, SO.sub.3R.sup.14, C(O)R.sup.15, CONR.sup.16R.sup.17 or CO.sub.2R.sup.18; each of R.sup.13-R.sup.18 is independently alkyl or aryl; and Z is alkl or aryl.

  1. Development of vanadium-phosphate catalysts for methanol production by selective oxidation of methane

    Energy Technology Data Exchange (ETDEWEB)

    McCormick, R.L. [Colorado School of Mines, Golden, CO (United States)

    1995-12-31

    The United States has vast natural gas reserves which could contribute significantly to our energy security if economical technologies for conversion to liquid fuels and chemicals were developed. Many of these reserves are small scale or in remote locations and of little value unless they can be transported to consumers. Transportation is economically performed via pipeline, but this route is usually unavailable in remote locations. Another option is to convert the methane in the gas to liquid hydrocarbons, such as methanol, which can easily and economically be transported by truck. Therefore, the conversion of methane to liquid hydrocarbons has the potential to decrease our dependence upon oil imports by opening new markets for natural gas and increasing its use in the transportation and chemical sectors of the economy. In this project, we are attempting to develop, and explore new catalysts capable of direct oxidation of methane to methanol. The specific objectives of this work are discussed.

  2. In situ vibrational spectroscopic investigation of C4 hydrocarbon selective oxidation over vanadium-phosphorus-oxide catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Xue, Zhi -Yang [Iowa State Univ., Ames, IA (United States)

    1999-05-10

    n-Butane selective oxidation over the VPO catalyst to maleic anhydride is the first and only commercialized process of light alkane selective oxidation. The mechanism of this reaction is still not well known despite over twenty years of extensive studies, which can partially be attributed to the extreme difficulties to characterize catalytic reactions real-time under typical reaction conditions. In situ spectroscopic characterization techniques such as Infrared spectroscopy and laser Raman spectroscopy were used in the current mechanistic investigations of n-butane oxidation over VPO catalysts. To identify the reaction intermediates, oxidation of n-butane, 1,3-butadiene and related oxygenates on the VPO catalyst were monitored using FTIR spectroscopy under transient conditions. n-Butane was found to adsorb on the VPO catalyst to form olefinic species, which were further oxidized to unsaturated, noncyclic carbonyl species. The open chain dicarbonyl species then experienced cycloaddition to form maleic anhydride. VPO catalyst phase transformations were investigated using in situ laser Raman spectroscopy. This report contains Chapter 1: General introduction; Chapter 2: Literature review; and Chapter 5: Conclusion and recommendations.

  3. Vanadium based amorphous mixed oxides used as negative electrodes of lithium batteries; Oxydes mixtes amorphes a base de vanadium comme electrodes negatives de batteries au lithium

    Energy Technology Data Exchange (ETDEWEB)

    Guyomard, D.; Leroux, F.; Sigala, C.; Le Gal La Salle, A.; Piffard, Y. [Institut des Materiaux de Nantes, 44 (France). Laboratoire de Chimie des Solides

    1996-12-31

    This paper presents recent results concerning the chemical and electrochemical synthesis, the electrochemical properties and the characterization of two new families of amorphous oxides of formula Li{sub x}MVO{sub 4} (1oxides allows the low potential reversible insertion of lithium and can be used as negative electrodes in high performance lithium-ion batteries. (J.S.) 19 refs.

  4. Lithium Storage in Microstructures of Amorphous Mixed-Valence Vanadium Oxide as Anode Materials.

    Science.gov (United States)

    Zhao, Di; Zheng, Lirong; Xiao, Ying; Wang, Xia; Cao, Minhua

    2015-07-08

    Constructing three-dimensional (3 D) nanostructures with excellent structural stability is an important approach for realizing high-rate capability and a high capacity of the electrode materials in lithium-ion batteries (LIBs). Herein, we report the synthesis of hydrangea-like amorphous mixed-valence VOx microspheres (a-VOx MSs) through a facile solvothermal method followed by controlled calcination. The resultant hydrangea-like a-VOx MSs are composed of intercrossed nanosheets and, thus, construct a 3 D network structure. Upon evaluation as an anode material for LIBs, the a-VOx MSs show excellent lithium-storage performance in terms of high capacity, good rate capability, and long-term stability upon extended cycling. Specifically, they exhibit very stable cycling behavior with a highly reversible capacity of 1050 mA h g(-1) at a rate of 0.1 A g(-1) after 140 cycles. They also show excellent rate capability, with a capacity of 390 mA h g(-1) at a rate as high as 10 A g(-1) . Detailed investigations on the morphological and structural changes of the a-VOx MSs upon cycling demonstrated that the a-VOx MSs went through modification of the local VO coordinations accompanied with the formation of a higher oxidation state of V, but still with an amorphous state throughout the whole discharge/charge process. Moreover, the a-VOx MSs can buffer huge volumetric changes during the insertion/extraction process, and at the same time they remain intact even after 200 cycles of the charge/discharge process. Thus, these microspheres may be a promising anode material for LIBs. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Ambient condition bias stress stability of vanadium (IV) oxide phthalocyanine based p-channel organic field-effect transistors

    Science.gov (United States)

    Obaidulla, Sk Md; Singh, Subhash; Mohapatra, Y. N.; Giri, P. K.

    2018-01-01

    High bias-stress stability and low threshold voltage (V th) shift under ambient conditions are highly desirable for practical applications of organic field-effect transistors (OFETs). We demonstrate here a 20-fold enhancement in the bias-stress stability for hexamethyledisilazane (HMDS) treated vanadium (IV) oxide phthalocyanine (VOPc) based OFETs as compared to the bare VOPc case under ambient conditions. VOPc based OFETs were fabricated on bare (non treated) SiO2 and a HMDS monolayer passivated SiO2 layer, with an operating voltage of 40 V. The devices with top contact gold (Au) electrodes exhibit excellent p-channel behavior with a moderate hole mobility for the HMDS-treated device. It is demonstrated that the time dependent ON-current decay and V th shift can be effectively controlled by using self-assembled monolayers of HMDS on the VOPc layer. For the HMDS-treated case, the bias stress stability study shows the stretched exponential decay of drain current by only ~15% during the long-term operation with constant bias voltage under ambient conditions, while it shows a large decay of  >70% for the nontreated devices operated for 1000 s. The corresponding characteric decay time constant (τ) is 104 s for the HMDS treated case, while that of the the non-treated SiO2 case is only ~480 s under ambient conditions. The inferior performance of the device with bare SiO2 is traced to the charge trapping at the voids in the inter-grain region of the films, while it is almost negligible for the HMDS-treated case, as confirmed from the AFM and XRD analyses. It is believed that HMDS treatment provides an excellent interface with a low density of traps and passivates the dangling bonds, which improve the charge transport characteristics. Also, the surface morphology of the VOPc film clearly influences the device performance. Thus, the HMDS treatment provides a very attractive approach for attaining long-term air stability and a low V th shift for the VOPc based OFET

  6. The critical role of phosphate in vanadium phosphate oxide for the catalytic activation and functionalization of n-butane to maleic anhydride.

    Science.gov (United States)

    Cheng, Mu-Jeng; Goddard, William A

    2013-03-27

    We used density functional theory to study the mechanism of n-butane oxidation to maleic anhydride on the vanadium phosphorus oxide (VPO) surface. We found that O(1)═P on the V(V)OPO4 surface is the active center for initiating the VPO chemistry through extraction of H from alkane C-H bonds. This contrasts sharply with previous suggestions that the active center is either the V-O bonds or else a chemisorbed O2 on the (V(IV)O)2P2O7 surface. The ability of O(1)═P to cleave alkane C-H bonds is due to its strong basicity coupled with large reduction potentials of nearby V(V) ions. We examined several pathways for the subsequent functionalization of n-butane to maleic anhydride and found that the overall barrier does not exceed 21.7 kcal/mol.

  7. Bronze railing from Mediana

    Directory of Open Access Journals (Sweden)

    Vasić Miloje R.

    2003-01-01

    Full Text Available The hoard containing components of bronze railing was discovered in trench 7 during excavations at Mediana in 2000. Railing consists of cancelli and herms with busts of deities between them. Railing was constructed in such a way that it was possible to disassemble and reassemble it. Three cancelli one fragmented semicancellus cast together with herm and herms, one with bust of Aesculapius and other with bust of Luna. It could be concluded that railing consisted of two segments with passage between them. Male deities were represented on the left segment of the railing and female deities on the right segment. Detailed analysis revealed that Aesculapius as well as Luna bear strong mark of classical Greek and Hellenistic art, which experienced some kind of renaissance in the time of Constantine I. It is very probable that we can recognize the portrait of Faustina, Constantine’s wife in the portrait of Luna. According to the historical events the railing could have been produced before 325 AD when Constantine definitively accepted Christianity at Council of Nicaea. It is difficult to say where the railing had been produced. It had been most probably brought to Mediana during the stay of emperor Julian in Niš in 361. The sculptures found in one room of the villa with peristyle had probably been brought at the same time. The apse of triclinium of this villa had most likely been arranged as small shrine with bronze railing at its entrance. The railing was buried in 378 after battle of Adrianople and invasion of Goths in diocese Dacia.

  8. XAS study of vanadium in fluid cracking catalysts

    Science.gov (United States)

    Woolery, G. L.; Chin, A. A.; Kirker, G. W.; Huss, A.

    1989-06-01

    X-ray absorption spectroscopy was used to investigate the oxidation state and local environment of vanadium in Fluid Catalytic Cracking (FCC) catalysts as a function of processing and deactivation conditions. Our results suggest that oxidation of vanadium to V+5 alone is not solely responsible for catalyst deactivation but that other factors such as vanadium location and mobility play a significant role in catalyst performance. Basic alkaline earth oxide passivators such as MgO were found to interact strongly with vanadium during the regeneration period leading to formation of a magnesium vanadate compound.

  9. Mummification in Bronze Age Britain

    OpenAIRE

    Booth, T. J.; Chamberlain, A.T.; Pearson, M.P.

    2015-01-01

    Intentional mummification is a practice usually associated with early Egyptian or Peruvian societies, but new evidence suggests that it may also have been widespread in prehistoric Britain, and possibly in Europe more generally. Following the discovery of mummified Bronze Age skeletons at the site of Cladh Hallan in the Western Isles of Scotland, a method of analysis has been developed that can consistently identify previously mummified skeletons. The results demonstrate that Bronze Age popul...

  10. Decorative layers on tin bronzes

    OpenAIRE

    Z. Konopka; M. Nadolski; A. Zyska; M. Łągiewka

    2010-01-01

    Decorative layers are decisive for aesthetic value of castings, therefore significant demands are raised towards such layers, e.g. pleasant durable colour, gloss, and smoothness. The work discusses the influence of the type of mechanical working applied to the surfaces of CuSn10 tin bronze castings on the quality and durability of a decorative coating. The scope of the work has included designing and manufacturing of cast samples of tin bronze, mechanical working of the surfaces in order to p...

  11. Solid-state transformation of single precursor vanadium complex nanostructures to V₂O₅ and VO₂: catalytic activity of V₂O₅ for oxidative coupling of 2-naphthol.

    Science.gov (United States)

    Pradhan, Mukul; Roy, Anindita; Sinha, Arun Kumar; Sahoo, Ramkrishna; Deb, Dibakar; Pal, Tarasankar

    2015-01-28

    A vanadium complex, [(C5H5N)2V2O3·H2O], of different morphologies has been obtained via a modified hydrothermal procedure using pyridine and VOSO4 salt as the starting material. The evolved [(C5H5N)2V2O3·H2O] nanobelts are of 50-200 nm in width and of a length up to several millimeters. At higher temperatures (600 °C), the solid [(C5H5N)2V2O3·H2O] nanostructures are converted to vanadium pentoxide (V2O5) and vanadium dioxide (VO2) when heated in air and nitrogen atmosphere, respectively. During growth, the mechanism of the evolution of octahedra, truncated octahedra, and hollow truncated octahedra of [(C5H5N)2V2O3·H2O] are reported for the first time. These types of well-structured morphology are also isolated while V2O5 and VO2 are evolved. The as-grown belt-like and octahedral morphologies of [(C5H5N)2V2O3·H2O] are retained during the solid-state transformation, suggesting a route to evolve crystalline nanomaterials. Again, the morphological evolution of the [(C5H5N)2V2O3·H2O] nanostructures has been examined to be pyridine and precursor vanadyl sulfate (VS) concentration dependent. Thus, we are able to isolate truncated octahedra as an intermediate during the formation of [(C5H5N)2V2O3·H2O] nanobelts and nanoflowers with a high pyridine (Py) concentration. Interestingly, longer reaction times successively featured the transformation of truncated octahedra into nanobelts. Nanobelt evolution is not observed at low pyridine concentrations. However, the formation of octahedral morphology takes place at low pyridine concentration. All of the nanostructures were critically examined and characterized thoroughly by various physical techniques to ascertain their purity, structure and composition. An interesting, thermodynamically stable, single crystalline product from DMF soluble [(C5H5N)2V2O3·H2O] has been characterized, which indirectly supports the composition of [(C5H5N)2V2O3·H2O]. Selectively, vanadium pentoxide nanobelts have been found to be an

  12. Linking Precursor Alterations to Nanoscale Structure and Optical Transparency in Polymer Assisted Fast-Rate Dip-Coating of Vanadium Oxide Thin Films

    Science.gov (United States)

    Glynn, Colm; Creedon, Donal; Geaney, Hugh; Armstrong, Eileen; Collins, Timothy; Morris, Michael A.; Dwyer, Colm O.'

    2015-06-01

    Solution processed metal oxide thin films are important for modern optoelectronic devices ranging from thin film transistors to photovoltaics and for functional optical coatings. Solution processed techniques such as dip-coating, allow thin films to be rapidly deposited over a large range of surfaces including curved, flexible or plastic substrates without extensive processing of comparative vapour or physical deposition methods. To increase the effectiveness and versatility of dip-coated thin films, alterations to commonly used precursors can be made that facilitate controlled thin film deposition. The effects of polymer assisted deposition and changes in solvent-alkoxide dilution on the morphology, structure, optoelectronic properties and crystallinity of vanadium pentoxide thin films was studied using a dip-coating method using a substrate withdrawal speed within the fast-rate draining regime. The formation of sub-100 nm thin films could be achieved rapidly from dilute alkoxide based precursor solutions with high optical transmission in the visible, linked to the phase and film structure. The effects of the polymer addition was shown to change the crystallized vanadium pentoxide thin films from a granular surface structure to a polycrystalline structure composed of a high density of smaller in-plane grains, resulting in a uniform surface morphology with lower thickness and roughness.

  13. Linking Precursor Alterations to Nanoscale Structure and Optical Transparency in Polymer Assisted Fast-Rate Dip-Coating of Vanadium Oxide Thin Films

    Science.gov (United States)

    Glynn, Colm; Creedon, Donal; Geaney, Hugh; Armstrong, Eileen; Collins, Timothy; Morris, Michael A.; Dwyer, Colm O’

    2015-01-01

    Solution processed metal oxide thin films are important for modern optoelectronic devices ranging from thin film transistors to photovoltaics and for functional optical coatings. Solution processed techniques such as dip-coating, allow thin films to be rapidly deposited over a large range of surfaces including curved, flexible or plastic substrates without extensive processing of comparative vapour or physical deposition methods. To increase the effectiveness and versatility of dip-coated thin films, alterations to commonly used precursors can be made that facilitate controlled thin film deposition. The effects of polymer assisted deposition and changes in solvent-alkoxide dilution on the morphology, structure, optoelectronic properties and crystallinity of vanadium pentoxide thin films was studied using a dip-coating method using a substrate withdrawal speed within the fast-rate draining regime. The formation of sub-100 nm thin films could be achieved rapidly from dilute alkoxide based precursor solutions with high optical transmission in the visible, linked to the phase and film structure. The effects of the polymer addition was shown to change the crystallized vanadium pentoxide thin films from a granular surface structure to a polycrystalline structure composed of a high density of smaller in-plane grains, resulting in a uniform surface morphology with lower thickness and roughness. PMID:26123117

  14. Glucose-6-Phosphate Dehydrogenase in the Pentose Phosphate Pathway Is Localized in Vanadocytes of the Vanadium-Rich Ascidian, Ascidia sydneiensis samea

    OpenAIRE

    Taro, Uyama; Kazuhiro, YAMAMOTO; Kan, Kanamori; Hitoshi, Michibata; Department of Chemistry, Toyama University; Mukaishima Marine Biological Laboratory, Faculty of Science and Laboratory of Marine Molecular Biology, Graduate School of Science, Hiroshima University

    1998-01-01

    Ascidians are sessile marine animals known to accumulate high levels of vanadium selectively in vanadium-containing blood cells(vanadocytes). Almost all the vanadium accumulated in the vacuoles of vanadocytes is reduced to the +3 oxidation state via the +4 oxidation state, although vanadium is dissolved in the +5 oxidation state in sea water. Some of the reducing agents that participate in the reduction have been proposed. By chemical study, vanadium in the +5 oxidation state was reported to ...

  15. Vanadium Bioleaching Behavior by Acidithiobacillus ferrooxidans from a Vanadium-Bearing Shale

    Directory of Open Access Journals (Sweden)

    Dunpei Wei

    2018-01-01

    Full Text Available This study investigated bioleaching behavior of vanadium from a vanadium-bearing shale using Acidithiobacillus ferrooxidans (A. ferrooxidans. Results showed a maximum recovery of 62% vanadium in 1.2-day bioleaching, which was 22.45% higher than the controls. Then, the vanadium leaching efficiency decreased significantly, only 24% of that was obtained on the tenth day. The vanadium extraction in 1.2 days was mainly attributed to the dissolution of vanadium in free oxides of shale. Fe3+ produced by A. ferrooxidans promoted the dissolution process. X-ray diffraction (XRD patterns of the leached residues confirmed the generation of jarosite. SEM-EDS analysis of the residues indicated that jarosite adsorbed on the shale and inhibited the further dissolution of vanadium. The relevance of V, Fe, S, O was quite good in the energy disperse X-ray spectrometry (EDS element mapping of jarosite, and acid-washing of the jarosite resulted in 31.6% of the vanadium in the precipitates desorption, indicating that the decrease of vanadium leaching efficiency in bioleaching process was caused by both adsorption and co-precipitation with jarosite.

  16. Vanadium oxide based nanostructured materials for catalytic oxidative dehydrogenation of propane : effect of heterometallic centers on the catalyst performance.

    Energy Technology Data Exchange (ETDEWEB)

    Khan, M. I.; Deb, S.; Aydemir, K.; Alwarthan, A. A.; Chattopadhyay, S.; Miller, J. T.; Marshall, C. L. (Chemical Sciences and Engineering Division); (Illinois Inst. of Tech.); (King Saud Univ.)

    2010-01-01

    Catalytic properties of a series of new class of catalysts materials-[Co{sub 3}(H{sub 2}O){sub 12}V{sub 18}O{sub 42} (XO{sub 4})].24H{sub 2}O (VNM-Co), [Fe{sub 3}(H{sub 2}O){sub 12}V{sub 18}O{sub 42}(XO{sub 4})].24H{sub 2}O (VNM-Fe) (X = V, S) and [H{sub 6}Mn{sub 3}(H{sub 2}O){sub 12}V{sub 18}O{sub 42}(VO{sub 4})].30H{sub 2}O for the oxidative dehydrogenation of propane is studied. The open-framework nanostructures in these novel materials consist of three-dimensional arrays of {l_brace}V{sub 18}O{sub 42}(XO{sub 4}){r_brace} (X = V, S) clusters interconnected by {l_brace}-O-M-O-{r_brace} (M = Mn, Fe, Co) linkers. The effect of change in the heterometallic center M (M = Mn, Co, Fe) of the linkers on the catalyst performance was studied. The catalyst material with Co in the linker showed the best performance in terms of propane conversion and selectivity at 350 C. The material containing Fe was most active but least selective and Mn containing catalyst was least active. The catalysts were characterized by Temperature Programmed Reduction (TPR), BET surface area measurement, Diffuse Reflectance Infrared Fourier Transform Spectroscopy, and X-ray Absorption Spectroscopy. TPR results show that all three catalysts are easily reducible and therefore are active at relatively low temperature. In situ X-ray absorption near edge spectroscopy (XANES) and extended X-ray absorption fine structure spectroscopy (EXAFS) studies revealed that the oxidation state of Co(II) remained unchanged up to 425 C (even after pretreatment). The reduction of Co(II) into metallic form starts at 425 C and this process is completed at 600 C.

  17. Recovery of Vanadium from a High Ca/V Ratio Vanadium Slag Using Sodium Roasting and Ammonia Leaching

    Science.gov (United States)

    Xu, Song; Long, Mujun; Chen, Dengfu; Fan, Helin; Chen, Yuting; Sun, Xue

    In order to seek an effective extraction process for vanadium, the recovery of vanadium from a high Ca/V ratio vanadium slag was studied by sodium roasting and ammonia leaching. In the present paper, the oxidation and leaching process of vanadium slag was investigated by X-ray diffraction (XRD), scanning electron microscopy and energy dispersive X-ray spectrometry (SEM/EDS) techniques. The effects of ammonium carbonate concentration, leaching temperature and leaching time on the leaching ratio of vanadium were discussed. As indicated in the experimental result, the optimal (NH4)2CO3 concentration was 120g/L, leaching temperature was 60°C and leaching time was 20 min. Approximately 92% of the vanadium was recovered under the optimal conditions. Furthermore, by means of X-ray diffraction analysis, the phase transformations of the vanadium slag during roasting and leaching processes were analyzed and discussed.

  18. Bronze amulet from Sidak

    Directory of Open Access Journals (Sweden)

    Smagulov Erbulat A.

    2014-03-01

    Full Text Available A bronze amulet in the shape of a horseman found on the citadel of the Sidak fortified settlement site in Turkestan district, Southern Kazakhstan oblast is described in the article. Similar findings are met on the vast Eurasian area ranging from Mongolia to the Urals. The published item may be referred to a series of similar finds from the handicraft centers located in the Syr Darya river basin, such as Khujand, Kanka, and, lately, Sidak. Handicraft centers of Sogdiana are traditionally regarded as places of their manufacture. However, no finds of the kind are mentioned at proper Sogdian towns (Penjikent, Paikend, Afrasyab, etc., which have been thoroughly studied. Hence, the author makes a conclusion that these amulets, as well as many other pieces of jewelry were manufactured in the 7th to 8th centuries AD at the handicraft centers of Chach, a state formation comprising the Middle Syr-Darya River oases at the time. This region was inhabited by the descendants of the ancient Kangju state inhabitants, who inherited cultural traditions of the past, including the myths about the hero-horseman.

  19. A study of tin dioxide and antimony tetroxide supported vanadium oxide catalysts by solid-state 51V and 1H NMR techniques.

    Science.gov (United States)

    Reddy, B M; Mastikhin, V M

    1992-12-01

    A series of vanadia catalysts with various V2O5 loadings supported on SnO2 and alpha-Sb2O4 are investigated by the application of X-ray diffraction and solid-state 51V and 1H NMR techniques. XRD results show no evidence for the formation of a crystalline vanadia phase on both supports. However, the 51V NMR spectra of the catalysts reveal the existence of two types of vanadia species on the surface of the support: one due to a dispersed vanadia phase at lower vanadia loadings and the other due to a crystalline vanadia phase at higher vanadium content. The quantity of the dispersed vanadia phase, however, depends on the nature of the support material. The 1H NMR results provide evidence for the existence or non-existence of a metal oxide support interaction through the support surface hydroxyl groups.

  20. Quasi-one-dimensional nanostructured cobalt (Co) intercalated vanadium oxide (V{sub 2}O{sub 5}): Peroxovanadate sol gel synthesis and structural study

    Energy Technology Data Exchange (ETDEWEB)

    Langie da Silva, Douglas, E-mail: douglas.langie@ufpel.edu.br [Departamento de Física, Universidade Federal de Pelotas, Caixa Postal 354, Pelotas 96010-900 (Brazil); Moreira, Eduardo Ceretta [Laboratório de Espectroscopia, Universidade Federal do Pampa, Campus Bagé, Bagé 96400-970 (Brazil); Dias, Fábio Teixeira; Neves Vieira, Valdemar das [Departamento de Física, Universidade Federal de Pelotas, Caixa Postal 354, Pelotas 96010-900 (Brazil); Brandt, Iuri Stefani; Cas Viegas, Alexandre da; Pasa, André Avelino [Laboratório de Filmes Finos e Superfícies, Universidade Federal de Santa Catarina, Caixa Postal 476, Florianópolis 88.040-900 (Brazil)

    2015-01-15

    Nanostructured cobalt vanadium oxide (V{sub 2}O{sub 5}) xerogels spread onto crystalline Si substrates were synthesized via peroxovanadate sol gel route. The resulting products were characterized by distinct experimental techniques. The surface morphology and the nanostructure of xerogels correlate with Co concentration. The decrease of the structural coherence length is followed by the formation of a loose network of nanopores when the concentration of intercalated species was greater than 4 at% of Co. The efficiency of the synthesis route also drops with the increase of Co concentration. The interaction between the Co(OH{sub 2}){sub 6}{sup 2+} cations and the (H{sub 2}V{sub 10}O{sub 28}){sup 4−} anions during the synthesis was suggested as a possible explanation for the incomplete condensation of the V{sub 2}O{sub 5} gel. Finally the experimental results points for the intercalation of Co between the bilayers of the V{sub 2}O{sub 5}. In this scenario two possible preferential occupation sites for the metallic atoms in the framework of the xerogel were proposed. - Graphical abstract: Quasi-one-dimensional nanostructured cobalt (Co) intercalated vanadium oxide (V{sub 2}O{sub 5}) nanoribbons synthesized by peroxovanadate sol gel route. - Highlights: • Nanostructured cobalt V{sub 2}O{sub 5} gel spread onto c{sub S}i were synthesized via peroxovanadate sol gel route. • The micro and nanostructure correlates with the cobalt content. • The efficiency of the synthesis route shows to be also dependent of Co content. • The experimental results points for the intercalation of Co between the bilayers of the V{sub 2}O{sub 5} xerogel.

  1. Vanadium recycling in the United States in 2004

    Science.gov (United States)

    Goonan, Thomas G.

    2011-01-01

    As one of a series of reports that describe the recycling of metal commodities in the United States, this report discusses the flow of vanadium in the U.S. economy in 2004. This report includes a description of vanadium supply and demand in the United States and illustrates the extent of vanadium recycling and recycling trends. In 2004, apparent vanadium consumption, by end use, in the United States was 3,820 metric tons (t) in steelmaking and 232 t in manufacturing, of which 17 t was for the production of superalloys and 215 t was for the production of other alloys, cast iron, catalysts, and chemicals. Vanadium use in steel is almost entirely dissipative because recovery of vanadium from steel scrap is chemically impeded under the oxidizing conditions in steelmaking furnaces. The greatest amount of vanadium recycling is in the superalloy, other-alloy, and catalyst sectors of the vanadium market. Vanadium-bearing catalysts are associated with hydrocarbon recovery and refining in the oil industry. In 2004, 2,850 t of vanadium contained in alloy scrap and spent catalysts was recycled, which amounted to about 44 percent of U.S. domestic production. About 94 percent of vanadium use in the United States was dissipative (3,820 t in steel/4,050 t in steel+fabricated products).

  2. Electro-thermal control of aluminum-doped zinc oxide/vanadium dioxide multilayered thin films for smart-device applications.

    Science.gov (United States)

    Skuza, J R; Scott, D W; Mundle, R M; Pradhan, A K

    2016-02-17

    We demonstrate the electro-thermal control of aluminum-doped zinc oxide (Al:ZnO) /vanadium dioxide (VO2) multilayered thin films, where the application of a small electric field enables precise control of the applied heat to the VO2 thin film to induce its semiconductor-metal transition (SMT). The transparent conducting oxide nature of the top Al:ZnO film can be tuned to facilitate the fine control of the SMT of the VO2 thin film and its associated properties. In addition, the Al:ZnO film provides a capping layer to the VO2 thin film, which inhibits oxidation to a more energetically favorable and stable V2O5 phase. It also decreases the SMT of the VO2 thin film by approximately 5-10 °C because of an additional stress induced on the VO2 thin film and/or an alteration of the oxygen vacancy concentration in the VO2 thin film. These results have significant impacts on technological applications for both passive and active devices by exploiting this near-room-temperature SMT.

  3. Vanadium Compounds as PTP Inhibitors

    Directory of Open Access Journals (Sweden)

    Elsa Irving

    2017-12-01

    Full Text Available Phosphotyrosine signaling is regulated by the opposing actions of protein tyrosine kinases (PTKs and protein tyrosine phosphatases (PTPs. Here we discuss the potential of vanadium derivatives as PTP enzyme inhibitors and metallotherapeutics. We describe how vanadate in the V oxidized state is thought to inhibit PTPs, thus acting as a pan-inhibitor of this enzyme superfamily. We discuss recent developments in the biological and biochemical actions of more complex vanadium derivatives, including decavanadate and in particular the growing number of oxidovanadium compounds with organic ligands. Pre-clinical studies involving these compounds are discussed in the anti-diabetic and anti-cancer contexts. Although in many cases PTP inhibition has been implicated, it is also clear that many such compounds have further biochemical effects in cells. There also remain concerns surrounding off-target toxicities and long-term use of vanadium compounds in vivo in humans, hindering their progress through clinical trials. Despite these current misgivings, interest in these chemicals continues and many believe they could still have therapeutic potential. If so, we argue that this field would benefit from greater focus on improving the delivery and tissue targeting of vanadium compounds in order to minimize off-target toxicities. This may then harness their full therapeutic potential.

  4. Analyzing optical properties of thin vanadium oxide films through semiconductor-to-metal phase transition using spectroscopic ellipsometry

    Science.gov (United States)

    Sun, Jianing; Pribil, Greg K.

    2017-11-01

    We investigated the optical behaviors of vanadium dioxide (VO2) films through the semiconductor-to-metal (STM) phase transition using spectroscopic ellipsometry. Correlations between film thickness and refractive index were observed resulting from the absorbing nature of these films. Simultaneously analyzing data at multiple temperatures using Kramers-Kronig consistent oscillator models help identify film thickness. Nontrivial variations in resulting optical constants were observed through STM transition. As temperature increases, a clear increase is observed in near infrared absorption due to Drude losses that accompany the transition from semiconducting to metallic phases. Thin films grown on silicon and sapphire substrate present different optical properties and thermal hysteresis due to lattice stress and compositional differences.

  5. Effect of vanadium substitution on structural and electrical properties of sol-gel grown nanostructured zinc oxide

    Science.gov (United States)

    Boricha, Hetal; Rajyaguru, Bhargav; Gadani, Keval; Rathod, K. N.; Shrimali, V. G.; Udeshi, Bhagyashree; Keshvani, M. J.; Joshi, A. D.; Pandya, D. D.; Solanki, P. S.; Shah, N. A.

    2017-05-01

    In the present communication, we report the results on the structural and electrical studies on nanostructured pure (ZnO) and Vanadium (V) doped Zn0.95V0.05O samples synthesized using low cost Sol-Gel technique. To understand the structural properties and their dependence on V substitution, X-Ray diffraction (XRD) measurement was carried out for both the samples understudy. XRD results reveal the single phasic wurtzite nature of both the samples showing hexagonal unit cell structure. A minor phase of ZnV2O6 is observed in V doped ZnO sample. Improved dielectric permittivity, enhanced ac conductivity (σac) and suppression in impedance have been discussed on the basis of structural modifications by the substitution of V in ZnO, enhanced charge carrier concentration, charge carrier polarization and correlated barrier hopping due to the localized state.

  6. Vanadium Pentoxide Nanobelt-Reduced Graphene Oxide Nanosheet Composites as High-Performance Pseudocapacitive Electrodes: ac Impedance Spectroscopy Data Modeling and Theoretical Calculations

    Directory of Open Access Journals (Sweden)

    Sanju Gupta

    2016-07-01

    Full Text Available Graphene nanosheets and graphene nanoribbons, G combined with vanadium pentoxide (VO nanobelts (VNBs and VNBs forming GVNB composites with varying compositions were synthesized via a one-step low temperature facile hydrothermal decomposition method as high-performance electrochemical pseudocapacitive electrodes. VNBs from vanadium pentoxides (VO are formed in the presence of graphene oxide (GO, a mild oxidant, which transforms into reduced GO (rGOHT, assisting in enhancing the electronic conductivity coupled with the mechanical robustness of VNBs. From electron microscopy, surface sensitive spectroscopy and other complementary structural characterization, hydrothermally-produced rGO nanosheets/nanoribbons are decorated with and inserted within the VNBs’ layered crystal structure, which further confirmed the enhanced electronic conductivity of VNBs. Following the electrochemical properties of GVNBs being investigated, the specific capacitance Csp is determined from cyclic voltammetry (CV with a varying scan rate and galvanostatic charging-discharging (V–t profiles with varying current density. The rGO-rich composite V1G3 (i.e., VO/GO = 1:3 showed superior specific capacitance followed by VO-rich composite V3G1 (VO/GO = 3:1, as compared to V1G1 (VO/GO = 1:1 composite, besides the constituents, i.e., rGO, rGOHT and VNBs. Composites V1G3 and V3G1 also showed excellent cyclic stability and a capacitance retention of >80% after 500 cycles at the highest specific current density. Furthermore, by performing extensive simulations and modeling of electrochemical impedance spectroscopy data, we determined various circuit parameters, including charge transfer and solution resistance, double layer and low frequency capacitance, Warburg impedance and the constant phase element. The detailed analyses provided greater insights into physical-chemical processes occurring at the electrode-electrolyte interface and highlighted the comparative performance of

  7. Decorative layers on tin bronzes

    Directory of Open Access Journals (Sweden)

    Z. Konopka

    2010-10-01

    Full Text Available Decorative layers are decisive for aesthetic value of castings, therefore significant demands are raised towards such layers, e.g. pleasant durable colour, gloss, and smoothness. The work discusses the influence of the type of mechanical working applied to the surfaces of CuSn10 tin bronze castings on the quality and durability of a decorative coating. The scope of the work has included designing and manufacturing of cast samples of tin bronze, mechanical working of the surfaces in order to prepare them for applying coating layers,generating decorative layers as a result of chemical reactions, and the quality assessment and comparison of the obtained coating. Theassessment of thickness and continuity of the obtained decorative layers based on metallographic examinations has been presented.

  8. A bronze amulet from Sidak

    OpenAIRE

    Smagulov Erbulat A.

    2014-01-01

    A bronze amulet in the shape of a horseman found on the citadel of the Sidak fortified settlement site in Turkestan district, Southern Kazakhstan oblast is described in the article. Similar findings are met on the vast Eurasian area ranging from Mongolia to the Urals. The published item may be referred to a series of similar finds from the handicraft centers located in the Syr Darya river basin, such as Khujand, Kanka, and, lately, Sidak. Handicraft centers of Sogdiana are traditionally regar...

  9. Vanadium phosphates on mesoporous supports: model catalysts for solid-state NMR studies of the selective oxidation of n-butane.

    Science.gov (United States)

    Frey, Jörg; Sang Ooi, Yean; Thomas, Bejoy; Reddy Marthala, V R; Bressel, Arne; Schölkopf, Thomas; Schleid, Thomas; Hunger, Michael

    2009-04-01

    SBA-15 was utilized as mesoporous support for the dispersion of vanadium phosphate (VPO) compounds. Loading of SBA-15 with VPO compounds was found to be accompanied by decreasing (29)Si MAS NMR signals of Q(2) (Si(2Si,2OH)) and Q(3) (Si(3Si,1OH)) silicon species, which indicates coverage of the mesoporous support by the guest compounds. The (51)V MAS NNR spectra of the activated VPO/SBA-15 catalysts consist of patterns typical for the alpha(II)- and beta-phases of vanadyl orthophosphate. In the (31)P MAS NMR spectra of the activated VPO/SBA-15 catalysts, signals of beta-, delta-, and alpha(II)-VOPO(4) phases could be identified. Upon conversion of n-butane-(13)C(4), a strong decrease of the (31)P MAS NMR signals characteristic for the delta-VOPO(4) phase occurred, while by (13)C MAS NMR spectroscopy the formation of maleic anhydride, carbon monoxide, and carbon dioxide was observed. This finding supports the active role of the delta-VOPO(4) phase in the selective oxidation of n-butane on VPO/SBA-15 catalysts.

  10. Quasi-one-dimensional nanostructured cobalt (Co) intercalated vanadium oxide (V2O5): Peroxovanadate sol gel synthesis and structural study

    Science.gov (United States)

    da Silva, Douglas Langie; Moreira, Eduardo Ceretta; Dias, Fábio Teixeira; Neves Vieira, Valdemar das; Brandt, Iuri Stefani; Cas Viegas, Alexandre da; Pasa, André Avelino

    2015-01-01

    Nanostructured cobalt vanadium oxide (V2O5) xerogels spread onto crystalline Si substrates were synthesized via peroxovanadate sol gel route. The resulting products were characterized by distinct experimental techniques. The surface morphology and the nanostructure of xerogels correlate with Co concentration. The decrease of the structural coherence length is followed by the formation of a loose network of nanopores when the concentration of intercalated species was greater than 4 at% of Co. The efficiency of the synthesis route also drops with the increase of Co concentration. The interaction between the Co(OH2)62+ cations and the (H2V10O28)4- anions during the synthesis was suggested as a possible explanation for the incomplete condensation of the V2O5 gel. Finally the experimental results points for the intercalation of Co between the bilayers of the V2O5. In this scenario two possible preferential occupation sites for the metallic atoms in the framework of the xerogel were proposed.

  11. Strengthening of Ceramic-based Artificial Nacre via Synergistic Interactions of 1D Vanadium Pentoxide and 2D Graphene Oxide Building Blocks

    Science.gov (United States)

    Knöller, Andrea; Lampa, Christian P.; Cube, Felix Von; Zeng, Tingying Helen; Bell, David C.; Dresselhaus, Mildred S.; Burghard, Zaklina; Bill, Joachim

    2017-01-01

    Nature has evolved hierarchical structures of hybrid materials with excellent mechanical properties. Inspired by nacre’s architecture, a ternary nanostructured composite has been developed, wherein stacked lamellas of 1D vanadium pentoxide nanofibres, intercalated with water molecules, are complemented by 2D graphene oxide (GO) nanosheets. The components self-assemble at low temperature into hierarchically arranged, highly flexible ceramic-based papers. The papers’ mechanical properties are found to be strongly influenced by the amount of the integrated GO phase. Nanoindentation tests reveal an out-of-plane decrease in Young’s modulus with increasing GO content. Furthermore, nanotensile tests reveal that the ceramic-based papers with 0.5 wt% GO show superior in-plane mechanical performance, compared to papers with higher GO contents as well as to pristine V2O5 and GO papers. Remarkably, the performance is preserved even after stretching the composite material for 100 nanotensile test cycles. The good mechanical stability and unique combination of stiffness and flexibility enable this material to memorize its micro- and macroscopic shape after repeated mechanical deformations. These findings provide useful guidelines for the development of bioinspired, multifunctional systems whose hierarchical structure imparts tailored mechanical properties and cycling stability, which is essential for applications such as actuators or flexible electrodes for advanced energy storage.

  12. Vanadium-Catalyzed Oxidative C(CO)-C(CO) Bond Cleavage for C-N Bond Formation: One-Pot Domino Transformation of 1,2-Diketones and Amidines into Imides and Amides.

    Science.gov (United States)

    Digwal, Chander Singh; Yadav, Upasana; Ramya, P V Sri; Sana, Sravani; Swain, Baijayantimala; Kamal, Ahmed

    2017-07-21

    A novel vanadium-catalyzed one-pot domino reaction of 1,2-diketones with amidines has been identified that enables their transformation into imides and amides. The reaction proceeds by dual acylation of amidines via oxidative C(CO)-C(CO) bond cleavage of 1,2-diketones to afford N,N'-diaroyl-N-arylbenzamidine intermediates. In the reaction, these intermediates are easily hydrolyzed into imides and amides through vanadium catalysis. This method provides a practical, simple, and mild synthetic approach to access a variety of imides as well as amides in high yields. Moreover, one-step construction of imide and amide bonds with a long-chain alkyl group is an attractive feature of this protocol.

  13. Vanadium pentoxide nanoparticles mimic vanadium haloperoxidases and thwart biofilm formation

    Science.gov (United States)

    Natalio, Filipe; André, Rute; Hartog, Aloysius F.; Stoll, Brigitte; Jochum, Klaus Peter; Wever, Ron; Tremel, Wolfgang

    2012-08-01

    Marine biofouling--the colonization of small marine microorganisms on surfaces that are directly exposed to seawater, such as ships' hulls--is an expensive problem that is currently without an environmentally compatible solution. Biofouling leads to increased hydrodynamic drag, which, in turn, causes increased fuel consumption and greenhouse gas emissions. Tributyltin-free antifouling coatings and paints based on metal complexes or biocides have been shown to efficiently prevent marine biofouling. However, these materials can damage the environment through metal leaching (for example, of copper and zinc) and bacteria resistance. Here, we show that vanadium pentoxide nanowires act like naturally occurring vanadium haloperoxidases to prevent marine biofouling. In the presence of bromide ions and hydrogen peroxide, the nanowires catalyse the oxidation of bromide ions to hypobromous acid (HOBr). Singlet molecular oxygen (1O2) is formed and this exerts strong antibacterial activity, which prevents marine biofouling without being toxic to marine biota. Vanadium pentoxide nanowires have the potential to be an alternative approach to conventional anti-biofouling agents.

  14. Dependence of Vanadium Recovery

    African Journals Online (AJOL)

    a large-scale vanadium processing or separation processes where vanadium is a contaminant. However, the ... in a separating funnel, swirled manually and later on a mechanical shaker operated at 120 rpm for 2 minutes ..... (40% v/v) TBP and the relevant scheme for extraction would be according to Equation 7. VOCl + n ...

  15. Oxidative dehydrogenation of n-butane over magnesium vanadate nano-catalysts supported on magnesia-zirconia: effect of vanadium content.

    Science.gov (United States)

    Lee, Jong Kwon; Hong, Ung Gi; Yoo, Yeonshick; Cho, Young-Jin; Lee, Jinsuk; Chang, Hosik; Song, In Kyu

    2013-12-01

    Magnesia-zirconia (MgO-ZrO2) support was prepared by a sol-gel method, and magnesium vanadate nano-catalysts supported on magnesia-zirconia (X-Mg3(VO4)2/MgO-ZrO2) were then prepared by a wet impregnation method with a variation of vanadium content (X = 6.6, 9.9, 12.8, 15.2, and 19.1 wt%). X-Mg3(VO4)2/MgO-ZrO2 nano-catalysts were applied to the oxidative dehydrogenation of n-butane to n-butene and 1,3-butadiene. The formation of X-Mg3(VO4)2/MgO-ZrO2 nano-catalysts was well confirmed by XRD, XPS, and ICP-AES analyses. 15.2-Mg3(VO4)2/MgO-ZrO2 and 19.1-Mg3(VO4)2/MgO-ZrO2 catalysts experienced a catalyst deactivation, while the other Mg3(VO4)2/MgO-ZrO2 catalysts showed a stable catalytic performance during the whole reaction time. The effect of oxygen property of X-Mg3(VO4)2/MgO-ZrO2 nano-catalysts on the catalytic performance in the oxidative dehydrogenation of n-butane was investigated. Experimental results revealed that oxygen capacity of the catalyst was closely related to the catalytic performance, while oxygen mobility of the catalyst played an important role in the catalyst stability. Among the catalysts tested, 12.8-Mg3(VO4)2/MgO-ZrO2 catalyst showed the best catalytic performance in terms of yield for TDP (total dehydrogenation products).

  16. A novel process for the recovery of iron, titanium, and vanadium from vanadium-bearing titanomagnetite: sodium modification-direct reduction coupled process

    Science.gov (United States)

    Zhang, Yi-min; Yi, Ling-yun; Wang, Li-na; Chen, De-sheng; Wang, Wei-jing; Liu, Ya-hui; Zhao, Hong-xin; Qi, Tao

    2017-05-01

    A sodium modification-direct reduction coupled process was proposed for the simultaneous extraction of V and Fe from vanadium- bearing titanomagnetite. The sodium oxidation of vanadium oxides to water-soluble sodium vanadate and the transformation of iron oxides to metallic iron were accomplished in a single-step high-temperature process. The increase in roasting temperature favors the reduction of iron oxides but disfavors the oxidation of vanadium oxides. The recoveries of vanadium, iron, and titanium reached 84.52%, 89.37%, and 95.59%, respectively. Moreover, the acid decomposition efficiency of titanium slag reached 96.45%. Compared with traditional processes, the novel process provides several advantages, including a shorter flow, a lower energy consumption, and a higher utilization efficiency of vanadium-bearing titanomagnetite resources.

  17. 75 FR 14257 - Pricing for Bronze Medals

    Science.gov (United States)

    2010-03-24

    ... From the Federal Register Online via the Government Publishing Office DEPARTMENT OF THE TREASURY United States Mint Pricing for Bronze Medals AGENCY: United States Mint, Department of the Treasury. ACTION: Notice. SUMMARY: The United States Mint is announcing the price of the 1\\5/16\\- inch bronze...

  18. The Bronze Age Smith as Individual

    DEFF Research Database (Denmark)

    Nørgaard, Heide Wrobel

    During 1550-1100 BC magnificent decorated bronze objects appear in grave and hoard finds in Northwest Europe. While investigating similarities in the decorative elements of bronze objects belonging to the female gender, it is possible to find traces of the production process. These distinctive fe...

  19. Behaviour of millscale reinforced Aluminium Bronze composite ...

    African Journals Online (AJOL)

    Despite the desirable characteristics exhibited by most aluminium bronze, the deficient responses in certain critical applications have necessitated improvement in the mechanical properties. The microstructural and mechanical properties of cast aluminium bronze reinforced with iron millscale particles were investigated in ...

  20. New Research on Bronze Age Textile Production

    DEFF Research Database (Denmark)

    Andersson, Eva Birgitta; Mårtensson, Linda; Nosch, Marie-Louise Bech

    2008-01-01

    presentation of the results from the systematic tests with Bronze Age textile tools. results concerning mesurements of lenght and time consumed.......presentation of the results from the systematic tests with Bronze Age textile tools. results concerning mesurements of lenght and time consumed....

  1. Structure and function of vanadium haloperoxidases

    NARCIS (Netherlands)

    Wever, R.; Michibata, H.

    2012-01-01

    Vanadium haloperoxidases contain the bare metal oxide vanadate as a prosthetic group and differ strongly from the heme peroxidases in substrate specificity and molecular properties. The substrates of these enzymes are limited to halides and sulfides, which in the presence of hydrogen peroxide are

  2. Role of vanadium in Keggin heteropoly molybdate supported on ...

    Indian Academy of Sciences (India)

    ated for oxidation of 1,2-benzenedimethanol using H2O2 and O2 as oxidants. .... C on oil bath. In the case of O2 as oxidant, reaction was conducted under O2 atmosphere. Progress of the reaction was monitored by using thin-layer chro- ... The role of vanadium in heteropoly molybdate catalysts for oxidation reactions. 469.

