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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. Storage of potassium ions in layered vanadium pentoxide nanofiber electrodes for aqueous pseudocapacitors.

    PubMed

    Yeager, Matthew P; Du, Wenxin; Bishop, Brendan; Sullivan, Matthew; Xu, Wenqian; Su, Dong; Senanayake, Sanjaya D; Hanson, Jonathan; Teng, Xiaowei

    2013-12-01

    Spaced out: This paper investigates potassium-ion storage in vanadium pentoxide nanofibers (VNFs, K0.33 V2 O5 ) with a layered architecture. In situ XRD experiments reveal that the interplanar space of VNF expands/contracts upon extraction/insertion of potassium ions during the redox process. PMID:24124048

  3. Polypyrrole-encapsulated vanadium pentoxide nanowires on a conductive substrate for electrode in aqueous rechargeable lithium battery.

    PubMed

    Liang, Chaowei; Fang, Dong; Cao, Yunhe; Li, Guangzhong; Luo, Zhiping; Zhou, Qunhua; Xiong, Chuanxi; Xu, Weilin

    2015-02-01

    Precursors of ammonium vanadium bronze (NH4V4O10) nanowires assembled on a conductive substrate were prepared by a hydrothermal method. After calcination at 360°C, the NH4V4O10 precursor transformed to vanadium pentoxide (V2O5) nanowires, which presented a high initial capacity of 135.0mA h g(-1) at a current density of 50mA g(-1) in 5M LiNO3 aqueous solution; while the specific capacity faded quickly over 50 cycles. By coating the surface of V2O5 nanowires with water-insoluble polypyrrole (PPy), the formed nanocomposite electrode exhibited a specific discharge capacity of 89.9mA h g(-1) at 50mA g(-1) (after 100 cycles). A V2O5@PPy //LiMn2O4 rechargeable lithium battery exhibited an initial discharge capacity of 95.2mA h g(-1); and after 100 cycles, a specific discharge capacity of 81.5mA h g(-1) could retain at 100mA g(-1). PMID:25463177

  4. Vanadium pentoxide nanotubes by eelectrospinning

    NASA Astrophysics Data System (ADS)

    Lala, Neeta L.; Jose, R.; Yusoff, M. M.

    2012-11-01

    Nanofibers of vanadium pentoxide (V2O5) were synthesized by electrospinning a polymeric solution containing vanadium ion and with subsequent sintering. Conventionally, electrospun TNFs were produced by using a co-axial spinneret; however, TNFs in the present study were obtained by manipulating the concentration ratio of the precursor solution, distance, humidity and flow rate during electrospinning using a single spinneret and sintering with time and temperature change. On the basis of this hypothesis, nanofibers could be altered from elongated 1-D nanofibers to nanowires, nanotubes, spheres and flakes respectively. The surface morphology, structure, roughness and the crystal structure were analyzed using Field Emission Scanning Electron Microscopy (FE-SEM), Transmission Electron Microscopy (TEM), and X-ray diffraction (XRD). The current work has demonstrated a case study for energy storage where V2O5 nanotubes when tested shows the capacitance of 190 Fg-1 in 2M KCl electrolyte indicating an example for the energy storage which may be applicable for other electrochemical devices such as Li-ion batteries, fuel cells, hydrogen storage etc.

  5. HEALTH AND ENVIRONMENTAL EFFECTS PROFILE FOR VANADIUM PENTOXIDE

    EPA Science Inventory

    The Health and Environmental Effects Profile for vanadium pentoxide was prepared by the Office of Health and Environmental Assessment, Environmental Criteria and Assessment Office, Cincinnati, OH for the Office of Solid Waste and Emergency Response to support listings of hazardou...

  6. 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. PMID:22751222

  7. 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.

  8. 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...

  9. 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...

  10. 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.

  11. 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. PMID:24716494

  12. Cation-Induced Coiling of Vanadium Pentoxide Nanobelts

    PubMed Central

    2010-01-01

    Single-crystalline V2O5·xH2O nanorings and microloops were chemically assembled via an ion-induced chemical spinning route in the designed hydrothermal system. The morphology and structure of products were investigated by means of scanning electron microscopy (SEM) and transmission electron microscopy (TEM). X-ray powder diffraction (XRD) measurement, energy-dispersive X-ray spectroscopy (EDS) microanalysis and thermal gravimetric analysis (TGA) revealed that the composition of nanorings and microloops is V2O5·1·1H2O. For these oxide nanorings and microloops, the cation-induced coiling growth mechanism of vanadium pentoxide nanobelts has been proposed on the basis of crystallographic structure of vanadium pentoxide. Our proposed chemical spinning process and the rational solution-phase synthesis route can also be extended to prepare novel 1D materials with layered or more complex structures. PMID:21076706

  13. Health and environmental-effects profile for vanadium pentoxide

    SciTech Connect

    Not Available

    1985-04-01

    The Health and Environmental Effects Profile for vanadium pentoxide was prepared by the Office of Health and Environmental Assessment, Environmental Criteria and Assessment Office, Cincinnati, OH for the Office of Solid Waste and Emergency Response to support listings of hazardous constituents of a wide range of waste streams under Section 3001 of the Resource Conservation and Recovery Act (RCRA) and to provide health-related limits for emergency actions under Section 101 of the Comprehensive Environmental Response, Compensation and Liability Act (CERCLA). Both published literature and information obtained from Agency program office files were evaluated as they pertained to potential human health, aquatic life, and environmental effects of hazardous-waste constituents. Quantitative estimates are presented, provided sufficient data are available. Existing data are insufficient to determine an Acceptable Daily Intake (ADI) or a carcinogenic potency factor for vanadium pentoxide. The Reportable Quantity (RQ) value of 1, 10, 100, 1000, or 5000 pounds is used to determine the quantity of a hazardous substance for which notification is required in the event of a release as specified by CERCLA based on chronic toxicity. The RQ value for vanadium pentoxide is 100.

  14. 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.

  15. 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

    ... vanadium pentoxide assessment in Federal Register Notices published September 30, 2011, (76 FR 60827) and November 9, 2011 (76 FR 69736). DATES: The peer review panel meeting on the draft assessment for Vanadium... Pennsylvania Avenue NW., Washington, DC 20460; telephone: (703) 347-8561; facsimile: (703) 347- 8691). If...

  16. Correlation between friction and thickness of vanadium-pentoxide nanowires

    NASA Astrophysics Data System (ADS)

    Kim, Taekyeong

    2015-11-01

    We investigated the correlation between friction and thickness of vanadium-pentoxide nanowires (V2O5 NWs) by using friction/atomic force microscopy (FFM/AFM). We observed that the friction signal generally increased with thickness in the FFM/AFM image of the V2O5 NWs. We constructed a two-dimensional (2D) correlation distribution of the frictional force and the thickness of the V2O5 NWs and found that they are strongly correlated; i.e., thicker NWs had higher friction. We also generated a histogram for the correlation factors obtained from each distribution and found that the most probable factor is ~0.45. Furthermore, we found that the adhesion force between the tip and the V2O5 NWs was about -3 nN, and that the friction increased with increasing applied load for different thicknesses of V2O5 NWs. Our results provide an understanding of tribological and nanomechanical studies of various one-dimensional NWs for future fundamental research.

  17. Electrical and optical properties of thin films of hydrated vanadium pentoxide featuring electrochromic effect

    NASA Astrophysics Data System (ADS)

    Yakovleva, D. S.; Malinenko, V. P.; Pergament, A. L.; Stefanovich, G. B.

    2007-12-01

    Thin films of hydrated vanadium pentoxide (V2O5 · nH2O) exhibit the phenomenon of electrochromism, whereby a film reversibly changes its color under the action of an applied electric field. A specific feature of this phenomenon is that it takes place in a “dry” planar system, in the absence of an electrolyte, which makes this system promising for various applications. We have studied changes in the optical and electrical properties of hydrated vanadium pentoxide films under the conditions of electrochromic coloration.

  18. 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.

  19. 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

  20. 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.

  1. 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

    2012-03-01

    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 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. PMID:22293666

  2. 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.

  3. 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

  4. Fabrication and Characteristics of Pentacene/Vanadium Pentoxide Field-Effect Transistors

    SciTech Connect

    Minagawa, M.; Nakai, K.; Baba, A.; Shinbo, K.; Kato, K.; Kaneko, F.; Lee, C.

    2011-12-23

    Organic field-effect transistors (OFETs) were fabricated using pentacene thin layer, and the effects of inserted Lewis-acid thin layers on electrical properties were investigated. The OFETs have active layers of pentacene and vanadium pentoxide (V{sub 2}O{sub 5}) as a Lewis-acid layer. Typical source-drain current (I{sub DS}) vs. source-drain voltage (V{sub DS}) curves were observed under negative gate voltages (V{sub G}S) application, and the shift of the threshold voltage for FET driving (V{sub t}) to positive side was also observed by V{sub 2}O{sub 5} layer insertion, that is, -2.5 V for device with V{sub 2}O{sub 5} layer and -5.7 V for device without V{sub 2}O{sub 5} layer. It was thought that charge transfer (CT) complexes which were formed at the interface between pentacene and V{sub 2}O{sub 5} layer were dissociated by the applied gate voltage, and the generated holes seem to contribute to drain current and the apparent V{sub t} improvement.

  5. 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.

  6. Factors influencing charge capacity of vanadium pentoxide thin films during lithium ion intercalation/deintercalation cycles

    SciTech Connect

    Alamarguy, D.; Castle, J. E.; Ibris, N.; Salvi, A. M.

    2007-11-15

    The intercalation of vanadium pentoxide by lithium ions leads to a change in optical properties, a process that is of value in thin-film electrochromic devices. In this study, films of V{sub 2}O{sub 5}, deposited on indium tin oxide (ITO) glass coupons by a sol-gel process, were challenged by increasing numbers of charge-discharge cycles ranging from 72 to 589 full cycles. The samples were characterized by x-ray photoelectron spectroscopy (XPS) and then examined in the deintercalated state by time-of-flight secondary ion mass spectroscopy (SIMS). XPS enabled measurement of the thickness and composition of the solid-electrolyte interface and provided evidence of the residual V{sup 4+} concentration within the top few nanometers of the surface. The SIMS profile gave direct information on the thickness of the films and on the thickness loss caused by rinsing the samples after the electrochemical exposure. Determination, by SIMS, of the concentration of lithium ions has enabled a correction to be made for the amount of inactive material within the electrochemically active region of the film. The SIMS depth profiles for lithium in the four samples are similar, with a marked buildup of Li at the interface with the ITO. This interphase zone had a thickness of {approx}27 nm and was electrochemically inactive, enabling a further correction to be made. Thus, by means of the XPS and the SIMS results the chemistry and thickness of the films could be fully characterized. The remaining inconsistency between capacity (between 35% and 100% of the anticipated charge) and number of cycles is ascribed to edge effects arising from the method used for production of the coupons.

  7. Vanadium pentoxide-coated ultrafine titanium dioxide particles induce cellular damage and micronucleus formation in V79 cells.

    PubMed

    Bhattacharya, K; Cramer, H; Albrecht, C; Schins, R; Rahman, Q; Zimmermann, U; Dopp, E

    2008-01-01

    Surface-treated titanium dioxide (TiO(2)) particles coated with vanadium pentoxide (V(2)O(5)) are used industrially for selective catalytic reactions such as the removal of nitrous oxide from exhaust gases of combustion power plants (SCR process) and in biomaterials for increasing the strength of implants. In the present study, untreated ultrafine TiO(2) particles (anatase, diameter: 30-50 nm) and vanadium pentoxide (V(2)O(5))-treated anatase particles were tested for their cyto- and genotoxic effects in V79 cells (hamster lung fibroblasts). Cytotoxic effects of the particles were assessed by trypan blue exclusion, while genotoxic effects were investigated by micronucleus (MN) assay. In addition, the generation of reactive oxygen species (ROS) was determined by the acellular method of electron spin resonance technique (ESR) and by the cellular technique of determination of thiobarbituric acid-reactive substances (TBARS). Our results demonstrate that V(2)O(5)-treated TiO(2) particles induce more potent cyto- and genotoxic effects than untreated particles. Further, acellular and cellular radical formation was more pronounced with V(2)O(5)-anatase than untreated anatase. Thus, data indicate that V(2)O(5)-treated TiO(2) particles were more reactive than natural anatase and capable of inducing DNA damage in mammalian cells through production of free radicals. PMID:18569605

  8. Vanadium pentoxide induces pulmonary inflammation and tumor promotion in a strain-dependent manner

    PubMed Central

    2010-01-01

    Background Elevated levels of air pollution are associated with increased risk of lung cancer. Particulate matter (PM) contains transition metals that may potentiate neoplastic development through the induction of oxidative stress and inflammation, a lung cancer risk factor. Vanadium pentoxide (V2O5) is a component of PM derived from fuel combustion as well as a source of occupational exposure in humans. In the current investigation we examined the influence of genetic background on susceptibility to V2O5-induced inflammation and evaluated whether V2O5 functions as a tumor promoter using a 2-stage (initiation-promotion) model of pulmonary neoplasia in mice. Results A/J, BALB/cJ (BALB), and C57BL/6J (B6) mice were treated either with the initiator 3-methylcholanthrene (MCA; 10 μg/g; i.p.) or corn oil followed by 5 weekly aspirations of V2O5 or PBS and pulmonary tumors were enumerated 20 weeks following MCA treatment. Susceptibility to V2O5-induced pulmonary inflammation was assessed in bronchoalveolar lavage fluid (BALF), and chemokines, transcription factor activity, and MAPK signaling were quantified in lung homogenates. We found that treatment of animals with MCA followed by V2O5 promoted lung tumors in both A/J (10.3 ± 0.9 tumors/mouse) and BALB (2.2 ± 0.36) mice significantly above that observed with MCA/PBS or V2O5 alone (P < 0.05). No tumors were observed in the B6 mice in any of the experimental groups. Mice sensitive to tumor promotion by V2O5 were also found to be more susceptible to V2O5-induced pulmonary inflammation and hyperpermeability (A/J>BALB>B6). Differential strain responses in inflammation were positively associated with elevated levels of the chemokines KC and MCP-1, higher NFκB and c-Fos binding activity, as well as sustained ERK1/2 activation in lung tissue. Conclusions In this study we demonstrate that V2O5, an occupational and environmentally relevant metal oxide, functions as an in vivo lung tumor promoter among different inbred

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

    NASA Astrophysics Data System (ADS)

    Kong, AiGuo; Ding, Yong Jie; Wang, Ping; Zhang, Heng Qiang; Yang, Fan; Shan, Yong Kui

    2011-02-01

    Novel alkylimidazolium-intercalated V 2O 5 compounds were synthesized by a redox reaction between iodide ion and V 2O 5. The X-ray photoelectron spectroscopy and the diffuse reflectance UV-vis spectrometry experiments reveal that the vanadium in the intercalated V 2O 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 2O 5 intercalation compounds have typical lamellar structure with different d100 interlayer spacing values and the special straw-like nanofiber morphology with the length of 0.5-10 μm. Systematic investigation indicates that new intercalation compounds possess the extraordinary adsorption performance for methylene blue in an aqueous solution.

  10. Confocal laser scanning microscopy measurement of the morphology of vanadium pentoxide nanorods grown by electron beam irradiation or thermal oxidation

    NASA Astrophysics Data System (ADS)

    Kang, Manil; Hong, Donghyuk; Kim, Taesung; Chu, Minwoo; Kim, Sok Won

    2013-01-01

    In order to observe the morphology of nanostructures at the submicroscale, we use a confocal laser scanning (CLS) microscope built in our laboratory. The theoretical resolution of the hand-made CLS microscope is 150 nm and the performance of the microscope is evaluated by observing a USAF target. Vanadium pentoxide nanorods grown by electron beam irradiation and thermal oxidation methods are used as nanostructures and the morphologies of the nanorods observed by confocal laser scanning microscopy (CLSM) are compared with those obtained by scanning electron microscopy. The magnification and resolution of the CLSM were estimated to be approximately 1500 and 800 nm, respectively. From the results, we confirm that the CLSM can be used to measure nanostructures at the sub-micro-scale without a preconditioning process.

  11. Transmission Electron Microscopy and First Principle Studies Investigating Intercalation Phenomenon Of Vanadium Pentoxide(V2O5) nanowire cathode

    NASA Astrophysics Data System (ADS)

    Mukherjee, Arijita; Asayesh Ardakani, Hasti; Yi, Tanghong; Kim, Cheon Jung; Andrews, Justin; Banerjee, Sarbajit; Cabana, Jordi; S Yassar, Reza; F Klie, Robert; Jcesr Collaboration

    Vanadium Pentoxide(V2O5) is an attractive intercalation compound due to its characteristic layered structure from weak vanadium-oxygen bonding which enables the intercalation of ions between the layers. Here, we will discuss an in-situ transmission electron microscopy and electron energy-loss spectroscopy approach investigating lithiation of orthorhombic α-V2O5 nanowires where the center of the nanowire undergoes a transformation to γ-Li2V2O5 phase. Since V2O5 has also been predicted as a potential cathode host for magnesium ion intercalation, we also investigate Mg intercalation in α-V2O5 nanowire and determine if our reaction pathway leads to the formation of ε-Mg0.5V2O5 phase, as predicted by density functional theory calculations. In-situ Li and Mg intercalation experiments into the new tunnel structured ζ- V2O5 nanowires will also be presented and the resulting phases will be compared with theoretical predictions. This work is supported by Joint Center for Energy Storage Research (JCESR).

  12. 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. PMID:25578410

  13. Inhalative Exposure to Vanadium Pentoxide Causes DNA Damage in Workers: Results of a Multiple End Point Study

    PubMed Central

    Ehrlich, Veronika A.; Nersesyan, Armen K.; Hoelzl, Christine; Ferk, Franziska; Bichler, Julia; Valic, Eva; Schaffer, Andreas; Schulte-Hermann, Rolf; Fenech, Michael; Wagner, Karl-Heinz; Knasmüller, Siegfried

    2008-01-01

    Background Inhalative exposure to vanadium pentoxide (V2O5) causes lung cancer in rodents. Objective The aim of the study was to investigate the impact of V2O5 on DNA stability in workers from a V2O5 factory. Methods We determined DNA strand breaks in leukocytes of 52 workers and controls using the alkaline comet assay. We also investigated different parameters of chromosomal instability in lymphocytes of 23 workers and 24 controls using the cytokinesis-block micronucleus (MN) cytome method. Results Seven of eight biomarkers were increased in blood cells of the workers, and vanadium plasma concentrations in plasma were 7-fold higher than in the controls (0.31 μg/L). We observed no difference in DNA migration under standard conditions, but we found increased tail lengths due to formation of oxidized purines (7%) and pyrimidines (30%) with lesion-specific enzymes (formamidopyrimidine glycosylase and endonuclease III) in the workers. Bleomycin-induced DNA migration was higher in the exposed group (25%), whereas the repair of bleomycin-induced lesions was reduced. Workers had a 2.5-fold higher MN frequency, and nucleoplasmic bridges (NPBs) and nuclear buds (Nbuds) were increased 7-fold and 3-fold, respectively. Also, apoptosis and necrosis rates were higher, but only the latter parameter reached statistical significance. Conclusions V2O5 causes oxidation of DNA bases, affects DNA repair, and induces formation of MNs, NPBs, and Nbuds in blood cells, suggesting that the workers are at increased risk for cancer and other diseases that are related to DNA instability. PMID:19079721

  14. Correlation between porous structure and electrochemical properties of porous nanostructured vanadium pentoxide synthesized by novel spray pyrolysis

    NASA Astrophysics Data System (ADS)

    Kong, Long; Taniguchi, Izumi

    2016-04-01

    Porous nanostructured vanadium pentoxide (V2O5) particles were successfully prepared by spray pyrolysis (SP) in a precursor solution with an ammonium nitrate (NH4NO3) additive. The correlation between the porous structure and the electrochemical properties of the V2O5 particles was investigated. The porous structure markedly changed upon increasing the concentration of NH4NO3 in the precursor solution from 0 to 0.408 mol L-1. Pore structure analysis based on N2 adsorption-desorption isotherm measurements indicated that porous nanostructured V2O5 particles with a pore size of less than 100 nm can be prepared by the novel SP method and that an increase in the NH4NO3 concentration in the precursor solution can enlarge the pores in the V2O5 particles, especially those with a size between 20 and 80 nm. The porous nanostructured V2O5 prepared with an NH4NO3 concentration of 0.272 mol L-1 exhibited a first discharge capacity of 400 mAh g-1 at 20 mA g-1. The unique porous structure of V2O5 particles significantly enhanced the rate performance and exhibited a first discharge capacity of 180 mAh g-1 at 1200 mA g-1, which is much higher than that of dense V2O5 particles (70 mAh g-1).

  15. 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. PMID:26562331

  16. Supercritical fluid deposition of vanadium pentoxide within carbon nanotube buckypaper for electrochemical capacitor

    NASA Astrophysics Data System (ADS)

    Do, Quyet Huu

    There is a pressing need from a broad range of industries for high-performance energy storage devices with high power, high energy capacity, light weight, long lifetime, high efficiency, and low cost. A typical energy storage device, current electrochemical capacitors do not possess sufficient energy density to meet the needs. Recently utilization of oxide materials as pseudocapacitance materials has attracted a great deal of interest. However obtaining a high pseudocapacitance using an affordable oxide, while maintaining the high rate performance, remains elusive. This dissertation work aims to develop high-performance carbon nanotube (CNT) vanadium oxide hybrid nanostructured electrode materials for electrochemical capacitors. The CNT was in a form of freestanding thin film buckypaper (BP), which served as the current collector whilst providing double-layer capacitance, and vanadium oxide, coated on the CNT, was the pseudocapacitance material. Using a novel supercritical fluid deposition process, ultrathin vanadium oxide were uniformly deposited throughout the buckypaper with exceptional conformity at relatively low temperature, enabled by the unique properties of the supercritical fluids such as high solvation power, high diffusivity and zero surface tension. This overcame many of the transport limitations associated with the vanadium oxide material and indeed excellent electrode performance, particularly high rate performance, was achieved. The deposition process, the morphology and structure, and the capacitance behaviors of the composites were studied in detail, and the processing-morphology-electrochemical properties of the composites were elucidated. A high-pressure deposition system was constructed first for this dissertation research. Thereafter several deposition processes were investigated: physical adsorption - annealing, and in-situ reactive deposition. In the physical adsorption approach, the V2O5-buckypaper composite electrodes were fabricated by

  17. Quantification of Kras mutant fraction in the lung DNA of mice exposed to aerosolized particulate vanadium pentoxide by inhalation.

    PubMed

    Banda, Malathi; McKim, Karen L; Haber, Lynne T; MacGregor, Judith A; Gollapudi, B Bhaskar; Parsons, Barbara L

    2015-08-01

    This study investigated whether Kras mutation is an early event in the development of lung tumors induced by inhalation of particulate vanadium pentoxide (VP) aerosols. A National Toxicology Program tumor bioassay of inhaled particulate VP aerosols established that VP-induced alveolar/bronchiolar carcinomas of the B6C3F1 mouse lung carried Kras mutations at a higher frequency than observed in spontaneous mouse lung tumors. Therefore, this study sought to: (1) characterize any Kras mutational response with respect to VP exposure concentration, and (2) investigate the possibility that amplification of preexisting Kras mutation is an early event in VP-induced mouse lung tumorigenesis. Male Big Blue B6C3F1 mice (6 mice/group) were exposed to aerosolized particulate VP by inhalation, 6h/day, 5 days/week for 4 or 8 weeks, using VP exposure concentrations of 0, 0.1, and 1 mg/m(3). The levels of two different Kras codon 12 mutations [GGT → GAT (G12D) and GGT → GTT (G12V)] were measured in lung DNAs by Allele-specific Competitive Blocker PCR (ACB-PCR). For both exposure concentrations (0.1 and 1.0mg/m(3)) and both time points (4 and 8 weeks), the mutant fractions observed in VP-exposed mice were not significantly different from the concurrent controls. Given that 8 weeks of inhalation of a tumorigenic concentration of particulate aerosols of VP did not result in a significant change in levels of lung Kras mutation, the data do not support either a direct genotoxic effect of VP on Kras or early amplification of preexisting mutation as being involved in the genesis of VP-induced mouse lung tumors under the exposure conditions used. Rather, the data suggest that accumulation of Kras mutation occurs later with chronic VP exposure and is likely not an early event in VP-induced mouse lung carcinogenesis. PMID:26232258

  18. 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

  19. 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. PMID:27010675

  20. 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

  1. 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

    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

  2. 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%).

  3. Reactive Uptake of Dinitrogen Pentoxide on Aqueous Ammonium Nitrate Aerosols: Dependence on the Nitrate Activity

    NASA Astrophysics Data System (ADS)

    Wahner, A.; Folkers, M.; Mentel, T. F.; Sebald, H.; ten Brink, H. M.; Jongejan, P. A.

    2001-12-01

    The heterogeneous conversion of N2O_5 to HNO3 is an important step in the removal of nitrogen oxides from the atmosphere. In the planetary boundary layer this heterogeneous process occurs on the surfaces of aqueous aerosols. The fraction of NH4NO_3 in secondary inorganic aerosols in western Europe and in the United States is increasing, due to decreasing SO2 emissions at nearly constant NOX source strength. This may become of importance, since increasing nitrate concentrations in aerosols can reduce the reaction probability γ N2O5 by up to an order of magnitude ("nitrate effect" [1,2]). We measured γ N2O5 on NH4NO_3, (NH4)_2SO_4 and NH4HSO_4 aerosols in the large aerosol chamber at the FZ-Jülich. The decrease of N2O_5 and the formation of gas-phase HNO3 was monitored by high resolution FTIR spectroscopy. Simultaneously, the aerosol composition was determined on-line by Steam Jet Aerosol Collection/Ion Chromatography. The aerosol surface area was calculated from measured size distributions in the range of 20 nm to 5 μ m. The γ N2O5 of 0.02(+/- 0.003) on (NH4)_2SO_4 and NH4HSO_4 droplets are independent of the relative humidity (RH), like for the corresponding sodium salts at similar conditions. The γ N2O5 on NH4NO_3 aerosol is decreasing from 0.02 at 80% RH to 0.007 at 60% RH with decreasing relative humidity, thus increasing nitrate concentration. The functional dependence of γ N2O5 on the RH or on the ionic strength is different for NH4NO_3 and NaNO3. However it can be unified by supposing direct dependence of γ N2O5 on the mean nitrate activity. [1] A. Wahner, Th. F. Mentel, M. Sohn, J. Stier , J. Geophys. Res., 103 (1999), 31,103 [2] Th. F. Mentel, M. Sohn, A. Wahner , Phys. Chem. Chem. Phys. 1 (1999), 5451

  4. Synthesis of titanium-vanadium oxide materials from aqueous solutions via co-deposition

    NASA Astrophysics Data System (ADS)

    Shyue, Jing-Jong

    Titania-supported vanadium oxide is an important heterogeneous catalyst in a variety of applications. Therefore, the synthesis of mixed titanium-vanadium oxide films may be of interest for potential catalysts. While most vanadium-based catalysts consist of a vanadium oxide phase deposited on the surface of an oxide support, mixed titanium-vanadium oxides were co-deposited from aqueous solutions in a single step. The chemical composition of the titanium-vanadium oxide thin films on organic self-assembled monolayers (SAMs) was manipulated by chelating agents, including lactic acid and oxalic acid. Based on the dependence of Ti:V ratio in the films on the oxalic acid concentration, it is concluded that oxalic acid chelates both titanium and vanadium, but preferentially vanadium. Therefore, from solutions with [oxalate]:[vanadium] < 1:1, titanium-enriched films were formed. However, with [oxalate]: [vanadium] > 1:1, excess oxalic acid chelates titanium as well. Consequently, the Ti:V ratio dropped back to that of films deposited in the absence of chelating agents. At high concentrations of oxalic acid, both titanium and vanadium was chelated excessively. Therefore, no films formed. Lactic acid can be oxidized by pentavalent vanadium, so that it cannot chelate cations. Therefore, when [lactate]: [vanadium] < 1:2, V4+ was formed. These V4+ ions increased the deposition rate of vanadium, and vanadium-rich films were formed. For [lactate]:[vanadium] > 1:2, the remaining lactic acid preferentially chelate vanadium and showed effects comparable to those seen with oxalic acid. The vanadium content in the mixed oxide films affected the thickness of films formed on the alkylammonium SAMs but had little or no effect on the films formed on amine SAMs. This result is consistent with the presence of a Stern layer, previously reported to form on amine-terminated surfaces. In addition to forming thin films, titanium-vanadium oxide solid-solution powders were also prepared via co

  5. 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.

  6. Recovery of cobalt, molybdenum, nickel and vanadium from an aqueous ammonia and ammonium salt solution by coextracting molybdenum and vanadium and sequential extraction of nickel and cobalt

    SciTech Connect

    Hubred, G.L.; Van Leirsburg, D.A.

    1984-02-28

    A method is claimed for recovering metal values from an aqueous stream. The metal values are preferably obtained from leaching spent hydroprocessing catalysts, and include nickel, cobalt, vanadium and molybdenum. The metal values are extracted, isolated and purified by liquid, liquid extraction techniques.

  7. Improved lithium-metal/vanadium pentoxide polymer battery incorporating crosslinked ternary polymer electrolyte with N-butyl-N-methylpyrrolidinium bis(perfluoromethanesulfonyl)imide

    NASA Astrophysics Data System (ADS)

    Osada, Irene; von Zamory, Jan; Paillard, Elie; Passerini, Stefano

    2014-12-01

    Li metal polymer batteries incorporating crosslinked ternary PEO/PYR14TFSI/LiTFSI solid polymer electrolyte (SPE) have been prepared, using V2O5 as active cathode material. As a result of the optimization of the SPE as well as the cell assembly and cycling conditions, V2O5 lithium metal polymer batteries allow reaching 796 Wh kg-1 (of V2O5) at C/10 at 40 °C and maintaining 663 Wh kg-1 after 200 cycles at 40 °C. This is higher than the theoretical specific energy of LiCoO2 vs. Li of 609 Wh kg-1. Cycling at 80 °C allows reaching 270 mAh g-1 at C/2 and 210 mAh g-1 at 1 C, while at 20 °C it is still possible to reach a discharge capacity of almost 100 mAh g-1 at low rates. Post-cycling SEM and EDX imaging showed that, after 200 cycles at 40 °C, if the plating of Li is not fully homogeneous, no sign of dendrite growth nor obvious vanadium dissolution and redeposition on the anode side occurred.

  8. Hydrothermal synthesis of vanadium pentoxide nanowires

    NASA Astrophysics Data System (ADS)

    Kumar, J. Santhosh; Thangadurai, P.

    2016-05-01

    Nanowires of V2O5 were prepared via hydrothermal route using NH4VO3 as precursor in the presence of sulfuric acid at 120°C for 24 h. This synthesis process is free of any templates and reducing agents. Thermal analysis showed a phase change at 350°C and the samples were annealed at 500°C. The XRD analysis showed the monoclinic phase for the as-prepared and orthorhombic phase of V2O5 when annealed at 500°C. Characteristic Raman peaks also expressed the same structural features. Microstructure analysis by SEM showed the nanowire structure of V2O5 with thickness in the range of 20-50 nm and length in micrometers. The possible mechanisms of formation of the nanowires were schematically explained based on the layered structure of V2O5.

