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Sample records for alloy anode catalysts

  1. Catalyst Alloys Processing

    Science.gov (United States)

    Tan, Xincai

    2014-10-01

    Catalysts are one of the key materials used for diamond formation at high pressures. Several such catalyst products have been developed and applied in China and around the world. The catalyst alloy most widely used in China is Ni70Mn25Co5 developed at Changsha Research Institute of Mining and Metallurgy. In this article, detailed techniques for manufacturing such a typical catalyst alloy will be reviewed. The characteristics of the alloy will be described. Detailed processing of the alloy will be presented, including remelting and casting, hot rolling, annealing, surface treatment, cold rolling, blanking, finishing, packaging, and waste treatment. An example use of the catalyst alloy will also be given. Industrial experience shows that for the catalyst alloy products, a vacuum induction remelt furnace can be used for remelting, a metal mold can be used for casting, hot and cold rolling can be used for forming, and acid pickling can be used for metal surface cleaning.

  2. Alloy catalyst material

    DEFF Research Database (Denmark)

    2014-01-01

    The present invention relates to a novel alloy catalyst material for use in the synthesis of hydrogen peroxide from oxygen and hydrogen, or from oxygen and water. The present invention also relates to a cathode and an electrochemical cell comprising the novel catalyst material, and the process use...

  3. Electrochemical Characteristics of LaNi4.5Al0.5 Alloy Used as Anodic Catalyst in a Direct Borohydride Fuel Cell

    Institute of Scientific and Technical Information of China (English)

    Lianbang Wang; Guobin Wu; Zhenzhen Yang; Yunfang Gao; Xinbiao Mao; Chun'an Ma

    2011-01-01

    Fuel cells using borohydride as the fuel have received much attention because of high energy density and theoretical working potential. In this work, LaNi4.5Al0.5 hydrogen storage alloy used as the anodic material has been investigated. It was found that the increasing; operation temperature was helpful to the open-circuit potential, the discharge potential and the power density, but showed a negative effect on the utilization of the fuel due to the accelerated hydrogen evolution. The high KOH concentration was favorable for high-rate discharge capability. The adsorption and transformation of hydrogen on LaNi4.5Al0.5 alloy electrode has been observed, but its contribution to the discharge capability during a high-rate discharge was small.

  4. New anodizing process for magnesium alloys

    Institute of Scientific and Technical Information of China (English)

    LUO Sheng-lian; DAI Lei; ZHOU Hai-hui; CHAI Li-yuan; KUANG Ya-fei

    2006-01-01

    Compact anodic films with high hardness and good corrosion resistance on magnesium alloys were prepared by a new constant voltage and arc-free anodizing process. The effects of anodizing parameters such as applied voltage and electrolyte temperature on the peak current density and the thickness of films were investigated. In addition, the morphologies and corrosion resistance of films were investigated by scanning electron microscopy and potentiodynamic polarization, respectively. The results show that the higher the applied voltage, the higher the peak current density and the thicker the films. However, too high applied voltage may result in breakdown of films and intense sparking which may deteriorate the properties of the anodic films and bring about unsafety. The new anodizing process can be applied in a wide range of temperature. The new anodic films have numbers of pores with the diameter of 0.5 - 5.0 μm which do not transverse the entire film.

  5. Low-Pt-Content Anode Catalyst for Direct Methanol Fuel Cells

    Science.gov (United States)

    Narayanan, Sekharipuram; Whitacre, Jay

    2008-01-01

    Combinatorial experiments have led to the discovery that a nanophase alloy of Pt, Ru, Ni, and Zr is effective as an anode catalyst material for direct methanol fuel cells. This discovery has practical significance in that the electronic current densities achievable by use of this alloy are comparable or larger than those obtained by use of prior Pt/Ru catalyst alloys containing greater amounts of Pt. Heretofore, the high cost of Pt has impeded the commercialization of direct methanol fuel cells. By making it possible to obtain a given level of performance at reduced Pt content (and, hence, lower cost), the discovery may lead to reduction of the economic impediment to commercialization.

  6. Optical Transmittance of Anodically Oxidized Aluminum Alloy

    Science.gov (United States)

    Saito, Mitsunori; Shiga, Yasunori; Miyagi, Mitsunobu; Wada, Kenji; Ono, Sachiko

    1995-06-01

    Optical transmittance and anisotropy of anodic oxide films that were made from pure aluminum and an aluminum alloy (A5052) were studied. The alloy oxide film exhibits an enhanced polarization function, particularly when anodization is carried out at a large current density. It was revealed by chemical analysis that the alloy oxide film contains a larger amount of unoxidized aluminum than the pure-aluminum oxide film. The polarization function can be elucidated by considering unoxidized aluminum particles that are arranged in the columnar structure of the alumina film. Electron microscope observation showed that many holes exist in the alloy oxide film, around which columnar cells are arranged irregularly. Such holes and irregular cell arrangement cause the increase in the amount of unoxidized aluminum, and consequently induces scattering loss.

  7. New development of anodizing process of magnesium alloys

    Institute of Scientific and Technical Information of China (English)

    BAI Li-qun; LI Di

    2004-01-01

    Magnesium alloy, a kind of environment-friendly material with promising and excellent properties, is a good choice for a number of applications. The research and development of anodizing on magnesium alloys and its application situation are reviewed, and the anodizing development trend on magnesium alloys is summarized.

  8. Preparation and influence of performance of anodic catalysts for direct methanol fuel cell

    Institute of Scientific and Technical Information of China (English)

    WANG Zhenbo; YIN Geping; SHI Pengfei

    2007-01-01

    This research aims at increasing the utilization of platinum-ruthenium alloy (Pt-Ru) catalysts and thus lowering the catalyst loading in anodes for methanol electrooxidation.The direct methanol fuel cell's (DMFC) anodic catalysts,Pt-Ru/C,were prepared by chemical reduction with a reducing agent added in two kinds of solutions under different circumstances.The reducing agent was added in hot solution with the protection of inert gases or just air,and in cold solution with inert gases.The catalysts were treated at different temperatures.Their performance was tested by cyclic voltammetry and potentiostatic polarization by utilizing their inherent powder microelectrode in 0.5 mol/L CH3OH and 0.5 mol/L H2SO4 solution.The structures and micro-surface images ofthe catalysts were determined and observed by X-ray diffraction and transmission electron microscopy,respectively.The catalyst prepared in inert gases showed a better catalytic performance for methanol electrooxidation than that prepared in air.It resulted in a more homogeneous distribution of the Pt-Ru alloy in carbon.Its size is small,only about 4.5 nm.The catalytic performance is affected by the order of the reducing agent added.The performance of the catalyst prepared by adding the reductant at constant temperature of the solution is better than that prepared by adding it in the solution at 0℃ and then heating it up to the reducing temperature.The structure of the catalyst was modified,and there was an increase in the conversion of ruthenium into the alloyed state and an increase in particle size with the ascension of heat treatment temperature.In addition,the stability of the catalyst was improved after heat treatment.

  9. Novel Anode Catalyst for Direct Methanol Fuel Cells

    Directory of Open Access Journals (Sweden)

    S. Basri

    2014-01-01

    Full Text Available PtRu catalyst is a promising anodic catalyst for direct methanol fuel cells (DMFCs but the slow reaction kinetics reduce the performance of DMFCs. Therefore, this study attempts to improve the performance of PtRu catalysts by adding nickel (Ni and iron (Fe. Multiwalled carbon nanotubes (MWCNTs are used to increase the active area of the catalyst and to improve the catalyst performance. Electrochemical analysis techniques, such as energy dispersive X-ray spectrometry (EDX, X-ray diffraction (XRD, field emission scanning electron microscopy (FESEM, and X-ray photoelectron spectroscopy (XPS, are used to characterize the kinetic parameters of the hybrid catalyst. Cyclic voltammetry (CV is used to investigate the effects of adding Fe and Ni to the catalyst on the reaction kinetics. Additionally, chronoamperometry (CA tests were conducted to study the long-term performance of the catalyst for catalyzing the methanol oxidation reaction (MOR. The binding energies of the reactants and products are compared to determine the kinetics and potential surface energy for methanol oxidation. The FESEM analysis results indicate that well-dispersed nanoscale (2–5 nm PtRu particles are formed on the MWCNTs. Finally, PtRuFeNi/MWCNT improves the reaction kinetics of anode catalysts for DMFCs and obtains a mass current of 31 A g−1 catalyst.

  10. Bacterial adherence to anodized titanium alloy

    Energy Technology Data Exchange (ETDEWEB)

    Peremarch, C Perez-Jorge; Tanoira, R Perez; Arenas, M A; Matykina, E; Conde, A; De Damborenea, J J; Gomez Barrena, E; Esteban, J, E-mail: cperemarch@fjd.es

    2010-11-01

    The aim of this study was to evaluate Staphylococcus sp adhesion to modified surfaces of anodized titanium alloy (Ti-6Al-4V). Surface modification involved generation of fluoride-containing titanium oxide nanotube films. Specimens of Ti-6Al-4V alloy 6-4 ELI-grade 23- meets the requirements of ASTM F136 2002A (AMS 2631B class A1) were anodized in a mixture of sulphuric/hydrofluoric acid at 20 V for 5 and 60 min to form a 100 nm-thick porous film of 20 nm pore diameter and 230 nm-thick nanotube films of 100 nm in diameter. The amount of fluorine in the oxide films was of 6% and of 4%, respectively. Collection strains and six clinical strains each of Staphylococcus aureus and Staphylococcus epidermidis were studied. The adherence study was performed using a previously published protocol by Kinnari et al. The experiments were performed in triplicates. As a result, lower adherence was detected for collection strains in modified materials than in unmodified controls. Differences between clinical strains were detected for both species (p<0.0001, Kruskal-Wallis test), although global data showed similar results to that of collection strains (p<0.0001, Kruskal-Wallis test). Adherence of bacteria to modified surfaces was decreased for both species. The results also reflect a difference in the adherence between S. aureus and S. epidermidis to the modified material. As a conclusion, not only we were able to confirm the decrease of adherence in the modified surface, but also the need to test multiple clinical strains to obtain more realistic microbiological results due to intraspecies differences.

  11. A predictive fatigue life model for anodized 7050 aluminium alloy

    OpenAIRE

    Chaussumier, Michel; Mabru, Catherine; Shahzad, Majid; Chieragatti, Rémy; Rezaï-Aria, Farhad

    2013-01-01

    International audience; The objective of this study is to predict fatigue life of anodized 7050 aluminum alloy specimens. In the case of anodized 7050-T7451 alloy, fractographic observations of fatigue tested specimens showed that pickling pits were the predominant sites for crack nucleation and subsequent failure. It has been shown that fatigue failure was favored by the presence of multiple cracks. From these experimental results, a fatigue life predictive model has been developed including...

  12. Surface Modification of a MCFC Anode by Electrochemical Alloying

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Considering the properties of the valve metal alloys with specific corrosion resistance and electrocatalytic ac tivity, an investigation was made to examine if nickel-niobium alloy could serve as the anode material for molten carbo nate fuel cell (MCFC). An attempt was made to produce nickel-niobium surface alloy by an electrochemical process in the molten fluorides and to testify its performance required by the MCFC anode. Experimental results indicated that the corrosion resistance as well as polarization performance of the nickel electrode was improved by the surface alloying.As far as the corrosion resistance and polarization performance is concerned, the nickel-niobium surface alloy can be considered as a candidate material for the anode of MCFC.

  13. In situ characterization of nanoscale catalysts during anodic redox processes

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Renu [National Institute of Standards and Technology; Crozier, Peter [Arizona State University; Adams, James [Arizona State University

    2013-09-19

    Controlling the structure and composition of the anode is critical to achieving high efficiency and good long-term performance. In addition to being a mixed electronic and ionic conductor, the ideal anode material should act as an efficient catalyst for oxidizing hydrogen, carbon monoxide and dry hydrocarbons without de-activating through either sintering or coking. It is also important to develop novel anode materials that can operate at lower temperatures to reduce costs and minimized materials failure associated with high temperature cycling. We proposed to synthesize and characterize novel anode cermets materials based on ceria doped with Pr and/or Gd together with either a Ni or Cu metallic components. Ceria is a good oxidation catalyst and is an ionic conductor at room temperature. Doping it with trivalent rare earths such as Pr or Gd retards sintering and makes it a mixed ion conductor (ionic and electronic). We have developed a fundamental scientific understanding of the behavior of the cermet material under reaction conditions by following the catalytic oxidation process at the atomic scale using a powerful Environmental Scanning Transmission Electron Microscope (ESTEM). The ESTEM allowed in situ monitoring of structural, chemical and morphological changes occurring at the cermet under conditions approximating that of typical fuel-cell operation. Density functional calculations were employed to determine the underlying mechanisms and reaction pathways during anode oxidation reactions. The dynamic behavior of nanoscale catalytic oxidation of hydrogen and methane were used to determine: ? Fundamental processes during anodic reactions in hydrogen and carbonaceous atmospheres ? Interfacial effects between metal particles and doped ceria ? Kinetics of redox reaction in the anode material

  14. Effects of electrolyte components on properties of Al alloy anode

    Institute of Scientific and Technical Information of China (English)

    MA Zheng-qing; ZUO Lie; PANG Xu; ZENG Su-min

    2009-01-01

    The effects of Na2SnO3, In(OH)3 and Na2SnO3+In(OH)3 on the properties of Al alloy anode were studied in alkaline medium at 25 ℃. The self-corrosion rate of Al alloy anode was studied by method of H2 immersed in aqueous medium, and the electrochemical properties of Al alloy anode were tested via galvanostatic discharge and dynamic potential methods. The results show that the self-corrosion rate of Al alloy anode in 4 mol/L NaOH+3 mol/L NaAlO2 medium can be minimized by adding Na2SnO3, In(OH)3 and Na2SnO3+ In(OH)3. Na2SnO3, In(OH)3 and Na2SnO3+In(OH)3 make Al anodic potential shift positively in galvanostatic discharging. The most effective additive of Al alloy anode in 4 mol/L NaOH+3 mol/L NaAlO2 medium is 0.075 mol/L Na2SnO3+0.005 mol/L In(OH)3, integrating self-corrosion rate and electrochemical properties.

  15. Bifunctional anode catalysts for direct methanol fuel cells

    DEFF Research Database (Denmark)

    Rossmeisl, Jan; Ferrin, Peter; Tritsaris, Georgios

    2012-01-01

    Using the binding energy of OH* and CO* on close-packed surfaces as reactivity descriptors, we screen bulk and surface alloy catalysts for methanol electro-oxidation activity. Using these two descriptors, we illustrate that a good methanol electro-oxidation catalyst must have three key properties......: (1) the ability to activate methanol, (2) the ability to activate water, and (3) the ability to react off surface intermediates (such as CO* and OH*). Based on this analysis, an alloy catalyst made up of Cu and Pt should have a synergistic effect facilitating the activity towards methanol electro....... Adding Cu to a Pt(111) surface increases the methanol oxidation current by more than a factor of three, supporting our theoretical predictions for improved electrocatalysts....

  16. Environmentally friendly anodization on AZ31 magnesium alloy

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A novel anodization which is environmentally friendly,low voltage and lOW energy consumption was developed to improve corrosion resistance of AZ31 magnesium alloy.The corrosion resistance of the anodic films was studied by electrochemical impedance spectroscopy(EIS)and potentiodynamic polarization techniques.The microstructure and compositions of films were examined by SEM,XPS and XRD.A new kind of organic additive used in the electrolyte is friendly to the environment.The compact,intact and uniform coating with high hardness can be prepared on AZ31 magnesium alloy by the environmentally friendly anodization,which enhances the corrosion resistance of AZ31 Mg alloy significantly.

  17. Electro-catalysts for hydrogen production from ethanol for use in SOFC anodes

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Marcos Aurelio da; Paz Fiuza, Raigenis da; Guedes, Bruna C.; Pontes, Luiz A.; Boaventura, Jaime Soares [UFBA, Salvador, Bahia (Brazil). Energy and Materials Science Group

    2010-07-01

    Nickel and cobalt catalysts, supported on YSZ, were prepared by wet impregnation, with and without citric acid; the metal load was 10 and 35% by weight. The catalyst composition was studied by XRF, XPS and SEM-EDS. At low metal concentration, the results of these techniques presented comparables figures; at high concentration, SEM-EDS suggested a non-uniform distribution. The analysis showed that the solids were mixed oxides and formed an alloy after reduction. The surface passivation was possible under controlled conditions. The catalytic test with the steam reforming of ethanol indicated that the metal load had almost no effect on the catalytic activity, but decreased its selectivity. Afterwards, a unitary SOFC was prepared with deposition of the cathode layer. AFM and EIS were used for the characterization of SOFC components. They showed that the electro-catalyst surface was almost all covered with the metal phase, including the large pore walls of the anode. The YSZ phase dominates the material conductance of the complete SOFC assembly (anode/electrolyte/cathode). The unitary SOFC was tested with hydrogen, gaseous ethanol or natural gas; the SOFC operating with ethanol and hydrogen fuel presented virtually no over-potential. (orig.)

  18. ANODE CATALYST MATERIALS FOR USE IN FUEL CELLS

    DEFF Research Database (Denmark)

    2002-01-01

    Catalyst materials having a surface comprising a composition M¿x?/Pt¿3?/Sub; wherein M is selected from the group of elements Fe, Co, Rh and Ir; or wherein M represent two different elements selected from the group comprising Fe, CO, Rh, Ir, Ni, Pd, CU, Ag, Au and Sn; and wherein Sub represents...... a substrate material selected from Ru and Os; the respective components being present within specific ranges, display improved properties for use inanodes for low-temperature fuel cell anodes for PENFC fuel cells and direct methanol fuel cells....

  19. Solid solution lithium alloy cermet anodes

    Science.gov (United States)

    Richardson, Thomas J.

    2013-07-09

    A metal-ceramic composite ("cermet") has been produced by a chemical reaction between a lithium compound and another metal. The cermet has advantageous physical properties, high surface area relative to lithium metal or its alloys, and is easily formed into a desired shape. An example is the formation of a lithium-magnesium nitride cermet by reaction of lithium nitride with magnesium. The reaction results in magnesium nitride grains coated with a layer of lithium. The nitride is inert when used in a battery. It supports the metal in a high surface area form, while stabilizing the electrode with respect to dendrite formation. By using an excess of magnesium metal in the reaction process, a cermet of magnesium nitride is produced, coated with a lithium-magnesium alloy of any desired composition. This alloy inhibits dendrite formation by causing lithium deposited on its surface to diffuse under a chemical potential into the bulk of the alloy.

  20. Highly efficient anode catalyst with a Ni@PdPt core–shell nanostructure for methanol electrooxidation in alkaline media

    Institute of Scientific and Technical Information of China (English)

    Pei-shu Yu; Chun-tao Liu; Bo Feng; Jia-feng Wan; Li Li; Chun-yu Du

    2015-01-01

    To enhance the electrocatalytic activity of anode catalysts used in alkaline-media direct methanol fuel cells (DMFCs), a Ni@PdPt electrocatalyst was successfully prepared using a three-phase-transfer method. The Ni@PdPt electrocatalyst was characterized by X-ray dif-fraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and high-resolution TEM (HRTEM) techniques. The experimental results indicate that the average particle size of the core–shell-structured Ni@PdPt electrocatalyst is approxi-mately 5.6 nm. The Ni@PdPt electrocatalyst exhibits a catalytic activity 3.36 times greater than that of PdPt alloys for methanol oxidation in alkaline media. The developed Ni@PdPt electrocatalyst offers a promising alternative as a highly electrocatalytically active anode catalyst for alkaline DMFCs.

  1. Effects of sodium tartrate anodizing on fatigue life of TA15 titanium alloy

    Directory of Open Access Journals (Sweden)

    Fu Chunjuan

    2015-08-01

    Full Text Available Anodizing is always used as an effective surface modification method to improve the corrosion resistance and wear resistance of titanium alloy. The sodium tartrate anodizing is a new kind of environmental anodizing method. In this work, the effects of sodium tartrate anodizing on mechanical property were studied. The oxide film was performed on the TA15 titanium alloy using sodium tartrate as the film former. The effects of this anodizing and the traditional acid anodizing on the fatigue life of TA15 alloy were compared. The results show that the sodium tartrate anodizing just caused a slight increase of hydrogen content in the alloy, and had a slight effect on the fatigue life. While, the traditional acid anodizing caused a significant increase of hydrogen content in the substrate and reduced the fatigue life of the alloy significantly.

  2. Pt-Ni and Pt-M-Ni (M = Ru, Sn Anode Catalysts for Low-Temperature Acidic Direct Alcohol Fuel Cells: A Review

    Directory of Open Access Journals (Sweden)

    Ermete Antolini

    2017-01-01

    Full Text Available In view of a possible use as anode materials in acidic direct alcohol fuel cells, the electro-catalytic activity of Pt-Ni and Pt-M-Ni (M = Ru, Sn catalysts for methanol and ethanol oxidation has been widely investigated. An overview of literature data regarding the effect of the addition of Ni to Pt and Pt-M on the methanol and ethanol oxidation activity in acid environment of the resulting binary and ternary Ni-containing Pt-based catalysts is presented, highlighting the effect of alloyed and non-alloyed nickel on the catalytic activity of these materials.

  3. Carbon Supported Polyaniline as Anode Catalyst: Pathway to Platinum-Free Fuel Cells

    CERN Document Server

    Zabrodskii, A G; Malyshkin, V G; Sapurina, I Y

    2006-01-01

    The effectiveness of carbon supported polyaniline as anode catalyst in a fuel cell (FC) with direct formic acid electrooxidation is experimentally demonstrated. A prototype FC with such a platinum-free composite anode exhibited a maximum room-temperature specific power of about 5 mW/cm2

  4. The corrosion protection of several aluminum alloys by chromic acid and sulfuric acid anodizing

    Science.gov (United States)

    Danford, M. D.

    1994-01-01

    The corrosion protection afforded 7075-T6, 7075-T3, 6061-T6, and 2024-T3 aluminum alloys by chromic acid and sulfuric acid anodizing was examined using electrochemical techniques. From these studies, it is concluded that sulfuric acid anodizing provides superior corrosion protection compared to chromic acid anodizing.

  5. Mixed phase Pt-Ru catalyst for direct methanol fuel cell anode by flame aerosol synthesis

    DEFF Research Database (Denmark)

    Chakraborty, Debasish; Bischoff, H.; Chorkendorff, Ib

    2005-01-01

    A spray-flame aerosol catalyzation technique was studied for producing Pt-Ru anode electrodes for the direct methanol fuel cell. Catalysts were produced as aerosol nanoparticles in a spray-flame reactor and deposited directly as a thin layer on the gas diffusion layer. The as-prepared catalyst......Ru1/Vulcan carbon. The kinetics of methanol oxidation on the mixed phase catalyst was also explored by electrochemical impedance spectroscopy. (c) 2005 The Electrochemical Society....

  6. Ni3Mo3C as anode catalyst for high-performance microbial fuel cells.

    Science.gov (United States)

    Zeng, Li-Zhen; Zhao, Shao-Fei; Li, Wei-Shan

    2015-03-01

    Ni3Mo3C was prepared by a modified organic colloid method and explored as anode catalyst for high-performance microbial fuel cell (MFC) based on Klebsiella pneumoniae (K. pneumoniae). The prepared sample was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and Brunauer-Emmett-Teller (BET). The activity of the sample as anode catalyst for MFC based on K. pneumoniae was investigated by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and polarization curve measurement. The results show that the adding of nickel in Mo2C increases the BET surface area of Mo2C and improves the electrocatalytic activity of Mo2C towards the oxidation of microbial fermentation products. The power density of MFC with 3 mg cm(-2) Ni3Mo3C anode is far higher than that of the MFC with carbon felt as anode without any catalyst, which is 19 % higher than that of Mo2C anode and produced 62 % as much as that of Pt anode, indicating that Ni3Mo3C is comparative to noble metal platinum as anode electrocatalyst for MFCs by increasing the loading.

  7. Influence of Metal Sulfides as Anode Catalysts on Performance of H2S SOFC

    Institute of Scientific and Technical Information of China (English)

    钟理; 刘曼; 韩国林; CHUANGKar

    2003-01-01

    Two anode catalysts with Pt, MoS2 and composite metal sulfides (MoS2+NiS), are investigated for electrochemical oxidation of hydrogen sulfide in solid oxide fuel cell (SOFC) at temperatures 750-850℃. The catalysts comprising MoS2 and MoS2+NiS exhibited good electrical conductivity and catalytic activity. MoS2 and composite catalysts were found to be more active than Pt, a widely used catalyst for high temperature H2S/O2 fuel cell at 750-850℃. However, MoS2 itself sublimes above 450℃. In contrast, composite catalysts containing both Mo and transition metal (Ni) are shown to be stable and effective in promoting the oxidation of H2S in SOFC up to 850℃. However, electric contact is poor between the platinum current collecting layer and the composite metal sulfide layer, so that the cell performance becomes worse. This problem is overcome by adding conductive Ag powder into the anode layer (forming MoS2+NiS+Ag anode material) to increase anode electrical conductance instead of applying a thin laver of platinum on the top of anode.

  8. Electrodeposited NiCu Alloy Catalysts for Glucose Oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Lim, Jieun; Park, Hansoo; Kim, Sookil [Chung-Ang Univ., Seoul (Korea, Republic of); Ahn, Sang Hyun; Jang, Jong Hyun [Korea Institute of Science and Technology, Seoul (Korea, Republic of)

    2014-07-15

    NiCu alloys have been suggested as potential candidates for catalysts in glucose oxidation. In this study, NiCu alloys with different compositions were prepared on a glassy carbon substrate by changing the electrodeposition potential to examine the effect of Ni/Cu ratios in alloys on catalytic activity toward glucose oxidation. Cyclic voltammetry and chronoamperometry showed that NiCu alloys had higher catalytic activity than pure Ni and Cu catalysts. Especially, Ni{sub 59}Cu{sub 41} had superior catalytic activity, which was about twice that of Ni at a given oxidation potential. X-ray analyses showed that the oxidation state of Ni in NiCu alloys was increased with the content of Cu by lattice expansion. Ni components in alloys with higher oxidation state were more effective in the oxidation of glucose.

  9. On the role of reactant transport and (surface) alloy formation for the CO tolerance of carbon supported PtRu polymer electrolyte fuel cell catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Kaiser, J.; Colmenares, L.; Jusys, Z.; Behm, R.J. [Abt. Oberflaechenchemie und Katalyse, Universitaet Ulm (Germany); Moertel, R.; Boennemann, H. [Max-Planck-Institut fuer Kohlenforschung, Muelheim a.d. Ruhr (Germany); Koehl, G.; Modrow, H.; Hormes, J. [Physikalisches Institut, Universitaet Bonn (Germany)

    2006-07-15

    The role of atomic scale intermixing for the electrocatalytic activity of bimetallic PtRu anode catalysts in reformate operated polymer electrolyte fuel cells (PEFC) was investigated, exploiting the specific properties of colloid based catalyst synthesis for the selective preparation of alloyed and non-alloyed bimetallic catalysts. Three different carbon supported PtRu catalysts with different degrees of Pt and Ru intermixing, consisting of (i) carbon supported PtRu alloy particles (PtRu/C), (ii) Pt and Ru particles co-deposited on the same carbon support (Pt+Ru/C), and (iii) a mixture of carbon supported Pt and carbon supported Ru (Pt/C+Ru/C) as well as the respective monometallic Pt/C and Ru/C catalysts were prepared and characterized by electron microscopy (TEM), X-ray absorption spectroscopy, and CO stripping. Their performance as PEFC anode catalysts was evaluated by oxidation of a H{sub 2}/2%CO gas mixture (simulated reformate) under fuel cell relevant conditions (elevated temperature, continuous reaction and controlled reactant transport) in a rotating disk electrode (RDE) set-up. The CO tolerance and H{sub 2} oxidation activity of the three catalysts is comparable and distinctly different from that of the monometallic catalysts. The results indicate significant transport of the reactants, CO{sub ad} and/or OH{sub ad}, between Pt and Ru surface areas and particles for all three catalysts, with only subtle differences from the alloy catalyst to the physical mixture. The high activity and CO tolerance of the bimetallic catalysts, through the formation of bimetallic surfaces, is explained, e.g., by contact formation in nanoparticle agglomerates or by material transport and subsequent surface decoration/surface alloy formation during catalyst preparation, conditioning, and operation. The instability and mobility of the catalysts under these conditions closely resembles concepts in gas phase catalysis. (Abstract Copyright [2006], Wiley Periodicals, Inc.)

  10. Surface nanotopography of an anodized Ti–6Al–7Nb alloy enhances cell growth

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Her-Hsiung [Department of Dentistry, National Yang-Ming University, Taipei 112, Taiwan (China); Graduate Institute of Basic Medical Science, China Medical University, Taichung 404, Taiwan (China); Department of Biomedical Informatics, Asia University, Taichung 413, Taiwan (China); Department of Stomatology, Taipei Veterans General Hospital, Taipei 112, Taiwan (China); Wu, Chia-Ping [Institute of Oral Biology, National Yang-Ming University, Taipei 112, Taiwan (China); Sun, Ying-Sui [Department of Dentistry, National Yang-Ming University, Taipei 112, Taiwan (China); Yang, Wei-En [Institute of Oral Biology, National Yang-Ming University, Taipei 112, Taiwan (China); Lee, Tzu-Hsin, E-mail: biomaterials@hotmail.com [School of Dentistry, Chung Shan Medical University, Taichung 402, Taiwan (China); Oral Medicine Center, Chung Shan Medical University Hospital, Taichung 402, Taiwan (China)

    2014-12-05

    Highlights: • An electrochemical anodization was applied to α/β-type Ti–6Al–7Nb alloy surface. • Anodized surface had a nontoxic nanoporous topography. • Anodized surface increased proteins adsorption due to nanotopography. • Anodized surface enhanced cell growth due to nanotopography. • Electrochemical anodization has potential as implant surface treatment. - Abstract: The α/β-type Ti–6Al–7Nb alloy is a potential replacement for α/β-type Ti–6Al–4V alloy, which is widely used in biomedical implant applications. The biological response to implant material is dependent on the surface characteristics of the material. In the present study, a simple and fast process was developed to perform an electrochemical anodization treatment on Ti–6Al–7Nb alloy. The proposed process yielded a thin surface nanotopography, which enhanced cell growth on the Ti–6Al–7Nb alloy. The surface characteristics, including the morphology, wettability, and protein adsorption, were investigated, and the cytotoxicity was evaluated according to International Organization for Standardization 10993-5 specifications. Cell adhesion of human bone marrow mesenchymal stem cells on the test specimens was observed via fluorescence microscopy and scanning electron microscopy. The anodization process produced a surface nanotopography (pore size <100 nm) on anodized Ti–6Al–7Nb alloy, which enhanced the wettability, protein adsorption, cell adhesion, cell migration, and cell mineralization. The results showed that the surface nanotopography produced using the proposed electrochemical anodization process enhanced cell growth on anodized Ti–6Al–7Nb alloy for implant applications.

  11. An anodic alumina supported Ni-Pt bimetallic plate-type catalysts for multi-reforming of methane, kerosene and ethanol

    KAUST Repository

    Zhou, Lu

    2014-05-01

    An anodic alumina supported Ni-Pt bimetallic plate-type catalyst was prepared by a two-step impregnation method. The trace amount 0.08 wt% of Pt doping efficiently suppressed the nickel particle sintering and improved the nickel oxides reducibility. The prepared Ni-Pt catalyst showed excellent performance during steam reforming of methane, kerosene and ethanol under both 3000 h stationary and 500-time daily start-up and shut-down operation modes. Self-activation ability of this catalyst was evidenced, which was considered to be resulted from the hydrogen spillover effect over Ni-Pt alloy. In addition, an integrated combustion-reforming reactor was proposed in this study. However, the sintering of the alumina support is still a critical issue for the industrialization of Ni-Pt catalyst. Copyright © 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

  12. Cell response of anodized nanotubes on titanium and titanium alloys.

    Science.gov (United States)

    Minagar, Sepideh; Wang, James; Berndt, Christopher C; Ivanova, Elena P; Wen, Cuie

    2013-09-01

    Titanium and titanium alloy implants that have been demonstrated to be more biocompatible than other metallic implant materials, such as Co-Cr alloys and stainless steels, must also be accepted by bone cells, bonding with and growing on them to prevent loosening. Highly ordered nanoporous arrays of titanium dioxide that form on titanium surface by anodic oxidation are receiving increasing research interest due to their effectiveness in promoting osseointegration. The response of bone cells to implant materials depends on the topography, physicochemistry, mechanics, and electronics of the implant surface and this influences cell behavior, such as adhesion, proliferation, shape, migration, survival, and differentiation; for example the existing anions on the surface of a titanium implant make it negative and this affects the interaction with negative fibronectin (FN). Although optimal nanosize of reproducible titania nanotubes has not been reported due to different protocols used in studies, cell response was more sensitive to titania nanotubes with nanometer diameter and interspace. By annealing, amorphous TiO2 nanotubes change to a crystalline form and become more hydrophilic, resulting in an encouraging effect on cell behavior. The crystalline size and thickness of the bone-like apatite that forms on the titania nanotubes after implantation are also affected by the diameter and shape. This review describes how changes in nanotube morphologies, such as the tube diameter, the thickness of the nanotube layer, and the crystalline structure, influence the response of cells.

  13. Surface integrity after pickling and anodization of Ti-6Al-4V titanium alloy

    Science.gov (United States)

    Vermesse, Eric; Mabru, Catherine; Arurault, Laurent

    2013-11-01

    The surface integrity of Ti-6Al-4V titanium alloy was studied at different stages of surface treatments, especially pickling and compact anodization, through surface characteristics potentially worsening fatigue resistance.

  14. Formation and dielectric properties of anodic oxide films on Zr–Al alloys

    OpenAIRE

    Koyama, Shun; Aoki, Yoshitaka; Nagata, Shinji; Habazaki, Hiroki

    2011-01-01

    Zr–Al alloys containing up to 26 at.% aluminum, prepared by magnetron sputtering, have been anodized in 0.1 mol dm−3 ammonium pentaborate electrolyte, and the structure and dielectric properties of the resultant anodic oxide films have been examined by grazing incidence X-ray diffraction, transmission electron microscopy, Rutherford backscattering spectroscopy, and AC impedance spectroscopy. The anodic oxide film formed on zirconium consists of monoclinic and tetragonal ZrO2 with the fo...