  3. Study of hydrogen in coals, polymers, oxides, and muscle water by nuclear magnetic resonance; extension of solid-state high-resolution techniques. [Hydrogen molybdenum bronze

    Energy Technology Data Exchange (ETDEWEB)

    Ryan, L.M.

    1981-10-01

    Nuclear magnetic resonance (NMR) spectroscopy has been an important analytical and physical research tool for several decades. One area of NMR which has undergone considerable development in recent years is high resolution NMR of solids. In particular, high resolution solid state /sup 13/C NMR spectra exhibiting features similar to those observed in liquids are currently achievable using sophisticated pulse techniques. The work described in this thesis develops analogous methods for high resolution /sup 1/H NMR of rigid solids. Applications include characterization of hydrogen aromaticities in fossil fuels, and studies of hydrogen in oxides and bound water in muscle.

  4. Kinetics of Vanadium Extraction from Hot Metal by Basic Slag

    Science.gov (United States)

    Zhang, Tao; Xie, Bing; Liu, Xuan; Diao, Jiang; Zhang, Zhen; Li, Hong-Yi

    Extracting vanadium from vanadium containing hot metal by LD process has been proven an effective solution for the utilization of vanadium-titanium magnetite ore, but the systematic analyses of vanadium extraction rate and mechanism by basic slag are seldom reported. In this study, mathematical model of vanadium transfer from metal to slag was formulated and the rates of vanadium extraction of hot metal with basic slag were investigated. The results indicated that the apparent vanadium extraction rate constant, k p , were in the range of 1.33˜9.07×10-4g/(cm3·s). And the rate constant was increased with the increase of final slag basicity, reaction temperature and stirring gas flow. The apparent of mass transfer parameter decreases significantly from 0.13 cm3/ s to 0 cm3/ s in 20min, and the data changed as negative due to the decrease of slag oxidation and recovery of vanadium from slag to metal.

  5. On the structural and electronic properties of hexanuclear vanadium oxide clusters V6On(-/0) (n=12-15): is V6O12 cluster planar or cage-like?

    Science.gov (United States)

    Wang, Ling-Fei; Xie, Lu; Fang, Hong-Ling; Li, Yun-Fei; Zhang, Xiao-Bin; Wang, Bin; Zhang, Yong-Fan; Huang, Xin

    2014-10-15

    Density functional theory (DFT) calculations are carried out to investigate the structural and electronic properties of a series of hexanuclear vanadium oxide clusters V6On(-/0) (n=12-15). Generalized Koopmans' theorem is applied to predict the vertical detachment energies (VDEs) and simulate the photoelectron spectra (PES) for V6On(-) (n=12-15) clusters. Extensive DFT calculations are performed in search of the lowest-energy structures for both the anions and neutrals. All of these clusters appear to prefer the polyhedral cage structures, in contrast to the planar star-like structures observed in prior model surface studies for the V6O12 cluster. Molecular orbitals are performed to analyze the chemical bonding in the hexanuclear vanadium oxide clusters and provide insights into the sequential oxidation of V6On(-) (n=12-15) clusters. The V6On(-) (n=12-15) clusters possess well-defined V(5+) and V(3+) sites, and may serve as molecular models for surface defects. Electron spin density analyses show that the unpaired electrons in V6On(-) (n=12-14) clusters are primarily localized on the V(3+) sites rather than on the V(5+) sites. The difference gas phase versus model surface structures of V6O12 hints the critical roles of cluster-substrate interactions in stabilizing the planar V6O12 cluster on model surfaces. Copyright © 2014 Elsevier B.V. All rights reserved.

  6. Vanadium Recovery from Oil Fly Ash by Carbon Removal and Roast-Leach Process

    Science.gov (United States)

    Jung, Myungwon; Mishra, Brajendra

    2017-11-01

    This research mainly focuses on the recovery of vanadium from oil fly ash by carbon removal and the roast-leach process. The oil fly ash contained about 85% unburned carbon and 2.2% vanadium by weight. A vanadium-enriched product was obtained after carbon removal, and the vanadium content of this product was 19% by weight. Next, the vanadium-enriched product was roasted with sodium carbonate to convert vanadium oxides to water-soluble sodium metavanadate. The roasted sample was leached with water at 60°C, and the extraction percentage of vanadium was about 92% by weight. Several analytical techniques, such as inductively coupled plasma atomic emission spectroscopy (ICP-AES), x-ray fluorescence (XRF), and thermogravimetric and differential thermal analysis (TG-DTA), were utilized for sample analyses. Thermodynamic modeling was also conducted with HSC chemistry software to explain the experimental results.

  7. Vanadium Recovery from Oil Fly Ash by Carbon Removal and Roast-Leach Process

    Science.gov (United States)

    Jung, Myungwon; Mishra, Brajendra

    2018-02-01

    This research mainly focuses on the recovery of vanadium from oil fly ash by carbon removal and the roast-leach process. The oil fly ash contained about 85% unburned carbon and 2.2% vanadium by weight. A vanadium-enriched product was obtained after carbon removal, and the vanadium content of this product was 19% by weight. Next, the vanadium-enriched product was roasted with sodium carbonate to convert vanadium oxides to water-soluble sodium metavanadate. The roasted sample was leached with water at 60°C, and the extraction percentage of vanadium was about 92% by weight. Several analytical techniques, such as inductively coupled plasma atomic emission spectroscopy (ICP-AES), x-ray fluorescence (XRF), and thermogravimetric and differential thermal analysis (TG-DTA), were utilized for sample analyses. Thermodynamic modeling was also conducted with HSC chemistry software to explain the experimental results.

  8. Pathway and Surface Mechanism Studies of 1,3-butadiene Selective Oxidation Over Vanadium-Molybdenum-Oxygen Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Schroeder, William David [Iowa State Univ., Ames, IA (United States)

    2001-01-01

    The partial oxidation of 1,3-butadiene has been investigated over VMoO catalysts synthesized by sol-gel techniques. Surface areas were 9-14 m2/g, and compositions were within the solid solution regime, i.e. below 15.0 mol % MoO3/(MoO3 + V2O5). Laser Raman Spectroscopy and XRD data indicated that solid solutions were formed, and pre- and post-reaction XPS data indicated that catalyst surfaces contained some V+4 and were further reduced in 1,3-butadiene oxidation. A reaction pathway for 1,3-butadiene partial oxidation to maleic anhydride was shown to involve intermediates such as 3,4-epoxy-1-butene, crotonaldehyde, furan, and 2-butene-1,4-dial. The addition of water to the reaction stream substantially increased catalyst activity and improved selectivity to crotonaldehyde and furan at specific reaction temperatures. At higher water addition concentrations, furan selectivity increased from 12% to over 25%. The catalytic effects of water addition were related to competitive adsorption with various V2O5-based surface sites, including the vanadyl V=O, corner sharing V-O-V and edge sharing V-O oxygen. Higher levels of water addition were proposed to impose acidic character by dissociative adsorption. In addition, a novel combinatorial synthesis technique for VMoO was used to investigate the phase transitions of V2O5, solid solutions of Mo in V2O5, V9Mo6O40, and other reduced VMoO compounds, characterized by laser Raman spectroscopy. The natural composition gradient imposed by the sputter deposition apparatus was used to create VMoO arrays containing 225 samples ranging from 7.0-42 mol% MoO3/(V2O5 + MoO3), determined by EDS analysis.

  9. Catalytic determination of vanadium in water

    Science.gov (United States)

    Fishman, M. J.; Skougstad, M.W.

    1964-01-01

    A rapid, accurate, and sensitive spectrophotometric method for the quantitative determination of trace amounts of vanadium in water is based on the catalytic effect of vanadium on the rate of oxidation of gallic acid by persulfate in acid solution. Under given conditions of concentrations of reactants, temperature, and reaction time, the extent of oxidation of gallic acid is proportional to the concentration of vanadium present. Vanadium is determined by measuring the absorbance of the sample at 415 m?? and comparison with standard solutions treated in an identical manner. Concentrations in the range of from 0.1 to 8.0 ??g. per liter may be determined with a standard deviation of 0.2 or less. By reducing the reaction time, the method may be extended to cover the range from 1 to 100 ??g. with a standard deviation of 0.8 or less. Several substances interfere, including chloride above 100 p.p.m., and bromide and iodide in much lower concentrations. Interference from the halides is eliminated or minimized by the addition of mercuric nitrate solution. Most other substances do not interfere at the concentration levels at which they commonly occur in natural waters.

  10. Population genomics of Bronze Age Eurasia.

    Science.gov (United States)

    Allentoft, Morten E; Sikora, Martin; Sjögren, Karl-Göran; Rasmussen, Simon; Rasmussen, Morten; Stenderup, Jesper; Damgaard, Peter B; Schroeder, Hannes; Ahlström, Torbjörn; Vinner, Lasse; Malaspinas, Anna-Sapfo; Margaryan, Ashot; Higham, Tom; Chivall, David; Lynnerup, Niels; Harvig, Lise; Baron, Justyna; Della Casa, Philippe; Dąbrowski, Paweł; Duffy, Paul R; Ebel, Alexander V; Epimakhov, Andrey; Frei, Karin; Furmanek, Mirosław; Gralak, Tomasz; Gromov, Andrey; Gronkiewicz, Stanisław; Grupe, Gisela; Hajdu, Tamás; Jarysz, Radosław; Khartanovich, Valeri; Khokhlov, Alexandr; Kiss, Viktória; Kolář, Jan; Kriiska, Aivar; Lasak, Irena; Longhi, Cristina; McGlynn, George; Merkevicius, Algimantas; Merkyte, Inga; Metspalu, Mait; Mkrtchyan, Ruzan; Moiseyev, Vyacheslav; Paja, László; Pálfi, György; Pokutta, Dalia; Pospieszny, Łukasz; Price, T Douglas; Saag, Lehti; Sablin, Mikhail; Shishlina, Natalia; Smrčka, Václav; Soenov, Vasilii I; Szeverényi, Vajk; Tóth, Gusztáv; Trifanova, Synaru V; Varul, Liivi; Vicze, Magdolna; Yepiskoposyan, Levon; Zhitenev, Vladislav; Orlando, Ludovic; Sicheritz-Pontén, Thomas; Brunak, Søren; Nielsen, Rasmus; Kristiansen, Kristian; Willerslev, Eske

    2015-06-11

    The Bronze Age of Eurasia (around 3000-1000 BC) was a period of major cultural changes. However, there is debate about whether these changes resulted from the circulation of ideas or from human migrations, potentially also facilitating the spread of languages and certain phenotypic traits. We investigated this by using new, improved methods to sequence low-coverage genomes from 101 ancient humans from across Eurasia. We show that the Bronze Age was a highly dynamic period involving large-scale population migrations and replacements, responsible for shaping major parts of present-day demographic structure in both Europe and Asia. Our findings are consistent with the hypothesized spread of Indo-European languages during the Early Bronze Age. We also demonstrate that light skin pigmentation in Europeans was already present at high frequency in the Bronze Age, but not lactose tolerance, indicating a more recent onset of positive selection on lactose tolerance than previously thought.

  11. Synthesis and characterization of sodium vanadium oxide gels: the effects of water (n) and sodium (x) content on the electrochemistry of Na(x)V2O5·nH2O.

    Science.gov (United States)

    Lee, Chia-Ying; Marschilok, Amy C; Subramanian, Aditya; Takeuchi, Kenneth J; Takeuchi, Esther S

    2011-10-28

    Sodium vanadium oxide gels, Na(x)V(2)O(5)·nH(2)O, of varying sodium content (0.12 n > 0.01) and interlayer spacing were found to be inversely proportional to the sodium level (x), thus control of sodium (x) content provided a direct, chimie douce approach for control of hydration level (n) and interlayer spacing, without the need for high temperature treatment to affect dehydration. Notably, the use of high temperatures to modify hydration levels can result in crystallization and collapse of the interlayer structure, highlighting the distinct advantage of our novel chimie douce synthesis strategy. Subsequent to synthesis and characterization, results from an electrochemical study of a series of Na(x)V(2)O(5)·nH(2)O samples highlight the significant impact of interlayer water on delivered capacity of the layered materials. Specifically, the sodium vanadium oxide gels with higher sodium content and lower water content provided higher capacities in lithium based cells, where capacity delivered to 2.0 V under C/20 discharge ranged from 170 mAh/g for Na(0.12)V(2)O(5)·0.23H(2)O to 300 mAh/g for Na(0.32)V(2)O(5)·0.01H(2)O. The capacity differences were maintained as the cells were cycled. This journal is © the Owner Societies 2011

  12. Population genomics of Bronze Age Eurasia

    OpenAIRE

    Allentoft Morten E.; Sikora Martin; Sjögren Karl-Göran; Rasmussen Simon; Rasmussen Morten; Stenderup Jesper; Damgaard Peter B.; Schroeder Hannes; Ahlström Torbjörn; Vinner Lasse; Malaspinas Anna-Sapfo; Margaryan Ashot; Higham Tom; Chivall David; Lynnerup Niels

    2015-01-01

    The Bronze Age of Eurasia (around 3000–1000 BC) was a period of major cultural changes. However there is debate about whether these changes resulted from the circulation of ideas or from human migrations potentially also facilitating the spread of languages and certain phenotypic traits. We investigated this by using new improved methods to sequence low coverage genomes from 101 ancient humans from across Eurasia. We show that the Bronze Age was a highly dynamic period involving large scale p...

  13. Glucose-6-Phosphate Dehydrogenase in the Pentose Phosphate Pathway Is Localized in Vanadocytes of the Vanadium-Rich Ascidian, Ascidia sydneiensis samea.

    Science.gov (United States)

    Uyama, T; Yamamoto, K; Kanamori, K; Michibata, H

    1998-08-01

    Ascidians are sessile marine animals known to accumulate high levels of vanadium selectively in vanadium-containing blood cells (vanadocytes). Almost all the vanadium accumulated in the vacuoles of vanadocytes is reduced to the +3 oxidation state via the +4 oxidation state, although vanadium is dissolved in the +5 oxidation state in sea water. Some of the reducing agents that participate in the reduction have been proposed. By chemical study, vanadium in the +5 oxidation state was reported to be reduced to the +4 oxidation state in the presence of NADPH. The present study revealed the existence of glucose-6-phosphodehydrogenase (G6PDH), the first enzyme to produce NADPH in the pentose phosphate pathway, in vanadocytes of a vanadium-rich ascidian. The results suggested that G6PDH conjugates the reduction of vanadium from the +5 through to the +4 oxidation state in vanadocytes of ascidians.

  14. Warm Spraying of High-Strength Ni-Al-Bronze: Cavitation Characteristics and Property Prediction

    Science.gov (United States)

    Krebs, Sebastian; Kuroda, Seiji; Katanoda, Hiroshi; Gaertner, Frank; Klassen, Thomas; Araki, Hiroshi; Frede, Simon

    2017-01-01

    Bronze materials such as Ni-Al-bronze show exceptional performances against cavitation erosion, due to their high fatigue strength and high strength. These materials are used for ship propellers, pump systems or for applications with alternating stresses. Usually, the respective parts are cast. With the aim to use resources more efficiently and to reduce costs, this study aimed to evaluate opportunities to apply bronze as a coating to critical areas of respective parts. The coatings should have least amounts of pores and non-bonded areas and any contaminations that might act as crack nuclei and contribute to material damages. Processes with low oxidation and high kinetic impacts fulfill these criteria. Especially warm spraying, a nitrogen-cooled HVOF process, with similar impact velocities as cold gas spraying but enhanced process temperature, allows for depositing high-strength Ni-Al-bronze. This study systematically simulates and evaluates the formation and performance of warm-sprayed Ni-Al-bronze coatings for different combustion pressures and nitrogen flow rates. Substrate preheating was used to improve coating adhesion for lower spray parameter sets. Furthermore, this study introduces an energy-based concept to compare spray parameter sets and to predict coating properties. Coatings with low porosities and high mechanical strengths are obtained, allowing for a cavitation resistance similar to bulk material.

  15. A coordination chemistry study of hydrated and solvated cationic vanadium ions in oxidation states +III, +IV, and +V in solution and solid state.

    Science.gov (United States)

    Krakowiak, Joanna; Lundberg, Daniel; Persson, Ingmar

    2012-09-17

    The coordination chemistry of hydrated and solvated vanadium(III), oxovanadium(IV), and dioxovanadium(V) ions in the oxygen-donor solvents water, dimethyl sulfoxide (DMSO), and N,N'-dimethylpropyleneurea (DMPU) has been studied in solution by extended X-ray absorption fine structure (EXAFS) and large-angle X-ray scattering (LAXS) and in the solid state by single-crystal X-ray diffraction and EXAFS. The hydrated vanadium(III) ion has a regular octahedral configuration with a mean V-O bond distance of 1.99 Å. In the hydrated and DMSO-solvated oxovanadium(IV) ions, vanadium binds strongly to an oxo group at ca. 1.6 Å. The solvent molecule trans to the oxo group is very weakly bound, at ca. 2.2 Å, while the remaining four solvent molecules, with a mean V-O bond distance of 2.0 Å, form a plane slightly below the vanadium atom; the mean O═V-O(perp) bond angle is ca. 98°. In the DMPU-solvated oxovanadium(IV) ion, the space-demanding properties of the DMPU molecule leave no solvent molecule in the trans position to the oxo group, which reduces the coordination number to 5. The O═V-O bond angle is consequently much larger, 107°, and the mean V═O and V-O bond distances decrease to 1.58 and 1.97 Å, respectively. The hydrated and DMSO-solvated dioxovanadium(V) ions display a very distorted octahedral configuration with the oxo groups in the cis position with a mean V═O bond distance of 1.6 Å and a O═V═O bond angle of ca. 105°. The solvent molecules trans to the oxo groups are weakly bound, at ca. 2.2 Å, while the remaining two have bond distances of 2.02 Å. The experimental studies of the coordination chemistry of hydrated and solvated vanadium(III,IV,V) ions are complemented by summarizing previously reported crystal structures to yield a comprehensive description of the coordination chemistry of vanadium with oxygen-donor ligands.

  16. Controlled synthesis and electrochemical properties of vanadium ...

    Indian Academy of Sciences (India)

    Vanadium oxides (V3O7.H2O and VO2) with different morphologies have been selectively synthesized by a facile hydrothermal approach using glucose as the reducing and structure-directing reagent. The as-obtained V3O7.H2O nanobelts have a length up to several tens of micrometers, width of about 60–150 nm and ...

  17. Bronze-mean hexagonal quasicrystal

    Science.gov (United States)

    Dotera, Tomonari; Bekku, Shinichi; Ziherl, Primož

    2017-10-01

    The most striking feature of conventional quasicrystals is their non-traditional symmetry characterized by icosahedral, dodecagonal, decagonal or octagonal axes. The symmetry and the aperiodicity of these materials stem from an irrational ratio of two or more length scales controlling their structure, the best-known examples being the Penrose and the Ammann-Beenker tiling as two-dimensional models related to the golden and the silver mean, respectively. Surprisingly, no other metallic-mean tilings have been discovered so far. Here we propose a self-similar bronze-mean hexagonal pattern, which may be viewed as a projection of a higher-dimensional periodic lattice with a Koch-like snowflake projection window. We use numerical simulations to demonstrate that a disordered variant of this quasicrystal can be materialized in soft polymeric colloidal particles with a core-shell architecture. Moreover, by varying the geometry of the pattern we generate a continuous sequence of structures, which provide an alternative interpretation of quasicrystalline approximants observed in several metal-silicon alloys.

  18. A bronze amulet from Sidak

    Directory of Open Access Journals (Sweden)

    Smagulov Erbulat A.

    2014-03-01

    Full Text Available A bronze amulet in the shape of a horseman found on the citadel of the Sidak fortified settlement site in Turkestan district, Southern Kazakhstan oblast is described in the article. Similar findings are met on the vast Eurasian area ranging from Mongolia to the Urals. The published item may be referred to a series of similar finds from the handicraft centers located in the Syr Darya river basin, such as Khujand, Kanka, and, lately, Sidak. Handicraft centers of Sogdiana are traditionally regarded as places of their manufacture. However, no finds of the kind are mentioned at proper Sogdian towns (Penjikent, Paikend, Afrasyab, etc., which have been thoroughly studied. Hence, the author makes a conclusion that these amulets, as well as many other pieces of jewelry were manufactured in the 7th to 8th centuries AD at the handicraft centers of Chach, a state formation comprising the Middle Syr-Darya River oases at the time. This region was inhabited by the descendants of the ancient Kangju state inhabitants, who inherited cultural traditions of the past, including the myths about the hero-horseman.

  19. Reductive mineralization of cellulose with vanadium, iron and tungsten chlorides and access to MxOymetal oxides and MxOy/C metal oxide/carbon composites.

    Science.gov (United States)

    Henry, Aurélien; Hesemann, Peter; Alauzun, Johan G; Boury, Bruno

    2017-10-15

    M x O y and M x O y /C composites (M=V, Fe and W) were obtained by mineralization of cellulose with several metal chlorides. Cellulose was used both as a templating agent and as an oxygen and a carbon source. Soluble chloride molecules (VOCl 3 and WCl 6 ) and a poorly soluble ionic chloride compound (FeCl 3 ) were chosen as metal oxide precursors. In a first time, primary metal oxide/cellulose composites were obtained via a thermal treatment by reacting urea impregnated filter paper with the corresponding metal chlorides in an autoclave at 150°C after 3days. After either pyrolysis or calcination steps of these intermediate materials, interesting metal oxides with various morphologies were obtained (V 2 O 5, V 2 O 3 , Fe 3 O 4 , WO 3, H 0.23 WO 3 ), composites (V 2 O 3 /C) as well as carbides (hexagonal W 2 C and WC, Fe 3 C) This result highlight the reductive role that can play cellulose during the pyrolysis step that allows to tune the composition of M x O y /C composites. The materials were characterized by FTIR, Raman, TGA, XRD and SEM. This study highlights that cellulose can be used for a convenient preparation of a variety of highly demanded M x O y and M x O y /C composites with original shapes and morphologies. Copyright © 2017 Elsevier Ltd. All rights reserved.

  20. Oxidative dehydrogenation of n-butane over vanadium magnesium oxide catalysts supported on nano-structured MgO and ZrO2: effect of oxygen capacity of the catalyst.

    Science.gov (United States)

    Lee, Howon; Lee, Jong Kwon; Hong, Ung Gi; Song, In Kyu; Yoo, Yeonshick; Cho, Young-Jin; Lee, Jinsuk; Chang, Hosik; Jung, Ji Chul

    2012-07-01

    Vanadium-magnesium oxide catalysts supported on nano-structured MgO and ZrO2 (Mg3(VO4)2/MgO/ZrO2) were prepared by a wet impregnation method with a variation of Mg:Zr ratio (8:1, 4:1, 2:1, and 1:1). For comparison, Mg3(VO4)2/MgO and Mg3(VO4)2/ZrO2 catalysts were also prepared by a wet impregnation method. The prepared catalysts were applied to the oxidative dehydrogenation of n-butane in a continuous flow fixed-bed reactor. Mg3(VO4)2/MgO/ZrO2 (Mg:Zr = 4:1, 2:1, and 1:1) and Mg3(VO4)2/ZrO2 catalysts showed a stable catalytic activity during the whole reaction time, while Mg3(VO4)2/MgO/ZrO2 (8:1) and Mg3(VO4)2/MgO catalysts experienced a severe catalyst deactivation. Deactivation of Mg3(VO4)2/MgO/ZrO2 (8:1) and Mg3(VO4)2/MgO catalysts was due to their low oxygen mobility. Effect of oxygen capacity (the amount of oxygen in the catalyst involved in the reaction) of the supported Mg3(V04)2 catalysts on the catalytic performance in the oxidative dehydrogenation of n-butane was investigated. Experimental results revealed that oxygen capacity of the catalyst was closely related to the catalytic activity in the oxidative dehydrogenation of n-butane. A large oxygen capacity of the catalyst was favorable for obtaining a high catalytic activity in this reaction. Among the catalysts tested, Mg3(VO4)2/MgO/ZrO2 (4:1) catalyst with the largest oxygen capacity showed the best catalytic performance.

  1. Synthesis of hydrogen tungsten bronzes H{sub x}WO{sub 3} by reactive mechanical milling of hexagonal WO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Castro, Facundo J. [Centro Atomico Bariloche (CNEA, CONICET), Instituto Balseiro (UNCuyo), Av. Bustillo 9500, San Carlos de Bariloche (Argentina); Tonus, Florent; Bobet, Jean-Louis [Institut de Chimie de la Matiere Condensee de Bordeaux (ICMCB), CNRS (UPR 9048), Universite de Bordeaux I, 87 Avenue du Dr. A. Schweitzer, 33608 Pessac Cedex (France); Urretavizcaya, Guillermina, E-mail: urreta@cab.cnea.gov.a [Centro Atomico Bariloche (CNEA, CONICET), Instituto Balseiro (UNCuyo), Av. Bustillo 9500, San Carlos de Bariloche (Argentina)

    2010-04-16

    Recently, we have reported the formation of hydrogen tungsten bronzes by reactive mechanical milling monoclinic tungsten (VI) oxide under hydrogen atmosphere. In this work we report the milling of hexagonal WO{sub 3} under H{sub 2} atmosphere. Our main results are the structural transformation of the hexagonal oxide to the high temperature polymorph of WO{sub 3} with orthorhombic structure, and the formation of different hydrogen tungsten bronzes at distinct milling times. The bronzes seem to be formed from the orthorhombic oxide, and compared with the bronzes obtained by milling monoclinic WO{sub 3} are rather unstable after short exposure to air. The materials are characterized by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and total hydrogen content determination.

  2. Extraction of Vanadium from Stone Coal by Microwave Assisted Sulfation Roasting

    Science.gov (United States)

    Wang, Mingyu; Xian, Pengfei; Wang, Xuewen; Li, Bowen

    2015-02-01

    The extraction of vanadium from stone coal was investigated by microwave-assisted sulfation roasting followed by water leaching. The results showed that this process is an effective method for the extraction of vanadium from stone coal. Microwave-assisted sulfation roasting promotes the reaction of sulfuric acid with vanadium oxides and decreases roasting time. Under optimized conditions (roasting temperature 200°C, heating rate of 10°C/min, 25% sulfuric acid addition, water leaching at 75°C for 1 h, and liquid/solid ratio of 1.5 ml/g), the leaching rate of vanadium reached 92.6%.

  3. Organometalic carbosilane polymers containing vanadium and their preparation

    Science.gov (United States)

    Yajima, S.; Okamura, K.; Shishido, T.; Fukuda, K.

    1983-01-01

    The present invention concerns a new organometallic polymer material containing in part a vanadium-siloxane linkage (V-0-Si), which has excellent resistance to heat and oxidation and a high residue ratio after high temperature treatment in a non-oxidizing atmosphere, for example, nitrogen, argon, helium, ammonia, or hydrogen.

  4. Studies on phase and morphological evolution of silver vanadium oxides as a function of pH: evaluation of electrochemical behavior towards quantification of Pb2+ and Cd2+ ions

    Science.gov (United States)

    Gangaiah, Vijayakumar; Shivappa Adarakatti, Prashanth; Siddaramanna, Ashoka; Malingappa, Pandurangappa; Thimmanna Chandrappa, Gujjarahalli

    2017-08-01

    The effect of pH on morphological and phase evolution of silver vanadium oxide nanostructures are investigated under hydrothermal process. The results of powder x-ray diffraction (PXRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) disclosed that the morphological evolution of nanobelts into nanoring structures occurs at pH in between 4 and 5 with Ag2V4O11 phase and nanobelt morphologies at pH from 6 to 7 with β-AgVO3 phase. The prepared Ag2V4O11 and β-AgVO3 have been evaluated for the simultaneous quantification of Pb2+ and Cd2+ ions in aqueous solution using differential pulse anodic stripping voltammetry. The results reveal that Ag2V4O11 shows better quantification result compared to β-AgVO3.

  5. 77 FR 14600 - Pricing for 2012 Kennedy Half-Dollar Bags and Rolls, Bronze Medals, the First Spouse Bronze Medal...

    Science.gov (United States)

    2012-03-12

    ... United States Mint Pricing for 2012 Kennedy Half-Dollar Bags and Rolls, Bronze Medals, the First Spouse.... SUMMARY: The United States Mint is announcing 2012 pricing for Kennedy Half-Dollar bags and rolls, bronze medals, the First Spouse Bronze Medal Set and the Birth Set. Product Retail price Kennedy Half-Dollar...

  6. Bismuth bronze from machu picchu, peru.

    Science.gov (United States)

    Gordon, R B; Rutledge, J W

    1984-02-10

    The decorative bronze handle of a tumi excavated at the Inca city of Machu Picchu, Peru, contains 18 percent bismuth and appears to be the first known example of the use of bismuth with tin to make bronze. The alloy is not embrittled by the bismuth because the bismuth-rich constituent does not penetrate the grain boundaries of the matrix phase. The use of bismuth facilitates the duplex casting process by which the tumi was made and forms an alloy of unusual color.

  7. An extraction process to recover vanadium from low-grade vanadium-bearing titanomagnetite.

    Science.gov (United States)

    Chen, Desheng; Zhao, Hongxin; Hu, Guoping; Qi, Tao; Yu, Hongdong; Zhang, Guozhi; Wang, Lina; Wang, Weijing

    2015-08-30

    An extraction process to recover vanadium from low-grade vanadium-bearing titanomagnetite was developed. In this study, a mixed solvent system of di(2-ethylhexyl) phosphate (D2EHPA) and tri-n-butyl phosphate (TBP) diluted with kerosene was used for the selective extraction of vanadium from a hydrochloric acid leaching solution that contained low vanadium concentration with high concentrations of iron and impurities of Ca, Mg, and Al. In the extraction process, the initial solution pH and the phase ratio had considerable functions in the extraction of vanadium from the hydrochloric acid leaching solution. Under optimal extraction conditions (i.e., 30-40°C for 10min, 1:3 phase ratio (O/A), 20% D2EHPA concentration (v/v), and 0-0.8 initial solution pH), 99.4% vanadium and only 4.2% iron were extracted by the three-stage counter-current extraction process. In the stripping process with H2SO4 as the stripping agent and under optimal stripping conditions (i.e., 20% H2SO4 concentration, 5:1 phase ratio (O/A), 20min stripping time, and 40°C stripping temperature), 99.6% vanadium and only 5.4% iron were stripped by the three-stage counter-current stripping process. The stripping solution contained 40.16g/LV2O5,0.691g/L Fe, 0.007g/L TiO2, 0.006g/L SiO2 and 0.247g/L CaO. A V2O5 product with a purity of 99.12% V2O5 and only 0.026% Fe was obtained after the oxidation, precipitation, and calcination processes. The total vanadium recovered from the hydrochloric acid leaching solution was 85.5%. Copyright © 2015 Elsevier B.V. All rights reserved.

  8. On the regiospecificity of vanadium bromoperoxidase.

    Science.gov (United States)

    Martinez, J S; Carroll, G L; Tschirret-Guth, R A; Altenhoff, G; Little, R D; Butler, A

    2001-04-11

    Vanadium haloperoxidase enzymes catalyze the oxidation of halide ions by hydrogen peroxide, producing an oxidized intermediate, which can halogenate an organic substrate or react with a second equivalent of hydrogen peroxide to produce dioxygen. Haloperoxidases are thought to be involved in the biogenesis of halogenated natural products isolated from marine organisms, including indoles and terpenes, of which many are selectively oxidized or halogenated. Little has been shown concerning the ability of the marine haloperoxidases to catalyze regioselective reactions. Here we report the regiospecific bromoperoxidative oxidation of 1,3-di-tert-butylindole by V-BrPO from the marine algae Ascophyllum nodosum and Corallina officinalis. Both enzymes catalyze the regiospecific oxidation of 1,3-di-tert-butylindole in a reaction requiring both H(2)O(2) and Br(-) as substrates, but which produce the unbrominated 1,3-di-tert-butyl-2-indolinone product exclusively, in near quantitative yield (i.e. one H(2)O(2) consumed per product). By contrast, reactions with the controlled addition of aqueous bromine solution (HOBr = Br(2) = Br(3)(-)) produce three monobromo and one dibromo-2-indolinone products, all of which differ from the V-BrPO-catalyzed product. Further, reactivities of 1,3-di-tert-butyl-2-indolinone with both aqueous bromine and V-BrPO differ significantly and shed light onto the possible nature of the oxidizing intermediate. This is the first example of a regiospecific bromination by a vanadium haloperoxidase and further extends their usefulness as catalysts.

  9. Population genomics of Bronze Age Eurasia

    DEFF Research Database (Denmark)

    Allentoft, Morten E.; Sikora, Martin; Sjögren, Karl-Göran

    2015-01-01

    investigated this by using new, improved methods to sequence low-coverage genomes from 101 ancient humans from across Eurasia. We show that the Bronze Age was a highly dynamic period involving large-scale population migrations and replacements, responsible for shaping major parts of present-day demographic...

  10. Determination of V(IV) and V(V) by electrothermal atomic absorption spectrometry following selective solid-phase extraction and the study on the change in the oxidation state of vanadium species in seawater during the sample storage.

    Science.gov (United States)

    Nukatsuka, Isoshi; Shimizu, Yutaka; Ohzeki, Kunio

    2002-09-01

    The changes in the oxidation state of vanadium in artificial and natural seawater samples were studied by electrothermal atomic absorption spectrometry (ETAAS) with a direct injection of a resin suspension. V(IV) and V(V) were extracted as the complex with Chromazurol B and with N-cinnamoyl-N-2,3-xylylhydroxylamine, respectively, using a suspension of an anion-exchange resin and determined by ETAAS independently. The detection limits of both methods were 0.02 ng ml(-1) for 40 ml of a sample solution. The recovery tests for an artificial seawater sample spiked with V(IV) and/or V(V) were carried out carefully. The results showed that the recoveries of V(IV) or V(V) were 99.2-109% and the standard deviations were 1-6%. The total V was also determined after V(V) was reduced by ascorbic acid. In artificial seawater at pH 7.8, V(V) was stable but V(IV) was oxidized rapidly. In acidified artificial seawater (pH 2.0), V(IV) was oxidized slowly but only a small tendency of such reduction of V(V) was observed. In a natural seawater sample, V(IV) was not detected. The acidification of the natural seawater sample resulted in the reduction of V(V).

  11. The sodium tungsten bronzes as plasmonic materials: fabrication, calculation and characterization

    Science.gov (United States)

    Tegg, Levi; Cuskelly, Dylan; Keast, Vicki J.

    2017-06-01

    The tungsten bronzes are non-stoichiometric transition metal oxides of the form M x WO3, where 0  ⩽  x  ⩽  1, and M is a dopant ion, most commonly an alkali metal. In this work, the sodium tungsten bronzes (Na x WO3) are investigated as materials for plasmonic applications. The bronzes were fabricated with a solid state reaction, the dielectric function calculated using density functional theory (DFT) and the nanoparticle responses calculated with the boundary element method (BEM). The results were compared to Au and Ag, the materials most widely used in plasmonic applications. It was shown that for x  >  0.5, the solid state fabrication method produces cube-shaped particles of diameter  ⩾1 µm, whose bulk optical properties are well described by a free-electron model and a rigid band structure. The addition of Na into the lattice increases the free electron density, increasing the bulk plasma frequency. Nanoparticle plasmon resonances are found to be highly tunable, and generally at a lower frequency than Au or Ag, and so sodium tungsten bronzes are predicted to be well suited to biomedical or chemical sensing applications.

  12. Structural and catalytic properties of a novel vanadium containing ...

    Indian Academy of Sciences (India)

    Abstract. A novel vanadium containing solid core mesoporous silica shell catalyst was synthesized with different Si/V ratios by sol-gel method under neutral conditions. The synthesized materials were characterized by various techniques and gas phase diphenyl methane oxidation reaction. The mesoporosity combined with ...

  13. Optical properties of zinc–vanadium glasses doped with samarium ...

    Indian Academy of Sciences (India)

    Zinc–vanadium glasses doped with samarium oxide having the chemical composition Sm2O3() ZnO(40-)V2O5(60) (where = 0.1–0.5 mol%) were prepared by melt quenching method. The density of these glasses was measured by Archimedes method; the corresponding molar volumes have also been calculated.

  14. Research and development on vanadium alloys for fusion applications

    Energy Technology Data Exchange (ETDEWEB)

    Zinkle, S.J.; Rowcliffe, A.F. [Oak Ridge National Lab., TN (United States); Matsui, H.; Abe, K. [Tohoku Univ. (Japan); Smith, D.L. [Argonne National Lab., IL (United States); Osch, E. van [NERF, Petten (Netherlands); Kazakov, V.A. [RIAR, Dimitrovgrad (Russian Federation)

    1998-03-01

    The current status of research and development on unirradiated and irradiated V-Cr-Ti alloys intended for fusion reactor structural applications is reviewed, with particular emphasis on the flow and fracture behavior of neutron-irradiated vanadium alloys. Recent progress on fabrication, joining, oxidation behavior, and the development of insulator coatings is also summarized. Fabrication of large (>500 kg) heats of V-4Cr-4Ti with properties similar to previous small laboratory heats has now been demonstrated. Impressive advances in the joining of thick sections of vanadium alloys using GTA and electron beam welds have been achieved in the past two years, although further improvements are still needed.

  15. Growth of Tungsten Bronze Family Crystals

    Science.gov (United States)

    1989-03-01

    Keesrer. Mater Res BuL 15 t]s , 13(5the discussions on this. research b\\ Profesor .f J[19] R R Neurgaonkar W.K Cot.s and J R (Oi,’e- I-errocl. s otncs 35...L" tic . 22 𔃻 als, demonstrated’ the growth of excellent qual;tv bronze !N’BO.0. substrates using thie LPL and sputtering techniques. C.Car. to gt

  16. Uncommon corrosion phenomena of archaeological bronze alloys

    Science.gov (United States)

    Ingo, G. M.; de Caro, T.; Riccucci, C.; Khosroff, S.

    2006-06-01

    In the framework of the EFESTUS project (funded by the European Commission, contract No. ICA3-CT-2002-10030) the corrosion products of a large number of archaeological bronze artefacts are investigated by means of the combined use of scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD) and optical microscopy (OM) and tentative correlation of their nature with the chemical composition of the artefacts and the burial context is proposed. The results provide good insight into the corrosion layers and evidence in some bronze Roman coins and artefacts; the occurrence of uncommon corrosion phenomena that give rise to the formation of a yellowish-green complex chlorine-phosphate of lead (pyromorphite, (PbCl)Pb4(PO4)3) and of a gold-like thick layer of an iron and copper sulphide (chalcopyrite, CuFeS2). The micro-chemical and micro-structural results show that the coins were buried in a soil enriched in phosphorus for the accidental presence of a large amount of decomposing fragments of bones or in an anaerobic and humus rich soil where the chalcopyrite layer has been produced via the interaction between the iron of the soil, the copper of the coin and the sulphur produced by the decomposition of organic matter in an almost oxygen free environment. Finally, some unusual periodic corrosion phenomena occurring in high tin bronze mirrors found at Zama (Tunisia) are described.

  17. Vanadium-modified molecular sieves: preparation, characterization and catalysis

    Directory of Open Access Journals (Sweden)

    Ângela A. Teixeira-Neto

    2009-01-01

    Full Text Available Vanadium-containing molecular sieves are redox catalysts and are good candidates as substitutes for oxide-supported V2O5 in a number of reactions. These materials have the advantage of presenting better dispersion of vanadium species, as well as shape-selective properties and controllable acidities. They may be prepared by one-pot synthesis or by post-synthesis methods and a number of techniques such as diffuse reflectance UV-visible spectroscopy, 51V nuclear magnetic resonance and electron paramagnetic resonance, to name but a few, have been used to characterize these materials. In this review, methods of preparation of vanadium-modified molecular sieves, their characterization and applications in catalysis are discussed.

  18. The determination of vanadium in brines by atomic absorption spectroscopy

    Science.gov (United States)

    Crump-Wiesner, Hans J.; Feltz, H.R.; Purdy, W.C.

    1971-01-01

    A standard addition method is described for the determination of vanadium in brines by atomic absorption spectroscopy with a nitrous oxide-acetylene flame. Sample pH is adjusted to 1.0 with concentrated hydrochloric acid and the vanadium is directly extracted with 5% cupferron in methyl isobutyl ketone (MIBK). The ketone layer is then aspirated into the flame and the recorded absorption values are plotted as a function of the concentration of the added metal. As little as 2.5 ??g l-1 of vanadium can be detected under the conditions of the procedure. Tungsten and tin interfere when present in excess of 5 and 10 ??g ml-1, respectively. The concentrations of the two interfering ions normally found in brines are well below interference levels. ?? 1971.

  19. Analysis and measurement of the electrolyte imbalance in a vanadium redox flow battery

    Science.gov (United States)

    Ngamsai, Kittima; Arpornwichanop, Amornchai

    2015-05-01

    Electrolyte imbalance in vanadium redox flow batteries is an important problem for its long-term operation as it leads to loss of energy. To address this problem, a modified open circuit voltage (OCV) cell is developed by adding a middle half cell between the negative and positive half cells of a conventional OCV cell and used to predict the oxidation state of vanadium in the electrolyte solution from the measured voltage in each side of the electrolyte (positive and negative). The correlation between the oxidation state of vanadium and cell voltage is explained by a basic electrochemical principle and the Nernst equation. The experimental results show that at different oxidation states of vanadium, the predicted OCV agrees reasonably with the experimental data. In addition, the effect of the state of charge (SOC) and electrolyte imbalance on the energy capacity of a cell is discussed.

  20. The role of vanadium in the chemical defense of the solitary tunicate, Phallusia nigra.

    Science.gov (United States)

    Odate, Shobu; Pawlik, Joseph R

    2007-03-01

    Ascidians (sea squirts) may defend themselves from predators, biofouling competitors, and bacterial infection by producing secondary metabolites or sequestering acid, but many species also accumulate heavy metals, most notably vanadium. The defensive functions of heavy metals in ascidians remain unclear, and to this end, the solitary Caribbean tunicate, Phallusia nigra, was studied to localize vanadium in its tissues and to assess the defensive properties of vanadium-containing compounds. As determined by flame atomic absorption spectroscopy, the internal tissues and blood contained the highest vanadium concentrations (mean values of 2280 and 1886 ppm dry mass, respectively), followed by the tunic surface (871 ppm dry mass). Results of laboratory feeding assays with the bluehead wrasse, Thalassoma bifasciatum, confirmed outcomes of past studies that demonstrated that vanadyl sulfate (VOSO4.6H20) and sodium vanadate (Na3VO4) were unpalatable to fish, although these salts do not accurately reflect the chelation environment or oxidation state of vanadium in living tunicates. Fresh preparations of whole tunic, internal tissues, and blood were unpalatable to fish, but freezing and thawing of internal tissues and blood rendered them palatable. Crude organic extracts of whole tunic and internal tissues contained vanadium metabolites (225 and 750 ppm dry mass, respectively) and were palatable to T. bifasciatum; crude extracts also exhibited no antimicrobial effects against a panel of four marine bacteria known to be pathogens of marine invertebrates (Vibrio parahaemolyticus, Vibrio harveyi, Leucothrix mucor, and Deleya marina). Nonacidic vanadium (+3) complexes neither deterred predation nor inhibited microbial growth, whereas acidic aqua vanadium (+3 and +4) complexes were unpalatable to 7 bifasciatum and exhibited antimicrobial activity. Difficulties in decoupling low pH from oxidation state and chelation environment of vanadium prevent definitive conclusions about the

  1. Impedance spectroscopy study and phase transition in phospho-vanadium mixed oxide LiZnV0.5P0.5O4

    Science.gov (United States)

    Rahal, A.; Megdiche Borchani, S.; Guidara, Kamel; Megdiche, Makram

    2017-08-01

    An X-ray crystallographic study has allowed us to identify a powder of the type LiZnV0.5P0.5O4, which contains 50% of vanadium and 50% of phosphore, inside the binary system LiZnVO4-LiZnPO4. The structure is isotypic with the phenacite like LiZnP04. X-ray diffraction patterns are indexed according to the lattice parameters of the rhombohedral system and the R3 space group. IR spectra show the presence of VO4 and PO4 groups in the network of this material. The experimental results indicate that σ_{AC}(ω) is proportional to ( {ωn } ). The activation energy found from the Arrhenius plot confirms that the conduction processing of the material is not due to simple hopping mechanism. The temperature dependence of frequency exponent n was investigated to understanding the conduction mechanism in LiZnV0.5P0.5O4. The non-overlapping small Polaron tunneling (NSPT) model can explain the temperature dependence of the frequency exponent. A phase transition at T = 623 K has been evidenced by Differential scanning calorimetry (DSC) and subsequently confirmed by the analysis of dielectric and electric properties.

  2. Nano crystalline Bi{sub 2}(VO{sub 5}) phases in lithium bismuth borate glasses containing mixed vanadium-nickel oxides

    Energy Technology Data Exchange (ETDEWEB)

    Yadav, Arti, E-mail: artidabhur@gmail.com; Khasa, S.; Dahiya, M. S. [Department of Physics, Deenbandhu Chhotu Ram University of Science and Technology, Murthal, India-131039 (India); Agarwal, A. [Department of Applied Physics, G. J. University of Science and Technology, Hisar, India-125001 (India)

    2016-05-23

    Glass composition 7V{sub 2}O{sub 5}·23Li{sub 2}O·20Bi{sub 2}O{sub 3}·50B{sub 2}O{sub 3} and x(2NiO·V{sub 2}O{sub 5})·(30-x)Li{sub 2}O·20Bi{sub 2}O{sub 3}·50B{sub 2}O{sub 3}, x=0, 2, 5, 7 and 10, were produced by conventional melt quenching technique. The quenched amorphous glass samples were annealed at temperatures 400°C and 500°C for 6 hours. The Bi{sub 2}(VO{sub 5}) crystallite were grown in all prepared glass matrix. Tn vanadium lithium bismuth borate glass (annealed), the some phrase of V{sub 2}O{sub 5}-crystal were observed along with the nano crystalline Bi{sub 2}(VO{sub 5}) phase. The sharp peaks in FTTR spectra of all annealed compositions were also compatible with the XRD diffraction peaks of the system under investigation. Average crystalline size (D) of the Bi{sub 2}(VO{sub 5}) nano-crystallite was ~30 nm for samples annealed at 400°C and ~42 nm for samples annealed at 500°C. Lattice parameter and the lattice strain for all the samples was also calculated corresponding to the (113) plane of Bi{sub 2}(VO{sub 5}) crystallite.