  9. Comparative electrochemical studies of a nanostructured vanadium oxide electrode material in aqueous electrolyte

    NASA Astrophysics Data System (ADS)

    Soghomonian, Victoria; Yuan, Qifan; Ren, Shaola; Zukowski, Julia

    Electrochemical energy storage plays an increasing role in energy solutions. We report on a new hydrothermally synthesized vanadium oxide nanostructured material and study its performance as electrode material for insertion of various ions from aqueous solutions. The as-synthesized product is in the form of nanosheets forming quasi-spherical 3-dimensional objects. Variable temperature resistivity measurements indicate a thermally activated behavior. Electrodes are constructed, and comparative electrochemical insertion reactions of Li, Na, K and NH4 cations, over different cycle numbers, investigated. Concomitantly, morphological and microstructural changes are characterized by scanning electron microscopy, providing physical input to the observed electrochemical behavior. Specific charge is calculated. For Li and K, the specific charge decreases as the cycle number increases, while the reverse is observed for Na and NH4 cations. The trends are correlated to the morphological changes observed. The specific charge in the case of ammonium reaches 180 mAh/g after 20 cycles and continues increasing, indicating that ammonium cations may be considered as viable charge carriers for electrical energy storage system, and moreover in an aqueous electrolyte. We acknowledge support from the National Science Foundation, Grant No. DMR-1206338.

  10. Recovery of cobalt molybdenum nickel tungsten and vanadium from an aqueous ammonia and ammonium salt solution by coextracting molybdenum tungsten and vanadium and sequential extraction of nickel and cobalt

    SciTech Connect

    Hubred, G. L.; Van Leirsburg, D. A.

    1985-04-30

    A method of recovering metal values from an aqueous stream. The metal values are preferably obtained from leaching spent hydroprocessing catalysts, and include nickel, cobalt, vanadium and molybdenum. The metal values are extracted, isolated and purified by liquid, liquid extraction techniques.

  11. 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.

  12. 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.

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

    NASA Astrophysics Data System (ADS)

    Hudak, Nicholas S.

    2014-12-01

    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. 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.

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

    DOE PAGESBeta

    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

  15. Direct effect of vanadium on citrate uptake by rat renal brush border membrane vesicles (BBMV).

    PubMed

    Sato, Kazuhiro; Kusaka, Yukinori; Akino, Hironobu; Kanamaru, Hiroshi; Okada, Kenichiro

    2002-07-01

    Vanadium pentoxide is used as a catalyst and a ferrovanadium alloy ingredient in automotive steels and in jet engines and airframes. In addition, vanadium is found in fuel oils. Thus, occupational exposures to vanadium pentoxide and trioxide may occur during the cleaning of oil-fired ship boilers, and from oil-fired power station boilers. Occupational exposure to vanadium pentoxide induces green tongue, asthmatic symptoms and albuminuria with cast. Urinary citrate is freely filtered at the glomerulus, and its reabsorption in the proximal tubule is the major determinant of the rate of renal excretion. In this study, we exposed rat renal brush border membrane vesicles (BBMV) to vanadium pentoxide and examined their citrate uptake characteristics. The preincubation of BBMV with 1 mM V2O5 for 8 hours significantly inhibited citrate uptake compared with that of BBMV without V2O5, preincubation. These findings indicate that the preincubation of BBMV with vanadium pentoxide results in a time-dependent inhibition of citrate uptake by BBMV. These findings might contribute to nephrotoxicity in vanadium exposure. PMID:12141377

  16. 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.

  17. 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.

  18. 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

  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

    ... From the Russian Federation, 60 FR 35550 (July 10, 1995). \\3\\ See Preliminary Negative Determination... Ferrovanadium and Nitrided Vanadium From the Russian Federation, 77 FR 6537, (February 8, 2012) (Preliminary... importation of vanadium pentoxide from the Russian Federation (Russia) by the Evraz Group,\\1\\ which is...

  20. 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. PMID:26720551

  1. Microbial Reduction and Precipitation of Vanadium by Shewanella oneidensis

    PubMed Central

    Carpentier, W.; Sandra, K.; De Smet, I.; Brigé, A.; De Smet, L.; Van Beeumen, J.

    2003-01-01

    Shewanella oneidensis couples anaerobic oxidation of lactate, formate, and pyruvate to the reduction of vanadium pentoxide (VV). The bacterium reduces VV (vanadate ion) to VIV (vanadyl ion) in an anaerobic atmosphere. The resulting vanadyl ion precipitates as a VIV-containing solid. PMID:12788772

  2. 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.

  3. Enhanced electrochromism in gyroid-structured vanadium pentoxide.

    PubMed

    Scherer, Maik R J; Li, Li; Cunha, Pedro M S; Scherman, Oren A; Steiner, Ullrich

    2012-03-01

    Manufacturing V(2)O(5) in a 3D periodic highly interconnected gyroid structure on the 10 nm length scale is shown to lead to a significant electrochromic performance enhancement. The structured devices surpass previous inorganic electrochromic materials in all relevant parameters: the switching speed, coloration contrast, and composite coloration efficiency. In particular, the 85 ms switching speed lies within a factor of two of video rate. Enhanced ion intercalation into the gyroid morphology can be extended to other transition-metal oxides and is therefore promising for lithium ion batteries, supercapacitors, and sensors. PMID:22287187

  4. Vanadium pentoxide nanochains for high-performance electrochemical supercapacitors.

    PubMed

    Umeshbabu, Ediga; Ranga Rao, G

    2016-06-15

    We have synthesized unique hierarchical one dimensional (1D) nanochains of V2O5 by employing simple hydrothermal method using cetyltrimethylammonium bromide (CTAB) as a soft template. The electrochemical performance of resulting V2O5 electrode materials was evaluated by cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy techniques. The V2O5 nanochains (V2O5-ctab) show maximum specific capacitance of 631Fg(-1) at a current density of 0.5Ag(-1) and retain 300Fg(-1) even at high current density of 15Ag(-1). In addition the V2O5 nanochains show good cyclic stability with 75% capacitance retention after 1200 charge-discharge cycles. The order of specific capacitance is commercial bulk-V2O5 (160Fg(-1))

  5. Structural and toxic effect investigation of vanadium pentoxide.

    PubMed

    Yuvakkumar, R; Hong, S I

    2016-08-01

    A facile inorganic complex synthesis route has been developed to synthesis V2O5 nanostructures. The effects of varying incubation time on the crystallinity and morphology of the V2O5 phase has been investigated. The obtained XRD result clearly revealed the pure orthorhombic V2O5 crystalline phase. Raman antiphase bridging VO and chaining VO stretching modes peaks at 686 and 521cm(-1) attributed orthorhombic V2O5 characteristics. The V2p3/2 peak at the binding energies of 517eV and V2p1/2 peak at 524eV assigned to V(5+) oxidation state. Bioinspired V2O5 nanostructures as a biocompatible material for anticancer agents show excellent cytotoxicity at higher V2O5 concentration. PMID:27157769

  6. 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.

  7. 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. PMID:25843361

  8. Part A. Neutron activation analysis of selenium and vanadium in biological matrices. Part B. Isomeric transition activation in aqueous solutions of alkyl bromides

    SciTech Connect

    Ebrahim, A.

    1988-01-01

    Several procedures were evaluated for determination of selenium in biological fluids and vanadium in biological tissues by neutron activation analysis (NAA) employing {sup 77m}Se and {sup 52}V isotopes, respectively. Procedures for determination of total selenium, trimethylselenonium (TMSe) ion and selenite (SeO{sub 3}{sup 2{minus}}) ion in urine and serum and for total selenoamino acids in urine were developed by utilizing anion exchange chromatography and molecular NAA. A pre-column derivatization of selenoamino acids with o-phthalaldehyde was necessary for their determination. Also an analytical approach was developed for determination of trace vanadium in liver samples from normal and diabetic rats as well as human and cow. Reactions of bromine-80 activated by radiative neutron capture and bromine-82 activated by isomeric transition were investigated in aqueous solutions of bromomethane and 1-bromobutane. Bromine-80 organic yields decreased with decreasing solute concentrations. The tendency for aggregation of the solute molecules diminished as the solute concentration approached zero where the probable state of the solute approached a monomolecular dispersion. Unlike reactions of {sup 80}Br born by {sup 79}Br(n,{gamma}){sup 80}Br reaction, the total organic product yields resulting from the {sup 82m}Br(I.T.){sup 82}Br process showed no solute concentration dependence.

  9. 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.

  10. Synthesis and characterization of vanadium(IV) complexes with cis-inositol in aqueous solution and in the solid-state.

    PubMed

    Morgenstern, Bernd; Kutzky, Barbara; Neis, Christian; Stucky, Stefan; Hegetschweiler, Kaspar; Garribba, Eugenio; Micera, Giovanni

    2007-05-14

    The complex formation of vanadium(IV) with cis-inositol (ino) and the corresponding trimethyl ether 1,3,5-trideoxy-1,3,5-trimethoxy-cis-inositol (tmci) was studied in aqueous solution and in the solid-state. With increasing pH, the formation of [VO(H-2L)], [(VO)2L2H-5]-, [VO(H-3L)]- (L = ino) or [(VO)2L2H-6]2- (L = tmci), [V(H-3L)2]2-, and [VO(H-3L)(OH)2]3- was observed. For the vanadium(IV)/ino system, [(VO)2L2H-7]3- was observed as an additional dinuclear species. The formation constants of these complexes were determined by potentiometric titrations (25 degrees C, 0.1 M KCl). In addition, the vanadium(IV)/ino system was investigated by means of UV-vis spectrophotometric methods. EPR spectroscopy and cyclic voltammetry confirmed this complexation scheme. EPR measurements indicated the formation of three distinct isomers of the non-oxo complex [V(H-3ino)2]2- in weakly basic solution. This type of isomerism, which is not observed for the vanadium(IV)/tmci system, was assigned to the ability of ino to bind the vanadium(IV) center with three alkoxo groups having either a 1,3,5-triaxial or an 1,2,3-axial-equatorial-axial arrangement. The structures of [V(H-3ino)2][K2(ino)2].4H2O (1) and [Na6V(H-3ino)2](SO4)2.6H2O (2) were determined by single-crystal X-ray analysis. In both compounds, the coordination of each ino molecule to the vanadium(IV) center via three axial deprotonated oxygen donors was confirmed. The centrosymmetric structure of the coordination spheres corresponds to an almost regular octahedral geometry with a twist angle of 60 degrees. The crystal structure of the potassium complex 1 represents an unusual 1:1 packing of [V(H-3ino)2]2- dianions and [K2(ino)2]2+ dications, in which both K+ ions have a coordination number of nine and are bonded simultaneously to a 1,3,5-triaxial and an 1,2,3-axial-equatorial-axial site of ino. In 2, the [V(H-3ino)2]2- complexes are surrounded by six Na+ counterions that are bonded to the axial alkoxo oxygens and to the

  11. Increasing the energy density of the non-aqueous vanadium redox flow battery with the acetonitrile-1,3-dioxolane-dimethyl sulfoxide solvent mixture

    NASA Astrophysics Data System (ADS)

    Herr, T.; Fischer, P.; Tübke, J.; Pinkwart, K.; Elsner, P.

    2014-11-01

    Different solvent mixtures were investigated for non-aqueous vanadium acetylacetonate (V(acac)3) redox flow batteries with tetrabutylammonium hexafluorophosphate as the supporting electrolyte. The aim of this study was to increase the energy density of the non-aqueous redox flow battery. A mixture of acetonitrile, dimethyl sulfoxide and 1-3-dioxolane nearly doubles the solubility of the active species. The proposed electrolyte system was characterized by Raman and FT-IR spectroscopy, cyclic voltammetry, electrochemical impedance spectroscopy and charge-discharge set-up. Spectroscopic methods were applied to understand the interactions between the solvents used and their impact on the solubility. The potential difference between oxidation and reduction of V(acac)3 measured by cyclic voltammetry was about 2.2 V. Impedance spectroscopy showed an electrolyte resistance of about 2400 Ω cm2. Experiments in a charge-discharge test cell achieved coulombic and energy efficiencies of ∼95% and ∼27% respectively. The highest discharge power density was 0.25 mW cm-2.

  12. 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.

  13. 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.

  14. 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.

  15. DNA damage induction in human cells exposed to vanadium oxides in vitro.

    PubMed

    Rodríguez-Mercado, Juan J; Mateos-Nava, Rodrigo A; Altamirano-Lozano, Mario A

    2011-12-01

    Vanadium and vanadium salts cause genotoxicity and elicit variable biological effects depending on several factors. In the present study, we analyzed and compared the DNA damage and repair processes induced by vanadium in three oxidation states. We used human blood leukocytes in vitro and in a single cell gel electrophoresis assay at two pH values. We observed that vanadium(III) trioxide and vanadium(V) pentoxide produced DNA single-strand breaks at all of the concentrations (1, 2, 4, or 8 μg/ml) and treatment times (2, 4, or 6 h) tested. Vanadium(IV) tetraoxide treatment significantly increased DNA damage at all concentrations for 4 or 6 h of treatment but not for 2 h of treatment. The DNA repair kinetics indicated that most of the cells exposed to vanadium III and V for 4 h recovered within the repair incubation time of 90 min; however, those exposed to vanadium(IV) repaired their DNA within 120 min. The data at pH 9 indicated that vanadium(IV) tetraoxide induced DNA double-strand breaks. Our results show that the genotoxic effect of vanadium can be produced by any of its three oxidation states. However, vanadium(IV) induces double-strand breaks, and it is known that these lesions are linked with forming structural chromosomal aberrations. PMID:21803147

  16. 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. PMID:26695325

  17. 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.

  18. Waveguide lasers in ytterbium-doped tantalum pentoxide on silicon.

    PubMed

    Aghajani, A; Murugan, G S; Sessions, N P; Apostolopoulos, V; Wilkinson, J S

    2015-06-01

    A waveguide laser in an ytterbium-doped tantalum pentoxide film is reported. The waveguide is formed of a rib of sputtered tantalum pentoxide on top of oxidized silicon with an over-cladding of silica. Emission at a wavelength of 1025 nm was achieved with an absorbed pump power threshold and slope efficiency of ≈29  mW and 27%, respectively, for a cavity formed by a high reflector mirror and an estimated 12% Fresnel reflection from the bare end-face at the output. PMID:26030554

  19. 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.

  20. Vanadium oxide/polypyrrole aerogel nanocomposites

    SciTech Connect

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

    1996-12-31

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

  1. Hybrid uranyl-vanadium nano-wheels.

    PubMed

    Senchyk, G A; Wylie, E M; Prizio, S; Szymanowski, J E S; Sigmon, G E; Burns, P C

    2015-06-25

    Hybrid uranyl-vanadium oxide clusters intermediate between transition metal polyoxometalates and uranyl peroxide cage clusters were obtained by dissolving uranyl nitrate in the ionic liquid 3-ethyl-1-methylimidazolium ethyl sulfate mixed with an aqueous solution containing vanadium. Where sulfate was present, wheel-shaped {U20V20} crystallized and contains ten sulfate tetrahedra, and in the absence of added sulfate, {U2V16}, a derivative of {V18}, was obtained. PMID:26008125

  2. Passivated iodine pentoxide oxidizer for potential biocidal nanoenergetic applications.

    PubMed

    Feng, Jingyu; Jian, Guoqiang; Liu, Qing; Zachariah, Michael R

    2013-09-25

    Iodine pentoxide (I2O5), also known as diiodine pentoxide, is a strong oxidizer which has been recently proposed as an iodine-rich oxidizer in nanoenergetic formulations, whose combustion products lead to molecular iodine as a biocidal agent. However, its highly hygroscopic nature hinders its performance as a strong oxidizer and an iodine releasing agent and prevents its implementation. In this work, we developed a gas phase assisted aerosol spray pyrolysis which enables creation of iron oxide passivated I2O5. Transmission electron microscopy elemental imaging as well as temperature-jump mass spectrometry confirmed the core shell nature of the material and the fact that I2O5 could be encapsulated in pure unhydrated form. Combustion performance finds an optimal coating thickness that enables combustion performance similar to a high performing CuO based thermite. PMID:23988006

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

    SciTech Connect

    Sydorchuk, V.; Zazhigalov, V.; Khalameida, S.; Diyuk, E.; Skubiszewska-Zieba, J.; Leboda, R.; Kuznetsova, L.

    2010-09-15

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

  4. 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.

  5. 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

    ... has released this draft assessment solely for the purpose of pre-dissemination peer review under... peer review of this draft assessment. The public comment period and external peer review meeting are... external peer review meeting will be scheduled at a later date and announced in the Federal...

  6. 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.

  7. 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

    ... that to gain entrance to this EPA building to attend the meeting, you must have photo identification and must register at the guard's desk in the lobby. The guard will retain your photo identification..., please return your visitor's badge to the guard and you will receive your photo identification....

  8. 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. PMID:26529244

  9. PROCESS FOR RECOVERING URANIUM FROM AQUEOUS PHOSPHORIC ACID LIQUORS

    DOEpatents

    Schmitt, J.M.

    1962-09-01

    A liquid-liquid extraction method is given for recovering uranium values from aqueous solutions. An acidic aqueous solution containing uranium values is contacted with an organic phase comprising an organic diluent and the reaction product of phosphorous pentoxide and a substantially pure dialkylphosphoric acid. The uranium values are transferred to the organic phase even from aqueous solutions containing a high concentration of strong uranium complexing agents such as phosphate ions. (AEC)

  10. 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}.

  11. 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.}

  12. Synthesis and Structural Characterization of Orthorhombic Vanadium Oxide Nanorods

    NASA Astrophysics Data System (ADS)

    Garcia, L. M.; Chavira, E.; Santiago-Jacinto, P.; Rendon, L.; Marinero, E. E.; Tejada, A.; Fregoso-Israel, E.; Flores, C.

    2012-02-01

    Nanorod structures for Li storage are of interest for rechargeable battery applications. Vanadium pentoxide is a promising battery cathode material and in this work we report on the synthesis of V2O5 orthorhombic single crystal and polycrystalline nanorods by the sol-gel polymerizing acryl amide method via ethylenediamine tetra acetic acid EDTA assisted hydrothermal process. In order to determine the thermodynamic stability of nanostructured polymorphs vanadates, heat treatments were performed from 450 C to 500 ^oC with annealing times ranging from 48 to 72 h. The morphologies and structures of the nanorods were characterized by XRD, SEM and HRTEM. Thermo Gravimetric Analysis (TGA) was employed to monitor reaction mass losses during the course of the synthesis. Nanorod diameters ranging from 50 to 150 nm were observed. The lengths and diameter of the rods depended on the conditions of the preparation, such as concentration, and reaction time.

  13. 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.

  14. 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.

  15. Adsorption of Pb(II), Cr(III), Cu(II), Cd(II) and Ni(II) onto a vanadium mine tailing from aqueous solution.

    PubMed

    Shi, Taihong; Jia, Shiguo; Chen, Ying; Wen, Yinghong; Du, Changming; Guo, Huilin; Wang, Zhuochao

    2009-09-30

    The adsorption of heavy metal cations Pb(II), Cr(III), Cu(II), Cd(II) and Ni(II) from aqueous solution by a mine tailing which mainly contains muscovite was investigated. The property of the mineral was investigated by using SEM, FT-IR, XRD and BET analysis. pH(pzc) was measured by an titration technique to give a value of 5.4+/-0.1. Kinetics experiments indicated that the processes can be simulated by pseudo-second-order model. Total adsorption amounts of the heavy metal increased, while the adsorption density decreased when the solid-to-liquid ratio (S/L) increased. Grain size did not affect the adsorption capacity significantly. The resulting isotherms can be described by Frendlich relationship. And the maximum adsorption capacity (molar basis) followed the order of Cr(III)>Pb(II)>Cu(II)>Ni(II)>Cd(II). Thermodynamic analysis showed that the adsorption processed were endothermic and may be chemical in nature with positive DeltaH(0). The positive DeltaS(0) suggested that dissociative processed were involved. Small positive DeltaG(0) suggested that the adsorption processes required a small amount of energy. Adsorption processes were slightly affected by electrolyte ion concentration but strongly dependent on pH value. The most possible mechanism of the adsorption processes involve the inner-sphere-complexions by the aluminol or silanol groups on the surface of the mineral. PMID:19427115

  16. 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.

  17. 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.

  18. Contractile effect of vanadate and other vanadium compounds on the rat vas deferens.

    PubMed

    Garcia, A G; Jurkiewicz, A; Jurkiewicz, N H

    1981-03-01

    Sodium metavanadate (NaVO3), vanadium pentoxide (V2O5) and vanadyl sulphate (VOSO4), evoked rhythmic and tonic contractions of the normal and reserpinized rat isolated vas deferens. Contractions were not observed by the use of vanadium trichloride (VCl3) The order of potency of these compounds, for their maximum contractile effects was NaVO3 greater than V2O5 greater than VOSO4 greater than VCl3. Differences in pD2 values were less than 0.5 long units in relation to the first compound. Vanadium-induced contractions were blocked by Ca2+ deprivation, nifedipine, Mg2+, Mn2+, Ni2+ and Co2+, indicating the involvement of a loosely bound or extracellular calcium-dependent mechanism. It is still unclear whether this calcium translocation was related, or not, to changes in Na+, K+-ATPase activity. Since ouabain blocked the action of vanadyl or vanadate non-competitively, it is concluded that vanadium compounds and ouabain induce their effects by interacting with different sites in vas deferens, both of which may or may not be located on the (Na+, K+)ATPase enzyme complex. PMID:6908559

  19. 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.

  20. 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

  1. 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

  2. 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. PMID:24362016

  3. 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

  4. Vanadium Nitrogenase Reduces CO*

    PubMed Central

    Lee, Chi Chung; Hu, Yilin; Ribbe, Markus W.

    2011-01-01

    Vanadium nitrogenase not only reduces dinitrogen to ammonia but also reduces carbon monoxide to ethylene, ethane, and propane. The parallelism between the two reactions suggests a potential link in mechanism and evolution between the carbon and nitrogen cycles on Earth. PMID:20689010

  5. Vanadium nitrogenase reduces CO.

    PubMed

    Lee, Chi Chung; Hu, Yilin; Ribbe, Markus W

    2010-08-01

    Vanadium nitrogenase not only reduces dinitrogen to ammonia but also reduces carbon monoxide to ethylene, ethane, and propane. The parallelism between the two reactions suggests a potential link in mechanism and evolution between the carbon and nitrogen cycles on Earth. PMID:20689010

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

    SciTech Connect

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

    1996-06-18

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

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

    SciTech Connect

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

    2014-05-14

    Thin films of V{sub 2}O{sub 5} 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 V{sub 2}O{sub 5}. 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.

  8. A study of structure-property correlation in vanadium pentoxide and titanium dioxide based thin films as functional materials

    NASA Astrophysics Data System (ADS)

    Thapa, Chandra

    The focus of this thesis is to study the structure-property correlation in thin films of V2O5 and TiO2 based transition metal oxides as functional materials. V2O5 is investigated as a cathode material for lithium ion battery and TiO2 as a high-k dielectric material. We studied V2O5 thin films prepared by spin coating using three different types of precursors, MOD precursor, sol-gel organic precursor and sol-gel inorganic precursor. On the basis of structural and electrochemical studies, we find that the capacity is dependent on the degree of non-stoichiometry. We have also studied the effect of addition of Ti. Although Ti doping enhances non-stoichiometry, the capacity was found to increase only in 5% Ti-doped sol-gel film. This means the optimal degree of non-stoichiometry is crucial to enhance the capacity. TiO2 is one of the possible high-k dielectric materials because of its very high dielectric constant. We studied leakage characteristics, the dielectric strength and frequency dependent behavior of dielectric constant of TiO2 thin films prepared by MOD, sputter deposition and annealed at different temperatures. We find dielectric constant increasing with the increase in annealing temperature and leakage current density improvement by almost one order of magnitude with each 100 °C increase in annealing temperature. Since TiO2 possess two distinct thermodynamic phases: anatase and rutile, which dramatically influences the values of dielectric constant and leakage current density, it is crucial to stabilize the phase of TiO2 by doping. We find that 20% Zr-doping completely stabilizes TiO2 phase in its anatase form. The dielectric constant of the films is independent of annealing temperature but the leakage current density improves by one order of magnitude with every 100 °C increase in annealing temperature.

  9. Synthesis and electrochemical properties of vanadium oxide materials and structures as Li-ion battery positive electrodes

    NASA Astrophysics Data System (ADS)

    McNulty, David; Buckley, D. Noel; O'Dwyer, Colm

    2014-12-01

    The electrochemical intercalation of lithium into vanadium pentoxide was first reported in the 1970's. Over the last 40 years vanadium oxides have continued to be the subject of much research due to their desirable physical properties. Initial results with bulk V2O5 and V2O5 gels demonstrated the potential for application as a cathode material for lithium batteries. Encouraging specific capacities exceeding 250 mAh g-1 were accompanied by severe capacity fading, which prevented widespread commercial application of V2O5-containing cathodes. Following the commercial release of the Li-ion battery, the development of layered materials that reversibly intercalated lithium, and the resurgence in nanoscale materials for Li-ion and alternative batteries, have opened new opportunities for the examination of the influence of material structure on cell performance. Recent decades have witnessed advances in the control of shape, structure and function of Li-ion battery materials. This review details the synthesis and structural properties of vanadium oxides, one of the model layered battery materials, and reviews the synthesis and structure of vanadium oxides and related polymorphs, bronzes and phases. Their electrochemical characteristics under a wide range of conditions are assessed and compared as positive electrode materials in lithium and lithium-ion batteries up to the present day.

  10. Slag recycling of irradiated vanadium

    SciTech Connect

    Gorman, P.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.

  11. 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. PMID:25478865

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

    NASA Astrophysics Data System (ADS)

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

    2014-11-01

    Tantalum pentoxide (Ta2O5) 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 Ta2O5 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 Ta2O5.

  13. 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.

  14. 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

  15. 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.

  16. 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.

  17. 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.

  18. 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

    2011-04-01

    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. PMID:21347465

  19. Template-assisted formation of porous vanadium oxide as high performance cathode materials for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Su, Yanhui; Pan, Anqiang; Wang, Yaping; Huang, Jiwu; Nie, Zhiwei; An, Xinxin; Liang, Shuquan

    2015-11-01

    Similar to carbonaceous materials, porous metal oxides have attracted wide attention in energy storage and conversion systems because of their structural advantages, including high activity and electrolyte accessibility. In this work, we report the novel preparation of porous vanadium pentoxide (V2O5) as high performance cathode material for lithium ion batteries. Ketjen black (KB), a porous carbon material, has been employed as hard templates to host precursor species in their porous structures. The porous V2O5 electrode material is prepared after removing the KB carbon framework by calcinating the composites in air. As cathode materials for lithium ion batteries, the porous V2O5 electrodes exhibit high capacity, good cycling stability and rate capability. An initial discharge capacity of 141.1 mA h g-1 is delivered at a current density of 100 mAg-1, very close to the theoretical capacity of 147 mA h g-1.

  20. 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.

  1. TDPAC study of complex structure semiconductor compounds; The case of niobium pentoxide

    SciTech Connect

    Shitu, J.; Renteria, M.; Massolo, C.P.; Bibiloni, A.G.; Desimonni, J. )

    1992-07-20

    In this paper, a new method for analyzing Time-Differential Perturbed Angular Correlation spectra is presented and applied to study the hyperfine interaction of {sup 100}Rh in the high temperature modification of niobium pentoxide. The measured quadrupole interactions are assigned to about 80% of the radioactive probes replacing niobium atoms in the lattice and about 20% located in perturbed sites. The origin of this perturbation, producing a high frequency component in the measured spectra is discussed and temptatively assigned to remaining radiation damage in the compound. The hyperfine interaction of {sup 111}Cd probes, introduced through thermal diffusion into niobium pentoxide, is also presented. The temperature dependence of the hyperfine parameters in this case is studied in the temperature range RT-800{degrees} C. The spectral analyzing method employed allows a direct comparison of experimental data with point charge model calculations and a simultaneous evaluation of the antishielding factor {beta}. The obtained values (27 for {sup 100}Rh and 15 for {sup 111}Cd) are discussed in terms of the compound and probe's characteristics.

  2. TDPAC study of complex structure semiconductor compounds; The case niobium pentoxide

    SciTech Connect

    Shitu, J.; Renteria, M.; Massolo, C.P.; Bibiloni, A.G.; Desimoni, J. )

    1992-07-10

    In this paper, a new method for analyzing Time-Differential Perturbed Angular Correlation spectra is presented and applied to study the hyperfine interaction of {sup 100}Rh in the high temperature modification of niobium pentoxide. The measured quadrupole interactions are assigned to about 80% of the radioactive probes replacing niobium atoms in the lattice and about 20% located in perturbed sites. The origin of this perturbation, producing a high frequency component in the measured spectra is discussed and temptatively assigned to remaining radiation damage in the compound. The hyperfine interaction of {sup 111}Cd probes, introduced through thermal diffusion into niobium pentoxide, is also presented. The temperature dependence of the hyperfine parameters in this case is studied in the temperature range RT-800{degrees}C. The spectral analyzing method employed allows a direct comparison of experimental data with point charge model calculations and a simultaneous evaluation of the anti-shielding factor {beta}. The obtained values (27 for {sup 100}Rh and 15 for {sup 111}Cd) are discussed in terms of the compound and probe's characteristics.

  3. 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.

  4. Electronic structure of crystalline phosphorus pentoxide and the effect of an Ag impurity

    NASA Astrophysics Data System (ADS)

    Abarenkov, I. V.; Tupitsyn, I. I.; Kuznetsov, V. G.; Payne, M. C.

    1999-09-01

    The phosphorus pentoxide crystal with Pnam symmetry containing four P2O5 molecules in the unit cell was calculated by ab initio density-functional theory in the local-density approximation with a plane-wave basis set using the CASTEP code. The calculated optimized geometry is in good agreement with experiment. The population analysis made in terms of Löwdin and Mulliken charges and Wiberg indexes showed that this crystal has a mixed chemical bonding, partly ionic, partly covalent. An Ag atom impurity in the phosphorus pentoxide crystal was investigated within the periodic model. The distortion of the lattice around the impurity was analyzed in terms of PO4 tetrahedra. The calculations showed that in spite of considerable deformation of the lattice, the Ag impurity does not break the P-O bonding network and changes the P-O bond order only a little. The Ag impurity atom is bound to the crystal with an almost pure ionic bond, the Ag atomic charge being 0.6 (Löwdin charge).

  5. 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}.