  15. Reactivity descriptors for direct methanol fuel cell anode catalysts

    DEFF Research Database (Denmark)

    Ferrin, Peter; Nilekar, Anand Udaykumar; Greeley, Jeff

    2008-01-01

    We have investigated the anode reaction in direct methanol fuel cells using a database of adsorption free energies for 16 intermediates on 12 close-packed transition metal surfaces calculated with periodic, self-consistent, density functional theory (DFT-GGA). This database, combined with a simple...

  16. Ultrasmall PdmMn1-mOx binary alloyed nanoparticles on graphene catalysts for ethanol oxidation in alkaline media

    Science.gov (United States)

    Ahmed, Mohammad Shamsuddin; Park, Dongchul; Jeon, Seungwon

    2016-03-01

    A rare combination of graphene (G)-supported palladium and manganese in mixed-oxides binary alloyed catalysts (BACs) have been synthesized with the addition of Pd and Mn metals in various ratios (G/PdmMn1-mOx) through a facile wet-chemical method and employed as an efficient anode catalyst for ethanol oxidation reaction (EOR) in alkaline fuel cells. The as prepared G/PdmMn1-mOx BACs have been characterized by several instrumental techniques; the transmission electron microscopy images show that the ultrafine alloyed nanoparticles (NPs) are excellently monodispersed onto the G. The Pd and Mn in G/PdmMn1-mOx BACs have been alloyed homogeneously, and Mn presents in mixed-oxidized form that resulted by X-ray diffraction. The electrochemical performances, kinetics and stability of these catalysts toward EOR have been evaluated using cyclic voltammetry in 1 M KOH electrolyte. Among all G/PdmMn1-mOx BACs, the G/Pd0.5Mn0.5Ox catalyst has shown much superior mass activity and incredible stability than that of pure Pd catalysts (G/Pd1Mn0Ox, Pd/C and Pt/C). The well dispersion, ultrafine size of NPs and higher degree of alloying are the key factor for enhanced and stable EOR electrocatalysis on G/Pd0.5Mn0.5Ox.

  17. Ceramic anode catalyst for dry methane type molten carbonate fuel cell

    Science.gov (United States)

    Tagawa, T.; Yanase, A.; Goto, S.; Yamaguchi, M.; Kondo, M.

    Oxide catalyst materials for methane oxidation were examined in order to develop the anode electrode for molten carbonate type fuel cell (MCFC). As a primary selection, oxides such as lanthanum (La 2O 3) and samarium (Sm 2O 3) were selected from screening experiments of TPD, TG and tubular reactor. Composite materials of these oxides with titanium fine powder were assembled into a cell unit for MCFC as the anode electrode. Steady-state activities were observed with these anode electrode materials when hydrogen was used as a fuel. When methane was directly charged to anode as a fuel (dry methane operation), a power generation with steady state was observed on both lanthanum and samarium composites after gradual decrease of open circuit electromotive force (OCV) and closed circuit current (CCI). The steady-state activity held as long as 144 h of continuous operation.

  18. Design of a surface alloy catalyst for steam reforming

    DEFF Research Database (Denmark)

    Besenbacher, F.; Chorkendorff, Ib; Clausen, B.S.;

    1998-01-01

    Detailed studies of elementary chemical processes on well-characterized single crystal surfaces have contributed substantially to the understanding of heterogeneous catalysis. insight into the structure of surface alloys combined with an understanding of the relation between the surface composition...... and reactivity is shown to lead directly to new ideas for catalyst design, The feasibility of such an approach is illustrated by the synthesis, characterization, and tests of a high-surface area gold-nickel catalyst for steam reforming....

  19. Effect of intermetallic phases on the anodic oxidation and corrosion of 5A06 aluminum alloy

    Science.gov (United States)

    Li, Song-mei; Li, Ying-dong; Zhang, You; Liu, Jian-hua; Yu, Mei

    2015-02-01

    Intermetallic phases were found to influence the anodic oxidation and corrosion behavior of 5A06 aluminum alloy. Scattered intermetallic particles were examined by scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) after pretreatment. The anodic film was investigated by transmission electron microscopy (TEM), and its corrosion resistance was analyzed by electrochemical impedance spectroscopy (EIS) and Tafel polarization in NaCl solution. The results show that the size of Al-Fe-Mg-Mn particles gradually decreases with the iron content. During anodizing, these intermetallic particles are gradually dissolved, leading to the complex porosity in the anodic film beneath the particles. After anodizing, the residual particles are mainly silicon-containing phases, which are embedded in the anodic film. Electrochemical measurements indicate that the porous anodic film layer is easily penetrated, and the barrier plays a dominant role in the overall protection. Meanwhile, self-healing behavior is observed during the long immersion time.

  20. Characterization and Tribological Properties of Hard Anodized and Micro Arc Oxidized 5754 Quality Aluminum Alloy

    Directory of Open Access Journals (Sweden)

    M. Ovundur

    2015-03-01

    Full Text Available This study was initiated to compare the tribological performances of a 5754 quality aluminum alloy after hard anodic oxidation and micro arc oxidation processes. The structural analyses of the coatings were performed using XRD and SEM techniques. The hardness of the coatings was determined using a Vickers micro-indentation tester. Tribological performances of the hard anodized and micro arc oxidized samples were compared on a reciprocating wear tester under dry sliding conditions. The dry sliding wear tests showed that the wear resistance of the oxide coating generated by micro arc oxidation is remarkably higher than that of the hard anodized alloy.

  1. ENVIRONMENTAL FRIENDLY ANODIZING ON AZ91D MAGNESIUM ALLOYS AND COATING CHARACTERISTICS

    Institute of Scientific and Technical Information of China (English)

    A. Saijo; M. Hino; M. Hiramatsu; T. Kanadani

    2005-01-01

    An environmental friendly anodizing treatment (Anomag) from a phosphate-based solution without heavy metals on AZ91D magnesium alloy was studied. The characteristics of the coatings,such as structure, composition and corrosion resistance were investigated. The effects of this anodizing treatment on the mechanical properties were examined. X-ray diffraction (XRD) analysis revealed that the structure of the coatings is amorphous or glassy. In salt spray tests coatings with an average thickness of 10μm had an anticorrosive performance of over 1000 hours. Fatigue tests revealed that anodizing onto AZ91D magnesium alloy does not affect the fatigue strength. These results demonstrate the utility of this anodizing treatment on magnesium alloy for application as a structural material, such as in the automotive field.

  2. Fabrication of the superhydrophobic surface on aluminum alloy by anodizing and polymeric coating

    Science.gov (United States)

    Liu, Wenyong; Luo, Yuting; Sun, Linyu; Wu, Ruomei; Jiang, Haiyun; Liu, Yuejun

    2013-01-01

    We reported the preparation of the superhydrophobic surface on aluminum alloy via anodizing and polymeric coating. Both the different anodizing processes and different polymeric coatings of aluminum alloy were investigated. The effects of different anodizing conditions, such as electrolyte concentration, anodization time and current on the superhydrophobic surface were discussed. The results showed that a good superhydrophobic surface was facilely fabricated by polypropylene (PP) coating after anodizing. The optimum conditions for anodizing were determined by orthogonal experiments. When the concentration of oxalic acid was 10 g/L, the concentration of NaCl was 1.25 g/L, anodization time was 40 min, and anodization current was 0.4 A, the best superhydrophobic surface on aluminum alloy with the contact angle (CA) of 162° and the sliding angle of 2° was obtained. On the other hand, the different polymeric coatings, such as polystyrene (PS), polypropylene (PP) and polypropylene grafting maleic anhydride (PP-g-MAH) were used to coat the aluminum alloy surface after anodizing. The results showed that the superhydrophobicity was most excellent by coating PP, while the duration of the hydrophobic surface was poor. By modifying the surface with the silane coupling agent before PP coating, the duration of the superhydrophobic surface was improved. The morphologies of the superhydrophobic surface were further confirmed by optical microscope (OM) and scanning electron microscope (SEM). Combined with the material of PP with the low surface free energy, the micro/nano-structures of the surface resulted in the superhydrophobicity of the aluminum alloy surface.

  3. Porous anodic film formation on an Al-3.5wt% Cu alloy

    Energy Technology Data Exchange (ETDEWEB)

    Paez, M. A.; Skeldon, P.; Thompson, G. E.; Saez, M.; Bustos, O.; Monsalve, A.

    2003-07-01

    The morphological development of porous anodic films in the initial stages is examined during anodizing an Al-3,5 wt% Cu alloy in phosphoric acid. Using transmission electron microscopy a sequence of ultramicrotomed anodic sections reveals the dynamic evolution of numerous features in the thickening film in the initial stages of anodizing. The morphological changes in the anodic oxides in the initial stages of its formation appears related to the formation of bubbles during film growth. From Rutherford backscattering spectroscopy (RBS) analysis of the film, the formation of the bubbles is associated with the enrichment of copper in the alloy due to growth of the anodic oxide. On the other hand, during constant current anodizing of Al-Cu in phosphoric acid, the current efficiency is considerably less than that for anodizing super pure aluminium under similar conditions. >From the contrasting results between the charge consumed calculated from RBS and the real charge consumed during anodizing, oxygen gas bubbles generation and copper oxidation seem to be of less importance on the low efficiency for film formation. It is apparent that the main cause of losing efficiency for film growth on Al-Cu is associated with generation of oxygen ar residual second phase, with the development of stresses in the film and, the consequence of these effects on film cracking during film growth. (Author) 10 refs.

  4. Photoelectrochemical evidence of nitrogen incorporation during anodizing sputtering--deposited Al-Ta alloys.

    Science.gov (United States)

    Zaffora, A; Santamaria, M; Di Franco, F; Habazaki, H; Di Quarto, F

    2016-01-01

    Anodic films were grown to 20 V on sputtering-deposited Al-Ta alloys in ammonium biborate and borate buffer solutions. According to glow discharge optical emission spectroscopy, anodizing in ammonium containing solution leads to the formation of N containing anodic layers. Impedance measurements did not evidence significant differences between the dielectric properties of the anodic films as a function of the anodizing electrolyte. Photoelectrochemical investigation allowed evidencing that N incorporation induces a red-shift in the light absorption threshold of the films due to the formation of allowed localized states inside their mobility gap. The estimated Fowler threshold for the internal photoemission processes of electrons resulted to be independent of the anodizing electrolyte confirming that N incorporation does not appreciably affect the density of states distribution close to the conduction band mobility edge. The transport of photogenerated carriers has been rationalized according to the Pai-Enck model of geminate recombination.

  5. Furfural Hydrogenation on Alloyed Copper Catalysts With Additives of Ferrosilicium

    Directory of Open Access Journals (Sweden)

    T. K. Akilov

    2015-12-01

    Full Text Available The present work is dedicated to the study of influence of ferrosilicium additives [FA*-ferroalloy containing (% mass: 46.8 Si, ~53,0 Fe, other are (C, P, S impurities] on the activity of alloyed Gu-Al = 50-50 catalyst in the reaction of furfural hydrogenation under hydrogen pressure. Components content varied (% mass: Cu- 40...49, aluminum- 50, FA* -1.0...10.0. The catalysts were prepared from 1g alloys by leaching it with 20% of aqueous solution of caustic soda in boiling water-bath during 1 hour. The phase composition and structure of alloys were investigated by means of roentgenographic and X-ray spectrum methods.

  6. Fabrication of the superhydrophobic surface on aluminum alloy by anodizing and polymeric coating

    Energy Technology Data Exchange (ETDEWEB)

    Liu Wenyong, E-mail: lwy@iccas.ac.cn [Key Laboratory of Advanced Materials and Technology for Packaging, Hunan University of Technology, Zhuzhou 412007 (China); College of Packaging and Materials Engineering, Hunan University of Technology, Zhuzhou 412007 (China); Luo Yuting; Sun Linyu [College of Packaging and Materials Engineering, Hunan University of Technology, Zhuzhou 412007 (China); Wu Ruomei, E-mail: cailiaodian2004@126.com [College of Packaging and Materials Engineering, Hunan University of Technology, Zhuzhou 412007 (China); Jiang Haiyun [College of Packaging and Materials Engineering, Hunan University of Technology, Zhuzhou 412007 (China); Liu Yuejun [Key Laboratory of Advanced Materials and Technology for Packaging, Hunan University of Technology, Zhuzhou 412007 (China); College of Packaging and Materials Engineering, Hunan University of Technology, Zhuzhou 412007 (China)

    2013-01-01

    Graphical abstract: The hydrophobic surface on aluminum alloy fabricated by anodizing and polymeric coating. Highlights: Black-Right-Pointing-Pointer Anodizing and polymeric coating were used to prepare a superhydrophobic surface on aluminum alloy. Black-Right-Pointing-Pointer Superhydrophobic surfaces with a high water contact angle of 162 Degree-Sign and a low rolling angle of 2 Degree-Sign were obtained. Black-Right-Pointing-Pointer The method is facile, and the materials are inexpensive, and is expected to be used widely. - Abstract: We reported the preparation of the superhydrophobic surface on aluminum alloy via anodizing and polymeric coating. Both the different anodizing processes and different polymeric coatings of aluminum alloy were investigated. The effects of different anodizing conditions, such as electrolyte concentration, anodization time and current on the superhydrophobic surface were discussed. The results showed that a good superhydrophobic surface was facilely fabricated by polypropylene (PP) coating after anodizing. The optimum conditions for anodizing were determined by orthogonal experiments. When the concentration of oxalic acid was 10 g/L, the concentration of NaCl was 1.25 g/L, anodization time was 40 min, and anodization current was 0.4 A, the best superhydrophobic surface on aluminum alloy with the contact angle (CA) of 162 Degree-Sign and the sliding angle of 2 Degree-Sign was obtained. On the other hand, the different polymeric coatings, such as polystyrene (PS), polypropylene (PP) and polypropylene grafting maleic anhydride (PP-g-MAH) were used to coat the aluminum alloy surface after anodizing. The results showed that the superhydrophobicity was most excellent by coating PP, while the duration of the hydrophobic surface was poor. By modifying the surface with the silane coupling agent before PP coating, the duration of the superhydrophobic surface was improved. The morphologies of the superhydrophobic surface were further confirmed

  7. Corrosion and anodic behaviour of zinc and its ternary alloys in alkaline battery electrolytes

    Science.gov (United States)

    Suresh Kannan, A. R.; Muralidharan, S.; Sarangapani, K. B.; Balaramachandran, V.; Kapali, V.

    Several attempts are being made to avoid the use of mercury-bearing zinc/zinc alloys as anodes in alkaline power sources. The work presented here suggests the possible use of some ternary alloys based on zinc of purity 99.9 to 99.95 wt.% as anodes in 10 M NaOH solution with sodium citrate, sodium stannate and calcium oxide as complexing agents and inhibitors. The corrosion of zinc and its alloys in 10 M NaOH solution is under cathodic control; in other alkaline electrolytes, it is under anodic control. Anode efficiency of up to 99.0% is achieved. The corrosion rates of zinc and its alloys are found to be comparable with those of mercury-bearing zinc in the chosen electrolytes. It is concluded that both dry cells and Zn-air batteries can be constructed with the above anodes and alkaline electrolytes. Thus, the presence of mercury, either in the anode or in the electrolyte, is avoided.

  8. Novel alloys to improve the electrochemical behavior of zinc anodes for zinc/air battery

    Science.gov (United States)

    Lee, Chang Woo; Sathiyanarayanan, K.; Eom, Seung Wook; Yun, Mun Soo

    In our continued efforts for improving the performance of zinc anodes for a Zn/air battery, we now report the preparation of three alloys and improved performances of anodes made up with these alloys. The alloys contained zinc, nickel, and indium with different weight percentages and were calcined at two different temperatures. Out of the six alloys, the alloy which has a composition of zinc 90%, nickel 7.5% and Indium 2.5% and fired at 500 °C is found to be the best. In the case of the hydrogen evolution reaction, this alloy had its potential shifted to a more negative potential. As far as the cyclic voltammograms were concerned, the difference between the anodic and cathodic part was minimal when compared with other alloys. Surprisingly, this alloy had reversibility even after 100 cycles of the cyclic voltammogram. This is a clear indication that dendrite formation was reduced to a considerable extent. Images taken with a scanning electron microscope also indicated reduced dendrite formation.

  9. Band gap structure modification of amorphous anodic Al oxide film by Ti-alloying

    DEFF Research Database (Denmark)

    Canulescu, Stela; Rechendorff, K.; Borca, C. N.;

    2014-01-01

    The band structure of pure and Ti-alloyed anodic aluminum oxide has been examined as a function of Ti concentration varying from 2 to 20 at. %. The band gap energy of Ti-alloyed anodic Al oxide decreases with increasing Ti concentration. X-ray absorption spectroscopy reveals that Ti atoms...... are not located in a TiO2 unit in the oxide layer, but rather in a mixed Ti-Al oxide layer. The optical band gap energy of the anodic oxide layers was determined by vacuum ultraviolet spectroscopy in the energy range from 4.1 to 9.2 eV (300–135 nm). The results indicate that amorphous anodic Al2O3 has a direct...

  10. Surface integrity after pickling and anodization of Ti–6Al–4V titanium alloy

    OpenAIRE

    Vermesse, Eric; Mabru, Catherine; Arurault, Laurent

    2013-01-01

    International audience; The surface integrity of Ti–6Al–4V titanium alloy was studied at different stages of surface treatments, especially pickling and compact anodization, through surface characteristics potentially worsening fatigue resistance. No significant changes of the equiaxe microstructure were detected between sample core and surface, or after the pickling and anodization steps. Surface hydrogen and oxygen superficial contents were found to remain unchanged. Roughness characteristi...

  11. Calcination/acid-activation treatment of an anodic oxidation TiO2/Ti film catalyst

    Institute of Scientific and Technical Information of China (English)

    YAO Zhongping; JIANG Yanli; JIANG Zhaohua; ZHU Hongkui; BAI Xuefeng

    2009-01-01

    The aim of this work was to investigate the effects of calcination/acid-activation on the composition, structure, and photocatalytic (PC) re-duction property of an anodic oxidation TiO2/Ti film catalyst. The surface morphology and phase composition were examined by scanning electron microscopy and X-ray diffraction. The catalytic property of the film catalysts was evaluated through the removal rate of potassium chromate during the PC reduction process. The results showed that the film catalysts were composed of anatase and mtile TiO2 with a mi-cro-porous surface structure. The calcination treatment increased the content of TiO2 in the film, changed the relative ratio of anatase and rutile TiO2, and decreased the size of the micro pores of the film cat.a/ysts. The removal rate of potassium chromate was related to the tech-nique parameters of calcination/acid-activation treatment. When the anodic oxidation TiO2Ti film catalyst was calcined at 873 K for 30 min and then acid-activated in the concentrated H2SO4 for 60 min, it presented the highest catalytic property, with the removal rate of potassium chromate of 96.3% during the PC reduction process under the experimental conditions.

  12. Effects of Alloying Element Ca on the Corrosion Behavior and Bioactivity of Anodic Films Formed on AM60 Mg Alloys

    Directory of Open Access Journals (Sweden)

    Anawati Anawati

    2016-12-01

    Full Text Available Effects of alloying element Ca on the corrosion behavior and bioactivity of films formed by plasma electrolytic oxidation (PEO on AM60 alloys were investigated. The corrosion behavior was studied by conducting electrochemical tests in 0.9% NaCl solution while the bioactivity was evaluated by soaking the specimens in simulated body fluid (SBF. Under identical anodization conditions, the PEO film thicknesses increased with increasing Ca content in the alloys, which enhanced the corrosion resistance in NaCl solution. Thicker apatite layers grew on the PEO films of Ca-containing alloys because Ca was incorporated into the PEO film and because Ca was present in the alloys. Improvement of corrosion resistance and bioactivity of the PEO-coated AM60 by alloying with Ca may be beneficial for biodegradable implant applications.

  13. Morphological and Chemical Relationships in Nanotubes Formed by Anodizing of Ti6al4v Alloy

    Directory of Open Access Journals (Sweden)

    Kaczmarek- Pawelska A.

    2014-12-01

    Full Text Available The electrochemical formation of oxide nanotubes on the Ti6Al4V alloy has been so far difficult due to easy dissolution of vanadium reach β-phase of the two phase material. Due to the topographical heterogeneity of the anodic layer in nano and microscale at anodizing of the Ti6Al4V alloy we focused to establish the relationships between nanotube diameters on both phases of the alloy and fluorides concentration in electrolyte. We studied the effect of fluoride concentration (0.5-0.7 wt.% in 99% ethylene glycol on morphological parameters of nanotube layer on the Ti6Al4V alloy anodized at 20V for 20 min. Nanotubes with diameter ~40-50 nm ±5nm on the entire Ti6Al4V alloy surface in electrolyte containing 0.6% wt. NH4F were obtained. Microscale roughness studies revealed that nanotubular layer on α-phase is thicker than on β-phase. The annealing of nanotube layers at 600°C for 2h in air, nitrogen and argon, typically performed to improve their electrical properties, influenced chemical composition and morphology of nanotubes on the Ti6Al4V alloy. The vanadium oxides (VO2, V2O3, V2O5 were present in surface nanotube layer covering both phases of the alloy and the shape of nanotubes was preserved after annealing in nitrogen.

  14. Highly Dispersed Alloy Catalyst for Durability

    Energy Technology Data Exchange (ETDEWEB)

    Murthi, Vivek S.; Izzo, Elise; Bi, Wu; Guerrero, Sandra; Protsailo, Lesia

    2013-01-08

    Achieving DOE's stated 5000-hr durability goal for light-duty vehicles by 2015 will require MEAs with characteristics that are beyond the current state of the art. Significant effort was placed on developing advanced durable cathode catalysts to arrive at the best possible electrode for high performance and durability, as well as developing manufacturing processes that yield significant cost benefit. Accordingly, the overall goal of this project was to develop and construct advanced MEAs that will improve performance and durability while reducing the cost of PEMFC stacks. The project, led by UTC Power, focused on developing new catalysts/supports and integrating them with existing materials (membranes and gas diffusion layers (GDLs)) using state-of-the-art fabrication methods capable of meeting the durability requirements essential for automotive applications. Specifically, the project work aimed to lower platinum group metals (PGM) loading while increasing performance and durability. Appropriate catalysts and MEA configuration were down-selected that protects the membrane, and the layers were tailored to optimize the movements of reactants and product water through the cell to maximize performance while maintaining durability.

  15. Influence of Mg and Ti on the microstructure and electrochemical performance of aluminum alloy sacrificial anodes

    Institute of Scientific and Technical Information of China (English)

    MA Jingling; WEN Jiuba; LI Xudong; ZHAO Shengli; YAN Yanfu

    2009-01-01

    The experiments focused on the influence of magnesium and titanium as additional alloying elements on the microstructure and electro-chemical behavior of Al-Zn-ln sacrificial anodes. The electrochemical behavior of the aluminum sacrificial anode with 3 wt.% sodium chlo-fide solution was studied by electrochemical impedance spectroscopy (EIS) tests. It was found that a microstructure with few precipitates and refined grains could be achieved by adding 1 wt.% Mg and 0.05 wt.% Ti to the Al-Zn-In alloy, resulting in the improved current capacity and efficiency of the alloy. The equivalent circuit based on the EIS experimental data revealed less corrosion and lower adsorbed corrosion pro-duction on the surface of the aluminum alloy with a combination of 1 wt.% Mg and 0.05 wt.% Ti, which suggested that the corrosion behav-ior seemed to be strongly related to the presence of precipitate particles in the aluminum alloy, and moderate amounts of precipitate particles could be beneficial to the electrochemical performance of the aluminum alloy sacrificial anode.

  16. PEO of pre-anodized Al–Si alloys: Corrosion properties and influence of sealings

    Energy Technology Data Exchange (ETDEWEB)

    Mohedano, M., E-mail: marta.mohedano@hzg.de [Helmholtz Zentrum Geesthacht, Magnesium Innovation Centre, Institute of Materials Research, Max-Planck-Str. 1, D-21502 Geesthacht (Germany); Matykina, E.; Arrabal, R.; Mingo, B.; Pardo, A. [Departamento de Ciencia de Materiales, Facultad de Ciencias Químicas, Universidad Complutense, 28040 Madrid (Spain)

    2015-08-15

    Highlights: • A356 gravity-cast and rheocast pre-anodized aluminium alloys were coated by PEO. • Different sealing techniques were applied after the coating process. • Iron-rich constituents of the substrate occlude the continuity of the porous anodic film. • PEO coatings consisted of a mixture of α-Al{sub 2}O{sub 3}, γ-Al{sub 2}O{sub 3} and mullite. • Post-treatments improved both hydrophobic and corrosion properties. - Abstract: Voltage-controlled PEO coatings were developed on A356 aluminum alloys (gravity-cast and rheocast) with a pre-anodized layer. The influence of the alloy manufacturing process and the effect of Si-rich phase on the structure and composition of the oxide layers were evaluated using SEM, EDS and XRD. The pre-anodized oxide layer preserves the microstructure of the substrate due to the presence of secondary phases that have a different behavior relative to the matrix during anodizing. PEO coatings consisted of a mixture of α-Al{sub 2}O{sub 3}, γ-Al{sub 2}O{sub 3} and mullite. The corrosion behavior and the effectiveness of different sealing techniques based on salts of nickel, cobalt, cerium and phosphonic acid were also studied. Post-treatments improved the hydrophobic properties of the coatings and showed a beneficial effect, significantly increasing the coating impedance and thereby reducing the susceptibility to corrosion.

  17. Production of NiTi shape memory alloys via electro-deoxidation utilizing an inert anode

    Energy Technology Data Exchange (ETDEWEB)

    Jiao Shuqiang, E-mail: sjiao@ustb.edu.c [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China)] [Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB2 3QZ (United Kingdom); Zhang Linlin; Zhu Hongmin [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Fray, Derek J., E-mail: djf25@cam.ac.u [Department of Materials Science and Metallurgy, University of Cambridge, Cambridge CB2 3QZ (United Kingdom)

    2010-09-30

    NiTi shape memory alloys (SMA) with equiatomic composition of Ni and Ti were prepared by electro-deoxidation, in molten calcium chloride, at 950 {sup o}C. Constant voltage electro-deoxidation was conducted using a NiTiO{sub 3} cathode, and either a carbon anode or a novel CaRuO{sub 3}/CaTiO{sub 3} composite inert anode. Both anode materials successfully allowed NiTi shape memory alloy to be obtained. The primary difference is that molecular oxygen was produced on the inert anode, instead of environmentally undesired CO{sub 2} greenhouse gases on the carbon anode. Indeed, it was found that carbon could successfully be substituted with conductive calcium titanate-calcium ruthenate composites for electro-deoxidation. Furthermore, DSC was used to analyze the phase transformation of NiTi shape memory alloys, with results revealing the existence of reversible martensite-austenite phase transformations during the cooling and heating process.

  18. Influence of bi modification of pt anode catalyst in direct formic acid fuel cells.

    Science.gov (United States)

    Kang, Sungjin; Lee, Jaeyoung; Lee, Jae Kwang; Chung, Seung-Young; Tak, Yongsug

    2006-04-13

    The influence of Bi modification of Pt anode catalyst on the performance of direct formic acid fuel cells was investigated. Compared with the unmodified Pt anode, the Bi modified Pt (PtBi(m)) electrode prepared by under-potential deposition (UPD) caused faster electrocatalytic oxidation of formic acid at the same value of the overpotential, and thus, PtBi(m) resulted in an increase in the power performance of direct formic acid fuel cells. Electrochemical impedance spectra helped to explain the difference of performance between the unmodified Pt and Bi modified Pt electrodes. Solution conductivity and dehydration phenomena occurring in highly concentrated formic acid solutions can also explain the higher power performance of PtBi(m).

  19. Anodic behaviour of oxidised Ni-Fe alloys in cryolite-alumina melts

    Energy Technology Data Exchange (ETDEWEB)

    Chapman, Vivien, E-mail: v.singleton@student.unsw.edu.a [Centre for Electrochemical and Mineral Processing, School of Chemical Engineering, University of New South Wales, Sydney 2052 (Australia); Welch, Barry J. [Welbank Consulting Ltd., PO Box 207, Whitianga 3542 (New Zealand); Skyllas-Kazacos, Maria [Centre for Electrochemical and Mineral Processing, School of Chemical Engineering, University of New South Wales, Sydney 2052 (Australia)

    2011-01-01

    Nickel-iron alloys have been identified as promising inert anode candidates for the Hall-Heroult process. In this study, binary Ni-Fe alloys of various compositions were subjected to short-term galvanostatic electrolysis in a cryolite-alumina bath at 960 {sup o}C. Prior to electrolysis, the anodes were oxidised at 800 {sup o}C for 48 h, forming a protective scale. Fe{sub 2}O{sub 3}, Ni{sub x}Fe{sub 3-x}O{sub 4} and Ni{sub x}Fe{sub 1-x}O were identified as the major scale components using a combination of X-ray diffraction (XRD) analysis and energy dispersive X-ray spectroscopy (EDX). Anodes having Ni content of 50-65 wt% performed adequately during short-term electrolysis, operating at a steady potential of 3-3.5 V vs. AlF{sub 3}/Al. Overall, it was found that the pre-formed oxide scale was effective in reducing anode wear and fluoridation. In the absence of a pre-formed scale, anodes were shown to undergo appreciable internal corrosion and/or passivation due to metal fluoride formation. Analysis of the anodes following electrolysis was performed using XRD and electron microprobe analysis (EPMA).

  20. Manganese Detection with a Metal Catalyst Free Carbon Nanotube Electrode: Anodic versus Cathodic Stripping Voltammetry.

    Science.gov (United States)

    Yue, Wei; Bange, Adam; Riehl, Bill L; Riehl, Bonnie D; Johnson, Jay M; Papautsky, Ian; Heineman, William R

    2012-10-01

    Anodic stripping voltammetry (ASV) and cathodic stripping voltammetry (CSV) were used to determine Mn concentration using metal catalyst free carbon nanotube (MCFCNT) electrodes and square wave stripping voltammetry (SWSV). The MCFCNTs are synthesized using a Carbo Thermal Carbide Conversion method which results in a material that does not contain residual transition metals. Detection limits of 120 nM and 93 nM were achieved for ASV and CSV, respectively, with a deposition time of 60 s. CSV was found to be better than ASV in Mn detection in many aspects, such as limit of detection and sensitivity. The CSV method was used in pond water matrix addition measurements.

  1. Manganese Detection with a Metal Catalyst Free Carbon Nanotube Electrode: Anodic versus Cathodic Stripping Voltammetry

    Science.gov (United States)

    Yue, Wei; Bange, Adam; Riehl, Bill L.; Riehl, Bonnie D.; Johnson, Jay M.; Papautsky, Ian; Heineman, William R.

    2013-01-01

    Anodic stripping voltammetry (ASV) and cathodic stripping voltammetry (CSV) were used to determine Mn concentration using metal catalyst free carbon nanotube (MCFCNT) electrodes and square wave stripping voltammetry (SWSV). The MCFCNTs are synthesized using a Carbo Thermal Carbide Conversion method which results in a material that does not contain residual transition metals. Detection limits of 120 nM and 93 nM were achieved for ASV and CSV, respectively, with a deposition time of 60 s. CSV was found to be better than ASV in Mn detection in many aspects, such as limit of detection and sensitivity. The CSV method was used in pond water matrix addition measurements. PMID:24235806

  2. Effect of equal-channel angular pressing on pitting corrosion resistance of anodized aluminum-copper alloy

    Institute of Scientific and Technical Information of China (English)

    In-Joon SON; Hiroaki NAKANO; Satoshi OUE; Shigeo KOBAYASHI; Hisaaki FUKUSHIMA; Zenji HORITA

    2009-01-01

    The effect of equal-channel angular pressing(ECAP) on the pitting corrosion resistance of anodized Al-Cu alloy was investigated by electrochemical techniques in a solution containing 0.2 mol/L AlCl3 and also by surface analysis. Anodizing was conducted for 20 min at 200 and 400 A/m2 in a solution containing 1.53 mol/L H2SO4 and 0.018 5 mol/L Al2(SO4)3-16H2O at 20 ℃. Anodized Al-Cu alloy was immediately dipped in boiling water for 20 min to seal the micro pores present in anodic oxide films. The time required before initiating pitting corrosion of anodized Al-Cu alloy is longer with ECAP than without, indicating that ECAP process improves the pitting corrosion resistance of anodized Al-Cu alloy. Second phase precipitates such as Si, Al-Cu-Mg and Al-Cu-Si-Fe-Mn intermetallic compounds are present in Al-Cu alloy and the size of these precipitates is greatly decreased by application of ECAP. Al-Cu-Mg intermetallic compounds are dissolved during anodization, whereas the precipitates composed of Si and Al-Cu-Si-Fe-Mn remain in anodic oxide films due to their more noble corrosion potential than Al. FE-SEM and EPMA observation reveal that the pitting corrosion of anodized Al-Cu alloy occurs preferentially around Al-Cu-Si-Fe-Mn intermetallic compounds, since the anodic oxide films are absent at the boundary between the normal oxide films and these impurity precipitates. The improvement of pitting corrosion resistance of anodized Al-Cu alloy processed by ECAP appears to be attributed to a decrease in the size of precipitates, which act as origins of pitting corrosion.

  3. Fabrication of the micro/nano-structure superhydrophobic surface on aluminum alloy by sulfuric acid anodizing and polypropylene coating.

    Science.gov (United States)

    Wu, Ruomei; Liang, Shuquan; Liu, Jun; Pan, Anqiang; Yu, Y; Tang, Yan

    2013-03-01

    The preparation of the superhydrophobic surface on aluminum alloy by anodizing and polypropylene (PP) coating was reported. Both the different anodizing process and different PP coatings of aluminum alloy were investigated. The effects of different anodizing conditions, such as electrolyte concentration, anodization time and current on the superhydrophobic surface were discussed. By PP coating after anodizing, a good superhydrophobic surface was facilely fabricated. The optimum conditions for anodizing were determined by orthogonal experiments. After the aluminium-alloy was grinded with 600# sandpaper, pretreated by 73 g/L hydrochloric acid solution at 1 min, when the concentration of sulfuric acid was 180 g/L, the concentration of oxalic acid was 5 g/L, the concentration of potassium dichromate was 10 g/L, the concentration of chloride sodium was 50 g/L and 63 g/L of glycerol, anodization time was 20 min, and anodization current was 1.2 A/dm2, anodization temperature was 30-35 degrees C, the best micro-nanostructure aluminum alloy films was obtained. On the other hand, the PP with different concentrations was used to the PP with different concentrations was used to coat the aluminum alloy surface after anodizing. The results showed that the best superhydrophobicity was achieved by coating PP, and the duration of the superhydrophobic surface was improved by modifying the coat the aluminum alloy surface after anodizing. The results showed that the best superhydrophobicity was surface with high concentration PP. The morphologies of micro/nano-structure superhydrophobic surface were further confirmed by scanning electron microscope (SEM). The material of PP with the low surface free energy combined with the micro/nano-structures of the surface resulted in the superhydrophobicity of the aluminum alloy surface.

