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Sample records for aqueous vanadium pentoxide

  1. Vanadium pentoxide

    Integrated Risk Information System (IRIS)

    Vanadium pentoxide ; CASRN 1314 - 62 - 1 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogen

  2. IRIS Toxicological Review of Vanadium Pentoxide (External ...

    EPA Pesticide Factsheets

    This vanadium pentoxide reassessment consists of an oral reference dose (RfD), an inhalation reference concentration (RfC), an inhalation unit risk (IUR) and a cancer weight of evidence descriptor. This is the first assessment developing an RfC or IUR for this compound. This assessment is intended to provide human health data to support agency regulatory decisions. EPA is reassessing its IRIS toxicological review of vanadium pentoxide (CASRN 1314-62-1). This vanadium pentoxide reassessment consists of an oral reference dose (RfD), an inhalation reference concentration (RfC), an inhalation unit risk (IUR) and a cancer weight of evidence descriptor. This is the first assessment developing an RfC or IUR for this compound. This assessment is intended to provide human health data to support agency regulatory decisions.

  3. IRIS Toxicological Review of Vanadium Pentoxide ...

    EPA Pesticide Factsheets

    On September 30, 2011, the draft Toxicological Review of Vanadium Pentoxide and the charge to external peer reviewers were released for external peer review and public comment. The Toxicological Review and charge were reviewed internally by EPA and by other federal agencies and White House Offices before public release. In the new IRIS process (May 2009), introduced by the EPA Administrator, all written comments on IRIS assessments submitted by other federal agencies and White House Offices will be made publicly available. Accordingly, interagency comments and the interagency science consultation draft of the IRIS Toxicological Review of Vanadium Pentoxide and the charge to external peer reviewers are posted on this site. EPA is reassessing its IRIS toxicological review of vanadium pentoxide (CASRN 1314-62-1). This vanadium pentoxide reassessment consists of an oral reference dose (RfD), an inhalation reference concentration (RfC), an inhalation unit risk (IUR) and a cancer weight of evidence descriptor. This is the first assessment developing an RfC or IUR for this compound. This assessment is intended to provide human health data to support agency regulatory decisions.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed

    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 ((1)O(2)) 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.

  6. IRIS Toxicological Review of Vanadium Pentoxide (External Review Draft)

    EPA Science Inventory

    This vanadium pentoxide reassessment consists of an oral reference dose (RfD), an inhalation reference concentration (RfC), an inhalation unit risk (IUR) and a cancer weight of evidence descriptor. This is the first assessment developing an RfC or IUR for this compound. This as...

  7. IRIS Toxicological Review of Vanadium Pentoxide (Interagency Science Consultation Draft)

    EPA Science Inventory

    On September 30, 2011, the draft Toxicological Review of Vanadium Pentoxide and the charge to external peer reviewers were released for external peer review and public comment. The Toxicological Review and charge were reviewed internally by EPA and by other federal agencies and W...

  8. Sol-gel derived PZT films doped with vanadium pentoxide

    SciTech Connect

    Shen Hongfang; Guo Qing; Zhao Zhiman; Cao Guozhong

    2009-11-15

    The present research investigated the sol-gel preparation, dielectric and ferroelectric properties of PZT films doped with 5 mol% vanadium oxide. Stable PZTV sols can be readily formed, and homogeneous, micrometer thick and pinhole-free PZTV films were obtained by using spin coating followed with rapid annealing. The X-ray diffraction patterns revealed that no parasitic or secondary phases were formed in the sol-gel PZT films with the addition of vanadium oxide. The material doped with vanadium pentoxide showed enhanced dielectric constant and remanent polarization with reduced loss tangent and coercive field.

  9. Hierarchically structured vanadium pentoxide-polymer hybrid materials.

    PubMed

    Tritschler, Ulrich; Zlotnikov, Igor; Zaslansky, Paul; Fratzl, Peter; Schlaad, Helmut; Cölfen, Helmut

    2014-05-27

    Biomimetic composite materials consisting of vanadium pentoxide (V2O5) and a liquid crystal (LC) "gluing" polymer were manufactured exhibiting six structural levels of hierarchy, formed through LC phases. The organic matrix was a polyoxazoline with pendant cholesteryl and carboxyl units, forming a lyotropic phase with the same structural orientation extending up to hundreds of micrometers upon shearing, and binding to V2O5 via hydrogen bridges. Composites consisting of V2O5-LC polymer hybrid fibers with a pronounced layered structuring were obtained. The V2O5-LC polymer hybrid fibers consist of aligned V2O5 ribbons, composed of self-assembled V2O5 sheets, encasing a chiral nematic polymer matrix. The structures of the V2O5-LC polymer composites strongly depend on the preparation method, i.e., the phase-transfer method from aqueous to organic medium, in which the polymer forms LC phases. Notably, highly defined micro- and nanostructures were obtained when initiating the synthesis using V2O5 tactoids with preoriented nanoparticle building units, even when using isotropic V2O5 dispersions. Shear-induced hierarchical structuring of the composites was observed, as characterized from the millimeter and micrometer down to the nanometer length scales using complementary optical and electron microscopy, SAXS, μCT, and mechanical nanoindentation.

  10. Plasma assisted synthesis of vanadium pentoxide nanoplates

    NASA Astrophysics Data System (ADS)

    Singh, Megha; Sharma, Rabindar Kumar; Kumar, Prabhat; Reddy, G. B.

    2015-08-01

    In this work, we report the growth of α-V2O5 (orthorhombic) nanoplates on glass substrate using plasma assisted sublimation process (PASP) and Nickel as catalyst. 100 nm thick film of Ni is deposited over glass substrate by thermal evaporation process. Vanadium oxide nanoplates have been deposited treating vanadium metal foil under high vacuum conditions with oxygen plasma. Vanadium foil is kept at fixed temperature growth of nanoplates of V2O5 to take place. Samples grown have been studied using XPS, XRD and HRTEM to confirm the growth of α-phase of V2O5, which revealed pure single crystal of α- V2O5 in orthorhombic crystallographic plane. Surface morphological studies using SEM and TEM show nanostructured thin film in form of plates. Uniform, vertically aligned randomly oriented nanoplates of V2O5 have been deposited.

  11. Plasma assisted synthesis of vanadium pentoxide nanoplates

    SciTech Connect

    Singh, Megha; Sharma, Rabindar Kumar; Kumar, Prabhat Reddy, G. B.

    2015-08-28

    In this work, we report the growth of α-V{sub 2}O{sub 5} (orthorhombic) nanoplates on glass substrate using plasma assisted sublimation process (PASP) and Nickel as catalyst. 100 nm thick film of Ni is deposited over glass substrate by thermal evaporation process. Vanadium oxide nanoplates have been deposited treating vanadium metal foil under high vacuum conditions with oxygen plasma. Vanadium foil is kept at fixed temperature growth of nanoplates of V{sub 2}O{sub 5} to take place. Samples grown have been studied using XPS, XRD and HRTEM to confirm the growth of α-phase of V{sub 2}O{sub 5}, which revealed pure single crystal of α- V{sub 2}O{sub 5} in orthorhombic crystallographic plane. Surface morphological studies using SEM and TEM show nanostructured thin film in form of plates. Uniform, vertically aligned randomly oriented nanoplates of V{sub 2}O{sub 5} have been deposited.

  12. Optical properties of vanadium dioxide and vanadium pentoxide thin films.

    PubMed

    Chain, E E

    1991-07-01

    Several oxides of vanadium undergo a transition from a semiconductor or insulating state to a metal phase at a critical temperature. Vanadium dioxide undergoes this transition near 68 degrees C, while V(2)O(5) undergoes a similar phase transition near 257 degrees C. During the transition a change in oxide crystal structure is accompanied by large changes in electrical and optical behavior. Thin films of vanadium oxides are capable of reversibly switching from the semiconductor to the metallic state at high speeds and with high spatial resolution. Therefore, these oxides have potential use, particularly in thin film form, for a wide variety of applications involving thermally activated electronic or optical switching devices. Such films are of considerable technical interest because of applications in chemical sensors, energy-conserving coatings, transparent conductors, and switching materials. The numerous potential electronic, optical, and optoelectronic device applications which have been suggested have stimulated work on the preparation of thin films by a variety of techniques, including chemical vapor deposition, solgel, evaporation, and sputter deposition. This paper reviews the optical properties of vanadium oxide coatings and stresses the dependence of film properties on sample preparation and resultant film microstructure.

  13. Enhanced Lithium-ion intercalation properties of coherent hydrous vanadium pentoxide-carbon cryogels nanocomposites

    SciTech Connect

    Pan, Anqiang; Liu, Dawei; Zhou, Xiaoyuan; Garcia, Betzaita Betalla; Liang, Shu-quan; Liu, Jun; Cao, Guozhong

    2010-06-01

    Coherent hydrous vanadium pentoxide (V2O5•nH2O) - carbon cryogels (CCs) nanocomposites were synthesized by electrodeposition of vanadium pentoxide onto the porous carbon scaffold which was derived from resorcinol (R) and formaldehyde (F) organic hydrogels. As-fabricated nanocomposites were characterized by scanning electron microscopy (SEM), along with EDAX and nitrogen sorption isotherms which suggested vanadium pentoxide incorporated in the pores of carbon cryogels. The nanocomposites showed much improved discharge capacity and better cyclic stability as compared to hydrous vanadium pentoxide films deposited on platinum foil. The discharge capacity of the nanocomposites reached 280 mAh/g based on the mass of the vandium pentoxide at a current density of 100mA/g and it possessed good cycle stability at different discharge rate. The results demonstrated that electrochemical performances, such as specific discharge capacitance and reversibility of the composite electrode, could be greatly enhanced by the introduction of carbon cryogels (CCs) scaffold with three-dimensionally interconnected porous structure in which V2O5•nH2O homogeneously dispersed.

  14. 77 FR 5797 - Draft Toxicological Review of Vanadium Pentoxide: In Support of Summary Information on the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-02-06

    ... Integrated Risk Information System (IRIS) AGENCY: Environmental Protection Agency (EPA). ACTION: Notice of... Vanadium Pentoxide: In Support of Summary Information on the Integrated Risk Information System (IRIS... Information on the Integrated Risk Information System (IRIS)'' is available primarily via the Internet on...

  15. 76 FR 60825 - Draft Toxicological Review of Vanadium Pentoxide: In Support of Summary Information on the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-30

    ... Integrated Risk Information System (IRIS) AGENCY: Environmental Protection Agency (EPA). ACTION: Notice of..., ``Toxicological Review of Vanadium Pentoxide: In Support of Summary Information on the Integrated Risk Information System (IRIS)'' (EPA/635/R-11/004A). The draft assessment was prepared by the National Center...

  16. An improved lithium-vanadium pentoxide cell and comparison with a lithium-thionyl chloride cell

    NASA Astrophysics Data System (ADS)

    Voorn, G.

    1985-03-01

    This paper describes a programme of experiments conducted to assess the effects of: (a) diluting the electrolyte in lithium-vanadium pentoxide cells; (b) optimizing the volume of electrolyte per unit cathode mass. This programme led to the development of an improved cell, the performance of which is compared with that of a lithium-thionyl chloride cell of similar configuration.

  17. Electrons and phonons in layered and monolayer vanadium pentoxide

    NASA Astrophysics Data System (ADS)

    Lambrecht, Walter R. L.

    Vanadium pentoxide (V2O5) is a layered material with the potential for interesting new properties when made in 2D mono- or few-layer form. Its band structure is characterized by a split-off conduction band. The lowest conduction band is separated from the rest of the conduction bands by about 1 eV and consists of V-dxy orbitals, non-bonding to the oxygens by symmetry. This narrow band has dispersion essentially along the direction of chains occurring in the layer. When this band becomes half-filled by doping, spin-splitting occurs accompanied by an antiferromagnetic coupling between nearest neighbors along the chain direction. This situation is well known to occur in the so-called ladder compound NaV2O5 , which was extensively studied in the late 90s as a potential spin-Peierls or charge ordering compound. However, the monolayer form of V2O5 may allow for other ways to control the doping by gating, removing vanadyl oxygens, adsorption of alkali metals, nanoribbon formation, etc. Our calculations predict a switch from antiferromagnetic to ferromagnetic coupling for doping slightly less than half filling of the split-off band. In this talk we will discuss our recent work on the electronic band structure of both bulk and monolayer V2O5 as well as the phonons. We find that the quasi-particle self-consistent GW method strongly overestimates the band gap. Lattice polarization corrections of the screening are required because of the large LO/TO phonon frequency ratios. Excitonic effects may also be expected to be fairly large. We find that some of the vibrational modes, notably the vanadyl-oxygen bond stretch perpendicular to the layer, unexpectedly shows a strong blue shift. This is explained in terms of reduced screening affecting the long-range dipole components of the force constants. Supported by AFOSR and DOE. Work done with Churna Bhandari, Mark van Schilfgaarde and Andre Schleiffe.

  18. First Steps Towards an Understanding of a Mode ofCarcinogenic Action for Vanadium Pentoxide

    PubMed Central

    Schuler, Detlef; Chevalier, Hans-Jörg; Merker, Mandy; Morgenthal, Katja; Ravanat, Jean-Luc; Sagelsdorff, Peter; Walter, Marc; Weber, Klaus; Mcgregor, Douglas

    2011-01-01

    Inhalation of vanadium pentoxide clearly increases the incidence of alveolar/bronchiolar neoplasms in male and female B6C3F1 mice at all concentrations tested (1, 2 or 4 mg/m3), whereas responses in F344/N rats was, at most, ambiguous. While vanadium pentoxide is mutagenic in vitro and possibly in vivo in mice, this does not explain the species or site specificity of the neoplastic response. A nose-only inhalation study was conducted in female B6C3F1 mice (0, 0.25, 1 and 4 mg/m3, 6 h/day for 16 days) to explore histopathological, biochemical (α-tocopherol, glutathione and F2-isoprostane) and genetic (comet assays and 9 specific DNA-oxo-adducts) changes in the lungs. No treatment related histopathology was observed at 0.25 mg/m3. At 1 and 4 mg/m3, exposure-dependent increases were observed in lung weight, alveolar histiocytosis, sub-acute alveolitis and/or granulocytic infiltration and a generally time-dependent increased cell proliferation rate of histiocytes. Glutathione was slightly increased, whereas there were no consistent changes in α-tocopherol or 8-isoprostane F2α. There was no evidence for DNA strand breakage in lung or BAL cells, but there was an increase in 8-oxodGuo DNA lesions that could have been due to vanadium pentoxide induction of the lesions or inhibition of repair of spontaneous lesions. Thus, earlier reports of histopathological changes in the lungs after inhalation of vanadium pentoxide were confirmed, but no evidence has yet emerged for a genotoxic mode of action. Evidence is weak for oxidative stress playing any role in lung carcinogenesis at the lowest effective concentrations of vanadium pentoxide. PMID:22272055

  19. Chemical Composition Study of Vanadium Pentoxide Xerogels Doped by Bovine Albumin

    NASA Astrophysics Data System (ADS)

    Sereika, R.; Kaciulis, S.; Mezzi, A.; Brucale, M.

    2016-06-01

    Metal-bioorganic compounds of vanadium pentoxide and bovine serum albumin (BSA) (Fraction V) were obtained by using sol-gel method. Series of the samples (BSA)xV2O5ṡnH2O, where x=0, 0.01 and 0.001, were originally produced by the synthesis of vanadium pentoxide xerogels and subsequent blending with water-dissolved BSA in appropriate molar ratios. It was evident that the gelation process does not occur for x>0.01. For the X-ray photoelectron spectroscopy (XPS) studies, the thin layers of these materials were prepared by drying the gel onto the glass and mica substrates. The surface morphology of the samples was characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM) techniques. It follows from the analysis of experimental XPS spectra of (BSA)xV2O5ṡnH2O that the nitrogen ions in pure albumin and in (BSA)0.01V2O5ṡnH2O are present in imine, amine and protonated amine groups. The additional protonated amine arises when the concentration of albumin in (BSA)xV2O5ṡnH2O is low (x=0.001). Increasing the amount of albumin results in decrease of the number of oxygen ions bonded to vanadium. At the same time (with increase of albumin), the component of oxygen bounded to carbon and nitrogen is increasing. In the samples with greater amount of albumin, the reduction of vanadium ions occurs. This means that the trivalent and tetravalent vanadium ions are present together with pentavalent ones.

  20. Dynamic optical limiting experiments on vanadium dioxide and vanadium pentoxide thin films irradiated by a laser beam.

    PubMed

    Wang, Weiping; Luo, Yongquan; Zhang, Dayong; Luo, Fei

    2006-05-10

    Vanadium dioxide (VO2) and vanadium pentoxide (V2O5) thin films are irradiated by a near-infrared continuous-wave laser beam and the dynamic optical limiting performance is measured. The temperature varying with time of the films induced by a laser beam is also recorded by an IR thermal sensor. Under the irradiation of a laser beam with an intensity of 255 W/cm2 and a spot diameter of 2 mm, the laser beam transmittance of the VO2 film decreases from 47% before phase transition to 28% after phase transition, and the response time is approximately 200 ms; the laser beam transmittance of the V2O5 film decreases from 51% before phase transition to 24% after phase transition, and the response time is approximately 40 ms. The optical limiting is realized by this laser heating-induced phase transition.

  1. Dynamic optical limiting experiments on vanadium dioxide and vanadium pentoxide thin films irradiated by a laser beam

    SciTech Connect

    Wang Weiping; Luo Yongquan; Zhang Dayong; Luo Fei

    2006-05-10

    Vanadium dioxide (VO2) and vanadium pentoxide (V2O5) thin films are irradiated by a near-infrared continuous-wave laser beam and the dynamic optical limiting performance is measured. The temperature varying with time of the films induced by a laser beam is also recorded by an IR thermal sensor. Under the irradiation of a laser beam with an intensity of 255 W/cm2 and a spot diameter of 2 mm, the laser beam transmittance of the VO2 film decreases from 47% before phase transition to 28% after phase transition, and the response time is {approx}200 ms; the laser beam transmittance of the V2O5 film decreases from 51% before phase transition to 24% after phase transition, and the response time is {approx}40 ms. The optical limiting is realized by this laser heating-induced phase transition.

  2. Continuous tubular nanofibers of vanadium pentoxide by electrospinning for energy storage devices

    NASA Astrophysics Data System (ADS)

    Lala, Neeta L.; Jose, Rajan; Yusoff, Mashitah M.; Ramakrishna, Seeram

    2012-11-01

    Tubular nanofibers (TNFs) of vanadium pentoxide (V2O5) were synthesized by electrospinning technique using a single spinneret for the first time by controlling the properties of the precursor solution. A partially miscible polymeric solution of vanadium oxytrihydroxide [VO(OH)3] was produced by hydrolysis of vanadyl acetylacetonate in Poly(vinylpyrrolidone) (PVP). The phase-separated polymer solution formed the core of the electrospun fibers whereas the VO(OH)3 formed the shell; the core PVP has been removed by controlled heat treatment. The TNFs had an inner diameter 60 nm and wall thickness ±100 nm. The capacitive behavior of the V2O5 TNFs was studied using cyclic voltammetry and galvanostatic cycling techniques. The studies showed ideal stable supercapacitive characteristics in the electrospun V2O5 TNFs.

  3. Production of large-scale, freestanding vanadium pentoxide nanobelt porous structures.

    PubMed

    Yun, Yong Ju; Kim, Byung Hoon; Hong, Won G; Kim, Chang Hee; Kim, Yark Yeon; Jeong, Eun-ju; Jang, Won Ick; Yu, Han Young

    2012-03-07

    Large-scale, freestanding, porous structures of vanadium pentoxide nanobelts (VPNs) were successfully prepared using the template-free freeze-drying method. The porous and multi-layered VPN macrostructures are composed of randomly oriented long nanobelts (over 100 μm) and their side length can be controlled up to a few tens of centimetres. Also, the bulk density and surface area of these macrostructures are 3-5 mg cm(-3) and 40-80 m(2) g(-1), respectively, which are similar to those of the excellent adsorbents. In addition, the removal efficiency measurements of ammonia molecules revealed that the VPN porous structures can adsorb the ammonia molecules with the combinations of van der Waals forces and strong chemical bonding by functional groups on the VPN surface.

  4. Production of large-scale, freestanding vanadium pentoxide nanobelt porous structures

    NASA Astrophysics Data System (ADS)

    Yun, Yong Ju; Kim, Byung Hoon; Hong, Won G.; Kim, Chang Hee; Kim, Yark Yeon; Jeong, Eun-Ju; Jang, Won Ick; Yu, Han Young

    2012-02-01

    Large-scale, freestanding, porous structures of vanadium pentoxide nanobelts (VPNs) were successfully prepared using the template-free freeze-drying method. The porous and multi-layered VPN macrostructures are composed of randomly oriented long nanobelts (over 100 μm) and their side length can be controlled up to a few tens of centimetres. Also, the bulk density and surface area of these macrostructures are 3-5 mg cm-3 and 40-80 m2 g-1, respectively, which are similar to those of the excellent adsorbents. In addition, the removal efficiency measurements of ammonia molecules revealed that the VPN porous structures can adsorb the ammonia molecules with the combinations of van der Waals forces and strong chemical bonding by functional groups on the VPN surface.

  5. Contactless Monitoring of Conductivity Changes in Vanadium Pentoxide Xerogel Layers Using Surface Acoustic Waves

    NASA Astrophysics Data System (ADS)

    Rimeika, Romualdas; Sereika, Raimundas; Čiplys, Daumantas; Bondarenka, Vladimiras; Sereika, Albertas; Shur, Michael

    The hydrated form of the vanadium pentoxide (V2O5 ·nH2O) deposited by the sol-gel method on the piezoelectric YZ-LiNbO3 substrate has been studied using surface acoustic waves (SAWs). Brush-deposited and spin-coated layers, differing in thickness by an order of magnitude (∼1 μm and ∼0.1 μm, respectively) were studied. The variations with time in the transmitted SAW amplitude and phase during the gel-to-xerogel transition of V2O5 ·nH2O were observed and attributed to the acoustoelectric interaction. The possibilities of using the SAWs for contactless monitoring of the layer sheet conductivity have been demonstrated.

  6. Effect of Annealing on the Properties of Vanadium Pentoxide Films Prepared by Sol-Gel Method

    NASA Astrophysics Data System (ADS)

    Liu, Yaqiang; Du, Xuelian; Liu, Xueqin

    2014-03-01

    The vanadium pentoxide (V2O5) films were obtained by using sol-gel procedure and then were annealed at different temperature in air. The effect of different annealing temperatures on the composition, the microstructure, the surface morphology and the optical properties of the films were characterized by methods such as by X-ray diffraction, Raman spectroscopy, scanning electron microscopy and spectral transmittance. The results revealed that the film annealed at 150°C has amorphous structure and dense with a smooth surface and the films annealed at 300°C and 450°C have a polycrystalline V2O5 structure with preferred growth orientation along (001) planes, the c-axis and perpendicular to the silicon substrate surface. From the spectral transmittance we determined the absorption edge using the Tauc plot. The results indicated that optical bandgap of V2O5 thin films decreased with annealing temperature.

  7. Genetic susceptibility to interstitial pulmonary fibrosis in mice induced by vanadium pentoxide (V2O5)

    PubMed Central

    Walters, Dianne M.; White, Kevin M.; Patel, Ushma; Davis, Martin J.; Veluci-Marlow, Roberta M.; Bhupanapadu Sunkesula, Solomon Raju; Bonner, James C.; Martin, Jessica R.; Gladwell, Wes; Kleeberger, Steven R.

    2014-01-01

    Interstitial lung diseases (ILDs) are characterized by injury, inflammation, and scarring of alveoli, leading to impaired function. The etiology of idiopathic forms of ILD is not understood, making them particularly difficult to study due to the lack of appropriate animal models. Consequently, few effective therapies have emerged. We developed an inbred mouse model of ILD using vanadium pentoxide (V2O5), the most common form of a transition metal found in cigarette smoke, fuel ash, mineral ores, and steel alloys. Pulmonary responses to V2O5, including dose-dependent increases in lung permeability, inflammation, collagen content, and dysfunction, were significantly greater in DBA/2J mice compared to C57BL/6J mice. Inflammatory and fibrotic responses persisted for 4 mo in DBA/2J mice, while limited responses in C57BL/6J mice resolved. We investigated the genetic basis for differential responses through genetic mapping of V2O5-induced lung collagen content in BXD recombinant inbred (RI) strains and identified significant linkage on chromosome 4 with candidate genes that associate with V2O5-induced collagen content across the RI strains. Results suggest that V2O5 may induce pulmonary fibrosis through mechanisms distinct from those in other models of pulmonary fibrosis. These findings should further advance our understanding of mechanisms involved in ILD and thereby aid in identification of new therapeutic targets.—Walters, D. M., White, K. M., Patel, U., Davis, M. J., Veluci-Marlow, R. M., Bhupanapadu Sunkesula, S. R., Bonner, J. C., Martin, J. R., Gladwell, W., Kleeberger, S. R. Genetic susceptibility to interstitial pulmonary fibrosis in mice induced by vanadium pentoxide (V2O5). PMID:24285090

  8. Ultrastructural findings in murine seminiferous tubules as a consequence of subchronic vanadium pentoxide inhalation.

    PubMed

    Fortoul, Teresa Imelda; Bizarro-Nevares, Patricia; Acevedo-Nava, Sandra; Piñón-Zárate, Gabriela; Rodríguez-Lara, Vianey; Colín-Barenque, Laura; Mussali-Galante, Patricia; Avila-Casado, Maria del Carmen; Avila-Costa, Maria-Rosa; Saldivar-Osorio, Liliana

    2007-06-01

    Vanadium (V) is a transition metal emitted to the atmosphere during the combustion of fossil fuels. Its current status as an atmospheric pollutant increases the need for information about the effects that this element might have on the reproductive health of exposed populations. The present study investigated changes in testicular ultrastructure following inhalation exposure of male mice to V (as vanadium pentoxide). Tissue V level was constant during the 12-week time period. We observed necrosis of spermatogonium, spermatocytes and Sertoli cells, as well as pseudo-nuclear inclusion and disruption of cellular junctions. Our findings stressed the importance of the hemato-testicular barrier in supporting the function of Sertoli cells and suggest as a possible target of V, tight junction proteins. Further analysis is needed in order to identify the role that reactive oxidative species (ROS) might have on these cellular junctions, and if a specific protein is the target of its toxic effects. The relevance of this report concerns the impact that metal air pollution could have on male fertility in dense cities with vehicular traffic problems.

  9. Morphology, structure and electrochemical properties of single phase electrospun vanadium pentoxide nanofibers for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Cheah, Yan L.; Gupta, Nutan; Pramana, Stevin S.; Aravindan, Vanchiappan; Wee, Grace; Srinivasan, Madhavi

    2011-08-01

    One-dimensional (1D) vanadium pentoxide (V2O5) nanofibers (VNF) are synthesized by electrospinning vanadium sol-gel precursors containing vanadyl acetylacetonate and poly(vinylpyrrolidone) followed by sintering. Crystal structure, molecular structure and morphology of electrospun VNF are analyzed using field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), selected area diffraction (SAED), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). Single-phase electrospun VNF ∼300-800 nm in diameter, 20-50 μm long (aspect ratio > 50) with porous interconnected fibrous morphology are revealed by FESEM and TEM analysis. Electrochemical properties of the sintered VNF, as a cathode in lithium-ion batteries, explored using cyclic voltammetry (CV), galvanostatic charge/discharge and electrochemical impedance spectroscopy (EIS) give rise to new understandings of the electrochemical processes occurring in these nanofibrous cathodes. Electrospun VNF exhibits initial discharge capacity ∼316 mAh g-1 (∼2.2 Li per V2O5) in the voltage range of 1.75 and 4.0 V vs. Li/Li+ at 0.1 C rate. When cycled at a reduced voltage range of 2.0-4.0 V vs. Li/Li+, less phase transitions occur, giving rise to the initial specific capacity of 308 mAh g-1 and improved cyclic retention of 74% after 50 cycles.

  10. Vanadium pentoxide (V2O5) induced mucin production by airway epithelium

    PubMed Central

    Yu, Dongfang; Walters, Dianne M.; Zhu, Lingxiang; Lee, Pak-Kei

    2011-01-01

    Exposure to environmental pollutants has been linked to various airway diseases and disease exacerbations. Almost all chronic airway diseases such as chronic obstructive pulmonary disease and asthma are caused by complicated interactions between gene and environment. One of the major hallmarks of those diseases is airway mucus overproduction (MO). Excessive mucus causes airway obstruction and significantly increases morbidity and mortality. Metals are major components of environmental particulate matters (PM). Among them, vanadium has been suggested to play an important role in PM-induced mucin production. Vanadium pentoxide (V2O5) is the most common commercial source of vanadium, and it has been associated with occupational chronic bronchitis and asthma, both of which are MO diseases. However, the underlying mechanism is not entirely clear. In this study, we used both in vitro and in vivo models to demonstrate the robust inductions of mucin production by V2O5. Furthermore, the follow-up mechanistic study revealed a novel v-raf-1 murine leukemia viral oncogene homolog 1-IKK-NF-κB pathway that mediated V2O5-induced mucin production. Most interestingly, the reactive oxygen species and the classical mucin-inducing epidermal growth factor receptor (EGFR)-MAPK pathway appeared not to be involved in this process. Thus the V2O5-induced mucin production may represent a novel EGFR-MAPK-independent and environmental toxicant-associated MO model. Complete elucidation of the signaling pathway in this model will not only facilitate the development of the treatment for V2O5-associated occupational diseases but also advance our understanding on the EGFR-independent mucin production in other chronic airway diseases. PMID:21531775

  11. Optoelectronic and Electrochemical Properties of Vanadium Pentoxide Nanowires Synthesized by Vapor-Solid Process

    PubMed Central

    Pan, Ko-Ying; Wei, Da-Hua

    2016-01-01

    Substantial synthetic vanadium pentoxide (V2O5) nanowires were successfully produced by a vapor-solid (VS) method of thermal evaporation without using precursors as nucleation sites for single crystalline V2O5 nanowires with a (110) growth plane. The micromorphology and microstructure of V2O5 nanowires were analyzed by scanning electron microscope (SEM), energy-dispersive X-ray spectroscope (EDS), transmission electron microscope (TEM) and X-ray diffraction (XRD). The spiral growth mechanism of V2O5 nanowires in the VS process is proved by a TEM image. The photo-luminescence (PL) spectrum of V2O5 nanowires shows intrinsic (410 nm and 560 nm) and defect-related (710 nm) emissions, which are ascribable to the bound of inter-band transitions (V 3d conduction band to O 2p valence band). The electrical resistivity could be evaluated as 64.62 Ω·cm via four-point probe method. The potential differences between oxidation peak and reduction peak are 0.861 V and 0.470 V for the first and 10th cycle, respectively. PMID:28335268

  12. Vanadium Pentoxide Alloyed with Graphite for Thin-Film Thermal Sensors

    NASA Astrophysics Data System (ADS)

    Bianchi, C.; Ferreira, L. M.; Loureiro, J.; Rodrigues, A.; Duarte, P.; Baptista, A. C.; Ferreira, I. M.

    2016-03-01

    The thermoelectric (TE) properties of vanadium pentoxide (V2O5) alloyed with graphite (G) were studied as a function of its incorporation percentage. Variable weight percentages of graphite powder (0-50%) were added to V2O5 powder and their mixtures were evaporated by a thermal evaporation technique to form thin films with a thickness in the range of 30-80 nm. In the infrared wavelength region, the transmittance of the obtained films increased as the G percentage was increased, while in the visible range, it decreased with G up to 10%. The TE properties were improved when G was in the range of 10-30%, while it decreased for the other percentages: Seebeck coefficient ( S) changed from 0.6 mV/K to 0.9 mV/K and was zero with a G of 50%; the electrical conductivity varied slightly from 5 (Ωm)-1 to 0.7 (Ωm)-1 while the mobility improved from 0.07 cm2/V s to 1.5 cm2/V s and the respective carrier concentration was reduced, from 1 × 1018 cm-3 to 4 × 1016 cm-3. These films were applied as temperature sensors evaluating the thermovoltage as a function of thermal gradient between two electrodes, in which one was maintained at room temperature.

  13. In-situ synthesis of vanadium pentoxide nanofibre/exfoliated graphene nanohybrid and its supercapacitor applications

    NASA Astrophysics Data System (ADS)

    Choudhury, Arup; Bonso, Jeliza S.; Wunch, Melissa; Yang, Kap Seung; Ferraris, John P.; Yang, Duck J.

    2015-08-01

    A novel nanohybrid material composed of vanadium pentoxide nanofibres (VNFs) and exfoliated graphene were prepared by in-situ growth of VNFs onto graphene nanosheets, and explicated as electrode material for supercapacitor applications. The existence of non-covalent interactions between VNFs and graphene surfaces was confirmed by Raman and Fourier transform infrared (FTIR) spectroscopes. Morphological analysis of the nanohybrid revealed that the VNF layer uniformly grown on the graphene surfaces, producing high specific surface area and good electronic or ionic conducing path. High crystalline structure with small d-spacing of the VNFs on graphene was observed in X-ray diffraction (XRD) analysis. Compared to pristine VNF, the VNF/graphene nanohybrid exhibited higher specific capacitance of 218 F g-1 at current density of 1 A g-1, higher energy density of 22 Wh kg-1 and power density of 3594 W kg-1. Asymmetric supercapacitor devices were prepared using the Spectracarb 2225 activated carbon cloth and VNF/graphene nanohybrid as positive and negative electrode, respectively. The asymmetric device exhibited capacitance of 279 F g-1 at 1 A g-1, energy density of 37.2 Wh kg-1 and power density of 3743 W kg-1, which are comparable and or superior to reported asymmetric devices consisting of carbon material and metal oxide as electrode components.

  14. Vanadium pentoxide prevents NK-92MI cell proliferation and IFNγ secretion through sustained JAK3 phosphorylation.

    PubMed

    Gallardo-Vera, Francisco; Diaz, Daniel; Tapia-Rodriguez, Miguel; Fortoul van der Goes, Teresa; Masso, Felipe; Rendon-Huerta, Erika; Montaño, Luis F

    2016-01-01

    Vanadium is a major air pollutant with toxic and carcinogenic effects; it also exercises immunosuppressive effects on the adaptive immune response. Its effect on the innate immune response is poorly explored. The aim of this study was to identify if vanadium pentoxide (V2O5) impairs the function of immunoregulatory NK cells and to determine possible mechanisms associated with this effect. Interleukin-2-independent NK-92MI cells were exposed to different V2O5 concentrations for 6, 12, or 24 h periods. Cell proliferation was then evaluated using CFSE staining, apoptosis by Annexin V binding, and necrosis by 7-AAD staining. The release of IL-2, -4, -6, -10, -17A, IFNγ, and TNFα by the cells were assessed using a human CBA kit. Expression of CD45, SOCS1, JAK3, pJAK3, STAT5, pSTAT5, IL-2R, IL-15R, Fas, and FasL in/on the cells was determined by flow cytometry; JAK3 and pJAK3 expression were also evaluated via confocal microscopy. The results indicated that V2O5 could inhibit NK-92MI cell proliferation and induce cell apoptosis in a dose- and time-related manner. V2O5 also inhibited IL-2, IL-10, and IFNγ secretion but mostly only after 24 h of exposure and with primarily the higher doses tested. V2O5 had no effect on expression of JAK3 and STAT5, but did cause an increase in pJAK3 and appeared to lead (trend) to reductions in levels of phosphorylated STAT5. V2O5 increased the expression of IL-2R, IL-15R, Fas, and FasL at concentrations above the 50-100 µM range. V2O5 had no effect on expression of the CD45 membrane phosphatase, but it did cause an increase in the expression of SOCS1. These results indicate that a key toxic effect of V2O5 on NK cells is a dysregulation of signaling pathways mediated by IL-2. These effects could help to explain the previously-reported deleterious effects on innate immune responses of hosts exposed to inhaled V2O5.

  15. Solubility of vanadium from manganese vanadates in aqueous solutions of soda ash

    NASA Astrophysics Data System (ADS)

    Khalezov, B. D.; Krasheninin, A. G.; Vatolin, N. A.; Ovchinnikova, L. A.

    2016-05-01

    It is shown that, in the course of developing the technology of pure vanadium pentoxide preparation from manganic vanadium-containing metallurgical slags, their oxidative roasting and cinder formation without alkaline additives are accompanied by the decomposition of spinelides with the formation of manganese meta- and pyrovanadates. Concentrated aqueous solutions of soda ash with an Na2CO3 concentration of 120-150 g/dm3 are accepted as a selective leaching reagent for vanadium from a cinder. Manganese metaand pyrovanadates are synthesized, and the procedure of their preparation is presented. The solubility of vanadium from manganese vanadates in aqueous solutions of soda ash at C_{Na_2 CO_3 } = 150 g/dm^3 is studied at 20-95°C for pyrovanadate and at 85-95°C for metavanadate. It is shown that vanadium should be leached from converter manganic slags roasted without alkaline metal additives at a leaching solution temperature higher than 95°C. There is a possibility to increase the vanadium content in a leaching solution to 60-80 g/dm3. The results obtained are used in the development of the technology of vanadium leaching.

  16. Scanning tunneling microscopy of the atomically smooth (001) surface of vanadium pentoxide V2O5 crystals

    NASA Astrophysics Data System (ADS)

    Muslimov, A. E.; Butashin, A. V.; Kanevsky, V. M.

    2017-01-01

    The (001) cleavage surface of vanadium pentoxide (V2O5) crystal has been studied by scanning tunneling spectroscopy (STM). It is shown that the surface is not reconstructed; the STM image allows geometric lattice parameters to be determined with high accuracy. The nanostructure formed on the (001) cleavage surface of crystal consists of atomically smooth steps with a height multiple of unit-cell parameter c = 4.37 Å. The V2O5 crystal cleavages can be used as references in calibration of a scanning tunneling microscope under atmospheric conditions both along the ( x, y) surface and normally to the sample surface (along the z axis). It is found that the terrace surface is not perfectly atomically smooth; its roughness is estimated to be 0.5 Å. This circumstance may introduce an additional error into the microscope calibration along the z coordinate.

  17. Novel alkylimidazolium/vanadium pentoxide intercalation compounds with excellent adsorption performance for methylene blue

    SciTech Connect

    Kong Aiguo; Ding Yongjie; Wang Ping; Zhang Hengqiang; Yang Fan; Shan Yongkui

    2011-02-15

    Novel alkylimidazolium-intercalated V{sub 2}O{sub 5} compounds were synthesized by a redox reaction between iodide ion and V{sub 2}O{sub 5}. The X-ray photoelectron spectroscopy and the diffuse reflectance UV-vis spectrometry experiments reveal that the vanadium in the intercalated V{sub 2}O{sub 5} products was partially reduced by an iodide ion and the resultant iodine can be removed in the final products. The transmission electron microscope observation and X-ray diffraction analysis testify that the prepared alkylimidazolium/V{sub 2}O{sub 5} intercalation compounds have typical lamellar structure with different d{sub 100} interlayer spacing values and the special straw-like nanofiber morphology with the length of 0.5-10 {mu}m. Systematic investigation indicates that new intercalation compounds possess the extraordinary adsorption performance for methylene blue in an aqueous solution. -- Graphical abstract: The alkylimidazolium-intercalated V{sub 2}O{sub 5} compounds with special straw-like nanofiber morphology were synthesized by a redox reaction between iodide ion and V{sub 2}O{sub 5}, which show the excellent adsorption performance for methylene blue in an aqueous medium. Display Omitted Research highlights: {yields} Novel alkylimidazolium-intercalated V{sub 2}O{sub 5} compounds. {yields} A simple preparation method by a redox reaction between iodide ion in ionic liquid and V{sub 2}O{sub 5}. {yields} The excellent adsorption performance for methylene blue in an aqueous medium.

  18. Flexible Hybrid Electrodes Containing Vanadium Pentoxide (V2O5) and an Electron- and Ion-Conducting Diblock Copolymer for Energy Storage

    NASA Astrophysics Data System (ADS)

    An, Hyosung; Mike, Jared; Smith, Kendall; Swank, Lisa; Lin, Yen-Hao; Pesek, Stacy; Verduzco, Rafael; Lutkenhaus, Jodie

    2015-03-01

    Vanadium pentoxide (V2O5) is a promising cathode material for Lithium-ion batteries due to its high capacity, high energy density, and cost-effectiveness. However, its low lithium-ion diffusion coefficient (10-12 - 10-13 cm2/s), low electronic conductivity (10-2 - 10-3 S/cm), and severe volumetric changes during cycling have hindered its application in practical devices. One way to address these problems is to design hybrid electrodes that incorporate a second active material. For this purpose, poly(3-hexylthiophene)-block-poly(ethylene oxide) (P3HT- b-PEO) block copolymer containing electron- and ion-conducting polymer blocks was introduced to a V2O5 electrode system. Cathodes are prepared by mixing aqueous dispersions of block copolymer, V2O5, and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) and drop casting. The V2O5 and P3HT- b-PEO hybrid electrode showed synergistic results, having improved electrochemical storage performance and mechanical property. We also demonstrated a flexible battery prototype using the P3HT- b-PEO/V2O5 cathode.

  19. Superior selectivity and enhanced response characteristics of palladium sensitized vanadium pentoxide nanorods for detection of nitrogen dioxide gas.

    PubMed

    Mane, A A; Suryawanshi, M P; Kim, J H; Moholkar, A V

    2017-06-01

    Vanadium pentoxide (V2O5) nanorods have been deposited onto the glass substrates by spraying 75ml of 30mM vanadium trichloride (VCl3) solution at optimized substrate temperature of 400°C. The XRD study confirms the formation of orthorhombic crystal structure of V2O5 nanorods. The FE-SEM micrograph shows the nanorods-like morphology of V2O5. The presence of palladium (Pd) in the Pd-sensitized V2O5 nanorods is confirmed using EDAX study. The gas sensing measurements show that the Pd-sensitized V2O5 sensing material is an outstanding candidate for nitrogen dioxide (NO2) gas detection. Obtained results demonstrate that the Pd-sensitized V2O5 nanorods show the superior selectivity for NO2 gas in comparison with other gases such as NH3, H2S, CO, CO2 and SO2 at an operating temperature of 200°C. It shows the 75% response for 100ppm NO2 gas concentration with response and recovery times of 22s and 126s, respectively. Finally, the gas sensing mechanism based on chemisorption process is proposed to illustrate how Pd nanoparticles affect the gas sensing characteristics (response and response-recovery times).

  20. Aqueous vanadium ion dynamics relevant to bioinorganic chemistry: A review.

    PubMed

    Kustin, Kenneth

    2015-06-01

    Aqueous solutions of the four highest vanadium oxidation states exhibit four diverse colors, which only hint at the diverse reactions that these ions can undergo. Cationic vanadium ions form complexes with ligands; anionic vanadium ions form complexes with ligands and self-react to form isopolyanions. All vanadium species undergo oxidation-reduction reactions. With a few exceptions, elucidation of the dynamics of these reactions awaited the development of fast reaction techniques before the kinetics of elementary ligation, condensation, reduction, and oxidation of the aqueous vanadium ions could be investigated. As the biological roles played by endogenous and therapeutic vanadium expand, it is appropriate to bring the results of the diverse kinetics studies under one umbrella. To achieve this goal this review presents a systematic examination of elementary aqueous vanadium ion dynamics.

  1. Ultrasensitive non-enzymatic immunosensor for carcino-embryonic antigen based on palladium hybrid vanadium pentoxide/multiwalled carbon nanotubes.

    PubMed

    Han, Jian; Jiang, Liping; Li, Faying; Wang, Ping; Liu, Qing; Dong, Yunhui; Li, Yueyun; Wei, Qin

    2016-03-15

    A novel and sensitive sandwich-type non-enzymatic electrochemical immunosensor was fabricated for quantitative monitoring of carcino-embryonic antigen (CEA). Nanocomposite of stannic oxide/reduced graphene oxide was used as substrate material to increase the specific surface area and enhance the conductivity of the glassy carbon electrode. Gold nanoparticles (Au NPs) were introduced to link substrate materials and primary antibodies (Ab1) and accelerate the electron transfer in this system. At the same time, the palladium nanoparticles (Pd NPs)-vanadium pentoxide (V2O5)/multiwalled carbon nanotubes (MWCNTs) were used as the label of secondary antibodies (Ab2). This composite label has shown excellent catalytic activity towards the reduction of H2O2. The nanomaterial-based signal amplification can improve the sensitivity and lower the limit of detection. The proposed immunosensor showed wide linear range from 0.5 pgmL(-1) to 25 ngmL(-1) with limit of detection of 0.17 pgmL(-1). This novel immunosensor was used to analyze serum sample. The results indicated that this immunosensor may find huge potential application for quantitative detection of CEA in the clinical diagnosis.

  2. Mica-like vanadium pentoxide-nanostructured thin film as high-performance cathode for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Yu, Danmei; Qiao, Yajuan; Zhou, Xiaoyuan; Wang, Jie; Li, Chao; Chen, Changguo; Huo, Qisheng

    2014-11-01

    Stable and homogeneous mica-like vanadium pentoxide (V2O5)-nanostructured thin films are prepared directly by simple anodic deposition from V2O5/H2O2 sol solution, and then dried at ambient temperature and annealed at 500 °C in air for 1 h. The films' crystal- and microstructures, surface morphology and Li-ion intercalation properties were characterized and analyzed by X-Ray diffraction (XRD), field emission scanning electron microscopy (FSEM), thermogravimetric analysis (TGA), and electrochemical techniques. When used as a lithium-ion battery (LIB) cathode, the films exhibit a large discharge capacity of 596 mAh g-1 at a current density of 1080 mA g-1, as well as excellent cyclic stability and a fading rate of 1% per cycle. Explanations for such significant enhancements in specific capacity, cyclic stability, and rate performance of mica-like V2O5-nanostructured thin films are demonstrated in this study.

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

    NASA Astrophysics Data System (ADS)

    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.

  4. Electrical current suppression in Pd-doped vanadium pentoxide nanowires caused by reduction in PdO due to hydrogen exposure

    NASA Astrophysics Data System (ADS)

    Kim, Byung Hoon; Oh, Soon-Young; Jeong, Hu Young; Yu, Han Young; Yun, Yong Ju; Kim, Yark Yeon; Hong, Won G.; Lee, Jeong Yong; Kim, Hae Jin

    2010-04-01

    Pd nanoparticle-doped vanadium pentoxide nanowires (Pd-VONs) were synthesized. Electrical current suppression was observed when the Pd-VON was exposed to hydrogen gas, which cannot be explained by the work function changes mentioned in previous report such as Pd-doped carbon nanotubes and SnO2 nanowires. Using the x-ray photoelectron spectroscopy, we found that the reduction in PdO due to hydrogen exposure plays an important role in the current suppression of the Pd-VON.

  5. Synthesis and characterization of sulfur–carbon–vanadium pentoxide composites for improved electrochemical properties of lithium–sulfur batteries

    SciTech Connect

    Kong, Long; Handa, Yusuke; Taniguchi, Izumi

    2016-01-15

    Highlights: • A wet ball milling was conducted to synthesis S–C–V{sub 2}O{sub 5} composite electrode. • V{sub 2}O{sub 5} additive led to further improve electrochemical performance of S-cathode. • S–C–V{sub 2}O{sub 5} composite electrode exhibited a first discharge capacity of 951 mAh g{sup −1}. • The electrode (60 wt.%—S, 30 wt.%—V{sub 2}O{sub 5}, 10 wt.%—C) showed best battery performance. - Abstract: Sulfur (S)–carbon (C)–vanadium pentoxide (V{sub 2}O{sub 5}) composites were prepared by wet ball milling, and their physical and electrochemical properties were evaluated. Firstly, the effect of the carbon content of S–C composite electrodes on their physical and electrochemical properties was investigated. The S–C composite electrode with 60 wt.% S delivers a first discharge capacity of 1077 mAh g{sup −1}. However, its capacity markedly decreases to 606 mAh g{sup −1} after 10 cycles, which corresponds to a capacity fading rate of 47 mAh g{sup −1} per cycle. To improve the electrochemical performance of the S–C composite electrode, carbon was partially replaced by V{sub 2}O{sub 5}. The S–C–V{sub 2}O{sub 5} composite electrode with a composition of 60 wt.%—S, 30 wt.%—V{sub 2}O{sub 5} and 10 wt.%—C exhibits a lower capacity fading rate of 23 mAh g{sup −1} per cycle in the first 10 cycles and better capacity retention than the S–C composite electrode over 50 cycles.

  6. Genomic analysis of human lung fibroblasts exposed to vanadium pentoxide to identify candidate genes for occupational bronchitis

    PubMed Central

    Ingram, Jennifer L; Antao-Menezes, Aurita; Turpin, Elizabeth A; Wallace, Duncan G; Mangum, James B; Pluta, Linda J; Thomas, Russell S; Bonner, James C

    2007-01-01

    Background Exposure to vanadium pentoxide (V2O5) is a cause of occupational bronchitis. We evaluated gene expression profiles in cultured human lung fibroblasts exposed to V2O5 in vitro in order to identify candidate genes that could play a role in inflammation, fibrosis, and repair during the pathogenesis of V2O5-induced bronchitis. Methods Normal human lung fibroblasts were exposed to V2O5 in a time course experiment. Gene expression was measured at various time points over a 24 hr period using the Affymetrix Human Genome U133A 2.0 Array. Selected genes that were significantly changed in the microarray experiment were validated by RT-PCR. Results V2O5 altered more than 1,400 genes, of which ~300 were induced while >1,100 genes were suppressed. Gene ontology categories (GO) categories unique to induced genes included inflammatory response and immune response, while GO catogories unique to suppressed genes included ubiquitin cycle and cell cycle. A dozen genes were validated by RT-PCR, including growth factors (HBEGF, VEGF, CTGF), chemokines (IL8, CXCL9, CXCL10), oxidative stress response genes (SOD2, PIPOX, OXR1), and DNA-binding proteins (GAS1, STAT1). Conclusion Our study identified a variety of genes that could play pivotal roles in inflammation, fibrosis and repair during V2O5-induced bronchitis. The induction of genes that mediate inflammation and immune responses, as well as suppression of genes involved in growth arrest appear to be important to the lung fibrotic reaction to V2O5. PMID:17459161

  7. Lung Deposition and Clearance of Inhaled Vanadium Pentoxide in Chronically Exposed F344 Rats and B6C3F1 Mice

    SciTech Connect

    Dill, Jeffrey A.; Lee, Kyeonghee M.; Mellinger, Kathleen H.; Bates, Derrick J.; Burka, Leo T.; Roycroft, Joseph H.

    2004-01-01

    Female F344 rats and B6C3F1 mice were exposed to vanadium pentoxide (V{sub 2}O{sub 5}) at concentrations of 0, 0.5, 1, or 2 mg/m{sup 3} (rats) and 0, 1, 2, or 4 mg/m{sup 3} (mice) for 6 h/day, 5 days/week (for up to 18 months), by whole-body inhalation. Lung weights and lung burdens of vanadium were determined for exposed animals after 1, 5, and 12 days and after 1, 2, 6, 12, and 18 months of V{sub 2}O{sub 5} exposure. Blood vanadium concentrations were determined at 1, 2, 6, 12, and 18 months for all animals including controls. A model that assumed a first-order deposition rate and a first-order elimination rate for vanadium was employed to fit the lung burden data. Comparisons between exposed groups indicated a progressive increase in lung weight with exposure concentration and time on exposure for both species. The vanadium lung burdens appeared to reach steady state in the lowest exposure groups (0.5 and 1 mg/m{sup 3} for rats and mice, respectively) but showed a decline in the higher exposure groups. This deposition pattern was similar between rats and mice but the maximum lung burdens were observed at different times (1 or 2 months in mice vs. 6 months in rats). The vanadium deposition rate decreased faster in mice, while the elimination half-lives of vanadium lung burdens were about six- to nine-fold shorter in mice than in rats at 1 and 2 mg/m{sup 3}. Thus, the retention of vanadium in the lungs at 18 months was lower in mice ({approx}2% retained) compared with rats (13-15% retained) at the common exposure concentrations of 1 and 2 mg/m{sup 3}. The lung burden data were approximately proportional to the exposure concentration in both species, likely due to concomitant decreases in deposition and elimination to a similar extent with increasing exposure. The area under the lung burden versus time curves and the area under the blood concentration (control-normalized) versus time curves were also proportional to exposure concentration. The progression of

  8. Mesoporous Hybrids of Reduced Graphene Oxide and Vanadium Pentoxide for Enhanced Performance in Lithium-Ion Batteries and Electrochemical Capacitors.

    PubMed

    Pandey, Gaind P; Liu, Tao; Brown, Emery; Yang, Yiqun; Li, Yonghui; Sun, Xiuzhi Susan; Fang, Yueping; Li, Jun

    2016-04-13

    Mesoporous hybrids of V2O5 nanoparticles anchored on reduced graphene oxide (rGO) have been synthesized by slow hydrolysis of vanadium oxytriisopropoxide using a two-step solvothermal method followed by vacuum annealing. The hybrid material possesses a hierarchical structure with 20-30 nm V2O5 nanoparticles uniformly grown on rGO nanosheets, leading to a high surface area with mesoscale porosity. Such hybrid materials present significantly improved electronic conductivity and fast electrolyte ion diffusion, which synergistically enhance the electrical energy storage performance. Symmetrical electrochemical capacitors with two rGO-V2O5 hybrid electrodes show excellent cycling stability, good rate capability, and a high specific capacitance up to ∼466 F g(-1) (regarding the total mass of V2O5) in a neutral aqueous electrolyte (1.0 M Na2SO4). When used as the cathode in lithium-ion batteries, the rGO-V2O5 hybrid demonstrates excellent cycling stability and power capability, able to deliver a specific capacity of 295, 220, and 132 mAh g(-1) (regarding the mass of V2O5) at a rate of C/9, 1C, and 10C, respectively. The value at C/9 rate matches the full theoretical capacity of V2O5 for reversible 2 Li(+) insertion/extraction between 4.0 and 2.0 V (vs Li/Li(+)). It retains ∼83% of the discharge capacity after 150 cycles at 1C rate, with only 0.12% decrease per cycle. The enhanced performance in electrical energy storage reveals the effectiveness of rGO as the structure template and more conductive electron pathway in the hybrid material to overcome the intrinsic limits of single-phase V2O5 materials.

  9. In Vivo Effects of Vanadium Pentoxide and Antioxidants (Ascorbic Acid and Alpha-Tocopherol) on Apoptotic, Cytotoxic, and Genotoxic Damage in Peripheral Blood of Mice

    PubMed Central

    García-Rodríguez, María del Carmen; Hernández-Cortés, Lourdes Montserrat; Altamirano-Lozano, Mario Agustín

    2016-01-01

    This study was conducted to investigate the effects of vanadium pentoxide (V2O5), ascorbic acid (AA), and alpha-tocopherol (α-TOH) on apoptotic, cytotoxic, and genotoxic activity. Groups of five Hsd:ICR mice were treated with the following: (a) vehicle, distilled water; (b) vehicle, corn oil; (c) AA, 100 mg/kg intraperitoneally (ip); (d) α-TOH, 20 mg/kg by gavage; (e) V2O5, 40 mg/kg by ip injection; (f) AA + V2O5; and (g) α-TOH + V2O5. Genotoxic damage was evaluated by examining micronucleated polychromatic erythrocytes (MN-PCE) obtained from the caudal vein at 0, 24, 48, and 72 h after treatments. Induction of apoptosis and cell viability were assessed at 48 h after treatment in nucleated cells of peripheral blood. Treatment with AA alone reduced basal MN-PCE, while V2O5 treatment marginally increased MN-PCE at all times after injection. Antioxidants treatments prior to V2O5 administration decreased MN-PCE compared to the V2O5 group, with the most significant effect in the AA + V2O5 group. The apoptotic cells increased with all treatments, suggesting that this process may contribute to the elimination of the cells with V2O5-induced DNA damage (MN-PCE). The necrotic cells only increased in the V2O5 group. Therefore, antioxidants such as AA and α-TOH can be used effectively to protect or reduce the genotoxic effects induced by vanadium compounds like V2O5. PMID:27413422

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed Central

    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. PMID:28102338

  12. Doping-free silicon thin film solar cells using a vanadium pentoxide window layer and a LiF/Al back electrode

    NASA Astrophysics Data System (ADS)

    Jung, Hyung Hwan; Kwon, Jung-Dae; Lee, Sunghun; Su Kim, Chang; Nam, Kee-Seok; Jeong, Yongsoo; Chung, Kwun-Bum; Yoon Ryu, Seung; Ocak, Tülay; Eray, Aynur; Kim, Dong-Ho; Park, Sung-Gyu

    2013-08-01

    This work describes the preparation of a doped layer-free hydrogenated amorphous silicon (a-Si:H) thin film solar cell consisting of a vanadium pentoxide (V2O5-x) window layer, an intrinsic a-Si:H absorber layer, and a lithium fluoride (LiF)/aluminum (Al) back electrode. The large difference between the work functions of the V2O5-x layer and the LiF/Al electrode permitted photogenerated carriers in the i-a-Si:H absorber layer to be effectively separated and collected. The effects of the V2O5-x layer thickness and the oxidation states on the photovoltaic performance were investigated in detail. X-ray photoelectron spectroscopy analysis confirmed that the major species of the sputtered V2O5-x thin films were V5+ and V4+. Optimization of the V2O5-x window layer yielded a power conversion efficiency of 7.04%, which was comparable to the power conversion efficiency of a typical a-Si:H solar cell (7.09%).

  13. Vanadium(V) removal from aqueous solution and real wastewater using quaternized pine sawdust.

    PubMed

    Leiviskä, T; Keränen, A; Vainionpää, N; Al Amir, J; Hormi, O; Tanskanen, J

    2015-01-01

    Cross-linked and quaternized pine sawdust was tested for vanadium removal from a synthetic aqueous solution as well as from real industrial wastewater which had a considerable amount of vanadium and other ions such as sulphate, ammonium and nickel. The maximum vanadium sorption capacity of the modified pine sawdust was found to be 130 mg/g in synthetic solution and 103 mg/g in real wastewater. Modified pine sawdust worked well over a wide range of pH. Column studies with real wastewater proved that vanadium was efficiently desorbed from the material with 2 M NaOH and that the material could be reused.

  14. Exploring electrolyte preference of vanadium nitride supercapacitor electrodes

    SciTech Connect

    Wang, Bo; Chen, Zhaohui; Lu, Gang; Wang, Tianhu; Ge, Yunwang

    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.

  15. Comparative ion insertion study into a nanostructured vanadium oxide in aqueous salt solutions

    SciTech Connect

    Yuan, Q.; Ren, S. L.; Zukowski, J.; Pomeroy, M.; Soghomonian, V.

    2014-07-07

    We present a comparative study for the electrochemical insertion of different cations into a nanostructured vanadium oxide material. The oxide is hydrothemally synthesized and electrically characterized by variable temperature measurements. The electrochemical reactions are performed in aqueous chloride solutions of lithium, sodium, potassium, and ammonium, and the electrochemical behavior of various cycles are correlated with visual changes in the vanadium oxide nanosheets as observed by scanning electron microscopy. We note an increase in the specific charge per cycle in the cases of sodium and ammonium ions only, correlated with minimal physical changes to the nanosheets. The differing behavior of the various ions has implications for their use in electrical energy storage applications.

  16. Structure, hydrolysis, and diffusion of aqueous vanadium ions from Car-Parrinello molecular dynamics

    NASA Astrophysics Data System (ADS)

    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.

  17. Optical properties of electrochromic vanadium pentoxide

    NASA Astrophysics Data System (ADS)

    Cogan, Stuart F.; Nguyen, Nguyet M.; Perrotti, Stephen J.; Rauh, R. David

    1989-08-01

    Electrochemical and spectroscopic measurements were used to characterize the electrochromic behavior of sputtered V2O5 films. In response to lithium intercalation, the fundamental optical absorption edge of V2O5 shifts to high energies by 0.20-0.31 eV as the lithium concentration increases from Li0.0V2O5 to Li0.86V2O5. There is a corresponding increase in the near-infrared absorption that exhibits Beer's law behavior at low lithium concentrations. The shift in absorption edge results in a large decrease in absorbance in the 350-450 nm wavelength range. This effect is most prevalent in thin films which exhibit a yellow to colorless optical modulation on lithium intercalation. The cathodic coloration in the near infrared is relatively weak with a maximum coloration efficiency of 35 cm2/C.

  18. Nanoparticles of Low-Valence Vanadium Oxyhydroxides: Reaction Mechanisms and Polymorphism Control by Low-Temperature Aqueous Chemistry.

    PubMed

    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.

  19. 77 FR 46712 - Ferrovanadium and Nitrided Vanadium From the Russian Federation: Negative Final Determination of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-08-06

    ... International Trade Administration Ferrovanadium and Nitrided Vanadium From the Russian Federation: Negative... importation of vanadium pentoxide from the Russian Federation (Russia) by the Evraz Group,\\1\\ which is toll... ferrovanadium and nitrided vanadium (ferrovanadium) from Russia, within the meaning of section 781(a) of...

  20. Ultra-fast aqueous Li-ion redox energy storage from vanadium oxide-carbon nanotube yarn electrodes

    NASA Astrophysics Data System (ADS)

    Smithyman, Jesse; Do, Quyet H.; Zeng, Changchun; Liang, Zhiyong

    2015-03-01

    Half-cell electrochemical characterizations were conducted on carbon nanotube-vanadium oxide (CNT-VOx) yarn electrodes in an 8 M LiCl aqueous electrolyte. A supercritical fluid deposition and in-situ oxidation process was utilized to deposit nanoscale coatings of vanadium oxide on carbon nanotube (CNT) surfaces throughout the porous structure of CNT yarns. The high surface area, interconnected pore structure and high electrical conductivity of the CNT yarn enabled extraordinary rate capabilities from the high capacity Li/VOx system. High-rate cyclic voltammetry scans, requiring current densities of hundreds of amperes per gram of electrode mass, produced rectangular voltammograms with distinguishable redox peaks from Li-ion intercalation/deintercalation. Capacitances of over 150 F g-1 were achieved at a scan rate of 5 V s-1 over a 1.2 V potential window resulting in an energy density of >32 Wh kg-1 (>30 Wh L-1) for the yarn electrode. The charge storage also showed good reversibility when cycled over this large potential window, maintaining 90% of the capacitance after 100 cycles at a scan rate of 2 V s-1. Electrochemical impedance spectroscopy shows the frequency dependent behavior is distinctly lacking of the characteristic responses from the rate-limiting processes associated with faradaic charge storage in VOx.