  6. Sex-based differences in lymphocyte proliferation in the spleen after vanadium inhalation.

    PubMed

    Rodriguez-Lara, Vianey; Muñiz-Rivera Cambas, Angelica; González Villalva, Adriana; Fortoul, Teresa I

    2016-07-01

    Vanadium (V) is a transition metal often adhered to particulate matter and released into the atmosphere as vanadium pentoxide (V2O5) by the burning of fossil fuels. This air pollutant causes adverse effects in the immune system. Lymphocytosis and splenomegaly have been reported with increased white pulp in mice after V inhalation. The effect of V on the immune system as related to sex has been poorly investigated. This study sought to determine if V inhalation (a) produced lymphoproliferation that could explain the changes previously observed in the spleen and in peripheral blood lymphocyte counts and (b) whether any observed effects differed due to gender. Immunohistochemical analyses of Ki-67, a specific proliferation marker, was made in the spleens of CD-1 male and female mice exposed for 1 h, twice a week, over a 12-week period to V2O5 (at 1.4 mg V2O5/m(3)) by whole-body inhalation; similar analyses were performed on spleens of control mice exposed to vehicle (filtered air). The results showed that in male mice there was a significant increase in percentage of Ki-67 immunopositive lymphocytes starting from the second week and until the end of the exposure. The Ki-67 signal was cytoplasmic and nuclear in the exposed males, while in controls the signal was only nuclear. In female mice, V inhalation singificantly increased the percentage of proliferating lymphocytes only after 1 week of exposure. Ki-67 signal was observed only in the nucleus of lymphocytes from the control and exposed females. The results here help to explain the splenomegaly and lymphocytosis observed previously in male mice and support the lymphoproliferative effect induced by V. Lastly, the finding that there was a sex difference in the effect of vanadium on lymphocyte proliferation suggests a role for sex hormones in potential protection against V immunotoxicity; however, further studies are needed to support this hypothesis. PMID:27043960

  7. 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.

  8. Impact-Driven Thermite Reactions with Iodine Pentoxide and Silver Oxide

    NASA Astrophysics Data System (ADS)

    Russell, R.; Bless, S.; Pantoya, M.

    2011-04-01

    Thermite reactions using aluminum (Al) fuel and either iodine pentoxide (I2O5) or silver oxide (Ag2O) were initiated by high-velocity impact or thermal initiation and examined for their flame propagation behavior. In the impact-ignition experiments, the Al-Ag2O reaction produced more energy than the Al-I2O5 reaction; in the thermal-ignition experiments, the I2O5 reaction produced higher flame propagation rates (1,305 m/s compared with 531 m/s). The energy released from impact-initiated reactions is significantly enhanced by reducing the size of the oxide particles. Results suggest that the reaction propagation mechanisms may be the same, even though ignition is spurred by two different stimuli (mechanically induced compaction versus thermal).

  9. Synthesis, characterization and reactivity of early transition metal neo-pentoxides

    SciTech Connect

    Boyle, T.J.; Alam, T.M.; Scott, B.; Ziller, J.W.

    1997-12-31

    Titanium neo-pentoxide was isolated by the alcoholysis exchange between Ti(OCHMe{sub 2}){sub 4} and ONep. The molecule, [Ti(ONep){sub 4}]{sub 2}, was characterized using X-ray analysis and solution {sup 17}O, and {sup 47},{sup 49}Ti NMR spectroscopy. This dinuclear complex is the smallest Ti(OR){sub 4} isolated wherein each metal center is 5-coordinated. The molecule is highly soluble in standard solvents and volatile. The reactivity of this compound has been undertaken to compare with the ubiquitous Ti(O-I-Pr){sub 4}. The various compounds isolated and further NMR studies will be reported. Analogous routes to other M(ONep){sub n} will be reported as well.

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. 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.

  15. New vanadium trap proven in commercial trials

    SciTech Connect

    Dougan, T.J. ); Alkemade, U.; Lakhanpal, B. ); Boock, L.T. )

    1994-09-26

    A vanadium trap technology called RV4+ has demonstrated in a variety of commercial fluid catalytic cracking (FCC) units its ability to reduce vanadium on equilibrium catalyst by more than 20%. Reducing vanadium loading increases microactivity and zeolite surface area retention, confirming that RV4+ protects zeolites from vanadium deactivation. Sulfur competition had prevented some previous traps from working commercially, but was not a factor with the new trap. The technology can save refiners millions of dollars per year in catalyst costs, or allow them to process feeds containing higher vanadium concentrations. The paper discusses vanadium traps, deactivation mechanism, history of traps, vanadium mobility, intraparticle mobility, interparticle mobility, measuring performance, commercial results, sulfur competition, and economic value.

  16. A composite film of reduced graphene oxide modified vanadium oxide nanoribbons as a free standing cathode material for rechargeable lithium batteries

    NASA Astrophysics Data System (ADS)

    Sun, Yi; Yang, Shu-Bin; Lv, Li-Ping; Lieberwirth, Ingo; Zhang, Lin-Chao; Ding, Chu-Xiong; Chen, Chun-Hua

    2013-11-01

    Hydrated vanadium pentoxide (V2O5·0.86H2O) nanoribbons modified with reduced graphene oxide (RGO) are synthesized by a hydrothermal process. These ribbons are 30 nm thick, 200 nm to 1 μm wide and above 50 μm long. Binder-free films are prepared by using these ribbons and annealed at 300 °C in nitrogen as the cathode for rechargeable lithium cells. The intertwining network of this free-standing VOx/RGO film provides efficient conduction pathways for electrons and short diffusion distances for Li ions. The electrochemical tests exhibit that this cathode film delivers a high reversible specific capacity (160 mAh g-1) and good cycling stability (133 mAh g-1 after 200 cycles) in the voltage range between 2.0 and 3.5 V.

  17. 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.

  18. 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.

  19. Dynamic shock studies of vanadium

    SciTech Connect

    Chhabildas, L.C.; Hills, C.R.

    1985-01-01

    Using gas-gun loading techniques and velocity interferometric techniques, time-resolved wave profiles have been obtained in vanadium over the stress range of 2.9 to 9.7 GPa. The risetime data indicate steepened shock structures with increasing shock amplitude. However, unlike aluminum, finite risetimes are determined even at 9.7 GPa, indicating a large effective viscosity for the material. The dynamic yield strength measured at the Hugoniot elastic limit is 0.8 GPa and is approximately twice the static yield strength. Material softening is evidenced through measurements of shock velocity and yield strength determinations in the shocked state. The yield strength of the material upon release from the shocked state is estimated to be approx.0.43 GPa and is comparable to the static yield strength. Strain-rate dependent processes may be responsible for a higher elastic shear stress sustained before relaxation to an equilibrium value. The primary mode of deformation in shocked vanadium appears to be cross slip, resulting in dislocation tangles. Deformation twins are also observed in shock-recovered specimens with an increasing number with increased shock stress. The thermal diffusivity for vanadium is low, and the shear-strength loss observed in this material is consistent with the strength loss observed for other materials which also have low thermal diffusivities. It is conceivable that the loss of shear strength may be due to long thermal recovery times resulting from inhomogeneous deformation process.

  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. 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. PMID:26702713

  2. The aluminium and iodine pentoxide reaction for the destruction of spore forming bacteria.

    PubMed

    Clark, Billy R; Pantoya, Michelle L

    2010-10-21

    The threat of biological weapons is a major concern in the present day and has led to studying methods to neutralize spore forming bacteria. A new technique involves the use of a thermite reaction that exhibits biocidal properties to limit bacterial growth. The objective was to examine the influence on bacteria growth upon spore exposure to thermite reactions with and without biocidal properties. Three thermites are considered: two that have biocidal properties (aluminium (Al) combined with iodine pentoxide (I(2)O(5)) and Al combined with silver oxide (Ag(2)O)); and, one that produces a highly exothermic reaction but has no biocidal properties (Al combined with iron oxide (Fe(2)O(3))). Results show that Al + I(2)O(5) is extremely effective at neutralizing spores after only one hour of exposure. The temperature generated by the reaction was not determined to be an influential factor affecting spore growth kinetics. Further analysis of the thermite reactions revealed that the Al + I(2)O(5) reaction produces iodine gas that effectively interacts with the spores and neutralizes bacteria growth, while the Al + Ag(2)O reaction temperature does not vaporize silver. In the condensed phase silver does not interact with the spores enough to neutralize bacteria growth. This study gives evidence that a thermite can be used as a stable transportation and delivery system for biocidal gas. PMID:20730185

  3. Nonvolatile memory devices prepared from sol-gel derived niobium pentoxide films.

    PubMed

    Baek, Hyunhee; Lee, Chanwoo; Choi, Jungkyu; Cho, Jinhan

    2013-01-01

    We report on the resistive switching nonvolatile memory (RSNM) properties of niobium pentoxide (Nb(2)O(5)) films prepared using sol-gel chemistry. A sol-gel derived solution of niobium ethoxide, a precursor to Nb(2)O(5), was spin-coated on to a platinum (Pt)-coated silicon substrate, and was then annealed at approximately 620 and 450 °C to form a Nb(2)O(5) film of polycrystalline and amorphous structure, respectively. A top electrode consisting of Ag, W, Au, or Pt was then coated onto the Nb(2)O(5) films to complete the fabrication. After a forming process of limited current compliance up to 10 mA, known as "electroforming", a resistive switching phenomenon, independent of voltage polarity (unipolar switching), was observed at low operating voltages (0.59 ± 0.05 V(RESET) and 1.03 ± 0.06 V(SET)) with a high ON/OFF current ratio above 10(8). The reported approach offers opportunities for preparing Nb(2)O(5)-based resistive switching memory devices from solution process. PMID:23210494

  4. 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.

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

    DOE PAGESBeta

    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

  6. 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.

  7. 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.

  8. 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.

  9. 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...

  10. Perspectives for vanadium in health issues.

    PubMed

    Rehder, Dieter

    2016-03-01

    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. PMID:26898507

  11. 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.

  12. Density Functional Theory simulations of shock compression of porous tantalum pentoxide

    NASA Astrophysics Data System (ADS)

    Cochrane, K.; Vogler, T.; Root, S.; Desjarlais, M.; Shulenburger, L.; Mattsson, T.

    2013-06-01

    Density Functional Theory (DFT) based molecular dynamics has been established as a method capable of yielding high fidelity results for many materials at a wide range of pressures and temperatures and has recently been applied to complex polymers such as polyethylene, compounds such as ethane or CO2, and oxides such as MgO. We use this method and a modification to the Rankine-Hugoniot relation inspired by the P-_crush model to extend the DFT approach to the calculation of the shock response of an initially porous tantalum pentoxide. The experimental data have initial densities of approximately 1 g/cc, 3 g/cc, and 7 g/cc, reduced from a normal density of 8.36 g/cc, with final pressures up to 200 GPa. The DFT results compare well with the 3 g/cc and 7 g/cc over a wide range of pressures. The agreement with the 1 g/cc Hugoniot experimental data is reasonable at lower pressures, but with some larger discrepancies at higher pressures. Finally, we calculate the Gruneisen gamma as a function of density and found that it is density dependent but pressure independent for the lower densities and higher pressures. These results show that DFT methods may be capable of dealing with highly distended material with the proper modifications. Sandia National Laboratories is a multi-program laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the U.S. DOE's National Nuclear Security Administration under contract DE-AC04-94AL85000.

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

    DOE PAGESBeta

    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 [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

  14. 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.

  15. Toxicity of vanadium in female Leghorn chickens.

    PubMed

    Kubena, L F; Phillips, T D

    1983-01-01

    A study was conducted to determine the influence of dietary vanadium, fed after the onset of production, on hen day egg production, body weight changes, and mortality in laying breed chickens. Calcium orthovanadate was fed to 29-week-old female laying breed chickens at calculated levels of 0, 12.5, 25, 50, and 100 ppm dietary vanadium for five consecutive 28-day laying periods. Hen-day egg production and hen body weights were not influenced by the addition of 12.5 or 25 ppm dietary vanadium. Overall hen body weights and the hen day egg production were decreased in hens fed diets to which 50 ppm vanadium was added with a severe reduction in both parameters at 100 ppm. There were no mortalities during the experiment in the groups fed the 0, 12.5, 25, or 50 ppm vanadium diets. Mortality in the group fed the 100 ppm vanadium diet was 11, 39, and 56% at the end of the 28-day Periods 3, 4, and 5, respectively. There were no significant differences in egg weights, although a trend existed for lower egg weights with increasing levels of dietary vanadium. PMID:6828413

  16. 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

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

    PubMed

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

    2016-07-01

    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. PMID:27295523

  18. 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.

  19. Nonaqueous catalytic fluorometric trace determination of vanadium based on the pyronine B-hydrogen peroxide reaction and flow injection after cloud point extraction.

    PubMed

    Paleologos, E K; Koupparis, M A; Karayannis, M I; Veltsistas, P G

    2001-09-15

    The catalytic effect of vanadium on the pyronine B-H2O2 system is examined. Enhancement of the catalytic reaction rate along with the efficiency and selectivity against vanadium is achieved in a formic acid environment in the presence of a nonionic surfactant (Triton X-114). Elimination of drastic interference caused by inorganic acids and aqueous matrix along with a 50-fold preconcentration of vanadium are facilitated through cloud point extraction of its neutral complex with 8-quinolinol in an acidic solution. Subsequent flow injection analysis (FIA) with fluorometric detection renders the proposed method ideal for selective and cost-effective determination of as little as 0.020 microng L(-1) vanadium in environmental, biological, and food substrates. The preconcentration step can be applied simultaneously to multiple samples, allowing for massive preparation prior to analysis, compensating, thus, for the time-consuming procedure. PMID:11575789

  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. PMID:25608665

  1. 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.

  2. Vanadium Dioxide Phase Change Switches

    NASA Astrophysics Data System (ADS)

    Field, Mark; Hillman, Christopher; Stupar, Philip; Hacker, Jonathan; Griffith, Zachary; Lee, Kang-Jin

    2015-03-01

    We have built RF switches using vanadium dioxide thin films fabricated within a section of inverted transmission line with integrated on chip heaters to provide local thermal control. On heating the films above the metal insulator transition we obtain record low switch insertion loss of -0.13 dB at 50 GHz and -0.5 dB at 110 GHz. We investigate the device physics of these switches including the effect of a deposited insulator on the VO2 switching characteristics, the self-latching of the devices under high RF powers and the effect of resistance change with temperature on the device linearity. Finally we show how these devices can be integrated with silicon germanium RF circuits to produce a field programmable device where the RF signal routing can be selected under external control. Supported under the DARPA RF-FPGA Program, Contract HR0011-12-C-0092.

  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

    ... master alloys, vanadium chemicals, vanadium waste and scrap, vanadium- bearing raw materials, such as... nitrided vanadium from Russia. \\1\\ See Ferrovanadium and Nitrided Vanadium From Russia, 77 FR 51825 (August... Antidumping Order: Ferrovanadium and Nitrided Vanadium from the Russian Federation, 60 FR 35550 (July 10,...

  4. 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

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

    PubMed

    Romaidi; Ueki, Tatsuya

    2016-06-01

    Isolation of naturally occurring bacterial strains from metal-rich environments has gained popularity due to the growing need for bioremediation technologies. In this study, we found that the vanadium concentration in the intestine of the vanadium-rich ascidian Ascidia sydneiensis samea could reach 0.67 mM, and thus, we isolated vanadium-resistant bacteria from the intestinal contents and determined the ability of each bacterial strain to accumulate vanadium and other heavy metals. Nine strains of vanadium-resistant bacteria were successfully isolated, of which two strains, V-RA-4 and S-RA-6, accumulated vanadium at a higher rate than did the other strains. The maximum vanadium absorption by these bacteria was achieved at pH 3, and intracellular accumulation was the predominant mechanism. Each strain strongly accumulated copper and cobalt ions, but accumulation of nickel and molybdate ions was relatively low. These bacterial strains can be applied to protocols for bioremediation of vanadium and heavy metal toxicity. PMID:27177911

  6. 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. PMID:23644591

  7. 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

  8. 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

  9. 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.

  10. Vertical Liquid Crystal Orientation on Amorphous Tantalum Pentoxide Surfaces Depending on Anisotropic Dipole-Dipole Interaction via Ion Beam Irradiation

    NASA Astrophysics Data System (ADS)

    Lee, Jong-Jin; Kim, Hyung-Jun; Kang, Young-Gu; Kim, Young-Hwan; Park, Hong-Gyu; Kim, Byoung-Yong; Seo, Dae-Shik

    2011-03-01

    We achieved vertically aligned (VA) liquid crystals (LCs) on amorphous tantalum pentoxide (Ta2O5) alignment films deposited by radio frequency (rf) magnetron sputtering using ion beam (IB) irradiation. By analyzing measurements by X-ray photoelectron spectroscopy (XPS), we confirmed the bond breaking, as detected from the O 1s spectra, which caused an isotropic dipole-dipole interaction between the LC molecules and the Ta2O5 alignment film to uniformly align the vertical LC molecular orientation as a function of IB energy density. Moreover, by examining the electro-optical (EO) characteristics of the Ta2O5 surfaces compared with those of the polyimide (PI) alignment layer, we confirmed that Ta2O5 has a low threshold voltage and a low power consumption when used as an LC alignment layer.

  11. Thermotransport of hydrogen and deuterium in vanadium-niobium, vanadium-titanium, and vanadium-chromium alloys

    NASA Astrophysics Data System (ADS)

    Peterson, D. T.; Smith, M. F.

    1983-04-01

    Thermotransport of hydrogen and deuterium in vanadium alloyed with either niobium, titanium, or chromium is much greater than in pure vanadium, and additions of vanadium to niobium similarly increase thermotransport of hydrogen and deuterium over that observed in pure niobium. In all cases, the heat of transport was positive and was significantly greater for deuterium than for hydrogen. The results are consistent with an atomistic model in which the temperature dependence of atomic jump frequencies is the dominant factor in thermotransport with a small bias in the direction of atomic jumps. There is evidence that differences between the heats of transport for hydrogen and deuterium may be related to isotope effects in the activation energies for diffusion.

  12. Noble metal/vanadium alloy catalyst and method for making

    SciTech Connect

    Jalan, V.M.

    1980-05-13

    A novel catalyst comprises an alloy of a noble metal and vanadium. The catalyst is particularly useful in an electrochemical cell cathode electrode. The method for making the alloy involves reacting a vanadium compound with sodium dithionite to form a sol of a finely dispersed vanadium sulfite complex, and then reacting noble metal particles with the complex in a reducing environment.

  13. Memory Deficit Recovery after Chronic Vanadium Exposure in Mice

    PubMed Central

    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. PMID:26962395

  14. 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.

  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. Porous structured vanadium oxide electrode material for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Reddy, Ravinder N.; Reddy, Ramana G.

    A nano porous vanadium oxide (V 2O 5) was prepared by sol-gel method. The preparation involved elutriation of aqueous sodium meta vanadate over a cation exchange resin. The product was characterized using X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy, surface area analysis and thermogravimetric analysis. Electrochemical characterization was done using cyclic voltammetry in a three electrode system consisting of a saturated calomel electrode as reference electrode, platinum mesh as a counter electrode, and V 2O 5 mounted on Ti mesh as the working electrode. Two molars of aqueous KCl, NaCl and LiCl were used as electrolytes. A maximum capacitance of 214 F g -1 was obtained at a scan rate of 5 mV s -1 in 2 M KCl. The effect of different electrolytes and the effect of concentration of KCl on the specific capacitance of V 2O 5 were studied. Specific capacitance faded rapidly over 100 cycles in 2 M KCl at a 5 mV s -1 scan rate.

  17. Electroslag remelt processing of irradiated vanadium alloys

    NASA Astrophysics Data System (ADS)

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

    1996-10-01

    This paper describes experimental efforts to investigate the potential of a slag remelting process for reducing radioactivity of irradiated vanadium alloys used in a fusion power production facility. The experiment determined the removal characteristics of four surrogate transmutation isotopes significant to accident safety expected in a V5Ti5Cr alloy irradiated under fusion conditions (Ca, Y, to simulate Sc, Mn, and Ar). Removal of these isotopes could decrease the accident risk of reprocessing irradiated vanadium and reusing it in fusion reactors. An electroslag remelt furnace was used in the experiment to melt and react the constituents using a calcium fluoride slag. The process achieved 90% removal of calcium and over 99% removal of yttrium. Analyses indicate that 40% of the manganese has been removed. Argon analysis of the refined ingots indicates that 99% of the argon was removed from the vanadium alloy.

  18. 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.

  19. 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.

  20. 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.

  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. PMID:25917693

  2. 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).

  3. Spectrophotometric determination of vanadium after extraction as vanadium(III) picolinate.

    PubMed

    Yatirajam, V; Arya, S P

    1979-01-01

    Vanadium(V) is conveniently reduced by sodium dithionite to vanadium(III) which is extracted as its picolinate complex into chloroform. Vanadium is determined spectrophotometrically by measuring the absorbance of the complex at 385 nm against a reagent blank, Beer's law being obeyed over the range 1-50 microg/ml. The method is one of the most selective, being free from interference by relatively high concentrations of almost all the important elements, titanium, chromium, manganese, iron, cobalt, nickel, zinc, copper, aluminium, molybdenum, tungsten and uranium, found in industrial alloys. Only bismuth interferes. The method is quite simple and rapid. It has been successfully applied for the analysis of vanadium in a variety of samples. PMID:18962377

  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%. PMID:25840036

  5. 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.

  6. 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.

  7. 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. PMID:26097040

  8. Posttranslational modification of a vanadium nitrogenase

    PubMed Central

    Heiniger, Erin K; Harwood, Caroline S

    2015-01-01

    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. PMID:26097040

  9. 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.

  10. Novel water soluble neutral vanadium(IV)-antibiotic complex: Antioxidant, immunomodulatory and molecular docking studies.

    PubMed

    Datta, Chitraniva; Das, Dharitri; Mondal, Paritosh; Chakraborty, Biswajit; Sengupta, Mahuya; Bhattacharjee, Chira R

    2015-06-01

    A novel water soluble five coordinate oxovanadium(IV) complex, [VO(C16H15N4O8S)HSO4] incorporating cefuroxime, a cephalosporin group of antibiotic have been prepared from an interaction of vanadyl sulfate and cefuroxime in aqueous solution. The compound was characterized by Fourier transform infrared spectroscopy (FTIR), CHN microanalyses, ultraviolet-visible spectroscopy (UV-Vis), fast atom bombardment (FAB) mass spectrometry and thermogravimetric analysis (TGA). Density Functional Theory (DFT) computation using Gaussian 09 program at B3LYP level revealed a distorted square pyramidal energy optimized geometry for the vanadyl(IV) complex. The molecular docking studies show that the interaction between the vanadium complex and protein receptor, clathrin is dominated by hydrophobic forces. The experimental (1)H nuclear magnetic resonance (NMR) features of the analogous Zn(II) complex matched well with the theoretically computed values further affirming the distorted square pyramidal geometry for the vanadyl(IV) complex. Cyclic voltammetry revealed a metal centered single-electron oxidation-reduction response for VO(IV)/VO(V) couple. The antioxidant activity of the vanadium(IV)-complex vis-à-vis the antibiotic has been assessed by 1,1-diphenyl-2-picrylhydrazyl (DPPH) method. The vanadium complex showed comparatively better radical scavenging ability compared to the antibiotic cefuroxime. The antimicrobial activity of the compound has been assayed for five different microbial strains using minimum inhibitory concentration (MIC) method. Immunomodulatory studies carried out using phagocytosis index, myeloperoxidase release and cytokine assay indicated the vanadium(IV)-complex to be immunosuppressant. The cytotoxicity of the compound was evaluated by MTT (3-(4, 5-dimethyl thiazol-2-yl)-2, 5-diphenyl tetrazolium bromide) reduction assay. PMID:25982330

  11. Aqueous production.

    PubMed

    Krupin, T; Wax, M; Moolchandani, J

    1986-01-01

    The formation of aqueous humour by the ciliary body is a complex process. Active transport of solutes by the ciliary process epithelium is an energy-dependent mechanism that selectively transports substances against an electrochemical gradient across the cell membranes. Water passively follows the active solute transport. In addition to these active transport processes, ultrafiltration contributes to the formation of aqueous humour. The ciliary epithelium contains enzyme systems that function in the production of aqueous humour. The enzymes sodium-potassium-activated adenosine triphosphatase [(Na+:K+)ATPase] and carbonic anhydrase participate in the active transport across this epithelium. Inhibition of these enzymes lowers intraocular pressure (IOP) by decreasing aqueous humour production. the ciliary epithelium contains both alpha- and beta-adrenergic receptors. Electrophysiologic studies on the isolated iris-ciliary body (I-CB) preparation provide a means to study direct effects of the adrenergic agents on transepithelial properties of the ciliary epithelium. This paper will discuss the enzymatic and adrenergic properties of the ciliary epithelium as they relate to active transport and thereby aqueous humour production. PMID:3026067

  12. 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. PMID:24997904

  13. Comparative analysis of electrophysical properties of ceramic tantalum pentoxide coatings, deposited by electron beam evaporation and magnetron sputtering methods

    NASA Astrophysics Data System (ADS)

    Donkov, N.; Mateev, E.; Safonov, V.; Zykova, A.; Yakovin, S.; Kolesnikov, D.; Sudzhanskaya, I.; Goncharov, I.; Georgieva, V.

    2014-12-01

    Ta2O5 ceramic coatings have been deposited on glass substrates by e-beam evaporation and magnetron sputtering methods. For the magnetron sputtering process Ta target was used. X-ray diffraction measurements show that these coatings are amorphous. XPS survey spectra of the ceramic Ta2O5 coatings were obtained. All spectra consist of well-defined XPS lines of Ta 4f, 4d, 4p and 4s; O 1s; C 1s. Ta 4f doublets are typical for Ta2O5 coatings with two main peaks. Scanning electron microscopy and atomic force microscopy images of the e-beam evaporated and magnetron sputtered Ta2O5 ceramic coatings have revealed a relatively flat surface with no cracks. The dielectric properties of the tantalum pentoxide coatings have been investigated in the frequency range of 100 Hz to 1 MHz. The electrical behaviour of e-beam evaporated and magnetron sputtered Ta2O5 ceramic coatings have also been compared. The deposition process conditions principally effect the structure parameters and electrical properties of Ta2O5 ceramic coatings. The coatings deposited by different methods demonstrate the range of dielectric parameters due to the structural and stoichiometric composition changes

  14. Evaluation of nickel-titanium oxide-niobium pentoxide metal ceramic composite as interconnect for solid oxide fuel cell

    NASA Astrophysics Data System (ADS)

    Budur, Abhijith

    With increasing importance for clean energy, fuel cells have gained great significance in recent decades. Solid oxide fuel cells are easy to transport due to presence of solid electrolyte and also have requisite electrical properties,but have been obstructed by their limitation to be used at only temperatures greater than 6000C and less than 8000C. To construct a stack of cells, materials that are good electrical conductors and having necessary mechanical strengths at that temperatures are being considered as interconnects between the cells. Evaluation of Nickel-Titanium dioxide-Niobium pentoxide (NTN) as interconnect and comparison to Stainless Steel 441 alloy has been made in this research. The criteria for evaluation are the resistance, long-term stability and the power density characteristics of the cell for each interconnect. Electrical measurements by impedance spectroscopy techniques were conducted at variousworking temperatures using a gas mixture of 10 % hydrogen and 90% nitrogen to evaluate both interconnect materials in the working range of fuel cells. Scanning Electron Microscopy images of Lanthanum Strontium Manganite paste before and after the fuel cell measurements are shown.The results showed that both NTN and Stainless Steel 441 interconnects exhibit similar electrical properties under operating conditions of the fuel cell. Since theNTN interconnect is less prone to corrosion and does not have the effect of chromium poisoning, it can be considered as a viable interconnect material for solid oxide fuel cells.

  15. Structure and function of vanadium compounds in living organisms.

    PubMed

    Rehder, D

    1992-01-01

    Vanadium has been recognized as a metal of biological importance only recently. In this mini-review, its main functions uncovered during the past few years are addressed. These encompass (i) the regulation of phosphate metabolizing enzymes (which is exemplified for the inhibition of ribonucleases by vanadate), (ii) the halogenation of organic compounds by vanadate-dependent non-heme peroxidases from seaweeds, (iii) the reductive protonation of nitrogen (nitrogen fixation) by alternative, i.e. vanadium-containing, nitrogenases from N2-fixing bacteria, (iv) vanadium sequestering by sea squirts (ascidians), and (v) amavadine, a low molecular weight complex of V(IV) accumulated in the fly agaric and related toadstools. The function of vanadium, while still illusive in ascidians and toadstools, begins to be understood in vanadium-enzyme interaction. Investigations into the structure and function of model compounds play an increasingly important role in elucidating the biological significance of vanadium. PMID:1392470

  16. Chloride supporting electrolytes for all-vanadium redox flow batteries.

    PubMed

    Kim, Soowhan; Vijayakumar, M; Wang, Wei; Zhang, Jianlu; Chen, Baowei; Nie, Zimin; Chen, Feng; Hu, Jianzhi; Li, Liyu; Yang, Zhenguo

    2011-10-28

    This paper examines vanadium chloride solutions as electrolytes for an all-vanadium redox flow battery. The chloride solutions were capable of dissolving more than 2.3 M vanadium at varied valence states and remained stable at 0-50 °C. The improved stability appeared due to the formation of a vanadium dinuclear [V(2)O(3)·4H(2)O](4+) or a dinuclear-chloro complex [V(2)O(3)Cl·3H(2)O](3+) in the solutions over a wide temperature range. The all-vanadium redox flow batteries with the chloride electrolytes demonstrated excellent reversibility and fairly high efficiencies. Only negligible, if any, gas evolution was observed. The improved energy capacity and good performance, along with the ease in heat management, would lead to substantial reduction in capital cost and life-cycle cost, making the vanadium chloride redox flow battery a promising candidate for stationary applications. PMID:21922094

  17. 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.

  18. Biotinylated vanadium and chromium sulfide nanoparticles as probes for colocalization of membrane proteins.

    PubMed

    Loukanov, Alexandre; Emin, Saim

    2016-09-01

    We report the microemulsion synthesis of vanadium and chromium sulfide nanoparticles (NPs) and their biological application as nanoprobes for colocalization of membrane proteins. Spherical V2 S3 and Cr2 S3 NPs were prepared in reverse microemulsion droplets, as nanoreactors, obtained by the surfactant sodium bis(2-ethylhexyl) sulfosuccinate (AOT) in nonpolar organic phase (heptane). Electron microscopic data indicated that the size distribution of the nanoparticles was uniform with an average diameter between 3 ÷ 5 nm. The prepared hydrophobic nanocrystals were transferred in aqueous phase by surface cap exchange of AOT with biotin-dihydrolipoic ligands. This substitution allows the nanoparticles solubility in aqueous solutions and confer their bioactivity. In addition, we report the conjugation procedure between α-Lipoic acid (LA) and biotin (abbreviated as biotin-LA). The biotin-LA structure was characterized by 1D and 2D NMR spectroscopy. The biotinylated vanadium and chromium sulfide nanoparticles were tested as probes for colocalization of glutamate receptors on sodium-dodecyl-sulfate-digested replica prepared from rat hippocampus. The method suggests their high labeling efficiency for study of membrane biological macromolecules. Microsc. Res. Tech. 79:799-805, 2016. © 2016 Wiley Periodicals, Inc. PMID:27312069

  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. 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. PMID:24442345

  1. Electrorefining of carbothermic and carbonitrothermic vanadium: a comparative study

    SciTech Connect

    Tripathy, P.K.; Rakhasia, R.H.; Hubli, R.C.; Suri, A.K

    2003-06-19

    Electrorefining is a very effective technique for transforming impure vanadium to a state of high purity. Besides being semi-continuous in nature, this process removes all the interstitial impurities to well below their respective tolerable limits, together with a number of commonly associated metallic impurities. Among different types of vanadium materials used for anode feed, carbothermic vanadium is not only relatively, less costly and easy to prepare, but also could be electrorefined into high purity vanadium. However, the presence of relatively high amount of carbon in the anode feed critically affects the electrorefining process resulting in lesser purity and poorer recovery of the vanadium. In the present study, a low-cost vanadium intermediate, essentially a solid solution of vanadium, nitrogen, carbon and oxygen was studied for electrorefining. The anode feed, containing {approx}94% vanadium, was prepared by nitridation-cum-denitridation of a mixture, comprised of V{sub 2}O{sub 5} and petroleum coke powders. The electrorefining was carried out in a LiCl-KCl-VCl{sub 2} bath at 893 K under high purity argon atmosphere. The current efficiency, vanadium recovery and purity were 90, 86, and 99.85%, respectively.

