WorldWideScience

Sample records for anodic niobium oxides

  1. Surfactant-assisted growth of anodic nanoporous niobium oxide with a grained surface

    Energy Technology Data Exchange (ETDEWEB)

    Yoo, Jeong Eun [Department of Chemical Engineering, Inha University, 253 Yonghyun Dong, Nam-Gu, Incheon 402-751 (Korea, Republic of); Choi, Jinsub, E-mail: jinsub@inha.ac.k [Department of Chemical Engineering, Inha University, 253 Yonghyun Dong, Nam-Gu, Incheon 402-751 (Korea, Republic of)

    2010-07-15

    Nanoporous niobium oxide film with a maximum thickness of 520 nm was prepared by anodizing niobium in a mixture of 1 wt% HF, 1 M H{sub 3}PO{sub 4}, and a small amount of Sodium Dodecyl Sulfate (SDS) surfactant. The porosity of the anodic niobium oxide prepared without SDS is irregular with the surface of the oxide suggesting a grained surface pattern rather than an ordered porous structure. A proper amount of SDS addition can prepare a pore arrangement with stripe patterns. The pore depth and surface pattern were strongly affected by the concentration of SDS and bath temperature. We found that the addition of SDS surfactant facilitated improvement in the chemical resistance of niobium oxide, leading to the formation of pores with a longer length compared to those prepared without a SDS surfactant. This can be in part ascribed to the protection of the surface by the physical adsorption of SDS on the surface due to a charge-charge interaction and be in part attributed to the formation of Nb=O bonding on the outermost oxide layer by SDS. When anodization was carried out for 4 h, the surface dissolution of niobium oxide was observed, which means that the maximum tolerance time against chemical dissolution was less than 4 h.

  2. X-ray spectral determination of chemical state of phosphorus and sulfur in anodic oxide films on niobium

    International Nuclear Information System (INIS)

    Bokij, L.P.; Kostikov, Yu.P.

    1989-01-01

    Chemical forms of phosphorus and sulfur in niobium oxide anodic film, obtained by electrochemical technique using niobium in H 2 SO 4 and H 3 PO 4 aqueous solutions, are determined using data on chemical shifts of X-ray emission lines. Films represent Nb 2 O 5(1-γ) (SO 4 ) 5γ and Nb 2 O 5(1-γ) (PO 4 ) 10γ/3 (γ -share of oxygen substituted by acid anion) composition oxosalts. Electrolyte role in formation of niobium anodic oxide structure and effect of phosphorus and sulfur compounds on anodic film conductivity are determined

  3. Influence of electropolishing and anodic oxidation on morphology, chemical composition and corrosion resistance of niobium.

    Science.gov (United States)

    Sowa, Maciej; Greń, Katarzyna; Kukharenko, Andrey I; Korotin, Danila M; Michalska, Joanna; Szyk-Warszyńska, Lilianna; Mosiałek, Michał; Zak, Jerzy; Pamuła, Elżbieta; Kurmaev, Ernst Z; Cholakh, Seif O; Simka, Wojciech

    2014-09-01

    The work presents results of the studies performed on electropolishing of pure niobium in a bath that contained: sulphuric acid, hydrofluoric acid, ethylene glycol and acetanilide. After the electropolishing, the specimens were subjected to anodic passivation in a 1moldm(-3) phosphoric acid solution at various voltages. The surface morphology, thickness, roughness and chemical composition of the resulting oxide layers were analysed. Thusly prepared niobium samples were additionally investigated in terms of their corrosion resistance in Ringer's solution. The electropolished niobium surface was determined to be smooth and lustrous. The anodisation led to the growth of barrier-like oxide layers, which were enriched in phosphorus species. Copyright © 2014 Elsevier B.V. All rights reserved.

  4. Nanoporous titanium niobium oxide and titanium tantalum oxide compositions and their use in anodes of lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Dai, Sheng; Guo, Bingkun; Sun, Xiao-Guang; Qiao, Zhenan

    2017-10-31

    Nanoporous metal oxide framework compositions useful as anodic materials in a lithium ion battery, the composition comprising metal oxide nanocrystals interconnected in a nanoporous framework and having interconnected channels, wherein the metal in said metal oxide comprises titanium and at least one metal selected from niobium and tantalum, e.g., TiNb.sub.2-x Ta.sub.xO.sub.y (wherein x is a value from 0 to 2, and y is a value from 7 to 10) and Ti.sub.2Nb.sub.10-vTa.sub.vO.sub.w (wherein v is a value from 0 to 2, and w is a value from 27 to 29). A novel sol gel method is also described in which sol gel reactive precursors are combined with a templating agent under sol gel reaction conditions to produce a hybrid precursor, and the precursor calcined to form the anodic composition. The invention is also directed to lithium ion batteries in which the nanoporous framework material is incorporated in an anode of the battery.

  5. Growth of anodic films on niobium

    International Nuclear Information System (INIS)

    Gomes, M.A.B.; Bulhoes, L.O.S.

    1988-01-01

    The analysis of the response of the galvanostatic growth of anodic films on niobium metal in aqueous solutions is shown. The first spark voltage showed a dependence upon value of current density that could be explained as the incorporation of anions into the film. (M.J.C.) [pt

  6. Anodic oxidation

    CERN Document Server

    Ross, Sidney D; Rudd, Eric J; Blomquist, Alfred T; Wasserman, Harry H

    2013-01-01

    Anodic Oxidation covers the application of the concept, principles, and methods of electrochemistry to organic reactions. This book is composed of two parts encompassing 12 chapters that consider the mechanism of anodic oxidation. Part I surveys the theory and methods of electrochemistry as applied to organic reactions. These parts also present the mathematical equations to describe the kinetics of electrode reactions using both polarographic and steady-state conditions. Part II examines the anodic oxidation of organic substrates by the functional group initially attacked. This part particular

  7. Niobium oxide compositions and methods for using same

    Science.gov (United States)

    Goodenough, John B; Han, Jian-Tao

    2014-02-11

    The disclosure relates a niobium oxide useful in anodes of secondary lithium ion batteries. Such niobium oxide has formula Li.sub.xM.sub.1-yNb.sub.yNb.sub.2O.sub.7, wherein 0.ltoreq.x.ltoreq.3, 0.ltoreq.y.ltoreq.1, and M represents Ti or Zr. The niobium oxide may be in the form of particles, which may be carbon coated. The disclosure also relates to an electrode composition containing at least one or more niobium oxides of formula Li.sub.xM.sub.1-yNb.sub.yNb.sub.2O.sub.7. The disclosure further relates to electrodes, such as anodes, and batteries containing at least one or more niobium oxides of formula Li.sub.xM.sub.1-yNb.sub.yNb.sub.2O.sub.7. Furthermore, the disclosure relates to methods of forming the above.

  8. Niobium Doped Lanthanum Strontium Ferrite as A Redox-Stable and Sulfur-Tolerant Anode for Solid Oxide Fuel Cells.

    Science.gov (United States)

    Li, Jingwei; Wei, Bo; Cao, Zhiqun; Yue, Xing; Zhang, Yaxin; Lü, Zhe

    2018-01-10

    The Nb-doped lanthanum strontium ferrite perovskite oxide La 0.8 Sr 0.2 Fe 0.9 Nb 0.1 O 3-δ (LSFNb) is evaluated as an anode material in a solid oxide fuel cell (SOFC). The effects of Nb partial substitution in the crystal structure, the electrical conductivity, and the valence of Fe ions are studied. LSFNb exhibits good structural stability in a severe reducing atmosphere at 800 °C, suggesting that high-valent Nb can effectively promote the stability of the lattice structure. The concentration of Fe 2+ increases after Nb doping, as confirmed by X-ray photoelectron spectroscopy. The maximum power density of a thick Sc-stabilized zirconia (ScSZ) electrolyte-supported single cell reached 241.6 mW cm -2 at 800 °C with H 2 as fuel. The cell exhibited excellent stability for 100 h continuous operation without detectable degeneration. Scanning electron microscopy clearly revealed exsolution on the LSFNb surface after operation. Meanwhile, LSFNb particles agglomerated significantly during long-term stability testing. Impedance spectra suggested that both the LSFNb anode and the (La 0.75 Sr 0.25 ) 0.95 MnO 3-δ /ScSZ cathode underwent an activation process during long-term testing, through which the charge transfer ability increased significantly. Meanwhile, low-frequency resistance (R L ) mainly attributed to the anode (80 %) significantly increased, probably due to the agglomeration of LSFNb particles. The LSFNb anode exhibits excellent anti-sulfuring poisoning ability and redox stability. These results demonstrate that LSFNb is a promising anode material for SOFCs. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  9. Anode properties of magnesium hydride catalyzed with niobium oxide for an all solid-state lithium-ion battery.

    Science.gov (United States)

    Ikeda, Suguru; Ichikawa, Takayuki; Kawahito, Koji; Hirabayashi, Kazuhiro; Miyaoka, Hiroki; Kojima, Yoshitsugu

    2013-08-18

    The anode properties of pristine MgH2 and MgH2 catalyzed with Nb2O5 have been investigated for an all solid-state lithium-ion battery. The catalytic effect stabilizes the plateau voltage as a result of kinetic improvement of the hydrogen transfer from the Mg phase to the Li phase.

  10. Free energy of hydration of niobium oxide

    International Nuclear Information System (INIS)

    Plodinec, M.J.

    1996-01-01

    Some of the glasses being formulated by SRTC researchers contain niobium oxide. In this report, the free energy of hydration of the oxide is calculated from the free energies of formation of the oxide, the hydroxide, and water. This value can be used in calculations of the free energy of hydration of glasses containing niobium

  11. Mesostructured niobium-doped titanium oxide-carbon (Nb-TiO2-C) composite as an anode for high-performance lithium-ion batteries

    Science.gov (United States)

    Hwang, Keebum; Sohn, Hiesang; Yoon, Songhun

    2018-02-01

    Mesostructured niobium (Nb)-doped TiO2-carbon (Nb-TiO2-C) composites are synthesized by a hydrothermal process for application as anode materials in Li-ion batteries. The composites have a hierarchical porous structure with the Nb-TiO2 nanoparticles homogenously distributed throughout the porous carbon matrix. The Nb content is controlled (0-10 wt%) to investigate its effect on the physico-chemical properties and electrochemical performance of the composite. While the crystalline/surface structure varied with the addition of Nb (d-spacing of TiO2: 0.34-0.36 nm), the morphology of the composite remained unaffected. The electrochemical performance (cycle stability and rate capability) of the Nb-TiO2-C composite anode with 1 wt% Nb doping improved significantly. First, a full cut-off potential (0-2.5 V vs. Li/Li+) of Nb-doped composite anode (1 wt%) provides a higher energy utilization than that of the un-doped TiO2-C anode. Second, Nb-TiO2-C composite anode (1 wt%) exhibits an excellent long-term cycle stability (100% capacity retention, 297 mAh/g at 0.5 C after 100 cycles and 221 mAh/g at 2 C after 500 cycles) and improved rate-capability (192 mAh/g at 5 C), respectively (1 C: 150 mA/g). The superior electrochemical performance of Nb-TiO2-C (1 wt%) could be attributed to the synergistic effect of improved electronic conductivity induced by optimal Nb doping (1 wt%) and lithium-ion penetration (high diffusion kinetics) through unique pore structures.

  12. Thermodynamic study on vapourization of niobium oxides from slag melts

    Science.gov (United States)

    Li, Qiujin

    The partitioning of niobium to slag and gaseous niobium oxide vapourizing from metal/slag may cause niobium losses and erratic recovery rates in steelmaking practices. Knowledge of the volatility and activities of niobium oxides in slag melts are of great value for both theoretical evaluation and practical applications in niobium microalloyed steels. Because of the multi-valence state of niobium ions in slags, the behaviour of niobium in metallurgical slags is complicated. So far, little systematic attempts have been made and activity data of niobium oxides in slags are extremely scarce. The aim of this study is to determine precise data on the vapour pressures of niobium oxides, and consequently, to obtain information on thermodynamic quantities of niobium oxides in slag melts. The thermodynamic properties of niobium oxide in CaO-SiO2-NbO x and CaO-SiO2-Al2O3-NbOx slag melts were determined by employing the transpiration method from 1800-1873K under a controlled atmosphere. To confirm the validity of the transpiration method for the measurement of thermodynamic properties, the binary alloy system silver-gold was chosen for a comparison with the same property which has been measured by other recognized procedures. The agreement with literature results confirmed that the measurement yields reliable results for thermodynamic activity data by the transpiration method. The vapourization of liquid Nb2O5 was studied as a function of partial pressure of oxygen in the system and this confirms that atmosphere control is the essential condition for the vapourization study. The gaseous niobium oxide species was verified to be NbO2; hence, Nb2O5 vapourizes by the reaction Nb2O 5 (l) =2NbO2(g) +1/202(g). Heat of vapourization was estimated by applying the second law method and comparison with the literature showed a fairly good agreement. The thermodynamic properties of niobium oxide in the slag system of CaO-SiO 2-NbOx and CaO-SiO2-Al2O3-NbO x were measured by varying the

  13. Niobium-doped strontium titanates as SOFC anodes

    DEFF Research Database (Denmark)

    Blennow Tullmar, Peter; Kammer Hansen, Kent; Wallenberg, L. Reine

    2008-01-01

    been synthesized with a recently developed modified glycine-nitrate process. The synthesized powders have been calcined and sintered in air or in 9% H(2) / N(2) between 800 - 1400 degrees C. After calcination the samples were single phase Nb-doped strontium titanate with grain sizes of less than 100 nm...... in diameter on average. The phase purity, defect structure, and microstructure of the materials have been analyzed with SEM, XRD, and TGA. The electrical conductivity of the Nb-doped titanate decreased with increasing temperature and showed a phonon scattering conduction mechanism with sigma > 120 S...... ability of the Nb-doped titanates to be used as a part of a SOFC anode. However, the catalytic activity of the materials was not sufficient and it needs to be improved if titanate based materials are to be realized as constituents in SOFC anodes....

  14. Development of a niobium-doped titania inert anode for titanium electrowinning in molten chloride salts.

    Science.gov (United States)

    Snook, Graeme A; McGregor, Katherine; Urban, Andrew J; Lanyon, Marshall R; Donelson, R; Pownceby, Mark I

    2016-08-15

    The direct electrochemical reduction of solid titanium dioxide in a chloride melt is an attractive method for the production of titanium metal. It has been estimated that this type of electrolytic approach may reduce the costs of producing titanium sponge by more than half, with the additional benefit of a smaller environmental footprint. The process utilises a consumable carbon anode which releases a mixture of CO2 and CO gas during electrolysis, but suffers from low current efficiency due to the occurrence of parasitic side reactions involving carbon. The replacement of the carbon anode with a cheap, robust inert anode offers numerous benefits that include: elimination of carbon dioxide emissions, more efficient cell operation, opportunity for three-dimensional electrode configurations and reduced electrode costs. This paper reports a study of Nb-doped titania anode materials for inert anodes in a titanium electrolytic reduction cell. The study examines the effect of niobium content and sintering conditions on the performance of Nb-doped TiO2 anodes in laboratory-scale electrolysis tests. Experimental findings, including performance in a 100 h laboratory electrolysis test, are described.

  15. Spectrographic determination of impurities in high-purity tantalum oxide and niobium oxide

    International Nuclear Information System (INIS)

    Anderson, S.T.G.; Russell, G.M.

    1990-01-01

    The development of spectrographic methods by direct current arc excitation and carrier distillation for the determination of impurities in tantalum and niobium oxides are described. Iron, silicon, aluminium, titanium, calcium, silver, tin, magnesium, and manganese can be determined in tantalum oxide and niobium oxide in concentrations ranging from 3 to 300 p.p.m. Niobium can be determined in tantalum oxide in concentrations ranging from 10 to 300 p.p.m. Tantalum cannot be determined in niobium oxide, and tungsten cannot be determined in either matrix as a result of the absence of sensitive lines in the spectra of these elements. Relative standard deviations of analyte element concentrations are in the region of 0,18 for tantalum oxide samples, and 0,13 for niobium oxide samples. A detailed laboratory method is included. 4 figs., 4 tabs., 3 refs

  16. Anodic oxide films on tungsten

    International Nuclear Information System (INIS)

    Di Paola, A.; Di Quarto, F.; Sunseri, C.

    1980-01-01

    Scanning electron microscopy was used to investigate the morphology of anodic oxide films on tungsten, obtained in various conditions of anodization. Studies were made of the growth of porous films, whose thickness increases with time and depends upon the current density. Temperature and electrolyte composition influence the film morphology. Gravimetric measurements of film dissolution at 70 0 C show that after a transient time, the rate of metal dissolution and that of film formation coincide. The porous films thicken because tungsten dissolves as WO 2 2+ and precipitates as WO 3 .H 2 O. (author)

  17. Evaluation of niobium dimethylamino-ethoxide for chemical vapour deposition of niobium oxide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Dabirian, Ali [Laboratory for Photonic Materials and Characterization, Ecole Polytechnique Fédérale de Lausanne (EPFL), Station 17, 1015 Lausanne (Switzerland); Kuzminykh, Yury, E-mail: yury.kuzminykh@empa.ch [Laboratory for Photonic Materials and Characterization, Ecole Polytechnique Fédérale de Lausanne (EPFL), Station 17, 1015 Lausanne (Switzerland); Laboratory for Advanced Materials Processing, Empa, Swiss Federal Laboratories for Materials Science and Technology, Feuerwerkerstrasse 39, 3602 Thun (Switzerland); Wagner, Estelle; Benvenuti, Giacomo [3D-Oxides, 70 Rue G. Eiffel Technoparc, 01630 St Genis Pouilly (France); ABCD Technology, 12 route de Champ-Colin, 1260 Nyon (Switzerland); Rushworth, Simon [Tyndall National Institute, Lee Maltings, Dyke Parade, Cork (Ireland); Hoffmann, Patrik, E-mail: patrik.hoffmann@empa.ch [Laboratory for Photonic Materials and Characterization, Ecole Polytechnique Fédérale de Lausanne (EPFL), Station 17, 1015 Lausanne (Switzerland); Laboratory for Advanced Materials Processing, Empa, Swiss Federal Laboratories for Materials Science and Technology, Feuerwerkerstrasse 39, 3602 Thun (Switzerland)

    2014-11-28

    Chemical vapour deposition (CVD) processes depend on the availability of suitable precursors. Precursors that deliver a stable vapour pressure are favourable in classical CVD processes, as they ensure process reproducibility. In high vacuum CVD (HV-CVD) process vapour pressure stability of the precursor is of particular importance, since no carrier gas assisted transport can be used. The dimeric Nb{sub 2}(OEt){sub 10} does not fulfil this requirement since it partially dissociates upon heating. Dimethylamino functionalization of an ethoxy ligand of Nb(OEt){sub 5} acts as an octahedral field completing entity and leads to Nb(OEt){sub 4}(dmae). We show that Nb(OEt){sub 4}(dmae) evaporates as monomeric molecule and ensures a stable vapour pressure and, consequently, stable flow. A set of HV-CVD experiments were conducted using this precursor by projecting a graded molecular beam of the precursor onto the substrate at deposition temperatures from 320 °C to 650 °C. Film growth rates ranging from 8 nm·h{sup −1} to values larger than 400 nm·h{sup −1} can be obtained in this system illustrating the high level of control available over the film growth process. Classical CVD limiting conditions along with the recently reported adsorption–reaction limited conditions are observed and the chemical composition, and microstructural and optical properties of the films are related to the corresponding growth regime. Nb(OEt){sub 4}(dmae) provides a large process window of deposition temperatures and precursor fluxes over which carbon-free and polycrystalline niobium oxide films with growth rates proportional to precursor flux are obtained. This feature makes Nb(OEt){sub 4}(dmae) an attractive precursor for combinatorial CVD of niobium containing complex oxide films that are finding an increasing interest in photonics and photoelectrochemical water splitting applications. The adsorption–reaction limited conditions provide extremely small growth rates comparable to an

  18. Evaluation of niobium dimethylamino-ethoxide for chemical vapour deposition of niobium oxide thin films

    International Nuclear Information System (INIS)

    Dabirian, Ali; Kuzminykh, Yury; Wagner, Estelle; Benvenuti, Giacomo; Rushworth, Simon; Hoffmann, Patrik

    2014-01-01

    Chemical vapour deposition (CVD) processes depend on the availability of suitable precursors. Precursors that deliver a stable vapour pressure are favourable in classical CVD processes, as they ensure process reproducibility. In high vacuum CVD (HV-CVD) process vapour pressure stability of the precursor is of particular importance, since no carrier gas assisted transport can be used. The dimeric Nb 2 (OEt) 10 does not fulfil this requirement since it partially dissociates upon heating. Dimethylamino functionalization of an ethoxy ligand of Nb(OEt) 5 acts as an octahedral field completing entity and leads to Nb(OEt) 4 (dmae). We show that Nb(OEt) 4 (dmae) evaporates as monomeric molecule and ensures a stable vapour pressure and, consequently, stable flow. A set of HV-CVD experiments were conducted using this precursor by projecting a graded molecular beam of the precursor onto the substrate at deposition temperatures from 320 °C to 650 °C. Film growth rates ranging from 8 nm·h −1 to values larger than 400 nm·h −1 can be obtained in this system illustrating the high level of control available over the film growth process. Classical CVD limiting conditions along with the recently reported adsorption–reaction limited conditions are observed and the chemical composition, and microstructural and optical properties of the films are related to the corresponding growth regime. Nb(OEt) 4 (dmae) provides a large process window of deposition temperatures and precursor fluxes over which carbon-free and polycrystalline niobium oxide films with growth rates proportional to precursor flux are obtained. This feature makes Nb(OEt) 4 (dmae) an attractive precursor for combinatorial CVD of niobium containing complex oxide films that are finding an increasing interest in photonics and photoelectrochemical water splitting applications. The adsorption–reaction limited conditions provide extremely small growth rates comparable to an atomic layer deposition (ALD) process

  19. The oxidative coupling of methane and the oxidative dehydrogenation of ethane over a niobium promoted lithium doped magnesium oxide catalyst

    NARCIS (Netherlands)

    Swaan, H.M.; Swaan, H.M.; Li, X.; Seshan, Kulathuiyer; van Ommen, J.G.; Ross, J.R.H.; Ross, J.R.H.

    1993-01-01

    The promoting effect of niobium in a Li/MgO catalyst for the oxidative coupling of methane (OCM) and for the oxidative dehydrogenation of ethane (ODHE) has been studied in some detail. It has been found that a Li/Nb/MgO catalyst with 16 wt % niobium showed the highest activity for the C2 production

  20. Catalysts Promoted with Niobium Oxide for Air Pollution Abatement

    Directory of Open Access Journals (Sweden)

    Wendi Xiang

    2017-05-01

    Full Text Available Pt-containing catalysts are currently used commercially to catalyze the conversion of carbon monoxide (CO and hydrocarbon (HC pollutants from stationary chemical and petroleum plants. It is well known that Pt-containing catalysts are expensive and have limited availability. The goal of this research is to find alternative and less expensive catalysts to replace Pt for these applications. This study found that niobium oxide (Nb2O5, as a carrier or support for certain transition metal oxides, promotes oxidation activity while maintaining stability, making them candidates as alternatives to Pt. The present work reports that the orthorhombic structure of niobium oxide (formed at 800 °C in air promotes Co3O4 toward the oxidation of both CO and propane, which are common pollutants in volatile organic compound (VOC applications. This was a surprising result since this structure of Nb2O5 has a very low surface area (about 2 m2/g relative to the more traditional Al2O3 support, with a surface area of 150 m2/g. The results reported demonstrate that 1% Co3O4/Nb2O5 has comparable fresh and aged catalytic activity to 1% Pt/γ-Al2O3 and 1% Pt/Nb2O5. Furthermore, 6% Co3O4/Nb2O5 outperforms 1% Pt/Al2O3 in both catalytic activity and thermal stability. These results suggest a strong interaction between niobium oxide and the active component—cobalt oxide—likely by inducing an oxygen defect structure with oxygen vacancies leading to enhanced activity toward the oxidation of CO and propane.

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

    Directory of Open Access Journals (Sweden)

    Sathler M.N.B.

    1998-01-01

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

  2. The Influence of Oxide on the Electrodeposition of Niobium from Alkali Fluoride Melts

    DEFF Research Database (Denmark)

    Christensen, Erik; Wang, Xingdong; Barner, Jens H. Von

    1994-01-01

    Electrodeposit of niobium metal from K2NbF7-LiF-NaF-KF-Na2O melts at 700-degrees-C has been investigated. It was found that the equilibrium oxidation state of niobium was four for initial O2-/Nb(V) ratios of up to at least one. On the other hand when a niobium metal sheet was used for the reduction...

  3. Biomimetic novel nanoporous niobium oxide coating for orthopaedic applications

    Energy Technology Data Exchange (ETDEWEB)

    Pauline, S. Anne; Rajendran, N., E-mail: nrajendran@annauniv.edu

    2014-01-30

    Niobium oxide was synthesized by sol–gel methodology and a crystalline, nanoporous and adherent coating of Nb{sub 2}O{sub 5} was deposited on 316L SS using the spin coating technique and heat treatment. The synthesis conditions were optimized to obtain a nanoporous morphology. The coating was characterized using attenuated total reflectance-Infrared spectroscopy (ATR-IR), X-ray diffraction analysis (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDX), atomic force microscopy (AFM) and transmission electron microscopy (TEM) and the formation of crystalline Nb{sub 2}O{sub 5} coating with nanoporous morphology was confirmed. Mechanical studies confirmed that the coating has excellent adherence to the substrate and the hardness value of the coating was excellent. Contact angle analysis showed increased hydrophilicity for the coated substrate. In vitro bioactivity test confirmed that the Nb{sub 2}O{sub 5} coating with nanoporous morphology facilitated the growth of hydroxyapatite (HAp). This was further confirmed by the solution analysis test where increased uptake of calcium and phosphorous ions from simulated body fluid (SBF) was observed. Electrochemical evaluation of the coating confirmed that the crystalline coating is insulative and protective in nature and offered excellent corrosion protection to 316L SS. Thus, this study confirmed that the nanoporous crystalline Nb{sub 2}O{sub 5} coating conferred bioactivity and enhanced corrosion resistance on 316L SS.

  4. Anodic oxidation of Ta/Fe alloys

    International Nuclear Information System (INIS)

    Mato, S.; Alcala, G.; Thompson, G.E.; Skeldon, P.; Shimizu, K.; Habazaki, H.; Quance, T.; Graham, M.J.; Masheder, D.

    2003-01-01

    The behaviour of iron during anodizing of sputter-deposited Ta/Fe alloys in ammonium pentaborate electrolyte has been examined by transmission electron microscopy, Rutherford backscattering spectroscopy, glow discharge optical emission spectroscopy and X-ray photoelectron spectroscopy. Anodic films on Ta/1.5 at.% Fe, Ta/3 at.% Fe and Ta/7 at.% Fe alloys are amorphous and featureless and develop at high current efficiency with respective formation ratios of 1.67, 1.60 and 1.55 nm V -1 . Anodic oxidation of the alloys proceeds without significant enrichment of iron in the alloy in the vicinity of the alloy/film interface and without oxygen generation during film growth, unlike the behaviour of Al/Fe alloys containing similar concentrations of iron. The higher migration rate of iron species relative to that of tantalum ions leads to the formation of an outer iron-rich layer at the film surface

  5. Oxygen release and exchange in niobium oxide MEHPPV hybrid solar cells

    DEFF Research Database (Denmark)

    Lira-Cantu, M.; Norrman, K.; Andreasen, J.W.

    2006-01-01

    We demonstrate that niobium oxide exchanges oxygen with the atmosphere when illuminated by simulated sunlight. The oxygen exchange was found to take place for pristine niobium oxide films when illuminated in an oxygen atmosphere and when illuminated in an operational hybrid solar cell. The oxygen...... exchange was demonstrated using O-18(2)-isotopic labeling in combination with time-of-flight secondary ion mass spectrometry (TOF-SIMS) imaging analysis of devices and oxide substrates. TOF-SIMS depth profiling confirmed O-18 incorporation throughout the device in hybrid solar cells. The results...... are discussed in the context of hybrid solar cell stability and illuminate one of the degradation paths....

  6. Transparent Aluminum Oxide Films by Edge Anodization

    Science.gov (United States)

    Stott, Jonathan; Greenwood, Thomas; Winn, David

    In this paper we present our recent work on manufacturing thin (3 - 5 μm) films of porous aluminum(III) oxide [PAO] using a novel edge-anodization technique. With this modified anodization process, we are able to create transparent PAO films on top of insulating substrates such as glass or plastic. By controlling the processing parameters, the index of refraction of PAO films can be engineered to match the substrate, which gives us a durable reflection-free and scratch-resistant coating over conventional optics or LCD displays. Eventually we hope to create ordered porous aluminum oxide cladding around an optical fiber core, which could have a number of interesting optical properties if the pore spacing can be matched to the wavelength of light in the fiber. This work was funded by Fairfield University startup funding.

  7. High reactivity of nanosized niobium oxide cluster cations in methane activation: A comparison with vanadium oxides.

    Science.gov (United States)

    Ding, Xun-Lei; Wang, Dan; Wu, Xiao-Nan; Li, Zi-Yu; Zhao, Yan-Xia; He, Sheng-Gui

    2015-09-28

    The reactions between methane and niobium oxide cluster cations were studied and compared to those employing vanadium oxides. Hydrogen atom abstraction (HAA) reactions were identified over stoichiometric (Nb2O5)N(+) clusters for N as large as 14 with a time-of-flight mass spectrometer. The reactivity of (Nb2O5)N(+) clusters decreases as the N increases, and it is higher than that of (V 2O5)N(+) for N ≥ 4. Theoretical studies were conducted on (Nb2O5)N(+) (N = 2-6) by density functional calculations. HAA reactions on these clusters are all favorable thermodynamically and kinetically. The difference of the reactivity with respect to the cluster size and metal type (Nb vs V) was attributed to thermodynamics, kinetics, the electron capture ability, and the distribution of the unpaired spin density. Nanosized Nb oxide clusters show higher HAA reactivity than V oxides, indicating that niobia may serve as promising catalysts for practical methane conversion.

  8. Multi-component titanium–copper–cobalt- and niobium nanostructured oxides as catalysts for ethyl acetate oxidation

    Czech Academy of Sciences Publication Activity Database

    Tsoncheva, T.; Henych, Jiří; Ivanova, R.; Kovacheva, D.; Štengl, Václav

    2015-01-01

    Roč. 116, č. 2 (2015), s. 397-408 ISSN 1878-5190 Institutional support: RVO:61388980 Keywords : Copper and cobalt oxides * Effect of support * Ethyl acetate combustion * Multicomponent oxides * Titania doped with niobium Subject RIV: CA - Inorganic Chemistry Impact factor: 1.265, year: 2015

  9. New porous titanium–niobium oxide for photocatalytic degradation of bromocresol green dye in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Chaleshtori, Maryam Zarei, E-mail: mzarei@utep.edu [Materials Research and Technology Institute (MRTI), University of Texas at El Paso, 500W. University Ave., El Paso, TX 79968 (United States); Hosseini, Mahsa; Edalatpour, Roya [Materials Research and Technology Institute (MRTI), University of Texas at El Paso, 500W. University Ave., El Paso, TX 79968 (United States); Masud, S.M. Sarif [Department of Chemistry, University of Texas at El Paso, 500W. University Ave., El Paso, TX 79968 (United States); Chianelli, Russell R., E-mail: chianell@utep.edu [Materials Research and Technology Institute (MRTI), University of Texas at El Paso, 500W. University Ave., El Paso, TX 79968 (United States)

    2013-10-15

    Graphical abstract: The photocatalytic activity of different porous titanium–niobium oxides was evaluated toward degradation of bromocresol green (BG) under UV light. A better catalytic activity was observed for all samples at lower pH. Catalysts have a stronger ability for degradation of BG in acid media than in alkaline media. - Highlights: • Different highly structured titanium–niobium oxides have been prepared using improved methods of synthesis. • Photo-degradation of bromocresol green dye (BG) with nanostructure titanium–niobium oxide catalysts was carried out under UV light. • The photo-catalytic activity of all catalysts was higher in lower pH. • Titanium–niobium oxide catalysts are considerably stable and reusable. - Abstract: In this study, high surface area semiconductors, non porous and porous titanium–niobium oxides derived from KTiNbO{sub 5} were synthesized, characterized and developed for their utility as photocatalysts for decontamination with sunlight. These materials were then used in the photocatalytic degradation of bromocresol green dye (BG) in aqueous solution using UV light and their catalytic activities were evaluated at various pHs. For all catalysts, the photocatalytic degradation of BG was most efficient in acidic solutions. Results show that the new porous oxides have large porous and high surface areas and high catalytic activity. A topotactic dehydration treatment greatly improves catalyst performance at various pHs. Stability and long term activity of porous materials (topo and non-topo) in photocatalysis reactions was also tested. These results suggest that the new materials can be used to efficiently purify contaminated water.

  10. Chemical interaction in resistors based on lead ruthenite with additions of niobium(5) oxide compounds

    International Nuclear Information System (INIS)

    Lozinskij, N.S.; Shevtsova, N.A.; Gruba, A.I.; Volkov, V.I.

    1986-01-01

    The method of X-ray phase analysis was used to study chemical interaction in isothermal cross-section of Pb 2 RU 2 O 6 -Nb 2 O 5 , Rbsub(2)Rusub(2)Osub(6)-NbWOsub(5.5) and Rb 2 Ru 2 O 6 -Pb 2 Nb 2 O 7 systems at 850 deg C as well as in models of real ruthenium resistors. Chemical interaction is stated to take place in systems with niobium (5) oxide and NbWOsub(5.5). Niobium (5) and tungsten (6) displace ruthenium (4) from its compounds with formation of their lead salts. Similar chemical interactions between current-carrying phase of the resistor and modifiers representing niobium-containing take place in models of components of the studied systems take place in models of resistors

  11. Electrochemical oxidation of syngas on nickel and ceria anodes

    NARCIS (Netherlands)

    Tabish, A.N.; Patel, H.C.; Purushothaman Vellayani, A.

    2017-01-01

    Fuel flexibility of solid oxide fuel cells enables the use of low cost and practical fuels like syngas. Understanding of the oxidation kinetics with syngas is essential for proper selection of anode material and its design optimization. Using nickel and ceria pattern anodes, we study the

  12. Reaction kinetics of oxygen on single-phase alloys, oxidation of nickel and niobium alloys

    International Nuclear Information System (INIS)

    Lalauze, Rene

    1973-01-01

    This research thesis first addresses the reaction kinetics of oxygen on alloys. It presents some generalities on heterogeneous reactions (conventional theory, theory of jumps), discusses the core reaction (with the influence of pressure), discusses the influence of metal self-diffusion on metal oxidation kinetics (equilibrium conditions at the interface, hybrid diffusion regime), reports the application of the hybrid diffusion model to the study of selective oxidation of alloys (Wagner model, hybrid diffusion model) and the study of the oxidation kinetics of an alloy forming a solid solution of two oxides. The second part reports the investigation of the oxidation of single phase nickel and niobium alloys (phase α, β and γ)

  13. Apatite grown in niobium by two-step plasma electrolytic oxidation.

    Science.gov (United States)

    Pereira, Bruno Leandro; Lepienski, Carlos Maurício; Mazzaro, Irineu; Kuromoto, Neide Kazue

    2017-08-01

    Plasma electrolytic oxidation (PEO) of niobium plates were done electrochemically in two steps with electrolytes containing phosphorous and calcium being observed the formation of crystalline apatite. All samples were submitted to a first step of PEO using an electrolyte containing phosphate ions. The second oxidization step was made using three different electrolytes. Some samples were oxidized by PEO in electrolyte containing calcium, while in other samples it was used two mixtures of phosphoric acid and calcium acetate monohydrate solutions. Three different surface layers were obtained. The morphology and chemical composition of the films were analyzed by scanning electronic microscopy (SEM), and energy dispersive spectroscopy (EDS) respectively. It was observed that all samples submitted to two-step oxidation shown porous surface and a calcium and phosphorus rich layer. Average surface roughness (Ra) was measured by a profilometer remaining in the sub-micrometric range. The contact angle by sessile drop technique, using 1μL of distilled water was performed with an optical goniometer. It was verified a higher hydrophilicity in all surfaces compared to the polished niobium. Orthorhombic Nb 2 O 5 was identified by XRD in the oxide layer. Crystalline apatite was identified by XRD in surfaces after the second oxidation made with the Ca-rich electrolyte and a mixture of an electrolyte richer in Ca compared to P. These results indicate that a two-step oxidized niobium surface present great features for applications in the osseointegration processes: favorable chemical composition that increase the biocompatibility, the formation of crystalline niobium pentoxide (orthorhombic), high hydrophilicity and formation of crystalline calcium phosphate (apatite) under adequate electrolyte composition. Copyright © 2016 Elsevier B.V. All rights reserved.

  14. Niobium powder synthesized by calciothermic reduction of niobium hydroxide for use in capacitors

    Science.gov (United States)

    Baba, Masahiko; Kikuchi, Tatsuya; Suzuki, Ryosuke O.

    2015-03-01

    Metallic niobium powder was produced for applications in electric capacitors via calciothermic reduction of niobium hydroxide in molten CaCl2. Sub-micrometer spherical metallic particles with coral-like morphologies reflected the particle size of the starting oxide powder. A fine powder was obtained from the mixtures of niobium hydroxide and CaO or Ca(OH)2, respectively. Sintered pellets of the metallic powder showed a higher capacitance (CV) than those of the simply reduced powder without pre-treatment, because the shrinkage during sintering was smaller. The CV was as large as that of commercially sintered pellets for tantalum capacitors. Therefore, this niobium powder would act as a higher-voltage capacitor by applying chemical anodic treatment at higher voltages, and lower oxygen content in the reduced power could realize a lower leak current.

  15. Redox Stable Anodes for Solid Oxide Fuel Cells

    Directory of Open Access Journals (Sweden)

    Guoliang eXiao

    2014-06-01

    Full Text Available Solid oxide fuel cells (SOFCs can convert chemical energy from the fuel directly to electrical energy with high efficiency and fuel flexibility. Ni-based cermets have been the most widely adopted anode for SOFCs. However, the conventional Ni-based anode has low tolerance to sulfur-contamination, is vulnerable to deactivation by carbon build-up (coking from direct oxidation of hydrocarbon fuels, and suffers volume instability upon redox cycling. Among these limitations, the redox instability of the anode is particularly important and has been intensively studied since the SOFC anode may experience redox cycling during fuel cell operations even with the ideal pure hydrogen as the fuel. This review aims to highlight recent progresses on improving redox stability of the conventional Ni-based anode through microstructure optimization and exploration of alternative ceramic-based anode materials.

  16. Functionalization of niobium electrodes for the construction of impedimetric biosensors

    International Nuclear Information System (INIS)

    Helali, S.; Abdelghani, A.; Hafaiedh, I.; Martelet, C.; Prodromidis, M.I.; Albanis, T.; Jaffrezic-Renault, N.

    2008-01-01

    This paper describes the development of an impedimetric immunosensor, based on niobium/niobium oxide (Nb/NbOxHy) electrodes, for the detection of atrazine. Niobium oxide was anodically formed onto niobium electrodes at 25 V in 1 M H 2 SO 4 . Hydrous oxide layers were then silanized with APTES, and using glutaraldehyde as a cross linker, Fab fragment k47 antibody was covalently immobilized onto the surface of the electrodes. Electrochemical impedance spectroscopy (EIS) was used to characterize the building-up of the immunosensors as well as the binding of atrazine to its specific antibody. In presence of ferricyanide redox species and under a cathodic polarization voltage (- 1.2 V versus SCE), the relationship between the concentration of atrazine and the change of the electron transfer resistance value was studied

  17. Study on thermo-oxide layers of uranium-niobium alloy

    International Nuclear Information System (INIS)

    Luo Lizhu; Yang Jiangrong; Zhou Ping

    2010-01-01

    Surface oxides structure of uranium-niobium alloys which were annealed under different temperatures (room temperature, 100, 200, 300 degree C, respectively)in air were studied by X-ray photoelectron spectroscopy (XPS) analysis and depth profile. Thickness of thermo-oxide layers enhance with the increasing oxide temperature, and obvious changes to oxides structure are observed. Under different delt temperatures, Nb 2 O 5 are detected on the initial surface of U-Nb alloys, and a layer of NbO mixed with some NbO x (0 2 O 5 and Nb metal. Dealing samples in air from room temperature to 200 degree C, non-stoichiometric UO 2+x (UO 2 + interstitial oxygen, P-type semiconductor) are found on initial surface of U-Nb alloys, which has 0.7 eV shift to lower binding energy of U 4f 7/2 characteristics comparing to that of UO 2 . Under room temperature, UO 2 are commonly detected in the oxides layer, while under temperature of 100 and 200 degree C, some P-type UO 2+x are found in the oxide layers,which has a satellite at binding energy of 396.6 eV. When annealing at 300 degree C, higher valence oxides, such as U 3 O 8 or UO x (2 5/2 and U 4f 7/2 peaks are 392.2 and 381.8 eV, respectively. UO 2 mixed uranium metal are the main compositions in the oxide layers. From the results, influence of temperature to oxidation of uranium is more visible than to niobium in uranium-niobium alloys. (authors)

  18. MEASUREMENT OF THE HIGH-FIELD Q-DROP IN A LARGE-GRAIN NIOBIUM CAVITY FOR DIFFERENT OXIDATION PROCESSES

    Energy Technology Data Exchange (ETDEWEB)

    Gianluigi Ciovati; Peter Kneisel; Alex Gurevich

    2008-01-23

    In this contribution, we present the results from a series of RF tests at 1.7 K and 2.0 K on a single-cell cavity made of high-purity large (with area of the order of few cm2) grain niobium which underwent various oxidation processes. After initial buffered chemical polishing, anodization, baking in pure oxygen atmosphere and baking in air up to 180 °C was applied with the objective of clearly identifying the role of oxygen and the oxide layer on the Q-drop. During each rf test a temperature mapping system was used allowing to measure the local temperature rise of the cavity outer surface due to RF losses, which gives information about the losses location, their field dependence and space distribution on the RF surface. The results confirmed that the depth affected by baking is about 20 – 30 nm from the surface and showed that the Q-drop did not re-appear in a previously baked cavity by further baking at 120 °C in pure oxygen atmosphere or in air up to 180 °C. A statistic of the position of the “hot-spots” on the cavity surface showed that grain-boundaries are not the preferred location. An interesting correlation was found between the Q-drop onset, the quench field and the low-field energy gap, which supports the hypothesis of thermo-magnetic instability governing the Q-drop and the baking effect.

  19. MEASUREMENT OF THE HIGH-FIELD Q-DROP IN A LARGE-GRAIN NIOBIUM CAVITY FOR DIFFERENT OXIDATION PROCESSES

    International Nuclear Information System (INIS)

    Gianluigi Ciovati; Peter Kneisel; Alex Gurevich

    2008-01-01

    In this contribution, we present the results from a series of RF tests at 1.7 K and 2.0 K on a single-cell cavity made of high-purity large (with area of the order of few cm2) grain niobium which underwent various oxidation processes. After initial buffered chemical polishing, anodization, baking in pure oxygen atmosphere and baking in air up to 180 C was applied with the objective of clearly identifying the role of oxygen and the oxide layer on the Q-drop. During each rf test a temperature mapping system was used allowing to measure the local temperature rise of the cavity outer surface due to RF losses, which gives information about the losses location, their field dependence and space distribution on the RF surface. The results confirmed that the depth affected by baking is about 20-30 nm from the surface and showed that the Q-drop did not re-appear in a previously baked cavity by further baking at 120 C in pure oxygen atmosphere or in air up to 180 C. A statistic of the position of the ''hot-spots'' on the cavity surface showed that grain-boundaries are not the preferred location. An interesting correlation was found between the Q-drop onset, the quench field and the low-field energy gap, which supports the hypothesis of thermomagnetic instability governing the Q-drop and the baking effect.

  20. The effect of ethylene glycol on pore arrangement of anodic aluminium oxide prepared by hard anodization

    Science.gov (United States)

    Guo, Yang; Zhang, Li; Han, Mangui; Wang, Xin; Xie, Jianliang; Deng, Longjiang

    2018-03-01

    The influence of the addition of ethylene glycol (EG) on the pore self-ordering process in anodic aluminium oxide (AAO) membranes prepared by hard anodization (HA) was investigated. It was illustrated that EG has a substantial effect on the pore arrangement of AAO, and it was found that a smaller pore size can be obtained with an EG concentration reaching 20 wt% in aqueous electrolyte. The number of estimated defects of AAO increases significantly with an increase in EG concentration to 50 wt%. Excellent ordering of pores was realized when the samples were anodized in the 30 wt%-EG-containing aqueous electrolyte.

  1. Electrochemical oxidation of biological pretreated and membrane separated landfill leachate concentrates on boron doped diamond anode

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Bo, E-mail: 357436235@qq.com [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); Yu, Zhiming, E-mail: zhiming@csu.edu.cn [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Wei, Qiuping, E-mail: qiupwei@csu.edu.cn [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Long, HangYu, E-mail: 55686385@qq.com [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); Xie, Youneng, E-mail: 1187272844@qq.com [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); Wang, Yijia, E-mail: 503630433@qq.com [School of Materials Science and Engineering, Central South University, Changsha 410083 (China)

    2016-07-30

    Highlights: • High quality boron-doped diamond film electrodes were synthesized on Nb substrates. • Electrochemical oxidation on boron-doped diamond anode is an effective method for treating landfill leachate concentrates. • Optimal operating conditions for electrochemical oxidation of landfill leachate concentrates is determined. • 87.5% COD removal and 74.06% NH{sub 3}−N removal were achieved after 6 h treatment. - Abstract: In the present study, the high quality boron-doped diamond (BDD) electrodes with excellent electrochemical properties were deposited on niobium (Nb) substrates by hot filament chemical vapor deposition (HFCVD) method. The electrochemical oxidation of landfill leachate concentrates from disc tube reverse osmosis (DTRO) process over a BDD anode was investigated. The effects of varying operating parameters, such as current density, initial pH, flow velocity and cathode material on degradation efficiency were also evaluated following changes in chemical oxygen demand (COD) and ammonium nitrogen (NH{sub 3}−N). The instantaneous current efficiency (ICE) was used to appraise different operating conditions. As a result, the best conditions obtained were as follows, current density 50 mA cm{sup −2}, pH 5.16, flow velocity 6 L h{sup −1}. Under these conditions, 87.5% COD and 74.06% NH{sub 3}−N removal were achieved after 6 h treatment, with specific energy consumption of 223.2 kWh m{sup −3}. In short, these results indicated that the electrochemical oxidation with BDD/Nb anode is an effective method for the treatment of landfill leachate concentrates.

  2. Catalytic role of transition metals supported on niobium oxide in O2 activation

    Science.gov (United States)

    Omidvar, Akbar

    2018-03-01

    Metal particles supported on metal oxides (MMO) are promising materials with versatile applications such as catalyst in fuel cell technologies. As one of the transition metal oxides, niobium oxide (NbO) demonstrates a wide interesting properties that make it a potentially applicable in MMO materials. Here, the catalytic activity for the O2 activation of transition metals (Fe, Co, Ni, Cu, Rh, Pd, Ag, Ir, Pt, and Au) supported on the NbO has been studied theoretically using density functional theory (DFT). The activation of O2 molecule and yielding two separated O atoms is an essential step for the oxygen reduction reaction. Our study demonstrates that the transition metals supported on the NbO can act as driving force for O2 dissociation. Consistent with the prediction of reactivity descriptors, the maximum catalytic activity toward O2 activation is related to the Pt-supported on the NbO metal oxide.

  3. Mesoporous Niobium Oxide Spheres as an Effective Catalyst for the Transamidation of Primary Amides with Amines

    KAUST Repository

    Ghosh, Subhash Chandra

    2014-02-06

    Mesoporous niobium oxide spheres (MNOS), conveniently prepared by a novel antisolvent precipitation approach, have been shown to be an effective catalyst for the transamidation of primary amides with amines. This novel transamidation can be efficiently carried out under solvent-free conditions and is applicable to a wide range of primary amides and amines to provide N-alkyl amides in good to excellent yields. The catalyst is highly stable and reusable. The application of this transamidation reaction has been demonstrated in the synthesis of antidepressant drug moclobemide and other druglike compounds. © 2014 Wiley-VCH Verlag GmbH&Co. KGaA, Weinheim.

  4. Development and characterization of the oxidation behavior of various high temperature niobium based alloys

    Science.gov (United States)

    Portillo, Benedict I., II

    The oxidation response of various niobium based refractory alloys from the Nb-Mo-Si-B-X alloy system has been examined at temperatures between 700 and 1400°C in air. The development of these alloys was part of an ongoing effort to develop and discover a new materials system capable of replacing nickel based super alloys. Additions of titanium were found to provide limited oxidation resistance. A discontinuous layer of TiO2 was observed to from at temperatures above 1100°C. Alloys containing titanium additions were observed to suffer from pest oxidation at low and intermediate temperatures due to the development of Nb2O5. Poor oxidation resistance at intermediate temperatures for alloys with titanium additions was attributed to a transformation in the structure of Nb2O5 formed. Additions of chromium were observed to increase oxidation resistance through the development of a layered oxide structure containing SiO2 and CrNbO4. An intermediate oxidation layer was observed to develop along the oxide metal interface in which the solid solution was not oxidized. These alloys were found to be susceptible to pest oxidation at intermediate and low oxidation temperatures between 700 and 1000°C. Boron and molybdenum content was modified and shown to suppress pest oxidation at 700°C. Modified molybdenum content led to the development of molybdenum based primary solid solution instead of niobium. Alloys with modified molybdenum and boron content were found to have the best oxidation resistance surviving 168 hours of cyclic oxidation at 1400°C. Transient oxidation behavior was observed in thermal gravimetric results collected at 1200°C in the alloys with modified boron and molybdenum content and attributed to the preferential oxidation of Nb5Si3. Oxidation behavior was characterized by the weight change per surface area method and by thermal gravimetric analysis. Oxidation products were characterized by x-ray diffraction and scanning electron microscopy in several modes

  5. Method of removing niobium from uranium-niobium alloy

    International Nuclear Information System (INIS)

    Pollock, E.N.; Schlier, D.S.; Shinopulos, G.

    1992-01-01

    This patent describes a method of removing niobium from a uranium-niobium alloy. It comprises dissolving the uranium-niobium alloy metal pieces in a first aqueous solution containing an acid selected from the group consisting of hydrochloric acid and sulfuric acid and fluoboric acid as a catalyst to provide a second aqueous solution, which includes uranium (U +4 ), acid radical ions, the acids insolubles including uranium oxides and niobium oxides; adding nitric acid to the insolubles to oxidize the niobium oxides to yield niobic acid and to complete the solubilization of any residual uranium; and separating the niobic acid from the nitric acid and solubilized uranium

  6. Anodic oxidation of InP in pure water

    International Nuclear Information System (INIS)

    Robach, Y.; Joseph, J.; Bergignat, E.; Hollinger, G.

    1989-01-01

    It is shown that thin InP native oxide films can be grown by anodization of InP in pure water. An interfacial phosphorus-rich In(PO 3 ) 3 -like condensed phosphate is obtained this way. This condensed phosphate has good passivating properties and can be used in electronic device technology. The chemical composition of these native oxides was found similar to that of an anodic oxide grown in an anodization in glycol and water (AGW) electrolyte. From the similarity between the two depth profiles observed in pure water and AGW electrolyte, they can conclude that dissolution phenomena do not seem to play a major role. The oxide growth seems to be controlled by the drift of ionic species under the electric field

  7. Unique Reduced Graphene Oxide as Efficient Anode Material in Li ...

    Indian Academy of Sciences (India)

    19

    Unique Reduced Graphene Oxide as Efficient Anode Material in Li Ion Battery. Sampath Kumar Puttapati1 ... Keywords: carbon materials; graphene oxide; energy storage; Li ion battery. *. Corresponding author. Tel: +91 40 2313 4453; .... Chowdari B V R 2014 J. Solid State Electrochem. 18 941. [4] Pei S -F and Cheng H -M ...

  8. Aerosol synthesis and electrochemical analysis of niobium mixed-metal oxides for the ethanol oxidation reaction in acid and alkaline electrolyte

    Science.gov (United States)

    Konopka, Daniel A.

    . For the first time, in situ FTIR measurements in acid electrolyte showed that highly dispersed Pt nanoparticles (2--5nm) on NbRuyO z (at% 8Nb:1Ru) catalyze the formation of CO2 from ethanol in greater yield, and 0.35--0.4V lower, than Pt(111). Compared to conventional Pt/carbon, this indicates that, (1) Pt supported on NbRuyO z can be more effective at splitting the C---C bond in ethanol and, (2) the scission occurs at potentials more ideal for a higher efficiency fuel cell anode. Ex situ-microscopy revealed the polarization-induced two- and three-dimensional formation of Pt-NbOx interfacial adsorption sites responsible for the facilitation of the total oxidation pathway of ethanol. The results show that synthesis and post-treatment of niobia supports can bias the utility of Pt/niobia systems towards the ethanol oxidation reaction at the anode or the oxygen reduction reaction at the cathode. Experimental and computational-theoretical analyses indicate that the mechanism of interfacial site formation is dependent upon the local oxygen concentration, as well as the availability of multiple, energetically accessible oxidation states like those inherent to niobia. Future directions for the development of highly active, niobium-based materials tailored for efficient catalysis of the total oxidation pathway of ethanol are discussed.

  9. Laser-pulsed plasma chemistry: Laser-initiated plasma oxidation of niobium

    Science.gov (United States)

    Marks, R. F.; Pollak, R. A.; Avouris, Ph.; Lin, C. T.; Théfaine, Y. J.

    1983-03-01

    We report the first observation of the chemical modification of a solid surface exposed to an ambient gas plasma initiated by the interaction of laser radiation with the same surface. A new technique, which we designate laser-pulsed plasma chemistry (LPPC), is proposed for activating heterogeneous chemical reactions at solid surfaces in a gaseous ambient by means of a plasma initiated by laser radiation. Results for niobium metal in one atmosphere oxygen demonstrate single-pulse, self-limiting oxide growth induced by a pulsed CO2 laser. X-ray photoelectron spectroscopy (XPS or ESCA) was used to monitor surface chemical composition changes and thickness control of thin (1 to 5 nm) reaction product layers. The dependence of single-pulse oxide growth upon laser fluence is observed to be monotonic for oxide thicknesses up to 5 nm. Composition of the oxide Nb2O5-δ, formed by such an optically driven plasma, is similar to that formed by low-temperature oxidation processes such as rf plasma oxidation; however, the valence defect δ of the LPPC oxide is a least two to five times lower. Interdiffusion at the oxide/metal interface becomes important at higher irradiances and is activated by direct optical coupling with the solid or by plasma-mediated thermal coupling. Under ultrahigh vacuum, CO2 laser irradiances greater than 0.9 J cm-2 per pulse thin the surface oxide.

  10. Fabrication of ultra thin anodic aluminium oxide membranes by low anodization voltages

    Science.gov (United States)

    Pastore, I.; Poplausks, R.; Apsite, I.; Pastare, I.; Lombardi, F.; Erts, D.

    2011-06-01

    Formation of ultrathin anodised aluminium oxide (AAO) membranes with high aspect ratio by Al anodization in sulphuric and oxalic acids at low potentials was investigated. Low anodization potentials ensure slow electrochemical reaction speeds and formation of AAO membranes with pore diameter and thickness below 20 nm and 70 nm respectively. Minimum time necessary for formation of continuous AAO membranes was determined. AAO membrane pore surface was covered with polymer Paraloid B72TM to transport it to the selected substrate. The fabricated ultra thin AAO membranes could be used to fabricate nanodot arrays on different surfaces.

  11. Anodes for Solid Oxide Fuel Cells Operating at Low Temperatures

    DEFF Research Database (Denmark)

    Abdul Jabbar, Mohammed Hussain

    An important issue that has limited the potential of Solid Oxide Fuel Cells (SOFCs) for portable applications is its high operating temperatures (800-1000 ºC). Lowering the operating temperature of SOFCs to 400-600 ºC enable a wider material selection, reduced degradation and increased lifetime....... On the other hand, low-temperature operation poses serious challenges to the electrode performance. Effective catalysts, redox stable electrodes with improved microstructures are the prime requisite for the development of efficient SOFC anodes. The performance of Nb-doped SrT iO3 (STN) ceramic anodes...... at 400ºC. The potential of using WO3 ceramic as an alternative anode materials has been explored. The relatively high electrode polarization resistance obtained, 11 Ohm cm2 at 600 ºC, proved the inadequate catalytic activity of this system for hydrogen oxidation. At the end of this thesis...

  12. Electrochemical Energy Storage Applications of CVD Grown Niobium Oxide Thin Films.

    Science.gov (United States)

    Fiz, Raquel; Appel, Linus; Gutiérrez-Pardo, Antonio; Ramírez-Rico, Joaquín; Mathur, Sanjay

    2016-08-24

    We report here on the controlled synthesis, characterization, and electrochemical properties of different polymorphs of niobium pentoxide grown by CVD of new single-source precursors. Nb2O5 films deposited at different temperatures showed systematic phase evolution from low-temperature tetragonal (TT-Nb2O5, T-Nb2O5) to high temperature monoclinic modifications (H-Nb2O5). Optimization of the precursor flux and substrate temperature enabled phase-selective growth of Nb2O5 nanorods and films on conductive mesoporous biomorphic carbon matrices (BioC). Nb2O5 thin films deposited on monolithic BioC scaffolds produced composite materials integrating the high surface area and conductivity of the carbonaceous matrix with the intrinsically high capacitance of nanostructured niobium oxide. Heterojunctions in Nb2O5/BioC composites were found to be beneficial in electrochemical capacitance. Electrochemical characterization of Nb2O5/BioC composites showed that small amounts of Nb2O5 (as low as 5%) in conjunction with BioCarbon resulted in a 7-fold increase in the electrode capacitance, from 15 to 104 F g(-1), while imparting good cycling stability, making these materials ideally suited for electrochemical energy storage applications.

  13. Anodic oxide growth on Zr in neutral aqueous solution

    Indian Academy of Sciences (India)

    anodization and cathodic reactions on metal surfaces. Our sample, specially pre- pared for neutron reflectometry, was a sputter-deposited film on a polished Si(1 1 1) substrate, sufficiently thick to imitate a bulk metal. Upon removal from the sput- tering chamber and exposure to air, a passive oxide layer grew on the film. An.

  14. A review of liquid metal anode solid oxide fuel cells

    Directory of Open Access Journals (Sweden)

    ALIYA TOLEUOVA

    2013-06-01

    Full Text Available This review discusses recent advances in a solid oxide fuel cell (SOFC variant that uses liquid metal electrodes (anodes with the advantage of greater fuel tolerance and the ability to operate on solid fuel. Key features of the approach are discussed along with the technological and research challenges that need to be overcome for scale-up and commercialisation.

  15. Investigation of anodic oxide coatings on zirconium after heat treatment

    International Nuclear Information System (INIS)

    Sowa, Maciej; Dercz, Grzegorz; Suchanek, Katarzyna; Simka, Wojciech

    2015-01-01

    Highlights: • Oxide layers prepared via PEO of zirconium were subjected to heat treatment. • Surface characteristics were determined for the obtained oxide coatings. • Heat treatment led to the partial destruction of the anodic oxide layer. • Pitting corrosion resistance of zirconium was improved after the modification. - Abstract: Herein, results of heat treatment of zirconium anodised under plasma electrolytic oxidation (PEO) conditions at 500–800 °C are presented. The obtained oxide films were investigated by means of SEM, XRD and Raman spectroscopy. The corrosion resistance of the zirconium specimens was evaluated in Ringer's solution. A bilayer oxide coatings generated in the course of PEO of zirconium were not observed after the heat treatment. The resulting oxide layers contained a new sublayer located at the metal/oxide interface is suggested to originate from the thermal oxidation of zirconium. The corrosion resistance of the anodised metal was improved after the heat treatment

  16. Cytotoxicity and Bioactivity of Calcium Silicate Cements Combined with Niobium Oxide in Different Cell Lines.

    Science.gov (United States)

    Mestieri, Leticia Boldrin; Gomes-Cornélio, Ana Lívia; Rodrigues, Elisandra Márcia; Faria, Gisele; Guerreiro-Tanomaru, Juliane Maria; Tanomaru-Filho, Mário

    2017-01-01

    The aim of this study was to evaluate the cytotoxicity and bioactivity of calcium silicate-based cements combined with niobium oxide (Nb2O5) micro and nanoparticles, comparing the response in different cell lines. This evaluation used four cell lines: two primary cultures (human dental pulp cells - hDPCs and human dental follicle cells - hDFCs) and two immortalized cultures (human osteoblast-like cells - Saos-2 and mouse periodontal ligament cells - mPDL). The tested materials were: White Portland Cement (PC), mineral trioxide aggregate (MTA), white Portland cement combined with microparticles (PC/Nb2O5µ) or nanoparticles (PC/Nb2O5n) of niobium oxide (Nb2O5). Cytotoxicity was evaluated by the methylthiazolyldiphenyl-tetrazolium bromide (MTT) and trypan blue exclusion assays and bioactivity by alkaline phosphatase (ALP) enzyme activity. Results were analyzed by ANOVA and Tukey test (a=0.05). PC/Nb2O5n presented similar or higher cell viability than PC/Nb2O5µ in all cell lines. Moreover, the materials presented similar or higher cell viability than MTA. Saos-2 exhibited high ALP activity, highlighting PC/Nb2O5µ material at 7 days of exposure. In conclusion, calcium silicate cements combined with micro and nanoparticles of Nb2O5 presented cytocompatibility and bioactivity, demonstrating the potential of Nb2O5 as an alternative radiopacifier agent for these cements. The different cell lines had similar response to cytotoxicity evaluation of calcium silicate cements. However, bioactivity was more accurately detected in human osteoblast-like cell line, Saos-2.

  17. Effect of sealing on the morphology of anodized aluminum oxide

    International Nuclear Information System (INIS)

    Hu, Naiping; Dong, Xuecheng; He, Xueying; Browning, James F.; Schaefer, Dale W.

    2015-01-01

    Highlights: • We explored structural change of anodizing aluminum oxide induced by sealing. • All sealing methods decrease pore size as shown by X-ray/neutron scattering. • Cold sealing and hot water sealing do not alter the aluminum oxide framework. • Hot nickel acetate sealing both fills the pores and deposits on air oxide interface. • Samples with hot nickel acetate sealing outperform other sealing methods. - Abstract: Ultra-small angle X-ray scattering (USAXS), small-angle neutron scattering (SANS), X-ray reflectometry (XRR) and neutron reflectometry (NR) were used to probe structure evolution induced by sealing of anodized aluminum. While cold nickel acetate sealing and hot-water sealing decrease pore size, these methods do not alter the cylindrical porous framework of the anodic aluminum oxide layer. Hot nickel acetate both fills the pores and deposits on the air surface (air–oxide interface), leading to low porosity and small mean pore radius (39 Å). Electrochemical impedance spectroscopy and direct current polarization show that samples sealed by hot nickel acetate outperform samples sealed by other sealing methods

  18. Titanium-Niobium Oxides as Non-Noble Metal Cathodes for Polymer Electrolyte Fuel Cells

    Directory of Open Access Journals (Sweden)

    Akimitsu Ishihara

    2015-07-01

    Full Text Available In order to develop noble-metal- and carbon-free cathodes, titanium-niobium oxides were prepared as active materials for oxide-based cathodes and the factors affecting the oxygen reduction reaction (ORR activity were evaluated. The high concentration sol-gel method was employed to prepare the precursor. Heat treatment in Ar containing 4% H2 at 700–900 °C was effective for conferring ORR activity to the oxide. Notably, the onset potential for the ORR of the catalyst prepared at 700 °C was approximately 1.0 V vs. RHE, resulting in high quality active sites for the ORR. X-ray (diffraction and photoelectron spectroscopic analyses and ionization potential measurements suggested that localized electronic energy levels were produced via heat treatment under reductive atmosphere. Adsorption of oxygen molecules on the oxide may be governed by the localized electronic energy levels produced by the valence changes induced by substitutional metal ions and/or oxygen vacancies.

  19. Measurement of the high-field Q-drop in a high-purity large-grain niobium cavity for different oxidation processes

    Energy Technology Data Exchange (ETDEWEB)

    Ciovati, Gianluigi; Kneisel, Peter; gurevich, alex

    2007-06-01

    The most challenging issue for understanding the performance of superconducting radio-frequency (rf) cavities made of high-purity (residual resistivity ratio > 200) niobium is due to a sharp degradation (“Q-drop”) of the cavity quality factor Q0(Bp) as the peak surface magnetic field (Bp) exceeds about 90 mT, in the absence of field emission. In addition, a low-temperature (100 – 140 C) “in-situ” baking of the cavity was found to be beneficial in reducing the Q-drop. In this contribution, we present the results from a series of rf tests at 1.7 K and 2.0 K on a single-cell cavity made of high-purity large (with area of the order of few cm2) grain niobium which underwent various oxidation processes, after initial buffered chemical polishing, such as anodization, baking in pure oxygen atmosphere and baking in air up to 180 °C, with the objective of clearly identifying the role of oxygen and the oxide layer on the Q-drop. During each rf test a temperature mapping system allows measuring the local temperature rise of the cavity outer surface due to rf losses, which gives information about the losses location, their field dependence and space distribution. The results confirmed that the depth affected by baking is about 20 – 30 nm from the surface and showed that the Q-drop did not re-appear in a previously baked cavity by further baking at 120 °C in pure oxygen atmosphere or in air up to 180 °C. These treatments increased the oxide thickness and oxygen concentration, measured on niobium samples which were processed with the cavity and were analyzed with Transmission Electron Microscope (TEM) and Secondary Ion Mass Spectroscopy (SIMS). Nevertheless, the performance of the cavity after air baking at 180 °C degraded significantly and the temperature maps showed high losses, uniformly distributed on the surface, which could be completely recovered only by a post-purification treatment at 1250 °C. A statistic of the position of the “hot-spots” on the

  20. Electrocatalyst for alcohol oxidation at fuel cell anodes

    Science.gov (United States)

    Adzic, Radoslav [East Setauket, NY; Kowal, Andrzej [Cracow, PL

    2011-11-02

    In some embodiments a ternary electrocatalyst is provided. The electrocatalyst can be used in an anode for oxidizing alcohol in a fuel cell. In some embodiments, the ternary electrocatalyst may include a noble metal particle having a surface decorated with clusters of SnO.sub.2 and Rh. The noble metal particles may include platinum, palladium, ruthenium, iridium, gold, and combinations thereof. In some embodiments, the ternary electrocatalyst includes SnO.sub.2 particles having a surface decorated with clusters of a noble metal and Rh. Some ternary electrocatalysts include noble metal particles with clusters of SnO.sub.2 and Rh at their surfaces. In some embodiments the electrocatalyst particle cores are nanoparticles. Some embodiments of the invention provide a fuel cell including an anode incorporating the ternary electrocatalyst. In some aspects a method of using ternary electrocatalysts of Pt, Rh, and SnO.sub.2 to oxidize an alcohol in a fuel cell is described.

  1. Photoconductivity of Germanium Nanowire Arrays Incorporated in Anodic Aluminum Oxide

    International Nuclear Information System (INIS)

    Polyakov, B; Prikulis, J; Grigorjeva, L; Millers, D; Daly, B; Holmes, J D; Erts, D

    2007-01-01

    Photoconductivity of germanium nanowire arrays of 50 and 100 nm diameter incorporated into Anodic Aluminum Oxide (AAO) membranes illuminated with visible light is investigated. Photocurrent response to excitation radiation with time constants faster than 10 -4 s were governed by absorption of incident light by nanowires, while photokinetics with time constants of the order of 10 -3 s originates from the photoluminescence of the AAO matrix. Possible applications of nanowire arrays inside AAO as photoresistors are discussed

  2. Microstructural evolution of nanograin nickel-zirconia cermet anode materials for solid oxide fuel cell applications

    International Nuclear Information System (INIS)

    Nayak, Bibhuti Bhusan

    2012-01-01

    The aim of the study is to study the structure, microstructure, porosity, thermal expansion, electrical conductivity and electrochemical behavior of the anode material thus synthesized in order to find its suitability for solid oxide fuel cell (SOFC) anode application

  3. Barrier and porous anodic oxides on InSb

    Energy Technology Data Exchange (ETDEWEB)

    Suleiman, A.; Hashimoto, T. [Corrosion and Protection Centre, School of Materials, University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom); Skeldon, P. [Corrosion and Protection Centre, School of Materials, University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom)], E-mail: peter.skeldon@manchester.ac.uk; Thompson, G.E. [Corrosion and Protection Centre, School of Materials, University of Manchester, P.O. Box 88, Manchester M60 1QD (United Kingdom); Echeverria, F. [Dpto de Ing. Metalurgica y de Materiales, Universidad de Antioquia, Oficina 18-240, Calle 67 No. 53-108, A.A. 1226, Medellin (Colombia); Graham, M.J.; Sproule, G.I.; Moisa, S. [Institute for Microstructural Sciences, National Research Council of Canada, Montreal Road, Ottawa, K1A 0R6 (Canada); Habazaki, H. [Graduate Engineering School, Hokkaido University, N13 W8, Kita-ku, Sapporo 060-8628 (Japan); Bailey, P.; Noakes, T.C.Q. [Daresbury Laboratory, Daresbury, Warrington WA4 4AD (United Kingdom)

    2008-05-15

    Anodizing of InSb at 5 mA cm{sup -2} in sodium tungstate electrolyte is shown to produce barrier-type amorphous oxide at relatively low voltages, to about 40 V, and porous-type amorphous oxide at increased voltages. The barrier-type amorphous oxide, consisting of units of In{sub 2}O{sub 3} and Sb{sub 2}O{sub 3}, distributed relatively uniformly throughout the film, develops at a formation ratio of 2.2 {+-} 0.2 nm V{sup -1}. The outer 15-20% of the film also contains tungsten species. The relatively high efficiency of barrier film growth reduces significantly with transition to porous oxide, which is associated additionally with generation of oxygen at the film surface. The final oxide, at 65 V, comprises pores, of typical diameter 80 nm, orientated approximately normal to the substrate and extending from a barrier region to the film surface.

  4. Decomposition of aluminum oxide, titanium(IV) oxide and niobium(V) oxide by fusion with ammonium sulfate

    International Nuclear Information System (INIS)

    Hashiba, Minoru; Miura, Eiji; Nurishi, Yukio; Hibino, Taizo

    1980-01-01

    A decomposition method with ammonium sulfate for Al 2 O 3 , TiO 2 and Nb 2 O 5 is presented. Al 2 O 3 and TiO 2 were fused at 400 and 450 0 C, for 2 h and 1 h, respectively, in the presence of ammonium sulfate (oxide/ammonium sulfate = 1/20 in weight). The fused products were dissolved and extracted into 4N H 2 SO 4 aqueous solution by warming on the water bath or gently boiling on asbestos. The degree of decomposition by fusion was confirmed from the amount of the oxides recovered in the following manner; with the aid of filter pulp, the residue was completely separated by filtration and washed thoroughly by hot water. To the filtrate was added ammonia water in order to precipitate aluminum and titanium hydroxide. The precipitates were ignited in platinum crucible at 1000 0 C and weighed in oxide form. Nb 2 O 5 was fused at 400 0 C for 1 h in the presence of ammonium sulfate (niobium pentoxide/ammonium sulfate = 1/10 in weight). The fused product was extracted with 20% tartaric acid aqueous solution. The degree of decomposition by fusion was confirmed from the amount of the oxide recovered as follows; after separation of the residue by a filter paper with the aid of filter pulp and washed thoroughly by 2% tartaric acid aqueous solution, freshly prepared 6% aqueous solution of cupferron was added to the filtrate and the precipitate formed was filtered immediately. The precipitate was ignited in platinum crucible at 1000 0 C and weighed as Nb 2 O 5 . The recovery of Al 2 O 3 , TiO 2 and Nb 2 O 5 by the present method was (99.2 +- 0.4), (100.1 +- 0.2) and (100.1 +- 0.2)%, respectively. It is concluded that Al 2 O 3 , TiO 2 and Nb 2 O 5 could be completely decomposed with ammonium sulfate. (author)

  5. Spatially uniform resistance switching of low current, high endurance titanium–niobium-oxide memristors

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, Suhas [Hewlett Packard Labs, Palo Alto, CA (United States); Davila, Noraica [Hewlett Packard Labs, Palo Alto, CA (United States); Wang, Ziwen [Stanford Univ., CA (United States); Huang, Xiaopeng [Hewlett Packard Labs, Palo Alto, CA (United States); Strachan, John Paul [Hewlett Packard Labs, Palo Alto, CA (United States); Vine, David [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); David Kilcoyne, A. L. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Nishi, Yoshio [Stanford Univ., CA (United States); Stanley Williams, R. [Hewlett Packard Labs, Palo Alto, CA (United States)

    2016-11-24

    Here we analyzed micrometer-scale titanium-niobium-oxide prototype memristors, which exhibited low write-power (< 3 μW) and energy (< 200 fJ per bit per μm2), low read-power (~nW), and high endurance ( > millions of cycles). To understand their physico-chemical operating mechanisms, we performed in operando synchrotron X-ray transmission nanoscale spectromicroscopy using an ultra-sensitive time-multiplexed technique. We observed only spatially uniform material changes during cell operation, in sharp contrast to the frequently detected formation of a localized conduction channel in transition-metal-oxide memristors. We also associated the response of assigned spectral features distinctly to non-volatile storage (resistance change) and writing of information (application of voltage and Joule heating). Lastly, these results provide critical insights into high-performance memristors that will aid in device design, scaling and predictive circuit-modeling, all of which are essential for the widespread deployment of successful memristor applications.

  6. Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles.

    Science.gov (United States)

    Mestieri, Leticia Boldrin; Tanomaru-Filho, Mário; Gomes-Cornélio, Ana Livia; Salles, Loise Pedrosa; Bernardi, Maria Inês Basso; Guerreiro-Tanomaru, Juliane Maria

    2014-01-01

    Mineral Trioxide Aggregate (MTA) is composed of Portland Cement (PC) and bismuth oxide (BO). Replacing BO for niobium oxide (NbO) microparticles (Nbµ) or nanoparticles (Nbη) may improve radiopacity and bioactivity. The aim of this study was to evaluate the radiopacity and cytotoxicity of the materials: (1) PC; (2) White MTA; (3) PC+30% Nbµ; (4) PC+30% Nbη. For the radiopacity test, specimens of the different materials were radiographed along an aluminum step-wedge. For cell culture assays, Saos-2 osteoblastic-cells (ATCC HTB-85) were used. Cell viability was evaluated through MTT assay, and bioactivity was assessed by alkaline phosphatase activity assay. The results demonstrated higher radiopacity for MTA, followed by Nbµ and Nbη, which had similar values. Cell culture analysis showed that PC and PC+NbO associations promoted greater cell viability than MTA. It was concluded that the combination of PC+NbO is a potential alternative for composition of MTA.