  4. Study of Composite Hardcoat Anodizing of Aluminum Alloy 6063 and Its Friction Behaviors

    Institute of Scientific and Technical Information of China (English)

    LIU Shi-yong; ZHANG Hui-chen; GAO Xue-min; LIU Wei; SHI Ya-qin

    2004-01-01

    A composite hard-anodized coating containing micro PTFE (polytetrafluoroethylene) particles on aluminum alloy 6063 was produced by adding micro PTFE particles into the traditional hardcoat anodizing solution. The size of the PTFE particles is around 2 μ m in diameter and the content of the PTFE particles in the composite coating is within 2%-3% by area percentage. Thickness of the composite coating can reach up to 70 μ m after one hour's anodizing. Surface hardness of the composite coating is between 400-480 HV0.1. The average friction coefficient of the composite coating against steel under dry friction test is 0.11, which is 17% lower than that obtained by traditional hardcoat anodizing.

  5. Study of Composite Hardcoat Anodizing of Aluminum Alloy 6063 and Its Friction Behaviors

    Institute of Scientific and Technical Information of China (English)

    LIUShi-yong; ZHANGHui-chen; GAOXue-min; LIUWei; SHIYa-qin

    2004-01-01

    A composite hard-anodized coating containing micro PTFE (polytetrafluoroethylene) particles on aluminum alloy 6063 was produced by adding micro PTFE particles into the traditional hardcoat anodizing solution. The size of the PTFE particles is around 2μm in diameter and the content of the PTFE particles in the composite coating is within 2%-3% by area percentage. Thickness of the composite coating cart reach up to 70μm after one hour's anodizing. Surface hardness of the composite coating is between 4(RI-480 HV0.1, The average friction coefficient of the composite coating against steel under dry friction tost is 0.11, which is 17% lower than that obtained by traditional hardcoat anodizing.

  6. The Microstructure and Capacitance Characterizations of Anodic Titanium Based Alloy Oxide Nanotube

    Directory of Open Access Journals (Sweden)

    Po Chun Chen

    2013-01-01

    Full Text Available This paper presents a simple anodization process to fabricate ordered nanotubes (NTs of titanium and its alloys (Ti-Mo and Ti-Ta. TiO2, MoO3, and Ta2O5 are high dielectric constant materials for ultracapacitor application. The anodic titanium oxide contains a compact layer on the NT film and a barrier layer under the NT film. However, the microstructure of oxide films formed by anodic Ti-Mo and Ti-Ta alloys contains six layers, including a continuous compact layer, a continuous partial porous layer, a porous layer, a net layer, an ordering NT film, and an ordering compact barrier layer. There are extra layers, which are a partial porous layer and a porous layer, not presented on the TiO2 NT film. In this paper, we fabricated very high surface area ordered nanotubes from Ti and its alloys. Based on the differences of alloys elements and compositions, we investigated and calculated the specific capacitance of these alloys oxide nanotubes.

  7. Property of anodic coatings obtained in an organic, environmental friendly electrolyte on aluminum alloy 2024-T3

    Science.gov (United States)

    Zhang, R. F.; Shi, H. W.; Liu, Z. L.; Zhang, S. F.; Zhang, Y. Q.; Guo, S. B.

    2014-01-01

    Anodic coatings were obtained by micro arc oxidation on aluminum alloy 2024-T3 in a solution containing only 10 g/L sodium phytate. The morphology, composition, structure and corrosion resistance of anodic coatings were systematically investigated. The results show that the working voltage continually increases during 3 min and bright sparks appear after 25 s. Anodic coatings are evenly formed on the substrate and about 2 μm thick. XPS and XRD analyses reveal that the obtained coatings are mainly composed of α-Al2O3 and γ-Al2O3. Compared with the substrate, the corrosion resistance of the anodized aluminum alloys is improved.

  8. Carbon treated commercial aluminium alloys as anodes for aluminium-air batteries in sodium chloride electrolyte

    Science.gov (United States)

    Pino, M.; Herranz, D.; Chacón, J.; Fatás, E.; Ocón, P.

    2016-09-01

    An easy treatment based in carbon layer deposition into aluminium alloys is presented to enhance the performance of Al-air primary batteries with neutral pH electrolyte. The jellification of aluminate in the anode surface is described and avoided by the carbon covering. Treated commercial Al alloys namely Al1085 and Al7475 are tested as anodes achieving specific capacities above 1.2 Ah g-1vs 0.5 Ah g-1 without carbon covering. The influence of the binder proportion in the treatment as well as different carbonaceous materials, Carbon Black, Graphene and Pyrolytic Graphite are evaluated as candidates for the covering. Current densities of 1-10 mA cm-2 are measured and the influence of the alloy explored. A final battery design of 4 cells in series is presented for discharges with a voltage plateau of 2 V and 1 Wh g-1 energy density.

  9. FeCrO Nanoparticles as Anode Catalyst for Ethane Proton Conducting Fuel Cell Reactors to Coproduce Ethylene and Electricity

    Directory of Open Access Journals (Sweden)

    Jian-Hui Li

    2011-01-01

    Full Text Available Ethylene and electrical power are cogenerated in fuel cell reactors with FeCr2O4 nanoparticles as anode catalyst, La0.7Sr0.3FeO3- (LSF as cathode material, and BaCe0.7Zr0.1Y0.2O3- (BCZY perovskite oxide as proton-conducting ceramic electrolyte. FeCr2O4, BCZY and LSF are synthesized by a sol-gel combustion method. The power density increases from 70 to 240 mW cm−2, and the ethylene yield increases from about 14.1% to 39.7% when the operating temperature of the proton-conducting fuel cell reactor increases from 650∘C to 750∘C. The FeCr2O4 anode catalyst exhibits better catalytic performance than nanosized Cr2O3 anode catalyst.

  10. ANODIC BEHAVIOR OF ALLOY 22 IN HIGH NITRATE BRINES AT TEMPERATURES HIGHER THAN 100C

    Energy Technology Data Exchange (ETDEWEB)

    G.O. LLEVBARE; J.C. ESTILL; A. YILMAZ; R.A. ETIEN; G.A. HUST M.L. STUART

    2006-04-20

    Alloy 22 (N06022) may be susceptible to crevice corrosion in chloride solutions. Nitrate acts as an inhibitor to crevice corrosion. Several papers have been published regarding the effect of nitrate on the corrosion resistance of Alloy 22 at temperatures 100 C and lower. However, very little is known about the behavior of this alloy in highly concentrated brines at temperatures above 100 C. In the current work, electrochemical tests have been carried out to explore the anodic behavior of Alloy 22 in high chloride high nitrate electrolytes at temperatures as high as 160 C at ambient atmospheres. Even though Alloy 22 may adopt corrosion potentials in the order of +0.5 V (in the saturated silver chloride scale), it does not suffer crevice corrosion if there is high nitrate in the solution. That is, the inhibitive effect of nitrate on crevice corrosion is active for temperatures higher than 100 C.

  11. Enhanced corrosion resistance and biocompatibility of β-type Ti–25Nb–25Zr alloy by electrochemical anodization

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Her-Hsiung [Department of Dentistry, National Yang-Ming University, Taipei, 112 Taiwan (China); Graduate Institute of Basic Medical Science, China Medical University, Taichung, 404 Taiwan (China); Department of Biomedical Informatics, Asia University, Taichung, 413 Taiwan (China); Department of Stomatology, Taipei Veterans General Hospital, Taipei, 112 Taiwan (China); Wu, Chia-Ping; Sun, Ying-Sui; Huang, Hsun-Miao [Institute of Oral Biology, National Yang-Ming University, Taipei, 112 Taiwan (China); Lee, Tzu-Hsin, E-mail: biomaterials@hotmail.com [School of Dentistry, Chung Shan Medical University, Taichung, 402 Taiwan (China); Oral Medicine Center, Chung Shan Medical University Hospital, Taichung, 402 Taiwan (China)

    2013-12-31

    The biocompatibility of implants is largely determined by their surface characteristics. This study presents a novel method for performing electrochemical anodization on β-type Ti–25Nb–25Zr alloy with a low elastic modulus (approximately 70 GPa). This method results in a thin hybrid layer capable of enhancing the surface characteristics of the implants. We investigated the surface topography and microstructure of the resulting Ti–25Nb–25Zr alloy. The corrosion resistance was evaluated using potentiodynamic polarization curve measurements in simulated body fluid. The cytotoxicity was evaluated according to International Organization for Standardization 10993–5 specification. Cell adhesion of human bone marrow mesenchymal stem cells on the test specimens was observed using scanning electron microscopy and fluorescence microscopy. The anodization produced a thin (approximately 40 nm-thick) hybrid oxide layer with a nanoporous outer sublayer (pore size < 15 nm) and a dense inner layer. The thin hybrid oxide layer increased the corrosion resistance of the Ti–25Nb–25Zr alloy by increasing the corrosion potential and decreasing both the corrosion rate and passive current. Ti–25Nb–25Zr alloys with and without anodization treatment were non-toxic. Surface nanotopography on the anodized Ti–25Nb–25Zr alloy enhanced protein adsorption and cell adhesion. Our results demonstrate that electrochemical anodization increases the corrosion resistance and cell adhesion of β-type Ti–25Nb–25Zr alloy while providing a lower elastic modulus suitable for implant applications. - Highlights: • An electrochemical anodization was applied to β-type Ti–25Nb–25Zr alloy surface. • Anodized surface had nanoscale hybrid oxide layer. • Anodized surface increased corrosion resistance due to dense inner sublayer. • Anodized surface enhanced cell adhesion due to nanoporous outer sublayer. • Electrochemical anodization has potential as implant surface treatment.

  12. Effect of temperature on the anodizing process of aluminum alloy AA 5052

    Science.gov (United States)

    Theohari, S.; Kontogeorgou, Ch.

    2013-11-01

    The effect of temperature (10-40 °C) during the anodizing process of AA 5052 for 40 min in 175 g/L sulfuric acid solution at constant voltage (15 V) was studied in comparison with pure aluminum. The incorporated magnesium species in the barrier layer result in the further increase of the minimum current density passed during anodizing, as the temperature increases, by about 42% up to 30 °C and then by 12% up to 40 °C. Then during the anodizing process for 40 min a blocking effect on oxide film growth was gradually observed as the temperature increased until 30 °C. The results of EDAX analysis on thick films reveal that the mean amount of the magnesium species inside the film is about 50-70% less than that in the bulk alloy, while it is higher at certain locations adjacent to the film surface at 30 °C. The increase of anodizing temperature does not influence the porosity of thin films (formed for short times) on pure aluminum, while it reduces it on the alloy. At 40 °C the above mentioned blocking effects disappear. It means that the presence of magnesium species causes an impediment to the effect of temperature on iss, on the film thickness and on the porosity of thin films, only under conditions where film growth takes place without significant loss of the anodizing charge to side reactions.

  13. Novel Carbon Nanotubes-supported NiB Amorphors Alloy Catalyst for Benzene Hydrogenation

    Institute of Scientific and Technical Information of China (English)

    Mei Hua YANG; Rong Bin ZHANG; Feng Yi LI

    2004-01-01

    The NiB amorphous alloy catalysts supported on CNTs and alumina were prepared by impregnation and chemical reduction. The gas-phase benzene hydrogenation was used as a probe reaction to evaluate the catalytic activity. The result showed that the NiB amorphous alloy catalyst supported on carbon nanotubes exhibited higher activity than that supported on alumina.

  14. Characteristics of Anodized Layer in Investment Cast Ni50Ti50 Shape Memory Alloy

    Directory of Open Access Journals (Sweden)

    Shimaa H. El-Hadad

    2014-01-01

    Full Text Available NiTi shape memory alloys are promising implant materials due to their shape memory effect and super elasticity. In the current study, some Ni50Ti50 (mass % SMAs samples were prepared by investment casting. These samples were then anodized and thermally treated to improve the surface properties. A fully saturated oxide layer was obtained. The structure and hardness properties of the anodized surfaces were then investigated. A hard porous layer with no free Ni atoms could be obtained which can be used as prebiomimetic surface for biological application.

  15. Surface Characteristics and Electrochemical Impedance Investigation of Spark-Anodized Ti-6Al-4V Alloy

    Science.gov (United States)

    Garsivaz jazi, M. R.; Golozar, M. A.; Raeissi, K.; Fazel, M.

    2014-04-01

    In this study, the surface characteristic of oxide films on Ti-6Al-4V alloy formed by an anodic oxidation treatment in H2SO4/H3PO4 electrolyte at potentials higher than the breakdown voltage was evaluated. Morphology of the surface layers was studied by scanning electron microscope. The results indicated that the diameter of pores and porosity of oxide layer increase by increasing the anodizing voltage. The thickness measurement of the oxide layers showed a linear increase of thickness with increasing the anodizing voltage. The EDS analysis of oxide films formed in H2SO4/H3PO4 at potentials higher than breakdown voltage demonstrated precipitation of sulfur and phosphor elements from electrolyte into the oxide layer. X-ray diffraction was employed to exhibit the effect of anodizing voltage on the oxide layer structure. Roughness measurements of oxide layer showed that in spark anodizing, the Ra and Rz parameters would increase by increasing the anodizing voltage. The structure and Corrosion properties of oxide layers were studied using electrochemical impedance spectroscopy (EIS) techniques, in 0.9 wt.% NaCl solution. The obtained EIS spectra and their interpretation in terms of an equivalent circuit with the circuit elements indicated that the detailed impedance behavior is affected by three regions of the interface: the space charge region, the inner compact layer, and outer porous layer.

  16. Identification of non-precious metal alloy catalysts for selective hydrogenation of acetylene

    DEFF Research Database (Denmark)

    Studt, Felix; Abild-Pedersen, Frank; Bligaard, Thomas

    2008-01-01

    The removal of trace acetylene from ethylene is performed industrially by palladium hydrogenation catalysts ( often modified with silver) that avoid the hydrogenation of ethylene to ethane. In an effort to identify catalysts based on less expensive and more available metals, density functional...... calculations were performed that identified relations in heats of adsorption of hydrocarbon molecules and fragments on metal surfaces. This analysis not only verified the facility of known catalysts but identified nickel- zinc alloys as alternatives. Experimental studies demonstrated that these alloys...

  17. Study of The Pd-B/γ-Al2O3 Amorphous Alloy Catalyst

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The Pd-B/γ-Al2O3 amorphous alloy catalyst and Pd/γ-Al2O3 crystalline metal catalyst were prepared by KBH4 reduction and routine impregnation, respectively. Pd-B/γ-A12O3 and Pd/γ-A12O3 catalysts were characterized by XRD and SEM. It was found that the catalytic activity of the Pd-B/γ-A12O3 amorphous alloy catalyst was higher than that of the Pd/γ-A12O3crystalline metal catalyst in the anthraquinone hydrogenation.

  18. Anodic Fabrication of Ti-Ni-O Nanotube Arrays on Shape Memory Alloy

    Directory of Open Access Journals (Sweden)

    Qiang Liu

    2014-04-01

    Full Text Available Surface modification with oxide nanostructures is one of the efficient ways to improve physical or biomedical properties of shape memory alloys. This work reports a fabrication of highly ordered Ti-Ni-O nanotube arrays on Ti-Ni alloy substrates through pulse anodization in glycerol-based electrolytes. The effects of anodization parameters and the annealing process on the microstructures and surface morphology of Ti-Ni-O were studied using scanning electron microscope and Raman spectroscopy. The electrolyte type greatly affected the formation of nanotube arrays. A formation of anatase phase was found with the Ti-Ni-O nanotube arrays annealed at 450 °C. The oxide nanotubes could be crystallized to rutile phase after annealing treatment at 650 °C. The Ti-Ni-O nanotube arrays demonstrated an excellent thermal stability by keeping their nanotubular structures up to 650 °C.

  19. Anodic Layer of Pb-Ca-Sn-Ce Alloy for Maintenance-Free Lead/Acid Batteries

    Institute of Scientific and Technical Information of China (English)

    Li Dangguo; Zhou Genshu; Lin Guanfa; Zheng Maosheng

    2005-01-01

    The anodic films of novel Pb-Ca-Sn-Ce alloy, traditional Pb-Ca-Sn and Pb-Sb alloys formed in sulfuric solution at anodic +0.9 V potential corrosion for 6 h were investigated by means of XPS, XRD methods and AC impedance measurement. The results show that the growth of Pb(Ⅱ) oxide on the new Pb-Ca-Sn-Ce alloy surface is inhibited. The AC impedance measurement shows that resistance of the corrosion layer of novel Pb-Ca-Sn-Ce alloy decreases. It is found that the novel Pb-Ca-Sn-Ce alloy can encourage the development of PbO2 in the scale, and enhance the conductivity of the anodic scale. Hence the deep recycling properties of the battery can be expected better.

  20. Corrosion behavior of Cu-Ni-Ag-Al alloy anodes in aluminium electrolysis

    Institute of Scientific and Technical Information of China (English)

    徐君莉; 石忠宁; 邱竹贤

    2004-01-01

    The behavior of Cu-Ni-Ag-Al alloy used as anode for aluminum electrolysis was directly visualized in a two-compartment see-through cell during electrolysis, and its performances were tested at 850℃ in acidic electrolyte molten salts consisting of 39.3 % NaF-43.7 % AlF3-8 % NaCl-5 % CAF2-4 % Al2 O3 for 40 h in a laboratory cell. The results show that nascent oxygen oxidizes the anodic surface to form oxide film at the beginning of electrolysis. X-ray diffraction analysis of alloy surface show that the oxide film on the anodic surface consists of CuO, NiO, Al2O3,CuAl2 O4 and NiAl2 O4. However, SEM image shows the oxide film is porous, loose and easy to fall into electrolyte and to contaminate aluminum. The corrosion mechanism of metal anodes was analyzed.

  1. Electrochemical Fabrication of Pd-Ag Alloy Nanowire Arrays in Anodic Alumina Oxide Template

    Institute of Scientific and Technical Information of China (English)

    Erhong YUE; Gang YU; Yuejun OUYANG; Baicheng WENG; Weiwei SI; Liyuan YE

    2008-01-01

    The synthesis of Pd-Ag alloy nanowires in nanopores of porous anodic aluminum oxide (AAO) template by electrochemical deposition technique was reported.Pd-Ag alloy nanowires with 16%-25% Ag content are expected to serve as candidates of useful nanomaterials for the hydrogen sensors.Scanning electron microscopy (SEM) and energy dispersed X-ray spectroscopy (EDX) were employed to characterize the morphologies and compositions of the Pd-Ag nanowires.X-ray diffraction (XRD) was used to characterize the phase properties of the Pd-Ag nanowires.Pd-Ag alloy nanowire arrays with 17.28%-23.76% Ag content have been successfully fabricated by applying potentials ranging from -0.8 to -1.0 V (vs SCE).The sizes of the alloy nanowires are in agreement with the diameter of AAO nanopores.The underpotential deposition of Ag+ on Pd and Au plays an important role in producing an exceptionally high Ag content in the alloy.Alloy compositions can still be controlled by adjusting the ion concentration ratio of Pd2+ and Ag+ and the electrodeposition processes.XRD shows that nanowires obtained are in the form of alloy of Pd and Ag.

  2. Study on the Rare Earth Sealing Procedure of the Porous Film of Anodized 2024 Aluminum Alloy

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The rare earth sealing procedure of the porous film of anodized aluminum alloy 2024 was studied with the fieldemission scanning electron microscope (SEM) and X-ray energy dispersive spectroscopy (EDS). The results show thatRE solution can form cerium oxide/hydroxides precipitation in the pores of the anodized coating at the beginning ofsealing. At the same time, the spherical deposits formed on the surface of the anodized coating created a barrierto the precipitation of RE solution in the pores. When the pore-structured anodizing film is covered all with thespherical deposits, RE conversion coating will form on the surface of the anodized coating. The reaction of thecoating formation was investigated by employing cyclic voltammetry. The results indicate that accelerator H2O2 actsas the source of O2 by carrying chemical reaction in course of coating formation. In the mean time, it maybe carrieselectrochemical reaction to generate alkaline condition to accelerate the coating formation. The porous structure ofthe film is beneficial to the precipitation of the cerium hydroxides film.

  3. Phosphorus-Based Alloy Materials for Advanced Potassium-Ion Battery Anode.

    Science.gov (United States)

    Zhang, Wenchao; Mao, Jianfeng; Li, Sean; Chen, Zhixin; Guo, Zaiping

    2017-02-22

    Potassium-ion batteries (PIBs) are interesting as one of the alternative metal-ion battery systems to lithium-ion batteries (LIBs) due to the abundance and low cost of potassium. We have herein investigated Sn4P3/C composite as a novel anode material for PIBs. The electrode delivered a reversible capacity of 384.8 mA h g(-1) at 50 mA g(-1) and a good rate capability of 221.9 mA h g(-1), even at 1 A g(-1). Its electrochemical performance is better than any anode material reported so far for PIBs. It was also found that the Sn4P3/C electrode displays a discharge potential plateau of 0.1 V in PIBs, slightly higher than for sodium-ion batteries (SIBs) (0.01 V), and well above the plating potential of metal. This diminishes the formation of dendrites during cycling, and thus Sn4P3 is a relatively safe anode material, especially for application in large-scale energy storage, where large amounts of electrode materials are used. Furthermore, a possible reaction mechanism of the Sn4P3/C composite as PIB anode is proposed. This work may open up a new avenue for further development of alloy-based anodes with high capacity and long cycle life for PIBs.

  4. Advanced image analysis of the surface pattern emerging in Ni3Al intermetallic alloys on anodization

    Directory of Open Access Journals (Sweden)

    Marco Salerno

    2016-07-01

    Full Text Available Anodization of Ni3Al alloy is of interest in the field of industrial manufacturing, thanks to the formation of protective oxide layer on the materials working in corrosive environments and high temperatures. However, homogeneous surface treatment is paramount for technological applications of this material. The anodization conditions have to be set outside the ranges of corrosion and burning, which is the electric field enhanced anodic dissolution of the metal. In order to check against occurrence of these events, proper quantitative means for assessing the surface quality have to be developed and established. We approached this task by advanced analysis of scanning electron microscope images of anodized Ni3Al plates. The anodization was carried out in 0.3 M citric acid at two temperatures of 0 and 30°C and at voltages in the range of 2 12 V. Different figures can be used to characterize the quality of the surface, in terms of uniformity. Here, the concept of regularity ratio spread is used for the first time on surfaces of technological interest. Additionally, the Minkowski parameters have been calculated and their meaning is discussed.

  5. Advanced image analysis of the surface pattern emerging in Ni3Al intermetallic alloys on anodization

    Science.gov (United States)

    Salerno, Marco; Stępniowski, Wojciech; Cieślak, Grzegorz; Norek, Małgorzata; Michalska-Domańska, Marta; Karczewski, Krzysztof; Chilimoniuk, Paulina; Polkowski, Wojciech; Jóźwik, Paweł; Bojar, Zbigniew

    2016-07-01

    Anodization of Ni3Al alloy is of interest in the field of industrial manufacturing, thanks to the formation of protective oxide layer on the materials working in corrosive environments and high temperatures. However, homogeneous surface treatment is paramount for technological applications of this material. The anodization conditions have to be set outside the ranges of corrosion and “burning”, which is the electric field enhanced anodic dissolution of the metal. In order to check against occurrence of these events, proper quantitative means for assessing the surface quality have to be developed and established. We approached this task by advanced analysis of scanning electron microscope images of anodized Ni3Al plates. The anodization was carried out in 0.3 M citric acid at two temperatures of 0 and 30°C and at voltages in the range of 2 12 V. Different figures can be used to characterize the quality of the surface, in terms of uniformity. Here, the concept of regularity ratio spread is used for the first time on surfaces of technological interest. Additionally, the Minkowski parameters have been calculated and their meaning is discussed.

  6. Surface characteristics and electrochemical corrosion behavior of a pre-anodized microarc oxidation coating on titanium alloy.

    Science.gov (United States)

    Cui, W F; Jin, L; Zhou, L

    2013-10-01

    A porous bioactive titania coating on biomedical β titanium alloy was prepared by pre-anodization followed by micro arc oxidation technology. The effects of pre-anodization on the phase constituent, morphology and electrochemical corrosion behavior of the microarc oxidation coating were investigated. The results show that pre-anodization has less influence on the phase constituent and the surface morphology of the microarc oxidation coating, but improves the inner layer density of the microarc oxidation coating. The decrease of plasma discharge strength due to the presence of the pre-anodized oxide film contributes to the formation of the compact inner layer. The pre-anodized microarc oxidation coating effectively inhibits the penetration of the electrolyte in 0.9% NaCl solution and thus increases the corrosion resistance of the coated titanium alloy in physiological solution.

  7. Formation of titanium dioxide nanotubes on Ti–30Nb–xTa alloys by anodizing

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Eun-Sil [Department of Dental Materials and Research Center of Nano-Interface Activation for Biomaterials, School of Dentistry, Chosun University, Gwangju (Korea, Republic of); Jeong, Yong-Hoon [Department of Dental Materials and Research Center of Nano-Interface Activation for Biomaterials, School of Dentistry, Chosun University, Gwangju (Korea, Republic of); Biomechanics and Tissue Engineering Laboratory, Division of Orthodontics, College of Dentistry, The Ohio State University, Columbus, OH (United States); Choe, Han-Cheol, E-mail: hcchoe@chosun.ac.kr [Department of Dental Materials and Research Center of Nano-Interface Activation for Biomaterials, School of Dentistry, Chosun University, Gwangju (Korea, Republic of); Brantley, William A. [Division of Restorative, Prosthetic and Primary Care Dentistry, College of Dentistry, The Ohio State University, Columbus, OH (United States)

    2013-12-31

    The goal of this study was to investigate the formation of titanium dioxide nanotubes on the surface of cast Ti–30Nb–xTa alloys by anodizing. The anodization technique for creating the nanotubes utilized a potentiostat and an electrolyte containing 1 M H{sub 3}PO{sub 4} with 0.8 wt.% NaF. The grain size of the Ti–30Nb–xTa alloys increased as the Ta content increased. Using X-ray diffraction, for the Ti–30Nb alloy the main peaks were identified as α″ martensite with strong peaks of β phase. The phases in the Ti–30Nb–xTa alloys changed from a duplex (α″ + β) microstructure to solely β phase with increasing Ta content. The nanotubes that formed on the surface of the Ti–30Nb–xTa alloys were amorphous TiO{sub 2} without an evidence of the crystalline anatase or rutile forms of TiO{sub 2}. Scanning electron microscopy revealed that the average diameters of the small and large nanotubes on the Ti–30Nb alloy not containing Ta were approximately 100 nm and 400 nm, respectively, whereas the small and large nanotubes on the alloy had diameters of approximately 85 nm and 300 nm, respectively. As the Ta content increased from 0 to 15 wt.%, the average lengths of the nanotubes increased from 2 μm to 3.5 μm. Energy-dispersive X-ray spectroscopy indicated that the nanotubes were principally composed of Ti, Nb, Ta, O and F. Contact angle measurements showed that the nanotube surface had good wettability by water droplets. - Highlights: • TiO{sub 2} nanotube layers on anodized Ti-30Nb-xTa alloys have been investigated. • Nanotube surface had an amorphous structure without heat treatment. • Nanotube diameter of Ti-30Nb-xTa decreased, whereas tube layer increased with Ta content. • The nanotube surface exhibited the low contact angle and good wettability.

  8. Electrocatalysis of fuel cells reaction on Pt and Pt-bimetallic anode catalysts: A selective review

    Directory of Open Access Journals (Sweden)

    Stamenković Vojislav

    2002-01-01

    Full Text Available In this review we selectively summarize recent progress, primarily from our laboratory, in the development of interrelationships between the kinetics of the fuel cells reactions and the structure/composition of anode catalysts. The focus is placed on two types of metallic surfaces: platinum single crystals and bimetallic surfaces based on Pt. In the first part it was illustrated that the hydcogen reaction is structure sensitive process, with Pt(110 being an order of magnitude more active than either of the atomically "flatter" (100 and (111 surfaces. The hydrogen reaction on Pt(hkl modified by pseudomorphic Pd (submonolayers shows the "volcano-like" behavior, having the maximum rate on Pt(111 modified by 1 ML of Pd. The Pt(111-Pd system is used to demonstrate how the energetics of intermediates formed in the hydrogen reaction is affected by interfacial bonding and energetic constraints produced between pseudomorphic Pd films and the Pt(111 substrate. In the second part it was shown that the oxidation of Ha in the presence of CO occurs concurrently with CO oxidation on Pt and Pt bimetallic surfaces. The Pt-Ru system is used to demonstrate that both the bifunctional effect and the ligand effect contribute to the influence of Ru on the CO oxidation rate and for Hz oxidation process in the presence of CO. The knowledge is then used to create the real-life catalyst with the catalytic activities which are, to the greatest extend possible similar to the tailor-made surface.

  9. Adhesive strength of medical polymer on anodic oxide nanostructures fabricated on biomedical β-type titanium alloy.

    Science.gov (United States)

    Hieda, Junko; Niinomi, Mitsuo; Nakai, Masaaki; Cho, Ken; Mohri, Tomoyoshi; Hanawa, Takao

    2014-03-01

    Anodic oxide nanostructures (nanopores and nanotubes) were fabricated on a biomedical β-type titanium alloy, Ti-29Nb-13Ta-4.6Zr alloy (TNTZ), by anodization in order to improve the adhesive strength of a medical polymer, segmented polyurethane (SPU), to TNTZ. TNTZ was anodized in 1.0M H3PO4 solution with 0.5 mass% NaF using a direct-current power supply at a voltage of 20V. A nanoporous structure is formed on TNTZ in the first stage of anodization, and the formation of a nanotube structure occurs subsequently beneath the nanoporous structure. The nanostructures formed on TNTZ by anodization for less than 3,600s exhibit higher adhesive strengths than those formed at longer anodization times. The adhesive strength of the SPU coating on the nanoporous structure formed on top of TNTZ by anodization for 1,200s improves by 144% compared to that of the SPU coating on as-polished TNTZ with a mirror surface. The adhesive strength of the SPU coating on the nanotube structure formed on TNTZ by anodization for 3,600s increases by 50%. These improvements in the adhesive strength of SPU are the result of an anchor effect introduced by the nanostructures formed by anodization. Fracture occurs at the interface of the nanoporous structure and the SPU coating layer. In contrast, in the case that SPU coating has been performed on the nanotube structure, fracture occurs inside the nanotubes.

  10. ROLE OF ULTRASOUND IN MECHANISMS OF ANODE-CATHODE INTERACTIONS DURING ELECTROSPARK ALLOYING

    Directory of Open Access Journals (Sweden)

    N. M. Chigrinova

    2016-01-01

    Full Text Available The paper reveals results of investigations on mass transfer kinetics and dynamics of coating formation while using integral electrospark alloying method with additional ultrasonic exposure at different stages of formation. Nowadays, a classical method for electrospark alloying with hard-alloy anodes and impulse AC voltage frequency on the vibration exciter coil from 20 to 1600 Hz has been mainly used for application of protective and strengthening coatings within permissible thickness and characteristics. The key aspect of ultrasonic exposure application (frequency 22–44 kHz during electrospark alloying is the possibility to increase further thickness of coatings to be formed even after reaching a brittle fracture threshold of the coating material. Methodology of the executed research activity has been based on integrated studies (gravimetric, metallographic, X-ray diffraction and electron microscopic of coatings which are to be formed through compositions produced while using method of high-energy hot compaction and a “refractory carbide (WC and a binding material“ system in the form of alloy based on nickel from the series of “colmonoy” Ni – Ni3B system which is alloyed with additions of copper and silicon. The initial surface treatment within ultrasonic frequency range (22–44 kHz contributes to a noticeable increase in the mass transfer rate, which is primarily determined by chemical composition and thermodynamic stability of anodes. It is due to surface activation in the process of its preliminary deformation at ultrasonic frequency which creates additional conditions for striking of a spark.The final ultrasonic treatment improves coating quality due to its additional forging that leads to an increase of its structure homogeneity and density.

  11. A Practical Anodic and Cathodic Curve Intersection Model to Understand Multiple Corrosion Potentials of Fe-Based Glassy Alloys in OH- Contained Solutions.

    Science.gov (United States)

    Li, Y J; Wang, Y G; An, B; Xu, H; Liu, Y; Zhang, L C; Ma, H Y; Wang, W M

    2016-01-01

    A practical anodic and cathodic curve intersection model, which consisted of an apparent anodic curve and an imaginary cathodic line, was proposed to explain multiple corrosion potentials occurred in potentiodynamic polarization curves of Fe-based glassy alloys in alkaline solution. The apparent anodic curve was selected from the measured anodic curves. The imaginary cathodic line was obtained by linearly fitting the differences of anodic curves and can be moved evenly or rotated to predict the number and value of corrosion potentials.

  12. Using Mechanical Alloying to Create Bimetallic Catalysts for Vapor-Phase Carbon Nanofiber Synthesis

    Directory of Open Access Journals (Sweden)

    Laura Guevara

    2015-10-01

    Full Text Available Carbon nanofibers were generated over bimetallic catalysts in an atmospheric pressure chemical vapor deposition (APCVD reactor. Catalyst compositions of Fe 30 at%, Cu and Ni 30 at% and Cu were mechanically alloyed using high-energy ball milling over durations of 4, 8, 12, 16, and 20 h. The catalyst powders were then used to produce carbon nanofibers in ethylene and hydrogen (4:1 at temperatures of 500, 550, and 600 °C. The microstructures of the catalysts were characterized as a function of milling time as well as at deposition temperature. The corresponding carbon deposition rates were assessed and are correlated to the microstructural features of each catalyst. The milling process directly determines the performance of each catalyst toward carbon deposition, and both catalysts performed comparably to those made by traditional co-precipitation methods. Considerations in miscible and immiscible nanostructured alloy systems are discussed.

  13. The Incorporation of Lithium Alloying Metals into Carbon Matrices for Lithium Ion Battery Anodes

    Science.gov (United States)

    Hays, Kevin A.