  1. Practical thermodynamic quantities for aqueous vanadium- and iron-based flow batteries

    SciTech Connect

    Hudak, Nicholas S.

    2013-12-31

    A simple method for experimentally determining thermodynamic quantities for flow battery cell reactions is presented. Equilibrium cell potentials, temperature derivatives of cell potential (dE/dT), Gibbs free energies, and entropies are reported here for all-vanadium, iron–vanadium, and iron–chromium flow cells with state-of-the-art solution compositions. Proof is given that formal potentials and formal temperature coefficients can be used with modified forms of the Nernst Equation to quantify the thermodynamics of flow cell reactions as a function of state-of-charge. Such empirical quantities can be used in thermo-electrochemical models of flow batteries at the cell or system level. In most cases, the thermodynamic quantities measured here are significantly different from standard values reported and used previously in the literature. The data reported here are also useful in the selection of operating temperatures for flow battery systems. Because higher temperatures correspond to lower equilibrium cell potentials for the battery chemistries studied here, it can be beneficial to charge a cell at higher temperature and discharge at lower temperature. As a result, proof-of-concept of improved voltage efficiency with the use of such non-isothermal cycling is given for the all-vanadium redox flow battery, and the effect is shown to be more pronounced at lower current densities.

  2. Practical thermodynamic quantities for aqueous vanadium- and iron-based flow batteries

    DOE PAGES

    Hudak, Nicholas S.

    2013-12-31

    A simple method for experimentally determining thermodynamic quantities for flow battery cell reactions is presented. Equilibrium cell potentials, temperature derivatives of cell potential (dE/dT), Gibbs free energies, and entropies are reported here for all-vanadium, iron–vanadium, and iron–chromium flow cells with state-of-the-art solution compositions. Proof is given that formal potentials and formal temperature coefficients can be used with modified forms of the Nernst Equation to quantify the thermodynamics of flow cell reactions as a function of state-of-charge. Such empirical quantities can be used in thermo-electrochemical models of flow batteries at the cell or system level. In most cases, the thermodynamic quantitiesmore » measured here are significantly different from standard values reported and used previously in the literature. The data reported here are also useful in the selection of operating temperatures for flow battery systems. Because higher temperatures correspond to lower equilibrium cell potentials for the battery chemistries studied here, it can be beneficial to charge a cell at higher temperature and discharge at lower temperature. As a result, proof-of-concept of improved voltage efficiency with the use of such non-isothermal cycling is given for the all-vanadium redox flow battery, and the effect is shown to be more pronounced at lower current densities.« less

  3. Method for preparing high purity vanadium

    DOEpatents

    Schmidt, F.; Carlson, O.N.

    1984-05-16

    A method for preparing high purity vanadium having a low silicon content has been developed. Vanadium pentoxide is reduced with a stoichiometric, or slightly deficient amount of aluminum to produce a vanadium-aluminum alloy containing an excess of oxygen. Silicon is removed by electron-beam melting the alloy under oxidizing conditions to promote the formation of SiO which is volatile at elevated temperatures. Excess oxygen is removed by heating the alloy in the presence of calcium metal to form calcium oxide.

  4. Method for preparing high purity vanadium

    DOEpatents

    Schmidt, Frederick; Carlson, O. Norman

    1986-09-09

    A method for preparing high purity vanadium having a low silicon content has been developed. Vanadium pentoxide is reduced with a stoichiometric, or slightly deficient amount of aluminum to produce a vanadium-aluminum alloy containing an excess of oxygen. Silicon is removed by electron-beam melting the alloy under oxidizing conditions to promote the formation of SiO which is volatile at elevated temperatures. Excess oxygen is removed by heating the alloy in the presence of calcium metal to form calcium oxide.

  5. Characterization of aqueous formulations of tetra- and pentavalent forms of vanadium in support of test article selection in toxicology studies.

    PubMed

    Mutlu, Esra; Cristy, Tim; Graves, Steven W; Hooth, Michelle J; Waidyanatha, Suramya

    2017-01-01

    Tetravalent (V(IV)) and pentavalent (V(V)) forms of vanadium were selected for testing by the National Toxicology Program via drinking water exposure due to potential human exposure. To aid in the test article selection, drinking water formulations (125-2000 mg/L) of vanadyl sulfate (V(IV)), sodium orthovanadate, and sodium metavanadate (V(V)) were characterized by ultraviolet/visible (UV/VIS) spectroscopy, mass spectrometry (MS), or (51)V nuclear magnetic resonance (NMR) spectroscopy. Aqueous formulations of orthovanadate, metavanadate, and vanadyl sulfate in general were basic, neutral, and acidic, respectively. Changes in vanadium speciation were investigated by adjusting formulation pH to acidic, neutral, or basic. There was no visible difference in UV/VIS spectra of pentavalent forms. NMR and MS analyses showed that the predominant oxidovanadate species in both ortho- and metavanadate formulations at basic and acidic pH, respectively, were the monomer and decamer, while, a mixture of oxidovanadates were present at neutral pH. Oxidovanadate species were not observed in vanadyl sulfate formulations at acidic pH but were observed at basic pH suggesting conversion of V(IV) to V(V). These data suggest that formulations of both ortho- and metavanadate form similar oxidovanadate species in acidic, neutral and basic pH and exist mainly in the V(V) form while vanadyl sulfate exists mainly as V(IV) in acidic pH. Therefore, the formulation stability overtime was investigated only for sodium metavanadate and vanadyl sulfate. Drinking water formulations (50 and 2000 mg/L) of metavanadate (~pH 7) and vanadyl sulfate (~pH 3.5) were ≥92 % of target concentration up to 42 days at ~5 °C and ambient temperature demonstrating the utility in toxicology studies.

  6. Vanadium Oxide Electrochemical Capacitors: An Investigation into Aqueous Capacitive Degradation, Alternate Electrolyte-Solvent Systems, Whole Cell Performance and Graphene Oxide Composite Electrodes

    NASA Astrophysics Data System (ADS)

    Engstrom, Allison Michelle

    Vanadium oxide has emerged as a potential electrochemical capacitor material due to its attractive pseudocapacitive performance; however, it is known to suffer from capacitive degradation upon sustained cycling. In this work, the electrochemical cycling behavior of anodically electrodeposited vanadium oxide films with various surface treatments in aqueous solutions is investigated at different pH. Quantitative compositional analysis and morphological studies provide additional insight into the mechanism responsible for capacitive degradation. Furthermore, the capacitance and impedance behavior of vanadium oxide electrochemical capacitor electrodes is compared for both aqueous and nonaqueous electrolyte-solvent systems. Alkali metal chloride and bromide electrolytes were studied in aqueous systems, and nonaqueous systems containing alkali metal bromides were studied in polar aprotic propylene carbonate (PC) or dimethyl sulfoxide (DMSO) solvents. The preferred aqueous and nonaqueous systems identified in the half-cell studies were utilized in symmetric vanadium oxide whole-cells. An aqueous system utilizing a 3.0 M NaCl electrolyte at pH 3.0 exhibited an excellent 96% capacitance retention over 3000 cycles at 10 mV s-1. An equivalent system tested at 500 mV s-1 displayed an increase in capacitance over the first several thousands of cycles, and eventually stabilized over 50,000 cycles. Electrodes cycled in nonaqueous 1.0 M LiBr in PC exhibited mostly non-capacitive charge-storage, and electrodes cycled in LiBr-DMSO exhibited a gradual capacitive decay over 10,000 cycles at 500 mV s-1. Morphological and compositional analyses, as well as electrochemical impedance modeling, provide additional insight into the cause of the cycing behavior. Lastly, reduced graphene oxide and vanadium oxide nanowire composites have been successfully synthesized using electrophoretic deposition for electrochemical capacitor electrodes. The composite material was found to perform with a

  7. An Ambient Temperature Molten Sodium-Vanadium Battery with Aqueous Flowing Catholyte.

    PubMed

    Liu, Caihong; Shamie, Jack S; Shaw, Leon L; Sprenkle, Vincent L

    2016-01-20

    In this study, we have investigated the key factors dictating the cyclic performance of a new type of hybrid sodium-based flow batteries (HNFBs) that can operate at room temperature with high cell voltages (>3 V), multiple electron transfer redox reactions per active ion, and decoupled design of power and energy. HNFBs are composed of a molten Na-Cs alloy anode, flowing aqueous catholyte, and a Na-β″-Al2O3 solid electrolyte as the separator. The surface functionalization of graphite felt electrodes for the flowing aqueous catholyte has been studied for its effectiveness in enhancing V(2+)/V(3+), V(3+)/V(4+), and V(4+)/V(5+) redox couples. The V(4+)/V(5+) redox reaction has been further investigated at different cell operation temperatures for its cyclic stability and how the properties of the solid electrolyte membrane play a role in cycling. These fundamental understandings provide guidelines for improving the cyclic performance and stability of HNFBs with aqueous catholytes. We show that the HNFB with aqueous V-ion catholyte can reach high storage capacity (∼70% of the theoretical capacity) with good Coulombic efficiency (90% ± 1% in 2-30 cycles) and cyclic performance (>99% capacity retention for 30 cycles). It demonstrates, for the first time, the potential of high capacity HNFBs with aqueous catholytes, good capacity retention and long cycling life. This is also the first demonstration that Na-β″-Al2O3 solid electrolyte can be used with aqueous electrolyte at near room temperature for more than 30 cycles.

  8. Ion-sensing properties of 1D vanadium pentoxide nanostructures

    PubMed Central

    2012-01-01

    The application of one-dimensional (1D) V2O5·nH2O nanostructures as pH sensing material was evaluated. 1D V2O5·nH2O nanostructures were obtained by a hydrothermal method with systematic control of morphology forming different nanostructures: nanoribbons, nanowires and nanorods. Deposited onto Au-covered substrates, 1D V2O5·nH2O nanostructures were employed as gate material in pH sensors based on separative extended gate FET as an alternative to provide FET isolation from the chemical environment. 1D V2O5·nH2O nanostructures showed pH sensitivity around the expected theoretical value. Due to high pH sensing properties, flexibility and low cost, further applications of 1D V2O5·nH2O nanostructures comprise enzyme FET-based biosensors using immobilized enzymes. PMID:22709724

  9. Atomistic mechanism of α - β phase transition in vanadium pentoxide

    NASA Astrophysics Data System (ADS)

    Smirnov, Mikhail B.; Kazimirov, Viatcheslav Yu.; Baddour-Hadjean, Rita; Smirnov, Konstantin S.; Pereira-Ramos, Jean-Pierre

    2014-01-01

    A mechanism of the α - β structural phase transition (SPT) in V2O5 is proposed. The driving force of the SPT is suggested to be the U5 shear strain transforming the orthorhombic unit cell of the α-phase into the monoclinic unit cell of the β-phase. According to the model, the SPT is characterized by a concerted displacement of V2O5 chains and is of martensitic type. Results of periodic DFT calculations performed for structures along the transformation path corroborate the proposed mechanism. The calculated height of the energy barrier is in a good agreement with the heat of transition determined experimentally for the inverse β - α transformation. Possible ways of the experimental verification of the proposed mechanism are discussed.

  10. Dimension meditated optic and catalytic performance over vanadium pentoxides

    NASA Astrophysics Data System (ADS)

    Su, Dezhi; Zhao, Yongjie; Zhang, Ruibo; Ning, Mingqiang; Zhao, Yuzhen; Zhou, Heping; Li, Jingbo; Jin, Haibo

    2016-12-01

    Morphologies and sizes of V2O5 had crucial effect on their optic and catalytic performance. Diverse dimensional V2O5 were successfully synthesized by the combination of a hydrothermal and post heat treatment method. The as-obtained samples were characterized by X-ray power diffraction, scanning electron microscopy, transmission electron microscopy and Raman spectra. Moreover, the optic properties of diverse dimensional V2O5 were examined by Fourier transform imaging spectrometer and UV-vis-spectrophotometer. It showed that the IR transmittance of nanowire (at 1019 cm-1 is 85%) and UV absorbance of microflowers (at 480 nm) were high. Furthermore, the catalytic properties of diverse dimensional V2O5 on the thermal decomposition of ammonium perchlorate were evaluated and compared by Thermo-Gravimetric Analysis and Differential Scanning Calorimetry. Moreover, the best catalytic performance was obtained with the morphology of nanowire. It showed the thermal decomposition temperatures of AP with nanowire, microflowers and microsphere were reduced to 373 °C, 382 °C and 376 °C (decreased by 52 °C, 43 °C and 49 °C).

  11. Anion exchange membrane prepared from simultaneous polymerization and quaternization of 4-vinyl pyridine for non-aqueous vanadium redox flow battery applications

    NASA Astrophysics Data System (ADS)

    Maurya, Sandip; Shin, Sung-Hee; Sung, Ki-Won; Moon, Seung-Hyeon

    2014-06-01

    A simple, single step and environmentally friendly process is developed for the synthesis of anion exchange membrane (AEM) by simultaneous polymerization and quaternization, unlike the conventional membrane synthesis which consists of separate polymerization and quaternization step. The membrane synthesis is carried out by dissolving polyvinyl chloride (PVC) in cyclohexanone along with 4-vinyl pyridine (4VP) and 1,4-dibromobutane (DBB) in the presence of thermal initiator benzoyl peroxide, followed by film casting to get thin and flexible AEMs. The membrane properties such as ion exchange capacity, ionic conductivity and swelling behaviour are tuned by varying the degree of crosslinking. These AEMs exhibit low vanadium permeability, while retaining good dimensional and chemical stability in an electrolyte solution, making them appropriate candidates for non-aqueous vanadium acetylacetonate redox flow battery (VRFB) applications. The optimized membrane displays ion exchange capacity and ionic conductivity of 2.0 mequiv g-1 and 0.105 mS cm-1, respectively, whereas the efficiency of 91.7%, 95.7% and 87.7% for coulombic, voltage and energy parameter in non-aqueous VRFB, respectively. This study reveals that the non-aqueous VRFB performance is greatly influenced by membrane properties; therefore the optimal control over the membrane properties is advantageous for the improved performance.

  12. Vanadium Flow Battery Electrolyte Synthesis via Chemical Reduction of V2O5 in Aqueous HCl and H2SO4.

    SciTech Connect

    Small, Leo J.; Pratt, Harry; Staiger, Chad; Martin, Rachel Irene; Anderson, Travis Mark; Chalamala, Babu; Soundappan, Thiagarajan; Tiwari, Monika; Subarmanian, Venkat R.

    2017-01-01

    We report a simple method to synthesize V 4+ (VO 2+ ) electrolytes as feedstock for all- vanadium redox flow batteries (RFB). By dissolving V 2 O 5 in aqueous HCl and H 2 SO 4 , subsequently adding glycerol as a reducing agent, we have demonstrated an inexpensive route for electrolyte synthesis to concentrations >2.5 M V 4+ (VO 2+ ). Electrochemical analysis and testing of laboratory scale RFB demonstrate improved thermal stability across a wider temperature range (-10-65 degC) for V 4+ (VO 2+ ) electrolytes in HCl compared to in H 2 SO 4 electrolytes.

  13. A global biogeochemical mass balance model for vanadium

    SciTech Connect

    Hope, B.K.

    1995-12-31

    Vanadium is a major trace metal in fossil fuels and combustion of these materials provides a significant source of vanadium in the environment. Close correlation exists between atmospheric vanadium concentration and fuel consumption, so that atmospheric vanadium pentoxide has been used as an indicator of human industrial activity. Little vanadium is retained in refined oil products, and vanadium contamination occurs as fallout from refining operations and burning of residual oils. This is the major cause for the approximate doubling of the environmental flux of vanadium as a result of human activity; other sources are products of coal combustion, leachates, and effluents from mining and milling of uranium and titanium. It was estimated in 1975 that the injection of vanadium into the atmosphere from anthropogenic sources equaled the input from natural sources. Such evidence that environmental levels of vanadium are increasing has raised concern over the injection of vanadium into the atmosphere from anthropogenic sources. A simple global mass balance model was developed to demonstrate the influence of anthropogenic vanadium on the global distribution of this trace metal. Vanadium in particulate emissions owing to man`s industrial activities were estimated to comprise {approx} 53% of total atmosphere vanadium loading and exceeded natural continental or volcanogenic dust by only a narrow margin. Oceanic deposition of vanadium adhering to anthropogenic particles was estimated to comprise {approx} 5% of total ocean vanadium loading. There is no suggestion that these inputs of anthropogenic vanadium pose a significant global environmental threat. It is entirely possible, however, that anthropogenic vanadium inputs could pose an environmental hazard given a more restricted area and a specific set of unfavorable circumstances.

  14. Toxicity of aqueous vanadium to zooplankton and phytoplankton species of relevance to the athabasca oil sands region.

    PubMed

    Schiffer, Stephanie; Liber, Karsten

    2017-03-01

    Vanadium (V) is an abundant trace metal present in bitumen from the Athabasca Oil Sands (AOS) region in Alberta, Canada. The upgrading of bitumen can result in the production of large volumes of a carbonaceous material referred to as petroleum coke that contains V at elevated levels compared to the native bitumen. Previous studies have shown that coke has the capacity to leach ecotoxicologically relevant levels of V into water it contacts, yet limited data are available on the toxicity of aqueous V to planktonic organisms. Therefore, this study set out to evaluate the acute and chronic toxicity of V (as vanadate oxyanions) to freshwater zooplankton and phytoplankton species that are either commonly-used laboratory species, or species more regionally-representative of northern Alberta. Four cladoceran (2-d and 21-d tests) and two algal (3-d tests) species were exposed to V to obtain both acute and chronic toxicity estimates. Acute V toxicity (LC50s) ranged from 0.60mgV/L for Ceriodaphnia quadrangula to 2.17mgV/L for Daphnia pulex. Chronic toxicity estimates (EC50s) for cladoceran survival and reproduction were nearly identical within species and ranged from a low of 0.13 to a high of 0.46mgV/L for Daphnia dentifera and D. pulex, respectively. The lack of sublethal V toxicity in daphnia suggests a direct mechanism of toxicity through ion imbalance. Growth inhibition (EC50) of green algae occurred at concentrations of 3.24 and 4.12mgV/L for Pseudokirchneriella subcapitata and Scenedesmus quadricauda, respectively. Overall, cladocerans were more sensitive to V than green algae, with survival of the field-collected D. dentifera being approximately 2.5 to 3.5 times more sensitive to acute and chronic V exposure than the standard test species D. pulex. However, there were no significant differences in V toxicity between the field-collected cladocerans Simocephalus serrulatus and C. quadrangula, compared to the respective standard species D. pulex and Ceriodaphnia dubia

  15. Thirty years through vanadium chemistry.

    PubMed

    Costa Pessoa, J

    2015-06-01

    The relevance of vanadium in biological systems is known for many years and vanadium-based catalysts have important industrial applications, however, till the beginning of the 80s research on vanadium chemistry and biochemistry did not receive much attention from the scientific community. The understanding of the broad bioinorganic implications resulting from the similarities between phosphate and vanadate(V) and the discovery of vanadium dependent enzymes gave rise to an enormous increase in interest in the chemistry and biological relevance of vanadium. Thereupon the last 30years corresponded to a period of enormous research effort in these fields, as well as in medicinal applications of vanadium and in the development of catalysts for use in fine-chemical synthesis, some of these inspired by enzymatic active sites. Since the 80s my group in collaboration with others made contributions, described throughout this text, namely in the understanding of the speciation of vanadium compounds in aqueous solution and in biological fluids, and to the transport of vanadium compounds in blood plasma and their uptake by cells. Several new types of vanadium compounds were also synthesized and characterized, with applications either as prospective therapeutic drugs or as homogeneous or heterogenized catalysts for the production of fine chemicals. The developments made are described also considering the international context of the evolution of the knowledge in the chemistry and bioinorganic chemistry of vanadium compounds during the last 30years. This article was compiled based on the Vanadis Award presentation at the 9th International Vanadium Symposium.

  16. Vanadium. Its role for humans.

    PubMed

    Rehder, Dieter

    2013-01-01

    Vanadium is the 21st most abundant element in the Earth's crust and the 2nd-to-most abundant transition metal in sea water. The element is ubiquitous also in freshwater and nutrients. The average body load of a human individual amounts to 1 mg. The omnipresence of vanadium hampers checks directed towards its essentiality. However, since vanadate can be considered a close blueprint of phosphate with respect to its built-up, vanadate likely takes over a regulatory function in metabolic processes depending on phosphate. At common concentrations, vanadium is non-toxic. The main source for potentially toxic effects caused by vanadium is exposure to high loads of vanadium oxides in the breathing air of vanadium processing industrial enterprises. Vanadium can enter the body via the lungs or, more commonly, the stomach. Most of the dietary vanadium is excreted. The amount of vanadium resorbed in the gastrointestinal tract is a function of its oxidation state (V(V) or V(IV)) and the coordination environment. Vanadium compounds that enter the blood stream are subjected to speciation. The predominant vanadium species in blood are vanadate and vanadyl bound to transferrin. From the blood stream, vanadium becomes distributed to the body tissues and bones. Bones act as storage pool for vanadate. The aqueous chemistry of vanadium(V) at concentration <10 μM is dominated by vanadate. At higher concentrations, oligovanadates come in, decavanadate in particular, which is thermodynamically stable in the pH range 2.3-6.3, and can further be stabilized at higher pH by interaction with proteins.The similarity between vanadate and phosphate accounts for the interplay between vanadate and phosphate-dependent enzymes: phosphatases can be inhibited, kinases activated. As far as medicinal applications of vanadium compounds are concerned, vanadium's mode of action appears to be related to the phosphate-vanadate antagonism, to the direct interaction of vanadium compounds or fragments thereof

  17. Understanding Aqueous Electrolyte Stability through Combined Computational and Magnetic Resonance Spectroscopy: A Case Study on Vanadium Redox Flow Battery Electrolytes

    SciTech Connect

    Vijayakumar, M.; Nie, Zimin; Walter, Eric D.; Hu, Jian Z.; Liu, Jun; Sprenkle, Vincent L.; Wang, Wei

    2015-02-01

    Redox flow battery (RFB) is a promising candidate for energy storage component in designing resilient grid scale power supply due to the advantage of the separation of power and energy. However, poorly understood chemical and thermal stability issues of electrolytes currently limit the performance of RFB. Designing of high performance stable electrolytes requires comprehensive knowledge about the molecular level solvation structure and dynamics of their redox active species. The molecular level understanding of detrimental V2O5 precipitation process led to successful designing of mixed acid based electrolytes for vanadium redox flow batteries (VRFB). The higher stability of mixed acid based electrolytes is attributed to the choice of hydrochloric acid as optimal co-solvent, which provides chloride anions for ligand exchange process in vanadium solvation structure. The role of chloride counter anion on solvation structure and dynamics of vanadium species were studied using combined magnetic resonance spectroscopy and DFT based theoretical methods. Finally, the solvation phenomenon of multiple vanadium species and their impact on VRFB electrolyte chemical stability were discussed.

  18. Influence of solvents on species crossover and capacity decay in non-aqueous vanadium redox flow batteries: Characterization of acetonitrile and 1, 3 dioxolane solvent mixture

    NASA Astrophysics Data System (ADS)

    Bamgbopa, Musbaudeen O.; Almheiri, Saif

    2017-02-01

    The importance of the choice of solvent in a non-aqueous redox flow battery (NARFB) cannot be overemphasized. Several studies demonstrated the influence of the solvent on electrolyte performance in terms of reaction rates, energy/power densities, and efficiencies. In this work, we investigate capacity decay as a direct consequence of varying reactant crossover rates through membranes in different solvent environments. Specifically, we demonstrate the superiority of an 84/16 vol% acetonitrile/1,3 dioxolane solvent mixture over pure acetonitrile in terms of energy efficiency (up to 89%) and capacity retention for vanadium NARFBs - while incorporating a Nafion 115 membrane. The permeability of Nafion to the vanadium acetylacetonate active species is an order of magnitude lower when pure acetonitrile is replaced by the solvent mixture. A method to estimate relative membrane permeability is formulated from numerical analysis of self-discharge experimental data. Furthermore, tests on a modified Nafion/SiO2 membrane, which generally offered low species permeability, also show that different solvents alter membrane permeability. Elemental and morphological analyses of cycled Nafion and NafionSi membranes in different solvent environments indicate that different crossover rates induced by the choice of solvent during cycling are due to changes in the membrane microstructure, intrinsic permeability, swelling rates, and chemical stability.

  19. Metal-insulator transition characteristics of vanadium dioxide thin films synthesized by ultrasonic nebulized spray pyrolysis of an aqueous combustion mixture

    NASA Astrophysics Data System (ADS)

    Bharathi, R.; Naorem, Rameshwari; Umarji, A. M.

    2015-08-01

    We report the synthesis of high quality vanadium dioxide (VO2) thin films by a novel spray pyrolysis technique, namely ultrasonic nebulized spray pyrolysis of aqueous combustion mixture (UNSPACM). This simple and cost effective two step process involves synthesis of a V2O5 film on an LaAlO3 substrate followed by a controlled reduction to form single phase VO2. The formation of M1 phase (P21/c) is confirmed by Raman spectroscopic studies. A thermally activated metal-insulator transition (MIT) was observed at 61 ^\\circ C, where the resistivity changes by four orders of magnitude. Activation energies for the low conduction phase and the high conduction phase were obtained from temperature variable resistance measurements. The infrared spectra also show a dramatic change in reflectance from 13% to over 90% in the wavelength range of 7-15 μ m. This indicates the suitability of the films for optical switching applications at infrared frequencies.

  20. International strategic minerals inventory summary report; vanadium

    USGS Publications Warehouse

    Goldberg, I.; Hammerbeck, E.C.I.; Labuschagne, L.S.; Rossouw, C.

    1992-01-01

    Major world resources of vanadium are described in this summary report of information in the International Strategic Minerals Inventory (ISMI). ISMI is a cooperative data-collection effort of earth-science and mineral-resource agencies in Australia, Canada, the Federal Republic of Germany, the Republic of South Africa, the United Kingdom, and the United States of America. This report, designed to benefit geologists and policy analysts, contains two parts. Part I presents an overview of the resources and potential supply of vanadium based on inventory information. Part II contains tables of some geologic information and mineral-resource and production data collected by ISMI participants. Vanadium's greatest application is as an additive in steel. During 1984, for example, 90 percent of the vanadium produced in the world was consumed in steelmaking. The Soviet Union and China are the only major steel producers of the world that meet significant proportions of their vanadium needs from domestic sources, albeit from relatively low-grade ores. Reliable economically exploitable world resources total greater than 22 million metric tons of vanadium pentoxide. Deposits of the titaniferous magnetite type are the most economically important, and of these the Bushveld Complex of South Africa is the principal vanadium resource. The high-grade tenor of the Bushveld ore renders South Africa the world's leader in vanadium resources and production. Present (1990) major primary production is confined to only four countries: South Africa, the Soviet Union (low-grade ore), the Peoples Republic of China (low-grade ore), and the United States (partly from imported materials). This production trend is likely to continue for many years.

  1. Development of a tantalum pentoxide Luneberg lens

    NASA Technical Reports Server (NTRS)

    Bryan, D. A.; Chubb, C. R.; Powers, J. K.; Reed, W. R.; Dalke, E. A.; Tomaschke, H. E.

    1982-01-01

    A process has been developed for the fabrication of a tantalum pentoxide waveguide Luneburg lens as the input collimator for an optical signal processing circuit on a silicon substrate, such as an integrated wavelength demultiplexer. The development of such a lens involved improvement of the deposition mask profile, reduction of surface scattering by underlaying the lens, reduction of edge scattering by using shims under the mask, and prediction and measurement of the TE-TM polarization aberration. It is shown that polarization aberration significantly affects the design of a demultiplexer system.

  2. Experimental studies and applications of vanadium oxides.

    NASA Technical Reports Server (NTRS)

    Williams, L., Jr.

    1972-01-01

    The electrical and electrochemical properties of V-5 and V-7 vanadium oxides were investigated. The effects of pressure, temperature and moisture on the bulk resistivity of the oxides in powder, sintered, and crystalline form were determined, and the static and dynamic volt-ampere characteristics were obtained. Sintered samples tested showed better electrical stability than the compressed powder samples. Two types of commercially available vanadium pentoxide were heat-treated to obtain various crystalline oxide forms which were mounted on alumina substrates and terminated by thick-film conductors for making electrical connections. Indications are that these materials could have applications as sensors, critical-temperature resistors, high-speed switches, and temperature-compensation elements in hybrid microelectronic circuits.

  3. Aqueous V(V)-peroxo-amino acid chemistry. Synthesis, structural and spectroscopic characterization of unusual ternary dinuclear tetraperoxo vanadium(V)-glycine complexes.

    PubMed

    Gabriel, C; Kaliva, M; Venetis, J; Baran, P; Rodriguez-Escudero, I; Voyiatzis, G; Zervou, M; Salifoglou, A

    2009-01-19

    Vanadium participation in cellular events entails in-depth comprehension of its soluble and bioavailable forms bearing physiological ligands in aqueous distributions of binary and ternary systems. Poised to understand the ternary V(V)-H(2)O(2)-amino acid interactions relevant to that metal ion's biological role, we have launched synthetic efforts involving the physiological ligands glycine and H(2)O(2). In a pH-specific fashion, V(2)O(5), glycine, and H(2)O(2) reacted and afforded the unusual complexes (H(3)O)(2)[V(2)(O)(2)(mu(2):eta(2):eta(1)-O(2))(2)(eta(2)-O(2))(2)(C(2)H(5)NO(2))] x 5/4 H(2)O (1) and K(2)[V(2)(O)(2)(mu(2):eta(2):eta(1)-O(2))(2)(eta(2)-O(2))(2)(C(2)H(5)NO(2))] x H(2)O (2). 1 crystallizes in the triclinic space group P1, with a = 7.805(4) A, b = 8.134(5) A, c = 12.010(7) A, alpha = 72.298(9) degrees, beta = 72.991(9) degrees, gamma = 64.111(9) degrees, V = 641.9(6) A(3), and Z = 2. 2 crystallizes in the triclinic space group P1, with a = 7.6766(9) A, b = 7.9534(9) A, c = 11.7494(13) A, alpha = 71.768(2) degrees, beta = 73.233(2) degrees, gamma = 65.660(2) degrees, V = 610.15(12) A(3), and Z = 2. Both complexes 1 and 2 were characterized by UV/visible, LC-MS, FT-IR, Raman, NMR spectroscopy, cyclic voltammetry, and X-ray crystallography. The structures of 1 and 2 reveal the presence of unusual ternary dinuclear vanadium-tetraperoxo-glycine complexes containing [(V(V)=O)(O(2))(2)](-) units interacting through long V-O bonds and an effective glycinate bridge. The latter ligand is present in the dianionic assembly as a bidentate moiety spanning both V(V) centers in a zwitterionic form. The collective physicochemical properties of the two ternary species 1 and 2 project the chemical role of the low molecular mass biosubstrate glycine in binding V(V)-diperoxo units, thereby stabilizing a dinuclear V(V)-tetraperoxo dianion. Structural comparisons of the anions in 1 and 2 with other known dinuclear V(V)-tetraperoxo binary anionic species provide insight

  4. Photochemical aerobic detoxification of aqueous phenol and chlorophenol solutions promoted by iron salts and iron, vanadium, and copper oxides

    SciTech Connect

    Nizova, G.V.; Bochkova, M.M.; Kozlova, N.B.; Shul`pin, G.B.

    1995-09-10

    Phenol, 2,4,5-trichlorophenol, and pentachlorophenol in air in the presence of soluble iron salts or insoluble V{sub 2}O{sub 5}, Fe{sub 2}O{sub 3}, and CuO decompose in aqueous solution when irradiated by a luminescent lamp. The degree and the rate of decomposition are strongly influenced by the nature of the substrate and metal-containing promoter. As a result of decomposition, toxicity of solutions containing 2,4,5-trichlorophenol with respect to two types of living organisms - Protozoa (Tetrahymena pyriformis) and bacteria (Beneckea harveyi) - decreases significantly.

  5. VANADIUM ALLOYS

    DOEpatents

    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.

  6. Automated determination of nitrate plus nitrite in aqueous samples with flow injection analysis using vanadium (III) chloride as reductant.

    PubMed

    Wang, Shu; Lin, Kunning; Chen, Nengwang; Yuan, Dongxing; Ma, Jian

    2016-01-01

    Determination of nitrate in aqueous samples is an important analytical objective for environmental monitoring and assessment. Here we report the first automatic flow injection analysis (FIA) of nitrate (plus nitrite) using VCl3 as reductant instead of the well-known but toxic cadmium column for reducing nitrate to nitrite. The reduced nitrate plus the nitrite originally present in the sample react with the Griess reagent (sulfanilamide and N-1-naphthylethylenediamine dihydrochloride) under acidic condition. The resulting pink azo dye can be detected at 540 nm. The Griess reagent and VCl3 are used as a single mixed reagent solution to simplify the system. The various parameters of the FIA procedure including reagent composition, temperature, volume of the injection loop, and flow rate were carefully investigated and optimized via univariate experimental design. Under the optimized conditions, the linear range and detection limit of this method are 0-100 µM (R(2)=0.9995) and 0.1 µM, respectively. The targeted analytical range can be easily extended to higher concentrations by selecting alternative detection wavelengths or increasing flow rate. The FIA system provides a sample throughput of 20 h(-1), which is much higher than that of previously reported manual methods based on the same chemistry. National reference solutions and different kinds of aqueous samples were analyzed with our method as well as the cadmium column reduction method. The results from our method agree well with both the certified value and the results from the cadmium column reduction method (no significant difference with P=0.95). The spiked recovery varies from 89% to 108% for samples with different matrices, showing insignificant matrix interference in this method.

  7. Vanadium corrosion studies. Final report, 1 February 1989-30 June 1993

    SciTech Connect

    Bornstein, N.; Roth, H.; Pike, R.

    1993-06-30

    Vanadium present in certain crude and residual fuel oils, is converted within the burner of the gas turbine engine to the refractory dioxide, which in flight is fully oxidized to the pentoxide. Yttrium oxide, stable in the presence of the oxides of sulfur is identified and verified as a corrosion inhibitor. A chelation process to produce a hydrolytic stable fuel soluble yttrium additive is described.... Vanadium oxide corrosion, Hot corrosion, Sulfidation corrosion, Hot corrosion attenuation, Fuel additives, Water stable fuel soluble yttrium compounds, Chelation.

  8. Flexible vanadium oxide film for broadband transparent photodetector

    NASA Astrophysics Data System (ADS)

    Kim, Hong-Sik; Chauhan, Khushbu R.; Kim, Joondong; Choi, Eun Ha

    2017-03-01

    A High-performing transparent and flexible photodetector was achieved by reactive sputtering method. Vanadium pentoxide (V2O5) thin films were deposited on flexible polyethylene terephthalate (PET) substrates at room temperature. The transparent and flexible photodetectors with the configurations V2O5/ZnO/ITO/PET showed high-performing photoresponse with a quick response time (4.9 ms) and high detectivity of 1.45 × 1012 Jones, under a light intensity of 1 mW/m2. We demonstrated high-performing V2O5 film-based transparent and flexible broadband photodetectors which may provide a promising approach for transparent electronic applications.

  9. Uptake of Nitric Acid, Dinitrogen Pentoxide, Ozone and The Nitrate Radical On A Single Liquid Drop

    NASA Astrophysics Data System (ADS)

    Schütze, M.; Herrmann, H.

    A novel technique for the investigation of uptake processes on gas-liquid interfaces will be presented. It allows the generation and analysis of single liquid drops inside a flow tube reactor. The in situ analysis of the drop is performed by broad band UV-VIS absorption spectroscopy. Using this set-up the uptake of nitric acid and dinitrogen pentoxide on pure water was measured by monitoring the occurrence of the nitrate band centered at a wavelength of 300 nm. The uptake of ozone on NaI solutions of various concentrations was followed by the formation of the triiodide ion which is a product of the oxidation of iodide by ozone. Using aqueous solutions of the dye Alizarin Red S, the uptake of the nitrate radical could be quantified. In order to extract information on fundamental parameters, e.g. the mass accommo- dation coefficients (= a) of the species, a computer model is applied. It solves the diffusion equation for the transport of gas phase species to the interface numerically. The result is a separation of the influence of this process on the rate of the overall uptake process. The mass accommodation coefficients a > 0.03, a = 0.011 and a > 0.02 were obtained for nitric acid, dinitrogen pentoxide and ozone, respectively.

  10. Tungsten-vanadium oxide sputtered films for Electrochromic Devices

    SciTech Connect

    Michalak, F.; Richardson, T.; Rubin, M.; Slack, J.; von Rottkay, K.

    1998-10-01

    Mixed vanadium and tungsten oxide films with compositions ranging from 0 to 100% vanadium (metals basis) were prepared by reactive sputtering from metallic vanadium and tungsten targets in an atmosphere of argon and oxygen. The vanadium content varied smoothly with the fraction of total power applied to the vanadium target. Films containing vanadium were more color neutral than pure tungsten oxide films, tending to gray-brown at high V fraction. The electrochromic switching performance of these films was investigated by in situ monitoring of their visible transmittance during lithium insertion/extraction cycling in a non-aqueous electrolyte (1M LiClO{sub 4} in propylene carbonate). The solar transmittance and reflectance was measured ex situ. Films with vanadium content greater than about 15% exhibited a marked decrease in switching range. Coloration efficiencies followed a similar trend.

  11. Synthesis, characterization, and thermodynamic parameters of vanadium dioxide

    SciTech Connect

    Qi Ji; Ning Guiling Lin Yuan

    2008-08-04

    A novel process was developed for synthesizing pure thermochromic vanadium dioxide (VO{sub 2}) by thermal reduction of vanadium pentoxide (V{sub 2}O{sub 5}) in ammonia gas. The process of thermal reduction of V{sub 2}O{sub 5} was optimized by both experiments and modeling of thermodynamic parameters. The product VO{sub 2} was characterized by means of X-ray diffraction (XRD), X-ray photoelectron spectrometry (XPS), scanning electron microscopy (SEM), thermogravimetric analysis (TG), and differential scanning calorimetry (DSC). The experimental results indicated that pure thermochromic VO{sub 2} crystal particles were successfully synthesized. The phase transition temperature of the VO{sub 2} is approximately 342.6 K and the enthalpy of phase transition is 44.90 J/g.

  12. Platinum–Vanadium Oxide Nanotube Hybrids

    PubMed Central

    2010-01-01

    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. PMID:20672065

  13. Kinetic characterization of barium titanate-bismuth oxide-vanadium pentoxide glasses

    NASA Astrophysics Data System (ADS)

    Al-Syadi, Aref M.; Yousef, El Sayed; El-Desoky, M. M.; Al-Assiri, M. S.

    2014-06-01

    The glasses with the composition (80 - x)V2O5·20Bi2O3·xBaTiO3 with x = 2.5, 5, 7.5 and 10 mol % were prepared by a melting technique. The crystallization behavior and the microstructure of the glasses were investigated by using differential scanning calorimetry (DSC), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The mean value of the activation energy of structural relaxation () decreased from 395 ± 3 to 369 ± 1.83 kJ/mol when BaTiO3 increased from 2.5 to 10 mol %. The activation energies obtained by the methods Kissinger and Ozawa were in the range from 213 ± 0.65 to 256 ± 1.23 kJ/mol. Different analysis methods were used to estimate the Avrami exponents. Their values range from 4.26 ± 0.6 to 2.62 ± 0.11 for the exothermic peak of the prepared glasses. Moreover, synthesized glasses-ceramic containing BaTi4O9 and Ba3TiV4O15 were estimated by using XRD.

  14. Programmable diode/resistor-like behavior of nanostructured vanadium pentoxide xerogel thin film.

    PubMed

    Wan, Zhenni; Darling, Robert B; Anantram, M P

    2015-11-11

    Electrical properties of a Cr/V2O5/Cr structure are investigated and switching of the device due to electrochemical reactions is observed at low bias (<1 V). Depending on the polarity of the first applied bias, the switched device can behave like a diode (forward sweep first) or a resistor (reverse sweep first). The switching is irreversible and persistent, lasting for more than one month. By performing environmental tests, we prove that water molecules in the atmosphere and intercalated in the xerogel film are involved in the electrochemical reactions. It is proposed that an interfacial layer with reduced oxidation state forms at the Cr/V2O5 interface, and creates a higher Schottky barrier due to rise of electron affinity. Different interfacial layer thicknesses in forward and reverse first sweeps are responsible for different I-V characteristics in subsequent sweeps. The results suggest future applications of these V2O5 thin films in low-power read-only memory devices and diode-resistor networks.

  15. Sol-Gel-Based Template Synthesis and Li-Insertion Rate Performance of Nanostructured Vanadium Pentoxide

    DTIC Science & Technology

    1999-06-01

    compared to a thin film electrode of similar V2O5 mass and geometric area. The Li(+) storage capacity of the thin film electrode was equivalent to that...capacity of the thin film electrode. Above 500 deg C the nanostructured electrode delivered four times the capacity of the thin film control electrode....effects of Li-ion diffusion distance and surface area on V2O5 rate capability. Nanowires of V2O5 were prepared by depositing a precursor into the pores

  16. Optimizing vanadium pentoxide thin films and multilayers from dip-coated nanofluid precursors.

    PubMed

    Glynn, Colm; Creedon, Donal; Geaney, Hugh; O'Connell, John; Holmes, Justin D; O'Dwyer, Colm

    2014-02-12

    Using an alkoxide-based precursor, a strategy for producing highly uniform thin films and multilayers of V2O5 is demonstrated using dip coating. Defect-free and smooth films of V2O5 on different surfaces can be deposited from liquid precursors. We show how pinholes are formed due to heterogeneous nucleation during hydrolysis as the precursor forms a nanofluid. Using knowledge of instability formation often found in composite nanofluid films and the influence of cluster formation on the stability of these films, we show how polymer-precursor mixtures provide optimum uniformity and very low surface roughness in amorphous V2O5 and also orthorhombic V2O5 after crystallization by heating. Pinhole and roughness instability formation during the liquid stage of the nanofluid on gold and ITO substrates is suppressed giving a uniform coating. Practically, understanding evolution pathways that involve dewetting processes, nucleation, decomposition, or hydrolysis in complex nanofluids provides a route for improved uniformity of thin films. The method could be extended to improve the consistency in sequential or iterative multilayer deposits of a range of liquid precursors for functional materials and coatings.

  17. Chloroaluminate molten salt electrolytes and vanadium pentoxide xerogel cathodes for high energy density batteries

    NASA Astrophysics Data System (ADS)

    Xie, Jian

    The work presented here is part of an effort to develop a new type of battery which uses an alkali metal such as lithium or sodium or the alkaline earth magnesium, as the anode, a V2O5 xerogel as cathode, and a 1-ethyl-3-methylimidazolium chloride/aluminum chloride room temperature molten salt as electrolyte. First, the stability of the electrolyte was studied. The electrochemistry of 1-ethyl-3-methylimidazolium chloride (EMIC), the organic component of the 1-ethyl-3-methylimidazolium chloride/aluminum chloride molten salt, was examined in acetonitrile. Cyclic voltammetry and differential pulse voltammetry were used to study the reduction of EMI+, the cation of EMIC. Controlled potential coulometry was used to determine the number of electrons involved in the EMI+ reduction process. EMI+ reduction was found to be a one-electron, diffusion controlled process occurring at -2.35V (vs. a reference electrode consisting of a Ag wire in 0.1 M tetra-n-butylammonium perchlorate (TBAP)/acetonitrile solution) in 0.1M TBAP/acetonitrile solution. Two products were generated from the reduction, which are oxidized at about -0.45 and -0.65V. Mass spectroscopy data for these two products suggest that they are degradation products of EMI+. The major products of EMI+ reduction are not electrochemically active within the available potential window. Thus, small amounts of these species should not have a serious effect on the operation of a cell using an EMIC/AlCl3 electrolyte. The second project was to develop a method for buffering a melt which contains free Mg2+ ion for insertion into a V2O 5 xerogel cathode. The buffering of melts with MgCl2 and Mg metal was investigated starting with both acidic and basic melts. The following reaction is proposed for the Mg ribbon in acidic melt: 8Al2Cl - 7+3Mg→2Al+3Mg2++14AlCl -4 This was verified by electrochemical and atomic emission spectroscopy inductively coupled plasma (AES/ICP) data. Finally, the intercalation of Li+, Na+, and Mg2+ ions into V2O5 xerogels in this room temperature molten salt system was investigated. Characterization of spin coated V2O5 xerogel electrodes was also carried out by atomic force microscopy (AFM), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). Electrochemical data showed that Li + insertion is quite feasible in the melts. Preliminary studies of Na+, and Mg2+ insertion in melts show some evidence for insertion but need to be studied further.

  18. 76 FR 69736 - Draft Toxicological Review of Vanadium Pentoxide: In Support of Summary Information on the...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-11-09

    ... Integrated Risk Information System (IRIS) AGENCY: Environmental Protection Agency (EPA). ACTION: Notice of... on the Integrated Risk Information System (IRIS)'' (EPA/635R-11/004A). EPA is extending the public... Information on the Integrated Risk Information System (IRIS)'' is available primarily via the Internet on...

  19. Lithium vanadium bronze thin films for electrochromic applications

    SciTech Connect

    Green, M.; Pita, K.

    1997-04-01

    Thin films of fine grained polycrystalline stoichiometric vanadium pentoxide (85{percent} of bulk density) have been prepared by vacuum evaporation. These films have been made into lithium vanadium bronze, Li{sub x}V{sub 2}O{sub 5}, by inserting lithium, either electrochemically or chemically. In addition, lithium vanadium bronze thin films have been prepared by co-evaporation of Li and V{sub 2}O{sub 5}. The optical properties, absorption and refractive index, have been measured from 2000 to about 200 nm. Strong absorption arises from indirect transitions across the main gap and is {approx}2.2 eV for x=0. The variation of the energy gap up to an x value of 2 has been obtained from the absorption data and the importance of irreversible phase changes noted. High x value bronze is useful as a counter electrode material in glazings, having an energy gap of about 3 eV. There is a considerable, technologically significant, band tail in the absorption spectrum thought to arise from polaronic-type states, perhaps modified by the presence of guest species ions. The optical behavior upon lithium electrochemical insertion has also been examined. It is found that nonstoichiometry gives rise to an overall reduction in optical change per guest atom inserted. These effects are fast compared with electrochemical insertion times. {copyright} {ital 1997 American Institute of Physics.}

  20. Nanometer sized tantalum pentoxide fibers prepared by electrospinning

    SciTech Connect

    Dharmaraj, N.; Kim, H.Y.

    2006-03-09

    Novel, porous tantalum pentoxide (Ta{sub 2}O{sub 5}) nanofibers with 150-250 nm diameter were obtained by high temperature calcination of the as-electrospun tantalum pentoxide/poly(vinyl acetate) (PVAc) composite fibers prepared by sol-gel processing and electrospinning technique. Surface analysis, structure and elemental composition of these as-electrospun and as-calcinated Ta{sub 2}O{sub 5} nanofibers have been studied by scanning electron microscope (SEM) equipped with an energy dispersive X-ray analysis (EDX), high resolution field emission scanning electron microscopy (FE-SEM), atomic force microscopy (AFM), X-ray diffraction patterns (XRD) and FT-IR. High-resolution FE-SEM images showed the porous nature of Ta{sub 2}O{sub 5} nanofibers. EDX analysis revealed the perfect stoichiometry of the nanofibers as Ta{sub 2}O{sub 5}. A linear correlation was noted between the calcination temperature and orthorhombic crystalline phase evolution of Ta{sub 2}O{sub 5}.

  1. Optimizing the synthesis of vanadium-oxygen nanostructures by plasma plume dynamics using optical imaging

    NASA Astrophysics Data System (ADS)

    Masina, Bathusile N.; Lafane, Slimane; Wu, Lorinda; Abdelli-Messaci, Samira; Kerdja, Tahar; Forbes, Andrew

    2015-03-01

    The effect of an oxygen atmosphere on the expansion dynamics of a laser-produced vanadium-oxygen plasma has been investigated using a fast intensified charged-coupled device camera. We find regimes of the plasma plume expansion ranging from a free plume at vacuum and low oxygen pressures, through collisional and shock-wave-like hydrodynamic regimes at intermediate oxygen pressure, finally reaching a confined plume with subsequent thermalization of the plume particles at the highest pressure of the oxygen gas. Vanadium oxide nanostructures thin films were synthesized from this plasma and the resulting vanadium oxide phases studied as a function of the plume dynamics. We found monoclinic vanadium dioxide (VO2) (M1) and VO2 (B) nanoparticles in thin films deposited at 0.05 mbar. Pure phases of vanadium trioxide (V2O3) smooth and pentoxide (V2O5) nanorods thin films were detected at 0.01 and 0.1 to 0.2 mbar, respectively. Thin films containing VO2 (M1) were found to have a reversible metal-to-insulator transition at 61°C. This work paves the way to VO phase control by judicious choice of laser and plasma conditions.

  2. Temperature coefficient of resistance and thermal conductivity of Vanadium oxide 'Big Mac' sandwich structure

    NASA Astrophysics Data System (ADS)

    Abdel-Rahman, M.; Ilahi, S.; Zia, M. F.; Alduraibi, M.; Debbar, N.; Yacoubi, N.; Ilahi, B.

    2015-07-01

    In this paper, we synthesize and characterize a thin film thermometer structure for infrared microbolometers. The structure is composed of alternating multilayers of Vanadium pentoxide (V2O5), 25 nm, and Vanadium (V), 5 nm, thin films deposited by rf magnetron and dc magnetron sputtering respectively and annealed for 20, 30 and 40 min at 300 °C in Nitrogen (N2) atmosphere. The best achieved temperature coefficient of resistance (TCR) was found to be -2.57%/K for 40 min annealed samples. Moreover, we apply, for the first time, the photo-thermal deflection (PTD) technique for measuring the thermal conductivity of the synthesized thin films. The thermal conductivity of the developed thin films reveals an increase in thermal conductivity from 2 W/m K to 5.8 W/m K for as grown and 40 min annealed samples respectively.

  3. SUPERCONDUCTING VANADIUM BASE ALLOY

    DOEpatents

    Cleary, H.J.

    1958-10-21

    A new vanadium-base alloy which possesses remarkable superconducting properties is presented. The alloy consists of approximately one atomic percent of palladium, the balance being vanadium. The alloy is stated to be useful in a cryotron in digital computer circuits.

  4. Characterization on RF magnetron sputtered niobium pentoxide thin films

    SciTech Connect

    Usha, N.; Sivakumar, R.; Sanjeeviraja, C.

    2014-10-15

    Niobium pentoxide (Nb{sub 2}O{sub 5}) thin films with amorphous nature were deposited on microscopic glass substrates at 100°C by rf magnetron sputtering technique. The effect of rf power on the structural, morphological, optical, and vibrational properties of Nb{sub 2}O{sub 5} films have been investigated. Optical study shows the maximum average transmittance of about 87% and the optical energy band gap (indirect allowed) changes between 3.70 eV and 3.47 eV. AFM result indicates the smooth surface nature of the samples. Photoluminescence measurement showed the better optical quality of the deposited films. Raman spectra show the LO-TO splitting of Nb-O stretching of Nb{sub 2}O{sub 5} films.

  5. Nitridation under ammonia of high surface area vanadium aerogels

    SciTech Connect

    Merdrignac-Conanec, Odile . E-mail: odile.merdrignac@univ-rennes1.fr; El Badraoui, Khadija; L'Haridon, Paul

    2005-01-15

    Vanadium pentoxide gels have been obtained from decavanadic acid prepared by ion exchange on a resin from ammonium metavanadate solution. The progressive removal of water by solvent exchange in supercritical conditions led to the formation of high surface area V{sub 2}O{sub 5}, 1.6H{sub 2}O aerogels. Heat treatment under ammonia has been performed on these aerogels in the 450-900 deg. C temperature range. The oxide precursors and oxynitrides have been characterized by XRD, SEM, TGA, BET. Nitridation leads to divided oxynitride powders in which the fibrous structure of the aerogel is maintained. The use of both very low heating rates and high surface area aerogel precursors allows a higher rate and a lower threshold of nitridation than those reported in previous works. By adjusting the nitridation temperature, it has been possible to prepare oxynitrides with various nitrogen enrichment and vanadium valency states. Whatever the V(O,N) composition, the oxidation of the oxynitrides in air starts between 250 and 300 deg. C. This determines their potential use as chemical gas sensors at a maximum working temperature of 250 deg. C.

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

    NASA Astrophysics Data System (ADS)

    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.

  7. Vanadium Induces Dopaminergic Neurotoxicity Via Protein Kinase C-Delta Dependent Oxidative Signaling Mechanisms: Relevance to Etiopathogenesis of Parkinson's Disease

    PubMed Central

    Afeseh Ngwa, Hilary; Kanthasamy, Arthi; Anantharam, Vellareddy; Song, Chunjuan; Witte, Travis; Houk, R. S.; Kanthasamy, Anumantha G.

    2009-01-01

    Environmental exposure to neurotoxic metals through various sources including exposure to welding fumes has been linked to an increased incidence of Parkinson's disease (PD). Welding fumes contain many different metals including vanadium typically present as particulates containing vanadium pentoxide (V2O5). However, possible neurotoxic effects of this metal oxide on dopaminergic neuronal cells are not well studied. In the present study, we characterized vanadium-induced oxidative stress-dependent cellular events in cell culture models of PD. V2O5 was neurotoxic to dopaminergic neuronal cells including primary nigral dopaminergic neurons and the EC50 was determined to be 37 μM in N27 dopaminergic neuronal cell model. The neurotoxic effect was accompanied by a time-dependent uptake of vanadium and upregulation of metal transporter proteins Tf and DMT1 in N27 cells. Additionally, vanadium resulted in a threefold increase in reactive oxygen species generation, followed by release of mitochondrial cytochrome c into cytoplasm and subsequent activation of caspase-9 (>fourfold) and caspase-3 (>ninefold). Interestingly, vanadium exposure induced proteolytic cleavage of native protein kinase Cdelta (PKCδ, 72-74 kDa) to yield a 41 kDa catalytically active fragment resulting in a persistent increase in PKCδ kinase activity. Co-treatment with pan-caspase inhibitor ZVAD-FMK significantly blocked vanadium-induced PKCδ proteolytic activation, indicating that caspases mediate PKCδ cleavage. Also, co-treatment with Z-VAD-FMK almost completely inhibited V2O5-induced DNA fragmentation. Furthermore, PKCδ knockdown using siRNA protected N27 cells from V2O5-induced apoptotic cell death. Collectively, these results demonstrate vanadium can exert neurotoxic effects in dopaminergic neuronal cells via caspase-3-dependent PKCδ cleavage, suggesting that metal exposure may promote nigral dopaminergic degeneration. PMID:19646462

  8. Vanadium induces dopaminergic neurotoxicity via protein kinase Cdelta dependent oxidative signaling mechanisms: Relevance to etiopathogenesis of Parkinson's disease

    SciTech Connect

    Afeseh Ngwa, Hilary; Kanthasamy, Arthi; Anantharam, Vellareddy; Song, Chunjuan; Witte, Travis; Houk, Robert; Kanthasamy, Anumantha G.

    2009-10-15

    Environmental exposure to neurotoxic metals through various sources including exposure to welding fumes has been linked to an increased incidence of Parkinson's disease (PD). Welding fumes contain many different metals including vanadium typically present as particulates containing vanadium pentoxide (V{sub 2}O{sub 5}). However, possible neurotoxic effects of this metal oxide on dopaminergic neuronal cells are not well studied. In the present study, we characterized vanadium-induced oxidative stress-dependent cellular events in cell culture models of PD. V{sub 2}O{sub 5} was neurotoxic to dopaminergic neuronal cells including primary nigral dopaminergic neurons and the EC{sub 50} was determined to be 37 {mu}M in N27 dopaminergic neuronal cell model. The neurotoxic effect was accompanied by a time-dependent uptake of vanadium and upregulation of metal transporter proteins Tf and DMT1 in N27 cells. Additionally, vanadium resulted in a threefold increase in reactive oxygen species generation, followed by release of mitochondrial cytochrome c into cytoplasm and subsequent activation of caspase-9 (> fourfold) and caspase-3 (> ninefold). Interestingly, vanadium exposure induced proteolytic cleavage of native protein kinase Cdelta (PKC{delta}, 72-74 kDa) to yield a 41 kDa catalytically active fragment resulting in a persistent increase in PKC{delta} kinase activity. Co-treatment with pan-caspase inhibitor Z-VAD-FMK significantly blocked vanadium-induced PKC{delta} proteolytic activation, indicating that caspases mediate PKC{delta} cleavage. Also, co-treatment with Z-VAD-FMK almost completely inhibited V{sub 2}O{sub 5}-induced DNA fragmentation. Furthermore, PKC{delta} knockdown using siRNA protected N27 cells from V{sub 2}O{sub 5}-induced apoptotic cell death. Collectively, these results demonstrate that vanadium can exert neurotoxic effects in dopaminergic neuronal cells via caspase-3-dependent PKC{delta} cleavage, suggesting that metal exposure may promote nigral

  9. Method of precipitating uranium from an aqueous solution and/or sediment

    SciTech Connect

    Tokunaga, Tetsu K; Kim, Yongman; Wan, Jiamin

    2013-08-20

    A method for precipitating uranium from an aqueous solution and/or sediment comprising uranium and/or vanadium is presented. The method includes precipitating uranium as a uranyl vanadate through mixing an aqueous solution and/or sediment comprising uranium and/or vanadium and a solution comprising a monovalent or divalent cation to form the corresponding cation uranyl vanadate precipitate. The method also provides a pathway for extraction of uranium and vanadium from an aqueous solution and/or sediment.

  10. Nutritional essentiality of vanadium

    SciTech Connect

    Nielsen, F.H.

    1986-02-01

    Evidence to support the essentiality of vanadium is inconclusive. Thus, it cannot be unequivocally stated that vanadium is an essential nutrient. The basis for this statement can be appreciated more fully if the following definitions are accepted. In this section, a substance is considered nutritionally essential if a dietary deficiency consistently results in a suboptimal biological function that is preventable or reversible by physiological amounts of the element. In this definition, physiological is construed as those quantities usually found in biological material. For vanadium, the usual amounts are measured in nanograms per gram, or parts per billion. The other term that should be defined is pharmacologic action. Here it means the effect of a relatively high dietary intake of a substance that alleviates an abnormality caused by something other than a nutritional deficiency.

  11. Vanadium exposure induces olfactory dysfunction in an animal model of metal neurotoxicity.

    PubMed

    Ngwa, Hilary Afeseh; Kanthasamy, Arthi; Jin, Huajun; Anantharam, Vellareddy; Kanthasamy, Anumantha G

    2014-07-01

    Epidemiological evidence indicates chronic environmental exposure to transition metals may play a role in chronic neurodegenerative conditions such as Parkinson's disease (PD). Chronic inhalation exposure to welding fumes containing metal mixtures may be associated with development of PD. A significant amount of vanadium is present in welding fumes, as vanadium pentoxide (V2O5), and incorporation of vanadium in the production of high strength steel has become more common. Despite the increased vanadium use in recent years, the neurotoxicological effects of this metal are not well characterized. Recently, we demonstrated that V2O5 induces dopaminergic neurotoxicity via protein kinase C delta (PKCδ)-dependent oxidative signaling mechanisms in dopaminergic neuronal cells. Since anosmia (inability to perceive odors) and non-motor deficits are considered to be early symptoms of neurological diseases, in the present study, we examined the effect of V2O5 on the olfactory bulb in animal models. To mimic the inhalation exposure, we intranasally administered C57 black mice a low-dose of 182μg of V2O5 three times a week for one month, and behavioral, neurochemical and biochemical studies were performed. Our results revealed a significant decrease in olfactory bulb weights, tyrosine hydroxylase (TH) levels, levels of dopamine (DA) and its metabolite, 3,4-dihydroxyphenylacetic acid (DOPAC) and increases in astroglia of the glomerular layer of the olfactory bulb in the treatment groups relative to vehicle controls. Neurochemical changes were accompanied by impaired olfaction and locomotion. These findings suggest that nasal exposure to V2O5 adversely affects olfactory bulbs, resulting in neurobehavioral and neurochemical impairments. These results expand our understanding of vanadium neurotoxicity in environmentally-linked neurological conditions.

  12. Vanadium Exposure Induces Olfactory Dysfunction in an Animal Model of Metal Neurotoxicity

    PubMed Central

    Ngwa, Hilary Afeseh; Kanthasamy, Arthi; Jin, Huajun; Anantharam, Vellareddy; Kanthasamy, Anumantha G.

    2014-01-01

    Epidemiological evidence indicates chronic environmental exposure to transition metals may play a role in chronic neurodegenerative conditions such as Parkinson’s disease (PD). Chronic inhalation exposure to welding fumes containing metal mixtures may be associated with development of PD. A significant amount of vanadium is present in welding fumes, as vanadium pentoxide (V2O5), and incorporation of vanadium in the production of high strength steel has become more common. Despite the increased vanadium use in recent years, the neurotoxicological effects of this metal are not well characterized. Recently, we demonstrated that V2O5 induces dopaminergic neurotoxicity via protein kinase C delta (PKCδ)-dependent oxidative signaling mechanisms in dopaminergic neuronal cells. Since anosmia (inability to perceive odors) and non-motor deficits are considered to be early symptoms of neurological diseases, in the present study, we examined the effect of V2O5 on the olfactory bulb in animal models. To mimic the inhalation exposure, we intranasally administered C57 black mice a low-dose of 182 µg of V2O5 three times a week for one month, and behavioral, neurochemical and biochemical studies were performed. Our results revealed a significant decrease in olfactory bulb weights, tyrosine hydroxylase (TH) levels, levels of dopamine (DA) and its metabolite, 3, 4-dihydroxyphenylacetic acid (DOPAC) and increases in astroglia of the glomerular layer of the olfactory bulb in the treatment groups relative to vehicle controls. Neurochemical changes were accompanied by impaired olfaction and locomotion. These findings suggest that nasal exposure to V2O5 adversely affects olfactory bulbs, resulting in neurobehavioral and neurochemical impairments. These results expand our understanding of vanadium neurotoxicity in environmentally-linked neurological conditions. PMID:24362016

  13. Electronic density-of-states of amorphous vanadium pentoxide films: Electrochemical data and density functional theory calculations

    NASA Astrophysics Data System (ADS)

    Lykissa, Iliana; Li, Shu-Yi; Ramzan, Muhammad; Chakraborty, Sudip; Ahuja, Rajeev; Granqvist, Claes G.; Niklasson, Gunnar A.