  7. Sol-Gel Synthesis and Characterization of Cubic Bismuth Zinc Niobium Oxide Nanopowders

    Directory of Open Access Journals (Sweden)

    Ganchimeg Perenlei

    2014-01-01

    Full Text Available Bismuth zinc niobium oxide (BZN was successfully synthesized by a diol-based sol-gel reaction utilizing metal acetate and alkoxide precursors. Thermal analysis of a liquid suspension of precursors suggests that the majority of organic precursors decompose at temperatures up to 150°C, and organic free powders form above 350°C. The experimental results indicate that a homogeneous gel is obtained at about 200°C and then converts to a mixture of intermediate oxides at 350–400°C. Finally, single-phased BZN powders are obtained between 500 and 900°C. The degree of chemical homogeneity as determined by X-ray diffraction and EDS mapping is consistent throughout the samples. Elemental analysis indicates that the atomic ratio of metals closely matches a Bi1.5ZnNb1.5O7 composition. Crystallite sizes of the BZN powders calculated from the Scherrer equation are about 33–98 nm for the samples prepared at 500–700°C, respectively. The particle and crystallite sizes increase with increased sintering temperature. The estimated band gap of the BZN nanopowders from optical analysis is about 2.60–2.75 eV at 500-600°C. The observed phase formations and measured results in this study were compared with those of previous reports.

  8. Radiopacity and cytotoxicity of Portland cement associated with niobium oxide micro and nanoparticles

    Directory of Open Access Journals (Sweden)

    Leticia Boldrin MESTIERI

    2014-12-01

    Full Text Available Objective Mineral Trioxide Aggregate (MTA is composed of Portland Cement (PC and bismuth oxide (BO. Replacing BO for niobium oxide (NbO microparticles (Nbµ or nanoparticles (Nbη may improve radiopacity and bioactivity. The aim of this study was to evaluate the radiopacity and cytotoxicity of the materials: 1 PC; 2 White MTA; 3 PC+30% Nbµ; 4 PC+30% Nbη. Material and Methods For the radiopacity test, specimens of the different materials were radiographed along an aluminum step-wedge. For cell culture assays, Saos-2 osteoblastic-cells (ATCC HTB-85 were used. Cell viability was evaluated through MTT assay, and bioactivity was assessed by alkaline phosphatase activity assay. Results The results demonstrated higher radiopacity for MTA, followed by Nbµ and Nbη, which had similar values. Cell culture analysis showed that PC and PC+NbO associations promoted greater cell viability than MTA. Conclusions It was concluded that the combination of PC+NbO is a potential alternative for composition of MTA.

  9. Coloration and bleaching mechanism of niobium oxide electrochromic thin films; Sanka niobu electromic usumaku no chakushoshoku mechanism

    Energy Technology Data Exchange (ETDEWEB)

    Yoshimura, K.; Miki, T.; Tazawa, M.; Jin, P.; Igarashi, K.; Tanemura, S. [National Industrial Research Institute of Nagoya, Nagoya (Japan)

    1997-11-25

    In order to search for the coloration and bleaching mechanism of niobium oxide, considerations were given on optical properties and electron conditions in niobium oxide thin films (glass plates as substrates coated with ITO) prepared by using the reactive DC magnetron sputtering process. The films were so grown that their thickness will all be 100 nm to facilitate data comparison. Coloration and bleaching of the grown test films were conducted by cyclic voltammetry. Electron spectra were measured by using XPS, and electron energy was analyzed. Coloration of niobium oxide occurs as a result of change in valency electron state from an Nb {sup 5+} state to an Nb {sup 4+} state, while change in the XPS spectra also corresponds with the above change. However, the XPS spectra differ greatly between crystalline samples and amorphous samples. The coloration and bleaching mechanism of the crystallized Nb2O5 film can be explained by a reaction formula similar to that for WO3. However, with regard to the amorphous Nb2O5 film, an independent reaction involving water in the film seems to occur together with the same reaction as in the crystallized film. 9 refs., 5 figs.

  10. Structural transformation of nickel hydroxide films during anodic oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Crocker, Robert W. [Univ. of California, Berkeley, CA (United States); Muller, Rolf H. [Univ. of California, Berkeley, CA (United States)

    1992-05-01

    The transformation of anodically formed nickel hydroxide/oxy-hydroxide electrodes has been investigated. A mechanism is proposed for the anodic oxidation reaction, in which the reaction interface between the reduced and oxidized phases of the electrode evolves in a nodular topography that leads to inefficient utilization of the active electrode material. In the proposed nodular transformation model for the anodic oxidation reaction, nickel hydroxide is oxidized to nickel oxy-hydroxide in the region near the metal substrate. Since the nickel oxy-hydroxide is considerably more conductive than the surrounding nickel hydroxide, as further oxidation occurs, nodular features grow rapidly to the film/electrolyte interface. Upon emerging at the electrolyte interface, the reaction boundary between the nickel hydroxide and oxy-hydroxide phases spreads laterally across the film/electrolyte interface, creating an overlayer of nickel oxy-hydroxide and trapping uncharged regions of nickel hydroxide within the film. The nickel oxy-hydroxide overlayer surface facilitates the oxygen evolution side reaction. Scanning tunneling microscopy of the electrode in its charged state revealed evidence of 80 - 100 Angstrom nickel oxy-hydroxide nodules in the nickel hydroxide film. In situ spectroscopic ellipsometer measurements of films held at various constant potentials agree quantitatively with optical models appropriate to the nodular growth and subsequent overgrowth of the nickel oxy-hydroxide phase. A two-dimensional, numerical finite difference model was developed to simulate the current distribution along the phase boundary between the charged and uncharged material. The model was used to explore the effects of the physical parameters that govern the electrode behavior. The ratio of the conductivities of the nickel hydroxide and oxy-hydroxide phases was found to be the dominant parameter in the system.

  11. Structural transformation of nickel hydroxide films during anodic oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Crocker, R.W.; Muller, R.H.

    1992-05-01

    The transformation of anodically formed nickel hydroxide/oxy-hydroxide electrodes has been investigated. A mechanism is proposed for the anodic oxidation reaction, in which the reaction interface between the reduced and oxidized phases of the electrode evolves in a nodular topography that leads to inefficient utilization of the active electrode material. In the proposed nodular transformation model for the anodic oxidation reaction, nickel hydroxide is oxidized to nickel oxy-hydroxide in the region near the metal substrate. Since the nickel oxy-hydroxide is considerably more conductive than the surrounding nickel hydroxide, as further oxidation occurs, nodular features grow rapidly to the film/electrolyte interface. Upon emerging at the electrolyte interface, the reaction boundary between the nickel hydroxide and oxy-hydroxide phases spreads laterally across the film/electrolyte interface, creating an overlayer of nickel oxy-hydroxide and trapping uncharged regions of nickel hydroxide within the film. The nickel oxy-hydroxide overlayer surface facilitates the oxygen evolution side reaction. Scanning tunneling microscopy of the electrode in its charged state revealed evidence of 80 {endash} 100 Angstrom nickel oxy-hydroxide nodules in the nickel hydroxide film. In situ spectroscopic ellipsometer measurements of films held at various constant potentials agree quantitatively with optical models appropriate to the nodular growth and subsequent overgrowth of the nickel oxy-hydroxide phase. A two-dimensional, numerical finite difference model was developed to simulate the current distribution along the phase boundary between the charged and uncharged material. The model was used to explore the effects of the physical parameters that govern the electrode behavior. The ratio of the conductivities of the nickel hydroxide and oxy-hydroxide phases was found to be the dominant parameter in the system.

  12. Atomic Layer Deposition of Lithium Niobium Oxides as Potential Solid-State Electrolytes for Lithium-Ion Batteries.

    Science.gov (United States)

    Wang, Biqiong; Zhao, Yang; Banis, Mohammad Norouzi; Sun, Qian; Adair, Keegan R; Li, Ruying; Sham, Tsun-Kong; Sun, Xueliang

    2018-01-17

    The development of solid-state electrolytes by atomic layer deposition (ALD) holds unparalleled advantages toward the fabrication of next-generation solid-state batteries. Lithium niobium oxide (LNO) thin films with well-controlled film thickness and composition were successfully deposited by ALD at a deposition temperature of 235 °C using lithium tert-butoxide and niobium ethoxide as Li and Nb sources, respectively. Furthermore, incorporation of higher Li content was achieved by increasing the Li-to-Nb subcycle ratio. In addition, detailed X-ray absorption near edge structure studies of the amorphous LNO thin films on the Nb L-edge revealed the existence of Nb as Nb 5+ in a distorted octahedral structure. The octahedrons in niobium oxide thin films experienced severe distortions, which could be gradually alleviated upon the introduction of Li atoms into the thin films. The ionic conductivities of the as-prepared LNO thin films were also measured, with the highest value achieving 6.39 × 10 -8 S cm -1 at 303 K with an activation energy of 0.62 eV.

  13. Characterization of Human Gingival Fibroblasts on Zirconia Surfaces Containing Niobium Oxide

    Directory of Open Access Journals (Sweden)

    Young-Dan Cho

    2015-09-01

    Full Text Available It was indicated that tetragonal zirconia polycrystal (TZP containing yttria (Y2O3 and niobium oxide (Nb2O5 ((Y,Nb-TZP could be an adequate dental material to be used at esthetically important sites. The (Y,Nb-TZP was also proved to possess its osteogenic potential comparable with those conventional dental implant material, titanium (Ti. The objective of the current study was to characterize cellular response of human gingival fibroblasts (HGFs to smooth and rough surfaces of the (Y,Nb-TZP disc, which were obtained by polishing and sandblasting, respectively. Various microscopic, biochemical, and molecular techniques were used to investigate the disc surfaces and cellular responses for the experimental (Y,Nb-TZP and the comparing Ti groups. Sandblasted rough (Y,Nb-TZP (Zir-R discs had the highest surface roughness. HGFs cultured on polished (Y,Nb-TZP (Zir showed a rounded cell morphology and light spreading at 6 h after seeding and its proliferation rate significantly increased during seven days of culture compared to other surfaces. The mRNA expressions of type I collagen, integrin α2 and β1 were significantly stimulated for the Zir group at 24 h after seeding. The current findings, combined with the previous results, indicate that (Y,Nb-TZP provides appropriate surface condition for osseointegration at the fixture level and for peri-implant mucosal sealing at the abutment level producing a suitable candidate for dental implantation with an expected favorable clinical outcome.

  14. Removal of organic contaminants from secondary effluent by anodic oxidation with a boron-doped diamond anode as tertiary treatment

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Segura, Sergi, E-mail: sergigarcia@ub.edu [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia); Laboratori d’Electroquímica dels Materials i del Medi Ambient, Departament de Química Física, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Keller, Jürg [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia); Brillas, Enric [Laboratori d’Electroquímica dels Materials i del Medi Ambient, Departament de Química Física, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Radjenovic, Jelena, E-mail: j.radjenovic@awmc.uq.edu.au [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia)

    2015-02-11

    Graphical abstract: - Highlights: • Mineralization of secondary effluent by anodic oxidation with BDD anode. • Complete removal of 29 pharmaceuticals and pesticides at trace level concentrations. • Organochlorine and organobromine byproducts were formed at low μM concentrations. • Chlorine species evolution assessed to evaluate the anodic oxidation applicability. - Abstract: Electrochemical advanced oxidation processes (EAOPs) have been widely investigated as promising technologies to remove trace organic contaminants from water, but have rarely been used for the treatment of real waste streams. Anodic oxidation with a boron-doped diamond (BDD) anode was applied for the treatment of secondary effluent from a municipal sewage treatment plant containing 29 target pharmaceuticals and pesticides. The effectiveness of the treatment was assessed from the contaminants decay, dissolved organic carbon and chemical oxygen demand removal. The effect of applied current and pH was evaluated. Almost complete mineralization of effluent organic matter and trace contaminants can be obtained by this EAOP primarily due to the action of hydroxyl radicals formed at the BDD surface. The oxidation of Cl{sup −} ions present in the wastewater at the BDD anode gave rise to active chlorine species (Cl{sub 2}/HClO/ClO{sup −}), which are competitive oxidizing agents yielding chloramines and organohalogen byproducts, quantified as adsorbable organic halogen. However, further anodic oxidation of HClO/ClO{sup −} species led to the production of ClO{sub 3}{sup −} and ClO{sub 4}{sup −} ions. The formation of these species hampers the application as a single-stage tertiary treatment, but posterior cathodic reduction of chlorate and perchlorate species may reduce the risks associated to their presence in the environment.

  15. Advances of the research evolution on aluminum electrochemical anodic oxidation technology

    Science.gov (United States)

    Yang, Z. B.; Hu, J. C.; Li, K. Q.; Zhang, S. Y.; Fan, Q. H.; Liu, S. A.

    2017-12-01

    This article gives an overview on the development of aluminum anodization technique in terms of fundamental aspects and practical applications in the past decades. Besides, the formation mechanism and structural characteristics of anodic alumina films as well as the factors affected the formation of porous anodic alumina films are also discussed. Anodic aluminum oxide (AAO) prepared by the anodization method can be divided into two categories: dense anodic alumina (DAA) and porous anodic alumina (PAA). This article also summarizes the optical properties, magnetic properties, solar absorption properties, and catalytic properties of porous anodic alumina film and its applications in nanomaterials, optical materials, magnetic materials, biosensors, solar cells, and so on. In addition, future developmental trend of porous anodic alumina film is covered.

  16. Electrochemical degradation of clofibric acid in water by anodic oxidation

    International Nuclear Information System (INIS)

    Sires, Ignasi; Cabot, Pere Lluis; Centellas, Francesc; Garrido, Jose Antonio; Rodriguez, Rosa Maria; Arias, Conchita; Brillas, Enric

    2006-01-01

    Aqueous solutions containing the metabolite clofibric acid (2-(4-chlorophenoxy)-2-methylpropionic acid) up to close to saturation in the pH range 2.0-12.0 have been degraded by anodic oxidation with Pt and boron-doped diamond (BDD) as anodes. The use of BDD leads to total mineralization in all media due to the efficient production of oxidant hydroxyl radical (·OH). This procedure is then viable for the treatment of wastewaters containing this compound. The effect of pH, apparent current density, temperature and metabolite concentration on the degradation rate, consumed specific charge and mineralization current efficiency has been investigated. Comparative treatment with Pt yields poor decontamination with complete release of stable chloride ion. When BDD is used, this ion is oxidized to Cl 2 . Clofibric acid is more rapidly destroyed on Pt than on BDD, indicating that it is more strongly adsorbed on the Pt surface enhancing its reaction with ·OH. Its decay kinetics always follows a pseudo-first-order reaction and the rate constant for each anode increases with increasing apparent current density, being practically independent of pH and metabolite concentration. Aromatic products such as 4-chlorophenol, 4-chlorocatechol, 4-chlororesorcinol, hydroquinone, p-benzoquinone and 1,2,4-benzenetriol are detected by gas chromatography-mass spectrometry (GC-MS) and reversed-phase chromatography. Tartronic, maleic, fumaric, formic, 2-hydroxyisobutyric, pyruvic and oxalic acids are identified as generated carboxylic acids by ion-exclusion chromatography. These acids remain stable in solution using Pt, but they are completely converted into CO 2 with BDD. A reaction pathway for clofibric acid degradation involving all these intermediates is proposed

  17. Microstructure and optical appearance of anodized friction stir processed Al - Metal oxide surface composites

    DEFF Research Database (Denmark)

    Gudla, Visweswara Chakravarthy; Jensen, Flemming; Bordo, Kirill

    2014-01-01

    Multiple-pass friction stir processing (FSP) was employed to impregnate Ti, Y and Ce oxide powders into the surface of an Aluminium alloy. The FSP processed surface composite was subsequently anodized with an aim to develop optical effects in the anodized layer owing to the presence of incorporated...... oxide particles which will influence the scattering of light. This paper presents the investigations on relation between microstructure of the FSP zone and optical appearance of the anodized layer due to incorporation of metal oxide particles and modification of the oxide particles due to the anodizing...

  18. Physicochemical and mechanical properties of zirconium oxide and niobium oxide modified Portland cement-based experimental endodontic sealers.

    Science.gov (United States)

    Viapiana, R; Flumignan, D L; Guerreiro-Tanomaru, J M; Camilleri, J; Tanomaru-Filho, M

    2014-05-01

    To evaluate the physicochemical and mechanical properties of Portland cement-based experimental sealers (ES) with different radiopacifying agents (zirconium oxide and niobium oxide micro- and nanoparticles) in comparison with the following conventional sealers: AH Plus, MTA Fillapex and Sealapex. The materials were tested for setting time, compressive strength, flow, film thickness, radiopacity, solubility, dimensional stability and formaldehyde release. Data were subjected to anova and Tukey tests (P 0.05) and lower solubility when compared with MTA Fillapex and Sealapex (P Portland cement-based experimental endodontic sealers presented physicochemical properties according to the specifications no 57 ANSI/ADA (ADA Professional Product Review, 2008) and ISO 6876 (Dentistry - Root Canal Sealing Materials, 2012, British Standards Institution, London, UK). The sealers had setting times and flow ability that was adequate for clinical use, satisfactory compressive strength and low solubility. Additional studies should be carried out with the purpose of decreasing the film thickness and to determine the ideal ratio of radiopacifying agents in Portland cement-based root canal sealers. © 2013 International Endodontic Journal. Published by John Wiley & Sons Ltd.

  19. Niobium electrodeposition from molten fluorides

    International Nuclear Information System (INIS)

    Sartori, A.F.

    1987-01-01

    Niobium electrodeposition from molten alkali fluorides has been studied aiming the application of this technic to the processes of electrorefining and galvanotechnic of this metal. The effects of current density, temperature, niobium concentration in the bath, electrolysis time, substrate nature, ratio between anodic and cathodic areas, electrodes separation and the purity of anodes were investigated in relation to the cathodic current efficiency, electrorefining, electroplating and properties of the deposit and the electrolytic solution. The work also gives the results of the conctruction and operation of a pilot plant for refractory metals electrodeposition and shows the electrorefining and electroplating compared to those obtained at the laboratory scale. (author) [pt

  20. Solid oxide fuel cell power plant with an anode recycle loop turbocharger

    Energy Technology Data Exchange (ETDEWEB)

    Saito, Kazuo; Skiba, Tommy; Patel, Kirtikumar H.

    2016-09-27

    An anode exhaust recycle turbocharger (100) has a turbocharger turbine (102) secured in fluid communication with a compressed oxidant stream within an oxidant inlet line (218) downstream from a compressed oxidant supply (104), and the anode exhaust recycle turbocharger (100) also includes a turbocharger compressor (106) mechanically linked to the turbocharger turbine (102) and secured in fluid communication with a flow of anode exhaust passing through an anode exhaust recycle loop (238) of the solid oxide fuel cell power plant (200). All or a portion of compressed oxidant within an oxidant inlet line (218) drives the turbocharger turbine (102) to thereby compress the anode exhaust stream in the recycle loop (238). A high-temperature, automotive-type turbocharger (100) replaces a recycle loop blower-compressor (52).

  1. Solid oxide fuel cell power plant with an anode recycle loop turbocharger

    Science.gov (United States)

    Saito, Kazuo; Skiba, Tommy; Patel, Kirtikumar H.

    2015-07-14

    An anode exhaust recycle turbocharger (100) has a turbocharger turbine (102) secured in fluid communication with a compressed oxidant stream within an oxidant inlet line (218) downstream from a compressed oxidant supply (104), and the anode exhaust recycle turbocharger (100) also includes a turbocharger compressor (106) mechanically linked to the turbocharger turbine (102) and secured in fluid communication with a flow of anode exhaust passing through an anode exhaust recycle loop (238) of the solid oxide fuel cell power plant (200). All or a portion of compressed oxidant within an oxidant inlet line (218) drives the turbocharger turbine (102) to thereby compress the anode exhaust stream in the recycle loop (238). A high-temperature, automotive-type turbocharger (100) replaces a recycle loop blower-compressor (52).

  2. OXIDATION OF DRY HYDROCARBONS AT HIGH-POWER DENSITY ANODES

    Energy Technology Data Exchange (ETDEWEB)

    K.Krist; O. Spaldon-Stewart; R. Remick

    2004-03-01

    This work builds upon discoveries by the University of Pennsylvania and others pertaining to the oxidation of dry hydrocarbon fuels in high temperature solid oxide fuel cells. The work reported here was restricted primarily to dry methane and confirms that YSZ-based cells, having ceria in the anode as a catalyst and copper in the anode as a current collector, can operate on dry methane for extended periods. Thirty-three lab-scale cells of various designs were fabricated and operated under a variety of conditions. The longest-lived cell gave stable performance on dry methane at 800 C for over 305 hours. Only slight carbon deposition was noted at the completion of the test. A corresponding nickel/YSZ-based anode would have lasted for less than an hour under these test conditions (which included open circuit potential measurements) before carbon fouling essentially destroyed the cell. The best performing cell achieved 112 mW/cm{sub 2} on dry methane at 800 C. Several problems were encountered with carbon fouling and declining open circuit voltages in many of the test cells after switching from operation on hydrogen to dry methane. Although not rigorously confirmed by experimentation, the results suggested that air infiltration through less than perfect perimeter seals or pinholes in the electrolytes, or both gave rise to conditions that caused the carbon fouling and OCV decline. Small amounts of air reacting with methane in a partial oxidation reaction could produce carbon monoxide that, in turn, would deposit the carbon. If this mechanism is confirmed, it implies that near perfect hardware is required for extended operation. Some evidence was also found for the formation of electrical shorts, probably from carbon deposits bridging the electrolyte. Work with odorized methane and with methane containing 100-ppm hydrogen sulfide confirmed that copper is stable at 800 C in dry hydrocarbon fuels in the presence of sulfur. In a number of cases, but not exclusively, the

  3. On the chemical transport of some niobium oxides with TeCl4. 2

    International Nuclear Information System (INIS)

    Ritschel, M.; Oppermann, H.; Mattern, N.

    1978-01-01

    A report is given on the transport behaviour of the equilibrium phases NbOsub(2.417) to NbOsub(2.483) and of niobium pentoxide during chemical transport with TeCl 4 . It became apparent that phase-pure NbOsub(2.417) and Nb 2 O 5 are deposited from the investigated equilibrium phases. Chemical transport of the phases NbOsub(2.453) to NbOsub(2.483) produces a mixture of several phases. This indicates a strong inhibition of the equilibration in the starting solid. Chemical transport of the niobium pentoxide caused the deposition of monocrystals of the upper and lower phase boundary. The experimental behaviour agrees very well with the calculated results. Monocrystals of the niobium pentoxide forms H, M, N, B and P are deposited in a well identifiable manner by variation of the temperatures (T 2 , T 1 ). (author)

  4. Formation of self-organized nanoporous anodic oxide from metallic gallium.

    Science.gov (United States)

    Pandey, Bipin; Thapa, Prem S; Higgins, Daniel A; Ito, Takashi

    2012-09-25

    This paper reports the formation of self-organized nanoporous gallium oxide by anodization of solid gallium metal. Because of its low melting point (ca. 30 °C), metallic gallium can be shaped into flexible structures, permitting the fabrication of nanoporous anodic oxide monoliths within confined spaces like the inside of a microchannel. Here, solid gallium films prepared on planar substrates were employed to investigate the effects of anodization voltage (1, 5, 10, 15 V) and H(2)SO(4) concentration (1, 2, 4, 6 M) on anodic oxide morphology. Self-organized nanopores aligned perpendicular to the film surface were obtained upon anodization of gallium films in ice-cooled 4 and 6 M aqueous H(2)SO(4) at 10 and 15 V. Nanopore formation could be recognized by an increase in anodic current after a current decrease reflecting barrier oxide formation. The average pore diameter was in the range of 18-40 nm with a narrow diameter distribution (relative standard deviation ca. 10-20%), and was larger at lower H(2)SO(4) concentration and higher applied voltage. The maximum thickness of nanoporous anodic oxide was ca. 2 μm. In addition, anodic formation of self-organized nanopores was demonstrated for a solid gallium monolith incorporated at the end of a glass capillary. Nanoporous anodic oxide monoliths formed from a fusible metal will lead to future development of unique devices for chemical sensing and catalysis.

  5. Catalytic properties of niobium compounds

    International Nuclear Information System (INIS)

    Tanabe, K.; Iizuka, T.

    1983-04-01

    The catalytic activity and selectivity of niobium compounds including oxides, salts, organometallic compounds and others are outlined. The application of these compounds as catalysts to diversified reactions is reported. The nature and action of niobium catalysts are characteristic and sometimes anomalous, suggesting the necessity of basic research and the potential use as catalysts for important processes in the chemical industry. (Author) [pt

  6. Removal of organic contaminants from secondary effluent by anodic oxidation with a boron-doped diamond anode as tertiary treatment.

    Science.gov (United States)

    Garcia-Segura, Sergi; Keller, Jürg; Brillas, Enric; Radjenovic, Jelena

    2015-01-01

    Electrochemical advanced oxidation processes (EAOPs) have been widely investigated as promising technologies to remove trace organic contaminants from water, but have rarely been used for the treatment of real waste streams. Anodic oxidation with a boron-doped diamond (BDD) anode was applied for the treatment of secondary effluent from a municipal sewage treatment plant containing 29 target pharmaceuticals and pesticides. The effectiveness of the treatment was assessed from the contaminants decay, dissolved organic carbon and chemical oxygen demand removal. The effect of applied current and pH was evaluated. Almost complete mineralization of effluent organic matter and trace contaminants can be obtained by this EAOP primarily due to the action of hydroxyl radicals formed at the BDD surface. The oxidation of Cl(-) ions present in the wastewater at the BDD anode gave rise to active chlorine species (Cl2/HClO/ClO(-)), which are competitive oxidizing agents yielding chloramines and organohalogen byproducts, quantified as adsorbable organic halogen. However, further anodic oxidation of HClO/ClO(-) species led to the production of ClO3(-) and ClO4(-) ions. The formation of these species hampers the application as a single-stage tertiary treatment, but posterior cathodic reduction of chlorate and perchlorate species may reduce the risks associated to their presence in the environment. Copyright © 2014 Elsevier B.V. All rights reserved.

  7. Selection of a Commercial Anode Oxide Coating for Electro-oxidation of Cyanide

    Directory of Open Access Journals (Sweden)

    Lanza Marcos Roberto V.

    2002-01-01

    Full Text Available This paper presents a study of the performance of two commercial dimensionally stable anode (DSA® oxide coatings in the electrochemical process for cyanide oxidation. The coatings studied were 70TiO2/30RuO2 and 55Ta2O5/45IrO2, on Ti substrate. The efficiency of both materials in the electro-oxidation of free cyanide was compared using linear voltammetry and electrolysis at constant potential. The 70TiO2/30RuO2 electrode shows a better performance in the electro-oxidation of free cyanide.

  8. Fano resonance in anodic aluminum oxide based photonic crystals.

    Science.gov (United States)

    Shang, Guo Liang; Fei, Guang Tao; Zhang, Yao; Yan, Peng; Xu, Shao Hui; Ouyang, Hao Miao; Zhang, Li De

    2014-01-08

    Anodic aluminum oxide based photonic crystals with periodic porous structure have been prepared using voltage compensation method. The as-prepared sample showed an ultra-narrow photonic bandgap. Asymmetric line-shape profiles of the photonic bandgaps have been observed, which is attributed to Fano resonance between the photonic bandgap state of photonic crystal and continuum scattering state of porous structure. And the exhibited Fano resonance shows more clearly when the sample is saturated ethanol gas than air-filled. Further theoretical analysis by transfer matrix method verified these results. These findings provide a better understanding on the nature of photonic bandgaps of photonic crystals made up of porous materials, in which the porous structures not only exist as layers of effective-refractive-index material providing Bragg scattering, but also provide a continuum light scattering state to interact with Bragg scattering state to show an asymmetric line-shape profile.

  9. Macrokinetic relationships between anodic processes in chlorine electrolysis on ruthenium-titanium oxide anodes

    International Nuclear Information System (INIS)

    Evdokimov, S.V.

    1999-01-01

    Effect of porosity on kinetics of the main (chlorine evolution) and side (oxygen evolution and anodic dissolution of ruthenium dioxide) reactions for chlorine electrolysis conditions has been analyzed. Making allowance for chlorine hydrolysis secondary reaction, the distribution of chlorine concentration, solution pH and current densities of the main and side processes over the porous anode depth, have been found. It is shown that solution acidification in the anode pores due to chlorine hydrolysis can bring about replacement of oxygen evolution and ruthenium dioxide dissolution side reactions toward the porous anode external sides thus affecting its selectivity and corrosion resistance [ru

  10. Antisolvent Precipitation for the Synthesis of Monodisperse Mesoporous Niobium Oxide Spheres as Highly Effective Solid Acid Catalysts

    KAUST Repository

    Li, Cheng Chao

    2012-03-20

    We have developed a low-cost reaction protocol to synthesize mesoporous Nb 2O 5-based solid acid catalysts with external shape control. In the synthesis, monodisperse glycolated niobium oxide spheres (GNOS) were prepared by means of a simple antisolvent precipitation approach and subsequently converted to mesoporous niobium oxide spheres (MNOS) with a large surface area of 312m 2g -1 by means of the hydrothermal treatment. The antisolvent acetone used to obtain GNOS was recovered through distillation at high purity. The obtained mesoporous MNOS were functionalized further with sulfate anions at different temperatures or incorporated with tungstophosphoric acid to obtain recyclable solid acid catalysts. These MNOS-based catalysts showed excellent performance in a wide range of acid-catalyzed reactions, such as Friedel-Crafts alkylation, esterification, and hydrolysis of acetates. As they are monodisperse spheres with diameters in the submicrometer range, the catalysts can be easily separated and reused. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Anodic ammonia oxidation to nitrogen gas catalyzed by mixed biofilms in bioelectrochemical systems

    International Nuclear Information System (INIS)

    Zhan, Guoqiang; Zhang, Lixia; Tao, Yong; Wang, Yujian; Zhu, Xiaoyu; Li, Daping

    2014-01-01

    In this paper we report ammonia oxidation to nitrogen gas using microbes as biocatalyst on the anode, with polarized electrode (+600 mV vs. Ag/AgCl) as electron acceptor. In batch experiments, the maximal rate of ammonia-N oxidation by the mixed culture was ∼ 60 mg L −1 d −1 , and nitrogen gas was the main products in anode compartment. Cyclic voltammetry for testing the electroactivity of the anodic biofilms revealed that an oxidation peak appeared at +600 mV (vs. Ag/AgCl), whereas the electrode without biofilms didn’t appear oxidation peak, indicating that the bioanode had good electroactivities for ammonia oxidation. Microbial community analysis of 16S rRNA genes based on high throughput sequencing indicated that the combination of the dominant genera of Nitrosomonas, Comamonas and Paracocus could be important for the electron transfer from ammonia oxidation to anode

  12. In-situ electrochemical doping of nanoporous anodic aluminum oxide with indigo carmine organic dye

    International Nuclear Information System (INIS)

    Stępniowski, Wojciech J.; Norek, Małgorzata; Budner, Bogusław; Michalska-Domańska, Marta; Nowak-Stępniowska, Agata; Bombalska, Aneta; Kaliszewski, Miron; Mostek, Anna; Thorat, Sanjay; Salerno, Marco; Giersig, Michael; Bojar, Zbigniew

    2016-01-01

    Nanoporous anodic aluminum oxide was formed in sulfuric acid with addition of indigo carmine. During anodizing, the organic dye was incorporated into the porous oxide walls. X-ray photoelectron spectroscopy revealed the presence of nitrogen and sulfur in the anodic aluminum oxide. Two types of incorporated sulfur were found: belonging to the sulfate anions SO 4 2− of the electrolyte and belonging to the C-SO 3 − side groups of the indigo carmine. Raman spectroscopy confirmed the incorporation and showed that the inorganic–organic hybrid material inherited optical properties from the indigo carmine. Typical modes from pyrrolidone rings, unique for indigo carmine in the investigated system (650 and 1585 cm −1 ), were found to be the strongest for the greatest anodizing voltages used. Despite the indigo carmine incorporation, the morphology of the oxide is still nanoporous and its geometry is still tuned by the voltage applied during aluminum anodization. This work presents an inexpensive and facile approach to doping an inorganic oxide material with organic compounds. - Highlights: • Nanoporous anodic alumina was formed in electrolyte with indigo carmine. • XPS confirmed the presence of N and S in anodic alumina. • Raman spectroscopy revealed indigo carmine bands in anodic alumina. • The higher the voltage, the more indigo carmine was incorporated.

  13. In-situ electrochemical doping of nanoporous anodic aluminum oxide with indigo carmine organic dye

    Energy Technology Data Exchange (ETDEWEB)

    Stępniowski, Wojciech J., E-mail: wojciech.stepniowski@wat.edu.pl [Department of Advanced Materials and Technology, Faculty of Advanced Technology and Chemistry, Military University of Technology, 2 Kaliskiego Str., 00-908 Warszawa (Poland); Norek, Małgorzata [Department of Advanced Materials and Technology, Faculty of Advanced Technology and Chemistry, Military University of Technology, 2 Kaliskiego Str., 00-908 Warszawa (Poland); Budner, Bogusław [Institute of Optoelectronics, Military University of Technology, 2 Kaliskiego Str., 00-908 Warszawa (Poland); Michalska-Domańska, Marta [Department of Advanced Materials and Technology, Faculty of Advanced Technology and Chemistry, Military University of Technology, 2 Kaliskiego Str., 00-908 Warszawa (Poland); Institute of Optoelectronics, Military University of Technology, 2 Kaliskiego Str., 00-908 Warszawa (Poland); Nowak-Stępniowska, Agata; Bombalska, Aneta; Kaliszewski, Miron [Institute of Optoelectronics, Military University of Technology, 2 Kaliskiego Str., 00-908 Warszawa (Poland); Mostek, Anna [Department of Advanced Materials and Technology, Faculty of Advanced Technology and Chemistry, Military University of Technology, 2 Kaliskiego Str., 00-908 Warszawa (Poland); Thorat, Sanjay; Salerno, Marco [Department of Nanophysics, Istituto Italiano di Tecnologia, via Morego 30, Genova I-16163 (Italy); Giersig, Michael [Institut für Experimentalphysik, Freie Universität Berlin, Arnimallee 14, 14195 Berlin (Germany); Bojar, Zbigniew [Department of Advanced Materials and Technology, Faculty of Advanced Technology and Chemistry, Military University of Technology, 2 Kaliskiego Str., 00-908 Warszawa (Poland)

    2016-01-01

    Nanoporous anodic aluminum oxide was formed in sulfuric acid with addition of indigo carmine. During anodizing, the organic dye was incorporated into the porous oxide walls. X-ray photoelectron spectroscopy revealed the presence of nitrogen and sulfur in the anodic aluminum oxide. Two types of incorporated sulfur were found: belonging to the sulfate anions SO{sub 4}{sup 2−} of the electrolyte and belonging to the C-SO{sub 3}{sup −} side groups of the indigo carmine. Raman spectroscopy confirmed the incorporation and showed that the inorganic–organic hybrid material inherited optical properties from the indigo carmine. Typical modes from pyrrolidone rings, unique for indigo carmine in the investigated system (650 and 1585 cm{sup −1}), were found to be the strongest for the greatest anodizing voltages used. Despite the indigo carmine incorporation, the morphology of the oxide is still nanoporous and its geometry is still tuned by the voltage applied during aluminum anodization. This work presents an inexpensive and facile approach to doping an inorganic oxide material with organic compounds. - Highlights: • Nanoporous anodic alumina was formed in electrolyte with indigo carmine. • XPS confirmed the presence of N and S in anodic alumina. • Raman spectroscopy revealed indigo carmine bands in anodic alumina. • The higher the voltage, the more indigo carmine was incorporated.

  14. Silicon oxide based high capacity anode materials for lithium ion batteries

    Science.gov (United States)

    Deng, Haixia; Han, Yongbong; Masarapu, Charan; Anguchamy, Yogesh Kumar; Lopez, Herman A.; Kumar, Sujeet

    2017-03-21

    Silicon oxide based materials, including composites with various electrical conductive compositions, are formulated into desirable anodes. The anodes can be effectively combined into lithium ion batteries with high capacity cathode materials. In some formulations, supplemental lithium can be used to stabilize cycling as well as to reduce effects of first cycle irreversible capacity loss. Batteries are described with surprisingly good cycling properties with good specific capacities with respect to both cathode active weights and anode active weights.

  15. Electrochemical synthesis of magnetic nanostructures using anodic aluminum oxide templates

    Science.gov (United States)

    Gong, Jie

    In this dissertation, template electrodeposition was employed to fabricate high quality magnetic nanostructures suited for the reliable investigation of novel spintronics phenomena such as CIMS, BMR, and CPP-GMR. Several critical aspects/steps relating to the synthesis process were investigated in this work. In order to obtain high quality magnetic nanostructures, free-standing and Si-supported anodic aluminum oxide templates with closely controlled pore diameters, lengths, as well as constriction sizes, were synthesized by anodization, followed by appropriate post-processing. The pore opening size on the barrier layer can be controlled down to 5 nm by ion beam etching. After optimization of the compositional, structural, and magnetic properties of homogeneous FeCoNiCu layers electrodeposited under different conditions, the pulsed deposition process of FeCoNI/Cu multilayers on n-Si was studied. The influence of Cu deposition potential and Fe2+ concentration on microstructure, chemical and electrochemical properties, magnetic properties, and hence magnetotransport properties were assessed. The dissolution of the FM layer during potential transition was minimized in order to control interface sharpness. Combined with the systematic sublayer thickness and FM layer composition optimization, unprecedented GMR sensitivity of 0.11%/Oe at 5-15 Oe was obtained. Growth of multilayer nanowires was performed, and contact to a single wire was attempted using an electrochemical technique. We succeeded in addressing a small number of nanowires and measured a CPP-GMR of 17%. Template electrodeposition thus provides a promising way to repeatably fabricate prototypes for spin dependent transport studies.

  16. Laser-pulsed Plasma Chemistry: Laser-initiated Plasma Oxidation Of Niobium

    OpenAIRE

    Marks R.F.; Pollak R.A.; Avouris Ph.; Lin C.T.; Thefaine Y.J.

    1983-01-01

    We report the first observation of the chemical modification of a solid surface exposed to an ambient gas plasma initiated by the interaction of laser radiation with the same surface. A new technique, which we designate laser-pulsed plasma chemistry (LPPC), is proposed for activating heterogeneous chemical reactions at solid surfaces in a gaseous ambient by means of a plasma initiated by laser radiation. Results for niobium metal in one atmosphere oxygen demonstrate single-pulse, self-limitin...

  17. Compositions and structures of niobium oxide cluster ions, NbmOn±, (m = 2-12), revealed by ion mobility mass spectrometry.

    Science.gov (United States)

    Wu, Jenna W J; Moriyama, Ryoichi; Nakano, Motoyoshi; Ohshimo, Keijiro; Misaizu, Fuminori

    2017-09-20

    Herein, the compositions and geometrical structures of niobium oxide cluster ions were studied and compared with those of the lighter Group 5 counterpart vanadium oxide cluster ions by ion-mobility mass spectrometry (IM-MS). As a result of collision-induced dissociation in IM-MS, the compositions were found to be dependent on an odd and even number of niobium atoms, whereby the ions with (NbO 2 )(Nb 2 O 5 ) (m-1)/2 + and (NbO 3 )(Nb 2 O 5 ) (m-1)/2 - were identified as stable compositions for an odd number of Nb atoms, whereas (Nb 2 O 5 ) m/2 ± and (Nb 2 O 6 )(Nb 2 O 5 ) (m-2)/2 - were identified as stable compositions for an even number of Nb atom clusters. Furthermore, structural transitions were observed between m = 8 and 9 for cluster cations and m = 7 and 8 for cluster anions for experimental collision cross-sections (CCSs), which were determined from the arrival times in the ion-mobility measurements. Quantum chemical calculations were conducted on several structural candidates of these compositions for m = 2-12. For cluster cations with the sizes between m = 2 and 8 and cluster anions with m = 2-7, the structures were found to be similar to those of vanadium oxide cluster ions upon comparing the experimental CCSs with the theoretical CCSs of optimized structures. As compared to the vanadium oxide cluster ions, niobium oxide cluster cations with m ≥ 9 and anions with m ≥ 8 consisted of structures where some niobium atoms had more than five oxygen-atom coordination; thus, compact structures could be achieved in the case of niobium oxide cluster ions.

  18. Ni modified ceramic anodes for direct-methane solid oxide fuel cells

    Science.gov (United States)

    Xiao, Guoliang; Chen, Fanglin

    2016-01-19

    In accordance with certain embodiments of the present disclosure, a method for fabricating a solid oxide fuel cell is described. The method includes synthesizing a composition having a perovskite present therein. The method further includes applying the composition on an electrolyte support to form an anode and applying Ni to the composition on the anode.

  19. FIB-SEM investigation of trapped intermetallic particles in anodic oxide films on AA1050 aluminium

    DEFF Research Database (Denmark)

    Jariyaboon, Manthana; Møller, Per; Dunin-Borkowski, Rafal E.

    2011-01-01

    Purpose - The purpose of this investigation is to understand the structure of trapped intermetallics particles and localized composition changes in the anodized anodic oxide film on AA1050 aluminium substrates. Design/methodology/approach - The morphology and composition of Fe-containing intermet...

  20. Platinum-Niobium(V Oxide/Carbon Nanocomposites Prepared By Microwave Synthesis For Ethanol Oxidation

    Directory of Open Access Journals (Sweden)

    Virginija KEPENIENĖ

    2016-05-01

    Full Text Available In the present work, Pt nanoparticles were deposited by means of microwave synthesis on the primary carbon supported Nb2O5 composite which was prepared in two different ways: (A by dispersion of Nb2O5 and carbon with the mass ratio equal to 1:1 in a 2-propanol solution by ultrasonication for 30 min. with further desiccation of the mixture and (B by heating the Nb2O5/C composite obtained according to the procedure (A at 500 °C for 2 h. The transmission electron microscopy was used to determine the shape and the size of catalyst particles. X-ray diffraction and inductively coupled plasma optical emission spectroscopy were employed to characterize the structure and composition of the synthesized catalysts. The electrocatalytic activity of the synthesized catalysts towards the oxidation of ethanol in an alkaline medium was investigated by means of cyclic voltammetry.DOI: http://dx.doi.org/10.5755/j01.ms.22.2.8609

  1. Anodic oxide growth on Zr in neutral aqueous solution

    Indian Academy of Sciences (India)

    Abstract. Anodization and subsequent cathodic reactions on a thin-film sample of Zr were studied with in-situ neutron reflectometry (NR) and electrochemical impedance spec- troscopy (EIS). The NR results during anodization showed the originally 485 Å thick Zr film generally behaved similar to a bulk electrode in neutral ...

  2. Unique Reduced Graphene Oxide as Efficient Anode Material in Li ...

    Indian Academy of Sciences (India)

    19

    SRGO) was explicated as anode material in ... motivation behind testing SRGO as anode material in LIB is owing to its previously reported characteristics [1-3] like high ... Cycling performance of SRGO is shown in Fig. 2 which clearly indicates that ...

  3. Detection of Chlorine in a Non-aqueous Solution via Anodic Oxidation and a Photochemical Reaction.

    Science.gov (United States)

    Nakagawa, Shogo; Nishimura, Hajime; Kodera, Fumihiro

    2018-01-01

    In this study, we developed a new chlorine gas detection method using anodic oxidation and a photochemical reaction. Chlorine gas was temporarily solvated with an aprotic polar solvent having an extensive potential range in the positive direction, and the solvated chlorine molecule was detected by an anodic oxidation reaction. In addition, when combined with ultraviolet light irradiation, we could detect high sensitivity using the photochemical reaction.

  4. Flux pinning by voids in surface-oxidized superconducting niobium and vanadium

    International Nuclear Information System (INIS)

    Meij, G.P. van der.

    1984-03-01

    The volume pinning force in several niobium and vanadium samples with voids is determined at various temperatures. Reasonable agreement is found with the collective pinning theory of Larkin and Ovchinnikov above the field of maximum pinning, if the flux line lattice is assumed to be amorphous in this region and if the elementary pinning force is calculated from the quasi-classical theory of Thuneberg, Kurkijaervi, and Rainer. Also some history and relaxation effects are studied in an alternating field. A qualitative explanation is given in terms of flux line dislocations, which reduce the shear strength of the flux line lattice. (Auth.)

  5. Flux pinning by voids in surface-oxidized superconducting niobium and vanadium

    International Nuclear Information System (INIS)

    Meij, G.P. van der.

    1984-01-01

    This thesis describes a study of flux pinning by small voids (roughly 10 nm) in the type II superconductors niobium and vanadium. These voids were created in rectangular foils (with typical dimensions of 30x3x0.2 mm) during an irradiation with fast neutrons in the High Flux Reactor at Petten at temperatures between 400 and 1000 0 C. The pinning force per unit volume is determined from the magnetic properties of the superconducting samples. The experiments were carried out in a slowly ramped magnetic field, as well as in a combination of a static and a much smaller alternating field. (Auth.)

  6. Conversion Reaction-Based Oxide Nanomaterials for Lithium Ion Battery Anodes.

    Science.gov (United States)

    Yu, Seung-Ho; Lee, Soo Hong; Lee, Dong Jun; Sung, Yung-Eun; Hyeon, Taeghwan

    2016-04-27

    Developing high-energy-density electrodes for lithium ion batteries (LIBs) is of primary importance to meet the challenges in electronics and automobile industries in the near future. Conversion reaction-based transition metal oxides are attractive candidates for LIB anodes because of their high theoretical capacities. This review summarizes recent advances on the development of nanostructured transition metal oxides for use in lithium ion battery anodes based on conversion reactions. The oxide materials covered in this review include oxides of iron, manganese, cobalt, copper, nickel, molybdenum, zinc, ruthenium, chromium, and tungsten, and mixed metal oxides. Various kinds of nanostructured materials including nanowires, nanosheets, hollow structures, porous structures, and oxide/carbon nanocomposites are discussed in terms of their LIB anode applications. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Enhanced electrical power generation using flame-oxidized stainless steel anode in microbial fuel cells and the anodic community structure.

    Science.gov (United States)

    Yamashita, Takahiro; Ishida, Mitsuyoshi; Asakawa, Shiho; Kanamori, Hiroyuki; Sasaki, Harumi; Ogino, Akifumi; Katayose, Yuichi; Hatta, Tamao; Yokoyama, Hiroshi

    2016-01-01

    Carbon-based materials are commonly used as anodes in microbial fuel cells (MFCs), whereas metal and metal-oxide-based materials are not used frequently because of low electrical output. Stainless steel is a low-cost material with high conductivity and physical strength. In this study, we investigated the power generation using flame-oxidized (FO) stainless steel anodes (SSAs) in single-chambered air-cathode MFCs. The FO-SSA performance was compared to the performance of untreated SSA and carbon cloth anode (CCA), a common carbonaceous electrode. The difference in the anodic community structures was analyzed using high-throughput sequencing of the V4 region in 16S rRNA gene. Flame oxidation of SSA produced raised node-like sites, predominantly consisting of hematite (Fe2O3), on the surface, as determined by X-ray diffraction spectroscopy. The flame oxidation enhanced the maximum power density (1063 mW/m(2)) in MFCs, which was 184 and 24 % higher than those for untreated SSA and CCA, respectively. The FO-SSA exhibited 8.75 and 2.71 times higher current production than SSA and CCA, respectively, under potentiostatic testing conditions. Bacteria from the genus Geobacter were detected at a remarkably higher frequency in the biofilm formed on the FO-SSA (8.8-9.2 %) than in the biofilms formed on the SSA and CCA (0.7-1.4 %). Bacterial species closely related to Geobacter metallireducens (>99 % identity in the gene sequence) were predominant (93-96 %) among the genus Geobacter in the FO-SSA biofilm, whereas bacteria with a 100 % identity to G. anodireducens were abundant (>55 %) in the SSA and CCA biofilms. This is the first demonstration of power generation using an FO-SSA in MFCs. Flame oxidation of the SSA enhances electricity production in MFCs, which is higher than that with the common carbonaceous electrode, CCA. The FO-SSA is not only inexpensive but also can be prepared using a simple method. To our knowledge, this study reveals, for the first time, that

  8. The initial stages of atomic force microscope based local anodic oxidation of silicon

    Science.gov (United States)

    Kozhukhov, A. S.; Scheglov, D. V.; Fedina, L. I.; Latyshev, A. V.

    2018-02-01

    In this paper, the initial stages of local anodic oxidation (LAO) process initiated by AFM probe are studied on the wide (˜100μm) terraces of the atomic-smooth Si (111) surface when creating dense array of local oxidation points. The dependence of LAO points height on the value of voltage initiating the oxidation is found to have a pronounced step-like feature with a characteristic period of 0.7 ± 0.1 nm. The presented analysis shows for the first time the realization of the step-layer mechanism of anodic oxide growth on the Si (111) surface.

  9. The anodization synthesis of copper oxide nanosheet arrays and their photoelectrochemical properties

    Energy Technology Data Exchange (ETDEWEB)

    Shu, Xia [School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Zheng, Hongmei [School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Key Laboratory of Advanced Functional Materials and Devices of Anhui Province, Hefei 230009 (China); Xu, Guangqing, E-mail: gqxu1979@hfut.edu.cn [School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Key Laboratory of Advanced Functional Materials and Devices of Anhui Province, Hefei 230009 (China); Zhao, Jiebo [School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Cui, Lihua [School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); School of Materials Science and Engineering, Beifang University of Nationalities, Yinchuan 750021 (China); Cui, Jiewu; Qin, Yongqiang; Wang, Yan [School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Zhang, Yong [School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Key Laboratory of Advanced Functional Materials and Devices of Anhui Province, Hefei 230009 (China); Wu, Yucheng, E-mail: ycwu@hfut.edu.cn [School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Key Laboratory of Advanced Functional Materials and Devices of Anhui Province, Hefei 230009 (China)

    2017-08-01

    Graphical abstract: Current-time and potential-time curves of the copper foil anodization process, CV of copper substrate in anodization solution and SEM morphologies of anodization products on Cu substrates obtained at different time. - Highlights: • Copper oxides nanosheet arrays were achieved via anodization method. • The growth mechanisms of the copper anodization process were studied. • Photoelectrochemical performances of copper oxides NSAs were studied. - Abstract: We studied the growth of copper oxide nanosheet arrays on copper foil via a simple anodization method. The structures, morphologies, and elemental compositions of the specimens were characterized with an X-ray diffractometer, scanning electron microscope, high resolution transmission electron microscope, and X-ray photoelectron spectrometer. The copper oxide (Cu{sub 2}O and CuO) nanosheet arrays were comprised of 30-nm-thick nanosheets that stand vertically on the Cu substrate. The anodizing parameters, such as the current density, temperature, and polyethylene glycol concentration, were optimized to obtain the regular nanosheet arrays. The optical absorption properties of the anodized products were evaluated using a diffuse reflectance spectrometer, and broad and strong optical absorption bands arising from the UV to visible region were observed. The photoelectrochemical performance of the nanosheet arrays was measured with chronoamperometry and cyclic voltammetry on an electrochemical workstation equipped with a Xe lamp (wavelength >400 nm). A negative photocurrent was obtained due to the p-type semiconductor of the copper oxides. The copper oxide nanosheet arrays achieve the highest photocurrent of 0.4 mA/cm{sup 2} at the current density of 1.0 A/dm{sup 2}, temperature of 70 °C, and polyethylene glycol concentration of 0.5 g/L.

  10. Other Oxides Pre-removed from Bangka Tin Slag to Produce a High Grade Tantalum and Niobium Oxides Concentrate

    Science.gov (United States)

    Permana, S.; Soedarsono, J. W.; Rustandi, A.; Maksum, A.

    2016-05-01

    Indonesia, as the second largest tin producer in the world, has a byproduct from the production of tin. This byproduct is in the forms of tin slag containing tantalum pentoxide (Ta2O5) and niobium pentoxide (Nb2O5). This study focuses on the recovery of tantalum pentoxide and niobium pentoxide from the tin slag. In the process, one part of the tin slag sample was sieved only (BTS), and the other was roasted at 900°C, water quenched and then sieved (BTS-RQS). Samples BTS and BTS-RQS were characterized by thermo gravimetric analysis (TGA) and X-ray flourence (XRF). One part of BTS-RQS sample was dissolved in hydrofluoric acid (HF) and the other was dissolved in hydrochloric acid (HCl), washed with distilled water, then dissolved into sodium hydroxide (NaOH). Each sample was characterized by using XRF. The BTS sample produced the highest recovery of 0.3807 and 0.6978% for Ta2O5 and Nb2O5, respectively, from the particle size of -1.00+0.71 and a fraction of 47.29%, while BTS-RQS produced the highest recovery of 0.3931 and 0.8994% for Ta2O5 and Nb2O5, respectively, on the particle size of -0.71+0350 and a fraction of 21%. BTS-RQS, dissolved with 8% hydro fluoride acid, yields tantalum pentoxide and niobium pentoxide with a ratio of 2.01 and 2.09, respectively. For the sample BTS-RQS dissolve first with 6M hydrochloric acid, washed with distilled water, then dissolved with sodium hydroxide 10M, the yield ratios are 1.60 and 1.84 for tantalum pentoxide and niobium pentoxide, respectively. In this study, it is found that the dissolution by using hydrofluoric acid 8% yields the best ratio.

  11. Corrosion protection of iron using porous anodic oxide/conducting polymer composite coatings.

    Science.gov (United States)

    Konno, Yoshiki; Tsuji, Etsushi; Aoki, Yoshitaka; Ohtsuka, Toshiaki; Habazaki, Hiroki

    2015-01-01

    Conducting polymers (CPs), including polypyrrole, have attracted attention for their potential in the protection of metals against corrosion; however, CP coatings have the limitation of poor adhesion to metal substrates. In this study, a composite coating, comprising a self-organized porous anodic oxide layer and a polypyrrole layer, has been developed on iron. Because of electropolymerization in the pores of the anodic oxide layer, the composite coating showed improved adhesion to the substrate along with prolonged corrosion protection in a NaCl aqueous corrosive environment. The anodic oxide layers are formed in a fluoride-containing organic electrolyte and contain a large amount of fluoride species. The removal of these fluoride species from the oxide layer and the metal/oxide interface region is crucial for improving the corrosion protection.

  12. Effects of the Molybdenum Oxide/Metal Anode Interfaces on Inverted Polymer Solar Cells

    International Nuclear Information System (INIS)

    Wu Jiang; Guo Xiao-Yang; Xie Zhi-Yuan

    2012-01-01

    Inverted polymer solar cells with molybdenum oxide (MoO 3 ) as an anode buffer layer and different metals (Al or Ag) as anodes are studied. It is found that the inverted cell with a top Ag anode demonstrates enhanced charge collection and higher power conversion efficiency (PCE) compared to the cell with a top Al anode. An 18% increment of PCE is obtained by replacing Al with Ag as the top anode. Further studies show that an interfacial dipole pointing from MoO 3 to Al is formed at MoO 3 /Al interfaces due to electron transfer from Al to MoO 3 while this phenomenon cannot be observed at MoO 3 /Ag interfaces. It is speculated that the electric field at the MoO 3 /Al interface would hinder hole extraction, and hence reduce the short-circuit current

  13. Niobium and tantalum

    Science.gov (United States)

    Schulz, Klaus J.; Piatak, Nadine M.; Papp, John F.; Schulz, Klaus J.; DeYoung,, John H.; Seal, Robert R.; Bradley, Dwight C.

    2017-12-19

    Niobium and tantalum are transition metals that are almost always found together in nature because they have very similar physical and chemical properties. Their properties of hardness, conductivity, and resistance to corrosion largely determine their primary uses today. The leading use of niobium (about 75 percent) is in the production of high-strength steel alloys used in pipelines, transportation infrastructure, and structural applications. Electronic capacitors are the leading use of tantalum for high-end applications, including cell phones, computer hard drives, and such implantable medical devices as pacemakers. Niobium and tantalum are considered critical and strategic metals based on the potential risks to their supply (because current production is restricted to only a few countries) and the significant effects that a restriction in supply would have on the defense, energy, high-tech industrial, and medical sectors.The average abundance of niobium and tantalum in bulk continental crust is relatively low—8.0 parts per million (ppm) niobium and 0.7 ppm tantalum. Their chemical characteristics, such as small ionic size and high electronic field strength, significantly reduce the potential for these elements to substitute for more common elements in rock-forming minerals and make niobium and tantalum essentially immobile in most aqueous solutions. Niobium and tantalum do not occur naturally as pure metals but are concentrated in a variety of relatively rare oxide and hydroxide minerals, as well as in a few rare silicate minerals. Niobium is primarily derived from the complex oxide minerals of the pyrochlore group ((Na,Ca,Ce)2(Nb,Ti,Ta)2(O,OH,F)7), which are found in some alkaline granite-syenite complexes (that is, igneous rocks containing sodium- or potassium-rich minerals and little or no quartz) and carbonatites (that is, igneous rocks that are more than 50 percent composed of primary carbonate minerals, by volume). Tantalum is derived mostly from the

  14. Contrastive study of anodic oxidation on carbon fibers and graphite fibers

    International Nuclear Information System (INIS)

    Liu Xin; Yang Changling; Lu Yonggen

    2012-01-01

    Anodic oxidation of polyacrylonitrile (PAN) graphite fibers was investigated in comparison with that of carbon fibers. The mechanical and interfacial properties of the treated fibers along with their surface structures were studied with X-ray photoelectron spectroscopy, atomic force microscope, contact angle analyzer, tensile strength instrument and Raman spectrometer. The results show that the graphite fibers were inactive during anodic oxidation for the higher graphitic carbon, while the carbon fibers were active and the surface oxygen content got saturated soon. The dynamics of anodic oxidation for the fibers can be described by a homogenous thickness reduction model, which indicated that the kinetic constant of anodic oxidation for the graphite fibers was only one sixth of that for the carbon fibers. Surface roughness contributed to the improvement on fiber/matrix adhesion as well as the surface oxygen content. The achievement of the surface treatment was proved by Raman spectroscopy mapping the stress of the fiber inside an epoxy resin droplet. The increase of interfacial shear strength from the untreated graphite fibers to the anodized graphite fibers was 160% (from 65 to 170 MPa), much higher than 70% that from untreated carbon fibers to the anodized ones (from 135 to 230 MPa).

  15. Contrastive study of anodic oxidation on carbon fibers and graphite fibers

    Science.gov (United States)

    Liu, Xin; Yang, Changling; Lu, Yonggen

    2012-03-01

    Anodic oxidation of polyacrylonitrile (PAN) graphite fibers was investigated in comparison with that of carbon fibers. The mechanical and interfacial properties of the treated fibers along with their surface structures were studied with X-ray photoelectron spectroscopy, atomic force microscope, contact angle analyzer, tensile strength instrument and Raman spectrometer. The results show that the graphite fibers were inactive during anodic oxidation for the higher graphitic carbon, while the carbon fibers were active and the surface oxygen content got saturated soon. The dynamics of anodic oxidation for the fibers can be described by a homogenous thickness reduction model, which indicated that the kinetic constant of anodic oxidation for the graphite fibers was only one sixth of that for the carbon fibers. Surface roughness contributed to the improvement on fiber/matrix adhesion as well as the surface oxygen content. The achievement of the surface treatment was proved by Raman spectroscopy mapping the stress of the fiber inside an epoxy resin droplet. The increase of interfacial shear strength from the untreated graphite fibers to the anodized graphite fibers was 160% (from 65 to 170 MPa), much higher than 70% that from untreated carbon fibers to the anodized ones (from 135 to 230 MPa).

  16. Electrophoretic deposition of PTFE particles on porous anodic aluminum oxide film and its tribological properties

    International Nuclear Information System (INIS)

    Zhang, Dongya; Dong, Guangneng; Chen, Yinjuan; Zeng, Qunfeng

    2014-01-01

    Polytetrafluoroethylene (PTFE) composite film was successfully fabricated by depositing PTFE particles into porous anodic aluminum oxide film using electrophoretic deposition (EPD) process. Firstly, porous anodic aluminum oxide film was synthesized by anodic oxidation process in sulphuric acid electrolyte. Then, PTFE particles in suspension were directionally deposited into the porous substrate. Finally, a heat treatment at 300 °C for 1 h was utilized to enhance PTFE particles adhesion to the substrate. The influence of anodic oxidation parameters on the morphology and micro-hardness of the porous anodic aluminum oxide film was studied and the PTFE particles deposited into the pores were authenticated using energy-dispersive spectrometer (EDS) and scanning electron microscopy (SEM). Tribological properties of the PTFE composite film were investigated under dry sliding. The experimental results showed that the composite film exhibit remarkable low friction. The composite film had friction coefficient of 0.20 which deposited in 15% PTFE emulsion at temperature of 15 °C and current density of 3 A/dm 2 for 35 min. In addition, a control specimen of porous anodic aluminum oxide film and the PTFE composite film were carried out under the same test condition, friction coefficient of the PTFE composite film was reduced by 60% comparing with the control specimen at 380 MPa and 100 mm/s. The lubricating mechanism was that PTFE particles embedded in porous anodic aluminum oxide film smeared a transfer film on the sliding path and the micro-pores could support the supplement of solid lubricant during the sliding, which prolonged the lubrication life of the aluminum alloys.

  17. Kinetic investigation of oxygen evolution at titanium-ruthenium oxide anodes. Oxygen evolution kinetics at RuO2 and titaniumruthenium oxide anodes in chloride solutions

    International Nuclear Information System (INIS)

    Kokoulina, D.V.

    1986-01-01

    Oxygen evolution kinetics was studied at 70 degrees C at RuO 2 and titaniumruthenium oxide anodes in chlorinated chloride solutions (1 M NaCl, pH 1.4 to 2.25) by recording polarization curves. The reaction orders were determined. The kinetics of anodic oxygen evolution is important for an understanding of electrode behavior and for an estimate of possible current yields of oxygen under the different conditions of electrolysis of NaCl solutions. The results obtained demonstrate that substantial oxygen evolution can occur in chlorinated chloride solutions at active electrodes because of the coupled reaction of chlorine reduction

  18. An Indium-Free Anode for Large-Area Flexible OLEDs: Defect-Free Transparent Conductive Zinc Tin Oxide

    NARCIS (Netherlands)

    Morales-Masis, M.; Dauzou, F.; Jeangros, Q.; Dabirian, A.; Lifka, H.; Gierth, R.; Ruske, M.; Moet, D.; Hessler-Wyser, A.; Ballif, C.

    2016-01-01

    Flexible large-area organic light-emitting diodes (OLEDs) require highly conductive and transparent anodes for efficient and uniform light emission. Tin-doped indium oxide (ITO) is the standard anode in industry. However, due to the scarcity of indium, alternative anodes that eliminate its use are

  19. The simulation of the temperature effects on the microhardness of anodic alumina oxide layers

    Directory of Open Access Journals (Sweden)

    M. Gombár

    2014-01-01

    Full Text Available In order to improve the mechanical properties of the layer deposited by anodic oxidation of aluminum on the material EN AW-1050 H24, in the contribution was investigated the microhardness of the deposited layer as a function of the physic-chemical factors affecting in the process of anodic oxidation at the constant anodic current density J = 3 A.dm-2 in electrolyte formed by sulfuric acid and oxalic acid, with the emphasis on the influence of electrolyte temperature in the range – 1,78 °C to 45,78 °C. The model of the studied dependence was compiled based on mathematical and statistical analysis of matrix from experimental obtained data from composite rotation plan of experiment with five independent variable factors (amount of sulfuric acid in the electrolyte, the amount of oxalic acid in the electrolyte, electrolyte, anodizing time and applied voltage.

  20. Friction stir processed Al - Metal oxide surface composites: Anodization and optical appearance

    DEFF Research Database (Denmark)

    Gudla, Visweswara Chakravarthy; Jensen, Flemming; Canulescu, Stela

    2014-01-01

    Multiple-pass friction stir processing (FSP) was employed to impregnate metal oxide (TiO2, Y2O3 and CeO2) particles into the surface of an Aluminium alloy. The surface composites were then anodized in a sulphuric acid electrolyte. The effect of anodizing parameters on the resulting optical...... appearance was studied. Microstructural and morphological characterization was performed using transmission electron microscopy (TEM). The surface appearance was analysed using an integrating sphere-spectrometer setup. Increasing the anodizing voltage changed the surface appearance of the composites from...

  1. The electrochemical oxidation of H{sub 2} and CO at patterned Ni anodes of SOFCs

    Energy Technology Data Exchange (ETDEWEB)

    Utz, Annika

    2011-07-01

    In this work, a deeper understanding of the electrochemical oxidation at SOFC anodes was gained by the experimental characterization of patterned Ni anodes in H{sub 2}-H{sub 2}O and CO-CO{sub 2} atmosphere. By high resolution data analysis, the Line Specific Resistance attributed to charge transfer and its dependencies on gas composition, temperature and polarization voltage were identified. Furthermore, the comparison of the performance of patterned and cermet anodes was enabled using a transmission line model. (orig.)

  2. Biocatalytic anode for glucose oxidation utilizing carbon nanotubes for direct electron transfer with glucose oxidase

    Energy Technology Data Exchange (ETDEWEB)

    Vaze, Abhay; Hussain, Nighat; Tang, Chi [Department of Chemistry, University of Connecticut, Storrs, CT 06269-3060 (United States); Leech, Donal [School of Chemistry, National University of Ireland, Galway (Ireland); Rusling, James [Department of Chemistry, University of Connecticut, Storrs, CT 06269-3060 (United States); Department of Cell Biology, University of Connecticut Health Center, Farmington, CT 06032 (United States); School of Chemistry, National University of Ireland, Galway (Ireland)

    2009-10-15

    Covalently linked layers of glucose oxidase, single-wall carbon nanotubes and poly-L-lysine on pyrolytic graphite resulted in a stable biofuel cell anode featuring direct electron transfer from the enzyme. Catalytic response observed upon addition of glucose was due to electrochemical oxidation of FADH{sub 2} under aerobic conditions. The electrode potential depended on glucose concentration. This system has essential attributes of an anode in a mediator-free biocatalytic fuel cell. (author)

  3. Highly durable anode supported solid oxide fuel cell with an infiltrated cathode

    DEFF Research Database (Denmark)

    Samson, Alfred Junio; Hjalmarsson, Per; Søgaard, Martin

    2012-01-01

    An anode supported solid oxide fuel cell with an La0.6Sr0.4Co1.05O3_δ (LSC) infiltrated-Ce0.9Gd0.1O1.95 (CGO) cathode that shows a stable performance has been developed. The cathode was prepared by screen printing a porous CGO backbone on top of a laminated and co-fired anode supported half cell...

  4. Development and Testing of High Surface Area Iridium Anodes for Molten Oxide Electrolysis

    Science.gov (United States)

    Shchetkovskiy, Anatoliy; McKechnie, Timothy; Sadoway, Donald R.; Paramore, James; Melendez, Orlando; Curreri, Peter A.

    2010-01-01

    Processing of lunar regolith into oxygen for habitat and propulsion is needed to support future space missions. Direct electrochemical reduction of molten regolith is an attractive method of processing, because no additional chemical reagents are needed. The electrochemical processing of molten oxides requires high surface area, inert anodes. Such electrodes need to be structurally robust at elevated temperatures (1400-1600?C), be resistant to thermal shock, have good electrical conductivity, be resistant to attack by molten oxide (silicate), be electrochemically stable and support high current density. Iridium with its high melting point, good oxidation resistance, superior high temperature strength and ductility is the most promising candidate for anodes in high temperature electrochemical processes. Several innovative concepts for manufacturing such anodes by electrodeposition of iridium from molten salt electrolyte (EL-Form? process) were evaluated. Iridium electrodeposition to form of complex shape components and coating was investigated. Iridium coated graphite, porous iridium structure and solid iridium anodes were fabricated. Testing of electroformed iridium anodes shows no visible degradation. The result of development, manufacturing and testing of high surface, inert iridium anodes will be presented.

  5. Interaction of Human Osteoblast-Like Saos-2 and MG-63 Cells with Thermally Oxidized Surfaces of a Titanium-Niobium Alloy

    Czech Academy of Sciences Publication Activity Database

    Vandrovcová, Marta; Jirka, Ivan; Novotná, Katarína; Lisá, Věra; Frank, Otakar; Kolská, Z.; Starý, V.; Bačáková, Lucie

    2014-01-01

    Roč. 9, č. 6 (2014), e100475 E-ISSN 1932-6203 R&D Projects: GA ČR(CZ) GAP108/10/1858; GA ČR(CZ) GAP107/12/1025; GA MPO FR-TI3/088 Institutional support: RVO:67985823 ; RVO:61388955 Keywords : thermally oxidized surface * titanium-niobium * TiO2 * osteoblast * macrophage Subject RIV: EI - Biotechnology ; Bionics Impact factor: 3.234, year: 2014

  6. Hydrogen Oxidation Reaction at the Ni/YSZ Anode of Solid Oxide Fuel Cells from First Principles

    Science.gov (United States)

    Cucinotta, Clotilde S.; Bernasconi, Marco; Parrinello, Michele

    2011-11-01

    By means of ab initio simulations we here provide a comprehensive scenario for hydrogen oxidation reactions at the Ni/zirconia anode of solid oxide fuel cells. The simulations have also revealed that in the presence of water chemisorbed at the oxide surface, the active region for H oxidation actually extends beyond the metal/zirconia interface unraveling the role of water partial pressure in the decrease of the polarization resistance observed experimentally.

  7. Experimental study of methane partial oxidation on Ni-YSZ anode of solid oxide fuel cells

    Science.gov (United States)

    Iwai, Hiroshi; Tada, Koshi; Kishimoto, Masashi; Saito, Motohiro; Yoshida, Hideo

    2017-08-01

    The effects of oxygen addition to methane directly supplied to solid oxide fuel cells were investigated. Fundamental experiments were conducted using Ni-YSZ (yttria-stabilized zirconia) cermet as a typical anode material, and Ni-YSZ catalysts having different streamwise lengths were fabricated on YSZ flat plates. A premixed gas of methane, oxygen, nitrogen and steam was supplied to a test catalyst set in a rectangular test channel. The exhaust gas compositions and the surface temperature distributions of the test catalysts were measured. It was found that the oxidation of methane prominently proceeded near the upstream edge of the catalyst followed by steam/dry reforming reactions downstream. This resulted in the formation of a high-temperature region, leading to a large temperature gradient in the streamwise direction.

  8. Air-Impregnated Nanoporous Anodic Aluminum Oxide Layers for Enhancing the Corrosion Resistance of Aluminum.

    Science.gov (United States)

    Jeong, Chanyoung; Lee, Junghoon; Sheppard, Keith; Choi, Chang-Hwan

    2015-10-13

    Nanoporous anodic aluminum oxide layers were fabricated on aluminum substrates with systematically varied pore diameters (20-80 nm) and oxide thicknesses (150-500 nm) by controlling the anodizing voltage and time and subsequent pore-widening process conditions. The porous nanostructures were then coated with a thin (only a couple of nanometers thick) Teflon film to make the surface hydrophobic and trap air in the pores. The corrosion resistance of the aluminum substrate was evaluated by a potentiodynamic polarization measurement in 3.5 wt % NaCl solution (saltwater). Results showed that the hydrophobic nanoporous anodic aluminum oxide layer significantly enhanced the corrosion resistance of the aluminum substrate compared to a hydrophilic oxide layer of the same nanostructures, to bare (nonanodized) aluminum with only a natural oxide layer on top, and to the latter coated with a thin Teflon film. The hydrophobic nanoporous anodic aluminum oxide layer with the largest pore diameter and the thickest oxide layer (i.e., the maximized air fraction) resulted in the best corrosion resistance with a corrosion inhibition efficiency of up to 99% for up to 7 days. The results demonstrate that the air impregnating the hydrophobic nanopores can effectively inhibit the penetration of corrosive media into the pores, leading to a significant improvement in corrosion resistance.

  9. Electrochemical Impedance Modeling of a Solid Oxide Fuel Cell Anode

    DEFF Research Database (Denmark)

    Mohammadi, R.; Søgaard, Martin; Ramos, Tania

    2014-01-01

    A simulation package for the impedance response of SOFC anodes is presented here. The model couples the gas transport in gas channels and within a porous electrode with the electrochemical kinetics. The gas phase mass transport is modeled using mass conservation equations. A transmission line mod...

  10. Optical properties of alumina membranes prepared by anodic oxidation process

    International Nuclear Information System (INIS)

    Li Zhaojian; Huang Kelong

    2007-01-01

    The luminescence property of anodic alumina membranes (AAMs) with ordered nanopore arrays prepared by electrochemically anodizing aluminum in oxalic acid solutions have been investigated. Photoluminescence emission (PL) measurement shows that a blue PL band occurs in the wavelength ranges of 300-600 nm. The PL intensity and peak position of AAMs depend markedly on the excitation wavelength. A new peak located at 518 nm can be observed under a monitoring wavelength at 429 nm in the photoluminescence excitation (PLE) spectra. Convincing evidences have been presented that the PLE would be associated with the residual aluminum ions in the membrane. The PLE and PL of AAMs, as a function of anodizing times, have been discussed. It is found that the oxalic impurities incorporated in the AAMs would have important influences on the optical properties of AAMs in the initial stage of anodization. The PL and PLE spectra obtained show that there are three optical centers, of which the first is originated from the F + centers in AAMs, the second is correlated with the oxalic impurities incorporated in the AAMs, and the third is associated with the excess aluminum ions in the membrane

  11. XPS characterization of the anodic oxide film formed on uranium metal in sodium hydroxide solution

    International Nuclear Information System (INIS)

    Fu Xiaoguo; Wang Xiaolin; Guo Huanjun; Wang Qingfu; Zhao Zhengping; Zhong Yongqiang

    2002-01-01

    X-ray photoelectron spectroscopy (XPS) is used to examine the anodic oxide film formed on uranium metal in 0.8 mol/L NaOH solution. The U4f 7/2 fitting spectra suggests that the anodic oxide film is composed of uranium trioxide and a small amount of UO 2+x . Under UHV condition, the U4f peak shifts to the lower binding energy, while a gradual increase in the intensity of U5f peak and the broad of U4f peak are also observed. All of these changes are due to reduction of uranium trioxide in the anodic oxide film. XPS quantitative analysis confirms the occurrence of reduction reaction

  12. A novel Ni/ceria-based anode for metal-supported solid oxide fuel cells

    Science.gov (United States)

    Rojek-Wöckner, Veronika A.; Opitz, Alexander K.; Brandner, Marco; Mathé, Jörg; Bram, Martin

    2016-10-01

    For optimization of ageing behavior, electrochemical performance, and sulfur tolerance of metal-supported solid oxide fuel cells a new anode concept is introduced, which is based on a Ni/GDC cermet replacing the established Ni/YSZ anodes. In the present work optimized processing parameters compatible with MSC substrates are specified by doing sintering studies on pressed bulk specimen and on real porous anode structures. The electrochemical performance of the Ni/GDC anodes was characterized by means of symmetrical electrolyte supported model-type cells. In this study, three main objectives are pursued. Firstly, the effective technical realization of the Ni/GDC concept is demonstrated. Secondly, the electrochemical behavior of Ni/GDC porous anodes is characterized by impedance spectroscopy and compared with the current standard Ni/YSZ anode. Further, a qualitative comparison of the sulfur poisoning behavior of both anode types is presented. Thirdly, preliminary results of a successful implementation of the Ni/GDC cermet into a metal-supported single cell are presented.

  13. Synergism between anodic oxidation with diamond anodes and heterogeneous catalytic photolysis for the treatment of pharmaceutical pollutants

    Directory of Open Access Journals (Sweden)

    Juan M. Peralta-Hernández

    2016-03-01

    Full Text Available The mineralization of diclofenac and acetaminophen has been studied by single anodic oxidation with boron-doped diamond (AO-BDD using an undivided electrolysis cell, by single heterogeneous catalytic photolysis with titanium dioxide (HCP-TiO2 and by the combination of both advanced oxidation processes. The results show that mineralization can be obtained with either single technology. The type of functional groups of the pollutant does not influence the results of the single AO-BDD process, but it has a significant influence on the results obtained with HCP-TiO2. A clear synergistic effect appears when both processes are combined showing improvements in the oxidation rate of more than 50% for diclofenac and nearly 200% for acetaminophen at the highest current exerted. Results obtained are explained in terms of the production of oxidants on the surface of BDD (primarily peroxodisulfate and the later homogeneous catalytic light decomposition of these oxidants in the bulk. This mechanism is consistent with the larger improvement observed at higher current densities, for which the production of oxidants is promoted.