  2. Thermochromic Vanadium Oxide Coatings Grown by APCVD at Low Temperatures

    NASA Astrophysics Data System (ADS)

    Louloudakis, Dimitris; Vernardou, Dimitra; Spanakis, Emmanuel; Katsarakis, Nikolaos; Koudoumas, Emmanuel

    Amorphous vanadium dioxide coatings were deposited on SnO2-precoated glass substrates at 400 oC by atmospheric pressure chemical vapor deposition for various vanadium precursor flow rates. The coatings were characterized by X-ray diffraction, Raman spectroscopy, Fourier transform infrared spectroscopy and scanning electron microscopy. Their thermochromic performance has been found to be independent on the vanadium (V) triisopropoxide flow rates. All vanadium dioxide films present a reversible transition behavior at 68 oC as derived from the transmittance studies.

  3. Mineralogy and geochemistry of vanadium in the Colorado Plateau

    USGS Publications Warehouse

    Weeks, A.D.

    1961-01-01

    The chief domestic source of vanadium is uraniferous sandstone in the Colorado Plateau. Vanadium is 3-, 4-, or 5-valent in nature and, as oxides or combined with other elements, it forms more than 40 minerals in the Plateau ores. These ores have been studied with regard to the relative amounts of vanadium silicates and oxide-vanadates, uranium-vanadium ratios, the progressive oxidation of black low-valent ores to high-valent carnotite-type ores, and theories of origin. ?? 1961.

  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. 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.

  6. 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. PMID:18963866

  7. Quantitative chemical state analysis of supported vanadium oxide catalysts by high resolution vanadium Kα spectroscopy.

    PubMed

    Yamamoto, Takashi; Nanbu, Fumitaka; Tanaka, Tsunehiro; Kawai, Jun

    2011-03-01

    Oxidation states of vanadium species on Al(2)O(3), SiO(2), and TiO(2) were quantitatively analyzed by least-squares fitting of V Kα spectra recorded with a two-crystal X-ray fluorescence spectrometer. Uncertainties of analytical results by the normalization procedure, and coefficient of validation and the reduction behavior of vanadium species by X-ray irradiation were discussed. The V(5+)/V(4+)/V(3+) ratios on Al(2)O(3), SiO(2), and TiO(2) calcined at 773 K in air were determined to be ca. 6/3/1, 3/6/1, and 5/4/1, respectively. The possible chemical states of vanadium species on supports were proposed. PMID:21302919

  8. Effect of neutron irradiation on vanadium alloys

    SciTech Connect

    Braski, D.N.

    1986-01-01

    Neutron-irradiated vanadium alloys were evaluated for their susceptibility to irradiation hardening, helium embrittlement, swelling, and residual radioactivity, and the results were compared with those for the austenitic and ferritic stainless steels. The VANSTAR-7 and V-15Cr-5Ti alloys showed the greatest hardening between 400 and 600/sup 0/C while V-3Ti-1Si and V-20Ti had lower values that were comparable to those of ferritic steels. The V-15Cr-5Ti and VANSTAR-7 alloys were susceptible to helium embrittlement caused by the combination of weakened grain boundaries and irradiation-hardened grain matrices. Specimen fractures were entirely intergranular in the most severe instances of embrittlement. The V-3Ti-1Si and V-20Ti alloys were more resistant to helium embrittlement. Except for VANSTAR-7 irradiated to 40 dpa at 520/sup 0/C, all of the vanadium alloys exhibited low swelling that was similar to the ferritic steels. Swelling was greater in specimens that were preimplanted with helium using the tritium trick. The vanadium alloys clearly exhibit lower residual radioactivity after irradiation than the ferrous alloys.

  9. 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. PMID:24641550

  10. Vanadium metabolism in sheep. I. Comparative and acute toxicity of vanadium compounds in sheep.

    PubMed

    Hansard, S L; Ammerman, C B; Henry, P R; Simpson, C F

    1982-08-01

    Twelve Florida native wethers were given ammonium metavandate, calcium orthovanadate and calcium pyrovanadate by capsule in a study to examine the toxicity of the compounds. The initial daily dosage of 100 mg elemental vanadium was increased by 50 mg at 2-d intervals for an assessment not only of the toxic effects, but also to determined the amount that caused a decline in feed intake to 25% of that of control animals. The initial decline in feed intake was observed at 400 to 500 mg vanadium/d (9.6 to 12 mg/kg body weight, 310 to 350 ppm); a rapid decline in feed intake was accompanied by diarrhea. One sheep fed 550 mg vanadium as calcium orthovanadate died 3 d after dosing. One animal on each of the other three treatments was killed and necropsied for immediate comparison. Extensive mucosal hemorrhage of the small intestine and diffuse or petechial subcapsular hemorrhages of the kidneys were observed for sheep fed all compounds. The three vanadium compounds appeared to be similar in toxicity, as determined by abrupt declines in feed intake and pathological changes of the intestine and kidney. For a determination of acute toxicosis, three sheep were given 40 mg/kg body weight of vanadium as NH4VO3 in gelatin capsules and two sheep were included as controls. Two of the treated animals died within 80 h after administration and the other three were killed at 96 h. Vanadium content of kidney, liver, bone, spleen, lung and muscle was elevated by treatment. PMID:6982890

  11. 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.

  12. 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).

  13. 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.

  14. 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

    2014-11-01

    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. PMID:25097094

  15. 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.

  16. Surface characterization and reactivity of vanadium-tin oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Wang, Chien-Tsung; Chen, Miao-Ting; Lai, De-Lun

    2011-03-01

    Surface state and reactivity of vanadium-tin mixed oxide nanoparticles (V/Sn ratios 0.05-0.2) were characterized by spectroscopic techniques and catalytic measurements. Analyses by X-ray photoelectron spectroscopy (XPS) and diffuse reflectance spectroscopy (DRS) revealed that the oxidation state and surface structure of vanadium oxide species and the electronic interaction between Sn and V atoms are dependent upon the vanadium content. These oxides were evaluated as catalysts for methanol oxidation in a fixed-bed reactor. Both reaction rate and formaldehyde selectivity increased with increasing the vanadium amount in catalyst. Results demonstrate that the V 5+ site in the bridging V-O-Sn structure exhibits a high redox activity to facilitate the transformation of adsorbed methoxy to formaldehyde and that the vanadium dispersion plays a crucial role in the surface reactivity. A mechanism that elucidates the catalytic redox process is proposed.

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

    PubMed

    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

  18. 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.

  19. 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.

  20. 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

  1. The vanadium-iron protein of vanadium nitrogenase from Azotobacter chroococcum contains an iron-vanadium cofactor.

    PubMed Central

    Smith, B E; Eady, R R; Lowe, D J; Gormal, C

    1988-01-01

    N-Methylformamide extracts of acid-treated precipitated VFe protein of the V-nitrogenase of Azotobacter chroococcum are yellow-brown in colour and contain vanadium, iron and acid-labile sulphur in the approximate proportions 1:6:5. E.p.r. spectra of the extracts exhibit a weak signal with g values near 4.5, 3.6 and 2.0 characteristic of an S = 3/2 metal-containing centre. The N-methylformamide extracts activated the MoFe protein polypeptides from mutants of nitrogen-fixing bacteria unable to synthesize FeMoco, the active centre of Mo-nitrogenase. The active hybrid protein exhibited the characteristic substrate-reducing phenotype associated with the VFe protein except that it could not reduce N2 to NH3. The above data are interpreted as demonstrating the existence of an iron- and vanadium-containing cofactor, FeVaco, within the VFe protein. It is suggested that nitrogen fixation requires specific interactions between FeVaco or FeMoco and their respective polypeptides. The biosynthesis of these cofactors is discussed. PMID:2833236

  2. 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.

  3. Vanadium induced ultrastructural changes and apoptosis in male germ cells.

    PubMed

    Aragón, M A; Ayala, M E; Fortoul, T I; Bizarro, P; Altamirano-Lozano, M

    2005-01-01

    Vanadium is a transition metal that is emitted to the atmosphere during combustion of fossil fuels. In the environment, vanadium occurs in the (V) oxidized form, but in the body it is found exclusively in the (IV) oxidized form. Vanadium tetraoxide is an inorganic chemical species in the (IV) oxidized form that has been shown to induce toxic effects in vitro and in vivo. The reproductive toxicity of vanadium in males was studied through monitoring germ cell apoptosis during spermatogenesis. We analyzed ultrastructural damage, and testosterone and progesterone concentrations following vanadium tetraoxide administered to male mice for 60 days. Spermatogenesis stages I-III and X-XII frequently showed apoptotic germ cells in control and treated animals; vanadium tetraoxide treatment induced an increase in the number of germ cell apoptosis in stages I-III and XII at 9.4 and 18.8 mg/kg, respectively. Although spermatogenesis is regulated by testosterone, in our study this hormone level was not modified by vanadium administration; thus, germ cell death was not related with testosterone concentration. At the ultrastructural level, we observed inclusion structures that varied as to location and content in the Sertoli and germ cells. PMID:15808796

  4. Acute toxicity of vanadium to the threespine stickleback, Gasterosteus aculeatus

    SciTech Connect

    Gravenmier, J.J.; Johnston, D.W.; Arnold, W.R.

    2005-02-15

    Vanadium is widely distributed, occurring in many types of minerals, coal, and petroleum. Anthropogenic sources of vanadium originate from the production, processing, and wastes of these materials. The aquatic toxicity of vanadium to fish species is not well characterized. This study focused on the three-spined stickleback, Gasterosteus aculeatus, a small and widely distributed euryhaline species of fish. The three-spined stickleback is used as an effluent-monitoring species in both Canada and the United States. Five 96-h static renewal acute toxicity tests were performed in moderately hard water with adult fish. The geometric mean and range of the five 96-h LC{sup 50}s based on measured concentrations of total vanadium in the test solution were 3.17 and 2.35-4.07 mg V/L, respectively. A conservative estimation of a safe concentration of vanadium that would not affect survival of adult three-spined sticklebacks over a 96-h exposure period in moderately hard water is approximately 0.30 mg V/L. A comparison with other fish species previously tested suggests that the three-spined stickleback is intermediate in sensitivity to vanadium. Information reported from this study may be useful in effluent toxicity identification evaluations and ecological risk assessments related to vanadium.

  5. Chemical state of vanadium in tin-based yellow pigment

    SciTech Connect

    Fujiyoshi, Kaichi; Yokoyama, Hisanori ); Ren, Feng; Ishida, Shingo . Dept. of Chemistry and Materials Technology)

    1993-04-01

    Vanadium-tin composite oxides are rather widely used as, for example, yellow pigments for coloring glazes and selective oxidation catalysts for hydrocarbons. Physicochemical states of vanadium in V-doped SnO[sub 2] were studied to clarify the origin of the color of vanadium-tin yellow pigment and its color instability when fired with glaze material. Precision measurements of lattice parameters of V-doped SnO[sub 2] revealed that vanadium was dissolved as V[sup 4+] and its solubility limit was 0.9 wt% as V[sub 2]O[sub 5]. It was found that the color of vanadium-tin yellow was produced by two types of undissolved vanadium on SnO[sub 2] grains. One is poorly crystallized vanadium oxide (v), (V[sub 2]O[sub 5])[prime], having a yellow color, and the other is orange-colored crystalline V[sub 2]O[sub 5]. The structure of (V[sub 2]O[sub 5])[prime] was discussed in connection with its color.

  6. V6O13 films by control of the oxidation state from aqueous precursor to crystalline phase.

    PubMed

    Peys, Nick; Ling, Yun; Dewulf, Daan; Gielis, Sven; De Dobbelaere, Christopher; Cuypers, Daniel; Adriaensens, Peter; Van Doorslaer, Sabine; De Gendt, Stefan; Hardy, An; Van Bael, Marlies K

    2013-01-28

    An aqueous deposition process for V(6)O(13) films is developed whereby the vanadium oxidation state is continuously controlled throughout the entire process. In the precursor stage, a controlled wet chemical reduction of the vanadium(V) source with oxalic acid is achieved and monitored by (51)Vanadium Nuclear Magnetic Resonance ((51)V-NMR) and Ultraviolet-Visible (UV-Vis) spectroscopy. The resulting vanadium(IV) species in the aqueous solution are identified as mononuclear citrato-oxovanadate(IV) complexes by Electron Paramagnetic Resonance (EPR) and Fourier Transform Infra-Red (FTIR) spectroscopy. This precursor is successfully employed for the deposition of uniform, thin films. The optimal deposition and annealing conditions for the formation of crystalline V(6)O(13), including the control of the vanadium oxidation state, are determined through an elaborate study of processing temperature and O(2) partial pressure. To ensure a sub 100 nm adjustable film thickness, a non-oxidative intermediate thermal treatment is carried out at the end of each deposition cycle, allowing maximal precursor decomposition while still avoiding V(IV) oxidation. The resulting surface hydrophilicity, indispensable for the homogeneous deposition of the next layer, is explained by an increased surface roughness and the increased availability of surface vanadyl groups. Crystalline V(6)O(13) with a preferential (002) orientation is obtained after a post deposition annealing in a 0.1% O(2) ambient for thin films with a thickness of 20 nm. PMID:23108392

  7. Separation of tracer titanium-44 from vanadium

    SciTech Connect

    Sajjad, M.; Lambrecht, R.M.

    1986-03-01

    The trend in medical radionuclide and radiopharmaceutical research and development is toward the use of short-lived neutron-deficient nuclides. Biomedical generators that deliver positron-emitting nuclides will be an important source of these nuclides. The /sup 44/Ti-/sup 44/Sc generator (/sup 44/Ti(t/sub 1/2/ = 4 years), /sup 44/Sc (t/sub 1/2/ = 3.93 h)) has been suggested previously. Titanium-44 produced by the /sup 45/Sc(p,2n)/sup 44/Ti reaction is commercially available only in very limited quantities. The authors have found that /sup 44/Ti can also be produced by the /sup 51/V(p,2p6n)/sup 44/Ti nuclear reaction by irradiating a vanadium target with high-energy protons. A new separation method was required in order to recover /sup 44/Ti without added carrier. The authors have developed a new method for the separation of titanium from vanadium.

  8. Vanadium alloys - overview and recent results

    NASA Astrophysics Data System (ADS)

    Muroga, T.; Nagasaka, T.; Abe, K.; Chernov, V. M.; Matsui, H.; Smith, D. L.; Xu, Z.-Y.; Zinkle, S. J.

    2002-12-01

    This paper reviews recent progress in research on vanadium alloys with emphasis on V-4Cr-4Ti as a reference composition. New high purity V-4Cr-4Ti ingots and products (NIFS-HEATs) were made. The improved purity of the alloys made a practical demonstration of enhanced feasibility of recycling as a method of handling after use in fusion reactors. Significant progress has been made in the understanding of physical metallurgy of V-4Cr-4Ti and effects of O, N and C on the alloy properties such as low and high temperature mechanical properties, welding properties and low temperature irradiation effects, by means of including the comparison of various large heats and model alloys with different impurity levels. The effects of other trace impurities on some of the properties are also discussed. Other current efforts to characterize V-4Cr-4Ti, to improve its properties and to explore advanced vanadium alloys are reviewed. Issues remaining for the future investigations are discussed.

  9. 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 .

  10. 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.

  11. 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.

  12. Determining vanadium in titanium alloys by extraction voltammetry

    SciTech Connect

    Ulakhovich, N.A.; Shaidarova, L.G.; Beloglazova, A.D.; Naida, N.E. Akhmetzyanova, I.R.; Barkhanova, D.E.

    1987-01-01

    This study is a continuation of the authors developments in solvent-extraction voltammetric methods of determining alloying components in layerwise alloy analysis. Titanium alloys are dissolved by electrolysis in an electrolyte containing methanol. Logarithms provided in the study give the separation constants for the vanadium mercaptoquinolinates which indicate that molten naphthalene is the most effective extraction agent. This method has been applied to VT-6ch titanium alloy containing vanadium and aluminum. The authors checked the results by using the slower atomic emission check method with coincidental results. Extraction ACV indicates that there is not more than 0.01% vanadium in the core of the specimen.

  13. Vanadium and nickel in petroleums of bituminous Tatar rocks

    SciTech Connect

    Aigistova, S.Kh.; Safiullina, G.Kh.; Sadykov, A.N.; Kharlamov, V.A.

    1984-01-01

    The vanadium and nickel contents of petroleum obtained from bituminous rock of Ashal'chinsk, Akhmat, Gorskii, Katerchinsk, Klinsk (Studeno-Klyuchev), West-Chumachkin, Mordovian-Karmal' and Pokrov deposits, was determined polarographically. The vanadium concentration range in these petroleums is 0.01-0.09 and nickel 0.009-0.05 wt.%. According to results previously obtained, vanadium and nickel contents in ordinary petroleum of this country are no higher than 0.010 and 0.0014 wt.%, respectively. 3 references, 1 table.

  14. Surfactant-Free Vanadium Oxides from Reverse Micelles and Organic Oxidants: Solution Processable Nanoribbons with Potential Applicability as Battery Insertion Electrodes Assembled in Different Configurations.

    PubMed

    Tartaj, Pedro; Amarilla, Jose M; Vazquez-Santos, Maria B

    2015-11-17

    Vanadium oxides similar to other metal transition oxides are prototypes of multifunctionality. Implementing new synthesis routes that lead to dry vanadium oxide nanomaterials with good functional and structural properties as well as good processing capabilities is thus of general interest. Here we report a facile method based on reverse micelles for the growth at room temperature and atmospheric pressure of surfactant-free vanadium oxide nanoribbons that retain after drying excellent solution-processable capabilities. Essential for the success of the method is the use of a soluble organic oxidant that acts as oxidant and cosurfactant during the synthesis, and facilitates surfactant removal with a simple washing protocol. Interestingly, this simple surfactant removal protocol could be of general applicability. As a proof-of-concept of the functional, structural, and processing capabilities of the dry vanadium oxide nanoribbons here prepared, we have checked their lithium insertion capabilities as battery cathodes built upon different configurations. Specifically, we show efficient insertion both in dry nanoribbons processed as films using doctor blade and organic solvents and in dry nanoribbons infiltrated in three-dimensional metal collectors from aqueous suspensions. PMID:26513340

  15. Vanadium K-edge XANES in vanadium-bearing model compounds: a full multiple scattering study.

    PubMed

    Benzi, Federico; Giuli, Gabriele; Della Longa, Stefano; Paris, Eleonora

    2016-07-01

    A systematic study is presented on a set of vanadium-bearing model compounds, representative of the most common V coordination geometries and oxidation states, analysed by means of vanadium K-edge X-ray absorption near-edge spectroscopy calculations in the full multiple scattering (FMS) framework. Analysis and calibration of the free parameters of the theory under the muffin-tin approximation (muffin-tin overlap and interstitial potential) have been carried out by fitting the experimental spectra using the MXAN program. The analysis shows a correlation of the fit parameters with the V coordination geometry and oxidation state. By making use of this correlation it is possible to approach the study of unknown V-bearing compounds with useful preliminary information. PMID:27359143

  16. The atomic configuration of graphene/vanadium carbide interfaces in vanadium carbide-encapsulating carbon nanocapsules.

    PubMed

    Yazaki, Gaku; Matsuura, Daisuke; Kizuka, Tokushi

    2014-03-01

    Carbon nanocapsules (CNCs) encapsulating vanadium carbide (VC) nanocrystals with a NaCI structure were synthesized by a gas-evaporation method using arc-discharge heating. The CNCs were observed by high-resolution transmission electron microscopy. The VC nanocrystals within the nanospaces of CNCs were truncated by low-index facets and were coated with several graphene layers, forming graphene/VC interfaces. The atomic configuration and interlayer spacings at the interfaces were found. PMID:24745251

  17. 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. PMID:26901732

  18. 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

  19. 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

  20. Influence of vanadium on serum lipid and lipoprotein profiles: a population-based study among vanadium exposed workers

    PubMed Central

    2014-01-01

    Background Some experimental animal studies reported that vanadium had beneficial effects on blood total cholesterol (TC) and triglyceride (TG). However, the relationship between vanadium exposure and lipid, lipoprotein profiles in human subjects remains uncertain. This study aimed to compare the serum lipid and lipoprotein profiles of occupational vanadium exposed and non-exposed workers, and to provide human evidence on serum lipid, lipoprotein profiles and atherogenic indexes changes in relation to vanadium exposure. Methods This cross-sectional study recruited 533 vanadium exposed workers and 241 non-exposed workers from a Steel and Iron Group in Sichuan, China. Demographic characteristics and occupational information were collected through questionnaires. Serum lipid and lipoprotein levels were measured for all participants. The ratios of total cholesterol to high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) to HDL-C and apoB to apoA-I were used as atherogenic indexes. A general linear model was applied to compare outcomes of the two groups while controlling possible confounders and multivariate logistic regression was performed to evaluate the relationship between low HDL-C level, abnormal atherogenic index and vanadium exposure. Results Higher levels of HDL-C and apoA-I could be observed in the vanadium exposed group compared with the control group (P < 0.05). Furthermore, atherogenic indexes (TC/HDL-C, LDL-C/HDL-C, and apoB/apoA-I ratios) were found statistically lower in the vanadium exposed workers (P < 0.05). Changes in HDL-C, TC/HDL-C, and LDL-C/HDL-C were more pronounced in male workers than that in female workers. In male workers, after adjusting for potential confounding variables as age, habits of smoking and drinking, occupational vanadium exposure was still associated with lower HDL-C (OR 0.41; 95% CI, 0.27-0.62) and abnormal atherogenic index (OR 0.38; 95% CI, 0.20-0.70). Conclusion Occupational

  1. 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. PMID:26361086

  2. 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

  3. Layered Vanadium and Molybdenum Oxides: Batteries and Electrochromics

    SciTech Connect

    Chernova, N. A.; Roppolo, M.; Dillon, A. C.; Whittingham, M. S.

    2009-01-01

    The layered oxides of vanadium and molybdenum have been studied for close to 40 years as possible cathode materials for lithium batteries or electrochromic systems. The highly distorted metal octahedra naturally lead to the formation of a wide range of layer structures, which can intercalate lithium levels exceeding 300 Ah/kg. They have found continuing success in medical devices, such as pacemakers, but many challenges remain in their application in long-lived rechargeable devices. Their high-energy storage capability remains an encouragement to researchers to resolve the stability concerns of vanadium dissolution and the tendency of lithium and vanadium to mix changing the crystal structure on cycling the lithium in and out. Nanomorphologies have enabled higher reactivities to be obtained for both vanadium and molybdenum oxides, and with the latter show promise for electrochromic displays.

  4. 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. PMID:25697901

  5. TEM investigation of ductile iron alloyed with vanadium.

    PubMed

    Dymek, S; Blicharski, M; Morgiel, J; Fraś, E

    2010-03-01

    This article presents results of the processing and microstructure evolution of ductile cast iron, modified by an addition of vanadium. The ductile iron was austenitized closed to the solidus (1095 degrees C) for 100 h, cooled down to 640 degrees C and held on at this temperature for 16 h. The heat treatment led to the dissolution of primary vanadium-rich carbides and their subsequent re-precipitation in a more dispersed form. The result of mechanical tests indicated that addition of vanadium and an appropriate heat treatment makes age hardening of ductile iron feasible. The precipitation processes as well as the effect of Si content on the alloy microstructure were examined by scanning and transmission electron microscopy. It was shown that adjacent to uniformly spread out vanadium-rich carbides with an average size of 50 nm, a dispersoid composed of extremely small approximately 1 nm precipitates was also revealed. PMID:20500418

  6. 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.

  7. Raoult's Law Study of Vanadium Pentafluoride in Uranium Hexafluoride.

    PubMed

    Shrewsberry, R C; Musulin, B

    1964-09-25

    Binary systems of liquid vanadium pentafluoride dissolved in liquid uranium hexafluoride are non-ideal, with negative deviations from Raoult's law in the temperature range 75 degrees to 92 degrees C. PMID:17838706

  8. 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%.

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. 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

  16. 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

  17. 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

  18. 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

  19. 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

  20. 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

  1. 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

  2. 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

  3. 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.

  4. Nanostructured Electrocatalysts for All-Vanadium Redox Flow Batteries.

    PubMed

    Park, Minjoon; Ryu, Jaechan; Cho, Jaephil

    2015-10-01

    Vanadium redox reactions have been considered as a key factor affecting the energy efficiency of the all-vanadium redox flow batteries (VRFBs). This redox reaction determines the reaction kinetics of whole cells. However, poor kinetic reversibility and catalytic activity towards the V(2+)/V(3+) and VO(2+)/VO2(+) redox couples on the commonly used carbon substrate limit broader applications of VRFBs. Consequently, modified carbon substrates have been extensively investigated to improve vanadium redox reactions. In this Focus Review, recent progress on metal- and carbon-based nanomaterials as an electrocatalyst for VRFBs is discussed in detail, without the intention to provide a comprehensive review on the whole components of the system. Instead, the focus is mainly placed on the redox chemistry of vanadium ions at a surface of various metals, different dimensional carbons, nitrogen-doped carbon nanostructures, and metal-carbon composites. PMID:25899910

  5. 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)

  6. 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.

  7. 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.

  8. Crystal chemistry of the natural vanadium bronzes

    USGS Publications Warehouse

    Evans, H.T., Jr.; 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

  9. Vanadium Nitrogenase: A Two-Hit Wonder?

    PubMed Central

    Hu, Yilin; Lee, Chi Chung; Ribbe, Markus W.

    2013-01-01

    Nitrogenase catalyzes the biological conversion of atmospheric dinitrogen to bioavailable ammonia. The molybdenum (Mo)- and vanadium (V)-dependent nitrogenases are two homologous members of this metalloenzyme family. However, despite their similarities in structure and function, the characterization of V-nitrogenase has taken a much longer and more winding path than that of its Mo-counterpart. From the initial discovery of this nitrogen-fixing system, to the recent finding of its CO-reducing capacity, V-nitrogenase has proven to be a two-hit wonder in the over-a-century-long research of nitrogen fixation. This perspective provides a brief account of the catalytic function and structural basis of V-nitrogenase, as well as a short discussion of the theoretical and practical potentials of this unique metalloenzyme. PMID:22101422

  10. Vanadium nitrogenase: a two-hit wonder?

    PubMed

    Hu, Yilin; Lee, Chi Chung; Ribbe, Markus W

    2012-01-28

    Nitrogenase catalyzes the biological conversion of atmospheric dinitrogen to bioavailable ammonia. The molybdenum (Mo)- and vanadium (V)-dependent nitrogenases are two homologous members of this metalloenzyme family. However, despite their similarities in structure and function, the characterization of V-nitrogenase has taken a much longer and more winding path than that of its Mo-counterpart. From the initial discovery of this nitrogen-fixing system, to the recent finding of its CO-reducing capacity, V-nitrogenase has proven to be a two-hit wonder in the over-a-century-long research of nitrogen fixation. This perspective provides a brief account of the catalytic function and structural basis of V-nitrogenase, as well as a short discussion of the theoretical and practical potentials of this unique metalloenzyme. PMID:22101422

  11. Stable Vanadium Isotope Fractionation at High Temperatures

    NASA Astrophysics Data System (ADS)

    Prytulak, J.; Parkinson, I. J.; Savage, P. S.; Nielsen, S. G.; Halliday, A. N.

    2011-12-01

    Vanadium is a redox sensitive transition metal existing in multiple valence states at terrestrial conditions. Stable vanadium isotopes (reported as δ51V in % relative to an Alfa Aesar standard [1]) are a potentially powerful tracer of oxidation-reduction processes. However, the determination of δ51V is analytically challenging, primarily due to the extreme abundance ratio between the only two stable isotopes (51V/50V ~ 400) and, also, significant isobaric interferences of 50Ti and 50Cr on the minor 50V isotope. We have developed the first method able to determine δ51V to a precision (2 s.d. ~ 0.15%, [1,2]) that enables application of this isotope system to geological processes. To usefully investigate high temperature processes using vanadium isotopes, knowledge of the isotope composition and range of values present in the ambient mantle is required. Here we discuss the first δ51V measured in igneous materials encompassing peridotites, MORB, and primitive mantle-derived melts such as picrites. This first dataset provides a preliminary reconnaissance of the magnitude of natural fractionation. We find little isotope fractionation in suites of peridotites and MORB (< 0.5 %). However, the small but analytically significant variation appears to be related to secondary processes, with extremely altered peridotites consistently displaying slightly heavier isotope compositions. We find no resolvable δ51V variation between fresh MORB glass and fresh peridotite. Intriguingly, a suite of subduction-related peridotites from the Mariana forearc, previously characterized for fO2 [3], do not display the predicted co-variation between δ51V and fO2, but instead also have compositions identical to MORB glass. This nominally supports recent indications that there is limited difference in the oxygen fugacity of the MORB source and the subarc mantle wedge [e.g., 4, 5]. Finally, we observe large δ51V variations (~ 2 %) in a suite of evolving lavas from Hekla volcano, Iceland

  12. Economics of vanadium redox flow battery membranes

    NASA Astrophysics Data System (ADS)

    Minke, Christine; Turek, Thomas

    2015-07-01

    The membrane is a key component of the vanadium redox flow battery (VRFB) in terms of electrochemical performance as well as costs. The standard material Nafion® is cost intensive and therefore several alternative materials are in the focus of research. In this paper a substantial analytical approach is presented in order to quantify bottom price limits for different types of membranes. An in-depth analysis of material and production cost allows statements concerning cost potentials of different ion exchange membranes (IEM) and nano filtration membranes (NFM). The final result reveals that expected costs of IEM and NFM at high production volumes differ by one order of magnitude. Moreover, an analysis of the current market situation is made to provide a framework for economic considerations at present.