    2014-05-01

    Thin films of V2O5 were prepared by sputter deposition onto transparent and electrically conducting substrates and were found to be X-ray amorphous. Their electrochemical density of states was determined by chronopotentiometry and displayed a pronounced low-energy peak followed by an almost featureless contribution at higher energies. These results were compared with density functional theory calculations for amorphous V2O5. Significant similarities were found between measured data and computations; specifically, the experimental low-energy peak corresponds to a split-off part of the conduction band apparent in the computations. Furthermore, the calculations approximately reproduce the experimental band gap observed in optical measurements.

  14. Slag recycling of irradiated vanadium

    SciTech Connect

    Gorman, Patrick K.

    1995-04-05

    An experimental inductoslag apparatus to recycle irradiated vanadium was fabricated and tested. An experimental electroslag apparatus was also used to test possible slags. The testing was carried out with slag materials that were fabricated along with impurity bearing vanadium samples. Results obtained include computer simulated thermochemical calculations and experimentally determined removal efficiencies of the transmutation impurities. Analyses of the samples before and after testing were carried out to determine if the slag did indeed remove the transmutation impurities from the irradiated vanadium.

  15. Vanadium distribution following decavanadate administration.

    PubMed

    Soares, S S; Martins, H; Aureliano, M

    2006-01-01

    An acute exposure of two vanadate solutions-metavanadate and decavanadate-containing different vanadate oligomers, induces different patterns of subcellular vanadium distribution in blood plasma, red blood cells (RBC), and cardiac muscle subcellular fractions of the fish Sparus aurata (gilthead seabream). The highest amount of vanadium was found in blood plasma 1 h after (5 mM) intravenous vanadate administration (295 +/- 64 and 383 +/- 104 microg V/g dry tissue, for metavanadate and decavanadate solutions, respectively), being 80-fold higher than in RBC. After 12 h of administration, the amount of vanadium in plasma, as well as in cardiac cytosol, decreased about 50%, for both vanadate solutions. During the period between 1 and 12 h, the ratio of vanadium in plasma/vanadium in RBC increased from 27 to 128 for metavanadate, whereas it remains constant (77) for decavanadate. Both vanadium solutions were primarily accumulated in the mitochondrial fraction (138 +/- 0 and 195 +/- 34 ng V/g dry tissue for metavanadate and decavanadate solutions, respectively, after 12 h exposure), rather than in cytosol. The amount of vanadium in cardiac mitochondria was twofold higher than in cytosol, earlier for metavanadate (6 h) than for decavanadate (12 h). It is concluded that, in fish cardiac muscle, the vanadium distribution is dependent on the administration of decameric vanadate, with vanadium being mainly distributed in plasma, before being accumulated into the mitochondrial fraction.

  16. Structural and silver/vanadium ratio effects on silver vanadium phosphorous oxide solution formation kinetics: impact on battery electrochemistry.

    PubMed

    Bock, David C; Takeuchi, Kenneth J; Marschilok, Amy C; Takeuchi, Esther S

    2015-01-21

    The detailed understanding of non-faradaic parasitic reactions which diminish battery calendar life is essential to the development of effective batteries for use in long life applications. The dissolution of cathode materials including manganese, cobalt and vanadium oxides in battery systems has been identified as a battery failure mechanism, yet detailed dissolution studies including kinetic analysis are absent from the literature. The results presented here provide a framework for the quantitative and kinetic analyses of the dissolution of cathode materials which will aid the broader community in more fully understanding this battery failure mechanism. In this study, the dissolution of silver vanadium oxide, representing the primary battery powering implantable cardioverter defibrillators (ICD), is compared with the dissolution of silver vanadium phosphorous oxide (Ag(w)VxPyOz) materials which were targeted as alternatives to minimize solubility. This study contains the first kinetic analyses of silver and vanadium solution formation from Ag0.48VOPO4·1.9H2O and Ag2VP2O8, in a non-aqueous battery electrolyte. The kinetic results are compared with those of Ag2VO2PO4 and Ag2V4O11 to probe the relationships among crystal structure, stoichiometry, and solubility. For vanadium, significant dissolution was observed for Ag2V4O11 as well as for the phosphate oxide Ag0.49VOPO4·1.9H2O, which may involve structural water or the existence of multiple vanadium oxidation states. Notably, the materials from the SVPO family with the lowest vanadium solubility are Ag2VO2PO4 and Ag2VP2O8. The low concentrations and solution rates coupled with their electrochemical performance make these materials interesting alternatives to Ag2V4O11 for the ICD application.

  17. Morphological and textural characterization of vanadium oxide supported on zirconia by ionic exchange

    NASA Astrophysics Data System (ADS)

    Gazzoli, Delia; De Rossi, Sergio; Ferraris, Giovanni; Valigi, Mario; Ferrari, Luisa; Selci, Stefano

    2008-12-01

    Zirconia-supported vanadium oxide samples containing vanadium up to 6.8 wt.% were prepared by ionic exchange using aqueous solution of peroxovanadate complexes and hydrous zirconium oxide. The samples, heated at 823 K for 5 h in air, were studied by several techniques, including X-ray diffraction, surface area determinations, diffuse reflectance spectroscopy (UV-vis), Raman spectroscopy, pore size distribution measurements and atomic force microscopy. The results showed that the preparation procedure applied leads to good vanadium dispersion. The interaction between the anchored surface species and the support affects some ZrO 2 properties, including texture and phase transition. Depending on the vanadium loading, several species formed. In the most diluted sample small polyvanadate entities predominate, whereas at increasing vanadium loading (up to about 6 V atoms nm -2) more condensed species formed yielding granular-type surface aggregates. At higher loading, granular-type particles and large flat structures, due to amorphous two- or three-dimensional polyvanadate species and ZrV 2O 7-like structures developed. Treatments with an ammonia solution specified that only a fraction of the vanadium species (in a polymeric form) interacts with the zirconia surface. Atomic force microscopy directly imaged the formation of vanadium aggregates (superimposed to the interacting species) at increasing vanadium content and their removal by the ammonia leaching.

  18. Picosecond laser structuring of thin film platinum layers covered with tantalum pentoxide isolation

    SciTech Connect

    Heise, Gerhard; Huber, Heinz; Trappendreher, Daniel; Ilchmann, Florian; Weiss, Robin S.; Wolf, Bernhard

    2012-07-01

    A thin film layer system consisting of platinum (Pt) as conductive layer on a glass substrate and tantalum pentoxide as isolating layer on top of the platinum is attractive for designing biocompatible conductor paths and contact pads for bio sensor chips. For the flexible and rapid patterning of the conductive and the isolating layers, both, the complete removal and the selective ablation of the individual thin films were investigated using ultra-short laser pulses with about 10 ps pulse duration and 1064 nm wavelength at low laser fluences. A platinum film covered with tantalum pentoxide shows a significantly lower ablation threshold than a single Pt film on glass alone when illuminated from the front side. Furthermore, we explored that the tantalum pentoxide film can be removed by glass side illumination from the Pt film, without affecting the Pt film and leaving the Pt film on the glass substrate intact. Those ablation phenomena occur at laser fluences of about 0.2 J/cm{sup 2}, far below the evaporation limit of platinum. We present a detailed ablation threshold value examination for the structuring of these layer systems by front side and glass side irradiation for different film thicknesses. Furthermore, we discuss the possible underlying physical mechanisms of these ablation phenomena.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed

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

    2015-06-30

    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.

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

    PubMed Central

    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

  2. Thin films of pure vanadium nitride: Evidence for anomalous non-faradaic capacitance

    NASA Astrophysics Data System (ADS)

    Bondarchuk, Oleksandr; Morel, Alban; Bélanger, Daniel; Goikolea, Eider; Brousse, Thierry; Mysyk, Roman

    2016-08-01

    An impressive gravimetric capacitance of 1300 F g-1 (surface capacitance ∼3.3 mF cm-2) reported by Choi et al., 2006 for nanosized vanadium nitride has stimulated considerable interest in vanadium nitride as a potential electrode material for energy storing systems - supercapacitors. The postulated mechanism of charge storage in vanadium nitride materials involves redox reactions in the thin surface layer of vanadium oxide while the core vanadium nitride serves exclusively as a conducting platform. In this study we have synthesized pure oxygen-free vanadium nitride films and have found that they are capable of delivering a surface capacitance of up to ∼3 mF cm-2 at a potential scan rate of 3 mV s-1 and ∼2 mF cm-2 at a potential scan rate of 1 V s-1 in aqueous electrolytes. Combining electrochemical testing with X-ray photoelectron spectroscopy characterization has revealed that redox reactions play no or little role in the electrochemical response of pure VN, in contrast to the common wisdom stemming from the electrochemical response of oxygen-containing films. An alternative charge storage mechanism - space charge accumulation in a subsurface layer of ∼100 nm - was put forward to explain the experimentally observed capacitance of VN films in aqueous electrolytes.

  3. FAST TRACK COMMUNICATION: Influence of doping on the properties of vanadium oxide gel films

    NASA Astrophysics Data System (ADS)

    Pergament, A. L.; Velichko, A. A.; Berezina, O. Ya; Kazakova, E. L.; Kuldin, N. A.; Artyukhin, D. V.

    2008-10-01

    The effect of doping with H and W on the properties of V2O5 and VO2 derived from V2O5 gel has been studied. It is shown that the treatment of V2O5 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~100 K, is observed. For W-doped VO2 films, it is shown that substitution of V4+ with W6+ results in a decrease of the temperature of the metal-insulator transition. Also, it has been shown that the doping of initial films with ~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 V2O5 gel films.

  4. Vanadium recycling for fusion reactors

    SciTech Connect

    Dolan, T.J.; Butterworth, G.J.

    1994-04-01

    Very stringent purity specifications must be applied to low activation vanadium alloys, in order to meet recycling goals requiring low residual dose rates after 50--100 years. Methods of vanadium production and purification which might meet these limits are described. Following a suitable cooling period after their use, the vanadium alloy components can be melted in a controlled atmosphere to remove volatile radioisotopes. The aim of the melting and decontamination process will be the achievement of dose rates low enough for ``hands-on`` refabrication of new reactor components from the reclaimed metal. The processes required to permit hands-on recycling appear to be technically feasible, and demonstration experiments are recommended. Background information relevant to the use of vanadium alloys in fusion reactors, including health hazards, resources, and economics, is provided.

  5. PILOT EVALUATION OF VANADIUM ALLOYS.

    DTIC Science & Technology

    ARCS, SHEETS, ROLLING(METALLURGY), HIGH TEMPERATURE, SCIENTIFIC RESEARCH, COMPRESSIVE PROPERTIES, DUCTILITY, CREEP, OXIDATION, COATINGS , SILICIDES , HARDNESS, WELDING, EXTRUSION, TANTALUM ALLOYS, MOLYBDENUM ALLOYS....VANADIUM ALLOYS, * NIOBIUM ALLOYS, MECHANICAL PROPERTIES, MECHANICAL PROPERTIES, TITANIUM ALLOYS, ZIRCONIUM ALLOYS, CARBON ALLOYS, MELTING, ELECTRIC

  6. Effects of dietary vanadium in mallard ducks

    USGS Publications Warehouse

    White, D.H.; Dieter, M.P.

    1978-01-01

    Adult mallard ducks fed 0, 1, 10, or 100 ppm vanadyl sulfate in the diet were sacrificed after 12 wk on treatment; tissues were analyzed for vanadium. No birds died during the study and body weights did not change. Vanadium accumulated to higher concentrations in the bone and liver than in other tissues. Concentrations in bones of hens were five times those in bones of drakes, suggesting an interaction between vanadium and calcium mobilization in laying hens. Vanadium concentrations in most tissues were significantly correlated and increased with treatment level. Lipid metabolism was altered in laying hens fed 100 ppm vanadium. Very little vanadium accumulated in the eggs of laying hens.

  7. Non-oxo vanadium(IV) alkoxide chemistry: solid state structures, aggregation equilibria and thermochromic behaviour in solution.

    PubMed

    Westrup, Kátia C M; Gregório, Thaiane; Stinghen, Danilo; Reis, Dayane M; Hitchcock, Peter B; Ribeiro, Ronny R; Barison, Andersson; Back, Davi F; de Sá, Eduardo L; Nunes, Giovana G; Soares, Jaísa F

    2011-04-07

    The reversible thermochromic behaviour of homoleptic [{V(OR)(4)}(n)] complexes in solution [R = Pr(i) (product I), Bu(s) (B(s)), Nep (N) and Cy (C)] is accounted for the existence of an aggregation equilibrium involving dimeric and monomeric species in which vanadium(iv) is respectively five- and four-coordinate. Bulky R groups such as Bu(t) and Pe(t) (tert-pentoxide) prevent aggregation and therefore give rise to exclusively mononuclear compounds (B(t) and P(t), respectively) that are not thermochromic. The complexes and their temperature-dependent interconversion were characterised by single crystal X-ray diffractometry, magnetic susceptibility measurements and electronic, FTIR and EPR spectroscopies in a wide temperature range. Equilibrium constants and enthalpy and entropy changes for the dimerization reactions have been determined and compared with literature data.

  8. Speciation of vanadium in soil.

    PubMed

    Połedniok, Justyna; Buhl, Franciszek

    2003-01-02

    A method for speciation of vanadium in soil is presented in this work. The sequential extraction analysis procedure of Tessier et al. for heavy metals was used for the vanadium separation. The method consists of sequential leaching of the soil samples to separate five fractions of metals: (1) exchangeable, (2) bound to carbonates, (3) bound to Fe-Mn oxides, (4) bound to organic matter and (5) residual. The leaching solutions of Tessier were used for the vanadium extraction, only for the residual fraction the HClO(4) was replaced with H(2)SO(4). The optimum conditions for leaching of vanadium from soil (weight of sample, concentration and volume of extractants, time of extraction) were chosen for each fraction. A sensitive, spectrophotometric method based on the ternary complex V(IV) with Chrome Azurol S and benzyldodecyldimethylammonium bromide (epsilon=7.1x10(4) l mol(-1) cm(-1)) was applied for the vanadium determination after separation of V(V) by solvent extraction using mesityl oxide and reduction of V(V) using ascorbic acid. This method was applied for vanadium speciation in soil from two different regions of Poland: Upper Silesia (industrial region) and Podlasie (agricultural region). The content of vanadium in the fractions of Upper Silesia soil was respectively (in 10(-3)%): I, 3.39; III, 4.53; IV, 10.70; V, 8.70 and it was the highest in the organic fraction, indicating input by anthropogenic activities. The content of vanadium in Podlasie soil was clearly lower and it was (in 10(-3)%): I, 2.07; III, 0.92; IV, 0.69; V, 1.23. The concentration of vanadium in fraction 2 of both soils was less than detection limit of applied method. The total content of vanadium in the five soil fractions was in good correlation with the total content of this element in both soils found after HF-H(2)SO(4) digestion. Analysis using the ICP-AES method gave comparable results.

  9. Evanescent field Sensors Based on Tantalum Pentoxide Waveguides – A Review

    PubMed Central

    Schmitt, Katrin; Oehse, Kerstin; Sulz, Gerd; Hoffmann, Christian

    2008-01-01

    Evanescent field sensors based on waveguide surfaces play an important role where high sensitivity is required. Particularly tantalum pentoxide (Ta2O5) is a suitable material for thin-film waveguides due to its high refractive index and low attenuation. Many label-free biosensor systems such as grating couplers and interferometric sensors as well as fluorescence-based systems benefit from this waveguide material leading to extremely high sensitivity. Some biosensor systems based on Ta2O5 waveguides already took the step into commercialization. This report reviews the various detection systems in terms of limit of detection, the applications, and the suitable surface chemistry. PMID:27879731

  10. Synthesis and thermal evolution of structure in alkoxide-derived niobium pentoxide gels

    NASA Technical Reports Server (NTRS)

    Bansal, Narottam P.

    1993-01-01

    Niobium pentoxide gels in the form of transparent monoliths and powder have been synthesized from the controlled hydrolysis and polycondensation of niobium pentaethoxide under different experimental conditions using various mole ratios of Nb(OC2H5)5:H2O:C2H5OH:HCl. Alcohol acted as the mutual solvent and HCl as the deflocculating agent. In the absence of HCl, precipitation of colloidal particles was encountered on the addition of any water to the alkoxide. The gels were subjected to various thermal treatments and characterized by differential thermal analysis, thermogravimetric analysis, x-ray diffraction, and infrared spectroscopy. After drying at 400 C, the gels were amorphous to x-rays. The amorphous powder crystallized into the low-temperature orthorhombic form of Nb2O5 at approximately 500 C, which transformed irreversibly into the high-temperature monoclinic alpha-Nb2O5 between 900 to 1000 C. The kinetics of crystallization of the amorphous niobium pentoxide have been investigated by non-isothermal differential scanning calorimetry. The crystallization activation energy was determined to be 399 kJ/mol.

  11. Electronic properties of tantalum pentoxide polymorphs from first-principles calculations

    SciTech Connect

    Lee, J.; Lu, W.; Kioupakis, E.

    2014-11-17

    Tantalum pentoxide (Ta{sub 2}O{sub 5}) is extensively studied for its attractive properties in dielectric films, anti-reflection coatings, and resistive switching memory. Although various crystalline structures of tantalum pentoxide have been reported, its structural, electronic, and optical properties still remain a subject of research. We investigate the electronic and optical properties of crystalline and amorphous Ta{sub 2}O{sub 5} structures using first-principles calculations based on density functional theory and the GW method. The calculated band gaps of the crystalline structures are too small to explain the experimental measurements, but the amorphous structure exhibits a strong exciton binding energy and an optical band gap (∼4 eV) in agreement with experiment. We determine the atomic orbitals that constitute the conduction band for each polymorph and analyze the dependence of the band gap on the atomic geometry. Our results establish the connection between the underlying structure and the electronic and optical properties of Ta{sub 2}O{sub 5}.

  12. Effects of the mineral phase and valence of vanadium on vanadium extraction from stone coal

    NASA Astrophysics Data System (ADS)

    Hu, Yang-jia; Zhang, Yi-min; Bao, Shen-xu; Liu, Tao

    2012-10-01

    The influence of roasting on the leaching rate and valence of vanadium was evaluated during vanadium extraction from stone coal. Vanadium in stone coal is hard to be leached and the leaching rate is less than 10% when the raw ore is leached by 4 mol/L H2SO4 at 90°C for 2 h. After the sample is roasted at 900°C for 2 h, the leaching rate of vanadium reaches the maximum, and more than 70% of vanadium can be leached. The crystal of vanadium-bearing mica minerals decomposes and the content of V(V) increases with the rise of roasting temperature from 600 to 900°C, therefore the leaching rate of vanadium increases significantly with the decomposition of the mica minerals. Some new phases, anorthite for example, form when the roasting temperature reaches 1000°C. A part of vanadium may be enwrapped in the sintered materials and newly formed phases, which may impede the oxidation of low valent vanadium and make the leaching rate of vanadium drop dramatically. The leaching rate of vanadium is not only determined by the valence state of vanadium but also controlled by the decomposition of vanadium-bearing minerals and the existence state of vanadium to a large extent.

  13. Peracute vanadium toxicity in cattle grazing near a vanadium mine.

    PubMed

    McCrindle, C M; Mokantla, E; Duncan, N

    2001-12-01

    Animals may act as bioindicators for potential human health problems associated with mining and refining. Eight cattle died after a vanadium mine dam collapsed close to the area in which they were grazing. Necropsies were conducted on five cattle. Affected animals had shown a watery bloody diarrhea, red urine and listlessness before collapsing. On necropsy (n = 5) there was a moderate bilateral multifocal granulomatous-like conjunctivitis. The most prominent lesions were eosinophillic granulomatous-like inflammation of the thymus, mediastinal and mesenteric lymph nodes, oesophagus, abomasum and colon. There was also marked hyperaemia of the abomasal mucosa with petechiation. Pulmonary and tracheal haemorrhage was also present. Histopathology showed severe inflammatory cell infiltration (mainly eosinophils with lesser numbers of neutrophils and macrophages) of lymphoid tissue associated with the thymus, lymph nodes, esophagus, abomasum, colon and conjunctiva. There were also areas of tissue necrosis, congested blood vessels and haemorrhage. Conjunctival lesions point to a systemic rather than a local effect as the cattle in this case died following ingestion rather than inhalation of vanadium. The causal relationship between intoxication and death is conventionally based on the level of that toxin present in tissues at necropsy. The variability in demonstrating vanadium in biological samples may have been due to the rapid excretion of vanadium by the living animal, or the solubility of the salts, which results in the substance leaching into the fluid portion of the samples. Cross-reactions with colorimetric tests for arsenic should also be noted.

  14. Removal of arsenic, vanadium and/or nickel compounds from spent catecholated polymer

    DOEpatents

    Fish, R.H.

    1987-04-21

    Described is a process for removing arsenic, vanadium, and/or nickel from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. For vanadium and nickel removal an amine, preferably a diamine is included. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic, vanadium, and/or nickel bound to it from contacting petroliferous liquid as described above and involves: treating the spent polymer containing any vanadium and/or nickel with an aqueous acid to achieve an acid pH; and, separating the solids from the liquid; and then treating said spent catecholated polystyrene, at a temperature in the range of about 20 to 100 C with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10; and, separating the solids and liquids from each other. Preferably the regeneration treatment of arsenic containing catecholated polymer is in two steps wherein the first step is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, the steps are repeated using a bicarbonate.

  15. Removal of arsenic, vanadium, and/or nickel compounds from petroliferous liquids

    DOEpatents

    Fish, Richard H.

    1986-01-01

    Described is a process for removing arsenic, vanadium, and/or nickel from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. For vanadium and nickel removal an amine, preferably a diamine is included. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic, vanadium, and/or nickel bound to it from contacting petroliferous liquid as described above and involves: treating the spent polymer containing any vanadium and/or nickel with an aqueous acid to achieve an acid pH; and, separating the solids from the liquid; and then treating said spent catecholated polystyrene, at a temperature in the range of about 20.degree. to 100.degree. C. with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10; and, separating the solids and liquids from each other. Preferably the regeneration treatment of arsenic containing catecholated polymer is in two steps wherein the first step is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, the steps are repeated using a bicarbonate.

  16. Removal of arsenic, vanadium and/or nickel compounds from spent catecholated polymer

    DOEpatents

    Fish, Richard H.

    1987-01-01

    Described is a process for removing arsenic, vanadium, and/or nickel from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. For vanadium and nickel removal an amine, preferably a diamine is included. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic, vanadium, and/or nickel bound to it from contacting petroliferous liquid as described above and involves: treating the spent polymer containing any vanadium and/or nickel with an aqueous acid to achieve an acid pH; and, separating the solids from the liquid; and then treating said spent catecholated polystyrene, at a temperature in the range of about 20.degree. to 100.degree. C. with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10; and, separating the solids and liquids from each other. Preferably the regeneration treatment of arsenic containing catecholated polymer is in two steps wherein the first step is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, the steps are repeated using a bicarbonate.

  17. Removal of arsenic, vanadium, and/or nickel compounds from petroliferous liquids

    DOEpatents

    Fish, R.H.

    1985-05-17

    Described is a process for removing arsenic, vanadium, and/or nickel from petroliferous derived liquids (shale oil, SRC, etc.) by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. For vanadium and nickel removal an amine, preferably a diamine is included. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic, vanadium, and/or nickel bound to it from contacting petroliferous liquid as described above and involves: treating the spent polymer containing any vanadium and/or nickel with an aqueous acid to achieve an acid pH; and, separating the solids from the liquid; and then treating said spent catecholated polystyrene, at a temperature in the range of about 20/sup 0/ to 100/sup 0/C with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10; and, separating the solids and liquids from each other. Preferably the regeneration treatment of arsenic containing catecholated polymer is in two steps wherein the first step is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, the steps are repeated using a bicarbonate.

  18. Insight into the adsorption mechanisms of vanadium(V) on a high-efficiency biosorbent (Ti-doped chitosan bead).

    PubMed

    Liu, Xin; Zhang, Lingfan

    2015-08-01

    In this present study, a new chitosan bead modified with titanium ions (TiCB) was prepared and employed for the adsorption of vanadium ions from aqueous solutions. Batch adsorption experiments were performed to research the effect of various factors, including pH, temperature, contact time and initial concentration of vanadium(V) ions. The adsorption of vanadium was followed by the pseudo second-order kinetic and the Langmuir isotherm model, with a remarkable maximum adsorption capacity of 210 mg/g. The analysis of thermodynamic parameters (ΔG°, ΔH° and ΔS°) revealed that the nature of adsorption was feasible, spontaneous (ΔG°<0) and endothermic (ΔH°>0) process. FTIR, EDS, EMI and XPS studies suggested that the mechanisms of adsorption were possibly attributed to electrostatic attraction, ligand-exchange and redox reaction between TiCB and vanadium ions.

  19. Selective Separation and Extraction of Vanadium (V) Over Manganese (II) from Co-Leaching Solution of Roasted Stone Coal and Pyrolusite Using Solvent Extraction

    NASA Astrophysics Data System (ADS)

    Cai, Z. L.; Feng, Y. L.; Zhou, Y. Z.; Li, H. R.; Wang, W. D.

    2013-11-01

    Based on the novel technology for selective separation and extraction of vanadium (V) over manganese (II) from co-leaching solution of roasted stone coal and pyrolusite using solvent extraction, the extraction effect of vanadium (V) and manganese (II) has been studied and many technical conditions have also been optimized. Meanwhile, countercurrent simulation experiments were conducted to verify the results of the experiments. The results indicated that with three countercurrent extraction stages, 99.21% vanadium (V) was extracted using 5% (v/v) N235 and 5% (v/v) secondary octyl alcohol at initial aqueous pH of 3.0 and O/A phase ratio of 1.0. Vanadium (V) could be completely stripped after three-stage countercurrent experiments with 20 wt.% NH4Cl at O/A phase ratio of 1.0. The process flow sheet for the recovery of vanadium (V), as well as manganese (II), was proposed.

  20. Synthesis and electrochemical properties of niobium pentoxide deposited on layered carbide-derived carbon

    NASA Astrophysics Data System (ADS)

    Zhang, Chuanfang (John); Maloney, Ryan; Lukatskaya, Maria R.; Beidaghi, Majid; Dyatkin, Boris; Perre, Emilie; Long, Donghui; Qiao, Wenming; Dunn, Bruce; Gogotsi, Yury

    2015-01-01

    Herein we report on the hydrothermal synthesis of niobium pentoxide on carbide-derived carbon (Nb2O5/CDC) with a layered structure. The presence of phenylphosphonic acid guides the deposition during preparation, leading to the formation of amorphous Nb2O5 particles which are 4-10 nm in diameter and homogeneously distributed on the CDC framework. Electrochemical testing of the Nb2O5/CDC electrode indicated that the highest capacitance and Coulombic efficiency occurred using an electrolyte comprised of 1 M lithium perchlorate in ethylene carbonate/dimethyl carbonate. Subsequent heat treatment of Nb2O5/CDC in CO2 environment led to crystallization of the Nb2O5, allowing reversible Li+ intercalation/de-intercalation. For sweep rates corresponding to charging and discharging in under 3 min, a volumetric charge of 180 C cm-3 and Coulombic efficiency of 99.2% were attained.

  1. Dissociative electron attachment to dinitrogen pentoxide, N{sub 2}O{sub 5}

    SciTech Connect

    Cicman, P.; Buchanan, G.A.; Marston, G.; Gulejova, B.; Skalny, J.D.; Mason, N.J.; Scheier, P.; Maerk, T.D.

    2004-11-22

    Electron attachment was studied in gaseous dinitrogen pentoxide, N{sub 2}O{sub 5}, for incident electron energies between a few meV and 10 eV. No stable parent anion N{sub 2}O{sub 5}{sup -} was observed but several anionic fragments (NO{sub 3}{sup -}, NO{sub 2}{sup -}, NO{sup -}, O{sup -}, and O{sub 2}{sup -}) were detected using quadrupole mass spectrometry. Many of these dissociative pathways were found to be coupled and provide detailed information on the dynamics of N{sub 2}O{sub 5} fragmentation. Estimates of the cross sections for production of each of the anionic fragments were made and suggest that electron attachment to N{sub 2}O{sub 5} is amongst the most efficient attachment reactions recorded for nonhalogenated polyatomic systems.

  2. A new way to make solid state chemistry: Spark plasma synthesis of copper or silver vanadium oxide bronzes

    NASA Astrophysics Data System (ADS)

    Galy, J.; Dolle, M.; Hungria, T.; Rozier, P.; Monchoux, J.-Ph.

    2008-08-01

    The spark plasma sintering technique for various materials, oxides, nitrides, carbides, metals, composites, etc. is undergoing a rapid development following pioneering work in Japan. Here, the technique is used to create a new route to make solid state chemistry. The M-V-O system (M = Cu, Ag, Zn) was selected and direct interaction of M with vanadium pentoxide was performed. Remarkable syntheses have been achieved within minutes, paving the way for new materials. The M xV 2O 5 phases formed with Cu and Ag belong to the mixed valence metal-vanadium oxide bronzes whose structures and electric properties are of interest for applications as electrode materials in lithium batteries. Their formation may also be used as a model for further investigations in order to follow the diffusion mechanisms of atoms in solids and to get a better understanding of the SPS process. In this experiment M atoms penetrate micro-crystals of V 2O 5 oxide at a high speed, shearing their crystal network and rebuilding simultaneously in the mean time the crystal structure of the prototype structures β, β', ɛ or δ M xV 2O 5.

  3. Chromatographic separation of vanadium, tungsten and molybdenum with a liquid anion-exchanger.

    PubMed

    Fritz, J S; Topping, J J

    1971-09-01

    In acidic solution only molybdenum(VI), tungsten(VI), vanadium(V), niobium(V) and tantalum(V) form stable, anionic complexes with dilute hydrogen peroxide. This fact has been used in developing an analytical method of separating molybdenum(VI), tungsten(VI) and vanadium(V) from other metal ions and from each other. Preliminary investigations using reversed-phase paper chromatography and solvent extraction led to a reversed-phase column Chromatographic separation technique. These metal-peroxy anions are retained by a column containing a liquid anion-exchanger (General Mills Aliquat 336) in a solid support. Then molybdenum(VI), tungsten(VI) and vanadium(V) are selectively eluted with aqueous solutions containing dilute hydrogen peroxide and varying concentrations of sulphuric acid.

  4. Reduction of vanadium(V) to vanadium(IV) by NADPH, and vanadium(IV) to vanadium(III) by cysteine methyl ester in the presence of biologically relevant ligands.

    PubMed

    Islam, Mohammad K; Tsuboya, Chieko; Kusaka, Hiroko; Aizawa, Sen-ichi; Ueki, Tatsuya; Michibata, Hitoshi; Kanamori, Kan

    2007-08-01

    To better understand the mechanism of vanadium reduction in ascidians, we examined the reduction of vanadium(V) to vanadium(IV) by NADPH and the reduction of vanadium(IV) to vanadium(III) by L-cysteine methyl ester (CysME). UV-vis and electron paramagnetic resonance spectroscopic studies indicated that in the presence of several biologically relevant ligands vanadium(V) and vanadium(IV) were reduced by NADPH and CysME, respectively. Specifically, NADPH directly reduced vanadium(V) to vanadium(IV) with the assistance of ligands that have a formation constant with vanadium(IV) of greater than 7. Also, glycylhistidine and glycylaspartic acid were found to assist the reduction of vanadium(IV) to vanadium(III) by CysME.

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

    PubMed

    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.

  6. Vanadium Respiration by Geobacter metallireducens: Novel Strategy for In Situ Removal of Vanadium from Groundwater

    PubMed Central

    Ortiz-Bernad, Irene; Anderson, Robert T.; Vrionis, Helen A.; Lovley, Derek R.

    2004-01-01

    Vanadium can be an important contaminant in groundwaters impacted by mining activities. In order to determine if microorganisms of the Geobacteraceae, the predominant dissimilatory metal reducers in many subsurface environments, were capable of reducing vanadium(V), Geobacter metallireducens was inoculated into a medium in which acetate was the electron donor and vanadium(V) was the sole electron acceptor. Reduction of vanadium(V) resulted in the production of vanadium(IV), which subsequently precipitated. Reduction of vanadium(V) was associated with cell growth with a generation time of 15 h. No vanadium(V) was reduced and no precipitate was formed in heat-killed or abiotic controls. Acetate was the most effective of all the electron donors evaluated. When acetate was injected into the subsurface to enhance the growth and activity of Geobacteraceae in an aquifer contaminated with uranium and vanadium, vanadium was removed from the groundwater even more effectively than uranium. These studies demonstrate that G. metallireducens can grow via vanadium(V) respiration and that stimulating the activity of Geobacteraceae, and hence vanadium(V) reduction, can be an effective strategy for in situ immobilization of vanadium in contaminated subsurface environments. PMID:15128571

  7. Mineral resource of the month: vanadium

    USGS Publications Warehouse

    Magyar, Michael J.

    2007-01-01

    Vanadium, the name of which comes from Vanadis, a goddess in Scandinavian mythology, is one of the most important ferrous metals. Vanadium has many uses, but the metal’s metallurgical applications, such as an alloying element in iron and steel, account for more than 85 percent of U.S. consumption. The dominant nonmetallurgical use of the metal is as a catalyst for the production of maleic anhydride and sulfuric acid, ceramics, vanadium chemicals and electronics.

  8. Is vanadium of human nutritional importance yet?

    PubMed

    Harland, B F; Harden-Williams, B A

    1994-08-01

    The trace element vanadium has been studied by the nutrition community for four decades, yet has not achieved essential status for human beings. It is found in compounds at valences of 2, 3, 4, or 5, with the tetravalent and pentavalent forms being the most common. In human beings, pharmacologic amounts of vanadium (ie, 10 to 100 times normal intake) affect cholesterol and triglyceride metabolism, influence the shape of erythrocytes, and stimulate glucose oxidation and glycogen synthesis in the liver. Vanadium's primary mode of action is as a cofactor that enhances or inhibits enzymes. Recent evidence suggests that vanadium may be essential for higher animals. After their mothers had been fed carefully formulated vanadium-deficient diets, second-generation goat kids suffered skeletal damage and died within 3 days of parturition. Although ubiquitous in air, soil, water, and the food supply, vanadium is generally found in nanogram or microgram quantities, which makes it difficult to measure. Estimates for the American intake of vanadium (based on a food intake of 500 g dry weight) are 10 to 60 micrograms/day. Vanadium levels in diets from five regions of the United States range from 30.9 +/- 1.5 in the Southeast to 50.5 +/- 1.5 micrograms/kg dry weight in the West. Although vanadium is thought to be essential for goats, new data may soon support its essentiality in human beings.

  9. Vanadium irradiation at ATR - neutronics aspects

    SciTech Connect

    Gomes, I.C.; Smith, D.L.

    1995-04-01

    Calculations were performed to estimate damage and transmutation rates in vanadium irradiated in the ATR (Advanced Test Reactor) located in Idaho. The main focuses of the study are to evaluate the transmutation of vanadium to chromium and to explore ways to design the irradiation experiment to avoid excessive transmutation. It was found that the A-hole of ATR produces damage rate of {approximately} 0.2%/dpa of vanadium to chromium. A thermal neutron filter can be incorporated into the design to reduce the vanadium-to-chromium transmutation rate to low levels. A filter 1-2 mm thick of gadolinium or hafnium can be used.

  10. Vanadium interactions in crystalline silicon

    NASA Astrophysics Data System (ADS)

    Backlund, D. J.; Gibbons, T. M.; Estreicher, S. K.

    2016-11-01

    The properties of interstitial vanadium (Vi) in Si and its interactions with the vacancy and the self-interstitial, as well as with hydrogen, are calculated using first-principles techniques. The stable configurations, gap levels, and binding energies agree well with the available experimental data. The nudged-elastic-band method is used to calculate the activation energies for diffusion of Vi in various charge states. They range from 1.46 (for Vi +) to 2.04 eV (for Vi -). The (trigonal) {Vi,H } pair has a binding energy of 1.15 eV, a donor level at Ec-0.61 eV , and possibly an acceptor level Ec-0.07 eV . Substitutional vanadium (Vs) can also trap H interstitials and form electrically active {Vs,H } and {Vs,H ,H } complexes.

  11. A genetic algorithm approach for evaluation of optical functions of very thin tantalum pentoxide films on Si substrate

    NASA Astrophysics Data System (ADS)

    Sharlandjiev, P. S.; Nazarova, D. I.

    2013-11-01

    The optical characteristics of tantalum pentoxide films, deposited on Si(100) substrate by reactive sputtering, are studied. These films are investigated as high-kappa materials for the needs of nano-electronics, i.e. design of dynamic random access memories, etc. One problem in their implementation is that metal oxides are thermodynamically unstable with Si and an interfacial layer is formed between the oxide film and the silicon substrate during the deposition process. Herein, the center of attention is on the optical properties of that interfacial layer, which is studied by spectral photometric measurements. The evaluation of the optical parameters of the structure is fulfilled with the genetic algorithm approach. The spectral range of evaluation covers deep UV to NIR. The equivalent physical thickness (2.5 nm) and the equivalent refractive index of the interfacial layer are estimated from 236 to 750 nm as well as the thickness of the tantalum pentoxide film (9.5 nm).

  12. Low-loss and high index-contrast tantalum pentoxide microring resonators and grating couplers on silicon substrates.

    PubMed

    Rabiei, Payam; Rao, Ashutosh; Chiles, Jeff; Ma, Jichi; Fathpour, Sasan

    2014-09-15

    A platform for high index-contrast integrated photonics based on tantalum pentoxide submicrometer waveguides on silicon substrates is introduced. The platform allows demonstration of microring resonators with loaded quality factor, Q, of 67,000 and waveguides with a propagation loss of 4.9 dB/cm. Grating couplers, with an insertion loss of ~6 dB per coupler and 3 dB bandwidth of ~50 nm, are also demonstrated and integrated with microring resonators.

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

    PubMed

    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 <1% of the total vanadium readily mobilised. Column experiments revealed that only <0.1% of 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.

  14. VANADIUM CHEMISTRY ESSENTIALS FOR TREATMENT STUDIES

    EPA Science Inventory

    The importance of vanadium occurrence and treatment in drinking water has been elevated by its inclusion in the Contaminant Candidate List. Though it is still too early to know the nature of new regulatory requirements for vanadium, if indeed it becomes regulated, a substantial u...

  15. Vanadium hydride deuterium-tritium generator

    DOEpatents

    Christensen, Leslie D.

    1982-01-01

    A pressure controlled vanadium hydride gas generator to provide deuterium-tritium gas in a series of pressure increments. A high pressure chamber filled with vanadium-deuterium-tritium hydride is surrounded by a heater which controls the hydride temperature. The heater is actuated by a power controller which responds to the difference signal between the actual pressure signal and a programmed pressure signal.

  16. Toxicity of vanadium to different freshwater organisms

    SciTech Connect

    Beusen, J.M.; Neven, B.

    1987-08-01

    The aim of this study is to determine the acute and subchronic toxicity of vanadium for various species of freshwater fish. The long-term toxicity and the effect of vanadium on the reproduction of Daphnia magna is also evaluated and compared with the toxicity of other metals.

  17. Perspectives for vanadium in health issues.

    PubMed

    Rehder, Dieter

    2016-01-01

    Vanadium is omnipresent in trace amounts in the environment, in food and also in the human body, where it might serve as a regulator for phosphate-dependent proteins. Potential vanadium-based formulations--inorganic and coordination compounds with organic ligands--commonly underlie speciation in the body, that is, they are converted to vanadate(V), oxidovanadium(IV) and to complexes with the body's own ligand systems. Vanadium compounds have been shown to be potentially effective against diabetes Type 2, malign tumors including cancer, endemic tropical diseases (such as trypanosomiasis, leishmaniasis and amoebiasis), bacterial infections (tuberculosis and pneumonia) and HIV infections. Furthermore, vanadium drugs can be operative in cardio- and neuro-protection. So far, vanadium compounds have not yet been approved as pharmaceuticals for clinical use.

  18. A search for the ground state structure and the phase stability of tantalum pentoxide.

    PubMed

    Pérez-Walton, S; Valencia-Balvín, C; Padilha, A C M; Dalpian, G M; Osorio-Guillén, J M

    2016-01-27

    Tantalum pentoxide (Ta2O5) is a wide-gap semiconductor that presents good catalytic and dielectric properties, conferring to this compound promising prospective use in a variety of technological applications. However, there is a lack of understanding regarding the relations among its crystalline phases, as some of them are not even completely characterized and there is currently no agreement about which models better explain the crystallographic data. Additionally, its phase diagram is unknown. In this work we performed first-principles density functional theory calculations to study the structural properties of the different phases and models of Ta2O5, the equation of state and the zone-centered vibrational frequencies. From our results, we conclude that the phases that are built up from only distorted octahedra instead of combinations with pentagonal and/or hexagonal bipyramids are energetically more favorable and dynamically stable. More importantly, this study establishes that, given the pressure range considered, the B-phase is the most favorable structure and there is no a crystallographic phase transition to another phase at high-pressure. Additionally, for the equilibrium volume of the B-phase and the λ-model, the description of the electronic structure and optical properties were performed using semi-local and hybrid functionals.

  19. Oxidation state and interfacial effects on oxygen vacancies in tantalum pentoxide

    DOE PAGES

    Bondi, Robert J.; Marinella, Matthew J.

    2015-02-28

    First-principles density-functional theory (DFT) calculations are used to study the atomistic structure, structural energetics, and electron density near the O monovacancy (VOn; n=0,1+,2+) in both bulk, amorphous tantalum pentoxide (a-Ta2O5) and also at vacuum and metallic Ta interfaces. We calculate multivariate vacancy formation energies to evaluate stability as a function of oxidation state, distance from interface plane, and Fermi energy. VOn of all oxidation states preferentially segregate at both Ta and vacuum interfaces, where the metallic interface exhibits global formation energy minima. In a-Ta2O5, VO0 are characterized by structural contraction and electron density localization, while VO2+ promote structural expansion andmore » are depleted of electron density. In contrast, interfacial VO0 and VO2+ show nearly indistinguishable ionic and electronic signatures indicative of a reduced VO center. Interfacial VO2+ extract electron density from metallic Ta indicating VO2+ is spontaneously reduced at the expense of the metal. This oxidation/reduction behavior suggests careful selection and processing of both oxide layer and metal electrodes for engineering memristor device operation.« less

  20. Oxidation state and interfacial effects on oxygen vacancies in tantalum pentoxide

    SciTech Connect

    Bondi, Robert J. Marinella, Matthew J.

    2015-02-28

    First-principles density-functional theory calculations are used to study the atomistic structure, structural energetics, and electron density near the O monovacancy (V{sub O}{sup n}; n = 0,1+,2+) in both bulk, amorphous tantalum pentoxide (a-Ta{sub 2}O{sub 5}), and also at vacuum and metallic Ta interfaces. We calculate multivariate vacancy formation energies to evaluate stability as a function of oxidation state, distance from interface plane, and Fermi energy. V{sub O}{sup n} of all oxidation states preferentially segregates at both Ta and vacuum interfaces, where the metallic interface exhibits global formation energy minima. In a-Ta{sub 2}O{sub 5}, V{sub O}{sup 0} is characterized by structural contraction and electron density localization, while V{sub O}{sup 2+} promotes structural expansion and is depleted of electron density. In contrast, interfacial V{sub O}{sup 0} and V{sub O}{sup 2+} show nearly indistinguishable ionic and electronic signatures indicative of a reduced V{sub O} center. Interfacial V{sub O}{sup 2+} extracts electron density from metallic Ta, indicating that V{sub O}{sup 2+} is spontaneously reduced at the expense of the metal. This oxidation/reduction behavior suggests careful selection and processing of both oxide layer and metal electrodes for engineering memristor device operation.

  1. Oxidation state and interfacial effects on oxygen vacancies in tantalum pentoxide

    SciTech Connect

    Bondi, Robert J.; Marinella, Matthew J.

    2015-02-28

    First-principles density-functional theory (DFT) calculations are used to study the atomistic structure, structural energetics, and electron density near the O monovacancy (VOn; n=0,1+,2+) in both bulk, amorphous tantalum pentoxide (a-Ta2O5) and also at vacuum and metallic Ta interfaces. We calculate multivariate vacancy formation energies to evaluate stability as a function of oxidation state, distance from interface plane, and Fermi energy. VOn of all oxidation states preferentially segregate at both Ta and vacuum interfaces, where the metallic interface exhibits global formation energy minima. In a-Ta2O5, VO0 are characterized by structural contraction and electron density localization, while VO2+ promote structural expansion and are depleted of electron density. In contrast, interfacial VO0 and VO2+ show nearly indistinguishable ionic and electronic signatures indicative of a reduced VO center. Interfacial VO2+ extract electron density from metallic Ta indicating VO2+ is spontaneously reduced at the expense of the metal. This oxidation/reduction behavior suggests careful selection and processing of both oxide layer and metal electrodes for engineering memristor device operation.

  2. A search for the ground state structure and the phase stability of tantalum pentoxide

    NASA Astrophysics Data System (ADS)

    Pérez-Walton, S.; Valencia-Balvín, C.; Padilha, A. C. M.; Dalpian, G. M.; Osorio-Guillén, J. M.

    2016-01-01

    Tantalum pentoxide (Ta2O5) is a wide-gap semiconductor that presents good catalytic and dielectric properties, conferring to this compound promising prospective use in a variety of technological applications. However, there is a lack of understanding regarding the relations among its crystalline phases, as some of them are not even completely characterized and there is currently no agreement about which models better explain the crystallographic data. Additionally, its phase diagram is unknown. In this work we performed first-principles density functional theory calculations to study the structural properties of the different phases and models of Ta2O5, the equation of state and the zone-centered vibrational frequencies. From our results, we conclude that the phases that are built up from only distorted octahedra instead of combinations with pentagonal and/or hexagonal bipyramids are energetically more favorable and dynamically stable. More importantly, this study establishes that, given the pressure range considered, the B-phase is the most favorable structure and there is no a crystallographic phase transition to another phase at high-pressure. Additionally, for the equilibrium volume of the B-phase and the λ-model, the description of the electronic structure and optical properties were performed using semi-local and hybrid functionals.

  3. Methods for making lithium vanadium oxide electrode materials

    DOEpatents

    Schutts, Scott M.; Kinney, Robert J.

    2000-01-01

    A method of making vanadium oxide formulations is presented. In one method of preparing lithium vanadium oxide for use as an electrode material, the method involves: admixing a particulate form of a lithium compound and a particulate form of a vanadium compound; jet milling the particulate admixture of the lithium and vanadium compounds; and heating the jet milled particulate admixture at a temperature below the melting temperature of the admixture to form lithium vanadium oxide.

  4. Toxicity and hazard of vanadium to mallard ducks (Anas platyrhynchos) and Canada geese (Branta canadensis)

    USGS Publications Warehouse

    Rattner, B.A.; McKernan, M.A.; Eisenreich, K.M.; Link, W.A.; Olsen, G.H.; Hoffman, D.J.; Knowles, K.A.; McGowan, P.C.

    2006-01-01

    A recent Canada goose (Branta canadensis) die-off at a petroleum refinery fly ash pond in Delaware was attributed to vanadium (V) toxicity. Because of the paucity of V toxicity data for wild birds, a series of studies was undertaken using the forms of V believed to have resulted in this incident. In 7-d single oral dose trials with mallard drakes (Anas platyrhynchos), the estimated median lethal dose (LD50) for vanadium pentoxide was 113 mg/kg body weight, while the LD50 for sodium metavanadate was 75.5 mg/kg. Sodium metavanadate was found to be even more potent (LD50 = 37.2 mg/kg) in male Canada geese. The most distinctive histopathological lesion of both forms of V was Iympho-granulocytic enteritis with hemorrhage into the intestinal lumen. Vanadium accumulation in liver and kidney was proportional to the administered dose, and predictive analyses based on these data suggest that V concentrations of 10 :g/g dry weight (dw) in liver and 25 ug/g dw in kidney are associated with mortality (>90% confidence that exposure is >LD50) in mallards acutely exposed to sodium metavanadate. Chronic exposure to increasing dietary concentrations of sodium metavanadate (38.5 to 2651 ppm) over 67 d resulted in V accumulation in liver and kidney (25.2 and 13.6 ug/g dw, respectively), mild intestinal hemorrhage, blood chemistry changes, and evidence of hepatic oxidative stress in mallards, although some of these responses may have been confounded by food avoidance and weight loss. Dietary exposure of mallards to 250 ppm sodium metavanadate for 4 wk resulted in modest accumulation of V in liver and kidney <5 ug/g dw) and mild intestinal hemorrhage. Based on these data and other observations, it is unlikely that chronic low-level dietary exposure to V poses a direct lethal hazard to wildlife. However, point sources, such as the V-laden fly ash pond encountered by geese at the petroleum refinery in Delaware, may pose a significant hazard to water birds.

  5. Vanadium toxicity in the thymic development

    PubMed Central

    Cui, Hengmin

    2015-01-01

    The purpose of this study was to define the toxic effects of vanadium on thymic development in broilers fed on diets supplemented with 0, 5, 15, 30, 45 and 60 mg/kg of vanadium for 42 days. We examined the changes of relative weight, cell cycle phase, apoptotic cells, and protein expression of Bcl-2, Bax, and caspase-3 in the thymus by the methods of flow cytometry, TUNEL (terminal-deoxynucleotidyl transferase mediated nick end labeling) and immunohistochemistry. The results showed that dietary high vanadium (30mg/kg, 45mg/kg and 60mg/kg) caused the toxic effects on thymic development, which was characterized by decreasing relative weight, increasing G0/G1 phase (a prolonged nondividing state), reducing S phase (DNA replication) and proliferating index (PI), and increasing percentages of apoptotic thymocytes. Concurrently, the protein expression levels of Bax and caspase-3 were increased, and protein expression levels of Bcl-2 were decreased. The thymic development suppression caused by dietary high vanadium further leads to inhibitive effects on T lymphocyte maturity and activity, and cellular immune function. The above-mentioned results provide new evidences for further understanding the vanadium immunotoxicity. In contrast, dietary 5 mg/kg vanadium promoted the thymic development by increasing relative weight, decreasing G0/G1 phase, increasing S phase and PI, and reducing percentages of apoptotic thymocytes when compared to the control group and high vanadium groups. PMID:26416460

  6. Vanadium Electrolyte Studies for the Vanadium Redox Battery-A Review.

    PubMed

    Skyllas-Kazacos, Maria; Cao, Liuyue; Kazacos, Michael; Kausar, Nadeem; Mousa, Asem

    2016-07-07

    The electrolyte is one of the most important components of the vanadium redox flow battery and its properties will affect cell performance and behavior in addition to the overall battery cost. Vanadium exists in several oxidation states with significantly different half-cell potentials that can produce practical cell voltages. It is thus possible to use the same element in both half-cells and thereby eliminate problems of cross-contamination inherent in all other flow battery chemistries. Electrolyte properties vary with supporting electrolyte composition, state-of-charge, and temperature and this will impact on the characteristics, behavior, and performance of the vanadium battery in practical applications. This Review provides a broad overview of the physical properties and characteristics of the vanadium battery electrolyte under different conditions, together with a description of some of the processing methods that have been developed to produce vanadium electrolytes for vanadium redox flow battery applications.

  7. Sulfatization of vanadium pentoxide in equilibrium gaseous mixtures containing SO{sub 2}, SO{sub 3}, and O{sub 2}

    SciTech Connect

    Ivanenko, S.V.; Dzhoraev, R.R.

    1994-07-01

    The sulfatization of V{sub 2}O{sub 5} supported on SiO{sub 2} and SiO{sub 2} + MgSO{sub 4} carriers in equilibrium gaseous SO{sub 2}-SO{sub 3}-O{sub 2}-N{sub 2} mixtures at P{sub SO{sub 3}} = 0.8 - 33 kPa and T {>=} 673 K is studied using a flow thermogravimetric setup. Sulfatization is accompanied by V{sub 2}O{sub 5} reduction and production of vanadyle sulfate VOSO{sub 4}, which can decay completely or partially, depending on the conditions. This is supported by hysteresis observed in the course of the sulfatization and desulfatization of the catalyst. The experimental data indicates the formation of surface sulfates with various formations heats, which is determined by the energetic heterogeneity of the surface.

  8. Effect of nitrogen doping on oxygen vacancies of titanium dioxide supported vanadium pentoxide for ammonia-SCR reaction at low temperature.

    PubMed

    Li, Hongyu; Zhang, Shule; Zhong, Qin

    2013-07-15

    A V2O5/N-doped TiO2 catalyst has been developed by partly substituting the lattice oxygen of TiO2 support with nitrogen, which showed a remarkable increase in activity for the reduction of NO with NH3 at low temperature. The catalyst was characterized by Brunauer-Emmett-Teller (BET), transmission electron microscope (TEM), photoluminescence (PL), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR). The results demonstrated that N doping cannot noticeably change the microscopic features but dramatically enhanced the formation of surface oxygen vacancies, which can play a vital role in the formation of superoxide ions to improve the SCR activity. The catalyst with [N]/[Ti]=1.0×10(-2) showed the highest NO removal efficiency in the SCR reaction at low temperature. Furthermore, the V1TiN1.0 catalyst showed better resistance to SO2 and H2O during the SCR of NO.

  9. Scale-Up of Vanadium Trineodecanoate.

    DTIC Science & Technology

    1984-02-01

    vanadium concentration can be lowered by extraction with a liquid ion exchange system. Alamine 336 , a (trademark) product of General Mills, is a liquid ion...exchanger developed for vanadium extractiop. It is a water insoluble tertiary amine dissolved in kerosene. Alamine extracts vanadium at pH 1.2-2 and... chemical equations are shown below: 800 . 900 V205 + 6HCl + 2HCOOH 2VC1 3 + 5H20 + 2C0 2 1000 - 1500 VCl 3 + 3C9H1gCOOH 1 V(CgH 19COO) 3 + 3HCl In the

  10. Topotactic synthesis of vanadium nitride solid foams

    SciTech Connect

    Oyama, S.T.; Kapoor, R.; Oyama, H.T.; Hofmann, D.J.; Matijevic, E. )

    1993-06-01

    Vanadium nitride has been synthesized with a surface area of 120 m[sup 2] g[sup [minus]1] by temperature programmed nitridation of a foam-like vanadium oxide (35 m[sup 2] g[sup [minus]1]), precipitated from vanadate solutions. The nitridation reaction was established to be topotactic and pseudomorphous by x-ray powder diffraction and scanning electron microscopy. The crystallographic relationship between the nitride and oxide was [l brace]200[r brace]//[l brace]001[r brace]. The effect of precursor geometry on the product size and shape was investigated by employing vanadium oxide solids of different morphologies.

  11. Electrical Resistivity of Vanadium and Zirconium.

    DTIC Science & Technology

    1982-12-01

    the Superconducting Properties of Vanadium - Aluminum and Vanadium Tin Solid Solutions,’ Zh. Eksp. Teot. Piz., JI(6). 2124-31 (1975): Egl. tranal.: Soy...Fluctuations on the Superconducting and Normal Properties of Alloys of Titanium Containing Vanadium, Niobium, or Tantalum.’ Zh. Eksp. Tot. Fit. §1(6... Properties of Alloy NTI2A5,’ Metalloved. Ter. (brab. Met., S, 51 (1976); Engl. transl.: Met. Sci. Heat Treat. Not., 11(5-6), 453-4 * (1976). 84. Kharoo

  12. Solvents and supporting electrolytes for vanadium acetylacetonate flow batteries

    NASA Astrophysics Data System (ADS)

    Shinkle, Aaron A.; Pomaville, Timothy J.; Sleightholme, Alice E. S.; Thompson, Levi T.; Monroe, Charles W.

    2014-02-01

    Properties of supporting electrolytes and solvents were examined for use with vanadium acetylacetonate - a member of the class of metal(β-diketonate) active species - in non-aqueous redox flow batteries. Twenty supporting-electrolyte/solvent combinations were screened for ionic conductivity and supporting-electrolyte solubility. Hexane, tetrahydrofuran, and dimethylcarbonate solvents did not meet minimal conductivity and solubility criteria for any of the electrolytes used, which included tetraethylammonium tetrafluoroborate, tetrabutylammonium tetrafluoroborate, tetrabutylammonium hexafluorophosphate, and (1-butyl, 3-methyl)imidazolium bis(trifluoromethanesulfonyl)imide. Ionic conductivities and solubilities for solutions of these electrolytes passed screening criteria in acetonitrile and dimethylformamide solvents, in which maximum supporting-electrolyte and active-species solubilities were determined. Active-species electrochemistry was found to be reversible in several solvent/support systems; for some systems the voltammetric signatures of unwanted side reactions were suppressed. Correlations between supporting-solution properties and performance metrics suggest that an optimal solvent for a vanadium acetylacetonate RFB should have a low solvent molar volume for active-species solubility, and a high Hansen polarity for conductivity.

  13. Synthesis, investigation and practical application in lithium batteries of some compounds based on vanadium oxides

    NASA Astrophysics Data System (ADS)

    Shembel, E.; Apostolova, R.; Nagirny, V.; Aurbach, D.; Markovsky, B.

    In this paper, we investigate the inter-relationship between the conditions of the electrochemical synthesis of vanadium oxide compounds, their structural and morphological characteristics, kinetic parameters of the redox processes, and charge-discharge performance of lithium batteries with vanadium oxide cathodes. The materials studied were V 2O 5- y oxides and those with inserted sodium ions (Na-vanadium oxide compounds, Na-VOC) obtained electrochemically in the form of compact deposits on a metal substrate. The electrochemical synthesis of the oxides has been performed from aqueous vanadyl sulphate solutions. Optimal synthesis conditions (current density, pH, temperature, vanadyl sulphate and sodium sulphate concentrations), and subsequent optimal thermal treatment of the oxides, which provide high electrochemical activity of the cathode material and good adhesion of the oxide to the metal substrate, have been elucidated. A correlation between the structure of the vanadium oxides and Na-VOC, their morphology, impedance characteristics of the cathode, and lithium-ion solid state diffusion in the host cathode bulk has been established and discussed. A combination of analytical techniques (XRD, IR spectroscopy, TGA, BET, SEM) and electrochemical methods (cyclic voltammetry, chronopotentiometry, GITT, EIS) has been used in this study.

  14. Low-Cost and Facile Synthesis of the Vanadium Oxides V2O3, VO2, and V2O5 and Their Magnetic, Thermochromic and Electrochromic Properties.

    PubMed

    Mjejri, Issam; Rougier, Aline; Gaudon, Manuel

    2017-02-06

    In this study, vanadium sesquioxide (V2O3), dioxide (VO2), and pentoxide (V2O5) were all synthesized from a single polyol route through the precipitation of an intermediate precursor: vanadium ethylene glycolate (VEG). Various annealing treatments of the VEG precursor, under controlled atmosphere and temperature, led to the successful synthesis of the three pure oxides, with sub-micrometer crystallite size. To the best of our knowledge, the synthesis of the three oxides V2O5, VO2, and V2O3 from a single polyol batch has never been reported in the literature. In a second part of the study, the potentialities brought about by the successful preparation of sub-micrometer V2O5, VO2, and V2O3 are illustrated by the characterization of the electrochromic properties of V2O5 films, a discussion about the metal to insulator transition of VO2 on the basis of in situ measurements versus temperature of its electrical and optical properties, and the characterization of the magnetic transition of V2O3 powder from SQUID measurements. For the latter compound, the influence of the crystallite size on the magnetic properties is discussed.

  15. A Safe High-Performance All-Solid-State Lithium-Vanadium Battery with a Freestanding V2O5 Nanowire Composite Paper Cathode.

    PubMed

    Zhang, Yue; Lai, Jingyuan; Gong, Yudong; Hu, Yongming; Liu, Jin; Sun, Chunwen; Wang, Zhong Lin

    2016-12-21

    The electronic conductivity and structural stability are still challenges for vanadium pentoxide (V2O5) as cathode materials in batteries. Here, we report a V2O5 nanowire-reduced graphene oxide (rGO) composite paper for direct use as a cathode without any additives for high-temperature and high-safety solid polymer electrolyte [PEO-MIL-53(Al)-LiTFSI] lithium-vanadium batteries. The batteries can show a fast and stable lithium-ion-storage performance in a wide voltage window of 1.0-4.0 V versus Li(+)/Li at 80 °C, in which with an average capacity of 329.2 mAh g(-1) at 17 mA g(-1) and a stable cycling performance over 40 cycles are achieved. The excellent electrochemical performance is mainly ascribed to integration of the electronic conductivity of rGO and interconnected networks of the V2O5 nanowires and solid electrolyte. This is a promising lithium battery for flexible and highly safe energy-storage devices.

  16. Alkali metal yttrium neo-pentoxide double alkoxide precursors to alkali metal yttrium oxide nanomaterials

    DOE PAGES

    Boyle, Timothy J.; Neville, Michael L.; Sears, Jeremiah Matthew; ...

    2016-03-15

    In this study, a series of alkali metal yttrium neo-pentoxide ([AY(ONep)4]) compounds were developed as precursors to alkali yttrium oxide (AYO2) nanomaterials. The reaction of yttrium amide ([Y(NR2)3] where R=Si(CH3)3) with four equivalents of H-ONep followed by addition of [A(NR2)] (A=Li, Na, K) or Ao (Ao=Rb, Cs) led to the formation of a complex series of AnY(ONep)3+n species, crystallographically identified as [Y2Li3(μ3-ONep)(μ3-HONep)(μ-ONep)5(ONep)3(HONep)2] (1), [YNa2(μ3-ONep)4(ONep)]2 (2), {[Y2K3(μ3-ONep)3(μ-ONep)4(ONep)2(ηξ-tol)2][Y4K2(μ4-O)(μ3-ONep)8(ONep)4]•ηx-tol]} (3), [Y4K2(μ4-O)(μ3-ONep)8(ONep)4] (3a), [Y2Rb3(μ4-ONep)3(μ-ONep)6] (4), and [Y2Cs4(μ6-O)(μ3-ONep)6(μ3-HONep)2(ONep)2(ηx-tol)4]•tol (5). Compounds 1–5 were investigated as single source precursors to AYOx nanomaterials following solvothermal routes (pyridine, 185 °C for 24h). The final products after thermal processing weremore » found by powder X-ray diffraction experiments to be Y2O3 with variable sized particles based on transmission electron diffraction. Energy dispersive X-ray spectroscopy studies indicated that the heavier alkali metal species were present in the isolated nanomaterials.« less

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

    PubMed

    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).