  14. A low-energy ion scattering (LEIS) study of the influence of the vanadium concentration on the activity of vanadium-niobium oxide catalysts for the oxidative dehydrogenation of propane

    NARCIS (Netherlands)

    Smits, R.H.H.; Smits, R.H.H.; Seshan, Kulathuiyer; Ross, J.R.H.; Ross, J.R.H.; van den Oetelaar, L.C.A.; Helwegen, J.H.J.M.; Anantharaman, M.R.; Brongersma, H.H.

    1995-01-01

    A series of vanadium-niobium oxide catalysts in which the vanadia content varies between 0.3 and 18 mol% was prepared by coprecipitation. These catalysts were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), low-energy ion scattering (LEIS), and by catalytic testing

  15. Coulometric titration of niobium in 1F sulfuric acid

    International Nuclear Information System (INIS)

    Pannu, S.S.

    1975-01-01

    A coulometric titration at constant current has been devised for Nb in 1F sulfuric acid. The titration was based on the oxidation of Nb(III) to Nb(V) by Fe(III) electrogenerated at a graphite anode. Both potentiometric and amperometric end points were used. The Nb(V) was prior reduced at a mercury cathode by exhaustive electrolysis at a current density of 15 ma/mc 2 for at least 10 hr. Ta,V,Ti and a working platinum anode interfered, but the separation of the potentials of Nb(V)/Nb(III) and Ti(IV)/Ti(III) permitted the titration of first Nb and then Ti. The average error for the titration of 0.30 to 13.00 mg of niobium in 100 ml of 1F sulfuric acid was + 0.57%. (author)

  16. Upgrading tantalum and niobium oxides content in Bangka tin slag with double leaching

    Science.gov (United States)

    Soedarsono, J. W.; Permana, S.; Hutauruk, J. K.; Adhyputra, R.; Rustandi, A.; Maksum, A.; Widana, K. S.; Trinopiawan, K.; Anggraini, M.

    2018-03-01

    Tantalum has become one of the 14 types of critical materials where the level of its availability is assumed as the midterm critical metal. Benefits of the element tantalum in the electronics field increased the deficit balance of supply / demand, as more variations of electronic products developed. The tantalum experts calculated the level of availability until 2020. Base on the previous studies, tin slag is a secondary source of tantalum and niobium. This study uses tin slag from Bangka, Indonesia, abbreviated, Bangka Tin Slag (BTS). BTS was roasted, water quenched and sieved, abbreviated BTS-RQS.BTS was roasted, water quenched and sieved, abbreviated BTS-RQS.BTS-RQS was roasted at a temperature 700□C given sample code BTS-R700QS, while roasted at 800°C given sample code BTS-R800QS.A variable leaching experiment on BTS-R700QS was solvent concentration variable and on BTS-R800QS was time variable. The entire residue was characterized by X-Ray Fluorescence (XRF), and the optimum results are on the BTS-R800QS leaching into 5 M NaOH for 20 min followed by 5M HCl for 50 min, with content of Ta2O5 and Nb2O51.56% and 1.11%, respectively. The result of XRF measurement showed was the increasing of TNO content due to the increasing solvent concentration and time of acid leaching. The discussion of thermodynamics this study used was HSC Chemistry 6 as a supporting data.

  17. Chemical characterization and bioactivity of epoxy resin and Portland cement-based sealers with niobium and zirconium oxide radiopacifiers.

    Science.gov (United States)

    Viapiana, Raqueli; Guerreiro-Tanomaru, Juliane Maria; Hungaro-Duarte, Marco Antonio; Tanomaru-Filho, Mário; Camilleri, Josette

    2014-09-01

    The purpose of this study was to characterize and to evaluate the bioactivity potential of experimental root canal sealers (ES) based on Portland cement, epoxy resin with nano- and micro-particles of niobium or zirconium oxide used as radiopacifiers in comparison to AH Plus and MTA Fillapex. Specimens of the sealers (10 mm in diameter×1 mm thick) were prepared and the radiopacity was evaluated according to ISO 6876 (2012) specifications. Characterization of the sealers was performed under the scanning electron microscope (SEM) immediately after setting and after immersion for 28 days in Hank's balanced salt solution (HBSS). In addition X-ray energy dispersive spectroscopy (EDS), X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) spectroscopy were also performed. The pH and calcium ion release were measured after 1, 7, 14, 21 and 28 days after completion of seating using a digital pH meter and an atomic absorption spectrophotometer, respectively. The experimental sealers exhibited an average radiopacity of 2.5 mm thickness of aluminum, which was similar to MTA Fillapex (P>0.05) and inferior to AH Plus (Pepoxy resin and radiopacifier exhibited a degree of bioactivity although no evidence of cement hydration was demonstrated on material characterization. The radiopacifier particle size had limited effect on the sealer microstructure and chemical properties. Copyright © 2014 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  18. Influence of the anode materials on the electrochemical oxidation efficiency.Aplication to oxidative degradation of the pharmaceutical amoxicillin

    OpenAIRE

    Rodrigo Rodrigo, Manuel Andrés; Sopaj, Flamur; Oturan, Nihal; Podvorica, Fetah I.; Pinson, Jean; Oturan, Mehmet

    2015-01-01

    In this study, the electro-oxidation capacities of several electrode materials such as carbon-felt, carbon-fiber, carbon-graphite, platinum, lead dioxide, DSA (Dimensionally Stable Anode), (Ti/RuO2-IrO2), and BDD (Boron-Doped Diamond) were tested for the destruction of the antibiotic amoxicillin (AMX) in aqueous medium. BDD anode was more efficient than DSA to oxidize and mineralize totally AMX in water. Moreover, for BDD electrode we obtained very high electrolysis efficiency for the initial...

  19. Acid blue 29 decolorization and mineralization by anodic oxidation with a cold gas spray synthesized Sn-Cu-Sb alloy anode.

    Science.gov (United States)

    do Vale-Júnior, Edilson; Dosta, Sergi; Cano, Irene Garcia; Guilemany, Josep Maria; Garcia-Segura, Sergi; Martínez-Huitle, Carlos Alberto

    2016-04-01

    The elevated cost of anodic materials used in the anodic oxidation for water treatment of effluents undermines the real application of these technologies. The study of novel alternative materials more affordable is required. In this work, we report the application of Sn-Cu-Sb alloys as cheap anodic material to decolorize azo dye Acid Blue 29 solutions. These anodes have been synthesized by cold gas spray technologies. Almost complete decolorization and COD abatement were attained after 300 and 600 min of electrochemical treatment, respectively. The influence of several variables such as supporting electrolyte, pH, current density and initial pollutant concentration has been investigated. Furthermore, the release and evolution of by-products was followed by HPLC to better understand the oxidative power of Sn-Cu-Sb electrodes. Copyright © 2016 Elsevier Ltd. All rights reserved.

  20. A Review of RedOx Cycling of Solid Oxide Fuel Cells Anode

    Science.gov (United States)

    Faes, Antonin; Hessler-Wyser, Aïcha; Zryd, Amédée; Van Herle, Jan

    2012-01-01

    Solid oxide fuel cells are able to convert fuels, including hydrocarbons, to electricity with an unbeatable efficiency even for small systems. One of the main limitations for long-term utilization is the reduction-oxidation cycling (RedOx cycles) of the nickel-based anodes. This paper will review the effects and parameters influencing RedOx cycles of the Ni-ceramic anode. Second, solutions for RedOx instability are reviewed in the patent and open scientific literature. The solutions are described from the point of view of the system, stack design, cell design, new materials and microstructure optimization. Finally, a brief synthesis on RedOx cycling of Ni-based anode supports for standard and optimized microstructures is depicted. PMID:24958298

  1. A Review of RedOx Cycling of Solid Oxide Fuel Cells Anode

    Directory of Open Access Journals (Sweden)

    Jan Van herle

    2012-08-01

    Full Text Available Solid oxide fuel cells are able to convert fuels, including hydrocarbons, to electricity with an unbeatable efficiency even for small systems. One of the main limitations for long-term utilization is the reduction-oxidation cycling (RedOx cycles of the nickel-based anodes. This paper will review the effects and parameters influencing RedOx cycles of the Ni-ceramic anode. Second, solutions for RedOx instability are reviewed in the patent and open scientific literature. The solutions are described from the point of view of the system, stack design, cell design, new materials and microstructure optimization. Finally, a brief synthesis on RedOx cycling of Ni-based anode supports for standard and optimized microstructures is depicted.

  2. Preparation and Evaluation of Multi-Layer Anodes of Solid Oxide Fuel Cell

    Science.gov (United States)

    Santiago, Diana; Farmer, Serene C.; Setlock, John A.

    2012-01-01

    The development of an energy device with abundant energy generation, ultra-high specific power density, high stability and long life is critical for enabling longer missions and for reducing mission costs. Of all different types of fuel cells, the solid oxide fuel cells (SOFC) is a promising high temperature device that can generate electricity as a byproduct of a chemical reaction in a clean way and produce high quality heat that can be used for other purposes. For aerospace applications, a power-to-weight of (is) greater than 1.0 kW/kg is required. NASA has a patented fuel cell technology under development, capable of achieving the 1.0 kW/kg figure of merit. The first step toward achieving these goals is increasing anode durability. The catalyst plays an important role in the fuel cells for power generation, stability, efficiency and long life. Not only the anode composition, but its preparation and reduction are key to achieving better cell performance. In this research, multi-layer anodes were prepared varying the chemistry of each layer to optimize the performance of the cells. Microstructure analyses were done to the new anodes before and after fuel cell operation. The cells' durability and performance were evaluated in 200 hrs life tests in hydrogen at 850 C. The chemistry of the standard nickel anode was modified successfully reducing the anode degradation from 40% to 8.4% in 1000 hrs and retaining its microstructure.

  3. Effect of Graphene-Graphene Oxide Modified Anode on the Performance of Microbial Fuel Cell

    Science.gov (United States)

    Yang, Na; Ren, Yueping; Li, Xiufen; Wang, Xinhua

    2016-01-01

    The inferior hydrophilicity of graphene is an adverse factor to the performance of the graphene modified anodes (G anodes) in microbial fuel cells (MFCs). In this paper, different amounts of hydrophilic graphene oxide (GO) were doped into the modification layers to elevate the hydrophilicity of the G anodes so as to further improve their performance. Increasing the GO doped ratio from 0.15 mg·mg−1 to 0.2 mg·mg−1 and 0.25 mg·mg−1, the static water contact angle (θc) of the G-GO anodes decreased from 74.2 ± 0.52° to 64.6 ± 2.75° and 41.7 ± 3.69°, respectively. The G-GO0.2 anode with GO doped ratio of 0.2 mg·mg−1 exhibited the optimal performance and the maximum power density (Pmax) of the corresponding MFC was 1100.18 mW·m−2, 1.51 times higher than that of the MFC with the G anode. PMID:28335302

  4. Anodic oxidation of chloride ions in 1-butyl-3-methyl-limidazolium tetrafluoroborate ionic liquid

    International Nuclear Information System (INIS)

    Zhang, Qibo; Hua, Yixin; Wang, Rui

    2013-01-01

    Highlights: • The anodic oxidation of Cl − in BMIMBF 4 is electrochemically irreversible with diffusion controlled. • The oxidation of Cl − in BMIMBF 4 is more likely to form tri-chloride ion, Cl 3 − but not chlorine, Cl 2 . • The minute amount of Cl 2 detected after electrolysis forms according to the equilibrium of Cl 2 + Cl − ⇌ Cl 3 − . -- Abstract: The oxidation behavior of chloride ions on platinum electrodes was investigated in a natural ionic liquid, 1-butyl-3-methyl-limidazolium tetrafluoroborate (BMIMBF 4 ) in the presence of high concentrations of 1-butyl-3-methyl-limidazolium chloride (BMIMCl). Analysis of the electrode reaction was explored using cyclic voltammetry, and chronoamperometry with a platinum micro-disk electrode, and bulk potentiostatic electrolysis and UV–vis spectroscopy. The anodic oxidation of chloride ions on the platinum micro-disk electrode in the mixture was considered to be an irreversible process with diffusion controlled as revealed by cyclic voltammetry. The diffusion coefficient, D, and the number of electrons transferred, n, for anodic oxidation of Cl − in BMIMBF 4 derived from results of chronoamperometry revealed that the oxidation of chloride ions was more likely to form tri-chloride ion, Cl 3 − but not chlorine, Cl 2 . Bulk electrolysis and UV–vis spectroscopy further confirmed that the tri-chloride ion was the main product from the overall oxidation of the chloride ion

  5. Unique reduced graphene oxide as efficient anode material in Li ion ...

    Indian Academy of Sciences (India)

    2018-03-29

    Mar 29, 2018 ... https://doi.org/10.1007/s12034-018-1575-5. Unique reduced graphene oxide as efficient anode material in Li ion battery. SAMPATH KUMAR PUTTAPATI1, VENKATARAMANA GEDELA1,. VADALI V S S SRIKANTH1,∗. , M V REDDY2,3, STEFAN ADAMS3 and B V R CHOWDARI2. 1School of Engineering ...

  6. Physical Properties of Mixed Conductor Solid Oxide Fuel Cell Anodes of Doped CeO2

    DEFF Research Database (Denmark)

    Mogensen, Mogens Bjerg; Lindegaard, Thomas; Hansen, Uffe Rud

    1994-01-01

    conductivity vs. oxygen partial pressure. For both typesof conductivity a dependence on dopant valency was observed. The electronic conductivity was independent of dopantradius in contrast to the ionic which was highly dependent. These measured physical properties are compared with the idealrequirements...... for solid oxide fuel cell anodes. Not all requirements are fulfilled. Measures to compensate for this arediscussed....

  7. Methane Steam Reforming over an Ni-YSZ Solid Oxide Fuel Cell Anode in Stack Configuration

    DEFF Research Database (Denmark)

    Mogensen, David; Grunwaldt, Jan-Dierk; Hendriksen, Peter Vang

    2014-01-01

    The kinetics of catalytic steam reforming of methane over an Ni-YSZ anode of a solid oxide fuel cell (SOFC) have been investigated with the cell placed in a stack configuration. In order to decrease the degree of conversion, a single cell stack with reduced area was used. Measurements were...

  8. Study of niobium corrosion in alkaline medium

    International Nuclear Information System (INIS)

    Almeida, S.H. de.

    1987-01-01

    A comparative study of niobium electrochemical behaviour in NaOH and KOH solution, with concentrations between 0,5 and 6,1M is presented. The studies were done through electrochemicals assays, consisting in the corrosion potential and anodic and cathodic polarization curves, complemented by loss of mass experiments. The niobium anodic behaviour in alkaline medium is characterized by passivation occurrence, with a stable film formation. The Na oH solution in alkaline medium are more corrosible to niobium than the KOH solution. The loss of mass assays showed that the corrosion velocit is more dependente of hydroxide concentration in KOH medium than the NaOH medium. (C.G.C.) [pt

  9. Influence of Formation Conditions on the Level of Arrays Ordering of Anodic Titanium Oxide Nanotubes

    Science.gov (United States)

    Kondrikov, N. B.; Titov, P. L.; Schegoleva, S. A.; Khorin, M. A.

    Nanotubular titanium oxide coatings with different morphology and dimensional parameters are formed by anodic oxidation under different voltage and time modes in fluorine aqueous-nonaqueous electrolytes containing glycerin as well as several surface-active agents (SAA). Their morphological peculiarities are examined and qualitative and quantitative analysis of obtained types of ordering is carried out, geometric configuration entropy are calculated on the base of analysis SEM images and theory of self-organization.

  10. Properties of anodic oxides grown on a hafnium–tantalum–titanium thin film library

    Directory of Open Access Journals (Sweden)

    Andrei Ionut Mardare

    2014-01-01

    Full Text Available A ternary thin film combinatorial materials library of the valve metal system Hf–Ta–Ti obtained by co-sputtering was studied. The microstructural and crystallographic analysis of the obtained compositions revealed a crystalline and textured surface, with the exception of compositions with Ta concentration above 48 at.% which are amorphous and show a flat surface. Electrochemical anodization of the composition spread thin films was used for analysing the growth of the mixed surface oxides. Oxide formation factors, obtained from the potentiodynamic anodization curves, as well as the dielectric constants and electrical resistances, obtained from electrochemical impedance spectroscopy, were mapped along two dimensions of the library using a scanning droplet cell microscope. The semiconducting properties of the anodic oxides were mapped using Mott–Schottky analysis. The degree of oxide mixing was analysed qualitatively using x-ray photoelectron spectroscopy depth profiling. A quantitative analysis of the surface oxides was performed and correlated to the as-deposited metal thin film compositions. In the concurrent transport of the three metal cations during oxide growth a clear speed order of Ti > Hf > Ta was proven.

  11. The effect of pre-oxidation treatments on the oxidation tolerance of Ni-yttria-stabilized zirconia anodes in solid oxide fuel cells

    Science.gov (United States)

    Young, J. L.; Molero, H.; Birss, V. I.

    2014-12-01

    When a Ni-YSZ (yttria-stabilized zirconia) anode-supported solid oxide fuel cell (SOFC) is exposed to air at high temperatures, the outcome can be catastrophic cell degradation (primarily YSZ electrolyte cracking), resulting from the 70% volume expansion of Ni as it forms NiO. Earlier work showed that the damage is less severe under conditions when no gradient in the NiO content into the Ni-YSZ support layer was allowed to develop during the oxidation process (e.g., oxidation at 600 °C). This was correlated with qualitative scanning electron microscopy observations, showing that NiO particles are ejected out of the Ni-YSZ/air surface. In the present work, XPS analysis confirmed the enrichment of NiO at the outer anode surface, suggesting that it may be possible to pre-oxidize the Ni-YSZ support layer at 600 °C to force some NiO out onto the anode surface and thus enhance cell oxidation tolerance. It is shown here that, following pre-oxidation at 600 °C, the amount of Ni oxidation tolerated prior to electrolyte cracking at 600 °C increased from 75% to 80%. For oxidation at 800 °C, following pre-oxidation at 600 °C, electrolyte cracking was less severe, but cracks still appeared before 50% of the Ni in the anode was oxidized.

  12. Influence of water on the anodic oxidation mechanism of ...

    African Journals Online (AJOL)

    Diethylenetriamine was oxidised in different electrolytes on platinum electrode. In non-aqueous electrolyte, an irreversible oxidation peak characteristic of DETA oxidation appears on the voltammogram followed by a constant current until the higher limit of the sweeping potential domain is attained. The following successive ...

  13. Spectrographic determination of niobium in uranium - niobium alloys

    International Nuclear Information System (INIS)

    Charbel, M.Y.; Lordello, A.R.

    1984-01-01

    A method for the spectrographic determination of niobium in uranium-niobium alloys in the concentration range 1-10% has been developed. The metallic sample is converted to oxide by calcination in a muffle furnace at 800 0 C for two hours. The standards are prepared synthetically by dry-mixing. One part of the sample or standard is added to nineteen parts of graphite powder and the mixture is excited in a DC arc. Hafnium has been used as internal standard. The precision of the method is + - 4.8%. (Author) [pt

  14. Organic photovoltaics using thin gold film as an alternative anode to indium tin oxide

    International Nuclear Information System (INIS)

    Haldar, Amrita; Yambem, Soniya D.; Liao, Kang-Shyang; Alley, Nigel J.; Dillon, Eoghan P.; Barron, Andrew R.; Curran, Seamus A.

    2011-01-01

    Indium Tin Oxide (ITO) is the most commonly used anode as a transparent electrode and more recently as an anode for organic photovoltaics (OPVs). However, there are significant drawbacks in using ITO which include high material costs, mechanical instability including brittleness and poor electrical properties which limit its use in low-cost flexible devices. We present initial results of poly(3-hexylthiophene): phenyl-C 61 -butyric acid methyl ester OPVs showing that an efficiency of 1.9% (short-circuit current 7.01 mA/cm 2 , open-circuit voltage 0.55 V, fill factor 0.49) can be attained using an ultra thin film of gold coated glass as the device anode. The initial I-V characteristics demonstrate that using high work function metals when the thin film is kept ultra thin can be used as a replacement to ITO due to their greater stability and better morphological control.

  15. Three-dimensional reticular tin-manganese oxide composite anode materials for lithium ion batteries

    International Nuclear Information System (INIS)

    Zhu, X.J.; Guo, Z.P.; Zhang, P.; Du, G.D.; Poh, C.K.; Chen, Z.X.; Li, S.; Liu, H.K.

    2010-01-01

    Tin-manganese oxide film with three-dimensional (3D) reticular structure has been prepared by electrostatic spray deposition (ESD). X-ray diffraction (XRD) and transmission electron microscopy (TEM) indicate that the film is amorphous. X-ray-photoemission spectroscopy (XPS) demonstrates that the 3D grid is composed of tin-manganese oxide. As an anode electrode for the lithium ion battery, the tin-manganese oxide film has 1188.3 mAh g -1 of initial discharge capacity and very good capacity retention of 656.2 mAh g -1 up to the 30th cycle. Such a composite film can be used as an anode for lithium ion batteries with higher energy densities.

  16. Formation and characterization of porous SiC by anodic oxidation using potassium persulfate solution

    Science.gov (United States)

    Iwasa, Y.; Kamiyama, S.; Iwaya, M.; Takeuchi, T.; Akasaki, I.

    2018-01-01

    The formation process of porous SiC by anodic oxidation was investigated, aiming at the generation of pure white light with a high color rendering index (CRI) and high luminous efficiency. The efficiency of white light emission from porous SiC and its wavelength are strongly dependent on the porous structure such as the average pore size and porosity. In this study, we examined the structure and optical properties of porous SiC by adding potassium persulfate (K2S2O8) as an oxidant in HF solution to control the porosity of porous SiC formed by anodic oxidation. By increasing the amount of the oxidant, we enhanced the integrated light emission intensity of porous SiC to 81 times that of bulk SiC. Through the study of porous SiC we demonstrated that the peak wavelength of the porous SiC could be controlled from 370 to 500 nm. Porous SiC created by anodic oxidation was thus proven to have great potential for realizing high-CRI white light generation using LEDs.

  17. Study for preparation of nanoporous titania on titanium by anodic oxidation

    International Nuclear Information System (INIS)

    Passos, Alessandra Pires

    2014-01-01

    Currently titanium is the most common material used in dental, orthopedic implants and cardiovascular applications. In the mid 1960s, prof. Braenemark and coworkers developed the concept of osseointegration, meaning the direct structural and functional connection between living bone and the surface of artificial implant. Thus, studies on the modification of the implant surface are widely distributed among them are the acid attack, blasting with particles of titanium oxide or aluminum oxide, coating with bioactive materials such as hydroxyapatite, and the anodic oxidation. The focus of this work was to investigate the treatment of titanium surface by anodic oxidation. The aim was to develop a nanoporous titanium oxide overlay with controlled properties over titanium substrates. Recent results have shown that such surface treatment improves the biological interaction at the interface bone-implant besides protecting the titanium further oxidation and allow a faster osseointegration. The anodizing process was done in the potentiostatic mode, using an electrolyte composed of 1.0 mol/L H 3 PO 4 and HF 0.5% m/I. The investigated process parameters were the electrical potential (Va) and the process time (T). The electric potential was varied from 10 V to 30 V and the process time was defined as 1.0 h, 1.5 h or 2.0 h. The treated Ti samples were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), energy dispersive spectroscopy X-ray (EDS), and X-ray diffraction (XRD). The results showed the formation of nanoporous titanium oxide by anodizing with electric potential (Va) in the range of 20 V to 30 V and process time in the range of 1 to 2 hours. The average pore diameter was in the range 94-128 nm. Samples anodized in electric potential lower than 20 V did not show the formation of the nanoporous surface. In the case of Va above 30 V, it was observed the formation of agglomerates of TiO 2 . The results obtained in this study showed no

  18. Effect of Different Binders on the Electrochemical Performance of Metal Oxide Anode for Lithium-Ion Batteries.

    Science.gov (United States)

    Wang, Rui; Feng, Lili; Yang, Wenrong; Zhang, Yinyin; Zhang, Yanli; Bai, Wei; Liu, Bo; Zhang, Wei; Chuan, Yongming; Zheng, Ziguang; Guan, Hongjin

    2017-10-30

    When testing the electrochemical performance of metal oxide anode for lithium-ion batteries (LIBs), binder played important role on the electrochemical performance. Which binder was more suitable for preparing transition metal oxides anodes of LIBs has not been systematically researched. Herein, five different binders such as polyvinylidene fluoride (PVDF) HSV900, PVDF 301F, PVDF Solvay5130, the mixture of styrene butadiene rubber and sodium carboxymethyl cellulose (SBR+CMC), and polyacrylonitrile (LA133) were studied to make anode electrodes (compared to the full battery). The electrochemical tests show that using SBR+CMC and LA133 binder which use water as solution were significantly better than PVDF. The SBR+CMC binder remarkably improve the bonding capacity, cycle stability, and rate performance of battery anode, and the capacity retention was about 87% after 50th cycle relative to the second cycle. SBR+CMC binder was more suitable for making transition metal oxides anodes of LIBs.

  19. Large Scale Inert Anode for Molten Oxide Electrolysis, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — Molten oxide electrolysis is a demonstrated laboratory-scale process for producing oxygen from the JSC-1a lunar simulant; however, critical subsystems necessary for...

  20. Analysis of peel strength of consisting of an aluminum sheet, anodic aluminum oxide and a copper foil laminate composite

    Science.gov (United States)

    Shin, Hyeong-Won; Lee, Hyo-Soo; Jung, Seung-Boo

    2017-01-01

    Laminate composites consisting of an aluminum sheet, anodic aluminum oxide, and copper foil have been used as heat-spreader materials for high-power light-emitting diodes (LEDs). These composites are comparable to the conventional structure comprising an aluminum sheet, epoxy adhesives, and copper foil. The peel strength between the copper foil and anodic aluminum oxide should be more than 1.0 kgf/cm in order to be applied in high-power LED products. We investigated the effect of the anodic aluminum oxide morphology and heat-treatment conditions on the peel strength of the composites. We formed an anodic aluminum oxide layer on a 99.999% pure aluminum sheet using electrochemical anodization. A Ti/Cu seed layer was formed using the sputtering direct bonding copper process in order to form a copper circuit layer on the anodic aluminum oxide layer by electroplating. The developed heat spreader, composed of an aluminum layer, anodic aluminum oxide, and a copper circuit layer, showed peel strengths ranging from 1.05 to 3.45 kgf/cm, which is very suitable for high-power LED applications.

  1. Performance Factors and Sulfur Tolerance of Metal Supported Solid Oxide Fuel Cells with Nanostructured Ni:GDC Infiltrated Anodes

    DEFF Research Database (Denmark)

    Nielsen, Jimmi; Sudireddy, Bhaskar Reddy; Hagen, Anke

    2016-01-01

    Two metal supported solid oxide fuel cells (active area 16 cm2) with nanostructured Ni:GDC infiltrated anodes, possessing different anode and support microstructures were studied in respect to sulfur tolerance at an operating temperature of 650°C. The studied MS-SOFCs are based on ferretic...

  2. Performance Factors and Sulfur Tolerance of Metal Supported Solid Oxide Fuel Cells with Nanostructured Ni:GDC Infiltrated Anodes

    DEFF Research Database (Denmark)

    Nielsen, Jimmi; Sudireddy, Bhaskar Reddy; Hagen, Anke

    2015-01-01

    Two metal supported solid oxide fuel cells (active area 16 cm2) with nanostructured Ni:GDC infiltrated anodes, but different anode and support microstructures were studied in respect to sulfur tolerance at the aimed operating temperature of 650ºC. The studied MS-SOFCs are based on ferretic...

  3. Invariance of the mobility edge in anodic titanium oxides

    International Nuclear Information System (INIS)

    Tit, N.; Halley, J.W.; Shore, H.B.

    1992-05-01

    We present a theoretical investigation to explain the electronic and optical properties of anodic rutile TiO 2 thin films of different thicknesses (ranging from 5nm to 20nm). There is experimental evidence that the observed gap state at 0.7eV below the edge of conduction-band is due to an oxygen vacancy. For this reason, oxygen vacancies are used as defects in our model. A comparison of the calculated bulk-photoconductivity to photospectroscopy experiment reveals that the films have bulk-like transport properties with a bandgap E g =3.0eV. On the other hand, a fit of the surface density of states to the scanning tunneling microscopy (STM) experiment on the (001) surfaces has suggested a surface defect density of 5% of oxygen vacancies. To resolve this discrepancy, we calculated the dc-conductivity where localization effects are included. Our results show an impurity band formation at about p c =9% of oxygen vacancies. We concluded that the studied films have defect densities below the threshold of impurity band formation. As a consequence the gap states seen in STM are localized (i.e. the oxygen vacancies are playing the role of trapping centers, deep levels) and the mobility edge is invariant. (author). 11 refs, 3 figs

  4. Characterization of Niobium Oxide Films Deposited by High Target Utilization Sputter Sources

    International Nuclear Information System (INIS)

    Chow, R; Ellis, A D; Loomis, G E; Rana, S I

    2007-01-01

    High quality, refractory metal, oxide coatings are required in a variety of applications such as laser optics, micro-electronic insulating layers, nano-device structures, electro-optic multilayers, sensors and corrosion barriers. A common oxide deposition technique is reactive sputtering because the kinetic mechanism vaporizes almost any solid material in vacuum. Also, the sputtered molecules have higher energies than those generated from thermal evaporation, and so the condensates are smoother and denser than those from thermally-evaporated films. In the typical sputtering system, target erosion is a factor that drives machine availability. In some situations such as nano-layered capacitors, where the device's performance characteristics depends on thick layers, target life becomes a limiting factor on the maximizing device functionality. The keen interest to increase target utilization in sputtering has been addressed in a variety of ways such as target geometry, rotating magnets, and/or shaped magnet arrays. Also, a recent sputtering system has been developed that generates a high density plasma, directs the plasma beam towards the target in a uniform fashion, and erodes the target in a uniform fashion. The purpose of this paper is to characterize and compare niobia films deposited by two types of high target utilization sputtering sources, a rotating magnetron and a high density plasma source. The oxide of interest in this study is niobia because of its high refractive index. The quality of the niobia films were characterized spectroscopically in optical transmission, ellipsometrically, and chemical stoichiometry with X-ray photo-electron spectroscopy. The refractive index, extinction coefficients, Cauchy constants were derived from the ellipsometric modeling. The mechanical properties of coating density and stress are also determined

  5. Synthesis of coral-like tantalum oxide films via anodization in mixed organic-inorganic electrolytes.

    Directory of Open Access Journals (Sweden)

    Hongbin Yu

    Full Text Available We report a simple method to fabricate nano-porous tantalum oxide films via anodization with Ta foils as the anode at room temperature. A mixture of ethylene glycol, phosphoric acid, NH4F and H2O was used as the electrolyte where the nano-porous tantalum oxide could be synthesized by anodizing a tantalum foil for 1 h at 20 V in a two-electrode configuration. The as-prepared porous film exhibited a continuous, uniform and coral-like morphology. The diameters of pores ranged from 30 nm to 50 nm. The pores interlaced each other and the depth was about 150 nm. After calcination, the as-synthesized amorphous tantalum oxide could be crystallized to the orthorhombic crystal system. As observed in photocatalytic experiments, the coral-like tantalum oxide exhibited a higher photocatalytic activity for the degradation of phenol than that with a compact surface morphology, and the elimination rate of phenol increased by 66.7%.

  6. The anodization synthesis of copper oxide nanosheet arrays and their photoelectrochemical properties

    Science.gov (United States)

    Shu, Xia; Zheng, Hongmei; Xu, Guangqing; Zhao, Jiebo; Cui, Lihua; Cui, Jiewu; Qin, Yongqiang; Wang, Yan; Zhang, Yong; Wu, Yucheng

    2017-08-01

    We studied the growth of copper oxide nanosheet arrays on copper foil via a simple anodization method. The structures, morphologies, and elemental compositions of the specimens were characterized with an X-ray diffractometer, scanning electron microscope, high resolution transmission electron microscope, and X-ray photoelectron spectrometer. The copper oxide (Cu2O and CuO) nanosheet arrays were comprised of 30-nm-thick nanosheets that stand vertically on the Cu substrate. The anodizing parameters, such as the current density, temperature, and polyethylene glycol concentration, were optimized to obtain the regular nanosheet arrays. The optical absorption properties of the anodized products were evaluated using a diffuse reflectance spectrometer, and broad and strong optical absorption bands arising from the UV to visible region were observed. The photoelectrochemical performance of the nanosheet arrays was measured with chronoamperometry and cyclic voltammetry on an electrochemical workstation equipped with a Xe lamp (wavelength >400 nm). A negative photocurrent was obtained due to the p-type semiconductor of the copper oxides. The copper oxide nanosheet arrays achieve the highest photocurrent of 0.4 mA/cm2 at the current density of 1.0 A/dm2, temperature of 70 °C, and polyethylene glycol concentration of 0.5 g/L.

  7. Treatment of methyl orange dye wastewater by cooperative electrochemical oxidation in anodic-cathodic compartment.

    Science.gov (United States)

    Pang, L; Wang, H; Bian, Z Y

    2013-01-01

    Electrochemical oxidation of methyl orange wastewater was studied using Ti/IrO(2)/RuO(2) anode and a self-made Pd/C O(2)-fed cathode in the divided cell with a terylene diaphragm. The result indicated that the appropriate rate of feeding air improved the methyl orange removal efficiency. The discoloration efficiency of methyl orange in the divided cell increased with increasing current density. The initial pH value had some effect on the discoloration of methyl orange, which became not obvious when the pH ranged from 2 to 10. However, the average removal efficiency of methyl orange wastewater in terms of total organic carbon (TOC) can reach 89.3%. The methyl orange structure had changed in the electrolytic process, and the characteristic absorption peak of methyl orange was about 470 nm. With the extension of electrolysis time, the concentration of methyl orange gradually reduced; wastewater discoloration rate increased gradually. The degradation of methyl orange was assumed to be cooperative oxidation by direct or indirect electrochemical oxidation at the anode and H(2)O(2), ·OH, O(2)(-)· produced by oxygen reduction at the cathode in the divided cell. Therefore, the cooperative electrochemical oxidation of methyl orange wastewater in the anodic-cathodic compartment had better degradation effects.

  8. Anodic Oxidative Modification of Egg White for Heat Treatment.

    Science.gov (United States)

    Takahashi, Masahito; Handa, Akihiro; Yamaguchi, Yusuke; Kodama, Risa; Chiba, Kazuhiro

    2016-08-31

    A new functionalization of egg white was achieved by an electrochemical reaction. The method involves electron transfer from thiol groups of egg white protein to form disulfide bonds. The oxidized egg white produced less hydrogen sulfide during heat treatment; with sufficient application of electricity, almost no hydrogen sulfide was produced. In addition, gels formed by heating electrochemically oxidized egg white exhibited unique properties, such as a lower gelation temperature and a softened texture, presumably due to protein aggregation and electrochemically mediated intramolecular disulfide bond formation.

  9. The iron and cerium oxide influence on the electric conductivity and the corrosion resistance of anodized aluminium

    International Nuclear Information System (INIS)

    Souza, Kellie Provazi de

    2006-01-01

    The influence of different treatments on the aluminum system covered with aluminum oxide is investigated. The aluminum anodization in sulphuric media and in mixed sulphuric and phosphoric media was used to alter the corrosion resistance, thickness, coverage degree and microhardness of the anodic oxide. Iron electrodeposition inside the anodic oxide was used to change its electric conductivity and corrosion resistance. Direct and pulsed current were used for iron electrodeposition and the Fe(SO 4 ) 2 (NH 4 ) 2 .6H 2 O electrolyte composition was changed with the addition of boric and ascorbic acids. To the sealing treatment the CeCl 3 composition was varied. The energy dispersive x-ray (EDS), the x-ray fluorescence spectroscopy (FRX) and the morphologic analysis by scanning electronic microscopy (SEM) allowed to verify that, the pulsed current increase the iron content inside the anodic layer and that the use of the additives inhibits the iron oxidation. The chronopotentiometric curves obtained during iron electrodeposition indicated that the boric and ascorbic acids mixture increased the electrodeposition process efficiency. The electrochemical impedance spectroscopy (EIE), the Vickers (Hv) microhardness measurements and morphologic analysis evidenced that the sealing treatment improves the corrosion resistance of the anodic film modified with iron. The electrical impedance (EI) technique allowed to prove the electric conductivity increase of the anodized aluminum with iron electrodeposited even after the cerium low concentration treatment. Iron nanowires were prepared by using the anodic oxide pores as template. (author)

  10. Structural and optical anisotropy of nanoporous anodic aluminum oxide

    NARCIS (Netherlands)

    Kooij, Ernst S.; Galca, A.C.; Wormeester, Herbert; Poelsema, Bene; Schwarz, James A.; Contescu, Cristian I.; Putyera, Karol

    2004-01-01

    Porous aluminum oxide has stimulated considerable interest as a nanostructural template, primarily because of the self-organized formation of extremely well-aligned cylindrical pores. One of the fascinating aspects is the tunability of the interpore distance and pore diameter by simple variation of

  11. Anodic oxide growth on Zr in neutral aqueous solution

    Indian Academy of Sciences (India)

    The thickened oxide eventually cracked when its thickness reached ∼ 120 Å, causing loss of passivation. ... Canadian Neutron Beam Centre, National Research Council Canada, Chalk River, Ontario, Canada K0J 1J0; Department of Chemistry, The University of Western Ontario, London, Ontario, Canada N6A 5B7 ...

  12. Surface patterned dielectrics by direct writing of anodic oxides using scanning droplet cell microscopy

    International Nuclear Information System (INIS)

    Siket, Christian M.; Mardare, Andrei Ionut; Kaltenbrunner, Martin; Bauer, Siegfried; Hassel, Achim Walter

    2013-01-01

    Highlights: • Scanning droplet cell microscopy was applied for local gate oxide writing. • Sharp lines are obtained at the highest writing speed of 1 mm min −1 . • 13.4 kC cm −3 was found as charge per volume for aluminium oxide. • High field constant of 24 nm V −1 and dielectric constant of 12 were determined for Al 2 O 3 by CV and EIS. -- Abstract: Scanning droplet cell microscopy was used for patterning of anodic oxide lines on the surface of Al thin films by direct writing. The structural modifications of the written oxide lines as a function of the writing speed were studied by analyzing the relative error of the line widths. Sharper lines were obtained for writing speeds faster than 1 mm min −1 . An increase in sharpness was observed for higher writing speeds. A theoretical model based on the Faraday law is proposed to explain the constant anodisation current measured during the writing process and yielded a charge per volume of 13.4 kC cm −3 for Al 2 O 3 . From calculated oxide film thicknesses the high field constant was found to be 24 nm V −1 . Electrochemical impedance spectroscopy revealed an increase of the electrical permittivity up to ε = 12 with the decrease of the writing speed of the oxide line. Writing of anodic oxide lines was proven to be an important step in preparing capacitors and gate dielectrics in plastic electronics

  13. Enhanced electroluminescence from nanoscale silicon p+ -n junctions made with an anodic aluminum oxide pattern.

    Science.gov (United States)

    Hong, T; Chen, T; Ran, G Z; Wen, J; Li, Y Z; Dai, T; Qin, G G

    2010-01-15

    An enhancement of the electroluminescence (EL) from nanoscale silicon p(+)-n junctions made with an anodic aluminum oxide (AAO) pattern was demonstrated. The nanoporous AAO pattern with a pore density of 1.4 x 10(10) cm(-2) and a pore diameter of 50 +/- 10 nm was fabricated by the two-step anodic oxidation method on a n-type silicon wafer. The nanoscale AAO patterned Si p(+)-n junctions achieved an EL enhancement factor up to about 5 compared to the unpatterned Si p(+)-n junctions. The enhancement may originate from a reduction of nonradiative recombination due to partial passivation of the Si surface by the AAO pattern and improvement of the light extraction due to surface nanotextures.

  14. NANOSTRUCTURED METAL OXIDES FOR ANODES OF LI-ION RECHARGEABLE BATTERIES

    Energy Technology Data Exchange (ETDEWEB)

    Au, M.

    2009-12-04

    The aligned nanorods of Co{sub 3}O{sub 4} and nanoporous hollow spheres (NHS) of SnO{sub 2} and Mn{sub 2}O{sub 3} were investigated as the anodes for Li-ion rechargeable batteries. The Co{sub 3}O{sub 4} nanorods demonstrated 1433 mAh/g reversible capacity. The NHS of SnO{sub 2} and Mn{sub 2}O{sub 3} delivered 400 mAh/g and 250 mAh/g capacities respectively in multiple galvonastatic discharge-charge cycles. It was found that high capacity of NHS of metal oxides is sustainable attributed to their unique structure that maintains material integrity during cycling. The nanostructured metal oxides exhibit great potential as the new anode materials for Li-ion rechargeable batteries with high energy density, low cost and inherent safety.

  15. A Review on Anodic Aluminum Oxide Methods for Fabrication of Nanostructures for Organic Solar Cells

    DEFF Research Database (Denmark)

    Goszczak, Arkadiusz Jaroslaw; Cielecki, Pawel Piotr

    2018-01-01

    , low fabrication cost and easy control over its nano-scale morphology, make AAO patterning methods an intriguing candidate for nanopatterning. Hence, in this work, we present a review on the fabrication techniques and on nanostructures from Anodic Aluminum Oxide (AAO) for OSC applications....... The versatility of such patterning technique is shown by pointing out the possibility of using an AAO template for the fabrication of nanowires by wetting, nanodots by evaporation, nanostructures by imprinting resists, organic layers and much more....

  16. Electrochemical treatment of pharmaceutical wastewater by combining anodic oxidation with ozonation.

    Science.gov (United States)

    Menapace, Hannes M; Diaz, Nicolas; Weiss, Stefan

    2008-07-01

    Wastewater effluents from sewage treatment plants (STP) are important point sources for residues of pharmaceuticals and complexing agents in the aquatic environment. For this reason a research project, which started in December 2006, was established to eliminate pharmaceutical substances and complexing agents found in wastewater as micropollutants. For the treatment process a combination of anodic oxidation by boron-doped diamond (BDD) electrodes and ozonation is examined and presented. For the ozone production a non-conventional, separate reactor was used, in which ozone was generated by electrolysis with diamond electrodes For the determination of the achievable remediation rates four complexing agents (e.g., EDTA, NTA) and eight pharmaceutical substances (e.g., diazepam, carbamazepin) were analyzed in several test runs under different conditions (varied flux, varied current density for the diamond electrode and the ozone producing electrode of the ozone generator, different packing materials for the column in the ozone injection system). The flowrates of the treated water samples were varied from 3 L/h up to 26 L/h. For the anodic oxidation the influence of the current density was examined in the range between 22.7 and 45.5 mA/cm(2), for the ozone producing reactor two densities (1.8 a/cm(2) and 2.0 A/cm(2)) were tested. Matrix effects were investigated by test runs with samples from the effluent of an STP and synthetic waste water. Therefore the impact of the organic material in the samples could be determined by the comparison of the redox potential and the achievable elimination rates of the investigated substances. Comparing both technologies anodic oxidation seems to be superior to ozonation in each investigated area. With the used technology of anodic oxidation elimination rates up to 99% were reached for the investigated pharmaceutical substances at a current density of 45.5 mA/cm(2) and a maximum sample flux of 26 L/h.

  17. Retarding of electrochemical oxidation of formate on the platinum anode by a coat of Nafion membrane

    Science.gov (United States)

    Zhang, Rui; Lv, Weixin; Li, Guanghua; Mezaal, Mohammed Adnan; Li, Xiaojing; Lei, Lixu

    2014-12-01

    It has been found that the faradaic efficiency is decreasing with the electrolysis time for electrochemical reduction of CO2 to formate on a Sn cathode with a Pt anode in an undivided electrolytic cell, because the oxidation of formed formate takes place on the Pt anode, which also limits seriously the highest concentration of formate in the system. Here, we report that a coat of Nafion membrane on the Pt anode can retard the oxidation of formate: even if the concentration of the formate in the electrolyte reaches to 0.12 mol L-1, the faradaic efficiency still maintains above 61.3%; in contrast, the oxidation reaction of the formate on the naked Pt electrode is very fast, when the concentration of the formate in the electrolyte reaches to 0.023 mol L-1, the faradaic efficiency decreases to 35.3%. This is very important because the separation of formic acid could not be economical when its concentration is not high enough, and it is also costly if the depleted solution allows too less of its concentration because the solution has to be reused in the electrochemical process.

  18. The effects of phosphorus implantation on the anodic oxidation of silicon

    International Nuclear Information System (INIS)

    Kisielewicz, M.

    1985-01-01

    The effect of phosphorus implantation on the anodic oxidation-rate of p-type silicon (the enhancement oxidation-rate) has been studied for a wide range of energies, doses, dose rates and anneal conditions. The procedure use in the work, i.e. step by step formation of thin films of silicon oxide by anodic oxidation of ion-implanted wafer and subsequent removal of the film by an etch with dilute hydrofluoric acid, gave information about the depth distribution of the oxide growth rate as a function of implant and anneal conditions. By means of comparison of the OGR profiles with those for ion and damage predicted theoretically, the effect of the high concentration of implanted atoms (for considerably high-dose implants) has been separated from the effect of enhanced oxidation-rate due to void agglomerates (at low and moderately low dose implants). The data for P-implanted Si is discussed together with results for N, Ne, Si, Ar, As, Kr, Xe and Au-implanted silicon. (author)

  19. A modified anode/electrolyte structure for a solid oxide electrochemical cell and a method for making said structure

    DEFF Research Database (Denmark)

    2013-01-01

    A novel modified anode/electrolyte structure for a solid oxide electrochemical cell is an assembly comprising (a) an anode consisting of a backbone of electronically conductive perovskite oxides selected from the group of doped strontium titanates and mixtures thereof, (b) a scandia and yttria...... treatments resulted in a distribution of the metallic and/or ceramic interlayers in the electrolyte/anode backbone junction taking place. The structure is prepared by (a) depositing a ceramic interlayer onto one side of the electrolyte, (b) optionally applying a metallic interlayer thereon, (c) repeating...

  20. Reactive co-sputter deposition of nanostructured cermet anodes for solid oxide fuel cells

    Science.gov (United States)

    Ionov, Igor V.; Solovyev, Andrey A.; Shipilova, Anna V.; Lebedynskiy, Alexey M.; Smolyanskiy, Egor A.; Lauk, Alexander L.; Semenov, Vyacheslav A.

    2018-01-01

    The impact of a nanostructured NiO/yttria-stabilized zirconia (NiO/YSZ) and NiO/gadolinia-doped ceria (NiO/GDC) anode functional layers on low- and intermediate-temperature solid oxide fuel cell (SOFC) performance is investigated. NiO/YSZ and NiO/GDC thin films were reactively sputter-deposited by pulsed direct current magnetron sputtering from the Ni, Zr–Y, and Ce–Gd targets onto commercial NiO/YSZ substrates. Anode-supported SOFCs based on magnetron sputtered YSZ and GDC electrolytes (∼4 µm) with and without the nanostructured anode layers are fabricated. A direct comparison of the YSZ- and GDC-based SOFCs in temperature range of 600–800 and 400–600 °C is made. The performance of cells with the nanostructured anode layers significantly increases as compared to that of the cell without it, especially at lower temperatures. Increase of cells performance was achieved by reduction of the total area-specific resistance by 26–30%.

  1. Oxidation of H2 and CO in a fuel cell with a Platinum-tin Anode

    Directory of Open Access Journals (Sweden)

    Javier González

    2004-05-01

    Full Text Available This report describes the construction and evolution of a fuel cell with a bi-metallic anode of Pt-Sn supported on carbon, as catalysts for oxidation of pure hydrogen, pure CO and a 2% CO in H2 mixture. Both, cathode and anode were made with a structure composed by a diffusive layer and a catalytic layer. The diffusive layer was made with a carbon cloth while the catalytic layer contained the platinum and tin supported on carbon. To test the performance of the catalytic mixture, a proton exchange membrane fuel cell (PEMFC was developed with an original design for the gas distributation plates. The reactants were feed to ambient temperature and 3 psig in the anode side, while 5 psig pure oxygen was used in the cathode. The anode catalytic load was 0.57 mg/cm2 of platinum and 0.08 mg/cm2 of tin. The catalytic load in cathode was 0.85 mg/cm2 of pure platinum. It was found that this caralytic mixture is tolerant to CO presence.

  2. Lithium intercalation and interfacial kinetics of composite anodes formed by oxidized graphite and copper

    Energy Technology Data Exchange (ETDEWEB)

    Mancini, M.; Nobili, F.; Dsoke, S.; Tossici, R.; Marassi, R. [Dipartimento di Scienze Chimiche, Universita di Camerino, Via S. Agostino, 1, 62032 Camerino (MC) (Italy); D' Amico, F. [Dipartimento di Fisica, Universita di Camerino, Via Madonna delle Carceri, 9, 62032 Camerino (MC) (Italy); Croce, F. [Dipartimento di Scienze del Farmaco, Universita degli Studi ' ' G. D' Annunzio' ' , Via dei Vestini, 31, 66013 Chieti (Italy)

    2009-05-01

    The electrochemical behavior of composite anodes prepared either by mixing partially oxidized graphite and Cu powders or by coating the pristine partially oxidized graphite electrodes with few-nanometer-thick Cu layers has been studied by slow-scan-rate cyclic voltammetry (SSCV) and galvanostatic charge/discharge cycles over the temperature range of -30 C to 20 C. The interfacial intercalation/deintercalation kinetics has also been investigated using electrochemical impedance spectroscopy (EIS). The role of the Cu in improving low-temperature performances and kinetics of graphite electrodes is discussed. (author)

  3. Electrocatalytic Materials and Techniques for the Anodic Oxidation of Various Organic Compounds

    Energy Technology Data Exchange (ETDEWEB)

    Treimer, Stephen Everett [Iowa State Univ., Ames, IA (United States)

    2001-01-01

    The focus of this thesis was first to characterize and improve the applicability of Fe(III) and Bi(V) doped PbO2 film electrodes for use in anodic O-transfer reactions of toxic and waste organic compounds, e.g. phenol, aniline, benzene, and naphthalene. Further, they investigated the use of alternative solution/electrode interfacial excitation techniques to enhance the performance of these electrodes for remediation and electrosynthetic applications. Finally, they have attempted to identify a less toxic metal oxide film that may hold promise for future studies in the electrocatalysis and photoelectrocatalysis of O-transfer reactions using metal oxide film electrodes.

  4. High performance fuel electrode for a solid oxide electrochemical cell

    DEFF Research Database (Denmark)

    2013-01-01

    perovskite oxides selected from the group consisting of niobium-doped strontium titanate, vanadium-doped strontium titanate, tantalum-doped strontium titanate and mixtures thereof, thereby obtaining a porous anode backbone, (b) sintering the coated electrolyte at a high temperature, such as 1200 DEG C...

  5. Conducting metal oxide and metal nitride nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    DiSalvo, Jr., Francis J.; Subban, Chinmayee V.

    2017-12-26

    Conducting metal oxide and nitride nanoparticles that can be used in fuel cell applications. The metal oxide nanoparticles are comprised of for example, titanium, niobium, tantalum, tungsten and combinations thereof. The metal nitride nanoparticles are comprised of, for example, titanium, niobium, tantalum, tungsten, zirconium, and combinations thereof. The nanoparticles can be sintered to provide conducting porous agglomerates of the nanoparticles which can be used as a catalyst support in fuel cell applications. Further, platinum nanoparticles, for example, can be deposited on the agglomerates to provide a material that can be used as both an anode and a cathode catalyst support in a fuel cell.

  6. The influence of humidity on the kinetics of local anodic oxidation

    International Nuclear Information System (INIS)

    BartosIk, M; Skoda, D; Tomanec, O; Kalousek, R; Jansky, P; Zlamal, J; Spousta, J; Sikola, T

    2007-01-01

    In this paper the influence of relative humidity on fabrication of nanostructures at GaAs (100) surfaces by local anodic oxidation (LAO) is reported. The attention was paid both to the dimensions of oxide nanolines prepared at different relative humidities for tip-surface voltages of 6 - 9 V and tip speeds of 10 - 200 nm/s, and to the profiles corresponding to line trenches (etched in HCl after the nanoxidation). Contrary to the expectations the height and the half-width of oxide nanolines did not increase with relative humidity in the whole interval from 35% to 90%, but for lower relative humidities (< 50%) the lines were comparable in size to those prepared at 90%. However, this was accompanied with instabilities in the oxidation process resulting most probably from enhanced size variations of the water meniscus between the tip and the surface at these low humidities

  7. Synthesis and properties of iridescent Zn-containing anodic aluminum oxide films

    Energy Technology Data Exchange (ETDEWEB)

    Jia, Xiaoxuan; Sun, Huiyuan, E-mail: huiyuansun@126.com; Liu, Lihu; Hou, Xue; Liu, Huiyuan

    2015-07-01

    A simple method of fabricating Zn-containing anodic aluminum oxide films for multifunctional anticounterfeit technology is reported. The resulting membranes were characterized with UV–vis illumination studies, natural light illumination color experiments, and electron microscopy analysis. Deposition of Zn in the nanopore region can enhance the color saturation of the thin alumina film with different colors dramatically. Both the anodization time and etching time have great influence on the structural color. The mechanisms for the emergence of this phenomenon are discussed and theoretical analysis further demonstrates the experimental results. - Highlights: • Iridescent PAA@Zn nanocomposite films were successfully fabricated. • A simple organics-assisted method is applied to making a series of fancy and multicolor patterns. • The color varies with the angle of incidence of the light used to view the film as is expected with Bragg–Snell formula. • Such colored films could be used in multifunctional anti-counterfeiting applications.

  8. Methane Steam Reforming over an Ni-YSZ Solid Oxide Fuel Cell Anode in Stack Configuration

    Directory of Open Access Journals (Sweden)

    D. Mogensen

    2014-01-01

    Full Text Available The kinetics of catalytic steam reforming of methane over an Ni-YSZ anode of a solid oxide fuel cell (SOFC have been investigated with the cell placed in a stack configuration. In order to decrease the degree of conversion, a single cell stack with reduced area was used. Measurements were performed in the temperature range 600–800°C and the partial pressures of all reactants and products were varied. The obtained rates could be well fitted with a power law expression (r ∝PCH40.7. A simple model is presented which is capable of predicting the methane conversion in a stack configuration from intrinsic kinetics of the anode support material. The predictions are compared with the stack measurements presented here, and good agreement is observed.

  9. Electrochemical combustion of indigo at ternary oxide coated titanium anodes

    Directory of Open Access Journals (Sweden)

    María I. León

    2014-12-01

    Full Text Available The film of iridium and tin dioxides doped with antimony (IrO2-SnO2–Sb2O5 deposited on a Ti substrate (mesh obtained by Pechini method was used for the formation of ·OH radicals by water discharge. Detection of ·OH radicals was followed by the use of the N,N-dimethyl-p-nitrosoaniline (RNO as a spin trap. The electrode surface morphology and composition was characterized by SEM-EDS. The ternary oxide coating was used for the electrochemical combustion of indigo textile dye as a model organic compound in chloride medium. Bulk electrolyses were then carried out at different volumetric flow rates under galvanostatic conditions using a filter-press flow cell. The galvanostatic tests using RNO confirmed that Ti/IrO2-SnO2-Sb2O5 favor the hydroxyl radical formation at current densities between 5 and 7 mA cm-2, while at current density of 10 mA cm-2 the oxygen evolution reaction occurs. The indigo was totally decolorized and mineralized via reactive oxygen species, such as (·OH, H2O2, O3 and active chlorine formed in-situ at the Ti/IrO2-SnO2-Sb2O5 surface at volumetric flow rates between 0.1-0.4 L min-1 and at fixed current density of 7 mA cm-2. The mineralization of indigo carried out at 0.2 L min-1 achieved values of 100 %, with current efficiencies of 80 % and energy consumption of 1.78 KWh m-3.

  10. Novel Size and Surface Oxide Effects in Silicon Nanowires as Lithium Battery Anodes

    KAUST Repository

    McDowell, Matthew T.

    2011-09-14

    With its high specific capacity, silicon is a promising anode material for high-energy lithium-ion batteries, but volume expansion and fracture during lithium reaction have prevented implementation. Si nanostructures have shown resistance to fracture during cycling, but the critical effects of nanostructure size and native surface oxide on volume expansion and cycling performance are not understood. Here, we use an ex situ transmission electron microscopy technique to observe the same Si nanowires before and after lithiation and have discovered the impacts of size and surface oxide on volume expansion. For nanowires with native SiO2, the surface oxide can suppress the volume expansion during lithiation for nanowires with diameters <∼50 nm. Finite element modeling shows that the oxide layer can induce compressive hydrostatic stress that could act to limit the extent of lithiation. The understanding developed herein of how volume expansion and extent of lithiation can depend on nanomaterial structure is important for the improvement of Si-based anodes. © 2011 American Chemical Society.

  11. Characterization and quantification of oxides generated by anodization on titanium for implantation purposes

    Science.gov (United States)

    Aloia Games, L.; Pastore, J.; Bouchet, A.; Ballarre, J.

    2011-12-01

    The use of titanium as implant material is widely known in the surgery field. The formation of natural or artificial compact and protective oxide is a convenient tool for metal protection and a good way to generate phosphate deposits to enhance biocompatibility and bone fixation with the existing tissue. The present work has the aim of superficially modify commercially pure titanium sheets used in orthopedics and odontology, with a potencistatic anodization process with an ammonium phosphate and ammonium fluoride solution as electrolyte. The objective is to generate titanium oxides doped with phosphorous on the surface, to promote bioactivity. The characterization and quantification of the generated deposits is presented as a starting point for the future application of these materials. The applied characterization methods are X ray diffraction, micro-Raman spectroscopy analysis for evaluating the chemical and phase composition on the modified surface and PDI image analysis techniques that allow the segmentation of SEM images and the measurement and quantification of the oxides generated by the anodization process. The samples with polished treated surface at 30V have the deposit of a phosphate rich thick layer covering almost all the surface and spherical-shaped titanium oxide crystals randomly placed (covering more than 20% of the surface area).

  12. Characterization and quantification of oxides generated by anodization on titanium for implantation purposes

    International Nuclear Information System (INIS)

    Games, L Aloia; Ballarre, J; Pastore, J; Bouchet, A

    2011-01-01

    The use of titanium as implant material is widely known in the surgery field. The formation of natural or artificial compact and protective oxide is a convenient tool for metal protection and a good way to generate phosphate deposits to enhance biocompatibility and bone fixation with the existing tissue. The present work has the aim of superficially modify commercially pure titanium sheets used in orthopedics and odontology, with a potencistatic anodization process with an ammonium phosphate and ammonium fluoride solution as electrolyte. The objective is to generate titanium oxides doped with phosphorous on the surface, to promote bioactivity. The characterization and quantification of the generated deposits is presented as a starting point for the future application of these materials. The applied characterization methods are X ray diffraction, micro-Raman spectroscopy analysis for evaluating the chemical and phase composition on the modified surface and PDI image analysis techniques that allow the segmentation of SEM images and the measurement and quantification of the oxides generated by the anodization process. The samples with polished treated surface at 30V have the deposit of a phosphate rich thick layer covering almost all the surface and spherical-shaped titanium oxide crystals randomly placed (covering more than 20% of the surface area).

  13. LOW-TEMPERATURE, ANODE-SUPPORTED HIGH POWER DENSITY SOLID OXIDE FUEL CELLS WITH NANOSTRUCTURED ELECTRODES

    Energy Technology Data Exchange (ETDEWEB)

    Professor Anil V. Virkar

    2003-05-23

    This report summarizes the work done during the entire project period, between October 1, 1999 and March 31, 2003, which includes a six-month no-cost extension. During the project, eight research papers have, either been, published, accepted for publication, or submitted for publication. In addition, several presentations have been made in technical meetings and workshops. The project also has provided support for four graduate students working towards advanced degrees. The principal technical objective of the project was to analyze the role of electrode microstructure on solid oxide fuel cell performance. Prior theoretical work conducted in our laboratory demonstrated that the particle size of composite electrodes has a profound effect on cell performance; the finer the particle size, the lower the activation polarization, the better the performance. The composite cathodes examined consisted of electronically conducting perovskites such as Sr-doped LaMnO{sub 3} (LSM) or Sr-doped LaCoO{sub 3} (LSC), which is also a mixed conductor, as the electrocatalyst, and yttria-stabilized zirconia (YSZ) or rare earth oxide doped CeO{sub 2} as the ionic conductor. The composite anodes examined were mixtures of Ni and YSZ. A procedure was developed for the synthesis of nanosize YSZ by molecular decomposition, in which unwanted species were removed by leaching, leaving behind nanosize YSZ. Anode-supported cells were made using the as-synthesized powders, or using commercially acquired powders. The electrolyte was usually a thin ({approx}10 microns), dense layer of YSZ, supported on a thick ({approx}1 mm), porous Ni + YSZ anode. The cathode was a porous mixture of electrocatalyst and an ionic conductor. Most of the cell testing was done at 800 C with hydrogen as fuel and air as the oxidant. Maximum power densities as high as 1.8 W/cm{sup 2} were demonstrated. Polarization behavior of the cells was theoretically analyzed. A limited amount of cell testing was done using liquid

  14. Nanostructured metal oxide-based materials as advanced anodes for lithium-ion batteries.

    Science.gov (United States)

    Wu, Hao Bin; Chen, Jun Song; Hng, Huey Hoon; Lou, Xiong Wen David

    2012-04-21

    The search for new electrode materials for lithium-ion batteries (LIBs) has been an important way to satisfy the ever-growing demands for better performance with higher energy/power densities, improved safety and longer cycle life. Nanostructured metal oxides exhibit good electrochemical properties, and they are regarded as promising anode materials for high-performance LIBs. In this feature article, we will focus on three different categories of metal oxides with distinct lithium storage mechanisms: tin dioxide (SnO(2)), which utilizes alloying/dealloying processes to reversibly store/release lithium ions during charge/discharge; titanium dioxide (TiO(2)), where lithium ions are inserted/deinserted into/out of the TiO(2) crystal framework; and transition metal oxides including iron oxide and cobalt oxide, which react with lithium ions via an unusual conversion reaction. For all three systems, we will emphasize that creating nanomaterials with unique structures could effectively improve the lithium storage properties of these metal oxides. We will also highlight that the lithium storage capability can be further enhanced through designing advanced nanocomposite materials containing metal oxides and other carbonaceous supports. By providing such a rather systematic survey, we aim to stress the importance of proper nanostructuring and advanced compositing that would result in improved physicochemical properties of metal oxides, thus making them promising negative electrodes for next-generation LIBs.

  15. Destination of organic pollutants during electrochemical oxidation of biologically-pretreated dye wastewater using boron-doped diamond anode

    International Nuclear Information System (INIS)

    Zhu, Xiuping; Ni, Jinren; Wei, Junjun; Xing, Xuan; Li, Hongna

    2011-01-01

    Electrochemical oxidation of biologically-pretreated dye wastewater was performed in a boron-doped diamond (BDD) anode system. After electrolysis of 12 h, the COD was decreased from 532 to 99 mg L -1 ( -1 , the National Discharge Standard of China). More importantly, the destination of organic pollutants during electrochemical oxidation process was carefully investigated by molecular weight distribution measurement, resin fractionation, ultraviolet-visible spectroscopy, HPLC and GC-MS analysis, and toxicity test. As results, most organic pollutants were completely removed by electrochemical oxidation and the rest was primarily degraded to simpler compounds (e.g., carboxylic acids and short-chain alkanes) with less toxicity, which demonstrated that electrochemical oxidation of biologically-pretreated dye wastewater with BDD anode was very effective and safe. Especially, the performance of BDD anode system in degradation of large molecular organics such as humic substances makes it very promising in practical applications as an advanced treatment of biologically-pretreated wastewaters.

  16. Adaptable silicon-carbon nanocables sandwiched between reduced graphene oxide sheets as lithium ion battery anodes.

    Science.gov (United States)

    Wang, Bin; Li, Xianglong; Zhang, Xianfeng; Luo, Bin; Jin, Meihua; Liang, Minghui; Dayeh, Shadi A; Picraux, S T; Zhi, Linjie

    2013-02-26

    Silicon has been touted as one of the most promising anode materials for next generation lithium ion batteries. Yet, how to build energetic silicon-based electrode architectures by addressing the structural and interfacial stability issues facing silicon anodes still remains a big challenge. Here, we develop a novel kind of self-supporting binder-free silicon-based anodes via the encapsulation of silicon nanowires (SiNWs) with dual adaptable apparels (overlapped graphene (G) sheaths and reduced graphene oxide (RGO) overcoats). In the resulted architecture (namely, SiNW@G@RGO), the overlapped graphene sheets, as adaptable but sealed sheaths, prevent the direct exposure of encapsulated silicon to the electrolyte and enable the structural and interfacial stabilization of silicon nanowires. Meanwhile, the flexible and conductive RGO overcoats accommodate the volume change of embedded SiNW@G nanocables and thus maintain the structural and electrical integrity of the SiNW@G@RGO. As a result, the SiNW@G@RGO electrodes exhibit high reversible specific capacity of 1600 mAh g⁻¹ at 2.1 A g⁻¹, 80% capacity retention after 100 cycles, and superior rate capability (500 mAh g⁻¹ at 8.4 A g⁻¹) on the basis of the total electrode weight.

  17. Thermal Cyclability of Reactive Air Braze Seals in Anode Supported Solid Oxide Fuel Cells

    Energy Technology Data Exchange (ETDEWEB)

    Hardy, John S.; Darsell, Jens T.; Coyle, Christopher A.; Birnbaum, Jerome C.; Weil, K. Scott

    2004-12-31

    The popularity of anode-supported solid oxide fuel cells (SOFC) has increased in tandem with the ability to fabricate thinner gas-tight yttrium-stabilized zirconia (YSZ) electrolyte layers, which can now be routinely produced on the order of 7 to 10 μm thick. While this has significantly improved power output and decreased the required fuel cell operating temperatures, the ability to reliably seal fuel cells remains a concern. The seals must be hermetic and be robust enough to retain their hermeticity even under the extreme operating conditions of SOFCs. Perhaps the largest contributor to stresses experienced by the seal is the fact that the SOFC is an assembly of many different materials with different thermal expansion properties. Although every effort is made to minimize thermal expansion mismatches across the seals, the stresses developed during thermal cycling still jeopardize seal integrity. Reactive air brazing (RAB), a method of joining that employs a metallic, and therefore non-brittle, seal material has been used to seal electrolyte/anode bilayers, such as those in anode-supported SOFCs, to Crofer-22 alloy. The results of rupture strength testing will be reported for as-brazed and thermally cycled samples and the effect of thermal cycling on the RAB seal microstructure will be shown

  18. Cycle Life of Commercial Lithium-Ion Batteries with Lithium Titanium Oxide Anodes in Electric Vehicles

    Directory of Open Access Journals (Sweden)

    Xuebing Han

    2014-07-01

    Full Text Available The lithium titanium oxide (LTO anode is widely accepted as one of the best anodes for the future lithium ion batteries in electric vehicles (EVs, especially since its cycle life is very long. In this paper, three different commercial LTO cells from different manufacturers were studied in accelerated cycle life tests and their capacity fades were compared. The result indicates that under 55 °C, the LTO battery still shows a high capacity fade rate. The battery aging processes of all the commercial LTO cells clearly include two stages. Using the incremental capacity (IC analysis, it could be judged that in the first stage, the battery capacity decreases mainly due to the loss of anode material and the degradation rate is lower. In the second stage, the battery capacity decreases much faster, mainly due to the degradation of the cathode material. The result is important for the state of health (SOH estimation and remaining useful life (RUL prediction of battery management system (BMS for LTO batteries in EVs.

  19. Effects of nanoporous anodic titanium oxide on human adipose derived stem cells

    Science.gov (United States)

    Malec, Katarzyna; Góralska, Joanna; Hubalewska-Mazgaj, Magdalena; Głowacz, Paulina; Jarosz, Magdalena; Brzewski, Pawel; Sulka, Grzegorz D; Jaskuła, Marian; Wybrańska, Iwona

    2016-01-01

    The aim of current bone biomaterials research is to design implants that induce controlled, guided, successful, and rapid healing. Titanium implants are widely used in dental, orthopedic, and reconstructive surgery. A series of studies has indicated that cells can respond not only to the chemical properties of the biomaterial, but also, in particular, to the changes in surface topography. Nanoporous materials remain in focus of scientific queries due to their exclusive properties and broad applications. One such material is nanostructured titanium oxide with highly ordered, mutually perpendicular nanopores. Nanoporous anodic titanium dioxide (TiO2) films were fabricated by a three-step anodization process in propan-1,2,3-triol-based electrolyte containing fluoride ions. Adipose-derived stem cells offer many interesting opportunities for regenerative medicine. The important goal of tissue engineering is to direct stem cell differentiation into a desired cell lineage. The influence of nanoporous TiO2 with pore diameters of 80 and 108 nm on cell response, growth, viability, and ability to differentiate into osteoblastic lineage of human adipose-derived progenitors was explored. Cells were harvested from the subcutaneous abdominal fat tissue by a simple, minimally invasive, and inexpensive method. Our results indicate that anodic nanostructured TiO2 is a safe and nontoxic biomaterial. In vitro studies demonstrated that the nanotopography induced and enhanced osteodifferentiation of human adipose-derived stem cells from the abdominal subcutaneous fat tissue. PMID:27789947

  20. Photocatalytic effect of anodic titanium oxide nanotubes on various cell culture media

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Chun-Kang; Hu, Kan-Hung; Wang, Shing-Hoa [National Taiwan Ocean University, Center for Marine Bioenvironment and Biotechnology, Keelung (China); National Taiwan Ocean University, Department of Mechanical and Mechatronic Engineering, Keelung (China); Hsu, Todd [National Taiwan Ocean University, Center for Marine Bioenvironment and Biotechnology, Keelung (China); National Taiwan Ocean University, Institute of Bioscience and Biotechnology, Keelung (China); Tsai, Huei-Ting [National Taiwan Ocean University, Institute of Bioscience and Biotechnology, Keelung (China); Chen, Chien-Chon [National United University, Department of Energy and Resources, Miaoli (China); Liu, Shiu-Mei [National Taiwan Ocean University, Center for Marine Bioenvironment and Biotechnology, Keelung (China); National Taiwan Ocean University, Institute of Marine Biology, Keelung (China); Lin, Tai-Yuan [National Taiwan Ocean University, Institute of Optoelectronic Sciences, Keelung (China); Chen, Chin-Hsing [National Chiao Tong University, Department of Applied Chemistry, Hsinchu (China)

    2011-02-15

    The use of titanium dioxide (TiO{sub 2}) in photodynamic therapy for the treatment of cancer cells has been proposed following studies of cultured cancer cells. In this work, an ordered channel array of anodic titanium oxide (ATO) was fabricated by anodizing titanium foil. The ATO layer of nanotubes with diameters of 100 nm was made in NH{sub 4}F electrolyte by anodization. The photocatalytic effect of ATO was examined on various culture media by ultraviolet A (UV-A) (366 nm) irradiation. After UV-A irradiation of the ATO layer, redox potential of Tris-HCl buffer (pH 7.5) and dilute acrylamide solution increased instantaneously. The redox potential of the serum-containing RPMI1640 medium also increased dramatically, while that of serum-containing MEM and DMEM media increased slightly. The UVA-induced high redox potential was correlated with the greater ability to break down plasmid DNA strands. These phenomena suggest that a culture medium, such as RPMI1640, with a greater ability to produce free radical may be associated with a stronger photocatalytic effect of ATO on cultured cancer cells reported previously. (orig.)

  1. Quantitative analysis of solid oxide fuel cell anode microstructure change during redox cycles

    Science.gov (United States)

    Shimura, Takaaki; Jiao, Zhenjun; Hara, Shotaro; Shikazono, Naoki

    2014-12-01

    In the present study, correlation between solid oxide fuel cell anode microstructure and electrochemical performance during redox cycles was investigated. Electrolyte-support cell with nickel/yttria stabilized zirconia composite anode was prepared and tested under discharge process with redox cycles. Redox treatment was basically conducted every 20 h during discharge process. Polarization resistance decreased just after redox treatment and increased during discharge process. Enhancement of cell performance after every redox cycles and faster degradation in the following discharge process were observed. Polarization resistance gradually increased as redox cycles were repeated. Focused ion beam-scanning electron microscopy (FIB-SEM) observation was conducted for reconstructing the three dimensional microstructures of the tested samples. From the three dimensional microstructure reconstruction, it is found that the shape of nickel particle got thinner and complicated after redox cycles. Triple phase boundary (TPB) length increased after redox treatment and decreased after discharge process. This TPB change was highly associated with Ni connectivity and Ni specific surface area. These microstructure changes are consistent with the change of cell performance enhancement after redox treatment and degradation after discharge process. However, TPB length density kept on increasing as redox cycles are repeated, which is inconsistent with the gradual degradation of anode performance.

  2. Niobium(v) chloride and imidazolium bromides as efficient dual catalyst systems for the cycloaddition of carbon dioxide and propylene oxide

    KAUST Repository

    Wilhelm, Michael E.

    2014-02-19

    The application of niobium(v) chloride and several imidazolium bromides as catalyst systems for the cycloaddition of propylene oxide (PO) with carbon dioxide to propylene carbonate (PC) is reported. A set of 31 different imidazolium bromides has been synthesized with varying substituents at all five imidazolium ring atoms, of which 17 have not been reported before. The impact of different substitution patterns (steric and electronic changes and solubility in PO) at the imidazolium ring on the catalytic activity was investigated. The optimisation of the catalyst structure allows for the valorisation of carbon dioxide under mild reaction conditions with high reaction rates in very good yield and selectivity for PC. This journal is © the Partner Organisations 2014.

  3. Niobium pentoxide coating replacing zinc phosphate coating

    OpenAIRE

    RODRIGUES, P.R.P.; TERADA, M.; JUNIOR, O.R.A.; LOPES, A.C.; COSTA, I.; BANCZEK, E.P.

    2015-01-01

    A new coating made of niobium pentoxide, obtained through the sol-gel process, was developed for the carbon steel (SAE 1010). The corrosion protection provided by this coating was evaluated through electrochemical tests such as: open circuit potential, electrochemical impedance spectroscopy and anodic potentiodynamic polarization in NaCl 0,5 mol L-1 solution. The morphology and composition of the coatings were analyzed using scanning electronic microscopy, energy dispersive spectroscopy and X...

  4. Anodic oxidation of anthraquinone dye Alizarin Red S at Ti/BDD electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Sun Jianrui; Lu Haiyan [College of Chemistry, Jilin University, Changchun 130012 (China); Du Lili [State Key Laboratory of Superhard Materials, Jilin University, Changchun 130012 (China); Lin Haibo, E-mail: lhb910@jlu.edu.cn [College of Chemistry, Jilin University, Changchun 130012 (China); State Key Laboratory of Theoretical and Computational Chemistry, Jilin University, Changchun 130012 (China); Li Hongdong, E-mail: hdli@jlu.edu.cn [State Key Laboratory of Superhard Materials, Jilin University, Changchun 130012 (China)

    2011-05-15

    The boron-doped diamond (BDD) thin-film electrode with high quality using industrially titanium plate (Ti/BDD) as substrate has been prepared and firstly used in the oxidation of anthraquinone dye Alizarin Red S (ARS) in wastewaters. The Ti/BDD electrodes are shown to have high concentration of sp{sup 3}-bonded carbon and wide electrochemical window. The results of the cyclic voltammetries show that BDD has unique properties such as high anodic stability and the production of active intermediates at the high potential. The oxidation regions of ARS and water are significantly separated at the Ti/BDD electrode, and the peak current increases linearly with increasing ARS concentration. The bulk electrolysis shows that removal of chemical oxygen demand (COD) and color can be completely reached and the electrooxidation of ARS behaves as a mass-transfer-controlled process at the Ti/BDD electrode. It is demonstrated that the performances of the Ti/BDD electrode for anodic oxidation ARS have been significantly improved with respect to the traditional electrodes.