  13. Advances in Development of Vanadium Alloys and MHD Insulator Coatings

    SciTech Connect

    Muroga, Takeo; Chen, J M; Chernov, V M; Fukumoto, K; Hoelzer, David T; Kurtz, Richard; Nagasaka, T; Pint, Bruce A; Satou, M; Suzuki, Akihiro; Watanabe, H

    2007-01-01

    Recent progress in the development of low activation vanadium alloys and MHD insulator coatings for a Li-self cooled blanket is reviewed. Research progress in vanadium alloys is highlighted by technology for fabricating creep tubes, comparison of thermal creep in vacuum and Li, understanding impurity transfer between vanadium alloys and Li and its impact on mechanical properties, behavior of hydrogen and hydrogen isotopes, low dose irradiation effects on weld joints, and exploration for advanced vanadium alloys. Major remaining issues for vanadium alloys are thermal and irradiation creep, helium effects on high-temperature mechanical properties and radiation effects on low-temperature fracture properties. Er2O3 showed good compatibility with Li, and is promising as a MHD insulator coating on vanadium alloys. Significant progress in coating technology for this material has been made. Recent efforts are focused on multi-layer and in-situ coatings. Tests under flowing lithium conditions with a temperature gradient are necessary for quantitative examination of coating performance.

  14. 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.

  15. 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.

  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). PMID:23611800

  17. 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.

  18. 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

    2008-07-01

    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. PMID:18510311

  19. 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.

  20. 76 FR 78888 - Final Results of Expedited Sunset Review: Ferrovanadium and Nitrided Vanadium From Russia

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-20

    ... scrap, vanadium- bearing raw materials, such as slag, boiler residues, fly ash, and vanadium oxides. The... Initiation of Five-Year (``Sunset'') Review, 76 FR 54430 (September 1, 2011). The Department received...

  1. 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.

  2. 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.

  3. 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...

  4. 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.

  5. 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...

  6. 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...

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

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 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...

  8. 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...

  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, 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...

  11. 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.

  12. 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.

  13. 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.

  14. Membrane Development for Vanadium Redox Flow Batteries

    SciTech Connect

    Schwenzer, Birgit; Zhang, Jianlu; Kim, Soowhan; Li, Liyu; Liu, Jun; Yang, Zhenguo

    2011-10-17

    Large-scale energy storage has become a 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{reg_sign} as the preferred membrane material is responsible for {approx}11% of the overall cost of a 1 MW/8 MWh system. Therefore in recent years two main membrane-related research threads have emerged: (a) chemical and physical modification of Nafion membranes to optimize their properties with regard to vanadium redox flow battery (VRFB) application; and (b) replacement of the Nafion membranes with different, less expensive materials. This review summarizes the underlying basic science 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.

  15. Magnetism in Bulk Vanadium Dioxide Compounds

    NASA Astrophysics Data System (ADS)

    Mengyan, P. W.; Lichti, R. L.; Baker, B. B.; Jayarathna, G.

    2015-03-01

    Vanadium dioxide (VO2) compounds show a metal-semiconductor transition (MST) near room temperature (stoichiometric VO2 is metallic T >TMST ~ 340 K and semiconducting T

  16. Hydrogen and deuterium diffusion in vanadium alloys

    SciTech Connect

    Herro, H.M.

    1982-01-01

    Hydrogen and deuterium diffusion coefficients were measured between 473 and 230 K in alloys of vanadium containing titanium or niobium. Boltzmann-Matano techniques allowed the measurement of the hydrogen concentration dependence of the diffusion coefficient. In addition, one of these techniques permitted a determination of the terminal hydrogen solid solubility which was greatly increased by alloying. Both the hydrogen and deuterium diffusion coefficients were found to decrease with hydrogen isotope concentration in all alloys at all temperatures. The effect of niobium additions was to markedly reduce the rate of hydrogen migration to a minimum in the 75 at. pct. Nb alloy. The rate of hydrogen migration decreased with titanium concentration up to 30 at. pct. Ti, the highest concentration examined in that alloy system. The diffusion coefficients exhibited an Arrhenius temperature dependence and the resulting diffusion activation energy and D/sub o/ values both increased with titanium and with niobium concentration to a maximum of 75 at. pct. Nb. Deuterium diffusion activation energies were larger than corresponding hydrogen values in all alloys. The diffusion behavior found in these alloys is not well represented by current local deep trapping models.

  17. Permeation of deuterium implanted into vanadium alloys

    SciTech Connect

    Anderl, R.A.; Longhurst, G.R.; Struttmann, D.A.

    1986-05-01

    Permeation of deuterium through the vanadium alloy, V-15Cr-5Ti, was investigated using 3-keV, D/sub 3//sup +/ ion beams from a small accelerator. The experiments consisted of measurements of the deuterium reemission and permeation rates as a function of implantation fluence for 0.5-mm thick specimens heated to tempertures from 623 to 823/sup 0/K. Implantation-side surface characterization was made by simultaneous measurements of sputtered ions with a secondary ion mass spectrometer (SIMS). Analyses of these measurements indicate that for the experimental conditions used, the steady-state deuterium permeation flux in V-15Cr-5Ti is approximately 18% of the implantation flux. This corresponds to approximately 1000 times that seen in the ferritic steel, HT-9, under comparable conditions. Measurement of deuterium diffusivity in V-15Cr-5Ti using permeation break-through times indicates D = 1.4 x 10/sup -8/ exp(-.11 eV/kT) (m/sup 2//s).

  18. 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. PMID:22102992

  19. 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.

  20. Process for improving phosphorus-vanadium oxide and phosphorus-vanadium-co-metal oxide catalysts

    SciTech Connect

    Edwards, R.C.

    1987-10-20

    A process is described for the improvement of a vanadium-phosphorus-oxygen catalyst having a phosphorus to vanadium atomic ratio of about 2:1 to about 0.8:1 which catalyst is present on a catalyst bed having a portion therof containing an initial exotherm of reaction. The catalyst is suitable for use in the manufacture of maleic anhydride from a feed gas stream comprising C/sub 4/ hydrocarbons, benzene, or butane which process comprises: applying to the catalyst bed, simultaneously with introduction of the feed gas stream thereon, water and a phosphorus compound in an amount sufficient to initiate (a) deactivation of the portion of the catalyst containing the initial exotherm, and (b) formation of a new exotherm downstream in the catalyst bed from the initial exotherm, and thereafter reducing or discontinuing application of the phosphorus compound at a point in time when the initial exotherm portion of the catalyst bed is still undergoing deactivation, thereby allowing the partially deactivated exotherm portion to reactivate by producing a more isothermal catalyst bed.

  1. Diffusion and electrotransport of hydrogen and deuterium in vanadium-titanium and vanadium-chromium alloys

    NASA Astrophysics Data System (ADS)

    Pine, David J.; Cotts, R. M.

    1983-07-01

    The diffusion coefficient D and electrotransport effective charge number Z* of hydrogen and deuterium in V, V1-xTix, and V1-yCry were measured as a function of temperature using resistance techniques. Measurements were performed for hydrogen (deuterium) concentrations of approximately 1 at.% and alloys with x=0.03 and 0.08 and y=0.04 and 0.10. Alloying vanadium with either titanium or chromium was found to lower both D and Z* over the entire temperature range studied (310-480 K). The diffusion data obey an Arrhenius relation, the alloys having larger activation energies for diffusion than pure vanadium. No currently existing microscopic theory seems capable of explaining the dependence of D on alloy composition, nor can the data be consistently explained by a simple two-state trapping model. In every sample, Z* was observed to decrease with increasing temperature and host-metal resistivity for both hydrogen and deuterium. In addition, Z* was found to be larger for deuterium than hydrogen.

  2. Is vanadate reduced by thiols under biological conditions? Changing the redox potential of V(V)/V(IV) by complexation in aqueous solution.

    PubMed

    Crans, Debbie C; Zhang, Boyan; Gaidamauskas, Ernestas; Keramidas, Anastasios D; Willsky, Gail R; Roberts, Chris R

    2010-05-01

    Although dogma states that vanadate is readily reduced by glutathione, cysteine, and other thiols, there are several examples documenting that vanadium(V)-sulfur complexes can form and be observed. This conundrum has impacted life scientists for more than two decades. Investigation of this problem requires an understanding of both the complexes that form from vanadium(IV) and (V) and a representative thiol in aqueous solution. The reactions of vanadate and hydrated vanadyl cation with 2-mercaptoethanol have been investigated using multinuclear NMR, electron paramagnetic resonance (EPR), and UV-vis spectroscopy. Vanadate forms a stable complex of 2:2 stoichiometry with 2-mercaptoethanol at neutral and alkaline pH. In contrast, vanadate can oxidize 2-mercaptoethanol; this process is favored at low pH and high solute concentrations. The complex that forms between aqueous vanadium(IV) and 2-mercaptoethanol has a 1:2 stoichiometry and can be observed at high pH and high 2-mercaptoethanol concentration. The solution structures have been deduced based on coordination induced chemical shifts and speciation diagrams prepared. This work demonstrates that both vanadium(IV) and (V)-thiol complexes form and that redox chemistry also takes place. Whether reduction of vanadate takes place is governed by a combination of parameters: pH, solute- and vanadate-concentrations and the presence of other complexing ligands. On the basis of these results it is now possible to understand the distribution of vanadium in oxidation states (IV) and (V) in the presence of glutathione, cysteine, and other thiols and begin to evaluate the forms of the vanadium compounds that exert a particular biological effect including the insulin-enhancing agents, antiamoebic agents, and interactions with vanadium binding proteins. PMID:20359175

  3. 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. PMID:27268980

  4. Dependence of electrophysical properties on structure of vanadium dioxide films

    SciTech Connect

    Aleksandrov, Yu.A.; Baryshnikov, Yu.Yu.; Zakharov, I.L.; Makin, G.I.; Terman, M.Yu.

    1988-02-01

    Among the inorganic materials with a metal-semiconductor phase transition (MSPT), vanadium dioxide attracts much theoretical and practical interest for two reasons. First, the maximum change in the electrical conductivity at the MSPT point is of order of magnitudes, and secondly, since the temperature T/sub P/ at the MSPT point is about 68/sup 0/C, neither high nor low temperature techniques are required for the utilization of VO/sub 2/. We study the mixture and structural-morphological condition of thin films (0.01-2 ..mu..m) of vanadium dioxide as well as the relation between the films and the change in the resistivity in the MSPT temperature range. The resistivity of the vanadium dioxide films was measured by a standard four probe method.

  5. 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.

  6. A molecular dynamics simulation study of defect production in vanadium

    SciTech Connect

    Morishita, K. |; Diaz de la Rubia, T.

    1995-01-23

    We performed molecular dynamics simulations to investigate the process of defect production in pure vanadium. The interaction of atoms was described by the EAM interatomic potential modified at short range to merge smoothly with the universal potential for description of the high energy recoils in cascades. The melting point of this EAM model of vanadium was found to be consistent with the experimental melting temperature. The threshold energies of displacement events in the model system are also consistent with experimental minimum threshold in vanadium, and its average was found to be 44 eV. We evaluated the efficiencies of defect production in the displacement events initiated by recoils with kinetic energy up to 5 keV, and found that the probability of cluster formation is smaller than that of simulated events in fcc metals reported in the literature.

  7. 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.

  8. 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.

  9. 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

  10. 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.

  11. 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.

  12. Vanadium oxide thin film with improved sheet resistance uniformity

    NASA Astrophysics Data System (ADS)

    Généreux, Francis; Provençal, Francis; Tremblay, Bruno; Boucher, Marc-André; Julien, Christian; Alain, Christine

    2014-06-01

    This paper reports on the deposition of vanadium oxide thin films with sheet resistance uniformity better than 2.5% over a 150 mm wafer. The resistance uniformity within the array is estimated to be less than 1%, which is comparable with the value reported for amorphous silicon-based microbolometer arrays. In addition, this paper also shows that the resistivity of vanadium oxide, like amorphous silicon, can be modeled by Arrhenius' equation. This result is expected to significantly ease the computation of the correction table required for TEC-less operation of VOx-based microbolometer arrays.

  13. Synthesis and electrochemical performance of hierarchical nano-vanadium oxide.

    PubMed

    Mjejri, I; Sediri, F

    2016-10-15

    Hierarchically structured nano-vanadium oxides with different morphologies have been synthesized via a template-free hydrothermal route by adjusting the organic precursor quantities. The effects of molar ratio on structure, morphology and crystallite sized were investigated. The possible growth mechanism is also proposed. When evaluated as a cathode material for lithium-ion batteries, the vanadium oxyhydroxide H2V3O8 samples deliver very high charging capacity, good reversibility and a better cycling stability. The excellent electrochemical performance is attributed to multiple advantageous structural features. PMID:27442146

  14. 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

    2014-09-01

    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. PMID:25006616

  15. 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.

  16. 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.

  17. 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.

  18. Lithiated Vanadium Oxide (LVO), gamma-lithium vanadium bronze (Gamma-LIV2O5) and vanadium dioxide (VO2) as thermal battery cathode materials

    NASA Astrophysics Data System (ADS)

    Richie, A. G.; Warner, K.

    1991-05-01

    Thermal batteries are high temperature reserve batteries, predominantly used in missiles. Modern designs use a lithium (or lithium alloy) anode, an immobilized molten salt electrolyte, and an iron-disulphide cathode. These batteries have many advantages: high reliability, long storage life without maintenance, wide temperature range of operation, and, sometimes, high power. However, the energy density is rather low and this could be improved if the individual cell voltage could be raised above the present 2.2 V/cell open circuit-voltage for the lithium iron-disulphide couple. A new cathode material, lithiated vanadium oxide (LVO), was invented at RAE and has the advantage of a much higher open-circuit voltage of 2.6 V/cell versus lithium. The properties of LVO have been investigated and it has been shown that LVO consists of vanadium dioxide as the major component. Some lithium bromide is also present.

  19. 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.

  20. [Adsorption of methylene blue onto vanadium-doped magnetite].

    PubMed

    Zhong, Yuan-Hong; Liang, Xiao-Liang; Zhu, Jian-Xi; He, Hong-Ping; Yuan, Peng

    2010-06-01

    A series of vanadium-doped magnetite (Fe3-x VxO4, x < 0.4) synthesized by an oxidation-precipitation method, were characterized using chemical analysis, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), as well as thermogravimetric and differential scanning calorimetry (TG-DSC) analyses. The obtained results show that the synthetic Fe3-x VxO4 has spinel structure while vanadium mostly replaces Fe3+ in the octahedral sites. The synthetic Fe3-x VxO4 is magnetic material, with crystal size ranging from 28 to 35 nm. The substitution of vanadium in the magnetite structure increases the amount of surface hydroxyls. The experimental adsorption results indicate that, in neutral pH condition, the maximum adsorption capacities of Fe3-x VxO4 increase obviously with the increase of vanadium concentration in magnetite while the adsorption isotherm complies well with the Langmuir model. The adsorption of methylene blue (MB) on Fe3-x VxO4 can get equilibrium in the first 25 min, supporting a pseudo-second order equation. Moreover, the rise of the solution pH value results in an increase of the adsorption capability of MB on Fe3-x VxO4. PMID:20698274

  1. Presence of a Vanadium Nitrogenase in Azotobacter paspali.

    PubMed

    Fallik, E; Hartel, P G; Robson, R L

    1993-06-01

    There have been no previous studies on the genetics of Azotobacter paspali, an aerobic bacterium which forms a highly specific diazotrophic association with Bahia grass (Paspalum notatum). We constructed A. paspali strains defective in the molybdenum nitrogenase so that alternative N(2)ases could be studied. The cosmid vector pTBE and genomic DNA fragments ( approximately 50 kb) of A. paspali ATCC 23367 were used to construct a gene library in Escherichia coli. Recombinant cosmids containing sequences homologous to molybdenum nitrogenase nifDK structural genes were identified by hybridization. A 2.9-kb fragment bearing the putative nifDK genes of A. paspali was subcloned and mutagenized in vitro by the insertion of a kanamycin resistance gene cassette. The mutation was recombined into the chromosome of A. paspali with the suicide vector pCU101. One resultant mutant strain, AP2, was incapable of diazotrophic growth in a molybdenum-containing medium (Nif) without vanadium but grew well in a molybdenum-deficient medium with vanadium. The nitrogenase system in AP2 reduced acetylene to ethylene and produced ethane as 2.4% of the total products. Molybdenum levels as low as 10 nM prevented the diazotrophic growth of AP2, even in the presence of vanadium at levels up to 10 muM. These results are consistent with the existence of a vanadium nitrogenase system in A. paspali. PMID:16348965

  2. Vanadium-catalyzed regioselective oxidative coupling of 2-hydroxycarbazoles.

    PubMed

    Liu, Lei; Carroll, Patrick J; Kozlowski, Marisa C

    2015-02-01

    The first regioselective oxidative coupling of 2-hydroxycarbazoles is described. With a vanadium catalyst and oxygen as the terminal oxidant, dimers with an ortho-ortho' coupling pattern were obtained with high selectivity. Further oxidation led to ortho'-ortho' coupling to generate a tetramer, which provided insight that the atropisomerization barriers of the unsymmetrical biaryl bonds are much lower than expected. PMID:25590578

  3. Formation of vanadium silicide by high dose ion implantation

    NASA Astrophysics Data System (ADS)

    Salvi, V. P.; Narsale, A. M.; Vidwans, S. V.; Rangwala, A. A.; Guzman, L.; Dapor, M.; Giunta, G.; Calliari, L.; Marchetti, F.

    1987-10-01

    The vanadium silicide system has been found to be of increasing interest because one of the silicide phases viz. V 3Si with the A-15 structure is often accompanied by a high temperature superconductivity. We have studied the formation of vanadium silicide layers by high dose ion implantation. 30 keV 51V + ions were implanted at room temperature onto thermally evaporated a-Si films on thermally grown SiO 2 substrates. The samples were annealed in vacuum to study the possible evolution of V-Si phases. Both Seeman-Bohlin X-ray diffraction and Auger/sputter profiling techniques were used to analyse these samples. The observed Auger depth profile of the annealed samples shows a more uniform vanadium distribution as compared to the vanadium distribution in as-implanted samples, along with the changes in the Si L 2,3VV lineshape. The X-ray diffraction results show the formation of V 3Si, V 5Si 3 and VSi 2 phases. After annealing the sample in vacuum, a more ordered growth of V 3Si phase is found to be accompanied by an increase in VSi 2 phase. This has been related to the possible changes ocurring in the a-Si layers due to annealing of the sample.

  4. Ab initio Investigation of Helium in Vanadium Oxide Nanoclusters

    NASA Astrophysics Data System (ADS)

    Danielson, Thomas; Tea, Eric; Hin, Celine

    Nanostructured ferritic alloys (NFAs) are strong candidate materials for the next generation of fission reactors and future fusion reactors. They are characterized by a large number density of oxide nanoclusters dispersed throughout a BCC iron matrix, where current oxide nanoclusters are primarily comprised of Y-Ti-O compounds. The oxide nanoclusters provide the alloy with high resistance to neutron irradiation, high yield strength and high creep strength at the elevated temperatures of a reactor environment. In addition, the oxide nanoclusters serve as trapping sites for transmutation product helium providing substantially increased resistance to catastrophic cracking and embrittlement. Although the mechanical properties and radiation resistance of the existing NFAs is promising, the problem of forming large scale reactor components continues to present a formidable challenge due to the high hardness and unpredictable fracture behavior of the alloys. An alternative alloy has been previously proposed and fabricated where vanadium is added in order to form vanadium oxide nanoclusters that serve as deflection sites for crack propagation. Although experiments have shown evidence that the fracture behavior of the alloys is improved, it is unknown whether or not the vanadium oxide nanoclusters are effective trapping sites for helium. We present results obtained using density functional theory investigating the thermodynamic stability of helium with the vanadium oxide matrix to make a comparison of trapping effectiveness to traditional Y-Ti-O compounds.

  5. 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.

  6. Vanadium Exposure-Induced Neurobehavioral Alterations among Chinese Workers

    PubMed Central

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

    2014-01-01

    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. PMID:23500660

  7. 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}.

  8. Physiological roles of peroxido-vanadium complexes: Leitmotif as their signal transduction pathway.

    PubMed

    Matsugo, Seiichi; Kanamori, Kan; Sugiyama, Hironori; Misu, Hirofumi; Takamura, Toshinari

    2015-06-01

    Evidence exists that supports the various physiological roles of vanadium compounds, although the amount of vanadium in our body is limited. This limited concentration in our body does not attract much attention of the biological chemists, although the fact is present; even in the 19th century, vanadium derivatives were used for the therapeutic reagents. In the middle of the 20th century, the main focus of vanadium chemistry is mainly on the chemical and material fields. After the first discovery of vanadium compounds expressing ATPase activity, oxidovanadium(IV) sulfate was reported to have insulin mimic activity. Additionally, because some vanadium compounds possess cellular toxicity, trials were also carried out to examine the possible use of vanadium compounds as cancer therapeutics. The application of vanadium complexes was extended in recent years especially in the 21st century. In this review, we briefly explain the historical background of vanadium chemistry and also summarize the physiological role of vanadium complexes mainly focusing on the synthesis and physiological role of peroxidovanadium compounds and their interactions with insulin signal transduction pathways. PMID:25912243

  9. The role of vanadium in gree plants. II. Vanadium in green algae--two sites of action.

    PubMed

    Meisch, H U; Benzschawel, H; Bielig, H J

    1977-07-26

    Cells of Chlorella pyrenoidosa, derived from vanadium free agar slants, respond with great sensitivity to microamounts of vanadium, added as NH4VO3 to autotrophic liquid cultures. Between 0.01 and 1 microgram V per litre nutrient medium (2-10(-10)-2-10(-8) g-at/1), the algae respond with a continuous incrase in dry weight. At higher V-concentrations, further enhancement in biomass is accompanied by a additional increase in chlorophyll content. Maximum V-effect on both parameters was found to be at 500 microgram V/1 (10(-5) G-AT/1). Dry weight as well as chlorophyll content of Chlorella are decreased by concentrations above 25 mg V/1; 100 mg V/1 (2-10(-3) g-at/1) stop growth and cause death of the cells. The toxic threshold for the V-content in the algae was determined to be at 150-200 microgram V/g (3-4-10(-6) g-at/g) dry weight. Two different pH-optima for a positive vanadium action on dry weight and chlorophyll biosynthesis were established, the first at pH 7, the other in the range pH 7.5--8. Two sites of vanadium action in green algae are discussed. PMID:20864

  10. 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

  11. 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.

  12. Cellular uptake of titanium and vanadium from addition of salts or fretting corrosion in vitro

    SciTech Connect

    Maurer, A.M.; Merritt, K.; Brown, S.A. . Dept. of Biomedical Engineering)

    1994-02-01

    The use of titanium and titanium-6% aluminum-4% vanadium alloy for dental and orthopedic implants has increased in the last decade. The implants are presumed to be compatible because oseointegration, bony apposition, and cell attachment are known. However, the cellular association of titanium and vanadium have remained unknown. This study examined the uptake of salts or fretting corrosion products. Titanium was not observed to be toxic to the cells. Vanadium was toxic at levels greater than 10[mu]g/mL. The percentage of cellular association of titanium was shown to be about 10 times that of vanadium. The percentage of cellular association of either element was greater from fretting corrosion than from the addition of salts. The presence of vanadium did not affect the cellular uptake of titanium. The presence of titanium decreased the cell association of vanadium.

  13. 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.

  14. 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

  15. 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. PMID:25796623

  16. 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.

  17. Atom probe study of vanadium interphase precipitates and randomly distributed vanadium precipitates in ferrite.

    PubMed

    Nöhrer, M; Zamberger, S; Primig, S; Leitner, H

    2013-01-01

    Atom probe tomography and transmission electron microscopy were used to examine the precipitation reaction in the austenite and ferrite phases in vanadium micro-alloyed steel after a thermo-mechanical process. It was observed that only in the ferrite phase precipitates could be found, whereupon two different types were detected. Thus, the aim was to reveal the difference between these two types. The first type was randomly distributed precipitates from V supersaturated ferrite and the second type V interphase precipitates. Not only the arrangement of the particles was different also the chemical composition. The randomly distributed precipitates consisted of V, C and N in contrast to that the interphase precipitates showed a composition of V, C and Mn. Furthermore the randomly distributed precipitates had maximum size of 20 nm and the interphase precipitates a maximum size of 15 nm. It was assumed that the reason for these differences is caused by the site in which they were formed. The randomly distributed precipitates were formed in a matrix consisting mainly of 0.05 at% C, 0.68 at% Si, 0.03 at% N, 0.145 at% V and 1.51 at% Mn. The interphase precipitates were formed in a region with a much higher C, Mn and V content. PMID:24041583

  18. 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.

  19. Graphene/vanadium oxide nanotubes composite as electrode material for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Fu, Meimei; Ge, Chongyong; Hou, Zhaohui; Cao, Jianguo; He, Binhong; Zeng, Fanyan; Kuang, Yafei

    2013-07-01

    Graphene/vanadium oxide nanotubes (VOx-NTs) composite was successfully synthesized through the hydrothermal process in which acetone as solvent and 1-hexadecylamine (HDA) as structure-directing template were used. Morphology, structure and composition of the as-obtained composite were investigated by scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy, nitrogen isothermal adsorption/desorption and thermo gravimetric analysis (TGA). The composite with the VOx-NTs amount of 69.0 wt% can deliver a specific capacitance of 210 F/g at a current density of 1 A/g in 1 M Na2SO4 aqueous solution, which is nearly twice as that of pristine graphene (128 F/g) or VOx-NTs (127 F/g), and exhibit a good performance rate. Compared with pure VOx-NTs, the cycle stability of the composite was also greatly improved due to the enhanced conductivity of the electrode and the structure buffer role of graphene.

  20. Vanadium distribution in melts intermediate to ferroalloy production from vanadiferous slag

    SciTech Connect

    Howard, R.L. ); Richards, S.R. ); Welch, B.J. . Dept. of Chemical and Materials Engineering); Moore, J.J. . Dept. of Metallurgical and Materials Engineering)

    1994-02-01

    Processing of vanadiferous slags through the pyrometallurgical process route appears to offer advantages both in terms of ferroalloy production and in the potential for efficient vanadium recovery from hot metal. In order to investigate the effect of slag composition on the phase distribution of vanadium, a series of laboratory smelting experiments was carried out. The effect of basicity adjustments on the slag/metal distribution of iron, vanadium, and manganese was investigated using carbon and FeSi as a reductant. A simulation of the final stage of slag reduction was also carried out to determine the efficiency of vanadium recovery during metallothermic smelting using aluminum and FeSi.

  1. 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. PMID:24927405

  2. 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%.

  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. 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.

  5. 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

    2016-01-01

    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

  6. Uncoupling binding of substrate CO from turnover by vanadium nitrogenase

    PubMed Central

    Lee, Chi Chung; Fay, Aaron W.; Weng, Tsu-Chien; Krest, Courtney M.; Hedman, Britt; Hodgson, Keith O.; Hu, Yilin; Ribbe, Markus W.

    2015-01-01

    Biocatalysis by nitrogenase, particularly the reduction of N2 and CO by this enzyme, has tremendous significance in environment- and energy-related areas. Elucidation of the detailed mechanism of nitrogenase has been hampered by the inability to trap substrates or intermediates in a well-defined state. Here, we report the capture of substrate CO on the resting-state vanadium-nitrogenase in a catalytically competent conformation. The close resemblance of this active CO-bound conformation to the recently described structure of CO-inhibited molybdenum-nitrogenase points to the mechanistic relevance of sulfur displacement to the activation of iron sites in the cofactor for CO binding. Moreover, the ability of vanadium-nitrogenase to bind substrate in the resting-state uncouples substrate binding from subsequent turnover, providing a platform for generation of defined intermediate(s) of both CO and N2 reduction. PMID:26515097

  7. Improved activation cross sections for vanadium and titanium

    SciTech Connect

    Muir, D.W.; Arthur, E.D.

    1983-01-01

    Vanadium alloys such as V-20Ti and V-Cr-Ti are attractive candidates for use as structural materials in fusion-reactor blankets. The virtual absence of long-lived activation products in these alloys suggest the possibility of reprocessing on an intermediate time scale. We have employed the modern Hauser-Feshbach nuclear-model code GNASH to calculate cross sections for neutron-activation reactions in /sup 50/V and /sup 51/V, to allow a more accurate assessment of induced radioactivity in vanadium alloys. In addition, cross sections are calculated for the reactions /sup 46/Ti(n,2n) and /sup 45/Ti(n,2n) in order to estimate the production of /sup 44/Ti, a 1.2-MeV gamma-ray source with a half-life of 47 years.

  8. Natural selectivity of Nickel and Vanadium in crude oil

    NASA Astrophysics Data System (ADS)

    Fernandez, Olienka Patricia De La O.

    Nickel and Vanadium have always been found in crude oil all around the world. The metal content is found mainly in porphyrin structures in the asphaltene fraction of the petroleum. In order to determine the reason for this natural preference, a set of experiments testing thermodynamics, kinetics, and other factors were performed. Candidate metalloporphyrins containing Vanadyl, Chromium, Iron, Nickel, Copper and Zinc were analyzed through chemical reactions characterized using Silica Column Chromatography, HPLC, MS and UV-Visible. Theoretical analysis of the stability of metalloporphyrins was conducted using DFT/NRLMOL for computational calculation. The analysis of all factors leads us to conclude that the presence of Nickel and Vanadium in petroleum depend on different factors, not only on the stability of the structures, but mainly on abundance in the medium rising from biological processes.

  9. 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.

  10. Low reflectance sputtered vanadium oxide thin films on silicon

    NASA Astrophysics Data System (ADS)

    Esther, A. Carmel Mary; Dey, Arjun; Rangappa, Dinesh; Sharma, Anand Kumar

    2016-07-01

    Vanadium oxide thin films on silicon (Si) substrate are grown by pulsed radio frequency (RF) magnetron sputtering technique at RF power in the range of 100-700 W at room temperature. Deposited thin films are characterized by field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) techniques to investigate microstructural, phase, electronic structure and oxide state characteristics. The reflectance and transmittance spectra of the films and the Si substrate are recorded at the solar region (200-2300 nm) of the spectral window. Substantial reduction in reflectance and increase in transmittance is observed for the films grown beyond 200 W. Further, optical constants viz. absorption coefficient, refractive index and extinction coefficient of the deposited vanadium oxide films are evaluated.

  11. A novel process for comprehensive utilization of vanadium slag

    NASA Astrophysics Data System (ADS)

    Liu, Li-ying; Du, Tao; Tan, Wen-jun; Zhang, Xin-pu; Yang, Fan

    2016-02-01

    Traditional processes for treating vanadium slag generate a huge volume of solid residue and a large amount of harmful gas, which cause serious environmental problems. In this study, a new process for the comprehensive utilization of vanadium slag was proposed, wherein zeolite A and a V2O5/TiO2 system were synthesized. The structural properties of the as-synthesized zeolite A and the V2O5/TiO2 system were characterized using various experimental techniques, including X-ray diffraction, X-ray fluorescence, scanning electron microscopy, and infrared spectroscopy. The results reveal that zeolite A and the V2O5/TiO2 system are successfully obtained with high purity. The results of gas adsorption measurements indicate that the prepared zeolite A exhibits high selectivity for CO2 over N2 and is a candidate material for CO2 capture from flue-gas streams.

  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. Present status of vanadium alloys for fusion applications

    NASA Astrophysics Data System (ADS)

    Muroga, T.; Chen, J. M.; Chernov, V. M.; Kurtz, R. 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.