    An increased interest in renewable energies and alternative fuels has led to recognition of the necessity of wide scale adoption of the electric vehicle. Automotive manufacturers have striven to produce an electric vehicle that can match the range of their petroleum-fueled counterparts. However, the state-of-the-art lithium ion batteries used to power the current offerings still do not come close to the necessary energy density. The energy and power densities of the lithium ion batteries must be increased significantly if they are going to make electric vehicles a viable option. The chemistry of the lithium ion battery, based on lithium cobalt oxide cathodes and graphite anodes, is limited by the amount of lithium the cathode can provide and the anode will accept. While these materials have proven themselves in portable electronics over the past two decades, plausible higher energy alternatives do exist. The focus is of this study is on anode materials that could achieve a capacity of more than 3 times greater than that of graphite anodes. The lithium alloying anode materials investigated and reported herein include tin, arsenic, and gallium arsenide. These metals were synthesized with nanoscale dimensions, improving their electrochemical and mechanical properties. Each exhibits their own benefits and challenges, but all display opportunities for incorporation in lithium ion batteries. Tin is incorporated in multilayer graphene nanoshells by introducing small amounts of metal in the core and, separately, on the outside of these spheres. Electrolyte decomposition on the anode limits cycle life of the tin cores, however, tin vii oxides introduced outside of the multilayer graphene nanoshells have greatly improved long term battery performance. Arsenic is a lithium alloying metal that has largely been ignored by the research community to date. One of the first long term battery performance tests of arsenic is reported in this thesis. Anodes were made from nanoscale

  14. Optimization of Manganese and Magnesium Contents in As-cast Aluminum-Zinc-Indium Alloy as Sacrificial Anode

    Institute of Scientific and Technical Information of China (English)

    Mohammed R. Saeri; Ahmad Keywni

    2011-01-01

    In this study, effects of manganese and magnesium content on the electrochemical properties of Al-Zn-ln sacrificial anode were studied in 0.5 mol/L NaCl solution (pH=5). The aluminum base alloy with different amounts of Mn and Mg were melted at 750℃, then casted at molds at 25℃. Corrosion experiments were mounted to determine the optimal effect of Mn and Mg on the efficiencies of the aluminum alloy anodes. The corroded and unexposed sample surfaces were subjected to microstructure characterization by optical and scanning electron microscopy. AI-Zn-ln alloy doped with 0%, 0.01%, 0.05%.0.2% and 0.3% by weights of Mn and 0%, 0.5%, 1.0%, 1.5%, 2.0%, 2.5% and 3.0% by weights of Mg were prepared to determine the effect of Mn and Mg on anode efficiency in the environment. The different microstructures of the evolved AI- Zn-ln-Mg-Mn alloy were correlated with the anode efficiencies. The Al-5.0%Zn-2.0%Mg-0.15%Mn-0.02%ln gave the best anode efficiency (about 83%). The microstructures of the corroded surface of the optimized alloy revealed decreased distribution of the pockets of localized attacks which are characteristics of pitting (or crevice) corrosion.

  15. Anodic galvanostatic polarization of AA2024-T3 aircraft alloy in conventional mineral acids

    Energy Technology Data Exchange (ETDEWEB)

    Kozhukharov, S., E-mail: stephko1980@abv.bg [Department of Chemical Sciences, University of Chemical Technology and Metallurgy, 8 “Kliment Okhridski” Blvd, 1756, Sofia (Bulgaria); Girginov, Ch. [Department of Chemical Sciences, University of Chemical Technology and Metallurgy, 8 “Kliment Okhridski” Blvd, 1756, Sofia (Bulgaria); Avramova, I. [Institute of General and Inorganic Chemistry, Bulgarian Academy of Science, 11 “Georgi Bonchev” Str., 1113, Sofia (Bulgaria); Machkova, M. [Department of Chemical Sciences, University of Chemical Technology and Metallurgy, 8 “Kliment Okhridski” Blvd, 1756, Sofia (Bulgaria)

    2016-09-01

    The present study is devoted to the determination of the impact of the anodization of AA2024-T3 alloys in HCl, HNO{sub 3}, H{sub 2}SO{sub 4} or H{sub 3}PO{sub 4} on the samples’ surface morphology and properties. Subsequent systematic assessments were performed by Scanning Electron Microscopy (SEM), Energy Dispersion X-Ray Spectroscopy (EDX) and X-ray Photoelectron Spectroscopy (XPS). These observations were combined with Linear Voltammetry (LVA) and Electrochemical Impedance Spectroscopy (EIS) after 48 and 168 h of exposure to a 3.5% NaCl model corrosive medium. The main result is, that completely different effects were observed in accordance to the acid used. It was established that the monoprotonic acids have a deep destructive effect due to dissolution of the alloy components, whereas the polyprotonic ones possess either indistinguishable influence, or surface film formation. - Highlights: • AA2024 was polarized anodically in 15%{sub wt} acid solutions at 15 mA cm{sup −2} for 2 h. • Four mineral acids were selected for investigation: HCl, HNO{sub 3}, H{sub 2}SO{sub 4} and H{sub 3}PO{sub 4}. • SEM, EDX and XPS were applied for morphological description. • Electrochemical characterizations were performed by EIS and linear voltammetry. • The acid used predetermines completely different interaction with the AA2024 alloy.

  16. Magnesium-Based Sacrificial Anode Cathodic Protection Coatings (Mg-Rich Primers for Aluminum Alloys

    Directory of Open Access Journals (Sweden)

    Michael D. Blanton

    2012-09-01

    Full Text Available Magnesium is electrochemically the most active metal employed in common structural alloys of iron and aluminum. Mg is widely used as a sacrificial anode to provide cathodic protection of underground and undersea metallic structures, ships, submarines, bridges, decks, aircraft and ground transportation systems. Following the same principle of utilizing Mg characteristics in engineering advantages in a decade-long successful R&D effort, Mg powder is now employed in organic coatings (termed as Mg-rich primers as a sacrificial anode pigment to protect aerospace grade aluminum alloys against corrosion. Mg-rich primers have performed very well on aluminum alloys when compared against the current chromate standard, but the carcinogenic chromate-based coatings/pretreatments are being widely used by the Department of Defense (DoD to protect its infrastructure and fleets against corrosion damage. Factors such as reactivity of Mg particles in the coating matrix during exposure to aggressive corrosion environments, interaction of atmospheric gases with Mg particles and the impact of Mg dissolution, increases in pH and hydrogen gas liberation at coating-metal interface, and primer adhesion need to be considered for further development of Mg-rich primer technology.

  17. Surface morphology, composition and thermal behavior of tungsten-containing anodic spark coatings on aluminium alloy

    Energy Technology Data Exchange (ETDEWEB)

    Lukiyanchuk, I.V.; Rudnev, V.S.; Kuryavyi, V.G.; Boguta, D.L.; Bulanova, S.B.; Gordienko, P.S

    2004-01-01

    Anodic spark coatings on aluminium alloy were prepared in aqueous electrolytes with sodium tungstate. The influence of boric acid addition in the electrolyte on the surface morphology, elemental and phase composition of the coatings was investigated. In both cases the coatings contained O, Al and W. The coatings obtained in electrolyte with boric acid and sodium tungstate contain also B at approximately 1 at.%. Scanning electron microscopy indicated that the coatings had three layers: the grey underlayer of anodic alumina, the second black layer of crystalline or amorphous aluminium tungstate agglomerated into fibers and the outer green layer of WO{sub 3}. It was proposed that isopoly- and heteropolyanions in the electrolyte used take part in the coating growth.

  18. Surface integrity after pickling and anodization of Ti–6Al–4V titanium alloy

    Energy Technology Data Exchange (ETDEWEB)

    Vermesse, Eric [Institut Clément Ader (ICA), Université de Toulouse, ISAE, Toulouse (France); Université de Toulouse, Institut Carnot CIRIMAT, UMR CNRS-UPS-INP 5085, Université Paul Sabatier, 118, route de Narbonne, 31062 Toulouse cedex 9 (France); Mabru, Catherine [Institut Clément Ader (ICA), Université de Toulouse, ISAE, Toulouse (France); Arurault, Laurent, E-mail: arurault@chimie.ups-tlse.fr [Université de Toulouse, Institut Carnot CIRIMAT, UMR CNRS-UPS-INP 5085, Université Paul Sabatier, 118, route de Narbonne, 31062 Toulouse cedex 9 (France)

    2013-11-15

    The surface integrity of Ti–6Al–4V titanium alloy was studied at different stages of surface treatments, especially pickling and compact anodization, through surface characteristics potentially worsening fatigue resistance. No significant changes of the equiaxe microstructure were detected between sample core and surface, or after the pickling and anodization steps. Surface hydrogen and oxygen superficial contents were found to remain unchanged. Roughness characteristics (i.e. R{sub a}, R{sub z} but also local K{sub t} factor) similarly showed only slight modifications, although SPM and SEM revealed certain random local surface defaults, i.e. pits about 400 nm in depth. Finally internal stresses, evaluated using X-ray diffraction, highlighted a significant decrease of the compressive internal stresses, potentially detrimental for fatigue resistance.

  19. Effects of graphite on Zn-Sb alloys as anode materials for lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The electrochemical properties of multiphases Zn4Sb3C7 and ZnSbC2 as new lithium-ion anode materials wereinvestigated. The composition and microstructures of these multiphase materials were analyzed by XRD and TEM. It wasfound that the addition of graphite modifies the microstructures of pure alloys. The capacities and the cycle stability of theanodes are greatly improved. The reversible capacity of Zn4Sb3C7 reaches as high as 510 mAh/g at the first cycle, andkeeps higher than 300 mAh/g after 10 charge/discharge cycles

  20. Alloyed Ni-Fe nanoparticles as catalysts for NH3 decomposition

    DEFF Research Database (Denmark)

    Simonsen, Søren Bredmose; Chakraborty, Debasish; Chorkendorff, Ib;

    2012-01-01

    A rational design approach was used to develop an alloyed Ni-Fe/Al2O3 catalyst for decomposition of ammonia. The dependence of the catalytic activity is tested as a function of the Ni-to-Fe ratio, the type of Ni-Fe alloy phase, the metal loading and the type of oxide support. In the tests with high...

  1. Dead lithium phase investigation of Sn-Zn alloy as anode materials for lithium ion battery

    Institute of Scientific and Technical Information of China (English)

    HUANG ZhaoWen; HU SheJun; HOU XianHua; RU Qiang; YU HongWen; ZHAO LingZhi; LI WeiShan

    2009-01-01

    In this work, based on First-principle plane wave pseudo-potential method, we have carried out an in-depth study on the possible dead lithium phase of Sn-Zn alloy as anode materials for lithium ion batteries. Through investigation, we found that the phases LixSn4Zn4(x = 2, 4, 6, 8) contributed to reversible capacity, while the phases LixSn4Zns-(x-4)(x = 4.74, 7.72) led to capacity loss due to high formation energy, namely, they were the dead lithium phases during the charge/discharge process. And we come up with a new idea that stable lithium alloy phase with high lithiation formation energy (dead lithium phase) can also result in high loss of active lithium ion, besides the traditional expression that the formation of solid electrolyte interface film leads to high capacity loss.

  2. Self-sealing anodization approach to enhance micro-Vickers hardness and corrosion protection of a die cast Al alloy

    Science.gov (United States)

    Lee, Chulho; Oh, Kiseok; Lee, Dongeun; Kim, Yelim; Yoon, Hyungsop; Park, Dong-Wha; Gab Kim, Moon; Lee, Kiyoung; Choi, Jinsub

    2017-04-01

    Die cast, high-Si content ADC12 Al alloy samples were successfully anodized without surface cracks. This was accomplished with a 0.3 M sulfuric acid electrolyte with a high concentration of sodium aluminate. During anodization, the AlO2- anions were attracted to the positively-charged Al substrate and deposited in the cracks formed by un-oxidized Si islands within the ADC12. Anodic films prepared in electrolytes with a high concentration of AlO2- drastically enhanced surface morphology, thickness uniformity, Vickers hardness, and corrosion behavior in comparison with anodic film prepared without AlO2- concentration. The simultaneous sealing mechanism by AlO2- anions during anodization is reported in detail.

  3. Effect of Silica Sol on Boric-sulfuric Acid Anodic Oxidation of LY12CZ Aluminum Alloy

    Directory of Open Access Journals (Sweden)

    LIU Hui-cong

    2016-07-01

    Full Text Available Aluminum alloy anodizing coatings were prepared for LY12CZ in the boric-sulfuric acid solution (45g/L sulfuric acid,8g/L boric acid with the addition of 10%,20%,30% (volume fractionsilica sol,with the gradient voltage of 15V. The current and voltage transients of the anodizing process were collected by data collection instrument. The surface morphologies,microstructure and chemical composition of the anodic coatings were characterized by scanning electron microscopy (SEM. The corrosion resistance was examined by neutral salt spray,electrochemical impedance spectroscopy (EIS test and titrating test. The results show that the different concentration of silica sol addition can influence the forming and dissolution of anodizing coatings,improve the compactness smoothness and corrosion resistance during the anodizing process in the boric-sulfuric acid solution.

  4. Improvement of corrosion resistance of AZ31 Mg alloy by anodizing with co-precipitation of cerium oxide

    Institute of Scientific and Technical Information of China (English)

    Salah Abdelghany SALMAN; Ryoichi ICHINO; Masazumi OKIDO

    2009-01-01

    Anodizing of AZ31 Mg alloy in NaOH solution by co-precipitation of cerium oxide was investigated. The chemical composition and phase structure of the coating film were determined via optical microscopy, SEM and XRD. The corrosion properties of the anodic film were characterized by using potentiodynamic polarization curves in 17 mmol/L NaCl and 0.1 mol/L Na2SO4 solution at 298 K. The corrosion resistance of AZ31 magnesium alloy is significantly improved by adding cerium oxide to alkaline solution. In addition, the surface properties are enhanced and the film contains no crack.

  5. Anode- electrolyte- cathode sets of unitary SOFC with electro-catalysts deposited on previously sintered porous support

    Energy Technology Data Exchange (ETDEWEB)

    Carvalho, L.F.V.; Souza, F.M.B.; Fiuza, R.P.; Alencar, M.G.F.; Silva, M.A.; Boaventura, J.S. [Chemistry Inst., Salvador (Brazil). Dept. of Physical Chemistry

    2009-07-01

    The solid oxide fuel cell (SOFC) can be used in a broad range of applications. YSZ (yttria stabilized zirconia) and GDC (gadolinia doped ceria) are components of the anode/electrolyte set and LSM (manganite of strontium and lanthanum) ink are components of the cathode. In this study, different combinations of sodium bicarbonate, graphite and citric acid were used to form the electrocatalyst on nickel and iron. After sintering, the set was characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and surface area by BET. The pellets had good porosity and the anode-cathode-electrolyte interfaces had good inter-layer adherence. The catalyst was evenly dispersed on the support. The final porous structure did not have any surface area loss compared to the original powder. The mixed agents were found to be good pore formatting agents, with characteristics that were favourable for achieving good sets of anode-cathode-electrolytes. The final structure had good pore distribution and formation. The anode had good surface area and good tack from the interface anode/electrolyte.

  6. Evaluation of shot peening on the fatigue strength of anodized Ti-6Al-4V alloy

    Directory of Open Access Journals (Sweden)

    Costa Midori Yoshikawa Pitanga

    2006-01-01

    Full Text Available The increasingly design requirements for modern engineering applications resulted in the development of new materials with improved mechanical properties. Low density, combined with excellent weight/strength ratio as well as corrosion resistance, make the titanium attractive for application in landing gears. Fatigue control is a fundamental parameter to be considered in the development of mechanical components. The aim of this research is to analyze the fatigue behavior of anodized Ti-6Al-4V alloy and the influence of shot peening pre treatment on the experimental data. Axial fatigue tests (R = 0.1 were performed, and a significant reduction in the fatigue strength of anodized Ti-6Al-4V was observed. The shot peening superficial treatment, which objective is to create a compressive residual stress field in the surface layers, showed efficiency to increase the fatigue life of anodized material. Experimental data were represented by S-N curves. Scanning electron microscopy technique (SEM was used to observe crack origin sites.

  7. TiO{sub 2} nanotubes promoted PT-NI/C catalyst with low PT content as anode catalyst for direct ethanol fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Shen, L.; Jiang, Q.Z.; Gan, T.G.; Ma, Z.F. [Shanghai Jiao Tong Univ., Shanghai (China). Dept. of Chemical Engineering; Shen, M. [Oklahoma Univ., Norman, OK (United States). School of Chemical, Biological and Materials Engineering, Sarkeys Energy Center; Rodriguez Varela, F.J. [Cinvestav Unidad Saltillo, Coahuila (Mexico). Grupo de Recursos Naturales y Energeticos; Ocampo, A.L. [Univ. Nacional Autonoma, Mexico City (Mexico). Dept. de Quimica Analitica

    2010-07-15

    Although direct ethanol fuel cells (DEFC) have more energy density than direct methanol fuel cells (DMFC), their widespread use has been hampered by the fact that metallic platinum (Pt) catalysts are readily poisoned by strongly absorbed reaction intermediates such as CO{sub ads} at low operating temperatures. The addition of a second transition metal or a metal oxide component has been considered as a means to improve performance of DEFCs by forming a binary anode based on Pt. In this study, titanium oxide (TiO{sub 2}) nanotubes (TiO{sub 2}NTs) were added into a low-platinum content Pt-Ni/C catalyst to improve its catalytic activity for the ethanol oxidation reaction (EOR). The promotion effect of TiO{sub 2}NTs on Pt-Ni/C catalyst was examined. Cyclic voltametry (CV) and chronoamperometry showed that TiO{sub 2}NTs can improve the catalytic activity of the Pt-Ni/C catalyst considerably. Compared to a commercial Pt-Ru/C catalyst, the Pt-Ni-TiO{sub 2}NT/C catalyst has a larger electrochemical active surface (EAS) and has lower onset potential for the EOR. The elemental composition and electronic structure of the catalyst were characterized by X-ray photoelectron spectroscopy, energy dispersive X-ray spectrometry, inductively coupled plasma-optical emission spectrometry and X-ray diffraction. High resolution transmission electron microscopy was used to characterize the morphological properties of these catalysts. The study showed that onset oxidation potential can be lowered by the presence of TiO{sub 2}NTs because they retain more of the Pt metallic species and provide more hydroxides groups. 35 refs., 2 tabs., 10 figs.

  8. Structured Ni catalysts on porous anodic alumina membranes for methane dry reforming: NiAl 2 O 4 formation and characterization

    KAUST Repository

    Zhou, Lu

    2015-06-29

    This communication presents the successful design of a structured catalyst based on porous anodic alumina membranes for methane dry reforming. The catalyst with a strong Ni-NiAl2O4 interaction shows both excellent activity and stability. This journal is © The Royal Society of Chemistry.

  9. Advances in aluminum anodizing

    Science.gov (United States)

    Dale, K. H.

    1969-01-01

    White anodize is applied to aluminum alloy surfaces by specific surface preparation, anodizing, pigmentation, and sealing techniques. The development techniques resulted in alloys, which are used in space vehicles, with good reflectance values and excellent corrosive resistance.

  10. Evolution of insoluble eutectic Si particles in anodic oxidation films during adipic-sulfuric acid anodizing processes of ZL114A aluminum alloys

    Science.gov (United States)

    Hua, Lei; Liu, Jian-hua; Li, Song-mei; Yu, Mei; Wang, Lei; Cui, Yong-xin

    2015-03-01

    The effects of insoluble eutectic Si particles on the growth of anodic oxide films on ZL114A aluminum alloy substrates were investigated by optical microscopy (OM) and scanning electron microscopy (SEM). The anodic oxidation was performed at 25°C and a constant voltage of 15 V in a solution containing 50 g/L sulfuric acid and 10 g/L adipic acid. The thickness of the formed anodic oxidation film was approximately 7.13 μm. The interpore distance and the diameters of the major pores in the porous layer of the film were within the approximate ranges of 10-20 nm and 5-10 nm, respectively. Insoluble eutectic Si particles strongly influenced the morphology of the anodic oxidation films. The anodic oxidation films exhibited minimal defects and a uniform thickness on the ZL114A substrates; in contrast, when the front of the oxide oxidation films encountered eutectic Si particles, defects such as pits and non-uniform thickness were observed, and pits were observed in the films.

  11. Miniature fuel cell with monolithically fabricated Si electrodes - Alloy catalyst formation -

    Science.gov (United States)

    Ogura, Daiki; Suzuki, Takahiro; Katayama, Noboru; Dowaki, Kiyoshi; Hayase, Masanori

    2013-12-01

    A novel Pd-Pt catalyst formation process was proposed for reduction of Pt usage. In our miniature fuel cells, porous Pt was used as the catalyst, and the Pt usage was quite high. To reduce the Pt usage, we have attempted to deposit Pt on porous Pd by galvanic replacement, and relatively large output was demonstrated. In this study, in order to reduce more Pt usage and explore the alloy catalyst formation process, atomic layer deposition by UPD-SLRR (Under Potential Deposition - Surface Limited Redox Replacement) was applied to the Pd-Pt catalyst formation. The new process was verified at each process steps by EDS elemental analysis, and the expected spectra were obtained. Prototype cells were constructed by the new process, and cell output was raised to 420mW/cm2 by the Pd-Pt catalyst from 125mW/cm2 with Pd catalyst.

  12. Applying ellipsometry to studying the effect of two kinds of rare earth metal salts on anodizing aluminum alloy

    Institute of Scientific and Technical Information of China (English)

    H00G Quan; QIAN Ying; LI Lingjie; ZHANG Shengtao

    2004-01-01

    The effects of rare earth metal salts (REMs), cerium(Ⅳ) salt and lanthanum (Ⅲ) salt, on the property of anodized coating of LD10 aluminum alloy are studied by corrosion tests including neutral salt spray test and copper accelerated acetic acid immersion test, polarization curves measurement, energy dispersion analyzer of X-Ray(EDAX) analysis, and in situ ellipsometry. The results show that the addition of either of the two REMs in anodizing solution hardly changes the composition of an anodized coating, while increases the thickness of barrier part and reduces the porosity of porous part, which contributed to the improvement of the corrosion resistance of the anodized coating. The results also demonstrate that the effect of cerium salt was better than that of lanthanum salt.

  13. Enhancement in open-circuit voltage of implantable CMOS-compatible glucose fuel cell by improving the anodic catalyst

    Science.gov (United States)

    Niitsu, Kiichi; Ando, Takashi; Kobayashi, Atsuki; Nakazato, Kazuo

    2017-01-01

    This paper presents an implantable CMOS-compatible glucose fuel cell that generates an open-circuit voltage (OCV) of 880 mV. The developed fuel cell is solid-catalyst-based and manufactured from biocompatible materials; thus, it can be implanted to the human body. Additionally, since the cell can be manufactured using a semiconductor (CMOS) fabrication process, it can also be manufactured together with CMOS circuits on a single silicon wafer. In the literature, an implantable CMOS-compatible glucose fuel cell has been reported. However, its OCV is 192 mV, which is insufficient for CMOS circuit operation. In this work, we have enhanced the performance of the fuel cell by improving the electrocatalytic ability of the anode. The prototype with the newly proposed Pt/carbon nanotube (CNT) anode structure successfully achieved an OCV of 880 mV, which is the highest ever reported.

  14. Nanostructured Platinum Alloys for Use as Catalyst Materials

    Science.gov (United States)

    Hays, Charles C. (Inventor); Narayan, Sri R. (Inventor)

    2015-01-01

    A series of binary and ternary Pt-alloys, that promote the important reactions for catalysis at an alloy surface; oxygen reduction, hydrogen oxidation, and hydrogen and oxygen evolution. The first two of these reactions are essential when applying the alloy for use in a PEMFC.

  15. Further studies of the anodic dissolution in sodium chloride electrolyte of aluminium alloys containing tin and gallium

    Science.gov (United States)

    Nestoridi, Maria; Pletcher, Derek; Wharton, Julian A.; Wood, Robert J. K.

    As part of a programme to develop a high power density, Al/air battery with a NaCl brine electrolyte, the high rate dissolution of an aluminium alloy containing tin and gallium was investigated in a small volume cell. The objective was to define the factors that limit aluminium dissolution in condition that mimic a high power density battery. In a cell with a large ratio of aluminium alloy to electrolyte, over a range of current densities the extent of dissolution was limited to ∼1000 C cm -2 of anode surface by a thick layer of loosely bound, crystalline deposit on the Al alloy anode formed by precipitation from solution. This leads to a large increase in impedance and acts as a barrier to transport of ions.

  16. Further studies of the anodic dissolution in sodium chloride electrolyte of aluminium alloys containing tin and gallium

    Energy Technology Data Exchange (ETDEWEB)

    Nestoridi, Maria; Pletcher, Derek [The School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ (United Kingdom); Wharton, Julian A.; Wood, Robert J.K. [School of Engineering Sciences, The University, Southampton SO17 1BJ (United Kingdom)

    2009-09-05

    As part of a programme to develop a high power density, Al/air battery with a NaCl brine electrolyte, the high rate dissolution of an aluminium alloy containing tin and gallium was investigated in a small volume cell. The objective was to define the factors that limit aluminium dissolution in condition that mimic a high power density battery. In a cell with a large ratio of aluminium alloy to electrolyte, over a range of current densities the extent of dissolution was limited to {proportional_to}1000 C cm{sup -2} of anode surface by a thick layer of loosely bound, crystalline deposit on the Al alloy anode formed by precipitation from solution. This leads to a large increase in impedance and acts as a barrier to transport of ions. (author)

  17. Electron microscopic studies of anodic oxide films on the AZ91HP alloy

    Directory of Open Access Journals (Sweden)

    D. Peixoto Barbosa

    2003-01-01

    Full Text Available A Mg-9wt.Al-1wt.%Zn-alloy was anodized up to 90 V with constant current/constant voltage in an electrolyte which contained the compounds of the HAE-process (KOH, Al(OH3, KF, Na3PO4 and KMnO4. Electron microscopic examinations revealed a highly porous and irregular film structure. The distribution of the elements in the film was measured with energy dispersive spectrometry on specimens prepared in cross section for the transmission electron microscope. The main characteristic found was a fluoride-enriched zone of about 100 nm thickness at the metal / film interface. Practically no manganese from the permanganate was detected in this fluoride-enriched zone.

  18. Elaboration, physical and electrochemical characterizations of CO tolerant PEMFC anode materials. Study of platinum-molybdenum and platinum-tungsten alloys and composites; Elaborations et caracterisations electrochimiques et physiques de materiaux d'anode de PEMFC peu sensibles a l'empoisonnement par CO: etude d'alliages et de composites a base de platine-molybdene et de platine-tungstene

    Energy Technology Data Exchange (ETDEWEB)

    Peyrelade, E.

    2005-06-15

    PEMFC development is hindered by the CO poisoning ability of the anode platinum catalyst. It has been previously shown that the oxidation potential of carbon monoxide adsorbed on the platinum atoms can be lowered using specific Pt based catalysts, either metallic alloys or composites. The objective is then to realize a catalyst for which the CO oxidation is compatible with the working potential of a PEMFC anode. In our approach, to enhance the CO tolerance of platinum based catalyst supported on carbon, we studied platinum-tungsten and platinum-molybdenum alloys and platinum-metal oxide materials (Pt-WO{sub x} and Pt-MoO{sub x}). The platinum based alloys demonstrate a small effect of the second metal towards the oxidation of carbon monoxide. The platinum composites show a better tolerance to carbon monoxide. Electrochemical studies on both Pt-MoO{sub x} and Pt-WO{sub x} demonstrate the ability of the metal-oxides to promote the ability of Pt to oxidize CO at low potentials. However, chrono-amperometric tests reveal a bigger influence of the tungsten oxide. Complex chemistry reactions on the molybdenum oxide surface make it more difficult to observe. (author)

  19. One-step electrolytic preparation of Si-Fe alloys as anodes for lithium ion batteries

    Science.gov (United States)

    Wang, Hailong; Sun, Diankun; Song, Qiqi; Xie, Wenqi; Jiang, Xu; Zhang, Bo

    2016-06-01

    One-step electrolytic formation of uniform crystalline Si-Fe alloy particles was successfully demonstrated in direct electro-reduction of solid mixed oxides of SiO2 and Fe2O3 in molten CaCl2 at 900∘C. Upon constant voltage electrolysis of solid mixed oxides at 2.8V between solid oxide cathode and graphite anode for 5h, electrolytic Si-Fe with the same Si/Fe stoichimetry of the precursory oxides was generated. The firstly generated Fe could function as depolarizers to enhance reduction rate of SiO2, resulting in the enhanced reduction kinetics to the electrolysis of individual SiO2. When evaluated as anode for lithium ion batteries, the prepared SiFe electrode showed a reversible lithium storage capacity as high as 470mAh g-1 after 100 cycles at 200mA g-1, promising application in high-performance lithium ion batteries.

  20. A Novel Ultrafine Ru-B Amorphous Alloy Catalyst for Glucose Hydrogenation to Sorbitol

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    An ultrafine Ru-B amorphous alloy catalyst was prepared by chemical reduction with KBH4 in aqueous solution, which exhibited perfect selectivity to sorbitol (~100%) and very high activity during the liquid phase glucose hydrogenation, much higher than the corresponding crystallized Ru-B, the pure Ru powder, and Raney Ni catalysts. The correlation of the catalytic activity to both the structural and surface electronic characteristics was discussed briefly.

  1. Amorphous Nickel Based Alloy Catalysts and Magnetically Stabilized Bed Hydrogenation Technology

    Institute of Scientific and Technical Information of China (English)

    MuXuhong; ZongBaoning; 等

    2002-01-01

    Amorphous nickel based alloy catalysts(denoted as the SRNA series catalysts)were prepared via rapid quenching method followed by alkali leaching and other activation procedures.The physicochemical characterizations show that nickel,the active component in these catalysts,exists in the amorphous state,and the catalyst particles possess many nanosized voids leading to large surface area(the highest is 145m2/g).The evaluation results in some model reactions show that the SRNA series catalysts have 2 to 4 times higher activity and selectivity than conventional Raney Ni catalyst for the hydrogenation of compounds with unsatur-ated functional groups.At present,the SRNA series catalysts have been successfully used in hydrogenation of glucose,hydrogenation of pharmaceutical intermediates and purification of caprolactam.In order to use these catalysts efficiently,a magnetically stabilized bed(MSB) technology has been developed by combining the ferromagnetic property of the catalyst with the good mass transfer characteristics of MSB.The demonstration unit of MSB hydrogenation technology has been set up and has kept running for 2800 hours.The results show that,after running 2800 hours,the catalyst still retained good activity; meanwhile,the hydrogenation effi-ciency had been improved 10 times in comparison with the traditional CSTR process.

  2. Effects of benzotriazole on anodized film formed on AZ31B magnesium alloy in environmental-friendly electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Guo Xinghua [School of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin (China); An Maozhong, E-mail: mzan@hit.edu.c [School of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin (China); Yang Peixia; Li Haixian; Su Caina [School of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin (China)

    2009-08-12

    An environmental-friendly electrolyte of silicate and borate, which contained an addition agent of 1H-benzotriazole (BTA) with low toxicity (LD50 of 965 mg/kg), was used to prepare an anodized film on AZ31B magnesium alloy under the constant current density of 1.5 A/dm{sup 2} at room temperature. Effects of BTA on the properties of the anodized film were studied by scanning electron microscopy (SEM), energy dispersion spectrometry (EDS), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), loss weight measurement, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS), respectively. The results demonstrated that anodized growth process, surface morphology, thickness, phase structure and corrosion resistance of the anodized film were strongly dependant on the BTA concentration, which might be attributed to the formation of an BTA adsorption layer on magnesium substrate surface. When the BTA concentration was 5 g/L in the electrolyte, a compact and thick anodized film could provide excellent corrosion resistance for AZ31B magnesium alloy.

  3. A Practical Anodic and Cathodic Curve Intersection Model to Understand Multiple Corrosion Potentials of Fe-Based Glassy Alloys in OH- Contained Solutions.

    Directory of Open Access Journals (Sweden)

    Y J Li

    Full Text Available A practical anodic and cathodic curve intersection model, which consisted of an apparent anodic curve and an imaginary cathodic line, was proposed to explain multiple corrosion potentials occurred in potentiodynamic polarization curves of Fe-based glassy alloys in alkaline solution. The apparent anodic curve was selected from the measured anodic curves. The imaginary cathodic line was obtained by linearly fitting the differences of anodic curves and can be moved evenly or rotated to predict the number and value of corrosion potentials.

  4. Sacrificial anode stability and polarization potential variation in a ternary Al-xZn-xMg alloy in a seawater-marine environment

    Science.gov (United States)

    Muazu, Abubakar; Aliyu, Yaro Shehu; Abdulwahab, Malik; Idowu Popoola, Abimbola Patricia

    2016-06-01

    In this paper, the effects of zinc (Zn) and magnesium (Mg) addition on the performance of an aluminum-based sacrificial anode in seawater were investigated using a potential measurement method. Anodic efficiency, protection efficiency, and polarized potential were the parameters used. The percentages of Zn and Mg in the anodes were varied from 2% to 8% Zn and 1% to 4% Mg. The alloys produced were tested as sacrificial anodes for the protection of mild steel in seawater at room temperature. Current efficiency as high as 88.36% was obtained in alloys containing 6% Zn and 1% Mg. The polarized potentials obtained for the coupled (steel/Al-based alloys) are as given in the Pourbaix diagrams, with steel lying within the immunity region/cathodic region and the sacrificial anodes within the anodic region. The protection offered by the sacrificial anodes to the steel after the 7th and 8th week was measured and protection efficiency values as high as 99.66% and 99.47% were achieved for the Al-6%Zn-1%Mg cast anode. The microstructures of the cast anodes comprise of intermetallic structures of hexagonal Mg3Zn2 and body-centered cubic Al2Mg3Zn3. These are probably responsible for the breakdown of the passive alumina film, thus enhancing the anode efficiency.

  5. Evaluation of Al and Some of Its Alloys as Anode Materials vs γ-MnO2 as Cathode Material and Ore Produced γ-MnO2 vs Zn Anode in KOH Solution

    Institute of Scientific and Technical Information of China (English)

    A.M.A.Hashem; Kh.S. Abou-El-Sherbini; S. Zein El Abedin; H. Abbas

    2006-01-01

    In this study electrochemical performance of Al and some of its alloys (Al-Zn, Al-Mg and Al-Mn) anodes vs MnO2 cathode were carried out in alkaline solution. The results show that the Al-Zn alloy anode has the best cell capacity among the other alloys. Cell capacity values go in the order Al-Zn>Al-Mg>Al>Al-Mn. This result is probably related to the nature of passive films formed on the surface of the alloys which examined by scanning electron microscopy (SEM). SEM morphologies of Al and its alloys showed coarse grains of passive films formed on the surface of these anode materials while Al-Mn morphology shows a needle-like structure.Electrolytic manganese dioxide (EMD) produced by electrodepositing on platinum anode from liquor resulting from reduction of low grade pyrolusite ore (β-MnO2) by sulfur slag was characterized as cathode in alkaline Zn-MnO2 batteries. Ore produced sample (EMD1) was performed well in comparison with EMD standard (EMD2) (commercial battery grade electrolytic manganese dioxide, TOSOH-Hellas GH-S). SEM morphology of Zn anode after cell reaction was carried out and showed that Zn anode has fine grains of passive film on its surface.