  18. Laser Fabricated Nanostructures on Vanadium Foils

    SciTech Connect

    Farkas, B.; Fuele, M.; Nanai, L.; Balint, A. M.

    2011-10-03

    In this work we present our results concerning to the nanostructure generation on vanadium surfaces by ultrashort pulsed laser irradiation. The melting free formation of these structures is very important in many fields of science and industry too. We obtain that the nanostructure forming process on vanadium surface is Stransky Krastanov type. The surface covering and the nano-tower shape are depending on the ambient of the laser matter reaction.

  19. Vanadium hydride deuterium-tritium generator

    DOEpatents

    Christensen, L.D.

    1980-03-13

    A pressure controlled vanadium hydride gas generator was designed to provide deuterium-tritium gas in a series of pressure increments. A high pressure chamber filled with vanadium-deuterium-tritium hydride is surrounded by a heater which controls the hydride temperature. The heater is actuated by a power controller which responds to the difference signal between the actual pressure signal and a programmed pressure signal.

  20. The role of vanadium in biology.

    PubMed

    Rehder, Dieter

    2015-05-01

    Vanadium is special in at least two respects: on the one hand, the tetrahedral anion vanadate(v) is similar to the phosphate anion; vanadate can thus interact with various physiological substrates that are otherwise functionalized by phosphate. On the other hand, the transition metal vanadium can easily expand its sphere beyond tetrahedral coordination, and switch between the oxidation states +v, +iv and +iii in a physiological environment. The similarity between vanadate and phosphate may account for the antidiabetic potential of vanadium compounds with carrier ligands such as maltolate and picolinate, and also for vanadium's mediation in cardiovascular and neuronal defects. Other potential medicinal applications of more complex vanadium coordination compounds, for example in the treatment of parasitic tropical diseases, may also be rooted in the specific properties of the ligand sphere. The ease of the change in the oxidation state of vanadium is employed by prokarya (bacteria and cyanobacteria) as well as by eukarya (algae and fungi) in respiratory and enzymatic functions. Macroalgae (seaweeds), fungi, lichens and Streptomyces bacteria have available haloperoxidases, and hence enzymes that enable the 2-electron oxidation of halide X(-) with peroxide, catalyzed by a Lewis-acidic V(V) center. The X(+) species thus formed can be employed to oxidatively halogenate organic substrates, a fact with implications also for the chemical processes in the atmosphere. Vanadium-dependent nitrogenases in bacteria (Azotobacter) and cyanobacteria (Anabaena) convert N2 + H(+) to NH4(+) + H2, but are also receptive for alternative substrates such as CO and C2H2. Among the enigmas to be solved with respect to the utilization of vanadium in nature is the accumulation of V(III) by some sea squirts and fan worms, as well as the purport of the nonoxido V(IV) compound amavadin in the fly agaric.

  1. Overview of environmental and occupational vanadium exposure and associated health outcomes: an article based on a presentation at the 8th International Symposium on Vanadium Chemistry, Biological Chemistry, and Toxicology, Washington DC, August 15-18, 2012.

    PubMed

    Fortoul, T I; Rojas-Lemus, M; Rodriguez-Lara, V; Gonzalez-Villalva, A; Ustarroz-Cano, M; Cano-Gutierrez, G; Gonzalez-Rendon, S E; Montaño, L F; Altamirano-Lozano, M

    2014-01-01

    Vanadium (V) has a variety of applications that make it suitable for use in ceramic production and decoration, production of pigments for a variety of products, an accelerator for drying paint, production of aniline black dye, and as a mordant in coloring textiles. Taking advantage of its hardness, resilience, ability to form alloys, and its resistance to corrosion, V is also used in the production of tools, steel, machinery, and surgical implants. V is employed in producing photographic developers, batteries, and semi-conductors, and in catalyst-based recycling processes. As technologies have evolved, the use of V has increased in jet aircraft and space technology, as well as in manufacture of ultraviolet filter glass to prevent radiation injury. Due to these myriad uses, the potential for occupational exposure to V is ever-evident. Similarly, there is an increased risk for environmental contamination by V agents themselves or as components of by-products released into the environment. For example, the use of V in sulfuric acid production results in the release of soot and/or fly ash rich in vanadium pentoxide. Petroleum refinery, smelting, welding, and cutting of V-rich steel alloy, the cleaning and repair of oil-fired boilers, and catalysis of chemical productions are other sources of increased airborne V-bearing particles in local/distant environments. Exposure of non-workers to V is an increasing health concern. Studies have demonstrated associations between exposure to airborne V-bearing particles (as part of air pollution) and increased risks of a variety of pathologies like hypertension, dysrhythmia, systemic inflammation, hyper-coagulation, cancers, and bronchial hyper-reactivity. This paper will provide a review of the history of V usage in occupational settings, documented exposure levels, environmental levels of V associated with pollution, epidemiologic data relating V exposure(s) to adverse health outcomes, and governmental responses to protect both

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

    USGS Publications Warehouse

    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

  3. Effects of metal compounds with distinct physicochemical properties on iron homeostasis and antibacterial activity in the lungs: chromium and vanadium.

    PubMed

    Cohen, Mitchell D; Sisco, Maureen; Prophete, Colette; Yoshida, Kotaro; Chen, Lung-chi; Zelikoff, Judith T; Smee, Jason; Holder, Alvin A; Stonehuerner, Jacqueline; Crans, Debbie C; Ghio, Andrew J

    2010-02-01

    In situ reactions of metal ions or their compounds are important mechanisms by which particles alter lung immune responses. The authors hypothesized that major determinants of the immunomodulatory effect of any metal include its redox behavior/properties, oxidation state, and/or solubility, and that the toxicities arising from differences in physicochemical parameters are manifest, in part, via differential shifts in lung iron (Fe) homeostasis. To test the hypotheses, immunomodulatory potentials for both pentavalent vanadium (VV; as soluble metavanadate or insoluble vanadium pentoxide) and hexavalent chromium (CrVI; as soluble sodium chromate or insoluble calcium chromate) were quantified in rats after inhalation (5h/day for 5 days) of each at 100 microg metal/m3. Differences in effects on local bacterial resistance between the two VV, and between each CrVI, agents suggested that solubility might be a determinant of in situ immunotoxicity. For the soluble forms, VV had a greater impact on resistance than CrVI, indicating that redox behavior/properties was likely also a determinant. The soluble VV agent was the strongest immunomodulant. Regarding Fe homeostasis, both VV agents had dramatic effects on airway Fe levels. Both also impacted local immune/airway epithelial cell Fe levels in that there were significant increases in production of select cytokines/chemokines whose genes are subject to regulation by HIF-1 (whose intracellular longevity is related to cell Fe status). Our findings contribute to a better understanding of the role that metal compound properties play in respiratory disease pathogenesis and provide a rationale for differing pulmonary immunotoxicities of commonly encountered ambient metal pollutants.

  4. Separation and solvent extraction of vanadium and uranium with n-propyl 2,3,4-trihydroxybenzoate.

    PubMed

    Jasim, F

    1969-06-01

    A spectrophotometric method is described for the separation and determination of trace quantities of vanadium(IV) and (V) from uranium(VI). Vanadium is selectively separated from uranium by extraction at pH 6.5 into n-propyl 2,3,4-trihydroxybenzoate (PTB) dissolved in t-pentanol. Up to 120 microg of vanadium can be determined by measuring the absorbance of the blue complex in the organic phase at 585 nm. Uranium(VI) remains in the aqueous layer and can be determined spectrophotometrically by its reaction with PTB in aqueous acetone to produce a brown-red colour at pH 7.6-8.8. Solutions containing 25-275 microg of uranium absorb at 370-380 nm according to Beer's law. By modification, this procedure can be used for the determination of the two metals in native phosphate rocks. The effects of diverse ions on the determination of vanadium and uranium have also been examined.

  5. Hazardous waste to materials: recovery of molybdenum and vanadium from acidic leach liquor of spent hydroprocessing catalyst using alamine 308.

    PubMed

    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.

  6. Removal of vanadium(III) and molybdenum(V) from wastewater using Posidonia oceanica (Tracheophyta) biomass.

    PubMed

    Pennesi, Chiara; Totti, Cecilia; Beolchini, Francesca

    2013-01-01

    The use of dried and re-hydrated biomass of the seagrass Posidonia oceanica was investigated as an alternative and -low-cost biomaterial for removal of vanadium(III) and molybdenum(V) from wastewaters. Initial characterisation of this biomaterial identified carboxylic groups on the cuticle as potentially responsible for cation sorption, and confirmed the toxic-metal bioaccumulation. The combined effects on biosorption performance of equilibrium pH and metal concentrations were investigated in an ideal single-metal system and in more real-life multicomponent systems. There were either with one metal (vanadium or molybdenum) and sodium nitrate, as representative of high ionic strength systems, or with the two metals (vanadium and molybdenum). For the single-metal solutions, the optimum was at pH 3, where a significant proportion of vanadium was removed (ca. 70%) while there was ca. 40% adsorption of molybdenum. The data obtained from the more real-life multicomponent systems showed that biosorption of one metal was improved both by the presence of the other metal and by high ionic strength, suggesting a synergistic effect on biosorption rather than competition. There data ware used for the development of a simple multi-metal equilibrium model based on the non-competitive Langmuir approach, which was successfully fitted to experimental data and represents a useful support tool for the prediction of biosorption performance in such real-life systems. Overall, the results suggest that biomass of P. oceanica can be used as an efficient biosorbent for removal of vanadium(III) and molybdenum(V) from aqueous solutions. This process thus offers an eco-compatible solution for the reuse of the waste material of leaves that accumulate on the beach due to both human activities and to storms at sea.

  7. Removal of Vanadium(III) and Molybdenum(V) from Wastewater Using Posidonia oceanica (Tracheophyta) Biomass

    PubMed Central

    Pennesi, Chiara; Totti, Cecilia; Beolchini, Francesca

    2013-01-01

    The use of dried and re-hydrated biomass of the seagrass Posidonia oceanica was investigated as an alternative and –low-cost biomaterial for removal of vanadium(III) and molybdenum(V) from wastewaters. Initial characterisation of this biomaterial identified carboxylic groups on the cuticle as potentially responsible for cation sorption, and confirmed the toxic-metal bioaccumulation. The combined effects on biosorption performance of equilibrium pH and metal concentrations were investigated in an ideal single-metal system and in more real-life multicomponent systems. There were either with one metal (vanadium or molybdenum) and sodium nitrate, as representative of high ionic strength systems, or with the two metals (vanadium and molybdenum). For the single-metal solutions, the optimum was at pH 3, where a significant proportion of vanadium was removed (ca. 70%) while there was ca. 40% adsorption of molybdenum. The data obtained from the more real-life multicomponent systems showed that biosorption of one metal was improved both by the presence of the other metal and by high ionic strength, suggesting a synergistic effect on biosorption rather than competition. There data ware used for the development of a simple multi-metal equilibrium model based on the non-competitive Langmuir approach, which was successfully fitted to experimental data and represents a useful support tool for the prediction of biosorption performance in such real-life systems. Overall, the results suggest that biomass of P. oceanica can be used as an efficient biosorbent for removal of vanadium(III) and molybdenum(V) from aqueous solutions. This process thus offers an eco-compatible solution for the reuse of the waste material of leaves that accumulate on the beach due to both human activities and to storms at sea. PMID:24204692

  8. Single-step preparation of mesoporous, anatase-based titanium-vanadium oxide and its application.

    PubMed

    Shyue, Jing-Jong; De Guire, Mark R

    2005-09-14

    Mesoporous solid solutions of anatase-based titanium-vanadium oxides were synthesized from aqueous solutions. The V/Ti ratio was determined by the composition of the deposition solution, while the morphology and nanoscale porosity were controlled using micelles of the surfactants cetyltrimethylammonium bromide (CTAB), or hexadecylamine (HDA). The use of CTAB resulted in mesoporous powders, whereas HDA yielded clusters of nanotubes. As compared to materials of the same composition made without the use of a surfactant, the catalyst made with CTAB had 50% higher catalytic activity, and that made with HDA had 70% higher activity. As compared to titania-supported vanadia catalysts with equivalent vanadium loading and synthesized using wet impregnation, the co-deposited materials exhibited significantly higher (up to 3.8x) catalytic activity.

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

    EPA Science Inventory

    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...

  10. Manufacturing development of low activation vanadium alloys

    SciTech Connect

    Smith, J.P.; Johnson, W.R.; Baxi, C.B.

    1996-10-01

    General Atomics is developing manufacturing methods for vanadium alloys as part of a program to encourage the development of low activation alloys for fusion use. The culmination of the program is the fabrication and installation of a vanadium alloy structure in the DIII-D tokamak as part of the Radiative Divertor modification. Water-cooled vanadium alloy components will comprise a portion of the new upper divertor structure. The first step, procuring the material for this program has been completed. The largest heat of vanadium alloy made to date, 1200 kg of V-4Cr-4Ti, has been produced and is being converted into various product forms. Results of many tests on the material during the manufacturing process are reported. Research into potential fabrication methods has been and continues to be performed along with the assessment of manufacturing processes particularly in the area of joining. Joining of vanadium alloys has been identified as the most critical fabrication issue for their use in the Radiative Divertor Program. Joining processes under evaluation include resistance seam, electrodischarge (stud), friction and electron beam welding. Results of welding tests are reported. Metallography and mechanical tests are used to evaluate the weld samples. The need for a protective atmosphere during different welding processes is also being determined. General Atomics has also designed, manufactured, and will be testing a helium-cooled, high heat flux component to assess the use of helium cooled vanadium alloy components for advanced tokamak systems. The component is made from vanadium alloy tubing, machined to enhance the heat transfer characteristics, and joined to end flanges to allow connection to the helium supply. Results are reported.

  11. Memory Deficit Recovery after Chronic Vanadium Exposure in Mice.

    PubMed

    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.

  12. 77 FR 51825 - Ferrovanadium and Nitrided Vanadium From Russia

    Federal Register 2010, 2011, 2012, 2013, 2014

    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...

  13. Quantitation and detection of vanadium in biologic and pollution materials

    NASA Technical Reports Server (NTRS)

    Gordon, W. A.

    1974-01-01

    A review is presented of special considerations and methodology for determining vanadium in biological and air pollution materials. In addition to descriptions of specific analysis procedures, general sections are included on quantitation of analysis procedures, sample preparation, blanks, and methods of detection of vanadium. Most of the information presented is applicable to the determination of other trace elements in addition to vanadium.

  14. Catalysis science of supported vanadium oxide catalysts.

    PubMed

    Wachs, Israel E

    2013-09-07

    Supported vanadium oxide catalysts contain a vanadium oxide phase deposited on a high surface area oxide support (e.g., Al2O3, SiO2, TiO2, etc.) and have found extensive applications as oxidation catalysts in the chemical, petroleum and environmental industries. This review of supported vanadium oxide catalysts focuses on the fundamental aspects of this novel class of catalytic materials (molecular structures, electronic structures, surface chemistry and structure-reactivity relationships). The molecular and electronic structures of the supported vanadium oxide phases were determined by the application of modern in situ characterization techniques (Raman, IR, UV-vis, XANES, EXAFS, solid state (51)V NMR and isotopic oxygen exchange). The characterization studies revealed that the supported vanadium oxide phase consists of two-dimensional surface vanadia sites dispersed on the oxide supports. Corresponding surface chemistry and reactivity studies demonstrated that the surface vanadia sites are the catalytic active sites for oxidation reactions by supported vanadia catalysts. Combination of characterization and reactivity studies demonstrate that the oxide support controls the redox properties of the surface vanadia sites that can be varied by as much as a factor of ~10(3).

  15. Extraction of vanadium from high calcium vanadium slag using direct roasting and soda leaching

    NASA Astrophysics Data System (ADS)

    Li, Xin-sheng; Xie, Bing

    2012-07-01

    The extraction of vanadium from high calcium vanadium slag was attempted by direct roasting and soda leaching. The oxidation process of the vanadium slag at different temperatures was investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). The effects of roasting temperature, roasting time, Na2CO3 concentration, leaching temperature, leaching time, and liquid to solid ratio on the extraction of vanadium were studied. The results showed that olivine phases and spinel phases in the vanadium slag were completely decomposed at 500 and 800°C, respectively. Vanadium-rich phases were formed at above 850°C. The leaching rate of vanadium reached above 90% under the optimum conditions: roasting temperature of 850°C, roasting time of 60 min, Na2CO3 concentration of 160 g/L, leaching temperature of 95°C, leaching time of 150 min, and liquid to solid ratio of 10:1 mL/g. The main impurities were Si and P in the leach liquor.

  16. Slag remelt purification of irradiated vanadium alloys

    SciTech Connect

    Carmack, W.J.; Smolik, G.R.; McCarthy, K.A.; Gorman, P.K.

    1995-07-01

    This paper describes theoretical and scoping experimental efforts to investigate the decontamination potential of a slag remelting process for decontaminating irradiated vanadium alloys. Theoretical calculations, using a commercial thermochemical computer code HSC Chemistry, determined the potential slag compositions and slag-vanadium alloy ratios. The experiment determined the removal characteristics of four surrogate transmutation isotopes (Ca, Y - to simulate Sc, Mn, and Ar) from a V-5Ti-5Cr alloy with calcium fluoride slag. An electroslag remelt furnace was used in the experiment to melt and react the constituents. The process achieved about a 90 percent removal of calcium and over 99 percent removal of yttrium. Analyses indicate that about 40 percent of the manganese may have been removed. Argon analyses indicates that 99.3% of the argon was released from the vanadium alloy in the first melt increasing to 99.7% during the second melt. Powder metallurgy techniques were used to incorporate surrogate transmutation products in the vanadium. A powder mixture was prepared with the following composition: 90 wt % vanadium, 4.7 wt % titanium, 4.7 wt % chromium, 0.35 wt % manganese, 0.35 wt % CaO, and 0.35 wt % Y{sub 2}O{sub 3}. This mixture was packed into 2.54 cm diameter stainless steel tubes. Argon was introduced into the powder mixture by evacuating and backfilling the stainless steel containers to a pressure of 20 kPa (0.2 atm). The tubes were hot isostatically pressed at 207 MPa (2000 atm) and 1473 K to consolidate the metal. An electroslag remelt furnace (crucible dimensions: 5.1 cm diameter by 15.2 cm length) was used to process the vanadium electrodes. Chemical analyses were performed on samples extracted from the slags and ingots. Ingot analyses results are shown below. Values are shown in percent removal of the four targeted elements of the initial compositions.

  17. Reduction of quinquevalent vanadium solutions by wood and lignite

    USGS Publications Warehouse

    Pommer, A.M.

    1957-01-01

    To determine whether reduced vanadium ores could have been deposited by reduction from supergene quinquevalent vanadium solutions, the reducing capacity of fresh wood, wood degraded by long burial, and lignite was determined experimentally at temperatures of 120?? and 150?? in closed containers. A precipitate obtained by reduction of quinquevalent vanadium solutions with wood gave an X-ray pattern identical with a recently discovered low-valent vanadium mineral. The evidence indicated that deposition of reduced vanadium minerals by this mechanism is possible. ?? 1957.

  18. Vanadium-catalyzed chlorination under molecular oxygen.

    PubMed

    Moriuchi, Toshiyuki; Fukui, Yasuhiro; Kato, Satoshi; Kajikawa, Tomomi; Hirao, Toshikazu

    2015-06-01

    A catalytic chlorination of ketones was performed by using a vanadium catalyst in the presence of Bu4NI and AlCl3 under atmospheric molecular oxygen. This catalytic chlorination could be applied to the chlorination of alkenes to give the corresponding vic-dichlorides. AlCl3 was found to serve as both a Lewis acid and a chloride source to induce the facile chlorination. A combination of Bu4NI and AlI3 in the presence of a vanadium catalyst under atmospheric molecular oxygen induced the iodination of ketones.

  19. Stereospecific formation of dinuclear vanadium(V) tartrato complexes.

    PubMed

    Gáliková, Jana; Schwendt, Peter; Tatiersky, Jozef; Tracey, Alan S; Zák, Zdirad

    2009-09-07

    The first dinuclear nonperoxido tartrato complexes of vanadium(V), (NMe(4))(2)[V(2)O(4)((2R,3R)-H(2)tart)(2)] x 6 H(2)O (1), (NMe(4))(2)[V(2)O(2)((2R,3R)-tart)((2S,3S)-tart)] (2), (NEt(4))(2)[V(2)O(2)((2R,3R)-tart)((2S,3S)-tart)] (3) (tart = tartrato(4-) = C(4)H(2)O(6)(4-)) have been prepared from water-ethanol medium and characterized by X-ray structure analysis and spectral methods. The formation of the complexes has been found to be stereospecific; the composition and structure of anions containing one or both enantiomers of the ligand are profoundly different. The structure of anions in 1-3 also differs significantly from the structure of other dinuclear vanadium(V) alpha-hydroxycarboxylato complexes, but, interestingly, the geometry of the [V(2)O(2)((2R,3R)-tart)((2S,3S)-tart)](2-) ion resembles the structure of the [(VO)(2)((2R,3R)-tart)((2S,3S)-tart)](4-) ion which has a vanadium(IV) center. Using Raman and (51)V NMR spectroscopy the solvent dependent mutual transformations of [V(4)O(8)((2R,3R)-tart)(2)](4-) (V(4)L(2)-RR), [V(4)O(8)((2S,3S)-tart)(2)](4-) (V(4)L(2)-SS), [V(2)O(4)((2R,3R)-H(2)tart)(2)](2-) (V(2)L(2)-RR), [V(2)O(4)((2S,3S)-H(2)tart)(2)](2-) (V(2)L(2)-SS), and [V(2)O(2)((2R,3R)-tart)((2S,3S)-tart)](2-) (V(2)L(2)-rac) have been established. In aqueous solution the following reactions take place; 2 V(2)L(2)-rac --> V(2)L(2)-RR + V(2)L(2)-SS followed by partial decomposition, V(2)L(2)-RR --> V(4)L(2)-RR + 2 L (V(2)L(2)-SS --> V(4)L(2)-SS + 2 L). On the other hand V(2)L(2)-rac is stable in CH(3)CN solution while V(2)L(2)-RR (V(2)L(2)-SS) decomposes into several species.

  20. Vanadium recycling in the United States in 2004

    USGS Publications Warehouse

    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).

  1. Vanadium bioavailability in soils amended with blast furnace slag.

    PubMed

    Larsson, Maja A; Baken, Stijn; Smolders, Erik; Cubadda, Francesco; Gustafsson, Jon Petter

    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(-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.

  2. Synthesis of Polyoxovanadates from Aqueous Solutions

    NASA Astrophysics Data System (ADS)

    Bouhedja, L.; Steunou, N.; Maquet, J.; Livage, J.

    2001-12-01

    Polyoxovanadates have been synthesized from aqueous solutions of VV in the presence of inorganic Na+ and organic [N(CH3)4]+ cations. Decavanadate crystals are precipitated at room temperature around pH 7, whereas layered compounds Na[V3O8].H2O and N(CH3)4[V4O10] are formed at the same pH under hydrothermal conditions. In situ51V NMR experiments show that upon heating solute decavanadate species are progressively transformed into cyclic metavanadates [V4O12]4-. A chemical mechanism is suggested for the formation of these layered vanadium oxides. It involves the ring-opening polymerization of cyclic metavanadates arising from co-ordination expansion favored by protonation or vanadium reduction.

  3. Reduction of Tantalum Pentoxide Using Graphite and Tin-Oxide-Based Anodes via the FFC-Cambridge Process

    NASA Astrophysics Data System (ADS)

    Barnett, Roger; Kilby, Kamal Tripuraneni; Fray, Derek J.

    2009-04-01

    An investigation into the electrochemical reduction of tantalum pentoxide (Ta2O5) to tantalum metal in molten calcium chloride was performed. The oxide was made the cathode, and either graphite or tin oxide rods were selected as the anodes. The experiments were terminated after 8 hours of potentiostatic electrolysis using a two-electrode setup, with the current and anodic potential recorded. The cathode products were analyzed by means of X-ray diffraction, scanning electron microscopy (SEM), and inert-gas fusion analysis. The key result is that tantalum can be produced using either anode, but the tin oxide anode leads to greater current efficiency and a cleaner melt with no significant differences in the product microstructure.

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

    PubMed

    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%.

  5. Distribution of vanadium(V) species between soil and plants in the vicinity of vanadium mine.

    PubMed

    Panichev, N; Mandiwana, K; Moema, D; Molatlhegi, R; Ngobeni, P

    2006-09-21

    The distribution of vanadium(V) species between soil and plants around the vanadium mine have been studied. The mine dam spilled water around this area after collapsing some time ago. V(V) species were determined by electrothermal atomic absorption spectrometry (ETAAS) after leaching of vanadium(V) compounds with 0.1M of Na2CO3, with a limit of detection 0.2 microg g(-1). The validity of V(V) determination had been confirmed by the spike recovery and of the total amount of vanadium by the analysis of CRM's with good correspondence of found to certified values. The concentration of V(V) species were found to be in the range of 620-1680 microg g(-1) in soil and 4-6 microg g(-1) in grass samples, respectively. The total amount of vanadium in soil varied from 1570 to 3600 microg g(-1) and from 8 to 13 microg g(-1) in grass. The results indicate that considerable amount of vanadium (about 50%) in soils and plants is present as V(V) species.

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

    NASA Astrophysics Data System (ADS)

    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%.

  7. Nuclear Magnetic Resonance Studies on Vanadium(IV) Electrolyte Solutions for Vanadium Redox Flow Battery

    SciTech Connect

    Vijayakumar, M.; Burton, Sarah D.; Huang, Cheng; Li, Liyu; Yang, Zhenguo; Graff, Gordon L.; Liu, Jun; Hu, Jian Z.; Skyllas-Kazacos, Maria

    2010-11-15

    The vanadium (IV) electrolyte solutions with various vanadium concentrations are studied by variable temperature 1H and 17O Nuclear Magnetic Resonance (NMR) spectroscopy. The structure and kinetics of vanadium (IV) species in the electrolyte solutions are explored with respect to vanadium concentration and temperature. It was found that the vanadium (IV) species exist as hydrated vanadyl ion, i.e. [VO(H2O)5]2+ forming an octahedral coordination with vanadyl oxygen in the axial position and the remaining positions occupied by water molecules. This hydrated vanadyl ion structure is stable in vanadium concentrations up to 3M and in the temperature range of 240 to 340 K. The sulfate anions in the electrolyte solutions are found to be weekly bound to this hydrated vanadyl ion and occupies its second coordination sphere. The possible effects of these sulfate anions in proton and water exchange between vanadyl ion and solvent molecules are discussed based on 1H and 17O NMR results.

  8. Precipitation and fine structure in medium-carbon vanadium and vanadium/niobium microalloyed steels

    NASA Astrophysics Data System (ADS)

    Thompson, S. W.; Krauss, G.

    1989-11-01

    Hot-rolled and continuously cooled, medium-carbon microalloyed steels containing 0.2 or 0.4 pct C with vanadium (0.15 pct) or vanadium (0.15 pct) plus niobium (0.04 pct) additions were investigated with light and transmission electron microscopy. Energy dispersive spectroscopy in a scanning transmission electron microscope was conducted on precipitates of the 0.4 pct C steel with vanadium and niobium additions. The vanadium steels contained fine interphase precipitates within ferrite, pearlite nodules devoid of interphase precipitates, and fine ferritic transformation twins. The vanadium plus niobium steels contained large Nb-rich precipitates, precipitates which formed in cellular arrays on deformed austenite substructure and contained about equal amounts of niobium and vanadium, and V-rich interphase precipitates. Transformation twins in the ferrite and interphase precipitates in the pearlitic ferrite were not observed in either of the steels containing both microalloying elements. Consistent with the effect of higher C concentrations on driving the microalloying precipitation reactions, substructure precipitation was much more frequently observed in the 0.4C-V-Nb steel than in the 0.2C-V-Nb steel, both in the ferritic and pearlitic regions of the microstructure. Also, superposition of interphase and substructure precipitation was more frequently observed in the high-C-V-Nb steel than in the similar low-C steel.

  9. Vanadium compounds as therapeutic agents: some chemical and biochemical studies.

    PubMed

    Faneca, H; Figueiredo, V A; Tomaz, Isabel; Gonçalves, Gisela; Avecilla, Fernando; Pedroso de Lima, M C; Geraldes, Carlos F G C; Pessoa, João Costa; Castro, M Margarida C A

    2009-04-01

    The behaviour of three vanadium(V) systems, namely the pyridinone (V(V)-dmpp), the salicylaldehyde (V(V)-salDPA) and the pyrimidinone (V(V)-MHCPE) complexes, is studied in aqueous solutions, under aerobic and physiological conditions using (51)V NMR, EPR and UV-Visible (UV-Vis) spectroscopies. The speciations for the V(V)-dmpp and V(V)-salDPA have been previously reported. In this work, the system V(V)-MHCPE is studied by pH-potentiometry and (51)V NMR. The results indicate that, at pH ca. 7, the main species present are (V(V)O(2))L(2) and (V(V)O(2))LH(-1) (L=MHCPE(-)) and hydrolysis products, similar to those observed in aqueous solutions of V(V)-dmpp. The latter species is protonated as the pH decreases, originating (V(V)O(2))L and (V(V)O(2))LH. All the V(V)-species studied are stable in aqueous media with different compositions and at physiological pH, including the cell culture medium. The compounds were screened for their potential cytotoxic activity in two different cell lines. The toxic effects were found to be incubation time and concentration dependent and specific for each compound and type of cells. The HeLa tumor cells seem to be more sensitive to drug effects than the 3T3-L1 fibroblasts. According to the IC(50) values and the results on reversibility to drug effects, the V(V)-species resulting from the V(V)-MHCPE system show higher toxicity in the tumor cells than in non-tumor cells, which may indicate potential antitumor activity.

  10. Posttranslational modification of a vanadium nitrogenase.

    PubMed

    Heiniger, Erin K; Harwood, Caroline S

    2015-08-01

    In microbes that fix nitrogen, nitrogenase catalyzes the conversion of N2 to ammonia in an ATP-demanding reaction. To help conserve energy some bacteria inhibit nitrogenase activity upon exposure to ammonium. The purple nonsulfur phototrophic bacterium Rhodopseudomonas palustris strain CGA009 can synthesize three functional nitrogenase isoenzymes: a molybdenum nitrogenase, a vanadium nitrogenase, and an iron nitrogenase. Previous studies showed that in some alphaproteobacteria, including R. palustris, molybdenum nitrogenase activity is inhibited by ADP-ribosylation when cells are exposed to ammonium. Some iron nitrogenases are also posttranslationally modified. However, the posttranslational modification of vanadium nitrogenase has not been reported. Here, we investigated the regulation of the alternative nitrogenases of R. palustris and determined that both its vanadium nitrogenase and its iron nitrogenase activities were inhibited and posttranslationally modified when cells are exposed to ammonium. Vanadium nitrogenase is not found in all strains of R. palustris, suggesting that it may have been acquired by horizontal gene transfer. Also, phylogenetic analyses of the three nitrogenases suggest that VnfH, the target of ADP-ribosylation, may be the product of a gene duplication of nifH, the molybdenum nitrogenase homolog.

  11. Vanadium concentrations in settled outdoor dust particles.

    PubMed

    Dundar, Mustafa S

    2006-12-01

    Atmospheric dustfall is an important aspect of urban dust studies. Vanadium is considered as the marker element of air pollution emitted from residual oil and coal combustion. In this study, vanadium levels of outdoor dust particles are determined. The studied area covers the six sites located in Adapazarí (Turkey), which represents an earthquake-hit environment. The mass deposition rate was calculated for each sampling plate over the 30-days collection periods. The deposition rates for the six places in Adapazarí ranged from 20.5 to 84.9 microg/cm2/day. The arithmetic mean deposition rate for all places was 45.3 microg/cm2/day. Total dust deposition and vanadium loadings typically increased in magnitude according to the area order: Kampus > Serdivan > Cark C. > Ozanlar > Erenler > Yeşiltepe and Kampus > Serdivan > Cark C. > Ozanlar > Erenler > Yeşiltepe, respectively. The results suggested that vanadium may be useful for assessing the level of environmental pollution.

  12. Catalytic determination of vanadium in water

    USGS Publications Warehouse

    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.

  13. Geochemistry of vanadium (V) in Chinese coals.

    PubMed

    Liu, Yuan; Liu, Guijian; Qu, Qinyuan; Qi, Cuicui; Sun, Ruoyu; Liu, Houqi

    2016-10-11

    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.

  14. Large-scale production of anhydrous nitric acid and nitric acid solutions of dinitrogen pentoxide

    DOEpatents

    Harrar, Jackson E.; Quong, Roland; Rigdon, Lester P.; McGuire, Raymond R.

    2001-01-01

    A method and apparatus are disclosed for a large scale, electrochemical production of anhydrous nitric acid and N.sub.2 O.sub.5. The method includes oxidizing a solution of N.sub.2 O.sub.4 /aqueous-HNO.sub.3 at the anode, while reducing aqueous HNO.sub.3 at the cathode, in a flow electrolyzer constructed of special materials. N.sub.2 O.sub.4 is produced at the cathode and may be separated and recycled as a feedstock for use in the anolyte. The process is controlled by regulating the electrolysis current until the desired products are obtained. The chemical compositions of the anolyte and catholyte are monitored by measurement of the solution density and the concentrations of N.sub.2 O.sub.4.

  15. Speciation of vanadium in Chinese cabbage (Brassica rapa L.) and soils in response to different levels of vanadium in soils and cabbage growth.

    PubMed

    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.

  16. Large area graphene ion sensitive field effect transistors with tantalum pentoxide sensing layers for pH measurement at the Nernstian limit

    SciTech Connect

    Fakih, Ibrahim Sabri, Shadi; Szkopek, Thomas; Mahvash, Farzaneh; Nannini, Matthieu; Siaj, Mohamed

    2014-08-25

    We have fabricated and characterized large area graphene ion sensitive field effect transistors (ISFETs) with tantalum pentoxide sensing layers and demonstrated pH sensitivities approaching the Nernstian limit. Low temperature atomic layer deposition was used to deposit tantalum pentoxide atop large area graphene ISFETs. The charge neutrality point of graphene, inferred from quantum capacitance or channel conductance, was used to monitor surface potential in the presence of an electrolyte with varying pH. Bare graphene ISFETs exhibit negligible response, while graphene ISFETs with tantalum pentoxide sensing layers show increased sensitivity reaching up to 55 mV/pH over pH 3 through pH 8. Applying the Bergveld model, which accounts for site binding and a Guoy-Chapman-Stern picture of the surface-electrolyte interface, the increased pH sensitivity can be attributed to an increased buffer capacity reaching up to 10{sup 14} sites/cm{sup 2}. ISFET response was found to be stable to better than 0.05 pH units over the course of two weeks.

  17. Electronic, thermoelectric and optical properties of vanadium oxides: VO2, V2O3 and V2O 5

    NASA Astrophysics Data System (ADS)

    Lamsal, Chiranjivi

    Correlated electrons in vanadium oxides are responsible for their extreme sensitivity to external stimuli such as pressure, temperature or doping. As a result, several vanadium oxides undergo insulator-to-metal phase transition (IMT) accompanied by structural change. Unlike vanadium pentoxide (V2O5), vanadium dioxide (VO2) and vanadium sesquioxide (V2O3) show IMT in their bulk phases. In this study, we have performed one electron Kohn-Sham electronic band-structure calculations of VO2, V2O3 and V2O 5 in both metallic and insulating phases, implementing a full ab-initio simulation package based on Density Functional Theory (DFT), Plane Waves and Pseudopotentials (PPs). Electronic band structures are found to be influenced by crystal structure, crystal field splitting and strong hybridization between O2p and V3d bands. "Intermediate bands", with narrow band widths, lying just below the higher conduction bands, are observed in V2O 5 which play a critical role in optical and thermoelectric processes. Similar calculations are performed for both metallic and insulating phases of bulk VO2 and V2O3. Unlike in the metallic phase, bands corresponding to "valence electrons" considered in the PPs are found to be fully occupied in the insulating phases. Transport parameters such as Seebeck coefficient, electrical conductivity and thermal (electronic) conductivity are studied as a function of temperature at a fixed value of chemical potential close to the Fermi energy using Kohn-Sham band structure approach coupled with Boltzmann transport equations. Because of the layered structure and stability, only V2O5 shows significant thermoelectric properties. All the transport parameters have correctly depicted the highly anisotropic electrical conduction in V2O 5. Maxima and crossovers are also seen in the temperature dependent variation of Seebeck coefficient in V2O5, which can be consequences of "specific details" of the band structure and anisotropic electron-phonon interactions

  18. Vanadium oxide electrode synthesized by electroless deposition for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Wu, Haoran; Lian, Keryn

    2014-12-01

    A thin film vanadium oxide electrode was synthesized by a simple electroless deposition method. Surface and structural analyses revealed that the deposited oxide is a mixture of amorphous V2O5 and VO2. Electrochemical characterizations of the synthesized vanadium oxide showed capacitive behavior with good cycle life. The electroless deposition of vanadium oxide is inexpensive, easy to process, and environmentally benign, offering a promising route for electrode development for electrochemical capacitors.

  19. Modified lithium vanadium oxide electrode materials products and methods

    DOEpatents

    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.

  20. Effect of vanadium compounds on acid phosphatase activity.

    PubMed

    Vescina, C M; Sálice, V C; Cortizo, A M; Etcheverry, S B

    1996-01-01

    The direct effect of different vanadium compounds on acid phosphatase (ACP) activity was investigated. Vanadate and vanadyl but not pervanadate inhibited the wheat germ ACP activity. These vanadium derivatives did not alter the fibroblast Swiss 3T3 soluble fraction ACP activity. Using inhibitors of tyrosine phosphatases (PTPases), the wheat germ ACP was partially characterized as a PTPase. This study suggests that the inhibitory ability of different vanadium derivatives to modulate ACP activity seems to depend on the geometry around the vanadium atom more than on the oxidation state. Our results indicate a correlation between the PTPase activity and the sensitivity to vanadate and vanadyl cation.

  1. Vanadium bioavailability and toxicity to soil microorganisms and plants.

    PubMed

    Larsson, Maja A; Baken, Stijn; Gustafsson, Jon Petter; Hadialhejazi, Golshid; Smolders, Erik

    2013-10-01

    Vanadium, V, is a redox-sensitive metal that in solution, under aerobic conditions, prevails as the oxyanion vanadate(V). There is little known regarding vanadium toxicity to soil biota, and the present study was set up to determine the toxicity of added vanadate to soil organisms and to investigate the relationship between toxicity and vanadium sorption in soils. Five soils with contrasting properties were spiked with 7 different doses (3.2-3200 mg V kg(-1)) of dissolved vanadate, and toxicity was measured with 2 microbial and 3 plant assays. The median effective concentration (EC50) thresholds of the microbial assays ranged from 28 mg added V kg(-1) to 690 mg added V kg(-1), and the EC50s in the plant assays ranged from 18 mg added V kg(-1) to 510 mg added V kg(-1). The lower thresholds were in the concentration range of the background vanadium in the untreated control soils (15-58 mg V kg(-1)). The vanadium toxicity to plants decreased with a stronger soil vanadium sorption strength. The EC50 values for plants expressed on a soil solution basis ranged from 0.8 mg V L(-1) to 15 mg V L(-1) and were less variable among soils than corresponding values based on total vanadium in soil. It is concluded that sorption decreases the toxicity of added vanadate and that soil solution vanadium is a more robust measure to determine critical vanadium concentrations across soils.

  2. Controlled coordination in vanadium(V) dimethylhydrazido compounds.

    PubMed

    Sakuramoto, Takashi; Moriuchi, Toshiyuki; Hirao, Toshikazu

    2016-11-01

    The vanadium(V) dimethylhydrazido compounds were structurally characterized to elucidate the effect of the alkoxide ligands in the coordination environment of vanadium(V) hydrazido center. The single-crystal X-ray structure determination of the vanadium(V) dimethylhydrazido compound with isopropoxide ligands revealed a dimeric structure with the V(1)-N(1) distance of 1.680(5)Å, in which each vanadium atom is coordinated in a distorted trigonal-bipyramidal geometry (τ5=0.81) with the hydrazido and bridging isopropoxide ligands in the apical positions. On the contrary, nearly tetrahedral arrangement around the vanadium metal center (τ4=0.06) with the V(1)-N(1) distance of 1.660(2)Å was observed in the vanadium(V) dimethylhydrazido compound with tert-butoxide ligands. The introduction of the 2,2',2″-nitrilotriethoxide ligand led to a pseudo-trigonal-bipyramidal geometry (τ5=0.92) at the vanadium center with the V(1)-N(1) distance of 1.691(5)Å, wherein vanadium atom is pulled out of the plane formed by the nitrilotriethoxide oxygen atoms in the direction of the hydrazido nitrogen. The coordination from the apical ligand in the vanadium(V) dimethylhydrazido compound was found to result in the longer V(1)-N(1) distance.

  3. Investigation on vanadium oxide thin films deposited by spray pyrolysis technique

    NASA Astrophysics Data System (ADS)

    Margoni, Mudaliar Mahesh; Mathuri, S.; Ramamurthi, K.; Babu, R. Ramesh; Sethuraman, K.

    2016-05-01

    Vanadium oxide thin films were deposited at 400 °C by spray pyrolysis technique using 0.1 M aqueous precursor solution of ammonium meta vanadate (AMV) with two different pH values. X-ray diffraction results showed that the film prepared using aqueous precursor AMV solution (solution A; pH 7) is amorphous in nature and the film prepared by adding HNO3 in the AMV aqua solution A (solution B; pH 3) is polycrystalline in nature. Vanadium oxide film prepared from the precursor solution B is in the mixed phases of V2O5 and V4O7. Crystallinity is improved for the film prepared using solution B when compared to film prepared from solution A. Crystallite size, strain and dislocation density calculated for the film prepared from solution B is respectively 72.1 nm, 0.4554 × 10-3 lin.-2m-4 and 1.7263 × 1014 lin.m-2. Morphology study revealed that the size of the flakes formed on the surface of the films is influenced by the pH of the precursor solution. Average Visible Transmittance and maximum transmittance of the deposited films exceed 70% and the direct optical band gap value calculated for the films deposited from A and B solution is 1.91 eV and 2.08 eV respectively.

  4. Irradiation creep of vanadium-base alloys

    SciTech Connect

    Tsai, H.; Billone, M.C.; Strain, R.V.; Smith, D.L.; Matsui, H.

    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.

  5. Cytotoxicity of Exfoliated Layered Vanadium Dichalcogenides.

    PubMed

    Latiff, Naziah Mohamad; Sofer, Zdeněk; Fisher, Adrian C; Pumera, Martin

    2017-01-12

    Transition-metal Group 5 vanadium dichalcogenides have shown promising properties for many applications, such as batteries, capacitors, electrocatalysts for hydrogen production and many more. However, their toxicological effects have not yet been well understood. Here, we studied the cytotoxicity of exfoliated VS2 , VSe2 and VTe2 by incubating various concentrations of the materials with human lung carcinoma (A549) cells for 24 h and measuring the remaining cell viabilities after the treatment. We found that these vanadium dichalcogenides are relatively more toxic compared to Group 6 transition-metal dichalcogenides (TMDs), namely MoS2 , WS2 and WSe2 . This study is important for a better understanding of the toxicity of TMDs in preparation for their actual commercialisation in the future.

  6. Oxygen diffusion in vanadium-based alloys

    SciTech Connect

    de Avillez, R.R.

    1981-01-01

    The experimental study of transport and equilibrium properties of oxygen in vanadium-based alloys was made by EMF measurements on solid electrolytic cells over the temperature range of 873 to 1423/sup 0/K. The oxygen diffusion in vanadium was not significantly modified by small additions of Ti, Cr, Ni, Nb and Ta. The increase in the activation energy for oxygen diffusion in the V-based alloys containing Cr, Ni, Nb and Ta probably reflects the effect of these substitutional solutes on the activity coefficient of oxygen. The oxygen activity was increased by the addition of 1 at % of Cr, Ni and Nb, and decreased by the addition of Ti and Ta. However, the effects in the alloys containing Nb and Ta are very small.

  7. Activation of Janus kinase/signal transducers and activators of transcription pathway involved in megakaryocyte proliferation induced by vanadium resembles some aspects of essential thrombocythemia.

    PubMed

    Gonzalez-Villalva, Adriana; Piñon-Zarate, Gabriela; Falcon-Rodriguez, Carlos; Lopez-Valdez, Nelly; Bizarro-Nevares, Patricia; Rojas-Lemus, Marcela; Rendon-Huerta, Erika; Colin-Barenque, Laura; Fortoul, Teresa I

    2016-05-01

    Vanadium (V) is an air pollutant released into the atmosphere by burning fossil fuels. Also, it has been recently evaluated for their carcinogenic potential to establish permissible limits of exposure at workplaces. We previously reported an increase in the number and size of platelets and their precursor cells and megakaryocytes in bone marrow and spleen. The aim of this study was to identify the involvement of Janus kinase/signal transducers and activators of transcription (JAK/STAT) pathway and thrombopoietin (TPO) receptor, and myeloproliferative leukemia virus oncogene (Mpl), in megakaryocyte proliferation induced by this compound. Mice were exposed twice a week to vanadium pentoxide inhalation (0.02 M) and were killed at 4th, 6th, and 8th week of exposure. Phosphorylated JAK2 (JAK2 ph), STAT3 (STAT3 ph), STAT5, and Mpl were identified in mice spleen megakaryocytes by cytofluorometry and immunohistochemistry. An increase in JAK2 ph and STAT3 ph, but a decrease in Mpl at 8-week exposure was identified in our findings. Taking together, we propose that the morphological findings, JAK/STAT activation, and decreased Mpl receptor induced by V leads to a condition comparable to essential thrombocythemia, so the effect on megakaryocytes caused by different mechanisms is similar. We also suggest that the decrease in Mpl is a negative feedback mechanism after the JAK/STAT activation. Since megakaryocytes are platelet precursors, their alteration affects platelet morphology and function, which might have implications in hemostasis as demonstrated previously, so it is important to continue evaluating the effects of toxics and pollutants on megakaryocytes and platelets.

  8. Is vanadium a biometal for boreal cyanolichens?

    PubMed

    Darnajoux, Romain; Constantin, Jérôme; Miadlikowska, Jolanta; Lutzoni, François; Bellenger, Jean-Philippe

    2014-05-01

    Molybdenum (Mo) nitrogenase has long been considered the predominant isoenzyme responsible for dinitrogen fixation worldwide. Recent findings have challenged the paradigm of Mo hegemony, and highlighted the role of alternative nitrogenases, such as the vanadium-nitrogenase. Here, we first characterized homeostasis of vanadium (V) along with other metals in situ in the dinitrogen fixing cyanolichen Peltigera aphthosa. These lichens were sampled in natural sites exposed to various levels of atmospheric metal deposition. These results were compared with laboratory experiments where Anabaena variabilis, which is also hosting the V-nitrogenase, and a relatively close relative of the lichen cyanobiont Nostoc, was subjected to various levels of V. We report here that V is preferentially allocated to cephalodia, specialized structures where dinitrogen fixation occurs in tri-membered lichens. This specific allocation is biologically controlled and tightly regulated. Vanadium homeostasis in lichen cephalodia exposed to various V concentrations is comparable to the one observed in Anabaena variabilis and other dinitrogen fixing organisms using V-nitrogenase. Overall, our findings support current hypotheses that V could be a more important factor in mediating nitrogen input in high latitude ecosystems than previously recognized. They invite the reassessment of current theoretical models linking metal dynamics and dinitrogen fixation in boreal and subarctic ecosystems.

  9. A method for the determination of vanadium and iron oxidation states in naturally occurring oxides and silicates

    USGS Publications Warehouse

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

    1985-01-01

    A valence-specific analytical method for determining V3+ in ore minerals has been developed that involves two steps: dissolution of a mineral sample without disturbing the V3+/Vtot ratio, followed by determination of V3+ in the presence of V4+. The samples are dissolved in a mixture of hydrofluoric and sulphuric acids at 100?? in Teflon-lined reaction vessels. Tervalent vanadium is then determined colorimetrically by formation of a V3+-thiocyanate complex in aqueous-acetone medium. Fe3+ is measured semi-quantitatively in the same solution. The method has been tested with two naturally occurring samples containing vanadium and iron. The results obtained were supported by those obtained by other methods, including electron spin resonance spectroscopy, thermogravimetric analysis, and Mo??ssbauer spectroscopy. ?? 1985.

  10. A method for the determination of vanadium and iron oxidation states in naturally occurring oxides and silicates.

    PubMed

    Wanty, R B; Goldhaber, M B

    1985-05-01

    A valence-specific analytical method for determining V(3+) in ore minerals has been developed that involves two steps: dissolution of a mineral sample without disturbing the V(3+)/V(tot) ratio, followed by determination of V(3+) in the presence of V(4+). The samples are dissolved in a mixture of hydrofluoric and sulphuric acids at 100 degrees in Teflon-lined reaction vessels. Tervalent vanadium is then determined colorimetrically by formation of a V(3+)-thiocyanate complex in aqueous-acetone medium. Fe(3+) is measured semi-quantitatively in the same solution. The method has been tested with two naturally occurring samples containing vanadium and iron. The results obtained were supported by those obtained by other methods, including electron spin resonance spectroscopy, thermogravimetric analysis, and Mössbauer spectroscopy.

  11. Reduction of vanadium(V) with Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans.

    PubMed

    Bredberg, Katarina; Karlsson, Hans T; Holst, Olle

    2004-03-01

    Biotechnological leaching has been proposed as a suitable method for extraction of vanadium from spent catalysts and oil ash. In the biological leaching process, the vanadium(V) can be reduced to vanadium(IV), which is a less toxic and more soluble form of the vanadium. The present investigation showed that Acidithiobacillus ferrooxidans efficiently reduced vanadium(V) in the form of vanadium pentaoxide, to vanadyl(IV) ions, and tolerated high concentrations of vanadium(IV) and vanadium(V). A. ferrooxidans was compared with Acidithiobacillus thiooxidans, which has previously been utilized for vanadium leaching and reduction. Vanadium pentaoxide and sodium vanadate were used as model compounds. The results of this study indicate possibilities to develop an economical and technically feasible process for biotechnological vanadium recovery.

  12. Mechanical mixtures of metal oxides and phosphorus pentoxide as novel precursors for the synthesis of transition-metal phosphides.

    PubMed

    Guo, Lijuan; Zhao, Yu; Yao, Zhiwei

    2016-01-21

    This study presents a new type of precursor, mechanical mixtures of metal oxides (MOs) and phosphorus pentoxide (P2O5) are used to synthesize Ni2P, Co2P and MoP phosphides by the H2 reduction method. In addition, this is first report of common solid-state P2O5 being used as a P source for the synthesis of metal phosphides. The traditional precursors are usually prepared via a complicated preparation procedure involving dissolution, drying and calcination steps. However, these novel MOs/P2O5 precursors can be obtained only by simple mechanical mixing of the starting materials. Furthermore, unlike the direct transformation from amorphous phases to phosphides, various specific intermediates were involved in the transformation from MOs/P2O5 to phosphides. It is worthy to note that the dispersions of Ni2P, Co2P and MoP obtained from MOs/P2O5 precursors were superior to those of the corresponding phosphides prepared from the abovementioned traditional precursors. It is suggested that the morphology of the as-prepared metal phosphides might be inherited from the corresponding MOs. Based on the results of XRD, XPS, SEM and TEM, the formation pathway of phosphides can be defined as MOs/P2O5 precursors → complex intermediates (metals, metal phosphates and metal oxide-phosphates) → metal phosphides.

  13. A well-defined terminal vanadium(III) oxo complex.

    PubMed

    King, Amanda E; Nippe, Michael; Atanasov, Mihail; Chantarojsiri, Teera; Wray, Curtis A; Bill, Eckhard; Neese, Frank; Long, Jeffrey R; Chang, Christopher J

    2014-11-03

    The ubiquity of vanadium oxo complexes in the V+ and IV+ oxidation states has contributed to a comprehensive understanding of their electronic structure and reactivity. However, despite being predicted to be stable by ligand-field theory, the isolation and characterization of a well-defined terminal mononuclear vanadium(III) oxo complex has remained elusive. We present the synthesis and characterization of a unique terminal mononuclear vanadium(III) oxo species supported by the pentadentate polypyridyl ligand 2,6-bis[1,1-bis(2-pyridyl)ethyl]pyridine (PY5Me2). Exposure of [V(II)(NCCH3)(PY5Me2)](2+) (1) to either dioxygen or selected O-atom-transfer reagents yields [V(IV)(O)(PY5Me2)](2+) (2). The metal-centered one-electron reduction of this vanadium(IV) oxo complex furnishes a stable, diamagnetic [V(III)(O)(PY5Me2)](+) (3) species. The vanadium(III) oxo species is unreactive toward H- and O-atom transfer but readily reacts with protons to form a putative vanadium hydroxo complex. Computational results predict that further one-electron reduction of the vanadium(III) oxo species will result in ligand-based reduction, even though pyridine is generally considered to be a poor π-accepting ligand. These results have implications for future efforts toward low-valent vanadyl chemistry, particularly with regard to the isolation and study of formal vanadium(II) oxo species.

  14. Powder metallurgy of vanadium and its alloys (review)

    SciTech Connect

    Radomysel'skii, I.D.; Solntsev, V.P.; Evtushenko, O.V.

    1987-10-01

    This article reviews the current powder metallurgy technology of vanadium and its alloys. Data are given on sintering, compacting, electrowinning and other current production techniques, as well as on the corrosion behavior and mechanical and physical properties of alloys produced by these different methods. The use of vanadium alloys as reactor and jet engine materials is also briefly discussed.

  15. Vanadium-pumped titanium x-ray laser

    DOEpatents

    Nilsen, Joseph

    1992-01-01

    A resonantly photo-pumped x-ray laser (10) is formed of a vanadium (12) and titanium (14) foil combination (16) that is driven by two beams (18, 20) of intense line focused (22, 24) optical laser radiation. Ground state neon-like titanium ions (34) are resonantly photo-pumped by line emission from fluorine-like vanadium ions (32).

  16. Vanadium-pumped titanium x-ray laser

    DOEpatents

    Nilsen, J.

    1992-05-26

    A resonantly photo-pumped x-ray laser is formed of a vanadium and titanium foil combination that is driven by two beams of intense line focused optical laser radiation. Ground state neon-like titanium ions are resonantly photo-pumped by line emission from fluorine-like vanadium ions. 4 figs.

  17. Anion-conductive membranes with ultralow vanadium permeability and excellent performance in vanadium flow batteries.

    PubMed

    Mai, Zhensheng; Zhang, Huamin; Zhang, Hongzhang; Xu, Wanxing; Wei, Wenping; Na, Hui; Li, Xianfeng

    2013-02-01

    Anion exchange membranes prepared from quaternized poly(tetramethyl diphenyl ether sulfone) (QAPES) were first investigated in the context of vanadium flow battery (VFB) applications. The membranes showed an impressive suppression effect on vanadium ions. The recorded vanadium permeability was 0.02×10(-7)-0.09×10(-7) cm(2) min(-1), which was two orders of magnitude lower than that of Nafion 115. The self-discharge duration of a VFB single cell with a QAPES membrane is four times longer than that of Nafion 115. The morphological difference in hydrophilic domains between QAPES and Nafion was confirmed by TEM. After soaking the membranes in VO(2)(+) solution, adsorbed vanadium ions can barely be found in QAPES, whereas the hydrophilic domains of Nafion were stained. In the ex situ chemical stability test, QAPES showed a high tolerance to VO(2)(+) and remained intact after immersion in VO(2)(+) solution for over 250 h. The performance of a VFB single cell assembled with QAPES membranes is equal to or even better than that of Nafion 115 and remains stable in a long-term cycle test. These results indicate that QAPES membranes can be an ideal option in the fabrication of high-performance VFBs with low electric capacity loss.

  18. Nitriding process for the recovery of vanadium from ferrovanadium

    SciTech Connect

    Singh, K.; Suri, A.K.; Gupta, C.K.

    1996-10-01

    A three step process based on nitriding-leaching-pyrovacuum decomposition has been developed to prepare vanadium-nitrogen alloy from ferro-vanadium. Recent investigations in the laboratory have shown that pure vanadium can be contained from such an alloy by fused salt electrorefining. The process essentially involves nitriding of ferrovanadium powder with ammonia at 950--1,000 C. Nitrided ferroalloy was then leached with 2N HCl at 50 C to leach out iron nitrides. The residue analyzing 2.1% Fe and 15.5% N was then treated at 1,550 C under a dynamic vacuum of 0.3 m torr to yield vanadium-nitrogen alloy analyzing about 5.76% N and 0.28% C. Adopting this process a few hundred grams of V-N alloy has been prepared for use as soluble anode in fused salt electrorefining cell to prepare vanadium metal.

  19. Vanadium Compounds as Pro-Inflammatory Agents: Effects on Cyclooxygenases

    PubMed Central

    Korbecki, Jan; Baranowska-Bosiacka, Irena; Gutowska, Izabela; Chlubek, Dariusz

    2015-01-01

    This paper discusses how the activity and expression of cyclooxygenases are influenced by vanadium compounds at anticancer concentrations and recorded in inorganic vanadium poisonings. We refer mainly to the effects of vanadate (orthovanadate), vanadyl and pervanadate ions; the main focus is placed on their impact on intracellular signaling. We describe the exact mechanism of the effect of vanadium compounds on protein tyrosine phosphatases (PTP), epidermal growth factor receptor (EGFR), PLCγ, Src, mitogen-activated protein kinase (MAPK) cascades, transcription factor NF-κB, the effect on the proteolysis of COX-2 and the activity of cPLA2. For a better understanding of these processes, a lot of space is devoted to the transformation of vanadium compounds within the cell and the molecular influence on the direct targets of the discussed vanadium compounds. PMID:26053397

  20. Metabolic problems in northeastern Thailand: possible role of vanadium.

    PubMed

    Sitprija, V; Tungsanga, K; Tosukhowong, P; Leelhaphunt, N; Kruerklai, D; Sriboonlue, P; Saew, O

    1993-01-01

    Common metabolic problems in northeastern Thailand include renal stone disease, distal renal tubular acidosis, hypokalemic periodic paralysis, sudden unexplained nocturnal death and malnutrition-related diabetes mellitus. There is evidence of decreased activity of Na,K-ATPase and H,K-ATPase. A preliminary study was made of the vanadium concentration in the soil and water in northeastern Thailand. The urinary and tissue vanadium concentrations were also determined in the northeastern villagers. The soil was found to have high vanadium content. The vanadium content was also high in the urine, kidneys and lungs of the villagers. It is postulated that these metabolic problems are attributed to the inhibition of Na,K-ATPase and H,K-ATPase activity by vanadium.

  1. Chemistry related to the procurement of vanadium alloys

    SciTech Connect

    Smith, H.M.; Chung H.M.; Tsai, H.C.

    1997-08-01

    Evaluation of trace element concentrations in vanadium alloys is important to characterize the low-activation characteristics and possible effects of trace elements on the properties. Detailed chemical analysis of several vanadium and vanadium alloy heats procured for the Argonne vanadium alloy development program were analyzed by Johnson-Matthey (UK) as part of a joint activity to evaluate trace element effects on the performance characteristics. These heats were produced by normal production practices for high grade vanadium. The analyses include approximately 60 elements analyzed in most cases by glow-discharge mass spectrometry. Values for molybdenum and niobium, which are critical for low-activation alloys, ranged from 0.4 to 60 wppm for the nine heats.

  2. Recent progress on gas tungsten arc welding of vanadium alloys

    SciTech Connect

    King, J.F.; Grossbeck, M.L.; Goodwin, G.M.; Alexander, D.J.

    1997-04-01

    This is a progress report on a continuing research project to acquire a fundamental understanding of the metallurgical processes in the welding of vanadium alloys. It also has the goal of developing techniques for welding structural vanadium alloys. The alloy V-4Cr-4Ti is used as a representative alloy of the group; it is also the prime candidate vanadium alloy for the U.S. Fusion Program at the present time. However, other alloys of this class were used in the research as necessary. The present work focuses on recent findings of hydrogen embrittlement found in vanadium alloy welds. It was concluded that the atmosphere in the inert gas glove box was insufficient for welding 6mm thick vanadium alloy plates.

  3. 77 FR 54897 - Ferrovanadium and Nitrided Vanadium from the Russian Federation: Revocation of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-09-06

    ... International Trade Administration Ferrovanadium and Nitrided Vanadium from the Russian Federation: Revocation...), that revocation of the antidumping duty order on ferrovanadium and nitrided vanadium from the Russian... nitrided vanadium from Russia. \\1\\ See Ferrovanadium and Nitrided Vanadium From Russia, 77 FR 51825...

  4. Anomalous negative resistance in superconducting vanadium nanowires

    NASA Astrophysics Data System (ADS)

    Jorritsma, J.; Mydosh, J. A.

    2000-10-01

    Low-temperature electrical transport measurements were performed on large arrays of 150-nm-wide superconducting vanadium (V) wires covered with either a thin layer of Au (V/Au) or Fe (V/Fe). The measurements were conducted using various electrical contact geometries. Our results show that a particular arrangement of the electrical contacts in combination with the superconducting proximity effect can result in a pronounced ``negative resistance'' anomaly below the resistive transition. We demonstrate that this ``negative resistance'' can be clearly reproduced by constructing resistor circuits based upon the particular contact arrangement.

  5. Photoinduced heterostructure in a vanadium dioxide film

    NASA Astrophysics Data System (ADS)

    Semenov, A. L.

    2017-02-01

    A photoinduced semiconductor-metal phase transition that occurs in a surface layer of vanadium dioxide film on an aluminum substrate within the time Δ t < 1 ps has been studied theoretically. A nonthermal mechanism of the development of instability has been considered. It has been shown that a heterophase structure containing metallic and semiconductor layers is formed in the VO2 film. The phase transition time τ has been calculated as a function of the distance z from the film surface. Comparison with the experiment has been carried out.