  14. 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. PMID:25843360

  15. Vanadium dioxide: a Peierls-Mott insulator stable against disorder.

    PubMed

    Weber, Cédric; O'Regan, David D; Hine, Nicholas D M; Payne, Mike C; Kotliar, Gabriel; Littlewood, Peter B

    2012-06-22

    Vanadium dioxide undergoes a first order metal-insulator transition at 340 K. In this Letter, we develop and carry out state-of-the-art linear scaling density-functional theory calculations refined with nonlocal dynamical mean-field theory. We identify a complex mechanism, a Peierls-assisted orbital selection Mott instability, which is responsible for the insulating M(1) phase, and which furthermore survives a moderate degree of disorder. PMID:23004627

  16. Vanadium-Catalyzed Regioselective Oxidative Coupling of 2-Hydroxycarbazoles

    PubMed Central

    2016-01-01

    The first regioselective oxidative coupling of 2-hydroxycarbazoles is described. With a vanadium catalyst and oxygen as the terminal oxidant, dimers with an ortho–ortho′ coupling pattern were obtained with high selectivity. Further oxidation led to ortho′–ortho′ coupling to generate a tetramer, which provided insight that the atropisomerization barriers of the unsymmetrical biaryl bonds are much lower than expected. PMID:25590578

  17. 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.

  18. Gas nitriding of high vanadium steels—experiments and simulations

    NASA Astrophysics Data System (ADS)

    Larsson, Henrik; Ågren, John

    2004-09-01

    Four experimental high vanadium alloys were gas nitrided in an ammonia-nitrogen atmosphere. The microstructure and concentration gradients have been investigated by means of several techniques. The nitriding process has been tentatively simulated using the DICTRA software. A precise process simulation does not seem possible at present; the reason for this is discussed. Instead, bounds for the carbon and nitrogen concentration profiles were obtained by applying different simulation conditions.

  19. Integrated method for extracting nickel and vanadium compounds from oils

    SciTech Connect

    Overfield, R.E.

    1987-02-17

    A method is described for the extraction of vanadium or nickel metaloporphyrinic compounds from an oil containing such compounds. The method comprises contacting oil with a solvent selected from the group of gammabutyrolactone, acetonitrile, phenol, furfural, 2-pyrrolidinones, dimethylsulfone, dimethylformamide, pyridine-water mixtures, ethylene carbonate, propylene carbonate, ethylene trithiocarbonate, and dimethyl sulfone to produce a solvent-metalloporphyrinic compound stream and a demetallated product oil stream, regenerating the solvent-metalloporphyrinic stream by contacting it with a highly aromatic oil stream.

  20. 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.

  1. Infrared photodissociation spectroscopy of vanadium oxide-carbonyl cations.

    PubMed

    Brathwaite, A D; Ricks, A M; Duncan, M A

    2013-12-19

    Mass selected vanadium oxide-carbonyl cations of the form VO(m)(CO)(n)(+) (m = 0-3 and n = 3-6) are studied via infrared laser photodissociation spectroscopy in the 600-2300 cm(-1) region. Insight into the structure and bonding of these complexes is obtained from the number of infrared active bands, their relative intensities and their frequency positions. Density functional theory calculations are carried out in support of the experimental data. The effect of oxidation on the carbonyl stretching frequencies of VO(CO)(n)(+), VO2(CO)(n)(+), and VO3(CO)(n)(+) complexes is investigated. All of these oxide-carbonyl species have C-O stretch vibrations blue-shifted from those of the pure vanadium ion carbonyls. The V-O stretches of these complexes are also investigated, revealing the effects of CO coordination on these vibrations. The oxide-carbonyls all have a hexacoordinate core analogous to that of V(CO)6(+). The fully coordinated vanadium monoxide-carbonyl species is VO(CO)5(+), and those of the dioxide and trioxide are VO2(CO)4(+) and VO3(CO)3(+), respectively. PMID:23927497

  2. Electronic properties of vanadium-doped TiO2.

    PubMed

    Islam, Mazharul M; Bredow, Thomas; Gerson, Andrea

    2011-12-01

    The electronic properties of vanadium-doped rutile TiO(2) are investigated theoretically with a Hartree-Fock/DFT hybrid approach. The most common oxidation states (V(2+), V(3+), V(4+), and V(5+)) in different spin states are investigated and their relative stability is calculated. The most stable spin states are quartet, quintet, doublet, and singlet for V(2+), V(3+), V(4+), and V(5+) doping, respectively. By comparing the formation energy with respect to the parent oxides and gas-phase oxygen (ΔE), we conclude that V(4+) (ΔE=145.3 kJ mol(-1)) is the most likely oxidation state for vanadium doping with the possibility of V(5+) doping (ΔE=283.5 kJ mol(-1)). The energetic and electronic properties are converged with dopant concentrations in the range of 0.9 to 3.2%, which is within the experimentally accessible range. The investigation of electronic properties shows that V(4+) doping creates both occupied and unoccupied vanadium states in the band gap and V(5+) doping creates unoccupied states at the bottom of the conduction band. In both cases there is a significant reduction of the band gap by 0.65 to 0.75 eV compared to that of undoped rutile TiO(2). PMID:22025455

  3. Electron affinity of cubic boron nitride terminated with vanadium oxide

    NASA Astrophysics Data System (ADS)

    Yang, Yu; Sun, Tianyin; Shammas, Joseph; Kaur, Manpuneet; Hao, Mei; Nemanich, Robert J.

    2015-10-01

    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 BF3 and N2 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 VO2, and the surfaces were found to be thermally stable, exhibiting an NEA. In comparison, the oxygen-terminated c-BN surface, where B2O3 was detected, showed a positive electron affinity of ˜1.2 eV. The B2O3 evidently acts as a negatively charged layer introducing a surface dipole directed into the c-BN. Through the interaction of VO2 with the B2O3 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 B2O3 is favorable for the formation of the B-O-V layer structure, which provides a thermally stable surface dipole and an NEA surface.

  4. 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.

  5. 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.

  6. Intragranular ferrite nucleation in medium-carbon vanadium steels

    SciTech Connect

    Ishikawa, Fusao; Takahashi, Toshihiko ); Ochi, Tatsurou . Muroran R D Lab.)

    1994-05-01

    In this study, the mechanism of intragranular ferrite nucleation is investigated. It is found that intragranular ferrite idiomorphs'' nucleate at vanadium nitrides which precipitate at manganese sulfide particles during cooling in the austenite region. It is observed that intragranular ferrite has the Baker-Nutting orientation relationship with vanadium nitride which precipitated at manganese sulfide. According to classical nucleation theory, the proeutectoid ferrite nucleation rate depends on the following factors: (1) the driving free energy for ferrite nucleation, (2) the diffusivity of carbon atoms in austenite, and (3) the increase in the interfacial energy associated with ferrite nucleation. In the Baker-Nutting orientation relationship, the lattice mismatch across the habit planes is likely to be very small. Depleted zones of solute atoms such as vanadium are assumed to be formed in the austenite matrix around precipitates. The effect of the depleted zones on factors (1) and (2) is estimated thermodynamically and it is proved that those effects are negligibly small. Thus, the authors conclude that the most important factor in nucleation kinetics of intragranular ferrite is the formation of precipitates which can develop coherent, low energy interfaces with ferrite.

  7. Spleen and bone marrow megakaryocytes as targets for inhaled vanadium.

    PubMed

    Fortoul, Teresa I; Piñón-Zarate, Gabriela; Diaz-Bech, Maria Eugenia; González-Villalva, Adriana; Mussali-Galante, Patricia; Rodriguez-Lara, Vianey; Colin-Barenque, Laura; Martinez-Pedraza, Michelle; Montaño, Luis F

    2008-11-01

    An increased incidence in ischemic and thromboembolic events in the population of cities with rising air suspended particle pollution has suggested the interaction of some of the components of these particles in the coagulation system. A previous report from our laboratory identified thrombocytosis as a consequence of the subacute and chronic inhalation of vanadium. With this preceding information we decided to evaluate the effects of this element in the spleen and bone marrow in a mouse experimental model. CD-1 male mice inhaled V2O5 0.02 M for one hour twice a week for twelve weeks. The spleen and bone marrow were processed for light microscopy. The increase in quantity and size of megakaryocytes (MKs) in the exposed group in both organs was striking. Also, modifications in the cytoplasm, granule content and nuclear ultrastructure were evident. Our results indicate the influence of vanadium on megakaryopoyesis, an effect which could be the onset of the thrombocytosis previously reported by our group. The modifications in MKs described here suggest that inhaled vanadium could induce megakaryocytic proliferation, which may result in increased production of platelets and increased risk for thromboembolic events. PMID:18785114

  8. Continuous Aqueous Tritium Monitoring

    SciTech Connect

    Hofstetter, K.J.

    1995-03-29

    Continuous monitoring for tritium in the aqueous effluents of selected Savannah River Site (SRS) facilities is performed using a custom designed system that includes an automated water purification system and a flow-through radiation detection system optimized for tritium. Beads of plastic scintillators coupled with coincidence electronics provide adequate sensitivity (=25kBz/L) for tritium break-through detection int he aqueous discharge stream from these facilities. The tritium effluent water monitors (TEWMs) at SRS provide early warning (within 30 minutes) of an unanticipated release of tritium, supplement the routine sampling surveillances, and mitigate the impact of aqueous plant discharges of tritium releases to the environment.

  9. Continuous aqueous tritium monitoring

    SciTech Connect

    Hofstetter, K.J.

    1995-10-01

    Continuous monitoring for tritium in the aqueous effluents of selected Savannah River Site (SRS) facilities is performed using a unique system that includes an automated water purification system and a flow-through radiation detection system optimized for tritium. Beads of plastic scintillator coupled with coincidence electronics provide adequate sensitivity (approx.25kBq/L) for tritium breakthrough detection in the aqueous discharge stream from these facilities. The tritium effluent water monitors (TEWMs) at SRS provide early warning (within 30 minutes) of an unanticipated release of tritium, supplement the routine sampling surveillances, and mitigate the impact of aqueous plant discharges of tritium to the environment. 4 refs., 4 figs., 1 tab.

  10. 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. PMID:16797093

  11. Influences of permeation of vanadium ions through PVDF-g-PSSA membranes on performances of vanadium redox flow batteries.

    PubMed

    Luo, Xuanli; Lu, Zhengzhong; Xi, Jingyu; Wu, Zenghua; Zhu, Wentao; Chen, Liquan; Qiu, Xinping

    2005-11-01

    The preparation and physical characterization of a poly(vinylidene fluoride)-graft-poly(styrene sulfonic acid) (PVDF-g-PSSA) membrane prepared by a solution-grafting method were described. These membranes exhibited high conductivity with a value 3.22 x 10(-2) S/cm at 30 degrees C. ICP studies revealed that the PVDF-g-PSSA membrane showed dramatically lower vanadium ion permeability compared to Nafion 117. Trivalent vanadium ions had the highest permeability through all these membranes in contrast to pentavalent vanadium ions with the lowest. The VRB with the low-cost PVDF-g-PSSA membrane exhibited a higher performance than that with Nafion 117 under the same operating conditions, and its energy efficiency reached 75.8% at 30 mA/cm(2). The performance of VRB with the PVDF-g-PSSA membrane can be maintained after more than 200 cycles at a current density of 60 mA/cm(2). PMID:16853627

  12. 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.

  13. Ferrocene and cobaltocene derivatives for non-aqueous redox flow batteries.

    PubMed

    Hwang, Byunghyun; Park, Min-Sik; Kim, Ketack

    2015-01-01

    Ferrocene and cobaltocene and their derivatives are studied as new redox materials for redox flow cells. Their high reaction rates and moderate solubility are attractive properties for their use as active materials. The cyclability experiments are carried out in a static cell; the results showed that these materials exhibit stable capacity retention and predictable discharge potentials, which agree with the potential values from the cyclic voltammograms. The diffusion coefficients of these materials are 2 to 7 times higher than those of other non-aqueous materials such as vanadium acetylacetonate, iron tris(2,2'-bipyridine) complexes, and an organic benzene derivative. PMID:25428116

  14. 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.

  15. 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. PMID:24295153

  16. Theoretical Study of High-Valent Vanadium Oxo-Porphyrins as a Dopant of Crude Oil

    SciTech Connect

    Salcedo, Roberto; Martinez, LMR; Martinez-Magadan, Jose M.

    2001-06-15

    The role played by the vanadyl porphyrinate as a dopant for zeolites in the refinement process of crude oil is analyzed using DFT calculations. The pair formed by the vanadium atom and its bonded oxygen atoms seems to be the responsible items in the dopant reaction. However, the present paper shows the participation of the vanadium atom as being the most important.

  17. Hydrothermal synthesis of vanadium nitride and modulation of its catalytic performance for oxygen reduction reaction

    NASA Astrophysics Data System (ADS)

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

    2014-07-01

    A creative hydrothermal synthesis method followed by calcination for vanadium nitride (VN) is reported. The oxygen reduction reaction (ORR) study of the catalyst shows that VN possesses a comparable catalytic performance to commercial Pt/C catalyst. The ORR catalytic activity study of vanadium nitride, vanadium carbonitride, and vanadium carbide reveals that tuning anions offers a promising route for the activity enhancement of the non-precious metal catalysts.A creative hydrothermal synthesis method followed by calcination for vanadium nitride (VN) is reported. The oxygen reduction reaction (ORR) study of the catalyst shows that VN possesses a comparable catalytic performance to commercial Pt/C catalyst. The ORR catalytic activity study of vanadium nitride, vanadium carbonitride, and vanadium carbide reveals that tuning anions offers a promising route for the activity enhancement of the non-precious metal catalysts. Electronic supplementary information (ESI) available: Experimental methods; SEM characterization of the catalysts; Tafel test of Pt/C catalyst; BET and cyclic performance tests of VN. See DOI: 10.1039/c4nr02646b

  18. 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.

  19. 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. PMID:25727928

  20. Novel catalytic effects of Mn3O4 for all vanadium redox flow batteries.

    PubMed

    Kim, Ki Jae; Park, Min-Sik; Kim, Jae-Hun; Hwang, Uk; Lee, Nam Jin; Jeong, Goojin; Kim, Young-Jun

    2012-06-01

    A new approach for enhancing the electrochemical performance of carbon felt electrodes by employing non-precious metal oxides is designed. The outstanding electro-catalytic activity and mechanical stability of Mn(3)O(4) are advantageous in facilitating the redox reaction of vanadium ions, leading to efficient operation of a vanadium redox flow battery. PMID:22540132

  1. Effect of Sulfuric and Triflic Acids on the Hydration of Vanadium Cations: An ab Initio Study.

    PubMed

    Sepehr, Fatemeh; Paddison, Stephen J

    2015-06-01

    Vanadium redox flow batteries (VRFBs) may be a promising solution for large-scale energy storage applications, but the crossover of any of the redox active species V(2+), V(3+), VO(2+), and VO2(+) through the ion exchange membrane will result in self-discharge of the battery. Hence, a molecular level understanding of the states of vanadium cations in the highly acidic environment of a VRFB is needed. We examine the effects of sulfuric and triflic (CF3SO3H) acids on the hydration of vanadium species as they mimic the electrolyte and functional group of perfluorosulfonic acid (PFSA) membranes. Hybrid density functional theory in conjunction with a continuum solvation model was utilized to obtain the local structures of the hydrated vanadium cations in proximity to H2SO4, CF3SO3H, and their conjugate anions. The results indicate that none of these species covalently bond to the vanadium cations. The hydration structure of V(3+) is more distorted than that of V(2+) in an acidic medium. The oxo-group of VO2(+) is protonated by either acid, in contrast to VO(2+) which is not protonated. The atomic partial charge of the four oxidation states of vanadium varies from +1.7 to +2.0. These results provide the local solvation structures of vanadium cations in the VRFBs environment that are directly related to the electrolytes stability and diffusion of vanadium ions into the membrane. PMID:25954916

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

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... uranium, radium and vanadium ores subcategory. 440.30 Section 440.30 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ORE MINING AND DRESSING POINT SOURCE CATEGORY Uranium, Radium and Vanadium Ores Subcategory § 440.30...

  3. 40 CFR 440.30 - Applicability; description of the uranium, radium and vanadium ores subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... uranium, radium and vanadium ores subcategory. 440.30 Section 440.30 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ORE MINING AND DRESSING POINT SOURCE CATEGORY Uranium, Radium and Vanadium Ores Subcategory § 440.30...

  4. 40 CFR 440.30 - Applicability; description of the uranium, radium and vanadium ores subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... uranium, radium and vanadium ores subcategory. 440.30 Section 440.30 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ORE MINING AND DRESSING POINT SOURCE CATEGORY Uranium, Radium and Vanadium Ores Subcategory § 440.30...

  5. 40 CFR 440.80 - Applicability; description of the vanadium ore subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

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

  6. 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 (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ORE MINING AND DRESSING POINT SOURCE CATEGORY Vanadium Ore Subcategory (Mined Alone and Not as a Byproduct) § 440.80 Applicability; description of...

  7. 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 (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS (CONTINUED) ORE MINING AND DRESSING POINT SOURCE CATEGORY Vanadium Ore Subcategory (Mined Alone and Not as a Byproduct) § 440.80 Applicability; description of...

  8. 40 CFR 440.30 - Applicability; description of the uranium, radium and vanadium ores subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... uranium, radium and vanadium ores subcategory. 440.30 Section 440.30 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ORE MINING AND DRESSING POINT SOURCE CATEGORY Uranium, Radium and Vanadium Ores Subcategory § 440.30 Applicability; description of...

  9. 40 CFR 440.30 - Applicability; description of the uranium, radium and vanadium ores subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... uranium, radium and vanadium ores subcategory. 440.30 Section 440.30 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS ORE MINING AND DRESSING POINT SOURCE CATEGORY Uranium, Radium and Vanadium Ores Subcategory § 440.30 Applicability; description of...

  10. Investigation of the Electrolyte Effects on Formation of Vanadium Carbide via Plasma Electrolytic Saturation Method (pes)

    NASA Astrophysics Data System (ADS)

    Ghorbanian, Babak; Khoie, Seyed Mohammad Mousavi; Rasouli, Mahmood; Doodran, Ramona Javadi

    2016-02-01

    One of the most important hardening methods of tool steel is the use of carbide coatings. During this process, vanadium atoms diffuse the specimen’s surface at high temperature and reacts with the available carbon in steel and create vanadium carbide with high hardness. During the plasma electrolytic saturation (PES) process, the vanadium element diffuses with the help of plasma and increases up to around 950∘ as a result of the temperature, providing conditions for the creation of vanadium carbide. The best combination of electrolyte is 4g vanadium oxide and 50mL hydrochloric acid and different concern of sodium hydroxide. The results indicate that the formed coating is about 30μm. As the conductivity increases, the condition for diffusion is provided; however, with increase in the temperature, the diffusion decreases. The coating formation is observed in the current at 9-11 A and hardness of this coating is about 1400vickers.

  11. 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

    2016-06-01

    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.%.

  12. Characterization of poly(L-lysine)-graft-poly(ethylene glycol) assembled monolayers on niobium pentoxide substrates using time-of-flight secondary ion mass spectrometry and multivariate analysis.

    PubMed

    Wagner, M S; Pasche, S; Castner, D G; Textor, M

    2004-03-01

    Control of protein adsorption onto solid surfaces is a critical area of biomaterials and biosensors research. Application of high performance surface analysis techniques to these problems can improve the rational design and understanding of coatings that control protein adsorption. We have used static time-of-flight secondary ion mass spectrometry (TOF-SIMS) to investigate several poly(L-lysine)-graft-poly(ethylene glycol) (PLL-g-PEG) adlayers adsorbed electrostatically onto negatively charged niobium pentoxide (Nb(2)O(5)) substrates. By varying the PEG graft ratio (i.e., the number of lysine monomers per grafted PEG chain) and the molecular weights of the PLL and PEG polymers, the amount of protein adsorption can be tailored between 1 and 300 ng/cm(2). Detailed multivariate analysis using principal component analysis (PCA) of the positive and negative ion TOF-SIMS spectra showed changes in the outermost surface of the polymer films that were related to the density and molecular weight of the PEG chains on the surface. However, no significant differences were noted due to PLL molecular weight, despite observed differences in the serum adsorption characteristics for adlayers of PLL-g-PEG polymers with different PLL molecular weights. From the PCA results, multivariate peak intensity ratios were developed that correlated with the thickness of the adlayer and the enrichment of the PEG chains and the methoxy terminus of the PEG chains at the outermost surface of the adlayer. Furthermore, partial least squares regression was used to correlate the TOF-SIMS spectra with the amount of protein adsorption, resulting in a predictive model for determining the amount of protein adsorption on the basis of the TOF-SIMS spectra. The accuracy of the prediction of the amount of serum adsorption depended on the molecular weight of the PLL and PEG polymers and the PEG graft ratio. The combination of multivariate analysis and static TOF-SIMS provides detailed information on the surface

  13. The enrichment of biomass of cyanobacteria with vanadium using the cation and anion forms of its compounds.

    PubMed

    Vasilieva, Svetlana Gennadievna; Tambiev, Alexander Khapachevich; Sedykh, Ivelina Maximovna; Lukyanov, Alexander Andrievich; Bannikh, Lidia Nicolaevna

    2011-04-01

    Compounds of the trace element vanadium have been shown to mimic insulin effects in in vitro and in vivo systems. Vanadium compounds have emerged as agents for potential use in diabetes therapy. In our work we show the possibility of obtaining enriched biomass of cyanobacteria genus Spirulina (S. platensis and S. maxima) with vanadium in organic form. We have investigated the accumulation of vanadium by the cells of cyanobacteria S. platensis and S. maxima by adding to cultural medium both the forms of vanadium in various concentrations and have defined the optimal concentrations of vanadium in the medium for maximum enrichment of the cells. We defined that S. maxima is more steady to increased concentration of vanadium(IV) and (V) in medium. Optimal concentration of vanadium(IV) in the medium for enrichment of S. platensis and S. maxima biomass was 1.5 g/L, at this vanadium concentration in medium the content of vanadium in the cells of S. platensis was 1245±105 μg/g and in the cells of S. maxima was 1550±75 μg/g. In the case of vanadium(V) addition, the optimal concentration for S. platensis enrichment was 1.5 g/L vanadium(V) in medium, and the intracellular concentration was 2855±254 μg/g. For S. maxima the optimal concentration was 1.0 g/L vanadium(V) in medium, at that concentration the content of vanadium in cells was 2650±206 μg/g. In addition, we revealed the alterations in macro- and microelemental compositions of both cultures caused by the increased concentration of vanadium compounds in cultural medium. PMID:21514809

  14. Effect of vanadium contamination on the framework and micropore structure of ultra stable Y-zeolite.

    PubMed

    Etim, U J; Xu, B; Ullah, Rooh; Yan, Z

    2016-02-01

    Y-zeolites are the main component of fluid catalytic cracking (FCC) catalyst for conversion of crude petroleum to products of high demand including transportation fuel. We investigated effects of vanadium which is present as one of the impurities in FCC feedstock on the framework and micropore structure of ultra-stable (US) Y-zeolite. The zeolite samples were prepared and characterized using standard techniques including: (1) X-ray diffraction, (2) N2 adsorption employing non local density functional theory method, NLDFT, (3) Transmittance and Pyridine FTIR, (4) Transmittance electron microscopy (TEM), and (5) (27)Al and (29)Si MAS-NMR. Results revealed that in the presence of steam, vanadium caused excessive evolution of non inter-crystalline mesopores and structural damage. The evolved mesopore size averaged about 25.0nm at 0.5wt.% vanadium loading, far larger than mesopore size in zeolitic materials with improved hydrothermal stability and performance for FCC catalyst. A mechanism of mesopore formation based on accelerated dealumination has been proposed and discussed. Vanadium immobilization experiments conducted to mitigate vanadium migration into the framework clearly showed vanadium is mobile at reaction conditions. From the results, interaction of vanadium with the passivator limits and decreases mobility and activity of vanadium into inner cavities of the zeolite capable of causing huge structure breakdown and acid sites destruction. This study therefore deepens insight into the causes of alteration in activity and selectivity of vanadium contaminated catalyst and hints on a possible mechanism of passivation in vanadium passivated FCC catalyst. PMID:26520826

  15. 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.

  16. Specific S-nitrosothiol (thionitrite) quantification as solution nitrite after vanadium(III) reduction and ozone-chemiluminescent detection.

    PubMed

    Ewing, J F; Janero, D R

    1998-09-01

    Increasing evidence suggests that S-nitrosothiols (thionitrites) might represent naturally occurring nitric oxide surrogates and function as intermediates in nitrogen monoxide metabolism. A facile, sensitive, and selective micromethod has been developed and validated for quantification of S-nitrosothiols as their mercury-displaceable nitrogen monoxide content. In this method, brief (5-min), room-temperature pretreatment of S-nitrosothiol with a molar excess of aqueous mercuric chloride was used to liberate into solution, quantitatively, the nitrogen monoxide moiety, which rapidly and quantitatively converted to its stable solution end-product, nitrite. Solution nitrite was reduced back to nitric oxide with vanadium(III), and the nitric oxide was detected by gas-phase chemiluminescence after reaction with ozone in a commercial nitric oxide analyzer. A linear relationship was observed between S-nitrosothiol-bound nitrogen monoxide and ozone-chemiluminescent detector response over a wide range (16.3-3500 pmol) of nitric oxide, as generated by reaction of vanadium(III) with either nitrite standard or mercury-treated S-nitrosothiol. Assay response was quantitatively identical for equivalent amounts of nitrite and S-nitrosothiol-bound nitrogen monoxide. The method displayed 96% selectivity for nitrite vs. nitrate and negligible (<2%) interference by nitrosated compounds bearing nitrogen monoxide moieties bound to either nitrogen or carbon. The lower limits of quantitative sensitivity and qualitative detection were below 50 and 20 pmol S-nitrosothiol-bound nitrogen monoxide-equivalents, respectively. The intraday and interday coefficients of variation did not exceed 8%. This technique has been applied to quantify structurally diverse natural and synthetic S-nitrosothiols with quantitative recovery from complex biological samples such as culture media and plasma at levels of nitrogen monoxide-equivalents undetectable by the popular Saville colorimetric method. PMID:9741600

  17. 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. PMID:26419760

  18. 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.

  19. 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.

  20. 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. PMID:23799776

  1. X-ray-induced persistent photoconductivity in vanadium dioxide

    SciTech Connect

    Dietze, S. H.; Marsh, M. J.; Wang, Siming; Ramírez, J. -G.; Cai, Z. -H.; Mohanty, J. R.; Schuller, Ivan K.; Shpyrko, O. G.

    2014-10-08

    The resistivity of vanadium dioxide (VO2) decreased by over one order of magnitude upon localized illumination with x rays at room temperature. Despite this reduction, the structure remained in the monoclinic phase and had no signature of the high-temperature tetragonal phase that is usually associated with the lower resistance. Once illumination ceased, relaxation to the insulating state took tens of hours near room temperature. However, a full recovery of the insulating state was achieved within minutes by thermal cycling. We show that this behavior is consistent with random local-potential fluctuations and random distribution of discrete recombination sites used to model residual photoconductivity.

  2. 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

  3. Electrical transport and quasipersistent photocurrent in vanadium oxide nanowire networks

    NASA Astrophysics Data System (ADS)

    Park, Jitae; Lee, Eunmo; Lee, Kyu Won; Lee, Cheol Eui

    2006-10-01

    Electrical conductivity and photoconductivity measurements were carried out on semiconducting vanadium oxide nanowire networks synthesized through the polycondensation of vanadic acid. The temperature-dependent conductivity was described well by Mott's optical multiphonon assisted hopping model at high temperatures and by the variable-range hopping mechanism at low temperatures. The photoconductivity showed a weak temperature dependence. Besides, quasipersistent photocurrent with a single-exponential decay behavior was observed right after switching off the light and was explained in terms of the random local-potential fluctuation model.

  4. Nanocrystalline vanadium dioxide: synthesis and mid-infrared properties

    NASA Astrophysics Data System (ADS)

    Guinneton, Frédéric; Valmalette, Jean-Christophe; Gavarri, Jean-Raymond

    2000-11-01

    This work describes the first successful synthesis of nanocrystalline thermochromic VO 2 powder using the low temperature irreversible structural transformation of the metastable VO 2(B). At this step, the transformation is associated with a total rearrangement of VO 6 octahedra, and a strong increasing of density. The reversible metal-insulator phase transition (MIPT) of vanadium dioxide ( Tt=68°C) is associated with strong changes in electrical, magnetic and optical properties. The contrast of the optical transition in mid-infrared (MIR) region and the optical transparency are remarkably increased for these nanosized particles. Modifications in coloration are also observed.

  5. Magnetic properties of pure and surface-treated vanadium

    SciTech Connect

    DeSchutter, F.; Bruynseraede, Y.; Gilabert, A.

    1983-05-01

    The very high surface pinning present in superconductors strongly hinders the analysis of fission fragment irradiation experiments which produce heavy damage in a surface layer of approximately 10 ..mu..m. In order to decrease this pinning effect, different treatments such as coating with a normal metal or oxygen diffusion can be used. In this paper we show that oxygen doping lowers the critical temperature T /SUB c/ of Vanadium and surface oxidation reduces drastically the irreversibility of magnetization curves. The authors show that the dependence of T /SUB c/ on the oxygen concentration combined with the measurement of the oxygen concentration gradient (obeying Fick's diffusion law) can explain their magnetic permeability data.

  6. 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.

  7. Hydrogen and deuterium diffusion in vanadium-titanium alloys

    NASA Astrophysics Data System (ADS)

    Peterson, D. T.; Herro, H. M.

    1987-02-01

    Hydrogen and deuterium diffusion coefficients were measured in vanadium-titanium alloys, containing up to 30 at. pct Ti, by Boltzmann-Matano techniques. Hydrogen and deuterium diffusivity decreased rapidly with titanium concentration. The diffusion coefficients showed an Arrhenius temperature dependence in each alloy between 230 and 473 K with activation energies that increased with titanium concentration. The diffusion coefficient decreased linearly with hydrogen concentration in all alloys. The terminal solid solubilities increased markedly with titanium concentration with deuterium showing a larger terminal solid solubility than hydrogen below ten percent titanium. The diffusion results do not fit a localized deep trapping of hydrogen by the titanium atoms.

  8. Hydrogen and deuterium diffusion in vanadium-titanium alloys

    SciTech Connect

    Peterson, D.T.; Herro, H.M.

    1987-02-01

    Hydrogen and deuterium diffusion coefficients were measured in vanadium-titanium alloys, containing up to 30 at. pct Ti, by Boltzmann-Matano techniques. Hydrogen and deutrium diffusivity decreased rapidly with titanium concentration. The diffusion coefficients showed an Arrhenius temperature dependence in each alloy between 230 and 473 K with activation energies that increased with titanium concentration. The diffusion coefficient decreased linearly with hydrogen concentration in all alloys. The terminal solid solubilities increased markedly with titanium concentration with deuterium showing a larger terminal solid solubility than hydrogen below ten percent titanium. The diffusion results do not fit a localized deep trapping of hydrogen by the titanium atoms.