  5. Active Pt-Pb Ox/C anodes to promote the formic acid oxidation in presence of sulfuric acid

    Energy Technology Data Exchange (ETDEWEB)

    Buzzo, Guilherme S.; Niquirilo, Rafael V.; Suffredini, Hugo B. [Universidade Federal do ABC (UFABC), Santo Andre, SP (Brazil). Centro de Ciencias Naturais e Humanas

    2010-07-01

    The performance of Pt-Pb Ox-based catalysts to promote the formic acid oxidation is described here. All materials were synthesized by a modified sol-gel method. Voltammetric studies showed that the Pt-Pb Ox/C anode starts the oxidation process at extremely low potentials. Quasi-stationary polarization experiments and current vs. time measurements confirmed this affirmation. (author)

  6. Surface and interface analysis of poly-hydroxyethylmethacrylate-coated anodic aluminium oxide membranes

    Energy Technology Data Exchange (ETDEWEB)

    Ali, Nurshahidah [School of Engineering and Information Technology, Murdoch University, WA 6150 (Australia); Murdoch Applied Nanotechnology Research Group, Murdoch University, WA 6150 (Australia); Duan, Xiaofei [School of Chemistry, The University of Melbourne, VIC 3010 (Australia); Jiang, Zhong-Tao, E-mail: Z.Jiang@murdoch.edu.au [School of Engineering and Information Technology, Murdoch University, WA 6150 (Australia); Goh, Bee Min [School of Engineering and Information Technology, Murdoch University, WA 6150 (Australia); Lamb, Robert [School of Chemistry, The University of Melbourne, VIC 3010 (Australia); Tadich, Anton [Australian Synchrotron, Clayton, VIC 3086 (Australia); Poinern, Gérrard Eddy Jai; Fawcett, Derek [Murdoch Applied Nanotechnology Research Group, Murdoch University, WA 6150 (Australia); Chapman, Peter [Department of Chemistry, Curtin University, WA 6102 (Australia); Singh, Pritam [School of Engineering and Information Technology, Murdoch University, WA 6150 (Australia)

    2014-01-15

    The surface and interface of poly (2-hydroxyethylmethacrylate) (PHEMA) and anodic aluminium oxide (AAO) membranes were comprehensively investigated using Near Edge X-ray Absorption Fine Structure (NEXAFS) spectroscopy. It was found that 1s→π* (C=O) and 1s→σ* (C-O) transitions were dominant on the surface of both bulk PHEMA polymer and PHEMA-surface coated AAO (AAO–PHEMA) composite. Findings from NEXAFS, Fourier-Transform Infrared (FTIR) and X-ray Photoelectron Spectroscopy (XPS) analyses suggest the possibility of chemical interaction between carbon from the ester group of polymer and AAO membrane.

  7. Solid-state electrochromic cell with anodic iridium oxide film electrodes

    International Nuclear Information System (INIS)

    Dautremont-Smith, W.C.; Beni, G.; Schiavone, L.M.; Shay, J.L.

    1979-01-01

    A new solid-state electrochromic cell has been fabricated using an anodic iridium oxide film (AIROF) display electrode. The cell has the symmetric sandwich structure AIROFvertical-barNafionvertical-barAIROF, with the Nafion solid electrolyte opacified by an in situ precipitation technique. A symmetric square-wave voltage of 1.5 V amplitude produces clearly perceivable color changes from pale to dark blue-gray in approx. =1 sec when viewed in diffuse reflection. Good open-circuit optical memory is exhibited:

  8. Efficient and stable polymer solar cells prepared using plasmonic graphene oxides as anode buffers

    Science.gov (United States)

    Chen, Chung-Lei; Chuang, Ming-Kai; Chen, Chyong-Hua; Chu, Chih-Wei; Keshtov, Muchamed L.; Chen, Fang-Chung

    2015-08-01

    Gold nanoparticle-decorated graphene oxides (AuNP-GOs) have been incorporated into inverted organic photovoltaic devices (OPVs) as anode interlayers. The OPVs fabricated with AuNP-GOs exhibited significant improvement in both the short-circuit current and fill factor compared to a reference device fabricated with neat GOs. We attribute the improvement in the efficiency of the device to the plasmonic effects of the AuNP-GO nanocomposites, which induced local enhancement of the electromagnetic field. More importantly, the inverted OPVs also exhibited better reliability after the use of AuNP-GO nanocomposites.

  9. Study of the phase composition of nanostructures produced by the local anodic oxidation of titanium films

    International Nuclear Information System (INIS)

    Avilov, V. I.; Ageev, O. A.; Konoplev, B. G.; Smirnov, V. A.; Solodovnik, M. S.; Tsukanova, O. G.

    2016-01-01

    The results of experimental studies of the phase composition of oxide nanostructures formed by the local anodic oxidation of a titanium thin film are reported. The data of the phase analysis of titanium-oxide nanostructures are obtained by X-ray photoelectron spectroscopy in the ion profiling mode of measurements. It is established that the surface of titanium-oxide nanostructures 4.5 ± 0.2 nm in height possesses a binding energy of core levels characteristic of TiO 2 (458.4 eV). By analyzing the titanium-oxide nanostructures in depth by X-ray photoelectron spectroscopy, the formation of phases with binding energies of core levels characteristic of Ti 2 O 3 (456.6 eV) and TiO (454.8 eV) is established. The results can be used in developing the technological processes of the formation of a future electronic-component base for nanoelectronics on the basis of titanium-oxide nanostructures and probe nanotechnologies.

  10. The influence of a thin gold film on the optical spectral characteristics of a porous anodic aluminum-oxide membrane

    Science.gov (United States)

    Ushakov, N. M.; Vasilkov, M. Yu.; Fedorov, F. S.

    2017-07-01

    We have experimentally studied how a thin mesostructured gold film, deposited onto one side of a porous anodic aluminum-oxide membrane, influences its optical spectral characteristics in a 200-900 nm wavelength range. It is established that the gold film only modifies the spectral characteristics of the composite membrane at light wavelengths above 500 nm. The presence of a thin gold film ensures the surface conductivity of membrane on a level of 3.4 × 106 Ω-1 m-1, retains optical transparency within 10-20%, leads to the appearance of anomalous dispersion in the long-wavelength part of the transmission spectrum, and reduces the bandgap width from 5.61 eV (in anodic aluminum oxide) to 4.51 eV (in the composite). The obtained anodic aluminum-oxide membranes with thin gold films can be used as transparent conducting electrodes in optoelectronic devices with large light transmitter/receiver active areas.

  11. Fabrication and characterization of anode-supported micro-tubular solide oxide fuel cell by phase inversion method

    Science.gov (United States)

    Ren, Cong

    Nowadays, the micro-tubular solid oxide fuel cells (MT-SOFCs), especially the anode supported MT-SOFCs have been extensively developed to be applied for SOFC stacks designation, which can be potentially used for portable power sources and vehicle power supply. To prepare MT-SOFCs with high electrochemical performance, one of the main strategies is to optimize the microstructure of the anode support. Recently, a novel phase inversion method has been applied to prepare the anode support with a unique asymmetrical microstructure, which can improve the electrochemical performance of the MT-SOFCs. Since several process parameters of the phase inversion method can influence the pore formation mechanism and final microstructure, it is essential and necessary to systematically investigate the relationship between phase inversion process parameters and final microstructure of the anode supports. The objective of this study is aiming at correlating the process parameters and microstructure and further preparing MT-SOFCs with enhanced electrochemical performance. Non-solvent, which is used to trigger the phase separation process, can significantly influence the microstructure of the anode support fabricated by phase inversion method. To investigate the mechanism of non-solvent affecting the microstructure, water and ethanol/water mixture were selected for the NiO-YSZ anode supports fabrication. The presence of ethanol in non-solvent can inhibit the growth of the finger-like pores in the tubes. With the increasing of the ethanol concentration in the non-solvent, a relatively dense layer can be observed both in the outside and inside of the tubes. The mechanism of pores growth and morphology obtained by using non-solvent with high concentration ethanol was explained based on the inter-diffusivity between solvent and non-solvent. Solvent and non-solvent pair with larger Dm value is benefit for the growth of finger-like pores. Three cells with different anode geometries was

  12. Graphene oxide-multiwalled carbon nanotubes composite as an anode for lithium ion batteries

    Directory of Open Access Journals (Sweden)

    Majchrzycki Łukasz

    2016-09-01

    Full Text Available Nowadays reduced graphene oxide (rGO is regarded as a highly interesting material which is appropriate for possible applications in electrochemistry, especially in lithium-ion batteries (LIBs. Several methods were proposed for the preparation of rGO-based electrodes, resulting in high-capacity LIBs anodes. However, the mechanism of lithium storage in rGO and related materials is still not well understood. In this work we focused on the proposed mechanism of favorable bonding sites induced by additional functionalities attached to the graphene planes. This mechanism might increase the capacity of electrodes. In order to verify this hypothesis the composite of non-reduced graphene oxide (GO with multiwalled carbon nanotubes electrodes was fabricated. Electrochemical properties of GO composite anodes were studied in comparison with similarly prepared electrodes based on rGO. This allowed us to estimate the impact of functional groups on the reversible capacity changes. As a result, it was shown that oxygen containing functional groups of GO do not create, in noticeable way, additional active sites for the electrochemical reactions of lithium storage, contrary to what has been postulated previously.

  13. Effect of copper oxide electrocatalyst on CO2 reduction using Co3O4 as anode

    Directory of Open Access Journals (Sweden)

    V.S.K. Yadav

    2016-09-01

    Full Text Available The reduction of carbon dioxide (CO2 to products electrochemically (RCPE in 0.5 M NaHCO3 and Na2CO3 liquid phase electrolyte solutions was investigated. Cobalt oxide (Co3O4 as anode and cuprous oxide (Cu2O as the cathode were considered, respectively. The impacts of applied potential with time of reaction during reduction of CO2 to products were studied. The anode and cathode were prepared by depositing electrocatalysts on the graphite plate. Ultra-fast liquid chromatography (UFLC was used to analyze the products obtained from the reduction of CO2. The feasible way of reduction by applying voltages with current densities was clearly correlated. The results illustrate the capability of electrocatalyst successfully to remove atmospheric CO2 in the form of valuable chemicals. Maximum Faradaic efficiency of ethanol was 98.1% at 2 V and for formic acid (36.6% at 1.5 V was observed in NaHCO3. On the other hand, in Na2CO3 electrolyte solution maximum efficiency for ethanol was 55.21% at 1.5 V and 25.1% for formic acid at 2 V. In both electrolytes other end products like methanol, propanol, formaldehyde and acetic acid were formed at various applied voltage and output current densities.

  14. Identification of chlorinated oligomers formed during anodic oxidation of phenol in the presence of chloride

    International Nuclear Information System (INIS)

    Chen, Linxi; Campo, Pablo; Kupferle, Margaret J.

    2015-01-01

    Graphical abstract: - Highlights: • By-products from anodic oxidation of phenol in the presence of chloride are investigated. • Chlorinated oligomer formation is demonstrated by LC-QTOF-MS. • They have structures similar to triclosan and polychlorinated dibenzo-p-dioxins. - Abstract: Chlorinated oligomer intermediates formed during the anodic electrochemical oxidation of phenol with a boron-doped diamond electrode were studied at two different concentrations of chloride (5 mM and 50 mM). Under the same ionic strength, with sodium sulfate being the make-up ion, a 10-fold increase in Cl − led to removal rates 10.8, 1.5, and 1.4 times higher for phenol, TOC, and COD, respectively. Mono-, di- and trichlorophenols resulting from electrophilic substitution were the identified by-products. Nevertheless, discrepancies between theoretical and measured TOC values along with gaps in the mass balance of chlorine-containing species indicated the formation of unaccounted-for chlorinated by-products. Accurate mass measurements by liquid chromatography quadrupole time-of-flight mass spectrometry and MS-MS fragmentation spectra showed that additional compounds formed were dimers and trimers of phenol with structures similar to triclosan and polychlorinated dibenzo-p-dioxins

  15. Identification of chlorinated oligomers formed during anodic oxidation of phenol in the presence of chloride

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Linxi; Campo, Pablo; Kupferle, Margaret J., E-mail: margaret.kupferle@uc.edu

    2015-02-11

    Graphical abstract: - Highlights: • By-products from anodic oxidation of phenol in the presence of chloride are investigated. • Chlorinated oligomer formation is demonstrated by LC-QTOF-MS. • They have structures similar to triclosan and polychlorinated dibenzo-p-dioxins. - Abstract: Chlorinated oligomer intermediates formed during the anodic electrochemical oxidation of phenol with a boron-doped diamond electrode were studied at two different concentrations of chloride (5 mM and 50 mM). Under the same ionic strength, with sodium sulfate being the make-up ion, a 10-fold increase in Cl{sup −} led to removal rates 10.8, 1.5, and 1.4 times higher for phenol, TOC, and COD, respectively. Mono-, di- and trichlorophenols resulting from electrophilic substitution were the identified by-products. Nevertheless, discrepancies between theoretical and measured TOC values along with gaps in the mass balance of chlorine-containing species indicated the formation of unaccounted-for chlorinated by-products. Accurate mass measurements by liquid chromatography quadrupole time-of-flight mass spectrometry and MS-MS fragmentation spectra showed that additional compounds formed were dimers and trimers of phenol with structures similar to triclosan and polychlorinated dibenzo-p-dioxins.

  16. Anodic aluminum oxide with fine pore size control for selective and effective particulate matter filtering

    Science.gov (United States)

    Zhang, Su; Wang, Yang; Tan, Yingling; Zhu, Jianfeng; Liu, Kai; Zhu, Jia

    2016-07-01

    Air pollution is widely considered as one of the most pressing environmental health issues. Particularly, atmospheric particulate matters (PM), a complex mixture of solid or liquid matter suspended in the atmosphere, are a harmful form of air pollution due to its ability to penetrate deep into the lungs and blood streams, causing permanent damages such as DNA mutations and premature death. Therefore, porous materials which can effectively filter out particulate matters are highly desirable. Here, for the first time, we demonstrate that anodic aluminum oxide with fine pore size control fabricated through a scalable process can serve as effective and selective filtering materials for different types of particulate matters (such as PM2.5, PM10). Combining selective and dramatic filtering effect, fine pore size control and a scalable process, this type of anodic aluminum oxide templates can potentially serve as a novel selective filter for different kinds of particulate matters, and a promising and complementary solution to tackle this serious environmental issue.

  17. Degradation of thiamethoxam by the synergetic effect between anodic oxidation and Fenton reactions.

    Science.gov (United States)

    Meijide, J; Gómez, J; Pazos, M; Sanromán, M A

    2016-12-05

    In this work, a comparative study using anodic oxidation, Fenton and electro-Fenton treatments was performed in order to determine the synergic effect for the removal of thiamethoxan. The results determined that electro-Fenton process showed high efficiency in comparison with Fenton or anodic oxidation. After that, this hybrid process was optimized and the influence of iron catalyst concentration and applied current intensity on the degradation and mineralization were evaluated. Degradation profiles were monitored by high performance liquid chromatography (HPLC) being satisfactorily described by pseudo-first order kinetic model. At the optimal experimental conditions (300mA and 0.2mM Fe(+2)), the complete degradation of thiamethoxam was achieved after 10min. On the other hand, mineralization of thiamethoxam was monitored by total organic carbon (TOC) decay reaching more than 92% of TOC removal after 8h. Furthermore, a plausible mineralization pathway for the thiamethoxam degradation was proposed based on the identification of by-products such as aromatic intermediates, carboxylic acids and inorganic ions released throughout electro-Fenton process. Copyright © 2016 Elsevier B.V. All rights reserved.

  18. Effect of electrolyte temperature on the thickness of anodic aluminium oxide (AAO layer

    Directory of Open Access Journals (Sweden)

    P. Michal

    2016-07-01

    Full Text Available Effect of electrolyte temperature on the thickness of resulting oxide layer has been studied. Unlike previous published studies this article was aimed to monitor the relationship between electrolyte temperature and resulting AAO layer thickness in interaction with other input factors affecting during anodizing process under special process condition, i.e. lower concentration of sulphuric acid, oxalic acid, boric acid and sodium chloride. According to Design of Experiments (DOE 80 individual test runs of experiment were carried out. Using statistical analysis and artificial intelligence for evaluation, the computational model predicting the thickness of oxide layer in the range from 5 / μm to 15 / μm with tolerance ± 0,5 / μm was developed.

  19. Electrolysis of metal oxides in MgCl2 based molten salts with an inert graphite anode.

    Science.gov (United States)

    Yuan, Yating; Li, Wei; Chen, Hualin; Wang, Zhiyong; Jin, Xianbo; Chen, George Z

    2016-08-15

    Electrolysis of solid metal oxides has been demonstrated in MgCl2-NaCl-KCl melt at 700 °C taking the electrolysis of Ta2O5 as an example. Both the cathodic and anodic processes have been investigated using cyclic voltammetry, and potentiostatic and constant voltage electrolysis, with the cathodic products analysed by XRD and SEM and the anodic products by GC. Fast electrolysis of Ta2O5 against a graphite anode has been realized at a cell voltage of 2 V, or a total overpotential of about 400 mV. The energy consumption was about 1 kW h kgTa(-1) with a nearly 100% Ta recovery. The cathodic product was nanometer Ta powder with sizes of about 50 nm. The main anodic product was Cl2 gas, together with about 1 mol% O2 gas and trace amounts of CO. The graphite anode was found to be an excellent inert anode. These results promise an environmentally-friendly and energy efficient method for metal extraction by electrolysis of metal oxides in MgCl2 based molten salts.

  20. Nano structured porous anodized aluminium oxide by using C2H2O4 for electronic applications: Study of the cell potential effects on formation of porous alumina

    International Nuclear Information System (INIS)

    Nur Hafiza Mohd Najib; Derman, M.N.M.; Nuzaihan, M.N.; Nazwa, T.; Azniza, A.

    2011-01-01

    In this research, a nano porous anodized aluminium oxide AAO thin film was successfully grown onto oxide layer on silicon substrate. The anodization of Si/ SiO 2 / Al substrate was conducted in a vigorous stirring oxalic acid bath solution. The rate of growth, morphology and also the kinetic study of the AAO thin film were investigated. The resulting array, pores structure and pores density of AAO strongly depends on an applied voltage of the anodizing process. (author)

  1. Ceria-Based Anodes for Next Generation Solid Oxide Fuel Cells

    Science.gov (United States)

    Mirfakhraei, Behzad

    Mixed ionic and electronic conducting materials (MIECs) have been suggested to represent the next generation of solid oxide fuel cell (SOFC) anodes, primarily due to their significantly enhanced active surface area and their tolerance to fuel components. In this thesis, the main focus has been on determining and tuning the physicochemical and electrochemical properties of ceria-based MIECs in the versatile perovskite or fluorite crystal structures. In one direction, BaZr0.1Ce0.7Y0.1 M0.1O3-delta (M = Fe, Ni, Co and Yb) (BZCY-M) perovskites were synthesized using solid-state or wet citric acid combustion methods and the effect of various transition metal dopants on the sintering behavior, crystal structure, chemical stability under CO2 and H 2S, and electrical conductivity, was investigated. BZCY-Ni, synthesized using the wet combustion method, was the best performing anode, giving a polarization resistance (RP) of 0.4 O.cm2 at 800 °C. Scanning electron microscopy and X-ray diffraction analysis showed that this was due to the exsolution of catalytic Ni nanoparticles onto the oxide surface. Evolving from this promising result, the effect of Mo-doped CeO 2 (nCMO) or Ni nanoparticle infiltration into a porous Gd-doped CeO 2 (GDC) anode (in the fluorite structure) was studied. While 3 wt. % Ni infiltration lowered RP by up to 90 %, giving 0.09 O.cm2 at 800 °C and exhibiting a ca. 5 times higher tolerance towards 10 ppm H2, nCMO infiltration enhanced the H2 stability by ca. 3 times, but had no influence on RP. In parallel work, a first-time study of the Ce3+ and Ce 4+ redox process (pseudocapacitance) within GDC anode materials was carried out using cyclic voltammetry (CV) in wet H2 at high temperatures. It was concluded that, at 500-600 °C, the Ce3+/Ce 4+ reaction is diffusion controlled, probably due to O2- transport limitations in the outer 5-10 layers of the GDC particles, giving a very high capacitance of ca. 70 F/g. Increasing the temperature ultimately

  2. Effective improvement of interface modified strontium titanate based solid oxide fuel cell anodes by infiltration with nano-sized palladium and gadolinium-doped cerium oxide

    DEFF Research Database (Denmark)

    Abdul Jabbar, Mohammed Hussain; Høgh, Jens Valdemar Thorvald; Zhang, Wei

    2013-01-01

    The development of low temperature solid oxide fuel cell (SOFC) anodes by infiltration of Pd/Gd-doped cerium oxide (CGO) electrocatalysts in Nb-doped SrTiO3 (STN) backbones has been investigated. Modification of the electrode/electrolyte interface by thin layer of spin-coated CGO (400-500 nm) con...

  3. Niobium based coatings for dental implants

    International Nuclear Information System (INIS)

    Ramirez, G.; Rodil, S.E.; Arzate, H.; Muhl, S.; Olaya, J.J.

    2011-01-01

    Niobium based thin films were deposited on stainless steel (SS) substrates to evaluate them as possible biocompatible surfaces that might improve the biocompatibility and extend the life time of stainless steel dental implants. Niobium nitride and niobium oxide thin films were deposited by reactive unbalanced magnetron sputtering under standard deposition conditions without substrate bias or heating. The biocompatibility of the surfaces was evaluated by testing the cellular adhesion and viability/proliferation of human cementoblasts during different culture times, up to 7 days. The response of the films was compared to the bare substrate and pieces of Ti6Al4V; the most commonly used implant material for orthopedics and osteo-synthesis applications. The physicochemical properties of the films were evaluated by different means; X-ray diffraction, Rutherford backscattering spectroscopy and contact angle measurements. The results suggested that the niobium oxide films were amorphous and of stoichiometric Nb 2 O 5 (a-Nb 2 O 5 ), while the niobium nitride films were crystalline in the FCC phase (c-NbN) and were also stoichiometric with an Nb to N ratio of one. The biological evaluation showed that the biocompatibility of the SS could be improved by any of the two films, but neither was better than the Ti6Al4V alloy. On the other hand, comparing the two films, the c-NbN seemed to be a better surface than the oxide in terms of the adhesion and proliferation of human cemetoblasts.

  4. Fabrication of TiO2 Crystalline Coatings by Combining Ti-6Al-4V Anodic Oxidation and Heat Treatments

    Directory of Open Access Journals (Sweden)

    María Laura Vera

    2015-01-01

    Full Text Available The bio- and hemocompatibility of titanium alloys are due to the formation of a TiO2 layer. This natural oxide may have fissures which are detrimental to its properties. Anodic oxidation is used to obtain thicker films. By means of this technique, at low voltages oxidation, amorphous and low roughness coatings are obtained, while, above a certain voltage, crystalline and porous coatings are obtained. According to the literature, the crystalline phases of TiO2, anatase, and rutile would present greater biocompatibility than the amorphous phase. On the other hand, for hemocompatible applications, smooth and homogeneous surfaces are required. One way to obtain crystalline and homogeneous coatings is by heat treatments after anodic oxidation. The aim of this study is to evaluate the influence of heat treatments on the thickness, morphology, and crystalline structure of the TiO2 anodic coatings. The characterization was performed by optical and scanning electron microscopy, X-ray diffraction, and X-ray reflectometry. Coatings with different colors of interference were obtained. There were no significant changes in the surface morphology and roughness after heat treatment of 500°C. Heat treated coatings have different proportions of the crystalline phases, depending on the voltage of anodic oxidation and the temperature of the heat treatment.

  5. Quasi–solid state rechargeable Na-CO2 batteries with reduced graphene oxide Na anodes

    Science.gov (United States)

    Hu, Xiaofei; Li, Zifan; Zhao, Yaran; Sun, Jianchao; Zhao, Qing; Wang, Jianbin; Tao, Zhanliang; Chen, Jun

    2017-01-01

    Na-CO2 batteries using earth-abundant Na and greenhouse gas CO2 are promising tools for mobile and stationary energy storage, but they still pose safety risks from leakage of liquid electrolyte and instability of the Na metal anode. These issues result in extremely harsh operating conditions of Na-CO2 batteries and increase the difficulty of scaling up this technology. We report the development of quasi–solid state Na-CO2 batteries with high safety using composite polymer electrolyte (CPE) and reduced graphene oxide (rGO) Na anodes. The CPE of PVDF-HFP [poly(vinylidene fluoride-co-hexafluoropropylene)]–4% SiO2/NaClO4–TEGDME (tetraethylene glycol dimethyl ether) has high ion conductivity (1.0 mS cm−1), robust toughness, a nonflammable matrix, and strong electrolyte-locking ability. In addition, the rGO-Na anode presents fast and nondendritic Na+ plating/stripping (5.7 to 16.5 mA cm−2). The improved kinetics and safety enable the constructed rGO-Na/CPE/CO2 batteries to successfully cycle in wide CO2 partial pressure window (5 to 100%, simulated car exhaust) and especially to run for 400 cycles at 500 mA g−1 with a fixed capacity of 1000 mA·hour g−1 in pure CO2. Furthermore, we scaled up the reversible capacity to 1.1 A·hour in pouch-type batteries (20 × 20 cm, 10 g, 232 Wh kg−1). This study makes quasi–solid state Na-CO2 batteries an attractive prospect. PMID:28164158

  6. Buffered Electrochemical Polishing of Niobium

    Energy Technology Data Exchange (ETDEWEB)

    Ciovati, Gianluigi [Thomas Jefferson National Accelerator Facility (TJNAF), Newport News, VA (United States); Tian, Hui [Thomas Jefferson National Accelerator Facility (TJNAF), Newport News, VA (United States); College of William and Mary, Williamsburg, VA (United States); Corcoran, Sean [Virginia Polytechnic Inst. and State Univ. (Virginia Tech), Blacksburg, VA (United States)

    2011-03-01

    The standard preparation of superconducting radio-frequency (SRF) cavities made of pure niobium include the removal of a 'damaged' surface layer, by buffered chemical polishing (BCP) or electropolishing (EP), after the cavities are formed. The performance of the cavities is characterized by a sharp degradation of the quality factor when the surface magnetic field exceeds about 90 mT, a phenomenon referred to as 'Q-drop.' In cavities made of polycrystalline fine grain (ASTM 5) niobium, the Q-drop can be significantly reduced by a low-temperature (? 120 °C) 'in-situ' baking of the cavity if the chemical treatment was EP rather than BCP. As part of the effort to understand this phenomenon, we investigated the effect of introducing a polarization potential during buffered chemical polishing, creating a process which is between the standard BCP and EP. While preliminary results on the application of this process to Nb cavities have been previously reported, in this contribution we focus on the characterization of this novel electrochemical process by measuring polarization curves, etching rates, surface finish, electrochemical impedance and the effects of temperature and electrolyte composition. In particular, it is shown that the anodic potential of Nb during BCP reduces the etching rate and improves the surface finish.

  7. Effect of Samarium Oxide on the Electrical Conductivity of Plasma-Sprayed SOFC Anodes

    Science.gov (United States)

    Panahi, S. N.; Samadi, H.; Nemati, A.

    2016-10-01

    Solid oxide fuel cells (SOFCs) are rapidly becoming recognized as a new alternative to traditional energy conversion systems because of their high energy efficiency. From an ecological perspective, this environmentally friendly technology, which produces clean energy, is likely to be implemented more frequently in the future. However, the current SOFC technology still cannot meet the demands of commercial applications due to temperature constraints and high cost. To develop a marketable SOFC, suppliers have tended to reduce the operating temperatures by a few hundred degrees. The overall trend for SOFC materials is to reduce their service temperature of electrolyte. Meanwhile, it is important that the other components perform at the same temperature. Currently, the anodes of SOFCs are being studied in depth. Research has indicated that anodes based on a perovskite structure are a more promising candidate in SOFCs than the traditional system because they possess more favorable electrical properties. Among the perovskite-type oxides, SrTiO3 is one of the most promising compositions, with studies demonstrating that SrTiO3 exhibits particularly favorable electrical properties in contrast with other perovskite-type oxides. The main purpose of this article is to describe our study of the effect of rare-earth dopants with a perovskite structure on the electrical behavior of anodes in SOFCs. Sm2O3-doped SrTiO3 synthesized by a solid-state reaction was coated on substrate by atmospheric plasma spray. To compare the effect of the dopant on the electrical conductivity of strontium titanate, different concentrations of Sm2O3 were used. The samples were then investigated by x-ray diffraction, four-point probe at various temperatures (to determine the electrical conductivity), and a scanning electron microscope. The study showed that at room temperature, nondoped samples have a higher electrical resistance than doped samples. As the temperature was increased, the electrical

  8. Early-stage osseointegration capability of a submicrofeatured titanium surface created by microroughening and anodic oxidation.

    Science.gov (United States)

    Yamada, Masahiro; Ueno, Takeshi; Minamikawa, Hajime; Ikeda, Takayuki; Nakagawa, Kaori; Ogawa, Takahiro

    2013-09-01

    The role of nanoscale/submicron morphological features in the process of osseointegration is largely unknown. This study reports the creation of a unique submicrofeatured titanium surface by a combination of anodic oxidation and sandblasting and determines how the addition of this submicrofeature to a microroughened surface affects the early-stage process of osseointegration. Nonmicroroughened implants were prepared by machining Ti-6Al-4V alloy in a cylindrical form (1 mm diameter and 2 mm long). Microroughened implants were prepared by sandblasting machined implants, while submicrofeatured implants were created by anodic oxidation of the sandblasted implants. Implants were placed into rat femurs and subjected to biomechanical, interfacial, and histological analyses at 1 and 2 weeks post-implantation (n = 6). The submicrotopography was characterized by 50-300 nm nodules and pits in addition to other submicron-level irregularities formed entirely within the sandblast-created microstructures. The biomechanical strength of osseointegration increased continuously from week 1 to 2 for the submicrofeatured implants but not for the microroughened implants. A significant increase in bone-implant contact and bone volume, as well as a reduction in soft tissue intervention, were commonly found for the microroughened surface and the submicrofeatured surface compared with the nonmicroroughened surface. However, there were no differences in these parameters between the microroughened surface and the submicrofeatured surface. An extensive area of bone tissue at the submicrofeatured implant interface was retained intact after biomechanical shear testing, while the microroughened implant-tissue interface showed a gap along the entire axis of the implant, leading to clear separation of the tissue during the shear procedure. This study demonstrates that a submicrofeatured titanium surface created by a combination of sandblasting and anodic oxidation enhances the strength of

  9. Proposal of a new biokinetic model for niobium

    International Nuclear Information System (INIS)

    Oliveira, Roges

    2006-01-01

    There are two niobium isotopes generated in nuclear power plants: 95 Nb and 94 Nb. Workers and members of the public are subjects to intake these radionuclides in accident situation. For dose calculation purpose, it is very important to develop a model that describes in a more realistic way the kinetics of niobium inside of the human body. Presently the model adopted by ICRP (ICRP, 1989) is based on animal studies and describes the behavior of niobium in human being in a simple manner. The new model proposal describes the kinetics of the niobium from the intake into the blood until the excretion, doing this in a more realistic form and considering not only data from animals but data from human beings as well. For this objective, a workers group of a niobium extraction and processing industry exposed to stable niobium (93 Nb) in oxide insoluble form with associated uranium, was monitored for uranium and niobium determination in urinary and fecal excretion, by mass spectrometry. Based in the ratios of the niobium concentration in urinary and faecal excretion of this workers and animal data study, a new biokinetic model for niobium was proposed, with the followings modifications relative to ICRP model: a new compartment that represents muscular tissue; the fractions which are deposited into the compartment are modified; a third component in the retention equation of the bone tissue; introduction of recirculation between organs and blood. The new model was applied for a case of accidental intake and described adequately the experimental data

  10. Realization of tin oxide like anode for the manufacture of the organic solar cells

    Directory of Open Access Journals (Sweden)

    Khelil A.

    2012-06-01

    Full Text Available The transparent oxides such as SnO2, In2O3 and ZnO continue to arouse a private interest for their various applications. The objective of the various studies being to carry out the layers which are simultaneously most transparent and most conducting possible. Thus in the field of the solar spectrum, the transmission of the layers must be higher than 80% and their conductivity exceeding 103 (Ohm.cm-1. Their transparency which is related to the value of their forbidden band must be higher than 3.7 e V. Their electric properties as for them depend on the composition of the layers and a possible doping. In this work, one characterized layers of SnO2 deposited by chemical pulverization, one carried out measurements by, electronic scan microscopy, diffraction of x-rays and also of the optical measurements and electronic. It results from it that the layers are conducting and transparent in the visible one but they are relatively rough, following its characterizations, one carried out organic photovoltaic cells using these layers of SnO2 and also of the commercial ITO like anode in these components. More particularly one was interested in the influence of the presence of a fine layer of gold between the anode and organic material.

  11. Cadmium, lead and silver adsorption in hydrous niobium oxide(V) prepared by precipitation in homogeneous solution method; Adsorcao de chumbo, cadmio e prata em oxido de niobio(V) hidratado preparado pelo metodo da precipitacao em solucao homogenea

    Energy Technology Data Exchange (ETDEWEB)

    Tagliaferro, Geronimo V.; Pereira, Paulo Henrique F.; Rodrigues, Liana Alvares; Silva, Maria Lucia Caetano Pinto da, E-mail: fernandes_eng@yahoo.com.b [Universidade de Sao Paulo (USP), Lorena, SP (Brazil). Escola de Engenharia. Dept. de Engenharia Quimica

    2011-07-01

    This paper describes the adsorption of heavy metals ions from aqueous solution by hydrous niobium oxide. Three heavy metals were selected for this study: cadmium, lead and silver. Adsorption isotherms were well fitted by Langmuir model. Maximum adsorption capacity (Q{sub 0}) for Pb{sup 2+}, Ag{sup +} and Cd{sup 2+} was found to be 452.5, 188.68 and 8.85 mg g{sup -1}, respectively. (author)

  12. Synthesis of bismuth (III oxide films based anodes for electrochemical degradation of reactive blue 19 and crystal violet

    Directory of Open Access Journals (Sweden)

    Petrović Milica M.

    2014-01-01

    Full Text Available The Bi2O3 films-based anodes were synthesized by electrodeposition of Bi on stainless steel substrate at constant current density and during different deposition times, fallowed by calcination, forming Bi2O3. The thickness of the films was determined by two methods: the observation under the microscope and by calculation from mass difference. Electrochemical proceses at the anodes were ivestigated by linear sweep voltammetry. At the anodes obtained within 2, 5, 10 and 15 minutes of deposition, two dyes, namely: Reactive Blue 19 and Crystal Violet, were decolorized by oxidation with •OH radical, generated from H2O2 decomposition at the anodes. Decoloration times of the anodes varied, and the shortest one was achieved with the anode obtained during 5 minutes of deposition, with the film thickness of 2.5±0.3 μm. The optimal H2O2 concentration for the dyes degradation was found to be 10 mmol dm-3. [Projekat Ministarstva nauke Republike Srbije, br. ТR 34008

  13. Bio-electro oxidation of indigo carmine by using microporous activated carbon fiber felt as anode and bioreactor support.

    Science.gov (United States)

    Garcia, Luane Ferreira; Rodrigues Siqueira, Ana Claudia; Lobón, Germán Sanz; Marcuzzo, Jossano Saldanha; Pessela, Benevides Costa; Mendez, Eduardo; Garcia, Telma Alves; de Souza Gil, Eric

    2017-11-01

    The bioremediation and electro-oxidation (EO) processes are included among the most promising cleaning and decontamination mechanisms of water. The efficiency of bioremediation is dictated by the biological actuator for a specific substrate, its suitable immobilization and all involved biochemical concepts. The EO performance is defined by the anode efficiency to perform the complete mineralization of target compounds and is highlighted by the low or null use of reagent. Recently, the combination of both technologies has been proposed. Thus, the development of high efficient, low cost and eco-friendly anodes for sustainable EO, as well as, supporting devices for immobilization of biological systems applied in bioremediation is an open field of research. Therefore, the aim of this work was to promote the bio-electrochemical remediation of indigo carmine dye (widely common in textile industry), using new anode based on a microporous activated carbon fiber felt (ACFF) and ACFF with immobilized Laccase (Lcc) from Pycnoporus sanguineus. The results were discolorations of 62.7% with ACFF anode and 83.60% with ACFF-MANAE-Lcc anode, both for 60 min in tap water. This remediation rates show that this new anode has low cost and efficiency in the degradation of indigo dye and can be applied for other organic pollutant. Copyright © 2017 Elsevier Ltd. All rights reserved.

  14. Corrosion resistance of the substrates for the cryogenic gyroscope and electrodeposition of the superconductive niobium coatings

    Science.gov (United States)

    Dubrovskiy, A. R.; Okunev, M. A.; Makarova, O. V.; Kuznetsov, S. A.

    2017-05-01

    The interaction of different materials with the niobium containing melt was investigated. As substrate materials the ceramics, beryllium and carbopyroceram were chosen. Several spherical ceramic and beryllium samples were coated with protective molybdenum and niobium films by magnetron sputtering and PVD, respectively. After the experiment (exposition time 10 min) the exfoliation of molybdenum film from ceramic samples was observed due to interaction of the substrate with the melt. The niobium protective coatings reacted with the melt with niobium oxide formation. The beryllium samples regardless of the shape and the presence of the protective films were dissolved in the niobium containing melt due to more negative electrode potential comparing with niobium one. The carbopyroceram samples were exposed in the melt during 3 and 12 h. It was found that the carbopyroceram not corrodes in the niobium containing melt. The optimal regimes for electrodeposition of smooth uniform niobium coatings with the thickness up to 50 μm on carbopyroceram spheres were found.

  15. Developing a Thermal- and Coking-Resistant Cobalt-Tungsten Bimetallic Anode Catalyst for Solid Oxide Fuel Cells

    NARCIS (Netherlands)

    Yan, N.; Pandey, J.; Zeng, Y.; Amirkhiz, B.S.; Hua, B.; Geels, N.J.; Luo, J.L.; Rothenberg, G.

    2016-01-01

    We report the development of a novel Co–W bimetallic anode catalyst for solid oxide fuel cells (SOFCs) via a facile infiltration-annealing process. Using various microscopic and spectroscopic measurements, we find that the formed intermetallic nanoparticles are highly thermally stable up to 900 °C

  16. Gallium oxide nanorods as novel, safe and durable anode material for Li- and Na-ion batteries

    NARCIS (Netherlands)

    Meligrana, Giuseppina; Lueangchaichaweng, Warunee; Colo, Francesca; Destro, Matteo; Fiorilli, Sonia; Pescarmona, Paolo P.; Gerbaldi, Claudio

    2017-01-01

    Gallium oxide nanorods prepared by template-free synthesis are reported for the first time as safe and durable anode material for lithium- and sodium-ion batteries. The ambient temperature electrochemical response of the nanorods, tested by cyclic voltammetry and constant-current reversible cycling,

  17. Anodized Aluminum Oxide Templated Synthesis of Metal-Organic Frameworks Used as Membrane Reactors.

    Science.gov (United States)

    Yu, Yifu; Wu, Xue-Jun; Zhao, Meiting; Ma, Qinglang; Chen, Junze; Chen, Bo; Sindoro, Melinda; Yang, Jian; Han, Shikui; Lu, Qipeng; Zhang, Hua

    2017-01-09

    The incorporation of metal-organic frameworks (MOFs) into membrane-shaped architectures is of great importance for practical applications. The currently synthesized MOF-based membranes show many disadvantages, such as poor compatibility, low dispersity, and instability, which severely limit their utility. Herein, we present a general, facile, and robust approach for the synthesis of MOF-based composite membranes through the in situ growth of MOF plates in the channels of anodized aluminum oxide (AAO) membranes. After being used as catalysis reactors, they exhibit high catalytic performance and stability in the Knoevenagel condensation reaction. The high catalytic performance might be attributed to the intrinsic structure of MOF-based composite membranes, which can remove the products from the reaction zone quickly, and prevent the aggregation and loss of catalysts during reaction and recycling process. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Effect of wastewater quality parameters on coliform inactivation by tin oxide anodes.

    Science.gov (United States)

    Teel, Amy L; Watts, Richard J

    2018-04-16

    The effect of six water quality constituents on wastewater effluent disinfection by tin oxide anodes (TOAs) was investigated in single cell laboratory reactors. Several concentrations of suspended solids, chemical oxygen demand (COD), alkalinity, ammonia-nitrogen, nitrite-nitrogen, and nitrate-nitrogen were added to media containing 10 6 total coliform bacteria mL -1 . Current was applied through the TOAs, and coliform bacteria viability was analyzed over time. Over 99.9% inactivation of coliform bacteria was found over 15 min in TOA reactors. Concentrations of the six water quality constituents typical of concentrations found in wastewaters had no effect on TOA disinfection efficacy. The results of this research demonstrate that TOAs, which could potentially be powered by solar panels, have potential as a sustainable disinfection process compared to chlorine, ozone, and ultraviolet light.

  19. Indium-Doped Zinc Oxide Thin Films as Effective Anodes of Organic Photovoltaic Devices

    Directory of Open Access Journals (Sweden)

    Ziyang Hu

    2011-01-01

    Full Text Available Indium-doped zinc oxide (IZO thin films were prepared by low-cost ultrasonic spray pyrolysis (USP. Both a low resistivity (3.13×10−3 Ω cm and an average direct transmittance (400∼1500 nm about 80% of the IZO films were achieved. The IZO films were investigated as anodes in bulk-heterojunction organic photovoltaic (OPV devices based on poly(3-hexylthiophene and [6,6]-phenyl C61-butyric acid methyl ester. The device fabricated on IZO film-coated glass substrate showed an open circuit voltage of 0.56 V, a short circuit current of 8.49 mA cm-2, a fill factor of 0.40, and a power conversion efficiency of 1.91%, demonstrating that the IZO films prepared by USP technique are promising low In content and transparent electrode candidates of low-cost OPV devices.

  20. Boron-doped diamond anodic oxidation of ethidium bromide: Process optimization by response surface methodology

    International Nuclear Information System (INIS)

    Zhang Chunyong; Yang Lijiao; Rong Fei; Fu Degang; Gu Zhongze

    2012-01-01

    Highlights: ► Boron-doped diamond was used to degrade ethidium bromide. ► The process was optimized by a central composite rotatable design coupled with response surface methodology. ► Applied current is proved to be the most significant variable. ► A possible reaction sequence involving all the detected byproducts was proposed. - Abstract: The degradation of ethidium bromide (EtBr), a DNA intercalating pollutant, had been studied by anodic oxidation on boron-doped diamond (BDD) electrode under galvanostatic conditions. A central composite rotatable design coupled with response surface methodology was implemented to optimize the various operating parameters involved, among initial pH, flow rate, applied current and supporting electrolyte concentration, on the treatment efficiency; the latter was assessed in terms of color removal, COD removal, specific energy consumption and general current efficiency. Of the four parameters involved, applied current had a considerable effect on all the response factors. Optimum EtBr degradation was achieved by applying a current of 0.90 A, 9.0 mM Na 2 SO 4 , flow rate of 400 ml min −1 and pH 6.2 at 60 min of electrolysis, being reduced color by 80.2% and COD by 29.7%, with an energy consumption of 398.32 kW h (kg COD) −1 and a general current efficiency of 10.1%. Under these optimized conditions, EtBr decays followed pseudo first-order kinetics. Moreover, HPLC analysis of the BDD-treated solution allowed the detection of a number of reaction intermediates, and a possible reaction sequence involving all the detected byproducts was proposed for the electrochemical oxidation of EtBr on BDD anode.

  1. An anode with aluminum doped on zinc oxide thin films for organic light emitting devices

    International Nuclear Information System (INIS)

    Xu Denghui; Deng Zhenbo; Xu Ying; Xiao Jing; Liang Chunjun; Pei Zhiliang; Sun Chao

    2005-01-01

    Doped zinc oxides are attractive alternative materials as transparent conducting electrode because they are nontoxic and inexpensive compared with indium tin oxide (ITO). Transparent conducting aluminum-doped zinc oxide (AZO) thin films have been deposited on glass substrates by DC reactive magnetron sputtering method. Films were deposited at a substrate temperature of 150-bar o C in 0.03 Pa of oxygen pressure. The electrical and optical properties of the film with the Al-doping amount of 2 wt% in the target were investigated. For the 300-nm thick AZO film deposited using a ZnO target with an Al content of 2 wt%, the lowest electrical resistivity was 4x10 -4 Ωcm and the average transmission in the visible range 400-700 nm was more than 90%. The AZO film was used as an anode contact to fabricate organic light-emitting diodes. The device performance was measured and the current efficiency of 2.9 cd/A was measured at a current density of 100 mA/cm 2

  2. Propham mineralization in aqueous medium by anodic oxidation using boron-doped diamond anode: influence of experimental parameters on degradation kinetics and mineralization efficiency.

    Science.gov (United States)

    Ozcan, Ali; Sahin, Yücel; Koparal, A Savaş; Oturan, Mehmet A

    2008-06-01

    This study aims the removal of a carbamate herbicide, propham, from aqueous solution by direct electrochemical advanced oxidation process using a boron-doped diamond (BDD) anode. This electrode produces large quantities of hydroxyl radicals from oxidation of water, which leads to the oxidative degradation of propham up to its total mineralization. Effect of operational parameters such as current, temperature, pH and supporting electrolyte on the degradation and mineralization rate was studied. The applied current and temperature exert a prominent effect on the total organic carbon (TOC) removal rate of the solutions. The mineralization of propham can be performed at any pH value between 3 and 11 without any loss in oxidation efficiency. The propham decay and its overall mineralization reaction follows a pseudo-first-order kinetics. The apparent rate constant value of propham oxidation was determined as 4.8 x 10(-4)s(-1) at 100 mA and 35 degrees C in the presence of 50mM Na(2)SO(4) in acidic media (pH: 3). A general mineralization sequence was proposed considering the identified oxidation intermediates.

  3. Fabrication of super slippery sheet-layered and porous anodic aluminium oxide surfaces and its anticorrosion property

    Science.gov (United States)

    Song, Tingting; Liu, Qi; Liu, Jingyuan; Yang, Wanlu; Chen, Rongrong; Jing, Xiaoyan; Takahashi, Kazunobu; Wang, Jun

    2015-11-01

    Inspired by natural plants such as Nepenthes pitcher plants, super slippery surfaces have been developed to improve the attributes of repellent surfaces. In this report, super slippery porous anodic aluminium oxide (AAO) surfaces have fabricated by a simple and reproducible method. Firstly, the aluminium substrates were treated by an anodic process producing micro-nano structured sheet-layered pores, and then immersed in Methyl Silicone Oil, Fluororalkylsilane (FAS) and DuPont Krytox, respectively, generating super slippery surfaces. Such a good material with excellent anti-corrosion property through a simple and repeatable method may be potential candidates for metallic application in anti-corrosion and extreme environment.

  4. Multi-electrolyte-step anodic aluminum oxide method for the fabrication of self-organized nanochannel arrays

    Science.gov (United States)

    2012-01-01

    Nanochannel arrays were fabricated by the self-organized multi-electrolyte-step anodic aluminum oxide [AAO] method in this study. The anodization conditions used in the multi-electrolyte-step AAO method included a phosphoric acid solution as the electrolyte and an applied high voltage. There was a change in the phosphoric acid by the oxalic acid solution as the electrolyte and the applied low voltage. This method was used to produce self-organized nanochannel arrays with good regularity and circularity, meaning less power loss and processing time than with the multi-step AAO method. PMID:22333268

  5. Evaluating tetracycline degradation pathway and intermediate toxicity during the electrochemical oxidation over a Ti/Ti4O7anode.

    Science.gov (United States)

    Wang, Jianbing; Zhi, Dan; Zhou, Hao; He, Xuwen; Zhang, Dayi

    2018-03-12

    Tetracycline (TC) is one of the most widely used antibiotics with significant impacts on human health and thus it needs appropriate approaches for its removal. In the present study, we evaluated the performance and complete pathway of the TC electrochemical oxidation on a Ti/Ti 4 O 7 anode prepared by plasma spraying. Morphological data and composition analysis indicated a compact coating layer on the anode, which had the characteristic peaks of Ti 4 O 7 as active constituent. The TC electrochemical oxidation on the Ti/Ti 4 O 7 anode followed a pseudo-first-order kinetics, and the TC removal efficiency reached 95.8% in 40 min. The influential factors on TC decay kinetics included current density, anode-cathode distance and initial TC concentration. This anode also had high durability and the TC removal efficiency was maintained over 95% after five times reuse. For the first time, we unraveled the complete pathway of the TC electrochemical oxidation using high-performance liquid chromatograph (HPLC) and gas chromatograph (GC) coupled with mass spectrometer (MS). ·OH radicals produced from electrochemical oxidation attack the double bond, phenolic group and amine group of TC, forming a primary intermediate (m/z = 461), secondary intermediates (m/z = 432, 477 and 509) and tertiary intermediates (m/z = 480, 448 and 525). The latter were further oxidized to the key downstream intermediate (m/z = 496), followed by further downstream intermediates (m/z = 451, 412, 396, 367, 351, 298 and 253) and eventually short-chain carboxylic acids. We also evaluated the toxicity change during the electrochemical oxidation process with bioluminescent bacteria. The bioluminescence inhibition ratio peaked at 10 min (55.41%), likely owing to the high toxicity of intermediates with m/z = 461, 432 and 477 as obtained from quantitative structure activity relationship (QSAR) analysis. The bioluminescence inhibition ratio eventually decreased to 16.78% in 40

  6. Solid oxide fuel cell bi-layer anode with gadolinia-doped ceria for utilization of solid carbon fuel

    Science.gov (United States)

    Kellogg, Isaiah D.; Koylu, Umit O.; Dogan, Fatih

    Pyrolytic carbon was used as fuel in a solid oxide fuel cell (SOFC) with a yttria-stabilized zirconia (YSZ) electrolyte and a bi-layer anode composed of nickel oxide gadolinia-doped ceria (NiO-GDC) and NiO-YSZ. The common problems of bulk shrinkage and emergent porosity in the YSZ layer adjacent to the GDC/YSZ interface were avoided by using an interlayer of porous NiO-YSZ as a buffer anode layer between the electrolyte and the NiO-GDC primary anode. Cells were fabricated from commercially available component powders so that unconventional production methods suggested in the literature were avoided, that is, the necessity of glycine-nitrate combustion synthesis, specialty multicomponent oxide powders, sputtering, or chemical vapor deposition. The easily-fabricated cell was successfully utilized with hydrogen and propane fuels as well as carbon deposited on the anode during the cyclic operation with the propane. A cell of similar construction could be used in the exhaust stream of a diesel engine to capture and utilize soot for secondary power generation and decreased particulate pollution without the need for filter regeneration.

  7. Degradation of 1-hydroxy-2,4-dinitrobenzene from aqueous solutions by electrochemical oxidation: role of anodic material.

    Science.gov (United States)

    Quiroz, Marco A; Sánchez-Salas, José L; Reyna, Silvia; Bandala, Erick R; Peralta-Hernández, Juan M; Martínez-Huitle, Carlos A

    2014-03-15

    Electrochemical oxidation (ECOx) of 1-hydroxy-2,4-dinitrobenzene (or 2,4-dinitrophenol: 2,4-DNP) in aqueous solutions by electrolysis under galvanostatic control was studied at Pb/PbO2, Ti/SnO2, Ti/IrxRuySnO2 and Si/BDD anodes as a function of current density applied. Oxidative degradation of 2,4-DNP has clearly shown that electrode material and the current density applied were important parameters to optimize the oxidation process. It was observed that 2,4-DNP was oxidized at few substrates to CO2 with different results, obtaining good removal efficiencies at Pb/PbO2, Ti/SnO2 and Si/BDD anodes. Trends in degradation way depend on the production of hydroxyl radicals (OH) on these anodic materials, as confirmed in this study. Furthermore, HPLC results suggested that two kinds of intermediates were generated, polyhydroxylated intermediates and carboxylic acids. The formation of these polyhydroxylated intermediates seems to be associated with the denitration step and substitution by OH radicals on aromatic rings, this being the first proposed step in the reaction mechanism. These compounds were successively oxidized, followed by the opening of aromatic rings and the formation of a series of carboxylic acids which were at the end oxidized into CO2 and H2O. On the basis of these information, a reaction scheme was proposed for each type of anode used for 2,4-D oxidation. Copyright © 2014 Elsevier B.V. All rights reserved.

  8. Behaviour of niobium during early Earth’s differentiation: insights from its local structure and oxidation state in silicate melts at high pressure

    Science.gov (United States)

    Sanloup, C.; Cochain, B.; de Grouchy, C.; Glazyrin, K.; Konôpkova, Z.; Liermann, H.-P.; Kantor, I.; Torchio, R.; Mathon, O.; Irifune, T.

    2018-02-01

    Niobium (Nb) is one of the key trace elements used to understand Earth’s formation and differentiation, and is remarkable for its deficiency relative to tantalum in terrestrial rocks compared to the building chondritic blocks. In this context, the local environment of Nb in silica-rich melts and glasses is studied by in situ x-ray absorption spectroscopy (XAS) at high pressure (P) up to 9.3 GPa and 1350 K using resistive-heating diamond-anvil cells. Nb is slightly less oxidized in the melt (intermediate valence between  +4 and  +5) than in the glass (+5), an effect evidenced from the shift of the Nb-edge towards lower energies. Changes in the pre-edge features are also observed between melt and glass states, consistently with the observed changes in oxidation state although likely enhanced by temperature (T) effects. The oxidation state of Nb is not affected by pressure neither in the molten nor glassy states, and remains constant in the investigated P-range. The Nb-O coordination number is constant and equal to 6.3+/-0.4 below 5 GPa, and only progressively increases up to 7.1+/-0.4 at 9.3 GPa, the maximum P investigated. If these findings were to similarly apply to basaltic melts, that would rule out the hypothesis of Nb/Ta fractionation during early silicate Earth’s differentiation, thus reinforcing the alternative hypothesis of fractionation during core formation on reduced pre-planetary bodies.

  9. NIR fluorescence spectroscopic investigations of Er{sup 3+}-ions doped borate based tellurium calcium zinc niobium oxide glasses

    Energy Technology Data Exchange (ETDEWEB)

    Ravi, O. [Department of Instrumentation, Sri Venkateswara University, Tirupati 517502 (India); Dhoble, S.J. [Department of Physics, RTM Nagpur University, Nagpur 440033 (India); Ramesh, B.; Devarajulu, G. [Department of Physics, Sri Venkateswara University, Tirupati 517502 (India); Reddy, C. Madhukar [Department of Physics, AP Model School, Yerravaripalem 517194 (India); Linganna, K. [Department of Physics, Sri Venkateswara University, Tirupati 517502 (India); Reddy, G. Rajasekhar [Department of Instrumentation, Sri Venkateswara University, Tirupati 517502 (India); Raju, B. Deva Prasad, E-mail: drdevaprasadraju@gmail.com [Department of Physics, Sri Venkateswara University, Tirupati 517502 (India); Department of Future Studies, Sri Venkateswara University, Tirupati 517502 (India)

    2015-08-15

    A series of Er{sup 3+} ions doped tellurium calcium zinc niobium borate glasses were prepared by the melt quenching technique. The prepared samples were investigated by optical absorption and near infrared fluorescence spectroscopic studies. The obtained Judd–Ofelt intensity parameters Ω{sub λ} (λ=2, 4 and 6) were determined through experimental and calculated oscillator strengths obtained from absorption spectra and their results are studied and compared with reported literature. The stark-level energies of {sup 4}I{sub 13/2} excited and {sup 4}I{sub 15/2} ground states were evaluated by using both the absorption and emission measurements. The effect of Er{sup 3+} ion concentration on the emission intensity of {sup 4}I{sub 13/2}→{sup 4}I{sub 15/2} transition was discussed. Intense and broad 1.53 µm infrared fluorescence is observed at 980 nm diode laser excitation. Photoluminescence (PL) and its decay behavior studies were carried out for the transition {sup 4}I{sub 13/2}→{sup 4}I{sub 15/2} at 1.53 µm emission. The broad emission together with higher values of the bandwidth (81 nm), stimulated emission cross-section (32.25×10{sup −22} cm{sup 2}) and lifetime (530 µs for 1.0 mol% of Er{sup 3+}) of level {sup 4}I{sub 13/2} make these glasses attractive for broadband amplifiers. From the analysis of spectroscopic data, the present glass is a prospective photonic material for practical applications in the visible and NIR region. - Highlights: • In this study we prepared TCZNB glasses doped with Er{sup 3+} ions. • Glasses are characterized with absorption, emission and lifetime analysis. • Judd–Ofelt theory is used to calculate radiative properties. • TCZNB glasses could be used as NIR lasers.

  10. Structural characterization of niobium oxide thin films grown on SrTiO3 (111) and (La,Sr)(Al,Ta)O3 (111) substrates

    Science.gov (United States)

    Dhamdhere, Ajit R.; Hadamek, Tobias; Posadas, Agham B.; Demkov, Alexander A.; Smith, David J.

    2016-12-01

    Niobium oxide thin films have been grown by molecular beam epitaxy on SrTiO3 (STO) (111) and (La0.18Sr0.82)(Al0.59Ta0.41)O3 (LSAT) (111) substrates. Transmission electron microscopy (TEM) confirmed the formation of high quality films with coherent interfaces. Films grown with higher oxygen pressure on STO (111) resulted in a (110)-oriented NbO2 phase with a distorted rutile structure, which can be described as body-centered tetragonal. The a lattice parameter of NbO2 was determined to be ˜13.8 Å in good agreement with neutron diffraction results published in the literature. Films grown on LSAT (111) at lower oxygen pressure produced the NbO phase with a defective rock salt cubic structure. The NbO lattice parameter was determined to be a ≈ 4.26 Å. The film phase/structure identification from TEM was in good agreement with in situ x-ray photoelectron spectroscopy measurements that confirmed the dioxide and monoxide phases, respectively. The atomic structure of the NbO2/STO and NbO/LSAT interfaces was determined based on comparisons between high-resolution electron micrographs and image simulations.

  11. Investigation of Metal Oxide/Carbon Nano Material as Anode for High Capacity Lithium-ion Cells

    Science.gov (United States)

    Wu, James Jianjun; Hong, Haiping

    2014-01-01

    NASA is developing high specific energy and high specific capacity lithium-ion battery (LIB) technology for future NASA missions. Current state-of-art LIBs have issues in terms of safety and thermal stability, and are reaching limits in specific energy capability based on the electrochemical materials selected. For example, the graphite anode has a limited capability to store Li since the theoretical capacity of graphite is 372 mAh/g. To achieve higher specific capacity and energy density, and to improve safety for current LIBs, alternative advanced anode, cathode, and electrolyte materials are pursued under the NASA Advanced Space Power System Project. In this study, the nanostructed metal oxide, such as Fe2O3 on carbon nanotubes (CNT) composite as an LIB anode has been investigated.

  12. Novel Mg-Doped SrMoO3 Perovskites Designed as Anode Materials for Solid Oxide Fuel Cells

    Directory of Open Access Journals (Sweden)

    Vanessa Cascos

    2016-07-01

    Full Text Available SrMo1−xMxO3−δ (M = Fe and Cr, x = 0.1 and 0.2 oxides have been recently described as excellent anode materials for solid oxide fuel cells at intermediate temperatures (IT-SOFC with LSGM as the electrolyte. In this work, we have improved their properties by doping with aliovalent Mg ions at the B-site of the parent SrMoO3 perovskite. SrMo1−xMgxO3−δ (x = 0.1, 0.2 oxides have been prepared, characterized and tested as anode materials in single solid-oxide fuel cells, yielding output powers near 900 mW/cm−2 at 850 °C using pure H2 as fuel. We have studied its crystal structure with an “in situ” neutron power diffraction (NPD experiment at temperatures as high as 800 °C, emulating the working conditions of an SOFC. Adequately high oxygen deficiencies, observed by NPD, together with elevated disk-shaped anisotropic displacement factors suggest a high ionic conductivity at the working temperatures. Furthermore, thermal expansion measurements, chemical compatibility with the LSGM electrolyte, electronic conductivity and reversibility upon cycling in oxidizing-reducing atmospheres have been carried out to find out the correlation between the excellent performance as an anode and the structural features.

  13. Kinetics of the electrolytic Fe+2/Fe+3 oxidation on various anode materials

    Directory of Open Access Journals (Sweden)

    Cifuentes, L.

    2003-08-01

    Full Text Available The kinetics of the electrolytic Fe+2/Fe+3 oxidation, relevant to hydro-electrometallurgical processing, have been studied on lead, platinum, ruthenium oxide, iridium oxide and graphite anodes in ferrous sulfate-sulfuric acid solutions. The oxidation rate depends on ferrous sulfate concentration, solution temperature and degree of agitation. Potentiodynamic studies show that: a the highest oxidation rate is obtained on platinum; b lead is unsuitable as anodic material for the said reaction; c the remaining anode materials show a similar and satisfactory performance.

    Se ha estudiado la cinética de la oxidación electrolítica Fe+2/Fe+3 -relevante para el procesamiento hidroelectrometalúrgico- sobre plomo, platino, óxido de rutenio, óxido de iridio y grafito en soluciones de sulfato ferroso en ácido sulfúrico. La velocidad de oxidación depende de la concentración de sulfato ferroso, la temperatura de la solución y el grado de agitación. Estudios potenciodinámicos demuestran que: a las mayores velocidades de oxidación se obtienen sobre platino; b el plomo es inadecuado como material anódico para la reacción mencionada; c los materiales anódicos restantes exhiben un desempeño similar y satisfactorio.

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

    Science.gov (United States)

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

    2015-07-08

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

  15. Polydopamine deposition with anodic oxidation for better connective tissue attachment to transmucosal implants.

    Science.gov (United States)

    Teng, F; Chen, H; Xu, Y; Liu, Y; Ou, G

    2018-04-01

    Nowadays, most designs for the transmucosal surface of implants are machined-smooth. However, connective tissue adhered to the smooth surface of an implant has poor mechanical resistance, which can render separation of tissue from the implant interface and induce epithelial downgrowth. Modification of the transmucosal surface of implants, which can help form a good seal of connective tissue, is therefore desired. We hypothesized that anodic oxidation (AO) and polydopamine (PD) deposition could be used to enhance the attachment between an implant and peri-implant connective tissue. We tested this hypothesis in the mandibles of Beagle dogs. AO and PD were used to modify the transmucosal region of transmucosal implants (implant neck). The surface microstructure, surface roughness and elemental composition were investigated in vitro. L929 mouse fibroblasts were cultured to test the effect of PD on cell adhesion. Six Beagle dogs were used for the in vivo experiment (n = 6 dogs per group). Three months after building the edentulous animal model, four groups of implants (control, AO, PD and AO + PD) were inserted. After 4 months of healing, samples were harvested for histometric analyses. The surfaces of anodized implant necks were overlaid with densely distributed pores, 2-7 μm in size. On the PD-modified surfaces, N1s, the chemical bond of nitrogen in PD, was detected using X-ray photoelectron spectroscopy. L929 developed pseudopods more quickly on the PD-modified surfaces than on the surfaces of the control group. The in vivo experiment showed a longer connective tissue seal and a more coronally located peri-implant soft-tissue attachment in the AO + PD group than in the control group (P < .05). The modification of AO + PD on the implant neck yielded better attachment between the implant and peri-implant connective tissue. © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

  16. The effect of H2S on the performance of Ni-YSZ anodes in solid oxide fuel cells

    DEFF Research Database (Denmark)

    Rasmussen, Jens Foldager Bregnballe; Hagen, Anke

    2009-01-01

    Biomass-derived fuel, e.g. biogas, is a potential fuel for solid oxide fuel cells (SOFCs). At operating temperature (850 °C) reforming of the carbon-containing biogas takes place over the Ni-containing anode. However, impurities in the biogas, e.g. H2S, can poison both the reforming...... and the electrochemical activity of the anode. Tests of single anode-supported planar SOFCs were carried out in the presence of H2S under current load at 850 °C. The cell voltage dropped as we periodically added 2–100 ppm H2S to an H2-containing fuel in 24 h intervals, but it regenerated to the initial value after we...... turned off the H2S. Evaluation of the changes of the cell voltage suggests that saturation coverage was reached at approximately 40 ppm H2S. A front-like movement of S-poisoning over the anode was seen by monitoring the in-plane voltage in the anode. Furthermore, impedance spectra showed that mainly...

  17. Nonradical oxidation from electrochemical activation of peroxydisulfate at Ti/Pt anode: Efficiency, mechanism and influencing factors.

    Science.gov (United States)

    Song, Haoran; Yan, Linxia; Ma, Jun; Jiang, Jin; Cai, Guangqiang; Zhang, Wenjuan; Zhang, Zhongxiang; Zhang, Jiaming; Yang, Tao

    2017-06-01

    Electrochemical activation of peroxydisulfate (PDS) at Ti/Pt anode was systematically investigated for the first time in this work. The synergistic effect produced from the combination of electrolysis and the addition of PDS demonstrates that PDS can be activated at Ti/Pt anode. The selective oxidation towards carbamazepine (CBZ), sulfamethoxazole (SMX), propranolol (PPL), benzoic acid (BA) rather than atrazine (ATZ) and nitrobenzene (NB) was observed in electrochemical activation of PDS process. Moreover, addition of excess methanol or tert-butanol had negligible impact on CBZ (model compound) degradation, demonstrating that neither sulfate radical (SO 4 - ) nor hydroxyl radical (HO) was produced in electrochemical activation of PDS process. Direct oxidation (PDS oxidation alone and electrolysis) and nonradical oxidation were responsible for the degradation of contaminants. The results of linear sweep voltammetry (LSV) and chronoamperometry suggest that electric discharge may integrate PDS molecule with anode surface into a unique transition state structure, which is responsible for the nonradical oxidation in electrochemical activation of PDS process. Adjustment of the solution pH from 1.0 to 7.0 had negligible effect on CBZ degradation. Increase of either PDS concentration or current density facilitated the degradation of CBZ. The presence of chloride ion (Cl - ) significantly enhanced CBZ degradation, while addition of bicarbonate (HCO 3 - ), phosphate (PO 4 3- ) and humic acid (HA) all inhibited CBZ degradation with the order of HA > HCO 3 -  > PO 4 3- . The degradation products of CBZ and chlorinated products were also identified. Electrochemical activation of PDS at Ti/Pt anode may serve as a novel technology for selective oxidation of organic contaminants in water and soil. Copyright © 2017. Published by Elsevier Ltd.

  18. Josephson tunnel junctions in niobium films

    International Nuclear Information System (INIS)

    Wiik, Tapio.

    1976-12-01

    A method of fabricating stable Josephson tunnel junctions with reproducible characteristics is described. The junctions have a sandwich structure consisting of a vacuum evaporated niobium film, a niobium oxide layer produced by the glow discharge method and a lead film deposited by vacuum evaporation. Difficulties in producing thin-film Josephson junctions are discussed. Experimental results suggest that the lower critical field of the niobium film is the most essential parameter when evaluating the quality of these junctions. The dependence of the lower critical field on the film thickness and on the Ginzburg-Landau parameter of the film is studied analytically. Comparison with the properties of the evaporated films and with the previous calculations for bulk specimens shows that the presented model is applicable for most of the prepared samples. (author)

  19. Parabens abatement from surface waters by electrochemical advanced oxidation with boron doped diamond anodes.

    Science.gov (United States)

    Domínguez, Joaquín R; Muñoz-Peña, Maria J; González, Teresa; Palo, Patricia; Cuerda-Correa, Eduardo M

    2016-10-01

    The removal efficiency of four commonly-used parabens by electrochemical advanced oxidation with boron-doped diamond anodes in two different aqueous matrices, namely ultrapure water and surface water from the Guadiana River, has been analyzed. Response surface methodology and a factorial, composite, central, orthogonal, and rotatable (FCCOR) statistical design of experiments have been used to optimize the process. The experimental results clearly show that the initial concentration of pollutants is the factor that influences the removal efficiency in a more remarkable manner in both aqueous matrices. As a rule, as the initial concentration of parabens increases, the removal efficiency decreases. The current density also affects the removal efficiency in a statistically significant manner in both aqueous matrices. In the water river aqueous matrix, a noticeable synergistic effect on the removal efficiency has been observed, probably due to the presence of chloride ions that increase the conductivity of the solution and contribute to the generation of strong secondary oxidant species such as chlorine or HClO/ClO - . The use of a statistical design of experiments made it possible to determine the optimal conditions necessary to achieve total removal of the four parabens in ultrapure and river water aqueous matrices.

  20. Magnetic nanostructures formation via local anodic oxidation and magnetron sputtering through lithographic mask

    Directory of Open Access Journals (Sweden)

    Lenka Pravdova

    2016-10-01

    Full Text Available Changes of magnetic properties of thin metallic films caused by the magnetron sputtering technique and by oxidation lithography were studied. The magnetic nanostructure formation was done via a lithography by sputtering the material through a mask. The anodic oxidation lithography (LAO via scanning probe microscopy (SPM device Ntegra Aura was used to attempt to create the magnetic nanostructures. At the beginning, the work has been scoped to the preparation and testing multilayered magnetic nanostructures based on different combinations in material composition of layers. The magnetic properties of these samples were examined by Kerr phenomenon. We observed increasing of the magnetic hardness of the magnetic nanostructure when the copper layer in the composition of ferromagnetic and antiferromagnetic multilayers has been replaced by an aluminium layer. Adding the aluminium layer onto the copper layer resulted in a decrease of magnetic hardness. This work was followed by creating of horizontal nanostructures by LAO. Changes induced by the LAO observed in the magnetic properties of the samples correspond mainly to topographical changes of the surface. Changes in the magnetic properties induced by LAO or by a variability of sputtered layers could lead to the further production of magnetic printed circuit or photonic nanostructures.

  1. Tribological performance of titanium samples oxidized by fs-laser radiation, thermal heating, or electrochemical anodization

    Science.gov (United States)

    Kirner, S. V.; Slachciak, N.; Elert, A. M.; Griepentrog, M.; Fischer, D.; Hertwig, A.; Sahre, M.; Dörfel, I.; Sturm, H.; Pentzien, S.; Koter, R.; Spaltmann, D.; Krüger, J.; Bonse, J.

    2018-04-01

    Commercial grade-1 titanium samples (Ti, 99.6%) were treated using three alternative methods, (i) femtosecond laser processing, (ii) thermal heat treatment, and (iii) electrochemical anodization, respectively, resulting in the formation of differently conditioned superficial titanium oxide layers. The laser processing (i) was carried out by a Ti:sapphire laser (pulse duration 30 fs, central wavelength 790 nm, pulse repetition rate 1 kHz) in a regime of generating laser-induced periodic surface structures (LIPSS). The experimental conditions (laser fluence, spatial spot overlap) were optimized in a sample-scanning setup for the processing of several square-millimeters large surface areas covered homogeneously by these nanostructures. The differently oxidized titanium surfaces were characterized by optical microscopy, micro Raman spectroscopy, variable angle spectroscopic ellipsometry, and instrumented indentation testing. The tribological performance was characterized in the regime of mixed friction by reciprocating sliding tests against a sphere of hardened steel in fully formulated engine oil as lubricant. The specific tribological performance of the differently treated surfaces is discussed with respect to possible physical and chemical mechanisms.

  2. Role of electrode materials for the anodic oxidation of a real landfill leachate--comparison between Ti-Ru-Sn ternary oxide, PbO(2) and boron-doped diamond anode.

    Science.gov (United States)

    Panizza, Marco; Martinez-Huitle, Carlos A

    2013-01-01

    In this paper the electrocatalytic properties of Ti-Ru-Sn ternary oxide (TiRuSnO(2)), PbO(2) and boron-doped diamond (BDD) anodes have been compared for the electrochemical oxidation of a real landfill leachate from an old municipal solid waste landfill (average values of COD 780 mg dm(-3) and NH(4)(+)-N266 mg dm(-3)). The experiments have been performed using an undivided flow cell equipped with a stainless steel cathode, under constant current of 2 A and flow-rate of 420 dm(3) h(-1). The performance of the electrodes has been compared measuring the time evolution of aromatic compounds, COD, ammonium, colour removal, current efficiency and energy consumption. The experimental results indicated that after 8 h of electrolyses TiRuSnO(2) anode yields only 35% COD, 52% colour and 65% ammonium removal. Using PbO(2) ammonium and colour were completely removed but a residual COD (i.e. 115 mg dm(-3)) was present. On the contrary BDD enables complete COD, colour and ammonium removal due to the electrogeneration of hydroxyl radicals from water discharge and active chlorine from chloride ions oxidation. BDD also exhibits greater current efficiency along with a significantly lower energy cost than other electrodes. These results indicated that the electrochemical oxidation with BDD anode is an effective process for the treatment of landfill leachate. Copyright © 2012 Elsevier Ltd. All rights reserved.

  3. Interlaboratory niobium dosimetry comparison

    International Nuclear Information System (INIS)

    Wille, P.

    1980-01-01

    For an interlaboratory comparison of neutron dosimetry using niobium the 93 sup(m)Nb activities of irradiated niobium monitors were measured. This work was performed to compare the applied techniques of dosimetry with Nb in different laboratories. The niobium monitors were irradiated in the fast breeder EBRII, USA and the BR2, Belgium. The monitors were dissolved and several samples were prepared. Their niobium contents were determined by the 94 Nb-count rates. since the original specific count rate was known. The KX radiations of the 93 sup(m)Nb of the samples and of a calibrated Nb-foil were compared. This foil was measured by PTB, Braunschweig and CBNM, Geel, which we additionally compared with the KX radiation of 88 Sr produced by a thin 88 Y source from a 88 Y-standard solution (PTB). (orig.) [de

  4. Introduction to Ingot Niobium

    International Nuclear Information System (INIS)

    Superconducting radiofrequency (SRF) technology using niobium accelerating cavities was first applied at large scale in the recirculating electron linear accelerator CEBAF--the Continuous Electron Beam Accelerator Facility in Newport News, Virginia, USA, at what is now called Thomas Jefferson National Accelerator Facility, or Jefferson Lab. Building on the high quality factors and peak magnetic fields found in low residual resistivity ratio (low-RRR) solid niobium in the 1970s, Jefferson Lab has reintroduced ingot niobium technology. High tantalum content in ingot niobium is not expected to negatively impact cavity performance, but will reduce the cost of accelerator structures considerably. Optimized low-cost CW linear accelerators built with ingot niobium will show the way for future R and D and industrial applications. This paper portrays the Jefferson Lab SRF context, reviews the early history of ingot niobium technology from over a third of a century ago, explains the technical advantages of that technology's recent reintroduction, and presents the outlook for further development.

  5. Catalytic applications of niobium compounds

    International Nuclear Information System (INIS)

    Wright, C.J.; England, W.A.