  3. Determination of Vanadium Binding Mode on Seawater-Contacted Polyamidoxime Adsorbents

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Zhicheng [Lawrence Berkeley National Laboratory (LBNL); Rao, Linfeng [Lawrence Berkeley National Laboratory (LBNL); Abney, Carter W. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Bryantsev, Vyacheslav [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Ivanov, Aleksandr [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2017-09-01

    Adsorbents developed for the recovery of uranium from seawater display poor selectivity over other transition metals present in the ocean, with vanadium particularly problematic. To improve selectivity, an indispensable step is the positive identification of metal binding environments following actual seawater deployment. In this work we apply x-ray absorption fine structure (XAFS) spectroscopy to directly investigate the vanadium binding environment on seawater-deployed polyamidoxime adsorbents. Comparison of the x-ray absorption near edge spectra (XANES) reveal marked similarities to recently a reported non-oxido vanadium (V) structure formed upon binding with cyclic imidedioxime, a byproduct of generating amidoxime functionalities. Density functional theory (DFT) calculations provided a series of putative vanadium binding environments for both vanadium (IV) and vanadium (V) oxidation states, and with both amidoxime and cyclic imidedioxime. Fits of the extended XAFS (EXAFS) data confirmed vanadium (V) is bound exclusively by the cyclic imidedioxime moiety in a 1:2 metal:ligand fashion, though a modest structural distortion is also observed compared to crystal structure data and computationally optimized geometries which is attributed to morphology effects from the polymer graft chain and the absence of crystal packing interactions. These results demonstrate that improved selectivity for uranium over vanadium can be achieved by suppressing the formation of cyclic imidedioxime during preparation of polyamidoxime adsorbents for seawater uranium recovery.

  4. Examination of Ife Bronze Casting Culture and Its Decline in ...

    African Journals Online (AJOL)

    Ile-Ife, the Yoruba ancient city is known for its vibrant cultural environment. This city of ancient civilization and one of the home for bronze casting in the Western region of Nigeria have made significant contributions to the world of culture through its great artistic traditions in terracotta, bead making, bronze and brass casting ...

  5. The thermal analysis and derivative bronzes cast to plaster moulds

    Directory of Open Access Journals (Sweden)

    B. Pisarek

    2009-07-01

    Full Text Available It plaster moulds gets casted the alloys of following metals: Al, Cu, Ag, Au in precise and artistic founding. The investigation of the crys-tallization of bronzes in hot plaster moulds the method of the thermal analysis and derivative (TDA was not realized out so far. Probe TDAg and tripod enabling the execution of measurements on inductive casting machine INDUTHERM-VC 500D were designed for this technology especially. It was confirmed that one the method TDA can identify the crystallization process of the bronze in hot plaster moulds. The investigations of the superficial distribution of the concentration of elements in the microstructure of the studied grades of the bronze on X-ray microanalizer were conducted. It results that they be subject to in bronze CuSn10-C (B10 and the CuSn5Zn5Pb5-C (B555 of strong microsegregation from conducted investigations: Pb, Sn and Sb. The single separates of intermetallic phase κ was identified in the bronze B10 rich first of all in Zn, Sn, Sb and Fe, and two intermetallic phase, one rich were identified in the bronze B555 first of all in Zn, Sb, (Nor, Fe and second rich in Sn, Sb, (Nor, Fe. The most homogeneous microstructure from the bronze CuAl10Fe5Ni5-C (BA1055 is characterizes among the studied grades of the bronze in the cast state.

  6. Vanadium As a Potential Membrane Material for Carbon Capture: Effects of Minor Flue Gas Species.

    Science.gov (United States)

    Yuan, Mengyao; Liguori, Simona; Lee, Kyoungjin; Van Campen, Douglas G; Toney, Michael F; Wilcox, Jennifer

    2017-10-03

    Vanadium and its surface oxides were studied as a potential nitrogen-selective membrane material for indirect carbon capture from coal or natural gas power plants. The effects of minor flue gas components (SO 2 , NO, NO 2 , H 2 O, and O 2 ) on vanadium at 500-600 °C were investigated by thermochemical exposure in combination with X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and in situ X-ray diffraction (XRD). The results showed that SO 2 , NO, and NO 2 are unlikely to have adsorbed on the surface vanadium oxides at 600 °C after exposure for up to 10 h, although NO and NO 2 may have exhibited oxidizing effects (e.g., exposure to 250 ppmv NO/N 2 resulted in an 2.4 times increase in surface V 2 O 5 compared to exposure to just N 2 ). We hypothesize that decomposition of surface vanadium oxides and diffusion of surface oxygen into the metal bulk are both important mechanisms affecting the composition and morphology of the vanadium membrane. The results and hypothesis suggest that the carbon capture performance of the vanadium membrane can potentially be strengthened by material and process improvements such as alloying, operating temperature reduction, and flue gas treatment.

  7. Thermal and Electrical Conductivity Measurements of CDA 510 Phosphor Bronze

    Science.gov (United States)

    Tuttle, James E.; Canavan, Edgar; DiPirro, Michael

    2009-01-01

    Many cryogenic systems use electrical cables containing phosphor bronze wire. While phosphor bronze's electrical and thermal conductivity values have been published, there is significant variation among different phosphor bronze formulations. The James Webb Space Telescope (JWST) will use several phosphor bronze wire harnesses containing a specific formulation (CDA 510, annealed temper). The heat conducted into the JWST instrument stage is dominated by these harnesses, and approximately half of the harness conductance is due to the phosphor bronze wires. Since the JWST radiators are expected to just keep the instruments at their operating temperature with limited cooling margin, it is important to know the thermal conductivity of the actual alloy being used. We describe an experiment which measured the electrical and thermal conductivity of this material between 4 and 295 Kelvin.

  8. Brain Metal Distribution and Neuro-Inflammatory Profiles after Chronic Vanadium Administration and Withdrawal in Mice

    OpenAIRE

    Folarin, Oluwabusayo R.; Snyder, Amanda M.; Peters, Douglas G.; Funmilayo Olopade; Connor, James R.; Olopade, James O

    2017-01-01

    Vanadium is a potentially toxic environmental pollutant and induces oxidative damage in biological systems including the central nervous system (CNS). Its deposition in brain tissue may be involved in the pathogenesis of certain neurological disorders which after prolonged exposure can culminate into more severe pathology. Most studies on vanadium neurotoxicity have been done after acute exposure but in reality some populations are exposed for a lifetime. This work was designed to ascertain n...

  9. Noise Spectroscopy in Strongly Correlated Oxides

    Science.gov (United States)

    Alsaqqa, Ali M.

    Strongly correlated materials are an interesting class of materials, thanks to the novel electronic and magnetic phenomena they exhibit as a result of the interplay of various degrees of freedom. This gives rise to an array of potential applications, from Mott-FET to magnetic storage. Many experimental probes have been used to study phase transitions in strongly correlated oxides. Among these, resistance noise spectroscopy, together with conventional transport measurements, provides a unique viewpoint to understand the microscopic dynamics near the phase transitions in these oxides. In this thesis, utilizing noise spectroscopy and transport measurements, four different strongly correlated materials were studied: (1) neodymium nickel oxide (NdNiO 3) ultrathin films, (2) vanadium dioxide (VO2) microribbons, (3) copper vanadium bronze (CuxV2O 5) microribbons and (4) niobium triselenide (NbSe3) microribbons. Ultra thin films of rare-earth nickelates exhibit several temperature-driven phase transitions. In this thesis, we studied the metal-insulator and Neel transitions in a series of NdNiO3 films with different lattice mismatches. Upon colling down, the metal-insulator phase transition is accompanied by a structural (orthorohombic to monoclinic) and magnetic (paramagnetic to antiferromagnetic) transitions as well, making the problem more interesting and complex at the same time. The noise is of the 1/f type and is Gaussian in the high temperature phase, however deviations are seen in the low temperature phases. Below the metal-insulator transition, noise magnitude increases by orders of magnitude: a sign of inhomogeneous electrical conduction as result of phase separation. This is further assured by the non-Gaussian noise signature. At very low temperatures (T noise behavior switches between Gaussian and non-Gaussian over several hours, possibly arising from dynamically competing ground states. VO2 is one of the most widely studied strongly correlated oxides and is

  10. Characterisation of artificial patinas on bronze sculptures of the Carlo Bilotti Museum (Rome)

    Science.gov (United States)

    Casanova Municchia, A.; Bellatreccia, F.; D'Ercoli, G.; Lo Mastro, S.; Reho, I.; Ricci, M. A.; Sodo, A.

    2016-12-01

    Two bronze sculptures, Ettore e Andromaca, a reproduction of a plaster model by Giorgio de Chirico, and Cardinale, a cast made from an original by Giacomo Manzù, stand outside the Carlo Bilotti contemporary art museum in Villa Borghese park (Rome). The composition of the artificial brown patina present on the statues' surface, which was applied for aesthetic purposes, is unknown. This paper reports analysis carried out to identify the composition of the artificial patina and describe the corrosion products formed in outdoor conditions. Raman spectroscopy and scanning electron microscopy equipped with X-ray microanalysis were performed on sample fragments and powder scrapings taken from the bronze statues. X-ray powder diffraction was used whenever possible and subject to conservation priorities. Our data revealed, in the artificial brown patina, the formation of copper oxides (cuprite and tenorite) on the surface of both sculptures as possible result of oxidisation treatments performed with a blowtorch before the artificial patination process began. Furthermore, a copper nitrate (gerhardtite) was identified as an ingredient in the preparation applied to the bronze surfaces. The green areas revealed the presence of corrosion products as copper sulphate hydroxide (brochantite) and copper sulphate-chloride (connellite), which form under acid rains conditions.

  11. Analysis of the Quintilii’s Villa Bronzes by Spectroscopy Techniques

    Directory of Open Access Journals (Sweden)

    Fabio Stranges

    2014-01-01

    Full Text Available The aim of this work is the characterization, with different diagnostic tests, of three fragments of bronze artefacts recovered from the Villa of the Quintilii (located in the south of Rome. In particular, the sample alloys were investigated by different chemical and morphological analysis. Firstly, an analysis of the alloy, implemented through the electronic spectroscopy, was taken to discriminate the bronze morphology and its elemental composition. Subsequently, a surface analysis was realized by molecular spectroscopy to identify the alteration patinas on surfaces (such as bronze disease. Two diagnostic techniques are used for the alloy analysis: scanning electron microscopy (SEM connected to the EDX spectroscopy (to study the morphology and alloy composition and Auger electron spectroscopy (AES (to identify the oxidation state of each element. Moreover, for the study of surface patinas, IR and Raman spectroscopies were implemented. All studies were performed on the “as received” samples, covered by a thin layer of excavated soil and on samples processed in an aqueous solution of sulphuric acid (10%, to remove patinas and alterations.

  12. Selective extraction of vanadium from the APV-precipitated waste water

    Science.gov (United States)

    Li, Cui; Li, Hong-Yi; Tu, Chun-Bin; Zhang, Tao; Fang, Hai-Xing; Xie, Bing

    In the process of precipitating ammonium polyvanadate (APV) to produce vanadium pentoxide in Pan-steel in China, rest waste water usually contains about 24 333mg/L V(V), 2 100g/L Cr(VI),20 500mg/L Si(IV) and 20 100g/L Na2SO4. In order to recover valuable and also toxic metal ions contained in the waste water, effective extraction method of using anion exchange resin was realized to extract Vanadium selectively, leading to effective separation between vanadium and chromium. To ensure vanadium was absorbed by the resin, V(V) and Cr(VI) were reduced to V(IV) and Cr(III) by NaHSO3, respectively, and then V(IV) was oxidized by H2O2 to V(V) anions. Effects of temperature, solution pH, concentration of ions and absorbing time on vanadium absorption rate were investigated. Chromium was precipitated from rest solution while vanadium was eluted from resin by NaOH solution and then precipitated. Results showed that vanadium recovery of 73% could be obtained in optimized condition. The resin could be regenerated by 3% hydrochloric acid, which indicated the recyclability of the resin and thus low cost of this established method.

  13. Corrosion investigation of fire-gilded bronze involving high surface resolution spectroscopic imaging

    Energy Technology Data Exchange (ETDEWEB)

    Masi, G., E-mail: giulia.masi5@unibo.it [Dipartimento di Ingegneria Civile, Chimica, Ambientale e dei Materiali, Università di Bologna, via Terracini 28, 40131 Bologna (Italy); Chiavari, C., E-mail: cristina.chiavari@unibo.it [Dipartimento di Ingegneria Civile, Chimica, Ambientale e dei Materiali, Università di Bologna, via Terracini 28, 40131 Bologna (Italy); C.I.R.I. (Centro Interdipartimentale Ricerca Industriale) Meccanica Avanzata e Materiali, Università di Bologna, Bologna, via Terracini 28, 40131 Bologna (Italy); Avila, J., E-mail: jose.avila@synchrotron-soleil.fr [Synchrotron SOLEIL, L’Orme des Merisiers, 91190 Saint-Aubin (France); Esvan, J., E-mail: jerome.esvan@ensiacet.fr [Centre Interuniversitaire de Recherche et d’Ingénierie des Matériaux, Université de Toulouse, 4 allée Emile Monso, 31030 Toulouse (France); Raffo, S., E-mail: simona.raffo2@unibo.it [Dipartimento di Chimica Industriale “Toso Montanari”, Università di Bologna, viale Risorgimento 4, 40136 Bologna (Italy); Bignozzi, M.C., E-mail: maria.bignozzi@unibo.it [Dipartimento di Ingegneria Civile, Chimica, Ambientale e dei Materiali, Università di Bologna, via Terracini 28, 40131 Bologna (Italy); Asensio, M.C., E-mail: maria-carmen.asensio@synchrotron-soleil.fr [Synchrotron SOLEIL, L’Orme des Merisiers, 91190 Saint-Aubin (France); Robbiola, L., E-mail: robbiola@univ-tlse2.fr [TRACES Lab (CNRS UMR5608), Université Toulouse Jean-Jaurès, 5, allées Antonio-Machado, 31058 Toulouse (France); and others

    2016-03-15

    Graphical abstract: - Highlights: • Fire-gilded bronze prepared by ancient methods (Au–Hg layer on Cu–Sn–Zn–Pb–Sb). • Heating during gilding induces Sn and Znenrichment in the top part of the gilded layer. • SR-HRPES mapping of corrosion craters (cross-section) after accelerated ageing. • Selective dissolution of Cu and Zn in the craters induces Sn species enrichment. • The main species in the craters are related to hydroxi-oxide compounds. - Abstract: Gilded bronzes are often affected by severe corrosion, due to defects in the Au layer and Au/Cu alloy galvanic coupling, stimulated by large cathodic area of the gilded layer. Galvanic corrosion, triggered by gilding defects, leads to products growth at the Au/bronze interface, inducing blistering or break-up of the Au layer. In this context, fire-gilded bronze replicas prepared by ancient methods (use of spreadable Au–Hg paste) was specifically characterised by compiling complementary spectroscopic and imaging information before/after accelerated ageing with synthetic rain. Fire-gilded bronze samples were chemically imaged in cross-section at nano-metric scale (<200 nm) using high energy and lateral resolution synchrotron radiation photoemission (HR-SRPES) of core levels and valence band after conventional characterisation of the samples by Glow Discharge optical Emission Spectroscopy (GD-OES) and conventional X-ray photoelectron spectroscopy (XPS). We have found a net surface enrichment in Zn and Sn after fire-gilding and presence of metallic Hg, Pb and Cu within the Au layer. Moreover, the composition distribution of the elements together with their oxidation has been determined. It was also revealed that metallic phases including Hg and Pb remain in the gilding after corrosion. Moreover, selective dissolution of Zn and Cu occurs in the crater due to galvanic coupling, which locally induces relative Sn species enrichment (decuprification). The feasibility advantages and disadvantages of

  14. Exploring the chemistry and biology of vanadium-dependent haloperoxidases.

    Science.gov (United States)

    Winter, Jaclyn M; Moore, Bradley S

    2009-07-10

    Nature has developed an exquisite array of methods to introduce halogen atoms into organic compounds. Most of these enzymes are oxidative and require either hydrogen peroxide or molecular oxygen as a cosubstrate to generate a reactive halogen atom for catalysis. Vanadium-dependent haloperoxidases contain a vanadate prosthetic group and utilize hydrogen peroxide to oxidize a halide ion into a reactive electrophilic intermediate. These metalloenzymes have a large distribution in nature, where they are present in macroalgae, fungi, and bacteria, but have been exclusively characterized in eukaryotes. In this minireview, we highlight the chemistry and biology of vanadium-dependent haloperoxidases from fungi and marine algae and the emergence of new bacterial members that extend the biological function of these poorly understood halogenating enzymes.

  15. Exploring the Chemistry and Biology of Vanadium-dependent Haloperoxidases*

    Science.gov (United States)

    Winter, Jaclyn M.; Moore, Bradley S.

    2009-01-01

    Nature has developed an exquisite array of methods to introduce halogen atoms into organic compounds. Most of these enzymes are oxidative and require either hydrogen peroxide or molecular oxygen as a cosubstrate to generate a reactive halogen atom for catalysis. Vanadium-dependent haloperoxidases contain a vanadate prosthetic group and utilize hydrogen peroxide to oxidize a halide ion into a reactive electrophilic intermediate. These metalloenzymes have a large distribution in nature, where they are present in macroalgae, fungi, and bacteria, but have been exclusively characterized in eukaryotes. In this minireview, we highlight the chemistry and biology of vanadium-dependent haloperoxidases from fungi and marine algae and the emergence of new bacterial members that extend the biological function of these poorly understood halogenating enzymes. PMID:19363038

  16. Improvement on Performance of Mg-C Refractories as Lining of Vanadium-Extraction Converters

    Science.gov (United States)

    Huang, Weijun; Xu, Lei; Zhang, Shuai; Chen, Min

    For the purpose of extending the service life of MgO-C bricks used as linings of vanadium-extraction converters, the effect of Fe addition on properties of MgO-C bricks was investigated. The results showed the addition of Fe could effectively improve the sinterability of the oxidized layer of the MgO-C refractory at 1400°C due to the effect of FeO (formed by oxidation of Fe) on formation of MgO-FeOss and modification of the microstructure, and excellent corrosion resistance against vanadium containing slag was also obtained due to the increase of compactness of the oxidized layer and concentration of FeO in the oxidized layer. Consequently, it is considered that MgO-C brick by introducing the new phase of Fe is a favorable substitute of MgO-C refractory to be used as linings of vanadium-extraction converters.

  17. The Cooling Ability Study on CO2 and O2 Mixed Injection in Vanadium Extraction Process

    Science.gov (United States)

    Li, Pengcheng; Wang, Yu; Du, Wei-Tong; Wen, Gang

    Carbon dioxide could be utilized as a weak oxidant and a kind of coolant to oxidize elements, meanwhile, helping control the temperature during the converter vanadium extraction process. However, the optimum content of CO2 and the cooling effect of CO2 at low content have not been reported. In this study, experimental research based on the influence of different CO2 contents from 0% to 25% injected to the vanadium-containing hot metal was carried out, as well as contrast experiments of O2-N2 mixed blowing. The results indicated that the optimum content of CO2 was 15%. Under the optimum condition, the oxidation of [C] was the lowest and the oxidation rate of [V] was 96.9%, while the temperature was also lower than the O2-N2 mixed blowing. This paper provide a potential property for utilizing CO2 during the converter vanadium extraction process.

  18. Conductive transition metal oxide nanostructured electrochromic material and optical switching devices constructed thereof

    Science.gov (United States)

    Mattox, Tracy M.; Koo, Bonil; Garcia, Guillermo; Milliron, Delia J.; Trizio, Luca De; Dahlman, Clayton

    2017-10-10

    An electrochromic device includes a nanostructured transition metal oxide bronze layer that includes one or more transition metal oxide and one or more dopant, a solid state electrolyte, and a counter electrode. The nanostructured transition metal oxide bronze selectively modulates transmittance of near-infrared (NIR) spectrum and visible spectrum radiation as a function of an applied voltage to the device.

  19. Optical properties of zinc–vanadium glasses doped with samarium ...

    Indian Academy of Sciences (India)

    Abstract. Zinc–vanadium glasses doped with samarium oxide having the chemical composition Sm2O3(x). ZnO(40−x)V2O5(60)(where x = 0·1–0·5 mol%) were prepared by melt quenching method. The density of these glasses was measured by Archimedes method; the corresponding molar volumes have also been ...

  20. Russian meteorite Bronze Age (rock record)

    CERN Document Server

    Vodolazhskaya, Larisa

    2013-01-01

    This paper presents the results of a study of petroglyphs found in the quartzite grotto near the Skelnovsky small village in the Northern Black Sea in the South of Russia. The aim of the study was the analysis and interpretation of the Early Bronze Age petroglyphs using archaeoastronomical methods. The article presents a comparative analysis of Skelnovsky grotto ancient images and contemporary eyewitness accounts of the Sikhote-Alin meteorite fall and meteorite shower. Some petroglyphs were interpreted by us using ethnographic and folklore material. In this study, the magnetic declination for the geographical coordinates Skelnovsky farm was calculated, and the projection of the whole picture Skelnovskih petroglyphs on the topographical map of the area was built. The proposed location of the meteorite fall was determined with this projection. It is confirmed by satellite pictures, on which are the distinguishable terrain features, typical for the meteorite fall, are visible including the possible impact crater...

  1. Bronze Age stone worlds of Bodmin Moor: excavating Leskernick

    Directory of Open Access Journals (Sweden)

    Sue Hamilton

    1999-11-01

    Full Text Available Most archaeological work on the British Bronze Age has been undertaken in Wessex. Here a team fr om UCL' s Institute of Archaeology and Department of Anthropology describe their investigation of a very different Bronze Age landscape on Bodmin Moor in Cornwall. Their project, at the site of Leskernick, is innovative in its methodology and in how it is presented to the public.

  2. Deformability of niobium and tin bronze during compression

    Science.gov (United States)

    Nikulin, S. A.; Rozhnov, A. B.; Aliev, R. M.; Rogachev, S. O.; Khatkevich, V. M.; Abdyukhanov, I. M.; Dergunova, E. A.; Traktirnikova, N. V.

    2015-10-01

    The deformability of Cu-14.5 wt % Sn-0.25 wt % Ti bronze and pure niobium (99.84%) is studied during compression tests. It is found that an increase in the strain rate or a decrease in the test temperature can improve the strength characteristics of both materials. The strength properties of bronze are more sensitive to a change in the temperature-rate deformation conditions.

  3. Characterization of vanadium flow battery

    Energy Technology Data Exchange (ETDEWEB)

    Bindner, H.; Ekman, C.; Gehrke, O.; Isleifsson, F.

    2010-10-15

    This report summarizes the work done at Risoe DTU testing a vanadium flow battery as part of the project 'Characterisation of Vanadium Batteries' (ForskEl project 6555) with the partners PA Energy A/S and OI Electric A/S under the Danish PSO energy research program. A 15kW/120kWh vanadium battery has been installed as part of the distributed energy systems experimental facility, SYSLAB, at Risoe DTU. A test programme has been carried out to get hands-on experience with the technology, to characterize the battery from a power system point of view and to assess it with respect to integration of wind energy in the Danish power system. The battery has been in operation for 18 months. During time of operation the battery has not shown signs of degradation of performance. It has a round-trip efficiency at full load of approximately 60% (depending on temperature and SOC). The sources of the losses are power conversion in cell stacks/electrolyte, power converter, and auxiliary power consumption from pumps and controller. The response time for the battery is limited at 20kW/s by the ramp rate of the power converter. The battery can thus provide power and frequency support for the power system. Vanadium battery is a potential technology for storage based services to the power system provided investment and O and M cost are low enough and long term operation is documented. (Author)

  4. Chemical speciation of vanadium in particulate matter emitted from diesel vehicles and urban atmospheric aerosols.

    Science.gov (United States)

    Shafer, Martin M; Toner, Brandy M; Overdier, Joel T; Schauer, James J; Fakra, Sirine C; Hu, Shaohua; Herner, Jorn D; Ayala, Alberto

    2012-01-03

    We report on the development and application of an integrated set of analytical tools that enable accurate measurement of total, extractable, and, importantly, the oxidation state of vanadium in sub-milligram masses of environmental aerosols and solids. Through rigorous control of blanks, application of magnetic-sector-ICPMS, and miniaturization of the extraction/separation methods we have substantially improved upon published quantification limits. The study focused on the application of these methods to particulate matter (PM) emissions from diesel vehicles, both in baseline configuration without after-treatment and also equipped with advanced PM and NO(x) emission controls. Particle size-resolved vanadium speciation data were obtained from dynamometer samples containing total vanadium pools of only 0.2-2 ng and provide some of the first measurements of the oxidation state of vanadium in diesel vehicle PM emissions. The emission rates and the measured fraction of V(V) in PM from diesel engines running without exhaust after-treatment were both low (2-3 ng/mile and 13-16%, respectively). The V(IV) species was measured as the dominant vanadium species in diesel PM emissions. A significantly greater fraction of V(V) (76%) was measured in PM from the engine fitted with a prototype vanadium-based selective catalytic reductors (V-SCR) retrofit. The emission rate of V(V) determined for the V-SCR equipped vehicle (103 ng/mile) was 40-fold greater than that from the baseline vehicle. A clear contrast between the PM size-distributions of V(V) and V(IV) emissions was apparent, with the V(V) distribution characterized by a major single mode in the ultrafine (vanadium-containing fine-particle PM from the V-SCR identified V(2)O(5) as the dominant vanadium species.

  5. Brain Metal Distribution and Neuro-Inflammatory Profiles after Chronic Vanadium Administration and Withdrawal in Mice

    Directory of Open Access Journals (Sweden)

    Oluwabusayo R. Folarin

    2017-07-01

    Full Text Available Vanadium is a potentially toxic environmental pollutant and induces oxidative damage in biological systems including the central nervous system (CNS. Its deposition in brain tissue may be involved in the pathogenesis of certain neurological disorders which after prolonged exposure can culminate into more severe pathology. Most studies on vanadium neurotoxicity have been done after acute exposure but in reality some populations are exposed for a lifetime. This work was designed to ascertain neurodegenerative consequences of chronic vanadium administration and to investigate the progressive changes in the brain after withdrawal from vanadium treatment. A total of 85 male BALB/c mice were used for the experiment and divided into three major groups of vanadium treated (intraperitoneally (i.p. injected with 3 mg/kg body weight of sodium metavanadate and sacrificed every 3 months till 18 months; matched controls; and animals that were exposed to vanadium for 3 months and thereafter the metal was withdrawn. Brain tissues were obtained after animal sacrifice. Sagittal cut sections of paraffin embedded tissue (5 μm were analyzed by the Laser ablation-inductively coupled plasma-mass spectrometry (LA–ICP–MS to show the absorption and distribution of vanadium metal. Also, Haematoxylin and Eosin (H&E staining of brain sections, and immunohistochemistry for Microglia (Iba-1, Astrocytes (GFAP, Neurons (Neu-N and Neu-N + 4′,6-diamidine-2′-pheynylindole dihydrochloride (Dapi Immunofluorescent labeling were observed for morphological and morphometric parameters. The LA–ICP–MS results showed progressive increase in vanadium uptake with time in different brain regions with prediction for regions like the olfactory bulb, brain stem and cerebellum. The withdrawal brains still show presence of vanadium metal in the brain slightly more than the controls. There were morphological alterations (of the layering profile, nuclear shrinkage in the prefrontal

  6. Electrochromic device containing metal oxide nanoparticles and ultraviolet blocking material

    Energy Technology Data Exchange (ETDEWEB)

    Garcia, Guillermo; Koo, Bonil; Gregoratto, Ivano; Basu, Sourav; Rosen, Evelyn; Holt, Jason; Thomsen, Scott

    2017-10-17

    An electrochromic device includes a nanostructured transition metal oxide bronze layer that includes one or more transition metal oxide and one or more dopant. The electrochromic device also includes nanoparticles containing one or more transparent conducting oxide (TCO), a solid state electrolyte, a counter electrode, and at least one protective layer to prevent degradation of the one or more nanostructured transition metal oxide bronze. The nanostructured transition metal oxide bronze selectively modulates transmittance of near-infrared (NIR) and visible radiation as a function of an applied voltage to the device.

  7. Metal-insulator and charge ordering transitions in oxide nanostructures

    Science.gov (United States)

    Singh, Sujay Kumar

    Strongly correlated oxides are a class of materials wherein interplay of various degrees of freedom results in novel electronic and magnetic phenomena. Vanadium oxides are widely studied correlated materials that exhibit metal-insulator transitions (MIT) in a wide temperature range from 70 K to 380 K. In this Thesis, results from electrical transport measurements on vanadium dioxide (VO2) and vanadium oxide bronze (MxV 2O5) (where M: alkali, alkaline earth, and transition metal cations) are presented and discussed. Although the MIT in VO2 has been studied for more than 50 years, the microscopic origin of the transition is still debated since a slew of external parameters such as light, voltage, and strain are found to significantly alter the transition. Furthermore, recent works on electrically driven switching in VO2 have shown that the role of Joule heating to be a major cause as opposed to electric field. We explore the mechanisms behind the electrically driven switching in single crystalline nanobeams of VO2 through DC and AC transport measurements. The harmonic analysis of the AC measurement data shows that non-uniform Joule heating causes electronic inhomogeneities to develop within the nanobeam and is responsible for driving the transition in VO2. Surprisingly, field assisted emission mechanisms such as Poole-Frenkel effect is found to be absent and the role of percolation is also identified in the electrically driven transition. This Thesis also provides a new insight into the mechanisms behind the electrolyte gating induced resistance modulation and the suppression of MIT in VO2. We show that the metallic phase of VO2 induced by electrolyte gating is due to an electrochemical process and can be both reversible and irreversible under different conditions. The kinetics of the redox processes increase with temperature; a complete suppression of the transition and the stabilization of the metallic phase are achievable by gating in the rutile metallic phase

  8. [The vanadium compounds: chemistry, synthesis, insulinomimetic properties].

    Science.gov (United States)

    Fedorova, E V; Buriakina, A V; Vorob'eva, N M; Baranova, N I

    2014-01-01

    The review considers the biological role of vanadium, its participation in various processes in humans and other mammals, and the anti-diabetic effect of its compounds. Vanadium salts have persistent hypoglycemic and antihyperlipidemic effects and reduce the probability of secondary complications in animals with experimental diabetes. The review contains a detailed description of all major synthesized vanadium complexes having antidiabetic activity. Currently, vanadium complexes with organic ligands are more effective and safer than the inorganic salts. Despite the proven efficacy of these compounds as the anti-diabetic agents in animal models, only one organic complex of vanadium is currently under the second phase of clinical trials. All of the considered data suggest that vanadium compound are a new promising class of drugs in modern pharmacotherapy of diabetes.

  9. Study of sulfur and vanadium in heavy petroleum products

    Energy Technology Data Exchange (ETDEWEB)

    Novelli, J.M.

    1982-10-01

    Sulfur compounds in heavy oil fractions (>450/sup 0/C) are studied in the first part of this work. After chemical oxidation by metachloroperbenzoic acid to obtain sulfones, sulfur compounds are analyzed by infrared spectroscopy for their qualitative and quantitative repartition. The method can be applied for the study of sulfur containing molecules before and after structural modifications of petroleum fractions by any chemical refining processes. In a second part vanadium is characterized in asphalt by physicochemical and chemical methods. 80% of the vanadium in a Boscan asphalt is under the form of porphyrins. Different associations are evidenced in petroleum fractions and metalloporphyrins, but the liaison between the vanadyl group and heterocondensate from asphalts is the more frequent.

  10. Is vanadium a more versatile target in the activity of primordial life forms than hitherto anticipated?

    Science.gov (United States)

    Rehder, Dieter

    2008-03-21

    The two predominant forms of vanadium occurring in the geo-, aqua- and biosphere, soluble vanadate(V) and insoluble oxovanadium(IV) (vanadyl), are subject to bacterial activity and transformation. Bacteria belonging to genera such as Shewanella, Pseudomonas and Geobacter can use vanadate as a primary electron acceptor in dissimilation or respiration, an important issue in the context of biomineralisation and soil detoxification. Azotobacter, which can employ vanadium as an essential element in nitrogen fixation, secretes a vanadophore which enables the uptake of vanadium(V). Siderophores secreted by other bacteria competitively (to ferric iron) take up vanadyl and thus interfere with iron supply, resulting in bacteriostasis. The halo-alkaliphilic Thioalkalivibrio nitratireducens possibly uses vanadium as a constituent of an alternative, molybdopterin-free nitrate reductase. Marine macro-algae can generate a variety of halogenated organic compounds by use of vanadate-dependent haloperoxidases, and a molecular vanadium compound, amavadin, from Amanita mushrooms has turned out to be an efficient catalyst in oxidation reactions. The present account is a focused and critical review of the current knowledge of the interplay of bacteria and other primitive forms of life (cyanobacteria, algae, fungi and lichens) with vanadium, with the aim to provide perspectives for applications and further investigations.

  11. Effects of a vanadium post-metallocene catalyst-induced polymer backbone inhomogeneity on UV oxidative degradation of the resulting polyethylene film

    KAUST Repository

    Atiqullah, M.

    2012-07-01

    A Group 5 post-metallocene precatalyst, (ONO)VCl(THF) 2 (ONO = a bis(phenolate)pyridine LX 2 pincer ligand), activated with modified methylaluminoxane (MMAO-3A) produced a linear ethylene homopolymer (nm-HomoPE)and an unusual inhomogeneous copolymer (nm-CopolyPE) with 1-hexene having very low backbone unsaturation. The nm-CopolyPE inhomogeneity was reflected in the distributions of short chain branches, 1-hexene composition, and methylene sequence length. The 1-hexene incorporation into the polyethylene backbone strongly depended on the molecular weight of the growing polymer chain. (ONO)VCl(THF) 2, because of site diversity and easier removal of a tertiary (vs. a secondary) hydrogen, produced a skewed short chain branching (SCB) profile, incorporating 1-hexene more efficiently in the low molecular weight region than in the high molecular weight region. The significant decrease in molecular weight by 1-hexene showed that the (ONO)VCl(THF) 2 catalytic sites were also highly responsive to chain-transfer directly to 1-hexene itself, producing vinyl and trans-vinylene termini. Subsequently, the effect of backbone inhomogeneity on the UV oxidative degradation of films made from both polyethylenes was investigated. The major functional group accumulated in the branched nm-CopolyPE film was carbonyl followed by carboxyl, then vinyl/ester, whereas that in the linear nm-HomoPE film was carboxyl. However, (carbonyl, carboxyl, vinyl, and ester) nm-CopolyPE film >> (carboxyl) nm-HomoPE film). The distributions of the tertiary C-H sites and methylene sequence length in the branched nm-CopolyPE film enhanced abstraction of H, decomposition of hydroperoxide group ROOH, and generation of carbonyl compounds as compared with those in the linear nm-HomoPE film. This clearly establishes the role played by the backbone inhomogeneity. The effect of short chain branches and sequence length distributions on peak melting temperature T pm, and most probably lamellar thickness L o, was

  12. Characterization of Vanadium Flow Battery

    DEFF Research Database (Denmark)

    Bindner, Henrik W.; Krog Ekman, Claus; Gehrke, Oliver

    This report summarizes the work done at Risø-DTU testing a vanadium flow battery as part of the project “Characterisation of Vanadium Batteries” (ForskEl project 6555) with the partners PA Energy A/S and OI Electric A/S under the Danish PSO energy research program. A 15kW/120kWh vanadium battery...... has been installed as part of the distributed energy systems experimental facility, SYSLAB, at Risø DTU. A test programme has been carried out to get hands-on experience with the technology, to characterize the battery from a power system point of view and to assess it with respect to integration...... of wind energy in the Danish power system. The battery has been in operation for 18 months. During time of operation the battery has not shown signs of degradation of performance. It has a round-trip efficiency at full load of approximately 60% (depending on temperature and SOC). The sources of the losses...

  13. Setup of Galvanic Sensors for the Monitoring of Gilded Bronzes

    Directory of Open Access Journals (Sweden)

    Sara Goidanich

    2014-04-01

    Full Text Available Traditional electrochemical techniques, such as linear polarization resistance (Rp, and electrochemical impedance spectroscopy (EIS, cannot be applied to gilded bronzes, as it may not be possible to interpret the results obtained due to the bimetallic nature of the studied material. The measurement of the macrocouple current generated by the gold/bronze galvanic couple can be used as an indicator of degradation processes. Nevertheless, this measurement cannot be performed directly on the original artifacts due to the systematic presence of short-circuits between the two metals. In the present work the use of galvanic sensors is proposed as a possible solution for the monitoring of gilded bronze artefacts. The sensors have been designed to simulate real gilded bronze surfaces in terms of composition and stratigraphy and have proved to be a reliable diagnostic tool for the in situ monitoring of the rates of deterioration of gilded bronze surfaces and to test new conservation treatments. Their set-up and application is reported and their performances discussed.

  14. Solvothermal synthesis of vanadium phosphates in the form of xerogels, aerogels and mesostructures

    Energy Technology Data Exchange (ETDEWEB)

    Sydorchuk, V.; Zazhigalov, V. [Institute of Sorption and Endoecology, National Academy of Sciences of Ukraine, 13 General Naumov Str., Kyiv 03164 (Ukraine); Khalameida, S., E-mail: svkhal@ukr.net [Institute of Sorption and Endoecology, National Academy of Sciences of Ukraine, 13 General Naumov Str., Kyiv 03164 (Ukraine); Diyuk, E. [Institute of Sorption and Endoecology, National Academy of Sciences of Ukraine, 13 General Naumov Str., Kyiv 03164 (Ukraine); Skubiszewska-Zieba, J.; Leboda, R. [Faculty of Chemistry, Maria Curie-Sklodowska University, Maria Curie-Sklodowska Sq. 3, 20-031 Lublin (Poland); Kuznetsova, L. [Institute of Sorption and Endoecology, National Academy of Sciences of Ukraine, 13 General Naumov Str., Kyiv 03164 (Ukraine)

    2010-09-15

    Regularities and peculiarities of physicochemical changes, first of all phase transformations, during solvothermal treatment (with conventional and microwave heating) of the vanadium pentoxide and orthophosphoric acid mixture in organic solvents in the presence of reducing agents have been studied. Hemihydrate of vanadium hydrophosphate - the precursor of vanadium pyrophosphate, the active phase for n-butane to maleic anhydride oxidation, and ion exchanger with variable physicochemical characteristics, i.e. crystal structure, specific surface area, crystallite size and acidic properties - has been synthesized in the temperature range 170-200 {sup o}C. The obtained phases were examined using XRD, DTA-TG, SEM, FTIR spectroscopy, nitrogen adsorption as well as gas chromatographic determination of acidity through organic bases adsorption. The catalytic activity of prepared samples for n-butane oxidation has been investigated.

  15. Adsorption of Vanadium (V) from SCR Catalyst Leaching Solution and Application in Methyl Orange.

    Science.gov (United States)

    Sha, Xuelong; Ma, Wei; Meng, Fanqing; Wang, Ren; Fuping, Tian; Wei, Linsen

    2016-12-01

      In this study, we explored an effective and low-cost catalyst and its adsorption capacity and catalytic capacity for Methyl Orange Fenton oxidation degradation were investigated. The catalyst was directly prepared by reuse of magnetic iron oxide (Fe3O4) after saturated adsorption of vanadium (V) from waste SCR (Selective Catalytic Reduction) catalyst. The obtained catalyst was characterized by FTIR, XPS and the results showed that vanadium (V) adsorption process of Fe3O4 nanoparticles was non-redox reaction. The effects of pH, adsorption kinetics and equilibrium isotherms of adsorption were assessed. Adsorption of vanadium (V) ions by Fe3O4 nanoparticles could be well described by the Sips isotherm model which controlled by the mixed surface reaction and diffusion (MSRDC) adsorption kinetic model. The results show that vanadium (V) was mainly adsorbed on external surface of the Fe3O4 nanoparticles. The separation-recovering tungsten (VI) and vanadium (V) from waste SCR catalyst alkaline solution through pH adjustment was also investigated in this study. The results obtained from the experiments indicated that tungsten (VI) was selectively adsorbed from vanadium (V)/tungsten (VI) mixed solution in certain acidic condition by Fe3O4 nanoparticle to realize their recovery. Tungsten (V) with some impurity can be obtained by releasing from adsorbent, which can be confirmed by ICP-AES. The Methyl Orange degradation catalytic performance illustrated that the catalyst could improve Fenton reaction effectively at pH = 3.0 compare to Fe3O4 nanoparticles alone. Therefore, Fe3O4 nanoparticle adsorbed vanadium (V) has a potential to be employed as a heterogeneous Fenton-like catalyst in the present contribution, and its catalytic activity was mainly evaluated in terms of the decoloration efficiency of Methyl Orange.

  16. Leaching characteristics of vanadium in mine tailings and soils near a vanadium titanomagnetite mining site.

    Science.gov (United States)

    Yang, Jinyan; Tang, Ya; Yang, Kai; Rouff, Ashaki A; Elzinga, Evert J; Huang, Jen-How

    2014-01-15

    A series of column leaching experiments were performed to understand the leaching behaviour and the potential environmental risk of vanadium in a Panzhihua soil and vanadium titanomagnetite mine tailings. Results from sequential extraction experiments indicated that the mobility of vanadium in both the soil and the mine tailings was low, with vanadium readily mobilised. Column experiments revealed that only vanadium in the soil and mine tailing was leachable. The vanadium concentrations in the soil leachates did not vary considerably, but decreased with the leachate volume in the mine tailing leachates. This suggests that there was a smaller pool of leachable vanadium in the mine tailings compared to that in the soil. Drought and rewetting increased the vanadium concentrations in the soil and mine tailing leachates from 20μgL(-1) to 50-90μgL(-1), indicating the potential for high vanadium release following periods of drought. Experiments with soil columns overlain with 4, 8 and 20% volume mine tailings/volume soil exhibited very similar vanadium leaching behaviour. These results suggest that the transport of vanadium to the subsurface is controlled primarily by the leaching processes occurring in soils. Copyright © 2013 Elsevier B.V. All rights reserved.

  17. Effect of Heat Treatment on Microstructural Changes in Aluminium Bronze

    Directory of Open Access Journals (Sweden)

    Hájek J.

    2016-09-01

    Full Text Available This paper attempts to summarise the microstructural changes which take place in aluminium bronzes during heat treatment. Another objective of this study was to map the potential of a certain type of aluminium bronzes for undergoing martensitic transformation. The methods, which were chosen for assessing the results of heat treatment with regard to their availability, included measurement of hardness and observation of microstructure using light and scanning electron microscopy, Additional tools for evaluation of microstructure comprised measurement of microhardness and chemical analysis by EDS. An important part of the experiment is observation of microstructural changes in the Jominy bar during the end-quench test. Upon completing experiments of this kind, one can define the heat treatment conditions necessary for obtaining optimum properties. In addition, the paper presents important findings on how to improve the corrosion resistance of aluminium bronzes by special heat treatment sequences.

  18. Fabrication of a Bronze Age Sword using Ancient Techniques

    Science.gov (United States)

    Sapiro, David; Webler, Bryan

    2016-12-01

    A khopesh was cast and forged for the TMS 2016 Bladesmithing Symposium. The khopesh was the first sword style, originating during the Bronze Age in the Near East. The manufacturing process used in this study closely followed Bronze Age techniques to determine the plausibility of open mold casting coupled with cold work and annealing cycles. Forging and annealing cycles substantially increased blade strength and diminished intergranular δ-phase inclusions. While a functional blade was not completed due to casting defects, the process gives valuable insight into the effort required to fabricate a khopesh during the Bronze Age. Forging and annealing cycles following casting were necessary to produce the mechanical properties desired in a sword.

  19. Functional and morphological olfactory bulb modifications in mice after vanadium inhalation.

    Science.gov (United States)

    Colín-Barenque, Laura; Pedraza-Chaverri, Jose; Medina-Campos, Omar; Jimenez-Martínez, Ruben; Bizarro-Nevares, Patricia; González-Villalva, Adriana; Rojas-Lemus, Marcela; Fortoul, Teresa I

    2015-02-01

    Neurodegenerative disorders, such as Parkinson's and Alzheimer's diseases, have olfaction impairment. These pathologies have also been linked to environmental pollutants. Vanadium is a pollutant, and its toxic mechanisms are related to the production of oxidative stress. In this study, we evaluated the effects of inhaled vanadium on olfaction, the olfactory bulb antioxidant, through histological and ultrastructural changes in granule cells. Mice in control group were made to inhale saline; the experimental group inhaled 0.02-M vanadium pentoxide (V2O5) for 1 hr twice a week for 4 weeks. Animals were sacrificed at 1, 2, 3, and 4 weeks after inhalation. Olfactory function was evaluated by the odorant test. The activity of glutathione peroxidase (GPx) and glutathione reductase (GR) was assayed in olfactory bulbs and processed for rapid Golgi method and ultrastructural analysis. Results show that olfactory function decreased at 4-week vanadium exposure; granule cells showed a decrease in dendritic spine density and increased lipofuscin, Golgi apparatus vacuolation, apoptosis, and necrosis. The activity of GPx and GR in the olfactory bulb was increased compared to that of the controls. Our results demonstrate that vanadium inhalation disturbs olfaction, histology, and the ultrastructure of the granule cells that might be associated with oxidative stress, a risk factor in neurodegenerative diseases. © 2014 by The Author(s).

  20. Protection against vanadium-induced testicular toxicity by testosterone propionate in rats.

    Science.gov (United States)

    Chandra, Amar K; Ghosh, Rituparna; Chatterjee, Aparajita; Sarkar, Mahitosh

    2010-07-01

    Vanadium is a well recognized industrial hazard known to adversely affect male reproductive functions. The intricate mechanistic aspects of this metal and the role of oxidative stress in the deterioration of testicular functions are investigated in the current study. The experiment also focused on the effects of testosterone propionate in testicular and sperm functions in the rat intoxicated with vanadate. Vanadium exposure resulted in a more prominent spermatogenic arrest and consistently abolished the conversion of round to mature spermatids along with decreased epididymal sperm number and increased percentage of abnormal sperm. This is followed by a precipitous decline in the level of serum testosterone and gonadotropins and consequently the testicular steroidogenic and antioxidant enzymes were inhibited. Vanadium induces degeneration in the genital organs of rats and exhibits high indices of lipid oxidative damage. In response to exogenous testosterone propionate (TP) administration, spermatogonial cell populations remained suppressed, while the spermatogenesis was restored quantitatively. In contrast, the hormone treatment had no effect on the dramatically decreased serum FSH level after vanadate treatment. Moreover, TP could ameliorate the toxicity, as indicated by decreased testicular lipid peroxidation with marginal but significant increase in the activities of all the measured enzymes following vanadate-treatment. Taken together all these studies establish that vanadium is a testicular toxicant that perturbs the male reproductive system adversely. However, hormone replacement therapy by testosterone propionate may provide partial protection. The results suggest the feasibility of using endocrine regimens to impede deleterious effects of vanadium on the male reproductive system.

  1. Vanadium and iron complexes for catalytic oxidation

    NARCIS (Netherlands)

    Ligtenbarg, Alette Gerda Jeannet

    2001-01-01

    anadium werd in 1802 in Mexico ontdekt door Andres Manuel del Rio als bestanddeel van een mineraal. Een Frans chemicus was echter van mening dat het hier ging om onzuiver chroom, en de ontdekking werd daarom weer ingetrokken. Het element werd herontdekt in 1831 door de Zweedse chemicus Nils Gabriel

  2. Archaeological investigations of the Bronze Age village of Bagnara di Romagna (RA

    Directory of Open Access Journals (Sweden)

    Maurizio Cattani

    2014-12-01

    Full Text Available This paper summarizes the results of researches carried out in the area next to the modern village of Bagnara di Romagna (RA, where several evidences related to a Bronze Age settlement have been collected. Recently test trenches and surface collections allowed to retrieve bronze and ceramics dating from the Middle Bronze Age (phase BM2 to the Recent Bronze Age (phase BR2. The analysis of landscape and the palaeoenvironmental reconstruction complete the outline of the region of Imola, Faenza and Lugo during the Bronze Age where are well known the ancient settlements of Solarolo, via Ordiere, Monte Castellaccio end S. Giuliano di Toscanella.