  9. 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%.

  10. Rechargeable hybrid aqueous batteries

    NASA Astrophysics Data System (ADS)

    Yan, Jing; Wang, Jing; Liu, Hao; Bakenov, Zhumabay; Gosselink, Denise; Chen, P.

    2012-10-01

    A new aqueous rechargeable battery combining an intercalation cathode with a metal (first order electrode) anode has been developed. The concept is demonstrated using LiMn2O4 and zinc metal electrodes in an aqueous electrolyte containing two electrochemically active ions (Li+ and Zn2+). The battery operates at about 2 V and preliminarily tests show excellent cycling performance, with about 90% initial capacity retention over 1000 charge-discharge cycles. Use of cation-doped LiMn2O4 cathode further improves the cyclability of the system, which reaches 95% capacity retention after 4000 cycles. The energy density for a prototype battery, estimated at 50-80 Wh kg-1, is comparable or superior to commercial 2 V rechargeable batteries. The combined performance attributes of this new rechargeable aqueous battery indicate that it constitutes a viable alternative to commercial lead-acid system and for large scale energy storage application.

  11. Responsive aqueous foams.

    PubMed

    Fameau, Anne-Laure; Carl, Adrian; Saint-Jalmes, Arnaud; von Klitzing, Regine

    2015-01-12

    Remarkable properties have emerged recently for aqueous foams, including ultrastability and responsiveness. Responsive aqueous foams refer to foams for which the stability can be switched between stable and unstable states with a change in environment or with external stimuli. Responsive foams have been obtained from various foam stabilizers, such as surfactants, proteins, polymers, and particles, and with various stimuli. Different strategies have been developed to design this type of soft material. We briefly review the two main approaches used to obtain responsive foams. The first approach is based on the responsiveness of the interfacial layer surrounding the gas bubbles, which leads to responsive foams. The second approach is based on modifications that occur in the aqueous phase inside the foam liquid channels to tune the foam stability. We will highlight the most sophisticated approaches, which use light, temperature, and magnetic fields and lead to switchable foam stability. PMID:25384466

  12. Rheology of aqueous foams

    NASA Astrophysics Data System (ADS)

    Dollet, Benjamin; Raufaste, Christophe

    2014-10-01

    Aqueous foams are suspensions of bubbles inside aqueous phases. Their multiphasic composition leads to a complex rheological behavior that is useful in numerous applications, from oil recovery to food/cosmetic processing. Their structure is very similar to the one of emulsions, so that both materials share common mechanical properties. In particular, the presence of surfactants at the gas-liquid interfaces leads to peculiar interfacial and dissipative properties. Foam rheology has been an active research topics and is already reported in several reviews, most of them covering rheometry measurements at the scale of the foam, coupled with interpretations at the local scale of bubbles or interfaces. In this review, we start following this approach, then we try to cover the multiscale features of aqueous foam flows, emphasizing regimes where intermediate length scales need to be taken into account or regimes fast enough regarding internal time scales so that the flow goes beyond the quasi-static limit. xml:lang="fr"

  13. Pentavalent vanadium at concentration of the underground water level enhances the sweet taste sense to glucose in college students.

    PubMed

    Nagai, Masanori; Saitoh, Junko; Ohno, Hiromi; Hitomi, Chiaki; Wada, Maki

    2006-02-01

    Underground water in volcanic areas contains vanadium when the basalt layer exists among igneous rocks. The concentration of vanadium in drinking water sometimes exceeds 0.8 microM in these areas, however, the physiological effects of vanadium, especially non-toxic effects, at concentrations lower than 1 microM are unknown. In the present experiments, we examined the effect of pentavalent vanadium and tetravalent vanadium at 0.8 and 8.0 microM concentrations on the recognition threshold to taste substances in healthy college students. Pentavalent vanadium, ammonium vanadate, lowered the sweet taste threshold to glucose at 0.8 and 8.0 microM as well. Tetravalent vanadium, vanadium sulfate, did not alter the threshold to glucose either at 8.0 microM or at 0.8 microM. Ammonium vanadate also decreased the sweet taste threshold to L-proline at 8.0 microM. Ammonium vanadate did not influence the sour taste threshold to hydrogen chloride. Neither ammonium sulfate nor ammonium bicarbonate altered the sweet taste threshold to glucose. Therefore, the effect of ammonium vanadate on the sweet taste threshold is attained by vanadium but not by ammonium. It was concluded that pentavalent vanadium at 0.8 microM intensifies the sweet taste sense to glucose rather specifically. We have first shown the physiological effect of vanadium at the concentration of the underground water level. PMID:16502326

  14. 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.

  15. Aqueous citrato-oxovanadate(IV) precursor solutions for VO2: synthesis, spectroscopic investigation and thermal analysis.

    PubMed

    Peys, Nick; Adriaensens, Peter; Van Doorslaer, Sabine; Gielis, Sven; Peeters, Ellen; De Dobbelaere, Christopher; De Gendt, Stefan; Hardy, An; Van Bael, Marlies K

    2014-09-01

    An aqueous precursor solution, containing citrato-VO(2+) complexes, is synthesized for the formation of monoclinic VO2. With regard to the decomposition of the VO(2+) complexes towards vanadium oxide formation, it is important to gain insights into the chemical structure and transformations of the precursor during synthesis and thermal treatment. Hence, the conversion of the cyclic [V4O12](4-) ion to the VO(2+) ion in aqueous solution, using oxalic acid as an acidifier and a reducing agent, is studied by (51)Vanadium nuclear magnetic resonance spectroscopy. The citrate complexation of this VO(2+) ion and the differentiation between a solution containing citrato-oxalato-VO(2+) and citrato-VO(2+) complexes are studied by electron paramagnetic resonance and Fourier transform infra-red spectroscopy. In both solutions, the VO(2+) containing complex is mononuclear and has a distorted octahedral geometry with a fourfold R-CO2(-) ligation at the equatorial positions and likely a fifth R-CO2(-) ligation at the axial position. Small differences in the thermal decomposition pathway between the gel containing citrato-oxalato-VO(2+) complexes and the oxalate-free gel containing citrato-VO(2+) complexes are observed between 150 and 200 °C in air and are assigned to the presence of (NH4)2C2O4 in the citrato-oxalato-VO(2+) solution. Both precursor solutions are successfully used for the formation of crystalline vanadium oxide nanostructures on SiO2, after thermal annealing at 500 °C in a 0.1% O2 atmosphere. However, the citrato-oxalato-VO(2+) and the oxalate-free citrato-VO(2+) solution result in the formation of monoclinic V6O13 and monoclinic VO2, respectively. PMID:25005054

  16. 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.

  17. 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.

  18. Vanadium alloys for the radiative divertor program of DIII-D

    SciTech Connect

    Smith, J.P.; Johnson, W.R.; Stambaugh, R.D.; Trester, P.W.; Smith, D.; Bloom, E.

    1995-10-01

    Vanadium alloys provide an attractive solution for fusion power plants as they exhibit a potential for low environmental impact due to low level of activation from neutron fluence and a relatively short half-life. They also have attractive material properties for use in a reactor. General Atomics along with Argonne National Laboratory (ANL) and Oak Ridge National Laboratory (ORNL), has developed a plan to utilize vanadium alloys as part of the Radiative Divertor Project (RDP) modification for the DIII-D tokamak. The goal for using vanadium alloys is to provide a meaningful step towards developing advanced materials for fusion power applications by demonstrating the in-service behavior of a vanadium alloy (V-4Cr-4Ti) in a tokamak in conjunction with developing essential fabrication technology for the manufacture of full-scale vanadium alloy components. A phased approach towards utilizing vanadium in DIII-D is being used starting with small coupons and samples, advancing to a small component, and finally a portion of the new double-null, slotted divertor will be fabricated from vanadium alloy product forms. A major portion of the program is research and development to support fabrication and resolve key issues related to environmental effects.

  19. 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.

  20. Effect of iron on vanadium (001) strained surface magnetism

    NASA Astrophysics Data System (ADS)

    Elzain, M.; Al-Barwani, M.; Gismelseed, A.; Al-Rawas, A.; Yousif, A.; Widatallah, H.; Bouziane, K.; Al-Omari, I.

    2010-03-01

    The magnetism of the vanadium (001) surface has been a controversial subject on both theoretical and experiment fronts. Both strongly ferromagnetic and paramagnetic phases were reported. We have used the first principle full-potential linearized-augmented plane waves (FP-LAPW) as implemented in WIEN2k package to study the magnetic properties of strained surfaces of vanadium films as a function of film thickness. We found that for films thicker than about 11 monolayers, the magnetism of the strained surfaces converge to a constant value of about 0.15μB. Introduction of Fe monolayers and impurities at the centre of the films affects the magnetic structure of thin films but has no influence on the surface magnetism of thicker films. For Fe monolayers positioned at the centre of thick films, the Fe atoms maintain magnetic moment of order 0.86μB, a quadruple splitting of order -0.3 mm/s and a small negative isomer shift, while an Fe impurity has vanishing hyperfine fields and magnetic moment. In addition we have varied the location of the Fe monolayer and impurity within the V films and found that their position affects the surface magnetism.

  1. Mechanical and electrochemical characterization of vanadium nitride (VN) thin films

    NASA Astrophysics Data System (ADS)

    Caicedo, J. C.; Zambrano, G.; Aperador, W.; Escobar-Alarcon, L.; Camps, E.

    2011-10-01

    Vanadium nitride (V-N) thin films were grown using a reactive d.c. magnetron sputtering process, from a vanadium target (99.999%) in an Ar/N 2 gas mixture at different deposition bias voltage. Films were deposited onto silicon (1 0 0) and RUS-3 steel substrates at 400 °C. Structural, compositional, mechanical and electrochemical characterizations were performed by X-ray diffraction (XRD), elastic forward analysis (EFA), nanoindentation, electrochemical impedance spectroscopy (EIS), and Tafel polarization curves, respectively. X-ray diffraction patterns show the presence of (1 1 1) and (2 0 0) crystallographic orientations associated to the V-N cubic phase. Nanoindentation measurements revealed that when the bias voltage increases from 0 V to -150 V the hardness and elastic modulus are increased from 11 GPa to 20 GPa and from 187 GPa to 221 GPa, respectively. EIS and Tafel curves showed that the corrosion rate of steel, coated with V-N single layer films deposited without bias voltage, diminishes 90% compared to the steel without this coating. On the other hand, when the V-N coating was deposited at the highest d.c. bias voltage (-150 V), the corrosion rate was greater than in the steel coated with zero-voltage (0 V) V-N films. This last result could be attributed to the formation of porosities produced by the ion bombardment during the deposition process.

  2. Phonon Entropy of Alloying in Dilute Vanadium Alloys

    NASA Astrophysics Data System (ADS)

    Delaire, Olivier; Swan-Wood, Tabitha; Kresch, Max; Fultz, Brent

    2005-03-01

    We investigate the entropic effects associated with changes in the phonon modes of vanadium upon dilute substitutional alloying. Using inelastic neutron scattering, we have measured the phonon DOS and the phonon entropy of mixing in V - 6%X, with X a transition metal impurity. We study trends for impurities across the d-series and down several columns of the periodic table. We show that for Ni, Pd and Pt impurities, the phonon entropy of alloying is large and negative, and in the case of Pt it results in a negative total entropy of mixing for 6% impurities. A Born-von Karman model was used to invert the experimental DOS curves and showed that the phonon stiffening down this column is associated with an increases in 1NN longitudinal inter-atomic force-constants. The changes in the phonon DOS for impurities across the 3d series are also correlated with the previously measured changes in the superconducting temperature Tc. Ab-initio DFT simulations were used to compute the effect of impurities on the electronic and phonon properties of vanadium, and are compared to the experimental results. This work was supported by DOE through the BES Grant DE-FG03-0346055 and BES-MS, W-31-109-ENG-38.

  3. 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. PMID:25194319

  4. Growth of ultrathin vanadium oxide films on Ag(100)

    NASA Astrophysics Data System (ADS)

    Nakamura, Takuya; Sugizaki, Yuichi; Ishida, Shuhei; Edamoto, Kazuyuki; Ozawa, Kenichi

    2016-07-01

    Vanadium oxide films were grown on Ag(100) by vanadium deposition in O2 and subsequent annealing at 450 °C. It was found that at least three types of ordered V oxide films, which showed (1 × 1), hexagonal, and (4 × 1) LEED patterns, were formed on Ag(100) depending on the O2 pressure during deposition and conditions during postannealing. The films with the hexagonal and (1 × 1) periodicities were characterized by photoelectron spectroscopy (PES) and near-edge X-ray absorption fine structure (NEXAFS) analysis. The film with the (1 × 1) periodicity was ascribed to a VO(100) film. On the other hand, the film with the hexagonal periodicity was found to be composed of V2O3, and the analysis of the LEED pattern revealed that the lattice parameter of the hexagonal lattice is 0.50 nm, which is very close to that of corundum V2O3(0001) (0.495 nm).

  5. 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}.

  6. 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.

  7. 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

  8. Reactivity of molybdovanadophosphoric acids: Influence of the presence of vanadium in the primary and secondary structure

    SciTech Connect

    Casarini, D.; Centi, G.; Lena, V.; Tvaruzkova, Z. ); Jiru, P. )

    1993-10-01

    The catalytic behavior in butadiene and n-butane oxidation of molybdovanadophosphoric acids with vanadium localized inside the primary (oxoanion) and/or the secondary structure is reported. The samples are characterized by infrared, [sup 31]P-NMR, [sup 51]V-NMR, and UV-visible diffuse reflectance spectroscopies in order to obtain information on the nature and localization of vanadium in the samples before reaction and the possible changes occurring during the course of the catalytic reaction. In particular, it is shown that vanadium localized initially in the secondary structure can exchange with the molybdenum atoms of the oxoanion during the catalytic reaction. Introduction of vanadium in the molybdophosphoric acid structure enhances the selective formation of maleic anhydride from the butadiene when vanadium is present both inside the oxoanion or localized in the secondary structure (before the catalytic tests), but the maximum in catalytic performance is found for different amounts of vanadium, depending on where the vanadium is localized initially. However, when present in the secondary structure, vanadium also has a negative influence on the activity of the heteropoly acid. On the contrary, in n-butane oxidation, the presence of vanadium enhances the rate of alkane activation due to the different rate-determining step. The presence of V ions also affects the maximum selectivity and yield to maleic anhydride from butane. V ions in the secondary structure are more selective at low conversion, while V ions inside the oxoanion are more selective at higher conversions and thus allow better maximum yields to maleic anhydride. 40 refs., 11 figs., 2 tabs.

  9. Influence of vanadium-doping on the magnetism of FeCo/SiO2 nanoparticle.

    PubMed

    Desautels, Ryan D; Rowe, Michael P; Freeland, John W; Jones, Michael; van Lierop, Johan

    2016-06-21

    FeCo nanoparticles (4 ± 1 nm), encapsulated by SiO2, were synthesized with and without a 2% (atomic ratio) vanadium doping. The impact from the presence of vanadium, an additive often used in the bulk to alter both physical and mechanical properties, on the nanomagnetism was probed by element-specific X-ray spectroscopy and magnetometry techniques. While the nanostructure was unaffected by the addition of 2% vanadium, the temperature dependent magnetic properties were altered significantly, such as the increased coercivity and an exchange bias field shift. PMID:27232274

  10. Thermal oxidation-grown vanadium dioxide thin films on FTO (Fluorine-doped tin oxide) substrates

    NASA Astrophysics Data System (ADS)

    Tong, Guoxiang; Li, Yi; Wang, Feng; Huang, Yize; Fang, Baoying; Wang, Xiaohua; Zhu, Huiqun; Li, Liu; Shen, Yujian; Zheng, Qiuxin; Liang, Qian; Yan, Meng; Qin, Yuan; Ding, Jie

    2013-11-01

    By deposition of metallic vanadium on FTO substrate in Argon atmosphere at room temperature, the sample was then annealed in furnace for 2 h at the temperature of 410 °C in air ambient. (1 1 0) -orientated vanadium dioxide films were prepared on the FTO surface. A maximum transmittance of ˜40% happened at 900-1250 nm region at room temperature. The change of optical transmittance at this region was ˜25% between semiconducting and metallic states. In particular, vanadium dioxide thin films on FTO exhibit semiconductor-metal phase transition at ˜51 °C, the width of the hysteresis loop is ˜8 °C.

  11. 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. PMID:12092761

  12. 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

  13. Kinetic study of the reaction of vanadium and vanadium-titanium oxide cluster anions with SO2.

    PubMed

    Janssens, Ewald; Lang, Sandra M; Brümmer, Mathias; Niedziela, Andrzej; Santambrogio, Gabriele; Asmis, Knut R; Sauer, Joachim

    2012-11-01

    The reactivity of mass-selected V(4)O(10)(-) cluster anions towards sulphur dioxide is investigated in an ion trap under multi-collision conditions. Gas phase reaction kinetics are studied as a function of temperature (T(R) = 150-275 K). The binding energy of SO(2) to V(4)O(10)(-) is obtained by analyzing the experimental low pressure rate constants, employing the Lindemann energy transfer model for association reactions in conjunction with statistical RRKM theory. In addition, infrared multiple photon dissociation spectroscopy is used in conjunction with density functional theory for the structural assignment of the [V(4)O(10)(-), SO(2)] complex, revealing a square pyramidal structure with the SO(2) molecule incorporated in the vanadium oxide framework. Energy profiles are calculated for the reaction between V(4)O(10)(-) and V(6)O(15)(-) with SO(2). Whereas the transition structures along the reaction pathway of V(4)O(10)(-) with SO(2) have energies below those of the separated partners, the reaction of V(6)O(15)(-) with SO(2) proceeds via a transition structure with energy higher than the educts. The role of cluster size and composition is investigated by studying the reaction kinetics of larger (V(6)O(15)(-) and V(8)O(20)(-)) and titanium doped (V(3)TiO(10)(-) and V(2)Ti(2)O(10)(-)) vanadium oxide clusters with SO(2). The observed cluster size and composition dependencies are discussed. PMID:23008835

  14. A Kinetics and Equilibrium Study of Vanadium Dissolution from Vanadium Oxides and Phosphates in Battery Electrolytes: Possible Impacts on ICD Battery Performance

    PubMed Central

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

    2013-01-01

    Silver vanadium oxide (Ag2V4O11, SVO) has enjoyed widespread commercial success over the past 30 years as a cathode material for implantable cardiac defibrillator (ICD) batteries. Recently, silver vanadium phosphorous oxide (Ag2VO2PO4, SVPO) has been studied as possibly combining the desirable thermal stability aspects of LiFePO4 with the electrical conductivity of SVO. Further, due to the noted insoluble nature of most phosphate salts, a lower material solubility of SVPO relative to SVO is anticipated. Thus, the first vanadium dissolution studies of SVPO in battery electrolyte solutions are described herein. The equilibrium solubility of SVPO was ~5 times less than SVO, with a rate constant of dissolution ~3.5 times less than that of SVO. The vanadium dissolution in SVO and SVPO can be adequately described with a diffusion layer model, as supported by the Noyes-Whitney equation. Cells prepared with vanadium-treated anodes displayed higher AC impedance and DC resistance relative to control anodes. These data support the premise that SVPO cells are likely to exhibit reduced cathode solubility and thus less affected by increased cell resistance due to cathode solubility compared to SVO based cells. PMID:25866437

  15. 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

  16. CO Adsorption study of V/SiO 2: the low vanadium coverage regime

    NASA Astrophysics Data System (ADS)

    Immaraporn, B.; Magg, N.; Kaya, S.; Wang, J.; Bäumer, M.; Freund, H.-J.

    2004-07-01

    Adsorption of CO and its isotopic mixtures on vanadium particles in the very low coverage growth regime (0.02-0.05 MLV) on an ultra-thin ordered silica film is monitored by IRAS at 60 K. At different CO exposures, development of different vibrational peaks was observed. These peaks are assigned to either mono- or tri-carbonyl species [V(CO) x; x=1,3] via isotopic mixture experiments. Comparing vanadium growth both on the alumina and silica films, it can be inferred from CO adsorption experiments that the metal-support interaction is weaker for vanadium growth on the silica film. The charge transfer between the vanadium metal center and the silica film is estimated based on a charge-frequency relationship to be +0.4e.

  17. 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.

  18. Extending the carbon chain: hydrocarbon formation catalyzed by vanadium/molybdenum nitrogenases.

    PubMed

    Hu, Yilin; Lee, Chi Chung; Ribbe, Markus W

    2011-08-01

    In a small-scale reaction, vanadium-dependent nitrogenase has previously been shown to catalyze reductive catenation of carbon monoxide (CO) to ethylene, ethane, propylene, and propane. Here, we report the identification of additional hydrocarbon products [α-butylene, n-butane, and methane (CH(4))] in a scaled-up reaction featuring 20 milligrams of vanadium-iron protein, the catalytic component of vanadium nitrogenase. Additionally, we show that the more common molybdenum-dependent nitrogenase can generate the same hydrocarbons from CO, although CH(4) was not detected. The identification of CO as a substrate for both molybdenum- and vanadium-nitrogenases strengthens the hypothesis that CO reduction is an evolutionary relic of the function of the nitrogenase family. Moreover, the comparison between the CO-reducing capacities of the two nitrogenases suggests that the identity of heterometal at the active cofactor site affects the efficiency and product distribution of this reaction. PMID:21817053

  19. Characterization of vanadium-doped mesoporous titania and its adsorption of gaseous benzene

    NASA Astrophysics Data System (ADS)

    Nguyen-Phan, Thuy-Duong; Song, Myoung Bock; Yun, Hyunran; Kim, Eui Jung; Oh, Eun-Suok; Shin, Eun Woo

    2011-01-01

    A series of vanadium-doped mesoporous titania with different metal contents was synthesized in the study via a sol-gel process with the assistance of a dodecylamine surfactant. The existence of vanadium ions not only suppressed crystallization and sintering but also enhanced the porosity of the mesoporous TiO 2. Varying the vanadium concentration led to significant changes in the chemical oxidation state of each component. The presence of metal dopants significantly improved the removal efficiency of benzene and the doping the titania with 5 mol% vanadium removed the most benzene, regardless of the adsorption temperature. The adsorption behavior was elucidated by the specific surface area, the interactions between surface hydroxyl groups and the π-electrons of benzene, and the formation of σ-bonding and d-π* back-donation between the adsorbent and organic compounds.

  20. 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.

  1. 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.

  2. Alloying effect of vanadium upon structure and strength of {delta}-phase titanium trialuminide

    SciTech Connect

    Takahashi, Tohru; Iwami, Kenji; Hasegawa, Tadashi

    1997-12-31

    Titanium trialuminide intermetallic compound Al{sub 3}Ti, is characterized by its low density and its high oxidation resistance. Such properties are potentially useful in light-weight and heat-resistant structures for aerospace applications. Here, the allying effect of vanadium upon {delta}-phase titanium trialuminide has been investigated using materials whose compositions were of the type Al{sub 3}(Ti,V). Six types of ternary aluminum-titanium-vanadium alloys, ranging from Al{sub 3}Ti to Al{sub 3}V at 5 atomic % intervals, have been prepared by arc melting. All the materials showed the DO{sub 22} tetragonal structure, suggesting vanadium atoms substitute titanium atoms. The 0.2% proof stress increased with increasing vanadium content up to about 10 atomic %, and then decreased toward that of Al{sub 3}V both at room temperature and at elevated temperatures. Such behavior can be interpreted as substitutional solid solution strengthening.

  3. Capacity decay and remediation of nafion-based all-vanadium redox flow batteries.

    PubMed

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

    2013-02-01

    The relationship between electrochemical performance of vanadium redox flow batteries (VRBs) and electrolyte composition is investigated, and the reasons for capacity decay over charge-discharge cycling are analyzed and discussed herein. The results show that the reasons for capacity fading over real charge-discharge cycling include not only the imbalanced vanadium active species, but also the asymmetrical valence of vanadium ions in positive and negative electrolytes. The asymmetrical valence of vanadium ions leads to a state-of-charge (SOC)-range decrease in positive electrolytes and a SOC-range increase in negative electrolytes. As a result, the higher SOC range in negative half-cells further aggravates capacity fading by creating a higher overpotential and possible hydrogen evolution. Based on this finding, we developed two methods for restoring lost capacity, thereby enabling long-term operation of VRBs to be achieved without the substantial loss of energy resulting from periodic total remixing of electrolytes. PMID:23208862

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

    NASA Astrophysics Data System (ADS)

    Ngamsai, Kittima; Arpornwichanop, Amornchai

    2015-05-01

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

  5. Thermal radiative near field transport between vanadium dioxide and silicon oxide across the metal insulator transition

    NASA Astrophysics Data System (ADS)

    Menges, F.; Dittberner, M.; Novotny, L.; Passarello, D.; Parkin, S. S. P.; Spieser, M.; Riel, H.; Gotsmann, B.

    2016-04-01

    The thermal radiative near field transport between vanadium dioxide and silicon oxide at submicron distances is expected to exhibit a strong dependence on the state of vanadium dioxide which undergoes a metal-insulator transition near room temperature. We report the measurement of near field thermal transport between a heated silicon oxide micro-sphere and a vanadium dioxide thin film on a titanium oxide (rutile) substrate. The temperatures of the 15 nm vanadium dioxide thin film varied to be below and above the metal-insulator-transition, and the sphere temperatures were varied in a range between 100 and 200 °C. The measurements were performed using a vacuum-based scanning thermal microscope with a cantilevered resistive thermal sensor. We observe a thermal conductivity per unit area between the sphere and the film with a distance dependence following a power law trend and a conductance contrast larger than 2 for the two different phase states of the film.

  6. 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.

  7. Correlation between molten vanadium salts and the structural degradation of HK-type steel superheater tubes

    NASA Astrophysics Data System (ADS)

    de Carvalho Nunes, Frederico; de Almeida, Luiz Henrique; Ribeiro, André Freitas

    2006-12-01

    HK steels are among the most used heat-resistant cast stainless steels, being corrosion-resistant and showing good mechanical properties at high service temperatures. These steels are widely used in reformer furnaces and as superheater tubes. During service, combustion gases leaving the burners come in contact with these tubes, resulting in corrosive attack and a large weight loss occurs due to the presence of vanadium, which forms low melting point salts, removing the protective oxide layer. In this work the external surface of a tube with dramatic wall thickness reduction was analyzed using light microscopy, scanning electron microscopy, and transmission electron microscopy. The identification of the phases was achieved by energy dispersive spectroscopy (EDS) analyses. The results showed oxides arising from the external surface. In this oxidized region vanadium compounds inside chromium carbide particles were also observed, due to inward vanadium diffusion during corrosion attack. A chemical reaction was proposed to explain the presence of vanadium in the metal microstructure.

  8. Mars aqueous chemistry experiment

    NASA Technical Reports Server (NTRS)

    Clark, Benton C.; Mason, Larry W.

    1993-01-01

    The Mars Aqueous Chemistry Experiment (MACE) is designed to conduct a variety of measurements on regolith samples, encompassing mineral phase analyses, chemical interactions with H2O, and physical properties determinations. From these data, much can be learned or inferred regarding the past weathering environment, the contemporaneous soil micro-environments, and the general chemical and physical state of the Martian regolith. By analyzing both soil and duricrust samples, the nature of the latter may become more apparent. Sites may be characterized for comparative purposes and criteria could be set for selection of high priority materials on future sample return missions. Progress for the first year MACE PIDDP is reported in two major areas of effort: (1) fluids handling concepts, definition, and breadboard fabrication and (2) aqueous chemistry ion sensing technology and test facility integration. A fluids handling breadboard was designed, fabricated, and tested at Mars ambient pressure. The breadboard allows fluid manipulation scenarios to be tested under the reduced pressure conditions expected in the Martian atmosphere in order to validate valve operations, orchestrate analysis sequences, investigate sealing integrity, and to demonstrate efficacy of the fluid handling concept. Additional fluid manipulation concepts have also been developed based on updated MESUR spacecraft definition. The Mars Aqueous Chemistry Experiment Ion Selective Electrode (ISE) facility was designed as a test bed to develop a multifunction interface for measurements of chemical ion concentrations in aqueous solution. The interface allows acquisition of real time data concerning the kinetics and heats of salt dissolution, and transient response to calibration and solubility events. An array of ion selective electrodes has been interfaced and preliminary calibration studies performed.

  9. Continuous aqueous tritium monitor

    DOEpatents

    McManus, G.J.; Weesner, F.J.

    1987-10-19

    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 are 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. 2 figs.

  10. 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.

  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. Effect of water intercalation on VOx layers in dodecylamine-intercalated vanadium oxide nanotubes

    NASA Astrophysics Data System (ADS)

    Kweon, Hyocheon; Lee, Kyu Won; Lee, Eun Mo; Park, Jitae; Kim, I.-M.; Lee, Cheol Eui; Jung, G.; Gedanken, A.; Koltypin, Yu.

    2007-07-01

    Dodecylamine-intercalated vanadium oxide nanotubes were obtained by distinct synthesis processes. Water intercalation in the nanotube structure was identified in a marked manner by the distortion of the VOx layers in the x-ray diffraction patterns and enhanced V4+O absorption in the Fourier-transform infrared spectra. Our electron spin resonance measurements sensitively reflect changes in the microscopic structure and magnetic interactions introduced by the water intercalation in the vanadium oxide nanotubes.

  13. The high-temperature analytical uses of vanadium(V) oxide.

    PubMed

    Nebesar, B

    1978-04-01

    The review surveys the available representative information from several fields, on high-temperature analytical uses of vanadium(V) oxide during the last half-century. A brief historical background is included. The three main fields of use are organic microchemical analysis, macrocombustion determinations, and pyrohydrolysis, and the review covers apparatus and equipment, reagents, chemical considerations, characteristics of vanadium(V) oxide, procedural details, and evaluation of the results. PMID:18962239

  14. Determination of trace vanadium (V) in seawater and fresh water by the catalytic kinetic spectrophotometric method

    NASA Astrophysics Data System (ADS)

    Ji, Hongwei; Sha, Yuanyuan; Xin, Huizhen; Li, Shuang

    2010-12-01

    A new kinetic spectrophotometric method has been developed for the determination of vanadium (V). The method is based on the catalytic effect of vanadium (V) on the oxidation of weak acid brilliant blue dye (RAWL) by KBrO3 using the citric acid as activation reagent. The obtained optimum conditions are: c (RAWL) = 1×10-4 molL-1, c (KBrO3) = 3×10-2 molL-1, c (citric acid) = 9×10-3 molL-1, pH = 2.50, the reaction time being 7.0 min and the temperature being 25.0°C. Under the optimum conditions, the proposed method allows the determination of vanadium (V) in the range of 0-70.0 ng mL-1 and the detection limit is down to 0.407 ng mL-1. For standard vanadium (V) solution determination, the recovery efficiency is in the range of 98.5%-102% and the RSD ranges from 0.76%-1.25%. Moreover, it is demonstrated that most cations and anions do not interfere with the determination of vanadium (V) under the analytical condition. The new method was successfully applied in the determination of vanadium (V) in fresh water and seawater samples with satisfactory results. Vanadium (V) in the seawater samples from Qingdao offshore was determined using the method and the distribution of vanadium (V) was mapped. Compared with other instrumental analytical methods, the proposed method shows good selectivity, sensitivity, simplicity, lower cost and rapidity. It can be employed on shipboard easily.