  6. Controllable Deposition of Alloy Clusters or Nanoparticles Catalysts on Carbon Surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Sasaki, K.; Ando, Y.; Su, D.; Adzic, R.

    2011-08-15

    We describe a simple method for controllably depositing Pt-Ru alloy nanoparticles on carbon surfaces that is mediated by Pb or Cu adlayers undergoing underpotential deposition and stripping during Pt and Ru codeposition at diffusion-limiting currents. The amount of surface Pt atoms deposited largely reflects the number of potential cycles causing the deposition and stripping of the metal adlayer at underpotentials, the metal species used as a mediator, and the scan rate of the potential cycles. We employed electrochemical methanol oxidation to gain information on the catalyst's activities. The catalysts with large amounts of surface Pt atoms have relatively high methanol-oxidation activity. Catalysts prepared using this method enhance methanol-oxidation activity per electrode surface area, while maintaining catalytic activity per surface Pt atom; thus, the amount of Pt is reduced in comparison with conventional methanol-oxidation catalysts. The method is suitable for efficient synthesizing various bimetallic catalysts.

  7. Porous anodic film formation on an Al-3.5 wt % Cu alloy

    Directory of Open Access Journals (Sweden)

    Páez, M. A.

    2003-12-01

    Full Text Available The morphological development of porous anodic films in the initial stages is examined during anodizing an Al-3.5 wt % Cu alloy in phosphoric acid. Using transmission electron microscopy a sequence of ultramicrotomed anodic sections reveals the dynamic evolution of numerous features in the thickening film in the initial stages of anodizing. The morphological changes in the anodic oxide in the initial stages of its formation appears related to the formation of bubbles during film growth. From Rutherford backscattering spectroscopy (RBS analysis of the film, the formation of the bubbles is associated with the enrichment of copper in the alloy due to growth of the anodic oxide. On the other hand, during constant current anodizing of Al-Cu in phosphoric acid, the current efficiency is considerably less than that for anodizing superpure aluminium under similar conditions. From the contrasting results between the charge consumed calculated from RBS and the real charge consumed during anodizing, oxygen gas bubbles generation and copper oxidation seem to be of less importance on the low efficiency for film formation. It is apparent that the main cause of losing efficiency for film growth on Al-Cu is associated with generation of oxygen at residual second phase, with the development of stresses in the film and, the consequence of these effects on film cracking during film growth.

    En este trabajo se examinó el desarrollo morfológico de películas anódicas porosas en los estados iniciales de la anodización de una aleación de aluminio Al-3,5 % p/p Cu. La observación de una secuencia de secciones ultramicrotomadas del metal y su película anódica, por microscopía electrónica de transmisión, revela la evolución dinámica de numerosos detalles morfológicos durante los inicios del crecimiento de la película anódica. Los cambios morfológicos en el óxido anódico, en los inicios de su formación, aparecen relacionados a la formación de

  8. Amorphous Nickel Based Alloy Catalysts and Magnetically Stabilized Bed Hydrogenation Technology

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Amorphous nickel based alloy catalysts (denoted as the SRNA series catalysts) were prepared viarapid quenching method followed by alkali leaching and other activation procedures. The physicochemicalcharacterizations show that nickel, the active component in these catalysts, exists in the amorphous state, andthe catalyst particles possess many nanosized voids leading to large surface area (the highest is 145m2/g). Theevaluation results in some model reactions show that the SRNA series catalysts have 2 to 4 times higheractivity and selectivity than conventional Raney Ni catalyst for the hydrogenation of compounds with unsatur-ated functional groups. At present, the SRNA series catalysts have been successfully used in hydrogenation ofglucose, hydrogenation of pharmaceutical intermediates and purification of caprolactam. In order to use thesecatalysts efficiently, a magnetically stabilized bed (MSB) technology has been developed by combining theferromagnetic property of the catalyst with the good mass transfer characteristics of MSB. The demonstrationunit of MSB hydrogenation technology has been set up and has kept running for 2800 hours. The results showthat, after running 2800 hours, the catalyst still retained good activity; meanwhile, the hydrogenation effi-ciency had been improved 10 times in comparison with the traditional CSTR process.

  9. Amorphous Nickel Based Alloy Catalysts and Magnetically Stabilized Bed Hydrogenation Technology

    Institute of Scientific and Technical Information of China (English)

    Mu Xuhong; Zong Baoning; Meng Xiangkun; Min Enze

    2002-01-01

    Amorphous nickel based alloy catalysts (denoted as the SRNAseries catalysts) were prepared viarapid quenching method followed by alkali leaching and other activation procedures. The physicochemicalcharacterizations show that nickel, the active component in these catalysts, exists in the amorphous state, andthe catalyst particles possess many nanosized voids leading to large surface area (the highest is 145m2/g). Theevaluation results in some model reactions show that the SRNA series catalysts have 2 to 4 times higheractivity and selectivity than conventional Raney Ni catalyst for the hydrogenation of compounds with unsatur-ated functional groups. At present, the SRNA series catalysts have been successfully used in hydrogenation ofglucose, hydrogenation of pharmaceutical intermediates and purification of caprolactam. In order to use thesecatalysts efficiently, a magnetically stabilized bed (MSB) technology has been developed by combining theferromagnetic property of the catalyst with the good mass transfer characteristics of MSB. The demonstrationunit of MSB hydrogenation technology has been set up and has kept running for 2800 hours. The results showthat, after running 2800 hours, the catalyst still retained good activity; meanwhile, the hydrogenation effi-ciency had been improved 10 times in comparison with the traditional CSTR process.

  10. Carbon-coated Ni 20Si 80 alloy-graphite composite as an anode material for lithium-ion batteries

    Science.gov (United States)

    Lee, Heon-Yong; Kim, Young-Lae; Hong, Moon-Ki; Lee, Sung-Man

    A carbon-coated Ni 20Si 80 alloy-graphite composite has been studied as the anode for lithium-ion batteries. The composite is prepared by simple heat-treatment of a mixture of coal tar pitch and a Ni 20Si 80-graphite composite at 900 °C and under argon. The Ni 20Si 80 alloy powders are synthesized by mechanical alloying. The composite demonstrates promising electrochemical properties such as high reversible capacity, excellent cycle performance, and sufficiently high initial charge-discharge coulombic efficiency. This suggests buffering and conductive actions on the main active material, viz., Ni 20Si 80 alloy, of the graphite. These two effects are strongly enhanced by the carbon coating treatment.

  11. Structure, activity, and stability of platinum alloys as catalysts for the oxygen reduction reaction

    DEFF Research Database (Denmark)

    Vej-Hansen, Ulrik Grønbjerg

    In this thesis I present our work on theoretical modelling of platinum alloys as catalysts for the Oxygen Reduction Reaction (ORR). The losses associated with the kinetics of the ORR is the main bottleneck in low-temperature fuel cells for transport applications, and more active catalysts...... are essential for wide-spread use of this technology. platinum alloys have shown great promise as more active catalysts, which are still stable under reaction conditions. We have investigated these systems on multiple scales, using either Density Functional Theory (DFT) or Effective Medium Theory (EMT...... and dealloying due to kinetic barriers, despite the thermodynamic driving force for dissolution. This is followed by our results on trying to decouple the strain and ligand effects for platinum skin structures, and determining whether there is any correlation between adsorption energy and surface stability...

  12. Skeletal Amorphous Nickel Based Alloy Catalysts and Magnetically Stabilized Bed Hydrogenation Technology

    Institute of Scientific and Technical Information of China (English)

    Min Enze

    2004-01-01

    Looking toward 21 century, smaller, cleaner and more energy-efficient technology will be an important trend in the development of chemical industry. In light of the new process requirements,a number of technology breakthroughs have occurred. One of these discoveries, the magnetically stabilized bed (MSB), has been proven a powerful process for intensification. Since its initial research in the late 1980's at Research Institute of Petroleum Processing (RIPP), the MSB technology and related catalytic material have matured rapidly through an intensive research and engineering program, primarily focused on its scaling-up.In this paper, we report the discovery of a novel skeletal amorphous nickel-based alloy and its use in magnetically stabilized bed (MSB). Amorphous alloys are new kinds of catalytic materials with short-range order but long-range disorder structure. In comparison with Raney Ni, the skeletal amorphous nickel-based alloy has an increasingly higher activity in the hydrogenation of reactive groups and compounds including nitro, nitrile, olefin, acetylene, aromatics, etc. Up to now, the amorphous nickel based alloy catalysts, SRNA series catalyst, one with high Ni ratio have been commercially manufactured more than four year. The new SRNA catalyst has been successfully implemented for hydrogenation applications in slurry reactor at Balin Petrochemical, SINOPEC.SRNA catalyst with further improvement in catalytic activity and stability raise its relative stability to 2~4 times of that of conventional catalyst. In the course of the long-cycle operation of SRNA-4 the excellent catalyst activity and stability can bring about such advantage as low reaction temperature, good selectivity and low catalyst resumption.Magnetically stabilized bed (MSB), a fluidized bed of magnetizable particles by applying a spatially uniform and time-invariant magnetic field oriented axially relative to the fluidizing fluid flow, had many advantages such as the low pressure drop and

  13. Growth characterization of anodic film on AZ91D magnesium alloy in an electrolyte of Na2SiO3 and KF

    Institute of Scientific and Technical Information of China (English)

    Weiping Li; Liqun Zhu; Yihong Li; Bo Zhao

    2006-01-01

    Anodization of AZ91D magnesium alloy in the electrolyte solution of 0.5 mol/L of sodium silicate and 1.0 mol/L of potassium fluoride was investigated. The anodic films were characterized using optical microscopy (OM), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The corrosion resistance of the various anodized alloys was evaluated by a fast corrosion test using the solution of hydrochloric acid and potassium dichromate. The results showed that the addition of KF resulted in the presence of NaF in the anodic film. The thickness of the anodic film formed under a constant current density of 20 mA/cm2 for 16 min at 60℃ exceeded 100 μm. The growth of the anodic film could be divided into three stages based on the anodizing time; the growth rate was much faster during stage Ⅱ than in stages Ⅰ and Ⅲ. The anodic film exhibited the highest corrosion resistance for the AZ91 alloy,which is attributed to the fact that the anodization was maintained until the end of stage Ⅱ.

  14. Highly redox-resistant solid oxide fuel cell anode materials based on La-doped SrTiO3 by catalyst impregnation strategy

    Science.gov (United States)

    Shen, X.; Sasaki, K.

    2016-07-01

    An anode backbone using 40 wt% (ZrO2)0.89(Sc2O3)0.1(CeO2)0.01 (SSZ)-Sr0.9La0.1TiO3 (SLT) cermet was prepared for SSZ electrolyte-supported SOFC single cells. 15 mgcm-2 Ce0.9Gd0.1O2 (GDC) was impregnated to totally cover the SSZ-SLT anode backbone surface acting as a catalyst, and the cell voltage achieved 0.865 V at 200 mAcm-2 using (La0.75Sr0.25)0.98MnO3 (LSM)-SSZ cathode in 3%-humidified hydrogen fuel at 800 °C. Cell performance was substantially improved from 0.865 V to >0.97 V when 0.03 mgcm-2 Pd or Ni was further incorporated as a secondary catalyst into the anode layer. 50 redox cycles were performed to investigate redox stability of this high performance anode. It was found that even after the 50 redox cycle long-term degradation test, cell voltage at 200 mAcm-2 was retained around 0.94 V, higher than the cell performance using the conventional Ni-SSZ cermet anode. The catalytically-active reaction sites at ceria-Pd or ceria-Ni may account for the excellent performance, and the extremely low metal catalyst concentration prevent serious metal aggregation in achieving excellent redox stability.

  15. Long-term performance of different aluminum alloy designs as sacrificial anodes for rebars

    Directory of Open Access Journals (Sweden)

    de Rincón, O.

    2003-12-01

    Full Text Available This paper presents the performance of various cathodic-protection designs using Aluminum alloys to protect prestressed piles. The results obtained with different system designs (bracelete type-Al/Zn/In alloy, thermosprayed aluminum (3-year evaluation and conventional Al/Zn/In anocies in an epoxy-painted steel bracelet (12-year evaluation, indicated that all of these systems may be used as sacrificial anodes for pile protection. However, the thermosprayed aluminum type can not be used in prestressed concrete piles because the very negative potentials ( < -1100 mV vs. Cu/CuSO4 they supply to the reinforcement could lead to hydrogen embrittlement.

    Este trabajo presenta la realización de varios diseños de protección catódica utilizando aleaciones de aluminio para la protección de pilotes pretensados. Los resultados obtenidos con diferentes diseños (aleación de Al/Zn/In, tipo brazalete y aluminio termorociado (3 años de evaluación y ánodos convencionales de Al/Zn/In colocados en un brazalete de acero pintado con epoxy (12 años de evaluación, indicaron que todos estos sistemas pueden ser utilizados como ánodos de sacrificio para la protección de los pilotes. Sin embargo, el sistema con aluminio termorociado no puede ser utilizado en pilotes de acero pretensado debido al potencial muy negativo alcanzado por la armadura (<-1100 mV vs Cu/CuSO4, lo cual podría inducir a daños por hidrógeno.

  16. Pt Monolayer Shell on Nitrided Alloy Core—A Path to Highly Stable Oxygen Reduction Catalyst

    Directory of Open Access Journals (Sweden)

    Jue Hu

    2015-07-01

    Full Text Available The inadequate activity and stability of Pt as a cathode catalyst under the severe operation conditions are the critical problems facing the application of the proton exchange membrane fuel cell (PEMFC. Here we report on a novel route to synthesize highly active and stable oxygen reduction catalysts by depositing Pt monolayer on a nitrided alloy core. The prepared PtMLPdNiN/C catalyst retains 89% of the initial electrochemical surface area after 50,000 cycles between potentials 0.6 and 1.0 V. By correlating electron energy-loss spectroscopy and X-ray absorption spectroscopy analyses with electrochemical measurements, we found that the significant improvement of stability of the PtMLPdNiN/C catalyst is caused by nitrogen doping while reducing the total precious metal loading.

  17. Carbon-supported platinum alloy catalysts for phenol hydrogenation for making industrial chemicals

    Energy Technology Data Exchange (ETDEWEB)

    Srinivas, S.T.; Song, C.

    1999-07-01

    Phenol is available in large quantities in liquids derived from coal and biomass. Phenol hydrogenation is an industrially important reaction to produce cyclohexanone and cyclohexanol. Cyclohexane, cyclohexene and benzene are obtained as minor products in this reaction. Cyclohexanone is an important intermediate in the production of caprolactam for nylon 6 and cyclohexanol for adipic acid production. In USA, cyclohexanol and cyclohexanone are produced by benzene hydrogenation to cyclohexane over nickel or noble metal catalysts, followed by oxidation of cyclohexane to produce a mixture of cyclohexanol and cyclohexanone. Then cyclohexanol is dehydrogenated in the presence of Cu-Zn catalyst to cyclohexanone. Usually phenol hydrogenation is also carried out by using Ni catalyst in liquid phase. However, a direct single-step vapor phase hydrogenation of phenol to give cyclohexanone selectively is more advantageous in terms of energy savings and process economics, since processing is simplified and the endothermic step of cyclohexanol dehydrogenation can be avoided, as demonstrated by Montedipe and Johnson Matthey using promoted Pd/Al{sub 2}O{sub 3} catalyst. While it is not the purpose of this paper to dwell on the relative merits of these routes, it is necessary to mention that while using monometallic catalysts, generally the problem of catalyst deactivation of sintering as well as coking is frequently encountered. Addition and alloying of noble metal (e.g. Pt) with a second metal can result in a catalyst with better selectivity and activity in the reaction which is more resistant to deactivation. This paper presents the results on the single-step vapor phase hydrogenation of phenol over carbon-supported Pt-M (M=Cr, V, Zr) alloy catalysts to yield mainly cyclohexanone or cyclohexanol.

  18. Alliages intermétalliques du magnésium, anodes pour MAFC ? Magnesium intermetallic alloys, anodes for MAFC?

    Directory of Open Access Journals (Sweden)

    Montagné Pierre

    2013-11-01

    Full Text Available Des composés intermétalliques sélectionnés ont été étudiés en vue d'une utilisation en remplacement de l'anode métallique dans des batteries de type métal air. Ces composés présentent des structures cristallines très différentes : structure lamellaire pour MgB2, structure covalente simple pour Mg2Si et structure complexe basée sur un empilement compact de polyèdres pour Mg2Al3. Les meilleurs résultats sont obtenus pour ce dernier composé avec une réactivité vis-à-vis des électrolytes testés sensiblement inférieure à celle du magnésium et une cinétique de réaction plus lente. Le potentiel en fonctionnement au sein de la batterie est sensiblement plus faible que celui du magnésium mais il présente une stabilité remarquable au cours du temps. Selected intermetallic compounds have been studied as anodic materials in metal air fuel cells. These compounds have different structural types, MgB2 displays a lamellar structure, Mg2Si a simple covalent structure while Mg2Al3 has a complex structure based on compact polyhedral packing. Best electrochemical results are obtained for the latter, with a lower reactivity towards magnesium in the two electrolytes and with lower kinetics of reaction. The operating potential of the battery with a Mg2Al3 anode is noticeably lower than with a Mg anode, but it presents a very good stability over time.

  19. Hierarchical Pd-Sn alloy nanosheet dendrites: an economical and highly active catalyst for ethanol electrooxidation.

    Science.gov (United States)

    Ding, Liang-Xin; Wang, An-Liang; Ou, Yan-Nan; Li, Qi; Guo, Rui; Zhao, Wen-Xia; Tong, Ye-Xiang; Li, Gao-Ren

    2013-01-01

    Hierarchical alloy nanosheet dendrites (ANSDs) are highly favorable for superior catalytic performance and efficient utilization of catalyst because of the special characteristics of alloys, nanosheets, and dendritic nanostructures. In this paper, we demonstrate for the first time a facile and efficient electrodeposition approach for the controllable synthesis of Pd-Sn ANSDs with high surface area. These synthesized Pd-Sn ANSDs exhibit high electrocatalytic activity and superior long-term cycle stability toward ethanol oxidation in alkaline media. The enhanced electrocataytic activity of Pd-Sn ANSDs may be attributed to Pd-Sn alloys, nanosheet dendrite induced promotional effect, large number of active sites on dendrite surface, large surface area, and good electrical contact with the base electrode. Because of the simple implement and high flexibility, the proposed approach can be considered as a general and powerful strategy to synthesize the alloy electrocatalysts with high surface areas and open dendritic nanostructures.

  20. Low Pt content direct methanol fuel cell anode catalyst: nanophase PtRuNiZr

    Science.gov (United States)

    Narayanan, Sekharipuram R. (Inventor); Whitacre, Jay F. (Inventor)

    2010-01-01

    A method for the preparation of a metallic material having catalytic activity that includes synthesizing a material composition comprising a metal content with a lower Pt content than a binary alloy containing Pt but that displays at least a comparable catalytic activity on a per mole Pt basis as the binary alloy containing Pt; and evaluating a representative sample of the material composition to ensure that the material composition displays a property of at least a comparable catalytic activity on a per mole Pt basis as a representative binary alloy containing Pt. Furthermore, metallic compositions are disclosed that possess substantial resistance to corrosive acids.

  1. Low-temperature, vapor-liquid-solid, laterally grown silicon films using alloyed catalysts

    Science.gov (United States)

    LeBoeuf, Jerome L.; Brodusch, Nicolas; Gauvin, Raynald; Quitoriano, Nathaniel J.

    2014-12-01

    Using amorphous oxide templates known as micro-crucibles which confine a vapor-liquid-solid catalyst to a specific geometry, two-dimensional silicon thin-films of a single orientation have been grown laterally over an amorphous substrate and defects within crystals have been necked out. The vapor-liquid-solid catalysts consisted nominally of 99% gold with 1% titanium, chromium, or aluminum, and each alloy affected the processing of micro-crucibles and growth within them significantly. It was found that chromium additions inhibited the catalytic effect of the gold catalysts, titanium changed the morphology of the catalyst during processing and aluminum stabilized a potential third phase in the gold-silicon system upon cooling. Two mechanisms for growing undesired nanowires were identified both of which hindered the VLS film growth, fast silane cracking rates and poor gold etching, which left gold nanoparticles near the gold-vapor interface. To reduce the silane cracking rates, growth was done at a lower temperature while an engineered heat and deposition profile helped to reduce NWs caused by the second mechanism. Through experimenting with catalyst compositions, the fundamental mechanisms which produce concentration gradients across the gold-silicon alloy within a given micro-crucible have been proposed. Using the postulated mechanisms, micro-crucibles were designed which promote high-quality, single crystal growth of semiconductors.

  2. Effects of Cryogenic Forging and Anodization on the Mechanical Properties of AA 7075-T73 Aluminum Alloys

    Science.gov (United States)

    Shih, Teng-Shih; Liao, Tien-Wei; Hsu, Wen-Nong

    2016-03-01

    In this study, high-strength AA7075 alloy samples were cryogenically forged after annealing and then subjected to solution and aging treatments. The cryogenically forged 7075-T73 alloy samples displayed equiaxed fine grains associated with abundant fine precipitates in their matrix. Compared with conventional 7075-T73 alloy samples, the cryogenically forged samples exhibited an 8-12% reduction in tensile strength and an increased fatigue strength and higher corrosion resistance. The fatigue strength measured at 107 cycles was 225 MPa in the bare samples; the strength was increased to 250 MPa in the cryogenically forged samples. The effect of anodization on the corrosion resistance of the bare samples was improved from (E corr) -0.80 to -0.61 V.

  3. Synthesis and Characterization of Niobium-doped TiO2 Nanotube Arrays by Anodization of Ti-20Nb Alloys

    Institute of Scientific and Technical Information of China (English)

    Zhengchao Xu; Qi Li; Shian Gao; Jianku Shangi

    2012-01-01

    Well crystallized niobium-doped TiO; nanotube arrays (TiNbO-NT) were successfully synthesized via the anodization of titanium/niobium alloy sheets, followed with a heat treatment at 550 ℃ for 2 h. Morphology analysis results demonstrated that both the titanium/niobium alloy microstructure and the dissolution strength of electrolyte played major roles in the formation of nanotube structure. A single-phase microstructure was more favorable to the formation of uniform nanotube arrays, while modulating the dissolution strength of electrolyte was required to obtain nanotube arrays from the alloys with multi-phase microstructures. X-ray diffraction (XRD) and X-ray photoelectron (XPS) analysis results clearly demonstrated that niobium dopants (Nb^5+) were successfully doped into TiO2 anatase lattice by substituting Ti^4+ in this approach.

  4. Nanoporous alumina formed by self-organized two-step anodization of Ni{sub 3}Al intermetallic alloy in citric acid

    Energy Technology Data Exchange (ETDEWEB)

    Stepniowski, Wojciech J., E-mail: wstepniowski@wat.edu.pl [Department of Advanced Materials and Technology, Faculty of New Technologies and Chemistry, Military University of Technology, Kaliskiego 2 Str., 00-908 Warszawa (Poland); Cieslak, Grzegorz; Norek, Malgorzata; Karczewski, Krzysztof; Michalska-Domanska, Marta; Zasada, Dariusz; Polkowski, Wojciech; Jozwik, Pawel; Bojar, Zbigniew [Department of Advanced Materials and Technology, Faculty of New Technologies and Chemistry, Military University of Technology, Kaliskiego 2 Str., 00-908 Warszawa (Poland)

    2013-01-01

    Highlights: Black-Right-Pointing-Pointer Anodic porous alumina was formed by Ni{sub 3}Al intermetallic alloy anodization. Black-Right-Pointing-Pointer The anodizations were conducted in 0.3 M citric acid. Black-Right-Pointing-Pointer Nanopores geometry depends on anodizing voltage. Black-Right-Pointing-Pointer No barrier layer was formed during anodization. - Abstract: Formation of the nanoporous alumina on the surface of Ni{sub 3}Al intermetallic alloy has been studied in details and compared with anodization of aluminum. Successful self-organized anodization of this alloy was performed in 0.3 M citric acid at voltages ranging from 2.0 to 12.0 V using a typical two-electrode cell. Current density records revealed different mechanism of the porous oxide growth when compared to the mechanism pertinent for the anodization of aluminum. Electrochemical impedance spectroscopy experiments confirmed the differences in anodic oxide growth. Surface and cross-sections of the Ni{sub 3}Al intermetallic alloy with anodic oxide were observed with field-emission scanning electron microscope and characterized with appropriate software. Nanoporous oxide growth rate was estimated from cross-sectional FE-SEM images. The lowest growth rate of 0.14 {mu}m/h was found for the anodization at 0 Degree-Sign C and 2.0 V. The highest one - 2.29 {mu}m/h - was noticed for 10.0 V and 30 Degree-Sign C. Pore diameter was ranging from 18.9 nm (2.0 V, 0 Degree-Sign C) to 32.0 nm (12.0 V, 0 Degree-Sign C). Interpore distance of the nanoporous alumina was ranging from 56.6 nm (2.0 V, 0 Degree-Sign C) to 177.9 nm (12.0 V, 30 Degree-Sign C). Pore density (number of pore occupying given area) was decreasing with anodizing voltage increase from 394.5 pores/{mu}m{sup 2} (2.0 V, 0 Degree-Sign C) to 94.9 pores/{mu}m{sup 2} (12.0 V, 0 Degree-Sign C). All the geometrical features of the anodic alumina formed by two-step self-organized anodization of Ni{sub 3}Al intermetallic alloy are depending on the

  5. Intermetallic Alloys as CO Electroreduction Catalysts-Role of Isolated Active Sites

    DEFF Research Database (Denmark)

    Karamad, Mohammadreza; Tripkovic, Vladimir; Rossmeisl, Jan

    2014-01-01

    binary bulk alloys forming from these elements have been investigated using density functional theory calculations. The electronic and geometric properties of the catalyst surface can be tuned by varying the size of the active centers and the elements forming them. We have identified six different...... potentially selective intermetallic surfaces on which CO can be reduced to methanol at potentials comparable to or even slightly positive than those for CO/CO2 reduction to methane on Cu. Common features shared by most of the selective alloys are single TM sites. The role of single sites is to block parasitic...

  6. Fabrication of Ni-Ti-O nanotube arrays by anodization of NiTi alloy and their potential applications

    Science.gov (United States)

    Hang, Ruiqiang; Liu, Yanlian; Zhao, Lingzhou; Gao, Ang; Bai, Long; Huang, Xiaobo; Zhang, Xiangyu; Tang, Bin; Chu, Paul K.

    2014-01-01

    Nickel-titanium-oxide (Ni-Ti-O) nanotube arrays (NTAs) prepared on nearly equiatomic NiTi alloy shall have broad application potential such as for energy storage and biomedicine, but their precise structure control is a great challenge because of the high content of alloying element of Ni, a non-valve metal that cannot form a compact electronic insulating passive layer when anodized. In the present work, we systemically investigated the influence of various anodization parameters on the formation and structure of Ni-Ti-O NTAs and their potential applications. Our results show that well controlled NTAs can be fabricated during relatively wide ranges of the anodization voltage (5–90 V), electrolyte temperature (10–50°C) and electrolyte NH4F content (0.025–0.8 wt%) but within a narrow window of the electrolyte H2O content (0.0–1.0 vol%). Through modulating these parameters, the Ni-Ti-O NTAs with different diameter (15–70 nm) and length (45–1320 nm) can be produced in a controlled manner. Regarding potential applications, the Ni-Ti-O NTAs may be used as electrodes for electrochemical energy storage and non-enzymic glucose detection, and may constitute nanoscaled biofunctional coating to improve the biological performance of NiTi based biomedical implants. PMID:25520180

  7. Fabrication of Ni-Ti-O nanotube arrays by anodization of NiTi alloy and their potential applications

    Science.gov (United States)

    Hang, Ruiqiang; Liu, Yanlian; Zhao, Lingzhou; Gao, Ang; Bai, Long; Huang, Xiaobo; Zhang, Xiangyu; Tang, Bin; Chu, Paul K.

    2014-12-01

    Nickel-titanium-oxide (Ni-Ti-O) nanotube arrays (NTAs) prepared on nearly equiatomic NiTi alloy shall have broad application potential such as for energy storage and biomedicine, but their precise structure control is a great challenge because of the high content of alloying element of Ni, a non-valve metal that cannot form a compact electronic insulating passive layer when anodized. In the present work, we systemically investigated the influence of various anodization parameters on the formation and structure of Ni-Ti-O NTAs and their potential applications. Our results show that well controlled NTAs can be fabricated during relatively wide ranges of the anodization voltage (5-90 V), electrolyte temperature (10-50°C) and electrolyte NH4F content (0.025-0.8 wt%) but within a narrow window of the electrolyte H2O content (0.0-1.0 vol%). Through modulating these parameters, the Ni-Ti-O NTAs with different diameter (15-70 nm) and length (45-1320 nm) can be produced in a controlled manner. Regarding potential applications, the Ni-Ti-O NTAs may be used as electrodes for electrochemical energy storage and non-enzymic glucose detection, and may constitute nanoscaled biofunctional coating to improve the biological performance of NiTi based biomedical implants.

  8. Anodic oxides on a beta type Nb-Ti alloy and their characterization by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Woldemedhin, Michael Teka; Hassel, Achim Walter [Max Planck Institut fuer Eisenforschung GmbH, Duesseldorf (Germany); Institute for Chemical Technology of Inorganic Materials, Johannes Kepler University, Linz (Austria); Raabe, Dierk [Max Planck Institut fuer Eisenforschung GmbH, Duesseldorf (Germany)

    2010-04-15

    Anodic oxides were grown on the surface of an electropolished (Ti-30 at% Nb) beta-titanium ({beta}-Ti) alloy by cyclic voltammetry. The scan rate was 100 mV s{sup -1} between 0 and 8 V in increments of l V in an acetate buffer of pH 6.0. Electrochemical impedance spectroscopy was carried out right after each anodic oxide growth increment to study the electronic properties of the oxide/electrolyte interface in a wide frequency range from 100 kHz to 10 MHz with an AC perturbation voltage of 10 mV. A film formation factor of 2.4 nm V{sup -1} was found and a relative permittivity number (dielectric constant) of 42.4 was determined for the oxide film formed. Mott-Schottky analysis on a potentiostatically formed 7 nm thick oxide film was performed to assess the semiconducting properties of the mixed anodic oxide grown on the alloy. A flat band potential of -0.47 V (standard hydrogen electrode, SHE) was determined, connected to a donor density of 8.2 x 10{sup 17} cm{sup -3}. {beta}-Ti being highly isotropic in terms of mechanical properties should be superior to the stiffer {alpha}-Ti compound. Its application, however, requires a passivation behaviour comparable or better than {alpha}-Ti which in fact is found. (Abstract Copyright [2010], Wiley Periodicals, Inc.)

  9. Effects of Anodic Voltages on Microstructure and Properties of Plasma Electrolytic Oxidation Coatings on Biomedical NiTi Alloy

    Institute of Scientific and Technical Information of China (English)

    Jilin Xu; Fu Liu; Junming Luo; Liancheng Zhao

    2013-01-01

    Plasma electrolytic oxidation (PEO) coatings,formed under various anodic voltages (320-440 V) on biomedical NiTi alloy,are mainly composed of γ-Al2O3 crystal phase.The evolution of discharging sparks during the PEO process under different anodic voltages was observed.The surface and cross-sectional morphologies,composition,bonding strength,wear resistance and corrosion resistance of the coatings were investigated by scanning electron microscopy (SEM),thin-film X-ray diffraction (TF-XRD),energy dispersive X-ray spectrometry (EDS),surface roughness,direct pull-off test,ball-on-disk friction and wear test and potentiodynamic polarization test,respectively.The results showed that the evolution of discharging sparks during the PEO process directly influenced the microstructure of the PEO coatings and further influences the properties.When the anodic voltage increased from 320 V to 400 V,the corrosion resistance and wear resistance of the coatings slowly increased,and all the bonding strength was higher than 60 MPa; further increasing the anodic voltages,especially up to 440 V,although the thickness and γ-Al2O3 crystallinity of the coatings further increased,the microstructure and properties of the coatings were obviously deteriorated.

  10. Hydrothermal Synthesis of Co-Ru Alloy Particle Catalysts for Hydrogen Generation from Sodium Borohydride

    Directory of Open Access Journals (Sweden)

    Marija Kurtinaitienė

    2013-01-01

    Full Text Available We report the synthesis of μm and sub-μm-sized Co, Ru, and Co-Ru alloy species by hydrothermal approach in the aqueous alkaline solutions (pH ≥ 13 containing CoCl2 and/or RuCl3, sodium citrate, and hydrazine hydrate and a study of their catalytic properties for hydrogen generation by hydrolysis of sodium borohydride solution. This way provides a simple platform for fabrication of the ball-shaped Co-Ru alloy catalysts containing up to 12 wt% Ru. Note that bimetallic Co-Ru alloy bowls containing even 7 at.% Ru have demonstrated catalytic properties that are comparable with the ones of pure Ru particles fabricated by the same method. This result is of great importance in view of the preparation of cost-efficient catalysts for hydrogen generation from borohydrides. The morphology and composition of fabricated catalyst particles have been characterized using scanning electron microscopy, energy dispersive X-ray diffraction, and inductively coupled plasma optical emission spectrometry.

  11. A Novel Carbon Nanotube-Supported NiP Amorphous Alloy Catalyst and Its Hydrogenation Activity

    Institute of Scientific and Technical Information of China (English)

    Yan Ju; Fengyi Li

    2006-01-01

    A carbon nanotube-supported NiP amorphous catalyst (NiP/CNT) was prepared by induced reduction. Benzene hydrogenation was used as a probe reaction for the study of catalytic activity. The effects of the support on the activity and thermal stability of the supported catalyst were discussed based on various characterizations, including XRD, TEM, ICP, XPS, H2-TPD, and DTA. In comparison with the NiP amorphous alloy, the benzene conversion on NiP/CNT catalyst was lower, but the specific activity of NiP/CNT was higher, which is attributed to the dispersion produced by the support, an electron-donating effect, and the hydrogen-storage ability of CNT. The NiP/CNT thermal stability was improved because of the dispersion and electronic effects and the good heat-conduction ability of the CNT support.