  3. Fast imaging of laser induced plasma emission of vanadium dioxide (VO2) target

    CSIR Research Space (South Africa)

    Masina, BN

    2013-10-01

    Full Text Available The main objective of this study is to fully optimise the synthesis of vanadium oxide nanostructures using pulsed laser deposition. We will attempt to realise this by studying the mechanism of the plasma formation and expansion during the pulsed...

  4. Particle size and kind of mica in synthesis of nontoxic bronze and gold pearlescent pigments based on nanoencapsulated hematite

    Directory of Open Access Journals (Sweden)

    Maryam Hosseini-Zori

    2015-12-01

    Full Text Available Nano-encapsulated iron oxide in Zirconium oxide-coated mica pigments are thermally stable,innocuous to human health, non-combustible, and they do not conduct electricity. They could beapplied in several industries such as thermoplastics, cosmetics, food packaging, children toys, paints,automobiles coating, security purposes, and banknotes. Nowadays, they are highly desirable inceramic decoration. In the present study, intensively dark gold to bronze colored mica clay pigments,which were based on mica flakes covered with a layer of nano-iron oxide-Zirconium oxide particles,were prepared by homogeneous precipitation of iron nitrate and Zirconium chloride ammonia in thepresence of mica flakes in two kinds of ore clay-based phlogopite and muscovite minerals. The finalcolor was obtained by thermal annealing of precipitates at a temperature of 800◦C. The pigments werecharacterized by X-Ray Diffraction, Particle size analysis, Scanning electron microscopy,Transmission electron microscopy, X-Ray fluorescence, and Simultaneous thermal analysis. Resultsindicate that nano-encapsulated iron oxide in zirconia particles have been formed on mica flakes andkinds of clay-mica can be related to obtained shade from dark gold to bronze pearl. Higher particlesize of mica flakes about phlogopite type of mica introduced pearl effects with higher L* changes indifferent angles. Muscovite performed higher hue and better pearl effect than phlogopite.

  5. Community Geothermal Technology Program: Silica bronze project. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Bianchini, H.

    1989-10-01

    Objective was to incorporate waste silica from the HGP-A geothermal well in Pohoiki with other refractory materials for investment casting of bronze sculpture. The best composition for casting is about 50% silica, 25% red cinders, and 25% brick dust; remaining ingredient is a binder, such as plaster and water.

  6. Alarm calls of Bronze Mannikins communicate predator size to ...

    African Journals Online (AJOL)

    These groups were exposed to latex terrestrial snakes and mounted aerial raptors, and their alarm calls and predator response behaviours recorded. The Bronze Mannikins were able to discriminate between predators of different sizes, and increased their calling rate and decreased the end frequency of the alarm call in ...

  7. Aromatic quinoxaline as corrosion inhibitor for bronze in aqueous ...

    Indian Academy of Sciences (India)

    Administrator

    Keywords. Bronze; inhibitors; quinoxalin compounds; chloride solution; electrochemical studies. 1. Introduction. Heterocyclic organic compounds containing nitrogen, sulphur or oxygen atoms are often used to protect copper and copper alloy metals from corrosion. Among them, azoles compounds like triazoles, imidazoles ...

  8. Corrosion behavior of leaded-bronze alloys in sea water

    Energy Technology Data Exchange (ETDEWEB)

    Zohdy, K.M., E-mail: khalzohdy@yahoo.com [Higher Technological Institute, 10" t" h of Ramadan City (Egypt); Sadawy, M.M. [Mining and Petroleum Engineering Department, Al-Azhar University, Nasr City, Cairo 11371 (Egypt); Ghanem, M. [Industrial Education, Suez University (Egypt)

    2014-10-15

    The corrosion behavior of leaded-bronze alloys (Cu–5Sn–5Zn–5Pb, Cu–8Sn–8Zn–8Pb and Cu–10Sn–10Zn–10Pb) in sea water was investigated using weight loss method, open-circuit potential measurements (OCP), polarization techniques and electrochemical impedance spectroscopy (EIS). The nature and morphology of the corrosion products were investigated by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The results showed that the corrosion resistance decreases with decreasing copper content. The XRD indicated that the composition of patina depends on the concentration of Cu, Sn, Zn and Pb in each alloy. - Highlights: • The corrosion potential of leaded bronze shifts to more noble potential. • The corrosion resistance increases with increasing amount of copper content in leaded bronze alloys. • The patina formed on Cu–5Sn–5Zn–5Pb is more uniform and protective than other alloys. • The composition of patina formed on leaded bronze depends on the concentration of Cu, Sn, Zn and Pb in the alloy.

  9. Foraging behaviour in tadpoles of the bronze frog Rana temporalis ...

    Indian Academy of Sciences (India)

    The ability of bronze frog Rana temporalis tadpoles (pure or mixed parental lines) to assess the profitability of food habitats and distribute themselves accordingly was tested experimentally using a rectangular choice tank with a non-continuous input design. Food (boiled spinach) was placed at two opposite ends of the ...

  10. Electrodeposited nanocrystalline bronze alloys as replacement for Ni

    NARCIS (Netherlands)

    Hovestad, A.; Tacken, R.A.; Mannetje, H.H.'t

    2008-01-01

    Nanocrystalline white-bronze, CuSn, electroplating was investigated as alternative to Ni plating as undercoat for noble metals in jewellery applications. A strongly acidic plating bath was developed with an organic additive to suppress hydrogen evolution and obtain bright coatings. Polarization

  11. Tribological study of a bronze obtained by Sintering proceeds ...

    African Journals Online (AJOL)

    ... of the lubricant, the atmosphere, and finally the time. In this work we present the effect of speed and load on the tribological characteristics of a Cu 8% Sn bronze pressure sintered self-lubricating mode for two lubricants with different viscosities. Keywords: sintering; powder metallurgy; tribology; lubrication; copper alloy.

  12. Interaction of vanadium and phosphorus in chicks.

    Science.gov (United States)

    Hill, C H

    1994-12-01

    Studies were carried out to determine the effect of dietary vanadium on chicks fed phosphorus deficient and control diets. Vanadium at 50 mg/kg of diet decreased growth of both control and deficient chicks. The high mortality among the phosphorus deficient chicks was significantly alleviated by the presence of vanadium. The increased relative ventricular weights found among the deficient chicks was also alleviated by the presence of dietary vanadium. Vanadium fed at 10 or 20 mg/kg diet did not reduce growth rate but significantly reduced mortality among chicks fed the deficient diet and decreased the relative ventricle weights. Time course studies revealed that chicks are hatched with high relative ventricular weights (.83% of body wt) and remain at that level among chicks fed the phosphorus deficient diet. The addition of vanadium or phosphate to the diet resulted in a progressive decrease in relative ventricular weights. The inclusion of vanadium in the diet resulted in increased serum phosphorus levels among the deficient chicks that may be related to the decrease in mortality and relative ventricle weights.

  13. Enhancing the Electronic Conductivity of Vanadium-tellurite Glasses by Tuning the Redox State

    DEFF Research Database (Denmark)

    Kjeldsen, Jonas; Yue, Yuanzheng

    Transition metal oxides are used in a variety of electronic purposes, e.g., vanadium tellurite as cathode material in high-power demanding batteries. By tuning the redox state of vanadium, it is possible to achieve a lower internal resistance within the entire battery unit, thus a higher capacity....... In this work we vary the redox state of a given vanadium tellurite system by performing post heat-treatment in controlled atmosphere. This process is in theory not limited only to varying electronic conductivity, but also varying the glass structure, and hence, changing properties of the glasses, e.g, thermal...... and mechanical properties. Finally we give insight into the relation between the redox state and electronic conductivity....

  14. Fascinating and challenging role of tungstate promoted vanadium phosphate towards solvent free esterification of oleic acid.

    Science.gov (United States)

    Behera, Gobinda Chandra; Parida, K M

    2012-01-28

    A novel solid acid catalyst has been extensively used for the esterification reaction. Herein, tungstate promoted vanadium phosphate material is fabricated from its precursor, VOHPO(4)·0.5H(2)O and its catalytic activities and structure are investigated in detail. This kind of catalyst is, for the first time, applied for the effective production of biodiesel from fatty acids. Although vanadium phosphate has been extensively used in gas phase oxidation reactions, it has not drawn much attention for its application in liquid phase reactions. Our recent results indicate that vanadium phosphate is an effective, minimally polluting and re-usable catalyst that is highly suited to the production of biodiesel from fatty acids. This work extends the possibility of using VPO in other liquid phase reactions.

  15. The influence of calcium, magnesium, phosphorus and silica on vanadium precipitation in acidic sulfate solutions

    Directory of Open Access Journals (Sweden)

    A. H. Martins

    2000-06-01

    Full Text Available The experimental research work was carried out in accordance with the Factorial Design Statistical Method to evaluate and analyze the influence of calcium, magnesium, silica and phosphorus on the precipitation of vanadates. Precipitation was performed by neutralization with H2SO4 of alkaline aqueous solutions containing vanadium pentoxide (V2O5 at 60± 2ºC. The experimental responses measured were percent of vanadium recovery and vanadium pentoxide content in the precipitate. These impurities are considered representative of those present in a leach liquor from the ore obtained at Campo Alegre de Lourdes (Brazil. The operational variables in this work were used under optimum conditions as determined by the statistical approach. Among the impurities under study, phosphorus exhibited the highest negative influence on the experimental responses. Phosphorus diminished the percent of vanadium recovered from 98.9 to 34.5 and the vanadium oxide content in the precipitate from 91.2 % to 39.3 %.

  16. Can Vanadium Be Substituted into LiFePO[subscript 4]?

    Energy Technology Data Exchange (ETDEWEB)

    Omenya, Fredrick; Chernova, Natasha A.; Upreti, Shailesh; Zavalij, Peter Y.; Nam, Kyung-Wan; Yang, Xiao-Qing; Whittingham, M. Stanley (Binghamton); (BNL); (Maryland)

    2015-10-15

    Vanadium is shown to substitute for iron in the olivine LiFePO{sub 4} up to at least 10 mol %, when the synthesis is carried out at 550 C. In the solid solution LiFe{sub 1-3y/2}V{sub y}PO{sub 4}, the a and b lattice parameters and cell volume decrease with increasing vanadium content, while the c lattice parameter increases slightly. However, when the synthesis is performed at 650 C, a NASICON phase, Li{sub 3}V{sub 2}(PO{sub 4}){sub 3}, is also formed, showing that solid solution is a function of the synthesis temperature. X-ray absorption near-edge structure indicates vanadium is in the 3+ oxidation state and in an octahedral environment. Magnetic studies reveal a shift of the antiferromagnetic ordering transition toward lower temperatures with increasing vanadium substitution, confirming solid solution formation. The addition of vanadium enhances the electrochemical performance of the materials especially at high current densities.

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

    NARCIS (Netherlands)

    Wever, R.; van der Horst, M.A.

    2013-01-01

    Vanadium haloperoxidases differ strongly from heme peroxidases in substrate specificity and stability and in contrast to a heme group they contain the bare metal oxide vanadate as a prosthetic group. These enzymes specifically oxidize halides in the presence of hydrogen peroxide into hypohalous

  18. Portable XRF on Prehistoric Bronze Artefacts: Limitations and Use for the Detection of Bronze Age Metal Workshops

    DEFF Research Database (Denmark)

    Nørgaard, Heide Wrobel

    2017-01-01

    Two different scientific analyses—one destructive and one non destructive—were conducted on two separate groups of bronze ornaments dating from 1500–1100 BC to investigate, amongst other traits, the metal composition of their copper-tin alloys. One group of artefacts was sampled, and polished thi...

  19. Development of analytical techniques of vanadium isotope in seawater

    Science.gov (United States)

    Huang, T.; Owens, J. D.; Sarafian, A.; Sen, I. S.; Huang, K. F.; Blusztajn, J.; Nielsen, S.

    2015-12-01

    Vanadium (V) is a transition metal with isotopes of 50V and 51V, and oxidation states of +2, +3, +4 and +5. The average concentration in seawater is 1.9 ppb, which results in a marine residence time of ~50 kyrs. Its various oxidation states make it a potential tool for investigating redox conditions in the ocean and sediments due to redox related changes in the valance state of vanadium. In turn, chemical equilibrium between different oxidation states of V will likely cause isotopic fractionation that can potentially be utilized to quantify past ocean redox states. In order to apply V isotopes as a paleo-redox tracer, it is required that we know the isotopic composition of seawater and the relation to marine sources and sinks of V. We developed a novel method for pre-concentrating V and measuring the isotope ratio in seawater samples. In our method, we used four ion exchange chromatography columns to separate vanadium from seawater matrix elements, in particular titanium and chromium, which both have an isobaric interference on 50V. The first column uses the NOBIAS resin, which effectively separates V and other transition metals from the majority of seawater matrix. Subsequent columns are identical to those utilized when separating V from silicate samples (Nielsen et al, Geostand. Geoanal. Res., 2011). The isotopic composition of the purified V is measured using a Thermo Scientific Neptune multiple collector inductively coupled plasma mass spectrometer (MC-ICP-MS) in medium resolution mode. This setup resolves all molecular interferences from masses 49, 50, 51, 52 and 53 including S-O species on mass 50. To test the new method, we spiked an open ocean seawater sample from the Bermuda Atlantic Time Series (BATS) station with 10-25 μg of Alfa Aesar vanadium solution, which has an isotopic composition of δ51V = 0 [where δ51V = 1000 × [(51V/50Vsample - 51V/50VAA)/51V/50VAA]. The average of six spiked samples is -0.03±0.19‰, which is within error of the true

  20. Effects of Basicity and MgO in Slag on the Behaviors of Smelting Vanadium Titanomagnetite in the Direct Reduction-Electric Furnace Process

    Directory of Open Access Journals (Sweden)

    Tao Jiang

    2016-05-01

    Full Text Available The effects of basicity and MgO content on reduction behavior and separation of iron and slag during smelting vanadium titanomagnetite by electric furnace were investigated. The reduction behaviors affect the separation of iron and slag in the direct reduction-electric furnace process. The recovery rates of Fe, V, and Ti grades in iron were analyzed to determine the effects of basicity and MgO content on the reduction of iron oxides, vanadium oxides, and titanium oxides. The chemical compositions of vanadium-bearing iron and main phases of titanium slag were detected by XRF and XRD, respectively. The results show that the higher level of basicity is beneficial to the reduction ofiron oxides and vanadium oxides, and titanium content dropped in molten iron with the increasing basicity. As the content of MgO increased, the recovery rate of Fe increased slightly but the recovery rate of V increased considerably. The grades of Ti in molten iron were at a low level without significant change when MgO content was below 11%, but increased as MgO content increased to 12.75%. The optimum conditions for smelting vanadium titanomagnetite were about 11.38% content of MgO and quaternary basicity was about 1.10. The product, vanadium-bearing iron, can be applied in the converter steelmaking process, and titanium slag containing 50.34% TiO2 can be used by the acid leaching method.

  1. Electrochemical lithium intercalation into vanadium pentoxide xerogel film electrode

    Energy Technology Data Exchange (ETDEWEB)

    Pyun, Su Il; Bae, Joon Sung [Korea Advanced Inst. of Science and Technology, Daejon (Korea, Republic of). Dept. of Materials Science and Engineering

    1997-10-01

    The lithium-ion transport in vanadium pentoxide xerogel film electrodes has been investigated by using cyclic voltammetry and electrochemical impedance spectroscopy. The oxide xerogel film electrodes were prepared by spin-coating a viscous gel on an indium tin oxide (ITO) substrate. The spin-coated xerogel films were dried under vacuum at 130 and 270 C, respectively. The lithium intercalation into the xerogel film electrode dried at 270 C is limited by the interfacial reaction at the electrolyte/electrode interface rather than the lithium-ion transport in the oxide electrode. On the other hand, lithium intercalation into the film electrode dried at 130 C is largely limited by the lithium transport in the oxide film, and the chemical diffusivity of the lithium ion in the oxide film was determined to decrease from 10{sup -10} to 10{sup -12} cm{sup 2} s{sup -1} as the electrode potential of the oxide film fell from 3.0 to 2.2 V{sub Li/Li{sup +}}. The tranition of the diffusion-controlled intercalation to the interfacial reaction-controlled intercalation into the oxide xerogel film with decreasing drying temperature was explained in terms of the modification of the oxide lattice to a more open-structured lattice by structural modification of the oxide film by water molecules incorporated into the film. (orig.)

  2. Model investigations for vanadium-protein interactions: vanadium(III) compounds with dipeptides and their oxovanadium(IV) analogues.

    Science.gov (United States)

    Tasiopoulos, Anastasios J; Tolis, Evangelos J; Tsangaris, John M; Evangelou, Angelos; Woollins, DerekJ; Slawin, Alexandra M Z; Pessoa, Costa; Correia, Isabel; Kabanos, Themistoklis A

    2002-04-01

    The reaction of VCl(3) with 1,10-phenanthroline and a series of dipeptides (H(2)dip), having aliphatic as well as aromatic side chains, in methyl alcohol and in the presence of triethylamine affords vanadium(III) compounds of the general formula [V(III)(dip)(MeOH)(phen)]Cl. Aerial oxidation/hydrolysis of the vanadium(III) species gives their oxovanadium(IV) analogues of the general formula [V(IV)O(dip)(phen)]. X-ray crystallographic characterization of the [V(IV)O(dip)(phen)] compounds (where dip(2-)=Gly- L-Ala, Gly- L-Val and Gly- L-Phe) revealed that the vanadium atom possesses a severely distorted octahedral coordination and is ligated to a tridentate dip(2-) ligand at the N(amine) atom, the deprotonated N(peptide) atom and one of the O(carboxylate) atoms, as well as an oxo group and two phenanthroline nitrogen atoms. Circular dichroism characterization of the V(III)/V(IV)O(2+)-dipeptide compounds revealed a strong signal for the V(IV)O(2+) species in the visible range of the spectrum, with a characteristic pattern which may be exploited to identify the N(am), N(pep) and O(car) ligation of a peptide or a protein to V(IV)O(2+) center, and a weak Cotton effect of opposite sign to their vanadium(III) analogues. The visible spectra of the V(III)-dipeptide compounds revealed two d-d bands with high intensity, thus indicating that the covalency of the metal-donor atoms is significant, i.e. the vanadium d orbitals are significantly mixed with the ligand orbitals, and this is confirmed by the low values of their Racah B parameters. The high-intensity band of the V(IV)O(2+)-dipeptide compounds at approximately 460 nm implies also a strong covalency of the metal with the equatorial donor atoms and this was supported by the EPR spectra of these compounds. Moreover, the V(III)/V(IV)O(2+)-dipeptide complexes were characterized by EPR and IR spectroscopies as well as conductivity and magnetic susceptibility measurements.

  3. Mesoporous Vanadium Nitride Synthesized by Chemical Routes

    National Research Council Canada - National Science Library

    Mishra, Pragnya P; Theerthagiri, J; Panda, Rabi N

    2014-01-01

    Nanocrystalline vanadium nitride (VN) materials are synthesized by two different routes, namely, the urea route and the ammonia route, using various V2O5 precursors obtained by citric acid–based sol–gel method...

  4. Vertical Administration of Vanadium through Lactation Induces ...

    African Journals Online (AJOL)

    The work investigated the protective role of vitamin E on vanadium induced neurotoxicity. Three adult female rats were divided into three groups, A-C with each dam and her pups forming a group. Group A served as control. The dam in Group B was given 3mg/kg b.w./day of vanadium from PND 1 while the Group C dam ...

  5. Comparison of hypoglycemic activity and toxicity of vanadium (IV) and vanadium (V) absorbed in fermented mushroom of Coprinus comatus.

    Science.gov (United States)

    Ma, Zhaoji; Fu, Qin

    2009-12-01

    This study was designed to evaluate the effect and toxicity of administration of vanadium (IV, V) absorbed by Coprinus comatus (VACC) on alloxan-induced and sucrosefed hyperglycemic mice, respectively. The blood glucose, lipid profile, and the organ masses of the mice were analyzed. After the mice were administered with VACC, the blood glucose and the lipid profile of hyperglycemic mice decreased, irrespective of the VACC produced by vanadium (IV) or vanadium (V). However, the organ masses of the mice were significantly different after the mice were treated with vanadium (IV) and vanadium (V) 9 weeks later. The results indicate both vanadium (IV) and vanadium (V) absorbed in C. comatus have hypoglycemic activity on hyperglycemic mice. However, vanadium (IV) absorbed in C. comatus is less toxic to mice than vanadium (V).

  6. Vanadium speciation by chromatographic separation of V(IV) and V ...

    African Journals Online (AJOL)

    A new method for vanadium speciation has been developed. The method is based on chromatographic separation of vanadium(IV) and vanadium(V) in acidic medium followed by the determination with ICP-OES. Vanadium species exist in acidic solution (pH < 3) as VO2+ for vanadium(IV) and VO2 + for vanadium(V).

  7. 77 FR 46712 - Ferrovanadium and Nitrided Vanadium From the Russian Federation: Negative Final Determination of...

    Science.gov (United States)

    2012-08-06

    ... are vanadium additives other than ferrovanadium and nitrided vanadium, such as vanadium-aluminum master alloys, vanadium chemicals, vanadium waste and scrap, vanadium-bearing raw materials, such as slag... the processing performed in the United States represents a small proportion of the value of the...

  8. Vanadium in landscape components of western Transbaikalia

    Science.gov (United States)

    Kashin, V. K.

    2017-10-01

    Vanadium in soil-forming rocks, soils, and vegetation of forest-steppe, steppe, and dry-steppe landscapes of Transbaikalia has been studied. The mean element contents in rocks and soils are equal to its mean natural abundances (clarke values). The content of vanadium in soils is strictly determined by its content in parent materials; its dependence on the vanadium concentration in plants and on the soil pH and humus is less pronounced. With respect to the coefficient of biological uptake by plants, vanadium is assigned to the group of elements of slight accumulation (0.10-0.33) on mineral soils and of moderate accumulation (1.1-1.5) on peat bog soils. The mean vanadium concentration in steppe, meadow, and cultivated vegetation exceeds the norm for animals by 1.7-2.6 times but does not rich toxic levels. Vanadium uptake by plants is most intensive in meadow cenoses and is less intensive in dry-steppe cenoses.

  9. Protective effect of alpha glucosyl hesperidin (G-hesperidin) on chronic vanadium induced testicular toxicity and sperm nuclear DNA damage in male Sprague Dawley rats.

    Science.gov (United States)

    Vijaya Bharathi, B; Jaya Prakash, G; Krishna, K M; Ravi Krishna, C H; Sivanarayana, T; Madan, K; Rama Raju, G A; Annapurna, A

    2015-06-01

    The study was conducted to evaluate the vanadium-induced testicular toxicity and its effect on sperm parameters, sperm nuclear DNA damage and histological alterations in Sprague Dawley rats and to assess the protective effect of G-hesperidin against this damage. Treatment of rats with vanadium at a dose of 1 mg kg bw(-1) for 90 days resulted in significant reduction in serum testosterone levels, sperm count and motility. Further, a parallel increase in abnormal sperm morphology and adverse histopathological changes in testis was also associated with vanadium administration when compared to normal control. Moreover, sperm chromatin dispersion assay revealed that vanadium induces sperm nuclear DNA fragmentation. A marked increase in testicular malondialdehyde levels and decreased activity of antioxidant enzymes such as superoxide dismutase and catalase indicates vanadium-induced oxidative stress. Co-administration of G-hesperidin at a dose of 25 and 50 mg kg bw(-1) significantly attenuated the sperm parameters and histological changes by restoring the antioxidant levels in rat testis. These results suggested that vanadium exposure caused reduced bioavailability of androgens to the tissue and increased free radical formation, thereby causing structural and functional changes in spermatozoa. G-hesperidin exhibited antioxidant effect by protecting the rat testis against vanadium-induced oxidative damage, further ensures antioxidant potential of bioflavonoids. © 2014 Blackwell Verlag GmbH.

  10. Recovery of Vanadium from H2SO4-HF Acidic Leaching Solution of Black Shale by Solvent Extraction and Precipitation

    Directory of Open Access Journals (Sweden)

    Xingbin Li

    2016-03-01

    Full Text Available The recovery of vanadium from sulfuric and hydrofluoric mixed acid solutions generated by the direct leaching of black shale was investigated using solvent extraction and precipitation methods. The process consisted of reduction, solvent extraction, and stripping, followed by precipitation and calcination to yield vanadium pentoxide. The influence of various operating parameters on the extraction and recovery of vanadium was studied. Vanadium (IV was selectively extracted using a mixture of 10% (v/v di(2-ethylhexylphosphoric acid and 5% (v/v tri-n-butylphosphate in sulfonated kerosene. Using six extraction and five stripping stages, the extraction efficiency for vanadium was 96.7% and the stripping efficiency was 99.7%. V2O5 with a purity of 99.52% was obtained by oxidation of the loaded strip solution and precipitation of ammonium polyvanadate at pH 1.8 to 2.2, followed by calcination of the dried precipitate at 550 °C for 2 h. It was concluded that the combination of solvent extraction and precipitation is an efficient method for the recovery of vanadium from a multi-element leach solution generated from black shale.

  11. Bioaccumulation of Vanadium by Vanadium-Resistant Bacteria Isolated from the Intestine of Ascidia sydneiensis samea.

    Science.gov (United States)

    Romaidi; Ueki, Tatsuya

    2016-06-01

    Isolation of naturally occurring bacterial strains from metal-rich environments has gained popularity due to the growing need for bioremediation technologies. In this study, we found that the vanadium concentration in the intestine of the vanadium-rich ascidian Ascidia sydneiensis samea could reach 0.67 mM, and thus, we isolated vanadium-resistant bacteria from the intestinal contents and determined the ability of each bacterial strain to accumulate vanadium and other heavy metals. Nine strains of vanadium-resistant bacteria were successfully isolated, of which two strains, V-RA-4 and S-RA-6, accumulated vanadium at a higher rate than did the other strains. The maximum vanadium absorption by these bacteria was achieved at pH 3, and intracellular accumulation was the predominant mechanism. Each strain strongly accumulated copper and cobalt ions, but accumulation of nickel and molybdate ions was relatively low. These bacterial strains can be applied to protocols for bioremediation of vanadium and heavy metal toxicity.

  12. Casting Simulation of an Austrian Bronze Age Sword Hilt

    Science.gov (United States)

    Pola, Annalisa; Mödlinger, Marianne; Piccardo, Paolo; Montesano, Lorenzo

    2015-07-01

    Bronze Age swords with a metal hilt can be considered the peak of Bronze Age casting technologies. To reconstruct the casting techniques used more than 3000 years ago, a metal hilted sword of the Schalenknauf type from Lower Austria was studied with the aid of macroscopic analyses and simulation of mold filling and casting solidification. A three-dimensional model of the hilt was created based on optical scanner measurements performed on a hilt recently discovered during archaeological excavations. Three different configurations of the gating system were considered, two on the pommel disk and one on the knob, and the effect of its location on the formation of casting defects was investigated. Three-dimensional computed tomography was used to detect internal defects, such as gas and shrinkage porosity, which were then compared with those calculated by simulation. The best match between actual and predicted hilt quality demonstrated the location of the gating system, which turned out to be on the pommel disk.

  13. Bronze Vessels with Over Vase Looped Handle of Capenate Manufacture

    Directory of Open Access Journals (Sweden)

    Nicolò Donati

    2012-10-01

    Full Text Available In the work presented we attempted to clarify the particular bronze vascular forms herein defined recipienti troncoconici ad ansa sormontante (“over vase loop handled frustoconical vessels”, often called mug, caccabus or kettle. Through a morphological analysis of the bronze vessel we proposed a hypothesized purpose of infusion or sauce preparation or a spiced wine container. The contextual analysis made it possible to date the articles between the mid-third and half of the second century BC, although some clues can extend the upper limit toward the end of the fourth century BC. The data context also allowed to suggest the site of Capena as production centre, since 31 of the 67 specimens come from the neighboring necropoles.

  14. Nettle as a distinct Bronze Age textile plant.

    Science.gov (United States)

    Bergfjord, C; Mannering, U; Frei, K M; Gleba, M; Scharff, A B; Skals, I; Heinemeier, J; Nosch, M-L; Holst, B

    2012-01-01

    It is generally assumed that the production of plant fibre textiles in ancient Europe, especially woven textiles for clothing, was closely linked to the development of agriculture through the use of cultivated textile plants (flax, hemp). Here we present a new investigation of the 2800 year old Lusehøj Bronze Age Textile from Voldtofte, Denmark, which challenges this assumption. We show that the textile is made of imported nettle, most probably from the Kärnten-Steiermark region, an area which at the time had an otherwise established flax production. Our results thus suggest that the production of woven plant fibre textiles in Bronze Age Europe was based not only on cultivated textile plants but also on the targeted exploitation of wild plants. The Lusehøj find points to a hitherto unrecognized role of nettle as an important textile plant and suggests the need for a re-evaluation of textile production resource management in prehistoric Europe.

  15. Thermodynamics and kinetics of reactions involving vanadium in natural systems: Accumulation of vanadium in sedimentary rocks

    Science.gov (United States)

    Wanty, R.B.; Goldhaber, M.B.

    1992-01-01

    A critical review of thermodynamic data for aqueous and solid V species is presented to evaluate dissolution, transport, and precipitation of V under natural conditions. Emphasis is given to results of experimental studies of V chemistry, especially those for which the experimental conditions are near those found in nature. Where possible, data are obtained for or corrected to the reference conditions of 298.15K, 1 atm (1.01325 bar) and zero ionic strength. Vanadium [IV] (VIV) and vanadium[V] (VV) are the most soluble forms of V in nature, and their complexes with fluoride, sulfate, and oxalate may act to increase V solubility under oxidizing conditions. Because redox behavior is of fundamental importance to understanding natural V chemistry, the kinetics of reduction of VIV to VIII H2S were studied. Although H2S is predicted from thermodynamic data to be capable of reducing VIV to VIII, this reaction has not been demonstrated experimentally. Experiments were carried out under conditions of temperature (45??C), pH (3.6-6.8), ionic strength (0.05-0.1 m), and V concentrations (9.8-240 ??molar) likely to be found in nature. Because the reaction is very slow, H2S concentrations in excess of natural conditions were used (8.1 ?? 10-4 to 0.41 atm). The results show that VIV is reduced to VIII under a variety of conditions. The rate increases with increasing pH, but is not appreciably affected by ionic strength (as represented by the concentration of KCl, which was used as the supporting electrolyte in all cases). Prior to initiation of the reaction, there is an induction period, the length of which increases with increasing KCl concentration or decreasing pH. Attempts to model the reaction mechanism by numerical methods have failed to produce a satisfying fit of the results, indicating partial reaction orders, a complex mechanism, or involvement of a variety of intermediate species. The results of the thermodynamic and kinetic studies were applied to understanding the

  16. Influence of titanium and vanadium on the hydrogen transport through amorphous alumina films

    Energy Technology Data Exchange (ETDEWEB)

    Palsson, G.K. [Department of Physics, Uppsala University, Box 530, S-751 21 Uppsala (Sweden); Wang, Y.T. [Department of Physics, Uppsala University, Box 530, S-751 21 Uppsala (Sweden); Azofeifa, D. [Centro de Investigacion en Ciencia e Ingenieria de Materiales and Escuela de Fisica, Universidad de Costa Rica, San Jose (Costa Rica); Raanaei, H. [Department of Physics, Uppsala University, Box 530, S-751 21 Uppsala (Sweden); Department of Physics, Persian Gulf University, Bushehr 75168 (Iran, Islamic Republic of); Sahlberg, M. [Department of Materials Chemistry, Uppsala University, Box 538, S-751 21 Uppsala (Sweden); Hjoervarsson, B. [Department of Physics, Uppsala University, Box 530, S-751 21 Uppsala (Sweden)

    2010-04-02

    The influence of titanium and vanadium on the hydrogen transport rate through thin amorphous alumina films is addressed. Only small changes in the transport rate are observed when the Al{sub 2}O{sub 3} are covered with titanium or vanadium. This is in stark contrast to results with a Pd overlayer, which enhances the transport by an order of magnitude. Similarly, when titanium is embedded into the alumina the transport rate is faster than for the covered case but still slower than the undoped reference. Embedding vanadium in the alumina does not yield an increase in uptake rate compared to the vanadium covered oxide layers. These results add to the understanding of the hydrogen uptake of oxidized metals, especially the alanates, where the addition of titanium has been found to significantly enhance the rate of hydrogen uptake. The current findings eliminate two possible routes for the catalysis of alanates by Ti, namely dissociation and effective diffusion short-cuts formed by Ti. Finally, no photocatalytic enhancement was noticed on the titanium covered samples.

  17. Rewriting the Central European Early Bronze Age Chronology: Evidence from Large-Scale Radiocarbon Dating.

    Science.gov (United States)

    Stockhammer, Philipp W; Massy, Ken; Knipper, Corina; Friedrich, Ronny; Kromer, Bernd; Lindauer, Susanne; Radosavljević, Jelena; Wittenborn, Fabian; Krause, Johannes

    2015-01-01

    The transition from the Neolithic to the Early Bronze Age in Central Europe has often been considered as a supra-regional uniform process, which led to the growing mastery of the new bronze technology. Since the 1920s, archaeologists have divided the Early Bronze Age into two chronological phases (Bronze A1 and A2), which were also seen as stages of technical progress. On the basis of the early radiocarbon dates from the cemetery of Singen, southern Germany, the beginning of the Early Bronze Age in Central Europe was originally dated around 2300/2200 BC and the transition to more complex casting techniques (i.e., Bronze A2) around 2000 BC. On the basis of 140 newly radiocarbon dated human remains from Final Neolithic, Early and Middle Bronze Age cemeteries south of Augsburg (Bavaria) and a re-dating of ten graves from the cemetery of Singen, we propose a significantly different dating range, which forces us to re-think the traditional relative and absolute chronologies as well as the narrative of technical development. We are now able to date the beginning of the Early Bronze Age to around 2150 BC and its end to around 1700 BC. Moreover, there is no transition between Bronze (Bz) A1 and Bronze (Bz) A2, but a complete overlap between the type objects of the two phases from 1900-1700 BC. We thus present a revised chronology of the assumed diagnostic type objects of the Early Bronze Age and recommend a radiocarbon-based view on the development of the material culture. Finally, we propose that the traditional phases Bz A1 and Bz A2 do not represent a chronological sequence, but regionally different social phenomena connected to the willingness of local actors to appropriate the new bronze technology.

  18. Rewriting the Central European Early Bronze Age Chronology: Evidence from Large-Scale Radiocarbon Dating.

    Directory of Open Access Journals (Sweden)

    Philipp W Stockhammer

    Full Text Available The transition from the Neolithic to the Early Bronze Age in Central Europe has often been considered as a supra-regional uniform process, which led to the growing mastery of the new bronze technology. Since the 1920s, archaeologists have divided the Early Bronze Age into two chronological phases (Bronze A1 and A2, which were also seen as stages of technical progress. On the basis of the early radiocarbon dates from the cemetery of Singen, southern Germany, the beginning of the Early Bronze Age in Central Europe was originally dated around 2300/2200 BC and the transition to more complex casting techniques (i.e., Bronze A2 around 2000 BC. On the basis of 140 newly radiocarbon dated human remains from Final Neolithic, Early and Middle Bronze Age cemeteries south of Augsburg (Bavaria and a re-dating of ten graves from the cemetery of Singen, we propose a significantly different dating range, which forces us to re-think the traditional relative and absolute chronologies as well as the narrative of technical development. We are now able to date the beginning of the Early Bronze Age to around 2150 BC and its end to around 1700 BC. Moreover, there is no transition between Bronze (Bz A1 and Bronze (Bz A2, but a complete overlap between the type objects of the two phases from 1900-1700 BC. We thus present a revised chronology of the assumed diagnostic type objects of the Early Bronze Age and recommend a radiocarbon-based view on the development of the material culture. Finally, we propose that the traditional phases Bz A1 and Bz A2 do not represent a chronological sequence, but regionally different social phenomena connected to the willingness of local actors to appropriate the new bronze technology.

  19. Prevention of Dealloying in Manganese Aluminium Bronze Propeller: Part II

    OpenAIRE

    Napachat Tareelap; Kaysinee Sriraksasin; Nakorn Srisukhumbowornchai; Swieng Thuanboon; Choochat Nitipanyawong

    2014-01-01

    Due to the failure of manganese aluminium bronze (MAB) propeller caused by dealloying corrosion as described in Part I [1], this work aims to study the prevention of dealloying corrosion using aluminium and zinc sacrificial anodes. The results indicated that both of the sacrificial anodes could prevent the propeller from dealloying. Moreover, the dealloying in seawater was less than that found in brackish water. It was possible that hydroxide ions, from cathodic reaction, reacted with calcium...

  20. An extraction-chromogenic system for vanadium(IV,V based on 2,3-dihydroxynaphtahlene

    Directory of Open Access Journals (Sweden)

    Gavazov Kiril B.

    2016-10-01

    Full Text Available A liquid-liquid extraction-chromogenic system for vanadium(IV, V containing 2,3-dihydroxynaphtahlene (DN, 2,3,5-triphenyl-2H-tetrazolium chloride (TTC, water and chloroform was studied in detail. When the vanadium is in the oxidation state of IV, the extracted species are aggregates containing three 1:2:1 (V:DN:TTC ion-pair units composed of triphenyltetrazolium cations (TT+ and chelate anions {[VIVO(DN(DNH]− (I and/or [VIV(OH(DN2]− (II}. When the initial oxidation state of vanadium is V and the DN concentration is high, vanadium(V is reduced by DN to a lower oxidation state, V(IV. However, at low DN concentration, vanadium(V can enter the organic phase as a part of an ion-pair consisting of TT+ and [VVO2(DN]− (III. The ground-state equilibrium geometries of the anions I, II, and III were optimized by quantum chemical calculations using BLYP/6-31++G⋆. The following characteristics were determined under the optimum conditions for VIV extraction: absorption maximum λmax = 333 nm, molar absorptivity ε333= 2.1x104 dm3 mol−1 cm−1, Sandell’s sensitivity SS = 2.4 ng cm−2, and fraction extracted E = 98%. The conditional extraction constant was calculated by two independent methods. The calibration graph was linear in the range 0.1-3.1 μg cm−3 (R2=0.9994 and the limit of detection was 0.03 μg cm−3.

  1. Model of Cu-Al-Fe-Ni Bronze Crystallization

    Directory of Open Access Journals (Sweden)

    Pisarek B. P.

    2013-09-01

    Full Text Available According to the analysis of the current state of the knowledge shows that there is little information on the process of phase transformations that occur during the cooling Cu-Al-Fe-Ni hypo-eutectoid bronzes with additions of Cr, Mo and/or W, made additions individually or together, for the determination of: the type of crystallizing phases, crystallizing phases, order and place of their nucleation. On the basis of recorded using thermal and derivative analysis of thermal effects phases crystallization or their systems, analysis of the microstructure formed during crystallization - observed on the metallographic specimen casting ATD10-PŁ probe, analysis of the existing phase equilibrium diagrams forming elements tested Cu-Al-Fe-Ni bronze, with additions of Cr, Mo, W and/or Si developed an original model of crystallization and phase transformation in the solid state, the casting of high quality Cu-Al-Fe-Ni bronze comprising: crystallizing type phase, crystallizing phase sequence, place of nucleation.

  2. Investigations on dry sliding of laser cladded aluminum bronze

    Directory of Open Access Journals (Sweden)

    Freiße Hannes

    2016-01-01

    Full Text Available The aim of this study was to investigate the tribological behaviour of laser cladded aluminum bronze tool surfaces for dry metal forming. In a first part of this work a process window for cladding aluminum bronze on steel substrate was investigated to ensure a low dilution. Therefore, the cladding speed, the powder feed rate, the laser power and the distance between the process head and the substrate were varied. The target of the second part was to investigate the influence of different process parameters on the tribological behaviour of the cladded tracks. The laser claddings were carried out on both aluminum bronze and cold work tool steel as substrate materials. Two different particle sizes of the cladding powder material were used. The cladding speed was varied and a post-processing laser remelting treatment was applied. It is shown that the tribological behaviour of the surface in a dry oscillating ball-on-plate test is highly dependent on the substrate material. In the third part a deep drawing tool was additively manufactured by direct laser deposition. Furthermore, the tool was applied to form circular cups with and without lubrication.

  3. Matisse to Picasso: a compositional study of modern bronze sculptures.

    Science.gov (United States)

    Young, Marcus L; Schnepp, Suzanne; Casadio, Francesca; Lins, Andrew; Meighan, Melissa; Lambert, Joseph B; Dunand, David C

    2009-09-01

    Inductively coupled plasma-optical emission spectroscopy (ICP-OES) was used to determine the bulk metal elemental composition of 62 modern bronze sculptures cast in Paris in the first half of the twentieth century from the collections of The Art Institute of Chicago and the Philadelphia Museum of Art. As a result, a comprehensive survey of the alloy composition of the sculptures of many prominent European artists of the early twentieth century is presented here for the first time. The sculptures in this study consist of predominantly copper with two main alloying elements (zinc and tin). By plotting the concentrations of these two elements (zinc and tin) against each other for all the sculptures studied, three clusters of data become apparent: (A) high-zinc brass; (B) low-zinc brass; (C) tin bronze. These clusters correlate to specific foundries, which used specific casting methods (sand or lost wax) that were influenced by individual preferences and technical skills of the foundry masters. For instance, the high-zinc brass alloys (with the highest levels of tin and zinc and the lowest melting temperature) correspond to most of the Picasso sculptures, correlate with the Valsuani foundry, and are associated with the most recent sculptures (post-WWII) and with the lost-wax casting method. By expanding the ICP-OES database of objects studied, these material correlations may become useful for identifying, dating, or possibly even authenticating other bronzes that do not bear foundry marks. Figure.

  4. Friction Stir Processing Parameters and Property Distributions in Cast Nickel Aluminum Bronze

    National Research Council Canada - National Science Library

    Rosemark, Brian P

    2006-01-01

    Cast nickel-aluminum bronze (NAB) alloy is specified for many marine applications, including ship propellers, due to its excellent corrosion-resistance combined with acceptable mechanical properties...

  5. Patina in the construction of the poetic bronze image: science of materials, art and philosophy

    National Research Council Canada - National Science Library

    Silva, Claudia; Vélez, Gabriel; Colorado, Henry A

    2017-01-01

    Bronze has been positioned as the medium par excellence for sculptural production bearing the aesthetic, symbolic and poetic values that have propitiated the construction of a metallurgical archetype...

  6. In situ electrical resistivity measurements of vanadium thin films performed in vacuum during different annealing cycles

    Science.gov (United States)

    Pedrosa, Paulo; Cote, Jean-Marc; Martin, Nicolas; Arab Pour Yazdi, Mohammad; Billard, Alain

    2017-02-01

    The present study describes a sputtering and in situ vacuum electrical resistivity setup that allows a more efficient sputtering-oxidation coupling process for the fabrication of oxide compounds like vanadium dioxide, VO2. After the sputtering deposition of pure V thin films, the proposed setup enables the sample holder to be transferred from the sputtering to the in situ annealing + resistivity chamber without venting the whole system. The thermal oxidation of the V films was studied by implementing two different temperature cycles up to 550 °C, both in air (using a different resistivity setup) and vacuum conditions. Main results show that the proposed system is able to accurately follow the different temperature setpoints, presenting clean and low-noise resistivity curves. Furthermore, it is possible to identify the formation of different vanadium oxide phases in air, taking into account the distinct temperature cycles used. The metallic-like electrical properties of the annealed coatings are maintained in vacuum whereas those heated in air produce a vanadium oxide phase mixture.

  7. Iron diminishes the in vitro biological effect of vanadium.

    Science.gov (United States)

    Mechanistic pathways underlying inflammatory injury following exposures to vanadium-containing compounds are not defined. We tested the postulate that the in vitro biological effect of vanadium results from its impact on iron homeostasis. Human bronchial epithelial (HBE) cells ex...

  8. [An in vitro study on toxic effect of vanadium-titanium-magnetite dust on alveolar macrophage in rabbits].

    Science.gov (United States)

    Song, Y; Chen, Q; Guan, Y

    1998-11-01

    To study the toxic effect of vanadium-titanium-magnetite (VTM) dust on alveolar macrophage (AM) and its hazardous extent. Survival rates, morphology and function of AM were compared in rabbits exposed to dust of VTM, vanadium oxide, titanium dioxide and silica in various doses and length of time with in vitro cell culture and putamen membrane cover glass transmission electron microscopy, and changes in activities of lactic dehydrogenase (LDH) and acid phosphatase (ACP) in cell culture were measured. Exposure to all the four kinds of dust could lead to decrease in survival rate of AM, increase in activities of LDH and ACP in the cell culture, and changes in their morphology and function to the extent dependent on the nature of dust. Toxic effect of exposure to VTM dust was lower than that to vanadium oxide and silica, but higher than that to titanium dioxide, which had slight toxic effect.

  9. 77 FR 51825 - Ferrovanadium and Nitrided Vanadium From Russia

    Science.gov (United States)

    2012-08-27

    ... COMMISSION Ferrovanadium and Nitrided Vanadium From Russia Determination On the basis of the record \\1... antidumping duty order on ferrovanadium and nitrided vanadium from Russia would not be likely to lead to... contained in USITC Publication 4345 (August 2012), entitled Ferrovanadium and Nitrided Vanadium from Russia...

  10. Memory Deficit Recovery after Chronic Vanadium Exposure in Mice

    Directory of Open Access Journals (Sweden)

    Oluwabusayo Folarin

    2016-01-01

    Full Text Available Vanadium is a transitional metal with an ability to generate reactive oxygen species in the biological system. This work was designed to assess memory deficits in mice chronically exposed to vanadium. A total of 132 male BALB/c mice (4 weeks old were used for the experiment and were divided into three major groups of vanadium treated, matched controls, and animals exposed to vanadium for three months and thereafter vanadium was withdrawn. Animals were tested using Morris water maze and forelimb grip test at 3, 6, 9, and 12 months of age. The results showed that animals across the groups showed no difference in learning but had significant loss in memory abilities after 3 months of vanadium exposure and this trend continued in all vanadium-exposed groups relative to the controls. Animals exposed to vanadium for three months recovered significantly only 9 months after vanadium withdrawal. There was no significant difference in latency to fall in the forelimb grip test between vanadium-exposed groups and the controls in all age groups. In conclusion, we have shown that chronic administration of vanadium in mice leads to memory deficit which is reversible but only after a long period of vanadium withdrawal.

  11. Determination of Leachable Vanadium (V) in Sediment | Mampuru ...

    African Journals Online (AJOL)

    A method for speciation of vanadium in solid samples was developed for quantification of vanadium(+5) in solid samples of sediment Certified Reference Materials (CRM) PACS-2 and MESS-3 (Trace Elements in Sediments) of known total vanadium content. The method relies on a classical analytical chemistry procedure ...