    1984-01-01

    This article examines the potential uses of niobium, and its compounds, as catalysts in chemical processing. The word potential is deliberately chosen because in 1978 none of the world's twenty-five major catalysts (1) contained niobium. On the other hand, catalysts containing molybdenum and vanadium, neighbors of niobium in the periodic table, realized over 80 x 10 6 of sales in that same year. At the same time many of the patents for niobium catalysts cover applications in which niobium improves the activity of, or substitutes for, molybdenum based compounds. With favorable cost differentials and improvements in understanding, niobium may be able to replace molybdenum in some its traditional uses

  6. Nanocrystalline Mn-Mo-Ce Oxide Anode Doped Rare Earth Ce and Its Selective Electro-catalytic Performance

    Directory of Open Access Journals (Sweden)

    SHI Yan-hua

    2017-09-01

    Full Text Available The anode oxide of nanocrystalline Mn-Mo-Ce was prepared by anode electro-deposition technology, and its nanostructure and selective electro-catalytic performance were investigated using the SEM, EDS, XRD, HRTEM, electrochemical technology and oxygen evolution efficiency testing. Furthermore, the selective electro-catalytic mechanism of oxygen evolution and chlorine depression was discussed. The results show that the mesh-like nanostructure Mn-Mo-Ce oxide anode with little cerium doped is obtained, and the oxygen evolution efficiency for the anode in the seawater is 99.51%, which means a high efficiency for the selective electro-catalytic for the oxygen evolution. Due to the structural characteristics of γ-MnO2, the OH- ion is preferentially absorbed, while Cl- absorption is depressed. OH- accomplishes the oxygen evolution process during the valence transition electrocatalysis of Mn4+/Mn3+, completing the selective electro-catalysis process. Ce doping greatly increases the reaction activity, and promotes the absorption and discharge; the rising interplanar spacing between active (100 crystalline plane promotes OH- motion and the escape of newborn O2, so that the selective electro-catalytic property with high efficient oxygen evolution and chlorine depression is achieved from the nano morphology effect.

  7. Evaluation of Ni/SDC as anode material for dry CH4 fueled Solid Oxide Fuel Cells

    Science.gov (United States)

    Wang, Zhiming; Li, Yongdan; Schwank, Johannes W.

    2014-02-01

    A Ni/Sm0.2Ce0.8O1.9 (SDC) composite was employed as anode material for direct electrochemical oxidation (DEO) of dry CH4 in a solid oxide fuel cell. The anodic performance was investigated at temperatures between 600 °C and 700 °C using SDC as electrolyte material and Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF) as cathode material. The single cell exhibited maximum power densities of 671 mW cm-2, 494 mW cm-2 and 305 mW cm-2 in dry CH4 at 700 °C, 650 °C and 600 °C, respectively. Remarkably, at 700 °C the power density in CH4 was higher than in H2, thanks to the carbon tolerance of the anode. Durability tests under constant 300 mA output current showed only 3.7% performance loss after 72 h operation. The results demonstrate that Ni/SDC can be used as anode for the DEO of dry CH4 even at temperatures as low as 600 °C.

  8. Degradation analysis of anode-supported intermediate temperature-solid oxide fuel cells under various failure modes

    Science.gov (United States)

    Lee, Tae-Hee; Park, Ka-Young; Kim, Ji-Tae; Seo, Yongho; Kim, Ki Buem; Song, Sun-Ju; Park, Byoungnam; Park, Jun-Young

    2015-02-01

    This study focuses on mechanisms and symptoms of several simulated failure modes, which may have significant influences on the long-term durability and operational stability of intermediate temperature-solid oxide fuel cells (IT-SOFCs), including fuel/oxidation starvation by breakdown of fuel/air supply components and wet and dry cycling atmospheres. Anode-supported IT-SOFCs consisting of a Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF)-Nd0.1Ce0.9O2-δ (NDC) composite cathode with an NDC electrolyte on a Ni-NDC anode substrate are fabricated via dry-pressings followed by the co-firing method. Comprehensive and systematic research based on the failure mode and effect analysis (FMEA) of anode-supported IT-SOFCs is conducted using various electrochemical and physiochemical analysis techniques to extend our understanding of the major mechanisms of performance deterioration under SOFC operating conditions. The fuel-starvation condition in the fuel-pump failure mode causes irreversible mechanical degradation of the electrolyte and cathode interface by the dimensional expansion of the anode support due to the oxidation of Ni metal to NiO. In contrast, the BSCF cathode shows poor stability under wet and dry cycling modes of cathode air due to the strong electroactivity of SrO with H2O. On the other hand, the air-depletion phenomena under air-pump failure mode results in the recovery of cell performance during the long-term operation without the visible microstructural transformation through the reduction of anode overvoltage.

  9. Ethylene glycol as a new sustainable fuel for solid oxide fuel cells with conventional nickel-based anodes

    International Nuclear Information System (INIS)

    Qu, Jifa; Wang, Wei; Chen, Yubo; Wang, Feng; Ran, Ran; Shao, Zongping

    2015-01-01

    Highlights: • Ethylene glycol could be used as a sustainable fuel for solid oxide fuel cells. • Ethylene glycol was beneficial in suppressing coke formation on Ni anode. • A high power output of 1200 mW cm −2 was obtained with ethylene glycol at 750 °C. • An excellent operational stability was obtained with ethylene glycol fuel. - Abstract: In this study, renewable ethylene glycol (EG) was exploited as a potential fuel for solid oxide fuel cells (SOFCs) with conventional nickel yttria-stabilized zirconia (Ni–YSZ) cermet anodes for sustainable electric power generation. Carbon deposition behaviors over Ni–YSZ anodes under different carbon-containing atmospheres such as EG, glycerol, ethanol and methane were characterized through thermodynamic prediction, oxygen-temperature programmed oxidation and SEM–EDX analysis. EG was observed to be better than acetic acid and glycerol and much better than methane and ethanol in terms of carbon deposition. A calculation of the open-circuit voltages of EG-fueled SOFCs suggested that EG is a suitable fuel for SOFCs. A maximum power output of 1200 mW cm −2 at 750 °C was obtained from a cell operating on EG-steam fuel, which is only a little lower than that from a cell based on hydrogen fuel. The cell was further operated stably on an EG-steam gas mixture for 200 h with no apparent performance degradation, carbon deposition over the anode, Ni agglomeration, or change in the morphology of the anodes. The current study confirmed the practical applicability of EG as a direct fuel for SOFCs, which may have a great effect on future energy systems

  10. Nanopore formation on the surface oxide of commercially pure titanium grade 4 using a pulsed anodization method in sulfuric acid.

    Science.gov (United States)

    Williamson, R S; Disegi, J; Griggs, J A; Roach, M D

    2013-10-01

    Titanium and its alloys form a thin amorphous protective surface oxide when exposed to an oxygen environment. The properties of this oxide layer are thought to be responsible for titanium and its alloys biocompatibility, chemical inertness, and corrosion resistance. Surface oxide crystallinity and pore size are regarded to be two of the more important properties in establishing successful osseointegration. Anodization is an electrochemical method of surface modification used for colorization marking and improved bioactivity on orthopedic and dental titanium implants. Research on titanium anodization using sulphuric acid has been reported in the literature as being primarily conducted in molarity levels 3 M and less using either galvanostatic or potentiostatic methods. A wide range of pore diameters ranging from a few nanometers up to 10 μm have been shown to form in sulfuric acid electrolytes using the potentiostatic and galvanostatic methods. Nano sized pores have been shown to be beneficial for bone cell attachment and proliferation. The purpose of the present research was to investigate oxide crystallinity and pore formation during titanium anodization using a pulsed DC waveform in a series of sulfuric acid electrolytes ranging from 0.5 to 12 M. Anodizing titanium in increasing sulfuric acid molarities showed a trend of increasing transformations of the amorphous natural forming oxide to the crystalline phases of anatase and rutile. The pulsed DC waveform was shown to produce pores with a size range from ≤0.01 to 1 μm(2). The pore size distributions produced may be beneficial for bone cell attachment and proliferation.

  11. High electrochemical activity of the oxide phase in model ceria-Pt and ceria-Ni composite anodes

    Science.gov (United States)

    Chueh, William C.; Hao, Yong; Jung, Woochul; Haile, Sossina M.

    2012-02-01

    Fuel cells, and in particular solid-oxide fuel cells (SOFCs), enable high-efficiency conversion of chemical fuels into useful electrical energy and, as such, are expected to play a major role in a sustainable-energy future. A key step in the fuel-cell energy-conversion process is the electro-oxidation of the fuel at the anode. There has been increasing evidence in recent years that the presence of CeO2-based oxides (ceria) in the anodes of SOFCs with oxygen-ion-conducting electrolytes significantly lowers the activation overpotential for hydrogen oxidation. Most of these studies, however, employ porous, composite electrode structures with ill-defined geometry and uncontrolled interfacial properties. Accordingly, the means by which electrocatalysis is enhanced has remained unclear. Here we demonstrate unambiguously, through the use of ceria-metal structures with well-defined geometries and interfaces, that the near-equilibrium H2 oxidation reaction pathway is dominated by electrocatalysis at the oxide/gas interface with minimal contributions from the oxide/metal/gas triple-phase boundaries, even for structures with reaction-site densities approaching those of commercial SOFCs. This insight points towards ceria nanostructuring as a route to enhanced activity, rather than the traditional paradigm of metal-catalyst nanostructuring.

  12. The surface oxidation kinetics of zirconium-niobium alloys and aα-Fe with prevailing cubical texture

    International Nuclear Information System (INIS)

    Mukhambetov, D.G.; Kargin, D.B.; Chalaya, O. V.; Berber, N.N.

    2002-01-01

    It is known, that the kinetics of oxidation of zirconium at formed heating is characterized by two consecutive stages. At the initial stage the thin protecting film will be derived. The relation of its depth from time h (t) is described predominantly by parabolic law. Some time later there can be a transition to the linear law of oxidation. The time moment divided these areas on the kinetic relation is called as a point of break. The film is formed at the second stage, has a developed grid of pores or cracks, can be flake away and be crumbled by losing its protective properties. At the oxidation of the surface shells of the heat generating elements and the technological channels of atomic boilers both stages are proceeded simultaneously. This phenomenon is called modular corrosion. Its consequences can be dangerous for the equipment. Its mechanism is not clear till now. Similar dependencies h(t), with the break point, beginning from which the thin film is transformed into the thick one were found by us at the oxidation α-Fe with prevailing cubical texture. The task of the work was to study the oxide film growth laws in order to clarify the mechanisms of transition of the thin film into the oxide layer on the α-Fe surface and Zr-Nb alloy modular corrosion emergence. Low-carbonate steel with contents 99.43 % of α-Fe was used as a model object of our research. In the texture of the steel surface planar direction [100] was prevalent. Its part accounted for about 40 %. The isothermal air oxidation was carried out in the interval of 450-500 deg. C . Phase composition of the film was determined with X-ray diffraction. The mathematical treatment of the dependencies h(t) obtained by experiment showed that the kinetics of the film growth can be conditionally divided into 4-stages. The initial stage is described by function logarithmic function, the other stages - by the power mode h n =A n ·t, namely, the second stage - is described by function close to cubical (n≅3

  13. The fabrication of high sensitivity gold nanorod H2S gas sensors utilizing the highly uniform anodic aluminum oxide template

    Directory of Open Access Journals (Sweden)

    Chien-Yu Li

    2016-12-01

    Full Text Available Gold nanorod were fabricated using anodic alumina oxide template for H2S gas detection. The nanorod gas sensor exhibits high surface density and contact area, which can increase detection sensitivity. The anodic alumina oxide template contains an array of pores, with a width of 70 nm and a length of 27μm. Au nanorod were obtained through electro-deposition under a pulse bias of −1 V. The resistance of the Au nanorod was recorded upon exposure to various concentrations of H2S. The resistance could be attributed to the high electron affinity between sulfide and Au nanorod. Au–sulfide bonds provide strong bonding, which could alter the conductivity of the sensor. The gas sensor exhibits high sensitivity and short response time for H2S detection at room temperature.

  14. Prediction of overpotential and effective thickness of Ni/YSZ anode for solid oxide fuel cell by improved species territory adsorption model

    Science.gov (United States)

    Nagasawa, Tsuyoshi; Hanamura, Katsunori

    2017-06-01

    The reliability of analytical model for hydrogen oxidation at Ni/YSZ anode in solid oxide fuel cell named as species territory adsorption model has been improved by introducing referenced thermodynamic and kinetic parameters predicted by density function theory calculations. The model can explicitly predict anode overpotential using unknown values of quantities of state for oxygen migration process in YSZ near a triple phase boundary (TPB), frequency factor for hydrogen oxidation, and effective anode thickness. The former two are determined through careful fitting process between the predicted and experimental results of Ni/YSZ cermet and Ni-patterned anodes. This makes it possible to estimate effective anode thickness, which tends to increase with temperature in six kinds of Ni/YSZ anodes in references. In addition, the comparison between the proposed model and a published numerical simulation indicates that the model can predict more precise dependence of anode overpotential on steam partial pressure than that by Butler-Volmer equation with empirical exchange current density. The introduction of present model into numerical simulation instead of Butler-Volmer equation can give more accurate prediction of anode polarization.

  15. Bonding of a niobium wire to a niobium thin film

    NARCIS (Netherlands)

    Jaszczuk, W.; Jaszczuk, W.; ter Brake, Hermanus J.M.; Flokstra, Jakob; Veldhuis, Dick; Stammis, R.; Rogalla, Horst

    1991-01-01

    A method for bonding a niobium wire to a niobium thin film is described. The bonds are to be used as superconducting connections between wire-wound gradiometers and thin-film coupling coils on DC SQUIDS. The method is characterized by two steps. Firstly, the hardness of the niobium wire is reduced

  16. Anodic oxidation of textile wastewaters on boron-doped diamond electrodes.

    Science.gov (United States)

    Abdessamad, NourElHouda; Akrout, Hanene; Bousselmi, Latifa

    2015-01-01

    The objective of this study is to investigate the potential application of the anodic oxidation (AO) on two electrolytic cells (monopolar (Cell 1) and bipolar (Cell 2)) containing boron-doped diamond electrodes on the treatment of real textile effluents to study the reuse possibility of treated wastewater in the textile industry process. AO is applied in the flocculation coagulation pretreatment of both upstream (BH) and downstream (BS) effluents. The chemical oxygen demand (COD) results show that the final COD removal obtained for the BH effluent in the case of Cell 1 and Cell 2 is 800 and 150 mg O₂L⁻¹ after 5 and 6 h of electrolysis, respectively. The treatments of the BS effluent allow for obtaining a final COD of 76 mg L⁻¹ for Cell 1 and a total mineralization for Cell 2. The obtained results demonstrate that the apparent mineralization kinetics of both effluents when using Cell 2 are about four times faster than the one obtained by Cell 1 and highlight the important contribution of the bipolar cell. Besides, the energy consumption values show that the treatment of the BH effluent by Cell 1 consumes 865 kWh kg COD⁻¹ against 411 kWh kg COD(-1) by Cell 2. Therefore, the use of Cell 2 decreases the energy cost by 2.1-6.65 times when compared to Cell 1 in the case of the BH and BS effluent treatment, respectively.

  17. Anodic oxidation of textile dyehouse effluents on boron-doped diamond electrode

    International Nuclear Information System (INIS)

    Tsantaki, Eleni; Velegraki, Theodora; Katsaounis, Alexandros; Mantzavinos, Dionissios

    2012-01-01

    The electrochemical oxidation of textile effluents over a boron-doped diamond anode was investigated in the present study. Experiments were conducted with a multi-component synthetic solution containing seventeen dyes and other auxiliary inorganics, as well as an actual effluent from a textile dyeing process. The effect of varying operating parameters, such as current density (4–50 mA/cm 2 ), electrolyte concentration (0.1–0.5 M HClO 4 ), initial solution pH (1–12.3) and temperature (22–43 °C), on process efficiency was investigated following changes in total organic carbon (TOC), chemical oxygen demand (COD) and color. Complete decolorization accompanied by significant mineralization (up to 85% depending on the conditions) could be achieved after 180 min of treatment. Performance was improved at higher electrolyte concentrations and lower pH values, while the effect of temperature was marginal. Energy consumption per unit mass of COD removed was favored at lower current densities, since energy was unnecessarily wasted to side reactions at higher densities.

  18. Anodic oxidation of textile dyehouse effluents on boron-doped diamond electrode.

    Science.gov (United States)

    Tsantaki, Eleni; Velegraki, Theodora; Katsaounis, Alexandros; Mantzavinos, Dionissios

    2012-03-15

    The electrochemical oxidation of textile effluents over a boron-doped diamond anode was investigated in the present study. Experiments were conducted with a multi-component synthetic solution containing seventeen dyes and other auxiliary inorganics, as well as an actual effluent from a textile dyeing process. The effect of varying operating parameters, such as current density (4-50 mA/cm2), electrolyte concentration (0.1-0.5 M HClO4), initial solution pH (1-12.3) and temperature (22-43 °C), on process efficiency was investigated following changes in total organic carbon (TOC), chemical oxygen demand (COD) and color. Complete decolorization accompanied by significant mineralization (up to 85% depending on the conditions) could be achieved after 180 min of treatment. Performance was improved at higher electrolyte concentrations and lower pH values, while the effect of temperature was marginal. Energy consumption per unit mass of COD removed was favored at lower current densities, since energy was unnecessarily wasted to side reactions at higher densities. Copyright © 2011 Elsevier B.V. All rights reserved.

  19. Polyrhodanine modified anodic aluminum oxide membrane for heavy metal ions removal.

    Science.gov (United States)

    Song, Jooyoung; Oh, Hyuntaek; Kong, Hyeyoung; Jang, Jyongsik

    2011-03-15

    Polyrhodanine was immobilized onto the inner surface of anodic aluminum oxide (AAO) membrane via vapor deposition polymerization method. The polyrhodanine modified membrane was applied to remove heavy metal ions from aqueous solution because polyrhodanine could be coordinated with specific metal ions. Several parameters such as initial metal concentration, contact time and metal species were evaluated systematically for uptake efficiencies of the fabricated membrane under continuous flow condition. Adsorption isotherms of Hg(II) ion on the AAO-polyrhodanine membrane were analyzed with Langmuir and Freundlich isotherm models. The adsorption rate of Hg(II) ion on the membrane was obeyed by a pseudo-second order equation, indicating the chemical adsorption. The maximum removal capacity of Hg(II) ion onto the fabricated membrane was measured to be 4.2 mmol/g polymer. The AAO-polyrhodanine membrane had also remarkable uptake performance toward Ag(I) and Pb(II) ions. Furthermore, the polyrhodanine modified membrane could be recycled after recovery process. These results demonstrated that the polyrhodanine modified AAO membrane provided potential applications for removing the hazardous heavy metal ions from wastewater. Copyright © 2011 Elsevier B.V. All rights reserved.

  20. Liquid crystal alignment in nanoporous anodic aluminum oxide layer for LCD panel applications.

    Science.gov (United States)

    Hong, Chitsung; Tang, Tsung-Ta; Hung, Chi-Yu; Pan, Ru-Pin; Fang, Weileun

    2010-07-16

    This paper reports the implementation and integration of a self-assembled nanoporous anodic aluminum oxide (np-AAO) film and liquid crystal (LC) on an ITO-glass substrate for liquid crystal display (LCD) panel applications. An np-AAO layer with a nanopore array acts as the vertical alignment layer to easily and uniformly align the LC molecules. Moreover, the np-AAO nanoalignment layer provides outstanding material properties, such as being inorganic with good transmittance, and colorless on ITO-glass substrates. In this application, an LCD panel, with the LC on the np-AAO nanoalignment layer, is successfully implemented on an ITO-glass substrate, and its performance is demonstrated. The measurements show that the LCD panel, consisting of an ITO-glass substrate and an np-AAO layer, has a transmittance of 60-80%. In addition, the LCD panel switches from a black state to a bright state at 3 V(rms), with a response time of 62.5 ms. In summary, this paper demonstrates the alignment of LC on an np-AAO layer for LCD applications.

  1. A solid oxide fuel cell with a gadolinia-doped ceria anode: Preparation and performance

    DEFF Research Database (Denmark)

    Marina, O.A.; Bagger, C.; Primdahl, S.

    1999-01-01

    ) electrolyte without detrimental reaction. Single SOFCs comprising the CG4 anode, a composite strontium-doped lanthanum manganite-based cathode and the YSZ electrolyte were manufactured and tested in H-2/H2O and CH4/H2O atmospheres vs. air in the temperature range of 800-1015 degrees C, An area specific...... internal resistance of 0.39 Ohm cm(2) at 0.71 V cell voltage and a power density of 470 mW/cm(2) was obtained at 1000 degrees C using H-2/H2O/N-2 = 9/1.2/89.8 as the fuel and air as oxidant. A current density of 0.25 A/cm(2) at an area specific internal resistance of 2 Ohm cm(2) was obtained with CH4/H2O....../N-2 = 33/3/64. No carbon deposition was found on CG4 after cell operation at a steam-to-carbon ratio of 0.3 for 1000 h. Cells sustained several rapid thermal cycles in the temperature interval 200-1000 degrees C and a full redox cycle without degradation. (C) 1999 Elsevier Science B.V. All rights...

  2. Biogas Catalytic Reforming Studies on Nickel-Based Solid Oxide Fuel Cell Anodes

    DEFF Research Database (Denmark)

    Johnson, Gregory B.; Hjalmarsson, Per; Norrman, Kion

    2016-01-01

    of experiments were performed to study catalytic activity and effect of sulfur poisoning: (i) CH4 and CO2 dissociation; (ii) biogas (60% CH4 and 40% CO2) temperature-programmed reactions (TPRxn); and (iii) steady-state biogas reforming reactions followed by postmortem catalyst characterization by temperature......-programmed oxidation and time-of-flight secondary ion mass spectrometry. Results showed thatNi/ScYSZ/Pd-CGO was more active for catalytic dissociation of CH4 at 750°C and subsequent reactivity of deposited carbonaceous species. Sulfur deactivated most catalytic reactions except CO2 dissociation at 750°C. The presence...... of Pd-CGO helped to mitigate sulfur deactivation effect; e.g. lowering the onset temperature (up to 190°C) for CH4 conversion during temperature-programmed reactions. Both Ni/ScYSZ and Ni/ScYSZ/Pd-CGO anode catalysts were more active for dry reforming of biogas than they were for steam reforming...

  3. Metal oxides and lithium alloys as anode materials for lithium-ion batteries

    CSIR Research Space (South Africa)

    Kebede, M

    2016-07-01

    Full Text Available -generation anode materials for lithium–ion batteries with high prospect of replacing graphite. Most of these anode materials have higher specific capacities between the range of 600-1000 mA h g(sup-1) compared with 340 mA h g(sup-1) of graphite. These high...

  4. Syntheses of rare-earth metal oxide nanotubes by the sol-gel method assisted with porous anodic aluminum oxide templates

    International Nuclear Information System (INIS)

    Kuang Qin; Lin Zhiwei; Lian Wei; Jiang Zhiyuan; Xie Zhaoxiong; Huang Rongbin; Zheng Lansun

    2007-01-01

    In this paper, we report a versatile synthetic method of ordered rare-earth metal (RE) oxide nanotubes. RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM, and X-ray diffraction (XRD) have been employed to characterize the morphology and composition of the as-prepared nanotubes. It is found that as-prepared RE oxides evolve into bamboo-like nanotubes and entirely hollow nanotubes. A new possible formation mechanism of RE oxide nanotubes in the AAO channels is proposed. These high-quantity RE oxide nanotubes are expected to have promising applications in many areas such as luminescent materials, catalysts, magnets, etc. - Graphical abstract: A versatile synthetic method for the preparation of ordered rare-earth (RE) oxide nanotubes is reported, by which RE (RE=Y, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Yb) oxide nanotubes were successfully prepared from corresponding RE nitrate solution via the sol-gel method assisted with porous anodic aluminum oxide (AAO) templates

  5. Enhanced performance of a novel anodic PdAu/VGCNF catalyst for electro-oxidation in a glycerol fuel cell.

    Science.gov (United States)

    Yahya, N; Kamarudin, S K; Karim, N A; Masdar, M S; Loh, K S

    2017-11-25

    This study presents a novel anodic PdAu/VGCNF catalyst for electro-oxidation in a glycerol fuel cell. The reaction conditions are critical issues affecting the glycerol electro-oxidation performance. This study presents the effects of catalyst loading, temperature, and electrolyte concentration. The glycerol oxidation performance of the PdAu/VGCNF catalyst on the anode side is tested via cyclic voltammetry with a 3 mm 2 active area. The morphology and physical properties of the catalyst are examined using X-ray diffraction (XRD), field emission scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy. Then, optimization is carried out using the response surface method with central composite experimental design. The current density is experimentally obtained as a response variable from a set of experimental laboratory tests. The catalyst loading, temperature, and NaOH concentration are taken as independent parameters, which were evaluated previously in the screening experiments. The highest current density of 158.34 mAcm -2 is obtained under the optimal conditions of 3.0 M NaOH concentration, 60 °C temperature and 12 wt.% catalyst loading. These results prove that PdAu-VGCNF is a potential anodic catalyst for glycerol fuel cells.

  6. Niobium based coatings for dental implants

    Energy Technology Data Exchange (ETDEWEB)

    Ramirez, G., E-mail: enggiova@hotmail.com [Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, Circuito Exterior s/n, CU, Mexico D.F. 04510 (Mexico); Facultad de Quimica, Departamento de Ingenieria Quimica, Universidad Nacional Autonoma de Mexico, Mexico D.F. 04510 (Mexico); Rodil, S.E. [Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, Circuito Exterior s/n, CU, Mexico D.F. 04510 (Mexico); Arzate, H. [Laboratorio de Biologia Celular y Molecular, Facultad de Odontologia, Universidad Nacional Autonoma de Mexico, CU, Mexico D.F. 04510 (Mexico); Muhl, S. [Instituto de Investigaciones en Materiales, Universidad Nacional Autonoma de Mexico, Circuito Exterior s/n, CU, Mexico D.F. 04510 (Mexico); Olaya, J.J. [Unidad de Materiales, Departamento de Ingenieria Mecanica y Mecatronica, Universidad Nacional de Colombia, Cra. 30 45-03 Bogota (Colombia)

    2011-01-15

    Niobium based thin films were deposited on stainless steel (SS) substrates to evaluate them as possible biocompatible surfaces that might improve the biocompatibility and extend the life time of stainless steel dental implants. Niobium nitride and niobium oxide thin films were deposited by reactive unbalanced magnetron sputtering under standard deposition conditions without substrate bias or heating. The biocompatibility of the surfaces was evaluated by testing the cellular adhesion and viability/proliferation of human cementoblasts during different culture times, up to 7 days. The response of the films was compared to the bare substrate and pieces of Ti6Al4V; the most commonly used implant material for orthopedics and osteo-synthesis applications. The physicochemical properties of the films were evaluated by different means; X-ray diffraction, Rutherford backscattering spectroscopy and contact angle measurements. The results suggested that the niobium oxide films were amorphous and of stoichiometric Nb{sub 2}O{sub 5} (a-Nb{sub 2}O{sub 5}), while the niobium nitride films were crystalline in the FCC phase (c-NbN) and were also stoichiometric with an Nb to N ratio of one. The biological evaluation showed that the biocompatibility of the SS could be improved by any of the two films, but neither was better than the Ti6Al4V alloy. On the other hand, comparing the two films, the c-NbN seemed to be a better surface than the oxide in terms of the adhesion and proliferation of human cemetoblasts.

  7. On direct internal methane steam reforming kinetics in operating solid oxide fuel cells with nickel-ceria anodes

    Science.gov (United States)

    Thallam Thattai, A.; van Biert, L.; Aravind, P. V.

    2017-12-01

    Major operating challenges remain to safely operate methane fuelled solid oxide fuel cells due to undesirable temperature gradients across the porous anode and carbon deposition. This article presents an experimental study on methane steam reforming (MSR) global kinetics for single operating SOFCs with Ni-GDC (gadolinium doped ceria) anodes for low steam to carbon (S/C) ratios and moderate current densities. The study points out the hitherto insufficient research on MSR global and intrinsic kinetics for operating SOFCs with complete Ni-ceria anodes. Further, it emphasizes the need to develop readily applicable global kinetic models as a subsequent step from previously reported state-of-art and complex intrinsic models. Two rate expressions of the Power law (PL) and Langmuir-Hinshelwood (LH) type have been compared and based on the analysis, limitations of using previously proposed rate expressions for Ni catalytic beds to study MSR kinetics for complete cermet anodes have been identified. Firstly, it has been shown that methane reforming on metallic (Ni) current collectors may not be always negligible, contrary to literature reports. Both PL and LH kinetic models predict significantly different local MSR reaction rate and species partial pressure distributions along the normalized reactor length, indicating a strong need for further experimental verifications.

  8. Electrochemical Synthesis of Binary and Ternary Niobium-Containing Oxide Electrodes Using the p-Benzoquinone/Hydroquinone Redox Couple.

    Science.gov (United States)

    Papa, Christopher M; Cesnik, Anthony J; Evans, Taylor C; Choi, Kyoung-Shin

    2015-09-01

    New electrochemical synthesis methods have been developed to obtain layered potassium niobates, KNb3O8 and K4Nb6O17, and perovskite-type KNbO3 as film-type electrodes. The electrodes were synthesized from aqueous solutions using the redox chemistry of p-benzoquinone and hydroquinone to change the local pH at the working electrode to trigger deposition of desired phases. In particular, the utilization of electrochemically generated acid via the oxidation of hydroquinone for inorganic film deposition was first demonstrated in this study. The layered potassium niobates could be converted to (H3O)Nb3O8 and (H3O)4Nb6O17 by cationic exchange, which, in turn, could be converted to Nb2O5 by heat treatment. The versatility of the new deposition method was further demonstrated for the formation of CuNb2O6 and AgNbO3, which were prepared by the deposition of KNb3O8 and transition metal oxides, followed by thermal and chemical treatments. Considering the lack of solution-based synthesis methods for Nb-based oxide films, the methods reported in this study will contribute greatly to studies involving the synthesis and applications of Nb-based oxide electrodes.

  9. Nucleophile-directed selectivity towards linear carbonates in the niobium pentaethoxide-catalysed cycloaddition of CO2 and propylene oxide

    KAUST Repository

    Dutta, Barnali

    2014-01-01

    Homoleptic Nb-complexes combined with selected organic nucleophiles generate very active catalytic systems for the cycloaddition of propylene oxide and CO2 under ambient conditions. An unprecedented reaction pathway towards an acyclic organic carbonate is observed when extending the study to [Nb(OEt)5] in combination with 4-dimethylamino-pyridine (DMAP) or tetra-n-butylammonium bromide (TBAB). Mechanistic insights of the reaction are provided based on experimental and spectroscopic evidences. This journal is © the Partner Organisations 2014.

  10. Diffusion of oxygen in niobium during bake-out

    International Nuclear Information System (INIS)

    Benvenuti, C.; Calatroni, S.; Ruzinov, V.

    2003-01-01

    Bake-outs at temperatures between 100 degC and 150 degC for duration up to two days have become customary for optimising the performance of bulk niobium cavities. This treatment results in the diffusion of oxygen, originating from the surface oxide, into the niobium. The theoretical oxygen profile has been simulated using the diffusion equations, and compared with some experimental results. (author)

  11. Conical tungsten stamps for the replication of pore arrays in anodic aluminium oxide films

    Science.gov (United States)

    LeClere, D. J.; Thompson, G. E.; Derby, B.

    2009-06-01

    A tungsten master stamp has been generated by applying a novel procedure that includes two-step anodizing, followed by sequential anodizing and pore widening to develop nominally funnelled pores. These conical-shaped pores were filled with tungsten by sputter coating to manufacture a master stamp. Under a pressure of 65 MPa, the master stamp successfully embossed the surface of annealed and electropolished aluminium. The embossed surface was then used to control the position of pores created by anodizing under the conditions used to produce the original pore array.

  12. Fabrication of Acrylonitrile-Butadiene-Styrene Nanostructures with Anodic Alumina Oxide Templates, Characterization and Biofilm Development Test for Staphylococcus epidermidis.

    Directory of Open Access Journals (Sweden)

    Camille Desrousseaux

    Full Text Available Medical devices can be contaminated by microbial biofilm which causes nosocomial infections. One of the strategies for the prevention of such microbial adhesion is to modify the biomaterials by creating micro or nanofeatures on their surface. This study aimed (1 to nanostructure acrylonitrile-butadiene-styrene (ABS, a polymer composing connectors in perfusion devices, using Anodic Alumina Oxide templates, and to control the reproducibility of this process; (2 to characterize the physico-chemical properties of the nanostructured surfaces such as wettability using captive-bubble contact angle measurement technique; (3 to test the impact of nanostructures on Staphylococcus epidermidis biofilm development. Fabrication of Anodic Alumina Oxide molds was realized by double anodization in oxalic acid. This process was reproducible. The obtained molds present hexagonally arranged 50 nm diameter pores, with a 100 nm interpore distance and a length of 100 nm. Acrylonitrile-butadiene-styrene nanostructures were successfully prepared using a polymer solution and two melt wetting methods. For all methods, the nanopicots were obtained but inside each sample their length was different. One method was selected essentially for industrial purposes and for better reproducibility results. The flat ABS surface presents a slightly hydrophilic character, which remains roughly unchanged after nanostructuration, the increasing apparent wettability observed in that case being explained by roughness effects. Also, the nanostructuration of the polymer surface does not induce any significant effect on Staphylococcus epidermidis adhesion.

  13. Effects of the buffer layer inserted between the transparent conductive oxide anode and the organic electron donor

    Energy Technology Data Exchange (ETDEWEB)

    Godoy, A.; Kouskoussa, B.; Benchouk, K.; Khelil, A. [Facultad Ciencias de la Salud, Universidad Diego Portales, Ejercito 141, Santiago de Chile (Chile); Cattin, L.; Soto, G.M. [Universite de Nantes, Nantes Atlantique Universites, Institut des Materiaux Jean Rouxel (IMN)-CNRS, Faculte des Sciences et Techniques, 2 rue de la Houssiniere, BP 92208, Nantes F-44000 (France); Toumi, L. [LPCM2E, Universite d' Oran Es-Senia, LPCM2E (Algeria); Diaz, F.R.; del Valle, M.A. [Laboratorio de Polimeros, Facultad de Quimica, Pontificia Universidad Catolica de Chile, Casilla 306, Correo 22, Santiago (Chile); Morsli, M.; Bernede, J.C. [Universite de Nantes, Nantes Atlantique Universites, LAMP, Faculte des Sciences et Techniques, 2 rue de la Houssiniere, BP 92208, Nantes F-44000 (France)

    2010-04-15

    In optoelectronic devices, the work function of the transparent conductive oxide, which is used as anode, does not match well the highest occupied molecular orbital of the organic material, which induces the formation of a barrier opposed to hole exchange at this interface. Therefore a thin buffer layer is often used to achieve good matching of the band structure at the interface. From experimental results it can be deduced that the main effects of the buffer layer consist in a better matching of the band structure at the interface anode/organic material and in a more homogeneous organic layer growth. We show that, whatever the nature of the buffer layer-metal, oxide, organic material - the classical Schottky-Mott model allows to anticipate, at least roughly, the behaviour of the contact, even if some dipole effect are often present. A good correlation between the ''metal/buffer layer'' work function and the barrier {phi}{sub b} for hole exchange at anode/organic electron donor interfaces is obtained, as expected by the model. (author)

  14. Electrochemical incineration of chloromethylphenoxy herbicides in acid medium by anodic oxidation with boron-doped diamond electrode

    International Nuclear Information System (INIS)

    Boye, Birame; Brillas, Enric; Marselli, Beatrice; Michaud, Pierre-Alain; Comninellis, Christos; Farnia, Giuseppe; Sandona, Giancarlo

    2006-01-01

    The electrochemical degradation of saturated solutions of herbicides 4-chloro-2-methylphenoxyacetic acid, 2-(4-chlorophenoxy)-2-methylpropionic acid and 2-(4-chloro-2-methylphenoxy)propionic acid in 1 M HClO 4 on a boron-doped diamond (BDD) thin film anode has been studied by chronoamperometry, cyclic voltammetry and bulk electrolysis. At low anodic potentials polymeric products are formed causing the fouling and deactivation of BDD. This is reactivated at high potentials when water decomposes producing hydroxyl radical as strong oxidant of organics. Electrolyses in a batch recirculation system at constant current density ≥8 mA cm -2 yielded overall decontamination of all saturated solution. The effect of current density and herbicide concentration on the degradation rate of each compound, the specific charge required for its total mineralization and instantaneous current efficiency have been investigated. Experimental results have been compared with those predicted by a theoretical model based on a fast anodic oxidation of initial herbicides, showing that at 30 mA cm -2 their degradation processes are completely controlled by mass transfer. Kinetic analysis of the change of herbicide concentration with time during electrolysis, determined by high-performance liquid chromatography, revealed that all compounds follow a pseudo first-order reaction. Aromatic intermediates and generated carboxylic acids have been identified using this technique and a general pathway for the electrochemical incineration of all herbicides on BDD is proposed

  15. Recent advances in nanostructured Nb-based oxides for electrochemical energy storage

    Science.gov (United States)

    Yan, Litao; Rui, Xianhong; Chen, Gen; Xu, Weichuan; Zou, Guifu; Luo, Hongmei

    2016-04-01

    For the past five years, nanostructured niobium-based oxides have emerged as one of the most prominent materials for batteries, supercapacitors, and fuel cell technologies, for instance, TiNb2O7 as an anode for lithium-ion batteries (LIBs), Nb2O5 as an electrode for supercapacitors (SCs), and niobium-based oxides as chemically stable electrochemical supports for fuel cells. Their high potential window can prevent the formation of lithium dendrites, and their rich redox chemistry (Nb5+/Nb4+, Nb4+/Nb3+) makes them very promising electrode materials. Their unique chemical stability under acid conditions is favorable for practical fuel-cell operation. In this review, we summarized recent progress made concerning the use of niobium-based oxides as electrodes for batteries (LIBs, sodium-ion batteries (SIBs), and vanadium redox flow batteries (VRBs)), SCs, and fuel cell applications. Moreover, crystal structures, charge storage mechanisms in different crystal structures, and electrochemical performances in terms of the specific capacitance/capacity, rate capability, and cycling stability of niobium-based oxides are discussed. Insights into the future research and development of niobium-based oxide compounds for next-generation electrochemical devices are also presented. We believe that this review will be beneficial for research scientists and graduate students who are searching for promising electrode materials for batteries, SCs, and fuel cells.

  16. Synthesis and electrochemical properties of stannous oxide clinopinacoid as anode material for lithium ion batteries.

    Science.gov (United States)

    Iqbal, M Zubair; Wang, Fengping; Rafique, M Yasir; Ali, Shujaat; Din, Rafi Ud; Farooq, M Hassan; Khan, Matiullah; Ali, Murad

    2013-03-01

    Tin monoxide is a significant functional semiconductor material which employed to a wide area of applications especially optical and energy storage devices. Presently, template free hydrothermal technique has been employing to synthesize stannous oxide (SnO) clinopinacoid type controlled morphology using SnCl2 x 2H2O, NH3, and H2O as raw materials. The crystalline phase, morphology, particle size and component were characterized by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS) and field-emission scanning electron microscopy (FESEM). FESEM results exhibited the large scale homogeneous growth of clinopinacoid architecture with the obvious size of 5 - 7 micrometers. The XRD results showed that the average crystallite size of the tetragonal phase romarchite SnO was about 29 nm calculated from the FWHM of X-ray diffraction pattern. The dominant Raman active modes A(1g) = 205 cm(-1), B(1g) = 105-107 cm(-1) and about 6 cm(-1) redshift were observed by the Raman spectroscopy, which further confirmed the existence of the nano tetragonal phase SnO. The electrochemical performance of as-synthesized SnO clinopinacoid structure as the anode material for lithium ion batteries was investigated. It was observed that the first discharge capacity of the two samples could reach a very high value of 1502 mA h g(-1) and 1422 mA h g(-1) respectively. The effect of nitrogen concentration on morphology as well as cyclic performance of Li-Ion-batteries was also discussed.

  17. Three-Phase Solid Oxide Fuel Cell Anode Microstructure Realization Using Two-Point Correlation Functions

    International Nuclear Information System (INIS)

    Baniassadi, Majid; Garmestani, Hamid; Li, Dongsheng; Ahzi, Said; Khaleel, Mohammad A.; Sun, Xin

    2011-01-01

    A Monte Carlo methodology is developed as a means for three-dimensional (3D) reconstruction of the microstructure of a three-phase anode used in solid oxide fuel cells, based on two-point statistical functions. The salient feature of the presented reconstruction methodology is the ability to realize the 3D microstructure from its 2D SEM image for a three-phase medium extendable to n-phase media. In the realization procedure, different phases of the heterogeneous medium are represented by different cells which are allowed to grow. The growth of cells, however, are controlled via several optimization parameters related to rotation, shrinkage, translation, distribution and growth rates of the cells. Indeed, the proposed realization algorithm can be categorized as a member of dynamic programming methods and is designed so comprehensive that can realize any desired microstructure. To be more specific, at first the initial 2D image is successfully reconstructed and then the final optimization parameters are used as the initial values for the initiation of the 3D reconstruction algorithm. This paper presents a novel hybrid stochastic methodology based on the colony and kinetic algorithm for the simulation of the virtual microstructure. The simulation procedure involves repeated realizations where each realization in turn consists of nucleation and growth of cells. For each of the subsequent realizations, the controlling parameters get updated by minimization of an objective function at the end of the preceding realization. Here, the objective function is defined based on the two-point correlation functions from the simulated and real microstructures. The kinetic growth algorithm is established on the cellular automata approach which facilitates the simulation procedure. Comparison of the two-point correlation functions from different sections of the final 3D reconstructed microstructure with the initial real microstructure shows a satisfactory agreement which confirms the

  18. Low-surface-area hard carbon anode for na-ion batteries via graphene oxide as a dehydration agent.

    Science.gov (United States)

    Luo, Wei; Bommier, Clement; Jian, Zelang; Li, Xin; Carter, Rich; Vail, Sean; Lu, Yuhao; Lee, Jong-Jan; Ji, Xiulei

    2015-02-04

    Na-ion batteries are emerging as one of the most promising energy storage technologies, particularly for grid-level applications. Among anode candidate materials, hard carbon is very attractive due to its high capacity and low cost. However, hard carbon anodes often suffer a low first-cycle Coulombic efficiency and fast capacity fading. In this study, we discover that doping graphene oxide into sucrose, the precursor for hard carbon, can effectively reduce the specific surface area of hard carbon to as low as 5.4 m(2)/g. We further reveal that such doping can effectively prevent foaming during caramelization of sucrose and extend the pyrolysis burnoff of sucrose caramel over a wider temperature range. The obtained low-surface-area hard carbon greatly improves the first-cycle Coulombic efficiency from 74% to 83% and delivers a very stable cyclic life with 95% of capacity retention after 200 cycles.

  19. Enhanced performance in organic photovoltaic devices with a KMnO4 solution treated indium tin oxide anode modification

    International Nuclear Information System (INIS)

    Yang Qian-Qian; Zhao Su-Ling; Xu Zheng; Zhang Fu-Jun; Yan Guang; Kong Chao; Fan Xing; Zhang Yan-Fei; Xu Xu-Rong

    2012-01-01

    The properties of poly(3-hexylthiophene):(6,6)-phenyl C 61 butyric acid methyl ester (P3HT:PCBM) organic photovoltaic devices (OPVs) with an indium tin oxide (ITO) anode treated by a KMnO 4 solution are investigated. The optimized KMnO 4 solution has a concentration of 50 mg/L, and ITO is treated for 15 min. The modification of ITO anode results in an enhancement of the power conversion efficiency (PCE) of the device, which is responsible for the increase of the photocurrent. The performance enhancement is attributed to the work function modification of the ITO substrate through the strong oxygenation of KMnO 4 , and then the charge collection efficiency is improved. (interdisciplinary physics and related areas of science and technology)

  20. Low-Surface-Area Hard Carbon Anode for Na-Ion Batteries via Graphene Oxide as a Dehydration Agent

    Energy Technology Data Exchange (ETDEWEB)

    Luo, W; Bommier, C; Jian, ZL; Li, X; Carter, R; Vail, S; Lu, YH; Lee, JJ; Ji, XL

    2015-02-04

    Na-ion batteries are emerging as one of the most promising energy storage technologies, particularly for grid-level applications. Among anode candidate materials, hard carbon is very attractive due to its high capacity and low cost. However, hard carbon anodes often suffer a low first-cycle Coulombic efficiency and fast capacity fading. In this study, we discover that doping graphene oxide into sucrose, the precursor for hard carbon, can effectively reduce the specific surface area of hard carbon to as low as 5.4 m(2)/g. We further reveal that such doping can effectively prevent foaming during caramelization of sucrose and extend the pyrolysis burnoff of sucrose caramel over a wider temperature range. The obtained low-surface-area hard carbon greatly improves the first-cycle Coulombic efficiency from 74% to 83% and delivers a very stable cyclic life with 95% of capacity retention after 200 cycles.

  1. A general strategy toward graphitized carbon coating on iron oxides as advanced anodes for lithium-ion batteries

    Science.gov (United States)

    Ding, Chunyan; Zhou, Weiwei; Wang, Bin; Li, Xin; Wang, Dong; Zhang, Yong; Wen, Guangwu

    2017-08-01

    Integration of carbon materials with benign iron oxides is blazing a trail in constructing high-performance anodes for lithium-ion batteries (LIBs). In this paper, a unique general, simple, and controllable strategy is developed toward in situ uniform coating of iron oxide nanostructures with graphitized carbon (GrC) layers. The basic synthetic procedure only involves a simple dip-coating process for the loading of Ni-containing seeds and a subsequent Ni-catalyzed chemical vapor deposition (CVD) process for the growth of GrC layers. More importantly, the CVD treatment is conducted at a quite low temperature (450 °C) and with extremely facile liquid carbon sources consisting of ethylene glycol (EG) and ethanol (EA). The GrC content of the resulting hybrids can be controllably regulated by altering the amount of carbon sources. The electrochemical results reveal remarkable performance enhancements of iron oxide@GrC hybrids compared with pristine iron oxides in terms of high specific capacity, excellent rate and cycling performance. This can be attributed to the network-like GrC coating, which can improve not only the electronic conductivity but also the structural integrity of iron oxides. Moreover, the lithium storage performance of samples with different GrC contents is measured, manifesting that optimized electrochemical property can be achieved with appropriate carbon content. Additionally, the superiority of GrC coating is demonstrated by the advanced performance of iron oxide@GrC compared with its corresponding counterpart, i.e., iron oxides with amorphous carbon (AmC) coating. All these results indicate the as-proposed protocol of GrC coating may pave the way for iron oxides to be promising anodes for LIBs.

  2. Controlled hydrodynamic conditions on the formation of iron oxide nanostructures synthesized by electrochemical anodization: Effect of the electrode rotation speed

    International Nuclear Information System (INIS)

    Lucas-Granados, Bianca; Sánchez-Tovar, Rita; Fernández-Domene, Ramón M.; García-Antón, Jose

    2017-01-01

    Highlights: • Novel iron anodization process under controlled dynamic conditions was evaluated. • Iron oxide nanostructures composed mainly by hematite were synthesized. • Different morphologies were obtained depending on the electrode rotation speed. • A suitable photocatalyst was obtained by stirring the electrode at 1000 rpm.. - Abstract: Iron oxide nanostructures are of particular interest because they can be used as photocatalysts in water splitting due to their advantageous properties. Electrochemical anodization is one of the best techniques to synthesize nanostructures directly on the metal substrate (direct back contact). In the present study, a novel methodology consisting of the anodization of iron under hydrodynamic conditions is carried out in order to obtain mainly hematite (α-Fe 2 O 3 ) nanostructures to be used as photocatalysts for photoelectrochemical water splitting applications. Different rotation speeds were studied with the aim of evaluating the obtained nanostructures and determining the most attractive operational conditions. The synthesized nanostructures were characterized by means of Raman spectroscopy, Field Emission Scanning Electron Microscopy, photoelectrochemical water splitting, stability against photocorrosion tests, Mott-Schottky analysis, Electrochemical Impedance Spectroscopy (EIS) and band gap measurements. The results showed that the highest photocurrent densities for photoelectrochemical water splitting were achieved for the nanostructure synthesized at 1000 rpm which corresponds to a nanotubular structure reaching ∼0.130 mA cm −2 at 0.54 V (vs. Ag/AgCl). This is in agreement with the EIS measurements and Mott-Schottky analysis which showed the lowest resistances and the corresponding donor density values, respectively, for the nanostructure anodized at 1000 rpm.

  3. Anodic selective functionalization of cyclic amine derivatives

    OpenAIRE

    Onomura, Osamu

    2012-01-01

    Anodic reactions are desirable methods from the viewpoint of Green Chemistry, since no toxic oxidants are necessary for the oxidation of organic molecules. This review introduces usefulness of anodic oxidation and successive reaction for selective functionalization of cyclic amine derivatives.

  4. Thermochemical effect of fission products on sodium - MOX fuel reaction: The case of niobium

    Science.gov (United States)

    Costin, Dan T.; Desgranges, Lionel; Cabello-Ortiga, Victor; Hedberg, Marcus; Halleröd, Jenny; Retegan, Teodora; Ekberg, Christian

    2018-03-01

    The influence of niobium on the sodium MOX fuel chemical interaction was studied by different heat treatments of airtight capsules containing fresh MOX, sodium and a niobium strip. The characterisation results evidenced a two-step process with first MOX oxidation and then MOX reduction. This result was interpreted by considering the formation of sodium niobiate that captures oxygen from the MOX. This interpretation is used to discuss the influence of niobium as fission product on the sodium -irradiated MOX fuel reaction.

  5. Electrochemical degradation of polycyclic aromatic hydrocarbons in creosote solution using ruthenium oxide on titanium expanded mesh anode

    International Nuclear Information System (INIS)

    Tran, Lan-Huong; Drogui, Patrick; Mercier, Guy; Blais, Jean-Francois

    2009-01-01

    In this study, expanded titanium (Ti) covered with ruthenium oxide (RuO 2 ) electrode was used to anodically oxidize polycyclic aromatic hydrocarbons (PAH) in creosote solution. Synthetic creosote-oily solution (COS) was prepared with distilled water and a commercial creosote solution in the presence of an amphoteric surfactant; Cocamidopropylhydroxysultaine (CAS). Electrolysis was carried out using a parallelepipedic electrolytic 1.5-L cell containing five anodes (Ti/RuO 2 ) and five cathodes (stainless steel, 316L) alternated in the electrode pack. The effects of initial pH, temperature, retention time, supporting electrolyte, current density and initial PAH concentration on the process performance were examined. Experimental results revealed that a current density of 9.23 mA cm -2 was beneficial for PAH oxidation. The sum of PAH concentrations for 16 PAHs could be optimally diminished up to 80-82% while imposing a residence time in the electrolysis cell of 90 min. There was not a significant effect of the electrolyte (Na 2 SO 4 ) concentration on oxidation efficiency in the investigated range of 500-4000 mg/L. However, an addition of 500 mg Na 2 SO 4 L -1 was required to reduce the energy consumption and the treatment cost. Besides, there was no effect of initial PAH concentration on oxidation efficiency in the investigated range of 270-540 mg PAH L -1 . Alkaline media was not favourable for PAH oxidation, whereas high performance of PAH degradation could be recorded without initial pH adjustment (original pH around 6.0). Likewise, under optimal conditions, 84% of petroleum hydrocarbon (C 10 -C 50 ) was removed, whereas removal yields of 69% and 62% have been measured for O and G and COD, respectively. Microtox and Daphnia biotests showed that electrochemical oxidation using Ti/RuO 2 could be efficiently used to reduce more than 90% of the COS toxicity.

  6. Electrochemical degradation of polycyclic aromatic hydrocarbons in creosote solution using ruthenium oxide on titanium expanded mesh anode.

    Science.gov (United States)

    Tran, Lan-Huong; Drogui, Patrick; Mercier, Guy; Blais, Jean-François

    2009-05-30

    In this study, expanded titanium (Ti) covered with ruthenium oxide (RuO(2)) electrode was used to anodically oxidize polycyclic aromatic hydrocarbons (PAH) in creosote solution. Synthetic creosote-oily solution (COS) was prepared with distilled water and a commercial creosote solution in the presence of an amphoteric surfactant; Cocamidopropylhydroxysultaine (CAS). Electrolysis was carried out using a parallelepipedic electrolytic 1.5-L cell containing five anodes (Ti/RuO(2)) and five cathodes (stainless steel, 316 L) alternated in the electrode pack. The effects of initial pH, temperature, retention time, supporting electrolyte, current density and initial PAH concentration on the process performance were examined. Experimental results revealed that a current density of 9.23 mA cm(-2) was beneficial for PAH oxidation. The sum of PAH concentrations for 16 PAHs could be optimally diminished up to 80-82% while imposing a residence time in the electrolysis cell of 90 min. There was not a significant effect of the electrolyte (Na(2)SO(4)) concentration on oxidation efficiency in the investigated range of 500-4000 mg/L. However, an addition of 500 mg Na(2)SO(4)L(-1) was required to reduce the energy consumption and the treatment cost. Besides, there was no effect of initial PAH concentration on oxidation efficiency in the investigated range of 270-540 mg PAHL(-1). Alkaline media was not favourable for PAH oxidation, whereas high performance of PAH degradation could be recorded without initial pH adjustment (original pH around 6.0). Likewise, under optimal conditions, 84% of petroleum hydrocarbon (C(10)-C(50)) was removed, whereas removal yields of 69% and 62% have been measured for O&G and COD, respectively. Microtox and Daphnia biotests showed that electrochemical oxidation using Ti/RuO(2) could be efficiently used to reduce more than 90% of the COS toxicity.

  7. Sulfur poisoning of Ni/Gadolinium-doped ceria anodes: A long-term study outlining stable solid oxide fuel cell operation

    Science.gov (United States)

    Riegraf, Matthias; Zekri, Atef; Knipper, Martin; Costa, Rémi; Schiller, Günter; Friedrich, K. Andreas

    2018-03-01

    This work presents an analysis of the long-term behavior of nickel/gadolinium-doped ceria (CGO) anode-based solid oxide fuel cells (SOFC) under sulfur poisoning conditions. A parameter study of sulfur-induced irreversible long-term degradation of commercial, high-performance single cells was carried out at 900 °C for different H2/N2/H2S fuel gas atmospheres, current densities and Ni/CGO anodes. The poisoning periods of the cells varied from 200 to 1500 h. The possibility of stable long-term Ni/CGO anode operation under sulfur exposure is established and the critical operating regime is outlined. Depending on the operating conditions, two degradation phenomena can be observed. Small degradation of the ohmic resistance was witnessed for sulfur exposure times of approximately 1000 h. Moreover, degradation of the anode charge transfer resistance was observed to be triggered by the combination of a small anodic potential step and high sulfur coverage on Ni. The microstructural evolution of altered Ni/CGO anodes was examined post-mortem by means of SEM and FIB/SEM, and is correlated to the anode performance degradation under critical operating conditions, establishing Ni depletion, porosity increase and a tripe phase boundary density decrease in the anode functional layer. It is shown that short-term sulfur poisoning behavior can be used to assess long-term stability.

  8. Electro oxidation of Phenol on a Ti/RuO{sub 2} anode: effect of some electrolysis parameters

    Energy Technology Data Exchange (ETDEWEB)

    Santos, Iranildes D. dos; Dutra, Achilles J.B. [Universidade Federal do Rio de Janeiro (PEMM/COPPE/UFRJ), RJ (Brazil). Coordenacao dos Programas de Pos-Graduacao de Engenharia. Programa de Engenharia Metalurgica e de Materiais; Afonso, Julio C., E-mail: julio@iq.ufrj.b [Universidade Federal do Rio de Janeiro (IQ/UFRJ), RJ (Brazil). Inst. de Quimica. Dept. de Quimica Analitica

    2011-07-01

    The influences of electrolysis time, anodic area, current density and supporting electrolyte on phenol and its byproducts degradation on a Ti/RuO{sub 2} anode were investigated. It was observed that phenol and its byproducts were rapidly broken down in the presence of chloride ions. Gas chromatography/mass spectrometry (GC/MS) data have shown that the presence of chloride ions lead to chlorophenols formation, due to reactions with Cl{sub 2} and/or OCl{sup -} generated during electrolysis. However, these intermediate products were also degraded later by the oxidizing agents. The standards established by the CONAMA (Brazilian National Council for the Environment) for phenols and chlorophenols in effluents were achieved after 360 min of electrolysis with a current density of 10 mA cm-2. Cyclic voltammograms obtained with the anodes before and after 436 h of electrolysis under severe salinity conditions (2 mol L-1) and current density (800 mA cm-2) showed that Ti/RuO{sub 2} did not lose its electrocatalytic properties. This fact indicates that Ti/RuO{sub 2} can be used for the treatment of effluents containing phenols in a chloride environment. (author)

  9. Compact-Nanobox Engineering of Transition Metal Oxides with Enhanced Initial Coulombic Efficiency for Lithium-Ion Battery Anodes.

    Science.gov (United States)

    Zhu, Yanfei; Hu, Aiping; Tang, Qunli; Zhang, Shiying; Deng, Weina; Li, Yanhua; Liu, Zheng; Fan, Binbin; Xiao, Kuikui; Liu, Jilei; Chen, Xiaohua

    2018-03-05

    A novel strategy is proposed to construct a compact-nanobox (CNB) structure composed of irregular nanograins (average diameter ≈ 10 nm), aiming to confine the electrode-electrolyte contact area and enhance initial Coulombic efficiency (ICE) of transition metal oxide (TMO) anodes. To demonstrate the validity of this attempt, CoO-CNB is taken as an example which is synthesized via a carbothermic reduction method. Benefiting from the compact configuration, electrolyte can only contact the outer surface of the nanobox, keeping the inner CoO nanograins untouched. Therefore, the solid electrolyte interphase (SEI) formation is reduced. Furthermore, the internal cavity leaves enough room for volume variation upon lithiation and delithiation, resulting in superior mechanical stability of the CNB structure and less generation of fresh SEI. Consequently, the SEI remains stable and spatially confined without degradation, and hence, the CoO-CNB electrode delivers an enhanced ICE of 82.2%, which is among the highest values reported for TMO-based anodes in lithium-ion batteries. In addition, the CoO-CNB electrode also demonstrates excellent cyclability with a reversible capacity of 811.6 mA h g -1 (90.4% capacity retention after 100 cycles). These findings open up a new way to design high-ICE electrodes and boost the practical application of TMO anodes.

  10. Solution processed transition metal oxide anode buffer layers for efficiency and stability enhancement of polymer solar cells

    Science.gov (United States)

    Ameen, M. Yoosuf; Shamjid, P.; Abhijith, T.; Reddy, V. S.

    2018-01-01

    Polymer solar cells were fabricated with solution-processed transition metal oxides, MoO3 and V2O5 as anode buffer layers (ABLs). The optimized device with V2O5 ABL exhibited considerably higher power conversion efficiency (PCE) compared to the devices based on MoO3 and poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) ABLs. The space charge limited current measurements and impedance spectroscopy results of hole-only devices revealed that V2O5 provided a very low charge transfer resistance and high hole mobility, facilitating efficient hole transfer from the active layer to the ITO anode. More importantly, incorporation of V2O5 as ABL resulted in substantial improvement in device stability compared to MoO3 and PEDOT:PSS based devices. Unencapsulated PEDOT:PSS-based devices stored at a relative humidity of 45% have shown complete failure within 96 h. Whereas, MoO3 and V2O5 based devices stored in similar conditions retained 22% and 80% of their initial PCEs after 96 h. Significantly higher stability of the V2O5-based device is ascribed to the reduction in degradation of the anode/active layer interface, as evident from the electrical measurements.

  11. Layered oxygen-deficient double perovskite as an efficient and stable anode for direct hydrocarbon solid oxide fuel cells.

    Science.gov (United States)

    Sengodan, Sivaprakash; Choi, Sihyuk; Jun, Areum; Shin, Tae Ho; Ju, Young-Wan; Jeong, Hu Young; Shin, Jeeyoung; Irvine, John T S; Kim, Guntae

    2015-02-01

    Different layered perovskite-related oxides are known to exhibit important electronic, magnetic and electrochemical properties. Owing to their excellent mixed-ionic and electronic conductivity and fast oxygen kinetics, cation layered double perovskite oxides such as PrBaCo2O5 in particular have exhibited excellent properties as solid oxide fuel cell oxygen electrodes. Here, we show for the first time that related layered materials can be used as high-performance fuel electrodes. Good redox stability with tolerance to coking and sulphur contamination from hydrocarbon fuels is demonstrated for the layered perovskite anode PrBaMn2O5+δ (PBMO). The PBMO anode is fabricated by in situ annealing of Pr0.5Ba0.5MnO3-δ in fuel conditions and actual fuel cell operation is demonstrated. At 800 °C, layered PBMO shows high electrical conductivity of 8.16 S cm(-1) in 5% H2 and demonstrates peak power densities of 1.7 and 1.3 W cm(-2) at 850 °C using humidified hydrogen and propane fuels, respectively.

  12. UV-treated graphene oxide as anode interfacial layers for P3HT : PCBM solar cells

    Science.gov (United States)

    Cheng, Cheng-En; Tsai, Cheng-Wei; Pei, Zingway; Lin, Tsung-Wu; Chang, Chen-Shiung; Shih-Sen Chien, Forest

    2015-06-01

    Solution-processable graphene oxide (GO) ultrathin films were introduced as anode interfacial layers (AILs) for polymer solar cells (PSCs). The photovoltaic performance of PSCs containing thermal- and UV-treated GO was comparable to that of PSCs with conventional poly(3,4-ethyledioxythiphene):poly(styrenesulfonate) AILs. UV treatment induced the surface activation of GO; an increase in the work function of UV-treated GO improved the energy band alignment at the GO/poly(3-hexylthiophene) interface, which accounted for the efficient hole collection and photovoltaic performance of PSCs with treated GO.

  13. Syntheses of Nd2O3 nanowires through sol-gel process assisted with porous anodic aluminum oxide (AAO) template

    International Nuclear Information System (INIS)

    Qu Xiaofei; Dai Jinhui; Tian Jintao; Huang Xiang; Liu Zhongfang; Shen Zhenlei; Wang Peipei

    2009-01-01

    The syntheses of Nd 2 O 3 nanowires were performed through sol-gel process assisted with porous anodic aluminum oxide (AAO) as a template. The morphology and the phase composition of the prepared nanowires were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and energy disperse spectroscopy (EDS). The results showed that the Nd 2 O 3 nanowires could be successfully synthesized by using this method. The nanowires had successfully grown into the nanochannels of the AAO template. The prepared nanowires were quite uniform. Both the XRD and EDS examinations revealed that the obtained nanowires were not others but Nd 2 O 3

  14. A High-Performing Sulfur-Tolerant and Redox-Stable Layered Perovskite Anode for Direct Hydrocarbon Solid Oxide Fuel Cells

    Science.gov (United States)

    Ding, Hanping; Tao, Zetian; Liu, Shun; Zhang, Jiujun

    2015-01-01

    Development of alternative ceramic oxide anode materials is a key step for direct hydrocarbon solid oxide fuel cells (SOFCs). Several lanthanide based layered perovskite-structured oxides demonstrate outstanding oxygen diffusion rate, favorable electronic conductivity, and good oxygen surface exchange kinetics, owing to A-site ordered structure in which lanthanide and alkali-earth ions occupy alternate (001) layers and oxygen vacancies are mainly located in [LnOx] planes. Here we report a nickel-free cation deficient layered perovskite, (PrBa)0.95(Fe0.9Mo0.1)2O5 + δ (PBFM), for SOFC anode, and this anode shows an outstanding performance with high resistance against both carbon build-up and sulfur poisoning in hydrocarbon fuels. At 800 °C, the layered PBFM showed high electrical conductivity of 59.2 S cm−1 in 5% H2 and peak power densities of 1.72 and 0.54 W cm−2 using H2 and CH4 as fuel, respectively. The cell exhibits a very stable performance under a constant current load of 1.0 A cm−2. To our best knowledge, this is the highest performance of ceramic anodes operated in methane. In addition, the anode is structurally stable at various fuel and temperature conditions, suggesting that it is a feasible material candidate for high-performing SOFC anode. PMID:26648509

  15. Engineering of the energetic structure of the anode of organic photovoltaic devices utilizing hot-wire deposited transition metal oxide layers

    Energy Technology Data Exchange (ETDEWEB)

    Vasilopoulou, M., E-mail: mariva@imel.demokritos.gr [Institute of Nanoscience and Nanotechnology, Department of Microelectronics, National Center for Scientific Research Demokritos, POB 60228, 15310 Agia Paraskevi, Attiki (Greece); Stathopoulos, N.A.; Savaidis, S.A. [Department of Electronics, Technological and Educational Institute (TEI) of Piraeus, Petrou Ralli & Thivon, 12244 Aegaleo (Greece); Kostis, I. [Institute of Nanoscience and Nanotechnology, Department of Microelectronics, National Center for Scientific Research Demokritos, POB 60228, 15310 Agia Paraskevi, Attiki (Greece); Department of Electronics, Technological and Educational Institute (TEI) of Piraeus, Petrou Ralli & Thivon, 12244 Aegaleo (Greece); Papadimitropoulos, G. [Institute of Nanoscience and Nanotechnology, Department of Microelectronics, National Center for Scientific Research Demokritos, POB 60228, 15310 Agia Paraskevi, Attiki (Greece); Davazoglou, D., E-mail: d.davazoglou@imel.demokritos.gr [Institute of Nanoscience and Nanotechnology, Department of Microelectronics, National Center for Scientific Research Demokritos, POB 60228, 15310 Agia Paraskevi, Attiki (Greece)

    2015-09-30

    Graphical abstract: In this work we perform successful engineering of the anode of organic photovoltaics based on poly(3-hexylthiophene):[6,6]-phenyl butyric acid methyl ester blends by using metal oxide transport layers exhibiting shallow gap states which act as a barrier-free path for hole transport toward the anode. - Highlights: • Interface engineering of the anode. • Organic photovoltaics (OPVs). • Shallow gap states. • Barrier-free hole transport. • Design rules for interface engineering in OPVs. - Abstract: In this work we use hydrogen deposited molybdenum and tungsten oxides (chemically described as H:MO{sub x}x ≤ 3 where M = Mo or W) to control the energetics at the anode of bulk heterojunction (BHJ) organic photovoltaics (OPVs) based on poly(3-hexylthiophene):[6,6]-phenyl butyric acid methyl ester (P3HT:PC{sub 71}BM) blends. Significantly improved current densities and open circuit voltages were achieved as a result of improved hole transport from the P3HT highest occupied molecular orbital (HOMO) toward indium tin oxide (ITO) anode. This was attributed to the formation of shallow gap states in these oxides which are located just below the Fermi level and above the polymer HOMO and thus may act as a barrier-free path for the extraction of holes. Consequently, these states can be used for controlling the energetic structure of the anode of OPVs. By using ultraviolet photoelectron spectroscopy it was found that dependent on the deposition conditions these gap states and work function of the metal oxides may be tailored to contribute to the precise alignment of the HOMO of the organic semiconductor (OSC) with the Fermi level of the anode electrode resulting in further enhancement of the device performance.

  16. Comparative analysis on surface property in anodic oxidation polishing of reaction-sintered silicon carbide and single-crystal 4H silicon carbide

    Science.gov (United States)

    Shen, Xinmin; Tu, Qunzhang; Deng, Hui; Jiang, Guoliang; He, Xiaohui; Liu, Bin; Yamamura, Kazuya

    2016-04-01

    For effective machining of difficult-to-machine materials, such as reaction-sintered silicon carbide (RS-SiC) and single-crystal 4H silicon carbide (4H-SiC), a novel polishing technique named anodic oxidation polishing was proposed, which combined with the anodic oxidation of substrate and slurry polishing of oxide. By scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM-EDX) observation and atomic force microscopy analysis, both the anodic oxidation behaviors of RS-SiC and 4H-SiC were investigated. Through comparison of the surfaces before and after hydrofluoric acid etching of the oxidized samples by the scanning white light interferometry (SWLI) measurement, the relationships between oxidation depth and oxidation time were obtained, and the calculated oxidation rate for RS-SiC was 5.3 nm/s and that for 4H-SiC was 5.8 nm/s based on the linear Deal-Grove model. Through anodic oxidation polishing of RS-SiC substrate and 4H-SiC substrate, respectively, the surface roughness rms obtained by SWLI was improved to 2.103 nm for RS-SiC and to 0.892 nm for 4H-SiC. Experimental results indicate that anodic oxidation polishing is an effective method for the machining of RS-SiC and 4H-SiC samples, which would improve the process level of SiC substrates and promote the application of SiC products in the fields of optics, ceramics, semiconductors, electronics, and so on.

  17. Electrochemical degradation of Novacron Yellow C-RG using boron-doped diamond and platinum anodes: Direct and Indirect oxidation

    International Nuclear Information System (INIS)

    Rocha, J.H. Bezerra; Gomes, M.M. Soares; Santos, E. Vieira dos; Moura, E.C. Martins de; Silva, D. Ribeiro da; Quiroz, M.A.; Martínez-Huitle, C.A.

    2014-01-01

    Graphical abstract: - Highlights: • Nature of electrode material decides the electrocatalytic mechanism followed. • Electrogenerated strong oxidants on BDD surface improve the color and organic load removal. • Chlorine active species act in solution cage oxidizing organic matter. - Abstract: The present study discusses the electrochemical degradation process of a textile dye, Novacron Yellow C-RG (NY), dissolved in synthetic wastewaters, via direct and indirect oxidation. Experiments were conducted using boron-doped diamond (BDD) and platinum supported on Ti (Pt/Ti) electrodes in the absence and presence of NaCl in the solution. The direct process for removing color is relatively similar for both anodes, while the electrochemical degradation is significantly accelerated by the presence of halogen salt in the solution. Interestingly, it does not depend on applied current density, but rather on NaCl concentration. Therefore, the electrochemical processes (direct/indirect) favor specific oxidation pathways depending on electrocatalytic material. Whereas, the Pt/Ti anode favors preferentially color removal by direct and indirect oxidation (100% of color removal) due to the fragmentation of the azo dye group; BDD electrode favors color and organic load removals in both processes (95% and up to 87%, respectively), due to the rupture of dye in different parts of its chemical structure. Parameters of removal efficiency and energy consumption for the electrochemical process were estimated. Finally, an explanation has been attempted for the role of halide, in relation with the oxygen evolution reaction, concomitant with the electrochemical incineration as well as electrocatalytic mechanisms, for each one of the electrodes used

  18. Surface preparation of niobium

    International Nuclear Information System (INIS)

    Kneisel, P.

    1980-01-01

    Any discussion of surface preparation for superconducting rf-surfaces is certainly connected with the question what is the best recipe for achieving high Q-values and high break-down fields. Since the break-down in a cavity is not understood so far and because several mechanisms play a role, it also is not possible to give one recipe which always works. Nevertheless in the past certain preparation techniques for niobium surfaces have been developed and certain rules for preparation can be applied. In the following the to-days state of the art will be described and it is attempted to give a short description of the surface in conjunction with the methods of surface treatments, which generally can be applied to niobium cavities. (orig./WTR)

  19. Nano integrated lithium polymer electrolytes based on anodic aluminum oxide (AAO) templates

    Science.gov (United States)

    Bokalawela, Roshan S. P.

    Since their discovery in the 1970s, polymer electrolytes have been actively studied because they have properties important for many device applications. However, even after 40 years, the detailed mechanisms of conductivity in these electrolytes are still not completely understood. Moreover, the conductivity in polymer electrolytes is one of the limiting factors of these devices so that different methods to enhance conductivity are actively being explored. One proposed method of enhancing the conductivity is to confine the polymer electrolyte in the nanoscale, but the study of material properties at the nanoscale is challenging in this area. In this work, we confine poly(ethylene oxide) lithium triflate (PEO:LiTf)(X:1)X=10,30 polymer electrolytes in carefully fabricated nanometer-diameter anodized aluminum oxide (AAO) pore structures. We demonstrate two orders of magnitude higher conductivity in the confined structures versus that of bulk films. Using x-ray characterization we show that this increased conductivity is associated with ordered PEO polymer chains aligned in the template pore direction. The activation energy of the AAO-confined polymer electrolyte is found to be smaller than that of the unconfined melt and about half that of the unconfined solid. This result indicates that not only is the room-temperature confined polymer ordered, but that this order persists at temperatures where the nano-confined polymer electrolyte is expected to be a liquid. The geometric bulk resistances of the electrolytes were obtained by AC-impedance spectra, from which the ionic conductivities were calculated. The Arrhenius plots of temperature dependent ionic conductivities showed that the usual melting temperature of the PEO phase in confined PEO:LiTf(X:1) X=10,30 is suppressed and a single activation energy was evident throughout the temperature range 25--90 °C. Wide-angle x-ray scattering (WAXS) patterns show that the polymer chains in both the pure PEO and PEO:LiTf(10

  20. Kinetics of Carbon Monoxide Electro-Oxidation in Solid-Oxide Fuel Cells from Ni-YSZ Patterned-Anode Measurements

    KAUST Repository

    Hanna, J.

    2013-04-17

    A mathematical model is developed around the framework of a reduced mechanism describing electrochemical oxidation of carbon monoxide on Ni-YSZ patterned anodes. The electro-oxidation mechanism involves three reactions, one describing adsorption/ desorption of COonNi, and two single-electron charge-transfer steps inwhich the surface adsorbate CO(Ni) participates directly. These steps are coupled with surface transport in a reaction-diffusion model for which analytic equilibrium and steady-state solutions are derived. As much as possible, we make use of existing, independent, published information about heterogeneous chemistry, surface transport, and other model parameters. The only unknowns in our model are taken to be the kinetic rate constants of the electrochemical reactions, which we evaluate by fitting the model predictions to previously published patterned-anode experiments [B. Habibzadeh, Ph.D. Thesis, University of Maryland, College Park, MD, USA (2007)]. The results show that diffusion of CO on the Ni surface to the three-phase boundary is the rate-controlling process for CO electro-oxidation. Moreover, from a reaction standpoint, the charge-transfer process is dominated by a slow step involving CO(Ni). These findings collectively demonstrate the critical dependence of the electro-oxidation process to the direct participation of CO. © 2013 The Electrochemical Society. All rights reserved.

  1. Development of materials for use in solid oxid fuel cells anodes using renewable fuels in direct operation

    International Nuclear Information System (INIS)

    Lima, D.B.P.L. de; Florio, D.Z. de; Bezerra, M.E.O.