  6. Observations of Dinitrogen Pentoxide and Nitryl Chloride at two inland sites in North China: Abundances, Origins, and Impact on Photochemistry

    NASA Astrophysics Data System (ADS)

    LI, Q.; Xue, L.; Tham, Y. J.; Wang, W.; Yun, H.; Wang, T.; Wang, Z.; Wang, X.; Zhang, L.; Yao, L.; Wen, L.; Lu, K.; Zhang, Y.; Wang, W.

    2015-12-01

    Dinitrogen pentoxide (N2O5) and nitryl chloride (ClNO2) are key players in the nocturnal tropospheric chemistry, and also have potential to perturb the next-day's photochemistry. We here present the first ambient measurements of N2O5 and ClNO2 in inland regions of northern China, which is suffering from severe photochemical smog and haze pollution. A chemical ionization mass spectrometer (CIMS) was deployed at a semi-rural site in Wangdu, Hebei and on the top of Mt Tai, Shandong (1500 m a.s.l.) during the summer of 2014. At Wangdu, significant levels of ClNO2 were observed persistently throughout the campaign, with the maximum concentration of up to 2.1 ppbv (1-min data). N2O5 were generally in small concentrations but on few occasions reached up to hundreds of pptv. Clear variation of ClNO2 and N2O5 from night to night suggests the variability of N2O5 heterogeneous reactivity under different conditions over the region. On the mountain-top, elevated ClNO2-laden plumes were frequently observed around mid-night with a 1-min maximum of 2.1 ppbv, whilst N2O5 was always in very low levels indicating a fast N2O5 hydrolysis. The elevated ClNO2 levels at both locations were significantly influenced by the high NOx-saturated urban plumes and non-oceanic sources of chloride like biomass burning and coal-fired power plants in the region. MCM (Master Chemical Mechanism) modeling analyses indicate the significance of ClNO2 photolysis to the daytime radical and ozone production. Our study implies that the N2O5 reactivity and chlorine activation are significant in North China, and should be also important in other non-marine regions of China where NOx and particle chloride are in great abundances.

  7. Essentiality and toxicity of vanadium supplements in health and pathology.

    PubMed

    Gruzewska, K; Michno, A; Pawelczyk, T; Bielarczyk, H

    2014-10-01

    The biological properties of vanadium complexes have become an object of interest due to their therapeutic potential in several diseases. However, the mechanisms of action of vanadium salts are still poorly understood. Vanadium complexes are cofactors for several enzymes and also exhibit insulin-mimetic properties. Thus, they are involved in the regulation of glucose metabolism, including in patients with diabetes. In addition, vanadium salts may also normalize blood pressure and play a key role in the metabolism of the thyroid and of iron as well as in the regulation of total cholesterol, cholesterol HDL and triglyceride (TG) levels in blood. Moreover, in cases of hypoxia, vanadium compounds may improve cardiomyocytes function. They may also exhibit both carcinogenic and anti-cancer properties. These include dose- and exposure-time-dependent induction and inhibition of the proliferation and survival of cancer cells. On the other hand, the balance between vanadium's therapeutic properties and its side effects has not yet been determined. Therefore, any studies on the potential use of vanadium compounds as supplements to support the treatment of a number of diseases must be strictly monitored for adverse effects.

  8. Vanadium grossular from the Mozambique metamorphic rocks, south Kenya

    NASA Astrophysics Data System (ADS)

    Suwa, Kanenori; Suzuki, Kazuhiro; Agata, Takashi

    Green vanadium grossulars occur as porphyroblasts in calc-silicate-graphite gneiss associated with marble, pelitic-psammitic gneiss and granitoid gneiss in the Mozambique metamorphic belt, south Kenya. Calc-silicate-graphite gneiss contains scapolite, vanadian zoisite, vanadian diopside, vanadian sphene and vanadian magnetite, in addition to vanadium grossular. The vanadium grossular porphyroblasts are mantled by a kelyphitic rim that consists mainly of symplectic intergrowth of fine-grained scapolite, vanadium grossular, vanadian diopside, vanadian sphene, vanadian magnetite, plagioclase, calcite and quartz. Vanadian minerals (vanadian muscovite, vanadian zoisite, vanadian sphene and vanadian rutile) also occur in the marble. The occurrence of scapolite and the enrichment in vanadium suggest that the protolith of calc-silicate-graphite gneiss was evaporite or related sediment. The mode of occurrence of vanadium grossular in Kenya is quite similar to that in the Sør Rondane Mountains, East Antarctica. The vanadium-grossular-bearing gneisses in Kenya might be correlated with those in Antarctica, since the Sør Rondane Mountains had continued from the Mozambique metamorphic belt before the breakup of Gondwanaland.

  9. Interstitial embrittlement in vanadium laser welds

    SciTech Connect

    Strum, M.J.; Wagner, L.M.

    1992-02-24

    Efficiencies of interstitial absorption during pulsed ND:YAG laser welding of vanadium were compared for nitrogen, oxygen, hydrogen, and water vapor. Influence of interstitial levels on the embrittlement of vanadium laser welds was also measured. For 1000 ppM contaminant levels in the weld atmosphere, weld hydrogen content increased 9 ppM, nitrogen content increased 190 ppM, and oxygen content increased from 500 ppM relative to baseplate levels. Welds in ultrahigh-purity argon atmospheres contained 3 ppM hydrogen, 40 ppM nitrogen, and 250 ppM oxygen. Longitudinal all-weld tensile specimens and notched-plate specimens were used to measure weld metal tensile properties at {minus}55C. All of the laser weld notch-strength ratios exceeded unity and weld metal tensile strengths all exceeded the baseplate values. For 1000 ppM atmosphere contaminant levels, the only significant decrease in ductility, as measured by reduction-in-area at fracture was for the weld atmosphere containing oxygen. Weld atmospheres containing 1% nitrogen also reduced the weld ductility, and resulted in the onset of cleavage fracture.

  10. Interstitial embrittlement in vanadium laser welds

    SciTech Connect

    Strum, M.J.; Wagner, L.M.

    1992-02-24

    Efficiencies of interstitial absorption during pulsed ND:YAG laser welding of vanadium were compared for nitrogen, oxygen, hydrogen, and water vapor. Influence of interstitial levels on the embrittlement of vanadium laser welds was also measured. For 1000 ppM contaminant levels in the weld atmosphere, weld hydrogen content increased 9 ppM, nitrogen content increased 190 ppM, and oxygen content increased from 500 ppM relative to baseplate levels. Welds in ultrahigh-purity argon atmospheres contained 3 ppM hydrogen, 40 ppM nitrogen, and 250 ppM oxygen. Longitudinal all-weld tensile specimens and notched-plate specimens were used to measure weld metal tensile properties at [minus]55C. All of the laser weld notch-strength ratios exceeded unity and weld metal tensile strengths all exceeded the baseplate values. For 1000 ppM atmosphere contaminant levels, the only significant decrease in ductility, as measured by reduction-in-area at fracture was for the weld atmosphere containing oxygen. Weld atmospheres containing 1% nitrogen also reduced the weld ductility, and resulted in the onset of cleavage fracture.

  11. Large Spin Hall Angle in Vanadium Film

    NASA Astrophysics Data System (ADS)

    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.

  12. Facile synthesis of vanadium oxide nanowires

    NASA Astrophysics Data System (ADS)

    Kysar, Jesse; Sekhar, Praveen Kumar

    2016-10-01

    A simple growth process is reported for the synthesis of vanadium (II) oxide nanowires with an average width of 65 nm and up to 5 μm in length for growth at 1000 °C for 3 h. The vanadium (II) oxide nanowires were grown on a gold-coated silicon substrate at ambient pressure using a single heat zone furnace with Ar as the carrier gas. Gold was utilized as a catalyst for the growth of the nanowires. The growth temperature and heating time were varied to observe the nanowire morphology. An increase in nanowire width was observed with an increase in the heating temperature. A ninefold increase in the number density of the nanowires was observed when the heating time was changed from 30 min to 3 h. This is the first time a simple growth process for producing VO nanowires at ambient pressure has been demonstrated. Such a scheme enables wider use of VO nanowires in critical applications such as energy storage, gas sensors, and optical devices.

  13. Metal Insulator transition in Vanadium Dioxide

    NASA Astrophysics Data System (ADS)

    Jovaini, Azita; Fujita, Shigeji; Suzuki, Akira; Godoy, Salvador

    2012-02-01

    MAR12-2011-000262 Abstract Submitted for the MAR12 Meeting of The American Physical Society Sorting Category: 03.9 (T) On the metal-insulator-transition in vanadium dioxide AZITA JOVAINI, SHIGEJI FUJITA, University at Buffalo, SALVADOR GODOY, UNAM, AKIRA SUZUKI, Tokyo University of Science --- Vanadium dioxide (VO2) undergoes a metal-insulator transition (MIT) at 340 K with the structural change from tetragonal to monoclinic crystal. The conductivity _/ drops at MIT by four orders of magnitude. The low temperature monoclinic phase is known to have a lower ground-state energy. The existence of the k-vector k is prerequisite for the conduction since the k appears in the semiclassical equation of motion for the conduction electron (wave packet). The tetragonal (VO2)3 unit is periodic along the crystal's x-, y-, and z-axes, and hence there is a three-dimensional k-vector. There is a one-dimensional k for a monoclinic crystal. We believe this difference in the dimensionality of the k-vector is the cause of the conductivity drop. Prefer Oral Session X Prefer .

  14. Vanadium-base alloys for fusion reactor applications

    SciTech Connect

    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.

  15. Nuclear reactor fuel element with vanadium getter on cladding

    DOEpatents

    Johnson, Carl E.; Carroll, Kenneth G.

    1977-01-01

    A nuclear reactor fuel element is described which has an outer cladding, a central core of fissionable or mixed fissionable and fertile fuel material and a layer of vanadium as an oxygen getter on the inner surface of the cladding. The vanadium reacts with oxygen released by the fissionable material during irradiation of the core to prevent the oxygen from reacting with and corroding the cladding. Also described is a method for coating the inner surface of small diameter tubes of cladding with a layer of vanadium.

  16. Gas-Phase Partial Oxidation of Lignin to Carboxylic Acids over Vanadium Pyrophosphate and Aluminum-Vanadium-Molybdenum.

    PubMed

    Lotfi, Samira; Boffito, Daria C; Patience, Gregory S

    2015-10-26

    Lignin is a complex polymer that is a potential feedstock for aromatic compounds and carboxylic acids by cleaving the β-O-4 and 5-5' linkages. In this work, a syringe pump atomizes an alkaline solution of lignin into a catalytic fluidized bed operating above 600 K. The vanadium heterogeneous catalysts convert all the lignin into carboxylic acids (up to 25 % selectivity), coke, carbon oxides, and hydrogen. Aluminum-vanadium-molybdenum mostly produced lactic acid (together with formic acid, acrylic acid, and maleic anhydride), whereas the vanadium pyrophosphate catalyst produced more maleic anhydride.

  17. Evaluation of the nanomechanical properties of vanadium and native oxide vanadium thin films prepared by RF magnetron sputtering

    NASA Astrophysics Data System (ADS)

    Mamun, M. A.; Zhang, K.; Baumgart, H.; Elmustafa, A. A.

    2015-12-01

    Polycrystalline vanadium thin films of 50, 75, and 100 nm thickness were deposited by magnetron sputtering of a vanadium metal target of 2 inch diameter with 99.9% purity on native oxide covered Si substrates. One set of the fabricated samples were kept in moisture free environment and the other set was exposed to ambient air at room temperature for a long period of time that resulted in formation of native oxide prior to testing. The crystal structure and phase purity of the vanadium and the oxidized vanadium thin films were characterized by X-ray diffraction (XRD). The XRD results yield a preferential (1 1 0), and (2 0 0) orientation of the polycrystalline V films and (0 0 4) vanadium oxide (V3O7). The vanadium films thickness were verified using field emission scanning electron microscopy and the films surface morphologies were inspected using atomic force microscopy (AFM). AFM images reveal surface roughness was observed to increase with increasing film thickness and also subsequent to oxidation at room temperature. The nanomechanical properties were measured by nanoindentation to evaluate the modulus and hardness of the vanadium and the oxidized vanadium thin films. The elastic modulus of the vanadium and the oxidized vanadium films was estimated as 150 GPa at 30% film thickness and the elastic modulus of the bulk vanadium target is estimated as 135 GPa. The measured hardness of the vanadium films at 30% film thickness varies between 9 and 14 GPa for the 100 and 50 nm films, respectively, exhibiting size effects, where the hardness increases as the film thickness decreases. The hardness of the oxidized films depicted less variation and is reported as ∼10 GPa at 30% film thickness for the three oxides. The scanning electron microscopy (SEM) imaging depicted a gradual progression of pile up as the film thickness increased from 75 to 100 nm. It is noticed that as the film thickness increases the films experience softening effect due to grain coarsening and the

  18. Novel Neo-Pentoxide Precursors for MOCVD Thin Films of TiO(2) and ZrO(2).[1

    SciTech Connect

    Boyle, Timothy J.; Francisco, Laila P.; Gallegos, Jesus J.; Rodriguez, Mark A.; Ward, Timothy L.

    1999-07-14

    Two novel Group IV precursors, titanium (IV) neo-pentoxide, [Ti({mu}-ONep)(ONep){sub 3}]{sub 2} (l), and zirconium (IV) neo-pentoxide, [Zr({mu}-ONep)(ONep){sub 3}]{sub 2} (2), were reported to possess relatively high volatility at low temperatures. These compounds were therefore investigated as MOCVD precursors using a lamp-heated cold-wall CVD reactor and direct sublimation without carrier gas. The ONep derivatives proved to be competitive precursors for the production of thin films of the appropriate MO{sub 2} (M = Ti or Zr) materials in comparison to other metallo-organic precursors. Compound 1 was found to sublime at 120 C with a deposition rate of {approximately}0.350 {mu}m/min onto a substrate at 330 C forming the anatase phase with < 1% residual C found in the final film. Compound 2 was found to sublime at 160 C and deposited as crystalline material at 300 C with < 1% residual C found in the final film. A comparison to standard alkoxide and {beta}-diketonates is presented where appropriate.

  19. Geochemistry of vanadium in an epigenetic, sandstone-hosted vanadium- uranium deposit, Henry Basin, Utah

    USGS Publications Warehouse

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

    1990-01-01

    The epigenetic Tony M vanadium-uranium orebody in south-central Utah is hosted in fluvial sandstones of the Morrison Formation (Upper Jurassic). Measurements of the relative amounts of V+3 and V +4 in ore minerals show that V+3 is more abundant. Thermodynamic calculations show that vanadium was more likely transported to the site of mineralization as V+4. The ore formed as V+4 was reduced by hydrogen sulfide, followed by hydrolysis and precipitation of V+3 in oxide minerals or chlorite. Uranium was transported as uranyl ion (U+6), or some complex thereof, and reduced by hydrogen sulfide, forming coffinite. Detrital organic matter in the rocks served as the carbon source for sulfate-reducing bacteria. Vanadium most likely was derived from the dissolution of iron-titanium oxides. Uranium probably was derived from the overlying Brushy Basin Member of the Morrison Formation. Previous studies have shown that the ore formed at the density-stratified interface between a basinal brine and dilute meteoric water. The mineralization processes described above occurred within the mixing zone between these two fluids. -from Authors

  20. Characterization of vanadium, manganese and iron model clusters by vibrational and optical spectroscopic methods

    NASA Astrophysics Data System (ADS)

    Ji, Wenbin

    1999-12-01

    The active ferryl intermediates in the catalytic cycles of heme proteins are subject to interactions from the proximal and distal amino acid residues which control their activities and affect the ν(FeIVO) frequency. The effects of sixth axial ligation, hydrogen bonding, and solvent induced polarization on the resonance Raman (RR) spectra of the ferryl porphyrin analogs, vanadyl (VIVO) porphyrins and their π-cation radicals, are characterized. ν(VIVO) stretching bands for (VO)TMPyP and (VO)PPIX are observed to be sensitive to the pH value of the aqueous solutions, and reveal a number of coexisting 5-coordinate (c) and 6- c vanadyl porphyrins in solution. Moreover, the ν(VIVO) bands for (VO)TMP and (VO)TPP porphyrins upshift to higher frequencies with the formation of their π-cation radicals, in agreement with that of the (VO)OEP radical. For both a1u (OEP) and a2u (TPP, TMP) type radicals, an increased positive charge on the porphyrin reduces the porphyrin --> vanadium electron donation, but enhances the oxo --> V donation. The UV-Vis absorption and RR spectroscopic studies on a series of oxo-bridged vanadium(III) and manganese (III, IV) complexes established spectrostructural correlations that are useful as monitors of the structure of vanadium(III) and manganese(III, IV) centers in biological systems. The linear and bent V-O-V dimers display distinctive RR and absorption spectra. The linear V-O-V bridge displays an intense μ-O --> V charge transfer (CT) absorption band and a strongly enhanced symmetric (νs) or antisymmetric (νas) V-O-V stretching band in RR spectra, depending upon terminal ligands. In contrast, the bent bridge shows two μ-O --> V CT bands and both νs and νas V- O-V stretches are observed in RR spectra. These νs and νas vibrations are used to indicate that the vanadium(III) oxo-bridged dimer intercalates with DNA. The Mn-O-Mn vibrational frequencies in the 400-700 cm -1 region of the oxo-bridged manganese(III, IV) dimers, trimers, and

  1. Adsorption and photocatalytic degradation of malachite green by vanadium doped zinc oxide nanoparticles.

    PubMed

    Khezami, L; Taha, Kamal K; Ghiloufi, Imed; El Mir, Lassaad

    2016-01-01

    Herein the degradation of malachite green (MG) dye from aqueous medium by vanadium doped zinc oxide (ZnO:V3%) nanopowder was investigated. The specific surface area and pore volume of the nanopowder was characterized by nitrogen adsorption method. Batch experimental procedures were conducted to investigate the adsorption and photocatalytic degradation of MG dye. Adsorption kinetics investigations were performed by varying the amount of the catalyst and the initial dye concentrations. Adsorption and photocatalytic degradation data were modeled using the Lagergren pseudo-first-order and second-order kinetic equation. The results showed that the ZnO:V3% nanopowder was particularly effective for the removal of MG and data were found to comply with Lagergreen pseudo-first-order kinetic model.

  2. Process development for economical processing of various vanadium bearing materials

    NASA Astrophysics Data System (ADS)

    Retelsdorf, H. J.; Rothmann, H.; Fichte, R.

    1982-06-01

    Three different vanadium bearing products were tested. It was proven feasible to recover a ferroalloy containing 73.5% of the vanadium contained in the leaching residues from blast furnace slags by reduction in an electric arc furnace. The composition of the obtained ferroalloy was 67% Fe, 2% V, 7% Cr, and 5.5% C. The vanadium recovery contained 0.5 to 6% in the fly ash, resulting from the combustion of fuel. Different fly ashes were tested by oxidation through roasting and subsequent basic leaching, or by reduction roasting with subsequent acid leaching, or bysoda roasting and leaching. The third source of vanadium tested was the waste salt, originating in alumina production, and containing about 4% V, 5% P, and 0.5% As. It was possible to produce a ferroalloy containing V2O5 and a secondary sodium phosphate, which could be applied in the phosphate processing industry.

  3. 1. VIEW TO NORTH, FRONT AND SIDE. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    1. VIEW TO NORTH, FRONT AND SIDE. - Vanadium Corporation of America (VCA) Naturita Mill, Laboratory, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  4. 4. DETAIL OF GEARWELL AND GENERATOR, WEST VIEW. Vanadium ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    4. DETAIL OF GEARWELL AND GENERATOR, WEST VIEW. - Vanadium Corporation of America (VCA) Naturita Mill, Grinding Rod Mill, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  5. 2. VIEW TO WEST, REAR AND SIDE. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    2. VIEW TO WEST, REAR AND SIDE. - Vanadium Corporation of America (VCA) Naturita Mill, Mechanic Shed, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  6. 2. VIEW TO SOUTH, REAR AND SIDE. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    2. VIEW TO SOUTH, REAR AND SIDE. - Vanadium Corporation of America (VCA) Naturita Mill, Laboratory, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  7. 2. INTERIOR, WEST VIEW OF SUPPLY BINS. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    2. INTERIOR, WEST VIEW OF SUPPLY BINS. - Vanadium Corporation of America (VCA) Naturita Mill, Mill Warehouse, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  8. 1. VIEW TO EAST, FRONT AND SIDE. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    1. VIEW TO EAST, FRONT AND SIDE. - Vanadium Corporation of America (VCA) Naturita Mill, Grinding Rod Mill, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  9. 1. VIEW TO EAST, FRONT AND SIDE. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    1. VIEW TO EAST, FRONT AND SIDE. - Vanadium Corporation of America (VCA) Naturita Mill, Mechanic Shed, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  10. 2. INTERIOR, SOUTHWEST VIEW (STORAGE COMPARTMENTS). Vanadium Corporation of ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    2. INTERIOR, SOUTHWEST VIEW (STORAGE COMPARTMENTS). - Vanadium Corporation of America (VCA) Naturita Mill, Mine Warehouse, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  11. 1. VIEW TO EAST, FRONT AND SIDE. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    1. VIEW TO EAST, FRONT AND SIDE. - Vanadium Corporation of America (VCA) Naturita Mill, Weighing Office & Station, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  12. 3. INTERIOR, SOUTHEAST VIEW. Vanadium Corporation of America (VCA) ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    3. INTERIOR, SOUTHEAST VIEW. - Vanadium Corporation of America (VCA) Naturita Mill, Grinding Rod Mill, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  13. 14. VIEW TO NORTHWEST, SMALL ROASTER (DISMANTLED). Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    14. VIEW TO NORTHWEST, SMALL ROASTER (DISMANTLED). - Vanadium Corporation of America (VCA) Naturita Mill, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  14. 1. VIEW TO NORTH, FRONT AND SIDE. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    1. VIEW TO NORTH, FRONT AND SIDE. - Vanadium Corporation of America (VCA) Naturita Mill, Office Building, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  15. 1. VIEW TO SOUTH, FRONT AND SIDE. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    1. VIEW TO SOUTH, FRONT AND SIDE. - Vanadium Corporation of America (VCA) Naturita Mill, Mine Warehouse, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  16. 1. VIEW TO NORTHWEST, FRONT AND SIDE. Vanadium Corporation ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    1. VIEW TO NORTHWEST, FRONT AND SIDE. - Vanadium Corporation of America (VCA) Naturita Mill, Mill Warehouse, 3 miles Northwest of Naturita, between Highway 141 & San Miguel River, Naturita, Montrose County, CO

  17. Vanadium removal from LD converter slag using bacteria and fungi.

    PubMed

    Mirazimi, S M J; Abbasalipour, Z; Rashchi, F

    2015-04-15

    Removal of vanadium from Linz-Donawits (LD) converter slag was investigated by means of three different species of microbial systems: Acidithiobacillus thiooxidans (autotrophic bacteria), Pseudomonas putida (heterotrophic bacteria) and Aspergillus niger (fungi). The bioleaching process was carried out in both one-step and two-step process and the leaching efficiencies in both cases were compared. Formation of inorganic and organic acids during the leaching process caused mobilization of vanadium. In order to reduce toxic effects of the metal species on the above mentioned microorganisms, a prolonged adaptation process was performed. Both bacteria, A. thiooxidans and P. putida were able to remove more than 90% of vanadium at slag concentrations of 1-5 g L(-1) after 15 days. Also, the maximum achievable vanadium removal in the fungal system was approximately 92% at a slag concentration of 1 g L(-1) after 22 days.

  18. Method to remove uranium/vanadium contamination from groundwater

    DOEpatents

    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.

  19. Ion Exchange Separation of the Oxidation State of Vanadium.

    ERIC Educational Resources Information Center

    Cornelius, Richard

    1980-01-01

    Describes an experiment that emphasizes the discrete nature of the different oxidation states of vanadium by the separation of ammonium metavanadate into all four species by ion exchange chromatography. (CS)

  20. Systematics of Vanadium in Olivine from Planetary Basalts

    NASA Technical Reports Server (NTRS)

    Karner, J. M.; Papike, J. J.; Shearer, C. K.

    2002-01-01

    The systematics of vanadium in olivines from the Earth, Moon and Mars allows for the comparison of planetary basalt origin and igneous setting and process. Additional information is contained in the original extended abstract.

  1. Method to Remove Uranium/Vanadium Contamination from Groundwater

    SciTech Connect

    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.

  2. Absorption behavior of vanadium in Nafion®

    NASA Astrophysics Data System (ADS)

    Cho, Hyun-Seok; Ohashi, Masato; Van Zee, J. W.

    2014-12-01

    The absorption of vanadium to Nafion® was investigated through ex-situ isotherm and conductivity measurements at 23 °C. The data show a maximum loss of ion exchange capacity (IEC) of 30% for all four oxidation states of vanadium. The affinity of vanadium for N115 was measured by back titration and atomic absorption (AA) and characterized by isotherms at 23 °C, and the affinity is highest for the divalent species and lowest for the pentavalent species in the following order: VO2+ (V5+) < VO2+ (V4+) < V3+ < V2+. Steric hindrance from the associated water complex may explain the lower absorption of vanadium compared to alkali metals. The conductivity for the VO2+ (minimum affinity)-exchanged membrane was 2-3× lower than the sodium-exchanged membrane at an approximate RH = 100%.

  3. Thermodynamic modeling of restoring items converter vanadium slag

    NASA Astrophysics Data System (ADS)

    Golodova, M. A.; Rogihina, I. D.; Nohrina, O. I.; Rybenko, I. A.

    2016-09-01

    Calculations of parameters for equilibrium processes of iron, manganese, vanadium and titanium reduction from converter vanadium slag by carbon from small-sized coke and silica from ferrosilicon were performed by the method of thermodynamic modeling using the program complex “Terra”. Calculations were made for each type of reductant separately and in combination. Dependences of process parameters on reducing agents consumption were drawn. The analysis of the results was carried out.

  4. Extraction of vanadium from athabasca tar sands fly ash

    NASA Astrophysics Data System (ADS)

    Gomez-Bueno, C. O.; Spink, D. R.; Rempel, G. L.

    1981-06-01

    The production of refinery grade oil from the Alberta tar sands deposits as currently practiced by Suncor (formally Great Canadian Oil Sands Ltd.—GCOS) generates a substantial amount of petroleum coke fly ash which contains appreciable amounts of valuable metals such as vanadium, nickel and titanium. Although the recovery of vanadium from petroleum ash is a well established commercial practice, it is shown in the present work that such processes are not suitable for recovery of vanadium from the GCOS fly ash. The fact that the GCOS fly ash behaves so differently when compared to other petroleum fly ash is attributed to its high silicon and aluminum contents which tie up the metal values in a silica-alumina matrix. Results of experiments carried out in this investigation indicate that such matrices can be broken down by application of a sodium chloride/water roast of the carbon-free fly ash. Based on results from a series of preliminary studies, a detailed investigation was undertaken in order to define optimum conditions for a vanadium extraction process. The process developed involves a high temperature (875 to 950 °C) roasting of the fly ash in the presence of sodium chloride and water vapor carried out in a rotary screw kiln, followed by dilute sodium hydroxide atmosphereic leaching (98 °C) to solublize about 85 pet of the vanadium originally present in the fly ash. It was found that the salt roasting operation, besides enhancing vanadium recovery, also inhibits silicon dissolution during the subsequent leaching step. The salt roasting treatment is found to improve vanadium recovery significantly when the fly ash is fully oxidized. This is easily achieved by burning off the carbon present in the “as received” fly ash under excess air. The basic leaching used in the new process selectively dissolves vanadium from the roasted ash, leaving nickel and titanium untouched.

  5. Corrosion behavior of vanadium alloys in flowing lithium

    SciTech Connect

    Chopra, O.K.; Smith, D.L.

    1987-08-01

    Corrosion data are presented for several vanadium alloys exposed to flowing lithium at 427, 482, and 538/sup 0/C. The corrosion behavior is evaluated by weight change measurements. Metallographic results and data on the nonmetallic element transfer in lithium-exposed specimens are also presented. The influence of alloy composition and exposure conditions on the corrosion behavior of vanadium alloys is discussed. 6 refs., 9 figs., 2 tabs.

  6. Precipitation and Recrystallization in Some Vanadium and Vanadium-Niobium Microalloyed Steels

    NASA Astrophysics Data System (ADS)

    Crooks, M. J.; Garratt-Reed, A. J.; Sande, J. B. Vander; Owen, W. S.

    1981-12-01

    Static precipitation and recrystallization following hot compression of austenite and the interactions between the two processes have been studied in a set of aluminum-killed HSLA steels containing 0.1 pct carbon, [0.016 - 0.026] pct nitrogen and 0.1 or 0.2 pct vanadium. Two steels containing both vanadium (0.1 and 0.2 pct) and niobium (0.03 pct) were included for purposes of comparison. The compression and the static tests were all carried out isothermally at temperatures between 800 and 900 °C. The course of recrystallization was followed by measurements of the rate of softening and by optical metallography of specimens quenched from the test temperature after different times. Precipitation was studied by measurements of the rate of hardening, by transmission electron microscopy of thin foils, carbon and aluminum extraction replicas, and by X-ray dispersion and energy-loss spectroscopy from individual precipitates. The temperature of the nose of the C-curve for precipitation in vanadium steels is much lower than that in niobium steels, as is the temperature, TR, below which no recrystallization occurs in short times. Precipitation occurs both at austenite grain boundaries and in the grains (matrix precipitation). The former starts early and the precipitates grow rapidly to an approximately constant size; the matrix precipitates grow more slowly and are responsible for the observed hardening of the austenite. The relevance of various models proposed for the retardation and arrest of recrystallization of austenite are discussed. In the steels containing vanadium and niobium the precipitates contain both heavy elements: (V,Nb) (C,N). The Nb/V ratio in the matrix precipitates is different than in the parent austenite. The grain-boundary precipitates, however, contain the same Nb/V ratio as the parent austenite. The rate of hardening exhibits a reverse C-curve behavior, being more rapid than in the corresponding vanadium steels at higher temperatures and about the

  7. Alkali metal yttrium neo-pentoxide double alkoxide precursors to alkali metal yttrium oxide nanomaterials

    SciTech Connect

    Boyle, Timothy J.; Neville, Michael L.; Sears, Jeremiah Matthew; Cramer, Roger

    2016-03-15

    In this study, a series of alkali metal yttrium neo-pentoxide ([AY(ONep)4]) compounds were developed as precursors to alkali yttrium oxide (AYO2) nanomaterials. The reaction of yttrium amide ([Y(NR2)3] where R=Si(CH3)3) with four equivalents of H-ONep followed by addition of [A(NR2)] (A=Li, Na, K) or Ao (Ao=Rb, Cs) led to the formation of a complex series of AnY(ONep)3+n species, crystallographically identified as [Y2Li33-ONep)(μ3-HONep)(μ-ONep)5(ONep)3(HONep)2] (1), [YNa23-ONep)4(ONep)]2 (2), {[Y2K33-ONep)3(μ-ONep)4(ONep)2(ηξ-tol)2][Y4K24-O)(μ3-ONep)8(ONep)4]•ηx-tol]} (3), [Y4K24-O)(μ3-ONep)8(ONep)4] (3a), [Y2Rb34-ONep)3(μ-ONep)6] (4), and [Y2Cs46-O)(μ3-ONep)63-HONep)2(ONep)2x-tol)4]•tol (5). Compounds 1–5 were investigated as single source precursors to AYOx nanomaterials following solvothermal routes (pyridine, 185 °C for 24h). The final products after thermal processing were found by powder X-ray diffraction experiments to be Y2O3 with variable sized particles based on transmission electron diffraction. Energy dispersive X-ray spectroscopy studies indicated that the heavier alkali metal species were present in the isolated nanomaterials.

  8. Electronic Transitions of Palladium and Vanadium Dimer

    NASA Astrophysics Data System (ADS)

    Qian, Yue; Ng, Y. W.; Cheung, A. S.-C.

    2013-06-01

    The laser induced fluorescence (LIF) spectrum of palladium dimer (Pd_{2}) in the visible region between 480 and 700 nm has been studied. Five vibrational bands were recorded and analyzed; they are assigned to a ^{3} Π _{g} - X^{3} Σ _{u} ^{+} system. The vibrational frequency of the ground X^{3} Σ _{u} ^{+} state has been determined to be 211.4 cm^{-1}. This is the first experimental observation of the LIF spectrum of Pd_{2}. In addition, the LIF spectrum of vanadium dimer (V_{2}) has also been studied; several new transition band systems were observed in the wavelength between 480 and 530 nm. The analysis of the spectra recorded for these two molecules will be presented.

  9. Crystal chemistry of the natural vanadium bronzes

    USGS Publications Warehouse

    Evans, H.T.; Hughes, J.M.

    1990-01-01

    The crystal chemistry of the natural vanadium bronze minerals is reviewed on the basis of published information and new studies (mainly by X-ray powder-diffraction methods) using type material wherever possible. The known V bronze minerals are divided into three categories: 1) the hewettite group, 2) the straczekite group, 3) other structure types including navajoite, schubnelite, fervanite, shcherbinaite, bannermanite, and melanovanadite. All known structures associated with the fibrous V bronzes (fiber spacing 3.6 A??) can be considered as various lateral linkages (into sheets or networks) of only two types of polyvanadate chains: 1) a divanadate chain (V2O6)n consisting of alternating square pyramids, and 2) a tetravanadate chain (V4O12)n consisting of four highly condensed single octahedral chains. -from Authors

  10. Study on leaching vanadium from roasted residue of stone coal

    SciTech Connect

    He, D.; Feng, Q.; Zhang, G.; Luo, W.; Ou, L.

    2008-11-15

    In China, the total reserves of vanadium, reported as V{sub 2}O{sub 5}, in stone coal is 118 Mt (130 million st). Recovering vanadium from such a large resource is very important to China's vanadium industry. The technology now being used to recover vanadium from stone coal has the following two problems in the leaching process: a low recovery of vanadium and high acid consumption. To resolve these problems, a new leaching technology is proposed. The effects of factors such as H{sub 2}SO{sub 4} concentration, liquid-solid ratio, temperature and time, and the types and additions of additives were studied. By adding 1.5% (by weight) CaF2 and leaching the roasted residue of stone coal with 5.4% (by weight) sulfuric acid at 90{sup o}C for 12 hours at a liquid-solid ratio of 2 mL/g, the leaching degree of vanadium reached 83.10%. This proposed leaching technology gives a feasible alternative for the processing of roasting residue of stone coal and can be applied in the comprehensive utilization of stone coal ores in China.

  11. Vanadium-based nanostructure materials for secondary lithium battery applications

    NASA Astrophysics Data System (ADS)

    Tan, Hui Teng; Rui, Xianhong; Sun, Wenping; Yan, Qingyu; Lim, Tuti Mariana

    2015-08-01

    Vanadium-based materials, such as V2O5, LiV3O8, VO2(B) and Li3V2(PO4)3 are compounds that share the characteristic of intercalation chemistry. Their layered or open frameworks allow facile ion movement through the interspaces, making them promising cathodes for LIB applications. To bypass bottlenecks occurring in the electrochemical performances of vanadium-based cathodes that derive from their intrinsic low electrical conductivity and ion diffusion coefficients, nano-engineering strategies have been implemented to ``create'' newly emerging properties that are unattainable at the bulk solid level. Integrating this concept into vanadium-based cathodes represents a promising way to circumvent the aforementioned problems as nanostructuring offers potential improvements in electrochemical performances by providing shorter mass transport distances, higher electrode/electrolyte contact interfaces, and better accommodation of strain upon lithium uptake/release. The significance of nanoscopic architectures has been exemplified in the literature, showing that the idea of developing vanadium-based nanostructures is an exciting prospect to be explored. In this review, we will be casting light on the recent advances in the synthesis of nanostructured vanadium-based cathodes. Furthermore, efficient strategies such as hybridization with foreign matrices and elemental doping are introduced as a possible way to boost their electrochemical performances (e.g., rate capability, cycling stability) to a higher level. Finally, some suggestions relating to the perspectives for the future developments of vanadium-based cathodes are made to provide insight into their commercialization.

  12. Vanadium contamination monitored by an arctic bivalve, Cyrtodaria kurriana

    SciTech Connect

    Bourgoin, B.P.; Risk, M.J.

    1987-12-01

    The trace element Vanadium enters the ocean principally through natural weathering processes, atmospheric fallout and man's activity. Although recent studies failed to detect any significant input of atmospheric Vanadium in the Arctic environment, local contamination is always possible. Tuktoyaktuk is a small Inuvialuit community situated on the eastern edge of the Mackenzie River Delta along the shore of Kugmallit Bay. It has one of the few good natural harbors in the Western Arctic, and serves as the principle support base for oil and gas industry operations. Residual oil, high in Vanadium content, powers the electric generators and is periodically sprayed over the dirt road surfaces to keep dust levels down. This, along with heavy ship traffic, may contribute to local Vanadium contamination in the marine system. The Arctic Propeller clam, Cyrtodaria kurriana (Dunker), is the most common filter feeding bivalve in Tuktoyaktuk Harbor and is a major component in the trophic chain. This study investigates the utility of this bivalve as a monitor for Vanadium contamination in the Arctic environment. The total Vanadium content of sediments was determined bu x-ray fluorescence spectrometry, and of claim tissues by short-decay instrumental neutron activation analysis.

  13. Plasma enhanced chemical vapor deposition (PECVD) method of forming vanadium oxide films and vanadium oxide thin-films prepared thereby

    DOEpatents

    Zhang, Ji-Guang; Tracy, C. Edwin; Benson, David K.; Turner, John A.; Liu, Ping

    2000-01-01

    A method is disclosed of forming a vanadium oxide film on a substrate utilizing plasma enhanced chemical vapor deposition. The method includes positioning a substrate within a plasma reaction chamber and then forming a precursor gas comprised of a vanadium-containing chloride gas in an inert carrier gas. This precursor gas is then mixed with selected amounts of hydrogen and oxygen and directed into the reaction chamber. The amounts of precursor gas, oxygen and hydrogen are selected to optimize the final properties of the vanadium oxide film An rf plasma is generated within the reaction chamber to chemically react the precursor gas with the hydrogen and the oxygen to cause deposition of a vanadium oxide film on the substrate while the chamber deposition pressure is maintained at about one torr or less. Finally, the byproduct gases are removed from the plasma reaction chamber.

  14. Selective recovery of vanadium and scandium by ion exchange with D201 and solvent extraction using P507 from hydrochloric acid leaching solution of red mud.

    PubMed

    Zhu, Xiaobo; Li, Wang; Tang, Sen; Zeng, Majian; Bai, Pengyuan; Chen, Lunjian

    2017-05-01

    D201 resin and P507 extractant diluted with sulfonated kerosene were used to respectively separate vanadium and scandium, and impurity ions from hydrochloric acid leaching solution of red mud. More than 99% of vanadium was selectively adsorbed from the hydrochloric acid leaching solution under the conditions of pH value of 1.8, volume ratio of leaching solution to resin of 10, and flow rate of 3.33 mL/min. Maximum extraction and separation of scandium was observed from the acid leaching solution at an aqueous pH value of 0.2. More than 99% of scandium can be selectively extracted using 15% P507, 5% TBP at the aqueous solution/organic phase (A/O) ratio of 10:1 for 6 min. The loaded organic phase was washed with 0.3 mol/L sulfuric acid, wherein most impurities were removed. After the process of desorption or stripping, precipitation, and roasting, high-purity V2O5 and Sc2O3 were obtained. Finally, a conceptual flow sheet was established to separate and recover vanadium and scandium from red mud hydrochloric acid leaching solution.

  15. Investigations on transfer of water and vanadium ions across Nafion membrane in an operating vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Sun, Chenxi; Chen, Jian; Zhang, Huamin; Han, Xi; Luo, Qingtao

    Diffusion coefficients of the vanadium ions across Nafion 115 (Dupont) in a vanadium redox flow battery (VRFB) are measured and found to be in the order of V 2+ > VO 2+ > VO 2 + > V 3+. It is found that both in self-discharge process and charge-discharge cycles, the concentration difference of vanadium ions between the positive electrolyte (+ve) and negative electrolyte (-ve) is the main reason causing the transfer of vanadium ions across the membrane. In self-discharge process, the transfer of water includes the transfer of vanadium ions with the bound water and the corresponding transfer of protons with the dragged water to balance the charges, and the transfer of water driven by osmosis. In this case, about 75% of the net transfer of water is caused by osmosis. In charge-discharge cycles, except those as mentioned in the case of self-discharge, the transfer of protons with the dragged water across the membrane during the electrode reaction for the formation of internal electric circuit plays the key role in the water transfer. But in the long-term cycles of charge-discharge, the net transfer of water towards +ve is caused by the transfer of vanadium ions with the bound water and the transfer of water driven by osmosis.

  16. Photocatalytic reduction of vanadium(V) in TiO₂ suspension: chemometric optimization and application to wastewaters.

    PubMed

    Sturini, Michela; Rivagli, Elisa; Maraschi, Federica; Speltini, Andrea; Profumo, Antonella; Albini, Angelo

    2013-06-15

    The photocatalytic reduction of V(V) to V(IV) over TiO₂ in aqueous solution is presented. Experiments were undertaken on air-equilibrated water spiked with V(V) (0.6-20 mgL(-1)), under UV-A or solar light. A chemometric study was performed to optimize the reduction yield, by considering the most important variables recognized to affect the photocatalytic process. Among pH, irradiation time and catalyst concentration, the two latter proved to be determinant. The good yields achieved (up to 98%), along with the possibility of working in aerated solution, make this procedure simple, rapid and efficient. Although a deep insight on the photochemical mechanisms was beyond our scope, the role of electron donors was investigated, proving the efficiency of 2-propanol, citric acid and formic acid in the acceleration and improvement of V(V) conversion. After irradiation, total vanadium and aqueous V(V) and V(IV) after solid-phase separation on Chelex-100 resin, were determined by inductively coupled plasma optical emission spectroscopy (ICP-OES). The procedure was applied to contaminated wastewaters, combining remediation and possible vanadium recovery as V(IV).

  17. Sarcoplasmic reticulum calcium ATPase is inhibited by organic vanadium coordination compounds: pyridine-2,6-dicarboxylatodioxovanadium(V), BMOV, and an amavadine analogue.

    PubMed

    Aureliano, Manuel; Henao, Fernando; Tiago, Teresa; Duarte, Rui O; Moura, J J G; Baruah, Bharat; Crans, Debbie C

    2008-07-07

    The general affinity of the sarcoplasmic reticulum (SR) Ca (2+)-ATPase was examined for three different classes of vanadium coordination complexes including a vanadium(V) compound, pyridine-2,6-dicarboxylatodioxovanadium(V) (PDC-V(V)), and two vanadium(IV) compounds, bis(maltolato)oxovanadium(IV) (BMOV), and an analogue of amavadine, bis( N-hydroxylamidoiminodiacetato)vanadium(IV) (HAIDA-V(IV)). The ability of vanadate to act either as a phosphate analogue or as a transition-state analogue with enzymes' catalysis phosphoryl group transfer suggests that vanadium coordination compounds may reveal mechanistic preferences in these classes of enzymes. Two of these compounds investigated, PDC-V(V) and BMOV, were hydrolytically and oxidatively reactive at neutral pH, and one, HAIDA-V(IV), does not hydrolyze, oxidize, or otherwise decompose to a measurable extent during the enzyme assay. The SR Ca (2+)-ATPase was inhibited by all three of these complexes. The relative order of inhibition was PDC-V(V) > BMOV > vanadate > HAIDA-V(IV), and the IC 50 values were 25, 40, 80, and 325 microM, respectively. Because the observed inhibition is more potent for PDC-V(V) and BMOV than that of oxovanadates, the inhibition cannot be explained by oxovanadate formation during enzyme assays. Furthermore, the hydrolytically and redox stable amavadine analogue HAIDA-V(IV) inhibited the Ca (2+)-ATPase less than oxovanadates. To gauge the importance of the lipid environment, studies of oxidized BMOV in microemulsions were performed and showed that this system remained in the aqueous pool even though PDC-V(V) is able to penetrate lipid interfaces. These findings suggest that the hydrolytic properties of these complexes may be important in the inhibition of the calcium pump. Our results show that two simple coordination complexes with known insulin enhancing effects can invoke a response in calcium homeostasis and the regulation of muscle contraction through the SR Ca (2+)-ATPase.

  18. In-situ Investigation of Vanadium Ion Transport in Redox Flow Battery

    SciTech Connect

    Luo, Qingtao; Li, Liyu; Nie, Zimin; Wang, Wei; Wei, Xiaoliang; Li, Bin; Chen, Baowei; Yang, Zhenguo

    2012-06-27

    We will show a new method to differentiate the vanadium transport from concentration gradient and that from electric field. Flow batteries with vanadium and iron redox couples as the electro-active species were employed to investigate the transport behavior of vanadium ions in the presence of electric field. It was shown that electric field accelerated the positive-to-negative and reduced the negative-to-positive vanadium ions transport in charge process and affected the vanadium ions transport in an opposite way in discharge process. In addition, a method was designed to differentiate the concentration gradient-driven vanadium ions diffusion and electric field-driven vanadium ions migration. Simplified mathematical model was established to simulate the vanadium ions transport in real charge-discharge operation of flow battery. The concentration gradient diffusion coefficients and electric-migration coefficients of V2+, V3+, VO2+, and VO2+ across Nafion membrane were obtained by fitting the experimental data.

  19. CATALYTIC PROMOTION OF THE ADSORPTION OF VANADIUM ON AN ANIONIC EXCHANGE RESIN

    DOEpatents

    Bailes, R.H.; Ellis, D.A.

    1958-08-26

    An improvement in the process for the recovery of vanadium from acidic phosphatic solutions is presented. In this process the vanadium is first oxidized to the pentavaleat state, and is then separated by contacting such solutions with an anion exchange resin whereby adsorption of the complexed pentavalent vanadium is effected. The improvement lies in the fact that adsorp tion of the vanadium complex by the anion exchange resin is promoted and improved by providing fiuoride ions in solution to be contacted.

  20. Surface modification of tantalum pentoxide coatings deposited by magnetron sputtering and correlation with cell adhesion and proliferation in in vitro tests

    NASA Astrophysics Data System (ADS)

    Zykova, A.; Safonov, V.; Goltsev, A.; Dubrava, T.; Rossokha, I.; Donkov, N.; Yakovin, S.; Kolesnikov, D.; Goncharov, I.; Georgieva, V.

    2016-03-01

    The effect was analyzed of surface treatment by argon ions on the surface properties of tantalum pentoxide coatings deposited by reactive magnetron sputtering. The structural parameters of the as-deposited coatings were investigated by means of transmission electron microscopy, atomic force microscopy and scanning electron microscopy. X-ray diffraction profiles and X-ray photoelectron spectra were also acquired. The total surface free energy (SFE), the polar, dispersion parts and fractional polarities, were estimated by the Owens-Wendt-Rabel-Kaeble method. The adhesive and proliferative potentials of bone marrow cells were evaluated for both Ta2O5 coatings and Ta2O5 coatings deposited by simultaneous bombardment by argon ions in in vitro tests.

  1. 40 CFR 440.30 - Applicability; description of the uranium, radium and vanadium ores subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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  2. 40 CFR 440.30 - Applicability; description of the uranium, radium and vanadium ores subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

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  6. 40 CFR 440.80 - Applicability; description of the vanadium ore subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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  7. 40 CFR 421.220 - Applicability: Description of the secondary molybdenum and vanadium subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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  8. 40 CFR 421.220 - Applicability: Description of the secondary molybdenum and vanadium subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... secondary molybdenum and vanadium subcategory. 421.220 Section 421.220 Protection of Environment... POINT SOURCE CATEGORY Secondary Molybdenum and Vanadium Subcategory § 421.220 Applicability: Description of the secondary molybdenum and vanadium subcategory. The provisions of this subpart are...

  9. 40 CFR 440.80 - Applicability; description of the vanadium ore subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... vanadium ore subcategory. 440.80 Section 440.80 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ORE MINING AND DRESSING POINT SOURCE CATEGORY Vanadium Ore Subcategory (Mined Alone and Not as a Byproduct) § 440.80 Applicability; description of the vanadium...

  10. 40 CFR 440.80 - Applicability; description of the vanadium ore subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... vanadium ore subcategory. 440.80 Section 440.80 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Vanadium Ore Subcategory (Mined Alone and Not as a Byproduct) § 440.80 Applicability; description of the vanadium ore subcategory. The provisions of this subpart H are applicable to discharges from (a) mines...

  11. 40 CFR 440.80 - Applicability; description of the vanadium ore subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... vanadium ore subcategory. 440.80 Section 440.80 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ORE MINING AND DRESSING POINT SOURCE CATEGORY Vanadium Ore Subcategory (Mined Alone and Not as a Byproduct) § 440.80 Applicability; description of the vanadium...

  12. Consolidation and fabrication techniques for vanadium-20 w/o titanium /TV-20/

    NASA Technical Reports Server (NTRS)

    Burt, W. R.; Karasek, F. J.; Kramer, W. C.; Mayfield, R. M.; Mc Gowan, R. D.

    1968-01-01

    Tests of the mechanical properties, fuel compatibility, sodium corrosion and irradiation behavior were made for vanadium and vanadium alloy. Improved methods for consolidation and fabrication of bar, rod, sheet, and high-quality, small diameter, thin-wall tubing of vanadium-20 without titanium are reported.

  13. 40 CFR 421.220 - Applicability: Description of the secondary molybdenum and vanadium subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... secondary molybdenum and vanadium subcategory. 421.220 Section 421.220 Protection of Environment... POINT SOURCE CATEGORY Secondary Molybdenum and Vanadium Subcategory § 421.220 Applicability: Description of the secondary molybdenum and vanadium subcategory. The provisions of this subpart are...

  14. 40 CFR 421.220 - Applicability: Description of the secondary molybdenum and vanadium subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... secondary molybdenum and vanadium subcategory. 421.220 Section 421.220 Protection of Environment... POINT SOURCE CATEGORY Secondary Molybdenum and Vanadium Subcategory § 421.220 Applicability: Description of the secondary molybdenum and vanadium subcategory. The provisions of this subpart are...

  15. 40 CFR 421.220 - Applicability: Description of the secondary molybdenum and vanadium subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... secondary molybdenum and vanadium subcategory. 421.220 Section 421.220 Protection of Environment... POINT SOURCE CATEGORY Secondary Molybdenum and Vanadium Subcategory § 421.220 Applicability: Description of the secondary molybdenum and vanadium subcategory. The provisions of this subpart are...

  16. Vanadium carcinogenic, immunotoxic and neurotoxic effects: a review of in vitro studies.

    PubMed

    Zwolak, Iwona

    2014-01-01

    Deleterious health effects induced by inorganic vanadium compounds are linked with carcinogenic, immunotoxic and neurotoxic insults. The goal of this review is to provide a summary of mammalian cell culture studies (from the 1990s to most recent) looking into the mode of the above-mentioned adverse actions of vanadium. Regarding the carcinogenicity potential, the key cell-based studies have evidenced the ability of vanadium to induce genotoxic lesions, cell morphological transformation and anti-apoptotic effects in a certain type of cells. Two contradictory effects of vanadium on the immune functions of cells have been observed in cell culture studies. The first effect involves reduction of cell immune responses such as vanadium-dependent inhibition of cytokine-inducible functions, which may underlie the mechanism of vanadium-induced immunosuppression. The second one involves stimulation of immune activity, for example, a vanadium-mediated increase in cytokine production, which may contribute to vanadium-related inflammation. So far, an in vitro evaluation of vanadium neurotoxicity has only been reported in few articles. These papers indicate probable cytotoxic mechanisms resulting from exposure of neurons and glial cells to vanadium. In summary, this literature review collects in vitro reports on adverse vanadium effects and thus provides vanadium researchers with a single, concise source of data.

  17. 40 CFR 440.80 - Applicability; description of the vanadium ore subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... vanadium ore subcategory. 440.80 Section 440.80 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Vanadium Ore Subcategory (Mined Alone and Not as a Byproduct) § 440.80 Applicability; description of the vanadium ore subcategory. The provisions of this subpart H are applicable to discharges from (a) mines...

  18. Vanadium-uranium extraction from Wyoming vanadiferoud silicates. Report of investigations/1983

    SciTech Connect

    Hayashi, M.; Nichols, I.L.; Huiatt, J.L.

    1983-11-01

    The Bureau of Mines conducted laboratory studies on low-grade vanadiferous silicates from the Pumpkin Buttes and Nine Mile Lake deposits of Wyoming to examine techniques for extracting vanadium and uranium. Recovery from low-grade sources such as these could contribute to future vanadium production and reduce reliance on vanadium imports.

  19. Vanadium promotes hydroxyl radical formation by activated human neutrophils.

    PubMed

    Fickl, Heidi; Theron, Annette J; Grimmer, Heidi; Oommen, Joyce; Ramafi, Grace J; Steel, Helen C; Visser, Susanna S; Anderson, Ronald

    2006-01-01

    This study was undertaken to investigate the effects of vanadium in the +2, +3, +4, and +5 valence states on superoxide generation, myeloperoxidase (MPO) activity, and hydroxyl radical formation by activated human neutrophils in vitro, using lucigenin-enhanced chemiluminescence (LECL), autoiodination, and electron spin resonance with 5,5-dimethyl-l-pyrroline N-oxide as the spin trap, respectively. At concentrations of up to 25 microM, vanadium, in the four different valence states used, did not affect the LECL responses of neutrophils activated with either the chemoattractant, N-formyl-l-methionyl-l-leucyl-l-phenylalanine (1 microM), or the phorbol ester, phorbol 12-myristate 12-acetate (25 ng/ml). However, exposure to vanadium in the +2, +3, and +4, but not the +5, valence states was accompanied by significant augmentation of hydroxyl radical formation by activated neutrophils and attenuation of MPO-mediated iodination. With respect to hydroxyl radical formation, similar effects were observed using cell-free systems containing either hydrogen peroxide (100 microM) or xanthine/xanthine oxidase together with vanadium (+2, +3, +4), while the activity of purified MPO was inhibited by the metal in these valence states. These results demonstrate that vanadium in the +2, +3, and +4 valence states interacts prooxidatively with human neutrophils, competing effectively with MPO for hydrogen peroxide to promote formation of the highly toxic hydroxyl radical.

  20. Vanadium Extraction from Refractory Stone Coal Using Novel Composite Additive

    NASA Astrophysics Data System (ADS)

    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.

  1. Geochemical controls on vanadium accumulation in fossil fuels

    USGS Publications Warehouse

    Breit, G.N.; Wanty, R.B.

    1989-01-01

    High vanadium contents in petroleum and other fossil fuels have been attributed to organic-matter type, organisms, volcanic emanations, diffusion of sea water, and epigenetic enrichment. However, these factors are inadequate to account for the high abundance of vanadium in some fossil fuels and the paucity in others. By examining vanadium deposits in sedimentary rocks with sparse organic matter, constraints are placed on processes controlling vanadium accumulation in organic-rich sediments. Vanadium, as vanadate (V(V)), entered some depositional basins in oxidizing waters from dry, subaerial environments. Upon contact with organic matter in anoxic waters, V(V) is reduced to vanadyl (V(IV)), which can be removed from the water column by adsorption. H2S reduces V(IV) to V(III), which hydrolyzes and precipitates. The lack of V(III) in petroleum suggests that reduction of V(IV) to V(III) is inhibited by organic complexes. In the absence of strong complexing agents, V(III) forms and is incorporated in clay minerals.

  2. Geochemical controls of vanadium accumulation in fossil fuels

    USGS Publications Warehouse

    Breit, G.N.; Wanty, R.B.

    1989-01-01

    High vanadium contents in petroleum and other fossil fuels have been attributed to organic-matter type, organisms, volcanic emanations, diffusion of sea water, and epigenetic enrichment. However, these factors are inadequate to account for the high abundance of vanadium in some fossil fuels and the paucity in others. By examining vanadium deposits in sedimentary rocks with sparse organic matter, constraints are placed on processes controlling vanadium accumulation in organic-rich sediments. Vanadium, as vanadate (V(V)), entered some depositional basins in oxidizing waters from dry, subaerial environments. Upon contact with organic matter in anoxic waters, V(V) is reduced to vanadyl (V(IV)), which can be removed from the water column by adsorption. H2S reduces V(IV) to V(III), which hydrolyzes and precipitates. The lack of V(III) in petroleum suggests that reduction of V(IV) to V(III) is inhibited by organic complexes. In the absence of strong complexing agents, V(III) forms and is incorporated in clay minerals.

  3. Can Vanadium Be Substituted into LiFePO4

    SciTech Connect

    Omenya F.; Nam K.; Chernova N.A.; Upreti S.; Zavalij P.Y.; Nam K.-W.; Yang X.-Q.; Whittingham M.S.

    2011-11-08

    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.

  4. Electrochemically Induced Transformations of Vanadium Dioxide Nanocrystals.

    PubMed

    Dahlman, Clayton J; LeBlanc, Gabriel; Bergerud, Amy; Staller, Corey; Adair, Jacob; Milliron, Delia J

    2016-10-12

    Vanadium dioxide (VO2) undergoes significant optical, electronic, and structural changes as it transforms between the low-temperature monoclinic and high-temperature rutile phases. Recently, alternative stimuli have been utilized to trigger insulator-to-metal transformations in VO2, including electrochemical gating. Here, we prepare and electrochemically reduce mesoporous films of VO2 nanocrystals, prepared from colloidally synthesized V2O3 nanocrystals that have been oxidatively annealed, in a three-electrode electrochemical cell. We observe a reversible transition between infrared transparent insulating phases and a darkened metallic phase by in situ visible-near-infrared spectroelectrochemistry and correlate these observations with structural and electronic changes monitored by X-ray absorption spectroscopy, X-ray diffraction, Raman spectroscopy, and conductivity measurements. An unexpected reversible transition from conductive, reduced monoclinic VO2 to an infrared-transparent insulating phase upon progressive electrochemical reduction is observed. This insulator-metal-insulator transition has not been reported in previous studies of electrochemically gated epitaxial VO2 films and is attributed to improved oxygen vacancy formation kinetics and diffusion due to the mesoporous nanocrystal film structure.

  5. Fabrication and design of vanadium oxide microbolometer

    NASA Astrophysics Data System (ADS)

    Abdel-Rahman, M.; Al-Khalli, N.; Zia, M. F.; Alduraibi, M.; Ilahi, B.; Awad, E.; Debbar, N.

    2017-02-01

    Vanadium oxide (VxOy) multilayer sandwich structures previously studied by our group were found to yield a sensitive thermometer thin film material suitable for microbolometer applications. In this work, we aim to estimate the performance of a proposed air-bridge microbolometer configuration based on VxOy multilayer sandwich structure thermometer thin films. For this purpose, a microbolometer was fabricated on silicon (Si) substrate covered with a silicon nitride (Si3N4) insulating layer using VxOy thermometer thin film material. The fabricated microbolometer was patterned using electron-beam lithography and liftoff techniques and it was characterized in terms of its voltage repsonsivity (Rv), signal to noise ratio (SNR), noise equivalent power (NEP) and detectivity D*. A model was then developed by the aid of numerical optical/thermal simulations and experimentally measured parameters to estimate the performance of the microbolometer when fabricated in an air-bridge configuration. The estimated D* was found to be 1.55×107 cm.√Hz/ W.

  6. Electroslag remelting of a vanadium alloy

    SciTech Connect

    Nafziger, R.H.; Smolik, G.R.; Carmack, W.J.

    1996-12-31

    The Bureau of Mines, in cooperation with the Idaho National Engineering Laboratory, has electroslag melted a V-5Ti-5Cr alloy using a fused CaF{sub 2} flux. The alloy is a candidate for use in future fusion reactors. One objective of this research was to evaluate the feasibility of the electroslag melting process in separating simulated radioactive isotopes from the V alloy to demonstrate recyclability. Small amounts of Ca, Y, and Mn were added as surrogates for radioactive isotopes. Results showed that this vanadium alloy can be electroslag melted satisfactorily. The impurities added intentionally were removed or decreased successfully. Among the major alloying constituents, Cr was retained but there were some Ti losses. The latter may be controlled with process refinements. This research suggests that the electroslag melting process could be a suitable method for recycling V alloys after use in future fusion reactors, or for processing other reactive metal alloys with more immediate applications. 3 refs., 1 fig., 5 tabs.

  7. Membrane development for vanadium redox flow batteries.

    PubMed

    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.

  8. Feasibility of using solid sampling graphite furnace atomic absorption spectrometry for speciation analysis of volatile and non-volatile compounds of nickel and vanadium in crude oil.

    PubMed

    Silva, Márcia M; Damin, Isabel C F; Vale, Maria Goreti R; Welz, Bernhard

    2007-03-30

    A method for the direct determination of volatile and non-volatile nickel and vanadium compounds in crude oil without previous treatment using direct solid sampling graphite furnace atomic absorption spectrometry is proposed. The crude oil samples were weighed directly onto solid sampling platforms using a microbalance and introduced into a transversely heated solid sampling graphite tube. In previous work of our group losses of volatile nickel and vanadium compounds have been detected, whereas other nickel and vanadium compounds were thermally stable up to 1300 and 1600 degrees C, respectively. In order to avoid this problem different chemical modifiers (conventional and permanent) have been investigated. With 400microg of iridium as permanent modifier, the signal started to drop already after two atomization cycles, possibly because of an interaction of nickel (which is a catalyst poison) with iridium. Twenty micrograms of palladium applied in each determination was found to be optimum for both elements. The palladium was deposited on the platform and submitted to a drying step at 150 degrees C for 75s. After that the sample was added onto the platform and submitted to the furnace program. The influence of sample mass on the linearity of the response and on potential measurement errors was also investigated using four samples with different nickel content. For the sample with the lowest nickel concentration the relationship between mass and integrated absorbance was found to be non-linear when a high sample mass was introduced. It was suspected that the modifier had not covered the entire platform surface, which resulted in analyte losses. This problem could be avoided by using 40microL of 0.5g L(-1) Pd with 0.05% Triton X-100. Calibration curves were established with and without modifier, with aqueous standards, oil-in-water emulsions and the certified reference material NIST SRM 1634c (trace metals in residual fuel oil). The sensitivity for aqueous standards

  9. Vanadium-Binding Ability of Nucleoside Diphosphate Kinase from the Vanadium-Rich Fan Worm, Pseudopotamilla occelata.

    PubMed

    Yamaguchi, Nobuo; Yoshinaga, Masafumi; Kamino, Kei; Ueki, Tatsuya

    2016-06-01

    Polychaete fan worms and ascidians accumulate high levels of vanadium ions. Several vanadiumbinding proteins, known as vanabins, have been found in ascidians. However, no vanadium-binding factors have been isolated from the fan worm. In the present study, we sought to identify vanadiumbinding proteins in the branchial crown of the fan worm using immobilized metal ion affinity chromatography. A nucleoside diphosphate kinase (NDK) homolog was isolated and determined to be a vanadium-binding protein. Kinase activity of the NDK homologue, PoNDK, was suppressed by the addition of V(IV), but was unaffected by V(V). The effect of V(IV) on PoNDK precedes its activation by Mg(II). This is the first report to describe the relationship between NDK and V(IV). PoNDK is located in the epidermis of the branchial crown, and its distribution is very similar to that of vanadium. These results suggest that PoNDK is associated with vanadium accumulation and metabolism in P. occelata.