  12. Memory Deficit Recovery after Chronic Vanadium Exposure in Mice.

    Science.gov (United States)

    Folarin, Oluwabusayo; Olopade, Funmilayo; Onwuka, Silas; Olopade, James

    2016-01-01

    Vanadium is a transitional metal with an ability to generate reactive oxygen species in the biological system. This work was designed to assess memory deficits in mice chronically exposed to vanadium. A total of 132 male BALB/c mice (4 weeks old) were used for the experiment and were divided into three major groups of vanadium treated, matched controls, and animals exposed to vanadium for three months and thereafter vanadium was withdrawn. Animals were tested using Morris water maze and forelimb grip test at 3, 6, 9, and 12 months of age. The results showed that animals across the groups showed no difference in learning but had significant loss in memory abilities after 3 months of vanadium exposure and this trend continued in all vanadium-exposed groups relative to the controls. Animals exposed to vanadium for three months recovered significantly only 9 months after vanadium withdrawal. There was no significant difference in latency to fall in the forelimb grip test between vanadium-exposed groups and the controls in all age groups. In conclusion, we have shown that chronic administration of vanadium in mice leads to memory deficit which is reversible but only after a long period of vanadium withdrawal.

  13. Simple Sensitive Spectrophotometric Determination of Vanadium in Biological and Environmental Samples

    Directory of Open Access Journals (Sweden)

    B. Krishna Priya

    2006-01-01

    Full Text Available Novel, rapid, highly sensitive and selective spectrophotometric method for the determination of traces of vanadium (V in environmental and biological samples, pharmaceutical and steel samples was studied. The method is based on oxidation of 2,4- dinitro phenyl hydrazine(2,4-DNPH by vanadium (V followed by coupling reaction with N-(1-naphthalene-1-ylethane-1,2-diamine-dihydrochloride (NEDA in acidic medium to give red colored derivative or on oxidation of 4-Amino Pyridine by vanadium (V followed by coupling reaction with NEDA in basic medium to give pink colored derivative. The red colored derivative having an λmax 495 nm which is stable for 8 days and the pink colored derivative with 525 nm is stable for more than 7 days at 350C. Beer's law is obeyed for vanadium (V in the concentration range of 0.02 - 3.5 μg mL–1 (red derivative and 0.03 – 4.5 μg mL–1 (pink derivative at the wave length of maximum absorption. The optimum reaction conditions and other analytical parameters were investigated to enhance the sensitivity of the present method. The detailed study of various interferences made the method more selective. The proposed method was successfully applied to the analysis of vanadium in natural water samples, plant material, soil samples, synthetic mixtures, pharmaceutical samples and biological samples. The results obtained were agreed with the reported methods at the 95 % confidence level. The performance of proposed method was evaluated in terms of Student's t-test and Variance ratio f-test which indicates the significance of proposed method over reported method.

  14. Polypyrrole-encapsulated vanadium pentoxide nanowires on a conductive substrate for electrode in aqueous rechargeable lithium battery.

    Science.gov (United States)

    Liang, Chaowei; Fang, Dong; Cao, Yunhe; Li, Guangzhong; Luo, Zhiping; Zhou, Qunhua; Xiong, Chuanxi; Xu, Weilin

    2015-02-01

    Precursors of ammonium vanadium bronze (NH4V4O10) nanowires assembled on a conductive substrate were prepared by a hydrothermal method. After calcination at 360°C, the NH4V4O10 precursor transformed to vanadium pentoxide (V2O5) nanowires, which presented a high initial capacity of 135.0mA h g(-1) at a current density of 50mA g(-1) in 5M LiNO3 aqueous solution; while the specific capacity faded quickly over 50 cycles. By coating the surface of V2O5 nanowires with water-insoluble polypyrrole (PPy), the formed nanocomposite electrode exhibited a specific discharge capacity of 89.9mA h g(-1) at 50mA g(-1) (after 100 cycles). A V2O5@PPy //LiMn2O4 rechargeable lithium battery exhibited an initial discharge capacity of 95.2mA h g(-1); and after 100 cycles, a specific discharge capacity of 81.5mA h g(-1) could retain at 100mA g(-1). Copyright © 2014 Elsevier Inc. All rights reserved.

  15. Atomic layer deposition of VO{sub 2} films with Tetrakis-dimethyl-amino vanadium (IV) as vanadium precursor

    Energy Technology Data Exchange (ETDEWEB)

    Lv, Xinrui [Key Laboratory of Inorganic Coating Materials CAS, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 201800 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Cao, Yunzhen, E-mail: yzhcao@mail.sic.ac.cn [Key Laboratory of Inorganic Coating Materials CAS, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 201800 (China); Yan, Lu; Li, Ying; Song, Lixin [Key Laboratory of Inorganic Coating Materials CAS, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 201800 (China)

    2017-02-28

    Highlights: • VO{sub 2} film was easily deposited by ALD using novel vanadium precursor V(NMe{sub 2}){sub 4}. • Deposition and annealing condition were systematically investigated. • Comparable transition properties of VO{sub 2} film on resistance and spectral transmittance were studied. - Abstract: VO{sub 2} thin films have been grown on Si(100) (VO{sub 2}/Si) and fused silica substrates (VO{sub 2}/SiO{sub 2}) by atomic layer deposition (ALD) using tetrakis-dimethyl-amino vanadium (IV) (TDMAV) as a novel vanadium precursor and water as reactant gas. The quartz crystal microbalance (QCM) measurement was performed to study the ALD process of VO{sub 2} thin film deposition, and a constant growth rate of about 0.95 Å/cycle was obtained at the temperature range of 150–200 °C. XRD measurement was performed to study the influence of deposition temperature and post-annealing condition on the crystallization of VO{sub 2} films, which indicated that the films deposited between 150 and 200 °C showed well crystallinity after annealing at 475 °C for 100 min in Ar atmosphere. XPS measurement verified that the vanadium oxidation state was 4+ for both as-deposited film and post-annealed VO{sub 2}/Si film. AFM was applied to study the surface morphology of VO{sub 2}/Si films, which showed a dense polycrystalline film with roughness of about 1 nm. The resistance of VO{sub 2}/Si films deposited between 150 °C and 200 °C as a function of temperature showed similar semiconductor-to-metal transition (SMT) characters with the transition temperature for heating branch (T{sub c,h}) of about 72 °C, a hysteresis width of about 10 °C and the resistance change of two orders of magnitude. The increase of T{sub c,h} compared with the bulk VO{sub 2} (68 °C) may be attributed to the tensile stress along the c-axis in the film. Transmittance measurement of VO{sub 2}/SiO{sub 2} films showed typical thermochromic property with a NIR switching efficiency of above 50% at 2 μm across

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

    Science.gov (United States)

    Soedjak, H S; Butler, A

    1990-08-28

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

  17. Evaluation of Non-Timber forest Products (NTFPs) In Bronze Casting ...

    African Journals Online (AJOL)

    Evaluation of NTFPs input in bronze casting at Igun Street in Benin City was carried out with the use of measurement of inputs and questionnaires. Fifty percent sampling intensity was used to obtain 42 from the total population of 84 Bronze Casters. Data were analyzed with the use of descriptive statistics of frequency, ...

  18. Evaluation of Non-Timber forest Products (NTFPs) In Bronze Casting ...

    African Journals Online (AJOL)

    Michael Horsfall

    Evaluation of Non-Timber forest Products (NTFPs) In Bronze Casting Enterprise at. Egun Street, Benin City, Edo state. *KALU, C; AIGBOBO, E N. Department of Forestry and Wildlife, Faculty of Agriculture, University of Benin, Benin City. ABSTRACT: Evaluation of NTFPs input in bronze casting at Igun Street in Benin City was ...

  19. The Origin and Development of the Guild of Bronze Casters of Benin ...

    African Journals Online (AJOL)

    The guild of bronze casters was the most important guild that existed in the kingdom partly because of its function of preserving the history of the kingdom in bronze for posterity sake. A role it continued to play until the late 19th century when Benin kingdom was invaded. The outcome of the invasion was the fizzling out of the ...

  20. Metallography and microstructure interpretation of some archaeological tin bronze vessels from Iran

    Energy Technology Data Exchange (ETDEWEB)

    Oudbashi, Omid, E-mail: o.oudbashi@aui.ac.ir [Department of Conservation of Historic Properties, Faculty of Conservation, Art University of Isfahan, Hakim Nezami Street, Sangtarashha Alley, P.O. Box 1744, Isfahan (Iran, Islamic Republic of); Davami, Parviz, E-mail: pdavami@razi-foundation.com [Faculty of Material Science and Engineering, Sharif University of Technology/Razi Applied Science Foundation, No. 27, Fernan St., Shahid Ghasem Asghari Blvd., km 21 of Karadj Makhsous Road, Tehran (Iran, Islamic Republic of)

    2014-11-15

    Archaeological excavations in western Iran have recently revealed a significant Luristan Bronzes collection from Sangtarashan archaeological site. The site and its bronze collection are dated to Iron Age II/III of western Iran (10th–7th century BC) according to archaeological research. Alloy composition, microstructure and manufacturing technique of some sheet metal vessels are determined to reveal metallurgical processes in western Iran in the first millennium BC. Experimental analyses were carried out using Scanning Electron Microscopy–Energy Dispersive X-ray Spectroscopy and Optical Microscopy/Metallography methods. The results allowed reconstructing the manufacturing process of bronze vessels in Luristan. It proved that the samples have been manufactured with a binary copper–tin alloy with a variable tin content that may relates to the application of an uncontrolled procedure to make bronze alloy (e.g. co-smelting or cementation). The presence of elongated copper sulphide inclusions showed probable use of copper sulphide ores for metal production and smelting. Based on metallographic studies, a cycle of cold working and annealing was used to shape the bronze vessels. - Highlights: • Sangtarashan vessels are made by variable Cu-Sn alloys with some impurities. • Various compositions occurred due to applying uncontrolled smelting methods. • The microstructure represents thermo-mechanical process to shape bronze vessels. • In one case, the annealing didn’t remove the eutectoid remaining from casting. • The characteristics of the bronzes are similar to other Iron Age Luristan Bronzes.

  1. ISOTOPES, PLANTS, AND RESERVOIR EFFECTS : CASE STUDY FROM THE CASPIAN STEPPE BRONZE AGE

    NARCIS (Netherlands)

    Shishlina, N.; Zazovskaya, E.; van der Plicht, J.; Sevastyanov, V.; Boaretto, E.; Rebollo Franco, N.R.

    2012-01-01

    Bronze Age human and animal bone collagen from several steppe Bronze Age cultures (i.e. Early Catacomb, East and West Manych Catacomb, and Lola cultures) shows large variations in delta C-13 and delta N-15 values. In general, we observed that the older the sample, the lower the delta C-13 and delta

  2. Excerpt from "IRL (In Real Life: The Bronze Documentary Project" [interview

    Directory of Open Access Journals (Sweden)

    Stephanie Tuszynski

    2011-03-01

    Full Text Available Excerpt from "IRL (In Real Life: The Bronze Documentary Project". One of the first feature-length documentary films to take on the subject of online relationships, "IRL (In Real Life" chronicles the life, death, and afterlife of an online community called The Bronze, made up of fans from the official Web site for Buffy, the Vampire Slayer.

  3. Impedance spectroscopy study and phase transition in phospho-vanadium mixed oxide LiZnV{sub 0.5}P{sub 0.5}O{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Rahal, A.; Guidara, Kamel; Megdiche, Makram [Sfax Universite, Laboratoire de Caracterisations Spectroscopiques et Optique des Materiaux (LaSCOM), Faculte des Sciences de Sfax, BP 1171, Sfax (Tunisia); Megdiche Borchani, S. [Sfax Universite, Laboratoire de Caracterisations Spectroscopiques et Optique des Materiaux (LaSCOM), Faculte des Sciences de Sfax, BP 1171, Sfax (Tunisia); Institut Superieur D' Informatique et de Multimedia de Sfax (ISIMS), Pole Technologique de Sfax, Sakiet Ezzit, BP 242, Sfax (Tunisia)

    2017-08-15

    An X-ray crystallographic study has allowed us to identify a powder of the type LiZnV{sub 0.5}P{sub 0.5}O{sub 4}, which contains 50% of vanadium and 50% of phosphor, inside the binary system LiZnVO{sub 4}-LiZnPO{sub 4}. The structure is isotypic with the phenacite like LiZnP0{sub 4}. X-ray diffraction patterns are indexed according to the lattice parameters of the rhombohedral system and the R3 space group. IR spectra show the presence of VO{sub 4} and PO{sub 4} groups in the network of this material. The experimental results indicate that σ{sub AC}(ω) is proportional to (ω{sup n}). The activation energy found from the Arrhenius plot confirms that the conduction processing of the material is not due to simple hopping mechanism. The temperature dependence of frequency exponent n was investigated to understanding the conduction mechanism in LiZnV{sub 0.5}P{sub 0.5}O{sub 4}. The non-overlapping small Polaron tunneling (NSPT) model can explain the temperature dependence of the frequency exponent. A phase transition at T = 623 K has been evidenced by Differential scanning calorimetry (DSC) and subsequently confirmed by the analysis of dielectric and electric properties. (orig.)

  4. Global biogeochemical cycle of vanadium.

    Science.gov (United States)

    Schlesinger, William H; Klein, Emily M; Vengosh, Avner

    2017-12-26

    Synthesizing published data, we provide a quantitative summary of the global biogeochemical cycle of vanadium (V), including both human-derived and natural fluxes. Through mining of V ores (130 × 109 g V/y) and extraction and combustion of fossil fuels (600 × 109 g V/y), humans are the predominant force in the geochemical cycle of V at Earth's surface. Human emissions of V to the atmosphere are now likely to exceed background emissions by as much as a factor of 1.7, and, presumably, we have altered the deposition of V from the atmosphere by a similar amount. Excessive V in air and water has potential, but poorly documented, consequences for human health. Much of the atmospheric flux probably derives from emissions from the combustion of fossil fuels, but the magnitude of this flux depends on the type of fuel, with relatively low emissions from coal and higher contributions from heavy crude oils, tar sands bitumen, and petroleum coke. Increasing interest in petroleum derived from unconventional deposits is likely to lead to greater emissions of V to the atmosphere in the near future. Our analysis further suggests that the flux of V in rivers has been incremented by about 15% from human activities. Overall, the budget of dissolved V in the oceans is remarkably well balanced-with about 40 × 109 g V/y to 50 × 109 g V/y inputs and outputs, and a mean residence time for dissolved V in seawater of about 130,000 y with respect to inputs from rivers.

  5. Bronze age settlement in churchyard of Gradac monastery

    Directory of Open Access Journals (Sweden)

    Peković Mirko

    2009-01-01

    Full Text Available During 2005 and 2008, a team from Republic Cultural Heritage Preservation Institute carried out preservative, sondage, archaeological and revision exploration of the Church of Holy Virgin in Gradac monastery. The 2005 exploration aim was to uncover geomorphology and characteristics of soil and its moisture penetration, to make insight in condition of ground zones, uncovering of attached structures and archaeological material, obtaining stratigraphic data, all in purpose of obtaining data for making the Main Project for preserving the Church of Holy Virgin from moisture. The first phase of work started in 2008, and it included work on western, north-western and south-western part of the church. During these explorations, 9 sondages were opened and a drainage pit, in total area of 130 m² and total depth of 3 m. Beside medieval cultural layer and medieval necropolis, a prehistoric layer of 0.5-0.6 m depth was found which was documented with four residential horizons as well with other belonging archaeological material originated in period of the end of Early Bronze Age and Middle Bronze Age. Pottery from older prehistoric layer in Gradac, which was documented with two residential horizons, mainly consists of fragments of pottery made of weaker, refined clay, with smooth surfaces and with range of colour from brownish to dark grey. These are fragments of dishes and larger spherical pots with two vertical handles on wider part of body. Some fragments are decorated with wartlike bulges or recesses made with fingers. From fine pottery, there are pear-shaped amphorae with thin sides, bowls and cups. Beside pottery, in this layer there were also few fragments of different shapes made of Rozhnac stone, flints and quartzite, part of stone axe with perforation whose upper part is shaped into secant and two fragmented millstones made of quartzlathyte, a mineral found in mountain Golija (Pl. I-III. Analogies to this pottery are found in sites in Milića Brdo

  6. Vanadium bioavailability in soils amended with blast furnace slag

    Energy Technology Data Exchange (ETDEWEB)

    Larsson, Maja A., E-mail: maja.larsson@slu.se [Department of Soil and Environment, Swedish University of Agricultural Sciences, P.O. Box 7014, 750 07 Uppsala (Sweden); Baken, Stijn, E-mail: stijn.baken@ees.kuleuven.be [Department of Earth and Environmental Sciences, Leuven University, Kasteelpark Arenberg 20 bus 2459, 3001 Leuven (Belgium); Smolders, Erik, E-mail: erik.smolders@ees.kuleuven.be [Department of Earth and Environmental Sciences, Leuven University, Kasteelpark Arenberg 20 bus 2459, 3001 Leuven (Belgium); Cubadda, Francesco, E-mail: francesco.cubadda@iss.it [Department of Food Safety and Veterinary Public Health, Istituto Superiore di Sanità, Viale Regina Elena 299, Rome 00161 (Italy); Gustafsson, Jon Petter, E-mail: jon-petter.gustafsson@slu.se [Department of Soil and Environment, Swedish University of Agricultural Sciences, P.O. Box 7014, 750 07 Uppsala (Sweden); Division of Land and Water Resources Engineering, KTH Royal Institute of Technology, Brinellvägen 28, 100 44 Stockholm (Sweden)

    2015-10-15

    Blast furnace (BF) slags are commonly applied as soil amendments and in road fill material. In Sweden they are also naturally high in vanadium. The aim of this study was to assess the vanadium bioavailability in BF slags when applied to soil. Two soils were amended with up to 29% BF slag (containing 800 mg V kg{sup −1}) and equilibrated outdoors for 10 months before conducting a barley shoot growth assay. Additional soil samples were spiked with dissolved vanadate(V) for which assays were conducted two weeks (freshly spiked) and 10 months (aged) after spiking. The BF slag vanadium was dominated by vanadium(III) as shown by V K-edge XANES spectroscopy. In contrast, results obtained by HPLC-ICP-MS showed that vanadium(V), the most toxic vanadium species, was predominant in the soil solution. Barley shoot growth was not affected by the BF slag additions. This was likely due to limited dissolution of vanadium from the BF slag, preventing an increase of dissolved vanadium above toxic thresholds. The difference in vanadium bioavailability among treatments was explained by the vanadium concentration in the soil solution. It was concluded that the vanadium in BF slag is sparingly available. These findings should be of importance in environmental risk assessment.

  7. Effect of degassing addition on the solidification segregation of nickel aluminum bronze

    Science.gov (United States)

    Syazwan, F.; Kavinjr, M.; Maghribi, S.; Ashraf, N.; Hadi, A.; Shayfull, Z.; Rashidi, M. M.

    2017-09-01

    The effect of degassing agent addition on the solidification segregation of Nickel Aluminum Bronze was investigated. The complex relationship between the development of the solidification microstructures and buildup of microsegregation in Nickel Aluminum Bronze was obtained by using microstructure analysis and EDS analysis. This experiment describes the characterization of microsegregation in Nickel Aluminum Bronze which was made using point to count microanalysis along the microstructure. With this method, the differences of elements distribution in alloys solidified in the microstructure were clearly evidenced. The results show a microstructure directly affected by segregation of elements in Nickel Aluminum Bronze matrix. There is segregation of elements in the Late To Freeze (LTF) region after solidification from melting. As for degassing treatment, higher degassing addition on the Nickel Aluminum Bronze increased the elements segregation.

  8. Partial Oxidation of n-Pentane over Vanadium Phosphorus Oxide ...

    African Journals Online (AJOL)

    NICOLAAS

    hydrocarbons using heterogeneous catalysts to produce these compounds ... catalysts produced dehydrogenated products. Here ... vation of n-pentane using V2O5 supported on hydroxyapatite as catalysts. V2O5 showed excellent redox capabilities. Selectivity towards the anhydrides (MA 40 % and PA 25 %) was obtained.

  9. Chisels in the italian Bronze Age: technological and typological aspects

    Directory of Open Access Journals (Sweden)

    Speciale, Claudia

    2010-12-01

    Full Text Available Bronze chisels are tools used “à percussion posée”; this means they need a minimum length and some functional parts (tang, body, blade; they could have a handle of perishable material and they were used with a hammer to work wood, bronze and other materials. Chisels can be classified following their functional parts; the first element is the shape (rod or socketed chisel; the second one is body section; the third one is tang section. Chronology and distribution of every type were identified to obtain a general view of this class of tools during the Italian Bronze Age.

    Los cinceles de bronce son herramientas que se utilizan en percusión apoyada (à percussion posée, por consiguiente, necesitan una longitud mínima y algunas partes funcionales (empuñadura, cuerpo, hoja; podrían tener un mango de material perecedero. Se utilizan con un martillo en el labrado de la madera, del bronce y de otros materiales. Los cinceles se pueden clasificar de acuerdo con los siguientes elementos funcionales: el primero es la forma (cincel de varilla o de cubo; el segundo es la sección del cuerpo; el tercero es la sección de la empuñadura. La cronología y la distribución de cada tipo se identificaron para obtener una visión general de esta clase de instrumentos durante la Edad del Bronce en Italia.

  10. The Effect of Chromium on the Roasting Process of Vanadium Extraction

    Directory of Open Access Journals (Sweden)

    Dong Liu

    2016-07-01

    Full Text Available We simulated the roasting process of chromium by mixing Cr2O3 and Na2CO3 to analyze the influence of chromium on roasting vanadium slag. Samples were characterized by XRD, thermal analysis and SEM at different temperatures: Cr2O3 and Na2CO3 began to react at 500 °C. When the chromium oxide content was about 3.2%, the conversion rate of V reached the maximum value of 95%.

  11. The Role of Vanadium Bromoperoxidase in the Biosynthesis of Halogenated Marine Natural Products

    OpenAIRE

    Franklin, Jayme N.

    2003-01-01

    The widespread occurrence of bromine- and chlorine-containing marine natural products has prompted investigations into the biosynthesis of halogenated marine metabolites. Halogenating enzymes, such as haloperoxidases, have long been thought to be involved in the biogenesis of halogenated marine natural products. Vanadium bromoperoxidases (V-BrPO) have been identified and isolated from all major classes of marine algae, and catalyze the two-electron oxidation of bromide by hydrogen peroxide. ...

  12. Prevention of Dealloying in Manganese Aluminium Bronze Propeller: Part II

    Directory of Open Access Journals (Sweden)

    Napachat Tareelap

    2014-03-01

    Full Text Available Due to the failure of manganese aluminium bronze (MAB propeller caused by dealloying corrosion as described in Part I [1], this work aims to study the prevention of dealloying corrosion using aluminium and zinc sacrificial anodes. The results indicated that both of the sacrificial anodes could prevent the propeller from dealloying. Moreover, the dealloying in seawater was less than that found in brackish water. It was possible that hydroxide ions, from cathodic reaction, reacted with calcium in seawater to form calcium carbonate film protecting the propeller from corrosion.

  13. Analysis of selective laser cleaning of patina on bronze coins

    Science.gov (United States)

    Buccolieri, G.; Nassisi, V.; Torrisi, L.; Buccolieri, A.; Castellano, A.; Di Giulio, M.; Giuffreda, E.; Delle Side, D.; Velardi, L.

    2014-04-01

    The patina, is the result of a large number of chemical, electrochemical and physical processes which occur spontaneously during interaction of metal surfaces with the environment. In this work we want to analyze and remove the patina in artefacts, exposed to atmosphere for various decades. Here, experimental results about the laser cleaning of bronze coins by KrF (248 nm) and Nd:YAG (532 nm) lasers are reported. Both laser wavelengths were efficient to reduce the chlorine concentration on the surface of the coins more than 80 %, as demonstrated by Energy Dispersive X-Ray Fluorescence analyses.

  14. Comparison of silica-supported MoO{sub 3} and V{sub 2}O{sub 5} catalysts in the selective partial oxidation of methane

    Energy Technology Data Exchange (ETDEWEB)

    Faraldos, M.; Banares, M.A.; Fierro, J.L.G. [Instituto de Catalisis y Petroleoquimica, Madrid (Spain)] [and others

    1996-05-01

    The catalytic effects of molybdenum oxide and vanadium oxide catalysts supported on silica have been investigated for a wide range of metal loadings in the selective oxidation of methane. Vanadium oxide catalysts tend to be more active, but produce less formaldehyde. 49 refs., 7 figs.

  15. Vanadium in marine mussels and algae.

    Science.gov (United States)

    Sperling, K R; Bahr, B; Ott, J

    2000-01-01

    A method is presented which is sensitive enough for the determination of vanadium (V) in marine organisms such as mussels and algae. It was sufficiently checked by a reference material and it was applied to V determination in blue mussels and brown algae from the German Bight.

  16. Geochemistry of vanadium (V) in Chinese coals.

    Science.gov (United States)

    Liu, Yuan; Liu, Guijian; Qu, Qinyuan; Qi, Cuicui; Sun, Ruoyu; Liu, Houqi

    2017-10-01

    Vanadium in coals may have potential environmental and economic impacts. However, comprehensive knowledge of the geochemistry of V in coals is lacking. In this study, abundances, distribution and modes of occurrence of V are reviewed by compiling >2900 reported Chinese coal samples. With coal reserves in individual provinces as the weighting factors, V in Chinese coals is estimated to have an average abundance of 35.81 μg/g. Large variation of V concentration is observed in Chinese coals of different regions, coal-forming periods, and maturation ranks. According to the concentration coefficient of V in coals from individual provinces, three regions are divided across Chinese coal deposits. Vanadium in Chinese coals is probably influenced by sediment source and sedimentary environment, supplemented by late-stage hydrothermal fluids. Specifically, hydrothermal fluids have relatively more significant effect on the enrichment of V in local coal seams. Vanadium in coals is commonly associated with aluminosilicate minerals and organic matter, and the modes of V occurrence in coal depend on coal-forming environment and coal rank. The Chinese V emission inventory during coal combustion is estimated to be 4906 mt in 2014, accounting for 50.55 % of global emission. Vanadium emissions by electric power plants are the largest contributor.

  17. Temperature dependence of thermal conductivity of vanadium ...

    Indian Academy of Sciences (India)

    Unknown

    . Cryogenic Engineering .... Thermal conductivity of vanadium substituted BPSCCO system. 441 trical resistivity as well as the small decrease ..... G, Marre D, Putti M and Siri A S 1997 Physica C273 314. Chawlek J M, Uher C, Whitaker J F and ...

  18. Role of vanadium in Bi-2223 ceramics

    Indian Academy of Sciences (India)

    Home; Journals; Pramana – Journal of Physics; Volume 54; Issue 2. Role of vanadium in Bi-2223 ceramics. D R Mishra ... higher magnetization scattering at the Cu site. The results were explained keeping in mind the liquid phase mechanism behind the formation of the 2223 phase and the possibility of magnetic scattering.

  19. An improved method of preparation of nanoparticular metal oxide catalysts

    DEFF Research Database (Denmark)

    2014-01-01

    The present invention concerns an improved method of preparation of nanoparticular vanadium oxide/anatase titania catalysts having a narrow particle size distribution. In particular, the invention concerns preparation of nanoparticular vanadium oxide/anatase titania catalyst precursors comprising...... combustible crystallization seeds upon which the catalyst metal oxide is coprecipitated with the carrier metal oxide, which crystallization seeds are removed by combustion in a final calcining step....

  20. Environmental Roots of the Late Bronze Age Crisis

    Science.gov (United States)

    Kaniewski, David; Van Campo, Elise; Guiot, Joël; Le Burel, Sabine; Otto, Thierry; Baeteman, Cecile

    2013-01-01

    The Late Bronze Age world of the Eastern Mediterranean, a rich linkage of Aegean, Egyptian, Syro-Palestinian, and Hittite civilizations, collapsed famously 3200 years ago and has remained one of the mysteries of the ancient world since the event’s retrieval began in the late 19th century AD/CE. Iconic Egyptian bas-reliefs and graphic hieroglyphic and cuneiform texts portray the proximate cause of the collapse as the invasions of the “Peoples-of-the-Sea” at the Nile Delta, the Turkish coast, and down into the heartlands of Syria and Palestine where armies clashed, famine-ravaged cities abandoned, and countrysides depopulated. Here we report palaeoclimate data from Cyprus for the Late Bronze Age crisis, alongside a radiocarbon-based chronology integrating both archaeological and palaeoclimate proxies, which reveal the effects of abrupt climate change-driven famine and causal linkage with the Sea People invasions in Cyprus and Syria. The statistical analysis of proximate and ultimate features of the sequential collapse reveals the relationships of climate-driven famine, sea-borne-invasion, region-wide warfare, and politico-economic collapse, in whose wake new societies and new ideologies were created. PMID:23967146

  1. The Umm Al Binni Structure and Bronze Age Catastrophes

    Science.gov (United States)

    Hamacher, Duane W.

    Archaeological excavations of sites dating from 2200 BCE and 1200 BCE in the Middle East, Asia Minor, and southeast Europe provide evidence that a large scale disaster affected Bronze Age civilizations. There are numerous debates as to whether this was caused by warfare, a large-scale natural disaster, or some other factor. In 2001, Sharad Master used satellite images to discover a possible Holocene impact structure in the Al 'Amarah marshes of southern Iraq, known as Umm al Binni lake. With an estimated age of impact, I show that although destructive forces would have damaged Sumerian cities within a few hundred km of the coast, it is unlikely that this single impact would have caused the large-scale destruction seen over the larger region. The impact origin of the structure is unconfirmed and any connection to Bronze Age catastrophes remains speculative. Errata: Table 4 provides a list of impact sites, three of which are associated with nickel-iron impactors and therefore cannot be from a "fragmented comet".

  2. Environmental roots of the late bronze age crisis.

    Science.gov (United States)

    Kaniewski, David; Van Campo, Elise; Guiot, Joël; Le Burel, Sabine; Otto, Thierry; Baeteman, Cecile

    2013-01-01

    The Late Bronze Age world of the Eastern Mediterranean, a rich linkage of Aegean, Egyptian, Syro-Palestinian, and Hittite civilizations, collapsed famously 3200 years ago and has remained one of the mysteries of the ancient world since the event's retrieval began in the late 19(th) century AD/CE. Iconic Egyptian bas-reliefs and graphic hieroglyphic and cuneiform texts portray the proximate cause of the collapse as the invasions of the "Peoples-of-the-Sea" at the Nile Delta, the Turkish coast, and down into the heartlands of Syria and Palestine where armies clashed, famine-ravaged cities abandoned, and countrysides depopulated. Here we report palaeoclimate data from Cyprus for the Late Bronze Age crisis, alongside a radiocarbon-based chronology integrating both archaeological and palaeoclimate proxies, which reveal the effects of abrupt climate change-driven famine and causal linkage with the Sea People invasions in Cyprus and Syria. The statistical analysis of proximate and ultimate features of the sequential collapse reveals the relationships of climate-driven famine, sea-borne-invasion, region-wide warfare, and politico-economic collapse, in whose wake new societies and new ideologies were created.

  3. The bronze signum from Timacum Maius and its cultic attribution

    Directory of Open Access Journals (Sweden)

    Petrović Vladimir

    2016-01-01

    Full Text Available The bronze signum discussed in this paper was discovered by archaeological ex­cavation on the site of Timacum Maius in 2010. Found in the area of a luxurious Roman-period building, the artefact shows a tapering body with a central conical socket similar to a spearhead socket. It is one of the twenty-three known signa of the so-called classical-type. Most of them were found in the context of the cult of Jupiter Dolichenus, and we also presume the cultic purpose of the bronze signum from Timacum Maius. A similar find comes from Jupiter Dolichenus’ shrine in Egeta on the Danube limes with an inscription that connects it directly with the Dolichenian cult, and with the First Cohort of Cretans (Cohors I Cretum, the unit which had previously been stationed at Timacus Maius. The signum from Timacum Maius is most likely also connected with the cult of Jupiter Dolichenus and chronologically belongs to a period which is much earlier than the Severan age. [Projekat Ministarstva nauke Republike Srbije, 177012: Society, spiritual and material culture and communications in prehistory and early history of the Balkans

  4. The KCaSrTa5O15 photocatalyst with tungsten bronze structure for water splitting and CO2 reduction.

    Science.gov (United States)

    Takayama, Tomoaki; Tanabe, Kentaro; Saito, Kenji; Iwase, Akihide; Kudo, Akihiko

    2014-11-28

    KCaSrTa5O15 with tungsten bronze structure and a band gap of 4.1 eV showed activity for water splitting without cocatalysts. The activity was improved by loading the NiO cocatalyst. The apparent quantum yield of optimized NiO-loaded KCaSrTa5O15 was 2.3% at 254 nm for water splitting. When CO2 gas was bubbled into the reactant aqueous solution, Ag cocatalyst-loaded KCaSrTa5O15 produced CO and H2 as reduction products of CO2 and H2O, respectively, and O2 as an oxidation product of H2O. The carbon source of CO was confirmed to be CO2 molecules by using (13)CO2. The ratio of the number of electrons to that of holes calculated from the amounts of products (CO, H2 and O2) was almost unity. Additionally, the ratio of the turnover number of electrons consumed for CO production to the total number of an Ag atom of the cocatalyst that was the active site for CO2 reduction was 8.6 at 20 h. These results indicate that water was consumed as an electron donor for this photocatalytic CO2 reduction in an aqueous medium. Thus, KCaSrTa5O15 with tungsten bronze structure has arisen as a new photocatalyst that is active for water splitting and CO2 reduction utilizing water as an electron donor.

  5. Electrochemistry of vanadium(II and the electrodeposition of aluminum-vanadium alloys in the aluminum chloride-1-ethyl-3-methylimidazolium chloride molten salt

    Directory of Open Access Journals (Sweden)

    Tsuda T.

    2003-01-01

    Full Text Available The electrochemical behavior of vanadium(II was examined in the 66.7-33.3 mole percent aluminum chloride-1-ethyl-3-methylimidazolium chloride molten salt containing dissolved VCl2 at 353 K. Voltammetry experiments revealed that V(II could be electrochemically oxidized to V(III and V(IV. However at slow scan rates the V(II/V(III electrode reaction is complicated by the rapid precipitation of V(III as VCl3. The reduction of V(II occurs at potentials considerably negative of the Al(III/Al electrode reaction, and Al-V alloys cannot be electrodeposited from this melt. However electrodeposition experiments conducted in VCl2-saturated melt containing the additive, 1-ethyl-3-methylimidazolium tetrafluoroborate, resulted in Al-V alloys. The vanadium content of these alloys increased with increasing cathodic current density or more negative applied potentials. X-ray analysis of Al-V alloys that were electrodeposited on a rotating copper wire substrate indicated that these alloys did not form or contain an intermetallic compound, but were non-equilibrium or metastable solid solutions. The chloride-pitting corrosion properties of these alloys were examined in aqueous NaCl by using potentiodynamic polarization techniques. Alloys containing ~10 a/o vanadium exhibited a pitting potential that was 0.3 V positive of that for pure aluminum.

  6. Palaeoethnobotanical Data from the High Mountainous Early Bronze Age Settlement of Tsaghkasar-1 (Mt. Aragats, Armenia

    Directory of Open Access Journals (Sweden)

    Roman Hovsepyan

    2011-09-01

    Full Text Available Palaeoethnobotanical investigations suggest that at least part of the Early Bronze Age population of Tsaghkasar was settled and practiced agriculture in the high mountainous zone. People there appear to have cultivated hexa‐ and tetraploid wheats (probably bread wheat and emmer and barley (possibly hulled. Bronze Age agriculture in the Southern Caucasus differs from earlier and later period when cultivation of pulses, oil‐producing plants, and other plants was common. This emphasis on the cultivation and use of certain cereal grains at Early Bronze sites such as Tsaghkasar can tentatively be added to a constellation of practices associated with the Kura‐Araxes culture in the South Caucasus.

  7. Speciation of vanadium in Chinese cabbage (Brassica rapa L.) and soils in response to different levels of vanadium in soils and cabbage growth.

    Science.gov (United States)

    Tian, Liyan; Yang, Jinyan; Alewell, Christine; Huang, Jen-How

    2014-09-01

    This study highlights the accumulation and speciation of vanadium in Chinese cabbage (Brassica rapa L.) in relation to the speciation of soil vanadium with pot experiments at 122-622mgVkg(-1) by spiking NH4VO3. Cabbage planting decreased the bioavailable and residual vanadium based on sequential extraction, leading to enrichment of oxalate-extractable vanadium in soils. The biomass production increased with increasing concentrations of soil vanadium from 122 to 372mgVkg(-1), probably due to the increasing nitrogen availability and low vanadium availability in our soils with a consequent low vanadium toxicity. Although the concentrations of root vanadium (14.4-24.9mgVkg(-1)) related positively with soil vanadium, the bio-dilution alleviated the increase of leaf vanadium (2.1-2.7mgVkg(-1)). The predominance of vanadium(IV) in leaves (∼60-80% of total vanadium) indicates bio-reduction of vanadium in Chinese cabbage, since the mobile vanadium in oxic soils was usually pentavalent. Approximately 15-20% of the leaf vanadium was associated with recalcitrant leaf tissues. The majority of leaf vanadium was water and ethanol extractable, which is considered mobile and may cause more toxic effects on Chinese cabbage. Copyright © 2014 Elsevier Ltd. All rights reserved.

  8. Geochemistry and mineralogy of vanadium in mine tailings at Berg Aukas, northeastern Namibia

    Science.gov (United States)

    Sracek, O.; Mihaljevič, M.; Kříbek, B.; Majer, V.; Filip, J.; Vaněk, A.; Penížek, V.; Ettler, V.; Mapani, B.

    2014-08-01

    Vanadium-rich mine tailings at Berg Aukas, site with a world-known vanadium mineralization in northeastern Namibia, were investigated using a combination of solid phase and mineralogical analyses, leaching tests and speciation modeling. Principal objective of the study was to determine, if vanadium can be released into the environment. In spite of >30 y of weathering and oxidation of tailings material to a maximum sampling depth of 2.4 m, a large portion of V still remains in the primary mineral descloizite, (Pb, Zn)2(OH)VO4. A part of V was mobilized and adsorbed/co-precipitated with ferric oxyhydroxides. Based on sequential extraction and 57Fe Mössbauer spectroscopy, a large amount of ferric iron is present in insoluble hematite and goethite, where V is effectively bound. Other potential contaminants are Zn, present mostly in the primary mineral willemite, Zn2SiO4, descloizite and also in secondary smithsonite, ZnCO3; and Pb, which was transferred from completely dissolved galena to cerussite, PbCO3 and is also partly present in primary descloizite. Conditions in the mine tailings are alkaline (pH generally >8.2) and oxidizing during dry period, but mobility of V is low due to low solubility of descloizite and secondary crystalline ferric phases such as hematite. In contrast, Zn and especially Pb in secondary carbonates, probably represent more serious environmental and health risks.

  9. Optimal Location of Vanadium in Muscovite and Its Geometrical and Electronic Properties by DFT Calculation

    OpenAIRE

    Qiushi Zheng; Yimin Zhang; Tao Liu; Jing Huang; Nannan Xue; Qihua Shi

    2017-01-01

    Vanadium-bearing muscovite is the most valuable component of stone coal, which is a unique source of vanadium manufacture in China. Numbers of experimental studies have been carried out to destroy the carrier muscovite’s structure for efficient extraction of vanadium. Hence, the vanadium location is necessary for exploring the essence of vanadium extraction. Although most infer that vanadium may substitute for trivalent aluminium (Al) as the isomorphism in muscovite for the similar atomic rad...

  10. History of a Bronze Age tell and its environment

    Science.gov (United States)

    Kovács, Gabriella; Füleky, György; Vicze, Magdolna

    2016-04-01

    Százhalombatta-Földvár is the most excessively researched Bronze Age tell site in Hungary. Parallel to the investigation of the settlement structure and activity patterns the changes of the landscape and the effect of human alteration is also studied. Significant changes of the landscape can be detected from the Bronze Age until the recent natural and cultural heritage protection of the area. Archaeological, soil analytical and thin section soil micromorphological methods are used to reconstruct the past 4000 years of the tell and its immediate surroundings. Prior to the Bronze Age the area was covered by forest vegetation, so the initial settling could only be realised after deforestation (2000 BC). The result of the soil corings and the prepared soil thin sections are solid proves of this action. It also became evident that at some areas - so far it seems that at locales where house floors were laid for the very first time - even the topsoil was removed so intensively that only the B horizon of the relict forest soil can be found. This observation needs to be further tested outside the habitation area to define the horizontal extension of the forest clearance and the topsoil removal. The northern side of the settlement is bordered by a natural erosion gully. At 2000 BC it was just a natural depression, but by 1500 BC it was deepened to serve as a fortification ditch. Around 1200 BC the ditch started to be filled in and by 1000 BC it was refilled to such an extent that its surface was utilised again. At about 600 BC (Late Iron Age) a smaller inner rampart was erected on the southern side of the ditch for inner separation. Not much is known about the Roman period of this area (200 AD) but the remnants of a watchtower indicate their presence. During the 18th century AD the area was used for grape cultivation and later for hobby gardens up until the protection of the area in the late 20th century. Since then species of the original vegetation started to grow back

  11. Extraction of Vanadium from Vanadium Slag Via Non-salt Roasting and Ammonium Oxalate Leaching

    Science.gov (United States)

    Li, Meng; Du, Hao; Zheng, Shili; Wang, Shaona; Zhang, Yang; Liu, Biao; Dreisinger, David Bruce; Zhang, Yi

    2017-10-01

    A clean method featuring non-salt roasting followed by (NH4)2C2O4 leaching to recover vanadium from vanadium slag was proposed. The carcinogenic Cr6+ compounds and exhaust gases were avoided, and the water generated from vanadate precipitation may be recycled and reused in this new leaching process. The leaching residues may be easily used by a blast furnace. Moreover, (NH4)2C2O4 solution was used as a leaching medium to avoid expensive and complicated ammonium controlling operations as a result of the stability of (NH4)2C2O4 at a high temperature. The transformation mechanisms of vanadium- and chromium-bearing phases were systematically investigated by x-ray diffraction analysis and scanning electron microscopy with energy-disperse x-ray spectrometry, respectively. In addition, the effects of oxygen concentration, roasting temperature, and holding time on vanadium recovery were investigated. Finally, the effects of leaching variables on the vanadium leaching rate were also examined.

  12. Discrepancy between theory and measurement of superconducting vanadium

    Science.gov (United States)

    Zheng, X. H.; Walmsley, D. G.

    2015-08-01

    We have extracted consistent phonon dispersion information out of rather inconsistent vanadium X-ray scattering data from synchrotron and vacuum tube sources. With this and a new theoretical approach we have made firm predictions for the tunnelling conductance of superconducting vanadium; it is in unusually poor agreement with experimentally measured values. We argue that the problem lies in the experimental measurement rather than the theory. The preparation of a suitable high quality tunnel barrier on vanadium represents an outstanding challenge.

  13. Chemical speciation of vanadium in coal bottom Ash

    Energy Technology Data Exchange (ETDEWEB)

    Aydin, Firat; Aydin, Isil; Hamamci, Candan [Science Faculty, Chemistry Department, Dicle University, Diyarbakir (Turkey); Saydut, Abdurrahman [Engineering Faculty, Mining Engineering Department, Dicle University, Diyarbakir (Turkey); Gunduz, Beniz [Science Faculty, Chemistry Department, Selcuk University, Konya (Turkey)

    2012-04-15

    Chemical speciation of vanadium is important to understand the true nature of this element in the environment as well as its biochemical pathways. Sample pretreatment, preparation, and chemical speciation methods were applied for vanadium in coal bottom ash here. Two-stage microwave acid digestion was used to preparation of samples. Determination of vanadium was performed using inductively coupled plasma-optical emission spectrometry (ICP-OES). Speciation of vanadium was carried out using a seven-step sequential extraction procedure of the coal bottom ash each releasing species of vanadium: Water soluble, exchangeable, carbonate, reducible, oxidizable, sulfide, and residual fractions. Total vanadium concentration in the coal bottom ash is 701 mg kg{sup -1} d.w. The most abundant form of vanadium in coal bottom ash is residual fraction of vanadium (196 mg kg{sup -1} d.w.). Relative abundances of the remaining vanadium fractions in coal bottom ash are as follows: Reducible (176 mg kg{sup -1} d.w.) > sulfide (176 mg kg{sup -1} d.w.) > carbonate (85 mg kg{sup -1} d.w.) > oxidizable (50 mg kg{sup -1} d.w.) > water soluble (10.6 mg kg{sup -1} d.w.) > exchangeable (9.0 mg kg{sup -1} d.w.). (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. Microadditions of boron and vanadium in ADI

    Directory of Open Access Journals (Sweden)

    Rzychoń T.

    2007-01-01

    Full Text Available In the second part of the study, describing the role of vanadium and boron microadditions in the process of structure formation in heavy-walled castings made from ADI, the results of own investigations were presented. Within this study two series of melts of the ductile iron were made, introducing microadditions of the above mentioned elements to both unalloyed ductile iron and the ductile iron containing high levels of nickel and copper (the composition typical of ADI. Melts were conducted with iron-nickel-magnesium master alloy. Thermal analysis of the solidification process of the cast keel blocks was conducted, the heat treatment of the alloys was carried out, and then the effect of the introduced additions of boron and vanadium on the hardenability of the investigated cast iron was examined and evaluated.

  15. Vanadium in fuel oil - a new solution

    Energy Technology Data Exchange (ETDEWEB)

    Czech, N. [Siemens, Muelheim (Germany); Finckh, H. [Siemens, Erlangen (Germany)

    1998-11-01

    Hot corrosion of the hot-gas-path components due to vanadium contamination is one of the hazards associated with heavy residual oil combustion in heavy-duty gas turbines. This economically attractive oil combustion process has benefited from the recently developed vanadium inhibition technique, which is currently being tested at the Valladolid 220 MWe combined cycle plant in Mexico. The method uses atomization of a dilute aqueous solution of Epsom salt (MgSO{sub 7},7H{sub 2}O) into very small droplets which are then injected onto the flame where intensive mixing takes place. The successful use of this new technique promises extended operating periods between cleanup operations, and cost reductions from the use of inexpensive materials, as well as the ability to operate advanced gas turbines on difficult fuels, not previously feasible. (UK)

  16. Irradiation creep of vanadium-base alloys

    Energy Technology Data Exchange (ETDEWEB)

    Tsai, H.; Billone, M.C.; Strain, R.V.; Smith, D.L. [Argonne National Lab., IL (United States); Matsui, H. [Tohoku Univ. (Japan)

    1998-03-01

    A study of irradiation creep in vanadium-base alloys is underway with experiments in the Advanced Test Reactor (ATR) and the High Flux Isotope Reactor (HFIR) in the United States. Test specimens are thin-wall sealed tubes with internal pressure loading. The results from the initial ATR irradiation at low temperature (200--300 C) to a neutron damage level of 4.7 dpa show creep rates ranging from {approx}0 to 1.2 {times} 10{sup {minus}5}/dpa/MPa for a 500-kg heat of V-4Cr-4Ti alloy. These rates were generally lower than reported from a previous experiment in BR-10. Because both the attained neutron damage levels and the creep strains were low in the present study, however, these creep rates should be regarded as only preliminary. Substantially more testing is required before a data base on irradiation creep of vanadium alloys can be developed and used with confidence.