    2016-01-01

    Fuel cells produce electrical current from the electrochemical combustion of a gas or liquid (H2, CH4, C2H5OH, CH3OH, etc.) inserted into the anode cell. An important class of fuel cells is the SOFC (Solid Oxide Cell Fuel). It has a ceramic electrolyte that transports protons (H +) or O-2 ions and operating at high temperatures (500-1000 °C) and mixed conductive electrodes (ionic and electronic) ceramics or cermets. This work aims to develop anodes for fuel cells of solid oxide (SOFC) in order to direct operations with renewable fuels and strategic for the country (such as bioethanol and biogas). In this context, it becomes important to study in relation to the ceramic materials, especially those that must be used in high temperatures. Some types of double perovskites such as Sr2MgMoO6 (or simply SMMO) have been used as anodes in SOFC. In this study were synthesized by the polymeric precursor method, analyzed and characterized different ceramic samples of families SMMO, doped with Nb, this is: Sr2 (MgMo)1-xNbxO6 with 0 ≤ x ≤ 0.2. The materials produced were characterized by various techniques such as, thermal analysis, X-ray diffraction and scanning electron microscopy, and electrical properties determined by dc and ac measurements in a wide range of temperature, frequency and partial pressure of oxygen. The results of this work will contribute to a better understanding of advanced ceramic properties with mixed driving (electronic and ionic) and contribute to the advancement of SOFC technology operating directly with renewable fuels. (author)

  2. An in situ near-ambient pressure X-ray Photoelectron Spectroscopy study of Mn polarised anodically in a cell with solid oxide electrolyte

    International Nuclear Information System (INIS)

    Bozzini, Benedetto; Amati, Matteo; Bocchetta, Patrizia; Dal Zilio, Simone; Knop-Gericke, Axel; Vesselli, Erik; Kiskinova, Maya

    2015-01-01

    This paper reports an in situ study of the anodic behavior of a model solid oxide electrolysis cell (SOEC) by means of near-ambient pressure X-ray Photoelectron Spectroscopy (XPS) combined with near edge X-ray absorption fine structure (NEXAFS) measurements. The focus is on the anodic surface chemistry of MnO x , a model anodic material already considered in cognate SOFC-related studies, during electrochemical operation in CO 2 , CO 2 /H 2 O and H 2 O ambients. The XPS and NEXAFS results we obtained, complemented by electrochemical measurements and SEM characterisation, reveal the chemical evolution of Mn under electrochemical control. MnO is the stable chemical form at open-circuit potential (OCP), while Mn 3 O 4 forms under anodic polarisation in all the investigated gas ambients. Carbon deposits are present on the Mn electrode at OCP, but they are readily oxidised under anodic conditions. Prolonged operation of the MnO x anode leads to pitting of the Mn films, damaging of the triple-phase boundary region and also to formation of discontinuities in the Mn patch. This is accompanied by chemical transformations of the electrolyte and formation of ZrC without impact on the surface chemistry of the Mn-based anode

  3. EQCM behavior of copper anodes in alkaline medium and characterization of the electrocatalysis of ethanol oxidation by Cu(III

    Directory of Open Access Journals (Sweden)

    Paixão Thiago R. L. C.

    2006-01-01

    Full Text Available The anodic oxidation of copper electrodes in alkaline solutions was investigated by using voltammetry, chronoamperometry, impedance measurements and the electrochemical quartz crystal microbalance (EQCM. Experiments were carried out in NaOH solutions in the 0.1 to 3.0 mol L-1 concentration range. The formation of soluble and insoluble species such as Cu(OH4(2- and Cu2O during the electrodic dissolution of copper anodes was characterized by analyzing potentiodynamic mass responses and the relationship between mass changes and charge. On the other hand, EQCM data were not effective to confirm the nature of other copper species proposed in literature named as CuO and Cu(OH2 because of viscoelastic changes in the film layer electrodeposited onto the quartz crystal. The participation of a Cu(III soluble species in the electrocatalytic oxidation of ethanol was proved by EQCM measurements, data providing valuable information on the mechanism of the electrode process and formation of a Cu(II insoluble species from the reaction of Cu(III with ethanol.

  4. Preparation of 3D nanoporous copper-supported cuprous oxide for high-performance lithium ion battery anodes.

    Science.gov (United States)

    Liu, Dequan; Yang, Zhibo; Wang, Peng; Li, Fei; Wang, Desheng; He, Deyan

    2013-03-07

    Three-dimensional (3D) nanoporous architectures can provide efficient and rapid pathways for Li-ion and electron transport as well as short solid-state diffusion lengths in lithium ion batteries (LIBs). In this work, 3D nanoporous copper-supported cuprous oxide was successfully fabricated by low-cost selective etching of an electron-beam melted Cu(50)Al(50) alloy and subsequent in situ thermal oxidation. The architecture was used as an anode in lithium ion batteries. In the first cycle, the sample delivered an extremely high lithium storage capacity of about 2.35 mA h cm(-2). A high reversible capacity of 1.45 mA h cm(-2) was achieved after 120 cycles. This work develops a promising approach to building reliable 3D nanostructured electrodes for high-performance lithium ion batteries.

  5. Electrodeposition of vertically standing Ag nanoplates and nanowires on transparent conductive electrode using porous anodic aluminum oxide template

    Science.gov (United States)

    Wang, Jue; Pan, Shanlin

    2017-10-01

    We report fabricating vertically standing Ag nanoplates and nanowires on a transparent conductive substrate of indium tin oxides (ITO) with the assistance of a porous anodic aluminum oxide (AAO) template. Two-dimensional Ag nanoplates can be electrodeposited onto an AAO covered ITO surface without using an adhesion layer. Ag nanoplates obtained using AAO templates have 3 × {222} superlattice fringes, different from the 3 × {422} superlattice fringes reported in the previous study. Ag nanowires can be electrodeposited onto ITO which is initially covered with an AAO template through a conductive polymer poly (3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS). The coverage, diameter, and thickness of Ag nanoplates are strongly dependent on the electrodeposition time. These Ag nanoplates and nanowires are used for surface enhanced Raman spectroscopy (SERS) and the influence of their shape, size, and coverage on SERS enhancement is studied.

  6. Microstructural degradation of Ni-YSZ anodes for solid oxide fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Thyden, K.

    2008-03-15

    Ni-YSZ cermets have been used as anode materials in SOFCs for more than 20 years. Despite this fact, the major cause of degradation within the Ni-YSZ anode, namely Ni sintering / coarsening, is still not fully understood. Even if microstructural studies of anodes in tested cells are of technological relevance, it is difficult to identify the effect from isolated parameters such as temperature, fuel gas composition and polarization. Model studies of high temperature aged Ni-YSZ cermets are generally performed in atmospheres containing relatively low concentrations of H2O. In this work, the microstructural degradation in both electrochemically longterm tested cells and high-temperature aged model materials are studied. Since Ni particle sintering / coarsening is attributed to be the major cause of anode degradation, this subject attains the primary focus. A large part of the work is focused on improving microstructural techniques and shows that the application of low acceleration voltages (<= 1 kV) in a FE-SEM makes it possible to obtain two useful types of contrast between the phases in Ni-YSZ composites. By changing between the ordinary lateral SE detector and the inlens detector, using similar microscope settings, two very different sample characteristics are probed: 1) The difference in secondary emission coefficient, delta, between the percolating and non-percolating Ni is maximized in the low-voltage range due to a high delta for the former and the suppression of delta by a positive charge for the latter. This difference yields a contrast between the two phases which is picked up by an inlens secondary electron detector. 2) The difference in backscatter coefficient, eta, between Ni and YSZ is shown to increase with decreasing voltage. The contrast is illustrated in images collected by the normal secondary detector since parts of the secondary signals are generated by backscattered electrons. High temperature aging experiments of model Ni-YSZ anode cermets show

  7. Apatite Formation and Biocompatibility of a Low Young’s Modulus Ti-Nb-Sn Alloy Treated with Anodic Oxidation and Hot Water

    Science.gov (United States)

    Tanaka, Hidetatsu; Mori, Yu; Noro, Atsushi; Kogure, Atsushi; Kamimura, Masayuki; Yamada, Norikazu; Hanada, Shuji; Masahashi, Naoya; Itoi, Eiji

    2016-01-01

    Ti-6Al-4V alloy is widely prevalent as a material for orthopaedic implants because of its good corrosion resistance and biocompatibility. However, the discrepancy in Young’s modulus between metal prosthesis and human cortical bone sometimes induces clinical problems, thigh pain and bone atrophy due to stress shielding. We designed a Ti-Nb-Sn alloy with a low Young’s modulus to address problems of stress disproportion. In this study, we assessed effects of anodic oxidation with or without hot water treatment on the bone-bonding characteristics of a Ti-Nb-Sn alloy. We examined surface analyses and apatite formation by SEM micrographs, XPS and XRD analyses. We also evaluated biocompatibility in experimental animal models by measuring failure loads with a pull-out test and by quantitative histomorphometric analyses. By SEM, abundant apatite formation was observed on the surface of Ti-Nb-Sn alloy discs treated with anodic oxidation and hot water after incubation in Hank’s solution. A strong peak of apatite formation was detected on the surface using XRD analyses. XPS analysis revealed an increase of the H2O fraction in O 1s XPS. Results of the pull-out test showed that the failure loads of Ti-Nb-Sn alloy rods treated with anodic oxidation and hot water was greater than those of untreated rods. Quantitative histomorphometric analyses indicated that anodic oxidation and hot water treatment induced higher new bone formation around the rods. Our findings indicate that Ti-Nb-Sn alloy treated with anodic oxidation and hot water showed greater capacity for apatite formation, stronger bone bonding and higher biocompatibility for osteosynthesis. Ti-Nb-Sn alloy treated with anodic oxidation and hot water treatment is a promising material for orthopaedic implants enabling higher osteosynthesis and lower stress disproportion. PMID:26914329

  8. Fabrication of porous tungsten oxide via anodizing in an ammonium nitrate/ethylene glycol/water mixture for visible light-driven photocatalyst

    Science.gov (United States)

    Kikuchi, Tatsuya; Kawashima, Jun; Natsui, Shungo; Suzuki, Ryosuke O.

    2017-11-01

    Fabrication of a nanoporous tungsten oxide film via anodizing of tungsten in an ammonium nitrate (NH4NO3)/ethylene glycol (EG)/water (H2O) mixture is reported for use as a visible light-driven photocatalyst. Anodizing of tungsten in a 1.0 M NH4NO3/EG solution containing less than 0.1 vol% H2O resulted in active dissolution of the tungsten substrate. As the H2O concentration increased to more than 25 vol%, a thin barrier oxide film was formed on the tungsten substrate. A thick porous tungsten oxide with numerous nanopores measuring several tens of nanometer in diameter was fabricated via anodizing at a moderate H2O concentration of 1.0 vol%. The porous oxide consisted of a double-layered structure with an outer porous layer and an inner dense layer, and the outer porous layer became thinner as the NH4NO3 concentration decreased. A uniform porous oxide film from the top surface to the bottom interface was fabricated via anodizing at 20 V in a 0.02 M NH4NO3/EG solution containing 1.0 vol% H2O at 313 K. The porous tungsten oxide exhibited visible light-driven photocatalytic activity for the photocatalytic decomposition of methylene blue.

  9. Rational Design of a Water-Storable Hierarchical Architecture Decorated with Amorphous Barium Oxide and Nickel Nanoparticles as a Solid Oxide Fuel Cell Anode with Excellent Sulfur Tolerance.

    Science.gov (United States)

    Song, Yufei; Wang, Wei; Ge, Lei; Xu, Xiaomin; Zhang, Zhenbao; Julião, Paulo Sérgio Barros; Zhou, Wei; Shao, Zongping

    2017-11-01

    Solid oxide fuel cells (SOFCs), which can directly convert chemical energy stored in fuels into electric power, represent a useful technology for a more sustainable future. They are particularly attractive given that they can be easily integrated into the currently available fossil fuel infrastructure to realize an ideal clean energy system. However, the widespread use of the SOFC technology is hindered by sulfur poisoning at the anode caused by the sulfur impurities in fossil fuels. Therefore, improving the sulfur tolerance of the anode is critical for developing SOFCs for use with fossil fuels. Herein, a novel, highly active, sulfur-tolerant anode for intermediate-temperature SOFCs is prepared via a facile impregnation and limited reaction protocol. During synthesis, Ni nanoparticles, water-storable BaZr 0.4 Ce 0.4 Y 0.2 O 3- δ (BZCY) perovskite, and amorphous BaO are formed in situ and deposited on the surface of a Sm 0.2 Ce 0.8 O 1.9 (SDC) scaffold. More specifically, a porous SDC scaffold is impregnated with a well-designed proton-conducting perovskite oxide liquid precursor with the nominal composition of Ba(Zr 0.4 Ce 0.4 Y 0.2 ) 0.8 Ni 0.2 O 3- δ (BZCYN), calcined and reduced in hydrogen. The as-synthesized hierarchical architecture exhibits high H 2 electro-oxidation activity, excellent operational stability, superior sulfur tolerance, and good thermal cyclability. This work demonstrates the potential of combining nanocatalysts and water-storable materials in advanced electrocatalysts for SOFCs.

  10. V{sub 2}O{sub 5}-ZrO{sub 2} catalysts for the oxidative dehydrogenation of propane - influence of the niobium oxide doping

    Energy Technology Data Exchange (ETDEWEB)

    Albrecht, S.; Hallmeier, K.H.; Wendt, G. [Leipzig Univ. (Germany). Fakultaet fuer Chemie und Mineralogie; Lippold, G. [Leipzig Univ. (Germany). Fakultaet fuer Physik und Geowissenschaften

    1998-12-31

    The oxidative dehydrogenation (ODH) of light alkanes is an alternative way for the production of olefins. A wide variety of catalytic systems has been investigated. Vanadium oxide based catalysts were described in the literature as effective catalysts for the ODH of propane. The catalytic activity and selectivity depend on the kind of support material, the kind of dopants and the formation of complex metal oxide phases. In recent papers it was claimed that both orthovanadate and/or pyrovanadate species are selective for the ODH of propane. Niobia based materials were investigated as catalysts for acidic and selective oxidation type reactions. In the ODH of propane niobia exhibited a high selectivity to propene but the conversion of propane was low. V{sub 2}O{sub 5}-Nb{sub 2}O{sub 5} catalysts proved to be catalytically active and selective and showed no formation of oxygenates. In the present study the influence of the niobia dopant of the catalytic properties of V{sub 2}O{sub 5}-ZrO{sub 2} catalysts in the ODH of propane was examined. The structural and textural properties of the catalysts were investigated using several methods. (orig.)

  11. Anodic formation of low-aspect-ratio porous alumina films for metal-oxide sensor application

    International Nuclear Information System (INIS)

    Gorokh, G.; Mozalev, A.; Solovei, D.; Khatko, V.; Llobet, E.; Correig, X.

    2006-01-01

    Thin nanoporous anodic alumina films, of low aspect ratio (1:1), with two distinctive pore sizes and morphologies were prepared by two-step constant-current anodising of aluminium layers on SiO 2 /Si substrates in 0.4 mol dm -3 tartaric (TA) and malonic acid (MA) electrolytes and then modified by open-circuit dissolution. The anodic films were employed as a support material for sputtering-deposition of thin WO 3 layers in view of exploiting their gas sensing properties. The films and deposits were characterized by scanning electron microscopy, X-ray diffraction and electric resistance measurements at fixed temperatures in the range of 100-300 deg. C upon NH 3 and CO gas exposures. Test sensors prepared from the annealed and stabilized alumina-supported WO 3 active layers were insensitive to CO but showed considerably enhanced responses to NH 3 at 300 deg. C, the sensitivity depending upon the anodic film nature, the pore size and the surface morphology. The increased sensor sensitivity is due to the substantially enlarged film surface area of the TA-supported WO 3 films and the nanostructured, camomile-like morphology of the MA-supported WO 3 films. Sensing mechanisms in the alumina-supported WO 3 active layers are discussed

  12. Scanning electron microscopy of heat treated TiO2 nanotubes arrays obtained by anodic oxidation

    Science.gov (United States)

    Naranjo, D. I.; García-Vergara, S. J.; Blanco, S.

    2017-12-01

    Scanning electron microscopy was used to investigate the anatase-rutile transformation of self-organized TiO2 nanotubes obtained on titanium foil by anodizing and subsequent heat treatment. The anodizing was carried out at 20V in an 1% v/v HF acid and ethylene glycol:water (50:50) electrolyte at room temperature. The anodized samples were initially pre-heat treated at 450°C for 4 hours to modify the amorphous structure of TiO2 nanotubes into anatase structure. Then, the samples were heated between 600 to 800°C for different times, in order to promote the transformation to rutile structure. The formation of TiO2 nanotubes is evident by SEM images. Notably, when the samples are treated at high temperature, the formation of rutile crystals starts to become evident at the nanotubes located on the originally grain boundaries of the titanium. Thus, the anatase - rutile transformation has a close relationship with the microstructure of the titanium, more exactly with grain boundaries.

  13. Electrochemical degradation of polycyclic aromatic hydrocarbons in creosote solution using ruthenium oxide on titanium expanded mesh anode

    Energy Technology Data Exchange (ETDEWEB)

    Tran, Lan-Huong; Drogui, Patrick; Mercier, Guy [Institut National de la Recherche Scientifique (Centre Eau Terre et Environnement), Universite du Quebec, 490 rue de la Couronne, C.P. 7500, Quebec, Qc G1K 9A9 (Canada); Blais, Jean-Francois, E-mail: blaisjf@ete.inrs.ca [Institut National de la Recherche Scientifique (Centre Eau Terre et Environnement), Universite du Quebec, 490 rue de la Couronne, C.P. 7500, Quebec, Qc G1K 9A9 (Canada)

    2009-05-30

    In this study, expanded titanium (Ti) covered with ruthenium oxide (RuO{sub 2}) electrode was used to anodically oxidize polycyclic aromatic hydrocarbons (PAH) in creosote solution. Synthetic creosote-oily solution (COS) was prepared with distilled water and a commercial creosote solution in the presence of an amphoteric surfactant; Cocamidopropylhydroxysultaine (CAS). Electrolysis was carried out using a parallelepipedic electrolytic 1.5-L cell containing five anodes (Ti/RuO{sub 2}) and five cathodes (stainless steel, 316L) alternated in the electrode pack. The effects of initial pH, temperature, retention time, supporting electrolyte, current density and initial PAH concentration on the process performance were examined. Experimental results revealed that a current density of 9.23 mA cm{sup -2} was beneficial for PAH oxidation. The sum of PAH concentrations for 16 PAHs could be optimally diminished up to 80-82% while imposing a residence time in the electrolysis cell of 90 min. There was not a significant effect of the electrolyte (Na{sub 2}SO{sub 4}) concentration on oxidation efficiency in the investigated range of 500-4000 mg/L. However, an addition of 500 mg Na{sub 2}SO{sub 4} L{sup -1} was required to reduce the energy consumption and the treatment cost. Besides, there was no effect of initial PAH concentration on oxidation efficiency in the investigated range of 270-540 mg PAH L{sup -1}. Alkaline media was not favourable for PAH oxidation, whereas high performance of PAH degradation could be recorded without initial pH adjustment (original pH around 6.0). Likewise, under optimal conditions, 84% of petroleum hydrocarbon (C{sub 10}-C{sub 50}) was removed, whereas removal yields of 69% and 62% have been measured for O and G and COD, respectively. Microtox and Daphnia biotests showed that electrochemical oxidation using Ti/RuO{sub 2} could be efficiently used to reduce more than 90% of the COS toxicity.

  14. Facile and large-scale preparation of sandwich-structured graphene-metal oxide composites as anode materials for Li-ion batteries

    International Nuclear Information System (INIS)

    Fang, Hongmei; Zhao, Li; Yue, Wenbo; Wang, Yuan; Jiang, Yang; Zhang, Yuan

    2015-01-01

    Graphene-based metal oxides are desirable as potential anode materials for lithium-ion batteries (LIBs) owing to their superior electrochemical properties. In this work, sandwich-structured graphene-metal oxide (ZnO, NiO) composites are facilely synthesized on a large scale through self-assembly of graphene oxide nanosheets and metal ammine complexes, and then thermal decomposition of the self-assembled products. ZnO or NiO nanoparticles with diameters of 5∼10 nm are immobilized between the layers of graphene nanosheets, which may provide the space for accommodating the volume change of metal oxides during cycles, and highly improve the electronic conductivity of the composites. Accordingly, these sandwich-structured composites exhibit enhanced electrochemical performances compared to metal oxide particles or stacked graphene nanosheets. This facile synthesis method is very suitable for the large-scale production of three-dimensional graphene-based composites as high-performance anodes for LIBs.

  15. A ZnS nanocrystal/reduced graphene oxide composite anode with enhanced electrochemical performances for lithium-ion batteries.

    Science.gov (United States)

    Feng, Yan; Zhang, Yuliang; Wei, Yuzhen; Song, Xiangyun; Fu, Yanbo; Battaglia, Vincent S

    2016-11-09

    A simple route for the preparation of ZnS nanocrystal/reduced graphene oxide (ZnS/RGO) by a hydrothermal synthesis process was achieved. The chemical composition, morphology, and structural characterization reveal that the ZnS/RGO composite is composed of sphalerite-phased ZnS nanocrystals uniformly dispersed on functional RGO sheets with a high specific surface area. The ZnS/RGO composite was utilized as an anode in the construction of a high-performance lithium-ion battery. The ZnS/RGO composite with appropriate RGO content exhibits a high reversible specific capacity (780 mA h g -1 ), excellent cycle stability over 100 cycles (71.3% retention), and good rate performance at 2C (51.2% of its capacity when measured at a 0.1C rate). To further investigate this ZnS/RGO anode for practical use in full Li-ion cells, we tested the electrochemical performance of the ZnS/RGO anode at different cut-off voltages for the first time. The presence of RGO plays an important role in providing high conductivity as well as a substrate with a high surface area. This helps alleviate the typically problems associated with volume expansion and shrinkage during prolonged cycling. Additionally, the RGO provides multiple nucleation points that result in a uniformly dispersed film of nanosized ZnS that covers its surface. Thus, the high surface area RGO enables high electronic conductivity and fast charge transfer kinetics for ZnS lithiation/delithiation.

  16. Design and optimization of a combined fuel reforming and solid oxide fuel cell system with anode off-gas recycling

    International Nuclear Information System (INIS)

    Lee, Tae Seok; Chung, J.N.; Chen, Yen-Cho

    2011-01-01

    Highlights: → In this work, an analytical, parametric study is performed to evaluate the feasibility and performance of a combined fuel reforming and SOFC system. → Specifically the effects of adding the anode off-gas recycling and recirculation components and the CO 2 absorbent unit are investigated. → The AOG recycle ratio increases with increasing S/C ratio and the addition of AOG recycle eliminates the need for external water consumption. → The key finding is that for the SOFC operating at 900 deg. C with the steam to carbon ratio at 5 and no AOG recirculation, the system efficiency peaks. - Abstract: An energy conversion and management concept for a combined system of a solid oxide fuel cell coupled with a fuel reforming device is developed and analyzed by a thermodynamic and electrochemical model. The model is verified by an experiment and then used to evaluate the overall system performance and to further suggest an optimal design strategy. The unique feature of the system is the inclusion of the anode off-gas recycle that eliminates the need of external water consumption for practical applications. The system performance is evaluated as a function of the steam to carbon ratio, fuel cell temperature, anode off gas recycle ratio and CO 2 adsorption percentage. For most of the operating conditions investigated, the system efficiency starts at around 70% and then monotonically decreases to the average of 50% at the peak power density before dropping down to zero at the limiting current density point. From an engineering application point of view, the proposed combined fuel reforming and SOFC system with a range of efficiency between 50% and 70% is considered very attractive. It is suggested that the optimal system is the one where the SOFC operates around 900 deg. C with S/C ratio higher than 3, maximum CO 2 capture, and minimum AOG recirculation.

  17. Probing anodic oxidation kinetics and nanoscale heterogeneity within TiO2 films by Conductive Atomic Force Microscopy and combined techniques

    International Nuclear Information System (INIS)

    Diamanti, M.V.; Souier, T.; Stefancich, M.; Chiesa, M.; Pedeferri, M.P.

    2014-01-01

    Graphical abstract: - Highlights: • Nanoscale anodic titanium oxides were investigated with multidisciplinary approach. • Oxide thickness was estimated via spectrophotometry and coulometry. • C-AFM identified nanometric conductivity heterogeneities, ascribed to oxide structure. • High conductivity areas exhibited local memristive behavior. - Abstract: Anodic oxidation of titanium in acid electrolytes allows to obtain a thin, compact oxide layer with thickness, structure, color, and electrical properties that vary with process parameters imposed, among which cell voltage has a key effect. Although oxidation kinetics have been investigated in several research works, a broader vision of oxide properties–including thickness and structure–still has to be achieved, especially in the case of very thin oxide films, few tens of nanometers thick. This is vital for engineered applications of nanostructured TiO 2 films, as in the field of memristive devices, where a precise control of oxide thickness, composition and structure is required to tune its electrical response. In this work, oxide films were produced on titanium with thickness ranging from few nanometers to 200 nm. Oxide thickness was estimated by coulometry and spectrophotometry. These techniques were then combined with C-AFM, which provided a deeper understanding of oxide thickness and uniformity of the metal surface and probed the presence of crystalline nano-domains within the amorphous oxide phase affecting the overall film electrical and optical properties

  18. Nano-Sized Structurally Disordered Metal Oxide Composite Aerogels as High-Power Anodes in Hybrid Supercapacitors.

    Science.gov (United States)

    Huang, Haijian; Wang, Xing; Tervoort, Elena; Zeng, Guobo; Liu, Tian; Chen, Xi; Sologubenko, Alla; Niederberger, Markus

    2018-03-27

    A general method for preparing nano-sized metal oxide nanoparticles with highly disordered crystal structure and their processing into stable aqueous dispersions is presented. With these nanoparticles as building blocks, a series of nanoparticles@reduced graphene oxide (rGO) composite aerogels are fabricated and directly used as high-power anodes for lithium-ion hybrid supercapacitors (Li-HSCs). To clarify the effect of the degree of disorder, control samples of crystalline nanoparticles with similar particle size are prepared. The results indicate that the structurally disordered samples show a significantly enhanced electrochemical performance compared to the crystalline counterparts. In particular, structurally disordered Ni x Fe y O z @rGO delivers a capacity of 388 mAh g -1 at 5 A g -1 , which is 6 times that of the crystalline sample. Disordered Ni x Fe y O z @rGO is taken as an example to study the reasons for the enhanced performance. Compared with the crystalline sample, density functional theory calculations reveal a smaller volume expansion during Li + insertion for the structurally disordered Ni x Fe y O z nanoparticles, and they are found to exhibit larger pseudocapacitive effects. Combined with an activated carbon (AC) cathode, full-cell tests of the lithium-ion hybrid supercapacitors are performed, demonstrating that the structurally disordered metal oxide nanoparticles@rGO||AC hybrid systems deliver high energy and power densities within the voltage range of 1.0-4.0 V. These results indicate that structurally disordered nanomaterials might be interesting candidates for exploring high-power anodes for Li-HSCs.

  19. Characterization and sintering of niobium-ATR alumina

    International Nuclear Information System (INIS)

    Sibuya, N.H.; Iwasaki, H.; Suzuki, C.K.; Pinatti, D.G.

    1987-01-01

    In the niobium aluminothermy a slag is produced, composed mostly of alumina and other compounds such as niobium oxide and silica. The phase composition of this ATR alumina was characterized by X-ray powder diffractometry, and afterwards this alumina was subjected to leaching processes. It was noticed that the original content of 70% α-alumina in slag rose to 95% after the calcination. ATR alumina (leached and calcined, and without any treatment) was used to make pressed bodies which were fired in air at 1200 to 1400 0 C for 1 to 10,5 hours; and in vacuum at 1550 to 1800$0C for 2 hours. Characterization was done by density measurements, X-ray diffractometry and ultrasonic analysis. Ultrasonic analysis of some vacuum fired bodies showed londitudinal velocities close to the value found in literature. Correlation of several techniques measurements disclosed the niobium oxide interference in sintering. (Author) [pt

  20. Understanding the Critical Role of the Ag Nanophase in Boosting the Initial Reversibility of Transition Metal Oxide Anodes for Lithium-Ion Batteries.

    Science.gov (United States)

    Lee, Daehee; Wu, Mihye; Kim, Dong-Hyun; Chae, Changju; Cho, Min Kyung; Kim, Ji-Young; Lee, Sun Sook; Choi, Sungho; Choi, Youngmin; Shin, Tae Joo; Chung, Kyung Yoon; Jeong, Sunho; Moon, Jooho

    2017-07-05

    The initial reversible capacity, a critical impediment in transition metal oxide-based anodes, is augmented in conversion-reaction-involved CoO anodes for lithium-ion batteries, by incorporating a chemically synthesized Ag nanophase. With an increase in the added amount of Ag nanophase from 5 to 15 wt %, the initial capacity loss decreases linearly up to 31.7%. The Ag nanophase maintains its pristine metallic nature without undergoing phase transformations, even during repeated vigorous electrochemical reactions of the active CoO phase. Complementary ex situ chemical/physical analyses suggest that the Ag nanophase promotes the catalytic generation of reversible gel-like/polymeric films wherein lithium ions are stored capacitively in the low-voltage region below 0.7 V during discharging. These scientific findings would provide a heretofore unrecognized pathway to resolving a major issue associated with the critical irreversibility in conversion-type transition metal oxide anodes.

  1. Electrochemical oxidation of quinoline aqueous solution on β-PbO2anode and the evolution of phytotoxicity on duckweed.

    Science.gov (United States)

    Ma, Xiangjuan; Bian, Lixia; Ding, Jingfeng; Wu, Yaping; Xia, Huilong; Li, Jionghui

    2017-04-01

    Electrochemical oxidation of quinoline on a β-PbO 2 electrode modified with fluoride resin and the comprehensive toxicity of intermediates formed during oxidation on duckweed were investigated in detail. The results showed that quinoline was initially hydroxylated at the C-2 and C-8 positions by hydroxyl radicals (·OH) electro-generated on a β-PbO 2 anode, yielding 2(1H)-quinolinone and 8-hydroxyquinoline, then undergoing ring cleavage to form pyridine, nicotinic acid, pyridine-2-carboxaldehyde and acetophenone, which were ultimately converted to biodegradable organic acids. NO 3 - was the final form of quinoline-N. The growth of duckweed exposed to the oxidized quinoline solution was gradually inhibited with the decrease in pH and the formation of intermediates. However, the growth inhibition of duckweed could be eliminated beyond 120 min of oxidation, indicating the comprehensive toxicity of the quinoline solution reduced when the amount of quinoline removed was above 80%. Additionally, the adjustment of the pH to 7.5 and the addition of nutrients to the treated quinoline solution before culturing duckweed could obviously alleviate the inhibition on duckweed. Thus, partial electrochemical degradation of quinoline offers a cost-effective and clean alternative for pretreatment of wastewater containing nitrogen-heterocyclic compounds before biological treatment. The duckweed test presents a simple method for assessing the comprehensive toxicity of intermediates.

  2. Fabrication of nanostructures on Si(1 0 0) and GaAs(1 0 0) by local anodic oxidation

    International Nuclear Information System (INIS)

    Cervenka, Jiri; Kalousek, Radek; Bartosik, Miroslav; Skoda, David; Tomanec, Ondrej; Sikola, Tomas

    2006-01-01

    Atomic force microscopes have become useful tools not only for observing surface morphology and nanostructure topography but also for fabrication of various nanostructures itself. In this paper, the application of AFM for fabrication of nanostructures by local anodic oxidation (LAO) of Si(1 0 0) and GaAs(1 0 0) surfaces is presented. A special attention is paid to finding relations between the size of oxide nanolines (height and half-width) and operational parameters as tip-sample voltage and tip writing speed. It was demonstrated that the formation of silicon oxide lines obeys the Cabrera-Mott theory, i.e. the height of the lines grow, linearly with tip-sample voltage and is inversely proportional to logarithm of tip writing speed. As for GaAs substrates, the oxide line height grows linearly with tip-sample voltage as well but LAO exhibits a certain deviation from this theory. It is shown that the selective chemical etching of Si or GaAs ultrathin films processed by LAO makes it possible to use these films as nanolithographic masks for further nanotechnologies, e.g. fabrication of metallic nanostructures by ion-beam bombardment. The ability to control LAO and tip motion can be utilized in fabrication of complex nanostructures finding their applications in nanoelectronic devices, nanophotonics and other high-tech areas

  3. Comparative electrochemical analysis of crystalline and amorphous anodized iron oxide nanotube layers as negative electrode for LIB.

    Science.gov (United States)

    Pervez, Syed Atif; Kim, Doohun; Farooq, Umer; Yaqub, Adnan; Choi, Jung-Hee; Lee, You-Jin; Doh, Chil-Hoon

    2014-07-23

    This work is a comparative study of the electrochemical performance of crystalline and amorphous anodic iron oxide nanotube layers. These nanotube layers were grown directly on top of an iron current collector with a vertical orientation via a simple one-step synthesis. The crystalline structures were obtained by heat treating the as-prepared (amorphous) iron oxide nanotube layers in ambient air environment. A detailed morphological and compositional characterization of the resultant materials was performed via transmission electron microscopy (TEM), field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), and Raman spectroscopy. The XRD patterns were further analyzed using Rietveld refinements to gain in-depth information on their quantitative phase and crystal structures after heat treatment. The results demonstrated that the crystalline iron oxide nanotube layers exhibit better electrochemical properties than the amorphous iron oxide nanotube layers when evaluated in terms of the areal capacity, rate capability, and cycling performance. Such an improved electrochemical response was attributed to the morphology and three-dimensional framework of the crystalline nanotube layers offering short, multidirectional transport lengths, which favor rapid Li(+) ions diffusivity and electron transport.

  4. Textured cermets of CeO{sub 2} (or GDC) with Co for solid oxide fuel cells anodes

    Energy Technology Data Exchange (ETDEWEB)

    Ortega-San-Martin, Luis; Pena, Jose Ignacio; Larrea, Angel; Gil, Vanesa; Orera, Victor M. [Instituto de Ciencia de Materiales de Aragon, CSIC-Universidad de Zaragoza, Fac de Ciencias, C/ Pedro Cerbuna 12, 50009-Zaragoza (Spain)

    2010-10-15

    Cermets composed of submicron size alternating lamellae of CeO{sub 2}, or 10% Gadolinia doped Ceria (GDC), and porous-metallic Cobalt have been prepared from eutectic oxide mixtures. A fine eutectic structure was obtained by fast directional solidification of the cobalt oxide-ceria oxide eutectic composite using the Laser Floating Zone (LFZ) technique. The resulting microstructure, with an interphase spacing down to 0.5 {mu}m, was obtained for solidification rates of 750 mm/h. Textured cermets were obtained by subsequent reduction under H{sub 2} containing atmosphere of the eutectic oxide composite. The reduction kinetics was studied in the 550-750 C temperature range and effective diffusion coefficients were obtained. The reduction process does not correspond to a typical thermally activated process. The cermets are composed of ceria lamellae of about 200 nm thickness alternated with porous-metallic cobalt lamellae of {<=}400 nm. The lamellar microstructure of the cermets favours oxygen ion mobility through ceria and its size can be controlled by solidification rate of the eutectic precursor. These materials are proposed as SOFC anodes. (author)

  5. Niobium and tantalum

    International Nuclear Information System (INIS)

    Polupanova, L.I.; Volkova, G.A.

    1983-01-01

    General mineralogical-geochemical and analytical characteristics of niobium and tantalum are presented. Potentialities of any analytical methods for determining these elements in various geologic samples are estimated. The following specific techniques are described: neutron + activation determination of Ta, fluorescence X-radiometric determination of Nb and Ta, fluorescence X-ray spectral determination of Nb and Ta, spectrographic determination of Nb and Ta, gravimetric determination of Nb and Ta, their extraction-photometric determination with various reagents (crystal violet, rhodamine 6 Y, butylrhodamine B)

  6. A silicon nanowire-reduced graphene oxide composite as a high-performance lithium ion battery anode material.

    Science.gov (United States)

    Ren, Jian-Guo; Wang, Chundong; Wu, Qi-Hui; Liu, Xiang; Yang, Yang; He, Lifang; Zhang, Wenjun

    2014-03-21

    Toward the increasing demands of portable energy storage and electric vehicle applications, silicon has been emerging as a promising anode material for lithium-ion batteries (LIBs) owing to its high specific capacity. However, serious pulverization of bulk silicon during cycling limits its cycle life. Herein, we report a novel hierarchical Si nanowire (Si NW)-reduced graphene oxide (rGO) composite fabricated using a solvothermal method followed by a chemical vapor deposition process. In the composite, the uniform-sized [111]-oriented Si NWs are well dispersed on the rGO surface and in between rGO sheets. The flexible rGO enables us to maintain the structural integrity and to provide a continuous conductive network of the electrode, which results in over 100 cycles serving as an anode in half cells at a high lithium storage capacity of 2300 mA h g(-1). Due to its [111] growth direction and the large contact area with rGO, the Si NWs in the composite show substantially enhanced reaction kinetics compared with other Si NWs or Si particles.

  7. Self-Assembly of Silicon@Oxidized Mesocarbon Microbeads Encapsulated in Carbon as Anode Material for Lithium-Ion Batteries.

    Science.gov (United States)

    Liu, Huitian; Shan, Zhongqiang; Huang, Wenlong; Wang, Dongdong; Lin, Zejing; Cao, Zongjie; Chen, Peng; Meng, Shuxian; Chen, Li

    2018-02-07

    The utilization of silicon/carbon composites as anode materials to replace the commercial graphite is hampered by their tendency to huge volumetric expansion, costly raw materials, and complex synthesis processes in lithium-ion batteries. Herein, self-assembly method is successfully applied to prepare hierarchical silicon nanoparticles@oxidized mesocarbon microbeads/carbon (Si@O-MCMB/C) composites for the first time, in which O-MCMB core and low-cost sucrose-derived carbon shell not only effectively enhance the electrical conductivity of the anode, but also mediate the dramatic volume change of silicon during cycles. At the same time, the carbon can act as "adhesive", which is crucial in enhancing the adhesive force between Si and O-MCMB in the composites. The as-obtained Si@O-MCMB/C delivers an initial reversible capacity of 560 mAh g -1 at 0.1 A g -1 , an outstanding cyclic retention of 92.8% after 200 cycles, and respectable rate capability. Furthermore, the synthetic route presented here is efficient, less expensive, simple, and easy to scale up for high-performance composites.

  8. Structural and magnetic properties of nickel nanowires grown in porous anodic aluminium oxide template by electrochemical deposition technique

    Science.gov (United States)

    Nugraha Pratama, Sendi; Kurniawan, Yudhi; Muhammady, Shibghatullah; Takase, Kouichi; Darma, Yudi

    2018-03-01

    We study the formation of nickel nanowires (Ni NWs) grown in porous anodic aluminium oxide (AAO) template by the electrochemical deposition technique. Here, the initial AAO template was grown by anodization of aluminium substrate in sulphuric acid solution. The cross-section, crystal structure, and magnetic properties of Ni NWs system were characterized by field-emission SEM, XRD, and SQUID. As a result, the highly-ordered Ni NWs are observed with the uniform diameter of 27 nm and the length from 31 to 163 nm. Based on XRD spectra analysis, Ni NWs have the face-centered cubic structure with the lattice parameter of 0.35 nm and average crystallite size of 17.19 nm. From SQUID measurement at room temperature, by maintaining the magnetic field perpendicular to Ni NWs axis, the magnetic hysteresis of Ni NWs system show the strong ferromagnetism with the coercivity and remanence ratio of ∼148 Oe and ∼0.23, respectively. The magnetic properties are also calculated by means of generalized gradient approximation methods. From the calculation result, we show that the ferromagnetism behavior comes from Ni NWs without any contribution from AAO template or the substrate. This study opens the potential application of Ni NWs system for novel functional magnetic devices.

  9. Modelling of CH4 multiple-reforming within the Ni-YSZ anode of a solid oxide fuel cell

    Science.gov (United States)

    Tran, Dang Long; Tran, Quang Tuyen; Sakamoto, Mio; Sasaki, Kazunari; Shiratori, Yusuke

    2017-08-01

    A new approach for the modelling of the simultaneous dry and steam reforming of CH4 (methane multiple-reforming (MMR)) within the Ni-YSZ anode of a solid oxide fuel cell (SOFC) is introduced in this paper. MMR is modelled by using artificial neural network (ANN) and fuzzy inference system (FIS) that can express the gas composition and temperature dependences of the consumption or the production rate of gaseous species involved in MMR. The necessary parameters for this approach are determined from the measured reforming kinetics for an anode-supported cell (ASC) fuelled by a CH4-CO2-H2O-N2 mixture. The developed MMR model is incorporated into a 3D-CFD planar ASC model to calculate the SOFC performance, and the calculated results match well with experimental values for the feed of simulated biogas (CH4/CO2 = 1) and H2. The established SOFC model considering MMR is a powerful tool to simulate the performance of internal reforming SOFC.

  10. Degradation of cathode current-collecting materials for anode-supported flat-tube solid oxide fuel cell

    Science.gov (United States)

    Kim, Jong-Hee; Song, Rak-Hyun; Chung, Dong-You; Hyun, Sang-Hoon; Shin, Dong-Ryul

    Different types of cathode current-collecting material for anode-supported flat-tube solid oxide fuel cells are fabricated and their electrochemical properties are characterized. Current collection for the cathode is achieved by winding Ag wire and by painting different conductive pastes of Ag-Pd, Pt, La 0.6Sr 0.4CoO 3 (LSCo), and La 0.6Sr 0.4Co 0.2Fe 0.8O 3 (LSCF) on the wire. Cell performance at the initial operation time is in the order of Pt > LSCo > LSCF > Ag-Pd. On the other hand, the performance degradation rate is in the order of LSCo Ag-Pd. LSCo paste as a cathode current-collector shows the most stable long-term performance of 0.8 V, 300 mA cm -2 at 750 °C, even under a thermal cycle condition with heating and cooling rates of 150 °C h -1. The performance degradation of the Ag-Pd and Pt pastes is caused by increased polarization resistance due to metal particle sintering. From these results, it is concluded that a cathode current-collector composed of wound silver wire with LSCo paste is useful for anode-supported flat-tube cells as it does not experience any significant degradation during a long operation time.

  11. Indirect anodic oxidation applied for treatment of simulated wastewater containing Cationic Red X-GRL and Disperse Red 3B

    Directory of Open Access Journals (Sweden)

    Bo Yang

    2017-06-01

    Full Text Available The treatment of simulated wastewater containing Cationic Red X-GRL (X-GRL or Disperse Red 3B (DR-3B dye was carried out by indirect anodic oxidation, using Ti/SnO2 electrodes as the anode. The influences of pH value, voltage, electrolysis time and sodium chloride dosage on the degradation performance were studied by single factor experiment. Furthermore the nitrogen states and UV-Vis spectra in dyes degradation were analyzed. The results showed that under the optimum condition (pH = 3, voltage = 20 V, NaCl = 2.5 g/L, the decolorization and chemical oxygen demand removal of X-GRL were 98% and 67%, respectively; and those of DR-3B were 51% and 61%, respectively. The azo double bond conjugated system in X-GRL is much more easily destroyed than the anthraquinone conjugated system in DR-3B; the aryl ring structures of them can be partially degraded.

  12. Porphyrin Dye-Sensitized Zinc Oxide Aggregated Anodes for Use in Solar Cells

    Directory of Open Access Journals (Sweden)

    Yu-Kai Syu

    2016-08-01

    Full Text Available Porphyrin YD2-o-C8-based dyes were employed to sensitize room-temperature (RT chemical-assembled ZnO aggregated anodes for use in dye-sensitized solar cells (DSSCs. To reduce the acidity of the YD2-o-C8 dye solution, the proton in the carboxyl group of a porphyrin dye was replaced with tetrabuthyl ammonium (TBA+ in this work. The short-circuit current density (Jsc of the YD2-o-C8-TBA-sensitized ZnO DSSCs is higher than that of the YD2-o-C8-sensitized cells, resulting in the improvement of the efficiency of the YD2-o-C8-based ZnO DSSCs. With an appropriate incorporation of chenodeoxycholic acid (CDCA as coadsorbate, the Jsc and efficiency of the YD2-o-C8-TBA-sensitized ZnO DSSC are enhanced due to the improvement of the incident-photon-to-current efficiency (IPCE values in the wavelength range of 400–450 nm. Moreover, a considerable increase in Jsc is achieved by the addition of a light scattering layer in the YD2-o-C8-TBA-sensitized ZnO photoanodes. Significant IPCE enhancement in the range 475–600 nm is not attainable by tuning the YD2-o-C8-TBA sensitization processes for the anodes without light scattering layers. Using the RT chemical-assembled ZnO aggregated anode with a light scattering layer, an efficiency of 3.43% was achieved in the YD2-o-C8-TBA-sensitized ZnO DSSC.

  13. Fracture properties of nickel-based anodes for solid oxide fuel cells

    DEFF Research Database (Denmark)

    Goutianos, Stergios; Frandsen, Henrik Lund; Sørensen, Bent F.

    2010-01-01

    Reliable assessment of structural integrity of fuel cells requires the knowledge of the mechanical properties of their individual components, in particular the fracture toughness. A technique is presented to measure the critical energy-release rate/fracture toughness of thin ceramic layers...... such as the anode material (NiO–YSZ) in a fuel cell. The approach involves a new specimen geometry which consists of a thin ceramic glued onto thick steel beams to form a double cantilever beam (DCB) specimen. The fracture toughness values, measured from truly sharp cracks, are obtained over a range of applied...

  14. Effect of redox treatments on Ce0.50Zr0.50O2 based solid oxide fuel cell anodes

    Science.gov (United States)

    Boaro, Marta; Pappacena, Alfonsina; Abate, Chiara; Ferluga, Matteo; Llorca, Jordi; Trovarelli, Alessandro

    2014-12-01

    This work investigates the activity of copper modified Ce0.50Zr0.50O2 (Cu-CZ) based anodes prepared through subsequent impregnation steps into a porous YSZ matrix. The ceria-zirconia oxide was reduced at increasing temperatures and the effect of structural changes on anode performance investigated at 973 K under humidified H2. Performance of all cells increased after one redox cycle due to a decrease of both the anode polarization and the ohmic resistance of the cell. The redox behaviour of Cu-CZ anode was investigated in a symmetrical cell configuration and it was observed that subsequent redox cycles lead to an activation and stabilization of the electrodes. SEM and EIS characterizations showed that this is mainly attributable to a rearrangement of the morphology and microstructure of the CZ oxide at the electrode/electrolyte interface and to an improvement of copper distribution into the porous electrode matrix. It is inferred that the interplay of copper and CZ favours the promotion of anode activity by increasing the number of active sites; moreover it stabilizes the redox behaviour of the electrode. An optimization of electrical and structural properties of Cu-CZ composites was also discussed.

  15. Initialization of a methane-fueled single-chamber solid-oxide fuel cell with NiO + SDC anode and BSCF + SDC cathode

    Science.gov (United States)

    Zhang, Chunming; Zheng, Yao; Ran, Ran; Shao, Zongping; Jin, Wanqin; Xu, Nanping; Ahn, Jeongmin

    2008-05-01

    The initialization of an anode-supported single-chamber solid-oxide fuel cell, with NiO + Sm0.2Ce0.8O1.9 anode and Ba0.5Sr0.5Co0.8Fe0.2O3-δ + Sm0.2Ce0.8O1.9 cathode, was investigated. The initialization process had significant impact on the observed performance of the fuel cell. The in situ reduction of the anode by a methane-air mixture failed. Although pure methane did reduce the nickel oxide, it also resulted in severe carbon coking over the anode and serious distortion of the fuel cell. In situ initialization by hydrogen led to simultaneous reduction of both the anode and cathode; however, the cell still delivered a maximum power density of ∼350 mW cm-2, attributed to the re-formation of the BSCF phase under the methane-air atmosphere at high temperatures. The ex situ reduction method appeared to be the most promising. The activated fuel cell showed a peak power density of ∼570 mW cm-2 at a furnace temperature of 600 °C, with the main polarization resistance contributed from the electrolyte.

  16. Anodic oxidation of wastewater containing the Reactive Orange 16 Dye using heavily boron-doped diamond electrodes

    International Nuclear Information System (INIS)

    Migliorini, F.L.; Braga, N.A.; Alves, S.A.; Lanza, M.R.V.; Baldan, M.R.; Ferreira, N.G.

    2011-01-01

    Highlights: → Electrochemical advanced oxidation process was studied using BDD based anodes with different boron concentrations. → The difference between the non-active and active anodes for organics degradation. → The influence of morphologic and structural properties of BDD electrodes on the RO-16 dye degradation. - Abstract: Boron-doped diamond (BDD) films grown on the titanium substrate were used to study the electrochemical degradation of Reactive Orange (RO) 16 Dye. The films were produced by hot filament chemical vapor deposition (HFCVD) technique using two different boron concentrations. The growth parameters were controlled to obtain heavily doped diamond films. They were named as E1 and E2 electrodes, with acceptor concentrations of 4.0 and 8.0 x 10 21 atoms cm -3 , respectively. The boron levels were evaluated from Mott-Schottky plots also corroborated by Raman's spectra, which characterized the film quality as well as its physical property. Scanning Electron Microscopy showed well-defined microcrystalline grain morphologies with crystal orientation mixtures of (1 1 1) and (1 0 0). The electrode efficiencies were studied from the advanced oxidation process (AOP) to degrade electrochemically the Reactive Orange 16 azo-dye (RO16). The results were analyzed by UV/VIS spectroscopy, total organic carbon (TOC) and high-performance liquid chromatography (HPLC) techniques. From UV/VIS spectra the highest doped electrode (E2) showed the best efficiency for both, the aromaticity reduction and the azo group fracture. These tendencies were confirmed by the TOC and chromatographic measurements. Besides, the results showed a direct relationship among the BDD morphology, physical property, and its performance during the degradation process.

  17. Characteristics of Sr0.92Y0.08Ti1-yNiyO3-δ anode and Ni-infiltrated Sr0.92Y0.08TiO3-δ anode using CH4 fuel in solid oxide fuel cells

    Science.gov (United States)

    Park, Eun Kyoung; Lee, Soonil; Yun, Jeong Woo

    2018-01-01

    Strontium titanium oxide co-doped with yttrium and nickel (SrxY1-xTiyNi1-yO3-δ; hereafter, SYTN), was investigated as an alternative anode material for solid oxide fuel cells. To improve the ionic conductivity of the Sr0.92Y0.08TiO3-δ (SYT) anode, Ni2+ was substituted into the B-site (initially occupied by Ti4+), thereby forming oxygen vacancies. To analyze the effects of Ni-doping in the SYT anode, the electrochemical properties of the SYTN anode were compared with those of the Ni-infiltrated SYT(Ni@SYT) using H2 and CH4 as fuels. The electrochemical reactions at the SYTN anode in the presence of both H2 and CH4 were limited by relatively slow reactions, such as non-charged processes including oxygen surface exchange and solid surface diffusion. The high electrical conductivity and excellent catalytic activity of the Ni nanoparticles in the Ni@SYT anode led to improved cell performance. CH4 decomposition at the Ni@SYT anode occurred via thermal pyrolysis of CH4 rather than by steam methane reforming, resulting in carbon deposition. In comparison, the poor inherent catalytic activity for CH4 oxidation exhibited by the SYTN anode minimized carbon deposition on the anode surface.

  18. Influence of water on the anodic oxidation mechanism of diethylenetriamine (deta on platinum electrode

    Directory of Open Access Journals (Sweden)

    Lassine Ouattara

    2006-12-01

    Full Text Available Diethylenetriamine was oxidised in different electrolytes on platinum electrode. In non-aqueous electrolyte, an irreversible oxidation peak characteristic of DETA oxidation appears on the voltammogram followed by a constant current until the higher limit of the sweeping potential domain is attained. The following successive scans showed a high decrease of the current intensity and that is due to the formation of an insulating coating layer on the electrode surface. When water is added to the non-aqueous electrolyte, a DETA oxidation wave appears on the voltammograms. That oxidation wave is observed on the following scans. Indeed, DETA oxidation mechanism seems to be different either the electrolyte is free or not of water. In non-aqueous electrolyte, DETA oxidation leads to electrode surface covering by a thin polymeric film but in water containing electrolyte, oxygen evolution occurs and DETA oxidation leads to uncoated surface by producing aldehyde and amine through imine hydrolysis.

  19. Preparation of mesoporous alumina films by anodization: Effect of pretreatments on the aluminum surface and MTBE catalytic oxidation

    International Nuclear Information System (INIS)

    Vazquez, A.L.; Carrera, R.; Arce, E.; Castillo, N.; Castillo, S.; Moran-Pineda, M.

    2009-01-01

    Mesoporous materials are both scientifically and technologically important because of the presence of voids of controllable dimensions at atomic, molecular, and nanometric scales. Over the last decade, there has been both an increasing interest and research effort in the synthesis and characterization of these types of materials. The purposes of this work are to study the physical and chemical changes in the properties of mesoporous alumina films produced by anodization in sulphuric acid by different pretreatments on the aluminium surface such as mechanical polishing [MP] and electropolishing [EP]; and to compare their properties such as morphology, structure and catalytic activity with those present in commercial alumina. The morphologic and physical characterizations of the alumina film samples were carried out by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The chemical evaluations were performed by the oxidation of methyl-tert-butyl-ether (MTBE) at 400 deg. C under O 2 /He oxidizing conditions (Praxair, 2.0% O 2 /He balance). According to the results, the samples that presented higher activities than those in Al 2 O 3 /Al [MP] and commercial alumina in the MTBE oxidation (69%), were those prepared by Al 2 O 3 /Al [EP]. The average mesoporous diameter was 17 nm, and the morphological shape was equiaxial; thus, that pore distribution was the smallest of all with a homogeneous distribution.

  20. Elementary kinetic modelling applied to solid oxide fuel cell pattern anodes and a direct flame fuel cell system

    Energy Technology Data Exchange (ETDEWEB)

    Vogler, Marcel

    2009-05-27

    In the course of this thesis a model for the prediction of polarisation characteristics of solid oxide fuel cells (SOFC) was developed. The model is based on an elementary kinetic description of electrochemical reactions and the fundamental conservation principles of mass and energy. The model allows to predict the current-voltage relation of an SOFC and offers ideal possibilities for model validation. The aim of this thesis is the identification of rate-limiting processes and the determination of the elementary pathway during charge transfer. The numerical simulation of experiments with model anodes allowed to identify a hydrogen transfer to be the most probable charge-transfer reaction and revealed the influence of diffusive transport. Applying the hydrogen oxidation kinetics to the direct flame fuel cell system (DFFC) showed that electrochemical oxidation of CO is possible based on the same mechanism. Based on the quantification of loss processes in the DFFC system, improvements on cell design, predicting 80% increase of efficiency, were proposed. (orig.)

  1. Controlling the shape and gap width of silicon electrodes using local anodic oxidation and anisotropic TMAH wet etching

    International Nuclear Information System (INIS)

    Rouhi, Jalal; Mahmud, Shahrom; Naderi, Nima; Abdullah, Mat Johar; Hutagalung, Sabar Derita; Kakooei, Saeid

    2012-01-01

    A simple method for fabricating silicon electrodes with various shapes and gap widths was designed using the special properties of anisotropic tetramethylammonium hydroxide (TMAH) wet etching and local anodic oxidation (LAO). A statistical system was used for the optimization of the parameters of the LAO process to facilitate a better understanding and precise analysis of the process. Analyses of the interaction effects among the significant factors of LAO showed that the relative humidity and applied voltage were interdependent. They had the strongest interaction effect on the dimensions of the oxide mask. TMAH with a concentration of 25% was used as an etchant solution in (1 0 0) silicon with a rectangular oxide mask. The observed undercutting at convex corners, tip shape of emitters and gap widths of electrodes were exactly consistent with theoretical studies. Combination of the LAO method and anisotropic TMAH wet etching was successfully used to fabricate Si nano-gap electrodes. This fabrication method of sharp and round tip emitters was simple, controllable and faster than common techniques. These results indicate that the method can be a new approach for studying the electrical properties of nano-gap electrodes. (paper)

  2. Synthesis of praseodymium doped cerium oxides by the polymerization-combustion method for application as anodic component in SOFC devices

    Science.gov (United States)

    Cruz Pacheco, A. F.; Gómez Cuaspud, J. A.; López, E. Vera

    2016-02-01

    This work reports the synthesis and the characterization of six oxides; it is based on Ce1-xPrxO2 (x=0.0, 0.2, 0.4, 0.6, 0.8 and 1.0) system, which is obtained by the polymerization- combustion technique for potential applications on design of advanced electrodic components, for solid oxide fuel cells (SOFC). Initially the solid precursors are characterized by infrared spectroscopy (FTIR) and thermal analysis (TGA-DTA), allowing to determine the formation of prevalent citrate species and the optimal temperature for the consolidation of the desired crystalline phases. The X-ray diffraction (XRD) and the transmission electron microscopy analysis (TEM) are performed over calcined samples which provided information about the formation of a fluorite phase with grain distribution, surface, textural and morphological properties consistent with the nanometric obtaining crystallites (30nm), it is oriented along the (1 1 1) facet, with d spacings of 0.31nm for the main diffraction signal. These results indicate the effectiveness of the proposed synthesis method for potential applications in the design of advanced anodic materials for solid oxide fuel cells.

  3. Preparation of mesoporous alumina films by anodization: Effect of pretreatments on the aluminum surface and MTBE catalytic oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Vazquez, A.L., E-mail: avazquezd@ipn.m [Departamento de Ingenieria Metalurgica, ESIQIE-IPN, AP 75-876, Mexico, D.F. (Mexico); Programa de Ingenieria Molecular, Instituto Mexicano del Petroleo, Eje Lazaro Cardenas 152, C.P. 07730, Mexico, D.F. (Mexico); Carrera, R. [Departamento de Ingenieria Metalurgica, ESIQIE-IPN, AP 75-876, Mexico, D.F. (Mexico); Programa de Ingenieria Molecular, Instituto Mexicano del Petroleo, Eje Lazaro Cardenas 152, C.P. 07730, Mexico, D.F. (Mexico); Arce, E. [Departamento de Ingenieria Metalurgica, ESIQIE-IPN, AP 75-876, Mexico, D.F. (Mexico); Castillo, N. [CINVESTAV, Departamento de Fisica. Av. IPN 2508, 07360, Mexico, D.F (Mexico); Castillo, S. [Departamento de Ingenieria Metalurgica, ESIQIE-IPN, AP 75-876, Mexico, D.F. (Mexico); Programa de Ingenieria Molecular, Instituto Mexicano del Petroleo, Eje Lazaro Cardenas 152, C.P. 07730, Mexico, D.F. (Mexico); Moran-Pineda, M. [Programa de Ingenieria Molecular, Instituto Mexicano del Petroleo, Eje Lazaro Cardenas 152, C.P. 07730, Mexico, D.F. (Mexico)

    2009-08-26

    Mesoporous materials are both scientifically and technologically important because of the presence of voids of controllable dimensions at atomic, molecular, and nanometric scales. Over the last decade, there has been both an increasing interest and research effort in the synthesis and characterization of these types of materials. The purposes of this work are to study the physical and chemical changes in the properties of mesoporous alumina films produced by anodization in sulphuric acid by different pretreatments on the aluminium surface such as mechanical polishing [MP] and electropolishing [EP]; and to compare their properties such as morphology, structure and catalytic activity with those present in commercial alumina. The morphologic and physical characterizations of the alumina film samples were carried out by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The chemical evaluations were performed by the oxidation of methyl-tert-butyl-ether (MTBE) at 400 deg. C under O{sub 2}/He oxidizing conditions (Praxair, 2.0% O{sub 2}/He balance). According to the results, the samples that presented higher activities than those in Al{sub 2}O{sub 3}/Al [MP] and commercial alumina in the MTBE oxidation (69%), were those prepared by Al{sub 2}O{sub 3}/Al [EP]. The average mesoporous diameter was 17 nm, and the morphological shape was equiaxial; thus, that pore distribution was the smallest of all with a homogeneous distribution.

  4. Preliminary Electrochemical Characterization of Anode Supported Solid Oxide Cell (AS-SOC) Produced in the Institute of Power Engineering Operated in Electrolysis Mode (SOEC)

    Science.gov (United States)

    Kupecki, Jakub; Motyliński, Konrad; Skrzypkiewicz, Marek; Wierzbicki, Michał; Naumovich, Yevgeniy

    2017-12-01

    The article discusses the operation of solid oxide electrochemical cells (SOC) developed in the Institute of Power Engineering as prospective key components of power-to-gas systems. The fundamentals of the solid oxide cells operated as fuel cells (SOFC - solid oxide fuel cells) and electrolysers (SOEC - solid oxide fuel cells) are given. The experimental technique used for electrochemical characterization of cells is presented. The results obtained for planar cell with anodic support are given and discussed. Based on the results, the applicability of the cells in power-to-gas systems (P2G) is evaluated.

  5. Technology of niobium and molybdenum refining by electron beam

    International Nuclear Information System (INIS)

    Conti, R.A.; Pinatti, D.G.; Sandim, H.R.Z.

    1988-01-01

    The uses of metals and alloys in superconductors (Nb46%Ti), aerospatial industry (Ti6Al4V), electroeletronic industry (Nb, Mo, W) and in surgical implants (Ti, Nb) are increasing nowadays. A refining process of niobium and molybdenum by electron beam technique, since the oxides reduction till the obtention of a high purity ingot is presented. (C.G.C.) [pt

  6. Accelerated creep in solid oxide fuel cell anode supports during reduction

    DEFF Research Database (Denmark)

    Frandsen, Henrik Lund; Makowska, Malgorzata Grazyna; Greco, Fabio

    2016-01-01

    studied previously. In this work a newly discovered creep phenomenon taking place during the reduction is reported. This relaxes stresses at a much higher rate (∼ x104) than creep during operation. The phenomenon was studied both in three-point bending and uniaxial tension. Differences between the two...... measurements could be explained by newly observed stress promoted reduction. Finally, samples exposed to a small tensile stress (∼ 0.004 MPa) were observed to expand during reduction, which is in contradiction to previous literature. These observations suggest that release of internal residual stresses between...... the NiO and the YSZ phases occurs during reduction. The accelerated creep should practically eliminate any residual stress in the anode support in an SOFC stack, as has previously been indirectly observed. This phenomenon has to be taken into account both in the production of stacks and in the simulation...

  7. Methane steam reforming kinetics over Ni-YSZ anode materials for Solid Oxide Fuel Cells

    DEFF Research Database (Denmark)

    Mogensen, David

    of internal reforming has to be carefully controlled. The objective of this thesis is to make such a careful control possible by examining the rate of internal steam reforming in SOFCs. The catalytic steam reforming activity of Ni-YSZ anode material was tested both in a packed bed reactor to determine...... energy. The overall efficiency of a fuel cell system operating on natural gas can be significantly improved by having part of the steam reforming take place inside the SOFC stack. In order to avoid large temperature gradients as a result of the highly endothermal steam reforming reaction, the amount...... accurately predict the steam reforming rate in a stack from the rate expression obtained from the packed bed experiments. During the experiments a previously unreported long term dynamic behavior of the catalyst was observed. After startup, the initial high reactivity was slowly reduced by a factor 5-10 over...

  8. Theoretical study of support effect of Au catalyst for glucose oxidation of alkaline fuel cell anode

    Energy Technology Data Exchange (ETDEWEB)

    Ishimoto, Takayoshi, E-mail: ishimoto@ifrc.kyushu-u.ac.jp [Frontier Energy Research Division, INAMORI Frontier Research Center, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395 (Japan); Hamatake, Yumi [Frontier Energy Research Division, INAMORI Frontier Research Center, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395 (Japan); Kazuno, Hiroki; Kishida, Takayuki [OLYMPUS Corporation, 2-3 Kuboyama-cho, Hachioji-shi, Tokyo 192-8512 (Japan); Koyama, Michihisa, E-mail: koyama@ifrc.kyushu-u.ac.jp [Frontier Energy Research Division, INAMORI Frontier Research Center, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395 (Japan); International Institute for Carbon-Neutral Energy Research, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395 (Japan)

    2015-01-01

    Highlights: • The catalytic activity of Au in alkaline solution is studied theoretically. • Carbon and oxide materials are used to estimate support effect for glucose oxidation. • The glucose oxidation on SnO{sub 2}(1 1 0) supported Au catalyst shows high activity. • The charge transfer from Au catalyst to support materials is dominant. - Abstract: We theoretically analyzed the glucose oxidation reaction mechanism and reaction activity of Au catalyst supported by carbon (graphite(0 0 0 1), (101{sup ¯}0), and (112{sup ¯}0)) and oxide (ZrO{sub 2}(1 1 1) and SnO{sub 2}(1 1 0)) in alkaline solution environment by using density functional theory method. We observed large stabilization of Au catalyst on support materials due to the electron transfer in the case of graphite(112{sup ¯}0) and SnO{sub 2}(1 1 0) systems. The catalytic activity for glucose oxidation reaction over Au supported by graphite(101{sup ¯}0) and (112{sup ¯}0) is calculated to be low in comparison with those of unsupported system. We found that SnO{sub 2}(1 1 0) supported Au catalyst shows high activity toward the glucose oxidation. One of the main factors for the observed high catalytic activity is charge transfer from Au catalyst to support materials. When the atomic charge of Au catalyst becomes positive by the support effect, the activity of glucose oxidation reaction on Au catalyst is improved.

  9. Morphology study of niobium pentoxide

    International Nuclear Information System (INIS)

    Romero, R.P.P.; Panta, P.C.; Araujo, A.O. de; Bergmann, C.P.

    2016-01-01

    Currently, Niobium pentoxide (Nb 2 O 5 ) has been studied due to physical properties and their use in obtaining electronic ceramics, optical lenses, pH sensors, special filters for TV receivers, among other applications. This study investigated the morphology of the niobium pentoxide obtained by hydrothermal synthesis from the precursor pentachloride niobium (NbCl 5 ), where the synthesis was carried out at a temperature of 150 and 200 °C for 130 min and the product obtained was calcined at temperatures 600, 800 and 1000 °C for 60 min. The following characterizations were performed for analysis of the material, among them, X-ray diffraction (XRD) for analysis of the crystal structure, thermal gravimetric analysis (TGA) for detecting the existing functional groups and scanning electron microscopy (SEM) for morphology of material. As a result, different morphologies were obtained and consequently different niobium pentoxide properties studied. (author)

  10. Investigation of ionic movements during anodic oxidation of superimposed metallic layers by the use of Rutherford backscattering techniques and nuclear micro analysis

    International Nuclear Information System (INIS)

    Perriere, J.; Siejka, J.; Rigo, S.

    1980-01-01

    Nuclear micro-analysis by the direct observation of nuclear reactions and of backscattered particles was used to study ionic movements during the anodization of superimposed metallic films (M 1 -M 2 systems). It has been shown that the order of cations is largely preserved during the anodization of Ta-Nb or Al-Nb systems while it is inverted in the case of Nb-Ta and Nb-Al systems. These results are discussed in terms of differences in jump probabilities of atoms. The oxygen movements in these systems were studied by 18 O tracing techniques; the results suggest that a correlation exists between oxygen and cationic migration during anodic oxide growth. The discussion of these results in terms of microscopic transport mechanisms is based on a neighbour to neighbour type propagation process for cationic as well as oxygen movement. (author)

  11. Carbon-coated Si nanoparticles/reduced graphene oxide multilayer anchored to nanostructured current collector as lithium-ion battery anode

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Zhengjiao; Guo, Pengqian; Liu, Boli; Xie, Wenhe; Liu, Dequan; He, Deyan, E-mail: hedy@lzu.edu.cn

    2017-02-28

    Silicon is the most promising anode material for the next-generation lithium-ion batteries (LIBs). However, the large volume change during lithiation/delithiation and low intrinsic conductivity hamper its electrochemical performance. Here we report a well-designed LIB anode in which carbon-coated Si nanoparticles/reduced graphene oxide (Si/rGO) multilayer was anchored to nanostructured current collector with stable mechanical support and rapid electron conduction. Furthermore, we improved the integral stability of the electrode through introducing amorphous carbon. The designed anode exhibits superior cyclability, its specific capacity remains above 800 mAh g{sup −1} after 350 cycles at a current density of 2.0 A g{sup −1}. The excellent electrochemical performance can be attributed to the fact that the Si/rGO multilayer is reinforced by the nanostructured current collector and the formed amorphous carbon, which can maintain the structural and electrical integrities of the electrode.

  12. Carbon-coated Si nanoparticles/reduced graphene oxide multilayer anchored to nanostructured current collector as lithium-ion battery anode

    Science.gov (United States)

    Liu, Zhengjiao; Guo, Pengqian; Liu, Boli; Xie, Wenhe; Liu, Dequan; He, Deyan

    2017-02-01

    Silicon is the most promising anode material for the next-generation lithium-ion batteries (LIBs). However, the large volume change during lithiation/delithiation and low intrinsic conductivity hamper its electrochemical performance. Here we report a well-designed LIB anode in which carbon-coated Si nanoparticles/reduced graphene oxide (Si/rGO) multilayer was anchored to nanostructured current collector with stable mechanical support and rapid electron conduction. Furthermore, we improved the integral stability of the electrode through introducing amorphous carbon. The designed anode exhibits superior cyclability, its specific capacity remains above 800 mAh g-1 after 350 cycles at a current density of 2.0 A g-1. The excellent electrochemical performance can be attributed to the fact that the Si/rGO multilayer is reinforced by the nanostructured current collector and the formed amorphous carbon, which can maintain the structural and electrical integrities of the electrode.

  13. Anodic and cathodic reactions in molten calcium chloride

    International Nuclear Information System (INIS)

    Fray, D.J.

    2002-01-01

    Calcium chloride is a very interesting electrolyte in that it is available, virtually free, in high purity form as a waste product from the chemical industry. It has a very large solubility for oxide ions, far greater than many alkali halides and other divalent halides and has the same toxicity as sodium chloride and also a very high solubility in water. Intuitively, on the passage of current, it is expected that calcium would be deposited at the cathode and chlorine would evolve at the anode. However, if calcium oxide is added to the melt, it is possible to deposit calcium and evolve oxygen containing gases at the anode, making the process far less polluting than when chlorine is evolved. This process is discussed in terms of the addition of calcium to molten lead. Furthermore, these reactions can be altered dramatically depending upon the electrode materials and the other ions dissolved in the calcium chloride. As calcium is only deposited at very negative cathodic potentials, there are several interesting cathodic reactions that can occur and these include the decomposition of the carbonate ion and the ionization of oxygen, sulphur, selenium and tellurium. For example, if an oxide is used as the cathode in molten calcium chloride, the favoured reaction is shown to be the ionization of oxygen O + 2e - → O 2- rather than Ca 2+ + 2 e- → Ca. The oxygen ions dissolve in the salt leaving the metal behind, and this leads to the interesting hypothesis that metal oxides can be reduced directly to the metal purely by the use of electrons. Examples are given for the reduction of titanium dioxide, zirconium dioxide, chromium oxide and niobium oxide and by mixing oxide powders together and reducing the mixed compact, alloys and intermetallic compounds are formed. Preliminary calculations indicate that this new process should be much cheaper than conventional metallothermic reduction for these elements. (author)

  14. Vanadium Oxide Thin Film Formation on Graphene Oxide by Microexplosive Decomposition of Ammonium Peroxovanadate and Its Application as a Sodium Ion Battery Anode.

    Science.gov (United States)

    Mikhaylov, Alexey A; Medvedev, Alexander G; Grishanov, Dmitry A; Sladkevich, Sergey; Gun, Jenny; Prikhodchenko, Petr V; Xu, Zhichuan J; Nagasubramanian, Arun; Srinivasan, Madhavi; Lev, Ovadia

    2018-02-27

    Formation of vanadium oxide nanofilm-coated graphene oxide (GO) is achieved by thermally induced explosive disintegration of a microcrystalline ammonium peroxovanadate-GO composite. GO sheets isolate the microcrystalline grains and capture and contain the microexplosion products, resulting in the deposition of the nanoscale products on the GO. Thermal treatment of the supported nanofilm yields a sequence of nanocrystalline phases of vanadium oxide (V 3 O 7 , VO 2 ) as a function of temperature. This is the first demonstration of microexplosive disintegration of a crystalline peroxo compound to yield a nanocoating. The large number of recently reported peroxide-rich crystalline materials suggests that the process can be a useful general route for nanofilm formation. The V 3 O 7 @GO composite product was tested as a sodium ion battery anode and showed high charge capacity at high rate charge-discharge cycling (150 mAh g -1 at 3000 mA g -1 vs 300 mAh g -1 at 100 mA g -1 ) due to the nanomorphology of the vanadium oxide.

  15. Study for preparation of nanoporous titania on titanium by anodic oxidation; Estudo da preparacao de titania nanoporosa sobre titanio por oxidacao anodica

    Energy Technology Data Exchange (ETDEWEB)

    Passos, Alessandra Pires

    2014-07-01

    Currently titanium is the most common material used in dental, orthopedic implants and cardiovascular applications. In the mid 1960s, prof. Braenemark and coworkers developed the concept of osseointegration, meaning the direct structural and functional connection between living bone and the surface of artificial implant. Thus, studies on the modification of the implant surface are widely distributed among them are the acid attack, blasting with particles of titanium oxide or aluminum oxide, coating with bioactive materials such as hydroxyapatite, and the anodic oxidation. The focus of this work was to investigate the treatment of titanium surface by anodic oxidation. The aim was to develop a nanoporous titanium oxide overlay with controlled properties over titanium substrates. Recent results have shown that such surface treatment improves the biological interaction at the interface bone-implant besides protecting the titanium further oxidation and allow a faster osseointegration. The anodizing process was done in the potentiostatic mode, using an electrolyte composed of 1.0 mol/L H{sub 3}PO{sub 4} and HF 0.5% m/I. The investigated process parameters were the electrical potential (Va) and the process time (T). The electric potential was varied from 10 V to 30 V and the process time was defined as 1.0 h, 1.5 h or 2.0 h. The treated Ti samples were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), energy dispersive spectroscopy X-ray (EDS), and X-ray diffraction (XRD). The results showed the formation of nanoporous titanium oxide by anodizing with electric potential (Va) in the range of 20 V to 30 V and process time in the range of 1 to 2 hours. The average pore diameter was in the range 94-128 nm. Samples anodized in electric potential lower than 20 V did not show the formation of the nanoporous surface. In the case of Va above 30 V, it was observed the formation of agglomerates of TiO{sub 2}. The results obtained in this study

  16. Extraction of tantalum (5) and niobium (5) by octanol from fluoride and fluoride-sulfuric acid solutions

    International Nuclear Information System (INIS)

    Majorov, V.G.; Nikolaev, A.I.; Konkov, V.K.

    2001-01-01

    Extractability of octanol and tributylphosphate in the processes of tantalum (5) and niobium (5) extraction from their concentrated fluoride and fluoride-sulfuric acid solutions, as well as in the course of tantalum (5) and niobium (5) separation and purification, was compared. The use of octanol in the extraction technology of tantalum (5) and niobium (5) separation was shown to be effective. Stability of the extractant in long-time contact with process solutions was pointed out among its important advantages. A flowsheet of extractional separation and purification of niobium (5) and tantalum (5) using octanol, which permits preparation of the elements pure oxides, was proposed [ru

  17. Niobium and tantalum: indispensable twins

    Science.gov (United States)

    Schulz, Klaus; Papp, John

    2014-01-01

    Niobium and tantalum are transition metals almost always paired together in nature. These “twins” are difficult to separate because of their shared physical and chemical properties. In 1801, English chemist Charles Hatchett uncovered an unknown element in a mineral sample of columbite; John Winthrop found the sample in a Massachusetts mine and sent it to the British Museum in London in 1734. The name columbium, which Hatchet named the new element, came from the poetic name for North America—Columbia—and was used interchangeably for niobium until 1949, when the name niobium became official. Swedish scientist Anders Ekberg discovered tantalum in 1802, but it was confused with niobium, because of their twinned properties, until 1864, when it was recognized as a separate element. Niobium is a lustrous, gray, ductile metal with a high melting point, relatively low density, and superconductor properties. Tantalum is a dark blue-gray, dense, ductile, very hard, and easily fabricated metal. It is highly conductive to heat and electricity and renowned for its resistance to acidic corrosion. These special properties determine their primary uses and make niobium and tantalum indispensable.

  18. In-situ study of the gas-phase composition and temperature of an intermediate-temperature solid oxide fuel cell anode surface fed by reformate natural gas

    Science.gov (United States)

    Santoni, F.; Silva Mosqueda, D. M.; Pumiglia, D.; Viceconti, E.; Conti, B.; Boigues Muñoz, C.; Bosio, B.; Ulgiati, S.; McPhail, S. J.