  10. An X-Ray Diffraction Investigation of alpha-Al2O2 Addition to Yttria Stabilized Zirconia (YSZ) Thermal Barrier Coatings Subject to Destabilizing Vanadium Pentoxide (V2O5) Exposure

    DTIC Science & Technology

    1993-09-01

    Stabilized Zirconia TZP - Tetragonal Stabilized Zirconia 6 The effect of ’alloying’ ceramic particles or fibers are clearly evident. The fracture toughness...TA!RL OF CONIMn3S I. INTRO.DUCTION . .. . . . 1 11. BACMWrJD .................... 2 A. CRYSTALLOGRAPHY OF ZIRCONIA .... ............ 2 1. Cubic ...7 1. ZrO2 -Y203 Phase Diagram ......... .......... 7 a. Monoclinic - Tetragonal Transformation 9 b. Cubic

  11. Amphiphilic block copolymer membrane for vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Wang, Fei; Sylvia, James M.; Jacob, Monsy M.; Peramunage, Dharmasena

    2013-11-01

    An amphiphilic block copolymer comprised of hydrophobic polyaryletherketone (PAEK) and hydrophilic sulfonated polyaryletherketone (SPAEK) blocks has been synthesized and characterized. A membrane prepared from the block copolymer is used as the separator in a single cell vanadium redox flow battery (VRB). The proton conductivity, mechanical property, VO2+ permeability and single VRB cell performance of this block copolymer membrane are investigated and compared to Nafion™ 117. The block copolymer membrane showed significantly improved vanadium ion selectivity, higher mechanical strength and lower conductivity than Nafion™ 117. The VRB containing the block copolymer membrane exhibits higher coulombic efficiency and similar energy efficiency compared to a VRB using Nafion™ 117. The better vanadium ion selectivity of the block copolymer membrane has led to a much smaller capacity loss during 50 charge-discharge cycles for the VRB.

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

    USGS Publications Warehouse

    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.

  13. Insulating phases of vanadium dioxide are Mott-Hubbard insulators

    NASA Astrophysics Data System (ADS)

    Huffman, T. J.; Hendriks, C.; Walter, E. J.; Yoon, Joonseok; Ju, Honglyoul; Smith, R.; Carr, G. L.; Krakauer, H.; Qazilbash, M. M.

    2017-02-01

    We present comprehensive broadband optical spectroscopy data on two insulating phases of vanadium dioxide (V O2 ): monoclinic M2 and triclinic. The main result of our work is that the energy gap and the electronic structure are essentially unaltered by the first-order structural phase transition between the M2 and triclinic phases. Moreover, the optical interband features in the M2 and triclinic phases are remarkably similar to those observed in the well-studied monoclinic M1 insulating phase of V O2 . As the energy gap is insensitive to the different lattice structures of the three insulating phases, we rule out vanadium-vanadium pairing (the Peierls component) as the dominant contributor to the opening of the gap. Rather, the energy gap arises primarily from intra-atomic Coulomb correlations.

  14. Novel hybrid materials based on the vanadium oxide nanobelts

    NASA Astrophysics Data System (ADS)

    Zabrodina, G. S.; Makarov, S. G.; Kremlev, K. V.; Yunin, P. A.; Gusev, S. A.; Kaverin, B. S.; Kaverina, L. B.; Ketkov, S. Yu.

    2016-04-01

    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 V2O5·nH2O gel with surfactants (TBAB, CTAB) used as structure-directing agents, where CTAB - cetyltrimethylammonium bromide, TBAB - tetrabutylammonium bromide. Hybrid materials were prepared decoration of (CTA)0.33V2O5 flexible nanobelts with cationic zinc phthalocyanine by the ion-exchange route. Investigations of the thermal stability, morphologies and structures of the (CTA)0.33V2O5, (TBA)0.16V2O5 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.

  15. Oxidative demethylation of 2-picolines on vanadium oxide catalysts

    SciTech Connect

    Suvorov, B.V.; Glubokovskikh, L.K.; Demin, V.V.; Kan, I.I.

    1988-07-10

    One of the known methods for the preparation of pyridine is based on the dealkylation of alkylpyridines in the presence of vanadium-containing catalysts, molecular oxygen and steam. By using the oxidative demethylation of 2-picoline in the presence of steam on a fused vanadium(V) oxide, pyridine can be obtained in a yield of up to 88% of theory. To lower the consumption of vanadium(V) oxide and increase the thermostability of the catalyst, they studied the possible use of V/sub 2/O/sub 5/ catalysts on various carriers (diatomite, silica gel, porcelain balls), including the industrially produced brand SVD and SVS catalysts. The SVS brand catalyst has a satisfactory activity and selectivity in the oxidation demethylation of 2-picoline into pyridine. Under optimal conditions, pyridine is formed on this catalyst in a yield of 88% of the theoretical.

  16. Structure and properties of bimetallic titanium and vanadium oxide clusters.

    PubMed

    Helmich, Benjamin; Sierka, Marek; Döbler, Jens; Sauer, Joachim

    2014-05-14

    By employing a genetic algorithm together with density functional theory (B3LYP), we investigate the most stable minimum structures of several bimetallic titanium and vanadium oxide clusters that contain four metal atoms. The following compositions are studied: VnTin-4O10(-) (n = 1-4), (TiO2)VOn(-) (n = 1-4), and (TiO2)VOn(+) (n = 1-3). Apart from (TiO2)3VO(-), vanadium oxo groups are always part of the most stable minimum structures when vanadium is present. Anti-ferromagnetic coupling lowers the energy substantially if spin centers are located at neighbored metal atoms rather than at distant oxygen radical sites. Vanadium-rich or oxygen-poor compositions prefer symmetric adamantane-like cage structures, some of which have already been proposed in a previous study. In contrast, vanadium-poor and oxygen-rich compositions show versatile structural motifs that cannot be intuitively derived from the symmetric cage motif. Particularly, for Ti4O10(-) there are several non-symmetric and distorted cages that have an up to 68 kJ mol(-1) lower energy than the symmetric adamantane-like cage structure. Nevertheless, for the adamantane-like cage the simulated infra-red spectrum (within the harmonic approximation) agrees best with the experimental vibrational spectrum. The oxidative power of the (TiO2)3VO3(-) and (TiO2)3VO2(+) clusters as measured by the energy of removing 1/2 O2 (297 and 227 kJ mol(-1), respectively) is less than that of the pure vanadium oxide clusters (V2O5)VO3(-) and (V2O5)VO2(+) (283 and 165 kJ mol(-1), respectively).

  17. Effect of dietary vanadium on intestinal microbiota in broiler.

    PubMed

    Wang, Kangping; Cui, Hengmin; Deng, Yuanxin; Peng, Xi; Zuo, Zhicai; Fang, Jing; Deng, Junliang; Cui, Wei; Wu, Bangyuan

    2012-11-01

    The purpose of this 42-day study was to examine the effect of dietary vanadium on intestinal microorganism diversity in the duodenum, ileum, cecum, and rectum segments of broilers by the plate count and polymerase chain reaction-denaturing gradient gel electrophoresis (DGGE). A total of 420 1-day-old avian broilers were divided into six groups and fed on a control diet or the same diet supplemented with vanadium at the doses of 5, 15, 30, 45, and 60 mg/kg in the form of ammonium metavanadate. In comparison with control group, the dietary vanadium at the doses of 45 and 60 mg/kg could decrease the counts of Bifidobacterium spp. in the intestinal tract at 21 and 42 days of age. With increasing level in dietary vanadium, the counts of Escherichia coli were significantly increased in the ileum, cecum, and rectum and were decreased in the duodenum at 21 and 42 days of age. However, the counts of Lactobacilli were decreased in the cecum and rectum and increased in the ileum of 45 and 60 mg/kg groups. The colonization of these three bacteria could be affected by dietary vanadium. DGGE analysis showed that the number of bands in duodenum, ileum, cecum, and rectum were obviously decreased in the 30, 45, and 60 mg/kg groups at 21 and 42 days of age. In conclusion, the dietary vanadium in excess of 30 mg/kg could alter the amount and diversity of intestinal bacteria in broilers, implying that the structure and initial balance in the intestinal microbiota were disrupted.

  18. Research and development on vanadium alloys for fusion applications

    SciTech Connect

    Zinkle, S.J.; Rowcliffe, A.F.; Matsui, H.; Abe, K.; Smith, D.L.; Osch, E. van; Kazakov, V.A.

    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.

  19. Fever and neutrophilic alveolitis caused by a vanadium based catalyst

    PubMed Central

    Vandenplas, O; Binard-Van, C; Gregoire, J; Brumagne, A; Larbanois, A

    2002-01-01

    Methods: The investigation included inhalation challenge with the suspected compound combined with monitoring of lung function tests and post-challenge bronchoalveolar lavage. Results: Exposure to the vanadium containing catalyst for 120 minutes resulted in a sustained decline in forced vital capacity and forced expiratory volume in one second, while the transfer factor for carbon monoxide did not change significantly. The subject developed fever and peripheral blood neutrophilia. Bronchoalveolar lavage performed 48 hours after the end of challenge exposure showed a marked increase in neutrophils (60% of total cell count). Conclusions: Exposure to vanadium can cause a metal fume fever-like syndrome associated with neutrophilic alveolitis. PMID:12409538

  20. Vanadium and Other Elements in Greenland Ice Cores

    DTIC Science & Technology

    1976-07-01

    Photograph by C’.C. Langway , Jr.) :1 CRREL Report 76-24 Vanadium and other elements in Greenland ice cores M.M. Herron, C.C. Langway , Jr., H.V. Weiss...Chemistry, San Diego State University; by Dr. C.C. Langway , Jr., Chairman of the Department of Geological Sciences, State University of New. York at Buffalo...the use of such commercial products. ij! 𔃼y\\ .j =3 VANADIUM AND OTHER ELEMENTS IN GREENLAND ICE CORES M.M. Herron;C.C. Langway , Jr., H.V.,Weiss, J

  1. A significantly improved membrane for vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Jia, Chuankun; Liu, Jianguo; Yan, Chuanwei

    A novel sandwich-type sulfonated poly(ether ether ketone) (SPEEK)/tungstophosphoric acid (TPA)/polypropylene (PP) composite membrane for a vanadium redox flow battery (VRB) has been developed with improved properties: the permeability of vanadium ions is greatly reduced and the performance of the VRB cell is greatly increased. The membrane is based on a traditional SPEEK membrane embedded with TPA but PP is used to enhance the membrane for the first time. Although its voltage efficiency (VE) is a little lower than that of a Nafion 212 membrane, it is expected to have good prospects for VRB systems because of its low cost and good performance.

  2. Sorption preconcentration of vanadium for its determination in sea water

    SciTech Connect

    Andreeva, I.Yu.; Lebedeva, L.I.; Izotova, Yu.A.; Danilova, E.Ya.

    1987-08-10

    This work is devoted to a study of the conditions of vanadium sorption by a fibrous sorbent with a view to evolving a procedure for its determination in sea water. The sorbent was the same as used by them earlier for molybdenum preconcentration. It is a fiber based on polyethylenepolyamine-modified polyacrylonitrile. The sorbent contained 80% tertiary and approx. = 20% primary and secondary amino groups. Static exchange capacity of the sorbent relative to HCl 2 mmole/g, swelling 34%, fiber diameter 0.016 mm. The vanadium content was determined photometrically using acidic chromium blue K.

  3. Vanadium(V) complexes of a tripodal ligand, their characterisation and biological implications.

    PubMed

    Maurya, Mannar R; Uprety, Bhawna; Avecilla, Fernando; Adão, Pedro; Costa Pessoa, J

    2015-10-28

    The reaction of the tripodal tetradentate dibasic ligand 6,6'-(2-(pyridin-2-yl)ethylazanediyl)bis(methylene)bis(2,4-di-tert-butylphenol), H2L(1)I, with [V(IV)O(acac)2] in CH3CN gives the V(V)O-complex, [V(V)O(acac)(L(1))] 1. Crystallisation of 1 in CH3CN at ∼0 °C gives dark blue crystals of 1, while at room temperature it affords dark green crystals of [{V(V)O(L(1))}2μ-O] 3. Upon prolonged treatment of 1 in MeOH, [V(V)O(OMe)(MeOH)(L(1))] 2 is obtained. All three complexes were analysed by single-crystal X-ray diffraction, depicting a distorted octahedral geometry around vanadium. In the reaction of H2L(1) with V(IV)OSO4 partial hydrolysis of the tripodal ligand results in the elimination of the pyridyl fragment of L(1) and the formation of H[V(V)O2(L(2))] 4 containing the ONO tridentate ligand 6,6'-azanediylbis(methylene)bis(2,4-di-tert-butylphenol), H2L(2)II. Compound 4, which was not fully characterised, undergoes dimerization in acetone yielding the hydroxido-bridged [{V(V)O(L(2))}2μ-(OH)2] 5 having a distorted octahedral geometry around each vanadium. In contrast, from a solution of 4 in acetonitrile, the dinuclear compound [{V(V)O(L(2))}2μ-O] 6 is obtained, with a trigonal bipyramidal geometry around each vanadium. The methoxido complex 2 is successfully employed as a functional catechol-oxidase mimic in the oxidation of catechol to o-quinone under air. The process was confirmed to follow a Michaelis-Menten type kinetics with respect to catechol, the Vmax and KM values obtained being 7.66 × 10(-6) M min(-1) and 0.0557 M, respectively, and the turnover frequency is 0.0541 min(-1). A similar reaction with the bulkier 3,5-di-tert-butylcatechol proceeded at a much slower rate. Complex 2 was also used as a catalyst precursor for the oxidative bromination of thymol in aqueous medium. The selectivity shows quite interesting trends, namely when not using excess of the primary oxidizing agent, H2O2, the para mono-brominated product corresponds to ∼93% of the

  4. Comparison of vanadium-rich activity of three species fungi of basidiomycetes.

    PubMed

    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 < 0.05) and the body weight of the alloxan-induced hyperglycemic mice was increased gradually. Thus, we selected C. comatus to absorb vanadium and chose 0.4% as the optimal concentration of vanadium for the pharmacological works.

  5. Vanadium-mediated lipid peroxidation in microsomes from human term placenta

    SciTech Connect

    Byczkowski, J.Z.; Wan, B.; Kulkarni, A.P.

    1988-11-01

    Vanadium is considered an essential element present in living organisms in trace amounts but it is toxic when introduced in excessive doses to animals and humans. Vanadium compounds are extensively used in modern industry and occupational exposure to high doses of vanadium is quite common. In pregnant mice, vanadium accumulates preferentially in the placenta and to lower extent in fetal skeleton and mammary gland during exposure to radioactive vanadium. Accumulation of vanadium in fetoplacental unit may present threat to the fetus by interacting with enzymes and ion-transporting systems in membranes. It is also possible that accumulation of vanadium with its concomitant reduction to vanadyl may lead to lipid peroxidation, followed by damage to biological membranes, lysosomal enzymes release and destruction of placental tissue. To explore some of these possibilities the authors decided to examine whether vanadate can undergo redox cycling in microsomes from human term placenta (HTP) that can lead to lipid peroxidation.

  6. Influence of vanadium concentration and temperature on the preparation of electrochromic thin films of ammonium intercalated vanadium(V) oxide xerogel nanoribbons.

    PubMed

    Najdoski, Metodija; Koleva, Violeta; Samet, Aksu

    2014-09-07

    A new and simple chemical method for deposition of thin films of ammonium intercalated V2O5·nH2O xerogels has been designed. The chemical deposition has been performed in aqueous solutions of ammonium metavanadate and acetic acid at temperatures between 50 and 85 °C. Depending on the vanadium concentration and deposition temperature xerogels with different composition have been prepared. The structure, morphology, electrochemical and electrochromic behaviour of the thin films with a composition of (NH4)0.15V2O5·1.3H2O have been examined. The film morphology comprises randomly oriented ribbon-like units (100 nm wide and about 500 nm long) which are composed of aggregated primary smaller particles in the nanoscale region of 50-100 nm. Two relatively stable redox pairs are observed in the cyclic voltammograms which correspond to the two-step electrochromism with colour transformations yellow/green and green/blue. The thin film thickness is found to have strong influence on the transmittance variance as deduced by the optical spectra of the reduced and oxidized states. The best result regarding the transmittance variance of 54% at 400 nm is achieved with thin films with thickness of about 200 nm which makes the prepared films very attractive for application in electrochromic devices.

  7. Interaction of trace levels of vanadium(IV) and vanadium(V) in biological systems

    SciTech Connect

    Crans, D.C.; Bunch, R.L.; Theisen, L.A. )

    1989-09-13

    Enzyme kinetics have been used to study interactions of trace-level concentrations of vanadate (V(V)) and vanadyl cation (V(IV)) in biological systems. A quantitative method based on the inhibition of alkaline or acid phosphatase by monomeric vanadate or vanadyl cation has been developed to determine the concentration of free monomeric vanadate or vanadyl cation at 10{sup {minus}5}-10{sup {minus}7} M vanadium concentrations. Interactions of vanadate and vanadyl cation with potential ligands including buffers, chelating agents, enzyme substrates, cofactors, amino acids, peptides, and proteins were examined. Seven out of 26 commonly used buffers were found to strongly complex vanadate, and an additional 11 buffers were found to complex vanadate to various degrees. The vanadyl cation generally interacts more strongly with these buffers than does vanadate.

  8. Effects of Microwave Roasting on the Kinetics of Extracting Vanadium from Vanadium Slag

    NASA Astrophysics Data System (ADS)

    Zhang, Guoquan; Zhang, Ting-an; Lü, Guozhi; Zhang, Ying; Liu, Yan; Zhang, Weiguang

    2016-02-01

    The kinetics of extracting vanadium (V) from microwave-roasted (MR) vanadium slag (V-slag) with concentrated H2SO4 were investigated. The microwave irradiation experiments were performed in a modified microwave muffle furnace at temperatures ranging from 150°C to 750°C. The x-ray diffraction analysis indicated that the spinel phase of the V-slag is destroyed after 10 min of roasting. The phase composition of the V-slag was changed by the roasting process, and a new Fe2O3 phase appeared in the samples roasted at higher temperatures. Compared to the raw slag, the surface area, pore volume, and pore size of the MR slags were much lower. It was easier to leach V from the MR samples than the raw sample with the H2SO4 solution, and the leaching process was accelerated in the MR samples. When the V-slag was roasted at 150°C and 350°C (MR@150 and MR@350, respectively), the apparent activation energy was decreased from 77.65 kJ/mol to 68.42 kJ/mol and 66.68 kJ/mol, respectively. The process of leaching V from the raw and MR slags was controlled by both the surface chemical reactions and internal diffusion. The reaction orders of the raw, MR@150, and MR@350 V-slags, with respect to the H2SO4 concentration, were 1.23, 0.75, and 0.70, respectively.

  9. Magnetic stirrer induced dispersive ionic-liquid microextraction for the determination of vanadium in water and food samples prior to graphite furnace atomic absorption spectrometry.

    PubMed

    Naeemullah; Kazi, Tasneem Gul; Tuzen, Mustafa

    2015-04-01

    A new dispersive liquid-liquid microextraction, magnetic stirrer induced dispersive ionic-liquid microextraction (MS-IL-DLLME) was developed to quantify the trace level of vanadium in real water and food samples by graphite furnace atomic absorption spectrometry (GFAAS). In this extraction method magnetic stirrer was applied to obtained a dispersive medium of 1-butyl-3-methylimidazolium hexafluorophosphate [C4MIM][PF6] in aqueous solution of (real water samples and digested food samples) to increase phase transfer ratio, which significantly enhance the recovery of vanadium - 4-(2-pyridylazo) resorcinol (PAR) chelate. Variables having vital role on desired microextraction methods were optimised to obtain the maximum recovery of study analyte. Under the optimised experimental variables, enhancement factor (EF) and limit of detection (LOD) were achieved to be 125 and 18 ng L(-1), respectively. Validity and accuracy of the desired method was checked by analysis of certified reference materials (SLRS-4 Riverine water and NIST SRM 1515 Apple leaves). The relative standard deviation (RSD) for 10 replicate determinations at 0.5 μg L(-1) of vanadium level was found to be <5.0%. This method was successfully applied to real water and acid digested food samples.

  10. Vanadium isotopic difference between the silicate Earth and meteorites

    NASA Astrophysics Data System (ADS)

    Nielsen, Sune G.; Prytulak, Julie; Wood, Bernard J.; Halliday, Alex N.

    2014-03-01

    It has been argued that the stable isotopic composition of the element vanadium (V) provides a potential indicator of the effects high-energy irradiation early in Solar System development. Such irradiation would produce enrichment in the minor isotope, 50V compared with the 400 times more abundant 51V (Gounelle et al., 2001; Lee et al., 1998). Here we show that the vanadium isotopic composition of the silicate Earth is enriched in 51V by ∼0.8‰ compared with carbonaceous and ordinary chondrites as well as achondrites from Mars and the asteroid 4 Vesta. Although V is depleted by core formation, experiments reveal no isotopic fractionation between metal and silicate that could account for the observed difference in V isotope composition between terrestrial and extraterrestrial materials. Nucleosynthetic provenance of the terrestrial vanadium isotope offset is inconsistent with anomalies of other nucleosynthetically produced isotopes in bulk meteorites, which are more variable than vanadium (Burkhardt et al., 2011; Carlson et al., 2007; Trinquier et al., 2009). Furthermore, V isotopes are unlikely to have been affected by volatilization, parent body alteration or impact erosion of Earth's surface. Therefore, the cause of the isotopic difference is unclear. One possibility is that Earth's isotopically heavier V reflects a deficit in material irradiated during the initial stages of Solar System formation. Whatever the cause, the terrestrial deficit in 50V implies that bulk Earth cannot be entirely reconstructed by mixtures of different meteorites.

  11. Vanadium based materials as electrode materials for high performance supercapacitors

    NASA Astrophysics Data System (ADS)

    Yan, Yan; Li, Bing; Guo, Wei; Pang, Huan; Xue, Huaiguo

    2016-10-01

    As a kind of supercapacitors, pseudocapacitors have attracted wide attention in recent years. The capacitance of the electrochemical capacitors based on pseudocapacitance arises mainly from redox reactions between electrolytes and active materials. These materials usually have several oxidation states for oxidation and reduction. Many research teams have focused on the development of an alternative material for electrochemical capacitors. Many transition metal oxides have been shown to be suitable as electrode materials of electrochemical capacitors. Among them, vanadium based materials are being developed for this purpose. Vanadium based materials are known as one of the best active materials for high power/energy density electrochemical capacitors due to its outstanding specific capacitance and long cycle life, high conductivity and good electrochemical reversibility. There are different kinds of synthetic methods such as sol-gel hydrothermal/solvothermal method, template method, electrospinning method, atomic layer deposition, and electrodeposition method that have been successfully applied to prepare vanadium based electrode materials. In our review, we give an overall summary and evaluation of the recent progress in the research of vanadium based materials for electrochemical capacitors that include synthesis methods, the electrochemical performances of the electrode materials and the devices.

  12. Organometalic carbosilane polymers containing vanadium and their preparation

    NASA Technical Reports Server (NTRS)

    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.

  13. Evaluation of lithium-vanadium oxide cells. Technical report

    SciTech Connect

    Hunger, H.F.

    1982-12-01

    Hermetically sealed lithium-vanadium oxide cells were evaluated after one year of storage. From cell capacity measurements, excellent charge retention was found. The energy to weight and volume ratios did not change substantially during storage. The rate capability observed is within practical limits. At 0 degrees C the rate is 31 percent of that at room temperature.

  14. Thermochemical hydrogen production by a vanadium/chlorine process

    NASA Astrophysics Data System (ADS)

    Knoche, K. F.; Schuster, P.; Ritterbex, T.

    A pure thermochemical cycle of the vanadium/chlorine family similar to the one proposed earlier by Funk et al. (1964) is investigated experimentally with respect to certain chemical reactions. A complete mass and energy balance of this cycle is given. The thermal efficiency is calculated to be approximately 40%.

  15. Vanadium exposure-induced neurobehavioral alterations among Chinese workers.

    PubMed

    Li, Hong; Zhou, Dinglun; Zhang, Qin; Feng, Chengyong; Zheng, Wei; He, Keping; Lan, Yajia

    2013-05-01

    Vanadium-containing products are manufactured and widely used in the modern industry. Yet the neurobehavioral toxicity due to occupational exposure to vanadium remained elusive. This cross-sectional study was designed to examine the neurotoxic effects of occupational vanadium exposure. A total of 463 vanadium-exposed workers (exposed group) and 251 non-exposed workers (control group) were recruited from a Steel and Iron Group in Sichuan, China. A WHO-recommended neurobehavioral core test battery (NCTB) and event-related auditory evoked potentials test (P300) were used to assess the neurobehavioral functions of all study subjects. A general linear model was used to compare outcome scores between the two groups while controlling for possible confounders. The exposed group showed a statistically significant neurobehavioral alteration more than the control group in the NCTB tests. The exposed workers also exhibited an increased anger-hostility, depression-dejection and fatigue-inertia on the profile of mood states (p<0.05). Performances in the simple reaction time, digit span, benton visual retention and pursuit aiming were also poorer among exposed workers as compared to unexposed control workers (p<0.05). Some of these poor performances in tests were also significantly related to workers' exposure duration. P300 latencies were longer in the exposed group than in the control (p<0.05). Longer mean reaction times and more counting errors were also found in the exposed workers (p<0.05). Given the findings of our study and the limitations of neurobehavioral workplace testing, we found evidence of altered neurobehavioral outcomes by occupational exposure to vanadium.

  16. Salinity dependence of vanadium toxicity against the brackish water hydroid Cordylophora caspia.

    PubMed

    Ringelband, U

    2001-01-01

    Vanadium, an abundant metal, enters the environment through natural rock weathering or by combustion of oil products. A third pathway is the leaching of vanadium-rich building materials. Stones made from steel industry residual slags, so-called slag stones, contain rather large amounts of vanadium. The increasing use of these slag stones in riverbank reinforcement has therefore led to increased interest in the toxicity of vanadium to aquatic organisms. The aim of the study was to determine the toxicity of vanadium to the brackish water hydroid Cordylophora caspia and the effect of vanadium on the membrane-bound enzyme Na, K-ATPase at various salinities. EC50 values for population growth inhibition were determined from 1.74 to 7.96 mg x L(-1) vanadium, depending on salinity. The maximum inhibition of population growth by vanadium was observed at low salinities. Correspondingly, maximum Na, K-ATPase inhibition was also measured at low salinities and decreased with increasing salinity. The present study suggests that the observed inhibition of population growth of C. caspia caused by vanadium-contaminated rearing water is due to the vanadium-induced inhibition of phosphatases.

  17. Synthesis and characterization of novel Wells-Dawson-type mono vanadium(V)-substituted tungsto-polyoxometalate isomers: 1- and 4-[S2VW17O62](5-).

    PubMed

    Ueda, Tadaharu; Ohnishi, Miho; Shiro, Motoo; Nambu, Jun-ichi; Yonemura, Toshiaki; Boas, John F; Bond, Alan M

    2014-05-19

    Two vanadium(V)-substituted tungsto-polyoxometalate isomers, 1- and 4-[S2VW17O62](5-), were prepared as their tetra-alkyl ammonium salts from a W(VI)-H2SO4-V(V) reaction mixture in aqueous CH3CN solution. X-ray crystallographic structural analysis revealed that both isomers have a Wells-Dawson-type structure with a higher occupancy of vanadium at polar sites and belt sites for 1- and 4-[S2VW17O62](5-), respectively. The isomers were also characterized by elemental analysis, infrared, Raman, UV-vis, and (51)V NMR spectroscopies as well as voltammetry, and the data obtained were compared with that derived from [S2W18O62](4-). Significantly, the reversible potentials for the vanadium(V/IV) couple for both 1- and 4-[S2VW17O62](5-) in CH3CN (0.1 M n-Bu4NPF6) are considerably more positive than the tungstate reduction process exhibited by the [S2W18O62](4-) framework, implying that the presence of vanadium should be useful in catalytic reactions. The one-electron-reduced [S2V(IV)W17O62](6-) forms of both isomers were prepared in solution by controlled potential bulk electrolysis and characterized by voltammetry and EPR spectroscopy.

  18. Molecular geometry of vanadium dichloride and vanadium trichloride: a gas-phase electron diffraction and computational study.

    PubMed

    Varga, Zoltán; Vest, Brian; Schwerdtfeger, Peter; Hargittai, Magdolna

    2010-03-15

    The molecular geometries of VCl2 and VCl3 have been determined by computations and gas-phase electron diffraction (ED). The ED study is a reinvestigation of the previously published analysis for VCl2. The structure of the vanadium dichloride dimer has also been calculated. According to our joint ED and computational study, the evaporation of a solid sample of VCl2 resulted in about 66% vanadium trichloride and 34% vanadium dichloride in the vapor. Vanadium dichloride is unambiguously linear in its 4Sigma(g)+ ground electronic state. For VCl3, all computations yielded a Jahn-Teller-distorted ground-state structure of C(2v) symmetry. However, it lies merely less than 3 kJ/mol lower than the 3E'' state (D(3h) symmetry). Due to the dynamic nature of the Jahn-Teller effect in this case, rigorous distinction cannot be made between the planar models of either D(3h) symmetry or C(2v) symmetry for the equilibrium structure of VCl3. Furthermore, the presence of several low-lying excited electronic states of VCl3 is expected in the high-temperature vapor. To our knowledge, this is the first experimental and computational study of the VCl3 molecule.

  19. 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}

    SciTech Connect

    Dong, Xinbo; Wang, Danjun; Li, Kebin; Zhen, Yanzhong; Hu, Huaiming; Xue, Ganglin

    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}.

  20. Assessing the solubility controls on vanadium in groundwater, northeastern San Joaquin Valley, CA

    USGS Publications Warehouse

    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

  1. Influence of vanadium-organic ligands treatment on selected metal levels in kidneys of STZ rats.

    PubMed

    Krośniak, Mirosław; Kowalska, Joanna; Francik, Renata; Gryboś, Ryszard; Blusz, Magdalena; Kwiatek, Wojciech M

    2013-06-01

    The objective of the study was to investigate the effects of five organic vanadium complexes supplement and a small dose of insulin injection on V, Fe, Cu, Zn, Mn, Ca, and K level in the streptozotocin diabetic rat's kidney during a 5-week treatment with the tested complexes. In all groups of animals, metal level in the lyophilized kidney organs was investigated by means of the proton induced X-ray emission method. Tissue vanadium level was naturally higher in vanadium-treated rats. The maximum level of vanadium was observed in the kidney (x(mean) = 16.6 μg/g). The influence of vanadium administration on other metal level in rat's tissue was also investigated. Spectacular influence of vanadium action was observed on copper and zinc level in examined tissue.

  2. Spectroscopic Investigations of the Fouling Process on Nafion Membranes in Vanadium Redox Flow Batteries

    SciTech Connect

    Vijayakumar, M.; Sivakumar, Bhuvaneswari M.; Nachimuthu, Ponnusamy; Schwenzer, Birgit; Kim, Soowhan; Yang, Zhenguo; Liu, Jun; Graff, Gordon L.; Thevuthasan, Suntharampillai; Hu, Jian Z.

    2011-01-01

    The Nafion-117 membrane used in vanadium redox flow battery (VRFB) is analyzed by X-ray photoelectron spectroscopy (XPS) and nuclear magnetic resonance (NMR) spectroscopy. The XPS study reveals the chemical identity and environment of vanadium cations accumulated at the surface due to their low diffusivity. On the other hand, the 17O NMR spectrum explores the diffused vanadium cation from the bulk part of Nafion and shows the chemical bonding of cation and the host membrane. The 19F NMR shows the basic Nafion structure is not altered due to the presence of diffused vanadium cation. Based on these spectroscopic studies, the chemical environment of diffused vanadium cation in the Nafion membrane is discussed. This study also shed light into the possible cause for the high diffusivity of certain vanadium cations inside the Nafion membranes.

  3. Atmospheric pressure chemical vapour deposition of vanadium oxides

    NASA Astrophysics Data System (ADS)

    Manning, Troy Darrell

    The APCVD of vanadium(IV) oxide thin films from halide precursors was investigated. It was found that the phase of vanadium oxide obtained could be controlled by the reactor temperature and precursor ratio. For vanadium(IV) chloride and water, reactor temperatures > 550 °C and an excess of water over VCI4 was required to produce VO2 thin films. For vanadium(V) oxytrichloride and water, reactor temperatures > 550 °C and an excess of water over VOCI3 also produced VO2 but required low total gas flow rates (< 1 L min 1) for complete coverage of the substrate. Vanadium(IV) oxide thin films doped with metal ions (W, Cr, Nb, Ti, Mo or Sn) were also prepared by the APCVD process in order to reduce the thermochromic transition temperature (TC) from 68 °C for the undoped material to < 30 °C. The most successful dopant was tungsten, introduced into the VOCl3, and water system as WCI6, which lowered T to 5 °C for a 3 atom% tungsten doped thin film. Tungsten (VI) ethoxide was introduced into the VCI4 and water system and reduced TC, of VO2, to 42 °C for a 1 atom% tungsten doped thin film. Chromium, introduced as CrCO2Cl2, formed a chromium vanadium oxide that did not display any thermochromic properties. Niobium, introduced as NbCl5 into the VOCl3 system, reduced TC of VO2, but the amount of niobium introduced could not be easily controlled. Molybdenum, introduced as MoCI5, also reduced TC of VO2, but the form of the molybdenum appeared to be different from that required for complete control of TC, Titanium, introduced as TiCl4, produced phase segregated films of VO2 and TiO2, with interesting multifunctional properties and a reduced TC. Tin, introduced as SnCl4, also formed a phase segregated material of VO2, and SnO2, with a slightly reduced TC.

  4. Vanadium oxide based materials: Synthesis, characterization and gas sensing properties

    NASA Astrophysics Data System (ADS)

    Ayesh, Samar I.

    In recent years, the demand for gas sensors based on safety and process control requirements has been expanding. The reason for such demand sterns from environmental and safety concerns since the toxic gases released from automobile exhausts and chemical plants can directly or indirectly pollute our environment and affect our health. Among the chemicals studied, nitrogen oxide (NOx) gases are among the most dangerous air pollutants. Transition metal oxide clusters (or polyoxometalates) provide an exciting opportunity for the design and synthesis of a new generation of materials for efficient NOx sensing. Polyoxometalates are an important and fast emerging class of compounds that exhibit many remarkable properties. Chapter 1 provides introduction and background of chemical sensors. It describes the need for gas sensors and the current status of research in the area of NOx gas sensors in particular. A description of polyoxmetalates and their relevance as potential novel gas sensor materials is also given. Chapter 2 describes the synthesis and characterization by FTIR spectroscopy, elemental analysis, thermogravimetric analysis, manganometric titration, bond valence sum calculation, temperature dependent magnetic properties studies, electron paramagnetic resonance, and complete single crystal X-ray diffraction analysis of newly prepared vanadium oxide based-systems that have been discovered during the course of this work. First, the system containing arrays of decavanadates networked by extensive hydrogen bonding with cyclic nitrogen bases are described. This is followed by the mixed-valence vanadium oxide cluster, [VV 13VIV3O42(Cl)]-7, containing a hitherto unknown vanadium oxide framework structure. Finally the synthesis of 3D-framework materials is described. These compounds have highly symmetrical closely related three-dimensional framework structures consisting vanadium oxide shells {V18O42(XO4)} linked via heterometallic atoms {M' = Cd, Zn} into three

  5. Comparison of damage microstructures in neutron-irradiated vanadium and iron

    SciTech Connect

    Horton, L.L.; Farrell, K.

    1983-01-01

    The cavity morphology and dislocation loop geometry in bcc vanadium are compared with the previously reported observations for neutron-irradiated iron. The specimens were vanadium (V) with 100 wppM of interstitial impurities and vanadium with boron carbide additions (V-B/sub 4/C) which were irradiated to approx. 1 dpa in the same Oak Ridge Research Reactor capsules as the iron specimens.

  6. The public health implications of farming cattle in areas with high background concentrations of vanadium.

    PubMed

    Gummow, B; Botha, C J; Noordhuizen, J P T M; Heesterbeek, J A P

    2005-12-12

    Forty-two adult Brahman-cross cattle farmed extensively in two groups, immediately adjacent to and 2 km from a vanadium processing plant respectively, were slaughtered over a 5 year period at a nearby abattoir. Cattle were being exposed to vanadium at close to no-adverse-effect levels. The dose of vanadium that cattle were taking in prior to slaughter was calculated for each animal from environmental and physiological data using a stochastic risk assessment model. The median exposure doses in the month prior to slaughter ranged from 0.55 to 2.73 mg vanadium/kg body weight/day. A range of tissues was taken from the cattle at slaughter for vanadium determination and tissue levels of vanadium in muscle, liver and kidney are reported. The concentrations of vanadium in the milk of cattle from the same farm sampled over 5 years are also reported. Concentrations were further modelled using a lognormal distribution function to look at possible extreme values that are likely to occur. The concentrations of vanadium in commonly consumed tissues ranged from <0.05 to 11.51 mg/kg (wet-mass basis). The median concentration of vanadium in milk was 0.23 mg vanadium/kg. People drinking milk were at highest risk. The potential oral daily intake of vanadium for people consuming these foodstuffs was modelled using a stochastic model. The model predicted that there is less than a 5% chance that the potential daily intake of vanadium from milk will be >0.44 microg/kg/day for adults. Based on this upper limit it was concluded from current knowledge of toxicity in humans that the tissue and milk residues from cattle should pose no health risk to the consumer.

  7. Vanadium accumulation in carbonaceous rocks: A review of geochemical controls during deposition and diagenesis

    USGS Publications Warehouse

    Breit, G.N.; Wanty, R.B.

    1991-01-01

    Published data relevant to the geochemistry of vanadium were used to evaluate processes and conditions that control vanadium accumulation in carbonaceous rocks. Reduction, adsorption, and complexation of dissolved vanadium favor addition of vanadium to sediments rich in organic carbon. Dissolved vanadate (V(V)) species predominate in oxic seawater and are reduced to vanadyl ion (V(IV)) by organic compounds or H2S. Vanadyl ion readily adsorbs to particle surfaces and is added to the sediment as the particles settle. The large vanadium concentrations of rocks deposited in marine as compared to lacustrine environments are the result of the relatively large amount of vanadium provided by circulating ocean water compared to terrestrial runoff. Vanadium-rich carbonaceous rocks typically have high contents of organically bound sulfur and are stratigraphically associated with phosphate-rich units. A correspondence between vanadium content and organically bound sulfur is consistent with high activities of H2S during sediment deposition. Excess H2S exited the sediment into bottom waters and favored reduction of dissolved V(V) to V(IV) or possibly V(III). The stratigraphic association of vanadiferous and phosphatic rocks reflects temporal and spatial shifts in bottom water chemistry from suboxic (phosphate concentrated) to more reducing (euxinic?) conditions that favor vanadium accumulation. During diagenesis some vanadium-organic complexes migrate with petroleum out of carbonaceous rocks, but significant amounts of vanadium are retained in refractory organic matter or clay minerals. As carbon in the rock evolves toward graphite during metamorphism, vanadium is incorporated into silicate minerals. ?? 1991.

  8. Vanadium chlorite from a sandstone-hosted vanadium-uranium deposit, Henry basin, Utah.

    USGS Publications Warehouse

    Whitney, G.; Northrop, H.R.

    1986-01-01

    This ore deposit formed by reduction and precipitation of U and V in the presence of organic matter at the interface between a stagnant brine and overlying circulating meteoric water. Some samples of the vanadium chlorite (heated before analysis) contain = or >10% V2O5; in fresh samples most of the V is in the V3+ state. XRD data suggest that Fe and V are concentrated preferentially in the interlayer hydroxide sheets of the chlorite. A d060 value of 1.52 A indicates that the chlorite probably has a dioctahedral structure distended by the presence of octahedral Fe and V; it is a IIb polytype. The V ore zone is flanked by peripheral zones with perfectly ordered chlorite/smectite containing much less V than the pure chlorite. Chemical analysis of a sample heated to 900oC before analysis gave SiO2 44.89, Al2O3 25.14, TiO2 0.35, Fe2O3 8.29, MgO 8.47, CaO 0.84, Na2O 0.27, K2O 2.18, Li2O 0.16, UO3 0.92, V2O5 9.14, = 100.65, together with Cr 10, Mn 200, Co 150, Ni 5.8, Cu 10, Zn 140 ppm; XRD, DTG, TG and IR curves are presented. -R.A.H.

  9. Transmutation-induced embrittlement of vanadium and several vanadium alloys in HFIR

    NASA Astrophysics Data System (ADS)

    Ohnuki, S.; Takahashi, H.; Garner, F. A.; Pawel, J. E.; Shiba, K.; Hishinuma, A.

    1996-10-01

    Vanadium, V1Ni, V10Ti and V10Ti1Ni (at%) were irradiated in HFIR to doses ranging from 18 to 30 dpa and temperatures between 300 and 600°C. Since the irradiation was conducted in a highly thermalized neutron spectrum without shielding against thermal neutrons, significant levels of chromium (15-22%) were formed by transmutation. The addition of such large chromium levels caused strong embrittlement. At higher irradiation temperatures radiation-induced segregation of transmutant Cr and solute Ti at specimen surfaces caused strong increases in the density of the alloy. The resultant shrinkage, possibly compounded by thermal cycling, led to cracks developing at all intersections of grain boundaries with the specimen surface. This caused specimens irradiated at 500°C or below to often fail during retrieval from the reactor, as well as during electropolishing and other handling operations. At 600°C, the cracking and embrittlement processes are so severe that only a fine dust, composed mostly of individual grains or chunks of grains, was found in the irradiation capsule.

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

    NASA Astrophysics Data System (ADS)

    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%.

  11. Neurobehavioral and cytotoxic effects of vanadium during oligodendrocyte maturation: a protective role for erythropoietin.

    PubMed

    Mustapha, Oluwaseun; Oke, Bankole; Offen, Nils; Sirén, Anna-Leena; Olopade, James

    2014-07-01

    Vanadium exposure has been known to lead to lipid peroxidation, demyelination and oligodendrocytes depletion. We investigated behaviour and glial reactions in juvenile mice after early neonatal exposure to vanadium, and examined the direct effects of vanadium in oligodendrocyte progenitor cultures from embryonic mice. Neonatal pups exposed to vanadium via lactation for 15 and 22 days all had lower body weights. Behavioural tests showed in most instances a reduction in locomotor activity and negative geotaxis. Brain analyses revealed astrocytic activation and demyelination in the vanadium exposed groups compared to the controls. In cell culture, exposure of oligodendrocytes to 300 μM sodium metavanadate significantly increased cell death. Expression of the oligodendrocyte specific proteins, 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNPase) and oligodendrocyte specific protein (OSP/Claudin) were reduced upon vanadium treatment while simultaneous administration of erythropoietin (EPO; 4-12 U/ml) counteracted vanadium-toxicity. The data suggest that oligodendrocyte damage may explain the increased vulnerability of the juvenile brain to vanadium and support a potential for erythropoietin as a protective agent against vanadium-toxicity during perinatal brain development and maturation.

  12. Montroseite, a new vanadium oxide from the Colorado plateaus

    USGS Publications Warehouse

    Weeks, Alice D.; Cisney, Evelyn A.; Sherwood, Alexander M.

    1953-01-01

    Montroseite, a new vanadium mineral named from Montrose County, Colorado, has been found in four mines in western Colorado and in two mines in eastern Utah. It is black, opaque, submetallic, and occurs in microscopic bladed crystals of the orthorhombic dipyramidal class. The axial ratio is a:b:c = 0.509:1:0.310, the common forms are b {010}, m {110}, p {121}, and a large vicinal form is approximately {0, 10, 1}. The observed specific gravity is 4.0 and the calculated specific gravity is 4.15. The composition is essentially VO(OH), with some iron commonly substituted for vanadium. Partial oxidation to VO2 has taken place. Chemical analyses and X-ray diffraction data are given. Single crystal study indicated that the space group symmetry is Pbnm(D2h16).

  13. Orientation of Vanadium Dioxide Grains on Various Substrates

    NASA Astrophysics Data System (ADS)

    Rivera, Felipe; Davis, Robert; Vanfleet, Richard

    2010-10-01

    Crystalline vanadium dioxide VO2 experiences a fast and reversible semiconductor-to-metal structural phase transition near 68^oC. The changes exhibited during this phase transition comprise a well known change in resistivity of several orders of magnitude, as well as a significant drop in optical transmittance in the infrared. Due to the changes in these optical and electronic properties, vanadium dioxide shows promise as a material to be used in many applications ranging from thermochromic window coatings to optoelectronic devices. However, since there is a structural component to the phase transition of VO2, it is of interest to study the orientation of the crystalline grains deposited. Substrates such as glass, SiO2, Sapphire, and TiO2 have been used for the deposition of this material. We used orientation imaging microscopy to study and characterize the orientation of the grains deposited on several of these substrates. Here we present results on this study.

  14. Hypoglycemic activity of Grifola frondosa rich in vanadium.

    PubMed

    Cui, Bo; Han, Linna; Qu, Jingran; Lv, Yingtao

    2009-11-01

    The hypoglycemic activity of fermented mushroom of Grifola frondosa rich in vanadium (GFRV) was studied in this paper. Alloxan- and adrenalin-induced hyperglycemic mice were used in the study. The blood glucose and the HbA1c of the mice were analyzed respectively. After the mice were administered (ig) with GFRV, the blood glucose and the HbA1c of alloxan-induced hyperglycemic mice decreased (p < 0.05, p < 0.01) and ascension of blood glucose induced by adrenalin was inhibited (p < 0.01). Also, the bodyweight of the alloxan-induced hyperglycemic mice was increased gradually. In the fermented mushroom of G. frondosa, vanadium at lower doses in combination with G. frondosa induced significant decreases of the blood glucose and HbA1c levels in hyperglycemic mice.

  15. New diketone based vanadium complexes as insulin mimetics.

    PubMed

    Sheela, A; Roopan, S Mohana; Vijayaraghavan, R

    2008-10-01

    Since 1985, when Heyliger et al. first reported the in vivo insulin mimetic activity of oral vanadate, extensive studies exploring vanadium chemistry, including the synthesis of novel complexes and their biological effects both in vitro and in vivo have been pursued. Such complexes have emerged as possible potential agents for diabetes therapy. Among the several existing compounds, diketone based vanadium complexes have been chosen for the current study. Two new complexes namely bisdimethylmalonatooxovanadium(IV) and bisdiethylmalonatooxovanadium(IV) have been synthesized and characterized by UV-visible, FTIR and mass spectral studies. The antidiabetic activity of the complexes was proved by animal study. The results show that the above complexes have comparable antidiabetic potential with respect to the standard drug as well as with bisacetylacetonatooxovanadium(IV) which has been studied earlier by Reul et al.

  16. Present Status of Vanadium Alloys for Fusion Applications

    SciTech Connect

    Muroga, Takeo; Chen, J. M.; Chernov, V. M.; Kurtz, Richard J.; Le Flem, M.

    2014-12-01

    Vanadium alloys are advanced options for low activation structural materials. After more than two decades of research, V-4Cr-4Ti has been emerged as the leading candidate, and technological progress has been made in reducing the number of critical issues for application of vanadium alloys to fusion reactors. Notable progress has been made in fabricating alloy products and weld joints without degradation of properties. Various efforts are also being made to improve high temperature strength and creep-rupture resistance, low temperature ductility after irradiation, and corrosion resistance in blanket conditions. Future research should focus on clarifying remaining uncertainty in the operating temperature window of V-4Cr-4Ti for application to near to middle term fusion blanket systems, and on further exploration of advanced materials for improved performance for longer-term fusion reactor systems.

  17. Impact of vanadium ions in barium borate glass.

    PubMed

    Abdelghany, A M; Hammad, Ahmed H

    2015-02-25

    Combined optical and infrared spectral measurements of prepared barium borate glasses containing different concentrations of V2O5 were carried out. Vanadium containing glasses exhibit extended UV-visible (UV/Vis.) bands when compared with base binary borate glass. UV/Vis. spectrum shows the presence of an unsymmetrical strong UV broad band centered at 214 nm attributed to the presence of unavoidable trace iron impurities within the raw materials used for the preparation of such glass. The calculated direct and indirect optical band gaps are found to decrease with increasing the vanadium content (2.9:137 for indirect and 3.99:2.01 for direct transition). This change was discussed in terms of structural changes in the glass network. Infrared absorption spectra of the glasses reveal the appearance of both triangular and tetrahedral borate units. Electron spin resonance analyses indicate the presence of unpaired species in sufficient quantity to be identified and to confirm the spectral data.

  18. Phonon triggered rhombohedral lattice distortion in vanadium at high pressure

    SciTech Connect

    Antonangeli, Daniele; Farber, Daniel L.; Bosak, Alexei; Aracne, Chantel M.; Ruddle, David G.; Krisch, Michael

    2016-08-19

    In spite of the simple body-centered-cubic crystal structure, the elements of group V, vanadium, niobium and tantalum, show strong interactions between the electronic properties and lattice dynamics. Further, these interactions can be tuned by external parameters, such as pressure and temperature. We used inelastic x-ray scattering to probe the phonon dispersion of single-crystalline vanadium as a function of pressure to 45 GPa. Our measurements show an anomalous high-pressure behavior of the transverse acoustic mode along the (100) direction and a softening of the elastic modulus C44 that triggers a rhombohedral lattice distortion occurring between 34 and 39 GPa. Lastly, our results provide the missing experimental confirmation of the theoretically predicted shear instability arising from the progressive intra-band nesting of the Fermi surface with increasing pressure, a scenario common to all transition metals of group V.

  19. Impact of vanadium ions in barium borate glass

    NASA Astrophysics Data System (ADS)

    Abdelghany, A. M.; Hammad, Ahmed H.

    2015-02-01

    Combined optical and infrared spectral measurements of prepared barium borate glasses containing different concentrations of V2O5 were carried out. Vanadium containing glasses exhibit extended UV-visible (UV/Vis.) bands when compared with base binary borate glass. UV/Vis. spectrum shows the presence of an unsymmetrical strong UV broad band centered at 214 nm attributed to the presence of unavoidable trace iron impurities within the raw materials used for the preparation of such glass. The calculated direct and indirect optical band gaps are found to decrease with increasing the vanadium content (2.9:137 for indirect and 3.99:2.01 for direct transition). This change was discussed in terms of structural changes in the glass network. Infrared absorption spectra of the glasses reveal the appearance of both triangular and tetrahedral borate units. Electron spin resonance analyses indicate the presence of unpaired species in sufficient quantity to be identified and to confirm the spectral data.

  20. Shunt current loss of the vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Xing, Feng; Zhang, Huamin; Ma, Xiangkun

    The shunt current loss is one of main factors to affect the performance of the vanadium redox flow battery, which will shorten the cycle life and decrease the energy transfer efficiency. In this paper, a stack-level model based on the circuit analog method is proposed to research the shunt current loss of the vanadium redox flow battery, in which the SOC (state of charge) of electrolyte is introduced. The distribution of shunt current is described in detail. The sensitive analysis of shunt current is reported. The shunt current loss in charge/discharge cycle is predicted with the given experimental data. The effect of charge/discharge pattern on the shunt current loss is studied. The result shows that the reduction of the number of single cells in series, the decrease of the resistances of manifold and channel and the increase of the power of single cell will be the further development for the VRFB stack.

  1. Phonon triggered rhombohedral lattice distortion in vanadium at high pressure.

    PubMed

    Antonangeli, Daniele; Farber, Daniel L; Bosak, Alexei; Aracne, Chantel M; Ruddle, David G; Krisch, Michael

    2016-08-19

    In spite of the simple body-centered-cubic crystal structure, the elements of group V, vanadium, niobium and tantalum, show strong interactions between the electronic properties and lattice dynamics. Further, these interactions can be tuned by external parameters, such as pressure and temperature. We used inelastic x-ray scattering to probe the phonon dispersion of single-crystalline vanadium as a function of pressure to 45 GPa. Our measurements show an anomalous high-pressure behavior of the transverse acoustic mode along the (100) direction and a softening of the elastic modulus C44 that triggers a rhombohedral lattice distortion occurring between 34 and 39 GPa. Our results provide the missing experimental confirmation of the theoretically predicted shear instability arising from the progressive intra-band nesting of the Fermi surface with increasing pressure, a scenario common to all transition metals of group V.

  2. Phonon triggered rhombohedral lattice distortion in vanadium at high pressure

    DOE PAGES

    Antonangeli, Daniele; Farber, Daniel L.; Bosak, Alexei; ...

    2016-08-19

    In spite of the simple body-centered-cubic crystal structure, the elements of group V, vanadium, niobium and tantalum, show strong interactions between the electronic properties and lattice dynamics. Further, these interactions can be tuned by external parameters, such as pressure and temperature. We used inelastic x-ray scattering to probe the phonon dispersion of single-crystalline vanadium as a function of pressure to 45 GPa. Our measurements show an anomalous high-pressure behavior of the transverse acoustic mode along the (100) direction and a softening of the elastic modulus C44 that triggers a rhombohedral lattice distortion occurring between 34 and 39 GPa. Lastly, ourmore » results provide the missing experimental confirmation of the theoretically predicted shear instability arising from the progressive intra-band nesting of the Fermi surface with increasing pressure, a scenario common to all transition metals of group V.« less

  3. Phonon triggered rhombohedral lattice distortion in vanadium at high pressure

    PubMed Central

    Antonangeli, Daniele; Farber, Daniel L.; Bosak, Alexei; Aracne, Chantel M.; Ruddle, David G.; Krisch, Michael

    2016-01-01

    In spite of the simple body-centered-cubic crystal structure, the elements of group V, vanadium, niobium and tantalum, show strong interactions between the electronic properties and lattice dynamics. Further, these interactions can be tuned by external parameters, such as pressure and temperature. We used inelastic x-ray scattering to probe the phonon dispersion of single-crystalline vanadium as a function of pressure to 45 GPa. Our measurements show an anomalous high-pressure behavior of the transverse acoustic mode along the (100) direction and a softening of the elastic modulus C44 that triggers a rhombohedral lattice distortion occurring between 34 and 39 GPa. Our results provide the missing experimental confirmation of the theoretically predicted shear instability arising from the progressive intra-band nesting of the Fermi surface with increasing pressure, a scenario common to all transition metals of group V. PMID:27539662

  4. Pressure-Temperature Phase Diagram of Vanadium Dioxide.

    PubMed

    Chen, Yabin; Zhang, Shuai; Ke, Feng; Ko, Changhyun; Lee, Sangwook; Liu, Kai; Chen, Bin; Ager, Joel W; Jeanloz, Raymond; Eyert, Volker; Wu, Junqiao

    2017-03-08

    The complexity of strongly correlated electron physics in vanadium dioxide is exemplified as its rich phase diagrams of all kinds, which in turn shed light on the mechanisms behind its various phase transitions. In this work, we map out the hydrostatic pressure-temperature phase diagram of vanadium dioxide nanobeams by independently varying pressure and temperature with a diamond anvil cell. In addition to the well-known insulating M1 (monoclinic) and metallic R (tetragonal) phases, the diagram identifies the existence at high pressures of the insulating M1' (monoclinic, more conductive than M1) phase and two metallic phases of X (monoclinic) and O (orthorhombic, at high temperature only). Systematic optical and electrical measurements combined with density functional calculations allow us to delineate their phase boundaries as well as reveal some basic features of the transitions.

  5. Preparation and characterization of chitosan-zirconium(IV) composite for adsorption of vanadium(V).

    PubMed

    Zhang, Lingfan; Liu, Xin; Xia, Wei; Zhang, Wenqing

    2014-03-01

    In this present study, an inorganic-biopolymer composite based on chitosan-zirconium(IV) was prepared and investigated as a biosorbent for the removal of vanadium(V) ions from aqueous solution. The resulting composite before and after adsorbed V(V) were characterized by using FT-IR, XRD, SEM and EDS, respectively. Various relevant parameters affecting the adsorption capacity such as pH, initial concentration, contact time, temperature and co-existing ions were evaluated. The results demonstrated that the optimum pH was found to be 4.0 and the equilibrium was achieved after 4h for V(V) adsorption. The Langmuir isotherm model could be well described the adsorption of V(V), with the maximum adsorption capacity of 208 mg g(-1) at 30 °C. The kinetics data were well fitted to pseudo-second-order equation, indicating that chemical sorption as the rate-limiting step of adsorption mechanism. The calculated thermodynamic parameters such as ΔG°, ΔH° and ΔS° indicated that the adsorption process was feasible, spontaneous and endothermic in nature. Moreover, co-existing ions including nitrate, chloride and sulfate had a certain effect on the uptake of V(V). The V(V) loaded chitosan-zirconium(IV) composite could be regenerated by 0.01 mol L(-1) sodium hydroxide, with efficiency greater than 95%.

  6. Continuously variable, electrically addressed beam splitter based on vanadium dioxide.

    PubMed

    Allogho, Guy-Germain; Hamam, Habib; Beydaghyan, Gisia; Alloul, Sofiane; Haché, Alain

    2013-01-10

    Vanadium dioxide (VO(2)) is used to implement an electrically addressable beam splitter with continuously variable splitting ratios. The electrical control of temperature in a thin VO(2) layer is used to vary its transmission/reflection behavior. The technique is characterized for various incidence angles, s- and p-polarizations, and the wavelength range of 400-2000 nm. Splitting ratios continuously tunable over four orders of magnitude are reported.

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

    PubMed

    Ghio, Andrew J; Stonehuerner, Jacqueline; Soukup, Joleen M; Dailey, Lisa A; Kesic, Matthew J; Cohen, Mitchell D

    2015-06-01

    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 exposed to vanadyl sulfate (VOSO4) showed a time- and dose-dependent increase in vanadium relative to PBS. HBE cells exposed to VOSO4 and then exposed to ferric ammonium citrate (FAC) significantly increased intracellular iron import supporting an interaction between the two metals. Following exposure to VOSO4, there was an increase (336±73%) in RNA for divalent metal transporter 1 (DMT1), a major iron importer. With inclusion of VOSO4 in the incubation, vanadium could be measured in the nuclear and mitochondrial fractions and the supernatant. Non-heme iron in the nuclear and mitochondrial fractions were decreased immediately following VOSO4 exposure while there was an increased concentration of non-heme iron in the supernatant. Provision of excess iron inhibited changes in the concentration of this metal provoked by VOSO4 exposures. Using Amplex Red, VOSO4 was shown to significantly increase oxidant generation by HBE cells in a time- and dose-dependent manner. HBE cells pre-treated with FAC and then exposed to VOSO4 demonstrated a decreased generation of oxidants. Similarly, activation of the transcription factor NF-ĸB promoter and release of interleukin-6 and -8 were increased following VOSO4 exposure and these effects were diminished by pre-treatment with FAC. We conclude that an initiating event in biological effect after exposure to vanadyl sulfate is a loss of requisite cell iron.

  8. Influence of site occupancy on diffusion of hydrogen in vanadium

    NASA Astrophysics Data System (ADS)

    Mooij, Lennard; Huang, Wen; Droulias, Sotirios A.; Johansson, Robert; Hartmann, Ola; Xin, Xiao; Palonen, Heikki; Scheicher, Ralph H.; Wolff, Max; Hjörvarsson, Björgvin

    2017-02-01

    We investigate the effect of site occupancy on the chemical diffusion of hydrogen in strained vanadium. The diffusion rate is found to decrease substantially, when hydrogen is occupying octahedral sites as compared to tetrahedral sites. Profound isotope effects are observed when comparing the diffusion rate of H and D. The changes in the diffusion rate are found to be strongly influenced by the changes in the potential energy landscape, as deduced from first-principles molecular dynamics calculations.

  9. Vanadium sorption by mineral soils: Development of a predictive model.

    PubMed

    Larsson, Maja A; Hadialhejazi, Golshid; Gustafsson, Jon Petter

    2017-02-01

    The toxicity of vanadium in soils depends on its sorption to soil components. Here we studied the vanadate(V) sorption properties of 26 mineral soils. The data were used to optimise parameters for a Freundlich equation with a pH term. Vanadium K-edge XANES spectroscopy for three selected soils confirmed that the added vanadate(V) had accumulated mostly as adsorbed vanadate(V) on Fe and Al hydrous oxides, with only minor contributions from organically complexed vanadium(IV). Data on pH-dependent V solubility for seven soils showed that on average 0.36 H(+) accompanied each V during adsorption and desorption. The resulting model provided reasonable fits to the V sorption data, with r(2) > 0.99 for 20 of 26 soils. The observed KdS value, i.e. the ratio of total to dissolved V, was strongly dependent on V addition and soil; it varied between 3 and 4 orders of magnitude. The model was used to calculate the Freundlich sorption strength (FSS), i.e. the amount of V sorbed at [V] = 2.5 mg L(-1), in the concentration range of observed plant toxicities. A close relationship between FSS and oxalate-extractable Fe and Al was found (r(2) = 0.85) when one acidic soil was removed from the regression. The FSS varied between 27 and 8718 mg V kg(-1), showing that the current environmental guidelines can be both under- and overprotective for vanadium.