  17. Hazardous waste to materials: recovery of molybdenum and vanadium from acidic leach liquor of spent hydroprocessing catalyst using alamine 308.

    Science.gov (United States)

    Sahu, K K; Agrawal, Archana; Mishra, D

    2013-08-15

    Recovery of valuable materials/metals from waste goes hand in hand with environmental protection. This paper deals with the development of a process for the recovery of metals such as Mo, V, Ni, Al from spent hydroprocessing catalyst which may otherwise cause a nuisance if dumped untreated. A detailed study on the separation of molybdenum and vanadium from the leach solution of spent hydroprocessing catalyst of composition: 27.15% MoO₃, 1.7% V₂O₅, 3.75% NiO, 54.3% Al₂O₃, 2.3% SiO₂ and 10.4% LOI is reported in this paper. The catalyst was subjected to roasting under oxidizing atmosphere at a temperature of about 550 °C and leaching in dilute sulphuric acid to dissolve molybdenum, vanadium, nickel and part of aluminium. Metals from the leach solution were separated by solvent extraction. Both molybdenum and vanadium were selectively extracted with a suitable organic solvent leaving nickel and dissolved aluminium in the raffinate. Various parameters such as initial pH of the aqueous feed, organic to aqueous ratio (O:A), solvent concentration etc. were optimized for the complete extraction and recovery of Mo and V. Molybdenum and vanadium from the loaded organic were stripped by ammonia solution. They were recovered as their corresponding ammonium salt by selective precipitation, and were further calcined to get the corresponding oxides in pure form. Copyright © 2013 Elsevier Ltd. All rights reserved.

  18. LAMQS analysis applied to ancient Egyptian bronze coins

    Energy Technology Data Exchange (ETDEWEB)

    Torrisi, L., E-mail: lorenzo.torrisi@unime.i [Dipartimento di Fisica dell' Universita di Messina, Salita Sperone, 31, 98166 Messina (Italy); Caridi, F.; Giuffrida, L.; Torrisi, A. [Dipartimento di Fisica dell' Universita di Messina, Salita Sperone, 31, 98166 Messina (Italy); Mondio, G.; Serafino, T. [Dipartimento di Fisica della Materia ed Ingegneria Elettronica dell' Universita di Messina, Salita Sperone, 31, 98166 Messina (Italy); Caltabiano, M.; Castrizio, E.D. [Dipartimento di Lettere e Filosofia dell' Universita di Messina, Polo Universitario dell' Annunziata, 98168 Messina (Italy); Paniz, E.; Salici, A. [Carabinieri, Reparto Investigazioni Scientifiche, S.S. 114, Km. 6, 400 Tremestieri, Messina (Italy)

    2010-05-15

    Some Egyptian bronze coins, dated VI-VII sec A.D. are analyzed through different physical techniques in order to compare their composition and morphology and to identify their origin and the type of manufacture. The investigations have been performed by using micro-invasive analysis, such as Laser Ablation and Mass Quadrupole Spectrometry (LAMQS), X-ray Fluorescence (XRF), Laser Induced Breakdown Spectroscopy (LIBS), Electronic (SEM) and Optical Microscopy, Surface Profile Analysis (SPA) and density measurements. Results indicate that the coins have a similar bulk composition but significant differences have been evidenced due to different constituents of the patina, bulk alloy composition, isotopic ratios, density and surface morphology. The results are in agreement with the archaeological expectations, indicating that the coins have been produced in two different Egypt sites: Alexandria and Antinoupolis. A group of fake coins produced in Alexandria in the same historical period is also identified.

  19. Microadditions of boron and vanadium in ADI

    OpenAIRE

    Rzychoń T.; Kiełbus A.; Szala J.

    2007-01-01

    In the second part of the study, describing the role of vanadium and boron microadditions in the process of structure formation in heavy-walled castings made from ADI, the results of own investigations were presented. Within this study two series of melts of the ductile iron were made, introducing microadditions of the above mentioned elements to both unalloyed ductile iron and the ductile iron containing high levels of nickel and copper (the composition typical of ADI). Melts were conducted ...

  20. Determination of Leachable Vanadium (V) in Sediment

    African Journals Online (AJOL)

    NICO

    USA) were used for the filtration of sample solutions. RESEARCH ... were transferred to a Teflon beaker and treated on a hot plate at about 110 °C ... Table 1 Thermal programme for the determination of vanadium using. ET-AAS. Step. Temperature/°C. Ramp/s–1. Hold/s–1. Internal gas flow/mL min–1. 1. 120. 1. 10. 250. 2.

  1. Characterization of vanadium flow battery. Revised

    Energy Technology Data Exchange (ETDEWEB)

    Bindner, H.; Ekman, C.; Gehrke, O.; Isleifsson, F.

    2011-02-15

    This report summarizes the work done at Risoe-DTU testing a vanadium flow battery as part of the project ''Characterisation of Vanadium Batteries'' (ForskEl project 6555) with the partners PA Energy A/S and OI Electric A/S under the Danish PSO energy research program. A 15kW/120kWh vanadium battery has been installed as part of the distributed energy systems experimental facility, SYSLAB, at Risoe DTU. A test programme has been carried out to get hands-on experience with the technology, to characterize the battery from a power system point of view and to assess it with respect to integration of wind energy in the Danish power system. The battery has been in operation for 18 months. During time of operation the battery has not shown signs of degradation of performance. It has a round-trip efficiency at full load of approximately 60% (depending on temperature and SOC). The sources of the losses are power conversion in cell stacks/electrolyte, power converter, and auxiliary power consumption from pumps and controller. The efficiency was not influenced by the cycling of the battery. The response time for the battery is limited at 20kW/s by the ramp rate of the power converter. The battery can thus provide power and frequency support for the power system. The battery was operated together with a 11kW stall-regulated Gaia wind turbine to smooth the output of the wind turbine and during the tests the battery proved capable of firming the output of the wind turbine. Vanadium battery is a potential technology for storage based services to the power system provided investment and O and M cost are low enough and long term operation is documented. (Author)

  2. Vanadium proton exchange membrane water electrolyser

    Science.gov (United States)

    Noack, Jens; Roznyatovskaya, Nataliya; Pinkwart, Karsten; Tübke, Jens

    2017-05-01

    In order to reverse the reactions of vanadium oxygen fuel cells and to regenerate vanadium redox flow battery electrolytes that have been oxidised by atmospheric oxygen, a vanadium proton exchange membrane water electrolyser was set up and investigated. Using an existing cell with a commercial and iridium-based catalyst coated membrane, it was possible to fully reduce V3.5+ and V3+ solutions to V2+ with the formation of oxygen and with coulomb efficiencies of over 96%. The cell achieved a maximum current density of 75 mA/cm2 during this process and was limited by the proximity of the V(III) reduction to the hydrogen evolution reaction. Due to the specific reaction mechanisms of V(IV) and V(III) ions, V(III) solutions were reduced with an energy efficiency of 61%, making this process nearly twice as energy efficient as the reduction of V(IV) to V(III). Polarisation curves and electrochemical impedance spectroscopy were used to further investigate the losses of half-cell reactions and to find ways of further increasing efficiency and performance levels.

  3. Influence Cr on Crystallization and the Phase Transformations of the Bronze BA1044

    Directory of Open Access Journals (Sweden)

    B. P. Pisarek

    2007-07-01

    Full Text Available The investigations were introduced in the paper, method of thermal and derivative analysis (TDA, the process of crystallization and phase transformation in the solid state of the aluminium bronze CuA110Fe4Ni4 (BA1044 and with the addition 0.3% Cr. Two intermetallic phase were identified in the microstructure of the bronze BA1044: κFel - rich in Fe and Cu and κFe2 - rich in Fe, and in the microstructure of the bronze BA1044+0.3 % Cr only one phase κFel - rich in Fe, Cu and Cr. The presence of chrome in the bronze BA1044 reduce size the primary crystals of the phase β, reduces the dynamics of the processes of thermal phase transformation in the solid state and lengthens the time their of duration.

  4. Characterisation of Late Bronze Age large size shield nails by EDXRF, micro-EDXRF and X-ray digital radiography

    Energy Technology Data Exchange (ETDEWEB)

    Figueiredo, E., E-mail: elin@itn.pt [Instituto Tecnologico e Nuclear, Estrada Nacional 10, 2686-953 Sacavem (Portugal); CENIMAT/I3N, Departamento de Ciencia dos Materiais, Faculdade de Ciencias e Tecnologia, Universidade Nova de Lisboa, 2829-516 Monte de Caparica (Portugal); Departamento de Conservacao e Restauro, Faculdade de Ciencias e Tecnologia, Universidade Nova de Lisboa, 2829-516 Monte de Caparica (Portugal); Araujo, M.F. [Instituto Tecnologico e Nuclear, Estrada Nacional 10, 2686-953 Sacavem (Portugal); Silva, R.J.C. [CENIMAT/I3N, Departamento de Ciencia dos Materiais, Faculdade de Ciencias e Tecnologia, Universidade Nova de Lisboa, 2829-516 Monte de Caparica (Portugal); Senna-Martinez, J.C. [Centro de Arqueologia (Uniarq), Faculdade de Letras, Universidade de Lisboa, 1600-214 Lisboa (Portugal); Ines Vaz, J.L. [Departamento de Letras, Universidade Catolica, Estrada da Circunvalacao, 3504-505 Viseu (Portugal)

    2011-09-15

    In the present study six exceptional large size metallic nails, a dagger and a sickle from the Late Bronze Age archaeological site of Figueiredo das Donas (Central Portugal) have been analysed by EDXRF, micro-EDXRF and X-ray digital radiography for the study of material composition and technology of fabrication. The combination of these analytical and examination techniques showed that all artefacts are made of bronze with As, Sb and Pb impurities, and that the nails were most likely manufactured using the casting-on technique. These results reinforce the use of binary bronze by Late Bronze Age in the region, and the incorporation of new fabrication technologies that resulted from ancient spheres of interaction. - Highlights: > EDXRF, micro-EDXRF and X-ray digital radiography in cultural heritage studies. > Archaeometallurgical study of a Late Bronze Age artefact collection from Portugal. > Practise of a specific and traditional bronze metallurgy. > Appearance of technological innovations as the casting-on technique.

  5. Fragility–structure–conductivity relations in vanadium tellurite glass

    DEFF Research Database (Denmark)

    Kjeldsen, Jonas; Yue, Yuanzheng; Rodrigues, Ana Candida Martins

    the ability to intercalate lithium-ions, it is a candidate as cathode material. Here, we investigate the correlation between liquid fragility, structure and electronic conductivity in a series of vanadium-tellurite glasses with varying vanadium concentration. We measure dynamic and thermodynamic fragility...

  6. Combined effect of vanadium and nickel on lipid peroxidation and ...

    African Journals Online (AJOL)

    use

    2011-12-12

    Dec 12, 2011 ... Signs of toxicity were observed following treatment with vanadium, not nickel nor combined vanadium and .... Kazakhstan. Animal treatment. Outbred 3-month-old male albino rats, weighing between 230 to. 235 g (mean) at the beginning of experiment, were obtained from ..... Vitamin E supplementation.

  7. Synergistic extraction of vanadium (V, IV) with dithizone

    Energy Technology Data Exchange (ETDEWEB)

    Akaiwa, H.; Kawamoto, H.; Hiyamuta, E. (Gunma Univ., Kiryu (Japan). Faculty of Technology)

    1981-11-01

    By employing the synergistic extraction technique, vanadium (V, IV) has been found to form the primary dithizonate in the presence of a synergist. The extraction of the element proceeds according to the following equations. VO/sub 2//sup +/ + H/sub 2/dz,sub(org) + TBPO sub(org) reversible VO/sub 2/(Hdz)(TBPO)sub(org) + H/sup +/, and VOOH/sup +/ + H/sub 2/dz,sub(org) + TOPO sub(org) reversible VOOH(Hdz)(TOPO)sub(org) + H/sup +/, where H/sub 2/dz, TBPO, and TOPO denote dithizone, tributylphosphine oxide and trioctylphosphine oxide, respectively, and the subscript org indicates the benzene phase. The resulting adduct VO/sub 2/(Hdz)(TBPO) has an absorption maximum at 503 nm and is stable for at least 1 h. However, the red color of VOOH(Hdz)(TOPO) in benzene fades away during the standing time, probably due to the dimerization of the initially extracted monomeric species.

  8. Vanadium Extraction from Shale via Sulfuric Acid Baking and Leaching

    Science.gov (United States)

    Shi, Qihua; Zhang, Yimin; Liu, Tao; Huang, Jing

    2018-01-01

    Fluorides are widely used to improve vanadium extraction from shale in China. Sulfuric acid baking-leaching (SABL) was investigated as a means of recovering vanadium which does not require the use of fluorides and avoids the productions of harmful fluoride-containing wastewater. Various effective factors were systematically studied and the experimental results showed that 90.1% vanadium could be leached from the shale. On the basis of phase transformations and structural changes after baking the shale, a mechanism of vanadium extraction from shale via SABL was proposed. The mechanism can be described as: (1) sulfuric acid diffusion into particles; (2) the formation of concentrated sulfuric acid media in the particles after water evaporation; (3) hydroxyl groups in the muscovite were removed and transient state [SO4 2-] was generated; and (4) the metals in the muscovite were sulfated by active [SO4 2-] and the vanadium was released. Thermodynamics modeling confirmed this mechanism.

  9. Exploring electrolyte preference of vanadium nitride supercapacitor electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Bo; Chen, Zhaohui; Lu, Gang [Department of Electrical Engineering and Automation, Luoyang Institute of Science and Technology, Luoyang 471023 (China); Wang, Tianhu [School of Electrical Information and Engineering, Jiangsu University of Technology, Changzhou 213001 (China); Ge, Yunwang, E-mail: ywgelit@126.com [Department of Electrical Engineering and Automation, Luoyang Institute of Science and Technology, Luoyang 471023 (China)

    2016-04-15

    Highlights: • Hierarchical VN nanostructures were prepared on graphite foam. • Electrolyte preference of VN supercapacitor electrodes was explored. • VN showed better capacitive property in organic and alkaline electrolytes than LiCl. - Abstract: Vanadium nitride hierarchical nanostructures were prepared through an ammonia annealing procedure utilizing vanadium pentoxide nanostructures grown on graphite foam. The electrochemical properties of hierarchical vanadium nitride was tested in aqueous and organic electrolytes. As a result, the vanadium nitride showed better capacitive energy storage property in organic and alkaline electrolytes. This work provides insight into the charge storage process of vanadium nitride and our findings can shed light on other transition metal nitride-based electrochemical energy storage systems.

  10. Vanadium and vanadium nitride thin films grown by high power impulse magnetron sputtering

    Science.gov (United States)

    Hajihoseini, H.; Gudmundsson, J. T.

    2017-12-01

    Thin vanadium and vanadium nitride films were grown on SiO2 by non-reactive and reactive high power impulse magnetron sputtering (HiPIMS), respectively. The film properties were compared to films grown by conventional dc magnetron sputtering (dcMS) at similar conditions. We explored the influence of the stationary magnetic confinement field strength on the film properties and the process parameters. The deposition rate is much lower for non-reactive sputtering by HiPIMS than for dcMS. Furthermore, for both dcMS and HiPIMS the deposition rate is lower for strong magnetic confinement. Structural characterization was carried out using x-ray diffraction and reflection methods as well as atomic force microscopy and scanning electron microscope. Both dcMS and HiPIMS grown vanadium films are polycrystalline with similar grain size regardless of magnetic field strength. For dcMS grown vanadium films the surface roughness is higher when a strong magnetic field is used. For both non-reactive growth of vanadium and reactive growth of vanadium nitride the HiPIMS process produces denser films with lower surface roughness than dcMS does. Lowering the magnetic field strength increases the deposition rate significantly for reactive HiPIMS while it increases only slightly in the reactive dcMS case. The films grown by HiPIMS with strong magnetic confinement exhibit higher density and lower roughness. We find that the operating pressure, growth temperature, discharge voltage and film thickness has influence on the properties of HiPIMS grown vanadium nitride films. The films are denser when grown at high temperature, high discharge voltage and low pressure. The density of those films is lower for thicker films and thicker films consist of larger grain size. For all the films explored, higher density coincides with lower surface roughness. Thus, the deposition method, magnetic field strength, growth temperature, discharge voltage, film thickness and growth pressure have a significant

  11. Mechanism of Enhancing Extraction of Vanadium from Stone Coal by Roasting with MgO

    Directory of Open Access Journals (Sweden)

    Fang Chen

    2017-02-01

    Full Text Available In this paper, the extraction of vanadium from stone coal by roasting with MgO and leaching with sulfuric acid has been investigated, and the mechanism analysis of stone coal roasting with MgO was studied. The results indicated that under the conditions that the mass fraction of the particles with grain size of 0–0.074 mm in raw ore was 75%, the roasting temperature was 500 °C, the roasting time was 1 h, MgO addition was 3 wt %, the sulfuric acid concentration was 20 vol %, the liquid-to-solid ratio was 1.5 mL/g, the leaching temperature was 95 °C, and leaching time was 2 h, resulting in a vanadium leaching efficiency of 86.63%, which increased by 7.73% compared with that of blank roasting. The mechanism analysis showed that the degree of calcite decomposition was low and, thus, magnesium vanadate was more easily formed than calcium vanadate below 500 °C. Moreover, magnesium vanadate was easier to dissolve than calcium vanadate during the sulfuric acid leaching process. Thus, the vanadium leaching efficiency was enhanced by using MgO as a roasting additive below 500 °C. Additionally, at high temperature the formation of tremolite would consume calcium oxide produced from the decomposition of calcite, thus, the formation of calcium vanadate was hindered, and V2O5 would react with MgO to form magnesium vanadate. Therefore, the vanadium leaching efficiency of roasting with MgO was higher than that of blank roasting at high temperature.

  12. 40 CFR 440.30 - Applicability; description of the uranium, radium and vanadium ores subcategory.

    Science.gov (United States)

    2010-07-01

    ... for the extraction of uranium, radium and vanadium. Only vanadium byproduct production from uranium... uranium, radium and vanadium ores subcategory. 440.30 Section 440.30 Protection of Environment... SOURCE CATEGORY Uranium, Radium and Vanadium Ores Subcategory § 440.30 Applicability; description of the...

  13. Vanadium bromoperoxidase-catalyzed biosynthesis of halogenated marine natural products.

    Science.gov (United States)

    Carter-Franklin, Jayme N; Butler, Alison

    2004-11-24

    Marine red algae (Rhodophyta) are a rich source of bioactive halogenated natural products. The biogenesis of the cyclic halogenated terpene marine natural products, in particular, has attracted sustained interest in part because terpenes are the biogenic precursors of many bioactive metabolites. The first enzymatic asymmetric bromination and cyclization of a terpene, producing marine natural products isolated from red algae, is reported. Vanadium bromoperoxidase (V-BrPO) isolated from marine red algae (species of Laurencia, Plocamium, Corallina) catalyzes the bromination of the sesquiterpene (E)-(+)-nerolidol producing alpha-, beta-, and gamma-snyderol and (+)-3beta-bromo-8-epicaparrapi oxide. alpha-Snyderol, beta-snyderol, and (+)-3beta-bromo-8-epicaparrapi oxide have been isolated from Laurencia obtusa, and each have also been isolated from other species of marine red algae. gamma-Snyderol is a proposed intermediate in other bicyclo natural products. Single diastereomers of beta-snyderol, gamma-snyderol, and mixed diastereomers of (+)-3beta-bromo-8-epicaparrapi oxide (de = 20-25%) are produced in the enzyme reaction, whereas two diastereomers of these compounds are formed in the synthesis with 2,4,4,6-tetrabromocyclohexa-2,5-dienone (TBCO). V-BrPO likely functions by catalyzing the two-electron oxidation of bromide ion by hydrogen peroxide producing a bromonium ion or equivalent in the active site that brominates one face of the terminal olefin of nerolidol. These results establish V-BrPO's role in the biosynthesis of brominated cyclic sesquiterpene structures from marine red algae for the first time.

  14. Necropolis on Bor lake: New reports on Bronze age burial

    Directory of Open Access Journals (Sweden)

    Kapuran Aleksandar

    2011-01-01

    Full Text Available This article deals with the social and anthropological aspects of burial rituals during the Middle Bronze Age in Timočka Krajina. Decades of systematic research of necropolises and reconnaissance in the basin of the Crni Timok proved an increase in number of sites around ore - rich areas of the east Kučaj mountains as well as around Romuliana site and the fertile valleys of Džanovo polje (Map. 1. The quantitative increase in settlements was reflected by the emergence of large necropolises, only three of which have been systematically explored; those in Trnjani, Magura and Bor Lake (Fig. 1; Plan 1. Analysis of geographical features of many settlements and their position in relation to natural resources helped define two communities, one of which carried out mining and metallurgical activities, while the other group engaged in the production of food. Both groups lived in the immediate vicinity and mutual dependence, functioning within a developed market for copper production. During the exploration of the necropolis near Bor Lake in 1997, the remains of burnt skeletons were collected from burial structures 2/97 and 13/97 (Fig. 2; Plans 2 and 3. Anthropological analysis of the cremated remains of the deceased showed that high temperatures were used during the cremation process, which we assume could have only been achieved in metallurgical furnaces. This is confirmed by the fact that the skeletal fragments contain traces of melted metal, as well as finds of bronze slag inside urns and grave structures in the necropolis in Trnjani (Figs. 3 and 4; Tables 1-4. Burial ritual of this kind was not proved by systematic archaeological research of necropolises in the basin of Crni Timok, although anthropological data collected from necropolises linked to metallurgical settlements may indicate some guidelines in the ritual cremation of prominent members of these communities. [Projekat Ministarstva nauke Republike Srbije, br. 177020: Arheologija Srbije

  15. Conductive porous vanadium nitride/graphene composite as chemical anchor of polysulfides for lithium-sulfur batteries

    Science.gov (United States)

    Sun, Zhenhua; Zhang, Jingqi; Yin, Lichang; Hu, Guangjian; Fang, Ruopian; Cheng, Hui-Ming; Li, Feng

    2017-03-01

    Although the rechargeable lithium-sulfur battery is an advanced energy storage system, its practical implementation has been impeded by many issues, in particular the shuttle effect causing rapid capacity fade and low Coulombic efficiency. Herein, we report a conductive porous vanadium nitride nanoribbon/graphene composite accommodating the catholyte as the cathode of a lithium-sulfur battery. The vanadium nitride/graphene composite provides strong anchoring for polysulfides and fast polysulfide conversion. The anchoring effect of vanadium nitride is confirmed by experimental and theoretical results. Owing to the high conductivity of vanadium nitride, the composite cathode exhibits lower polarization and faster redox reaction kinetics than a reduced graphene oxide cathode, showing good rate and cycling performances. The initial capacity reaches 1,471 mAh g-1 and the capacity after 100 cycles is 1,252 mAh g-1 at 0.2 C, a loss of only 15%, offering a potential for use in high energy lithium-sulfur batteries.

  16. Dynamic modelling of the effects of ion diffusion and side reactions on the capacity loss for vanadium redox flow battery

    Science.gov (United States)

    Tang, Ao; Bao, Jie; Skyllas-Kazacos, Maria

    The diffusion of vanadium ions across the membrane along with side reactions can have a significant impact on the capacity of the vanadium redox flow battery (VFB) over long-term charge-discharge cycling. Differential rates of diffusion of the vanadium ions from one half-cell into the other will facilitate self-discharge reactions, leading to an imbalance between the state-of-charge of the two half-cell electrolytes and a subsequent drop in capacity. Meanwhile side reactions as a result of evolution of hydrogen or air oxidation of V 2+ can further affect the capacity of the VFB. In this paper, a dynamic model is developed based on mass balances for each of the four vanadium ions in the VFB electrolytes in conjunction with the Nernst Equation. This model can predict the capacity as a function of time and thus can be used to determine when periodic electrolyte remixing or rebalancing should take place to restore cell capacity. Furthermore, the dynamic model can be potentially incorporated in the control system of the VFB to achieve long term optimal operation. The performance of three different types of membranes is studied on the basis of the above model and the simulation results together with potential operational issues are analysed and discussed.

  17. Thermolysis of Half-Sandwich Vanadium(V) Imido Complexes to Generate Vanadium(III) Imido Species via a Vanadium(IV) Intermediate

    NARCIS (Netherlands)

    Batinas, Aurora A.; Dam, Jeroen; Meetsma, Auke; Hessen, Bart; Bouwkamp, Marco W.

    2010-01-01

    Thermolysis of half-sandwich vanadium imido complexes Cp(RN)V(i-Pr(2)N)Me (R = p-Tol, 1a; R = t-Bu, 1b) results in a mixture of products, including vanadium(IV) dimers [CpVMe](2)(mu-RN)(2), i-Pr(2)NH, i-PrNCMe(2), CH(4), and one or more paramagnetic species. In the presence of dmpe (dmpe =

  18. Effects of gamma irradiations on reactive pulsed laser deposited vanadium dioxide thin films

    Science.gov (United States)

    Madiba, I. G.; Émond, N.; Chaker, M.; Thema, F. T.; Tadadjeu, S. I.; Muller, U.; Zolliker, P.; Braun, A.; Kotsedi, L.; Maaza, M.

    2017-07-01

    Vanadium oxide films are considered suitable coatings for various applications such as thermal protective coating of small spacecrafts because of their thermochromic properties. While in outer space, such coating will be exposed to cosmic radiations which include γ-rays. To study the effect of these γ-rays on the coating properties, we have deposited vanadium dioxide (VO2) films on silicon substrates and subjected them to extensive γ-irradiations with typical doses encountered in space missions. The prevalent crystallographic phase after irradiation remains the monoclinic VO2 phase but the films preferential orientation shifts to lower angles due to the presence of disordered regions caused by radiations. Raman spectroscopy measurements also evidences that the VO2 structure is slightly affected by gamma irradiation. Indeed, increasing the gamma rays dose locally alters the crystalline and electronic structures of the films by modifying the V-V inter-dimer distance, which in turns favours the presence of the VO2 metallic phase. From the XPS measurements of V2p and O1s core level spectra, an oxidation of vanadium from V4+ towards V5+ is revealed. The data also reveal a hydroxylation upon irradiation which is corroborated by the vanishing of a low oxidation state peak near the Fermi energy in the valence band. Our observations suggest that gamma radiations induce the formation of Frenkel pairs. Moreover, THz transmission measurements show that the long range structure of VO2 remains intact after irradiation whilst the electrical measurements evidence that the coating resistivity decreases with gamma irradiation and that their transition temperature is slightly reduced for high gamma ray doses. Even though gamma rays are only one of the sources of radiations that are encountered in space environment, these results are very promising with regards to the potential of integration of such VO2 films as a protective coating for spacecrafts.

  19. Laser recleaning of a Bronze Age prehistoric dolmen

    Science.gov (United States)

    Daurelio, G.; Andriani, S. E.; Catalano, I. M.; Albanese, A.

    2007-05-01

    Dolmen La Chianca (XVI-XV century B.C.) is one of the most important megalithic buildings in Europe for its state of conservation and for the great number of findings that were discovered there (human remains, ceramic vases, pendants, bronze objects, obsidian and silica blades etc.). The building was defaced by many writings made using different markers (permanent black, correction ink pen, ballpoint pen, pencil, water-based coloured markers). The writings were removed by using a Nd-YAG laser source (λ 1064 nm with pulse duration; t 8 ns ; f 2 to 20 Hz ; energy per impulse up to 280 mJ). Degradation mapping and laser cleaning with photographs, taken before, during and after the process in situ, were carried out, then different laser parameters and techniques were used to remove different ink types. A first laser cleaning was operated on the same building in 1999 by Daurelio, but vandals defaced newly the monument, then a new restoration became necessary.

  20. Tracing the dynamic life story of a Bronze Age Female

    Science.gov (United States)

    Margarita Frei, Karin; Mannering, Ulla; Kristiansen, Kristian; Allentoft, Morten E.; Wilson, Andrew S.; Skals, Irene; Tridico, Silvana; Louise Nosch, Marie; Willerslev, Eske; Clarke, Leon; Frei, Robert

    2015-05-01

    Ancient human mobility at the individual level is conventionally studied by the diverse application of suitable techniques (e.g. aDNA, radiogenic strontium isotopes, as well as oxygen and lead isotopes) to either hard and/or soft tissues. However, the limited preservation of coexisting hard and soft human tissues hampers the possibilities of investigating high-resolution diachronic mobility periods in the life of a single individual. Here, we present the results of a multidisciplinary study of an exceptionally well preserved circa 3.400-year old Danish Bronze Age female find, known as the Egtved Girl. We applied biomolecular, biochemical and geochemical analyses to reconstruct her mobility and diet. We demonstrate that she originated from a place outside present day Denmark (the island of Bornholm excluded), and that she travelled back and forth over large distances during the final months of her life, while consuming a terrestrial diet with intervals of reduced protein intake. We also provide evidence that all her garments were made of non-locally produced wool. Our study advocates the huge potential of combining biomolecular and biogeochemical provenance tracer analyses to hard and soft tissues of a single ancient individual for the reconstruction of high-resolution human mobility.

  1. Bronze baby syndrome and the risk of kernicterus.

    Science.gov (United States)

    Bertini, Giovanna; Dani, Carlo; Fonda, Claudio; Zorzi, Carlo; Rubaltelli, Firmino F

    2005-07-01

    The problem of kernicterus in infants with bronze baby syndrome (BBS) has been reviewed on the basis of cases reported in the literature. In addition, a new case concerning an infant with severe Rh haemolytic disease, who presented with BBS and who has developed neurological manifestations of kernicterus with magnetic resonance images showing basal ganglia abnormalities, is presented. In this patient, the total serum bilirubin (TSB) concentration ranged from 18.0 to 22.8 mg/dl (306 to 388 micromol/l) and the bilirubin/albumin (B/A) ratio was 6.0 (mg/g) (6.8 is the value at which an exchange transfusion should be considered). The case presented is important due to the fact that kernicterus appeared after an exchange transfusion was performed when the TSB level reached 22.8 mg/dl (388 micromol/l) on 6th day of life while the haematocrit was 30%. From this case and from other cases reported in the literature, we must stress that, even if the level at which hyperbilirubinemia poses a threat remains undefined, BBS may constitute an additional risk of developing kernicterus. The possible strategies for implementing an approach to the management of hyperbilirubinemia (especially the haemolytic kind) in the presence of BBS may include an exchange transfusion carried out at lower TSB concentration than previously recommended or an early administration of Sn-mesoporphyrin.

  2. Separation of Molybdenum, Vanadium and Nickel by Liquid-Liquid Extraction

    OpenAIRE

    COŞAR, T.

    2014-01-01

    Elements in the ash of asphaltites that is used in thermal central for power generation units are Mo, V, U, Ti and Ni. The main goal of this study was to separate molybdenum, vanadium and nickel from the aqueous solution. The quantities of the above elements in solution were in the range of 50-80 ppm. The separate these elements from solution, the liquid-liquid extraction method was applied to samples. Alamine 336 was used as extractant. During the reduction-oxidation processes, single and mu...

  3. Electrical quadruple hysteresis in Pd-doped vanadium pentoxide nanowires due to water adsorption

    Directory of Open Access Journals (Sweden)

    Byung Hoon Kim, Soon-Young Oh, Han Young Yu, Won G Hong, Yong Ju Yun, Yark Yeon Kim and Hae Jin Kim

    2010-01-01

    Full Text Available Humidity-dependent current–voltage (I–V characteristics of Pd-doped vanadium pentoxide nanowires (Pd-VONs were investigated. Electrical quadruple hysteresis (QH was observed and attributed to the large amount of water molecules adsorbed on the nanowires. Using QH in Pd-VONs, the reaction of water with PdO was interpreted as the water molecules are desorbed and then dissociated with increasing bias voltage. Owing to the dissociated H+ and OH− ions, PdO is reduced and oxidized. As a result, water molecules recombine as the bias voltage is decreased.

  4. Dating simple flakes: Early Bronze Age flake production technology on the Middle Euphrates Steppe, Syria

    Directory of Open Access Journals (Sweden)

    Yoshihiro Nishiaki

    2014-03-01

    Full Text Available Aceramic flint scatters, comprising very crude cores or flakes and no formalised tools, are frequently found on the Middle Euphrates steppe of northern Syria. Previous studies suggest that many of them are residues of short-term activities by the nomads or shepherds of the Early Bronze Age. In order to verify this interpretation, a more precise chronological framework needs to be established for the Early Bronze Age lithic industry. This paper analyses stratified flake assemblages of the Early Bronze Age at Tell Ghanem al-Ali, a securely radiocarbon-dated settlement on the Middle Euphrates, and examines which occupation level yields assemblages most similar to those of the steppe. Results demonstrate that the lithic industry of this period underwent significant diachronic changes in terms of core reduction technology. Based on the chronological framework developed at Tell Ghanem al-Ali, the steppe assemblages in question can be assigned to different phases of the Early Bronze Age. This finding will help identify processes at the beginning of the extensive exploitation of the steppe, which is regarded as one of the most important socioeconomic changes that occurred among Early Bronze Age communities of the Middle Euphrates.

  5. Corrosion of Bronzes by Extended Wetting with Single versus Mixed Acidic Pollutants.

    Science.gov (United States)

    Gianni, Liliana; Gigante, Giovanni E; Cavallini, Mauro; Adriaens, Annemie

    2014-04-28

    The corrosion of bronzes was examined in the context of single-acid versus mixed-acid (as in urban acid rain) solutions. Two bi-component bronzes (copper with either 3% Sn or 7% Sn) that closely represent those of historic artifacts were immersed for five weeks in conditions designed to replicate those experienced by statues and ornaments in cities where rainfall and humidity constantly produce an electrolyte layer on the surfaces of bronzes. Ions, acids, and particles of pollutants can dissolve in this layer, resulting in a variety of harsh corrosion processes. The kinetics of corrosion and the properties of the resulting patinas were monitored weekly by electrochemical impedance spectroscopy and open-circuit potential measurements. The sizes and appearances of the corrosion products were monitored and used to estimate the progress of the corrosion, whose crystalline structures were visualized using scanning electron microscopy with energy dispersive spectroscopy, identified by X-ray diffraction, and characterized by spectrocolorimetry. The electrochemical measurements demonstrated that greater damage (in terms of color change and corrosion product formation) did not correspond to deficiencies in protection. The mixed-acid solution did not corrode the bronzes, as would be expected from the additive effects of the single acids. The postulated mechanisms of metal dissolution appear to be specific to a particular bronze alloy, with the tin component playing an important role.

  6. Propolis as a green corrosion inhibitor for bronze in weakly acidic solution

    Science.gov (United States)

    Varvara, Simona; Bostan, Roxana; Bobis, Otilia; Găină, Luiza; Popa, Florin; Mena, Vicente; Souto, Ricardo M.

    2017-12-01

    In the present work, the inhibitive action of natural propolis on bronze corrosion in a weakly acidic solution containing Na2SO4 and NaHCO3 at pH 5 was evaluated using multiscale electrochemical techniques, namely potentiodynamic polarization, electrochemical impedance spectroscopy and scanning vibrating electrode technique measurements. The major constituents of propolis were identified by HPLC. Surface characterization was performed by SEM-EDX and AFM analysis. Experiments were performed as a function of the propolis concentration and immersion time in the corrosive electrolyte. The obtained results showed that propolis presents good anticorrosive properties on bronze, acting as a mixed-type inhibitor, but its protective effectiveness is time-dependent. The highest inhibiting efficiency of 98.9% was obtained in the presence of 100 ppm propolis, after about 12 h of exposure to inhibitor-containing electrolyte through the stabilization of Cu2O on the bronze surface. The inhibitive properties of propolis on bronze corrosion are likely due to the adsorption of its main constituents (flavonoids and phenolic compounds), through the oxygen atoms in their functional groups and aromatic rings, which have been evidenced by FT-IR spectra. The adsorption of propolis on bronze was found to follow Langmuir adsorption isotherm.

  7. Corrosion of Bronzes by Extended Wetting with Single versus Mixed Acidic Pollutants

    Directory of Open Access Journals (Sweden)

    Liliana Gianni

    2014-04-01

    Full Text Available The corrosion of bronzes was examined in the context of single-acid versus mixed-acid (as in urban acid rain solutions. Two bi-component bronzes (copper with either 3% Sn or 7% Sn that closely represent those of historic artifacts were immersed for five weeks in conditions designed to replicate those experienced by statues and ornaments in cities where rainfall and humidity constantly produce an electrolyte layer on the surfaces of bronzes. Ions, acids, and particles of pollutants can dissolve in this layer, resulting in a variety of harsh corrosion processes. The kinetics of corrosion and the properties of the resulting patinas were monitored weekly by electrochemical impedance spectroscopy and open-circuit potential measurements. The sizes and appearances of the corrosion products were monitored and used to estimate the progress of the corrosion, whose crystalline structures were visualized using scanning electron microscopy with energy dispersive spectroscopy, identified by X-ray diffraction, and characterized by spectrocolorimetry. The electrochemical measurements demonstrated that greater damage (in terms of color change and corrosion product formation did not correspond to deficiencies in protection. The mixed-acid solution did not corrode the bronzes, as would be expected from the additive effects of the single acids. The postulated mechanisms of metal dissolution appear to be specific to a particular bronze alloy, with the tin component playing an important role.

  8. Experimental Investigation of Friction Coefficient and Wear Rate of Brass and Bronze under Lubrication Conditions

    Directory of Open Access Journals (Sweden)

    S. Senhadji

    2016-03-01

    Full Text Available The present study is conducted in order to compare the frictional and wear behaviour under mixed lubrication of two pins: bronze (CuSn9P and brass (CuZn39Pb2, sliding on a steel disc (XC42. The selection of this type of brass and bronze was made because they are not large differences in microhardness, however, have a completely different microstructure. All tests were carried out by using a pin-on-disc tribometer, with a plane contact mode and a pure sliding velocity. The results indicate that friction coefficient and the wear coefficient of brass are significantly higher in comparison to bronze for the two studied roughness (Ra = 2 and 0.15 μm. We also note that for the brass the friction is slightly affected by the roughness of the discs, and the running time is reduced. Regarding bronze, the friction passes from 0.17 for the rough disc (Ra = 2 μm to 0.02 for the smooth disc (Ra = 0.15 μm with a time of running about 2000 s; the low value of friction corresponds to the transition to a hydrodynamic regime. The analysis of the microstructure of brass shows a high shear of the surface layers, with a severe plastic deformation, which is not the case for the bronze that is not affected by observable deformations.

  9. Large Spin Hall Angle in Vanadium Film

    Science.gov (United States)

    Wang, Tao; Fan, Xin; Wang, Wenrui; Xie, Yunsong; Warsi, Muhammad A.; Wu, Jun; Chen, Yunpeng; Lorenz, Virginia O.; Xiao, John Q.

    We report the large spin Hall angle observed in Vanadium film with small grain size and distorted lattice parameter. The spin Hall angle is quantified by measuring current-induced spin-orbit torque in V/CoFeB bilayer using optical spin torque magnetometer based on polar magneto-optical Kerr effect (MOKE). The spin Hall angle as large as θSH = -0.071 has been observed in V/CoFeB bilayer Structural analysis, using X-ray diffraction (XRD), transmission electron microscopy (TEM) and selected area electron diffraction (SAED), confirms films grown at room temperature have very small grain size and enlarged lattice parameter. The Vanadium films with distorted crystal structure also have high resistivity (>200 μΩ cm) and long spin diffusion length (~16.3 nm) measured via spin pumping experiment. This finding of spin Hall effect enhancement in more disordered structure will provide insights for understanding and exploiting materials with strong spin orbit interaction, especially in light 3d transition metals which promise long spin diffusion length.

  10. Roll-to-Roll Processing of Inverted Polymer Solar Cells using Hydrated Vanadium(VOxide as a PEDOT:PSS Replacement

    Directory of Open Access Journals (Sweden)

    Frederik C. Krebs

    2011-01-01

    Full Text Available The use of hydrated vanadium(Voxide as a replacement of the commonly employed hole transporting material PEDOT:PSS was explored in this work. Polymer solar cells were prepared by spin coating on glass. Polymer solar cells and modules comprising 16 serially connected cells were prepared using full roll-to-roll (R2R processing of all layers. The devices were prepared on flexible polyethyleneterphthalate (PET and had the structure PET/ITO/ZnO/P3HT:PCBM/V2O5·(H2On/Ag. The ITO and silver electrodes were processed and patterned by use of screen printing. The zinc oxide, P3HT:PCBM and vanadium(Voxide layers were processed by slot-die coating. The hydrated vanadium(Voxide layer was slot-die coated using an isopropanol solution of vanadyl-triisopropoxide (VTIP. Coating experiments were carried out to establish the critical thickness of the hydrated vanadium(Voxide layer by varying the concentration of the VTIP precursor over two orders of magnitude. Hydrated vanadium(Voxide layers were characterized by profilometry, scanning electron microscopy, energy dispersive X-ray spectroscopy, and grazing incidence wide angle X-ray scattering. The power conversion efficiency (PCE for completed modules was up to 0.18%, in contrast to single cells where efficiencies of 0.4% were achieved. Stability tests under indoor and outdoor conditions were accomplished over three weeks on a solar tracker.

  11. Vanadium and nickel in petroleums of bituminous Tatar rocks

    Energy Technology Data Exchange (ETDEWEB)

    Aigistova, S.Kh.; Safiullina, G.Kh.; Sadykov, A.N.; Kharlamov, V.A.

    1984-01-01

    The vanadium and nickel contents of petroleum obtained from bituminous rock of Ashal'chinsk, Akhmat, Gorskii, Katerchinsk, Klinsk (Studeno-Klyuchev), West-Chumachkin, Mordovian-Karmal' and Pokrov deposits, was determined polarographically. The vanadium concentration range in these petroleums is 0.01-0.09 and nickel 0.009-0.05 wt.%. According to results previously obtained, vanadium and nickel contents in ordinary petroleum of this country are no higher than 0.010 and 0.0014 wt.%, respectively. 3 references, 1 table.

  12. Vanadium-base alloys for fusion reactor applications

    Energy Technology Data Exchange (ETDEWEB)

    Smith, D.L.; Loomis, B.A.; Diercks, D.R.

    1984-10-01

    Vanadium-base alloys offer potentially significant advantages over other candidate alloys as a structural material for fusion reactor first wall/blanket applications. Although the data base is more limited than that for the other leading candidate structural materials, viz., austenitic and ferritic steels, vanadium-base alloys exhibit several properties that make them particularly attractive for the fusion reactor environment. This paper presents a review of the structural material requirements, a summary of the materials data base for selected vanadium-base alloys, and a comparison of projected performance characteristics compared to other candidate alloys. Also, critical research and development (R and D) needs are defined.

  13. Of farms and fields : the Bronze Age and Iron Age settlement and Celtic field at Hijken-Hijkerveld

    NARCIS (Netherlands)

    Arnoldussen, S.; de Vries, Karen M.

    2014-01-01

    Between 1969 and 1973, excavations were undertaken at Hijken, the Netherlands. An area of 3 hectares within a cultural landscape replete with barrows and Celtic field banks was opened-up and yielded Late Neolithic graves, a Bronze Age palisade and several Middle Bronze Age houses. During the Late

  14. Building the Bronze Age : Architectural and social change on the Greek mainland during Early Helladic III, Middle Helladic and Late Helladic I

    NARCIS (Netherlands)

    Wiersma, Corien

    2014-01-01

    Communities living on the Greek Mainland during the end of the Early Bronze Age (EBA. ca. 2200-2000 BC) and the earlier Middle Bronze Age (MBA, ca. 2000-1800 BC) were thought to be relatively simple and egalitarian, while during the later MBA and early Late Bronze Age (LBA, ca. 1700-1600 BC),

  15. Selenium, Vanadium, and Chromium as Micronutrients to Improve Metabolic Syndrome.

    Science.gov (United States)

    Panchal, Sunil K; Wanyonyi, Stephen; Brown, Lindsay

    2017-03-01

    Trace metals play an important role in the proper functioning of carbohydrate and lipid metabolism. Some of the trace metals are thus essential for maintaining homeostasis, while deficiency of these trace metals can cause disorders with metabolic and physiological imbalances. This article concentrates on three trace metals (selenium, vanadium, and chromium) that may play crucial roles in controlling blood glucose concentrations possibly through their insulin-mimetic effects. For these trace metals, the level of evidence available for their health effects as supplements is weak. Thus, their potential is not fully exploited for the target of metabolic syndrome, a constellation that increases the risk for cardiovascular disease and type 2 diabetes. Given that the prevalence of metabolic syndrome is increasing throughout the world, a simpler option of interventions with food supplemented with well-studied trace metals could serve as an answer to this problem. The oxidation state and coordination chemistry play crucial roles in defining the responses to these trace metals, so further research is warranted to understand fully their metabolic and cardiovascular effects in human metabolic syndrome.

  16. Numerical modeling of an all vanadium redox flow battery.

    Energy Technology Data Exchange (ETDEWEB)

    Clausen, Jonathan R.; Brunini, Victor E.; Moffat, Harry K.; Martinez, Mario J.

    2014-01-01

    We develop a capability to simulate reduction-oxidation (redox) flow batteries in the Sierra Multi-Mechanics code base. Specifically, we focus on all-vanadium redox flow batteries; however, the capability is general in implementation and could be adopted to other chemistries. The electrochemical and porous flow models follow those developed in the recent publication by [28]. We review the model implemented in this work and its assumptions, and we show several verification cases including a binary electrolyte, and a battery half-cell. Then, we compare our model implementation with the experimental results shown in [28], with good agreement seen. Next, a sensitivity study is conducted for the major model parameters, which is beneficial in targeting specific features of the redox flow cell for improvement. Lastly, we simulate a three-dimensional version of the flow cell to determine the impact of plenum channels on the performance of the cell. Such channels are frequently seen in experimental designs where the current collector plates are borrowed from fuel cell designs. These designs use a serpentine channel etched into a solid collector plate.

  17. Boiling heat transfer on single phosphor bronze and copper mesh microstructures

    Directory of Open Access Journals (Sweden)

    Orman Łukasz J.

    2014-03-01

    Full Text Available The paper presents experimental results of boiling heat transfer of distilled water and ethyl alcohol on surfaces covered with single layers of wire mesh structures made of phosphor bronze and copper. For each material two kinds of structures have been considered (higher and lower in order to determine the impact of the height of the structure on boiling heat transfer. The wire diameter of the copper meshes was 0,25 mm and 0,32 mm, while of the bronze meshes: 0,20 mm and 0,25 mm. The structures had the same mesh aperture (distance between the wires – 0,50 mm for copper and 0,40 for bronze but different wire diameter and, consequently, different height of the layers. The tests have been performed under ambient pressure in the pool boiling mode. The obtained results indicate a visible impact of the layer height on the boiling heat transfer performance of the analysed microstructures.