    2017-12-01

    An innovative experimental setup is used for in-depth and in-operando characterization of solid oxide fuel cell anodic processes. This work focuses on the heterogeneous reactions taking place on a 121 cm2 anode-supported cell (ASC) running with a H2, CH4, CO2, CO and steam gas mixture as a fuel, using an operating temperature of 923 K. The results have been obtained by analyzing the gas composition and temperature profiles along the anode surface in different conditions: open circuit voltage (OCV) and under two different current densities, 165 mA cm-2 and 330 mA cm-2, corresponding to 27% and 54% of fuel utilization, respectively. The gas composition and temperature analysis results are consistent, allowing to monitor the evolution of the principal chemical and electrochemical reactions along the anode surface. A possible competition between CO2 and H2O in methane internal reforming is shown under OCV condition and low current density values, leading to two different types of methane reforming: Steam Reforming and Dry Reforming. Under a current load of 40 A, the dominance of exothermic reactions leads to a more marked increase of temperature in the portion of the cell close to the inlet revealing that current density is not uniform along the anode surface.

  19. Hydrogen oxidation mechanisms on Ni/yttria stabilized zirconia anodes: Separation of reaction pathways by geometry variation of pattern electrodes

    Science.gov (United States)

    Doppler, M. C.; Fleig, J.; Bram, M.; Opitz, A. K.

    2018-03-01

    Nickel/yttria stabilized zirconia (YSZ) electrodes are affecting the overall performance of solid oxide fuel cells (SOFCs) in general and strongly contribute to the cell resistance in case of novel metal supported SOFCs in particular. The electrochemical fuel conversion mechanisms in these electrodes are, however, still only partly understood. In this study, micro-structured Ni thin film electrodes on YSZ with 15 different geometries are utilized to investigate reaction pathways for the hydrogen electro-oxidation at Ni/YSZ anodes. From electrodes with constant area but varying triple phase boundary (TPB) length a contribution to the electro-catalytic activity is found that does not depend on the TPB length. This additional activity could clearly be attributed to a yet unknown reaction pathway scaling with the electrode area. It is shown that this area related pathway has significantly different electrochemical behavior compared to the TPB pathway regarding its thermal activation, sulfur poisoning behavior, and H2/H2O partial pressure dependence. Moreover, possible reaction mechanisms of this reaction pathway are discussed, identifying either a pathway based on hydrogen diffusion through Ni with water release at the TPB or a path with oxygen diffusion through Ni to be a very likely explanation for the experimental results.

  20. Electrochemical oxidation of tramadol in low-salinity reverse osmosis concentrates using boron-doped diamond anodes.

    Science.gov (United States)

    Lütke Eversloh, Christian; Schulz, Manoj; Wagner, Manfred; Ternes, Thomas A

    2015-04-01

    The electrochemical treatment of low-salinity reverse osmosis (RO) concentrates was investigated using tramadol (100 μM) as a model substance for persistent organic contaminants. Galvanostatic degradation experiments using boron-doped diamond electrodes at different applied currents were conducted in RO concentrates as well as in ultra-pure water containing either sodium chloride or sodium sulfate. Kinetic investigations revealed a significant influence of in-situ generated active chlorine besides direct anodic oxidation. Therefore, tramadol concentrations decreased more rapidly at elevated chloride content. Nevertheless, reduction of total organic carbon (TOC) was found to be comparatively low, demonstrating that transformation rather than mineralization was taking place. Early stage product formation could be attributed to both direct and indirect processes, including demethylation, hydroxylation, dehydration, oxidative aromatic ring cleavage and halogenation reactions. The latter led to various halogenated derivatives and resulted in AOX (adsorbable organic halogens) formation in the lower mg/L-range depending on the treatment conditions. Characterisation of transformation products (TPs) was achieved via MS(n) experiments and additional NMR measurements. Based on identification and quantification of the main TPs in different matrices and on additional potentiostatic electrolysis, a transformation pathway was proposed. Copyright © 2014 Elsevier Ltd. All rights reserved.

  1. Novel synthesis of holey reduced graphene oxide (HRGO) by microwave irradiation method for anode in lithium-ion batteries

    Science.gov (United States)

    Alsharaeh, Edreese; Ahmed, Faheem; Aldawsari, Yazeed; Khasawneh, Majdi; Abuhimd, Hatem; Alshahrani, Mohammad

    2016-07-01

    In this work, holey reduced graphene oxide (HRGO) was synthesized by the deposition of silver (Ag) nanoparticles onto the reduced graphene oxide (RGO) sheets followed by nitric acid treatment to remove Ag nanoparticles by microwave irradiation to form a porous structure. The HRGO were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), ultra violet-visible spectroscopy (UV-Vis), thermogravimetric analysis (TGA), and Raman spectroscopy. These novel HRGO exhibited high rate capability with excellent cycling stability as an anode material for lithium-ion batteries. The results have shown an excellent electrochemical response in terms of charge/discharge capacity (423 mAh/g at 100 mA/g). The cyclic performance was also exceptional as a high reversible capacity (400 mAh/g at 100 mA/g) was retained for 100 charge/discharge cycles. This fascinating electrochemical performance can be ascribed to their specific porous structure (2-5 nm pores) and high surface area (457 m2/g), providing numerous active sites for Li+ insertion, high electrical conductivity, low charge-transfer resistance across the electrolyte-electrode interface, and improved structural stability against the local volume change during Li+ insertion-extraction. Such electrodes are envisioned to be mass scalable with relatively simple and low-cost fabrication procedures, thereby providing a clear pathway toward commercialization.

  2. Fabrication of Polymeric Antireflection Film Manufactured by Anodic Aluminum Oxide Template on Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Jenn-Kai Tsai

    2017-03-01

    Full Text Available In this study, high energy conversion efficient dye-sensitized solar cells (DSSCs were successfully fabricated by attaching a double anti-reflection (AR layer, which is composed of a subwavelength moth-eye structured polymethyl methacrylate (PMMA film and a polydimethylsiloxane (PDMS film. An efficiency of up to 6.79% was achieved. The moth-eye structured PMMA film was fabricated by using an anodic aluminum oxide (AAO template which is simple, low-cost and scalable. The nano-pattern of the AAO template was precisely reproduced onto the PMMA film. The photoanode was composed of Titanium dioxide (TiO2 nanoparticles (NPs with a diameter of 25 nm deposited on the fluorine-doped tin oxide (FTO glass substrate and the sensitizer N3. The double AR layer was proved to effectively improve the short-circuit current density (JSC and conversion efficiency from 14.77 to 15.79 mA/cm2 and from 6.26% to 6.79%, respectively.

  3. Hierarchical structured graphene/metal oxide/porous carbon composites as anode materials for lithium-ion batteries

    International Nuclear Information System (INIS)

    Guo, Rong; Yue, Wenbo; Ren, Yu; Zhou, Wuzong

    2016-01-01

    Highlights: • CeO 2 and Co 3 O 4 nanoparticles display different behavior within CMK-3. • CMK-3-CeO 2 and Co 3 O 4 show various electrochemical properties • CMK-3-CeO 2 and Co 3 O 4 are further wrapped by graphene nanosheets. • Graphene-encapsulated composites show better electrochemical performances. - Abstract: As a novel anode material for lithium-ion batteries, CeO 2 displays imperceptible volumetric and morphological changes during the lithium insertion and extraction processes, and thereby exhibits good cycling stability. However, the low theoretical capacity and poor electronic conductivity of CeO 2 hinder its practical application. In contrast, Co 3 O 4 possesses high theoretical capacity, but undergoes huge volume change during cycling. To overcome these issues, CeO 2 and Co 3 O 4 nanoparticles are formed inside the pores of CMK-3 and display various electrochemical behaviors due to the different morphological structures of CeO 2 and Co 3 O 4 within CMK-3. Moreover, the graphene/metal oxide/CMK-3 composites with a hierarchical structure are then prepared and exhibit better electrochemical performances than metal oxides with or without CMK-3. This novel synthesis strategy is hopefully employed in the electrode materials design for Li-ion batteries or other energy conversion and storage devices.

  4. High-Temperature Stable Anatase Titanium Oxide Nanofibers for Lithium-Ion Battery Anodes.

    Science.gov (United States)

    Lee, Sangkyu; Eom, Wonsik; Park, Hun; Han, Tae Hee

    2017-08-02

    Control of the crystal structure of electrochemically active materials is an important approach to fabricating high-performance electrodes for lithium-ion batteries (LIBs). Here, we report a methodology for controlling the crystal structure of TiO 2 nanofibers by adding aluminum isopropoxide to a common sol-gel precursor solution utilized to create TiO 2 nanofibers. The introduction of aluminum cations impedes the phase transformation of electrospun TiO 2 nanofibers from the anatase to the rutile phase, which inevitably occurs in the typical annealing process utilized for the formation of TiO 2 crystals. As a result, high-temperature stable anatase TiO 2 nanofibers were created in which the crystal structure was well-maintained even at high annealing temperatures of up to 700 °C. Finally, the resulting anatase TiO 2 nanofibers were utilized to prepare LIB anodes, and their electrochemical performance was compared to pristine TiO 2 nanofibers that contain both anatase and rutile phases. Compared to the electrode prepared with pristine TiO 2 nanofibers, the electrode prepared with anatase TiO 2 nanofibers exhibited excellent electrochemical performances such as an initial Coulombic efficiency of 83.9%, a capacity retention of 89.5% after 100 cycles, and a rate capability of 48.5% at a current density of 10 C (1 C = 200 mA g -1 ).

  5. Characteristics of anodic polarization of solid oxide fuel cells under pressurized conditions

    Energy Technology Data Exchange (ETDEWEB)

    Kikuchi, Ryuji; Yano, Tatsuya; Eguchi, Koichi [Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8510 (Japan); Takeguchi, Tatsuya [Catalysis Research Center, Hokkaido University, Kita-ku, Sapporo 001-0021 (Japan)

    2004-10-29

    AC impedance measurements were carried out under pressurized conditions by using a Ni-Y{sub 2}O{sub 3}-stabilized zirconia (YSZ)/YSZ half cell in order to investigate anodic polarization at high-pressure conditions. AC impedance spectra were measured at 900 and 1000C in H{sub 2}-H{sub 2}O system with a constant H{sub 2}/H{sub 2}O ratio, or a constant partial pressure of H{sub 2} or H{sub 2}O for different total pressures of 1 to 10 atm. At high pressures, the resistance characterized by the semicircle at high frequency was lowered, whereas that at low frequency was raised. A model based on one-dimensional diffusion was developed to estimate concentration polarization based on the impedance measurements, and activation polarization was evaluated using a linear current-potential relation derived from the Butler-Volmer equation. The activation overvoltage was at most 40 mV at 10 mA/cm{sup 2}, irrespective of the total pressure. Concentration polarization was computed to increase as the total pressure was raised, whereas it was almost constant for temperature change. Large voltage drop at small current densities was calculated for the system with low partial pressure of oxygen.

  6. A comprehensive CFD model of anode-supported solid oxide fuel cells

    International Nuclear Information System (INIS)

    Jeon, Dong Hyup

    2009-01-01

    The two-dimensional comprehensive CFD model of anode-supported SOFCs operating at intermediate temperature has been presented. This model provides transport phenomena of gas species with electrochemical characteristics and micro-structural properties, and predicts SOFC performance. The mathematical model solves conservation of electrons and ions, continuity equation, conservation of momentum, conservation of mass, and conservation of energy. A continuum micro-scale model based on statistical properties together with a mole-based conservation model was employed. CFD technique was used to solve the set of governing equations. The cell performance was decomposed with contributions of each overpotential and was presented at several operating temperatures with analysis of effective diffusivity. It was found that the contribution of potential gain due to temperature rising was considerably high. However it became non-significant at high operating temperature due to decreasing of effective diffusivity in AFL. These results showed that the performance and the distributions of current density, overpotentials, and mole fractions of gas species have a strong dependence upon temperature. From these results, it was concluded that the conservation of energy should be accommodated in comprehensive SOFC model. Also the useful information for the effect of parameters on cell performance and transport phenomena was provided

  7. A robust NiO-Sm0.2Ce0.8O1.9 anode for direct-methane solid oxide fuel cell

    KAUST Repository

    Tian, Dong

    2015-07-02

    In order to directly use methane without a reforming process, NiO-Sm0.2Ce0.8O1.9 (NiO-SDC) nanocomposite anode are successfully synthesized via a one-pot, surfactant-assisted co-assembly approach for direct-methane solid oxide fuel cells. Both NiO with cubic phase and SDC with fluorite phase are obtained at 550 °C. Both NiO nanoparticles and SDC nanoparticles are highly monodispersed in size with nearly spherical shapes. Based on the as-synthesized NiO-SDC, two kinds of single cells with different micro/macro-porous structure are successfully fabricated. As a result, the cell performance was improved by 40%-45% with the new double-pore NiO-SDC anode relative to the cell performance with the conventional NiO-SDC anode due to a wider triple-phase-boundary (TPB) area. In addition, no significant degradation of the cell performance was observed after 60 hours, which means an increasing of long term stability. Therefore, the as-synthesized NiO-SDC nanocomposite is a promising anode for direct-methane solid oxide fuel cells.

  8. Developing the photovoltaic performance of dye-sensitized solar cells (DSSCs) using a SnO2-doped graphene oxide hybrid nanocomposite as a photo-anode

    Science.gov (United States)

    Sasikumar, Ragu; Chen, Tse-Wei; Chen, Shen-Ming; Rwei, Syang-Peng; Ramaraj, Sayee Kannan

    2018-05-01

    Tin(IV) oxide nanoparticles (SnO2 NPs) doped on the surface of graphene oxide (GO) sheets for application in Dye-Sensitized Solar Cells (DSSCs). The effective incorporation of SnO2 on the surface of GO sheets were confirmed by powder X-ray diffraction (PXRD), Fourier transform infra-red spectroscopy (FT-IR), thermogravimetric analysis (TGA), electrochemical impedance spectroscopy (EIS), and Raman spectroscopy. The morphology of the GO/SnO2 hybrid nanocomposite was confirmed by field emission scanning electron microscopy (FE-SEM) analysis. This current study involvement with the effect of different photo-anodes such as GO, SnO2, and GO/SnO2 hybrid nanocomposite on the power conversion efficiency (PCE) of the triiodide electrolyte based DSSCs. Remarkably, GO/SnO2 hybrid nanocomposite based photo-anode for DSSC observed PCE of 8.3% and it is about 12% higher than that of un-doped TiO2 photo-anode. The equivalent short-circuit photocurrent density (Jsc) of 16.67 mA cm-2, open circuit voltage (Voc) of 0.77 V, and fill factor (FF) of 0.65 respectively. The achieved results propose that the hybrid nanocomposite is an appropriate photo-anodic material for DSSCs applications.

  9. Tuning the charge state of Ag and Au atoms and clusters deposited on oxide surfaces by doping: a DFT study of the adsorption properties of nitrogen- and niobium-doped TiO2 and ZrO2.

    Science.gov (United States)

    Schlexer, Philomena; Ruiz Puigdollers, Antonio; Pacchioni, Gianfranco

    2015-09-14

    The charge state of Ag and Au atoms and clusters (Ag4 and Au4, Ag5 and Au5) adsorbed on defective TiO2 anatase(101) and tetragonal ZrO2(101) has been systematically investigated as a function of oxide doping and defectivity using a DFT+U approach. As intrinsic defects, we have considered the presence of oxygen vacancies. As extrinsic defects, substitutional nitrogen- and niobium-doping have been investigated, respectively. Both surface and sub-surface defects and dopants have been considered. Whereas on surfaces with oxygen vacancies or Nb-doping, atoms and clusters may become negatively charged, N-doping always leads to the formation of positively charged adsorbates, independently of the supporting material (TiO2 or ZrO2). This suggests the possibility to tune the electronic properties of supported metal clusters by selective doping of the oxide support, an effect that may result in complete changes in chemical reactivity.

  10. Kinetic Analysis of the Anodic Carbon Oxidation Mechanism in a Molten Carbonate Medium

    International Nuclear Information System (INIS)

    Allen, Jessica A.; Tulloch, John; Wibberley, Louis; Donne, Scott W.

    2014-01-01

    The oxidation mechanism for carbon in a carbonate melt was modelled using an electrochemical kinetic approach. Through the Butler-Volmer equation for electrode kinetics, a series of expressions was derived assuming each step of the proposed carbon oxidation mechanism is in turn the rate determining step (RDS). Through the derived expressions the transfer coefficient and Tafel slope were calculated for each possible RDS of the proposed mechanism and these were compared with real data collected on carbon based electrodes including graphite and coal. It was established that the RDS of the electrochemical oxidation process is dependent on both the carbon type and the potential region of oxidation. The simplified kinetic analysis suggested that the RDS in the main oxidation region is likely to be the first or second electron transfer on a graphite electrode surface, which occurs following initial adsorption of an oxygen anion to an active carbon site. This is contrary to previous suggestions that adsorption of the second anion to the carbon surface will be rate determining. It was further shown that use of a coal based carbon introduces a change in mechanism with an additional reaction region where a different mechanism is proposed to be operating

  11. Electrochemical Oxidation of Resorcinol in Aqueous Medium Using Boron-Doped Diamond Anode: Reaction Kinetics and Process Optimization with Response Surface Methodology.

    Science.gov (United States)

    Körbahti, Bahadır K; Demirbüken, Pelin

    2017-01-01

    Electrochemical oxidation of resorcinol in aqueous medium using boron-doped diamond anode (BDD) was investigated in a batch electrochemical reactor in the presence of Na 2 SO 4 supporting electrolyte. The effect of process parameters such as resorcinol concentration (100-500 g/L), current density (2-10 mA/cm 2 ), Na 2 SO 4 concentration (0-20 g/L), and reaction temperature (25-45°C) was analyzed on electrochemical oxidation using response surface methodology (RSM). The optimum operating conditions were determined as 300 mg/L resorcinol concentration, 8 mA/cm 2 current density, 12 g/L Na 2 SO 4 concentration, and 34°C reaction temperature. One hundred percent of resorcinol removal and 89% COD removal were obtained in 120 min reaction time at response surface optimized conditions. These results confirmed that the electrochemical mineralization of resorcinol was successfully accomplished using BDD anode depending on the process conditions, however the formation of intermediates and by-products were further oxidized at much lower rate. The reaction kinetics were evaluated at optimum conditions and the reaction order of electrochemical oxidation of resorcinol in aqueous medium using BDD anode was determined as 1 based on COD concentration with the activation energy of 5.32 kJ/mol that was supported a diffusion-controlled reaction.

  12. Electrochemical Oxidation of Resorcinol in Aqueous Medium Using Boron-Doped Diamond Anode: Reaction Kinetics and Process Optimization with Response Surface Methodology

    Directory of Open Access Journals (Sweden)

    Bahadır K. Körbahti

    2017-10-01

    Full Text Available Electrochemical oxidation of resorcinol in aqueous medium using boron-doped diamond anode (BDD was investigated in a batch electrochemical reactor in the presence of Na2SO4 supporting electrolyte. The effect of process parameters such as resorcinol concentration (100–500 g/L, current density (2–10 mA/cm2, Na2SO4 concentration (0–20 g/L, and reaction temperature (25–45°C was analyzed on electrochemical oxidation using response surface methodology (RSM. The optimum operating conditions were determined as 300 mg/L resorcinol concentration, 8 mA/cm2 current density, 12 g/L Na2SO4 concentration, and 34°C reaction temperature. One hundred percent of resorcinol removal and 89% COD removal were obtained in 120 min reaction time at response surface optimized conditions. These results confirmed that the electrochemical mineralization of resorcinol was successfully accomplished using BDD anode depending on the process conditions, however the formation of intermediates and by-products were further oxidized at much lower rate. The reaction kinetics were evaluated at optimum conditions and the reaction order of electrochemical oxidation of resorcinol in aqueous medium using BDD anode was determined as 1 based on COD concentration with the activation energy of 5.32 kJ/mol that was supported a diffusion-controlled reaction.

  13. Degradation of trans-ferulic acid in acidic aqueous medium by anodic oxidation, electro-Fenton and photoelectro-Fenton

    Energy Technology Data Exchange (ETDEWEB)

    Flores, Nelly; Sirés, Ignasi; Garrido, José Antonio; Centellas, Francesc; Rodríguez, Rosa María; Cabot, Pere Lluís; Brillas, Enric, E-mail: brillas@ub.edu

    2016-12-05

    Highlights: • trans-Ferulic acid degradation by EAOPs using a stirred BDD/air-diffusion cell. • Slow substrate abatement and poor mineralization by AO-H{sub 2}O{sub 2}. • 98% Mineralization by PEF, but with rapid and similar substrate decay than by EF. • Quicker degradation by SPEF due to the more potent photolytic action of sunlight. • Reaction pathway with four primary aromatic products and three final carboxylic acids. - Abstract: Solutions of pH 3.0 containing trans-ferulic acid, a phenolic compound in olive oil mill wastewater, have been comparatively degraded by anodic oxidation with electrogenerated H{sub 2}O{sub 2} (AO-H{sub 2}O{sub 2}), electro-Fenton (EF) and photoelectro-Fenton (PEF). Trials were performed with a BDD/air-diffusion cell, where oxidizing ·OH was produced from water discharge at the BDD anode and/or in the solution bulk from Fenton’s reaction between cathodically generated H{sub 2}O{sub 2} and added catalytic Fe{sup 2+}. The substrate was very slowly removed by AO-H{sub 2}O{sub 2}, whereas it was very rapidly abated by EF and PEF, at similar rate in both cases, due to its fast reaction with ·OH in the bulk. The AO-H{sub 2}O{sub 2} process yielded a slightly lower mineralization than EF, which promoted the accumulation of barely oxidizable products like Fe(III) complexes. In contrast, the fast photolysis of these latter species under irradiation with UVA light in PEF led to an almost total mineralization with 98% total organic carbon decay. The effect of current density and substrate concentration on the performance of all treatments was examined. Several solar PEF (SPEF) trials showed its viability for the treatment of wastewater containing trans-ferulic acid at larger scale. Four primary aromatic products were identified by GC–MS analysis of electrolyzed solutions, and final carboxylic acids like fumaric, acetic and oxalic were detected by ion-exclusion HPLC. A reaction sequence for trans-ferulic acid mineralization

  14. Ni-YSZ solid oxide fuel cell anode behavior upon redox cycling based on electrical characterization

    DEFF Research Database (Denmark)

    Klemensø, Trine; Mogensen, Mogens Bjerg

    2006-01-01

    Ni-YSZ cermets are a prevalent material used for solid oxide fuel cells. However, the cermet degrades upon redox cycling. The degradation is related to microstructural changes, but knowledge of the mechanisms has been limited. DC conductivity measurements were performed on cermets and cermets......, where the Ni component was removed, before, during and after redox cycling the cermet. The cermet conductivity degraded over time due to sintering of the nickel phase. Following oxidizing events, the conductivity of the cermets improved, whereas the conductivity of the YSZ phase decreased. A model...

  15. Ni-YSZ solid oxide fuel cell anode behavior upon redox cycling based on electrical characterization

    DEFF Research Database (Denmark)

    Klemensø, Trine; Mogensen, Mogens Bjerg

    2007-01-01

    Nickel (Ni)—yttria-stabilized zirconia (YSZ) cermets are a prevalent material used for solid oxide fuel cells. The cermet degrades upon redox cycling. The degradation is related to microstructural changes, but knowledge of the mechanisms has been limited. Direct current conductivity measurements...... were performed on cermets and cermets where the Ni component was removed. Measurements were carried out before, during, and after redox cycling the cermet. The cermet conductivity degraded over time due to sintering of the nickel phase. Following oxidizing events, the conductivity of the cermets...

  16. Self-sealing of unsealed aluminium anodic oxide films in very different atmospheres

    Directory of Open Access Journals (Sweden)

    González, J. A.

    2003-12-01

    Full Text Available It is widely believed that the corrosion resistance behaviour of bare aluminium in natural environments is superior to that of unsealed anodised aluminium. However, results obtained in the exposure of unsealed anodised aluminium specimens with three different film thicknesses, in 9 atmospheres of Ibero-America with salinity levels between 3.9 and 517 mg.m-2.d-1 chloride, clearly shows the reverse to be true. After a sufficient time, which is shorter the higher the precipitation rate and the environmental relative humidity, a self-sealing process takes place, leading to coatings that surpass the quality standards demanded in industrial practice. Anodic films, sealed and unsealed, are protective coatings whose quality improves with ageing in most natural environments.

    Está muy difundida la idea de que el comportamiento del aluminio es superior al del aluminio anodizado y sin sellar, desde el punto de vista de la resistencia a la corrosión, en los ambientes naturales. Sin embargo, los resultados obtenidos en la exposición de anodizados sin sellar, de tres espesores diferentes, a 9 atmósferas de Iberoamérica, con salinidades comprendidas entre 3,9 y 517 mg.m-2.d-1 de cloruros, muestran, sin lugar a dudas, lo contrario. Con tiempo suficiente, tanto más rápidamente cuanto mayor sean las precipitaciones y la humedad relativa ambiental, tiene lugar un proceso de autosellado que conduce a recubrimientos que superan las normas de calidad exigidas en la práctica industrial. Los anodizados, sellados y sin sellar, son recubrimientos protectores que mejoran su calidad, en la mayoría de los ambientes naturales, con el envejecimiento.

  17. Degradation of some ceria electrolytes under hydrogen contact nearby anode in solid oxide fuel cells (SOFCs

    Directory of Open Access Journals (Sweden)

    Malta Luiz Fernando Brum

    2004-01-01

    Full Text Available This work is concerned with thermodynamic analysis of the stability of some ceria electrolytes under contact with hydrogen gas nearby anode in fuel cells. It was considered the following types of ceria-electrolytes: pure ceria, strontium-doped ceria, calcium-doped ceria and calcium-bismuth-doped ceria. The equilibrium Log (pH2O/pH2 vs. T diagrams were constructed for x = 0.1 and 0.01, where x is the fraction of initial ceria converted to Ce2O3 (proportional to the ratio between activities of Ce3+ and Ce4+ in the ceria electrolyte, which is proportional to the fraction of electronic conduction in the electrolyte at a given temperature. The predictions of the diagrams are as follows: (a Ce1.9Ca0.1Bi0.8O5.1 and Ce0.9Sr0.1O1.9 are less stable than pure ceria for the whole temperature range (from 0 to 1000 °C; (b Ce0.9Ca0.1O1.9 is more stable than pure ceria below about 650 °C for x = 0.1 and below about 400 °C for x = 0.01; (c at each temperature in the considered range the pressure ratio pH2O(g/pH2(g has to be higher than thermodynamically predicted in order to keep CeO2 stable in the electrolyte contacting hydrogen gas. Thermodynamic predictions are entirely capable of explaining experimental data published on the subject (irreversible cell degradation in the case of SrO-doped ceria; weight loss from doped-ceria electrolyte above 700 °C; oxygen gas release during sintering of ceria.

  18. The iron and cerium oxide influence on the electric conductivity and the corrosion resistance of anodized aluminium; A influencia do ferro e do oxido de cerio sobre a condutividade eletrica e a resistencia a corrosao do aluminio anodizado

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Kellie Provazi de

    2006-07-01

    The influence of different treatments on the aluminum system covered with aluminum oxide is investigated. The aluminum anodization in sulphuric media and in mixed sulphuric and phosphoric media was used to alter the corrosion resistance, thickness, coverage degree and microhardness of the anodic oxide. Iron electrodeposition inside the anodic oxide was used to change its electric conductivity and corrosion resistance. Direct and pulsed current were used for iron electrodeposition and the Fe(SO{sub 4}){sub 2}(NH{sub 4}){sub 2}.6H{sub 2}O electrolyte composition was changed with the addition of boric and ascorbic acids. To the sealing treatment the CeCl{sub 3} composition was varied. The energy dispersive x-ray (EDS), the x-ray fluorescence spectroscopy (FRX) and the morphologic analysis by scanning electronic microscopy (SEM) allowed to verify that, the pulsed current increase the iron content inside the anodic layer and that the use of the additives inhibits the iron oxidation. The chronopotentiometric curves obtained during iron electrodeposition indicated that the boric and ascorbic acids mixture increased the electrodeposition process efficiency. The electrochemical impedance spectroscopy (EIE), the Vickers (Hv) microhardness measurements and morphologic analysis evidenced that the sealing treatment improves the corrosion resistance of the anodic film modified with iron. The electrical impedance (EI) technique allowed to prove the electric conductivity increase of the anodized aluminum with iron electrodeposited even after the cerium low concentration treatment. Iron nanowires were prepared by using the anodic oxide pores as template. (author)

  19. Sulfur Poisoning of the Water Gas Shift Reaction on Anode Supported Solid Oxide Fuel Cells

    DEFF Research Database (Denmark)

    Hagen, Anke

    2013-01-01

    resistance increased both in the high and low frequency region, which indicates a strong poisoning of the water gas shift reaction and thus a lack of hydrogen fuel in addition to the poisoning of the electrochemical hydrogen oxidation. All poisoning effects are reversible under the applied operating...

  20. Strontium Titanate-based Composite Anodes for Solid Oxide Fuel Cells

    DEFF Research Database (Denmark)

    Blennow Tullmar, Peter; Kammer Hansen, Kent; Wallenberg, L.R.

    2008-01-01

    Surfactant-assisted infiltration of Gd-doped ceria (CGO) in Nb-doped SrTiO3 (STN) was investigated as a potential fuel electrode for solid oxide fuel cells (SOFC). An electronically conductive backbone structure of STN was first fabricated at high temperatures and then combined with the mixed con...

  1. Long term performance degradation analysis and optimization of anode supported solid oxide fuel cell stacks

    International Nuclear Information System (INIS)

    Parhizkar, Tarannom; Roshandel, Ramin

    2017-01-01

    Highlights: • A degradation based optimization framework is developed. • The cost of electricity based on degradation of solid oxide fuel cells is minimized. • The effects of operating conditions on degradation mechanisms are investigated. • Results show 7.12% lower cost of electricity in comparison with base case. • Degradation based optimization is a beneficial concept for long term analysis. - Abstract: The main objective of this work is minimizing the cost of electricity of solid oxide fuel cell stacks by decelerating degradation mechanisms rate in long term operation for stationary power generation applications. The degradation mechanisms in solid oxide fuel cells are caused by microstructural changes, reactions between lanthanum strontium manganite and electrolyte, poisoning by chromium, carburization on nickel particles, formation of nickel sulfide, nickel coarsening, nickel oxidation, loss of conductivity and crack formation in the electrolyte. The rate of degradation mechanisms depends on the cell operating conditions (cell voltage and fuel utilization). In this study, the degradation based optimization framework is developed which determines optimum operating conditions to achieve a minimum cost of electricity. To show the effectiveness of the developed framework, optimization results are compared with the case that system operates at its design point. Results illustrate optimum operating conditions decrease the cost of electricity by 7.12%. The performed study indicates that degradation based optimization is a beneficial concept for long term performance degradation analysis of energy conversion systems.

  2. Set potential regulation reveals additional oxidation peaks of Geobacter sulfurreducens anodic biofilms

    KAUST Repository

    Zhu, Xiuping

    2012-08-01

    Higher current densities produced in microbial fuel cells and other bioelectrochemical systems are associated with the presence of various Geobacter species. A number of electron transfer components are involved in extracellular electron transfer by the model exoelectrogen, Geobacter sulfurreducens. It has previously been shown that 5 main oxidation peaks can be identified in cyclic voltammetry scans. It is shown here that 7 separate oxidation peaks emerged over relatively long periods of time when a larger range of set potentials was used to acclimate electroactive biofilms. The potentials of oxidation peaks obtained with G. sulfurreducens biofilms acclimated at 0.60 V (vs. Ag/AgCl) were different from those that developed at - 0.46 V, and both of their peaks were different from those obtained for biofilms incubated at - 0.30 V, 0 V, and 0.30 V. These results expand the known range of potentials for which G. sulfurreducens produces identifiable oxidation peaks that could be important for extracellular electron transfer. © 2012 Elsevier B.V.

  3. Multi-metallic anodes for solid oxide fuel cell applications; Anodos multi-metalicos para aplicacoes em celulas a combustivel de oxido solido

    Energy Technology Data Exchange (ETDEWEB)

    Restivo, T.A. Guisard; Mello-Castanho, S.R.H. [Instituto de Pesquisas Energeticas e Nucleares (CCTM/IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Centro de Ciencia e Tecnologia dos Materiais; Leite, D. Will [Instituto de Pesquisas e Estudos Industriais (IPEI/FEI), Sao Bernardo do Campo, SP (Brazil). Fac. de Engenharia Industrial

    2009-07-01

    A new method for direct preparation of materials for solid oxide fuel cell anode - Ni- YSZ cermets - based on mechanical alloying (MA) of the original powders is developed, allowing to admix homogeneously any component. Additive metals are selected from thermodynamic criteria, leading to compacts consolidation through sintering by activated surface (SAS). The combined process MA-SSA can reduce the sintering temperature by 300 deg C, yielding porous anodes. Densification mechanisms are discussed from quasi-isothermal sintering kinetics results. Doping with Ag, W, Cu, Mo, Nb, Ta, in descending order, promotes the densification of pellets through liquid phase sintering and evaporation of metals and oxides, which allow reducing the sintering temperature. Powders and pellets characterization by electronic microscopy and X-ray diffraction completes the result analyses. (author)

  4. Thermal cycling and electrochemical characteristics of solid oxide fuel cell supported on stainless steel with a new 3-phase composite anode

    Science.gov (United States)

    Dayaghi, Amir Masoud; Kim, Kun Joong; Kim, Sun Jae; Kim, Sunwoong; Bae, Hongyeul; Choi, Gyeong Man

    2017-06-01

    We report design, fabrication method, and fast thermal-cycling ability of solid oxide fuel cells (SOFCs) that use stainless steel (STS) as a support, and a new 3-phase anode. La and Ni co-doped SrTiO3 (La0.2Sr0.8Ti0.9Ni0.1O3-d, LSTN), replaces some of the Ni in conventional Ni-yttria stabilized zirconia (YSZ) anode; the resultant LSTN-YSZ-Ni 3-phase-composite anode is tested as a new reduction (or decomposition)-resistant anode of STS-supported SOFCs that can be co-fired with STS. A multi-layered cell with YSZ electrolyte (thickness ∼5 μm), composite anode, STS-cermet contact-layer, and STS support is designed, then fabricated by tape casting, lamination, and co-firing at 1250 °C in reducing atmosphere. The maximum power density (MPD) is 325 mW cm-2 at 650 °C; this is one of the highest among STS-supported cells fabricated by co-firing. The cell also shows stable open-circuit voltage and Ohmic resistance during 100 rapid thermal cycles between 170 and 600 °C. STS support minimizes stress and avoids cracking of electrolyte during rapid thermal cycling. The excellent MPD and stability during thermal cycles, and promising characteristics of SOFC as a power source for vehicle or mobile devices that requires rapid thermal cycles, are attributed to the new design of the cell with new anode structure.

  5. Reduction of Al2O3 in niobium--lithium systems at 10000C

    International Nuclear Information System (INIS)

    Selle, J.E.; DeVan, J.H.

    1977-07-01

    Various grades of aluminum oxide (Al 2 O 3 ) were sealed inside capsules of niobium and niobium-1% zirconium alloy which were then exposed to liquid lithium for 3000 hr at 1000 0 C. Similar unsealed capsules were exposed to a high vacuum. Reduction of the Al 2 O 3 occurred in the lithium-treated capsules, but no reaction occurred in the vacuum-treated capsules. Metallography and electron-microprobe analysis showed that reaction products in the form of compounds of niobium, aluminum, and zirconium were formed. Lithium acted as a sink for oxygen

  6. Synthesis of niobium nitride by pyrolysis of niobium pentachloride ammines

    International Nuclear Information System (INIS)

    Grebtsova, O.M.; Shulga, Y.M.; Troitskii, V.N.

    1986-01-01

    This paper investigates the conditions for the preparation of niobium nitride in the thermal decomposition of niobium nitride in the thermal decomposition of niobium pentachloride ammines. The synthesis of the ammines was accomplished by the reaction of powdered NbC1 5 with dry ammonia at 210 K. Thermography and x-ray diffraction, spectral, and chemical analyses were used to identify the ammonolysis products. It was established that the products of ammonolysis of NbC1 5 are a mixture of the x-ray-amorphous complex Nb (NH 2 ) /SUB 5-x/ - (NG 3 ) 3 CL 3 (x≅) and 2 moles of NH 4 C1. The steps in the thermal decomposition of this mixture were studied. The phase transition that is observed in the case of further vacuum heat treatment at 1100-1300 K is presented

  7. Degradation of 4,6-dinitro-o-cresol from water by anodic oxidation with a boron-doped diamond electrode

    International Nuclear Information System (INIS)

    Flox, Cristina; Garrido, Jose Antonio; Rodriguez, Rosa Maria; Centellas, Francesc; Cabot, Pere-Lluis; Arias, Conchita; Brillas, Enric

    2005-01-01

    Anodic oxidation of 4,6-dinitro-o-cresol (DNOC) has been studied in a cell of 100 ml with a boron-doped diamond anode and a graphite cathode, both of 3-cm 2 area. Solutions containing up to approximately 240 mg l -1 of compound in the pH range 2.0-12.0 have been treated at 100, 300 and 450 mA between 15 and 50 deg C. Total mineralization is always achieved due to the great amount of hydroxyl radical (·OH) produced as oxidant on the anode surface. Total organic carbon is more rapidly removed in acid medium, being the optimum pH 3.0. The degradation rate increases when temperature, current and DNOC concentration increase. However, at 100 mA depollution becomes more effective from 71 mg l -1 of initial pollutant. A pseudo first-order kinetics for DNOC decay is always found by reversed-phase chromatography, with a rate constant practically independent of pH, as expected if the same electroactive species is oxidized in all media. Ion-exclusion chromatography allowed the detection of oxalic acid as the ultimate carboxylic acid. The mineralization process leads to the complete release of NO 3 - ions from the destruction of nitroderivative intermediates. These products are oxidized simultaneously with accumulated oxalic acid up to the end of electrolyses. Comparative treatment of the same solutions with a Pt anode yields a quite poor depollution because of the generation of much lower amounts of reactive ·OH on its surface

  8. Formation of double ring patterns on Co2MnSi Heusler alloy thin film by anodic oxidation under scanning probe microscope

    OpenAIRE

    Toutam, Vijaykumar; Pandey, Himanshu; Singh, Sandeep; Budhani, R. C.

    2013-01-01

    Double ring formation on Co2MnSi (CMS) films is observed at electrical breakdown voltage during local anodic oxidation (LAO) using atomic force microscope (AFM). Corona effect and segregation of cobalt in the vicinity of the rings is studied using magnetic force microscopy and energy dispersive spectroscopy. Double ring formation is attributed to the interaction of ablated material with the induced magnetic field during LAO. Steepness of forward bias transport characteristics from the unpertu...

  9. Double-layer anti-reflection coating containing a nanoporous anodic aluminum oxide layer for GaAs solar cells.

    Science.gov (United States)

    Yang, Tianshu; Wang, Xiaodong; Liu, Wen; Shi, Yanpeng; Yang, Fuhua

    2013-07-29

    Multilayer anti-reflection (AR) coatings can be used to improve the efficiency of Gallium Arsenide (GaAs) solar cells. We propose an alternate method to obtain optical thin films with specified refractive indices, which is using a self-assembled nanoporous anodic aluminum oxide (AAO) template as an optical thin film whose effective refractive index can be tuned by pore-widening. Different kinds of double-layer AR coatings each containing an AAO layer were designed and investigated by finite difference time domain (FDTD) method. We demonstrate that a λ /4n - λ /4n AR coating consisting of a TiO(2) layer and an AAO layer whose effective refractive index is 1.32 realizes a 96.8% light absorption efficiency of the GaAs solar cell under AM1.5 solar spectrum (400 nm-860 nm). We also have concluded some design principles of the double-layer AR coating containing an AAO layer for GaAs solar cells.

  10. Reforming results of a novel radial reactor for a solid oxide fuel cell system with anode off-gas recirculation

    Science.gov (United States)

    Bosch, Timo; Carré, Maxime; Heinzel, Angelika; Steffen, Michael; Lapicque, François

    2017-12-01

    A novel reactor of a natural gas (NG) fueled, 1 kW net power solid oxide fuel cell (SOFC) system with anode off-gas recirculation (AOGR) is experimentally investigated. The reactor operates as pre-reformer, is of the type radial reactor with centrifugal z-flow, has the shape of a hollow cylinder with a volume of approximately 1 L and is equipped with two different precious metal wire-mesh catalyst packages as well as with an internal electric heater. Reforming investigations of the reactor are done stand-alone but as if the reactor would operate within the total SOFC system with AOGR. For the tests presented here it is assumed that the SOFC system runs on pure CH4 instead of NG. The manuscript focuses on the various phases of reactor operation during the startup process of the SOFC system. Startup process reforming experiments cover reactor operation points at which it runs on an oxygen to carbon ratio at the reactor inlet (ϕRI) of 1.2 with air supplied, up to a ϕRI of 2.4 without air supplied. As confirmed by a Monte Carlo simulation, most of the measured outlet gas concentrations are in or close to equilibrium.

  11. Online gas composition estimation in solid oxide fuel cell systems with anode off-gas recycle configuration

    Science.gov (United States)

    Dolenc, B.; Vrečko, D.; Juričić, Ð.; Pohjoranta, A.; Pianese, C.

    2017-03-01

    Degradation and poisoning of solid oxide fuel cell (SOFC) stacks are continuously shortening the lifespan of SOFC systems. Poisoning mechanisms, such as carbon deposition, form a coating layer, hence rapidly decreasing the efficiency of the fuel cells. Gas composition of inlet gases is known to have great impact on the rate of coke formation. Therefore, monitoring of these variables can be of great benefit for overall management of SOFCs. Although measuring the gas composition of the gas stream is feasible, it is too costly for commercial applications. This paper proposes three distinct approaches for the design of gas composition estimators of an SOFC system in anode off-gas recycle configuration which are (i.) accurate, and (ii.) easy to implement on a programmable logic controller. Firstly, a classical approach is briefly revisited and problems related to implementation complexity are discussed. Secondly, the model is simplified and adapted for easy implementation. Further, an alternative data-driven approach for gas composition estimation is developed. Finally, a hybrid estimator employing experimental data and 1st-principles is proposed. Despite the structural simplicity of the estimators, the experimental validation shows a high precision for all of the approaches. Experimental validation is performed on a 10 kW SOFC system.

  12. Coupling digestion in a pilot-scale UASB reactor and electrochemical oxidation over BDD anode to treat diluted cheese whey.

    Science.gov (United States)

    Katsoni, Alphathanasia; Mantzavinos, Dionissios; Diamadopoulos, Evan

    2014-11-01

    The efficiency of the anaerobic treatment of cheese whey (CW) at mesophilic conditions was investigated. In addition, the applicability of electrochemical oxidation as an advanced post-treatment for the complete removal of chemical oxygen demand (COD) from the anaerobically treated cheese whey was evaluated. The diluted cheese whey, having a pH of 6.5 and a total COD of 6 g/L, was first treated in a 600-L, pilot-scale up-flow anaerobic sludge blanket (UASB) reactor. The UASB process, which was operated for 87 days at mesophilic conditions (32 ± 2 °C) at a hydraulic retention time (HRT) of 3 days, led to a COD removal efficiency between 66 and 97 %, while the particulate matter of the wastewater was effectively removed by entrapment in the sludge blanket of the reactor. When the anaerobic reactor effluent was post-treated over a boron-doped diamond (BDD) anode at 9 and 18 A and in the presence of NaCl as the supporting electrolyte, complete removal of COD was attained after 3-4 h of reaction. During electrochemical experiments, three groups of organochlorinated compounds, namely trihalomethanes (THMs), haloacetonitriles (HANs), and haloketons (HKs), as well as 1,2-dichloroethane (DCA) and chloropicrin were identified as by-products of the process; these, alongside free chlorine, are thought to increase the matrix ecotoxicity to Artemia salina.

  13. Direct ceramic inkjet printing of yttria-stabilized zirconia electrolyte layers for anode-supported solid oxide fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Tomov, R.I.; Hopkins, S.C. [Applied Superconductivity and Cryoscience Group, Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB4 3QZ (United Kingdom); Krauz, M.; Kluczowski, J.R. [Institute of Power Engineering, Ceramic Department CEREL, 36-040 Boguchwala (Poland); Jewulski, J. [Institute of Power Engineering, Fuel Cells Department, 02-981 Warsaw (Poland); Glowacka, D.M. [Detector Physics Group, Cavendish Laboratory, University of Cambridge, Cambridge CB3 0HE (United Kingdom); Glowacki, B.A. [Applied Superconductivity and Cryoscience Group, Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB4 3QZ (United Kingdom); Institute of Power Engineering, Fuel Cells Department, 02-981 Warsaw (Poland)

    2010-11-01

    Electromagnetic drop-on-demand direct ceramic inkjet printing (EM/DCIJP) was employed to fabricate dense yttria-stabilized zirconia (YSZ) electrolyte layers on a porous NiO-YSZ anode support from ceramic suspensions. Printing parameters including pressure, nozzle opening time and droplet overlapping were studied in order to optimize the surface quality of the YSZ coating. It was found that moderate overlapping and multiple coatings produce the desired membrane quality. A single fuel cell with a NiO-YSZ/YSZ ({proportional_to}6 {mu}m)/LSM + YSZ/LSM architecture was successfully prepared. The cell was tested using humidified hydrogen as the fuel and ambient air as the oxidant. The cell provided a power density of 170 mW cm{sup -2} at 800 C. Scanning electron microscopy (SEM) revealed a highly coherent dense YSZ electrolyte layer with no open porosity. These results suggest that the EM/DCIJP inkjet printing technique can be successfully implemented to fabricate electrolyte coatings for SOFC thinner than 10 {mu}m and comparable in quality to those fabricated by more conventional ceramic processing methods. (author)

  14. The effect of anodic oxide coating on the fatigue behaviour of AA6082 with an ultrafine-grained microstructure

    Energy Technology Data Exchange (ETDEWEB)

    Koehler, L.; Haendel, M.; Halle, T.; Nickel, D.; Alisch, G.; Lampke, T. [Technische Universitaet Chemnitz, Institut fuer Werkstoffwissenschaft und Werkstofftechnik, Chemnitz (Germany); Hockauf, K.

    2011-07-15

    In this work, the high-cycle fatigue behaviour of the precipitation hardening aluminium wrought alloy AA6082 was investigated for a conventionally-grained and an ultrafine-grained substrate condition, with each a hard and a soft electrolytic anodic oxide (EAO) coating. The investigations were focused on the susceptibility of the coatings to anodising- and fatigue-induced cracking of the coatings and its impact on the fatigue life. For both substrate materials, the fatigue strength of the coated specimens was significantly reduced compared to the uncoated materials. Considering the resistance to crack initiation in the coating, the soft-anodised coatings were found to be superior compared to the hard-anodised ones. Moreover, the coatings on the ultrafine-grained substrate showed an enhanced resistance to anodising-induced as well as fatigue-induced cracking. However, it is supposed that the lower resistance to crack transition from the coating into the substrate is one of the most important factors which strongly limits the fatigue life of the EAO-coated specimens. This might be the reason why the fatigue strength of the ultrafine-grained substrates is relatively low, despite their higher resistance to crack initiation. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  15. Nickel oxide crystalline nano flakes: synthesis, characterization and their use as anode in lithium-ion batteries

    Science.gov (United States)

    Ahmadi, Majid; Younesi, Reza; Vegge, Tejs; J-F Guinel, Maxime

    2014-04-01

    Nickel oxide crystalline nano flakes (NONFs)—only about 10 nm wide—were produced using a simple and inexpensive chemistry method followed by a short annealing in ambient air. In a first step, Ni(OH)2 sheets were synthesized by adding sodium hydroxide (NaOH) drop-wise in a Ni(NO3)2 aqueous solution that was then sonicated for up to 60 min, washed and vigorously stirred overnight in deionized water. In a second step, the products of this reaction were annealed in ambient air in the temperature range 285-450 °C producing the desired NONFs. The products were characterized using x-ray diffraction, scanning electron microscopy and high resolution transmission electron microscopy including electron diffraction and electron energy-loss spectroscopy. Electrochemical investigations showed that anodes made of these NONFs provided significantly higher discharge capacities (70 to 100% higher) compared to commercial nanometric NiO nanopowder used under the same conditions. Moreover, these NONFs had higher initial capacity retentions at both low and high current densities compared to the same NiO nanopowder.

  16. Enhanced water vapour flow in silica microchannels and interdiffusive water vapour flow through anodic aluminium oxide (AAO) membranes

    Science.gov (United States)

    Lei, Wenwen; McKenzie, David R.

    2015-12-01

    Enhanced liquid water flows through carbon nanotubes reinvigorated the study of moisture permeation through membranes and micro- and nano-channels. The study of water vapour through micro-and nano-channels has been neglected even though water vapour is as important as liquid water for industry, especially for encapsulation of electronic devices. Here we measure moisture flow rates in silica microchannels and interdiffusive water vapour flows in anodic aluminium oxide (AAO) membrane channels for the first time. We construct theory for the flow rates of the dominant modes of water transport through four previously defined standard configurations and benchmark it against our new measurements. The findings show that measurements of leak behaviour made using other molecules, such as helium, are not reliable. Single phase water vapour flow is overestimated by a helium measurement, while Washburn or capillary flow is underestimated or for all channels when boundary slip applies, to an extent that depends on the slip length for the liquid phase flows.

  17. A Macroporous TiO2 Oxygen Sensor Fabricated Using Anodic Aluminium Oxide as an Etching Mask

    Directory of Open Access Journals (Sweden)

    Sheng-Po Wu

    2010-01-01

    Full Text Available An innovative fabrication method to produce a macroporous Si surface by employing an anodic aluminium oxide (AAO nanopore array layer as an etching template is presented. Combining AAO with a reactive ion etching (RIE processes, a homogeneous and macroporous silicon surface can be effectively configured by modulating AAO process parameters and alumina film thickness, thus hopefully replacing conventional photolithography and electrochemical etch methods. The hybrid process integration is considered fully CMOS compatible thanks to the low-temperature AAO and CMOS processes. The gas-sensing characteristics of 50 nm TiO2 nanofilms deposited on the macroporous surface are compared with those of conventional plain (or non-porous nanofilms to verify reduced response noise and improved sensitivity as a result of their macroporosity. Our experimental results reveal that macroporous geometry of the TiO2 chemoresistive gas sensor demonstrates 2-fold higher (~33% improved sensitivity than a non-porous sensor at different levels of oxygen exposure. In addition, the macroporous device exhibits excellent discrimination capability and significantly lessened response noise at 500 °C. Experimental results indicate that the hybrid process of such miniature and macroporous devices are compatible as well as applicable to integrated next generation bio-chemical sensors.

  18. Mechanical strenght and niobium and niobium-base alloys substructures

    International Nuclear Information System (INIS)

    Monteiro, W.A.; Andrade, A.H.P. de

    1986-01-01

    Niobium and some of its alloys have been used in several fields of technological applications such as the aerospace, chemical and nuclear industries. This is due to its excelent mechanical stringth at high temperatures and reasonable ductility at low temperatures. In this work, we review the main features of the relationship mechanical strength - substructure in niobium and its alloys, taking into account the presence of impurities, the influence of initial thermal and thermo - mechanical treatments as well as the irradiation by energetic particles. (Author) [pt

  19. Porous Co3O4 nanofibers surface-modified by reduced graphene oxide as a durable, high-rate anode for lithium ion battery

    International Nuclear Information System (INIS)

    Hu, Renzong; Zhang, Houpo; Bu, Yunfei; Zhang, Hanyin; Zhao, Bote; Yang, Chenghao

    2017-01-01

    Here we report our findings in synthesis and characterization of porous Co 3 O 4 nanofibers coated with a surface-modification layer, reduced graphene oxide. The unique porous Co 3 O 4 @rGO architecture enables efficient stress relaxation and fast Li + ions and electron transport during discharge/charge cycling. When tested in a half cell, the Co 3 O 4 @rGO electrodes display high Coulombic efficiency, enhanced cyclic stability, and high rate capability (∼900 mAh/g at 1A/g, and ∼600 mAh/g at 5 A/g). The high capacity is contributed by a stable capacity yielded from reversible conversion reactions above 0.8 V vs. Li/Li + , and a increasing capacity induced by the electrolyte decomposition and interfacial storage between 0.8 0.01 V during discahrge. A full cell constructed from a Co 3 O 4 @rGO anode and a LiMn 2 O 4 cathode delivers good capacity retention with operation voltage of ∼2.0 V. These performances are better than those of other full cells using alloy or metal oxide anodes. Our work is a preliminary attempt for practicality of high capacity metal oxide anodes in Li-ion batteries used for the electronic devices.

  20. Proposal of a new biokinetic model for niobium; Proposta de um novo modelo biocinetico para o niobio

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Roges

    2006-07-01

    There are two niobium isotopes generated in nuclear power plants: 95 Nb and 94 Nb. Workers and members of the public are subjects to intake these radionuclides in accident situation. For dose calculation purpose, it is very important to develop a model that describes in a more realistic way the kinetics of niobium inside of the human body. Presently the model adopted by ICRP (ICRP, 1989) is based on animal studies and describes the behavior of niobium in human being in a simple manner. The new model proposal describes the kinetics of the niobium from the intake into the blood until the excretion, doing this in a more realistic form and considering not only data from animals but data from human beings as well. For this objective, a workers group of a niobium extraction and processing industry exposed to stable niobium (93 Nb) in oxide insoluble form with associated uranium, was monitored for uranium and niobium determination in urinary and fecal excretion, by mass spectrometry. Based in the ratios of the niobium concentration in urinary and faecal excretion of this workers and animal data study, a new biokinetic model for niobium was proposed, with the followings modifications relative to ICRP model: a new compartment that represents muscular tissue; the fractions which are deposited into the compartment are modified; a third component in the retention equation of the bone tissue; introduction of recirculation between organs and blood. The new model was applied for a case of accidental intake and described adequately the experimental data.

  1. Development and manufacturing of tape casted, anode-supported solid oxide fuel cells; Entwicklung und Herstellung von foliengegossenen, anodengestuetzten Festoxidbrennstoffzellen

    Energy Technology Data Exchange (ETDEWEB)

    Schafbauer, Wolfgang

    2010-07-01

    Solid oxide fuel cells offer high potential in transforming the chemical energy of hydrogen or natural gas into electrical energy. Due to the high efficiency of fuel cells, lots of effort has been made in the improvement of net efficiency and in materials development during the last years. Recently, the introduction of high performance, low-cost production technologies become more and more important. At the Institute of Energy Research IEF-1 of Forschungszentrum Julich, standard SOFCs were processed by time and work consuming methods. On the way to market entrance, product costs have to be reduced drastically. The aim of this thesis is the introduction of a high efficient low-cost processing route for the SOFC manufacturing. Therefore, the well-known and well established shaping technology tape casting was used for generating the anode substrates. As the first goal of this approach, two different tape casting slurries were developed in order to get substrates in the thickness range from 300 to 500 {mu}m after sintering. After shaping of the substrates, sinter regimes for the different necessary coatings were adapted to the novel substrate types in order to obtain cells with high performance and strength. Therefore, the different coating technologies like screen printing and vacuum slip casting were used for cell manufacturing. The optimization of the different coating steps during cell manufacturing led to high performance SOFCs with a 10% higher power output compared to the Julich state-of-the-art SOFC. Additional experiments verified the workability of the novel tape cast substrates for the manufacturing of near-net-shape SOFC. Finally, the novel cell types based on tape cast substrates were assembled to stacks with up to ten repeating units. Stack tests showed identical performance and degradation compared to stacks containing state-of-the-art SOFCs. Thus, the complete lifetime circle of a SOFC starting from powder preparation to stack assembly has been

  2. A process for electrodeposition of layers of niobium, vanadium, molybdenum or tungsten, or of their alloys

    International Nuclear Information System (INIS)

    Diepers, H.; Schmidt, O.

    1976-01-01

    An improvement is proposed for the process for electrodeposition of layers of niobium, vanadium, molybdenum or tungsten or of their alloys from molten-salt electrolytes (fluorid melts) which is to increase the quality of layers in order to obtain regular thickness and smooth surfaces. According to the invention, a pre-separation is executed on an auxiliary cathode before the (preheated) cathode is immersed. The cathode is only charged for separation after the adjustment of a constant anode potential. It is an advantage that the auxiliary cathode is mechanically and electrically connected with the cathode. As an electrolyte, a mixture of niobium fluorides and a eustetic mixture of potassium fluorides, sodium fluorides and lithium fluorides are particularly suitable for the electrodeposition of niobium. (UWI) [de

  3. Niobium LEP 2 accelerating cavities

    CERN Multimedia

    An accelerating cavity from LEP. This could be cut open to show the layer of niobium on the inside. Operating at 4.2 degrees above absolute zero, the niobium is superconducting and carries an accelerating field of 6 million volts per metre with negligible losses. Each cavity has a surface of 6 m2. The niobium layer is only 1.2 microns thick, ten times thinner than a hair. Such a large area had never been coated to such a high accuracy. A speck of dust could ruin the performance of the whole cavity so the work had to be done in an extremely clean environment. These challenging requirements pushed European industry to new achievements. 256 of these cavities were used in an upgrade of the LEP accelerator to double the energy of the particle beams.

  4. Micromechanical Modeling of Solid Oxide Fuel Cell Anode Supports based on Three-dimensional Reconstructions

    DEFF Research Database (Denmark)

    Kwok, Kawai; Jørgensen, Peter Stanley; Frandsen, Henrik Lund

    2014-01-01

    The efficiency and lifetime of solid oxide fuel cells (SOFCs) is compromised by mechanical failure of cells in the system. Improving the mechanical reliability is a major step in ensuring feasibility of the technology. To quantify the stress in a cell, mechanical properties of the different layers...... need to be accurately known. Since the mechanical properties are heavily dependent on the microstructures of the materials, it is highly advantageous to understand the impact of microstructures and to be able to determine accurate effective mechanical properties for cell or stack scale analyses...

  5. Fabrication and tests of anode supported solid oxide fuel cell; Fabricacao e testes de celula a combustivel de oxido solido suportada no anodo

    Energy Technology Data Exchange (ETDEWEB)

    Florio, D.Z. de [UNESP, Araraquara, SP (Brazil)], e-mail: dzflorio@ipen.br; Fonseca, F.C.; Franca, Y.V.; Muccillo, E.N.S.; Muccillo, R. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Berton, M.A.C.; Garcia, C.M. [LACTEC - Instituto de Tecnologia para o Desenvolvimento, Curitiba, PR (Brazil)

    2006-07-01

    A laboratory setup was designed and put into operation for the development of solid oxide fuel cells (SOFCs). Ceramic single cells were fabricated by low-cost methods, and emphasis was given to the use of ready available raw materials. The whole project consisted of the preparation of the component materials - anode, cathode, and electrolyte - and the buildup of a hydrogen leaking-free sample chamber with platinum leads and current collectors for measuring the electrochemical properties of single SOFCs. Anode-supported single SOFCs of the type (ZrO{sub 2}:Y{sub 2}O{sub 3} + NiO) anode / (ZrO{sub 2}:Y{sub 2}O{sub 3}) electrolyte / (La{sub 0.65}Sr{sub 0.35}MnO{sub 3} + ZrO{sub 2}:Y{sub 2}O{sub 3}) cathode have been prepared and tested at 700 deg C and 800 deg C after in situ H{sub 2} anode reduction. The main results show that the slurry coating method resulted in single-cells with good reproducibility and reasonable performance, suggesting that this method can be considered for fabrication of SOFCs. (author)

  6. Electrochemical performance and stability of Ni1-xCox-based cermet anode for direct methane-fuelled solid oxide fuel cells

    Directory of Open Access Journals (Sweden)

    Nicharee Wongsawatgul

    2017-01-01

    Full Text Available Carbon deposition on Ni-based anode is well-known as a major barrier for the practical use and commercialization of hydrocarbon-fuelled solid oxide fuel cells (SOFCs. In this work, Co alloying in Ni-YSZ was studied as an alternative anode material for using CH4 as a fuel. The Ni-YSZ and Ni-Co alloyed-YSZ were prepared by the traditional impregnation method without further mixing processes. After sintering and reduction in H2 atmosphere, the introduced Co can completely dissolved into the Ni lattice and changed the morphology with an increase in the Ni-YSZ grain size and showed a better uniform microstructure. The Co alloying also enhanced the electrochemical performance under CH4 fuel by reducing the resistance and anodic overvoltage. Moreover, the Co addition enhanced the stability of the cell with CH4 a constant load current of 80 mA for 60 h. This performance related to the carbon deposition on the anode surface. The Co alloying showed a high efficiency to suppress the carbon deposition and improved the electrochemical performance of an SOFC cell operating under CH4 fuel.

  7. Unique Cobalt Sulfide/Reduced Graphene Oxide Composite as an Anode for Sodium-Ion Batteries with Superior Rate Capability and Long Cycling Stability.

    Science.gov (United States)

    Peng, Shengjie; Han, Xiaopeng; Li, Linlin; Zhu, Zhiqiang; Cheng, Fangyi; Srinivansan, Madhavi; Adams, Stefan; Ramakrishna, Seeram

    2016-03-09

    Exploitation of high-performance anode materials is essential but challenging to the development of sodium-ion batteries (SIBs). Among all proposed anode materials for SIBs, sulfides have been proved promising candidates due to their unique chemical and physical properties. In this work, a facile solvothermal method to in situ decorate cobalt sulfide (CoS) nanoplates on reduced graphene oxide (rGO) to build CoS@rGO composite is described. When evaluated as anode for SIBs, an impressive high specific capacity (540 mAh g(-1) at 1 A g(-1) ), excellent rate capability (636 mAh g(-1) at 0.1 A g(-1) and 306 mAh g(-1) at 10 A g(-1)), and extraordinarily cycle stability (420 mAh g(-1) at 1 A g(-1) after 1000 cycles) have been demonstrated by CoS@rGO composite for sodium storage. The synergetic effect between the CoS nanoplates and rGO matrix contributes to the enhanced electrochemical performance of the hybrid composite. The results provide a facile approach to fabricate promising anode materials for high-performance SIBs. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. 10-fold enhancement in light-driven water splitting using niobium oxynitride microcone array films

    KAUST Repository

    Shaheen, Basamat

    2016-03-26

    We demonstrate, for the first time, the synthesis of highly ordered niobium oxynitride microcones as an attractive class of materials for visible-light-driven water splitting. As revealed by the ultraviolet photoelectron spectroscopy (UPS), photoelectrochemical and transient photocurrent measurements, the microcones showed enhanced performance (~1000% compared to mesoporous niobium oxide) as photoanodes for water splitting with remarkable stability and visible light activity. © 2016 Elsevier B.V. All rights reserved.

  9. Properties of Stimulated Emission of the PM567 Dye in Pores of Anodized Aluminum Oxide

    Science.gov (United States)

    Aimukhanov, A. K.; Ibrayev, N. Kh.; Esimbek, A. M.

    2018-02-01

    Properties of the stimulated emission of the PM567 dye in porous aluminum oxide are investigated. It is established that when PM567 molecules are doped into aluminum oxide pores, a small part of dye molecules forms aggregates. The quantum yield of fluorescence of PM567 in Al2O3 is V f = 0.85. The stimulated emission of PM567 in the Al2O3 film is observed in the short-wavelength maximum of the fluorescence band. The threshold of the stimulated emission is 2 MW/cm2. The kinetics of the decay of stimulated emission is measured. It is demonstrated that low-Q lasing of the stimulated emission of PM567 in the film with Q ≥ 1·102 is caused by the fact that the geometry of rays in pores does not correspond to that of complete internal reflection, and hence, the radiative losses increase. The efficiency of lasing of PM567 in Al2O3 is 0.3%.

  10. Photonic Crystals with Large Complete Bandgap Composed of an Approximately Ordered Array of Laurel-Crown-Like Structures Fabricated by Employing Anodic Aluminum Oxide Template

    Science.gov (United States)

    Chan, Der-Sheng; Chau, Yuan-Fong

    2013-01-01

    An innovative fabrication processes of a photonic crystal composed of an approximately ordered array of laurel-crown-like structures by employing an anodic aluminum oxide (AAO) template is presented. We found that the intensity of the electric field is affected by the microstructure and surface morphology of aluminum foil after etching the scalloped barrier oxide layer (BOL). In addition, the electric current is strongly dependent on the electric field distribution in the scalloped BOL at the pore bottoms. By using a different step potential (DSP) of 30-60 V in series, the proposed photonic crystal is fabricated and possesses a large complete photonic bandgap.

  11. Ultrasound-assisted anodization of aluminum in oxalic acid

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Rong; Jiang Kaiming [Department of Physics, Shanghai Maritime University, 1550 Pudong Avenue, Shanghai 200135 (China); Zhu Yun [State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, 865 Changning Road, Shanghai 200050 (China); Qi Haiyang [Department of Physics, Shanghai Maritime University, 1550 Pudong Avenue, Shanghai 200135 (China); Ding Guqiao, E-mail: gqding@mail.sim.ac.cn [State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology, Chinese Academy of Sciences, 865 Changning Road, Shanghai 200050 (China)

    2011-10-15

    Porous anodic alumina is an important nanoscale template for fabrication of various nanostructures. We report a new ultrasound-assisted anodization process in oxalic acid. Under the continuous irradiation of ultrasound, the one-step-anodized sample has a smooth and clean surface, and two-step-anodization brings ordered porous anodic alumina with higher growth rate of 52 {mu}m/h. The ultrasound applied during the anodization can clean the surface and enhance the nanopore growth since it can accelerate the oxide dissolving on the electrolyte/oxide interface. The ultrasound-assisted anodization may be utilized for other anodizations.

  12. Spray coated indium-tin-oxide-free organic photodiodes with PEDOT:PSS anodes

    Directory of Open Access Journals (Sweden)

    Morten Schmidt

    2014-10-01

    Full Text Available In this paper we report on Indium Tin Oxide (ITO-free spray coated organic photodiodes with an active layer consisting of a poly(3-hexylthiophen (P3HT and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM blend and patterned poly(3,4-ethylenedioxythiophene:poly(styrenesulfonate (PEDOT:PSS electrodes. External quantum efficiency and current voltage characteristics under illuminated and dark conditions as well as cut-off frequencies for devices with varying active and hole conducting layer thicknesses were measured in order to characterize the fabricated devices. 60% quantum efficiency as well as nearly four orders of magnitude on-off ratios have been achieved. Those values are comparable with standard ITO devices.

  13. Effect of inlet fuel type on the degradation of Ni/YSZ anode of solid oxide fuel cell by carbon deposition

    Directory of Open Access Journals (Sweden)

    Suttichai Assabumrungrat

    2006-11-01

    Full Text Available According to the high operating temperature of Solid Oxide Fuel Cell (SOFC (700-1100ºC, it is known that some hydrocarbon fuels can be directly used as inlet fuel instead of hydrogen by feeding straight to the anode. This operation is called a direct internal reforming SOFC (DIR-SOFC. However, the major difficulty of this operation is the possible degradation of anode by the carbon deposition, as the carbon species are easily formed. In the present work, the effect of inlet fuel (i.e. H2, synthesis gas (H2+CO, CH4, CH4+H2O, CH3OH+H2O, and C2H5OH+H2O on the degradation of nickel cermet (Ni/YSZ, which is the most common anode material of SOFC, was studied.It was found from the work that hydrogen and synthesis gas (CO+H2 are proper to be used as direct inlet fuels for DIR-SOFC with Ni/YSZ anode, since the carbon formation on Ni/YSZ occurred in the small quantity. The mixture of methane and steam (CH4+H2O can also be used as the inlet feed, but the H2O/CH4 ratio plays an important role. In contrast, pure methane (CH4, methanol with steam (CH3OH+H2O and ethanol with steam (C2H5OH+H2O are not suitable for using as direct inlet fuel for DIR-SOFC with Ni/YSZ anode even the higher H2O/CH3OH and H2O/C2H5OH ratios were applied.

  14. Electrochemical improvement of low-temperature petroleum cokes by chemical oxidation with H2O2 for their use as anodes in lithium ion batteries

    International Nuclear Information System (INIS)

    Concheso, A.; Santamaria, R.; Menendez, R.; Jimenez-Mateos, J.M.; Alcantara, R.; Lavela, P.; Tirado, J.L.

    2006-01-01

    The electrochemical performance of non-graphitized petroleum cokes has been improved by mild oxidation using hydrogen peroxide, a procedure used for the first time in these materials. For this purpose, various carbonisation temperatures and H 2 O 2 treatments were tested. For low sulfur content cokes, the aqueous oxidative treatment significantly increases the capacity values above 372 mAh/g during the first cycles. In contrast, cokes with a sulfur content of ca. 5%, did not shown a real improvement. The former results have been interpreted in terms of an effective oxidation of the particles surface, which removes unorganized carbon, where lithium can be irreversibly trapped. Moreover, a stable and less resistive passivating layer grows during the first discharge of lithium, as revealed by impedance spectroscopy. Therefore, chemical procedures, as mild oxidation, open an interesting field of research for the improvement of disordered carbons as anode materials in lithium ion batteries

  15. Control of indium tin oxide anode work function modified using Langmuir-Blodgett monolayer for high-efficiency organic photovoltaics

    Directory of Open Access Journals (Sweden)

    Yuya Yokokura

    2017-08-01

    Full Text Available The use of Langmuir-Blodgett (LB monolayers to modify the indium tin oxide (ITO work function and thus improve the performance of zinc phthalocyanine (ZnPc/fullerene (C60-based and boron subphthalocyanine chloride (SubPc/C60-based small molecule organic photovoltaic devices (OPVs was examined. In general, LB precursor compounds contain one or more long alkyl chain substituents that can act as spacers to prevent electrical contact with adjoining electrode surfaces. As one example of such a compound, arachidic acid (CH3(CH218COOH was inserted in the forms of one-layer, three-layer or five-layer LB films between the anode ITO layer and the p-type layer in ZnPc-C60-based OPVs to investigate the effects of the long alkyl chain group when it acts as an electrically insulating spacer. The short-circuit current density (Jsc values of the OPVs with the three- and five-layer inserts (1.78 mA·cm−2 and 0.61 mA·cm−2, respectively were reduced dramatically, whereas the Jsc value for the OPV with the single-layer insertion (2.88 mA·cm−2 was comparable to that of the OPV without any insert (3.14 mA·cm-2. The ITO work function was shifted positively by LB deposition of a surfactant compound, C9F19C2H4-O-C2H4-COOH (PFECA, which contained a fluorinated head group. This positive effect was maintained even after formation of an upper p-type organic layer. The Jsc and open-circuit voltage (Voc of the SubPc-C60-based OPV with the LB-modified ITO layers were effectively enhanced. As a result, a 42% increase in device efficiency was achieved.

  16. H2O2 assisted room temperature oxidation of Ti2C MXene for Li-ion battery anodes

    KAUST Repository

    Ahmed, Bilal

    2016-03-08

    Herein we demonstrate that a prominent member of the MXene family, Ti2C, undergoes surface oxidation at room temperature when treated with hydrogen peroxide (H2O2). The H2O2 treatment results in opening up of MXene sheets and formation of TiO2 nanocrystals on their surface, which is evidenced by the high surface area of H2O2 treated MXene and X-ray diffraction (XRD) analysis. We show that the reaction time and the amount of hydrogen peroxide used are the limiting factors, which determine the morphology and composition of the final product. Furthermore, it is shown that the performance of H2O2 treated MXene as an anode material in Li ion batteries (LIBs) was significantly improved as compared to as-prepared MXenes. For instance, after 50 charge/discharge cycles, specific discharge capacities of 389 mA h g−1, 337 mA h g−1 and 297 mA h g−1 were obtained for H2O2 treated MXene at current densities of 100 mA g−1, 500 mA g−1 and 1000 mA g−1, respectively. In addition, when tested at a very high current density, such as 5000 mA g−1, the H2O2 treated MXene showed a specific capacity of 150 mA h g−1 and excellent rate capability. These results clearly demonstrate that H2O2 treatment of Ti2C MXene improves MXene properties in energy storage applications, such as Li ion batteries or capacitors.

  17. Manipulation of stored charge in anodic aluminium oxide/SiO2 dielectric stacks by the use of pulsed anodisation

    International Nuclear Information System (INIS)

    Lu, Zhong; Ouyang, Zi; Grant, Nicholas; Wan, Yimao; Yan, Di; Lennon, Alison

    2016-01-01

    Graphical abstract: - Highlights: • Pulse anodisation was used to grow AAO layers with controllable stored charge. • Stored charge density ranging from −5.2 × 10 11 to 2.5 × 10 12 q/cm 2 was demonstrated. • Enhancement in surface passivation was demonstrated with charge management. • Annealing significantly reduces the positive stored charge and the interface defect. - Abstract: A method of fabricating anodic aluminium oxide (AAO) with the capability of manipulating its stored charge is reported. This method involves the use of a pulsed current source to anodise aluminium layers instead of the typically used constant current/voltage source, with the test structures experiencing positive and negative cycles periodically. By tuning the positive cycle percentage, it is demonstrated that the effective stored charge density can be manipulated in a range from −5.2 × 10 11 to 2.5 × 10 12 q/cm 2 when the AAO is formed over a 12 nm SiO 2 layer. An investigation of the stored charge distribution in the dielectric stacks indicates a positive fixed charge at the SiO 2 /Si interface, a negative fixed charge at the AAO/SiO 2 interface and a positive bulk charge within the AAO layer. The effective stored charge density and interface states were found to be affected by annealing conditions and it is suggested that oxygen annealing can reduce the bulk positive charge while post-metallisation anneal is most effective in reducing silicon interface defects. Charge manipulation using pulsed anodisation is shown to reduce carrier recombination on boron-diffused silicon surfaces highlighting the potential of the process to be used to tune the electrical properties of dielectric layers so that they can reduce surface recombination on silicon surfaces having different dopant polarity and concentrations.

  18. Control of indium tin oxide anode work function modified using Langmuir-Blodgett monolayer for high-efficiency organic photovoltaics

    Science.gov (United States)

    Yokokura, Yuya; Dogase, Tomomichi; Shinbo, Tatsuki; Nakayashiki, Yuya; Takagi, Yusuke; Ueda, Kazuyoshi; Sarangerel, Khayankhyarvaa; Delgertsetseg, Byambasuren; Ganzorig, Chimed; Sakomura, Masaru

    2017-08-01

    The use of Langmuir-Blodgett (LB) monolayers to modify the indium tin oxide (ITO) work function and thus improve the performance of zinc phthalocyanine (ZnPc)/fullerene (C60)-based and boron subphthalocyanine chloride (SubPc)/C60-based small molecule organic photovoltaic devices (OPVs) was examined. In general, LB precursor compounds contain one or more long alkyl chain substituents that can act as spacers to prevent electrical contact with adjoining electrode surfaces. As one example of such a compound, arachidic acid (CH3(CH2)18COOH) was inserted in the forms of one-layer, three-layer or five-layer LB films between the anode ITO layer and the p-type layer in ZnPc-C60-based OPVs to investigate the effects of the long alkyl chain group when it acts as an electrically insulating spacer. The short-circuit current density (Jsc) values of the OPVs with the three- and five-layer inserts (1.78 mA.cm-2 and 0.61 mA.cm-2, respectively) were reduced dramatically, whereas the Jsc value for the OPV with the single-layer insertion (2.88 mA.cm-2) was comparable to that of the OPV without any insert (3.14 mA.cm-2). The ITO work function was shifted positively by LB deposition of a surfactant compound, C9F19C2H4-O-C2H4-COOH (PFECA), which contained a fluorinated head group. This positive effect was maintained even after formation of an upper p-type organic layer. The Jsc and open-circuit voltage (Voc) of the SubPc-C60-based OPV with the LB-modified ITO layers were effectively enhanced. As a result, a 42% increase in device efficiency was achieved.