  10. Specific heat of vanadium dioxide at helium temperatures

    NASA Astrophysics Data System (ADS)

    Surikov, Vad. I.; Kuznetsova, Yu. V.; Lyakh, O. V.; Surikov, Val. I.; Kondratova, Yu. E.

    2013-08-01

    Results are reported of measurements of the specific heat СР of a series of samples of vanadium dioxide in the temperature range from 4.2 to 25 K. Analysis of the results shows that at these temperatures an appreciable contribution to the specific heat comes from the specific heat of the crystalline lattice and defects of the crystalline lattice, the presence of which is a consequence of the method of synthesis of the materials.

  11. Carbonitride precipitation in niobium/vanadium microalloyed steels

    NASA Astrophysics Data System (ADS)

    Speer, J. G.; Michael, J. R.; Hansen, S. S.

    1987-02-01

    A detailed study of carbonitride precipitation in niobium/vanadium microalloyed steels is presented. A thermodynamic model is developed to predict the austenite/carbonitride equilibrium in the Fe-Nb-V-C-N system, using published solubility data and the Hillert/Staffansson model for stoichiometric phases. The model can be used to estimate equilibrium austenite and carbonitride compositions, and the amounts of each phase, as a function of steel composition and temperature. The model also provides a method to estimate the carbonitride solution temperatures for different steel compositions. Actual carbonitride precipitation behavior in austenite is then examined in two experimental 0.03Nb steels containing 0.05V and 0.20V, respectively. Samples were solution treated, rolled at 954 °C (20 pct or 50 pct), held isothermally for times up to 10,000 seconds at 843 °C, 954 °C, or 1066 °C, and brine quenched. The process of carbonitride precipitation in deformed austenite is followed by analytical electron microscopy (AEM) of carbon extraction replicas. Precipitates are. observed at prior-austenite grain boundaries, and also within the grains (presumably at substructure introduced by the rolling deformation). Analysis of the grain-boundary and matrix precipitate compositions by AEM indicates that the grain-boundary precipitates are consistently richer in vanadium than the matrix precipitates, although compositional trends with holding time and temperature are similar for the two types of precipitates. The compositions of both the grain-boundary and matrix precipitates are not significantly influenced by the rolling reduction or the holding time at temperature. As predicted by the thermodynamic model, the precipitates become more vanadium-rich as the vanadium level in the steel is increased and as the temperature is reduced. The agreement between the measured and predicted precipitate compositions is quite good for the grain-boundary precipitates, although the matrix

  12. Terahertz spectroscopy of the metal insulator transition in vanadium dioxide

    NASA Astrophysics Data System (ADS)

    Hilton, David; Prasankumar, Rohit; Cavalleri, Andrea; Fourmaux, Sylvain; Kieffer, Jean-Claude; Taylor, Antoinette; Averitt, Richard

    2006-03-01

    We employ terahertz spectroscopy to study the metal-insulator phase transition in vanadium dioxide (VO2 ). We measure the terahertz frequency conductivity in the metallic phase that has a real conductivity of 1000 &-1circ; cm-1 and a negligible imaginary conductivity. The observed conductivity dynamics are consistent with a photoinduced transition in spatially inhomogeneous regions of the film, followed by a thermally driven transition to the maximum conductivity.

  13. Corrosion resistance investigation of vanadium alloys in liquid lithium

    NASA Astrophysics Data System (ADS)

    Borovitskaya, I. V.; Lyublinskiy, I. E.; Bondarenko, G. G.; Paramonova, V. V.; Korshunov, S. N.; Mansurova, A. N.; Lyakhovitskiy, M. M.; Zharkov, M. Yu.

    2016-12-01

    A major concern in using vanadium alloys for first wall/blanket systems in fusion reactors is their activity with regard to nonmetallic impurities in the coolants. This paper presents the results of studying the corrosion resistance in high-purity liquid lithium (with the nitrogen and carbon content of less than 10-3 wt %) of vanadium and vanadium alloys (V-1.86Ga, V-3.4Ga-0.62Si, V-4.81Ti-4.82Cr) both in the initial state and preliminarily irradiated with Ar+ ions with energy of 20 keV to a dose of 1022 m-2 at an irradiation temperature of 400°C. The degree of corrosion was estimated by measuring the changes in the weight and microhardness. Corrosion tests were carried out under static isothermal conditions at a temperature of 600°C for 400 h. The identity of corrosion mechanisms of materials both irradiated with Ar ions and not irradiated, which consisted in an insignificant penetration of nitrogen into the materials and a substantial escape of oxygen from the materials, causing the formation of a zone with a reduced microhardness near the surface, was established. The influence of the corrosive action of lithium on the surface morphology of the materials under study was found, resulting in the manifestation of grain boundaries and slip lines on the sample surface, the latter being most clearly observed in the case of preliminary irradiation with Ar ions.

  14. A dynamic model for the global cycling of anthropogenic vanadium

    NASA Astrophysics Data System (ADS)

    Hope, Bruce K.

    2008-12-01

    Vanadium is a major trace metal in fossil fuels. Combustion of residual fuel oils and coal in industrialized economies is recognized as the major source of anthropogenic vanadium. A dynamic mass balance model assessed the influence of anthropogenic inputs on the global distribution and cycling of vanadium between 1700 and 2400 assuming different fossil fuel consumption and V production (mining) scenarios. Anthropogenic V sources were divided into fossil fuel combustion, industrial, and domestic (nonindustrial human activity). By 2050, inputs of anthropogenic V could comprise ≈75-85% of those to the atmosphere, ≈21-33% to ocean dissolved, ≈9-13% to ocean particulate, and ≈28-43% of inputs to land; with between ≈61-64% of all anthropogenic inputs attributable to fossil fuel combustion. Contributions from combustion and industrial sources, although dominant relative to contributions from domestic sources between 1900 and 2100, were estimated to peak between 2000 and 2050. Accumulation of anthropogenic V on land and in the ocean apparently occurs because natural removal processes are unable to cope with increasing amounts and rates of anthropogenic contributions. Impacts or hazards associated with anthropogenic inputs are unlikely to be discernible or significant on a global scale, but may be measurable and meaningful at smaller scales (coastal waters, continental shelves, and bays), in the locality of specific sources, or given an unfavorable exposure scenario.

  15. Vanadium haloperoxidases from brown algae of the Laminariaceae family.

    PubMed

    Almeida, M; Filipe, S; Humanes, M; Maia, M F; Melo, R; Severino, N; da Silva, J A; Fraústo da Silva, J J; Wever, R

    2001-07-01

    Vanadium haloperoxidases were extracted, purified and characterized from three different species of Laminariaceae--Laminaria saccharina (Linné) Lamouroux, Laminaria hyperborea (Gunner) Foslie and Laminaria ochroleuca de la Pylaie. Two different forms of the vanadium haloperoxidases were purified from L. saccharina and L. hyperborea and one form from L. ochroleuca species. Reconstitution experiments in the presence of several metal ions showed that only vanadium(V) completely restored the enzymes activity. The stability of some enzymes in mixtures of buffer solution and several organic solvents such as acetone, ethanol, methanol and 1-propanol was noteworthy; for instance, after 30 days at least 40% of the initial activity for some isoforms remained in mixtures of 3:1 buffer solution/organic solvent. The enzymes were also moderately thermostable, keeping full activity up to 40 degrees C. Some preliminary steady-state kinetic studies were performed and apparent Michaelis-Menten kinetic parameters were determined for the substrates iodide and hydrogen peroxide. Histochemical studies were also performed in fresh tissue sections from stipe and blade of L. hyperborea and L. saccharina, showing that haloperoxidase activity was concentrated in the external cortex near the cuticle, although some activity was also observed in the inner cortical region.

  16. Synthesis, immunomodulation and cytotoxic effects of vanadium (IV) complexes.

    PubMed

    Ashiq, Uzma; Jamal, Rifat Ara; Mesaik, Mohammad Ahmed; Mahroof-Tahir, Muhammad; Shahid, Saba; Khan, Khalid Mohammed

    2014-05-01

    Vanadium is known to exhibit several bioactivities and shows potential as a pharmaceutical drug. The current studies were conducted with the goal of synthesizing a new generation of oxovanadium(IV) complexes, investigating their effects on cancer cell proliferation and their immunomodulatory properties, and predicting possible structure activity relationships. The elucidation of the structures of the synthesized complexes was achieved using elemental analysis, conductivity measurements, magnetic property measurements, and IR and electronic spectroscopies. These studies suggest that the synthesized complexes have a binuclear structure. All of the complexes were evaluated on different cancer cell lines, including HeLa, PC-3, and C33A, and on the normal 3T3 fibroblast cells. Some of the compounds exhibited prominent inhibitory activities on the cervical cancer cell lines and the prostate cancer PC-3 cells. The immunomodulatory activity of the vanadium compounds was evaluated on human phagocytes for ROS (reactive oxygen species) production using luminol- and lucigenin-based chemiluminescence assays. No potent effect was exerted by the majority of the tested compounds on whole blood oxidative burst activity. A study of human T-cells proliferation in vitro on vanadium complexes was also conducted. The majority of the compounds were observed to exhibit potent inhibitory effects. The superoxide, nitric oxide and DPPH (2,2-diphenyl-1-picrylhydrazyl) radical scavenging properties were also determined.

  17. Peak power prediction of a vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Yu, V. K.; Chen, D.

    2014-12-01

    The vanadium redox flow battery (VRFB) is a promising grid-scale energy storage technology, but future widespread commercialization requires a considerable reduction in capital costs. Determining the appropriate battery size for the intended power range can help minimize the amount of materials needed, thereby reducing capital costs. A physics-based model is an essential tool for predicting the power range of large scale VRFB systems to aid in the design optimization process. This paper presents a modeling framework that accounts for the effects of flow rate on the pumping losses, local mass transfer rate, and nonuniform vanadium concentration in the cell. The resulting low-order model captures battery performance accurately even at high power densities and remains computationally practical for stack-level optimization and control purposes. We first use the model to devise an optimal control strategy that maximizes battery life during discharge. Assuming optimal control is implemented, we then determine the upper efficiency limits of a given VRFB system and compare the net power and associated overpotential and pumping losses at different operating points. We also investigate the effects of varying the electrode porosity, stack temperature, and total vanadium concentration on the peak power.

  18. High power density self-cooled lithium-vanadium blanket.

    SciTech Connect

    Gohar, Y.; Majumdar, S.; Smith, D.

    1999-07-01

    A self-cooled lithium-vanadium blanket concept capable of operating with 2 MW/m{sup 2} surface heat flux and 10 MW/m{sup 2} neutron wall loading has been developed. The blanket has liquid lithium as the tritium breeder and the coolant to alleviate issues of coolant breeder compatibility and reactivity. Vanadium alloy (V-4Cr-4Ti) is used as the structural material because it can accommodate high heat loads. Also, it has good mechanical properties at high temperatures, high neutron fluence capability, low degradation under neutron irradiation, good compatibility with the blanket materials, low decay heat, low waste disposal rating, and adequate strength to accommodate the electromagnetic loads during plasma disruption events. Self-healing electrical insulator (CaO) is utilized to reduce the MHD pressure drop. A poloidal coolant flow with high velocity at the first wall is used to reduce the peak temperature of the vanadium structure and to accommodate high surface heat flux. The blanket has a simple blanket configuration and low coolant pressure to reduce the fabrication cost, to improve the blanket reliability, and to increase confidence in the blanket performance. Spectral shifter, moderator, and reflector are utilized to improve the blanket shielding capability and energy multiplication, and to reduce the radial blanket thickness. Natural lithium is used to avoid extra cost related to the lithium enrichment process.

  19. Increasing the heat resistance of vanadium by siliciding

    SciTech Connect

    Lyutyi, E.M.; Tsvikilevich, O.S.; Shirokov, V.V.; Stepanishin, V.I.

    1988-01-01

    The purpose of this article was to evaluate the influence of modifier metals on the protective properties of silicide coatings in heating of vanadium in air and also on the mechanical properties of type VnM-2 unalloyed vanadium and VTsU alloy. Coatings were produced by diffusion impregnation from molten sodium with silicon or silicides of the modifying elements. The silicides of titanium, zirconium, hafnium, niobium, tantalum, molybdenum, chromium, tungsten, rhenium, and nickel were investigated using x-ray spectrometric and hardness investigations and x-ray diffractometric analysis. The protective properties of the coatings were determined from the relative change in weight of the samples with and without coatings during isothermal oxidation in air at 1073/sup 0/K and also by differential thermal analysis. The influence of the coating on the mechanical properties of the material was also investigated using a borosilicide coating. High-temperature vacuum annealing was assessed as a method for restoring the plastic properties and relieving the stresses of vanadium and VTsU alloy subsequent to coating.

  20. Dramatic performance gains of a novel circular vanadium flow battery

    NASA Astrophysics Data System (ADS)

    Zheng, Qiong; Xing, Feng; Li, Xianfeng; Liu, Tao; Lai, Qinzhi; Ning, Guiling; Zhang, Huamin

    2015-03-01

    Vanadium flow battery (VFB) holds great promise for use in large scale energy storage applications. However, one major issue that limits the battery performance is the energy storage capacity loss due to insufficient use of electrolyte. The battery structure design is flexible and acceptable to solve the issue. Based on the mass transport limitation of the conventional rectangular vanadium flow battery (RFB), a novel circular vanadium flow battery (CFB) was firstly proposed in the research. Without increasing pump consumption, the new structure of CFB is effective to achieve mass transport enhancement and concentration polarization reduction. The charge-discharge test confirmed the performance advantage of CFB, presenting a significant increment of 10.52% at 40 mA cm-2 and 30.46% at 160 mA cm-2 in the utilization of electrolyte and improved energy storage capacity by 12.56% at 40 mA cm-2 and a 2.55 times of that for RFB at 160 mA cm-2. The performance advantage of CFB becomes exceptionally evident at high current densities.

  1. A stochastic exposure assessment model to estimate vanadium intake by beef cattle used as sentinels for the South African vanadium mining industry.

    PubMed

    Gummow, B; Kirsten, W F A; Gummow, R J; Heesterbeek, J A P

    2006-10-17

    This paper presents an environmental exposure assessment model for estimating chronic intake of vanadium (a transition metal) by cattle farmed extensively in areas contaminated by vanadium pollutants. The exposure model differs from most other models in several ways: (1) it does not rely heavily on extrapolating information from the point source (e.g. stack height, exit velocity, exit diameter) to the point of exposure. (2) It incorporates the physiological constraints of the species exposed. (3) It takes into account oral as well as inhalation exposure. (4) It addresses terrain, by using measurements at the point of exposure. (5) It accounts for existing background concentrations of pollutants and pollutants from multiple sources. (6) It uses a stochastic process with distribution functions to account for variability in the data over time. Environmental inputs into the model included aerial fall-out sample vanadium (n=566), unwashed grass sample vanadium (n=342) and soluble soil sample vanadium (n=342). Physiological cattle inputs were derived from two cohorts of Brahman-cross sentinel cattle (n=30). The model provided an estimate of the chronic external exposure dose of vanadium for two separate groups of cattle grazing over a 5-year period (1999-2004) immediately adjacent (median dose=2.14mg vanadium/kg body weight/day) and 2km away (median dose=1.07mg/kg/day) from a South African vanadium-processing plant, respectively. The final output of the model is a distribution curve of the probable vanadium intake based on the variability within the inputs over the 5-year period of the study. The model is adaptable enough for application to other transition metals and species (including man), and could be used as an alternative to plume-dispersion modelling.

  2. Influence of transmutation on microstructure, density change, and embrittlement of vanadium and vanadium alloys irradiated in HFIR

    SciTech Connect

    Ohnuki, S.; Takahashi, H.; Shiba, K.; Hishinuma, A.; Pawel, J.; Garner, F.A.

    1994-06-01

    Addition of 1 at.% nickel to vanadium and V-10Ti, followed by irradiation along with the nickel-free metals in HFIR to 2.3 {times} 10{sup 22}n cm{sup {minus}2}, E > 0.1MeV (corresponding to 17.7 dpa) at 400 C, has been used to study the influence of helium on microstructural evolution and embrittlement. Approximately 15.3% of the vanadium transmuted to chromium in these alloys. The {approximately}50 appm helium generated from the {sup 58}Ni(n,{gamma}){sup 59}Ni(n,{alpha}){sup 56}Fe sequence was found to exert much less influence than either the nickel directly or the chromium formed by transmutation. The V-10Ti and V-10Ti-1Ni alloys developed an extreme fragility and broke into smaller pieces in response to minor physical insults during density measurements. A similar behavior was not observed in pure V or V-1Ni. Helium`s role in determination of mechanical properties and embrittlement of vanadium alloys in HFIR is overshadowed by the influence of alloying elements such as titanium and chromium. Both elements have been shown to increase the ductile-to-brittle transition temperature (DBTT) rather rapidly in the region of 10% (Cr + Ti). Since Cr is produced by transmutation of V, this is a possible mechanism for the embrittlement. Large effects on the DBTT may have also resulted from uncontrolled accumulation of interstitial elements such as C, N, and O during irradiation.

  3. Ultra-low vanadium ion diffusion amphoteric ion-exchange membranes for all-vanadium redox flow batteries

    NASA Astrophysics Data System (ADS)

    Liao, J. B.; Lu, M. Z.; Chu, Y. Q.; Wang, J. L.

    2015-05-01

    An amphoteric ion-exchange membrane (AIEM) from fluoro-methyl sulfonated poly(arylene ether ketone) bearing content-controlled benzimidazole moiety, was firstly fabricated for vanadium redox flow battery (VRB). The AIEM and its covalently cross-linked membrane (AIEM-c) behave the highly suppressed vanadium-ion crossover and their tested VO2+ permeability are about 638 and 1117 times lower than that of Nafion117, respectively. This is further typically verified by the lower VO2+ concentration inside AIEM that is less than half of that inside Nafion117 detected by energy dispersive X-ray spectrometry, in addition of the nearly 3 times longer battery self-discharge time. The ultra-low vanadium ion diffusion could be ascribed to the narrower ion transporting channel originated from the acid-base interactions and the rebelling effect between the positively-charged benzimidazole structure and VO2+ ions. It is found that, VRB assembled with AIEM exhibits the equal or higher Coulombic efficiency (99.0% vs. 96.4%), voltage efficiency (90.7% vs. 90.7%) and energy efficiency (89.8% vs. 87.4%) than that with Nafion117 and keeps continuous 220 charge-discharge cycles for over 25 days, confirming that the AIEM of this type is a potentially suitable separator for VRB application.

  4. Vanadium diaphragm electrode serves as hydrogen diffuser in lithium hydride cell

    NASA Technical Reports Server (NTRS)

    Crouthamel, C. E.; Heinrich, R. R.; Johnson, C. E.

    1967-01-01

    Lithium hydride cell uses vanadium diaphragm electrode as a hydrogen diffuser. Vanadium is high in hydrogen gas solubility and permeability, is least sensitive to adverse surface effects, maintains good mechanical strength in hydrogen atmospheres, and appears to be compatible with all alkali-halide electrolytes and lithium metals.

  5. Uptake and speciation of vanadium in the benthic invertebrate Hyalella azteca.

    PubMed

    Jensen-Fontaine, Madeleine; Norwood, Warren P; Brown, Mitra; Dixon, D George; Le, X Chris

    2014-01-01

    Vanadium has the potential to leach into the environment from petroleum coke, an oil sands byproduct. To determine uptake of vanadium species in the biota, we exposed the benthic invertebrate Hyalella azteca with increasing concentrations of two different vanadium species, V(IV) and V(V), for seven days. The concentrations of vanadium in the H. azteca tissue increased with the concentration of vanadium in the exposure water. Speciation analysis revealed that V(IV) in the exposure water was oxidized to V(V) between renewal periods, and therefore the animals were mostly exposed to V(V). Speciation analysis of the H. azteca tissue showed the presence of V(V), V(IV), and an unidentified vanadium species. These results indicate the uptake and metabolism of vanadium by H. azteca. Because H. azteca are widely distributed in freshwater systems and are an important food supply for many fish, determining the uptake and metabolism of vanadium allows for a better understanding of the potential environmental effects on invertebrates.

  6. Protective effects of Sesamum indicum extract against oxidative stress induced by vanadium on isolated rat hepatocytes.

    PubMed

    Hosseini, Mir-Jamal; Shahraki, Jafar; Tafreshian, Saman; Salimi, Ahmad; Kamalinejad, Mohammad; Pourahmad, Jalal

    2016-08-01

    Vanadium toxicity is a challenging problem to human and animal health with no entirely understanding cytotoxic mechanisms. Previous studies in vanadium toxicity showed involvement of oxidative stress in isolated liver hepatocytes and mitochondria via increasing of ROS formation, release of cytochrome c and ATP depletion after incubation with different concentrations (25-200 µM). Therefore, we aimed to investigate the protective effects of Sesamum indicum seed extract (100-300 μg/mL) against oxidative stress induced by vanadium on isolated rat hepatocytes. Our results showed that quite similar to Alpha-tocopherol (100 µM), different concentrations of extract (100-300 μg/mL) protected the isolated hepatocyte against all oxidative stress/cytotoxicity markers induced by vanadium in including cell lysis, ROS generation, mitochondrial membrane potential decrease and lysosomal membrane damage. Besides, vanadium induced mitochondrial/lysosomal toxic interaction and vanadium reductive activation mediated by glutathione in vanadium toxicity was significantly (P < 0.05) ameliorated by Sesamum indicum extracts. These findings suggested a hepato-protective role for extracts against liver injury resulted from vanadium toxicity. © 2015 Wiley Periodicals, Inc. Environ Toxicol 31: 979-985, 2016.

  7. The assessment of biomarkers in sentinel cattle for monitoring vanadium exposure.

    PubMed

    Gummow, B; van den Broek, J; Kirsten, W F A; Botha, C J; Noordhuizen, J P T M; Heesterbeek, J A P

    2006-04-01

    Various potential biomarkers were sampled for vanadium every 3-4 months from Bos indicus beef cattle farmed extensively immediately adjacent (high exposure (HE) group) and two km away (low exposure (LE) group) from a vanadium processing plant, respectively. Vanadium intake (mg vanadium kg(-1) bwt d(-1)) was modelled using environmental and physiological data as inputs. The vanadium intake ranged from 0.57 to 5.44 mg vanadium kg(-1) bwt d(-1) in the HE group and 0.41 to 2.61 mg vanadium kg(-1) bwt d(-1) in the LE group over a five-year period of monitoring. Samples collected from live sentinel animals over the five-year period included caudal coccygeal vertebrae, tail-switch hair, milk, urine, faeces, rib-bone biopsies and a wide range of blood clinical pathology and haematological parameters. The data was analysed for differences in response between the HE and LE groups. Where differences were found, a linear mixed-effects regression model was fitted to model the relationship between the exposure dose and the response variable. The model included the effects of age, duration of exposure and response, and allowed the prediction of the exposure dose given these inputs. Moreover, forty-two adult cattle were slaughtered over the five years. A wide range of tissue samples, rumen content and whole blood were taken from the cattle at slaughter for vanadium determination. In live animals, a difference in response was found between the HE group and LE group with respect to serum albumin (n = 36), monocyte (n = 36) and thrombocyte (n = 36) counts, and hair (n = 2) and faeces (n = 34) vanadium concentrations. No difference in vanadium concentrations could be shown for urine (n = 36), the traditional occupational health biomarker. Regression models are described for serum albumin, monocyte counts, faeces and hair, which showed the most promise as biomarkers. Average concentrations of vanadium in the tissues of slaughtered cattle ranged from 0.08 to 2.94 mg kg(-1) (wet

  8. Effects of Iron Sand Ratios on the Basic Characteristics of Vanadium Titanium Mixed Ores

    NASA Astrophysics Data System (ADS)

    Liu, Dong-hui; Zhang, Jian-liang; Liu, Zheng-jian; Wang, Yao-zu; Xue, Xun; Yan, Jie

    2016-09-01

    Effects of iron sand ratios on the basic characteristics of vanadium titanium mixed ores were investigated using micro-sinter and grey relational analysis methods. The results show that iron sand presents poor assimilability, poor liquid flow capability, and low bonding phase strength. As the iron sand ratio in vanadium titanium mixed ores increases, the mixed ore's assimilation temperature increases, the fluidity index of liquid decreases, and the bonding phase strength first rises and then decreases. The comprehensive index of basic characteristic (CI) improves and then deteriorates with increasing iron sand ratio. The CI of vanadium titanium mixed ores is optimized when the iron sand ratio is 9 wt.%. In order to make full use of low-price iron-bearing materials and improve the sintering characteristics of vanadium titanium magnetite, the iron sand ratio in vanadium titanium mixed ores should be controlled within 9-12 wt.%.

  9. A comparison of hypoglycemic activity of three species of basidiomycetes rich in vanadium.

    PubMed

    Han, Chunchao; Liu, Tongjun

    2009-02-01

    The hypoglycemic activity of fermented mushroom of three fungi of basidiomycetes rich in vanadium was studied in this paper. Alloxan- and adrenalin-induced hyperglycemic mice were used in the study. The blood glucose and the sugar tolerance were determined. After the mice were administered (ig) with Coprinus comatus rich in vanadium, the blood glucose of alloxan-induced hyperglycemic mice decreased (p < 0.05), ascension of blood glucose induced by adrenalin was inhibited (p < 0.01) and the sugar tolerance of the normal mice was improved. However, the same result did not occur in Ganoderma lucidum and Grifola frondosa group. Compared with Ganoderma rich in vanadium and Grifola frondosa rich in vanadium, the hypoglycemic effects of Coprinus comatus rich in vanadium on hyperglycemic animals are significant; it may be used as a hypoglycemic food or medicine for hyperglycemic people.

  10. The protective effect of vanadium against diabetic cataracts in diabetic rat model.

    PubMed

    Sun, Lei; Shi, De-Jing; Gao, Xiang-Chun; Mi, Shu-Yong; Yu, Ying; Han, Qing

    2014-05-01

    The present study was designed to investigate the effect of vanadium in alloxan-induced diabetes and cataract in rats. Different doses of vanadium was administered once daily for 8 weeks to alloxan-induced diabetic rats. To know the mechanism of action of vanadium, lens malondialdehyde (MDA), protein carbonyl content, activity of superoxide dismutase (SOD), activities of aldose reductase (AR), and sorbitol levels were assayed, respectively. Supplementation of vanadium to alloxan-induced diabetic rats decreased the blood glucose levels due to hyperglycemia, inhibited the AR activity, and delayed cataract progression in a dose-dependent manner. The observed beneficial effects may be attributed to polyol pathway activation but not decreased oxidative stress. Overall, the results of this study demonstrate that vanadium could effectively reduce the alloxan-induced hyperglycemia and diabetic cataracts in rats.

  11. Synthesis of vanadium(V) hydrazido complexes with tris(2-hydroxyphenyl)amine ligands.

    PubMed

    Moriuchi, Toshiyuki; Ikeuchi, Kousuke; Hirao, Toshikazu

    2013-09-07

    The reaction of the oxidovanadium(V) complexes with N,N-dimethylhydrazine was demonstrated to afford the corresponding vanadium(V) dimethylhydrazido complexes. The substituent at the 3-position of the tris(2-hydroxyphenyl)amine ligand was found to influence the electronic environment of the vanadium center. The crystal structure of the non-substituted vanadium(V) dimethylhydrazido complex exhibited a distorted trigonal bipyramidal geometry with phenolate oxygen atoms in equatorial positions and the near-linear V(1)-N(2)-N(3) angle. The vanadium(V) diphenylhydrazido complexes could be obtained by the reaction of the oxidovanadium(V) complexes with N,N-diphenylhydrazine. A distorted trigonal bipyramidal geometry with phenolate oxygen atoms in equatorial positions was also observed in the crystal structure of the non-substituted vanadium(V) diphenylhydrazido complex.

  12. Non-noble metal vanadium phosphites with broad absorption for photocatalytic hydrogen evolution

    SciTech Connect

    Song, Jun-Ling; Zhang, Jian-Han; Mao, Jiang-Gao

    2016-05-15

    We reported the synthesis and crystal structures of alkali metal and alkali-earth metal phosphite, namely, CsV{sub 2}(H{sub 3}O)(HPO{sub 3}){sub 4} (1), and Ba{sub 3}V{sub 2}(HPO{sub 3}){sub 6} (2). Both compounds were prepared by hydrothermal reactions and feature unique new structures. They both exhibit 3D complicated frameworks based on VO{sub 6} octahedra which are connected by HPO{sub 3} tetrahedra via corner-sharing. Alkali or alkali earth metal cations are filled in the different channels of the frameworks. Topological analysis shows that the framework of CsV{sub 2}(H{sub 3}O) (HPO{sub 3}){sub 4} (1) is a new 3,3,3,4,5-connected network with the Schläfli symbol of {4.6"2}{sub 2}{4"2.6"6.8"2}{6"3}{6"5.8}. The investigations of X-ray photoelectron spectroscopy (XPS) and magnetic measurement on CsV{sub 2}(H{sub 3}O)(HPO{sub 3}){sub 4} suggest a +3 oxidation state of the vanadium ions in compound 1. Photocatalytic performance was evaluated by photocatalytic H{sub 2} evolution and degradation of methylene blue, which shows that both compounds exhibit activity under visible-light irradiation. IR spectrum, UV–vis-NIR spectrum and thermogravimetric analysis (TGA) of compounds were also investigated. - Graphical abstract: Metal vanadium phosphites with broad absorption for photocatalytic hydrogen evolution and the degradation of methylene blue aqueous solution. - Highlights: • Two new vanadium phosphites, CsV{sub 2}(H{sub 3}O)(HPO{sub 3}){sub 4} and Ba{sub 3}V{sub 2}(HPO{sub 3}){sub 6}, are reported. • CsV{sub 2}(H{sub 3}O)(HPO{sub 3}){sub 4} and Ba{sub 3}V{sub 2}(HPO{sub 3}){sub 6} feature complicated 3D framework structures with different channels. • CsV{sub 2}(H{sub 3}O)(HPO{sub 3}){sub 4} and Ba{sub 3}V{sub 2}(HPO{sub 3}){sub 6} exhibit strong and broad absorptions in the visible and Near IR region. • Photocatalytic properties of CsV{sub 2}(H{sub 3}O)(HPO{sub 3}){sub 4} and Ba{sub 3}V{sub 2}(HPO{sub 3}){sub 6} are investigated. • The magnetic

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

    PubMed

    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

  14. Enrichment, Distribution of Vanadium-Containing Protein in Vanadium-Enriched Sea Cucumber Apostichopus japonicus and the Ameliorative Effect on Insulin Resistance.

    PubMed

    Liu, Yanjun; Zhou, Qingxin; Zhao, Yanlei; Wang, Yiming; Wang, Yuming; Wang, Jingfeng; Xu, Jie; Xue, Changhu

    2016-05-01

    Sea cucumbers are a potential source of natural organic vanadium that may improve insulin resistance. In this work, vanadium was accumulated rapidly in blood, body wall, and intestine by sea cucumber Apostichopus japonicus. Furthermore, water-soluble vanadium-containing proteins, the main form of the organic vanadium, were tentatively accumulated and isolated by a bioaccumulation experiment. It was also designed to evaluate the beneficial effect of vanadium-containing proteins (VCPs) from sea cucumber rich in vanadium on the development of hyperglycemia and insulin resistance in C57BL/6J mice fed with a high-fat high-sucrose diet (HFSD). HFSD mice treated with VCPs significantly decreased fasting blood glucose, serum insulin, and HOMA-IR values as compared to HFSD mice, respectively. Serum adiponectin, resistin, TNF-α, and leptin levels in insulin-resistant mice were dramatically reduced by a VCP supplement. These results show an ameliorative effect on insulin resistance by treatment with VCPs. Such compound seems to be a valuable therapy to achieve and/or maintain glycemic control and therapeutic agents in the treatment arsenal for insulin resistance and type 2 diabetes.

  15. Leaching of vanadium, sodium, and silicon from molten V-Ti-bearing slag obtained from low-grade vanadium-bearing titanomagnetite

    NASA Astrophysics Data System (ADS)

    Zhu, Yuan-yuan; Yi, Ling-yun; Zhao, Wei; Chen, De-sheng; Zhao, Hong-xin; Qi, Tao

    2016-08-01

    The water leaching process of vanadium, sodium, and silicon from molten vanadium-titanium-bearing (V-Ti-bearing) slag obtained from low-grade vanadium-bearing titanomagnetite was investigated systematically. The results show that calcium titanate, sodium aluminosilicate, sodium oxide, silicon dioxide and sodium vanadate are the major components of the molten V-Ti-bearing slag. The experimental results indicate that the liquid-solid (L/S) mass ratio significantly affects the leaching process because of the respective solubilities and diffusion rates of the components. A total of 83.8% of vanadium, 72.8% of sodium, and 16.1% of silicon can be leached out via a triple counter-current leaching process under the optimal conditions of a particle size below 0.074 mm, a temperature of 90°C, a leaching time of 20 min, an L/S mass ratio of 4:1, and a stirring speed of 300 r/min. The kinetics of vanadium leaching is well described by an internal diffusion-controlled model and the apparent activation energy is 11.1 kJ/mol. The leaching mechanism of vanadium was also analyzed.

  16. Electron affinity of cubic boron nitride terminated with vanadium oxide

    SciTech Connect

    Yang, Yu; Sun, Tianyin; Shammas, Joseph; Hao, Mei; Nemanich, Robert J.; Kaur, Manpuneet

    2015-10-28

    A thermally stable negative electron affinity (NEA) for a cubic boron nitride (c-BN) surface with vanadium-oxide-termination is achieved, and its electronic structure was analyzed with in-situ photoelectron spectroscopy. The c-BN films were prepared by electron cyclotron resonance plasma-enhanced chemical vapor deposition employing BF{sub 3} and N{sub 2} as precursors. Vanadium layers of ∼0.1 and 0.5 nm thickness were deposited on the c-BN surface in an electron beam deposition system. Oxidation of the metal layer was achieved by an oxygen plasma treatment. After 650 °C thermal annealing, the vanadium oxide on the c-BN surface was determined to be VO{sub 2}, and the surfaces were found to be thermally stable, exhibiting an NEA. In comparison, the oxygen-terminated c-BN surface, where B{sub 2}O{sub 3} was detected, showed a positive electron affinity of ∼1.2 eV. The B{sub 2}O{sub 3} evidently acts as a negatively charged layer introducing a surface dipole directed into the c-BN. Through the interaction of VO{sub 2} with the B{sub 2}O{sub 3} layer, a B-O-V layer structure would contribute a dipole between the O and V layers with the positive side facing vacuum. The lower enthalpy of formation for B{sub 2}O{sub 3} is favorable for the formation of the B-O-V layer structure, which provides a thermally stable surface dipole and an NEA surface.

  17. Optimized anion exchange membranes for vanadium redox flow batteries.

    PubMed

    Chen, Dongyang; Hickner, Michael A; Agar, Ertan; Kumbur, E Caglan

    2013-08-14

    In order to understand the properties of low vanadium permeability anion exchange membranes for vanadium redox flow batteries (VRFBs), quaternary ammonium functionalized Radel (QA-Radel) membranes with three ion exchange capacities (IECs) from 1.7 to 2.4 mequiv g(-1) were synthesized and 55-60 μm thick membrane samples were evaluated for their transport properties and in-cell battery performance. The ionic conductivity and vanadium permeability of the membranes were investigated and correlated to the battery performance through measurements of Coulombic efficiency, voltage efficiency and energy efficiency in single cell tests, and capacity fade during cycling. Increasing the IEC of the QA-Radel membranes increased both the ionic conductivity and VO(2+) permeability. The 1.7 mequiv g(-1) IEC QA-Radel had the highest Coulombic efficiency and best cycling capacity maintenance in the VRFB, while the cell's voltage efficiency was limited by the membrane's low ionic conductivity. Increasing the IEC resulted in higher voltage efficiency for the 2.0 and 2.4 mequiv g(-1) samples, but the cells with these membranes displayed reduced Coulombic efficiency and faster capacity fade. The QA-Radel with an IEC of 2.0 mequiv g(-1) had the best balance of ionic conductivity and VO(2+) permeability, achieving a maximum power density of 218 mW cm(-2) which was higher than the maximum power density of a VRFB assembled with a Nafion N212 membrane in our system. While anion exchange membranes are under study for a variety of VRFB applications, this work demonstrates that the material parameters must be optimized to obtain the maximum cell performance.

  18. Direct determination of sodium, potassium, chromium and vanadium in biodiesel fuel by tungsten coil atomic emission spectrometry.

    PubMed

    Dancsak, Stacia E; Silva, Sidnei G; Nóbrega, Joaquim A; Jones, Bradley T; Donati, George L

    2014-01-02

    High levels of sodium and potassium can be present in biodiesel fuel and contribute to corrosion, reduced performance and shorter engine lifetime. On the other hand, trace amounts of chromium and vanadium can increase the emission of pollutants during biodiesel combustion. Sample viscosity, immiscibility with aqueous solutions and high carbon content can compromise biodiesel analyzes. In this work, tungsten filaments extracted from microscope light bulbs are used to successively decompose biodiesel's organic matrix, and atomize and excite the analytes to determine sodium, potassium, chromium and vanadium by tungsten coil atomic emission spectrometry (WCAES). No sample preparation other than simple dilution in methanol or ethanol is required. Direct analysis of 10-μL sample aliquots using heating cycles with less than 150 s results in limits of detection (LOD) as low as 20, 70, 70 and 90 μg kg(-1) for Na, K, Cr and V, respectively. The procedure's accuracy is checked by determining Na and K in a biodiesel reference sample and carrying out spike experiments for Cr and V. No statistically significant differences were observed between reference and determined values for all analytes at a 95% confidence level. The procedure was applied to three different biodiesel samples and concentrations between 6.08 and 95.6 mg kg(-1) for Na and K, and between 0.22 and 0.43 mg kg(-1) for V were obtained. The procedure is simple, fast and environmentally friendly. Small volumes of reagents, samples and gases are used and no residues are generated. Powers of detection are comparable to other traditional methods.

  19. Development of analytical techniques of vanadium isotope in seawater

    NASA Astrophysics Data System (ADS)

    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. Cobalt vanadium oxide thin nanoplates: primary electrochemical capacitor application

    PubMed Central

    Zhang, Youjuan; Liu, Yuanying; Chen, Jing; Guo, Qifei; Wang, Ting; Pang, Huan

    2014-01-01

    Co3V2O8 thin nanoplates are firstly described as a kind of electrode material for supercapacitors. More importantly, from electrochemical measurements, the obtained Co3V2O8 nanoplate electrode shows a good specific capacitance (0.5 A g−1, 739 F g−1) and cycling stability (704 F g−1 retained after 2000 cycles). This study essentially offers a new kind of metal vanadium oxides as electrochemical active material for the development of supercapacitors. PMID:25023373

  1. Low temperature electrolytes for lithium/silver vanadium oxide cells

    NASA Technical Reports Server (NTRS)

    Tuhovak, Denise R.; Takeuchi, Esther S.

    1991-01-01

    Combinations of methyl formate (MF) and propylene carbonate (PC) using salt concentrations of 0.6 to 2.4 M, with lithium hexafluoroarsenate and lithium tetrafluoroborate in a five to one molar ratio, were investigated as electrolytes in lithium/silver vanadium oxide batteries. The composition of the electrolyte affected cell performance at low temperature, self-discharge and abuse resistance as characterized by short circuit and crush testing. The electrolyte that provided the best combination of good low temperature performance, low cell self-discharge and abuse resistance was 0.6 M salt in 10:90 PC/MF.

  2. Pulsating electrolyte flow in a full vanadium redox battery

    NASA Astrophysics Data System (ADS)

    Ling, C. Y.; Cao, H.; Chng, M. L.; Han, M.; Birgersson, E.

    2015-10-01

    Proper management of electrolyte flow in a vanadium redox battery (VRB) is crucial to achieve high overall system efficiency. On one hand, constant flow reduces concentration polarization and by extension, energy efficiency; on the other hand, it results in higher auxiliary pumping costs, which can consume around 10% of the discharge power. This work seeks to reduce the pumping cost by adopting a novel pulsing electrolyte flow strategy while retaining high energy efficiency. The results indicate that adopting a short flow period, followed by a long flow termination period, results in high energy efficiencies of 80.5% with a pumping cost reduction of over 50%.

  3. Vanadium Flow Battery for Energy Storage: Prospects and Challenges.

    PubMed

    Ding, Cong; Zhang, Huamin; Li, Xianfeng; Liu, Tao; Xing, Feng

    2013-04-18

    The vanadium flow battery (VFB) as one kind of energy storage technique that has enormous impact on the stabilization and smooth output of renewable energy. Key materials like membranes, electrode, and electrolytes will finally determine the performance of VFBs. In this Perspective, we report on the current understanding of VFBs from materials to stacks, describing the factors that affect materials' performance from microstructures to the mechanism and new materials development. Moreover, new models for VFB stacks as well as structural design will be summarized as well. Finally, the challenges, the overall cost evaluation, and future research directions will be briefly proposed.

  4. Determination of total vanadium and vanadium(V) in groundwater from Mt. Etna and estimate of daily intake of vanadium(V) through drinking water.

    PubMed

    Arena, Giovanni; Copat, Chiara; Dimartino, Angela; Grasso, Alfina; Fallico, Roberto; Sciacca, Salvatore; Fiore, Maria; Ferrante, Margherita

    2015-06-01

    Vanadium(V) can be found in natural waters in the form of V(IV) and V(V) species, which have different biological properties and toxicity. The purpose of this study was to determine the concentrations of total V and V(V) in groundwater from the area of Mt. Etna and to assess the estimated daily intake (EDI) of V(V) of adults and children through drinking water. Water was sampled monthly at 21 sites in 2011. Total vanadium was determined by inductively coupled plasma-mass spectrometry (ICP-MS) and speciation by ion chromatography-ICP-MS (IC-ICP-MS). The concentration of V(V) species ranged from 62.8 to 98.9% of total V, with significantly higher concentrations in samples from the S/SW slope of Mt. Etna. The annual mean concentrations of total V exceeded the Italian legal limit of 140 μg/L at four sites on the S/SW slope. In the absence of thresholds for V(V) intake, only the Environmental Protection Agency (EPA) has calculated a reference dose. Children's EDI of V(V) at the sites with the higher V concentrations exceeded EPA thresholds (9 μg/kg/day). In particular, we found in Camporotondo, Mascalucia, Ragalna and San Pietro Clarenza sites children's EDIs of 11, 9.3, 11 and 9.9, respectively. The EDI of V(V) was significantly higher than the literature range (0.09-0.34 μg/kg/day).

  5. MIPs in Aqueous Environments.

    PubMed

    Wan, Ying-chun; Ma, Hui-ting; Lu, Bin

    2015-01-01

    When organic solvent-compatible molecularly imprinted polymers (MIPs) are used in aqueous environment, how to reduce nonspecific binding is a major challenge. By modifying the binding solvents and introducing appropriate washing and elution steps, even relatively hydrophobic MIPs can gain optimal rebinding selectivity in aqueous conditions. Furthermore, water-compatible MIPs that can be used to treat aqueous samples directly have been prepared. The use of hydrophilic co-monomers, the controlled surface modification through controlled radical polymerization, and the new interfacial molecular imprinting methods are different strategies to prepare water-compatible MIPs. By combining MIPs with other techniques, both organic solvent-compatible and water-compatible MIPs can display better functional performances in aqueous conditions. Intensive studies on MIPs in aqueous conditions can provide new MIPs with much-improved compatibilities that will lead to more interesting applications in biomedicine and biotechnology.

  6. Atomic layer deposition of VO2 films with Tetrakis-dimethyl-amino vanadium (IV) as vanadium precursor

    NASA Astrophysics Data System (ADS)

    Lv, Xinrui; Cao, Yunzhen; Yan, Lu; Li, Ying; Song, Lixin

    2017-02-01

    VO2 thin films have been grown on Si(100) (VO2/Si) and fused silica substrates (VO2/SiO2) 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 VO2 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 VO2 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 VO2/Si film. AFM was applied to study the surface morphology of VO2/Si films, which showed a dense polycrystalline film with roughness of about 1 nm. The resistance of VO2/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 (Tc,h) of about 72 °C, a hysteresis width of about 10 °C and the resistance change of two orders of magnitude. The increase of Tc,h compared with the bulk VO2 (68 °C) may be attributed to the tensile stress along the c-axis in the film. Transmittance measurement of VO2/SiO2 films showed typical thermochromic property with a NIR switching efficiency of above 50% at 2 μm across the transition.

  7. Effects of vanadium on population growth and Na-K-ATPase activity of the brackish water hydroid Cordylophora caspia

    SciTech Connect

    Ringelband, U.; Karbe, L.

    1996-07-01

    Vanadium, a relatively abundant heavy metal, enters the environment naturally through rock weathering. A large fraction of vanadium input is of human origin. The combustion of petroleum- and coal-products, which contain relatively high concentrations of vanadium, is one of the most important sources of the enrichment of vanadium in the environment. As it is used as an alloy, and vanadium rich iron-ores of various origin are used in steel production, the residual slag-stones of the steel industry can contain considerable vanadium concentrations. Wherever slag-stones serve as a cheap and convenient material in riverbank reinforcement, vanadium can leach into the aquatic environment. Vanadium is regarded as an essential trace element for higher animals. Cantley et al. indicated a regulatory function of vanadate in vivo. Although considerable information is available on the toxic effects of vanadium on humans, very little is known about the toxicity of vanadium towards aquatic organisms, especially invertebrates. Bell and Sargent have shown an inhibition of Na-K-ATPase activity in gills of the eel Anguilla anguilla. Holleland and Towle have demonstrated the inhibition of Na-K-ATPase activity in the gills of the shore crab Carcinus maenas. The aim of this study was to determine the toxicity of vanadium towards the brackish water hydroid Cordylophora caspia. Hydroids are known to be particularly sensitive to heavy metals and their asexual reproduction can be used in a well-established population growth test. Furthermore, the effects of vanadium on Na-K-ATPase activity in hydroids were studied in in vivo experiments, wherein the animals were exposed to sublethal concentrations of vanadium. In addition, the inhibition of Na-K-ATPase was measured in vitro, by adding vanadium to a microsomal preparation. 16 refs., 4 figs.

  8. Inverse association of plasma vanadium levels with newly diagnosed type 2 diabetes in a Chinese population.

    PubMed

    Wang, Xia; Sun, Taoping; Liu, Jun; Shan, Zhilei; Jin, Yilin; Chen, Sijing; Bao, Wei; Hu, Frank B; Liu, Liegang

    2014-08-15

    Vanadium compounds have been proposed to have beneficial effects on the pathogenesis and complications of type 2 diabetes. Our objective was to evaluate the association between plasma vanadium levels and type 2 diabetes. We performed a case-control study involving 1,598 Chinese subjects with or without newly diagnosed type 2 diabetes (December 2004-December 2007). Cases and controls were frequency-matched by age and sex. Plasma vanadium concentrations were measured and compared between groups. Analyses showed that plasma vanadium concentrations were significantly lower in cases with newly diagnosed type 2 diabetes than in controls (P = 0.001). Mean plasma vanadium levels in participants with and without diabetes were 1.0 μg/L and 1.2 μg/L, respectively. Participants in the highest quartile of plasma vanadium concentration had a notably lower risk of newly diagnosed type 2 diabetes (odds ratio = 0.26, 95% confidence interval: 0.19, 0.35; P < 0.001), compared with persons in the lowest quartile. The trend remained significant after adjustment for known risk factors and in further stratification analyses. Our results suggested that plasma vanadium concentrations were inversely associated with newly diagnosed type 2 diabetes in this Chinese population.

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

    NASA Astrophysics Data System (ADS)

    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.

  10. Water adsorption on polycrystalline vanadium from ultra-high vacuum to ambient relative humidity

    NASA Astrophysics Data System (ADS)

    Rameshan, C.; Ng, M. L.; Shavorskiy, A.; Newberg, J. T.; Bluhm, H.

    2015-11-01

    We have studied the reaction of water vapor with a polycrystalline vanadium surface using ambient pressure X-ray photoelectron spectroscopy (AP-XPS) which allows the investigation of the chemical composition of the vanadium/water vapor interface at p(H2O) in the Torr range. Water dissociation on the vanadium surface was studied under isobaric conditions at p(H2O) ranging from 0.01 to 0.50 Torr and temperatures from 625 K to 260 K, i.e. up to a relative humidity (RH) of 15%. Water vapor exposure leads to oxidation and hydroxylation of the vanadium foil already at a pressure of 1 × 10- 6 Torr at 300 K (RH 4 × 10- 6%). The vanadium oxide layer on the surface has a stoichiometry of V2O3. Initial adsorption of molecular water on the surface is observed at RH > 0.001%. Above a RH of 0.5% the amount of adsorbed water increases markedly. Experiments at increasing temperatures show that the water adsorption process is reversible. Depth profile measurements show a thickness for the vanadium oxide layer of 3-5 mono layers (ML) and for vanadium hydroxide of 1-1.5 ML over the whole RH range in the isobar experiments. The thickness of the adsorbed water layer was found to be in the sub-ML range for the investigated RH's.

  11. Chelation therapy and vanadium: effect on reproductive organs in rats.

    PubMed

    Shrivastava, Sadhana; Jadon, Anjana; Shukla, Sangeeta; Mathur, Ramesh

    2007-06-01

    Present investigation was planned to evaluate the therapeutic effectiveness of chelating agents against vanadium intoxication on blood and reproductive organs of rats. Male and female albino rats were injected vanadyl sulphate (7.5 mg/kg, po, for 21 days, 5 days in a week). Chelating agents tiron (T) alone and in combination with lipoic acid (LA), vitamin E (vit E) and selenium (Se) were given for 2 days/week. With the administration of vanadyl sulphate to rats fructose level in seminal vesicles was significantly (P< or =0.05) declined. The activities of alkaline phosphatase and adenosine triphosphatase were also decreased, whereas glycogen content and acid phosphatase activity increased in testis, seminal vesicles, ovaries and uterus after toxicant exposure. Significant changes in serum transaminases, serum alkaline phosphatase and lactate dehydrogenase were recouped by chelation therapy. Lipid peroxidation, reduced glutathione level and triglycerides levels altered significantly after exposure to vanadium in rats. The ultrastructural damage in spermatogenic stages in treated animals showed recovery pattern after therapy. Co-treatment with antioxidants restored these activities. The most effective combination was tiron + selenium followed by tiron + vitamin E, and tiron + lipoic acid.

  12. Structural investigation of phosphate - bismuth glasses with vanadium

    NASA Astrophysics Data System (ADS)

    Stǎnescu, R.; Vedeanu, N.; Cozar, I. B.; Mǎgdaş, A.

    2013-11-01

    The xV2O5(1-dx)[0.5P2O5ṡ0.5Bi2O3] glass system with 0 ≤ x ≤ 50 mol% is investigated by IR and Raman spectroscopy. Both P2O5 and Bi2O3 oxides are known as network formers, but Bi2O3 is an unconventional one. At low content of vanadium oxide (x ≤ 5 mol%), both IR and Raman spectra are dominated by vibration bands characteristics to structural groups of phosphate and bismuthate lattices. Due to the network modifier role, vanadium oxide acts mainly on the Bi2O3 network allowing the phosphate groups to impose their characteristics absorption bands in spectra. These bands are strongly reduced for x ≥ 20 mol% due to the phosphate network depolymerization and the appearance of new vibrations characteristic to P-O-V, Bi-O-V and V-O-V groups showing the network former role of V2O5.

  13. Structural investigation of phosphate - bismuth glasses with vanadium

    SciTech Connect

    Stănescu, R.; Vedeanu, N.; Cozar, I. B.; Măgdaş, A.

    2013-11-13

    The xV{sub 2}O{sub 5}(1−dx)[0.5P{sub 2}O{sub 5}⋅0.5Bi{sub 2}O{sub 3}] glass system with 0 ≤ x ≤ 50 mol% is investigated by IR and Raman spectroscopy. Both P{sub 2}O{sub 5} and Bi{sub 2}O{sub 3} oxides are known as network formers, but Bi{sub 2}O{sub 3} is an unconventional one. At low content of vanadium oxide (x ≤ 5 mol%), both IR and Raman spectra are dominated by vibration bands characteristics to structural groups of phosphate and bismuthate lattices. Due to the network modifier role, vanadium oxide acts mainly on the Bi{sub 2}O{sub 3} network allowing the phosphate groups to impose their characteristics absorption bands in spectra. These bands are strongly reduced for x ≥ 20 mol% due to the phosphate network depolymerization and the appearance of new vibrations characteristic to P-O-V, Bi-O-V and V-O-V groups showing the network former role of V{sub 2}O{sub 5}.

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

    SciTech Connect

    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.

  15. First-principles investigation of vanadium isotope fractionation in solution and during adsorption

    NASA Astrophysics Data System (ADS)

    Wu, Fei; Qin, Tian; Li, Xuefang; Liu, Yun; Huang, Jen-How; Wu, Zhongqing; Huang, Fang

    2015-09-01

    Equilibrium fractionation factors of vanadium (V) isotopes among tri- (V(III)), tetra- (V(IV)) and penta-valent (V(V)) inorganic V species in aqueous system and during adsorption of V(V) to goethite are estimated using first-principles calculation. Our results highlight the dependence of V isotope fractionation on valence states and the chemical binding environment. The heavy V isotope (51V) is enriched in the main V species following a sequence of V(III) < V(IV) < V(V). According to our calculations, at 25 °C, the equilibrium isotope fractionation factor between [V5+O2(OH)2]- and [V4+O(H2O)5]2+ (ln ⁡α V (V)- V (IV)) is 3.9‰, and the equilibrium isotope fractionation factor between [V5+O2(OH)2]- and [V3+(OH)3(H2O)3] (ln ⁡α V (V)- V (III)) is 6.4‰. In addition, isotope fractionation between +5 valence species [V5+O2(OH)2]- and [V5+O2(H2O)4]+ is 1.5‰ at 25 °C, which is caused by their different bond lengths and coordination numbers (CN). Theoretical calculations also show that light V isotope (50V) is preferentially adsorbed on the surface of goethite. Our work reveals that V isotopes can be significantly fractionated in the Earth's surface environments due to redox reaction and mineral adsorption, indicating that V isotope data can be used to monitor toxic V(V) attenuation processes through reduction or adsorption in natural water systems. In addition, a simple mass balance model suggests that V isotope composition of seawater might vary with change of ambient oxygen levels. Thus our theoretical investigations imply a promising future for V isotopes as a potential new paleo-redox tracer.

  16. Processing of Egyptian boiler-ash for extraction of vanadium and nickel.

    PubMed

    Amer, A M

    2002-01-01

    Proposed technique in this investigation is given for vanadium and nickel enrichment in the Egyptian boiler ash. Among the various concepts for recovery of vanadium and nickel from boiler ash, the pyro-metallurgical approach is technically feasible, but is not cost-effective from an operational economy standpoint. Another technically viable process which, however, needs further development and presented in this investigation, is the hydrometallurgical processing that involves acid leaching under oxygen pressure of ground ash, followed by electrolytic separation of nickel from sulphate solution and vanadium is then neutralized and precipitated by adjustment the pH value and calcined to produce V2O5.

  17. Magnetic and luminescent properties of vanadium-doped ZnSe crystals

    NASA Astrophysics Data System (ADS)

    Radevici, Ivan; Nedeoglo, Natalia; Sushkevich, Konstantin; Huhtinen, Hannu; Nedeoglo, Dmitrii; Paturi, Petriina

    2016-12-01

    Magnetic and photoluminescence properties of vanadium-doped ZnSe crystals with impurity concentrations varied by changing the V amount in the source material from 0.03 to 0.30 at% are studied in 5-300 K temperature range. Investigation of magnetic properties shows that the studied concentrations of vanadium impurity that should not disturb crystal lattice are insignificant for observing ferromagnetic behaviour even at low temperatures. The contribution of V impurity to edge emission and its influence on infra-red emission are discussed. Similarities of magnetic and luminescent properties induced by vanadium and other transition metal impurities are discussed.

  18. Study and characterization of positive electrolytes for application in the aqueous all-copper redox flow battery

    NASA Astrophysics Data System (ADS)

    Sanz, Laura; Lloyd, David; Magdalena, Eva; Palma, Jesús; Anderson, Marc; Kontturi, Kyösti

    2015-03-01

    In recent studies, the employment of the aqueous solution system comprised of Cu(II)-Cu(I)-Cl system was addressed for massive energy storage in Redox Flow Batteries (RFBs) [5,6], providing important practical advantages compared to the widespread all-vanadium or Zn/Br systems [5]. The substitution of vanadium electrolytes by copper-chloride electrolytes allows the simplification of the process and notably reduces the cost, allowing for a better commercialization of RFBs. Here, a complete physico-chemical characterization of positive copper electrolytes and their electrochemical performance using different supporting electrolytes, HCl and CaCl2, is presented. Once the physical properties and the electrochemical performance of each one of the supporting electrolytes were determined, the final composition of supporting electrolyte for this Cu(II)/Cu(I) redox couple could be optimized by mixing different sources of chloride, regarding its practical application in the all-copper RFB.

  19. MCM-41-supported oxo-vanadium(IV) complex: a highly selective heterogeneous catalyst for the bromination of hydroxy aromatic compounds in water.

    PubMed

    Bhunia, Susmita; Saha, Debraj; Koner, Subratanath

    2011-12-20

    An ecofriendly solid catalyst has been synthesized by anchoring vanadium(IV) into organically modified MCM-41. First, the surface of Si-MCM-41 was modified with 3-aminopropyl-triethoxysilane (3-APTES), the amine group of which upon condensation with ortho-hydroxy-acetophenone affords a N(2)O(2)-type Schiff base moiety in the mesoporous matrix. The Schiff base moieties were used to anchor oxo-vanadium(IV) ions. The prepared catalyst has been characterized by UV-vis, IR spectroscopy, small-angle X-ray diffraction (SAX), nitrogen sorption, and transmission electron microscopy (TEM) studies. It is observed that the mesostructure has not been destroyed in the multistep synthesis procedure, as evidenced by SAX and TEM measurements. The catalyst has shown unprecedented high conversion as well as para selectivity toward the bromination of hydroxy aromatic compounds using aqueous 30% H(2)O(2)/KBr in water. The reaction proceeds according to the stoichiometric ratio, and the monobrominated product was obtained as the major product using a stoichiometric amount of the bromine source. The immobilized complex does not leach or decompose during the catalytic reactions, showing practical advantages over the free metal complex.

  20. Antidiabetic Bis-Maltolato-OxoVanadium(IV): Conversion of inactive trans- to bioactive cis-BMOV for possible binding to target PTP-1B

    PubMed Central

    Scior, Thomas; Mack, Hans-Georg; García, José Antonio Guevara; Koch, Wolfhard

    2008-01-01

    The postulated transition of Bis-Maltolato-OxoVanadium(IV) (BMOV) from its inactive trans- into its cis-aquo-BMOV isomeric form in solution was simulated by means of computational molecular modeling. The rotational barrier was calculated with DFT – B3LYP under a stepwise optimization protocol with STO-3G, 3-21G, 3-21G*, and 6-31G ab initio basis sets. Our computed results are consistent with reports on the putative molecular mechanism of BMOV triggering the insulin-like cellular response (insulin mimetic) as a potent inhibitor of the protein tyrosine phosphatase-1B (PTP-1B). Initially, trans-BMOV is present in its solid dosage form but in aqueous solution, and during oral administration, it is readily converted into a mixture of “open-type” and “closed-type” complexes of cis-aquo-BMOV under equilibrium conditions. However, in the same measure as the “closed-type” complex binds to the cytosolic PTP-1B, it disappears from solution, and the equilibrium shifts towards the “closed-type” species. In full accordance, the computed binding mode of cis-BMOV is energetically favored over sterically hindered trans-BMOV. In view of our earlier report on prodrug hypothesis of vanadium organic compounds the present results suggest that cis-BMOV is the bioactive species. PMID:19920909

  1. Reflectance of aqueous solutions

    NASA Technical Reports Server (NTRS)

    Querry, M. R.

    1972-01-01

    The optical properties and optical constants of water and aqueous solutions were studied to develop an accurate tabulation of graphical representations of the optical constants through a broad spectrum. Manuscripts of articles are presented concerning extinction coefficients, relative specular reflectance, and temperature effect on the water spectrum. Graphs of absolute reflectance, phase shifts, index of refraction, and extinction coefficients for water, heavy water and aqueous solutions are included.

  2. Phase formation at bonded vanadium and stainless steel interfaces

    SciTech Connect

    Summers, T.S.E.

    1992-01-01

    The interface between vanadium bonded to stainless steel was studies to determine whether a brittle phase formed during three joining operations. Inertia friction welds between V and 21-6-9 stainless steel were examined using TEM. In the as-welded condition, a continuous, polygranular intermetallic layer about 0.25 {mu}m thick was present at the interface. This layer grew to about 50 {mu}m thick during heat treatment at 1000{degrees}C for two hours. Analysis of electron diffraction patterns confirmed that this intermetallic was the {omega} phase. The interface between vanadium and type 304, SANDVIK SAF 2205, and 21-6-9 stainless steel bonded by a co-extrusion process had intermetallic particles at the interface in the as-extruded condition. Heat treatment at 1000{degrees}C for two hours caused these particles to grow into continuous layers in all three cases. Based on the appearance, composition and hardness of this interfacial intermetallic, it was also concluded to be {omega} phase. Bonding V to type 430 stainless steel by co-extrusion caused V-rich carbides to form at the interface due to the higher concentration of C in the type 430 than in the other stainless steels investigated. The carbide particles initially present grew into a continuous layer during a two-hour heat treatment at 1000{degrees}C. Co-hipping 21-6-9 stainless steel tubing with V rod resulted in slightly more concentric specimens than the co-extruded ones, but a continuous layer of the {omega} phase formed during the hipping operation. This brittle layer could initiate failure during subsequent forming operations. The vanadium near the stainless steel interface in the co-extruded and co-hipped tubing in some cases was harder than before heat treatment. It was concluded that this hardening was due to thermal straining during cooling following heat treatment and that thermal strains might present a greater problem than seen here when longer tubes are used in actual applications.