  15. 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.

  16. 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.

  17. 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.

  18. 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.

  19. Vanadium dioxide nanomaterial for smart thermochromic glazing of windows

    NASA Astrophysics Data System (ADS)

    Li, Xiaoping; Chen, Sihai; Wang, Shuangbao; Lai, Jianjun; Chen, Changhong; Yi, Xinjian

    2004-02-01

    Nanostructural vanadium dioxide thin films are investigated as intelligent window coatings. The films are fabricated using reactive sputtering and post annealing. A reversible semiconductor to metal phase transition for as-deposited VO2 nanostructure films with grain size of ~8nm takes place at a temperature of 35°C, which lowers about 33°C in comparison with a phase transition temperature of 68°C in conventional VO2 films with a grain size of 1-2 μm. The results indicate that the nanostructural VO2 films are more suitable to the application for smart thermochromic glazing of windows than that of conventional VO2 films.

  20. FM-AFM crossover in vanadium oxide nanomaterials

    NASA Astrophysics Data System (ADS)

    Demishev, S. V.; Chernobrovkin, A. L.; Glushkov, V. V.; Grigorieva, A. V.; Goodilin, E. A.; Sluchanko, N. E.; Samarin, N. A.; Semeno, A. V.

    2010-01-01

    The magnetic properties of nanomaterials based on vanadium oxide (multiwall nanotubes, nanorods, and nanolayers) have been investigated in the temperature range of 1.8-220 K by high-frequency (60-GHz) EPR. A transition from a ferromagnetic temperature dependence to an antiferromagnetic temperature dependence has been observed in nanorods and nanotubes with a decrease in the temperature. The FM-AFM crossover observed near T C ˜ 110 K is accompanied by a low-temperature increase in the Curie constant by a factor of 2.7-7. The comparison of the experimental data for various VO x nanoparticles indicates that the most probable cause of the change in the type of magnetic interaction is a change in the concentration of V4+ magnetic ions.

  1. 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.

  2. Plasmonic properties of metal-vanadium dioxide nanostructures

    NASA Astrophysics Data System (ADS)

    Suh, Jae Yong

    This research is concerned with the fabrication of vanadium dioxide in the form of thin films and nanoparticles, and its effect on optical functionality when joined with two kinds of metallic nanostructures. As for the underlying physical phenomena, the metal-insulator phase transition in VO2 and the optical properties are studied. For the modulation of extraordinary transmission, metal-VO2 double-layer subwavelength aperture arrays were fabricated. For the modulation of the localized surface plasmon resonance of noble metal nanoparticles, gold nanoparticle arrays enveloped in a VO 2 thin film were created. These two-dimensional metal nanostructures incorporating a VO2 thin film exhibit a reverse hysteretic behavior and a plasmon resonance shift, respectively. Experimental measurements and simulations confirm that the complex dielectric functions of VO2 play an essential role in controlling the plasmonic properties of metal nanostructures.

  3. 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.

  4. 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.

  5. 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.

  6. 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. PMID:27464181

  7. 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.

  8. The trapping of hydrogen ions in vanadium and titanium

    NASA Astrophysics Data System (ADS)

    Arbuzov, V. L.; Vykhodets, V. B.; Raspopova, G. A.

    1996-10-01

    The accumulation of implanted deuterium has been investigated at room temperature in vanadium, titanium and their alloys up to (2-15) × 10 17 ions cm -2 fluences by means of D(d, p)T reaction. The amount of accumulated D was measured using a 700 KeV D + ion beam during implantation. It is found that concentration of implanted deuterium in irradiated samples nonmonotonously increases the increasing fluence and in a complicated manner depends upon VTi alloy composition. These data are explained by concentration dependence of D diffusion coefficient in VTi alloys, structural ion irradiation induced inhomogeneity of alloys with > 5-8 at.% Ti, and irradiation-enhanced diffusion of deuterium.

  9. Negative entropy of mixing for vanadium-platinum solutions.

    PubMed

    Delaire, O; Swan-Wood, T; Fultz, B

    2004-10-29

    The phonon densities of states for pure vanadium and the solid solutions V-6.25% Ni, Pd, Pt were determined from inelastic neutron scattering measurements. The solute atoms caused a large stiffening of the phonons, resulting in large, negative vibrational entropies of mixing. For V-6.25%Pt, the negative vibrational entropy of mixing exceeds the conventional positive chemical entropy of mixing. This negative total entropy of mixing should extend to lower concentrations of Pt, and the effect on the bcc solvus line is discussed. The experimental data were inverted to obtain interatomic force constants by using a Born-von Kármán model with an iterative optimization algorithm. The stiffening of bonds responsible for the decrease of entropy was found to occur mainly in first-nearest-neighbor solute-host bonds, and correlates in part with the solute metallic radius. PMID:15525182

  10. Negative Entropy of Mixing for Vanadium-Platinum Solutions

    NASA Astrophysics Data System (ADS)

    Delaire, O.; Swan–Wood, T.; Fultz, B.

    2004-10-01

    The phonon densities of states for pure vanadium and the solid solutions V-6.25% Ni, Pd, Pt were determined from inelastic neutron scattering measurements. The solute atoms caused a large stiffening of the phonons, resulting in large, negative vibrational entropies of mixing. For V-6.25%Pt, the negative vibrational entropy of mixing exceeds the conventional positive chemical entropy of mixing. This negative total entropy of mixing should extend to lower concentrations of Pt, and the effect on the bcc solvus line is discussed. The experimental data were inverted to obtain interatomic force constants by using a Born von Kármán model with an iterative optimization algorithm. The stiffening of bonds responsible for the decrease of entropy was found to occur mainly in first-nearest-neighbor solute-host bonds, and correlates in part with the solute metallic radius.

  11. Neutron radiography of a root growing in soil with vanadium

    NASA Astrophysics Data System (ADS)

    Furukawa, J.; Nakanishi, T. M.; Matsubayashi, M.

    1999-11-01

    We show how the root activity of water uptake is inhibited by the presence of vanadium in soil. A soybean seedling was grown in an aluminum container where water absorbing polymer with V was imbedded with soil. The sample was irradiated with thermal neutrons to get the radiograph on an X-ray film. Through image analysis, the water uptake manner both around the main root and side root was studied. When the water uptake along the main root was measured, the effect of V was observed as early as two days whilst no observable change in morphological development of main root as well as side root was detected. Since the microscopic research of water movement around the root is not well studied, this result is expected to be applied further, especially in constructing water absorbing model of the root.

  12. 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. PMID:25898154

  13. Vanadium isotopic composition of the sea squirt (Ciona savignyi).

    PubMed

    Nomura, Masao; Nakamura, Mana; Soeda, Ryosuke; Kikawada, Yoshikazu; Fukushima, Michiko; Oi, Takao

    2012-09-01

    Vanadium (V) in the sea squirt (Ciona savignyi) from Onagawa Bay, Miyagi, Japan, was isolated and purified through adsorption on a diamine resin and anion and cation exchanges after the dissolution of sea squirt samples with nitric acid and hydrogen peroxide. The (50)V/(51)V isotope ratio of V thus obtained was mass-spectrometrically determined to be from 2.51×10(-3) to 2.55×10(-3) with the average of 2.53×10(-3) by the thermal ionisation technique. This value agreed with those of vanadyl chloride and vanadyl nitrate both prepared from vanadyl sulphate (Wako Pure Chemical Industries, Ltd., Japan) and of V in coastal seawater (Shimokita Peninsula, Aomori, Japan) within experimental uncertainties (standard deviation of±0.04), which suggested that no appreciable V isotope fractionation occurs accompanying V uptake by the sea squirt from sea water. PMID:22462478

  14. 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}

  15. A basic study on the biological monitoring for vanadium-effects of vanadium on Vero cells and the evaluation of intracellular vanadium contents.

    PubMed

    Mochizuki, Mariko; Kudo, Eiko; Kikuchi, Mitsuho; Takano, Takashi; Taniuchi, Yojiro; Kitamura, Tomoya; Hondo, Ryo; Ueda, Fukiko

    2011-07-01

    A high concentration of vanadium (V) has toxic effects on human and animals and is one of environmental pollutants. In the present study, we have conducted a fundamental study using cultured Vero cells from monkey kidney for the future environmental monitoring. Orthovanadate (VAN), one of V compounds, of 10(-10) and 10(-8) M did not affect the cell growth although the higher concentration of above 10(-6) M VAN inhibited the cell growth accompanied with the decrease in cell numbers and morphological changes. Given that the washing method with ice-cold Li is also effective for determination of the cellular Na content, we used this method for the determination of the V content of the Vero cells. The V distributions in Vero cell; in the 10(-3) M VAN solution, extracellular and intracellular were obtained as 1:0.564:0.036 and 1:0.662:0.098 at 60 and 120 min after the treatment of VAN. The intracellular V content was 10% of the applied concentration of VAN. Consequently, it was suggested that V concentration of 10(-7) and 10(-6) M in the tissue and environment, respectively, might become the threshold concentration; a criterion of the environmental contamination when we carry out environmental monitoring. PMID:20556539

  16. 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.

  17. 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.

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

    NASA Astrophysics Data System (ADS)

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

    2003-12-01

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

  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. AN UPDATE ON BIAXIAL THERMAL CREEP OF VANADIUM ALLOYS

    SciTech Connect

    Kurtz, Richard J.; Ermi, August M.

    2002-09-01

    A study of the thermal creep properties of two vanadium alloys was performed using pressurized tube specimens. Creep tubes nominally 4.57 mm OD by 0.25 mm wall thickness were pressurized with high-purity helium gas to mid-wall effective stresses below the effective (Von Mises) yield strength. Specimens were fabricated from V-4Cr-4Ti (Heat No. 832665) and a V-3Fe-4Ti alloy. The samples were heated to 650, 700, 725, and 800 degrees C in an ultra-high vacuum furnace and periodically removed to measure the change in tube outer diameter with a high-precision laser profilometer. The normalized minimum creep rate was found to be power-law dependent on the modulus compensated applied stress. The value of the stress exponent varied with the applied stress. At normalized stresses ranging from 0.002 to 0.008 the stress exponent was about 4 and the activation energy was about 300 kJ/mole, which is quite close to the activation energy for self-diffusion in pure vanadium. These results suggest that the predominant mechanism of creep in this regime is climb-assisted dislocation motion. At lower stresses the value of the stress exponent is near unity suggesting that viscous creep mechanisms such as Coble creep or grain boundary sliding may be operative, but the data are too sparse to be conclusive. The reported creep rates from uniaxial tests [1] in vacuum are several times higher than the creep rates measured here. This is probably due to the larger interstitial oxygen concentration of the creep tubing (699 wppm) compared to the sheet stock (310 wppm) used for tensile specimen fabrication. Finally, the creep strength of V-4Cr-4Ti at 700 and 800 degrees C was superior to the V-3Fe-4Ti alloy.

  1. Vanadium and niobium additions in pressure vessel steels

    SciTech Connect

    Xu, Peiyuan.

    1992-01-01

    A statistically designed series of vanadium and niobium microalloyed C-Mn HSLA steels was used for an investigation of heat-affected zone (HAZ) toughness in multipass welds. The vanadium additions were in the range 0.005 to 0.097 Wt.% and the niobium additions were in the range 0.004 to 0.06 Wt.%. GMAW processes with welding heat inputs of 3kJ/mm and 5kJ/mm and post-weld heat treatments (PWHT) at additions of microalloy elements V and Nb on multipass HAZ toughness in the as-welded and PWHT conditions was confirmed. the 50 Joule transition temperature (TT50J) for HAZs in all weld conditions correlated with maximum HAZ hardness. Increases in HAZ hardness and TT50J caused by PWHT were observed. Hence PWHT is not recommended for V/Nb microalloyed HLSA steels. The randomly distributed precipitation of V and Nb carbides (V,Nb)C, including dislocation precipitation and matrix precipitation with particle sizes of 5-15nm, is the predominant alloy carbide precipitate morphology in these steels. Banded morphology of (V,Nb)C precipitation is rarely observed in the HAZ. The volume fraction of (V,Nb)C precipitates increases as increasing V and/or Nb contents in the experimental heats. The volume fraction of precipitates also increases with increasing the PWHT time. The crack initiation sites in Charpy specimens of HAZs tested at the approximate transition temperature are shifted from the highest stress triaxiality location to a higher hardness location. This is found to be characteristic of fracture in the multipass HAZ of the microalloyed steel. An analytical study shows that the influences of additions of microalloy elements V and Nb on yield stress, [sigma][sub y8], and fracture stress, [sigma][sub f], eventuate in the increase of transition temperature in these materials.

  2. Vanadium and columbium additions in pressure vessel steels

    SciTech Connect

    Xu, P.; Somers, B.R.; Pense, A.W.

    1994-09-01

    A statistically designed series of vanadium and columbium microalloyed C-Mn HSLA steels was used for an investigation of heat-affected zone (HAZ) toughness in post weld heat treated (PWHT) multi-pass welds. The vanadium additions were in the range 0.005 to 0.097 Wt.% and the columbium additions were in the range 0.004 to 0.06 Wt.% GMAW processes with welding heat inputs of 3kJ/mm and 5kJ/mm and post-weld heat treatments at 620 C for 2 10 hours were employed. A degradation of the HAZ toughness with additions of microalloy elements V and Cb in the as-welded and PWHT conditions was revealed. The 50 Joule (37 ft-lb) transition temperature (TT50J) for HAZs in all weld conditions correlated with maximum HAZ hardness. Increases in HAZ hardness and TT50J caused by PWHT were observed. Hence PWHT in some situations may not beneficial for V/Cb microalloyed HLSA steels. The randomly distributed precipitation of V and Cb carbides (V, Cb)C, including dislocation precipitation and matrix precipitation with particle sizes of 5--15 nm, is the predominant alloy carbide precipitate morphology in these steels. The crack initiation sites in Charpy specimens of HAZs tested at the approximate transition temperature are shifted from the highest stress triaxiality, mid-specimen location to an off center higher hardness location. This is found to be characteristic of fracture in the multipass HAZ of the microalloyed steel.

  3. 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.

  4. Effect of Vanadium Addition on Reliability and Microstructure of BaTiO3-Based Multilayer Ceramic Capacitors

    NASA Astrophysics Data System (ADS)

    Natsui, Hidesada; Shibahara, Takeshi; Yonezawa, Yu; Kido, Osamu

    2012-09-01

    The vanadium distribution in multilayer ceramic capacitors (MLCCs), sintered under a reducing atmosphere, was investigated using scanning transmission electron microscopy-electron energy loss spectroscopy (STEM-EELS), and insulation resistance degradation was analyzed using impedance spectroscopy in highly accelerated lifetime tests to clarify the effects of vanadium on both the electrical properties and microstructure of MLCCs. Vanadium mitigated insulation resistance degradation and increased the reliability of MLCCs. Moreover, vanadium content increased and insulation resistance at the ceramic/electrode interface decreased slowly. This change in dynamics directly resulted in an improved lifetime of MLCCs. The results of STEM-EELS analysis showed that vanadium distributed along the grain boundary and grain boundary junction, but substituted into BaTiO3 at the ceramic/electrode interface. Therefore, it is considered that vanadium substitution at the ceramic/electrode interface improves the reliability of MLCCs.

  5. Review of Advances in Development of Vanadium Alloys and MHD Insulator Coatings

    SciTech Connect

    Muroga, T.; Chen, J. M.; Chernov, V. M.; Fukumoto, Kenichi; Hoelzer, D. T.; Kurtz, Richard J.; Nagasaka, T.; Pint, Bruce A.; Satou, M.; Suzuki, Atsuyuki; Watanabe, Hideo

    2007-08-01

    In this paper, recent progress in the development of low activation vanadium alloys and MHD insulator coatings for Li-self cooled blanket is overviewed. The research progress in vanadium alloys is highlighted by technology of fabricating creep tubes, comparison of thermal creep in vacuum and Li, understanding on impurity transfer between vanadium alloys and Li and its impact on mechanical properties, behavior of hydrogen and hydrogen isotopes, low dose irradiation effects on weld joints and exploration for advanced vanadium alloys. Major remaining issues of vanadium alloys are thermal and irradiation creep, helium effects on high temperature mechanical properties and radiation effects on low temperature fracture properties. A new promising candidate of Er2O3, which showed good compatibility with Li, was identified for MHD insulator coating on vanadium alloys. The coating technology has made a significant progressed for the new candidate material. Recent efforts are being focused on multi-layer coating and in-situ coating. Tests in flowing lithium conditions with temperature gradient are necessary for quantitative examination of the performance.

  6. Influence of vanadium doping on the supercapacitance performance of hexagonal birnessite

    NASA Astrophysics Data System (ADS)

    Liu, Lihu; Min, Min; Liu, Fan; Yin, Hui; Zhang, Yashan; Qiu, Guohong

    2015-03-01

    Nanostructured birnessite, promising candidate for supercapacitor electrode materials, shows greatly improved discharge capacity and cyclic stability with vanadium doping. The influence of vanadium doping on the physicochemical properties and supercapacitance performance of birnessite-type manganese oxides is investigated. Crystal structures, micromorphologies, bond lengths and chemical compositions of vanadium doped birnessites are characterized by XRD, SEM, XPS, TGA, and titration. The electrochemical properties are analyzed using galvanostatic charge-discharge test, cyclic voltammetry, and electrochemical impedance spectroscopy. The results exhibit that V/Mn molar ratio can reach 0.16:1 when Mn(IV) and K+ are partially substituted by V(V) in birnessite. The thickness of disk-shaped crystal, bond length of Mn-O1 and manganese average oxidation state decreases first and then increases with an increase in V/Mn molar ratio in synthesis system. Charge-transfer resistance decreases after doping vanadium, and increases with an increase in the content of vanadium in birnessite. Diffusion resistance increases first and then decreases due to the change of particle size and pore size distribution. The highest specific capacitance of 245 F g-1 is obtained with excellent cyclic stability for doped birnessite with V/Mn molar ratio of 0.14:1. Our study indicates that vanadium remarkably affects micromorphology, substructure, and electrochemical properties of manganese dioxides.

  7. 51V solid-state magic angle spinning NMR spectroscopy of vanadium chloroperoxidase.

    PubMed

    Pooransingh-Margolis, Neela; Renirie, Rokus; Hasan, Zulfiqar; Wever, Ron; Vega, Alexander J; Polenova, Tatyana

    2006-04-19

    We report 51V solid-state NMR spectroscopy of the 67.5-kDa vanadium chloroperoxidase, at 14.1 T. We demonstrate that, despite the low concentration of vanadium sites in the protein (one per molecule, 1 mumol of vanadium spins in the entire sample), the spinning sideband manifold spanning the central and the satellite transitions is readily detectable. The quadrupolar and chemical shift anisotropy tensors have been determined by numerical simulations of the spinning sideband envelopes and the line shapes of the individual spinning sidebands corresponding to the central transition. The observed quadrupolar coupling constant C(Q) of 10.5 +/- 1.5 MHz and chemical shift anisotropy delta(sigma) of -520 +/- 13 ppm are sensitive reporters of the geometric and electronic structure of the vanadium center. Density functional theory calculations of the NMR spectroscopic observables for an extensive series of active site models indicate that the vanadate cofactor is most likely anionic with one axial hydroxo- group and an equatorial plane consisting of one hydroxo- and two oxo- groups. The work reported in this manuscript is the first example of 51V solid-state NMR spectroscopy applied to probe the vanadium center in a protein directly. This approach yields the detailed coordination environment of the metal unavailable from other experimental measurements and is expected to be generally applicable for studies of diamagnetic vanadium sites in metalloproteins. PMID:16608356

  8. 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.

  9. A novel comprehensive utilization of vanadium slag: As gamma ray shielding material.

    PubMed

    Dong, Mengge; Xue, Xiangxin; Yang, He; Liu, Dong; Wang, Chao; Li, Zhefu

    2016-11-15

    New exploration of vanadium slag as gamma ray shielding material was proposed, the shielding properties of vanadium slag was higher than concrete when the energy of photons was in 0.0001MeV-100000MeV. Vanadium slag/epoxy resin composites were prepared, shielding and material properties of materials were tested by (60)Co gamma ray, simultaneous DSC-TGA, electronic universal testing machine and scanning electron microscopy, respectively. The results showed that the shielding properties of composite would be better with the increase of vanadium slag addition amount. The HVL (half value layer thickness) of vanadium slag was between Lead and concrete while composite was higher than concrete when the addition amount of vanadium slag was 900 used as material to shield (60)Co gamma ray, also the resistance temperature of composite was about 215°C and the bending strength was over 10MPa. The composites could be used as injecting mortar for cracks developed in biological concrete shields, coating for the floor of the nuclear facilities, and shielding materials by itself. PMID:27343141

  10. Influence of intoxication with vanadium compounds on the intestinal absorption of calcium in the rat

    SciTech Connect

    Witkowska, D.; Oledzka, R.; Pietrzyk, B.

    1986-12-01

    Calcium is transferred to the plasma after absorption from the gastrointestinal tract and by resorption from the bone. It is recognized that many environmental poisons, e.g. heavy metal, pesticides etc. cause alterations in calcium homeosthasis in human beings and experimental animals. Although vanadium is not considered to be as important a health hazard to man as lead or cadmium it must be nevertheless regarded as a dangerous pollutant. There exists an obvious risk of pollution by and poisoning due to the high vanadium content of crude oil and the industrial use of vanadium as a steel additive. The toxic effects of this element and its compounds in many biological systems have been reviewed in detail but little is known about vanadium influence on calcium metabolism. The present study was undertaken to determine the effect of various treatments with vanadium compounds, containing vanadium as VO/sup 2 +/ (VOSO/sub 4/) and VO/sub 3/ (NaVO/sub 3/) ions, exert on calcium transport through the rat duodenum.

  11. Detection of capacity imbalance in vanadium electrolyte and its electrochemical regeneration for all-vanadium redox-flow batteries

    NASA Astrophysics Data System (ADS)

    Roznyatovskaya, Nataliya; Herr, Tatjana; Küttinger, Michael; Fühl, Matthias; Noack, Jens; Pinkwart, Karsten; Tübke, Jens

    2016-01-01

    A vanadium electrolyte for redox-flow batteries (VRFB) with different VIII and VIV mole fractions has been studied by UV-vis spectroscopy. Spectrophotometric detection enables a rough estimate of the VIV and VIII content, which can be used to detect an electrolyte capacity imbalance, i.e. a deviation in the mole fraction of VIV or VIII away from 50%. The isosbestic point at 600 nm can be used as a reference point in the analysis of common VRFB electrolyte batches. The VRFB electrolyte is observed to have an imbalance after prolonged storage (a couple of years) in a tank under ambient conditions. A regeneration procedure, which involves pre-charging the unbalanced electrolyte and mixing part of it with a portion of initial unbalanced electrolyte, has been tested. The resulting rebalanced electrolyte has been compared with a common electrolyte in a charge-discharge cell test and is shown to be suitable for cell operation.

  12. 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.

  13. New homoleptic organometallic derivatives of vanadium(III) and vanadium(IV): synthesis, characterization, and study of their electrochemical behaviour.

    PubMed

    Alonso, Pablo J; Forniés, Juan; García-Monforte, M Angeles; Martín, Antonio; Menjón, Babil

    2005-08-01

    The arylation of [VCl3(thf)3] with LiR(Cl), where R(Cl) is a polychlorinated phenyl group [C6Cl5, 2,4,6-trichlorophenyl(tcp), or 2,6-dichlorophenyl (dcp)] gives four-coordinate, homoleptic organovanadium(III) derivatives with the formula [Li(thf)(4)][V(III)(R(Cl))(4)] (R(Cl) = C(6)Cl(5) (1), tcp (2), dcp (3)). The anion [V(III)(C6Cl5)4]- has an almost tetrahedral geometry, as observed in the solid-state structure of [NBu4][V(C6Cl5)4] (1') (X-ray diffraction). Compounds 1-3 are electrochemically related to the neutral organovanadium(IV) species [V(IV)(R(Cl))4] (R(Cl) = C6Cl5 (4), tcp (5), dcp (6)). The redox potentials of the V(IV)/V(III) semisystems in CH2Cl2 decrease with decreasing chlorination of the phenyl ring (E(1/2) = 0.84 (4/1), 0.42 (5/2), 0.25 V (6/3)). All the [V(IV)(R(Cl))4] derivatives involved in these redox couples could also be prepared and isolated by chemical methods. The arylation of [VCl(3)(thf)(3)] with LiC6F5 also gives a homoleptic organovanadium(III) compound, but with a different stoichiometry: [NBu4]2[V(III)(C6F5)5] (7). In this five-coordinate species, the C6F5 groups define a trigonal bipyramidal environment for the vanadium atom (X-ray diffraction). EPR spectra for the new organovanadium compounds 1-6 are also given and analysed in terms of an elongated tetrahedral structure with C(2v) local symmetry. It is suggested that the R(Cl) groups exert a protective effect towards the vanadium centre. PMID:15915520

  14. Vanadium contamination of lichens and tree foliage in the vicinity of three oil-fired power plants in Eastern Canada

    SciTech Connect

    Juichang, R.; Freedman, B.; Coles, C.; Zwicker, B.; Holzbecker, J.; Chatt, A.

    1995-06-01

    Vanadium concentrations were determined by neutron activation analysis in samples of epiphytic lichens and tree foliage collected at sites along 10 transects in the vicinity of three oil-fired power plants in eastern Canada. The vanadium concentrations in plants decreased exponentially with increasing distance from the power plants. Substantially larger concentrations of vanadium occurred in lichen tissues than in tree foliage. Lichens clearly are more suitable for biomonitoring environmental contamination with vanadium near oil-fired power plants. 2 refs., 1 fig., 2 tabs.

  15. Vanadium compounds for the treatment of human diabetes mellitus: A scientific curiosity? A review of thirty years of research.

    PubMed

    Domingo, José L; Gómez, Mercedes

    2016-09-01

    In the second part of the 1980s, and in the 1990s, a number of investigators demonstrated -mainly in streptozotocin-induced (STZ) diabetic rats-that the vanadate and vanadyl forms of vanadium possessed a number of insulin-like effects in various cells. It was hypothesized that oral vanadium could be an alternative treatment to parenteral insulin in the therapy of diabetes mellitus. However, the long-term and/or chronic administration of vanadium compounds should also mean tissue vanadium accumulation and risks of toxicity. The purpose of this review was to revise the current-state-of-the-art on the use of vanadium in the treatment of human diabetes. It has been conducted more than three decades after the first report on the beneficial insulin-mimetic effects of oral vanadium administration in STZ-diabetic rats. Although the antidiabetic effects of vanadium in STZ-diabetic rodents are well supported, in the few studies on human patients with positive results, that are available in the literature, vanadium compounds were administered during very short periods. We conclude that vanadium administration for the treatment of human diabetes is misplaced. PMID:27417449

  16. Mars aqueous chemistry experiment

    NASA Technical Reports Server (NTRS)

    Clark, Benton C.; Mason, Larry W.

    1994-01-01

    Mars Aqueous Chemistry Experiment (MACE) is designed to conduct a variety of measurements on regolith samples, encompassing mineral phase analyses, chemical interactions with H2O, and physical properties determinations. From these data, much can be learned or inferred regarding the past weathering environment, the contemporaneous soil micro-environments, and the general chemical and physical state of the Martian regolith. By analyzing both soil and duricrust samples, the nature of the latter may become more apparent. Sites may be characterized for comparative purposes and criteria could be set for selection of high priority materials on future sample return missions. The second year of the MACE project has shown significant progress in two major areas. MACE Instrument concept definition is a baseline design that has been generated for the complete MACE instrument, including definition of analysis modes, mass estimates and thermal model. The design includes multiple reagent reservoirs, 10 discrete analysis cells, sample manipulation capability, and thermal control. The MACE Measurement subsystems development progress is reported regarding measurement capabilities for aqueous ion sensing, evolved gas sensing, solution conductivity measurement, reagent addition (titration) capabilities, and optical sensing of suspended particles.

  17. Aqueous cleaning design presentation

    NASA Technical Reports Server (NTRS)

    Maltby, Peter F.

    1995-01-01

    The phase-out of CFC's and other ozone depleting chemicals has prompted industries to re-evaluate their present methods of cleaning. It has become necessary to find effective substitutes for their processes as well as to meet the new cleaning challenges of improved levels of cleanliness and to satisfy concerns about environmental impact of any alternative selected. One of the most popular alternatives being selected is aqueous cleaning. This method offers an alternative for removal of flux, grease/oil, buffing compound, particulates and other soils while minimizing environmental impact. What I will show are methods that can be employed in an aqueous cleaning system that will make it environmentally friendly, relatively simple to maintain and capable of yielding an even higher quality of cleanliness than previously obtained. I will also explore several drying techniques available for these systems and other alternatives along with recent improvements made in this technology. When considering any type of cleaning system, a number of variables should be determined before selecting the basic configuration. Some of these variables are: (1) Soil or contaminants being removed from your parts; (2) The level of cleanliness required; (3) The environmental considerations of your area; (4) Maintenance requirements; and (5) Operating costs.

  18. 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. PMID:27154842

  19. 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.

  20. NMR investigation of the interaction of vanadate with carbasilatranes in aqueous solutions.

    PubMed

    Evgeniou, Evgenios M; Pergantis, Spyros A; Leontidis, Epameinondas; Keramidas, Anastasios D

    2005-10-17

    Reaction of vanadate with carbasilatranes [methoxy{N,N',N' '-2,2',3-[bis(1-methylethanolato)(propyl)]amino}silane (1), methoxy{N,N',N' '-2,2',3-[bis(1-ethanolethanolato)(propyl)]amino}silane (2), and {N,N',N' '-2,2',2-[bis(ethanolato)(glycolpropyl ether)]amino}silane (3)] in aqueous solution results in the formation of vanadosilicates and five-coordinated chelate vanadium(V) complexes as evidenced by 51V, 1H, and 13C NMR spectroscopy. Chiral carbasilatrane S,S-1 was characterized in the solid state by X-ray diffraction, revealing a trigonal bipyramidal geometry around the metal ion, with one unidentate methoxy group and one atrane nitrogen atom at the axial positions and one carbon and two atrane oxygen atoms at the equatorial plane of the bipyramid. Crystal data (Mo Kalpha; 100(2) K) are as follows: orthorhombic space group P2(1)2(1)2(1); a = 8.8751(6), b = 9.7031(7), c = 14.2263(12) A; Z = 4. The complexation of vanadium either with 1 or 2 is stereoselective yielding approximately 94% of the complex containing ligand in the S,R-configuration. The lower ability of the S,S- and R,R-diastereoisomers of 1 and 2 to ligate vanadate was attributed to stereochemical factors, dictating a square pyramidal geometry for the chelated complexes. A dynamic process between the vanadium chelate complexes and the respective carbasilatranes was evaluated by 2D {1H} EXSY NMR spectroscopy. These spectra show that the vanadate complexes with the open carbasilatranes exchange more slowly with the free ligand compared to the respective alcohol aminate complexes. PMID:16212377