  12. Influence of annealing and deformation on optical properties of ultra precision diamond turned and anodized 6060 aluminium alloy

    DEFF Research Database (Denmark)

    Tabrizian-Ghalehno, Naja; Hansen, Hans Nørgaard; Hansen, P.E.;

    2010-01-01

    function (BRDF), an optical instrument. Results indicated that the post-forging heat treatment had a great influence on the appearance of the anodized layer, which was also a function of the deformation introduced prior to heat treatment. The effect was assumed to be attributed to the change...... in microstructure, especially the distribution and the amount of the intermetallic particles such as elemental Si and Mg2Si. Roughness of the oxide film was also found to be a function of the heat treatment and deformation condition.......Influence of cold forging, and subsequent heat treatment and diamond turning on optical quality of anodized film on 6060 (AlMgSi) alloy was investigated and compared with microstructural changes. Heat treatment of the samples was carried out either prior to forging, post-forging, or both...

  13. Influence of voltage waveform on anodic film of AZ91 Mg alloy via plasma electrolytic oxidation: Microstructural characteristics and electrochemical responses

    Energy Technology Data Exchange (ETDEWEB)

    Ko, Young Gun [School of Materials Science and Engineering, Yeungnam University, Gyeongsan 712-749 (Korea, Republic of); Lee, Eung Seok [Department of Metallurgy and Materials Engineering, Hanyang University, Ansan 426-791 (Korea, Republic of); Shin, Dong Hyuk, E-mail: dhshin@hanyang.ac.kr [Department of Metallurgy and Materials Engineering, Hanyang University, Ansan 426-791 (Korea, Republic of)

    2014-02-15

    Highlights: • The effect of voltage waveform on the anodic film structure is significant. • The anodic film by asymmetric-sine wave is denser than that by half-sine wave. • Asymmetric-sine wave results in excellent electrochemical properties. -- Abstract: The present study investigated how the voltage waveform influenced the microstructural characteristics and electrochemical responses of the anodic film on AZ91 Mg alloy coated by plasma electrolytic oxidation (PEO). PEO coatings of AZ91 Mg alloy were performed for 600 s in an alkaline silicate electrolyte with respect to the voltage waveform such as half-sine and asymmetric-sine waveforms. Microstructural observations on cross section of the anodic film utilizing scanning electron microscope revealed that the anodic film formed via asymmetric-sine wave was much denser in structure than that via half-sine counterpart since the occurrence of the cathodic breakdown between the anodic pulses could effectively suppress the formation of the micro-pores and discharge channels in the anodic films. Thereby, the hardness and corrosion properties of the anodic film formed by asymmetric-sine wave were found to be superior to those by half-sine wave. In addition, electrochemical responses were interpreted in relation to the equivalent circuit model consisting of resistor and capacitor elements within an electrical cell.

  14. Apatite Formation and Biocompatibility of a Low Young's Modulus Ti-Nb-Sn Alloy Treated with Anodic Oxidation and Hot Water.

    Directory of Open Access Journals (Sweden)

    Hidetatsu Tanaka

    Full Text Available 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.

  15. Effect of anodic polarization on the free-floating parts at Pt/YSZ catalyst electrode

    Energy Technology Data Exchange (ETDEWEB)

    Toghan, Arafat, E-mail: arafat.toghan@yahoo.com [Lehrstuhl für Physikalische Chemie II, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstrasse 3, D-91058 Erlangen (Germany); Chemistry Department, Faculty of Science, South Valley University, 83523 Qena (Egypt); Institut für Physikalische Chemie und Elektrochemie, Leibniz-Universität Hannover, Callinstrasse 3-3a, D-30167 Hannover (Germany); Imbihl, R. [Institut für Physikalische Chemie und Elektrochemie, Leibniz-Universität Hannover, Callinstrasse 3-3a, D-30167 Hannover (Germany)

    2015-09-30

    Photoemission electron microscopy (PEEM) was used as spatially resolving method to explore the effect of electrochemical pumping with a positive voltage to porous platinum electrodes interfaced as working electrode to yttrium stabilized zirconia (YSZ). The experiments were conducted under UHV conditions (p ≈ 10{sup −9} mbar). In PEEM a uniform rapid darkening of the Pt surface was observed during anodic polarization followed by the appearance of bright spots on a dark background. The bright spots observed in PEEM images are due to zirconia reduction around electrically isolated Pt islands.

  16. Methanol-Tolerant Cathode Catalyst Composite For Direct Methanol Fuel Cells

    Science.gov (United States)

    Zhu, Yimin; Zelenay, Piotr

    2006-03-21

    A direct methanol fuel cell (DMFC) having a methanol fuel supply, oxidant supply, and its membrane electrode assembly (MEA) formed of an anode electrode and a cathode electrode with a membrane therebetween, a methanol oxidation catalyst adjacent the anode electrode and the membrane, an oxidant reduction catalyst adjacent the cathode electrode and the membrane, comprises an oxidant reduction catalyst layer of a platinum-chromium alloy so that oxidation at the cathode of methanol that crosses from the anode through the membrane to the cathode is reduced with a concomitant increase of net electrical potential at the cathode electrode.

  17. Characterization and reactivity of Pd Pt bimetallic supported catalysts obtained by laser vaporization of bulk alloy

    Science.gov (United States)

    Rousset, J. L.; Cadete Santos Aires, F. J.; Bornette, F.; Cattenot, M.; Pellarin, M.; Stievano, L.; Renouprez, A. J.

    2000-09-01

    Bimetallic Pd-Pt clusters produced by laser vaporization of bulk alloy have been deposited on high surface alumina. Energy dispersive X-ray (EDX) analysis and transmission electron microscopy (TEM) show that they have a perfectly well-defined stoichiometry and a narrow range of size. Therefore, they constitute ideal systems to investigate alloying effects towards reactivity. Pd-Pt alloys are already known for their applications in the hydrogenation of unsaturated hydrocarbons, especially aromatics, because this system is highly resistant to sulfur and nitrogen poisoning. In this context, the catalytic properties of this system have been investigated in the hydrogenation of tetralin in the presence of hydrogen sulfide. Preliminary results show that this model catalyst is more sulfur-resistant than each of the pure supported metals prepared by chemical methods.

  18. Pre-coating of LSCM perovskite with metal catalyst for scalable high performance anodes

    KAUST Repository

    Boulfrad, Samir

    2013-07-01

    In this work, a highly scalable technique is proposed as an alternative to the lab-scale impregnation method. LSCM-CGO powders were pre-coated with 5 wt% of Ni from nitrates. After appropriate mixing and adequate heat treatment, coated powders were then dispersed into organic based vehicles to form a screen-printable ink which was deposited and fired to form SOFC anode layers. Electrochemical tests show a considerable enhancement of the pre-coated anode performances under 50 ml/min wet H2 flow with polarization resistance decreased from about 0.60cm2 to 0.38 cm2 at 900 C and from 6.70 cm2 to 1.37 cm2 at 700 C. This is most likely due to the pre-coating process resulting in nano-scaled Ni particles with two typical sizes; from 50 to 200 nm and from 10 to 40 nm. Converging indications suggest that the latter type of particle comes from solid state solution of Ni in LSCM phase under oxidizing conditions and exsolution as nanoparticles under reducing atmospheres. Copyright © 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

  19. High throughput evaluation of perovskite-based anode catalysts for direct methanol fuel cells

    Science.gov (United States)

    Deshpande, Kishori; Mukasyan, Alexander; Varma, Arvind

    Liquid feed direct methanol fuel cells (DMFC) are promising candidates for portable power applications. However, owing to the problems associated with expensive Pt-based catalysts, viz., CO poisoning, a promising approach is to use complex oxides of the type ABO 3 (A = Sr, Ce, La, etc. and B = Co, Fe, Ni, Pt, Ru, etc.). In the current work, a variety of ABO 3 and A 2BO 4 type non-noble and partially substituted noble metal high surface area compounds were synthesized by an effective and rapid aqueous combustion synthesis (CS). Their catalytic activity was evaluated by using "High Throughput Screening Unit"-NuVant System, which compares up to 25 compositions simultaneously under DMFC conditions. It was found that the Sr-based perovskites showed performance comparable with the standard Pt-Ru catalyst. Further, it was observed that the method of doping SrRuO 3 with Pt influenced the activity. Specifically, platinum added during aqueous CS yielded better catalyst than when added externally at the ink preparation stage. Finally, it was also demonstrated that the presence of SrRuO 3 significantly enhanced the catalytic properties of Pt, leading to superior performance even at lower noble metal loadings.

  20. Effects of Al and Sn on electrochemical properties of Mg-6%Al-1%Sn (mass fraction) magnesium alloy as anode in 3.5%NaCl solution

    Institute of Scientific and Technical Information of China (English)

    黄俏; 余琨; 杨士海; 文利; 戴翼龙; 乔雪岩

    2014-01-01

    Mg-6%Al-1%Sn (mass fraction) alloy is a newly developed anode material for seawater activated batteries. The electrochemical properties of Mg-1%Sn, Mg-6%Al and Mg-6%Al-1%Sn alloys are measured by galvanostatic and potentiodynamic tests. Scanning electron microscopy (SEM) with energy dispersive spectrometry (EDS) is used to characterize the microstructures of the experimental alloys. The results show that the Mg-6%Al-1%Sn alloy obtains more negative discharge potential (−1.38 V (vs SCE)) in hot-rolled condition. This is attributed to the fine dynamically recrystallized grains during the hot rolling process. After the experimental alloys are annealed at 473 K for 1 h, the discharge potentials of Mg-6%Al-1%Sn alloy are more negative than those of Mg-6%Al alloy under different current densities. After annealing at 673 K, the discharge potentials of Mg-6%Al-1%Sn alloy become more positive than those of Mg-6%Al alloy. Such phenomenon is due to the coarse grains and the second phase Mg2Sn. The discharge potentials of Mg-1%Sn shift positively obviously in the discharge process compared with Mg-6%Al-1%Sn alloy. This is due to the corrosion products pasting on the discharge surface, which leads to anode polarization.

  1. Nanotemplated platinum fuel cell catalysts and copper-tin lithium battery anode materials for microenergy devices

    OpenAIRE

    Rohan, James F.; Hasan, Maksudul; Holubowitch, Nicolas E.

    2011-01-01

    Nanotemplated materials have significant potential for applications in energy conversion and storage devices due to their unique physical properties. Nanostructured materials provide additional electrode surface area beneficial for energy conversion or storage applications with short path lengths for electronic and ionic transport and thus the possibility of higher reaction rates. We report on the use of controlled growth of metal and alloy electrodeposited templated nanostructures for energy...

  2. Partial oxidation of dimethyl ether using the structured catalyst Rh/Al2O3/Al prepared through the anodic oxidation of aluminum.

    Science.gov (United States)

    Yu, B Y; Lee, K H; Kim, K; Byun, D J; Ha, H P; Byun, J Y

    2011-07-01

    The partial oxidation of dimethyl ether (DME) was investigated using the structured catalyst Rh/Al2O3/Al. The porous Al2O3 layer was synthesized on the aluminum plate through anodic oxidation in an oxalic-acid solution. It was observed that about 20 nm nanopores were well developed in the Al2O3 layer. The thickness of Al2O3 layer can be adjusted by controlling the anodizing time and current density. After pore-widening and hot-water treatment, the Al2O3/Al plate was calcined at 500 degrees C for 3 h. The obtained delta-Al2O3 had a specific surface area of 160 m2/g, making it fit to be used as a catalyst support. A microchannel reactor was designed and fabricated to evaluate the catalytic activity of Rh/Al2O3/Al in the partial oxidation of DME. The structured catalyst showed an 86% maximum hydrogen yield at 450 degrees C. On the other hand, the maximum syngas yield by a pack-bed-type catalyst could be attained by using a more than fivefold Rh amount compared to that used in the structured Rh/Al2O3/Al catalyst.

  3. First-principles study of interphase Ni3Sn in Sn-Ni alloy for anode of lithium ion battery

    Institute of Scientific and Technical Information of China (English)

    Hou Xian-Hua; Hu She-Jun; Li Wei-Shan; Ru Qiang; Yu Hong-Wen; Huang Zhao-Wen

    2008-01-01

    This paper investigates the mechanism of Li insertion into interphase NiaSn in Ni-Sn alloy for the anode of lithium ion battery by means of the first-principles plane-wave pseudopotential.Compared with other phases,it is found that the Ni3Sn has larger relative expansion ratio and lower electrochemical potential,with its specific plateaus voltage around 0.3 eV when lithium atoms are filled in all octahedral interstitial sites.and the relative expansion ratio increasing dramatically when the lithiated phase transits from octahedral interstitial sites to tetrahedral interstitial sites.So this phase is a devastating phase for whole alloy electrode materials.

  4. The effects of hydrogen sulfide on the polymer electrolyte membrane fuel cell anode catalyst: H2S-Pt/C interaction products

    Science.gov (United States)

    Lopes, Thiago; Paganin, Valdecir A.; Gonzalez, Ernesto R.

    2011-08-01

    The performance of a polymer electrolyte membrane fuel cell (PEMFC) operating on a simulated hydrocarbon reformate is described. The anode feed stream consisted of 80% H2, ∼20% N2, and 8 ppm hydrogen sulfide (H2S). Cell performance losses are calculated by evaluating cell potential reduction due to H2S contamination through lifetime tests. It is found that potential, or power, loss under this condition is a result of platinum surface contamination with elemental sulfur. Electrochemical mass spectroscopy (EMS) and electrochemical techniques are employed, in order to show that elemental sulfur is adsorbed onto platinum, and that sulfur dioxide is one of the oxidation products. Moreover, it is demonstrated that a possible approach for mitigating H2S poisoning on the PEMFC anode catalyst is to inject low levels of air into the H2S-contaminated anode feeding stream.

  5. Determination of sulfuric acid concentration for anti-cavitation characteristics of Al alloy by two step anodizing process to forming nano porous.

    Science.gov (United States)

    Lee, Seung-Jun; Kim, Seong-Kweon; Jeong, Jae-Yong; Kim, Seong-Jong

    2014-12-01

    Al alloy is a highly active metal but forms a protective oxide film having high corrosion resistance in atmosphere environment. However, the oxide film is not suitable for practical use, since the thickness of the film is not uniform and it is severly altered with formation conditions. This study focused on developing an aluminum anodizing layer having hardness, corrosion resistance and abrasion resistance equivalent to a commercial grade protective layer. Aluminum anodizing layer was produced by two-step aluminum anodizing oxide (AAO) process with different sulfuric acid concentrations, and the cavitation characteristics of the anodized coating layer was investigated. In hardness measurement, the anodized coating layer produced with 15 vol.% of sulfuric acid condition had the highest value of hardness but exhibited poor cavitation resistance due to being more brittle than those with other conditions. The 10 vol.% of sulfuric acid condition was thus considered to be the optimum condition as it had the lowest weight loss and damage depth.

  6. Effect of sodium tartrate concentrations on morphology and characteristics of anodic oxide film on titanium alloy Ti–10V–2Fe–3Al

    Directory of Open Access Journals (Sweden)

    Ma Kun

    2016-08-01

    Full Text Available The effect of sodium tartrate concentrations on morphology and characteristics of anodic oxide film on titanium alloy was investigated. The alloy substrates were anodized in different concentration solutions of sodium tartrate with the addition of PTFE emulsion and their morphology and characteristics were analyzed. The anodic oxide film presented a uniform petaloid drums and micro-cracks morphology. Additionally, micro-cracks dramatically swelled with the increase of the tartrate concentrations. The thickness of the anodic oxide film increased with the concentrations until the concentration reached 15 g/L. The results of Raman analysis illustrate that all samples have similarity in the crystal structure, consisting of mainly amorphous TiO2, some anatase TiO2 and a small amount of rutile TiO2. And the ratios of anatase TiO2 and rutile TiO2 increase with the concentrations until it reaches 15 g/L. Furthermore, the intensity of the peaks increases with enhanced concentrations until the concentration reaches 15 g/L. The corrosion resistance of the anodic oxide film is increased by the sodium tartrate with higher concentrations before 15 g/L. The coefficient of friction of the anodic oxide film reduces with the concentrations until the concentration reaches 15 g/L, then the coefficient of friction of the anodic oxide film increases with the concentrations.

  7. Amide group anchored glucose oxidase based anodic catalysts for high performance enzymatic biofuel cell

    Science.gov (United States)

    Chung, Yongjin; Ahn, Yeonjoo; Kim, Do-Heyoung; Kwon, Yongchai

    2017-01-01

    A new enzyme catalyst is formed by fabricating gold nano particle (GNP)-glucose oxidase (GOx) clusters that are then attached to polyethyleneimine (PEI) and carbon nanotube (CNT) with cross-linkable terephthalaldehyde (TPA) (TPA/[CNT/PEI/GOx-GNP]). Especially, amide bonds belonging to TPA play an anchor role for incorporating rigid bonding among GNP, GOx and CNT/PEI, while middle size GNP is well bonded with thiol group of GOx to form strong GNP-GOx cluster. Those bonds are identified by chemical and electrochemical characterizations like XPS and cyclic voltammogram. The anchording effect of amide bonds induces fast electron transfer and strong chemical bonding, resulting in enhancements in (i) catalytic activity, (ii) amount of immobilized GOx and (ii) performance of enzymatic biofuel cell (EBC) including the catalyst. Regarding the catalytic activity, the TPA/[CNT/PEI/GOx-GNP] produces high electron transfer rate constant (6 s-1), high glucose sensitivity (68 μA mM-1 cm-2), high maximum current density (113 μA cm-2), low charge transfer resistance (17.0 Ω cm2) and long-lasting durability while its chemical structure is characterized by XPS confirming large portion of amide bond. In EBC measurement, it has high maximum power density (0.94 mW cm-2) compatible with catalytic acitivity measurements.

  8. Effect of Solution Temperature for Al Alloy Anodizing on Cavitation Characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Seung-Jun [Kunsan National University, Kunsan (Korea, Republic of); Lee, Jung Hyung; Kim, Seong Jong [Mokpo National Maritime University, Haeyangdaehak-ro 91, Mokpo (Korea, Republic of)

    2015-06-15

    The commercialization of aluminum had been delayed than other metals because of its high oxygen affinity. Anodizing is a process in which oxide film is formed on the surface of a valve metal in an electrolyte solution by anodic oxidation reaction. Aluminum has thin oxide film on surface but the oxide film is inhomogeneous having a thickness only in the range of several nanometers. Anodizing process increases the thickness of the oxide film significantly. In this study, porous type oxide film was produced on the surface of aluminum in sulfuric acid as a function of electrolyte temperature, and the optimum condition were determined for anodizing film to exhibit excellent cavitation resistance in seawater environment. The result revealed that the oxide film formed at 10 ℃ represented the highest cavitation resistance, while the oxide film formed at 15 ℃ showed the lowest resistance to cavitation in spite of its high hardness.

  9. Ethane dehydrogenation over nano-Cr 2O 3 anode catalyst in proton ceramic fuel cell reactors to co-produce ethylene and electricity

    Science.gov (United States)

    Fu, Xian-Zhu; Luo, Xiao-Xiong; Luo, Jing-Li; Chuang, Karl T.; Sanger, Alan R.; Krzywicki, Andrzej

    Ethane and electrical power are co-generated in proton ceramic fuel cell reactors having Cr 2O 3 nanoparticles as anode catalyst, BaCe 0.8Y 0.15Nd 0.05O 3- δ (BCYN) perovskite oxide as proton conducting ceramic electrolyte, and Pt as cathode catalyst. Cr 2O 3 nanoparticles are synthesized by a combustion method. BaCe 0.8Y 0.15Nd 0.05O 3- δ (BCYN) perovskite oxides are obtained using a solid state reaction. The power density increases from 51 mW cm -2 to 118 mW cm -2 and the ethylene yield increases from about 8% to 31% when the operating temperature of the solid oxide fuel cell reactor increases from 650 °C to 750 °C. The fuel cell reactor and process are stable at 700 °C for at least 48 h. Cr 2O 3 anode catalyst exhibits much better coke resistance than Pt and Ni catalysts in ethane fuel atmosphere at 700 °C.

  10. Magnetically stabilized bed reactor for selective hydrogenation of olefins in reformate with amorphous nickel alloy catalyst

    Institute of Scientific and Technical Information of China (English)

    Xuhong Mu; Enze Min

    2007-01-01

    A magnetically stabilized bed (MSB) reactor for selective hydrogenation of olefins in reformate was developed by combining the advantages of MSB and amorphous nickel alloy catalyst. The effects of operating conditions, such as temperature, pressure, liquid space velocity, hydrogen-to-oil ratio, and magnetic field intensity on the reaction were studied. A mathematical model of MSB reactor for hydrogenation of olefins in reformate was established. A reforming flow scheme with a post-hydrogenation MSB reactor was proposed. Finally, MSB hydrogenation was compared with clay treatment and conventional post-hydrogenation.

  11. The features of CNT growth on catalyst-content amorphous alloy layer by CVD-method

    Science.gov (United States)

    Dubkov, S.; Bulyarskii, S.; Pavlov, A.; Trifonov, A.; Kitsyuk, E.; Mierczynski, P.; Maniecki, T.; Ciesielski, R.; Gavrilov, S.; Gromov, D.

    2016-12-01

    This work is devoted to the CVD-synthesis of arrays of carbon nanotubes (CNTs) on Co-Zr-N-(O), Ni-Nb-N-(O), Co- Ta-N-(O) catalytic alloy films from gas mixture of C2H2+NH3+Ar at a substrate temperature of about 550°C.Heating of the amorphous alloy causes its crystallization and squeezing of the catalytic metal onto the surface. As a result, small catalyst particles are formed on the surface. The CNT growth takes place after wards on these particles. It should be noted that the growth of CNT arrays on these alloys is insensitive to the thickness of alloy film, which makes this approach technically attractive. In particular, the possibility of local CNT growth at the ends of the Co-Ta-N-(O) film and three-level CNT growth at the end of more complex structure SiO2/Ni-Nb-N-O/SiO2/Ni-Nb-N-O/SiO2/Ni-Nb-N-O/SiO2 is demonstrated.

  12. The Integration of a Structural Water Gas Shift Catalyst with a Vanadium Alloy Hydrogen Transport Device

    Energy Technology Data Exchange (ETDEWEB)

    Barton, Thomas; Argyle, Morris; Popa, Tiberiu

    2009-06-30

    This project is in response to a requirement for a system that combines water gas shift technology with separation technology for coal derived synthesis gas. The justification of such a system would be improved efficiency for the overall hydrogen production. By removing hydrogen from the synthesis gas stream, the water gas shift equilibrium would force more carbon monoxide to carbon dioxide and maximize the total hydrogen produced. Additional benefit would derive from the reduction in capital cost of plant by the removal of one step in the process by integrating water gas shift with the membrane separation device. The answer turns out to be that the integration of hydrogen separation and water gas shift catalysis is possible and desirable. There are no significant roadblocks to that combination of technologies. The problem becomes one of design and selection of materials to optimize, or at least maximize performance of the two integrated steps. A goal of the project was to investigate the effects of alloying elements on the performance of vanadium membranes with respect to hydrogen flux and fabricability. Vanadium was chosen as a compromise between performance and cost. It is clear that the vanadium alloys for this application can be produced, but the approach is not simple and the results inconsistent. For any future contracts, large single batches of alloy would be obtained and rolled with larger facilities to produce the most consistent thin foils possible. Brazing was identified as a very likely choice for sealing the membranes to structural components. As alloying was beneficial to hydrogen transport, it became important to identify where those alloying elements might be detrimental to brazing. Cataloging positive and negative alloying effects was a significant portion of the initial project work on vanadium alloying. A water gas shift catalyst with ceramic like structural characteristics was the second large goal of the project. Alumina was added as a

  13. The Integration of a Structural Water Gas Shift Catalyst with a Vanadium Alloy Hydrogen Transport Device

    Energy Technology Data Exchange (ETDEWEB)

    Barton, Thomas; Argyle, Morris; Popa, Tiberiu

    2009-06-30

    This project is in response to a requirement for a system that combines water gas shift technology with separation technology for coal derived synthesis gas. The justification of such a system would be improved efficiency for the overall hydrogen production. By removing hydrogen from the synthesis gas stream, the water gas shift equilibrium would force more carbon monoxide to carbon dioxide and maximize the total hydrogen produced. Additional benefit would derive from the reduction in capital cost of plant by the removal of one step in the process by integrating water gas shift with the membrane separation device. The answer turns out to be that the integration of hydrogen separation and water gas shift catalysis is possible and desirable. There are no significant roadblocks to that combination of technologies. The problem becomes one of design and selection of materials to optimize, or at least maximize performance of the two integrated steps. A goal of the project was to investigate the effects of alloying elements on the performance of vanadium membranes with respect to hydrogen flux and fabricability. Vanadium was chosen as a compromise between performance and cost. It is clear that the vanadium alloys for this application can be produced, but the approach is not simple and the results inconsistent. For any future contracts, large single batches of alloy would be obtained and rolled with larger facilities to produce the most consistent thin foils possible. Brazing was identified as a very likely choice for sealing the membranes to structural components. As alloying was beneficial to hydrogen transport, it became important to identify where those alloying elements might be detrimental to brazing. Cataloging positive and negative alloying effects was a significant portion of the initial project work on vanadium alloying. A water gas shift catalyst with ceramic like structural characteristics was the second large goal of the project. Alumina was added as a

  14. 锂离子电池Sn基合金负极材料%Tin-Based Alloy Anode Materials for Lithium Ion Batteries

    Institute of Scientific and Technical Information of China (English)

    褚道葆; 李建; 袁希梅; 李自龙; 魏旭; 万勇

    2012-01-01

    Development of high safety, high energy, low cost and long service life Li ion rechargeable batteries is current a tremendous challenge for power battery application. The performance of the battery mainly depends on the nature of anode and cathode materials. Tin-based alloy is an industrially promising anode material for lithium ion batteries due to its high energy capacity and safety characteristics. In this review, the recent progress in Sn-based alloy anode materials for lithium ion batteries are reviewed. The different preparation methods of Sn- based alloy anodes are summarized. This review focuses on the problems in electrochemical properties of the Sn- based alloy anode and their causes, including the effect of loss of active material, SEI film and oxide film formation, aggregation of alloy particles and generation of dead lithium in the process of the intercalation of lithium ions on the charge and discharge performance of the alloy anode. The research trends in improving the electrochemical performance of the Sn-based alloy anode are prospected.%发展高安全性、高能量、低成本、长寿命锂离子电池是当前动力电池应用面临的巨大挑战。电池的性能主要取决于正负极电极材料的性能。Sn基合金负极具有高能量和安全特性,是一种很有产业化前景的锂离子电池负极材料。本文综述了Sn基合金电极作为锂离子电池负极的最新研究进展,对Sn基合金负极的不同制备方法进行了总结,重点介绍了锡基合金负极材料在电化学性能方面所存在的问题及其原因,包括锡基活性物质的损失、SEI膜和氧化膜的形成、纳米粒子的团聚和锂离子嵌入过程中死锂的产生等影响合金充放电性能的因素,最后展望了以提高Sn基合金负极电化学性能为目的的研究趋势。

  15. Bi-Sn alloy catalyst for simultaneous morphology and doping control of silicon nanowires in radial junction solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Zhongwei [National Laboratory of Solid State Microstructures and School of Electronics Science and Engineering/Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093 (China); School of Science, Nantong University, Nantong 226000 (China); Lu, Jiawen; Qian, Shengyi; Xu, Jun; Xu, Ling; Wang, Junzhuan; Shi, Yi; Chen, Kunji [National Laboratory of Solid State Microstructures and School of Electronics Science and Engineering/Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093 (China); Misra, Soumyadeep; Roca i Cabarrocas, Pere [LPICM, CNRS, Ecole Polytechnique, Université Paris-Saclay, 91128 Palaiseau (France); Yu, Linwei, E-mail: yulinwei@nju.edu.cn, E-mail: linwei.yu@polytechnique.edu [National Laboratory of Solid State Microstructures and School of Electronics Science and Engineering/Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093 (China); LPICM, CNRS, Ecole Polytechnique, Université Paris-Saclay, 91128 Palaiseau (France)

    2015-10-19

    Low-melting point metals such as bismuth (Bi) and tin (Sn) are ideal choices for mediating a low temperature growth of silicon nanowires (SiNWs) for radial junction thin film solar cells. The incorporation of Bi catalyst atoms leads to sufficient n-type doping in the SiNWs core that exempts the use of hazardous dopant gases, while an easy morphology control with pure Bi catalyst has never been demonstrated so far. We here propose a Bi-Sn alloy catalyst strategy to achieve both a beneficial catalyst-doping and an ideal SiNW morphology control. In addition to a potential of further growth temperature reduction, we show that the alloy catalyst can remain quite stable during a vapor-liquid-solid growth, while providing still sufficient n-type catalyst-doping to the SiNWs. Radial junction solar cells constructed over the alloy-catalyzed SiNWs have demonstrated a strongly enhanced photocurrent generation, thanks to optimized nanowire morphology, and largely improved performance compared to the reference samples based on the pure Bi or Sn-catalyzed SiNWs.

  16. Effect of Fluoride Ions on the Anodic Behavior of Mill Annealed and Aged Alloy 22

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez, M A; Carranza-, R M; Rebak, R B

    2003-10-07

    Alloy 22 (N06022) is the current candidate alloy to fabricate the external wall of the high level nuclear waste containers for the Yucca Mountain repository. It was of interest to study and compare the general and localized corrosion susceptibility of Alloy 22 in saturated NaF solutions ({approx} 1 M NaF) at 90 C. Standard electrochemical tests such as cyclic potentiodynamic polarization, amperometry, potentiometry, and electrochemical impedance spectroscopy were used. Studied variables included the solution pH and the alloy microstructure (thermal aging). Results show that Alloy 22 is highly resistant to general and localized corrosion in pure fluoride solutions. Thermal aging is not detrimental and even seems to be slightly beneficial for general corrosion in alkaline solutions.

  17. Studies on anodic oxide coating with low absorptance and high emittance on aluminum alloy 2024

    Energy Technology Data Exchange (ETDEWEB)

    Siva Kumar, C. [Department of Post-graduate studies in Chemistry, Central College, Bangalore (India); Sharma, A.K. [Thermal Process Section, ISRO Satellite Centre, Vimanapura Post, Bangalore (India); Mahendra, K.N.; Mayanna, S.M. [Department of Post-graduate studies in Chemistry, Central College, Bangalore (India)

    2000-01-01

    Anodization of AA 2024 in sulfuric acid bath containing glycerol, lactic acid and ammonium metavenadate has been studied to develop white anodic oxide coating. Investigation on the influence of various operating parameters - coating thickness, current density and ammonium metavenadate concentration on the optical properties was carried out to optimize the process. Infrared, atomic absorption spectroscopic techniques and scanning electron micrograph were used to characterize the coating. The obtained oxide coating provides a ratio of solar absorptance ({alpha}) to infrared emittance ({epsilon}), as low as 0.2. The optical properties and hardness values measured under optimum experimental conditions support its use as a thermal control coating.

  18. Effect of nickel content on the anodic dissolution and passivation of zinc–nickel alloys in alkaline solutions by potentiodynamic and potentiostatic techniques

    Indian Academy of Sciences (India)

    Abdel-Rahman El-Sayed; Hany M Abd El-Lateef; Hossnia S Mohran

    2015-04-01

    The effect of systematic increase of Ni on the anodic dissolution and passivation of Zn–Ni alloys in various concentrations of KOH solution (0.1–1 M) was investigated. The anodic dissolution and passivation behaviour for each pure Zn and Ni in the same studied solutions was also investigated, and the obtained data were compared. Potentiodynamic and potentiostatic methods were used, and the corrosion layer formed on each electrode surface was characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). The results of the anodic potentiodynamic measurements exhibited that the polarization curves showed active/passive transition in the case of Ni and active/pseudopassive in the case of both Zn and its alloys. The results showed that the increase in Ni content increases the activation energy (a) and decreases the dissolution rate of the alloys in KOH solution, and the lowest dissolution rate was obtained at 10% Ni. The results of both potentiodynamic and potentiostatic measurements exhibit sudden increase in current density which is observed at certain positive potential (+0.42 V .SCE) in the case of the investigated alloys. This indicates that the addition of Ni to Zn promotes the electrochemical reaction (in the passive region). However, the passivation potential shifted to more positive direction with the increase in Ni content in the alloy.

  19. Activity and Stability of Rare Earth-Based Hydride Alloys as Catalysts of Hydrogen Absorption-Oxidation Reactions

    Institute of Scientific and Technical Information of China (English)

    Ying Taokai(应桃开); Gao Xueping(高学平); Hu Weikang(胡伟康); Noréus Dag

    2004-01-01

    Rare earth-based AB5-type hydrogen storage alloys as catalysts of hydrogen-diffusion electrodes for hydrogen absorption and oxidation reactions in alkaline fuel cells were investigated. It is demonstrated that the meta-hydride hydrogen-diffusion electrodes could be charged by hydrogen gas and electrochemically discharged at the same time to retain a stable oxidation potential for a long period. The catalytic activities and stability are almost comparable with a Pt catalyst on the active carbon. Further improvement of performances is expected via reduction of catalyst size into nanometers.

  20. Fabrication and characterization of anodic oxide films on a Ti-10V-2Fe-3Al titanium alloy

    Institute of Scientific and Technical Information of China (English)

    Jian-hua Liu; Jun-lan Yi; Song-mei Li; Mei Yu; Yong-zhen Xu

    2009-01-01

    Anodic oxide films of the titanium alloy Ti-10V-2Fe-3Al in ammonium tartrate electrolyte without hydrofluoric acid or fluoride were fabricated.The morphology,components,and microstructure of the films were characterized by scanning electron mi-croscopy (SEM),X-ray photoelectron spectroscopy (XPS),X-ray diffraction (XRD),and Raman spectroscopy.The results showed that the films were thick,uniform,and nontransparent.Such films exhibited sedimentary morphology,with a thickness of about 3 μm,and the pore diameters of the deposits ranged from several hundred nanometers to 1.5 μm.The films were mainly titanium dioxide.Some coke-like deposits,which may contain or be changed by OH,NH,C-C,C-O,and C=O groups,were doped in the firms.The films were mainly amorphous with a small amount of anatase and rutile phase.

  1. Investigation of carbon supported PtW catalysts as CO tolerant anodes at high temperature in proton exchange membrane fuel cell

    Science.gov (United States)

    Hassan, Ayaz; Paganin, Valdecir A.; Ticianelli, Edson A.