  18. DEGRADATION WORKS OF MONUMENTAL ART CAST BRONZE UNDER THE INFLUENCE OF ENVIRONMENTAL FACTORS

    Directory of Open Access Journals (Sweden)

    Delia NICA-BADEA

    2012-11-01

    Full Text Available Intensive pollution, combined with the lack of conservation of monuments exposed to these environments make the main cause of deterioration of cultural objects to atmospheric corrosion metal. This paper proposes a study of the main factors leading to degradation Bronze alloy, cast bronze monuments exposed to open atmosphere: corrosive environmental factors, stability and products of corrosion of bronze. In general, all corrosion products present on a metal surface are indicated as 'skate', can be composed of single-layer or multilayer products. The paper also includes a case study on the influence of environmental factors on degradation Matthias monument statue in Cluj-Napoca, Romania. Visual inspection of the monument informs us that have white spots, gray, reddish not consistent with the base color green patina, surfaces showing depigmentation, the rain washed areas, crystallization, deposition of air-borne particles.

  19. Craftmanship, Production and Distribution of Metalwork in the Early and Middle Northern Bronze Age

    DEFF Research Database (Denmark)

    Nørgaard, Heide Wrobel

    possible to compare these traits between different bronze objects. Using a group of bronze objects who are already critically analyzed with regard to the formal characteristics gives a unique opportunity to recognize the workshops and their distribution areas and will be the base of the project.......Workshops and their sphere of influence is an important factor in the identification of social groups who are related to what we term workshop. Here the specialization within the workshop based on certain forms and behaviours can be linked to the knowledge of social groups. Statements about...... the origin of foreign objects can help to clarify social interaction in Bronze Age Europe. The project aims not only to find the centres of production and their distribution areas but also to examine their role in the creation of social identities. The aim is furthermore to examine the techniques used...

  20. Medical image registration algorithms assesment: Bronze Standard application enactment on grids using the MOTEUR workflow engine.

    Science.gov (United States)

    Glatard, Tristan; Montagnat, Johan; Pennec, Xavier

    2006-01-01

    Medical image registration is pre-processing needed for many medical image analysis procedures. A very large number of registration algorithms are available today, but their performance is often not known and very difficult to assess due to the lack of gold standard. The Bronze Standard algorithm is a very data and compute intensive statistical approach for quantifying registration algorithms accuracy. In this paper, we describe the Bronze Standard application and we discuss the need for grids to tackle such computations on medical image databases. We demonstrate MOTEUR, a service-based workflow engine optimized for dealing with data intensive applications. MOTEUR eases the enactment of the Bronze Standard and similar applications on the EGEE production grid infrastructure. It is a generic workflow engine, based on current standards and freely available, that can be used to instrument legacy application code at low cost.

  1. Medical image registration algorithms assesment Bronze Standard application enactment on grids using the MOTEUR workflow engine

    CERN Document Server

    Glatard, T; Pennec, X

    2006-01-01

    Medical image registration is pre-processing needed for many medical image analysis procedures. A very large number of registration algorithms are available today, but their performance is often not known and very difficult to assess due to the lack of gold standard. The Bronze Standard algorithm is a very data and compute intensive statistical approach for quantifying registration algorithms accuracy. In this paper, we describe the Bronze Standard application and we discuss the need for grids to tackle such computations on medical image databases. We demonstrate MOTEUR, a service-based workflow engine optimized for dealing with data intensive applications. MOTEUR eases the enactment of the Bronze Standard and similar applications on the EGEE production grid infrastructure. It is a generic workflow engine, based on current standards and freely available, that can be used to instrument legacy application code at low cost.

  2. THE CHARACTERIZATION OF A CORRODED EGYPTIAN BRONZE STATUE AND A STUDY OF THE DEGRADATION PHENOMENA

    Directory of Open Access Journals (Sweden)

    Mohamed GHONIEM

    2011-06-01

    Full Text Available This paper presents the results of scientific examinations carried out on an Egyptian bronze statue discovered buried in Sais. Optical Microscopy (OM, Scanning Electron Microscopy (SEM coupled with Energy Dispersive Spectroscopy (EDS and X-ray Diffraction (XRD were used to understand the corrosive morphological characteristics of the patina, to investigate the corrosion products, analyze the elementary composition of the statue and to identify the corrosive factors with effects on the alteration processes. The results indicated that the statue was made of bronze alloy, with copper as the main element, besides lead and tin. Three layers of alteration products with various composition and morphology covered the substrate of the bronze alloy. XRD results indicated that the statue was subjected to many corrosive ions such as sulfur and chloride, and buried in wet soil, rich in oxygen and carbon. This study provides useful information for the restoration and protection of the statue.

  3. Mesoporous tungsten oxynitride as electrocatalyst for promoting redox reactions of vanadium redox couple and performance of vanadium redox flow battery

    Science.gov (United States)

    Lee, Wonmi; Jo, Changshin; Youk, Sol; Shin, Hun Yong; Lee, Jinwoo; Chung, Yongjin; Kwon, Yongchai

    2018-01-01

    For enhancing the performance of vanadium redox flow battery (VRFB), a sluggish reaction rate issue of V2+/V3+ redox couple evaluated as the rate determining reaction should be addressed. For doing that, mesoporous tungsten oxide (m-WO3) and oxyniride (m-WON) structures are proposed as the novel catalysts, while m-WON is gained by NH3 heat treatment of m-WO3. Their specific surface area, crystal structure, surface morphology and component analysis are measured using BET, XRD, TEM and XPS, while their catalytic activity for V2+/V3+ redox reaction is electrochemically examined. As a result, the m-WON shows higher peak current, smaller peak potential difference, higher electron transfer rate constant and lower charge transfer resistance than other catalysts, like the m-WO3, WO3 nanoparticle and mesoporous carbon, proving that it is superior catalyst. Regarding the charge-discharge curve tests, the VRFB single cell employing the m-WON demonstrates high voltage and energy efficiencies, high specific capacity and low capacity loss rate. The excellent results of m-WON are due to the reasons like (i) reduced energy band gap, (ii) reaction familiar surface functional groups and (ii) greater electronegativity.

  4. Nomadic pastoralism in the Early Bronze Age of the central Balkans evaluation of background knowledge

    Directory of Open Access Journals (Sweden)

    Porčić Marko

    2008-01-01

    Full Text Available The aim of the paper is to examine background knowledge about the orga­nizational properties of mobile pastoral groups in order to assess the likelihood of the existence of pastoral nomads in the Early Bronze Age in the central Balkans. The patterning found by A. L. Johnson (2002 is taken as a point of departure for the cross-cultural analysis conducted in this study. Johnson’s findings are in the main corroborated. Acquired knowledge about the workings of pastoral societies suggests that highly mobile pastoral groups should not be expected in the Early Bronze Age of the central Balkans.

  5. Non-invasive chemical and phase analysis of Roman bronze artefacts from Thamusida (Morocco)

    Energy Technology Data Exchange (ETDEWEB)

    Gliozzo, Elisabetta, E-mail: gliozzo@unisi.i [Dipartimento di Scienze della Terra, Universita di Siena, via Laterina 8, 53100 Siena (Italy); Arletti, Rossella, E-mail: rarletti@unimore.i [Dipartimento di Scienze della Terra, Universita di Modena e Reggio Emilia, Largo S. Eufemia 19, 41100 Modena (Italy); Cartechini, Laura, E-mail: laura@thch.unipg.i [Istituto di Scienze e Tecnologie Molecolari del CNR (CNR-ISTM), c/o Dipartimento di Chimica, Universita di Perugia, via Elce di Sotto 8, 06123 Perugia (Italy); Dipartimento di Chimica, Universita di Perugia, via Elce di Sotto 8, 06123 Perugia (Italy); Imberti, Silvia, E-mail: Silvia.Imberti@stfc.ac.u [Science and Technology Facilities Council, Rutherford Appleton Laboratory, Harwell Science and Innovation Campus, Didcot, OX11 0QX (United Kingdom); Kockelmann, Winfried A., E-mail: Winfried.Kockelmann@stfc.ac.u [Science and Technology Facilities Council, Rutherford Appleton Laboratory, Harwell Science and Innovation Campus, Didcot, OX11 0QX (United Kingdom); Memmi, Isabella, E-mail: memmi@unisi.i [Dipartimento di Scienze della Terra, Universita di Siena, via Laterina 8, 53100 Siena (Italy); Rinaldi, Romano, E-mail: rrinaldi@unipg.i [Dipartimento di Chimica, Universita di Perugia, via Elce di Sotto 8, 06123 Perugia (Italy); Tykot, Robert H., E-mail: rtykot@cas.usf.ed [Department of Anthropology, University of South Florida, Tampa, FL 33620 (United States)

    2010-12-15

    A repertory of Roman military bronze equipment (1st- 3rd century AD) found at the archaeological site of Thamusida (Rabat, Morocco) was analysed by non-destructive X-ray fluorescence and time of flight neutron diffraction (TOF-ND). Most objects are made of leaded alloys, where copper is combined with tin and/or zinc and, in six cases, to arsenic as well. A mixed technology was employed, making a limited use of 'pure' semi-finished materials if compared with the large utilization of recycled materials (brass and bronze).

  6. Vanadium - investigations on supply and demand of mineral raw materials

    Energy Technology Data Exchange (ETDEWEB)

    Eggert, P.; Kippenberger, C.; Kruszona, M.; Schmidt, H.; Wettig, E.

    1981-11-01

    Conclusions which are drawn in the latest report of the Federal Institute for Geosciences and Mineral Resources, Hanover, and the German Institute for Economic Research, Berlin, on the steel additive vanadium are presented.

  7. Method to Remove Uranium/Vanadium Contamination from Groundwater

    Energy Technology Data Exchange (ETDEWEB)

    Metzler, Donald R.; Morrison Stanley

    2004-07-27

    A process for removing uranium/vanadium-based contaminants from groundwater using a primary in-ground treatment media and a pretreatment media that chemically adjusts the groundwater contaminant to provide for optimum treatment by the primary treatment media.

  8. Exploring a novel approach to fabricate vanadium carbide ...

    Indian Academy of Sciences (India)

    -shell structure; composite materials; mesoporous material; solid-state reaction. ... A novel approach to the fabrication of vanadium carbide encapsulated into carbon nanotube (VC@C) core-shell structured composite by thermal treatment with ...

  9. Remobilization of pentavalent antimony and vanadium from a granular iron hydroxide material--a comparative study of different leaching systems.

    Science.gov (United States)

    Kolbe, Falko; Weiss, Holger; Wennrich, Rainer; Lorenz, Wilhelm Georg; Daus, Birgit

    2011-09-30

    The remobilization of antimony and vanadium from previously loaded commercial granular ferric-hydroxide GEH material (intended for water treatment) was examined by using a sequential extraction procedure and three different leaching systems to evaluate their physicochemical mobility and potential availability under different simulated environmental conditions. A classical batch extraction, an extraction cell (EC) and rotating-coiled columns (RCC) were used as extraction systems. For each system it could be shown that the content of ion-exchangeable antimony and vanadium in previously loaded material is negligible (extraction time and the possibility of generating information to the leaching kinetics. It is shown that the efficiency of the three leaching systems is quite different employing Wenzel's sequential fractionation protocol. Only by working with RCC, the iron (hydr)oxide matrix was completely dissolved within four steps resulting in the total mobilization of antimony and vanadium. EC seems to be less suitable for leaching studies of Sb and V sorbed on iron(hydr)oxide. The remobilizable proportion of the several fractions was lower in comparison to batch and RCC and seems to be a result of an agglomeration of the GEH in the EC device. Copyright © 2011 Elsevier B.V. All rights reserved.

  10. A new vanadium(V) persulfide complex: (NEt[sub 4])[VO(S[sub 2])[sub 2](bpy)

    Energy Technology Data Exchange (ETDEWEB)

    Castro, S.L.; Martin, J.D.; Christou, G. (Indiana Univ., Bloomington, IN (United States))

    1993-06-23

    Over the last several years, the authors have been investigating nonorganometallic vanadium/sulfide chemistry, concentrating on the higher metal oxidation states (III-V). They have found this area to be rich in structural types and reactivity characteristics. Together with related efforts by others, an impressive pool of complexes has now been made available spanning a variety of nuclearities and oxidation levels, including mixed valency. The authors' interest in this area stems from the conversion of crude oil vanadyl impurities to polymeric vanadium sulfides under the sulfur-rich conditions present during catalytic hydrodesulfurization and hydrodemetalation processes. A variety of discrete V/S species are probably forming as intermediates, and the characterization of V/S species thus becomes of relevance to the understanding of these transformations. The area of impact of the present work is vanadium persulfide chemistry. A number of V complexes of various metal nuclearities are now known that contain S[sub 2][sup 2[minus

  11. Tackling capacity fading in vanadium flow batteries with amphoteric membranes

    Science.gov (United States)

    Oldenburg, Fabio J.; Schmidt, Thomas J.; Gubler, Lorenz

    2017-11-01

    Capacity fading and poor electrolyte utilization caused by electrolyte imbalance effects are major drawbacks for the commercialization of vanadium flow batteries (VFB). The influence of membrane type (cationic, anionic, amphoteric) on these effects is studied by determining the excess and net flux of each vanadium ion in an operating VFB assembled with a cation exchange membrane (CEM), Nafion® NR212, an anion exchange membrane (AEM), Fumatech FAP-450, and an amphoteric ion exchange membrane (AIEM) synthesized in-house. It is shown that the net vanadium flux, accompanied by water transport, is directed towards the positive side for the CEM and towards the negative side for the AEM. The content of cation and anion exchange groups in the AIEM is adjusted via radiation grafting to balance the vanadium flux between the two electrolyte sides. With the AIEM the net vanadium flux is significantly reduced and capacity fading due to electrolyte imbalances can be largely eliminated. The membrane's influence on electrolyte imbalance effects is characterized and quantified in one single charge-discharge cycle by analyzing the content of the four different vanadium species in the two electrolytes. The experimental data recorded herewith conclusively explains the electrolyte composition after 80 cycles.

  12. The effects of surface modification on carbon felt electrodes for use in vanadium redox flow batteries

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Ki Jae; Kim, Young-Jun; Kim, Jae-Hun [Advanced Batteries Research Center, Korea Electronics Technology Institute, Seongnam, Gyeonggi 463-816 (Korea, Republic of); Park, Min-Sik, E-mail: parkms@keti.re.kr [Advanced Batteries Research Center, Korea Electronics Technology Institute, Seongnam, Gyeonggi 463-816 (Korea, Republic of)

    2011-12-15

    Highlights: Black-Right-Pointing-Pointer We observed the physical and chemical changes on the surface of carbon felts after various surface modifications. Black-Right-Pointing-Pointer The surface area and chemistry of functional groups formed on the surface of carbon felt are critical to determine the kinetics of the redox reactions of vanadium ions. Black-Right-Pointing-Pointer By incorporation of the surface modifications into the electrode preparation, the electrochemical activity of carbon felts could be notably enhanced. - Abstract: The surface of carbon felt electrodes has been modified for improving energy efficiency of vanadium redox flow batteries. For comparative purposes, the effects of various surface modifications such as mild oxidation, plasma treatment, and gamma-ray irradiation on the electrochemical properties of carbon felt electrodes were investigated at optimized conditions. The cell energy efficiency was improved from 68 to 75% after the mild oxidation of the carbon felt at 500 Degree-Sign C for 5 h. This efficiency improvement could be attributed to the increased surface area of the carbon felt electrode and the formation of functional groups on its surface as a result of the modification. On the basis of various structural and electrochemical characterizations, a relationship between the surface nature and electrochemical activity of the carbon felt electrodes is discussed.

  13. Nanoparticles of Low-Valence Vanadium Oxyhydroxides: Reaction Mechanisms and Polymorphism Control by Low-Temperature Aqueous Chemistry.

    Science.gov (United States)

    Besnardiere, Julie; Petrissans, Xavier; Ribot, François; Briois, Valérie; Surcin, Christine; Morcrette, Mathieu; Buissette, Valérie; Le Mercier, Thierry; Cassaignon, Sophie; Portehault, David

    2016-11-07

    An aqueous synthetic route at 95 °C is developed to reach selectively three scarcely reported vanadium oxyhydroxides. Häggite V2O3(OH)2, Duttonite VO(OH)2, and Gain's hydrate V2O4(H2O)2 are obtained as nanowires, nanorods, and nanoribbons, with sizes 1 order of magnitude smaller than previously reported. X-ray absorption spectroscopy provides evidence that vanadium in these phases is V+IV. Combined with FTIR, XRD, and electron microscopy, it yields the first insights into formation mechanisms, especially for Häggite and Gain's hydrate. This study opens the way for further investigations of the properties of novel V+IV (oxyhydr)oxides nanostructures.

  14. Localization of Vanabins, Vanadium-Binding Proteins, in the Blood Cells of the Vanadium-Rich Ascidian, Ascidia sydneiensis samea(Physiology)

    OpenAIRE

    Nobuo, Yamaguchi; Yuko, Amakawa; Hiroshi, Yamada; Tatsuya, Ueki; Hitoshi, Michibata; Marine Biological Laboratory, Graduate School of Science, Hiroshima University; Department of Neuroscience, Graduate School of Medicine and Dentistry, Okayama University; Molecular Physiology Laboratory, Department of Biological Science, Graduate School of Science, Hiroshima University

    2006-01-01

    Some species of the family Ascidiidae accumulate vanadium in concentrations in excess of 350mM, which is about 10^7-fold higher than the concentration of vanadium in seawater. In these species, signet ring cells with a single large vacuole in which vanadium ions are contained function as vanadium-accumulating cells. These have been termed vanadocytes. We recently isolated five vanadium-binding proteins, which we named Vanabinl, Vanabin2, Vanabin3, Vanabin4, and VanabinP, from vanadocytes of t...

  15. Comparison of Ultrasound-Assisted and Regular Leaching of Vanadium and Chromium from Roasted High Chromium Vanadium Slag

    Science.gov (United States)

    Wen, Jing; Jiang, Tao; Gao, Huiyang; Liu, Yajing; Zheng, Xiaole; Xue, Xiangxin

    2018-02-01

    Ultrasound-assisted leaching (UAL) was used for vanadium and chromium leaching from roasted material obtained by the calcification roasting of high-chromium-vanadium slag. UAL was compared with regular leaching. The effect of the leaching time and temperature, acid concentration, and liquid-solid ratio on the vanadium and chromium leaching behaviors was investigated. The UAL mechanism was determined from particle-size-distribution and microstructure analyses. UAL decreased the reaction time and leaching temperature significantly. Furthermore, 96.67% vanadium and less than 1% chromium were leached at 60°C for 60 min with 20% H2SO4 at a liquid-solid ratio of 8, which was higher than the maximum vanadium leaching rate of 90.89% obtained using regular leaching at 80°C for 120 min. Ultrasonic waves broke and dispersed the solid sample because of ultrasonic cavitation, which increased the contact area of the roasted sample and the leaching medium, the solid-liquid mass transfer, and the vanadium leaching rate.

  16. Hittites and "barbarians" in the Late Bronze Age: regional survey in northern Turkey

    OpenAIRE

    Matthews, Roger

    1999-01-01

    The Hittites have attracted less attention from British archaeologists than other Bronze Age states of ancient Southwest Asia, and yet in the second millennium BC they controlled most of Anatolia and at the peak of their power they even conquered Babylon. Here the Director of the British Institute of Archaeology at Ankara describes new research on the northwest frontier of the Hittite empire.

  17. Study on surface properties of gilt-bronze artifacts, after Nd:YAG laser cleaning

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Hyeyoun [Division of Restoration Technology, National Research Institute of Cultural Heritage, Daejeon (Korea, Republic of); Cho, Namchul, E-mail: nam1611@hanmail.net [Department of Cultural Heritage Conservation Science, Kongju National University, Gongju, 314-701 (Korea, Republic of); Lee, Jongmyoung [Laser Engineering Group, IMT Co. Ltd, Gyeonggi (Korea, Republic of)

    2013-11-01

    As numerous pores are formed at plating gilt-bronze artifacts, the metal underlying the gold is corroded and corrosion products are formed on layer of gold. Through this study, the surfaces of gilt-bronze are being investigated before and after the laser irradiation to remove corrosion products of copper by using Nd:YAG laser. For gilt-bronze specimens, laser and chemical cleaning were performed, and thereafter, surface analysis with SEM-EDS, AFM, and XPS were used to determine the surface characteristics. Experimental results show that chemical cleaning removes corrosion products of copper through dissolution but it was not removed uniformly and separated the metal substrate and the gold layer. Nevertheless, through laser cleaning, some of the corrosions were removed with some damaged areas due to certain conditions and brown residues remained. Brown residues were copper corrosion products mixed with soil left within the gilt layer. It was due to surface morphology of uneven and rough gilt layer. Hence, they did not react effectively to laser beams, and thus, remained as residues. The surface properties of gilt-bronze should be thoroughly investigated with various surface analyses to succeed in laser cleaning without damages or residues.

  18. Characterisation of a Proto-historic bronze collection by micro-EDXRF

    Energy Technology Data Exchange (ETDEWEB)

    Figueiredo, Elin, E-mail: elin@itn.pt [IST/ITN, Instituto Superior Técnico, Universidade Técnica de Lisboa, Estrada Nacional 10, 2686-953 Sacavém (Portugal); CENIMAT/I3N, Departamento de Ciência dos Materiais, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica (Portugal); Araújo, M. Fátima [IST/ITN, Instituto Superior Técnico, Universidade Técnica de Lisboa, Estrada Nacional 10, 2686-953 Sacavém (Portugal); Silva, Rui J.C. [CENIMAT/I3N, Departamento de Ciência dos Materiais, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Caparica (Portugal); Vilaça, Raquel [CEAUCP-FCT, Instituto de Arqueologia, Departamento de História, Arqueologia e Artes, Faculdade de Letras, Universidade de Coimbra, Palácio de Sub-Ripas, 3000-395 Coimbra (Portugal)

    2013-02-01

    Highlights: ► A collection of Proto-historic metal artefacts was analysed by micro-EDXRF. ► Composition of major and minor elements has been determined. ► Artefacts were manufactured in a bronze alloy with a low impurity pattern. ► The alloy shows parallels with indigenous Late Bronze Age Iberian productions. -- Abstract: Studies concerning European Proto-historic metallic artefacts can provide important clues about technological transfers during a period of time characterised by diverse cultural interactions. A collection of Proto-historic metallic artefacts from Medronhal (western Iberian Peninsula) composed by rings, bracelets and a fibula related to different cultural affiliations were investigated by micro-EDXRF to provide a major and a minor elemental characterisation. Results show that the Medronhal collection was manufactured in a Cu–Sn alloy (binary bronze) with similar Sn contents among the various types of artefacts and a low impurity pattern. Results of the type and quality of metal were compared to other artefact collections to infer about metallurgical parallels. Strong parallels with indigenous Late Bronze Age Iberian metallurgical productions were found.

  19. Isotopic dietary reconstruction of humans from Middle Bronze Age Lerna, Argolid, Greece

    NARCIS (Netherlands)

    Triantaphyllou, S.; Richards, M. P.; Zerner, C.; Voutsaki, S.

    2008-01-01

    This study presents the results of a carbon and nitrogen stable isotope analysis of 39 human bone and 8 animal samples from Middle Bronze Age (or Middle Helladic, MH, ca. 2100-1700 BC) Lerna, Greece. The isotopic data indicate that the humans had a C-3 terrestrial diet while certain individuals

  20. Antibacterial drugs as corrosion inhibitors for bronze surfaces in acidic solutions

    Energy Technology Data Exchange (ETDEWEB)

    Rotaru, Ileana [Department of Chemical Engineering, “Babes-Bolyai” University, 11 Arany-Janos St., 400028 Cluj-Napoca (Romania); Varvara, Simona, E-mail: svarvara@uab.ro [Department of Exact Sciences and Engineering, “1 Decembrie 1918” University, 11-13 Nicolae Iorga St., 510009 Alba Iulia (Romania); Gaina, Luiza [Department of Chemical Engineering, “Babes-Bolyai” University, 11 Arany-Janos St., 400028 Cluj-Napoca (Romania); Muresan, Liana Maria, E-mail: limur@chem.ubbcluj.ro [Department of Chemical Engineering, “Babes-Bolyai” University, 11 Arany-Janos St., 400028 Cluj-Napoca (Romania)

    2014-12-01

    Graphical abstract: - Highlights: • All four investigated antibacterial drugs act as corrosion inhibitors for bronze surface. • In the presence of antibiotics, a 3RC electric circuit simulates the corrosion system. • The electrochemical results indicate as best inhibitors Doxy, followed by Strepto. • HOMO–LUMO energy gap increases in the order: Doxy > Strepto > Cipro > Amoxi. • The thin protective film on bronze is reinforced by the presence of the antibiotics. - Abstract: The present study is aiming to investigate the effect of four antibiotics (amoxicillin, ciprofloxacin, doxycycline and streptomycin,) belonging to different classes of antibacterial drugs on bronze corrosion in a solution simulating an acid rain (pH 4). Due to their ability to form protective films on the metal surface, the tested antibiotics act as corrosion inhibitors for bronze. The antibiotics were tested at various concentrations in order to determine the optimal concentration range for the best corrosion inhibiting effect. In evaluating the inhibition efficiency, polarization curves, electrochemical impedance spectroscopy, SEM and XPS measurements were used. Moreover, a correlation between the inhibition efficiency of some antibacterial drugs and certain molecular parameters was determined by quantum chemical computations. Parameters like energies E{sub HOMO} and E{sub LUMO} and HOMO–LUMO energy gap were used for correlation with the corrosion data.

  1. Strangers in a strange land: Egyptians in southern Palestine during the Bronze Age

    Directory of Open Access Journals (Sweden)

    Rachael Sparks

    2002-10-01

    Full Text Available When the Institute of Archaeology was formally established in 1937, it became responsible for housing Sir Flinders Petrie’s collection of archaeological material from Palestine. This unique inheritance has great value as a research collection, as its curator demonstrates here in her discussion of interaction between Egypt and Palestine in the Bronze Age.

  2. Genetic variation of the bronze locus (MC1R in turkeys from Southern Brazil

    Directory of Open Access Journals (Sweden)

    Josmael Corso

    2017-03-01

    Full Text Available Abstract Domestic turkeys present several color phenotypes controlled by at least five genetic loci, but only one of these has been identified precisely: the bronze locus, which turned out to be the melanocortin-1 receptor (MC1R gene. MC1R variation is important for breeders interested in maintaining or developing different color varieties. In this study, we sequenced most of the MC1R gene from 16 White Holland (the main commercial turkey variety and 19 pigmented turkeys from southern Brazil with two purposes. The first was to describe the MC1R diversity in White Holland turkeys, which may serve as reservoirs of genetic diversity at this locus. The second was to test whether the traditional color classification used by Brazilian breeders is related to previously known MC1R alleles. White Holland turkeys had four different haplotypes corresponding to the bronze (b+ and black-winged bronze (b1 alleles. Pigmented turkeys also had four haplotypes corresponding to the b+ and b1 alleles, but different haplotypes represent the most common b+ allele in these two groups. The black (B allele was absent from our samples. Overall, our results suggest that white and pigmented individuals form two different populations, and that the traditional color classification used by Brazilian breeders cannot accurately predict the genotypes at the bronze locus.

  3. Genetic variation of the bronze locus (MC1R) in turkeys from Southern Brazil.

    Science.gov (United States)

    Corso, Josmael; Hepp, Diego; Ledur, Mônica C; Peixoto, Jane O; Fagundes, Nelson J R; Freitas, Thales R O

    2017-01-01

    Domestic turkeys present several color phenotypes controlled by at least five genetic loci, but only one of these has been identified precisely: the bronze locus, which turned out to be the melanocortin-1 receptor (MC1R) gene. MC1R variation is important for breeders interested in maintaining or developing different color varieties. In this study, we sequenced most of the MC1R gene from 16 White Holland (the main commercial turkey variety) and 19 pigmented turkeys from southern Brazil with two purposes. The first was to describe the MC1R diversity in White Holland turkeys, which may serve as reservoirs of genetic diversity at this locus. The second was to test whether the traditional color classification used by Brazilian breeders is related to previously known MC1R alleles. White Holland turkeys had four different haplotypes corresponding to the bronze (b+) and black-winged bronze (b1) alleles. Pigmented turkeys also had four haplotypes corresponding to the b+ and b1 alleles, but different haplotypes represent the most common b+ allele in these two groups. The black (B) allele was absent from our samples. Overall, our results suggest that white and pigmented individuals form two different populations, and that the traditional color classification used by Brazilian breeders cannot accurately predict the genotypes at the bronze locus.

  4. Electrodeposition and corrosion resistance of nanocrystalline white bronze (CuSn) coatings

    NARCIS (Netherlands)

    Hovestad, A.; Lekka, M.; Willemsen, R.M.R.; Tacken, R.A.; Bonora, P.L.

    2008-01-01

    For jewellery applications electroplated white bronze (CuSn) was investigated as undercoating for noble metal finishes as alternative to nickel. A strongly acidic plating bath was developed with an organic additive to suppress hydrogen evolution and obtain bright coatings. An electrochemical study

  5. La médaille de bronze du CNRS à un physicien clermontois

    CERN Multimedia

    2005-01-01

    Evey year, the National center for scientific research (CNRS), rewards around fifty of searchers at various stages of their career. The bronze medal rewards the first work of a searcher, making of him a specialist in his field; Philippe Crochet was awarded this medal

  6. Exposition and Synthesis of Benin Bronze Casting: Emphasis on the Olotan Casters of Benin

    Science.gov (United States)

    Ifeta, Chris Funke

    2016-01-01

    The introduction of Western education to Nigeria has brought in its wake great strides toward development. Changes in Benin dates far back to the dawn of the 20th century. This paper investigates the critical role of education in development. The paper integrates interview data collected from bronze casters in Benin. The first section of the paper…

  7. The Agro Pontino region, refuge after the Early Bronze Age Avellino eruption of Mount Vesuvius, Italy?

    NARCIS (Netherlands)

    Bakels, C.; Sevink, J.; Kuijper, W.; Kamermans, H.

    2015-01-01

    In recent years it was discovered that the Middle to Late Holocene infi ll of the Agro Pontino graben (Central Italy) held a tephra layer originating from the Avellino eruption of the Vesuvius volcano. The eruption is dated to 1995 ± 10 calBC and took therefore place during the Early Bronze Age.

  8. Cold Spraying of Cu-Al-Bronze for Cavitation Protection in Marine Environments

    Science.gov (United States)

    Krebs, S.; Gärtner, F.; Klassen, T.

    2015-01-01

    Traveling at high speeds, ships have to face the problem of rudder cavitation-erosion. At present, the problem is countered by fluid dynamically optimized rudders, synthetic, and weld-cladded coatings on steel basis. Nevertheless, docking and repair is required after certain intervals. Bulk Cu-Al-bronzes are in use at ships propellers to withstand corrosion and cavitation. Deposited as coatings with bulk-like properties, such bronzes could also enhance rudder life times. The present study investigates the coating formation by cold spraying CuAl10Fe5Ni5 bronze powders. By calculations of the impact conditions, the range of optimum spray parameters was preselected in terms of the coating quality parameter η on steel substrates with different temperatures. As-atomized and annealed powders were compared to optimize cavitation resistance of the coatings. Results provide insights about the interplay between the mechanical properties of powder and substrate for coating formation. Single particle impact morphologies visualize the deformation behavior. Coating performance was assessed by analyzing microstructures, bond strength, and cavitation resistance. These first results demonstrate that cold-sprayed bronze coatings have a high potential for ensuring a good performances in rudder protection. With further optimization, such coatings could evolve towards a competitive alternative to existing anti-cavitation procedures.

  9. A tunable hybrid metamaterial absorber based on vanadium oxide films

    Science.gov (United States)

    Wen, Qi-Ye; Zhang, Huai-Wu; Yang, Qing-Hui; Chen, Zhi; Long, Yang; Jing, Yu-Lan; Lin, Yuan; Zhang, Pei-Xin

    2012-06-01

    A tunable hybrid metamaterial absorber (MA) in the microwave band was designed, fabricated and characterized. The hybrid MA was realized by incorporating a VO2 film into the conventional resonant MA. By thermally triggering the insulator-metal phase transition of the VO2 film, the impedance match condition was broken and a deep amplitude modulation of about 63.3% to the electromagnetic wave absorption was achieved. A moderate blue-shift of the resonance frequency was observed which is promising for practical applications. This VO2-based MA exhibits many advantages such as strong tunability, frequency agility, simple fabrication and ease of scaling to the terahertz band.

  10. Adsorption of ammonia on vanadium-antimony mixed oxides

    Energy Technology Data Exchange (ETDEWEB)

    Seitz, Hernan; German, Estefania [Departamento e Instituto de Fisica del Sur, Universidad Nacional del Sur-CONICET, Avda. Alem 1253, (8000) Bahia Blanca (Argentina); Juan, Alfredo, E-mail: cajuan@uns.edu.ar [Departamento e Instituto de Fisica del Sur, Universidad Nacional del Sur-CONICET, Avda. Alem 1253, (8000) Bahia Blanca (Argentina); Irigoyen, Beatriz [Departamento de Ingenieria Quimica, Facultad de Ingenieria, Universidad de Buenos Aires, Pabellon de Industrias, Ciudad Universitaria, (1428) Ciudad Autonoma de Buenos Aires (Argentina)

    2012-02-01

    We analyzed the adsorption of ammonia (NH{sub 3}) on the VSbO{sub 4}(1 1 0) catalyst surface using density functional theory (DFT) calculations. We followed the evolution of the chemical bonds between different atoms of the resulting NH{sub 3}/VSbO{sub 4} system and the changes in the electronic structure of the catalyst. NH{sub 3} preferential adsorption geometries were analyzed through the crystal orbital overlap population (COOP) concept and the density of states (DOS) curves. The VSbO{sub 4}(1 1 0) surface exhibits Lewis and Bronsted acid sites on which the ammonia molecule can interact. On the Lewis acid site, NH{sub 3} adsorption resulted in the interaction between the N and a surface V-isolated cation. On Bronsted acid site, N interacted with a surface H coming from the chemical dissociation of water. The COOP analysis indicate that NH{sub 3} interaction on the VSbO{sub 4}(1 1 0) surface is weak. In addition, the DOS curves show more developed electronic interactions for NH{sub 3} adsorption on Lewis acid site than over Bronsted acid site.

  11. Structure, hydrolysis, and diffusion of aqueous vanadium ions from Car-Parrinello molecular dynamics

    Science.gov (United States)

    Jiang, Zhen; Klyukin, Konstantin; Alexandrov, Vitaly

    2016-09-01

    A molecular level understanding of the properties of electroactive vanadium species in aqueous solution is crucial for enhancing the performance of vanadium redox flow batteries. Here, we employ Car-Parrinello molecular dynamics simulations based on density functional theory to investigate the hydration structures, first hydrolysis reaction, and diffusion of aqueous V2+, V3+, VO2+, and VO 2+ ions at 300 K. The results indicate that the first hydration shell of both V2+ and V3+ contains six water molecules, while VO2+ is coordinated to five and VO 2+ to three water ligands. The first acidity constants (pKa) estimated using metadynamics simulations are 2.47, 3.06, and 5.38 for aqueous V3+, VO 2+ , and VO2+, respectively, while V2+ is predicted to be a fairly weak acid in aqueous solution with a pKa value of 6.22. We also show that the presence of chloride ions in the first coordination sphere of the aqueous VO 2+ ion has a significant impact on water hydrolysis leading to a much higher pKa value of 4.8. This should result in a lower propensity of aqueous VO 2+ for oxide precipitation reaction in agreement with experimental observations for chloride-based electrolyte solutions. The computed diffusion coefficients of vanadium species in water at room temperature are found to increase as V 3 + < VO 2 + < V O 2 + < V 2 + and thus correlate with the simulated hydrolysis constants, namely, the higher the pKa value, the greater the diffusion coefficient.

  12. X-ray absorption of Azotobacter vinelandii vanadium nitrogenase

    Energy Technology Data Exchange (ETDEWEB)

    George, G.N.; Coyle, C.L.; Hales, B.J.; Cramer, S.P.

    1988-06-08

    Evidence for the existence of a vanadium-containing nitrogenase has existed for more than half a century, but progress in understanding this enzyme has only come recently. In 1980, Bishop and co-workers proposed that an alternative nitrogen-fixing enzyme exists in Azotobacter vinelandii and subsequently proposed that vanadium was involved. In 1986, Robson et al. demonstrated clearly that the alternate nitrogenase from Azotobacter chroococcum, Acl*, contained vanadium instead of molybdenum. Hales et al. have shown the vanadium is also found in the Azotobacter vinelandii alternative component I, Avl'. The molybdenum and vanadium nitrogenase proteins are similar in many respects. Like the molybdenum enzyme, both Acl* and Avl' exhibit an EPR spectrum characteristic of a species with an S = 3/2 ground state; Avl' also contains the so-called P-clusters. Additionally Acl* has recently been shown to possess an N-methylformamide soluble cofactor, FeVco, analogous to the well-known iron-molybdenum cofactor FeMoco. Arber et al. have reported X-ray absorption spectra for the Acl* enzyme and interpreted the EXAFS as evidence for a V-Fe-S cluster. The local vanadium structure is proposed to resemble a recently synthesized cubane-like VFe/sub 3/S/sub 4/ cluster, and analogies are drawn with the EXAFS-derived structure reported for the molybdenum nitrogenases. The authors report herein an X-ray absorption spectroscopic study of A. vinelandii vanadium nitrogenase, Avl', which supports and extends the work of Arber et al.

  13. Critical Commodities: Tracing Greek Trade in Oil and Wine from the Late Bronze Age to the Archaic Period

    OpenAIRE

    Pratt, Catherine Elizabeth

    2014-01-01

    Most studies of the Greek oil and wine industry focus either on the Late Bronze Age or the Classical Period, rarely mentioning the Early Iron Age (so often cast as a Dark Age) between the two. This dissertation attempts to fill this gap by investigating evidence for the continuity of a surplus economy between the Late Bronze Age and the Archaic period. Specifically, I examine what type of oil and wine economy existed in the Late Bronze Age (LBA), how this economy continued into the Early Iron...

  14. Vanadium-Catalyzed Enantioselective Desymmetrization of meso-Secondary Allylic Alcohols and Homoallylic Alcohols

    OpenAIRE

    Li, Zhi; Zhang, Wei; Hisashi Yamamoto, H.

    2008-01-01

    Vanadium-catalyzed epoxidation has extended substrate scope. In addition to various bis-allylic alcohols, bis-homoallylic alcohols can also be desymmetrized using our Vanadium-Bis-hydroxamic acid complexes.

  15. Complexation of vanadium with amidoxime and carboxyl groups. Uncovering the competitive role of vanadium in uranium extraction from seawater

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Cong-Zhi; Wu, Qun-Yan; Lan, Jian-Hui; Shi, Wei-Qun [Chinese Academy of Sciences, Beijing (China). Inst. of High Energy Physics; Chai, Zhi-Fang [Chinese Academy of Sciences, Beijing (China). Inst. of High Energy Physics; Soochow Univ., Suzhou (China). School of Radiological and Interdisciplinary Sciences (RAD-X); Wu, Guo-Zhong [Chinese Academy of Sciences, Shanghai (China). Shanghai Inst. of Applied Physics

    2017-09-01

    At present, amidoxime-based adsorbents are considered to be the most promising materials for extraction of uranium from seawater. However, the high concentrations of transition metals especially vanadium strongly compete with uranium in the sequestration process, which is extremely limited the commercial use of amidoxime-based adsorbents. In this work, the coordination modes, bonding nature, and stabilities of possible vanadium(IV) (VO{sup 2+}) and (V) (VO{sub 2}{sup +}, VO{sup 3+}, V{sup 5+}) complexes with amidoximate (AO{sup -}), carboxyl (Ac{sup -}), glutarimidedioximate (HA{sup -}) and deprotonated glutarimidedioximate (A{sup 2-}) on single and double alkyl chains (R=C{sub 13}H{sub 26}) are systematically explored by quantum chemical calculations. Different from the uranyl (UO{sub 2}{sup 2+}) complexes, the AO{sup -} groups of the vanadium(IV) and (V) complexes prefer to coordinate as monodentate and chelate ligands, while few species with AO{sup -} groups in η{sup 2}-binding mode have been observed in the vanadium complexes. Besides, the vanadium complexes are predicted to have obvious covalent metal-ligand bonds. According to thermodynamic stability analysis, all the vanadium complexes with AO{sup -}, Ac{sup -}, HA{sup -} and A{sup 2-} ligands on double alkyl chains are found to be more stable than corresponding complexes with ligands on a single chain. The synergistic effect of the amidoxime and carboxyl groups can be observed in most of VO{sub 2}{sup +} and VO{sup 3+} complexes with mixed ligands (AO{sup -}/Ac{sup -}). The vanadium(IV) and (V) complexes are more stable than the corresponding uranyl complexes, and the adsorption capability of the amidoxime-based adsorbents toward vanadium(V) ions decrease in the order of VO{sub 2}{sup +}>VO{sup 3+}> V{sup 5+}. The dioxovanadium cation VO{sub 2}{sup +} is predicted to form multinuclear vanadium complex in the sequestration process, possibly resulting in higher stable VO{sub 2}{sup +} complexes. Therefore

  16. Vanadium uptake by biomass of Coprinus comatus and their effect on hyperglycemic mice.

    Science.gov (United States)

    Han, Chunchao; Cui, Bo; Wang, Yingzi

    2008-07-01

    The Vanadium uptake by Coprinus comatus and their co-effect on hyperglycemic mice were studied. By fermentation and AAS analysis, the optimal concentration of vanadium in medium was 0.4%, and the content of vanadium accumulated in the mycelia was 3,528.0 microg/g. At the concentration of 0.4%, the vanadium-associated toxicity was reduced, and its anti-diabetic effects were maintained.

  17. A Novel Eco-Friendly Vanadium Precipitation Method by Hydrothermal Hydrogen Reduction Technology

    OpenAIRE

    Guobin Zhang; Yimin Zhang; Shenxu Bao; Jing Huang; Liuhong Zhang

    2017-01-01

    In view of the serious pollution problems caused by the traditional vanadium precipitation process, the eco-friendly technology of hydrothermal hydrogen reduction was first applied to precipitate phase pure vanadium sesquioxide (V2O3) products from stripped pentavalent vanadium (V (V)) solution extracted from vanadium-bearing shale. Thermodynamic analysis demonstrate the method of hydrothermal hydrogen reduction is feasible for precipitating V2O3 from V (V) solution at a suitable pH range, an...

  18. The Vanadium Iodoperoxidase from the marine flavobacteriaceae species Zobellia galactanivorans reveals novel molecular and evolutionary features of halide specificity in the vanadium haloperoxidase enzyme family.

    Science.gov (United States)

    Fournier, Jean-Baptiste; Rebuffet, Etienne; Delage, Ludovic; Grijol, Romain; Meslet-Cladière, Laurence; Rzonca, Justyna; Potin, Philippe; Michel, Gurvan; Czjzek, Mirjam; Leblanc, Catherine

    2014-12-01

    Vanadium haloperoxidases (VHPO) are key enzymes that oxidize halides and are involved in the biosynthesis of organo-halogens. Until now, only chloroperoxidases (VCPO) and bromoperoxidases (VBPO) have been characterized structurally, mainly from eukaryotic species. Three putative VHPO genes were predicted in the genome of the flavobacterium Zobellia galactanivorans, a marine bacterium associated with macroalgae. In a phylogenetic analysis, these putative bacterial VHPO were closely related to other VHPO from diverse bacterial phyla but clustered independently from eukaryotic algal VBPO and fungal VCPO. Two of these bacterial VHPO, heterogeneously produced in Escherichia coli, were found to be strictly specific for iodide oxidation. The crystal structure of one of these vanadium-dependent iodoperoxidases, Zg-VIPO1, was solved by multiwavelength anomalous diffraction at 1.8 Å, revealing a monomeric structure mainly folded into α-helices. This three-dimensional structure is relatively similar to those of VCPO of the fungus Curvularia inaequalis and of Streptomyces sp. and is superimposable onto the dimeric structure of algal VBPO. Surprisingly, the vanadate binding site of Zg-VIPO1 is strictly conserved with the fungal VCPO active site. Using site-directed mutagenesis, we showed that specific amino acids and the associated hydrogen bonding network around the vanadate center are essential for the catalytic properties and also the iodide specificity of Zg-VIPO1. Altogether, phylogeny and structure-function data support the finding that iodoperoxidase activities evolved independently in bacterial and algal lineages, and this sheds light on the evolution of the VHPO enzyme family. Copyright © 2014, American Society for Microbiology. All Rights Reserved.

  19. A new sensitive electrochemical method for the determination of vanadium(IV) and vanadium(V) in Benfield sample.

    Science.gov (United States)

    Qureshi, Munawar Saeed; Mohd Yusoff, Abdull Rahim bin; Shah, Afzal; Nafady, Ayman; Sirajuddin

    2015-01-01

    Vanadium(IV) and vanadium(V) can be determined by using differential pulse cathodic stripping voltammetry technique (DPCSV). Cupferron (ammonium N-nitrosophenylhydroxylamine) was used as ligand to form complex compounds with vanadium ions in Britton-Robinson buffer (BRB) solution. At concentration lower than 1.0×10(-6) M, both V(IV) and V(V) cupferron complexes showed a single cathodic peak at -0.576 V in BRB of pH 4; thus V(IV) and V(V) ions cannot be differentiated at low concentration. However, the ionic species of vanadium can be differentiated at high concentration in the presence of cupferron. Parameters including pH of BRB solution, initial potential and accumulation potential were optimized. Under the optimized parameters, the limit of detection (LOD) was 0.09 nM, and the peak current was linear in the concentration range 0.01-0.9 µM total vanadium ions. The determination of V(IV) and V(V) ions was carried out at higher concentration in the sample using calibration plot method. At higher concentration range of 10-60 µM V(IV) and V(V) ions were determined with LOD of 1.2 and 1.1 µM, respectively. The developed method was successfully applied to 10,00,000 fold diluted Benfield sample and 0.6227 M total vanadium ions were determined. The determination of V(IV) and V(V) ions were also successfully carried out in artificial sample as well as Benfield sample (dilution factor, 10,000). The concentration of V(IV) and V(V) ions was 22.52 µM and 38.91 µM, respectively, giving total vanadium concentration of 0.6143 M in Benfield sample. Copyright © 2014 Elsevier B.V. All rights reserved.