  3. A disposable alkaline phosphatase-based biosensor for vanadium chronoamperometric determination.

    PubMed

    Alvarado-Gámez, Ana Lorena; Alonso-Lomillo, María Asunción; Domínguez-Renedo, Olga; Arcos-Martínez, María Julia

    2014-02-24

    A chronoamperometric method for vanadium ion determination, based on the inhibition of the enzyme alkaline phosphatase, is reported. Screen-printed carbon electrodes modified with gold nanoparticles were used as transducers for the immobilization of the enzyme. The enzymatic activity over 4-nitrophenyl phosphate sodium salt is affected by vanadium ions, which results in a decrease in the chronoamperometric current registered. The developed method has a detection limit of 0.39 ± 0.06 µM, a repeatability of 7.7% (n = 4) and a reproducibility of 8% (n = 3). A study of the possible interferences shows that the presence of Mo(VI), Cr(III), Ca(II) and W(VI), may affect vanadium determination at concentration higher than 1.0 mM. The method was successfully applied to the determination of vanadium in spiked tap water.

  4. Direct and selective spectrophotometric method for the determination of vanadium in steel, environmental and biological samples

    NASA Astrophysics Data System (ADS)

    Mathew, Sunitha B.; Pataila, Girija; Pillai, Ajai K.; Gupta, V. K.

    2011-10-01

    A simple, direct and selective spectrophotometric method for determination of vanadium is described. The present methodology is based on the strong oxidizing power of vanadium (V). Vanadium (V) selectively oxidizes leucocrystal violet (LCV) to crystal violet in the presence of phosphoric acid. The violet colored dye obtained shows maximum absorbance at 590 nm. Beer's law is obeyed in the concentration range 0.06-0.6 μg ml -1. The molar absorptivity and Sandell's sensitivity are found to be 6.78 × 10 4 l mol -1 cm -1 and 0.0044 μg cm -2, respectively. The proposed method is simple, direct, and sensitive. It has been successfully applied for the determination of vanadium in various environmental, biological and steel samples.

  5. Molten salt synthesis and localized surface plasmon resonance study of vanadium dioxide nanopowders

    SciTech Connect

    Wang Fu; Liu Yun; Liu Chunyan

    2009-12-15

    Rutile-type vanadium dioxide nanopowders with four different sizes were successfully synthesized by carbothermal reducing V{sub 2}O{sub 5} in KCl-LiCl molten salt. XRD and TEM characterizations suggested that vanadium dioxide particles formed by a broken and reunited process of vanadium oxide. Molten salt and organic carbon sources are crucial to the size of final particles. In the presence of the molten salt, the organic carbon with a shorter chain length would induce smaller particles. The UV-VIS-IR spectral measurements for as-prepared vanadium dioxide announced an obvious localized surface plasmon resonance band in the near infrared region at 90 deg. C. - Graphical abstract: Schematic illustration of the formation mechanism of VO{sub 2}(M) nanoparticles in molten salt, particles size can be controlled by choosing organic carbon sources with different chain length.

  6. ATR-A1 irradiation experiment on vanadium alloys and low activation steels

    SciTech Connect

    Tasi, H.; Strain, R.V.; Gomes, I.; Hins, A.G.; Smith, D.L.

    1996-04-01

    To study the mechanical properties of vanadium alloys under neutron irradiation at low temperatures, an experiment was designed and constructed for irradiation in the Advanced Test Reactor (ATR). The experiment contained Charpy, tensile, compact tension, TEM, and creep specimens of vanadium alloys. It also contained limited low-activation ferritic steel specimens as part of the collaborative agreement with Monbusho of Japan. The design irradiation temperatures for the vanadium alloy specimens in the experiment are {approx}200 and 300{degrees}C, achieved with passive gap-gap sizing and fill gas blending. To mitigate vanadium-to-chromium transmutation from the thermal neutron flux, the test specimens are contained inside gadolinium flux filters. All specimens are lithium-bonded. The irradiation started in Cycle 108A (December 3, 1995) and is expected to have a duration of three ATR cycles and a peak influence of 4.4 dpa.

  7. Chemical vapour deposition of thermochromic vanadium dioxide thin films for energy efficient glazing

    SciTech Connect

    Warwick, Michael E.A.; Binions, Russell

    2014-06-01

    Vanadium dioxide is a thermochromic material that undergoes a semiconductor to metal transitions at a critical temperature of 68 °C. This phase change from a low temperature monoclinic structure to a higher temperature rutile structure is accompanied by a marked change in infrared reflectivity and change in resistivity. This ability to have a temperature-modulated film that can limit solar heat gain makes vanadium dioxide an ideal candidate for thermochromic energy efficient glazing. In this review we detail the current challenges to such glazing becoming a commercial reality and describe the key chemical vapour deposition technologies being employed in the latest research. - Graphical abstract: Schematic demonstration of the effect of thermochromic glazing on solar radiation (red arrow represents IR radiation, black arrow represents all other solar radiation). - Highlights: • Vanadium dioxide thin films for energy efficient glazing. • Reviews chemical vapour deposition techniques. • Latest results for thin film deposition for vanadium dioxide.

  8. Vanadium K-edge X-ray absorption spectroscopy of bromoperoxidase from Ascophyllum nodosum

    SciTech Connect

    Arber, J.M.; de Boer, E.; Garner, C.D.; Hasnain, S.S.; Wever, R. )

    1989-09-19

    Bromoperoxidase from Ascophyllum nodusum was the first vanadium-containing enzyme to be isolated. X-ray absorption spectra have now been collected in order to investigate the coordination of vanadium in the native, native plus bromide, native plus hydrogen peroxide, and dithionite-reduced forms of the enzyme. The edge and X-ray absorption near-edge structures show that, in the four samples studied, it is only on reduction of the native enzyme that the metal site is substantially altered. In addition, these data are consistent with the presence of vanadium(IV) in the reduced enzyme and vanadium(V) in the other samples. Extended X-ray absorption fine structure data confirm that there are structural changes at the metal site on reduction of the native enzyme, notably a lengthening of the average inner-shell distance, and the presence of terminal oxygen together with histidine and oxygen-donating residues.

  9. A Disposable Alkaline Phosphatase-Based Biosensor for Vanadium Chronoamperometric Determination

    PubMed Central

    Alvarado-Gámez, Ana Lorena; Alonso-Lomillo, María Asunción; Domínguez-Renedo, Olga; Arcos-Martínez, María Julia

    2014-01-01

    A chronoamperometric method for vanadium ion determination, based on the inhibition of the enzyme alkaline phosphatase, is reported. Screen-printed carbon electrodes modified with gold nanoparticles were used as transducers for the immobilization of the enzyme. The enzymatic activity over 4-nitrophenyl phosphate sodium salt is affected by vanadium ions, which results in a decrease in the chronoamperometric current registered. The developed method has a detection limit of 0.39 ± 0.06 μM, a repeatability of 7.7% (n = 4) and a reproducibility of 8% (n = 3). A study of the possible interferences shows that the presence of Mo(VI), Cr(III), Ca(II) and W(VI), may affect vanadium determination at concentration higher than 1.0 mM. The method was successfully applied to the determination of vanadium in spiked tap water. PMID:24569772

  10. Disassembly of irradiated lithium-bonded capsules containing vanadium alloy specimens

    SciTech Connect

    Tsai, H.; Strain, R.V.

    1996-04-01

    Capsules containing vanadium alloy specimens from irradiation experiments in FFTF and EBR-II are being processed to remove the lithium bond and retrieve the specimens for testing. The work has progressed smoothly.

  11. Molecular based magnets comprising vanadium tetracyanoethylene complexes for shielding electromagnetic fields

    DOEpatents

    Epstein, Arthur J.; Morin, Brian G.

    1998-01-01

    The invention presents a vanadium tetracyanoethylene solvent complex for electromagnetic field shielding, and a method for blocking low frequency and magnetic fields using these vanadium tetracyanoethylene compositions. The compositions of the invention can be produced at ambient temperature and are light weight, low density and flexible. The materials of the present invention are useful as magnetic shields to block low frequency fields and static fields, and for use in cores in transformers and motors.

  12. Utilization of vanadium alloys in the DIII-D Radiative Divertor Program

    SciTech Connect

    Smith, J.P.; Johnson, W.R.; Stambaugh, R.D.; Trester, P.W.; Smith, D.; Bloom, E.

    1995-10-01

    Vanadium alloys are attractive candidate structural materials for fusion power plants because of their potential for minimum environmental impact due to low neutron activation and rapid activation decay. They also possess favorable material properties for operation in a fusion environment. General Atomics (GA), in conjunction with Argonne National Laboratory (ANL) and Oak Ridge National Laboratory (ORNL), has developed a plan for the utilization of vanadium alloys as part of the Radiative Divertor (RD) upgrade for the DIII-D tokamak. The plan will be carried out in conjunction with General Atomics and the Materials Program of the US Department of Energy (DOE). This application of a vanadium alloy will provide a meaningful step in the development of advanced materials for fusion power devices by: (1) developing necessary materials processing technology for the fabrication of large vanadium alloy components, and (2) demonstrating the in-service behavior of a vanadium alloy (V-4Cr-4Ti) in a tokamak environment. The program consists of three phases: first, small vanadium alloy coupon samples will be exposed in DIII-D at positions in the vessel floor and within the pumping plenum region of the existing divertor structure; second, a small vanadium alloy component will be installed in the existing divertor, and third, during the forthcoming Radiative Divertor modification, scheduled for completion in mid-1997, the upper section of the new double-null, slotted divertor will be fabricated from vanadium alloy product forms. This program also includes research and development (R and D) efforts to support fabrication development and to resolve key issues related to environmental effects.

  13. Vanadium doping of LiMnPO4: Vibrational spectroscopy and first-principle studies

    NASA Astrophysics Data System (ADS)

    Kellerman, D.; Medvedeva, N.; Mukhina, N.; Semenova, A.; Baklanova, I.; Perelyaeva, L.; Gorshkov, V.

    2014-01-01

    The samples of pure and 10% vanadium-doped LiMnPO4 have been synthesized by the solid-state reaction technique. The results of Raman and infrared absorption spectroscopy show that the vanadium atoms replace phosphorus giving rise to LiMn(PO4)1-x(VO4)x solid solutions. This conclusion is confirmed by the first-principle studies.

  14. Molecular based magnets comprising vanadium tetracyanoethylene complexes for shielding electromagnetic fields

    DOEpatents

    Epstein, A.J.; Morin, B.G.

    1998-10-13

    The invention presents a vanadium tetracyanoethylene solvent complex for electromagnetic field shielding, and a method for blocking low frequency and magnetic fields using these vanadium tetracyanoethylene compositions. The compositions of the invention can be produced at ambient temperature and are light weight, low density and flexible. The materials of the present invention are useful as magnetic shields to block low frequency fields and static fields, and for use in cores in transformers and motors. 21 figs.

  15. Thermochromic modulation of surface plasmon polaritons in vanadium dioxide nanocomposites.

    PubMed

    Jostmeier, Thorben; Mangold, Moritz; Zimmer, Johannes; Karl, Helmut; Krenner, Hubert J; Ruppert, Claudia; Betz, Markus

    2016-07-25

    We propose and implement a new concept for thermochromic plasmonic elements. It is based on vanadium dioxide (VO2) nanocrystals located in the near field of surface plasmon polaritons supported by an otherwise unstructured gold thin film. When the VO2 undergoes the metal-insulator phase transition, the coupling conditions for conversion of light into propagating surface plasmon polaritons change markedly. In particular, we realize thermochromic plasmonic grating couplers with substantial switching contrast as well as tunable plasmonic couplers in a Kretschmann configuration. The use of VO2 nanocrystals permits highly repetitive switching and room temperature operation. Simulations based on the actual dielectric function of our VO2 nanocrystals agree well with the experiment.

  16. Thermochromic vanadium oxide thin films: Electronic and optical properties

    NASA Astrophysics Data System (ADS)

    Niklasson, G. A.; Li, S.-Y.; Granqvist, C. G.

    2014-11-01

    Vanadium dioxide, VO2, is a widely studied thermochromic material with potential applications in energy efficient window technology. It undergoes a first-order metal-to- insulator transition, accompanied by a crystal structure transformation from monoclinic to tetragonal rutile, at a critical temperature of 68 °C. Below this temperature, VO2 is semiconducting and infrared transmitting whereas it is metallic and infrared reflecting above the transition temperature. However, in order to achieve significant thermochromic switching, the luminous transmittance of thin films will typically be less than 50%. Here we report on recent research to improve the luminous transmittance as well as the transmittance change at the transition temperature. We systematically evaluate the effect of antireflection coatings, doping with Mg and the performance of coatings comprising thermochromic nanoparticles in a transparent matrix. The last option is shown to give the best performance and holds great promise for practical applications.

  17. Materials design using correlated oxides: Optical properties of vanadium dioxide

    NASA Astrophysics Data System (ADS)

    Tomczak, J. M.; Biermann, S.

    2009-05-01

    Materials with strong electronic Coulomb interactions play an increasing role in modern materials applications. "Thermochromic" systems, that exhibit thermally induced changes in their optical response, provide a particularly interesting case. The optical switching associated with the metal-insulator transition of vanadium dioxide (VO2), for example, has been proposed for use in "intelligent" windows that selectively filter radiative heat in hot weather conditions. In this work, we develop the theoretical tools for describing such a behaviour. Using a novel scheme for the calculation of the optical conductivity of correlated materials, we obtain quantitative agreement with experiments for both phases of VO2. On the example of an optimized energy-saving window setup, we further demonstrate that theoretical materials design has now come into reach, even for the particularly challenging class of correlated electron systems.

  18. Vanadium oxide bronzes containing rare-earth elements

    SciTech Connect

    Volkov, V.L.; Zubkov, V.G.; Fedyukov, A.S.; Zainulin, Yu.G.

    1988-05-01

    We attempted to make phases having the general formula Ln/sub x/V/sub 2/O/sub 5/ (Ln = La, Eu, Yb) without success; the specimens usually consisted of three phases: the rare-earth orthovanadate LnVO/sub 4/, vanadium(V) oxide, and VO/sub 2/. To shift the process to give Ln/sub x/V/sub 2/O/sub 5/, heat treatment was applied to mixtures of the initial high-purity substances. The x-ray patterns were recorded with a DRON-UM1 apparatus with Cr K..cap alpha.. radiation and were processed by the Poroshok program. The IR spectra were recorded with UR-20 spectrometer with oil mulls.

  19. X-ray induced photoconductivity in Vanadium Dioxide samples

    NASA Astrophysics Data System (ADS)

    Dietze, Sebastian; Mohanty, Jyoti; Marsh, Moses; Kim, Jong Woo; West, Kevin; Schuller, Ivan K.; Shpyrko, Oleg G.

    2011-03-01

    Vanadium Dioxide (VO2) goes through a first-order phase transition at approximately 340K, exhibiting both an insulator to metal transition (IMT) and a structural phase transition (SPT), with a monoclinic (M1) insulating phase at low temperatures and a rutile (R) metallic phase at high temperatures. We show an anomalous behavior of x-ray induced persistent photoconductivity (PPC) well below the temperature induced phase transition in VO2 devices. We present conductivity and X-ray Diffraction (XRD) measurements, revealing a large enhancement of conductivity due to photo-induced carriers. Moreover, with the addition of nominal electric fields, we are able to fully transition into the rutile metallic phase at room temperature. This effect is completely reversible, allowing the monoclinic insulating phase to be recovered via annealing.

  20. Ion-assisted evaporation of vanadium dioxide thin films

    NASA Astrophysics Data System (ADS)

    Zou, Mengyang; Ni, Chuan; Sarangan, Andrew

    2016-09-01

    Vanadium dioxide (VO2) is a polycrystalline thin film that reversibly changes from a semiconductor to a metallic state at 68°C, and has important applications in thermal detection and actuation as well as in reconfigurable photonic circuitry. In this work, we have produced VO2 thin films by oxygen ion-assisted electron-beam evaporation. Compared to prior work, the phase change temperature is as low as 54°C, which we believe arise due to the oxygen implantation from the ion-assisted process. The films were deposited on c-cut sapphire substrates, and their properties were measured using a four-point probe electrical sheet resistance measurement.

  1. Application of vanadium hydride compressors for Joule-Thomson cryocoolers

    NASA Astrophysics Data System (ADS)

    Bowman, R. C., Jr.; Freeman, B. D.; Phillips, J. R.

    The Joule-Thomson expansion of hydrogen gas offers efficient and reliable cryocoolers to produce temperatures between 10 and 50 K. A critical component to the development of these devices is the metal hydride storage bed that provides a nonmechanical method to compress hydrogen gas via the reversible absorption by appropriate metals or alloys. A thermodynamic model has been used to calculate the impact of operational parameters such as input/output pressure ratios and bed temperature on energy balance and system efficiency. Detailed comparisons are reported for a compressor which utilizes vanadium metal as the sorbent for either hydrogen or deuterium where the unusually large isotope differences between the phase diagrams and thermal properties for VH(x) and VD(x) have been considered. The sensitivity of heat input requirements to the uncertainties in primary variables are described.

  2. Calculation of 3s photoemission spectra of vanadium on graphite

    SciTech Connect

    Krueger, P.; Taguchi, M.; Parlebas, J.C.; Kotani, A.

    1997-06-01

    A few years ago, a satellite structure in the vanadium 3s x-ray photoemission spectroscopy (XPS) spectrum of V clusters upon graphite was observed and attributed to the presence of magnetic moments on the V surface. Here, we present calculations of these spectra using a cluster model that takes into account intra-atomic d-d and d{endash}core electron correlation and hybridization between V d and graphite {pi} states. When the V-graphite distance is increased from 1.5 to 2.0 {Angstrom} the system undergoes a low-to-high spin transition, which is clearly evidenced in the evolution of the XPS line shape. Although direct comparison with experiment is difficult, our study suggests that the observed satellite is due to core hole screening rather than a magnetic moment on the V atom. {copyright} {ital 1997} {ital The American Physical Society}

  3. Microstructure and mechanical properties of vanadium alloys after thermomechanical treatments

    SciTech Connect

    Grinyaev, Konstantin V. Ditenberg, Ivan A.; Smirnov, Ivan V.; Tyumentsev, Alexander N.; Tsverova, Anastasiya S.; Chernov, Vyacheslav M.; Potapenko, Mikhail M.

    2015-10-27

    The results of investigation of dispersion strengthening effect on parameters of structural-phase states and characteristics of short-term strength and ductility of vanadium alloys of V–4Ti–4Cr, V–2.4Zr–0.25C, V–1.2Zr–8.8Cr and V–1.7Zr–4.2Cr–7.6W systems with different concentration of interstitial elements after optimized thermomechanical treatment mode were summarized. It was shown that for effective realization of dispersion strengthening by Orowan-type mechanism at least 25–50% of the initial volume fraction of coarse particles should be transformed into fine-disperse state and redistributed over the volume of material.

  4. Structural and optical properties of hydrothermally synthesized vanadium oxides nanobelts

    NASA Astrophysics Data System (ADS)

    Derkaoui, I.; Khenfouch, M.; Elmokri, I.; Mothudi, B. M.; Dhlamini, M. S.; Moloi, S. J.; Zorkani, I.; Jorio, A.; Maaza, M.

    2017-03-01

    Nanostructured metal oxides have attracted a lot of attention recently owning to their unique structural advantages, and demonstrated promising chemical and physical properties for various applications. In this study, we report the structural and optical properties of vanadium oxide nanoparticles (VO-NPs) prepared via a hydrothermal method. Our results are revealing that the components of VO-NPs films are having a belt-like shape with a uniform size distribution. The nanobelts with very smooth and flat surfaces have a typical length of up to 1μm and a width of about 9-14 nm. Moreover, The UV-Visible spectroscopy revealed an excellent optical propertiesshowing clearly the good stoichiometry and crystallinity of our VO-NPs films. This synthesis method provides a new simple route to fabricate one-dimensional nanostructured metal oxides which is suitable for a large field of applications.

  5. Geometric constraints on phase coexistence in vanadium dioxide single crystals

    NASA Astrophysics Data System (ADS)

    McGahan, Christina; Gamage, Sampath; Liang, Jiran; Cross, Brendan; Marvel, Robert E.; Haglund, Richard F.; Abate, Yohannes

    2017-02-01

    The appearance of stripe phases is a characteristic signature of strongly correlated quantum materials, and its origin in phase-changing materials has only recently been recognized as the result of the delicate balance between atomic and mesoscopic materials properties. A vanadium dioxide (VO2) single crystal is one such strongly correlated material with stripe phases. Infrared nano-imaging on low-aspect-ratio, single-crystal VO2 microbeams decorated with resonant plasmonic nanoantennas reveals a novel herringbone pattern of coexisting metallic and insulating domains intercepted and altered by ferroelastic domains, unlike previous reports on high-aspect-ratio VO2 crystals where the coexisting metal/insulator domains appear as alternating stripe phases perpendicular to the growth axis. The metallic domains nucleate below the crystal surface and grow towards the surface with increasing temperature as suggested by the near-field plasmonic response of the gold nanorod antennas.

  6. Low temperature performance of lithium/silver vanadium oxide cells

    NASA Technical Reports Server (NTRS)

    Takeuchi, E. S.; Tuhovak, D. R.; Post, C. J.

    1990-01-01

    Lithium/silver vanadium oxide cells for low temperature applications have been developed. Prismatic and spirally wound AA cells were tested under constant load discharge of 0.3 to 1.8 amps or pulse discharge of 0.225 or 1.0 amps at temperatures from -40 to 25 C. At -40 C with current densities of 2.5 mA/cm2, 23 percent of theoretical capacity was achieved under constant load discharge and 40 percent of theoretical capacity was achieved under pulse test. Self-discharge estimates of 0.7 percent per year at 25 C were obtained from microcalorimetry. Preliminary safety testing of the cells revealed no violent performance under short circuit or crush tests.

  7. Vanadium, recent advancements and research prospects: A review.

    PubMed

    Imtiaz, Muhammad; Rizwan, Muhammad Shahid; Xiong, Shuanglian; Li, Hailan; Ashraf, Muhammad; Shahzad, Sher Muhammad; Shahzad, Muhammad; Rizwan, Muhammad; Tu, Shuxin

    2015-07-01

    Metal pollution is an important issue worldwide, with various documented cases of metal toxicity in mining areas, industries, coal power plants and agriculture sector. Heavy metal polluted soils pose severe problems to plants, water resources, environment and nutrition. Among all non-essential metals, vanadium (V) is becoming a serious matter of discussion for the scientists who deals with heavy metals. Due to its mobility from soil to plants, it causes adverse effects to human beings. This review article illustrates briefly about V, its role and shows the progress about V research so far done globally in the light of the previous work which may assist in inter-disciplinary studies to evaluate the ecological importance of V toxicity.

  8. Experimental investigation of radiative thermal rectifier using vanadium dioxide

    SciTech Connect

    Ito, Kota; Nishikawa, Kazutaka; Iizuka, Hideo; Toshiyoshi, Hiroshi

    2014-12-22

    Vanadium dioxide (VO{sub 2}) exhibits a phase-change behavior from the insulating state to the metallic state around 340 K. By using this effect, we experimentally demonstrate a radiative thermal rectifier in the far-field regime with a thin film VO{sub 2} deposited on the silicon wafer. A rectification contrast ratio as large as two is accurately obtained by utilizing a one-dimensional steady-state heat flux measurement system. We develop a theoretical model of the thermal rectifier with optical responses of the materials retrieved from the measured mid-infrared reflection spectra, which is cross-checked with experimentally measured heat flux. Furthermore, we tune the operating temperatures by doping the VO{sub 2} film with tungsten (W). These results open up prospects in the fields of thermal management and thermal information processing.

  9. Capacitive network near the metal insulator transition in Vanadium Dioxide

    NASA Astrophysics Data System (ADS)

    Ramirez, J. G.; Patino, E. J.; Schmidt, R.; Sharoni, A.; Gomez, M. E.; Schuller, I. K.

    2011-03-01

    Recent infrared spectroscopy and transport measurements in nano-scaled junction of VO2 have revealed the existence of phase separation into metallic and insulating phases. Here we present Impedance spectroscopy measurements performed in high quality Vanadium dioxide (VO2) thin films for the first time. This technique allows distinguishing between the resistive and capacitive response of the VO2 films and provides the dielectric properties across the metal-insulator transition (MIT). The film capacitance exhibits an unusual increase close to the MIT which implies the formation of a capacitor network produced by the nanoscale phase separation of metallic and insulating phases. This work has been supported by AFOSR, COLCIENCIAS, CENM and Ramon y Cajal Fellowship.

  10. Optical transmission in thin films of vanadium compounds

    NASA Astrophysics Data System (ADS)

    Karimov, Kh. S.; Mahroof-Tahir, M.; Saleem, M.; Ahmad, N.; Rashid, A.

    2014-07-01

    Thin films of five vanadium compounds/composite: (1) VO2(3-fl) (3-fl = 3-Hydroxyflavone), (2) VO(pbd)2 (pbd = 1-Phenyl-1, 3-butadione), (3) VO(dbm)2 (dbm = Dibenzoylmethane), (4) VPc (Vanadyl Phthalocyanine) and (5) V2O5-PEPC (V2O5- poly-N-epoxypropylcarbazole composite), were deposited by the drop-casting method from the solution in benzene. The transmittance—irradiance relationships were investigated and the transmission in the visible spectrum and optical images were obtained as well. It was found that the transmittance of the VO2(3-fl), VO(pbd)2, VO(dbm)2 and VPc, was practically independent of the irradiance; whereas the transmittance of V2O5-PEPC decreased by 4% for thin and 9% for thick films with an increase of the irradiance.

  11. Development of laser welding techniques for vanadium alloys

    SciTech Connect

    Strain, R.V.; Leong, K.H.; Smith, D.L.

    1996-04-01

    Laser welding is potentially advantageous because of its flexibility and the reduced amount of material affected by the weld. Lasers do not require a vacuum (as do electron beam welders) and the welds they produce high depth-to-width ratios. Scoping with a small pulsed 50 J YAG laser indicated that lasers could produce successful welds in vanadium alloy (V-5%Cr-5%Ti) sheet (1 mm thick) when the fusion zone was isolated from air. The pulsed laser required an isolating chamber filled with inert gas to produce welds that did not contain cracks and showed only minor hardness increases. Following the initial scoping tests, a series of tests were preformed with a 6 kW continuous CO{sub 2} laser. Successful bead-on-plate welds were made on V-4%Cr-4%Ti and V-5%Cr-5%Ti alloys to depths of about 4 mm with this laser.

  12. Anomalously low electronic thermal conductivity in metallic vanadium dioxide

    NASA Astrophysics Data System (ADS)

    Lee, Sangwook; Hippalgaonkar, Kedar; Yang, Fan; Hong, Jiawang; Ko, Changhyun; Suh, Joonki; Liu, Kai; Wang, Kevin; Urban, Jeffrey J.; Zhang, Xiang; Dames, Chris; Hartnoll, Sean A.; Delaire, Olivier; Wu, Junqiao

    2017-01-01

    In electrically conductive solids, the Wiedemann-Franz law requires the electronic contribution to thermal conductivity to be proportional to electrical conductivity. Violations of the Wiedemann-Franz law are typically an indication of unconventional quasiparticle dynamics, such as inelastic scattering, or hydrodynamic collective motion of charge carriers, typically pronounced only at cryogenic temperatures. We report an order-of-magnitude breakdown of the Wiedemann-Franz law at high temperatures ranging from 240 to 340 kelvin in metallic vanadium dioxide in the vicinity of its metal-insulator transition. Different from previously established mechanisms, the unusually low electronic thermal conductivity is a signature of the absence of quasiparticles in a strongly correlated electron fluid where heat and charge diffuse independently.

  13. Tc anisotropy and phase separation in strained Vanadium Dioxide films

    NASA Astrophysics Data System (ADS)

    Liu, Mengkun; Wagner, Martin; Abreu, Elsa; Kittiwatanakul, Salinporn; McLeod, Alexander; Goldflam, Michael; Fei, Zhe; Dai, Siyuan; Fogler, Michael; Lu, Jiwei; Wolf, Stuart; Averitt, Richard; Basov, D. N.

    2013-03-01

    We report Infrared near field study on strain induced transition temperature (Tc) anisotropy in vanadium dioxide (VO2) films via direct visualization of a spontaneous structural and electronic phase separation. The films are epitaxially grown on [110]R or [100]R TiO2 substrates and exhibit large uniaxial strain. By mapping the film topography with AFM and electronic percolation with Infrared scattering scanning near-field optical microscopy, a temperature dependent electron-lattice correlation can be clearly observed. Our work sheds a new light onto the nature of the Tc anomaly in metal-insulator transition and leads to the possibility of controlling the material's properties through strain induced phase separation.

  14. Decomposition of peracetic acid catalyzed by vanadium complexes

    SciTech Connect

    Makarov, A.P.; Gekhman, A.E.; Moiseev, I.I.; Polotryuk, O.Y.

    1986-02-01

    This paper studies the decomposition of peracetic acid (AcOOH) in acetic acid (AcOH) catalyzed by vanadium complexes. It is shown that peractic acid in acetic acid solutions of ammonium anadate decomposes with the predominant formation of 0/sub 2/ and small amounts of CO/sub 2/, the yield of which increases with increasing temperature and peracetic acid concentration. Both reactions proceed without the formation of free radicals in amounts detectable by ESR spectroscopy. The rate of oxygen release under conditions in which the formation of CO/sub 2/ is insignificant obeys a kinetic equation indicating the intermediate formation of a complex between V/sup 5 +/ ions and peracetic acid and the slow conversion of this complex into the observed products.

  15. Anomalously low electronic thermal conductivity in metallic vanadium dioxide.

    PubMed

    Lee, Sangwook; Hippalgaonkar, Kedar; Yang, Fan; Hong, Jiawang; Ko, Changhyun; Suh, Joonki; Liu, Kai; Wang, Kevin; Urban, Jeffrey J; Zhang, Xiang; Dames, Chris; Hartnoll, Sean A; Delaire, Olivier; Wu, Junqiao

    2017-01-27

    In electrically conductive solids, the Wiedemann-Franz law requires the electronic contribution to thermal conductivity to be proportional to electrical conductivity. Violations of the Wiedemann-Franz law are typically an indication of unconventional quasiparticle dynamics, such as inelastic scattering, or hydrodynamic collective motion of charge carriers, typically pronounced only at cryogenic temperatures. We report an order-of-magnitude breakdown of the Wiedemann-Franz law at high temperatures ranging from 240 to 340 kelvin in metallic vanadium dioxide in the vicinity of its metal-insulator transition. Different from previously established mechanisms, the unusually low electronic thermal conductivity is a signature of the absence of quasiparticles in a strongly correlated electron fluid where heat and charge diffuse independently.

  16. Evaluation of Solid-Solution Hardening of Fe-27 at. pct Al by Vanadium and Comparison to Precipitation Strengthening by Vanadium Carbides

    NASA Astrophysics Data System (ADS)

    Kratochvíl, Petr; Pešička, Josef; Král, Robert; Švec, Martin; Palm, Martin

    2015-11-01

    The compressive yield stress of Fe-27Al- xV(-C) ( x = 0 to 4 at. pct) at 1073 K (800 °C) has been determined. The increase of the yield stress of Fe-Al by increasing vanadium content is explained by solid-solution hardening. The experimentally observed values of the yield stress at 1073 K (800 °C) are compared with the strengthening given by theories evaluating the interaction between solute atoms and dislocations. The experimental results fit well the increase of the yield stress by the interaction of the solute atoms with screw dislocations. Further increase in yield strength in similar alloys due to vanadium carbides is documented. Precipitated carbides were identified by transmission electron microscopy and Kikuchi patterns. Although precipitation of vanadium carbides increases the compressive yield stress, they also could result in premature failure in tension as their highly anisotropic shape may facilitate crack nucleation.

  17. Tantalum and vanadium response to shock-wave loading at normal and elevated temperatures. Non-monotonous decay of the elastic wave in vanadium

    SciTech Connect

    Zaretsky, E. B.; Kanel, G. I.

    2014-06-28

    The evolution of the elastic precursor waves in pure tantalum and vanadium is presented at normal and elevated temperatures over propagation distances that ranged from 0.125 to 3 mm. Measurements were performed in order to obtain experimental data about the temperature-rate dependence of the yield stress of the two metals. With increasing propagation distance, the rate of the decay of elastic precursor decreases, as the shear stress in the elastic precursor wave approaches the Peierls stresses. It has been found that the decay, with propagation distance, of the post-spike minimum of the spike-like elastic precursor wave in vanadium is essentially non-monotonous. The experiments also revealed that annealing of tantalum and vanadium increases their Hugoniot elastic limit. The anomalous increase of the high strain rate yield stress with temperature, as observed earlier for some FCC and HCP metals, has not been detected in these measurements.

  18. Oxidation potential and state of some vanadium ores and the relation of woody material to their deposition

    USGS Publications Warehouse

    Pommer, Alfred Michael

    1956-01-01

    Oxidation potential studies with a multiple pH-potential recorder designed and constructed for this purpose demonstrated that some uranium-vanadium ores in the Colorado Plateau were in a reduced state when deposited. Any oxidation which took place occurred after deposition. Experimental and theoretical reducing studies on fresh wood, wood degraded by burial for 450 years, and lignite, indicate that such ores may have been deposited by reduction of oxidized vanadium solutions by woody material. A vanadium (III) mineral, V2O(OH)4, was prepared synthetically by reduction of a vanadium (V) solution with wood. This is the only reported synthesis of any reduced vanadium mineral by any method. It was shown that the origin of almost all vanadium deposits currently of commercial importance involves life processes and products.

  19. Vanadium oxides nanostructures: Hydrothermal synthesis and electrochemical properties

    SciTech Connect

    Mjejri, I.; Etteyeb, N.; Sediri, F.

    2014-12-15

    Highlights: • Vanadium oxides nanostructures were synthesized hydrothermally. • Reversible redox behavior with doping/dedoping process. • Doping/dedoping is easier for Li{sup +} to Na{sup +}. • Energy-related applications such as cathodes in lithium batteries. - Abstract: A facile and template-free one-pot strategy is applied to synthesize nanostructured vanadium oxide particles via a hydrothermal methodology. X-ray diffraction (XRD), scanning electron microscope (SEM), Fourier transforms infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) have been used to characterize the structure and morphology of the samples. The products are gradually changed from sheet-shaped VO{sub 2}(B) to rod-like V{sub 3}O{sub 7}·H{sub 2}O with decreasing cyclohexanediol as both protective and reducing agent. The specific surface area of the VO{sub 2}(B) nanosheets and V{sub 3}O{sub 7}·H{sub 2}O nanorods was found to be 22 and 16 m{sup 2} g{sup −1}, respectively. Thin films of VO{sub 2}(B) and V{sub 3}O{sub 7}·H{sub 2}O deposited on ITO substrates were electrochemically characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The voltammograms show reversible redox behavior with doping/dedoping process corresponding to reversible cation intercalation/de-intercalation into the crystal lattice of the nanorods/nanosheets. This process is easier for the small Li{sup +} cation than larger ones Na{sup +}.

  20. Terahertz coded aperture mask using vanadium dioxide bowtie antenna array

    NASA Astrophysics Data System (ADS)

    Nadri, Souheil; Percy, Rebecca; Kittiwatanakul, Lin; Arsenovic, Alex; Lu, Jiwei; Wolf, Stu; Weikle, Robert M.

    2014-09-01

    Terahertz imaging systems have received substantial attention from the scientific community for their use in astronomy, spectroscopy, plasma diagnostics and security. One approach to designing such systems is to use focal plane arrays. Although the principle of these systems is straightforward, realizing practical architectures has proven deceptively difficult. A different approach to imaging consists of spatially encoding the incoming flux of electromagnetic energy prior to detection using a reconfigurable mask. This technique is referred to as "coded aperture" or "Hadamard" imaging. This paper details the design, fabrication and testing of a prototype coded aperture mask operating at WR-1.5 (500-750 GHz) that uses the switching properties of vanadium dioxide(VO2). The reconfigurable mask consists of bowtie antennas with vanadium dioxide VO2 elements at the feed points. From the symmetry, a unit cell of the array can be represented by an equivalent waveguide whose dimensions limit the maximum operating frequency. In this design, the cutoff frequency of the unit cell is 640 GHz. The VO2 devices are grown using reactive-biased target ion beam deposition. A reflection coefficient (S11) measurement of the mask in the WR-1.5 (500-750 GHz) band is conducted. The results are compared with circuit models and found to be in good agreement. A simulation of the transmission response of the mask is conducted and shows a transmission modulation of up to 28 dB. This project is a first step towards the development of a full coded aperture imaging system operating at WR-1.5 with VO2 as the mask switching element.

  1. Current status and associated human health risk of vanadium in soil in China.

    PubMed

    Yang, Jie; Teng, Yanguo; Wu, Jin; Chen, Haiyang; Wang, Guoqiang; Song, Liuting; Yue, Weifeng; Zuo, Rui; Zhai, Yuanzheng

    2017-03-01

    A detailed assessment of vanadium contamination characteristics in China was conducted based on the first national soil pollution survey. The map overlay analysis was used to evaluate the contamination level of vanadium and the non-carcinogenic risk assessment model was calculated to quantify the vanadium exposure risks to human health. The results showed that, due to the drastically increased mining and smelting activities, 26.49% of soils were contaminated by vanadium scattered in southwest of China. According to Canadian soil quality guidelines, about 8.6% of the national soil pollution survey samples were polluted, and pose high non-carcinogenic risks to the public, especially to children living in the vicinity of heavily polluted mining areas. We propose the area near the boundary of Yunnan, Guizhou, Guangxi, and Sichuan provinces as priority control areas due to their higher geochemical background or higher health risks posed to the public. Finally, recommendations for management are proposed, including minimization of contaminant inputs, establishing stringent monitoring program, using phytoremediation, and strengthening the enforcement of relevant laws. Therefore, this study provides a comprehensive assessment of soil vanadium contamination in China, and the results will provide valuable information for China's soil vanadium management and risk avoidance.

  2. Vanadium in particles and sediments of the northern Saronikos Gulf, Greece.

    PubMed

    Kalogeropoulos, N; Scoullos, M; Vassilaki-Grimani, M; Grimanis, A P

    1989-04-01

    This study provides data for total and non-residual vanadium distributions in the northern Saronikos Gulf and shows that close to the Athens sewage outfall (ASO), the combined domestic and industrial wastes have resulted in a considerable increase in concentrations of vanadium in sediments and suspended solids. This appears to be the main vanadium source in the area; a second major source is a fertilizer plant (FP) near the entrance of Piraeus Harbour (PH), the impact of which is also important. Atmospheric inputs from the Piraeus industrial site and frequent crude oil spillages from ships and land-based sources seem to contribute significantly to the observed vanadium distribution, which is clearly affected by the prevailing circulation of surface waters and winds. The high percentage of the 0.5 NHCl-leachable vanadium fraction in the most polluted sediments, together with positive correlation with organic carbon and certain other trace metals (i.e. Ag, Co, Cr, Fe, Zn) and negative correlation coefficients with Al and Sc, indicate that a considerable portion of the vanadium is of "anthropogenic" origin not related to lithogenous particles. It enters the system in association with relatively large organic aggregates, either authigenic or derived from sewage.

  3. Lactational Vitamin E Protects Against the Histotoxic Effects of Systemically Administered Vanadium in Neonatal Rats.

    PubMed

    Olaolorun, F A; Obasa, A A; Balogun, H A; Aina, O O; Olopade, J O

    2014-12-29

    The work investigated the protective role of lactational vitamin E administration on vanadium-induced histotoxicity. Three groups of Wistar rats, with each group comprising of two dams and their pups, were used in this study. Group I pups were administered intraperitoneal injection of sterile water at volumes corresponding to the dose rate of the vanadium (sodium metavanadate) treated group from postnatal day (PND) 1-14 while those in Group II were administered intraperitoneal injection of 3mg/kg vanadium from PND 1-14. Group III pups were administered intraperitoneal injection of 3mg/kg vanadium while the dam received oral vitamin E (500 mg) concurrently every 72 hours. The results showed that group II pups exhibited histopathological changes which included seminiferous tubule disruption of the testes characterised by vacuolar degeneration and coagulative necrosis of spermatogonia and Sertoli cells with reduction in mitosis, and areas of interstitial thickening with fibroblast proliferation. In addition, the lungs showed disruption of the bronchiolar wall and denudation of the bronchiolar respiratory epithelium while the liver showed hydropic degeneration and coagulative necrosis of the centrilobular hepatocytes. These histotoxic changes were ameliorated in the vanadium + vitamin E group. We conclude that lactational vitamin E protects against the histotoxic effects of vanadium and could be a consideration for supplementation in the occupationally and environmentally exposed neonates. However, caution should be taken in vitamin E supplementation because there is still equivocal evidence surrounding its benefits as a supplement at the moment.

  4. Investigation of crossover processes in a unitized bidirectional vanadium/air redox flow battery

    NASA Astrophysics Data System (ADS)

    grosse Austing, Jan; Nunes Kirchner, Carolina; Komsiyska, Lidiya; Wittstock, Gunther

    2016-02-01

    In this paper the losses in coulombic efficiency are investigated for a vanadium/air redox flow battery (VARFB) comprising a two-layered positive electrode. Ultraviolet/visible (UV/Vis) spectroscopy is used to monitor the concentrations cV2+ and cV3+ during operation. The most likely cause for the largest part of the coulombic losses is the permeation of oxygen from the positive to the negative electrode followed by an oxidation of V2+ to V3+. The total vanadium crossover is followed by inductively coupled plasma mass spectroscopy (ICP-MS) analysis of the positive electrolyte after one VARFB cycle. During one cycle 6% of the vanadium species initially present in the negative electrolyte are transferred to the positive electrolyte, which can account at most for 20% of the coulombic losses. The diffusion coefficients of V2+ and V3+ through Nafion® 117 are determined as DV2+ ,N 117 = 9.05 ·10-6 cm2 min-1 and DV3+ ,N 117 = 4.35 ·10-6 cm2 min-1 and are used to calculate vanadium crossover due to diffusion which allows differentiation between vanadium crossover due to diffusion and migration/electroosmotic convection. In order to optimize coulombic efficiency of VARFB, membranes need to be designed with reduced oxygen permeation and vanadium crossover.

  5. Low-temperature direct synthesis of mesoporous vanadium nitrides for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Lee, Hae-Min; Jeong, Gyoung Hwa; Kim, Sang-Wook; Kim, Chang-Koo

    2017-04-01

    Mesoporous vanadium nitrides are directly synthesized by a one-step chemical precipitation method at a low temperature (70 °C). Structural and morphological analyses reveal that vanadium nitride consist of long and slender nanowhiskers, and mesopores with diameters of 2-5 nm. Compositional analysis confirms the presence of vanadium in the VN structure, along with oxidized vanadium. The cyclic voltammetry and charge-discharge tests indicate that the obtained material stores charges via a combination of electric double-layer capacitance and pseudocapacitance mechanisms. The vanadium nitride electrode exhibits a specific capacitance of 598 F/g at a current density of 4 A/g. After 5000 charge-discharge cycles, the electrode has an equivalent series resistance of 1.42 Ω and retains 83% of its initial specific capacitance. This direct low-temperature synthesis of mesoporous vanadium nitrides is a simple and promising method to achieve high specific capacitance and low equivalent series resistance for electrochemical capacitor applications.

  6. Impacts of heterogeneous uptake of dinitrogen pentoxide and chlorine activation on ozone and reactive nitrogen partitioning: improvement and application of the WRF-Chem model in southern China

    NASA Astrophysics Data System (ADS)

    Li, Qinyi; Zhang, Li; Wang, Tao; Tham, Yee Jun; Ahmadov, Ravan; Xue, Likun; Zhang, Qiang; Zheng, Junyu

    2016-12-01

    The uptake of dinitrogen pentoxide (N2O5) on aerosol surfaces and the subsequent production of nitryl chloride (ClNO2) can have a significant impact on the oxidising capability and thus on secondary pollutants such as ozone. The range of such an impact, however, has not been well quantified in different geographical regions. In this study, we applied the Weather Research and Forecasting coupled with Chemistry (WRF-Chem) model to investigate the impact of the N2O5 uptake processes in the Hong Kong-Pearl River Delta (HK-PRD) region, where the highest ever reported N2O5 and ClNO2 concentrations were observed in our recent field study. We first incorporated into the WRF-Chem an aerosol thermodynamics model (ISORROPIA II), recent parameterisations for N2O5 heterogeneous uptake and ClNO2 production and gas-phase chlorine chemistry. The revised model was then used to simulate the spatiotemporal distribution of N2O5 and ClNO2 over the HK-PRD region and the impact of N2O5 uptake and Cl activation on ozone and reactive nitrogen in the planetary boundary layer (PBL). The updated model can generally capture the temporal variation of N2O5 and ClNO2 observed at a mountaintop site in Hong Kong, but it overestimates N2O5 uptake and ClNO2 production. The model results suggest that under average conditions, elevated levels of ClNO2 (> 0.25 ppb within the PBL) are present in the south-western PRD, with the highest values (> 1.00 ppb) predicted near the ground surface (0-200 m above ground level; a.g.l.). In contrast, during the night when very high levels of ClNO2 and N2O5 were measured in well-processed plumes from the PRD, ClNO2 is mostly concentrated within the residual layer ( ˜ 300 m a.g.l.). The addition of N2O5 heterogeneous uptake and Cl activation reduces the NO and NO2 levels by as much as 1.93 ppb ( ˜ 7.4 %) and 4.73 ppb ( ˜ 16.2 %), respectively, and it increases the total nitrate and ozone concentrations by up to 13.45 µg m-3 ( ˜ 57.4 %) and 7.23 ppb ( ˜ 16

  7. Investigation of structure-dielectric property relationships in zirconium oxide, tantalum pentoxide, and oxide-polymer laminate films for high energy density capacitor applications

    NASA Astrophysics Data System (ADS)

    Sethi, Guneet

    Pulsed power applications involve transformation of electrical energy into high-peak power pulses through capacitors. There is an immediate need for fast-response capacitors with decreased volume, weight, and cost for pulsed power applications and power distribution systems. This research challenge is dominated by energy density. Energy density is directly related to dielectric properties such as dielectric polarization, conductivity and breakdown strength of the capacitor dielectric. This research work correlates processing and microstructure of single and multiple component dielectric films with their dielectric properties. The inorganic materials studied in this dissertation include zirconium oxide (ZrO2) and tantalum pentoxide (Ta 2O5) reactive sputtered films. Film crystallization & structure was studied as a function of sputtering growth variables such as sputtering power, sputtering pressure, source frequency, oxygen pressure, substrate temperature, substrate material, and post-deposition annealing temperature. Polycrystalline phase of ZrO2 and amorphous phase of Ta2O 5 were obtained for most sputtering growth variables. Although the amorphous films have lower permittivity (32 for amorphous & 51 for polycrystalline at 1 kHz), they also have lower AC and DC conductivities (3.4x10-8 S/m for amorphous & 12.2x10 -8 S/m for polycrystalline at 1 kHz), which result in high breakdown strength than polycrystalline films. Amorphous Ta2O5 films are found to be ideal for high-energy density capacitors with energy density of 14 J/cm3 because of their high permittivity, low leakage current density, and high dielectric breakdown strength. Oxide films were combined with different polymers (polyvinyldene flouride-triflouroethylene, polypropylene and polyethylene terephthalate) to produce two different kinds of laminate composites---oxide on polymer and polymer on oxide. Permittivity and conductivity differences in the polymer and oxide films result in an impedance contrast

  8. Influence of concentration and volume of precursor on the electrochemical properties of vanadium oxide thin films prepared by spray pyrolysis

    NASA Astrophysics Data System (ADS)

    Ingole, R. S.; Fugare, B. Y.; Lokhande, B. J.

    2016-04-01

    Vanadium oxide (V2O5) thin films have been prepared by spray pyrolysis using different concentrations and volumes of precursor solution via aqueous route at 673K deposition temperature. The influences of concentration and volume on the structural, morphological and electrochemical properties of the deposited samples are studied well. X - ray diffraction study shows orthorhombic crystal structure with V2O5 phase, confirmed by FTIR spectroscopy. Scanning electron microscopy shows granular, homogeneous and dense surface morphology. Cyclic voltammetery of all samples carried at all scan rates. Samples prepared using 0.05M, 40 ml of precursor solution shows highest specific capacitance 428.25 F/gm at 5 mV/s, Charge discharge behavior exhibits specific energy 18.73 Wh/kg, specific power 36.00 kW/kg, columbic efficiency 87.50 %. Impedance spectroscopy study was carried in the frequency range 1mHz - 1MHz, reveals pseudocapacitive behavior of the electrode exhibiting internal resistance 1.34 ohm.

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

    PubMed

    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.

  10. Catalytic destruction of PCDD/Fs over vanadium oxide-based catalysts.

    PubMed

    Yu, Ming-Feng; Lin, Xiao-Qing; Li, Xiao-Dong; Yan, Mi; Prabowo, Bayu; Li, Wen-Wei; Chen, Tong; Yan, Jian-Hua

    2016-08-01

    Vanadium oxide-based catalysts were developed for the destruction of vapour phase PCDD/Fs (polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans). A vapour phase PCDD/Fs generating system was designed to supply stable PCDD/Fs steam with initial concentration of 3.2 ng I-TEQ Nm(-3). Two kinds of titania (nano-TiO2 and conventional TiO2) and alumina were used as catalyst supports. For vanadium-based catalysts supported on nano-TiO2, catalyst activity is enhanced with operating temperature increasing from 160 to 300 °C and then reduces with temperature rising further to 350 °C. It is mainly due to the fact that high volatility of organic compounds at 350 °C suppresses adsorption of PCDD/Fs on catalysts surface and then further inhibits the reaction between catalyst and PCDD/Fs. The optimum loading of vanadium on nano-TiO2 support is 5 wt.% where vanadium oxide presents highly dispersed amorphous state according to the Raman spectra and XRD patterns. Excessive vanadium will block the pore space and form microcrystalline V2O5 on the support surface. At the vanadium loading of 5 wt.%, nano-TiO2-supported catalyst performs best on PCDD/Fs destruction compared to Al2O3 and conventional TiO2. Chemical states of vanadium in the fresh, used and reoxidized VOx(5 %)/TiO2 catalysts at different operating temperature are also analysed by XPS.

  11. Chemical bath deposition and characterization of electrochromic thin films of sodium vanadium bronzes

    SciTech Connect

    Najdoski, Metodija; Koleva, Violeta; Demiri, Sani

    2012-03-15

    Highlights: Black-Right-Pointing-Pointer We report a new chemical bath method for the deposition of vanadium bronze thin films. Black-Right-Pointing-Pointer The films are phase mixture of NaV{sub 6}O{sub 15} and Na{sub 1.1}V{sub 3}O{sub 7.9} with 10.58% lattice water. Black-Right-Pointing-Pointer The as-deposited vanadium bronze films exhibit two-step electrochromism. Black-Right-Pointing-Pointer They change their yellow-orange color to green and then from green to blue color. Black-Right-Pointing-Pointer The method allows the preparation of films on substrates with low melting point. -- Abstract: Thin yellow-orange films of sodium vanadium oxide bronzes have been prepared from a sodium-vanadium solution (1:1) at 75 Degree-Sign C and pH = 3. The composition, structure and morphology of the films have been studied by XRD, IR spectroscopy, TG and SEM-EDX analyses. It has been established that the prepared films are a phase mixture of hydrated NaV{sub 6}O{sub 15} (predominant component) and Na{sub 1.1}V{sub 3}O{sub 7.9} with total water content of 10.58%. The sodium vanadium bronze thin films exhibit two-step electrochromism followed by color change from yellow-orange to green, and then from green to blue. The cyclic voltammetry measurements on the as-deposited and annealed vanadium bronze films reveal the existence of different oxidation/reduction vanadium sites which make these films suitable for electrochromic devices. The annealing of the films at 400 Degree-Sign C changes the composition, optical and electrochemical properties.

  12. Synthesis, Characterization, Antioxidant Status, and Toxicity Study of Vanadium-Rutin Complex in Balb/c Mice.

    PubMed

    Roy, Souvik; Majumdar, Sumana; Singh, Amit Kumar; Ghosh, Balaram; Ghosh, Nilanjan; Manna, Subhadip; Chakraborty, Tania; Mallick, Sougato

    2015-08-01

    A new trend was developed for the formation of a complex between vanadium and flavonoid derivatives in order to increase the intestinal absorption and to reduce the toxicity of vanadium compounds. The vanadium-rutin complex was characterized by several spectroscopic techniques like ultraviolet (UV)-visible, Fourier transform infrared (FTIR), NMR, mass spectrometry, and microscopic evaluation by scanning electron microscopy. The mononuclear complex was formed by the interaction between vanadium and rutin with 1:2 metal to ligand stoichiometry. Antioxidant activity of the complex was evaluated by 1,1-diphenyl-2 picrylhydrazyl, ferric-reducing power, and 2,2'-azin-obis 3-ethylbenzothiazoline-6-sulphonic acid methods. It was shown that radical scavenging activity and ferric-reducing potential of free rutin was lower as compared with vanadium-rutin complex. The study was also investigated for oral acute toxicity and 28 days repeated oral subacute toxicity study of vanadium-rutin complex in balb/c mice. The vanadium-rutin complex showed mortality at a dose of 120 mg/kg in the balb/c mice. In 28 days repeated oral toxicity study, vanadium-rutin complex was administered to both sex of balb/c mice at dose levels of 90, 45, and 20 ppm, respectively. In addition, subacute toxicity study of vanadium-rutin complex (at 90 ppm dose level) showed increase levels of white blood cell (WBC), total bilirubin, alanine aminotransferase (ALT), alkaline phosphatase (ALP), aspartate aminotransferase (AST), creatinine, and blood urea nitrogen and decrease level of total protein (TP) as compared with control group. Histopathological study of vanadium-rutin showed structural alteration in the liver, kidney, and stomach at 90 ppm dose level. No observed toxic level of vanadium-rutin complex at 20 ppm dose level could be good for further study.

  13. Continuous aqueous tritium monitor

    DOEpatents

    McManus, Gary J.; Weesner, Forrest J.

    1989-05-30

    An apparatus for a selective on-line determination of aqueous tritium concentration is disclosed. A moist air stream of the liquid solution being analyzed is passed through a permeation dryer where the tritium and moisture and selectively removed to a purge air stream. The purge air stream is then analyzed for tritium concentration, humidity, and temperature, which allows computation of liquid tritium concentration.

  14. Evaluation of additive formulations to inhibit precipitation of positive electrolyte in vanadium battery

    NASA Astrophysics Data System (ADS)

    Rahman, Faizur; Skyllas-Kazacos, M.

    2017-02-01

    A comprehensive study has been performed to develop blended additive formulations based on organic and inorganic compounds to prevent the precipitation of supersaturated V(V) species in the Vanadium Flow Battery at high temperatures around 50 °C. It was found that organic formulations are oxidized by the strong oxidizing effect of V(V) species and are hence ineffective. The inorganic additive formulation KS11 which consists of 1 wt% of K3PO4+ 1 wt% of SHMP appears to be very effective with a vanadium solution of composition 3.5 M V(V) in total sulphate/bisulphate concentration of 5.7 M up to a temperature of 40 °C. The phosphate ions (PO43-) released from K3PO4 and PO3- ions from SHMP (NaPO3)6 are believed to adsorb onto the nucleating ions, thus inhibiting the precipitation of scale forming species, or adsorption onto the growing crystals, deforming and/or inhibiting further formation of vanadium crystals. Although the electrochemical activity of 3.5 M V solutions was unaffected in the presence of the KS11, increasing vanadium concentration above 3.5 M and total sulphate/bisulphate concentration above 6 M is probably increasing the formation of electrochemically inactive complexes of vanadium-sulphate and polyvanadic species. This results in increased solution viscosity and subsequently reduces the electrochemical activity exponentially.

  15. Elucidating the Higher Stability of Vanadium (V) Cations in Mixed Acid Based Redox Flow Battery Electrolytes

    SciTech Connect

    Vijayakumar, M.; Wang, Wei; Nie, Zimin; Sprenkle, Vincent L.; Hu, Jian Z.

    2013-11-01

    The Vanadium (V) cation structures in mixed acid based electrolyte solution were analysed by density functional theory (DFT) based computational modelling and 51V and 35Cl Nuclear Magnetic Resonance (NMR) spectroscopy. The Vanadium (V) cation exists as di-nuclear [V2O3Cl2.6H2O]2+ compound at higher vanadium concentrations (≥1.75M). In particular, at high temperatures (>295K) this di-nuclear compound undergoes ligand exchange process with nearby solvent chlorine molecule and forms chlorine bonded [V2O3Cl2.6H2O]2+ compound. This chlorine bonded [V2O3Cl2.6H2O]2+ compound might be resistant to the de-protonation reaction which is the initial step in the precipitation reaction in Vanadium based electrolyte solutions. The combined theoretical and experimental approach reveals that formation of chlorine bonded [V2O3Cl2.6H2O]2+ compound might be central to the observed higher thermal stability of mixed acid based Vanadium (V) electrolyte solutions.

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

    SciTech Connect

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

    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. Vanadium(IV/V) complexes of Triapine and related thiosemicarbazones: Synthesis, solution equilibrium and bioactivity.

    PubMed

    Kowol, Christian R; Nagy, Nóra V; Jakusch, Tamás; Roller, Alexander; Heffeter, Petra; Keppler, Bernhard K; Enyedy, Éva A

    2015-11-01

    The stoichiometry and thermodynamic stability of vanadium(IV/V) complexes of Triapine and two related α(N)-heterocyclic thiosemicarbazones (TSCs) with potential antitumor activity have been determined by pH-potentiometry, EPR and (51)V NMR spectroscopy in 30% (w/w) dimethyl sulfoxide/water solvent mixtures. In all cases, mono-ligand complexes in different protonation states were identified. Dimethylation of the terminal amino group resulted in the formation of vanadium(IV/V) complexes with considerably higher stability. Three of the most stable complexes were also synthesized in solid state and comprehensively characterized. The biological evaluation of the synthesized vanadium complexes in comparison to the metal-free ligands in different human cancer cell lines revealed only minimal influence of the metal ion. Thus, in addition the coordination ability of salicylaldehyde thiosemicarbazone (STSC) to vanadium(IV/V) ions was investigated. The exchange of the pyridine nitrogen of the α(N)-heterocyclic TSCs to a phenolate oxygen in STSC significantly increased the stability of the complexes in solution. Finally, this also resulted in increased cytotoxicity activity of a vanadium(V) complex of STSC compared to the metal-free ligand.

  18. Chemistry, urease inhibition, and phytotoxic studies of binuclear vanadium(IV) complexes.

    PubMed

    Ara, Rifat; Ashiq, Uzma; Mahroof-Tahir, Mohammad; Maqsood, Zahida Tasneem; Khan, Khalid Mohammed; Lodhi, Muhammad Arif; Choudhary, Muhammad Iqbal

    2007-01-01

    Vanadium plays an important role in biological systems and exhibits a variety of bioactivities. In an effort to uncover the chemistry and biochemistry of vanadium with nitrogen- and oxygen-containing ligands, we report herein the synthesis and spectroscopic characterization of vanadium(IV) complexes with hydrazide ligands. Substituents on these ligands exhibit systematic variations of electronic and steric factors. Elemental and spectral data indicate the presence of a dimeric unit with two vanadium(IV) ions coordinated with two hydrazide ligands along with two H(2)O molecules. The stability studies of these complexes over time in coordinating solvent, DMSO, indicates binding of the solvent molecules to give [V2O2L2(H2O)2(DMSO)2]2+ (L=hydrazide ligand) and then conversion of it to a monomeric intermediate species, [VOL(DMSO)3]1+. Hydrazide ligands are inactive against urease, whereas vanadium(IV) complexes of these ligands show significant inhibitory potential against this enzyme and are found to be non-competitive inhibitors. These complexes also show low phytotoxicity indicating their usefulness for soil ureases. Structure-activity relationship studies indicate that the steric and/or electronic effects that may change the geometry of the complexes play an important role in their inhibitory potential and phytotoxicity.

  19. Temperature dependence of the damage microstructures in neutron-irradiated vanadium

    SciTech Connect

    Horton, L.L.; Farrell, K.

    1983-01-01

    Vanadium and vanadium with boron carbide additions (V-B/sub 4/C) were irradiated to approx. 1 dpa in the Oak Ridge Research Reactor at controlled temperatures ranging from 455 to 925 K. The V-B/sub 4/C alloy was enriched in /sup 10/B, which produced approx. 3900 at. ppM helium. In the vanadium specimens, the dislocation microstructures varied from clusters of small (< 50 nm diam) dislocation loops (455 to 625 K) to larger, homogeneously distributed loops at higher temperatures. Their Burgers vectors were a/2<111>. The V-B/sub 4/C specimens contained only tangled dislocation segments. Cavities were observed in all specimens. The cavity concentration decrease and the average diameter increased with increasing irradiation temperature. At 725 K, the maximum swelling was observed in both the vanadium (0.1%) and V-B/sub 4/C (1.4%). At comparable temperatures the cavities in the V-B/sub 4/C specimens were smaller and more numerous than those in the vanadium specimens. Helium bubbles were found on the grain boundaries in all of the V-B/sub 4/ specimens.

  20. Determination of vanadium accumulation in onion root cells (Allium cepa L.) and its correlation with toxicity.

    PubMed

    Marcano, Letty; Carruyo, Ingrid; Fernández, Yusmary; Montiel, Xiomara; Torrealba, Zaida

    2006-08-01

    The vanadium is a metal that presents great interest from the toxicological point of view, because of the numerous alterations that can take place in different biological systems. This work evaluated the capacity of vanadium accumulation and its correlation with genotoxic effects in root cells of Allium cepa L. The bulbs were cultivated in renovated filtered water each 24 h, at a temperature of 25 +/- 0.5 degrees C, in darkness and constant aeration. Treatments were carried out under the same experimental conditions, using water solutions of vanadium of 25, 50, 75 and 100 microg/g for 0, 12, 24, 48 and 72 h. A control was carried out where metal solution was substituted by distilled water. After the treatment, the meristems were fixed with alcohol--acetic acid (3:1) and stained according to the technique of Feulgen. The capacity of accumulation was determined by GFAAS. The analysis of the results revealed an accumulation of the metal for all times and concentrations. No correlation was presented among vanadium accumulation, growth and mitotic index; however, positive correlation was given with the induction of chromosomic aberrations. In conclusion, vanadium is able to induce cytotoxic effect in the exposed roots, but only genotoxic effect was correlated with metal accumulation.