    2016-09-01

    The CO tolerance mechanism and the stability of carbon supported PtW electrocatalysts are evaluated in the anode of a proton exchange membrane fuel cell (PEMFC) at two different temperatures. The electrocatalysts are characterized by energy dispersive spectroscopy, X-ray diffraction, and transmission electron spectroscopy. Employed electrochemical techniques include cyclic voltammetry, CO stripping, fuel cell polarization, and online mass spectrometry. At a cell temperature of 85 °C, the PtW/C catalyst shows higher CO tolerance compared to Pt/C due an electronic effect of WOx in the Pt 5d band, which reduces the CO adsorption. An increase in hydrogen oxidation activity in the presence of CO is observed for both the catalysts at a higher temperature, due to the decrease of the Pt-CO coverage. A reduction in the current densities occurs for the PtW/C catalyst in both polarization curves and cyclic voltammograms after 5000 cycles of the anode in the range of 0.1-0.7 V vs. RHE at 50 mVs-1. This decrease in performance is assigned to the dissolution of W, with a consequent increase in the membrane resistivity. However, the observed decline of performance is small either in the presence of pure H2 or in the presence of H2/CO.

  2. Electrically conductive anodized aluminum coatings

    Science.gov (United States)

    Alwitt, Robert S. (Inventor); Liu, Yanming (Inventor)

    2001-01-01

    A process for producing anodized aluminum with enhanced electrical conductivity, comprising anodic oxidation of aluminum alloy substrate, electrolytic deposition of a small amount of metal into the pores of the anodized aluminum, and electrolytic anodic deposition of an electrically conductive oxide, including manganese dioxide, into the pores containing the metal deposit; and the product produced by the process.

  3. Rhenium Nanochemistry for Catalyst Preparation

    Directory of Open Access Journals (Sweden)

    Vadim G. Kessler

    2012-08-01

    Full Text Available The review presents synthetic approaches to modern rhenium-based catalysts. Creation of an active center is considered as a process of obtaining a nanoparticle or a molecule, immobilized within a matrix of the substrate. Selective chemical routes to preparation of particles of rhenium alloys, rhenium oxides and the molecules of alkyltrioxorhenium, and their insertion into porous structure of zeolites, ordered mesoporous MCM matrices, anodic mesoporous alumina, and porous transition metal oxides are considered. Structure-property relationships are traced for these catalysts in relation to such processes as alkylation and isomerization, olefin metathesis, selective oxidation of olefins, methanol to formaldehyde conversion, etc.

  4. Synthesis And Electrochemical Characteristics Of Mechanically Alloyed Anode Materials SnS2 For Li/SnS2 Cells

    Directory of Open Access Journals (Sweden)

    Hong J.H.

    2015-06-01

    Full Text Available With the increasing demand for efficient and economic energy storage, tin disulfide (SnS2, as one of the most attractive anode candidates for the next generation high-energy rechargeable Li-ion battery, have been paid more and more attention because of its high theoretical energy density and cost effectiveness. In this study, a new, simple and effective process, mechanical alloying (MA, has been developed for preparing fine anode material tin disulfides, in which ammonium chloride (AC, referred to as process control agents (PCAs, were used to prevent excessive cold-welding and accelerate the synthesis rates to some extent. Meanwhile, in order to decrease the mean size of SnS2 powder particles and improve the contact areas between the active materials, wet milling process was also conducted with normal hexane (NH as a solvent PCA. The prepared powders were both characterized by X-ray diffraction, Field emission-scanning electron microscopeand particle size analyzer. Finally, electrochemical measurements for Li/SnS2 cells were takenat room temperature, using a two-electrode cell assembled in an argon-filled glove box and the electrolyte of 1M LiPF6 in a mixture of ethylene carbonate(EC/dimethylcarbonate (DMC/ethylene methyl carbonate (EMC (volume ratio of 1:1:1.

  5. Preparation of Uniform Ni-B Amorphous Alloy Catalyst on CNTs and its Performance for Acetylene Selective Hydrogenation

    Institute of Scientific and Technical Information of China (English)

    Chang Yuan HU; Feng Yi LI; Rong Bin ZHANG; Li HUA

    2006-01-01

    Uniform Ni-B amorphous alloys about 14 nm have been prepared on CNTs-A support,named Ni-B/CNTs-A. In comparison with the Ni-B/CNTs amorphous catalyst, Ni-B/CNTs-A showed higher nickel loading, determined by ICP and better catalytic activity and ethylene selectivity in the acetylene hydrogenation reaction.

  6. Influence of molybdate species on the tartaric acid/sulphuric acid anodic films grown on AA2024 T3 aerospace alloy

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Rubio, M. [Departamento de Quimica-Fisica Aplicada, Universidad Autonoma de Madrid, 28049 Madrid (Spain); Department of Surface Technologies, Engineering of Materials and Processes, Airbus Spain, Av. John Lennon s/n 28906 Getafe (Spain); Ocon, P. [Departamento de Quimica-Fisica Aplicada, Universidad Autonoma de Madrid, 28049 Madrid (Spain)], E-mail: pilar.ocon@uam.es; Climent-Font, A. [Departamento de Fisica Aplicada, Universidad Autonoma de Madrid (UAM), 28049 Madrid (Spain); Centro de Micro-Analisis de Materiales (CMAM), Universidad Autonoma de Madrid (UAM), 28049 Madrid (Spain); Smith, R.W. [Unidad de Microanalisis de Materiales, Parque Cientifico de Madrid (PCM), Campus de Cantoblanco, 28049 Madrid (Spain); Curioni, M.; Thompson, G.E.; Skeldon, P. [Corrosion and Protection Centre, School of Materials, University of Manchester, M60 1QD England (United Kingdom); Lavia, A.; Garcia, I. [Department of Surface Technologies, Engineering of Materials and Processes, Airbus Spain, Av. John Lennon s/n 28906 Getafe (Spain)

    2009-09-15

    AA2024 T3 alloy specimens have been anodised in tartaric acid/sulphuric media and tartaric acid/sulphuric media containing sodium molybdate; molybdate species were added to the anodising bath to enhance further the protection provided by the porous anodic film developed over the macroscopic alloy surface. Morphological characterisation of the anodic films formed in both electrolytes was undertaken using scanning electron and transmission electron microscopies; the chemical compositions of the films were determined by Rutherford backscattering spectroscopy that was complemented by elemental depth profiling using rf-glow discharge optical emission spectrometry. The electrochemical behaviour was evaluated using potentiodynamic polarisations and electrochemical impedance spectroscopy; the corrosion performance was examined after salt spray testing. The porous anodic film morphology was little influenced by the addition of molybdate salt, although thinner films were generated in its presence. Chemical composition of the anodic film was roughly similar; however, addition of sodium molybdate in the anodizing bath resulted in residues of molybdate species in the porous skeleton and improved corrosion resistance measured by electrochemical techniques that was confirmed by salt spray testing.

  7. High-performance core-shell PdPt@Pt/C catalysts via decorating PdPt alloy cores with Pt

    Science.gov (United States)

    Wu, Yan-Ni; Liao, Shi-Jun; Liang, Zhen-Xing; Yang, Li-Jun; Wang, Rong-Fang

    A core-shell structured low-Pt catalyst, PdPt@Pt/C, with high performance towards both methanol anodic oxidation and oxygen cathodic reduction, as well as in a single hydrogen/air fuel cell, is prepared by a novel two-step colloidal approach. For the anodic oxidation of methanol, the catalyst shows three times higher activity than commercial Tanaka 50 wt% Pt/C catalyst; furthermore, the ratio of forward current I f to backward current I b is high up to 1.04, whereas for general platinum catalysts the ratio is only ca. 0.70, indicating that this PdPt@Pt/C catalyst has high activity towards methanol anodic oxidation and good tolerance to the intermediates of methanol oxidation. The catalyst is characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The core-shell structure of the catalyst is revealed by XRD and TEM, and is also supported by underpotential deposition of hydrogen (UPDH). The high performance of the PdPt@Pt/C catalyst may make it a promising and competitive low-Pt catalyst for hydrogen fueled polymer electrolyte membrane fuel cell (PEMFC) or direct methanol fuel cell (DMFC) applications.

  8. AB5-type Hydrogen Storage Alloy Modified with Ti/Zr Used as Anodic Materials in Borohydride Fuel Cell

    Institute of Scientific and Technical Information of China (English)

    Lianbang WANG; Chunan MA; Xinbiao MAO; Yuanming SUN; Seijiro SUDA

    2005-01-01

    Fuel cell using borohydride as the fuel has received much attention. AB5-type hydrogen storage alloy used as the anodic material instead of noble metals has been investigated. In order to restrain the generation of hydrogen and enhance the utilization of borohydride, Ti/Zr metal powders has been added into the parent LmNi4.78Mn0.22 (where Lm is La-richened mischmetal) alloy (LNM) by ball milling and heat treatment methods. It is found that the addition of Ti/Zr metal powders lowers the electrochemical catalytic activity of the electrodes, at the same time, restrains the generation of hydrogen and enhances the utilization of the fuel. All the results show that the hydrogen generation rate or the utilization of the fuel is directly relative to the electrochemical catalytic activity or the discharge capability of the electrodes. The utilization of the fuel increases with discharge current density. It is very important to find a balance between the discharge capability and the utilization of the fuel.

  9. Effects of acidity and alkalinity on corrosion behaviour of Al-Zn-Mg based anode alloy

    Science.gov (United States)

    Ma, Jingling; Wen, Jiuba; Li, Quanan; Zhang, Qin

    2013-03-01

    Effects of 1 M HCl, 0.6 M NaCl with different pH values and 4 M NaOH solutions on the corrosion behaviour of Al-5Zn-1Mg-0.02In-0.05Ti-0.5Mn (wt%) alloy have been investigated using measurements of self-corrosion, potentiodynamic polarization, cyclic polarization experiment combined with open circuit potential technique and scanning electron microscopy. The corrosion behaviour of the alloy was found to be dependant on the Cl-, OH- ions and pH value. In acidic or slightly neutral solutions, general and pitting corrosion occurred simultaneously. In contrast, exposure to alkaline solutions results in general corrosion which was traced back to the dissolution of the resistive oxidation film on the surface of the alloy. Experience revealed that the alloy was susceptible to pitting corrosion in all chloride solution. The alloy undergoes two types of localized corrosion process, leading to the formation of hemispherical and crystallographic pits. Polarization resistance measurements which are in good agreement with those of self-corrosion, show that the corrosion kinetic is minimized in slightly neutral solutions (pH = 7).

  10. Influence of Ga and Hg on microstructure and electrochemical corrosion behavior of Mg alloy anode materials

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The effects of Hg and Ga on the electrochemical corrosion behavior of Mg-5%Hg (molar fraction) alloys were investigated by the measurement of polarization curves and galvanostatic test. The microstructure of the alloys and the corroded surface of the specimens were investigated by scanning electron microscopy, X-ray diffractometry and emission spectrum analysis. It can be concluded that the addition of 1%Ga (molar fraction) reduces corrosion current density from 26.98 mA/cm2 to 2.34 mA/cm2;while the addition of 1%Hg (molar fraction) increases corrosion current density. The addition of Ga and Hg both promotes the electrochemical activity of the alloys and the influence of Ga is more effective than Hg. Mg-5%Hg-1%Ga alloy has the best electrochemical activity, showing mean potential of-1.992 V. The activation mechanism of the magnesium alloy produced by Hg and Ga was put forward. Magnesium atoms are dissolved in liquid Hg and Ga to form amalgam and undergo severe oxidation at the amalgam/electrolyte interface.

  11. Oxidation of Fe-W Alloy Electrodeposits for Application to Anodes as Lithium Ion Batteries

    Science.gov (United States)

    Su, Changwei; Ye, Mengchao; Zhon, Linxing; Hou, Jianping; Li, Junmin; Guo, Junming

    2016-12-01

    A citrate-ammonia bath was selected to electrodeposit Fe-W alloys, which exhibit a crystalline structure even if the content of W in the Fe-W alloy is up to 37.8wt%. Those alloys could be oxidized partly at 700∘C. Resultant oxides were composed of Fe2O3, Fe3O4 and amorphous products. The composite oxides presented better electrochemical properties than those of the Fe2O3 and Fe3O4 composite formed by oxidation of Fe deposits. For instance, such an electrode demonstrates the reversible capacity of up to 2438.3mAhg-1 (in terms of incremental oxygen) after 100 charge-discharge cycles, while the electrodes of Fe2O3 and Fe3O4 composites formed by oxidation of Fe deposits were of only 667.5mAhg-1.

  12. Effect of the Pd/MWCNTs anode catalysts preparation methods on their morphology and activity in a direct formic acid fuel cell

    Science.gov (United States)

    Lesiak, B.; Mazurkiewicz, M.; Malolepszy, A.; Stobinski, L.; Mierzwa, B.; Mikolajczuk-Zychora, A.; Juchniewicz, K.; Borodzinski, A.; Zemek, J.; Jiricek, P.

    2016-11-01

    Impact of Pd/MWCNTs catalysts preparation method on the catalysts morphology and activity in a formic acid electrooxidation reaction was investigated. Three reduction methods of Pd precursor involving reduction in a high pressure microwave reactor (Pd1), reduction with NaBH4 (Pd2) and microwave-assisted polyol method (Pd3) were used in this paper. Crystallites size and morphology were studied using the scanning transmission electron microscopy (STEM), X-ray diffraction (XRD), whereas elemental composition, Pd chemical state and functional groups content by the X-ray photoelectron spectroscopy (XPS). The prepared catalysts were tested in a direct formic acid fuel cell (DFAFC) as an anode material. The catalytic activity was correlated with a mean fraction of the total Pd atoms exposed at the surface (FE). The value of FE was calculated from the crystallites size distribution determined by the STEM measurements. Non-linear dependence of a current density versus FE, approaching the maximum at FE≈0.25 suggests that the catalytic process proceeded at Pd nanocrystallites faces, with inactive edges and corners. Pd2 catalyst exhibited highest activity due to its smallest Pd crystallites (3.2 nm), however the absence of Pd crystallites aggregation and low content of carbon in PdCx phase, i.e. x = 4 at.% may also affect the observed.

  13. Effect of the Pd/MWCNTs anode catalysts preparation methods on their morphology and activity in a direct formic acid fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    Lesiak, B., E-mail: blesiak-orlowska@ichf.edu.pl [Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warszawa (Poland); Mazurkiewicz, M.; Malolepszy, A. [Faculty of Chemical and Process Engineering, Warsaw University of Technology, Waryńskiego 1, 00-645 Warszawa (Poland); Stobinski, L. [Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warszawa (Poland); Faculty of Chemical and Process Engineering, Warsaw University of Technology, Waryńskiego 1, 00-645 Warszawa (Poland); Mierzwa, B.; Mikolajczuk-Zychora, A.; Juchniewicz, K.; Borodzinski, A. [Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warszawa (Poland); Zemek, J.; Jiricek, P. [Institute of Physics, Academy of Sciences of the Czech Republic, 162-53 Prague 6, Cukrovarnicka 10 (Czech Republic)

    2016-11-30

    Highlights: • Catalysts properties studied by XRD, STEM, XPS methods. • Differences in Pd particle size, content of Pd, functional groups, PdC{sub x.}. • Catalytic activity studied in a Direct Formic Acid Fuel Cell. • Highest activity–catalyst prepared using a strong reducing agent (NaBH{sub 4}). - Abstract: Impact of Pd/MWCNTs catalysts preparation method on the catalysts morphology and activity in a formic acid electrooxidation reaction was investigated. Three reduction methods of Pd precursor involving reduction in a high pressure microwave reactor (Pd1), reduction with NaBH{sub 4} (Pd2) and microwave-assisted polyol method (Pd3) were used in this paper. Crystallites size and morphology were studied using the scanning transmission electron microscopy (STEM), X-ray diffraction (XRD), whereas elemental composition, Pd chemical state and functional groups content by the X-ray photoelectron spectroscopy (XPS). The prepared catalysts were tested in a direct formic acid fuel cell (DFAFC) as an anode material. The catalytic activity was correlated with a mean fraction of the total Pd atoms exposed at the surface (FE). The value of FE was calculated from the crystallites size distribution determined by the STEM measurements. Non-linear dependence of a current density versus FE, approaching the maximum at FE≈0.25 suggests that the catalytic process proceeded at Pd nanocrystallites faces, with inactive edges and corners. Pd2 catalyst exhibited highest activity due to its smallest Pd crystallites (3.2 nm), however the absence of Pd crystallites aggregation and low content of carbon in PdC{sub x} phase, i.e. x = 4 at.% may also affect the observed.

  14. A Pd/C-CeO2 Anode Catalyst for High-Performance Platinum-Free Anion Exchange Membrane Fuel Cells.

    Science.gov (United States)

    Miller, Hamish A; Lavacchi, Alessandro; Vizza, Francesco; Marelli, Marcello; Di Benedetto, Francesco; D'Acapito, Francesco; Paska, Yair; Page, Miles; Dekel, Dario R

    2016-05-10

    One of the biggest obstacles to the dissemination of fuel cells is their cost, a large part of which is due to platinum (Pt) electrocatalysts. Complete removal of Pt is a difficult if not impossible task for proton exchange membrane fuel cells (PEM-FCs). The anion exchange membrane fuel cell (AEM-FC) has long been proposed as a solution as non-Pt metals may be employed. Despite this, few examples of Pt-free AEM-FCs have been demonstrated with modest power output. The main obstacle preventing the realization of a high power density Pt-free AEM-FC is sluggish hydrogen oxidation (HOR) kinetics of the anode catalyst. Here we describe a Pt-free AEM-FC that employs a mixed carbon-CeO2 supported palladium (Pd) anode catalyst that exhibits enhanced kinetics for the HOR. AEM-FC tests run on dry H2 and pure air show peak power densities of more than 500 mW cm(-2) .

  15. Pd-Au bimetallic catalysts: understanding alloy effects from planar models and (supported) nanoparticles.

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Feng; Goodman, Wayne D.

    2012-12-21

    Pd-Au bimetallic catalysts often display enhanced catalytic activities and selectivities compared with Pd-alone catalysts. This enhancement is often caused by two alloy effects, i.e., ensemble and ligand effects. The ensemble effect is dilution of surface Pd by Au. With increasing surface Au coverages, contiguous Pd ensembles disappear and isolated Pd ensembles form. For certain reactions, for example vinyl acetate synthesis, this effect is responsible for reaction rate enhancement via the formation of highly active surface sites, e.g., isolated Pd pairs. The disappearance of contiguous Pd ensembles also switches off side reactions catalyzed by these sites. This explains selectivity increase of certain reactions, for example direct H2O2 synthesis. The ligand effect is electronic perturbation of Au to Pd. By direct charge transfer or affecting bond length, the ligand effect causes the Pd d band to be more filled and the d-band center away from the Fermi level. Both changes make Pd more "atomic like" therefore binding reactants and products weaker. For certain reactions, this eliminates the so-called "self poisoning" and enhances activity/selectivity.

  16. Microstructural characterization and mechanical property of active soldering anodized 6061 Al alloy using Sn-3.5Ag-xTi active solders

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Wei-Lin, E-mail: wangwl77@gmail.com; Tsai, Yi-Chia, E-mail: tij@itri.org.tw

    2012-06-15

    Active solders Sn-3.5Ag-xTi varied from x = 0 to 6 wt.% Ti addition were prepared by vacuum arc re-melting and the resultant phase formation and variation of microstructure with titanium concentration were analyzed using X-ray diffraction, optical microscopy and scanning electron microscopy. The Sn-3.5Ag-xTi active solders are used as metallic filler to join with anodized 6061 Al alloy for potential applications of providing a higher heat conduction path. Their joints and mechanical properties were characterized and evaluated in terms of titanium content. The mechanical property of joints was measured by shear testing. The joint strength was very dependent on the titanium content. Solder with a 0.5 wt.% Ti addition can successfully wet and bond to the anodized aluminum oxide layers of Al alloy and posses a shear strength of 16.28 {+-} 0.64 MPa. The maximum bonding strength reached 22.24 {+-} 0.70 MPa at a 3 wt.% Ti addition. Interfacial reaction phase and chemical composition were identified by a transmission electron microscope with energy dispersive spectrometer. Results showed that the Ti element reacts with anodized aluminum oxide to form Al{sub 3}Ti-rich and Al{sub 3}Ti phases at the joint interfaces. - Highlights: Black-Right-Pointing-Pointer Active solder joining of anodized Al alloy needs 0.5 wt.% Ti addition for Sn-3.5Ag. Black-Right-Pointing-Pointer The maximum bonding strength occurs at 3 wt.% Ti addition. Black-Right-Pointing-Pointer The Ti reacts with anodized Al oxide to form Al{sub 3}Ti-rich and Al{sub 3}Ti at joint interface.

  17. Hydriding/dehydriding properties of NdMgNi alloy with catalyst CeO2

    Institute of Scientific and Technical Information of China (English)

    李霞; 张羊换; 杨泰; 许剑轶; 赵栋梁

    2016-01-01

    Hydrogen storage composites Nd2Mg17-50 wt.%Ni-x wt.%CeO2 (x=0, 0.5, 1.0, 1.5, 2.0) were obtained by induction-ball milling method. The catalytic effect of CeO2 on hydriding kinetics of Nd2Mg17-50 wt.%Ni composite was investigated. X-ray diffrac-tion (XRD) and high resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED) analyses showed that Nd2Mg17-50 wt.%Ni alloy had a multiphase structure, consisting of NdMg12, NdMg2Ni, Mg2Ni and Ni phases and the addition of catalyst CeO2 prompted the composites to be partly transformed into amorphous strucutre. The CeO2 improved the maxi-mum hydrogen capacity of Nd2Mg17-50 wt.%Ni alloy from 3.192 wt.% to 3.376 wt.% (x=1.0). What’s more, the increment of diffu-sion coefficientD led to the faster hydriding kinetics, which was calculated by Avrami-Erofeev equation. The dehydrogenation tem-perature reduced from 515.54 to 504.72 K was mainly caused by the decrease of activation energy from 93.28 to 69.36 kJ/mol, which was proved by the Kissinger equation.

  18. PREPARATION AND CHARACTERIZATION OF SPHERICAL PP/PB ALLOYS WITH MgCl2-SUPPORTED ZIEGLER-NATTA CATALYST

    Institute of Scientific and Technical Information of China (English)

    Ai-hua He; Yang-wei Shi; Guo-qing Liu; Wei Yao; Bao-chen Huang

    2012-01-01

    Polypropylene (PP)/polybutene-1 (PB) alloys within reactor were prepared by MgCl2-supported Ziegler-Natta catalyst with sequential two-stage polymerization technology.First,propylene homo-polymerizations were carried out to form isotactic polypropylene (iPP) particles containing active catalyst.Then,butene-1 was subsequently polymerized to form polybutene-1 phase inside the iPP particles.Finally,iPP/PB alloys with spherical shape and adjustable PB content were synthesized.The catalytic activity and catalytic stereospecificity of the Z-N catalyst in the two-stage polymerization process are discussed.The composition and physical properties of the PP alloys were characterized by FT-IR,13C-NMR,SEM,DSC and XRD.It was found that the in-reactor PP alloys are mainly composed of PP and PB with a little amount of poly(buteneco-propylene) random copolymers and poly(butene-block-propylene) block copolymers.SEM measurements verified that the PB phases with size in the range of 300-400 nm dispersed in the PP matrix uniformly.The incorporation of PB upon the PP matrix affects the properties of final products greatly.

  19. 高活性、高抗毒性的甲酸燃料电池阳极催化剂%Highly Active and Highly Poison Tolerant Anodic Catalysts for Direct Formic Acid Fuel Cells

    Institute of Scientific and Technical Information of China (English)

    卢学毅; 廖世军; 宋慧宇

    2012-01-01

    甲酸燃料电池是一种近年发展起来的新型燃料电池,具有极好的商业化前景,但其发展受到很多因素的制约,其中阳极催化剂是影响其性能的关键因素。本文从催化剂的制备方法、催化剂载体和掺杂其他元素等方面介绍了近年来国内外在提高催化剂的活性和抗毒性方面所做的重要研究工作。具体包括:电沉积法、有机溶胶法等重要制备方法,碳纳米管、石墨烯和复合材料作为催化剂载体的研究以及通过掺杂其他元素制备合金催化剂和复合催化剂来提高催化剂活性和抗毒性的相关研究工作。本文还对甲酸燃料电池的发展做了展望。%Formic acid fuel cell is a kind of fuel cell developed in recent years with promising commercial prospects. However, its development and commercialization are restricted by some factors, in which anodic catalyst is recognized as one of the most important factors. In this paper, some significant researches and attempts of promoting catalytic activity and poison tolerance are introduced, including novel preparation approaches, usage of novel supporting materials, as well as the design of multi-component catalyst by doping hetero elements. Concretely, the researches cover synthetic methods such as electrolytic deposition, organic colloid method, impregnation, study of using carbon nanotubes, graphene and complex materials as supports, and relevant work of adding other elements to prepare alloy catalysts and complex catalysts. Furthermore, the future development of formic acid fuel cell is also prospected.

  20. Cu-Ni-YSZ anodes for solid oxide fuel cell by mechanical alloying processing

    Energy Technology Data Exchange (ETDEWEB)

    Guisard Restivo, Thomaz A.; Mello-Castanho, Sonia R.H. [IPEN, Inst. of Energetic and Nuclear Research, Sao Paulo, SP (Brazil)

    2010-01-15

    The work shows some results concerning a new cermet material 40 vol.% [(Cu)-Ni]-YSZ processed by mechanical alloying followed by Sintering by Activated Surface method. The projected cermet microstructure for this application is expected to possess microstructural characteristics that lead to better electric and ionic percolating, higher electrocatalytic activity and fuel reforming. The powder samples prepared by mechanical alloying optimized conditions show a homogeneous mixture. Transmission and scanning electron microscope analysis have demonstrated the powder particles are nanosized after 2 h of milling, showing lamellar internal structure aggregates. Suitable sintered pellets are obtained from these powders, within the required porosity and microstructure. Sintering kinetics studies for pellets of Ni-YSZ and Ni-Cu-YSZ indicate 2-step sintering processes. Copper additive promotes sintering and refines the microstructure. (orig.)

  1. The anodic and cathodic dissolution of Al and Al-Cu-Mg alloy

    Energy Technology Data Exchange (ETDEWEB)

    Mokaddem, M.; Volovitch, P. [Laboratoire de physicochimie des surfaces, UMR7045, Ecole Nationale Superieure de Chimie de Paris, ParisTech, 11, rue Pierre et Marie Curie, Paris (France); Rechou, F.; Oltra, R. [Institut CARNOT de Bourgogne, Electrochimie Interfaciale-Corrosion, UMR5209, Universite de Bourgogne, Dijon (France); Ogle, K., E-mail: kevin-ogle@enscp.f [Laboratoire de physicochimie des surfaces, UMR7045, Ecole Nationale Superieure de Chimie de Paris, ParisTech, 11, rue Pierre et Marie Curie, Paris (France)

    2010-04-15

    Atomic emission spectroelectrochemistry (AESEC) was used to monitor the release of Al from 99.99% aluminum (1199 alloy) and Al, Mg, and Cu from 2024 Al alloy in 30 g/l NaCl electrolyte as a function of pH. The cathodic dissolution of Al was demonstrated and attributed to an increase in the pH at the interface due to the water reduction reaction. The dissolution of Mg was also observed but was a more complex function of current probably depending on the interfacial pH and the Al dissolution rate. The detachment of copper-rich particles was observed as very rapid spectroscopic emission transients (peak width < 10 ms).

  2. Development of Fe-Ni/YSZ-GDC electro-catalysts for application as SOFC anodes. XRD and TPR characterization, and evaluation in ethanol steam reforming reaction

    Energy Technology Data Exchange (ETDEWEB)

    Paz Fiuza, Raigenis da; Silva, Marcos Aurelio da; Boaventura, Jaime Soares [UFBA, Salvador, Bahia (Brazil). Energy and Materials Science Group

    2010-07-01

    Electro-catalysts based on Fe-Ni alloys were prepared using physical mixture and modified Pechini methods; they were supported on a composite of Yttria Stabilized Zirconia (YSZ) and Gadolinia Doped Ceria (GDC). The composites had compositions of 35% metal load and 65% support (70% wt. YSZ and 30% wt. GDC mixture) (cermets). The samples were characterized by Temperature-Programmed Reduction (TPR) and X-Ray Diffraction (XRD) and evaluated in ethanol steam reforming at 650 C for six hours and in the temperature range 300 - 900 C. The XRD results showed that the bimetallic sample calcined at 800 C formed a mixed oxide (NiFe{sub 2}O{sub 4}) in spinel structure; after reducing the sample in hydrogen, Ni-Fe alloys were formed. The presence of Ni decreased the final reduction temperature of the NiFe{sub 2}O{sub 4} species. The addition of Fe to Ni anchored to YSZ-GDC increased the hydrogen production and inhibits the carbon deposition. The bimetallic 30Fe5Ni samples reached an ethanol conversion of about 95%, and a hydrogen yield up to 48% at 750 C. In general, the ethanol conversion and hydrogen production were independent of the metal content in the electro-catalyst. However, the substitution of Ni for Fe significantly reduced the carbon deposition on the electro-catalyst: 74, 31 and 9 wt. % in the 35Ni, 20Fe15Ni, and 30Fe5Ni samples, respectively. (orig.)

  3. First-principle study on phase Al0.8NiaSn0.2 in Sn-Ni-Al alloy as anode for lithium ion battery

    Institute of Scientific and Technical Information of China (English)

    Huang Zhao-Wen; Hu She-Jun; Hou Xian-Hua; Zhao Ling-Zhi; Ru Qiang; Li Wei-Shan; Zhang Zhi-Wen

    2010-01-01

    The mechanism of lithium interealation/deintercalation for phase Al0.8Ni3Sn0.2 as anode material used in lithium ion battery was studied carefully based on the first-principle plane wave pseudo-potential method.The calculated results indicated that Sn-Ni-Al alloy had high theoretical capacity when used as anode material,however,there was high initial irreversible capacity loss because of the large volume expansion.Therefore the technological parameters during preparing the Sn-Ni-Al anode should be controlled strictly to make the content of Al0.8NiaSn0.2 phase as low as possible and to make the anode consist of promising Sn-Ni and Al-Ni phases.For comparison,an experiment based on magnetron sputtering was done.The result showed that the calculation is in good agreement with the experiment.We found that the first-principle investigation method is of far-reaching significance in synthesising new commercial anode materials with high capacity and good cycle performance.

  4. Enhancing the power generation in microbial fuel cells with effective utilization of goethite recovered from mining mud as anodic catalyst.

    Science.gov (United States)

    Jadhav, Dipak A; Ghadge, Anil N; Ghangrekar, Makarand M

    2015-09-01

    Catalytic effect of goethite recovered from iron-ore mining mud was studied in microbial fuel cells (MFCs). Characterization of material recovered from mining mud confirms the recovery of iron oxide as goethite. Heat treated goethite (550 °C) and untreated raw goethite were coated on stainless-steel anode of MFC-1 and MFC-2, respectively; whereas, unmodified stainless-steel anode was used in MFC-3 (control). Fivefold increment in power was obtained in MFC-1 (17.1 W/m(3) at 20 Ω) than MFC-3 (3.5 W/m(3)). MFC with raw goethite coated anode also showed enhanced power (11 W/m(3)). Higher Coulombic efficiency (34%) was achieved in MFC-1 than control MFC-3 (13%). Decrease in mass-transport losses and higher redox current during electrochemical analyses support improved electron transfer with the use of goethite on anode. Cheaper goethite coating kinetically accelerates the electron transfer between bacteria and anode, proving to be a novel approach for enhancing the electricity generation along with organic matter removal in MFC.

  5. Semiconducting behavior of the anodically passive films formed on AZ31B alloy

    OpenAIRE

    A. Fattah-alhosseini; M. Sabaghi Joni

    2014-01-01

    This work includes determination of the semiconductor character and estimation of the dopant levels in the passive film formed on AZ31B alloy in 0.01 M NaOH, as well as the estimation of the passive film thickness as a function of the film formation potential. Mott–Schottky analysis revealed that the passive films displayed n-type semiconductive characteristics, where the oxygen vacancies and interstitials preponderated. Based on the Mott–Schottky analysis, it was shown that the calculated do...

  6. Confined-space alloying of nanoparticles for the synthesis of efficient PtNi fuel-cell catalysts.

    Science.gov (United States)

    Baldizzone, Claudio; Mezzavilla, Stefano; Carvalho, Hudson W P; Meier, Josef Christian; Schuppert, Anna K; Heggen, Marc; Galeano, Carolina; Grunwaldt, Jan-Dierk; Schüth, Ferdi; Mayrhofer, Karl J J

    2014-12-15

    The efficiency of polymer electrolyte membrane fuel cells is strongly depending on the electrocatalyst performance, that is, its activity and stability. We have designed a catalyst material that combines both, the high activity for the decisive cathodic oxygen reduction reaction associated with nanoscale Pt alloys, and the excellent durability of an advanced nanostructured support. Owing to the high specific activity and large active surface area, the catalyst shows extraordinary mass activity values of 1.0 A mgPt(-1). Moreover, the material retains its initial active surface area and intrinsic activity during an extended accelerated aging test within the typical operation range. This excellent performance is achieved by confined-space alloying of the nanoparticles in a controlled manner in the pores of the support.

  7. Influence of the heat treatment condition of alloy AlCu4Mg1 on the microstructure and properties of anodic oxide layers

    Science.gov (United States)

    Morgenstern, R.; Dietrich, D.; Sieber, M.; Lampke, T.

    2017-03-01

    Due to their outstanding specific mechanical properties, high-strength, age-hardenable aluminum alloys offer a high potential for lightweight security-related applications. However, the use of copper-alloyed aluminum is limited because of their susceptibility to selective corrosion and their low wear resistance. These restrictions can be overcome and new applications can be opened up by the generation of protective anodic aluminum oxide layers. In contrast to the anodic oxidation of unalloyed aluminum, oxide layers produced on copper-rich alloys exhibit a significantly more complex pore structure. It is the aim of the investigation to identify the influence of microstructural parameters such as size and distribution of the strengthening precipitations on the coating microstructure. The aluminum alloy EN AW-2024 (AlCu4Mg1) in different heat treatment conditions serves as substrate material. The influence of the strengthening precipitations’ size and distribution on the development of the pore structure is investigated by the use of high-resolution scanning electron microscopy. Integral coating properties are characterized by non-destructive and light-microscopic thickness measurements and instrumented indentation tests.