  20. Effects of gamma irradiations on reactive pulsed laser deposited vanadium dioxide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Madiba, I.G., E-mail: madibagiven@gmail.com [UNESCO-UNISA Africa Chair in Nanosciences/Nanotechnology, College of Graduate Studies, University of South Africa (UNISA), Muckleneuk Ridge, P O Box 392, Pretoria (South Africa); Empa, Swiss Federal Laboratories Materials Science and Technology, CH-8600 Dübendorf (Switzerland); Émond, N.; Chaker, M. [Institut National de la Recherche Scientifique (INRS),1650 Blvd. Lionel-Boulet, Varennes, Québec J3X1S2 (Canada); Thema, F.T. [UNESCO-UNISA Africa Chair in Nanosciences/Nanotechnology, College of Graduate Studies, University of South Africa (UNISA), Muckleneuk Ridge, P O Box 392, Pretoria (South Africa); iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa); Tadadjeu, S.I. [iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa); Department of Electrical, Electronics and Computer Engineering, French South African Institute of Technology/Cape Peninsula University of Technology, Bellville campus, PO Box 1906, Bellville, 7530 (South Africa); Muller, U.; Zolliker, P. [Empa, Swiss Federal Laboratories Materials Science and Technology, CH-8600 Dübendorf (Switzerland); Braun, A. [ETH Zurich, Swiss Federal Institute of Technology, CH-8057, Zurich (Switzerland); Empa, Swiss Federal Laboratories Materials Science and Technology, CH-8600 Dübendorf (Switzerland); Kotsedi, L. [iThemba LABS-National Research Foundation, 1 Old Faure Road, Somerset West 7129, PO Box 722, Somerset West, Western Cape Province (South Africa); and others

    2017-07-31

    Highlights: • Synthesis of VO{sub 2} thin films by Reactive pulsed laser deposition has been achieved. • Properties VO{sub 2} remain mainly unaffected when subjected to gamma ray doses similar to those encountered during space missions. • The long range crystal structure of VO{sub 2} remains intact upon irradiation on different doses up to 100 kGy. • XPS reveals a shift from V{sup 4+} to V{sup 5+} oxidation state upon irradiation, due to the frenkel pair formation on the surface. • Irradiated films show the characteristic SMT of VO{sub 2}, although the electrical and optical properties are slightly affected. - Abstract: Vanadium oxide films are considered suitable coatings for various applications such as thermal protective coating of small spacecrafts because of their thermochromic properties. While in outer space, such coating will be exposed to cosmic radiations which include γ-rays. To study the effect of these γ-rays on the coating properties, we have deposited vanadium dioxide (VO{sub 2}) films on silicon substrates and subjected them to extensive γ-irradiations with typical doses encountered in space missions. The prevalent crystallographic phase after irradiation remains the monoclinic VO{sub 2} phase but the films preferential orientation shifts to lower angles due to the presence of disordered regions caused by radiations. Raman spectroscopy measurements also evidences that the VO{sub 2} structure is slightly affected by gamma irradiation. Indeed, increasing the gamma rays dose locally alters the crystalline and electronic structures of the films by modifying the V–V inter-dimer distance, which in turns favours the presence of the VO{sub 2} metallic phase. From the XPS measurements of V2p and O1s core level spectra, an oxidation of vanadium from V{sup 4+} towards V{sup 5+} is revealed. The data also reveal a hydroxylation upon irradiation which is corroborated by the vanishing of a low oxidation state peak near the Fermi energy in the

  1. Gastroprotective effect of vanadium in rats - the roles of gastric acid ...

    African Journals Online (AJOL)

    Vanadium (various forms) has been proven to be beneficial in the treatment of certain diseases, especially diabetes. Reports have it that vanadium may protect the stomach from gastric ulcerogens such as ethanol and acid. This study was designed to investigate the probable mechanism Vanadium exerts its' ...

  2. Method for Vanadium Speciation in Aqueous Samples by HPLC-ICP ...

    African Journals Online (AJOL)

    Method for Vanadium Speciation in Aqueous Samples by HPLC-ICP-OES. M Hu, PP Coetzee. Abstract. A method for vanadium speciation is proposed. The method uses a low concentration eluent, 10 mmol L–1 EDTA and 14 mmol L–1 sodium carbonate, for the ion chromatographic separation of vanadium species at a ...

  3. Method for Vanadium Speciation in Aqueous Samples by HPLC-ICP ...

    African Journals Online (AJOL)

    NJD

    methods can only measure the total concentration of vanadium, or one of the two vanadium species, particularly V(V).4–6 Some two-step methods for the determination of the two vanadium species7–10 have been proposed by several groups. These methods normally measure one of the two species in one step, and in the.

  4. Vanadium Extraction from Refractory Stone Coal Using Novel Composite Additive

    Science.gov (United States)

    Cai, Z. L.; Zhang, Y. M.; Liu, T.; Huang, J.

    2015-11-01

    Based on the novel composite additive BaCO3/CaO for the vanadium extraction from the refractory stone coal, the vanadium leaching effect has been investigated and many technical conditions have also been optimized. The results indicated that an optimum vanadium leaching efficiency of 81.07% can be obtained under the conditions that the mass ratio of BaCO3 to CaO was 1:9 with the total proportion of the raw ore was 5 wt.%, the roasting temperature was 850°C, the roasting time was 2 h, the sulfuric acid concentration was 15% (v/v), the leaching temperature was 95°C, the liquid-to-solid ratio was 4 mL/g, and the leaching time was 3 h. Meanwhile, the vanadium leaching mechanisms demonstrated that the composite additive BaCO3/CaO can destroy the lattice structure of muscovite and phlogopite with the production of BaSi4O9 and Ca2Al2SiO7 during the roasting process, which can therefore facilitate the release and extraction of vanadium.

  5. Imaging of Vanadium in Microfossils: A New Potential Biosignature

    Science.gov (United States)

    Marshall, Craig P.; Marshall, Alison Olcott; Aitken, Jade B.; Lai, Barry; Vogt, Stefan; Breuer, Pierre; Steemans, Philippe; Lay, Peter A.

    2017-11-01

    The inability to unambiguously distinguish the biogenicity of microfossil-like structures in the ancient rock record is a fundamental predicament facing Archean paleobiologists and astrobiologists. Therefore, novel methods for discriminating biological from nonbiological chemistries of microfossil-like structures are of the utmost importance in the search for evidence of early life on Earth. This, too, is important for the search for life on Mars by in situ analyses via rovers or sample return missions for future analysis here on Earth. Here, we report the application of synchrotron X-ray fluorescence imaging of vanadium, within thermally altered organic-walled microfossils of bona fide biological origin. From our data, we demonstrate that vanadium is present within microfossils of undisputable biological origin. It is well known in the organic geochemistry literature that elements such as vanadium are enriched and contained within crude oils, asphalts, and black shales that have been formed by diagenesis of biological organic material. It has been demonstrated that the origin of vanadium is due to the diagenetic alteration of precursor chlorophyll and heme porphyrin pigment compounds from living organisms. We propose that, taken together, microfossil-like morphology, carbonaceous composition, and the presence of vanadium could be used in tandem as a biosignature to ascertain the biogenicity of putative microfossil-like structures.

  6. Membrane development for vanadium redox flow batteries.

    Science.gov (United States)

    Schwenzer, Birgit; Zhang, Jianlu; Kim, Soowhan; Li, Liyu; Liu, Jun; Yang, Zhenguo

    2011-10-17

    Large-scale energy storage has become the main bottleneck for increasing the percentage of renewable energy in our electricity grids. Redox flow batteries are considered to be among the best options for electricity storage in the megawatt range and large demonstration systems have already been installed. Although the full technological potential of these systems has not been reached yet, currently the main problem hindering more widespread commercialization is the high cost of redox flow batteries. Nafion, as the preferred membrane material, is responsible for about 11% of the overall cost of a 1 MW/8 MWh system. Therefore, in recent years two main membrane related research threads have emerged: 1) chemical and physical modification of Nafion membranes to optimize their properties with regard to vanadium redox flow battery (VRFB) application; and 2) replacement of the Nafion membranes with different, less expensive materials. This review summarizes the underlying basic scientific issues associated with membrane use in VRFBs and presents an overview of membrane-related research approaches aimed at improving the efficiency of VRFBs and making the technology cost-competitive. Promising research strategies and materials are identified and suggestions are provided on how materials issues could be overcome.

  7. X-ray Photoelectron Spectroscopy as a tool to investigate silane-based coatings for the protection of outdoor bronze: The role of alloying elements

    Science.gov (United States)

    Masi, G.; Balbo, A.; Esvan, J.; Monticelli, C.; Avila, J.; Robbiola, L.; Bernardi, E.; Bignozzi, M. C.; Asensio, M. C.; Martini, C.; Chiavari, C.

    2018-03-01

    Application of a protective coating is the most widely used conservation treatment for outdoor bronzes (cast Cu-Sn-Zn-Pb-Sb alloys). However, improving coating protectiveness requires detailed knowledge of the coating/substrate chemical bonding. This is particularly the case for 3-mercapto-propyl-trimethoxy-silane (PropS-SH) applied on bronze, exhibiting a good protective behaviour in outdoor simulated conditions. The present work deals with X-Ray Photoelectron Spectroscopy (XPS) and Electron Microscopy (FEG-SEM + FIB (Focused Ion Beam)) characterization of a thin PropS-SH film on bronze. In particular, in order to better understand the influence of alloying elements on coating performance, PropS-SH was studied first on pure Cu and Sn substrates then on bronzes with increasing alloy additions: Cu8Sn as well as a quinary Cu-Sn-Zn-Pb-Sb bronze. Moreover, considering the real application of this coating on historical bronze substrates, previously artificially aged ("patinated") bronze samples were prepared and a comparison between bare and "patinated" quinary bronzes was performed. In the case of coated quinary bronze, the free surface of samples was analysed by High Resolution Photoelectron Spectroscopy using Synchrotron Radiation (HR-SRPES) at ANTARES (Synchrotron SOLEIL), which offers a higher energy and lateral resolution. By compiling complementary spectroscopic and imaging information, a deeper insight into the interactions between the protective coating and the bronze substrate was achieved.

  8. Atomic XAFS as a Tool To Probe the Reactivity of Metal Oxide Catalysts: Quantifying Metal Oxide Support Effects

    NARCIS (Netherlands)

    Keller, D.E.; Airaksinen, S.M.K.; Krause, A.O.I.; Weckhuysen, B.M.|info:eu-repo/dai/nl/285484397; Koningsberger, D.C.|info:eu-repo/dai/nl/073704342

    2007-01-01

    The potential of atomic XAFS (AXAFS) to directly probe the catalytic performances of a set of supported metal oxide catalysts has been explored for the first time. For this purpose, a series of 1 wt % supported vanadium oxide catalysts have been prepared differing in their oxidic support material

  9. Comparison of Microstructural and Tribological Effects of Low Vanadium-Low Titanium Additions to a Gray Cast Iron

    Science.gov (United States)

    Hassani, A.; Habibolahzadeh, A.; Sadeghinejad, S.

    2013-01-01

    Effects of low amounts of vanadium and titanium additions on the microstructure, tribological properties of a gray cast iron were studied and an overall comparison was made between these two alloys. Pin-on-disk tests were performed on the specimens at three different loads and two sliding speeds. SEM was utilized to study the worn surfaces and the mechanisms under which wear occurred. Local chemical analyses were conducted on the specific spots in the wear tracks by EDX. Wear mechanisms were determined and the quantitative amounts of the elements in the tribochemical films formed on the wear tracks were evaluated. Both vanadium-treated and untreated samples exhibited oxidative wear mechanism under mild regimes and adhesive wear mechanism under severe wear regime. The wear rate was reduced up to 85% when the vanadium-treated sample was tested; it showed the best wear resistance. The alloy having titanium, however, showed the least wear resistance compared to the others. It could be due to the formation of type-D graphite in its microstructure.

  10. Preliminary Study of Corrosion Status on Bronzes Excavated from Qin Dynasty Tombs at Xinfeng Town in China

    Directory of Open Access Journals (Sweden)

    Qian-li Fu

    2012-01-01

    Full Text Available From 2007 to 2008, many bronze wares of Qin Dynasty were excavated from tombs at Xinfeng town. Being an important finding, these bronze wares attracted people’s attention, especially for their conservation. Therefore, the corrosive products were explored by using Scanning Electron Microscope with Energy Dispersive X-ray Detector (SEM/EDS, X-Ray diffraction (XRD, and Raman spectroscopy (RM, which provided much valuable information on the conservation of these bronze wares. According to tested results, the corrosive products of bronzes were found to be comprised of cuprite (Cu2O, covellite (CuS, lead carbonate (PbCO3, and malachite (CuCO3·Cu(OH2. Meantime, the multilayer corrosive structure was found in some samples due to the cracks in Cu2O layer which had formed many microchannels to promote the material migration.

  11. Chromium, nickel and vanadium mobility in soils derived from fluvioglacial sands.

    Science.gov (United States)

    Agnieszka, Jeske; Barbara, Gworek

    2012-10-30

    The presented study was focused on soils developed from fluvioglacial sands from the Puszcza Borecka forest complex. The mobility of chromium, nickel and vanadium was evaluated with regard to litho- and pedogenic factors. The aim of the study was to determine with which soil constituents fractions of heavy metals are bound with particular attention drawn on the mobile fractions (F1+F2). Heavy metal fractions in the soils were determined using the sequential extraction method of Tessier et al. The purpose of sequential extraction methods to soil samples provides relevant information about possible toxicity when they are discharged into the soil environment. Chromium, nickel, and vanadium occurred predominantly in the fraction bound with iron and manganese oxides and in the residual fraction, thus showed low mobility. With regard to mobility, the elements studied can be arranged as follows: V

  12. Photolytic Release of Dissolved Vanadium and Copper from Resuspended Coastal Marine Sediments

    Science.gov (United States)

    Skrabal, S. A.; Hammaker, S. N.; McBurney, A. W.; Avery, G. B., Jr.; Kieber, R. J.; Mead, R. N.

    2016-02-01

    Sunlight photolysis engenders release of dissolved vanadium (V), copper (Cu), and dissolved organic carbon (DOC) from a wide variety of resuspendable coastal marine sediments. Net photoreleases after 6 h of simulated sunlight were as high as 12 nM for Cu and as high as 15 nM for V. Release of Cu significantly correlated with sediment Cu. Photoreleased Cu (but not V) correlated with sediment Fe content, suggesting that photoreduction of Fe oxide carrier phases may be an important photoproduction mechanism for Cu. Longer term experiments showed continued release of metals that were not immediately readsorbed back onto sediments after 24 h of irradiation suggesting that photoproduced metals persist in the dissolved phase and are not immediately scavenged onto particles. Experiments utilizing differing total suspended sediment (TSS) levels show that, although higher TSS causes more photoproduction of Cu and V, the amount produced per mass of sediment is greatest at the lowest TSS. Vanadium photoproduction increased in Macondo oil-amended sediments compared to controls after a one-month incubation period suggesting that the oil may be a source of this metal to the water column. These results imply that photoproduction is an unrecognized source of the micronutrient metals Cu and V to coastal waters.

  13. Axial coordination in nickel and vanadium porphyrins: Transient and difference raman spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Shelnutt, J.; Alston, K.; Findsen, E.; Ondrias, M.

    1986-04-01

    Nickel and vanadium tetrapyrroles occurring in coal and petroleum are of biological origin and their present day molecular structures provide a valuable chemical fossil marker of the diagenesis of the deposits. Both Ni- and V-porphyrins add axial ligands at the metal site. The authors have investigated the equilibrium properties and nanosecond dynamics of axial ligation in Ni(II)- and V(IV)-porphyrin complexes, Ni-porphyrin-reconstituted heme proteins, and Ni-porphyrin polymers using resonance Raman spectroscopy. The state of axial coordination is recognized by characteristic frequencies of Raman oxidation-state and core-size marker lines arising from the vibrations of the porphyrin ring, and the frequencies distinguish between 4-, 5-, and 6-coordination. For the Ni-porphyrins, 4- and 6-coordinate species are observed in coordinating solvents, while 5-coordinate Ni occurs only in the protein matrix. The axial ligand-Ni stretching mode frequency is influenced by the conformation of the protein matrix. Ligand affinity is affected by porphyrin structure, ligand basicity, and the porphyrin's environment. The authors also investigated photoinduced ligand-release and ligand binding kinetics using transient Raman spectroscopy. The protein matrix has a strong influence on the kinetics of ligand rebinding. For vanadium porphyrins, similar shifts in the marker lines characterize 5- and 6-coordinate forms.

  14. Biodesulfurization of vanadium-bearing titanomagnetite concentrates and pH control of bioleaching solution

    Science.gov (United States)

    Liu, Xiao-rong; Jiang, Sheng-cai; Liu, Yan-jun; Li, Hui; Wang, Hua-jun

    2013-10-01

    Vanadium-bearing titanomagnetite concentrates were desulfurized with Acidithiobacillus ferrooxidans ( A. ferrooxidans). The sulfur content of the concentrates was reduced from 0.69wt% to 0.14wt% after bioleaching for 15 d with a 10% pulp density at 30°C. Maintaining a stable pH value during biodesulfurization was critical because of high acid consumption, resulting from a combination of nonoxidative and oxidative dissolution of pyrrhotite in acid solution. It is discovered that the citric acid-disodium hydrogen phosphate buffer of pH 2.0 can control the solution pH value smoothly in the optimal range of 2.0-3.0 for A. ferrooxidans growth. Using the buffer in the volume fraction range of 5.0%-15.0% stimulates A. ferrooxidans growth and improves the biodesulfurization efficiency. Compared with the buffer-free control case, the maximum increase of biodesulfurization rate is 29.7% using a 10.0vol% buffer. Bioleaching provides an alternative process for desulfurization of vanadium-bearing titanomagnetite ores.

  15. Assessing the solubility controls on vanadium in groundwater, northeastern San Joaquin Valley, CA

    Science.gov (United States)

    Wright, Michael T.; Stollenwerk, Kenneth G.; Belitz, Kenneth

    2014-01-01

    The solubility controls on vanadium (V) in groundwater were studied due to concerns over possible harmful health effects of ingesting V in drinking water. Vanadium concentrations in the northeastern San Joaquin Valley ranged from 25 μg/L) and lowest in samples collected from anoxic groundwater (70% 2VO4−. Adsorption/desorption reactions with mineral surfaces and associated oxide coatings were indicated as the primary solubility control of V5+ oxyanions in groundwater. Environmental data showed that V concentrations in oxic groundwater generally increased with increasing groundwater pH. However, data from adsorption isotherm experiments indicated that small variations in pH (7.4–8.2) were not likely as an important a factor as the inherent adsorption capacity of oxide assemblages coating the surface of mineral grains. In suboxic groundwater, accurate SM modeling was difficult since Eh measurements of source water were not measured in this study. Vanadium concentrations in suboxic groundwater decreased with increasing pH indicating that V may exist as an oxycationic species [e.g. V(OH)3+]. Vanadium may complex with dissolved inorganic and organic ligands under suboxic conditions, which could alter the adsorption behavior of V in groundwater. Speciation modeling did not predict the existence of V-inorganic ligand complexes and organic ligands were not collected as part of this study. More work is needed to determine processes governing V solubility under suboxic groundwater conditions. Under anoxic groundwater conditions, SM predicts that aqueous V exists as the uncharged V(OH)3 molecule. However, exceedingly low V concentrations show that V is sparingly soluble in anoxic conditions. Results indicated that V may be precipitating as V3+- or mixed V3+/Fe3+-oxides in anoxic groundwater, which is consistent with results of a previous study. The fact that V appears insoluble in anoxic (Fe reducing) redox conditions indicates that the behavior of V is different than

  16. Direct Acid Leaching of Vanadium from Stone Coal

    Science.gov (United States)

    Zhang, Bo; Gao, Zhaoguo; Liu, Hongzhao; Wang, Wei; Cao, Yaohua

    2017-09-01

    This paper focused on optimizing the process conditions of direct acid leaching process to enhance the leaching efficiency of leaching vanadium from the stone coal. Orthogonal experiments and single factor experiments were conducted to investigate the effect of the influential factors of direct acid leaching on vanadium leaching ratio. The results showed that the vanadium leaching ratio reached the maximum value of 89.22 % under the optimal process conditions of CaF2 dosage 5 mass%, H2SO4 dosage 40 mass%, leaching temperature 95 °C and leaching time 10 h. Furthermore, the reaction mechanisms of the main influencing factors were analyzed. Finally, the two-stage counter-current leaching process was adopted to decrease the consumption of sulfuric acid and neutralizer, and the results indicated that the consumption of sulfuric acid decreased 12.50 % as well as neutralizer decreased 35.80 %.

  17. Complex research of vanadium dioxide in the homoginuity field

    Science.gov (United States)

    Surikov, Vad I.; Semenyuk, N. A.; Surikov, Val I.; Kuznetsova, Y. V.; Pavlovskaya, O. Y.

    2018-01-01

    The complex research results of vanadium dioxide VÜ2±x obtained with X-ray analysis method, a method of vacuum adiabatic calorimeter and Faraday method are discussed. The samples temperature dependences of electrical resistivity, heat capacity, and also magnetic susceptibility are presented and they prove that these characteristics jump abruptly in the phase transition area. Thermophysical, electrical, magnetic properties of vanadium dioxide are established to vary with the oxygen content in the samples. Values of Debye characteristic temperatures θD for samples VO2±x determined at temperature 150 K are presented. Values of entropy change as an amount of electronic and phonon components at phase transition were calculated. The results obtained allow to consider the phase transition of a metal semiconductor as a Mott-Peierls transition, and also to use vanadium dioxide in temperature sensors manufacture.

  18. Adsorption kinetics and isotherm of vanadium with melamine.

    Science.gov (United States)

    Peng, Hao; Liu, Zuohua; Tao, Changyuan

    2017-05-01

    Melamine, possessing three free amino groups and three aromatic nitrogen atoms in its molecule, has great potential as an adsorbent for metal ions. We investigated three impact factors of the adsorption process: the initial pH of the vanadium solution, contact time and reaction temperature. The adsorption kinetics could be accurately described by the pseudo-second-order kinetic model. Langmuir and Freundlich models fitted well with the experimental equilibrium data, and the maximal adsorption capacity was found to be 1,428.57 mg vanadium/g melamine, and the Freundlich model showed the adsorption is privilege type.

  19. Flowerlike vanadium sesquioxide: solvothermal preparation and electrochemical properties.

    Science.gov (United States)

    Liu, Haimei; Wang, Yonggang; Li, Huiqiao; Yang, Wensheng; Zhou, Haoshen

    2010-10-25

    A novel 3D hierarchical flowerlike vanadium sesquioxide (V(2)O(3)) nano/microarchitecture consisting of numerous nanoflakes is prepared via a solvothermal approach followed by an appropriate heating treatment. The as-obtained nanostructured V(2)O(3) flower is characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) analysis, and transmission electron microscopy (TEM) (or/and high-resolution TEM, HRTEM), and it is found that the V(2)O(3) flower is constructed by single-crystalline nanoflakes. Furthermore, it is demonstrated that the surface of the flowerlike V(2)O(3) material is composed of nanostructured pores, which derive from the adsorption/desorption of nitrogen, and that the pore-size distribution depends on the unique three-dimensional interconnection between nanoflakes and on their intrinsic properties. The electrochemical behavior of the V(2)O(3) flower for lithium-ion insertion/extraction in non-aqueous solution as well as the faradaic capacitance for pesudocapacitors in a neutral aqueous solution are also investigated. A reversible discharge capacity as high as 325 mA h g(-1) is obtained at a current density of 0.02 A g(-1) from a LiClO(4)/EC:DEC electrolyte solution (i.e. LiClO(4) in ethyl carbonate and diethyl carbonate). When used as the cathode material of pesudocapacitors in Li(2)SO(4), the flowerlike oxide displayed a very high initial capacitance of 218 F g(-1) at a current density of 0.05 A g(-1). We believe that the good performance of the flowerlike V(2)O(3) electrode is most probably due to its unique 3D hierarchical nano/microarchitecture, which shows that the electrochemical properties of a cathodic material do not only depend on the oxidation state of that material but also-to a large extent-on its crystalline structure and morphology. The aforementioned properties suggest that the present V(2)O(3) flower materials may have a great potential to be employed as electrode materials in

  20. Absorption of hydrogen in vanadium, enhanced by ion bombardment; Ionenbeschussunterstuetzte Absorption des Wasserstoffs in Vanadium

    Energy Technology Data Exchange (ETDEWEB)

    Paulus, H.; Lammers, M. [Inst. fuer Technologie- und Wissenstransfer, Soest (Germany); Mueller, K.H. [Inst. fuer Technologie- und Wissenstransfer, Soest (Germany)]|[Paderborn Univ. (Gesamthochschule), Soest (Germany). Fachbereich 16 - Elektrische Energietechnik; Kiss, G.; Kemeny, Z. [Technical Univ. Budapest (Hungary)

    1998-12-31

    Prior to hydrogen implantation into vanadium, the vanadium specimen usually is exposed to an activation process and is then heated at 1 atm hydrogen to temperatures between 500 and 600 C, subsequently cooled down in several steps. Within this temperature range, hydrogen solubility increases with declining temperature. A decisive factor determining hydrogen absorption is the fact that at temperatures above 250 C, oxygen desorbs from the material surface and thus no longer inhibits hydrogen absorption. Therefore a different approach was chosen for the experiments reported: Hydrogen absorption under UHV conditions at room temperature. After the usual activation process, the vanadium surface was cleaned by 5 keV Ar{sup +} ion bombardment. Thus oxygen absorption at the specimen surface (and new reactions with oxygen from the remaining gas) could be avoided, or removed. By means of thermal desorption mass spectrometry (TDMS), hydrogen absorption as a function of argon ion dose was analysed. TDMS measurements performed for specimens treated by ion bombardment prior to H{sup 2} exposure showed two H{sup 2} desorption peaks, in contrast to the profiles measured with specimens not exposed to ion bombardment. It is assumed that the ion bombardment disturbs the crystal structure so that further sites for hydrogen absorption are produced. (orig./CB) [Deutsch] Bei der Beladung von Vandium mit Wasserstoff wird ueblicherweise die Probe nach einer Aktivierungsprozedur bei 1 atm Wasserstoff auf Temperaturen im Bereich von 500 bis 600 C hochgeheizt und danach schrittweise abgekuehlt. In diesem Temperaturbereich nimmt die Wasserstoffloeslichkeit mit abnehmender Temperatur zu. Entscheidend fuer die Beladung ist aber auch die Tatsache, dass bei Temperaturen groesser 250 C Sauerstoff von der Oberflaeche desorbiert und dadurch die Absorption von Wasserstoff nicht mehr blockieren kann. Im Rahmen der hier beschriebenen Untersuchungen sollte die Wasserstoffbeladung unter UHV-Bedingungen bei

  1. Carbon-carbon bond cleavage of 1,2-hydroxy ethers b7 vanadium(V) dipicolinate complexes

    Energy Technology Data Exchange (ETDEWEB)

    Hanson, Susan K [Los Alamos National Laboratory; Gordon, John C [Los Alamos National Laboratory; Thorn, David L [Los Alamos National Laboratory; Scott, Brian L [Los Alamos National Laboratory; Baker, R Tom [Los Alamos National Laboratory

    2009-01-01

    The development of alternatives to current petroleum-based fuels and chemicals is becoming increasingly important due to concerns over climate change, growing world energy demand, and energy security issues. Using non-food derived biomass to produce renewable feedstocks for chemicals and fuels is a particularly attractive possibility. However, the majority of biomass is in the form of lignocellulose, which is often not fully utilized due to difficulties associated with breaking down both lignin and cellulose. Recently, a number of methods have been reported to transform cellulose directly into more valuable materials such as glucose, sorbitol, 5-(chloromethyl)furfural, and ethylene glycol. Less progress has been made with selective transformations of lignin, which is typically treated in paper and forest industries by kraft pulping (sodium hydroxide/sodium sulfide) or incineration. Our group has begun investigating aerobic oxidative C-C bond cleavage catalyzed by dipicolinate vanadium complexes, with the idea that a selective C-C cleavage reaction of this type could be used to produce valuable chemicals or intermediates from cellulose or lignin. Lignin is a randomized polymer containing methoxylated phenoxy propanol units. A number of different linkages occur naturally; one of the most prevalent is the {beta}-O-4 linkage shown in Figure 1, containing a C-C bond with 1,2-hydroxy ether substituents. While the oxidative C-C bond cleavage of 1,2-diols has been reported for a number of metals, including vanadium, iron, manganese, ruthenium, and polyoxometalate complexes, C-C bond cleavage of 1,2-hydroxy ethers is much less common. We report herein vanadium-mediated cleavage of C-C bonds between alcohol and ether functionalities in several lignin model complexes. In order to explore the scope and potential of vanadium complexes to effect oxidative C-C bond cleavage in 1,2-hydroxy ethers, we examined the reactivity of the lignin model complexes pinacol monomethyl ether (A

  2. Optimal Location of Vanadium in Muscovite and Its Geometrical and Electronic Properties by DFT Calculation

    Directory of Open Access Journals (Sweden)

    Qiushi Zheng

    2017-02-01

    Full Text Available Vanadium-bearing muscovite is the most valuable component of stone coal, which is a unique source of vanadium manufacture in China. Numbers of experimental studies have been carried out to destroy the carrier muscovite’s structure for efficient extraction of vanadium. Hence, the vanadium location is necessary for exploring the essence of vanadium extraction. Although most infer that vanadium may substitute for trivalent aluminium (Al as the isomorphism in muscovite for the similar atomic radius, there is not enough experimental evidence and theoretical supports to accurately locate the vanadium site in muscovite. In this study, the muscovite model and optimal location of vanadium were calculated by density functional theory (DFT. We find that the vanadium prefers to substitute for the hexa-coordinated aluminum of muscovite for less deformation and lower substitution energy. Furthermore, the local geometry and relative electronic properties were calculated in detail. The basal theoretical research of muscovite contained with vanadium are reported for the first time. It will make a further influence on the technology development of vanadium extraction from stone coal.

  3. Comparison of vanadium-rich activity of three species fungi of basidiomycetes.

    Science.gov (United States)

    Han, Chunchao; Cui, Bo; Qu, Jingran

    2009-03-01

    A comparison of vanadium-rich activity of three species fungi of Basidiomycetes, Ganoderma lucidum, Coprinus comatus, and Grifola frondosa, was studied. By fermentation and atomic absorption spectroscopy analysis, the biomass of G. lucidum and G. frondosa declined rapidly when the concentration of vanadium exceeded 0.3% but the biomass of C. comatus did not decline rapidly until the concentration of vanadium exceeded 0.4% and the content of vanadium accumulated in the mycelia was 3529.3 microg/g. After the mice were administered (intragastrically) with vanadium-rich C. comatus, the blood glucose of alloxan-induced hyperglycemic mice was decreased (p comatus to absorb vanadium and chose 0.4% as the optimal concentration of vanadium for the pharmacological works.

  4. Combined effects of graphite and sulfide on the tribological properties of bronze under dry conditions

    Directory of Open Access Journals (Sweden)

    Yoshimasa Hirai

    2016-12-01

    Full Text Available The present study describes the tribological properties of penetrated-graphite bronze containing micro-sized sulfide under dry conditions. The graphite penetration was carried out by means of roller burnishing. Micro shot peening was also applied in order to fabricate micro dimples in the penetrated graphite. The graphite area fraction was approximately 50%. The tribological properties were evaluated using a face-to-face type testing apparatus under dry conditions. The results showed that the friction coefficient of the sulfide-containing bronze decreased and the seizure resistance properties significantly increased. The friction distance until seizure occurrence was improved to more than 2.5 times. Furthermore, the friction coefficient was low and stable until the end of the experiment. It was inferred that the friction resistance was decreased and stabilized when the transfer layer was without Fe content.

  5. Palaeodemographic and palaeopathological characteristics of individuals buried in three Bronze Age sites from southern Croatia

    Directory of Open Access Journals (Sweden)

    M. Novak

    2011-12-01

    Full Text Available The purpose of this study is to reconstruct paleodemographic and paleopathological characteristics of sixteen individuals (three subadults, seven males and six females buried in three Bronze Age sites (Crip, Matkovići, and Veliki Vanik located in southern Croatia. The analysed sample is characterised by the presence of pathological changes which are often associated with stressful episodes such as anaemia, inadequate nutrition, infectious diseases and the occurrence of parasites. Cribra orbitalia, dental enamel hypoplasia, porotic hyperostosis and periostitis were observed in seven out of sixteen analysed skeletons. One ulnar “parry” fracture and three fractures of the frontal bone strongly suggest the presence of deliberate interpersonal violence within the studied communities. The average life span of the adults, as well as the number and character of the observed pathologies, suggest a relatively poor life quality and harsh living conditions in the studied region during the Bronze Age.

  6. Effect of Microstructure on Mechanical Properties of BA1055 Bronze Castings

    Directory of Open Access Journals (Sweden)

    Łabanowski J.

    2014-06-01

    Full Text Available The article presents research results performed on aluminum bronze CuAl10Fe5Ni5 (BA1055 castings used for marine propellers. Metallographic studies were made on light microscope and a scanning electron microscope to assess quantitatively and qualitatively the alloy microstructure. It has been shown that the shape, size and distribution of the iron-rich к−phase precipitates in bronze microstructure significantly affect its mechanical properties. With an increase in the number of small к−phase precipitates increases the tensile strength of castings, while the presence of large globular precipitates improves ductility. Fragmentation and shape of κ−phase precipitates depends on many factors, particularly on the chemical composition of the alloy, Fe/Ni ratio, cooling rate and casting technology.

  7. Connections: the relationships between Neolithic and Bronze Age Megalithic Astronomy in Britain

    CERN Document Server

    Higginbottom, Gail

    2015-01-01

    It has already been empirically verified that for many Bronze Age monuments erected in Scotland between 1400-900 BC, there was a concerted effort on behalf of the builders to align their monuments to astronomical bodies on the horizon. It has also been found that there are two common sets of complex landscape and astronomical patternings, combining specific horizon qualities, like distance and elevation, with the rising and setting points of particular astronomical phenomena. However, it has only been very recently demonstrated by us that that the visible astronomical-landscape variables found at Bronze Age sites on the inner isles and mainland of western Scotland were first established nearly two millennia earlier, with the erection of the mooted first standing-stone 'great circles' in Britain: Callanish and Stenness of Scotland (see G. Higginbottom and R. Clay, The Origins of Standing Stone Astronomy in Britain submitted to Journal of Archaeological Science & available on ArXiv). In the current paper we...

  8. An AMS dated late Bronze Age grave from the mound necropolis at Paulje

    Directory of Open Access Journals (Sweden)

    Gligorić Rada

    2016-01-01

    Full Text Available The subject of the paper is a closed entity - an incineration grave from northwest Serbia, dated to the developed Bronze Age, with an absolute date obtained by AMS (Accelerator mass spectrometry. The sample was taken from the wooden support on which the urn with the bones of the deceased and bronze jewellery was placed. The date obtained corresponds to the 14th century B.C. and confirms earlier proposed suppositions concerning the chronological determination of the necropolises from the territory of Jadar, Podgorina and Lower Podrinje. [Projekat Ministarstva nauke Republike Srbije, br. OI177020: Archaeology of Serbia: cultural identity, integration factors, technological processes and the role of Central Balkans in the development of European prehistory

  9. XRF and micro-PIXE studies of inhomogeneity of ancient bronze and silver alloys

    Science.gov (United States)

    Vasilescu, A.; Constantinescu, B.; Stan, D.; Talmatchi, G.; Ceccato, D.

    2017-09-01

    New results regarding alloy composition and microstructure for a series of ancient bronze and silver items by X-ray Fluorescence and micro-Particle Induced X-ray Emission spectrometry were obtained in the framework of an extensive numismatic project (Scythian-type arrowheads, arrowhead-shaped monetary signs and wheel coins produced by Histria, 7th-4th century of BCE, and Dacian Radulesti-Hunedoara-type silver tetradrachms, 2nd-1st century of BCE). In Histria, warfare arrowheads were used for trade with Barbarian neighbors at first, then mechanically modified, next melted and cast as dedicated monetary signs, being, in the end, replaced by wheel coins. Three different types of alloys have been identified, and Cu-Mn and Cu-Pb segregation shown. In a blank for Radulesti-Hunedoara-type coins, Ag-(Cu+Pb) segregation has been demonstrated, suggesting an imperfectly alloyed silver-leaded bronze.

  10. CHARACTERIZATION OF SHORT E-GLASS FIBER REINFORCEDGRAPHITE AND BRONZE FILLED EPOXY MATRIX COMPOSITES

    Directory of Open Access Journals (Sweden)

    N. Patil

    2016-03-01

    Full Text Available The mechanical characterization of short E- glass fiber reinforced, graphite and sintered bronze filled epoxy composite was carried out in this study. The aim of the present study was to develop tribological engineering material. In this study the flexural strength, theoretical and experimental density, Hardness and Impact strength of composites was investigated experimentally. The results showed that the increased percentage of graphite (10 to 15%Vol and Eglass fiber (10 to 15%Vol enhanced flexural strength (149 MPa of the composite and the maximum flexural modulus (13.3 GPa and 13.1 GPa was obtained for composite C2 and C5 respectively. Maximum hardness (84 on L scale and impact energy (90 Joule was obtained for the composite C6 with increased percentage of glass fiber and graphite filler. The metallurgical electron microscopic images were discussed to interpret the effect of graphite and sintered bronze on mechanical characterization of composite

  11. Cold spraying of aluminum bronze on profiled submillimeter cermet structures formed by laser cladding

    Science.gov (United States)

    Ryashin, N. S.; Malikov, A. G.; Shikalov, V. S.; Gulyaev, I. P.; Kuchumov, B. M.; Klinkov, S. V.; Kosarev, V. F.; Orishich, A. M.

    2017-10-01

    The paper presents results of the cold spraying of aluminum bronze coatings on substrates profiled with WC/Ni tracks obtained by laser cladding. Reinforcing cermet frames shaped as grids with varied mesh sizes were clad on stainless steel substrates using a CO2 laser machine "Siberia" (ITAM SB RAS, Russia). As a result, surfaces/substrates with heterogeneous shape, composition, and mechanical properties were obtained. Aluminum bronze coatings were deposited from 5lF-NS powder (Oerlikon Metco, Switzerland) on those substrates using cold spraying equipment (ITAM SB RAS). Data of profiling, microstructure diagnostics, EDS analysis, and mechanical tests of obtained composites is reported. Surface relief of the sprayed coatings dependence on substrate structure has been demonstrated.

  12. Archaeometallurgical Characterization of Some Ancient Copper and Bronze Artifacts from Albania

    Science.gov (United States)

    Dilo, T.; Civici, N.; Stamati, F.; Cakaj, O.

    2010-01-01

    Ancient copper and bronze artifacts from different Albanian archaeological sites have been analyzed by X-ray-fluorescence analysis to determine the type of alloy and elemental composition and by Optical Microscopy for the investigation of corrosion products and microstructure of the bulk metal. Three bronze coins excavated in Dyrrahu, dating to the IIIrd-IInd century B.C, are composed of copper, tin and lead. Both studied nails, one excavated in Dyrrahu (IVrth-IIIrd century B.C), and the other one found inside an amphora in a ancient ship close to the coast of Saranda (VIth-IVrth century B.C), are composed of copper. The strata-graphical morphology and microstructure images from microscopic examinations allowed us to identify different corrosion products and the diverse stages of metallurgical and mechanical treatment during their manufacture.

  13. The Content of Vanadium in the Egg of the Ascidian, Halocynthia roretzi and Its Changes during the Development

    OpenAIRE

    堀, 令司; 沼宮内, 隆晴; 道端, 斉; Reiji, Hori; Takaharu, Numakunai; Hitoshi, Michibata; 東北大学理学部付属浅虫臨海実験所; 富山大学理学部生物学教室; Asamushi marine biological station, Tohoku University; Biological Institute, Faculty of Science, University of Kanazawa

    1981-01-01

    The vanadium content of the egg and embryo of the ascidian, Halocynthia roretzi was determined by activation analysis. The content of vanadium in an egg remained unchanged during the cleavage. A remarkable increase in the amount of vanadium in the embryo was observed during metamorphosis. Vanadium content in the larva one year after spawning amounted to about 820,000 times of that of the unfertilized egg. The accumulation of vanadium by the ascidian was discussed in comparison with phosphorus.

  14. Hittites and "barbarians" in the Late Bronze Age: regional survey in northern Turkey

    Directory of Open Access Journals (Sweden)

    Roger Matthews

    1999-11-01

    Full Text Available The Hittites have attracted less attention from British archaeologists than other Bronze Age states of ancient Southwest Asia, and yet in the second millennium BC they controlled most of Anatolia and at the peak of their power they even conquered Babylon. Here the Director of the British Institute of Archaeology at Ankara describes new research on the northwest frontier of the Hittite empire.

  15. Ancient bronze coins from Mediterranean basin: LAMQS potentiality for lead isotopes comparative analysis with former mineral

    Energy Technology Data Exchange (ETDEWEB)

    Torrisi, L., E-mail: Lorenzo.Torrisi@unime.it [Department of Physics Science - MIFT, Messina University, V.le F.S. d’Alcontres 31, 98166 S. Agata, Messina (Italy); Italiano, A. [INFN, Sezione di Catania, Gruppo collegato di Messina (Italy); Torrisi, A. [Institute of Optoelectronics, Military University of Technology, 2 Kaliskiego Str., 00-908 Warsaw (Poland)

    2016-11-30

    Highlights: • Surface and bulk compositional elements in ancient bronze coins were investigated using XRF analysis. • Lead stable isotope {sup 204}Pb, {sup 206}Pb, {sup 207}Pb and {sup 208}Pb were measured in ancient coins with LAMQS analysis. • Lead ratios {sup 208}Pb/{sup 206}Pb and {sup 207}Pb/{sup 206}Pb, measured by LAMQS, were compared with Brettscaife.net geological database relative to the minerals in different mines of Mediterranean basin. • Bronze coins were correlated to possible ancient mining sites of minerals from which lead was extracted. - Abstract: Bronze coins coming from the area of the Mediterranean basin, dated back the II–X Cent. A.D., were analyzed using different physical analytical techniques. Characteristic X-ray fluorescence was used with electrons and photons, in order to investigate the elemental composition of both the surface layers and bulk. Moreover, the quadrupole mass spectrometry coupled to laser ablation (LAMQS technique) in high vacuum was used to analyse typical material compounds from surface contamination. Mass spectrometry, at high resolution and sensitivity, extended up to 300 amu, allowed measuring the {sup 208}Pb/{sup 206}Pb and {sup 207}Pb/{sup 206}Pb isotopic ratios into the coins. Quantitative relative analyses of these isotopic ratios identify the coin composition such as a “fingerprint” depending on the mineral used to extract the lead. Isotopic ratios in coins can be compared to those of the possible minerals used to produce the bronze alloy. A comparison between the measured isotope ratios in the analyzed coins and the literature database, related to the mineral containing Pb as a function of its geological and geophysical extraction mine, is presented. The analysis, restricted to old coins and the mines of the Mediterranean basin, indicates a possible correlation between the coin compositions and the possible geological sites of the extracted mineral.

  16. Human paleodiet and animal utilization strategies during the Bronze Age in northwest Yunnan Province, southwest China.

    Directory of Open Access Journals (Sweden)

    Lele Ren

    Full Text Available Reconstructing ancient diets and the use of animals and plants augment our understanding of how humans adapted to different environments. Yunnan Province in southwest China is ecologically and environmentally diverse. During the Neolithic and Bronze Age periods, this region was occupied by a variety of local culture groups with diverse subsistence systems and material culture. In this paper, we obtained carbon (δ13C and nitrogen (δ15N isotopic ratios from human and faunal remains in order to reconstruct human paleodiets and strategies for animal exploitation at the Bronze Age site of Shilinggang (ca. 2500 Cal BP in northwest Yunnan Province. The δ13C results for human samples from Shilinggang demonstrate that people's diets were mainly dominated by C3-based foodstuffs, probably due to both direct consumption of C3 food and as a result of C3 foddering of consumed animals. Auxiliary C4 food signals can also be detected. High δ15N values indicate that meat was an important component of the diet. Analysis of faunal samples indicates that people primarily fed pigs and dogs with human food waste, while sheep/goats and cattle were foddered with other food sources. We compare stable isotope and archaeobotanical data from Shilinggang with data from other Bronze Age sites in Yunnan to explore potential regional variation in subsistence strategies. Our work suggests that people adopted different animal utilization and subsistence strategies in different parts of Yunnan during the Bronze Age period, probably as local adaptations to the highly diversified and isolated environments in the region.

  17. Neolithic and Bronze Age migration to Ireland and establishment of the insular Atlantic genome.

    Science.gov (United States)

    Cassidy, Lara M; Martiniano, Rui; Murphy, Eileen M; Teasdale, Matthew D; Mallory, James; Hartwell, Barrie; Bradley, Daniel G

    2016-01-12

    The Neolithic and Bronze Age transitions were profound cultural shifts catalyzed in parts of Europe by migrations, first of early farmers from the Near East and then Bronze Age herders from the Pontic Steppe. However, a decades-long, unresolved controversy is whether population change or cultural adoption occurred at the Atlantic edge, within the British Isles. We address this issue by using the first whole genome data from prehistoric Irish individuals. A Neolithic woman (3343-3020 cal BC) from a megalithic burial (10.3× coverage) possessed a genome of predominantly Near Eastern origin. She had some hunter-gatherer ancestry but belonged to a population of large effective size, suggesting a substantial influx of early farmers to the island. Three Bronze Age individuals from Rathlin Island (2026-1534 cal BC), including one high coverage (10.5×) genome, showed substantial Steppe genetic heritage indicating that the European population upheavals of the third millennium manifested all of the way from southern Siberia to the western ocean. This turnover invites the possibility of accompanying introduction of Indo-European, perhaps early Celtic, language. Irish Bronze Age haplotypic similarity is strongest within modern Irish, Scottish, and Welsh populations, and several important genetic variants that today show maximal or very high frequencies in Ireland appear at this horizon. These include those coding for lactase persistence, blue eye color, Y chromosome R1b haplotypes, and the hemochromatosis C282Y allele; to our knowledge, the first detection of a known Mendelian disease variant in prehistory. These findings together suggest the establishment of central attributes of the Irish genome 4,000 y ago.

  18. Friction stir processing of nickel aluminum propeller bronze in comparison to fusion welds

    OpenAIRE

    Murray, David L.

    2005-01-01

    Friction Stir Processing (FSP) is currently being considered for use in manufacture of the Navy's NiAl bronze propellers. Incorporating this technology may improve service performance and enable reduction of manufacturing time and cost. This program of research has employed miniature tensile sample designs to examine the distributions of longitudinal properties through the various regimes in a fusion weld. Also, the distributions of both longitudinal and transverse properties throughout t...

  19. Middle and Late Bronze Age settlement on the South Downs: the case study of Black Patch

    OpenAIRE

    Tapper, Richard Quinn

    2012-01-01

    By integrating the corpus of existing knowledge with new information gained by applying geo-archaeological techniques as well as more traditional techniques to fresh archaeological investigations at Black Patch and elsewhere, the aims of the research are to look at the economy, social organization and ritual behaviour of life in the Middle and Late Bronze Age on the South Downs in the light of modern archaeological theory to consider the questions ‘Why were these areas chosen for settlement?’...

  20. Compositional analyses of a Reutlingen Bronze Age sword discovered at Giurgiu, Romania

    OpenAIRE

    Olariu, Agata; Alexandrescu, Emilian; Avram, Alexandru; Badica, Teodor

    2003-01-01

    The compositional scheme of a Bronze Age sword, found near the town of Giurgiu in Romania has been determined by the method of particle-induced X-ray emission (PIXE), at the tandem accelerator of the National Institute for Physics and Nuclear Engineering from Bucharest, Magurele, Romania. The results of the analyses and the comparison with the composition of other swords from the same geographic area, the Danubian plane from Bulgaria and Transylvania regions, show that the sword from Giurgiu ...