  19. Flame-Oxidized Stainless-Steel Anode as a Probe in Bioelectrochemical System-Based Biosensors to Monitor the Biochemical Oxygen Demand of Wastewater.

    Science.gov (United States)

    Liang, Qiaochu; Yamashita, Takahiro; Yamamoto-Ikemoto, Ryoko; Yokoyama, Hiroshi

    2018-02-16

    Biochemical oxygen demand (BOD) is a widely used index of water quality in wastewater treatment; however, conventional measurement methods are time-consuming. In this study, we analyzed a novel flame-oxidized stainless steel anode (FO-SSA) for use as the probe of bioelectrochemical system (BES)-based biosensors to monitor the BOD of treated swine wastewater. A thinner biofilm formed on the FO-SSA compared with that on a common carbon-cloth anode (CCA). The FO-SSA was superior to the CCA in terms of rapid sensing; the response time of the FO-SSA to obtain the value of R2 > 0.8 was 1 h, whereas the CCA required 4 h. These results indicate that the FO-SSA offers better performance than traditional CCAs in BES biosensors and can be used to improve biomonitoring of wastewater.

  20. Flame-Oxidized Stainless-Steel Anode as a Probe in Bioelectrochemical System-Based Biosensors to Monitor the Biochemical Oxygen Demand of Wastewater

    Directory of Open Access Journals (Sweden)

    Qiaochu Liang

    2018-02-01

    Full Text Available Biochemical oxygen demand (BOD is a widely used index of water quality in wastewater treatment; however, conventional measurement methods are time-consuming. In this study, we analyzed a novel flame-oxidized stainless steel anode (FO-SSA for use as the probe of bioelectrochemical system (BES-based biosensors to monitor the BOD of treated swine wastewater. A thinner biofilm formed on the FO-SSA compared with that on a common carbon-cloth anode (CCA. The FO-SSA was superior to the CCA in terms of rapid sensing; the response time of the FO-SSA to obtain the value of R2 > 0.8 was 1 h, whereas the CCA required 4 h. These results indicate that the FO-SSA offers better performance than traditional CCAs in BES biosensors and can be used to improve biomonitoring of wastewater.

  1. Evaluation of niobium as candidate electrode material for dc high voltage photoelectron guns

    Directory of Open Access Journals (Sweden)

    M. BastaniNejad

    2012-08-01

    Full Text Available The field emission characteristics of niobium electrodes were compared to those of stainless steel electrodes using a DC high voltage field emission test apparatus. A total of eight electrodes were evaluated: two 304 stainless steel electrodes polished to mirrorlike finish with diamond grit and six niobium electrodes (two single-crystal, two large-grain, and two fine-grain that were chemically polished using a buffered-chemical acid solution. Upon the first application of high voltage, the best large-grain and single-crystal niobium electrodes performed better than the best stainless steel electrodes, exhibiting less field emission at comparable voltage and field strength. In all cases, field emission from electrodes (stainless steel and/or niobium could be significantly reduced and sometimes completely eliminated, by introducing krypton gas into the vacuum chamber while the electrode was biased at high voltage. Of all the electrodes tested, a large-grain niobium electrode performed the best, exhibiting no measurable field emission (<10  pA at 225 kV with 20 mm cathode/anode gap, corresponding to a field strength of 18.7  MV/m.

  2. Deposition efficiency in the preparation of ozone-producing nickel and antimony doped tin oxide anodes

    Directory of Open Access Journals (Sweden)

    Staffan Sandin

    2017-03-01

    Full Text Available The influence of precursor salts in the synthesis of nickel and antimony doped tin oxide (NATO electrodes using thermal decomposition from dissolved chloride salts was investigated. The salts investigated were SnCl4×5H2O, SnCl2×2H2O, SbCl3 and NiCl2×6H2O. It was shown that the use of SnCl4×5H20 in the preparation process leads to a tin loss of more than 85 %. The loss of Sb can be as high as 90 % while no indications of Ni loss was observed. As a consequence, the concentration of Ni in the NATO coating will be much higher than in the precursor solution. This high and uncontrolled loss of precursors during the preparation process will lead to an unpredictable composition in the NATO coating and will have negative economic and environmental effects. It was found that using SnCl2×2H20 instead of SnCl4×5H2O can reduce the tin loss to less than 50 %. This tin loss occurs at higher temperatures than when using SnCl4×5H2O where the tin loss occurs from 56 – 147 °C causing the composition to change both during the drying (80 – 110 °C and calcination (460 -550 °C steps of the preparation process. Electrodes coated with NATO based on the two different tin salts were investigated for morphology, composition, structure, and ozone electrocatalytic properties.

  3. Paired removal of color and COD from textile dyeing wastewater by simultaneous anodic and indirect cathodic oxidation

    International Nuclear Information System (INIS)

    Wang, Chih-Ta; Chou, Wei-Lung; Kuo, Yi-Ming; Chang, Fu-Lin

    2009-01-01

    The anodic and indirect cathodic removals of color and COD from real dyeing wastewater were investigated simultaneously using a stacked Pt/Ti screen anode and a graphite packed-bed cathode in a divided flow-by electrochemical reactor. The anodically generated hypochlorite and cathodically generated hydrogen peroxide were the main species used to remove color and COD in the wastewater. Various experimental operating factors that can affect the removal efficiency were investigated, including the applied current density, the amount of NaCl added, the solution pH in alkaline ranges and the temperature. The color and COD removal efficiencies in the anodic chamber were much higher than those in the cathodic chamber. The overall (anodic plus cathodic) removal efficiencies increased with the applied current density, the amount of NaCl added and the temperature. In contrast, increasing the solution pH decreased the overall removal efficiency. The anodic and cathodic current efficiencies at 20 mA/cm 2 were 63.50% and 19.57%, respectively. In this work the total treatment cost for removing 1 g COD was US $0.643 when an air cylinder was used.

  4. High-efficiency, nickel-ceramic composite anode current collector for micro-tubular solid oxide fuel cells

    Science.gov (United States)

    Li, Tao; Wu, Zhentao; Li, K.

    2015-04-01

    High manufacturing cost and low-efficient current collection have been the two major bottlenecks that prevent micro-tubular SOFCs from large-scale application. In this work, a new nickel-based composite anode current collector has been developed for anode-supported MT-SOFC, addressing reduced cost, manufacturability and current collection efficiencies. Triple-layer hollow fibers have been successfully fabricated via a phase inversion-assisted co-extrusion process, during which a thin nickel-based inner layer was uniformly coated throughout the interior anode surface for improved adhesion with superior process economy. 10 wt.% CGO was added into the inner layer to prevent the excessive shrinkage of pure NiO, thus helping to achieve the co-sintering process. The electrochemical performance tests illustrate that samples with the thinnest anodic current collector (15% of the anode thickness) displayed the highest power density (1.07 W cm-2). The impedance analysis and theoretical calculations suggest that inserting the anodic current collector could dramatically reduce the percentage of contact loss down to 6-10 % of the total ohmic loss (compared to 70% as reported in literatures), which proves the high efficiencies of new current collector design. Moreover, the superior manufacturability and process economy suggest this composite current collector suitable for mass-scale production.

  5. Process for anodizing aluminum foil

    International Nuclear Information System (INIS)

    Ball, J.A.; Scott, J.W.

    1984-01-01

    In an integrated process for the anodization of aluminum foil for electrolytic capacitors including the formation of a hydrous oxide layer on the foil prior to anodization and stabilization of the foil in alkaline borax baths during anodization, the foil is electrochemically anodized in an aqueous solution of boric acid and 2 to 50 ppm phosphate having a pH of 4.0 to 6.0. The anodization is interrupted for stabilization by passing the foil through a bath containing the borax solution having a pH of 8.5 to 9.5 and a temperature above 80 0 C. and then reanodizing the foil. The process is useful in anodizing foil to a voltage of up to 760 V

  6. Tantalum(V) impurity extraction by octanol from niobium(V) fluoride solutions

    International Nuclear Information System (INIS)

    Majorov, V.G.; Nikolaev, A.I.; Kopkov, V.K.

    2002-01-01

    The conditions of the niobium and tantalum extraction separation by octanol in the fluoride solutions, depending on the metals and free hydrofluoric acid concentration as well as on the organic and water phases voluminous relation, are studied for the purpose of developing the technology of niobium deep purification from the tantalum impurities. The technological scheme of the niobium solutions(V) extraction purification from the tantalum impurities(V), which provides for obtaining the niobium oxide(V), containing less than 0.005 mass % Ta 2 O 5 , is proposed on the basis of the established optimal separation conditions. The possibility of using the developed technology by the pyrochlore reprocessing is indicated [ru

  7. Negligible degradation upon in situ voltage cycling of a PEMFC using an electrospun niobium-doped tin oxide supported Pt cathode.

    Science.gov (United States)

    Savych, Iuliia; Subianto, Surya; Nabil, Yannick; Cavaliere, Sara; Jones, Deborah; Rozière, Jacques

    2015-07-14

    Novel platinum-catalysed, corrosion-resistant, loose-tube-structured electrocatalysts for proton exchange membrane fuel cells have been obtained using single-needle electrospinning associated with a microwave-assisted polyol method. Monodisperse platinum particles supported on Nb-SnO2 demonstrated higher electrochemical stability than conventional Pt/C electrodes during ex situ potential cycling and comparable activity in the oxygen reduction reaction. In situ fuel cell operation under accelerated stress test conditions of a membrane electrode assembly elaborated using a Pt/C anode and Pt/Nb-SnO2 cathode confirmed that the voltage loss is significantly lower for the novel cathode than for an MEA prepared using conventional Pt/C supported electrocatalysts. Furthermore, the Nb-SnO2 stabilised the supported platinum nanoparticles against dissolution, migration and reprecipitation in the membrane. Pt/Nb-SnO2 loose-tubes constitute a mitigation strategy for two known degradation mechanisms in PEMFC: corrosion of the carbon support at the cathode, and dissolution of Pt at high cell voltages.

  8. Three-dimensional sandwich-structured NiMn2O4@reduced graphene oxide nanocomposites for highly reversible Li-ion battery anodes

    Science.gov (United States)

    Huang, Jiarui; Wang, Wei; Lin, Xirong; Gu, Cuiping; Liu, Jinyun

    2018-02-01

    A sandwich-structured NiMn2O4@reduced graphene oxide (NiMn2O4@rGO) nanocomposite consisting of ultrathin NiMn2O4 sheets uniformly anchored on both sides of a three-dimensional (3D) porous rGO is presented. The NiMn2O4@rGO nanocomposites prepared through a dipping process combining with a hydrothermal method show a good electrochemical performance including a high reversible capability of 1384 mAh g-1 at 1000 mA g-1 over 1620 cycles, and an superior rate performance. Thus, a full cell consisting of a commercial LiCoO2 cathode and the NiMn2O4@rGO anode delivers a stable capacity of about 1046 mAh g-1 (anode basis) after cycling at 50 mA g-1 for 60 times. It is demonstrated that the 3D porous composite structure accommodates the volume change during the Li+ insertion/extraction process and facilitates the rapid transport of ions and electrons. The high performance would enable the presented NiMn2O4@rGO nanocomposite a promising anode candidate for practical applications in Li-ion batteries.

  9. Homogeneous growth of TiO2-based nanotubes on nitrogen-doped reduced graphene oxide and its enhanced performance as a Li-ion battery anode.

    Science.gov (United States)

    Mehraeen, Shayan; Taşdemir, Adnan; Gürsel, Selmiye Alkan; Yürüm, Alp

    2018-06-22

    The pursuit of a promising replacement candidate for graphite as a Li-ion battery anode, which can satisfy both engineering criteria and market needs has been the target of researchers for more than two decades. In this work, we have investigated the synergistic effect of nitrogen-doped reduced graphene oxide (NrGO) and nanotubular TiO 2 to achieve high rate capabilities with high discharge capacities through a simple, one-step and scalable method. First, nanotubes of hydrogen titanate were hydrothermally grown on the surface of NrGO sheets, and then converted to a mixed phase of TiO 2 -B and anatase (TB) by thermal annealing. Specific surface area, thermal gravimetric, structural and morphological characterizations were performed on the synthesized product. Electrochemical properties were investigated by cyclic voltammetry and cyclic charge/discharge tests. The prepared anode showed high discharge capacity of 150 mAh g -1 at 1 C current rate after 50 cycles. The promising capacity of synthesized NrGO-TB was attributed to the unique and novel microstructure of NrGO-TB in which long nanotubes of TiO 2 have been grown on the surface of NrGO sheets. Such architecture synergistically reduces the solid-state diffusion distance of Li + and increases the electronic conductivity of the anode.

  10. Multi-length scale tomography for the determination and optimization of the effective microstructural properties in novel hierarchical solid oxide fuel cell anodes

    Science.gov (United States)

    Lu, Xuekun; Taiwo, Oluwadamilola O.; Bertei, Antonio; Li, Tao; Li, Kang; Brett, Dan J. L.; Shearing, Paul R.

    2017-11-01

    Effective microstructural properties are critical in determining the electrochemical performance of solid oxide fuel cells (SOFCs), particularly when operating at high current densities. A novel tubular SOFC anode with a hierarchical microstructure, composed of self-organized micro-channels and sponge-like regions, has been fabricated by a phase inversion technique to mitigate concentration losses. However, since pore sizes span over two orders of magnitude, the determination of the effective transport parameters using image-based techniques remains challenging. Pioneering steps are made in this study to characterize and optimize the microstructure by coupling multi-length scale 3D tomography and modeling. The results conclusively show that embedding finger-like micro-channels into the tubular anode can improve the mass transport by 250% and the permeability by 2-3 orders of magnitude. Our parametric study shows that increasing the porosity in the spongy layer beyond 10% enhances the effective transport parameters of the spongy layer at an exponential rate, but linearly for the full anode. For the first time, local and global mass transport properties are correlated to the microstructure, which is of wide interest for rationalizing the design optimization of SOFC electrodes and more generally for hierarchical materials in batteries and membranes.

  11. Rate and Selectivity Control in Thioether and Alkene Oxidation with H 2 O 2 over Phosphonate-Modified Niobium(V)-Silica Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Thornburg, Nicholas E.; Notestein, Justin M. (NWU)

    2017-09-05

    Supported metal oxide catalysts are versatile materials for liquid-phase oxidations, including alkene epoxidation and thioether sulfoxidation with H2O2. Periodic trends in H2O2 activation was recently demonstrated for alkene epoxidation, highlighting Nb-SiO2 as a more active and selective catalyst than Ti-SiO2. Three representative catalysts are studied consisting of NbV, TiIV, and ZrIV on silica, each made through a molecular precursor approach that yields highly dispersed oxide sites, for thioanisole oxidation by H2O2. Initial rates trend Nb>Ti>>Zr, as for epoxidation, and Nb outperforms Ti for a number of other thioethers. In contrast, selectivity to sulfoxide vs. sulfone trends Ti>Nb>>Zr at all conversions. Modifying the Nb-SiO2 catalyst with phenylphosphonic acid does not completely remove sulfoxidation reactivity, as it did for photooxidation and epoxidation, and results in an unusual material active for sulfoxidation but neither epoxidation nor overoxidation to the sulfone.

  12. Bilayer electrolyte-anode for solid oxide fuel cell; Obtencao de bicamadas eletrolito-anodo para pilhas a combustivel de oxido solido

    Energy Technology Data Exchange (ETDEWEB)

    Crochemore, G.B.; Marcomini, R.F.; Souza, D.P.F. de [Universidade Federal de Sao Carlos (GEMM/UFSCAR), Sao Carlos, SP (Brazil). Programa de Pos Graduacao em Ciencia e Engenharia de Materiais], Email: dulcina@ufscar.br; Rabelo, A.A. [Universidade Federal do Para (UFPA), Belem, PA (Brazil). Fac. de Engenharia de Materiais

    2010-07-01

    Solid oxide fuel cell is a high efficient device hence it plays a very important role in the hydrogen economy. However, the cell operation temperature must be lower than 800 deg C, what is attainable for thin Yttria stabilized zirconia (YSZ) electrolytes. The tape casting process is the most used technique because it allows a very fine tuning of the tape thickness. In this work it were investigated the processing conditions for obtaining electrolyte-anode (YSZ/ YSZ-NiO) bilayers with no lamination after the sintering process. (author)

  13. Formation of double ring patterns on Co2MnSi Heusler alloy thin film by anodic oxidation under scanning probe microscope

    International Nuclear Information System (INIS)

    Toutam, Vijaykumar; Singh, Sandeep; Pandey, Himanshu; Budhani, R. C.

    2013-01-01

    Double ring formation on Co 2 MnSi (CMS) films is observed at electrical breakdown voltage during local anodic oxidation (LAO) using atomic force microscope (AFM). Corona effect and segregation of cobalt in the vicinity of the rings is studied using magnetic force microscopy and energy dispersive spectroscopy. Double ring formation is attributed to the interaction of ablated material with the induced magnetic field during LAO. Steepness of forward bias transport characteristics from the unperturbed region of the CMS film suggest a non equilibrium spin contribution. Such mesoscopic textures in magnetic films by AFM tip can be potentially used for memory storage applications.

  14. Formation of double ring patterns on Co2MnSi Heusler alloy thin film by anodic oxidation under scanning probe microscope

    Directory of Open Access Journals (Sweden)

    Vijaykumar Toutam

    2013-02-01

    Full Text Available Double ring formation on Co2MnSi (CMS films is observed at electrical breakdown voltage during local anodic oxidation (LAO using atomic force microscope (AFM. Corona effect and segregation of cobalt in the vicinity of the rings is studied using magnetic force microscopy and energy dispersive spectroscopy. Double ring formation is attributed to the interaction of ablated material with the induced magnetic field during LAO. Steepness of forward bias transport characteristics from the unperturbed region of the CMS film suggest a non equilibrium spin contribution. Such mesoscopic textures in magnetic films by AFM tip can be potentially used for memory storage applications.

  15. Formation of double ring patterns on Co2MnSi Heusler alloy thin film by anodic oxidation under scanning probe microscope

    Science.gov (United States)

    Toutam, Vijaykumar; Pandey, Himanshu; Singh, Sandeep; Budhani, R. C.

    2013-02-01

    Double ring formation on Co2MnSi (CMS) films is observed at electrical breakdown voltage during local anodic oxidation (LAO) using atomic force microscope (AFM). Corona effect and segregation of cobalt in the vicinity of the rings is studied using magnetic force microscopy and energy dispersive spectroscopy. Double ring formation is attributed to the interaction of ablated material with the induced magnetic field during LAO. Steepness of forward bias transport characteristics from the unperturbed region of the CMS film suggest a non equilibrium spin contribution. Such mesoscopic textures in magnetic films by AFM tip can be potentially used for memory storage applications.

  16. Formation of double ring patterns on Co{sub 2}MnSi Heusler alloy thin film by anodic oxidation under scanning probe microscope

    Energy Technology Data Exchange (ETDEWEB)

    Toutam, Vijaykumar; Singh, Sandeep [National Physical Laboratory, New Delhi - 110012 (India); Pandey, Himanshu [Condensed Matter - Low Dimensional Systems Laboratory, Department of Physics, Indian Institute of Technology, Kanpur - 208016 (India); Budhani, R. C. [National Physical Laboratory, New Delhi - 110012 (India); Condensed Matter - Low Dimensional Systems Laboratory, Department of Physics, Indian Institute of Technology, Kanpur - 208016 (India)

    2013-02-15

    Double ring formation on Co{sub 2}MnSi (CMS) films is observed at electrical breakdown voltage during local anodic oxidation (LAO) using atomic force microscope (AFM). Corona effect and segregation of cobalt in the vicinity of the rings is studied using magnetic force microscopy and energy dispersive spectroscopy. Double ring formation is attributed to the interaction of ablated material with the induced magnetic field during LAO. Steepness of forward bias transport characteristics from the unperturbed region of the CMS film suggest a non equilibrium spin contribution. Such mesoscopic textures in magnetic films by AFM tip can be potentially used for memory storage applications.

  17. Indium doped niobium phosphates as intermediate temperature proton conductors

    DEFF Research Database (Denmark)

    Huang, Yunjie; Li, Qingfeng; Anfimova, Tatiana

    2013-01-01

    Indium doped niobium phosphates were prepared from precursors of trivalent indium oxide, pentavalent niobium oxide and phosphoric acid. The obtained materials were characterized by X-ray diffraction, impedance spectroscopy, FT-IR spectroscopy and scanning electron microscopy. It was found...... that the indium doping promoted formation of the cubic Nb2P4O15 phase instead of the monoclinic Nb5P7O30 phase in the pristine niobium phosphates and enhanced the preservation of OH functional groups in the phosphates. The preserved OH functionalities in the phosphates after the heat treatment at 650 °C...... contributed to the anhydrous proton conductivity. The Nb0.9In0.1 phosphate exhibited a proton conductivity of five times higher than that of the un-doped analog at 250 °C. The conductivity was stabilized at a level of above 0.02 S cm−1 under dry atmosphere at 250 °C during the stability evaluation for 3 days....

  18. Core-shell tin oxide, indium oxide, and indium tin oxide nanoparticles on silicon with tunable dispersion: electrochemical and structural characteristics as a hybrid Li-ion battery anode.

    Science.gov (United States)

    Osiak, Michal J; Armstrong, Eileen; Kennedy, Tadhg; Torres, Clivia M Sotomayor; Ryan, Kevin M; O'Dwyer, Colm

    2013-08-28

    Tin oxide (SnO2) is considered a very promising material as a high capacity Li-ion battery anode. Its adoption depends on a solid understanding of factors that affect electrochemical behavior and performance such as size and composition. We demonstrate here, that defined dispersions and structures can improve our understanding of Li-ion battery anode material architecture on alloying and co-intercalation processes of Lithium with Sn from SnO2 on Si. Two different types of well-defined hierarchical Sn@SnO2 core-shell nanoparticle (NP) dispersions were prepared by molecular beam epitaxy (MBE) on silicon, composed of either amorphous or polycrystalline SnO2 shells. In2O3 and Sn doped In2O3 (ITO) NP dispersions are also demonstrated from MBE NP growth. Lithium alloying with the reduced form of the NPs and co-insertion into the silicon substrate showed reversible charge storage. Through correlation of electrochemical and structural characteristics of the anodes, we detail the link between the composition, areal and volumetric densities, and the effect of electrochemical alloying of Lithium with Sn@SnO2 and related NPs on their structure and, importantly, their dispersion on the electrode. The dispersion also dictates the degree of co-insertion into the Si current collector, which can act as a buffer. The compositional and structural engineering of SnO2 and related materials using highly defined MBE growth as model system allows a detailed examination of the influence of material dispersion or nanoarchitecture on the electrochemical performance of active electrodes and materials.

  19. Investigation of the Reversible Lithiation of an Oxide Free Aluminum Anode by a LiBH4 Solid State Electrolyte

    Directory of Open Access Journals (Sweden)

    Jason A. Weeks

    2017-11-01

    Full Text Available In this study, we analyze and compare the physical and electrochemical properties of an all solid-state cell utilizing LiBH4 as the electrolyte and aluminum as the active anode material. The system was characterized by galvanostatic lithiation/delithiation, cyclic voltammetry (CV, X-ray diffraction (XRD, energy dispersive X-ray spectroscopy (EDS, Raman spectroscopy, electrochemical impedance spectroscopy (EIS, and scanning electron microscopy (SEM. Constant current cycling demonstrated that the aluminum anode can be reversibly lithiated over multiple cycles utilizing a solid-state electrolyte. An initial capacity of 895 mAh/g was observed and is close to the theoretical capacity of aluminum. Cyclic voltammetry of the cell was consistent with the constant current cycling data and showed that the reversible lithiation/delithiation of aluminum occurs at 0.32 V and 0.38 V (vs. Li+/Li respectively. XRD of the aluminum anode in the initial and lithiated state clearly showed the formation of a LiAl (1:1 alloy. SEM-EDS was utilized to examine the morphological changes that occur within the electrode during cycling. This work is the first example of reversible lithiation of aluminum in a solid-state cell and further emphasizes the robust nature of the LiBH4 electrolyte. This demonstrates the possibility of utilizing other high capacity anode materials with a LiBH4 based solid electrolyte in all-solid-state batteries.

  20. Efficiency gain of solid oxide fuel cell systems by using anode offgas recycle - Results for a small scale propane driven unit

    Science.gov (United States)

    Dietrich, Ralph-Uwe; Oelze, Jana; Lindermeir, Andreas; Spitta, Christian; Steffen, Michael; Küster, Torben; Chen, Shaofei; Schlitzberger, Christian; Leithner, Reinhard

    The transfer of high electrical efficiencies of solid oxide fuel cells (SOFC) into praxis requires appropriate system concepts. One option is the anode-offgas recycling (AOGR) approach, which is based on the integration of waste heat using the principle of a chemical heat pump. The AOGR concept allows a combined steam- and dry-reforming of hydrocarbon fuel using the fuel cell products steam and carbon dioxide. SOFC fuel gas of higher quantity and quality results. In combination with internal reuse of waste heat the system efficiency increases compared to the usual path of partial oxidation (POX). The demonstration of the AOGR concept with a 300 Wel-SOFC stack running on propane required: a combined reformer/burner-reactor operating in POX (start-up) and AOGR modus; a hotgas-injector for anode-offgas recycling to the reformer; a dynamic process model; a multi-variable process controller; full system operation for experimental proof of the efficiency gain. Experimental results proof an efficiency gain of 18 percentage points (η·POX = 23%, η·AOGR = 41%) under idealized lab conditions. Nevertheless, further improvements of injector performance, stack fuel utilization and additional reduction of reformer reformer O/C ratio and system pressure drop are required to bring this approach into self-sustaining operation.

  1. Monodispersed FeCO3 nanorods anchored on reduced graphene oxide as mesoporous composite anode for high-performance lithium-ion batteries

    Science.gov (United States)

    Xu, Donghui; Liu, Weijian; Zhang, Congcong; Cai, Xin; Chen, Wenyan; Fang, Yueping; Yu, Xiaoyuan

    2017-10-01

    The development of advanced 1D/2D hierarchical nanocomposites for high-performance lithium-ion batteries is important and promising. Herein, monodispersed FeCO3 nanorods anchored on reduced graphene oxide (RGO) are prepared via a facile and efficient one-pot hydrothermal synthesis. The influence of RGO content on the morphology and electrochemical performances of the mesoporous FeCO3/reduced graphene oxide (FeCO3/RGO) composites are systematically studied. Optimized FeCO3/RGO composite shows good cycling stability. It delivers an initial discharge capacity of 1449 mAh·g-1 at the current density of 200 mA g-1 and maintained a capacity of 789 mAh·g-1 after 80 cycles. A moderate amount of RGO sheets can not only provide more conductive channels to improve the electrode conductivity, but also effectively buffer the large volume variation of FeCO3 during continuous charge/discharge process. The combination of FeCO3 nanorods with RGOs synergistically contribute to enhanced capacity and durability of the composite anode. It demonstrates that RGO anchored-FeCO3 nanorods should be an attractive candidate as anode material for high-performance lithium-ion batteries.

  2. Immediate Function of Anodically Oxidized Surface Implants (TiUnite™) for Fixed Prosthetic Rehabilitation: Retrospective Study with 10 Years of Follow-Up

    Science.gov (United States)

    Maló, Paulo; Gonçalves, Yolande; Lopes, Armando; Ferro, Ana

    2016-01-01

    Purpose. To report the long-term outcome at 10 years of fixed prosthetic rehabilitation supported by dental implants with anodically oxidized surfaces in immediate function. Materials and Methods. This retrospective cohort study included 75 consecutive patients (44 females and 31 males; 14 bruxers; 21 smokers; 14 systemic compromised), with average age of 60 years, rehabilitated with 264 implants. Outcome measures were implant cumulative survival rates (calculated through life tables) and marginal bone level at 10 years. Results. Twenty-one patients with 66 implants (25%) were lost to follow-up. Six patients lost 12 implants (MkIII implants: n = 9; MkIV implants: n = 3). The overall implant cumulative survival rate at 10 years was 95.2% (maxilla: 95.6%; mandible: 94.7%). The average (standard deviation) marginal bone level at 10 years was 1.96 mm (1.50 mm), with 1.92 mm (1.31 mm) for the maxilla and 2.00 mm (1.71 mm) for the mandible, with a significant difference between nonsmokers (average = 1.60 mm) and smokers (average = 2.95 mm). Conclusions. Within the limitations of this study, it can be concluded that fixed prosthetic rehabilitation supported by implants with anodically oxidized surface in immediate function is a viable and safe treatment option for both jaws. PMID:28119922

  3. Immediate Function of Anodically Oxidized Surface Implants (TiUnite™ for Fixed Prosthetic Rehabilitation: Retrospective Study with 10 Years of Follow-Up

    Directory of Open Access Journals (Sweden)

    Paulo Maló

    2016-01-01

    Full Text Available Purpose. To report the long-term outcome at 10 years of fixed prosthetic rehabilitation supported by dental implants with anodically oxidized surfaces in immediate function. Materials and Methods. This retrospective cohort study included 75 consecutive patients (44 females and 31 males; 14 bruxers; 21 smokers; 14 systemic compromised, with average age of 60 years, rehabilitated with 264 implants. Outcome measures were implant cumulative survival rates (calculated through life tables and marginal bone level at 10 years. Results. Twenty-one patients with 66 implants (25% were lost to follow-up. Six patients lost 12 implants (MkIII implants: n=9; MkIV implants: n=3. The overall implant cumulative survival rate at 10 years was 95.2% (maxilla: 95.6%; mandible: 94.7%. The average (standard deviation marginal bone level at 10 years was 1.96 mm (1.50 mm, with 1.92 mm (1.31 mm for the maxilla and 2.00 mm (1.71 mm for the mandible, with a significant difference between nonsmokers (average = 1.60 mm and smokers (average = 2.95 mm. Conclusions. Within the limitations of this study, it can be concluded that fixed prosthetic rehabilitation supported by implants with anodically oxidized surface in immediate function is a viable and safe treatment option for both jaws.

  4. Anodic Concentration Polarization in SOFCs

    Energy Technology Data Exchange (ETDEWEB)

    Williford, Rick E.; Chick, Lawrence A.; Maupin, Gary D.; Simner, Steve P.; Stevenson, Jeffry W.; Khaleel, Mohammad A.; Wachsman, ED, et al

    2003-08-01

    Concentration polarization is important because it determines the maximum power output of a solid oxide fuel cell (SOFC) at high fuel utilization. Anodic concentration polarization occurs when the demand for reactants exceeds the capacity of the porous ceramic anode to supply them by gas diffusion mechanisms. High tortuosities (bulk diffusion resistances) are often assumed to explain this behavior. However, recent experiments show that anodic concentration polarization originates in the immediate vicinity of the reactive triple phase boundary (TPB) sites near the anode/electrolyte interface. A model is proposed to describe how concentration polarization is controlled by two localized phenomena: competitive adsorption of reactants in areas adjacent to the reactive TPB sites, followed by relatively slow surface diffusion to the reactive sites. Results suggest that future SOFC design improvements should focus on optimization of the reactive area, adsorption, and surface diffusion at the anode/electrolyte interface.

  5. Monolithic Gyroidal Mesoporous Mixed Titanium–Niobium Nitrides

    Science.gov (United States)

    2015-01-01

    Mesoporous transition metal nitrides are interesting materials for energy conversion and storage applications due to their conductivity and durability. We present ordered mixed titanium–niobium (8:2, 1:1) nitrides with gyroidal network structures synthesized from triblock terpolymer structure-directed mixed oxides. The materials retain both macroscopic integrity and mesoscale ordering despite heat treatment up to 600 °C, without a rigid carbon framework as a support. Furthermore, the gyroidal lattice parameters were varied by changing polymer molar mass. This synthesis strategy may prove useful in generating a variety of monolithic ordered mesoporous mixed oxides and nitrides for electrode and catalyst materials. PMID:25122534

  6. Pure niobium sheet formability limits hydroforming

    International Nuclear Information System (INIS)

    Collard, J.; Daumas, M.T.

    1986-04-01

    Sheets of niobium of 3 different thicknesses (0.1 mm, 1 mm and 2 mm) are deep-drawn by isostatic forming, influence of plane anisotropy and thickness are studied and deformation of the hydroformed niobium is observed. Forming limit curves are determined [fr

  7. Influence of temperature and atmosphere on the strength and elastic modulus of solid oxide fuel cell anode supports

    DEFF Research Database (Denmark)

    Ni, De Wei; Charlas, Benoit; Kwok, Kawai

    2016-01-01

    need to be characterized to ensure reliable operation. In this study, the effect of reduction temperature on microstructural stability, high temperature strength and elastic modulus of Ni-YSZ anode supports were investigated. The statistical distribution of strength was determined from a large number...... of samples (∼30) at each condition to ensure high statistical validity. It is revealed that the microstructure and mechanical properties of the Ni-YSZ strongly depend on the reduction temperature. Further studies were conducted to investigate the temperature dependence of the strength and elastic modulus...... for both the unreduced and reduced Ni(O)-YSZ anode supports. With increasing temperature, the strength and elastic modulus of the reduced Ni-YSZ specimens drop almost linearly. In contrast, the strength and elastic modulus of the unreduced NiO-YSZ remain almost constant over the investigated temperature...

  8. Shot peening as a pre-treatment to anodic oxidation coating process of AW 6082 aluminum for fatigue life improvement

    Czech Academy of Sciences Publication Activity Database

    Hadzima, B.; Nový, F.; Trško, L.; Pastorek, F.; Jambor, M.; Fintová, Stanislava

    2017-01-01

    Roč. 93, 9-12 (2017), s. 3315-3323 ISSN 0268-3768 R&D Projects: GA MŠk(CZ) LQ1601 Institutional support: RVO:68081723 Keywords : Fatigue life * AW 6082 aluminum alloy * Anodizing * Shot peening * Ultrasonic fatigue testing Subject RIV: JL - Materials Fatigue, Friction Mechanics OBOR OECD: Audio engineering, reliability analysis Impact factor: 2.209, year: 2016 https://link.springer.com/content/pdf/10.1007%2Fs00170-017-0776-1.pdf

  9. Steady-state oxygen-solubility in niobium

    International Nuclear Information System (INIS)

    Schulze, K.; Jehn, H.

    1977-01-01

    During annealing of niobium in oxygen in certain temperature and pressure ranges steady states are established between the absorption of molecular oxygen and the evaporation of volatile oxides. The oxygen concentration in the niobium-oxygen α-solid solution is a function of oxygen pressure and temperature and has been redetermined in the ranges 10 -5 - 10 -2 Pa O 2 and 2,070 - 2,470 K. It follows differing from former results the equation csub(o) = 9.1 x 10 -6 x sub(po2) x exp (502000/RT) with csub(o) in at.-ppm, sub(po2) in Pa, T in K, R = 8.31 J x mol -1 x K -1 . The existence of steady states is limited to a temperature range from 1870 to 2470 K and to oxygen concentrations below the solubility limit given by solidus and solvus lines in the T-c diagram. In the experiments high-purity niobium wires with a specific electrical ratio rho (273 K)/rho(4.2 K) > 5,000 have been gassed under isothermal-isobaric conditions until the steady state has been reached. The oxygen concentration has been determined analytically by vacuum fusion extraction with platinum-flux technique as well as by electrical residual resistivity measurements at 4.2 K. (orig.) [de

  10. Electrochemical behaviour and surface conductivity of niobium carbide-modified austenitic stainless steel bipolar plate

    Science.gov (United States)

    Wang, Lixia; Sun, Juncai; Kang, Bin; Li, Song; Ji, Shijun; Wen, Zhongsheng; Wang, Xiaochun

    2014-01-01

    A niobium carbide diffusion layer with a cubic NbC phase surface layer (∼6 μm) and a Nb and C diffusion subsurface layer (∼1 μm) is fabricated on the surface of AISI 304 stainless steel (304 SS) bipolar plate in a proton exchange membrane fuel cell (PEMFC) using plasma surface diffusion alloying. The electrochemical behaviour of the niobium carbide diffusion-modified 304 SS (Nb-C 304 SS) is investigated in simulated PEMFC environments (0.5 M H2SO4 and 2 ppm HF solution at 80 °C). Potentiodynamic, potentiostatic polarisation and electrochemical impedance spectroscopy measurements reveal that the niobium carbide diffusion layer considerably improves the corrosion resistance of 304 SS compared with untreated samples. The corrosion current density of Nb-C 304 SS is maintained at 0.058 μA cm-2 and 0.051 μA cm-2 under simulated anodic and cathodic conditions, respectively. The interfacial contact resistance of Nb-C 304 SS is 8.47 mΩ cm2 at a compaction force of 140 N cm-2, which is significantly lower than that of the untreated sample (100.98 mΩ cm2). Moreover, only a minor increase in the ICR of Nb-C 304 SS occurs after 10 h potentiostatic tests in both cathodic and anodic environments.

  11. Surface analyses of electropolished niobium samples for superconducting radio frequency cavity

    Energy Technology Data Exchange (ETDEWEB)

    Tyagi, P. V.; Nishiwaki, M.; Saeki, T.; Sawabe, M.; Hayano, H.; Noguchi, T.; Kato, S. [GUAS, Tsukuba, Ibaraki 305-0801 (Japan); KEK, Tsukuba, Ibaraki 305-0801 (Japan); KAKEN Inc., Hokota, Ibaraki 311-1416 (Japan); GUAS, Tsukuba, Ibaraki 305-0801 (Japan) and KEK, Tsukuba, Ibaraki 305-0801 (Japan)

    2010-07-15

    The performance of superconducting radio frequency niobium cavities is sometimes limited by contaminations present on the cavity surface. In the recent years extensive research has been done to enhance the cavity performance by applying improved surface treatments such as mechanical grinding, electropolishing (EP), chemical polishing, tumbling, etc., followed by various rinsing methods such as ultrasonic pure water rinse, alcoholic rinse, high pressure water rinse, hydrogen per oxide rinse, etc. Although good cavity performance has been obtained lately by various post-EP cleaning methods, the detailed nature about the surface contaminants is still not fully characterized. Further efforts in this area are desired. Prior x-ray photoelectron spectroscopy (XPS) analyses of EPed niobium samples treated with fresh EP acid, demonstrated that the surfaces were covered mainly with the niobium oxide (Nb{sub 2}O{sub 5}) along with carbon, in addition a small quantity of sulfur and fluorine were also found in secondary ion mass spectroscopy (SIMS) analysis. In this article, the authors present the analyses of surface contaminations for a series of EPed niobium samples located at various positions of a single cell niobium cavity followed by ultrapure water rinsing as well as our endeavor to understand the aging effect of EP acid solution in terms of contaminations presence at the inner surface of the cavity with the help of surface analytical tools such as XPS, SIMS, and scanning electron microscope at KEK.

  12. Differences in the electrochemical behavior of ruthenium and iridium oxide in electrocatalytic coatings of activated titanium anodes prepared by the sol–gel procedure

    Directory of Open Access Journals (Sweden)

    VLADIMIR V. PANIĆ

    2010-10-01

    Full Text Available The electrochemical characteristics of Ti0.6Ir0.4O2/Ti and Ti0.6Ru0.4O2/Ti anodes prepared by the sol–gel procedure from the corresponding oxide sols, obtained by force hydrolysis of the corresponding metal chlorides, were compared. The voltammetric properties in H2SO4 solution indicate that Ti0.6Ir0.4O2/Ti has more pronounced pseudocapacitive characteristics, caused by proton-assisted, solid state surface redox transitions of the oxide. At potentials negative to 0.0 VSCE, this electrode is of poor conductivity and activity, while the voltammetric behavior of the Ti0.6Ru0.4O2/Ti electrode is governed by proton injection/ejection into the oxide structure. The Ti0.6Ir0.4O2/Ti electrode had a higher electrocatalytical activity for oxygen evolution, while the investigated anodes were of similar activity for chlorine evolution. The potential dependence of the impedance characteristics showed that the Ti0.6Ru0.4O2/Ti electrode behaved like a capacitor over a wider potential range than the Ti0.6Ir0.4O2/Ti electrode, with fully-developed pseudocapacitive properties at potentials positive to 0.60 VSCE. However, the impedance characteristics of the Ti0.6Ir0.4O2/Ti electrode changed with increasing potential from resistor-like to capacitor-like behavior.

  13. Anode Fall Formation in a Hall Thruster

    International Nuclear Information System (INIS)

    Dorf, Leonid A.; Raitses, Yevgeny F.; Smirnov, Artem N.; Fisch, Nathaniel J.

    2004-01-01

    As was reported in our previous work, accurate, nondisturbing near-anode measurements of the plasma density, electron temperature, and plasma potential performed with biased and emissive probes allowed the first experimental identification of both electron-repelling (negative anode fall) and electron-attracting (positive anode fall) anode sheaths in Hall thrusters. An interesting new phenomenon revealed by the probe measurements is that the anode fall changes from positive to negative upon removal of the dielectric coating, which appears on the anode surface during the course of Hall thruster operation. As reported in the present work, energy dispersion spectroscopy analysis of the chemical composition of the anode dielectric coating indicates that the coating layer consists essentially of an oxide of the anode material (stainless steel). However, it is still unclear how oxygen gets into the thruster channel. Most importantly, possible mechanisms of anode fall formation in a Hall thruster with a clean and a coated anodes are analyzed in this work; practical implication of understanding the general structure of the electron-attracting anode sheath in the case of a coated anode is also discussed

  14. Electrochemical treatment of landfill leachate: Oxidation at Ti/PbO{sub 2} and Ti/SnO{sub 2} anodes

    Energy Technology Data Exchange (ETDEWEB)

    Cossu, R.; Polcaro, A.M.; Mascia, M.; Palmas, S.; Renoldi, F. [Univ. of Cagliari (Italy); Lavagnolo, M.C. [CISA, Cagliari (Italy)

    1998-11-15

    Leachate originating in landfills where municipal solid wastes are disposed is a wastewater with a complex composition that could have a high environmental impact. The primary goal of this research was to investigate the feasibility of removing refractory organic pollutants and ammonium nitrogen from landfill leachate by electrochemical oxidation. The effects of current density, pH, and chloride concentration on the removal of both chemical oxygen demand (COD) and ammonium nitrogen were investigated. Titanium coated with lead dioxide (PbO{sub 2}) or tin dioxide (SnO{sub 2}) was used as the anode. An effective process was achieved in which the leachate was decolorized, COD was removed up to a value of 100 mg L{sup {minus}1}, and ammonia was totally eliminated. Average current efficiency of about 30% was measured for a decrease of COD from 1200 to 150 mg L{sup {minus}1}, while efficiency of about 10% was measured for a near complete removal of ammonium nitrogen, starting from an initial value of 380 mg L{sup {minus}1}. Results indicated that the organic load was removed by both direct and indirect oxidation. Indirect oxidation by chlorine or hypochlorite originating from oxidation of chlorides is believed to be mainly responsible for the nitrogen removal.

  15. A new lithium-ion battery using 3D-array nanostructured graphene-sulfur cathode and silicon oxide-based anode.

    Science.gov (United States)

    Benítez, Almudena; Di Lecce, Daniele; Elia, Giuseppe Antonio; Caballero, Álvaro; Morales, Julián; Hassoun, Jusef

    2018-02-28

    In this work we report an efficient lithium-ion battery using enhanced sulfur-based cathode and silicon oxide-based anode as novel energy-storage system. The sulfur-carbon composite, exploiting graphene carbon with 3D array (3DG-S), is synthesized by reduction step and microwave-assisted solvothermal technique and fully characterized in terms of structure, morphology, thereby revealing suitable features for lithium-cell application. Electrochemical tests indicate the 3DG-S electrode as very stable and performing cathode in lithium half-cell, with capacity ranging from 1200 to 1000 mAh g-1 at C/10 and 1C rates, respectively. Remarkably, the Li-alloying anode, namely a LiySiOx-C prepared by the sol-gel method and lithiated by surface treatment, shows a suitable performance in lithium half-cell using an electrolyte designed for lithium-sulfur battery. The LiySiOx-C/3DG-S battery reveals very promising results with a capacity of about 460 mAh gS-1 delivered at average voltage of about 1.5 V over 200 cycles, suggesting the characterized materials as suitable candidates for low-cost and high-energy storage application. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Graphene oxide-confined synthesis of Li4Ti5O12 microspheres as high-performance anodes for lithium ion batteries

    International Nuclear Information System (INIS)

    Zhang, Jiawei; Cai, Yurong; Wu, Jun; Yao, Juming

    2015-01-01

    This paper reports a graphene oxide (GO) confined strategy to synthesize reduced GO-coated lithium titanate (Li 4 Ti 5 O 12, LTO) microspheres using as-prepared TiO 2 microspheres and GO as raw materials. The obtained samples are characterized by X-ray diffraction, field emission scanning electron microscopy and spectrophotometer. Results show that the spherical LTO is formed with approximate 1 μm diameter after hydrothermal reactions, which is due to a confined effect of GO on the surface of TiO 2 spheres. Electrochemical tests reveal that the presence of rGO can increase the capacity and cycling stability of LTO anodes, especially at higher C rate. The 3 wt% rGO-coated LTO anodes present a higher reversible Li-ion storage with a specific discharge capacity of 131.6 mAh g −1 at 5 C and 97% retention even after 500 cycles, which are more excellent than those of pristine LTO. The GO-confined method is anticipated to synthesize other electrode materials with high electrochemical performances

  17. Scalable Dry Production Process of a Superior 3D Net-Like Carbon-Based Iron Oxide Anode Material for Lithium-Ion Batteries.

    Science.gov (United States)

    Li, Min; Du, Haoran; Kuai, Long; Huang, Kuangfu; Xia, Yuanyuan; Geng, Baoyou

    2017-10-02

    Carbon-based transition-metal oxides are considered as an appropriate anode material candidate for lithium-ion batteries. Herein, a simple and scalable dry production process is developed to produce carbon-encapsulated 3D net-like FeO x /C materials. The process is simply associated with the pyrolysis of a solid carbon source, such as filter paper, adsorbed with ferrite nitrate. The carbon derived from filter paper induces a carbothermal reduction to form metallic Fe, the addition of carbon and iron increase the conductivity of this material. As expected, this 3D net-like FeO x /C composite delivers an excellent charge capacity of 851.3 mAh g -1 after 50 cycles at 0.2 A g -1 as well as high stability and rate performance of 714.7 mAh g -1 after 300 cycles at 1 A g -1 . Superior performance, harmlessness, low costs, and high yield may greatly stimulate the practical application of the products as anode materials in lithium-ion batteries. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Electrostatic Self-Assembly of Fe3O4 Nanoparticles on Graphene Oxides for High Capacity Lithium-Ion Battery Anodes

    Directory of Open Access Journals (Sweden)

    Jung Kyoo Lee

    2013-09-01

    Full Text Available Magnetite, Fe3O4, is a promising anode material for lithium ion batteries due to its high theoretical capacity (924 mA h g−1, high density, low cost and low toxicity. However, its application as high capacity anodes is still hampered by poor cycling performance. To stabilize the cycling performance of Fe3O4 nanoparticles, composites comprising Fe3O4 nanoparticles and graphene sheets (GS were fabricated. The Fe3O4/GS composite disks of mm dimensions were prepared by electrostatic self-assembly between negatively charged graphene oxide (GO sheets and positively charged Fe3O4-APTMS [Fe3O4 grafted with (3-aminopropyltrimethoxysilane (APTMS] in an acidic solution (pH = 2 followed by in situ chemical reduction. Thus prepared Fe3O4/GS composite showed an excellent rate capability as well as much enhanced cycling stability compared with Fe3O4 electrode. The superior electrochemical responses of Fe3O4/GS composite disks assure the advantages of: (1 electrostatic self-assembly between high storage-capacity materials with GO; and (2 incorporation of GS in the Fe3O4/GS composite for high capacity lithium-ion battery application.

  19. Carbon-wrapped MnO nanodendrites interspersed on reduced graphene oxide sheets as anode materials for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Boli; Li, Dan; Liu, Zhengjiao; Gu, Lili; Xie, Wenhe; Li, Qun; Guo, Pengqian; Liu, Dequan; He, Deyan, E-mail: hedy@lzu.edu.cn

    2017-02-01

    Highlights: • The C-MnO/rGO composites were anchored on nickel foam by a facile vacuum filtration and a subsequent thermal treatment. • The novel architecture of anodes effectively improved the electrochemical performance of lithium ion battery. • The active MnO nanodendrites became smaller nanoparticles still wrapped in graphene sheets after cycles. - Abstract: Carbon-wrapped MnO nanodendrites interspersed on reduced graphene oxide sheets (C-MnO/rGO) were prepared on nickel foam by a facile vacuum filtration and a subsequent thermal treatment. As a binder-free anode of lithium-ion battery, the nanodendritic structure of C-MnO accommodates the huge volume expansion and shortens the diffusion length for lithium ion and electron, rGO sheets prevent C-MnO nanodendites from aggregation and offer a good electronic conduction. As a result, the electrode with such a novel architecture delivers superior electrochemical properties including high reversible capacity, excellent rate capability and cycle stability. Moreover, MnO nanodendrites change to nanoparticles wrapped in graphene sheets during the lithiation/delithiation process, which is a more beneficial microstructure to further increase the specific capacity and cycle life of the electrode.

  20. Enhanced Efficiency of GaAs Single-Junction Solar Cells with Inverted-Cone-Shaped Nanoholes Fabricated Using Anodic Aluminum Oxide Masks

    Directory of Open Access Journals (Sweden)

    Kangho Kim

    2013-01-01

    Full Text Available The GaAs solar cells are grown by low-pressure metalorganic chemical vapor deposition (LP-MOCVD and fabricated by photolithography, metal evaporation, annealing, and wet chemical etch processes. Anodized aluminum oxide (AAO masks are prepared from an aluminum foil by a two-step anodization method. Inductively coupled plasma dry etching is used to etch and define the nanoarray structures on top of an InGaP window layer of the GaAs solar cells. The inverted-cone-shaped nanoholes with a surface diameter of about 50 nm are formed on the top surface of the solar cells after the AAO mask removal. Photovoltaic and optical characteristics of the GaAs solar cells with and without the nanohole arrays are investigated. The reflectance of the AAO nanopatterned samples is lower than that of the planar GaAs solar cell in the measured range. The short-circuit current density increased up to 11.63% and the conversion efficiency improved from 10.53 to 11.57% under 1-sun AM 1.5 G conditions by using the nanohole arrays. Dependence of the efficiency enhancement on the etching depth of the nanohole arrays is also investigated. These results show that the nanohole arrays fabricated with an AAO technique may be employed to improve the light absorption and, in turn, the conversion efficiency of the GaAs solar cell.

  1. Niobium Nb and tantalum Ta

    International Nuclear Information System (INIS)

    Busev, A.I.; Tiptsova, V.G.; Ivanov, V.M.

    1978-01-01

    The basic methods for determining niobium and tantalum in various objects are described. Nb and Ta are separated with the aid of N-benzoyl-N-phenylhydroxylamine by precipitating Nb(5) from a tartaric acid solution with subsequent precipitation of Ta from the filtrate. The gravimetric determination of Nb and Ta in steels is based on their quantitative separation from a diluted solution by way of hydrolysis with subsequent after-precipitation with phenylarsonic acid (in the absence of W). The gravimetric determination of Nb in the presence of W is carried out with the aid of Cupferron. To determine Nb in its carbide, Nb(5) reduced to Nb(3) is titrated with a solution of K 2 Cr 2 O 7 in the presence of phenyl-anthranilic acid. The photometric determination of Nb in tungsten-containing steels and in ores containing Ti, W, Mo and Cr is based on the rhodanide method. Nb is determined in alloys with Zr and Ti photometrically with the aid of 4-(2-pyridylazo)-resorcin and in alloyed steels with the aid of benzhydroxamic acid. The latter complex is extracted with chloroform. This method is used to determine Nb in rocks. The photometric determination of Ta in TiCl 4 is carried out with the aid of pyrogallol, in commercial niobium with the aid of methyl violet, and in steel with the aid of 4-(-pyridylazo)-resorcin. Also described is the polarographic determination of Nb in tantalum pentoxide

  2. Lamellar titanates: a breakthrough in the search for new solid oxide fuel cell anode materials operating on methane

    Energy Technology Data Exchange (ETDEWEB)

    Perillat-Merceroz, Cedric; Rosini, Sebastien; Gauthier, Gilles [CEA/LITEN, Laboratoire d' innovation technologique et des, energies nouvelles 17 rue des Martyrs, 38054 Grenoble (France); Roussel, Pascal; Vannier, Rose-Noelle [Universite Lille Nord de France, CNRS, UMR8181, UCCS, Unite de catalyse et de chimie du solide ENSCL-USTL, BP90108, 59652 Villeneuve d' Ascq (France); Gelin, Patrick [Universite Lyon1, CNRS, UMR5256, IRCELYON, Institut de recherches sur la catalyse et l' environnement, de Lyon 2 avenue Albert Einstein, 69626 Villeurbanne (France)

    2011-07-15

    Decreasing the dimensionality of the La{sub x}Sr{sub 1-x}TiO{sub 3+{delta}} family structure from 3D to 2D by increasing the La content greatly enhances the electrochemical performance of the material as an SOFC anode. This is attested to by the strong decrease in the polarization resistance values deduced from the complex impedance spectra (Nyquist plot) recorded at 900 C in H{sub 2}/H{sub 2}O(3%) on a symmetrical cell. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  3. Nanoporous niobium nitride (Nb2N) with enhanced electrocatalytic performance for hydrogen evolution

    Science.gov (United States)

    Li, Yan; Zhang, Jianli; Qian, Xingyue; Zhang, Yue; Wang, Yining; Hu, Rudan; Yao, Chao; Zhu, Junwu

    2018-01-01

    The transition metal nitrides (TMNs) with nanoporous structure have shown great promise as potential electrocatalysts for the hydrogen evolution reaction (HER). Herein, self-organized nanoporous Nb2N was first successfully synthesized through the anodization of niobium in mixed oxalic acid/HF electrolyte, followed by a simple annealing treatment in the ammonia atmosphere. Due to the highly ordered nanoporous structure with abundant active sites and the enhanced electrical conductivity, the Nb2N exhibits a high catalytic current (326.3 mA cm-2) and low onset potential (96.3 mV), which is almost 3.9 times and 4.2 times better than that of Nb2O5, respectively. Meanwhile, the Nb2N also presents low Tafel slope (92 mV dec-1), and excellent cycling durability. More importantly, this study will provide more opportunities for designing and fabricating niobium compounds as an innovative HER catalysts.

  4. Initial stages of anodic oxidation of silver in sodium hydroxide solution studied by potential sweep voltammetry and ellipsometry

    NARCIS (Netherlands)

    Droog, J.M.M.; Alderliesten, P.T.; Bootsma, G.A.

    1979-01-01

    The first stages of the oxidation of polycrystalline silver electrodes in NaOH solutions were studied by potential sweep voltammetry and ellipsometry. Formation of bulk Ag2O was found to be preceded by dissolution of silver species and deposition of a surface oxide. The equilibrium oxide coverage

  5. Investigation of electronic band structure and charge transfer mechanism of oxidized three-dimensional graphene as metal-free anodes material for dye sensitized solar cell application

    Science.gov (United States)

    Loeblein, Manuela; Bruno, Annalisa; Loh, G. C.; Bolker, Asaf; Saguy, Cecile; Antila, Liisa; Tsang, Siu Hon; Teo, Edwin Hang Tong

    2017-10-01

    Dye-sensitized solar cells (DSSCs) offer an optimal trade-off between conversion-efficiency and low-cost fabrication. However, since all its electrodes need to fulfill stringent work-function requirements, its materials have remained unchanged since DSSC's first report early-90s. Here we describe a new material, oxidized-three-dimensional-graphene (o-3D-C), with a band gap of 0.2 eV and suitable electronic band-structure as alternative metal-free material for DSSCs-anodes. o-3D-C/dye-complex has a strong chemical bonding via carboxylic-group chemisorption with full saturation after 12 sec at capacity of ∼450 mg/g (600x faster and 7x higher than optimized metal surfaces). Furthermore, fluorescence quenching of life-time by 28-35% was measured demonstrating charge-transfer from dye to o-3D-C.

  6. Effect of foreign anions on the kinetics of chlorine and oxygen evolution on ruthenium-titanium oxide anodes under the conditions of chlorine electrolysis

    International Nuclear Information System (INIS)

    Bune, N.Ya.; Filatov, V.P.; Losev, V.V.; Portnova, M. Yu.

    1985-01-01

    Polarization measurements and gas chromatographic analysis of the composition of gaseous electrolysis products were used to investigate the effect of phosphate, sulfate and perchlorate on the kinetics of the evolution of chlorine and oxygen at ruthenium-titanium oxide anodes (ORTA) under the conditions of chlorine electrolysis. It was found that at i = 0.2 A/cm 2 the addition of NaH 2 PO 4 and Na 2 SO 4 to the chloride solution inhibits the evolution of chlorine, indicating the predominant adsorption of phosphate and sulfate ions on the ORTA surface. At a constant potential, the evolution rate of oxygen from solutions of NaClO 4 , NaH 2 PO 4 , Na 2 SO 4 and NaCl of equal concentration with a pH approximately 1.6 decreases in the order perchlorate greater than chloride greater than sulfate greater than phosphate

  7. Persistent cyclestability of carbon coated Zn–Sn metal oxide/carbon microspheres as highly reversible anode material for lithium-ion batteries

    International Nuclear Information System (INIS)

    Fang, Guoqing; Kaneko, Shingo; Liu, Weiwei; Xia, Bingbo; Sun, Hongdan; Zhang, Ruixue; Zheng, Junwei; Li, Decheng

    2013-01-01

    Development of high-capacity anode materials equipped with strong cyclestability is a great challenge for use as practical electrode for high-performance lithium-ion rechargeable battery. In this study, we synthesized a carbon coated Zn–Sn metal nanocomposite oxide and carbon spheres (ZTO@C/CSs) via a simple glucose hydrothermal reaction and subsequent carbonization approach. The carbon coated ZTO/carbon microspheres composite maintained a reversible capacity of 680 mAh g −1 after 345 cycles at a current density of 100 mA g −1 , and furthermore the cell based on the composite exhibited an excellent rate capability of 470 mAh g −1 even when the cell was cycled at 2000 mA g –1 . The thick carbon layer formed on the ZTO nanoparticles and carbon spheres effectively buffered the volumetric change of the particles, which thus prolonged the cycling performance of the electrodes

  8. Electric charging/discharging characteristics of super capacitor, using de-alloying and anodic oxidized Ti-Ni-Si amorphous alloy ribbons.

    Science.gov (United States)

    Fukuhara, Mikio; Sugawara, Kazuyuki

    2014-01-01

    Charging/discharging behaviors of de-alloyed and anodic oxidized Ti-Ni-Si amorphous alloy ribbons were measured as a function of current between 10 pA and 100 mA, using galvanostatic charge/discharging method. In sharp contrast to conventional electric double layer capacitor (EDLC), discharging behaviors for voltage under constant currents of 1, 10 and 100 mA after 1.8 ks charging at 100 mA show parabolic decrease, demonstrating direct electric storage without solvents. The supercapacitors, devices that store electric charge on their amorphous TiO2-x surfaces that contain many 70-nm sized cavities, show the Ragone plot which locates at lower energy density region near the 2nd cells, and RC constant of 800 s (at 1 mHz), which is 157,000 times larger than that (5 ms) in EDLC.

  9. Nanocomposite anode materials for sodium-ion batteries

    Science.gov (United States)

    Manthiram, Arumugam; Kim Il, Tae; Allcorn, Eric

    2016-06-14

    The disclosure relates to an anode material for a sodium-ion battery having the general formula AO.sub.x--C or AC.sub.x--C, where A is aluminum (Al), magnesium (Mg), titanium (Ti), vanadium (V), chromium (Cr), manganese (Mn), iron (Fe), cobalt (Co), nickel (Ni), zirconium (Zr), molybdenum (Mo), tungsten (W), niobium (Nb), tantalum (Ta), silicon (Si), or any combinations thereof. The anode material also contains an electrochemically active nanoparticles within the matrix. The nanoparticle may react with sodium ion (Na.sup.+) when placed in the anode of a sodium-ion battery. In more specific embodiments, the anode material may have the general formula M.sub.ySb-M'O.sub.x--C, Sb-MO.sub.x--C, M.sub.ySn-M'C.sub.x--C, or Sn-MC.sub.x--C. The disclosure also relates to rechargeable sodium-ion batteries containing these materials and methods of making these materials.

  10. Photocatalytic activity of ferric oxide/titanium dioxide nanocomposite films on stainless steel fabricated by anodization and ion implantation

    Science.gov (United States)

    Zhan, Wei-ting; Ni, Hong-wei; Chen, Rong-sheng; Yue, Gao; Tai, Jun-kai; Wang, Zi-yang

    2013-08-01

    A simple surface treatment was used to develop photocatalytic activity for stainless steel. AISI 304 stainless steel specimens after anodization were implanted by Ti ions at an extracting voltage of 50 kV with an implantation dose of 3 × 1015 atoms·cm-2 and then annealed in air at 450°C for 2 h. The morphology was observed by scanning electron microscopy. The microstructure was characterized by X-ray diffraction and X-ray photoelectron spectroscopy. The photocatalytic degradation of methylene blue solution was carried out under ultraviolet light. The corrosion resistance of the stainless steel was evaluated in NaCl solution (3.5 wt%) by electrochemical polarization curves. It is found that the Ti ions depth profile resembles a Gaussian distribution in the implanted layer. The nanostructured Fe2O3/TiO2 composite film exhibits a remarkable enhancement in photocatalytic activity referenced to the mechanically polished specimen and anodized specimen. Meanwhile, the annealed Ti-implanted specimen remains good corrosion resistance.

  11. Modified surface morphology of a novel Ti-24Nb-4Zr-7.9Sn titanium alloy via anodic oxidation for enhanced interfacial biocompatibility and osseointegration.

    Science.gov (United States)

    Li, Xiang; Chen, Tao; Hu, Jing; Li, Shujun; Zou, Qin; Li, Yunfeng; Jiang, Nan; Li, Hui; Li, Jihua

    2016-08-01

    The Ti-24Nb-4Zr-7.9Sn titanium alloy (Ti2448) has shown potential for use in biomedical implants, because this alloy possesses several important mechanical properties, such as a high fracture strength, low elastic modulus, and good corrosion resistance. In this study, we aimed to produce a hierarchical nanostructure on the surface of Ti2448 to endow this alloy with favorable biological properties. The chemical composition of Ti2448 (64.0wt% Ti, 23.9wt% Nb, 3.9wt% Zr, and 8.1wt% Sn) gives this material electrochemical properties that lead to the generation of topographical features under standard anodic oxidation. We characterized the surface properties of pure Ti (Ti), nanotube-Ti (NT), Ti2448, and nanotube-Ti2448 (NTi2448) based on surface morphology (scanning electron microscopy and atomic force microscopy), chemical and phase compositions (X-ray diffraction and X-ray photoelectron spectroscopy), and wettability (water contact angle). We evaluated the biocompatibility and osteointegration of implant surfaces by observing the behavior of bone marrow stromal cells (BMSCs) cultured on the surfaces in vitro and conducting histological analysis after in vivo implantation of the modified materials. Our results showed that a hierarchical structure with a nanoscale bone-like layer was achieved along with nanotube formation on the Ti2448 surface. The surface characterization data suggested the superior biocompatibility of the NTi2448 surface in comparison with the Ti, NT, and Ti2448 surfaces. Moreover, the NTi2448 surface showed better biocompatibility for BMSCs in vitro and better osteointegration in vivo. Based on these results, we conclude that anodic oxidation facilitated the formation of a nanoscale bone-like structure and nanotubes on Ti2448. Unlike the modified titanium surfaces developed to date, the NTi2448 surface, which presents both mechanical compatibility and bioactivity, offers excellent biocompatibility and osteointegration, suggesting its potential for

  12. Hydrothermal synthesis of red phosphorus @reduced graphene oxide nanohybrid with enhanced electrochemical performance as anode material of lithium-ion battery

    Science.gov (United States)

    Zhu, Xing; Yuan, Zewei; Wang, Xiaobo; Jiang, Guodong; Xiong, Jian; Yuan, Songdong

    2018-03-01

    Red phosphorus @reduced graphene oxide (P @rGO) nanohybrid was synthesized via a two-step hydrothermal process. The obtained P @rGO nanohybrid was characterized by TEM, SEM, Raman, XRD and XPS. It was found that the nano-scale red phosphorus encapsulated in the reduced graphene oxide and the existence of phosphorus promote the reduction of graphene oxide. The electrochemical performance of P @rGO nanohybrid as an anode material was investigated by galvanostatic charge/discharge, rate performance, cyclic voltammetry and AC impedance test. With increasing the mass of rGO, the electrochemical performance of P @rGO nanohybrid was significantly enhanced. The first discharge/charge specific capacity of the nanohybrid prepared at optimum condition (P:GO = 7:3) could achieve approximately 2400 mAh/g and 1600 mAh/g respectively and still retained ∼1000 mAh/g after 80 cycles and the coulombic efficiency maintained almost 100%. The enhancement in P @rGO nanohybrid was attributed to the introduction of graphene, which led to the elimination of volume effect and the enhancement of conductively of pure red phosphorus.

  13. Solvent transfer of graphene oxide for synthesis of tin mono-sulfide graphene composite and application as anode of lithium-ion battery

    International Nuclear Information System (INIS)

    Tripathi, Alok M.; Mitra, Sagar

    2016-01-01

    Graphical abstract: Destabilization of graphene oxide colloid and SnS graphene composite preparation for lithium-ion battery. - Abstract: Tin mono sulfide (SnS) graphene composite has been synthesized for anode of lithium-ion battery. For synthesis of composite, graphene oxide (GO)-water (H 2 O) colloid has been destabilized and ensured the complete transfer of graphene oxide into another organic solvent N, N-dimethyl formamide (DMF). Mechanism for the destabilization of GO-H 2 O colloid is established. Surface to surface attachment of SnS on graphene sheet is achieved by solvothermal solution phase assembly of graphene sheets and SnS nanoparticles in DMF solvent. Graphene plays role in nanoparticle formation in composite. Such confined composite has been cycled reversibly at current rate of 160 mA g −1 , in voltage region of 0.01–2.5 V and exhibit a superior discharge capacity of 630 mAh g −1 after 50th cycle. Ex situ TEM analysis of used electrode reveal that the SnS nanoparticle-graphene composite with CMC binder perform better due to proper shape retention of electroactive materials during electrochemical cycling.

  14. Amorphous vanadium oxide matrixes supporting hierarchical porous Fe3O4/graphene nanowires as a high-rate lithium storage anode.

    Science.gov (United States)

    An, Qinyou; Lv, Fan; Liu, Qiuqi; Han, Chunhua; Zhao, Kangning; Sheng, Jinzhi; Wei, Qiulong; Yan, Mengyu; Mai, Liqiang

    2014-11-12

    Developing electrode materials with both high energy and power densities holds the key for satisfying the urgent demand of energy storage worldwide. In order to realize the fast and efficient transport of ions/electrons and the stable structure during the charge/discharge process, hierarchical porous Fe3O4/graphene nanowires supported by amorphous vanadium oxide matrixes have been rationally synthesized through a facile phase separation process. The porous structure is directly in situ constructed from the FeVO4·1.1H2O@graphene nanowires along with the crystallization of Fe3O4 and the amorphization of vanadium oxide without using any hard templates. The hierarchical porous Fe3O4/VOx/graphene nanowires exhibit a high Coulombic efficiency and outstanding reversible specific capacity (1146 mAh g(-1)). Even at the high current density of 5 A g(-1), the porous nanowires maintain a reversible capacity of ∼500 mAh g(-1). Moreover, the amorphization and conversion reactions between Fe and Fe3O4 of the hierarchical porous Fe3O4/VOx/graphene nanowires were also investigated by in situ X-ray diffraction and X-ray photoelectron spectroscopy. Our work demonstrates that the amorphous vanadium oxides matrixes supporting hierarchical porous Fe3O4/graphene nanowires are one of the most attractive anodes in energy storage applications.

  15. Method of low tantalum amounts determination in niobium and its compounds by ICP-OES technique.

    Science.gov (United States)

    Smolik, Marek; Turkowska, Magdalena

    2013-10-15

    A method of determination of low amounts of tantalum in niobium and niobium compounds without its prior separation by means of inductively coupled plasma optical emission spectrometry (ICP-OES) has been worked out. The method involves dissolution of the analyzed samples of niobium as well as its various compounds (oxides, fluorides, chlorides, niobates(V)) in fluoride environments, precipitation of sparingly soluble niobic(tantalic) acid (Nb2O5(Ta2O5) · xH2O), converting them into soluble complex compounds by means of oxalic acid with addition of hydrogen peroxide and finally analyzing directly obtained solutions by ICP-OES. This method permits determination of Ta in niobium at the level of 10(-3)% with relatively good precision (≤ 8% RSD) and accuracy (recovery factor: 0.9-1.1). Relative differences in the results obtained by two independent methods (ICP-OES and ICP-MS) do not exceed 14%, and other elements present in niobium compounds (Ti, W, Zr, Hf, V, Mo, Fe, Cr) at the level of 10(-2)% do not affect determination. © 2013 Elsevier B.V. All rights reserved.

  16. Study of optics anisotropy of niobium oxide

    International Nuclear Information System (INIS)

    Ferreira, N.G.; Decker, F.; Fracastoro-Decker, M.

    1988-01-01

    This work shows the use of ''in-situ'' optical techniques in electrochemical experiments to determine the refractive indexes of an anisotropic film. ''In situ'' reflectance measurements allow to study the behavior of a film during its growth process: in our case, since Nb 2 O 5 films are anisotropic only in the presence of an electric field, an ''in-situ'' technique is the only one appropriate to detect this phenomenon. (author) [pt

  17. Understanding Quality Factor Degradation in Superconducting Niobium Cavities at Low Microwave Field Amplitudes

    Science.gov (United States)

    Romanenko, A.; Schuster, D. I.

    2017-12-01

    In niobium superconducting radio frequency (SRF) cavities for particle acceleration, a decrease of the quality factor at lower fields—a so-called low field Q slope or LFQS—has been a long-standing unexplained effect. By extending the high Q measurement techniques to ultralow fields, we discover two previously unknown features of the effect: (i) saturation at rf fields lower than Eacc˜0.1 MV /m ; (ii) strong degradation enhancement by growing thicker niobium pentoxide. Our findings suggest that the LFQS may be caused by the two level systems in the natural niobium oxide on the inner cavity surface, thereby identifying a new source of residual resistance and providing guidance for potential nonaccelerator low-field applications of SRF cavities.

  18. Degreasing and cleaning superconducting RF Niobium cavities

    Energy Technology Data Exchange (ETDEWEB)

    Rauchmiller, Michael; Kellett, Ron; /Fermilab

    2011-09-01

    The purpose and scope of this report is to detail the steps necessary for degreasing and cleaning of superconducting RF Niobium cavities in the A0 clean room. It lists the required equipment and the cleaning procedure.

  19. Electrochemical oxidation of trace organic contaminants in reverse osmosis concentrate using RuO2/IrO2-coated titanium anodes.

    Science.gov (United States)

    Radjenovic, Jelena; Bagastyo, Arseto; Rozendal, René A; Mu, Yang; Keller, Jürg; Rabaey, Korneel

    2011-02-01

    During membrane treatment of secondary effluent from wastewater treatment plants, a reverse osmosis concentrate (ROC) containing trace organic contaminants is generated. As the latter are of concern, effective and economic treatment methods are required. Here, we investigated electrochemical oxidation of ROC using Ti/Ru(0.7)Ir(0.3)O(2) electrodes, focussing on the removal of dissolved organic carbon (DOC), specific ultra-violet absorbance at 254 nm (SUVA(254)), and 28 pharmaceuticals and pesticides frequently encountered in secondary treated effluents. The experiments were conducted in a continuously fed reactor at current densities (J) ranging from 1 to 250 A m(-2) anode, and a batch reactor at J = 250 A m(-2). Higher mineralization efficiency was observed during batch oxidation (e.g. 25.1 ± 2.7% DOC removal vs 0% removal in the continuous reactor after applying specific electrical charge, Q = 437.0 A h m(-3) ROC), indicating that DOC removal is depending on indirect oxidation by electrogenerated oxidants that accumulate in the bulk liquid. An initial increase and subsequent slow decrease in SUVA(254) during batch mode suggests the introduction of auxochrome substituents (e.g. -Cl, NH(2)Cl, -Br, and -OH) into the aromatic compounds. Contrarily, in the continuous reactor ring-cleaving oxidation products were generated, and SUVA(254) removal correlated with applied charge. Furthermore, 20 of the target pharmaceuticals and pesticides completely disappeared in both the continuous and batch experiments when applying J ≥ 150 A m(-2) (i.e. Q ≥ 461.5 A h m(-3)) and 437.0 A h m(-3) (J = 250 A m(-2)), respectively. Compounds that were more persistent during continuous oxidation were characterized by the presence of electrophilic groups on the aromatic ring (e.g. triclopyr) or by the absence of stronger nucleophilic substituents (e.g. ibuprofen). These pollutants were oxidized when applying higher specific electrical charge in batch mode (i.e. 1.45 kA h m(-3) ROC

  20. Effect of niobium addition in support catalysts applied in satellite propulsion

    Energy Technology Data Exchange (ETDEWEB)

    Soares, M.S., E-mail: marciosteinmetz@hotmail.com.br [Space Research National Institute, Combustion & Propulsion Associated Laboratory (Brazil); University of São Paulo, Lorena Engineering School, Materials Engineering Dept. (Brazil); Barbosa, R.D. [Space Research National Institute, Combustion & Propulsion Associated Laboratory (Brazil); University of São Paulo, Lorena Engineering School, Chemical Engineering Dept. (Brazil); Cruz, G.M. da; Rodrigues, J.A.J. [Space Research National Institute, Combustion & Propulsion Associated Laboratory (Brazil); Ribeiro, S. [University of São Paulo, Lorena Engineering School, Materials Engineering Dept. (Brazil)

    2017-03-01

    Catalysts composed of iridium as the active phase dispersed in aluminum oxide (Ir/Al{sub 2}O{sub 3}) are used in propulsion systems that employ hydrazine as monopropellant in the control of satellite orbit and attitude. The aluminum oxide (Al{sub 2}O{sub 3}) utilized as support must present high values of specific surface area, pore volume, and crush strength. The niobium effect was evaluated in this work, in its oxide form (Nb{sub 2}O{sub 5}), by 3 different methods: with the employment of a NbCl{sub 5} precursor solution, by wet impregnation and dry impregnation of an alumina obtained from a mixture of gibbsite and boehmite and by physical mixing of gibbsite and hydrated niobium oxide, both autoclaved separately. Aluminum oxides were prepared in both cases containing Nb{sub 2}O{sub 5} contents of 10, 20, and 30% w/w. The acid impregnating NbCl{sub 5} solution in the wet impregnation method caused a strong attack to the Al{sub 2}O{sub 3} support, altering and compromising its initial structure and morphology. This process did not occur in the supports prepared by dry impregnation. However, results indicated that the use of this methodology with Nb{sub 2}O{sub 5} contents of 20% and 30%, caused an extensive coverage of the support by Nb{sub 2}O{sub 5}, modifying the nature and amount of alumina sites responsible for anchorage of the iridium precursor. In the case of supports prepared through physical mixture (Nb{sub 2}O{sub 5}-Al{sub 2}O{sub 3}) from aluminum hydroxide and niobium acid precursor compounds, with both being previously autoclaved separately, the 20% and 30% Nb{sub 2}O{sub 5} contents presented the most promising properties, since the binder effect caused by amorphous Nb{sub 2}O{sub 5} increased the crush strength of the support, without compromising the aluminum oxide morphology and texture. Despite of existence of stronger acid sites due to the addition of niobium oxide to aluminum oxide, no increase in the acidity of the materials was observed due