  8. Performance Enhancement of Silicon Alloy-Based Anodes Using Thermally Treated Poly(amide imide) as a Polymer Binder for High Performance Lithium-Ion Batteries.

    Science.gov (United States)

    Yang, Hwi Soo; Kim, Sang-Hyung; Kannan, Aravindaraj G; Kim, Seon Kyung; Park, Cheolho; Kim, Dong-Won

    2016-04-05

    The development of silicon-based anodes with high capacity and good cycling stability for next-generation lithium-ion batteries is a very challenging task due to the large volume changes in the electrodes during repeated cycling, which results in capacity fading. In this work, we synthesized silicon alloy as an active anode material, which was composed of silicon nanoparticles embedded in Cu-Al-Fe matrix phases. Poly(amide imide)s, (PAI)s, with different thermal treatments were used as polymer binders in the silicon alloy-based electrodes. A systematic study demonstrated that the thermal treatment of the silicon alloy electrodes at high temperature made the electrodes mechanically strong and remarkably enhanced the cycling stability compared to electrodes without thermal treatment. The silicon alloy electrode thermally treated at 400 °C initially delivered a discharge capacity of 1084 mAh g(-1) with good capacity retention and high Coulombic efficiency. This superior cycling performance was attributed to the strong adhesion of the PAI binder resulting from enhanced secondary interactions, which maintained good electrical contacts between the active materials, electronic conductors, and current collector during cycling. These findings are supported by results from X-ray photoelectron spectroscopy, scanning electron microscopy, and a surface and interfacial cutting analysis system.

  9. Improved Osteoblast and Chondrocyte Adhesion and Viability by Surface-Modified Ti6Al4V Alloy with Anodized TiO2 Nanotubes Using a Super-Oxidative Solution

    OpenAIRE

    Ernesto Beltrán-Partida; Aldo Moreno-Ulloa; Benjamín Valdez-Salas; Cristina Velasquillo; Monica Carrillo; Alan Escamilla; Ernesto Valdez; Francisco Villarreal

    2015-01-01

    Titanium (Ti) and its alloys are amongst the most commonly-used biomaterials in orthopedic and dental applications. The Ti-aluminum-vanadium alloy (Ti6Al4V) is widely used as a biomaterial for these applications by virtue of its favorable properties, such as high tensile strength, good biocompatibility and excellent corrosion resistance. TiO2 nanotube (NTs) layers formed by anodization on Ti6Al4V alloy have been shown to improve osteoblast adhesion and function when compared to non-anodized m...

  10. A microstructural investigation of gas atomized Raney type Al-27.5 at.% Ni catalyst precursor alloys

    Energy Technology Data Exchange (ETDEWEB)

    Mullis, A.M., E-mail: a.m.mullis@leeds.ac.uk [Institute for Materials Research, University of Leeds, Leeds LS2 9JT (United Kingdom); Bigg, T.D., E-mail: t.bigg@leeds.ac.uk [Institute for Materials Research, University of Leeds, Leeds LS2 9JT (United Kingdom); Adkins, N.J., E-mail: n.j.e.adkins@bham.ac.uk [IRC in Materials Processing, University of Birmingham, Edgbaston, Birmingham B15-2TT (United Kingdom)

    2015-11-05

    Quantitative image analysis has been used to investigate the phase composition of gas atomized powders of a Raney type Ni catalyst precursor alloys of composition Al-27.5 at.% Ni in the powder size range 150–212 μm. We find that there are considerable variations in phase composition both between powders from the same batch and as a function distance from the particle surface within individual particles. Such variations may have significant implications for the future production and uptake of such catalysts, including the necessity for post-production crushing of gas atomized powders. Models are proposed to account for both variations. - Highlights: • The phase composition of powder Raney-Ni catalysts has been investigated. • Image analysis is used to quantify differences between and within particles. • Phase composition can vary by up to 10% between the particle surface and centre. • Differences of up to 10% in the mean composition are also found between particles.

  11. Possibility of Wastewater Treatment Using MFC with Ni-Co Catalyst of Fuel Electrode

    Directory of Open Access Journals (Sweden)

    Włodarczyk Paweł P.

    2016-06-01

    Full Text Available One of the problems with microbial fuel cells is a low current density of those energy sources. Nonetheless, it is possible to increase the current density by using the catalyst for fuel electrode (anode - as long as a low cost catalyst can be found. The possibility of wastewater treatment using the Ni-Co alloy as catalyst for MFC’s is presented in this paper. The alloys were obtained with different concentrations of Co (15 and 50% of Co. The increase of current density with Ni-Co catalyst is approximately 0,1 mA/cm2. So, a fundamental possibility wastewater treatment using the Ni-Co alloy as catalyst for microbial fuel cells was presented.

  12. Possibility of Wastewater Treatment Using MFC with Ni-Co Catalyst of Fuel Electrode

    Science.gov (United States)

    Włodarczyk, Paweł P.; Włodarczyk, Barbara

    2016-06-01

    One of the problems with microbial fuel cells is a low current density of those energy sources. Nonetheless, it is possible to increase the current density by using the catalyst for fuel electrode (anode) - as long as a low cost catalyst can be found. The possibility of wastewater treatment using the Ni-Co alloy as catalyst for MFC's is presented in this paper. The alloys were obtained with different concentrations of Co (15 and 50% of Co). The increase of current density with Ni-Co catalyst is approximately 0,1 mA/cm2. So, a fundamental possibility wastewater treatment using the Ni-Co alloy as catalyst for microbial fuel cells was presented.

  13. Semiconducting behavior of the anodically passive films formed on AZ31B alloy

    Directory of Open Access Journals (Sweden)

    A. Fattah-alhosseini

    2014-12-01

    Full Text Available This work includes determination of the semiconductor character and estimation of the dopant levels in the passive film formed on AZ31B alloy in 0.01 M NaOH, as well as the estimation of the passive film thickness as a function of the film formation potential. Mott–Schottky analysis revealed that the passive films displayed n-type semiconductive characteristics, where the oxygen vacancies and interstitials preponderated. Based on the Mott–Schottky analysis, it was shown that the calculated donor density increases linearly with increasing the formation potential. Also, the electrochemical impedance spectroscopy (EIS results indicated that the thickness of the passive film was decreased linearly with increasing the formation potential. The results showed that decreasing the formation potential offer better conditions for forming the passive films with higher protection behavior, due to the growth of a much thicker and less defective films.

  14. EFFECT OF ALLOY ELEMENTS ON ELECTROCHEMICAL PERFORMANCE OF ALUMINUM SACRIFICIAL ANODE%合金元素对铝基牺牲阳极性能的影响

    Institute of Scientific and Technical Information of China (English)

    李威力; 闫永贵; 陈光; 马力

    2012-01-01

    通过合金化方法,在Al-Zn-In三元牺牲阳极中依次添加Mg、Ti、Ga、Mn、Sn等元素,炼制不同成分的铝合金牺牲阳极。采用电化学性能测试、极化曲线测量及扫描电子显微镜分析等手段分析了合金元素对铝合金牺牲阳极性能的影响。结果表明,随着添加元素种类的增加,牺牲阳极电化学性能提高。在Al-Zn-In三元阳极中加入Mg和Ti,阳极溶解形貌更加均匀;加入Ga与Sn后,阳极的开路电位与工作电位负移;加入Mn后阳极的电流效率提高。%Elements such as Mg,Ti,Ga,Mn and Sn were added to the Al-Zn-In based ternary anode in order using alloying method and the aluminum sacrificial anodes with different incorporated elements were cast.The electrochemical performance test,polarization plots and scanning electron microscope technique were carried out to analyze the influence of several familiar elements to the performance of the aluminum anode.The experiment results indicated that with the increase of the adding element the anode electrochemical performance was improved.When the elements of Mg and Ti were added to Al-Zn-In ternary anode the dissolution morphology was more uniform.When Ga and Sn were added,the anode open-circuit potential and closed-circuit potential were more negative.When Mn was added,the current efficiency was promoted.

  15. Self-Organizing Evolution of Anodized Oxide Films on Ti-25Nb-3Mo-2Sn-3Zr Alloy and Hydrophilicity

    Institute of Scientific and Technical Information of China (English)

    何芳; 李立军; 陈利霞; 李凤娇; 黄远

    2014-01-01

    In the present work, hierarchical nanostructured titanium dioxide (TiO2) films were fabricated on Ti-25Nb-3Mo-2Sn-3Zr (TLM) alloy for biomedical applications via one-step anodization process in ethylene glycol-based electrolyte containing 0.5wt%NH4F. The nanostructured TiO2 films exhibited three distinct types depending on the anodization time:top irregular nanopores (INP)/beneath regular nanopores (RNP), top INP/middle regular nano-tubes (RNT)/bottom RNP and top RNT with underlying RNP. The evolution of the nanostructured TiO2 films with anodization time demonstrated that self-organizing nanopores formed at the very beginning and individual nanotubes originated from underlying nanopore dissolution. Furthermore, a modified two-stage self-organizing mechanism was introduced to illustrate the growth of the nanostructured TiO2 films. Compared with TLM titanium alloy matrix, the TiO2 films with special nano-structure hold better hydrophilicity and higher specific surface area, which lays the foun-dation for their biomedical applications.

  16. Reversible conversion-alloying of Sb2O3 as a high-capacity, high-rate, and durable anode for sodium ion batteries.

    Science.gov (United States)

    Hu, Meijuan; Jiang, Yinzhu; Sun, Wenping; Wang, Hongtao; Jin, Chuanhong; Yan, Mi

    2014-11-12

    Sodium ion batteries are attracting ever-increasing attention for the applications in large/grid scale energy storage systems. However, the research on novel Na-storage electrode materials is still in its infancy, and the cycling stability, specific capacity, and rate capability of the reported electrode materials cannot satisfy the demands of practical applications. Herein, a high performance Sb(2)O(3) anode electrochemically reacted via the reversible conversion-alloying mechanism is demonstrated for the first time. The Sb(2)O(3) anode exhibits a high capacity of 550 mAh g(-1) at 0.05 A g(-1) and 265 mAh g(-1) at 5 A g(-1). A reversible capacity of 414 mAh g(-1) at 0.5 A g(-1) is achieved after 200 stable cycles. The synergistic effect involving conversion and alloying reactions promotes stabilizing the structure of the active material and accelerating the kinetics of the reaction. The mechanism may offer a well-balanced approach for sodium storage to create high capacity and cycle-stable anode materials.

  17. Mechanical alloying of a hydrogenation catalyst used for the remediation of contaminated compounds

    Science.gov (United States)

    Quinn, Jacqueline W. (Inventor); Clausen, Christian A. (Inventor); Geiger, Cherie L. (Inventor); Aitken, Brian S. (Inventor)

    2012-01-01

    A hydrogenation catalyst including a base material coated with a catalytic metal is made using mechanical milling techniques. The hydrogenation catalysts are used as an excellent catalyst for the dehalogenation of contaminated compounds and the remediation of other industrial compounds. Preferably, the hydrogenation catalyst is a bimetallic particle including zero-valent metal particles coated with a catalytic material. The mechanical milling technique is simpler and cheaper than previously used methods for producing hydrogenation catalysts.

  18. Influence of Black Annealing Oxide Scale on the Anodic Behavior of Alloy 22

    Energy Technology Data Exchange (ETDEWEB)

    Rebak, R B; Etien, R A; Gordon, S R; Ilevbare, G O

    2006-05-22

    The resistance of Alloy 22 (N06022) to localized corrosion, mainly crevice corrosion, has been extensively investigated in the last few years. The effect of influencing variables such as temperature, applied potential, chloride concentration and nitrate inhibitor concentration have been addressed previously. At this time, it was important to address the effect an oxide film or scale that forms during the high temperature annealing process or solution heat treatment (SHT) and its subsequent water quenching. Electrochemical tests such as cyclic potentiodynamic polarization (CPP) have been carried out to determine the repassivation potential for localized corrosion and to assess the mode of attack on the specimens. Tests have been carried out in parallel using mill annealed (MA) specimens free from oxide on the surface. The comparative testing was carried out in six different electrolyte solutions at temperatures ranging from 60 C to 100 C. Results show that the repassivation potential of the specimens containing the black anneal oxide film on the surface was practically the same or higher as the repassivation potential for oxide-free specimens.

  19. TiN@nitrogen-doped carbon supported Pt nanoparticles as high-performance anode catalyst for methanol electrooxidation

    Science.gov (United States)

    Zhang, Jun; Ma, Li; Gan, Mengyu; Fu, Shenna; Zhao, Yi

    2016-08-01

    In this paper, TiN@nitrogen-doped carbons (NDC) composed of a core-shell structure are successfully prepared through self-assembly and pyrolysis treatment using γ-aminopropyltriethoxysilane as coupling agent, polyaniline as carbon and nitrogen source, respectively. Subsequently, TiN@NDC supporting Pt nanoparticles (Pt/TiN@NDC) are obtained by a microwave-assisted polyol process. The nitrogen-containing functional groups and TiN nanoparticles play a critical role in decreasing the average particle size of Pt and improving the electrocatalytic activity of Pt/TiN@NDC. Transmission electron microscope results reveal that Pt nanoparticles are uniformly dispersed in the TiN@NDC surface with a narrow particle size ranging from 1 to 3 nm in diameter. Moreover, the Pt/TiN@NDC catalyst shows significantly improved catalytic activity and high durability for methanol electrooxidation in comparison with Pt/NDC and commercial Pt/C catalysts, revealed by cyclic voltammetry and chronoamperometry. Strikingly, this novel Pt/TiN@NDC catalyst reveals a better CO tolerance related to Pt/NDC and commercial Pt/C catalysts, which due to the bifunctional mechanism and strong metal-support interaction between Pt and TiN@NDC. In addition, the probable reaction steps for the electrooxidation of CO adspecies on Pt NPs on the basis of the bifunctional mechanism are also proposed. These results indicate that the TiN@NDC is a promising catalyst support for methanol electrooxidation.

  20. Effect of aluminium alloy surface heterogeneities on anodic layer growth and properties; Efecto de las heterogeneidades superficiales de las aleaciones de aluminio sobre el crecimiento y propiedades de las capas anodicas

    Energy Technology Data Exchange (ETDEWEB)

    Bartolome, M. J.; Feliu, J.V.; Lopez, E.; Gonzalez, J. A.; Feliu, S.

    2007-07-01

    In the present work, X-ray photoelectron spectroscopy (XPS) is used to study sealed and unsealed anodic coatings obtained on pure-Al and on Al-Cu, Al-Mg-Si and Al-Mg alloys. In general, the sealing process is seen to produce a significant increase in the O/A ratio in the anodic coatings. this increase is more considerable with the Al-Cu and Al-Mg alloys than with the pure Al and the Al-Mg-Si alloy, perhaps due to the greater porosity of the coatings obtained on the former. An attempt is made to establish possible relationships between anodic film characteristics and surface heterogeneities, which also act in the phase prior to anodising. According to the results of this work, these heterogeneities affect the degree of dissolution of the metallic substrate during the anodising operation. (Author)

  1. Formation of Sn-M (M=Fe, Al, Ni) alloy nanoparticles by DC arc-discharge and their electrochemical properties as anodes for Li-ion batteries

    Science.gov (United States)

    Gao, Song; Huang, Hao; Wu, Aimin; Yu, Jieyi; Gao, Jian; Dong, Xinglong; Liu, Chunjing; Cao, Guozhong

    2016-10-01

    A direct current arc-discharge method was applied to prepare the Sn-M (M=Fe, Al, Ni) bi-alloy nanoparticles. Thermodynamic is introduced to analyze the energy circumstances for the formation of the nanoparticles during the physical condensation process. The electrochemical properties of as-prepared Sn-M alloy nanoparticles are systematically investigated as anodes of Li-ion batteries. Among them, Sn-Fe nanoparticles electrode exhibits high Coulomb efficiency (about 71.2%) in the initial charge/discharge (257.9 mA h g-1/366.6 mA h g-1) and optimal cycle stability (a specific reversible capacity of 240 mA h g-1 maintained after 20 cycles) compared with others. Large differences in the electrochemical behaviors indicate that the chemical composition and microstructure of the nanoparticles determine the lithium-ion storage properties and the long-term cyclic stability during the charge/discharge process.

  2. Non-noble catalysts and catalyst supports for phosphoric acid fuel cells

    Science.gov (United States)

    Mcalister, A. J.

    1981-01-01

    Tungsten carbide, which is active for hydrogen oxidation, is CO tolerant and has a hexagonal structure is discussed. Titanium carbide is inactive and has a cubic structure. Four different samples of the cubic alloys W sub x-1Ti sub XC sub 1-y were found to be active and CO tolerant. When the activities of these cubic alloys are weighted by the reciprocal of the square to those of highly forms of WC. They offer important insight into the nature of the active sites on W-C anode catalysts for use in phosphoric acid fuel cells.

  3. Investigation of Co3O4 nanorods supported Pd anode catalyst for methanol oxidation in alkaline solution

    Institute of Scientific and Technical Information of China (English)

    Yanbiao Ren; Shichao Zhang∗; Hua Fang; Xin Wei; Puheng Yang

    2014-01-01

    A Co3 O4 nanorod supported Pd electro-catalyst for the methanol electro-oxidation (MEO) has been fabricated by the combination of hydrother-mal synthesis and microwave-assisted polyol reduction processes. The crystallographic property and microstructure have been characterized using XRD, SEM and TEM. The results demonstrate that Pd nanoparticles (PdNPs) with a narrow particle size distribution (3−5 nm) are uni-formly deposited onto the surface of Co3O4 nanorods. Electrochemical measurements show that this catalyst having a larger electrochemically active surface area and a more negative onset-potential exhibits enhanced catalytic activity of 504 mA/mg Pd for MEO comparing with the Pd/C catalyst (448 mA/mg Pd). The dependency of logI against logv reveals that MEO on Pd-Co3O4 electrode is under a diffusion control. Electrochemical impedance spectroscopy (EIS) measurement agrees well with the CV results. The minimum charge transfer resistance of MEO on Pd-Co3 O4 is observed at−0.05 V, which coincides with the potential of MEO peak.

  4. Performance of Pt-Co alloys and CoTPP catalysts for the reduction of oxygen in AFC

    Energy Technology Data Exchange (ETDEWEB)

    Kiros, Y. [Royal Institute of Technology, Stockholm (Sweden); Sampathrajan, A.; Ramanathan, M. [Tamil Nadu Agricultural Univ., Coimbatore (India)

    1996-12-31

    One of the primary problems of the oxygen reduction reaction (ORR) for especially low and medium temperature fuel cells such as AFC, PEFC and PAFC is the high activation overpotential. This high overpotential is due to the complicated nature of the ORR and the morphological properties of the catalyst particles. High catalyst dispersion on the carbon support and small particle sizes, non-agglomeration and/or non-dissolution of the electrocatalyst is desired for the long-term operation of the electrodes. In this study electrodes were tested at different temperatures and concentrations in order to substantiate their influences on the activity and stability of the electrocatalysts, i.e.; cobalt tetraphenylporphyrin (CoTPP) and alloys of platinum and cobalt.

  5. Morphology and performances of the anodic oxide films on Ti6Al4V alloy formed in alkaline-silicate electrolyte with aminopropyl silane addition under low potential

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jiali; Wang, Jinwei, E-mail: wangjw@ustb.edu.cn; Yuan, Hongye

    2013-11-01

    Oxide films on Ti6Al4V alloy are prepared using sodium hydroxide–sodium silicate as the base electrolyte with addition of aminopropyl trimethoxysilane (APS) as additive by potentiostatic anodizing under 10 V. APS is incorporated into the films during anodizing and the surface morphology of the oxide films is changed from particle stacked to honeycomb-like porous surfaces as shown by scanning electron microscopy (SEM) with Energy Disperse Spectroscopy (EDX). The surface roughness and aminopropyl existence on the oxide films result in their differences in wettability as tested by the surface profile topography and contact angle measurements. The anti-abrasive ability of the anodic films is improved with the addition of APS due to its toughening effects and serving as lubricants in the ceramic oxide films as measured by ball-on-disk friction test. Also, potentiodynamic corrosion test proves that their anticorrosive ability in 3.5 wt.% NaCl is greatly improved as reflected by their much lower corrosion current (I{sub corr}) and higher corrosion potential (E{sub corr}) than those of the substrate.

  6. Influence of Zr Addition on Structure and Performance of Rare Earth Mg-Based Alloys as Anodes in Ni/MH Battery

    Directory of Open Access Journals (Sweden)

    Shujun Qiu

    2015-04-01

    Full Text Available In this study, the substitution of Mg with Zr in La0.7Mg0.3(Ni0.85Co0.153.5 was carried out with the purpose of improving the electrochemical performances. The structural and hydrogen storage properties in both gas-solid reaction and the electrochemical system were systematically studied on La0.7(Mg0.3−xZrx(Ni0.85Co0.153.5 (x = 0.05, 0.1, 0.2, 0.3 alloys. Each tested alloy is composed of LaNi3 phase, LaNi5 phase and ZrNi3 phase with different phase abundances. The electrochemical studies indicated that all Zr-substituted anodes possessed a much higher cycling capacity retention than pristine La0.7Mg0.3(Ni0.85Co0.153.5. However, the maximum discharge capacity was reduced with the increase of Zr content. The potential-step tests showed that the diffusion of hydrogen atoms inside the anodes was decelerated after the introduction of Zr.

  7. Highly cost-effective and sulfur/coking resistant VOx-grafted TiO2 nanoparticles as an efficient anode catalyst for direct conversion of dry sour methane in solid oxide fuel cells

    NARCIS (Netherlands)

    Garcia, A.; Yan, N.; Vincent, A.; Singh, A.; Hill, J.M.; Chuang, K. T.; Luo, J.L.

    2015-01-01

    In this work, we show that grafted metal oxide can be a highly cost-effective and active anode for solid oxide fuel cells for sour methane conversion. The developed electro-catalyst was composed of vanadium oxide grafted TiO2 nanoparticles (VOx/TiO2) infiltrated into a porous La0.4Sr0.5Ba0.1TiO3+δ e

  8. Enhancing the cyclability of Li-O2 batteries using PdM alloy nanoparticles anchored on nitrogen-doped reduced graphene as the cathode catalyst

    Science.gov (United States)

    Leng, Limin; Li, Jing; Zeng, Xiaoyuan; Song, Huiyu; Shu, Ting; Wang, Haishui; Liao, Shijun

    2017-01-01

    An efficient ORR/OER catalyst was developed by anchoring highly dispersed bimetallic PdM (M = Fe, Co, Ni) alloy nanoparticles on nitrogen-doped reduced graphene oxide (N-rGO). This new type of catalyst exhibited excellent ORR/OER activity, and the addition of transition metals also significantly improved catalytic stability, with the catalyst containing Fe (PdFe/N-rGO) exhibiting the best stability. A battery using this PdFe/N-rGO catalyst was capable of long-term stable cycling for 400 cycles (2000 h) with a limited capacity of 1000 mAh g-1 at 400 mA g-1, which was much longer than a battery with Pd/N-rGO as the catalyst (only 80 cycles, 400 h). We attribute the high performance of these catalysts to the high surface area of N-rGO, the anchoring of highly dispersed Pd alloy nanoparticles, and the prevention of Pd alloy nanoparticle aggregation and dissolution by the presence of the transition metals.

  9. Improved Osteoblast and Chondrocyte Adhesion and Viability by Surface-Modified Ti6Al4V Alloy with Anodized TiO2 Nanotubes Using a Super-Oxidative Solution

    Directory of Open Access Journals (Sweden)

    Ernesto Beltrán-Partida

    2015-03-01

    Full Text Available Titanium (Ti and its alloys are amongst the most commonly-used biomaterials in orthopedic and dental applications. The Ti-aluminum-vanadium alloy (Ti6Al4V is widely used as a biomaterial for these applications by virtue of its favorable properties, such as high tensile strength, good biocompatibility and excellent corrosion resistance. TiO2 nanotube (NTs layers formed by anodization on Ti6Al4V alloy have been shown to improve osteoblast adhesion and function when compared to non-anodized material. In his study, NTs were grown on a Ti6Al4V alloy by anodic oxidation for 5 min using a super-oxidative aqueous solution, and their in vitro biocompatibility was investigated in pig periosteal osteoblasts and cartilage chondrocytes. Scanning electron microscopy (SEM, energy dispersion X-ray analysis (EDX and atomic force microscopy (AFM were used to characterize the materials. Cell morphology was analyzed by SEM and AFM. Cell viability was examined by fluorescence microscopy. Cell adhesion was evaluated by nuclei staining and cell number quantification by fluorescence microscopy. The average diameter of the NTs was 80 nm. The results demonstrate improved cell adhesion and viability at Day 1 and Day 3 of cell growth on the nanostructured material as compared to the non-anodized alloy. In conclusion, this study evidences the suitability of NTs grown on Ti6Al4V alloy using a super-oxidative water and a short anodization process to enhance the adhesion and viability of osteoblasts and chondrocytes. The results warrant further investigation for its use as medical implant materials.

  10. Performance of metal alloys as hydrogen evolution reaction catalysts in a microbial electrolysis cell

    NARCIS (Netherlands)

    Jeremiasse, A.W.; Bergsma, J.; Kleijn, J.M.; Saakes, M.; Buisman, C.J.N.; Cohen Stuart, M.A.; Hamelers, H.V.M.

    2011-01-01

    H2 can be produced from organic matter with a microbial electrolysis cell (MEC). To decrease the energy input and increase the H2 production rate of an MEC, a catalyst is used at the cathode. Platinum is an effective catalyst, but its high costs stimulate searching for alternatives, such as non-nobl

  11. Alloyed Ni-Fe nanoparticles as catalysts for NH3 decomposition

    DEFF Research Database (Denmark)

    Simonsen, Søren Bredmose; Chakraborty, Debasish; Chorkendorff, Ib

    2012-01-01

    temperatures and a low NH3-to-H2 ratio, the catalytic activity of the best Ni-Fe/Al2O3 catalyst was found to be comparable or even better to that of a more expensive Ru-based catalyst. Small Ni-Fe nanoparticle sizes are crucial for an optimal overall NH3 conversion because of a structural effect favoring...

  12. Preparation of low-platinum-content platinum-nickel, platinum-cobalt binary alloy and platinum-nickel-cobalt ternary alloy catalysts for oxygen reduction reaction in polymer electrolyte fuel cells

    Science.gov (United States)

    Li, Mu; Lei, Yanhua; Sheng, Nan; Ohtsuka, Toshiaki

    2015-10-01

    A series of low-platinum-content platinum-nickel (Pt-Ni), platinum-cobalt (Pt-Co) binary alloys and platinum-nickel-cobalt (Pt-Ni-Co) ternary alloys electrocatalysts were successfully prepared by a three-step process based on electrodeposition technique and studied as electrocatalysts for oxygen reduction reaction (ORR) in polymer-electrolyte fuel cells. Kinetics of ORR was studied in 0.5 M H2SO4 solution on the Pt-Ni, Pt-Co and Pt-Ni-Co alloys catalysts using rotating disk electrode technique. Both the series of Pt-Ni, Pt-Co binary alloys and the Pt-Ni-Co ternary alloys catalysts exhibited an obvious enhancement of ORR activity in comparison with pure Pt. The significant promotion of ORR activities of Pt-Ni and Pt-Co binary alloys was attributed to the enhancement of the first electron-transfer step, whereas, Pt-Ni-Co ternary alloys presented a more complicated mechanism during the electrocatalysis process but a much more efficient ORR activities than the binary alloys.

  13. Unsupported NiPt alloy metal catalysts prepared by water-in-oil (W/O) microemulsion method for methane cracking

    KAUST Repository

    Zhou, Lu

    2016-05-18

    Unsupported NiPt metal catalyst with Ni/Pt molar ratio of 88/12 is prepared by water-in-oil (W/O) microemulsion method in this study. Compared to monometallic Ni and Pt catalysts, the NiPt catalyst exhibits superior activity and stability for methane cracking. By XRD (X-ray powder diffraction), XPS (X-ray photoelectron spectroscopy) and TEM (Transmission electron microscopy) analyses, the formation of Ni(0)Pt(0) alloy is believed to be the main reason for the reactivity improvement of this catalyst. Carbon nano tube (CNT) with Ni(0)Pt(0) particles anchored on the top of tube are found for the NiPt catalyst. © 2016 Elsevier Ltd.

  14. Synthesis of Ordered Mesoporous CuO/CeO2 Composite Frameworks as Anode Catalysts for Water Oxidation

    Directory of Open Access Journals (Sweden)

    Vassiliki Markoulaki Ι

    2015-11-01

    Full Text Available Cerium-rich metal oxide materials have recently emerged as promising candidates for the photocatalytic oxygen evolution reaction (OER. In this article, we report the synthesis of ordered mesoporous CuO/CeO2 composite frameworks with different contents of copper(II oxide and demonstrate their activity for photocatalytic O2 production via UV-Vis light-driven oxidation of water. Mesoporous CuO/CeO2 materials have been successfully prepared by a nanocasting route, using mesoporous silica as a rigid template. X-ray diffraction, electron transmission microscopy and N2 porosimetry characterization of the as-prepared products reveal a mesoporous structure composed of parallel arranged nanorods, with a large surface area and a narrow pore size distribution. The molecular structure and optical properties of the composite materials were investigated with Raman and UV-Vis/NIR diffuse reflectance spectroscopy. Catalytic results indicated that incorporation of CuO clusters in the CeO2 lattice improved the photochemical properties. As a result, the CuO/CeO2 composite catalyst containing ~38 wt % CuO reaches a high O2 evolution rate of ~19.6 µmol·h−1 (or 392 µmol·h−1·g−1 with an apparent quantum efficiency of 17.6% at λ = 365 ± 10 nm. This OER activity compares favorably with that obtained from the non-porous CuO/CeO2 counterpart (~1.3 µmol·h−1 and pure mesoporous CeO2 (~1 µmol·h−1.

  15. Mesoporous Silicon-Based Anodes

    Science.gov (United States)

    Peramunage, Dharmasena

    2015-01-01

    For high-capacity, high-performance lithium-ion batteries. A new high-capacity anode composite based on mesoporous silicon is being developed. With a structure that resembles a pseudo one-dimensional phase, the active anode material will accommodate significant volume changes expected upon alloying and dealloying with lithium (Li).

  16. Catalytic Hydrogenation of Levulinic Acid in Water into g-Valerolactone over Bulk Structure of Inexpensive Intermetallic Ni-Sn Alloy Catalysts

    Directory of Open Access Journals (Sweden)

    Rodiansono Rodiansono

    2015-07-01

    Full Text Available A bulk structure of inexpensive intermetallic nickel-tin (Ni-Sn alloys catalysts demonstrated highly selective in the hydrogenation of levulinic acid in water into g-valerolactone. The intermetallic Ni-Sn catalysts were synthesized via a very simple thermochemical method from non-organometallic precursor at low temperature followed by hydrogen treatment at 673 K for 90 min. The molar ratio of nickel salt and tin salt was varied to obtain the corresponding Ni/Sn ratio of 4.0, 3.0, 2.0, 1.5, and 0.75. The formation of Ni-Sn alloy species was mainly depended on the composition and temperature of H2 treatment. Intermetallics Ni-Sn that contain Ni3Sn, Ni3Sn2, and Ni3Sn4 alloy phases are known to be effective heterogeneous catalysts for levulinic acid hydrogenation giving very excellence g-valerolactone yield of >99% at 433 K, initial H2 pressure of 4.0 MPa within 6 h. The effective hydrogenation was obtained in H2O without the formation of by-product. Intermetallic Ni-Sn(1.5 that contains Ni3Sn2 alloy species demonstrated very stable and reusable catalyst without any significant loss of its selectivity. © 2015 BCREC UNDIP. All rights reserved. Received: 26th February 2015; Revised: 16th April 2015; Accepted: 22nd April 2015  How to Cite: Rodiansono, R., Astuti, M.D., Ghofur, A., Sembiring, K.C. (2015. Catalytic Hydrogenation of Levulinic Acid in Water into g-Valerolactone over Bulk Structure of Inexpensive Intermetallic Ni-Sn Alloy Catalysts. Bulletin of Chemical Reaction Engineering & Catalysis, 10 (2: 192-200. (doi:10.9767/bcrec.10.2.8284.192-200Permalink/DOI: http://dx.doi.org/10.9767/bcrec.10.2.8284.192-200  

  17. Studies on the properties of anodic oxidation film on aluminum alloy%铝合金阳极氧化膜的性能研究

    Institute of Scientific and Technical Information of China (English)

    许旋; 罗一帆; 林国辉

    2001-01-01

    在硫酸电解液中加入适量由羧酸和有机化合物组成的添加剂,制得铝合金阳极氧化膜。研究了温度对所得氧化膜厚度和硬度和影响,并利用扫描电镜观察了氧化膜的结构。结果表明,高温下形成的氧化膜结构松散,厚度和硬度低,而加入添加剂后,氧化膜溶解减慢,在高温下所形成的氧化膜的厚度和硬度大大增加。%Anodic oxidation film was prepared on aluminum alloy in sulfuricacid electrolyte. An additive was developed which consists of carboxylic acids and organic compounds. The effect of temperature on thickness and hardness of the obtained anodic oxidation film was studied, structure of the oxidation film was analyzed by SEM. The results show that oxidation film obtained at high temperature has loose structure. Thickness and hardness of the film decrease with the increase of temperature, while the addition of the additive reduces the dissolution of the oxidation film, and increases film thickness and hardness greatly at high temperature.

  18. Development of Ultra-Low Platinum Alloy Cathode Catalysts for PEM Fuel Cells

    Energy Technology Data Exchange (ETDEWEB)

    Popov, Branko N. [Univ. of South Carolina, Columbia, SC (United States). Dept. of Chemical Engineering; Weidner, John [Univ. of South Carolina, Columbia, SC (United States)

    2016-01-07

    The goal of this project is to synthesize a low cost PEM fuel cell cathode catalyst and support with optimized average mass activity, stability of mass activity, initial high current density performance under H2/air (power density), and catalyst and support stability able to meet 2017 DOE targets for electrocatalysts for transportation applications. Pt*/ACCS-2 catalyst was synthesized according to a novel methodology developed at USC through: (i) surface modification, (ii) metal catalyzed pyrolysis and (iii) chemical leaching to remove excess meal used to dope the support. Pt* stands for suppressed platinum catalyst synthesized with Co doped platinum. The procedure results in increasing carbon graphitization, inclusion of cobalt in the bulk and formation of non-metallic active sites on the carbon surface. Catalytic activity of the support shows an onset potential of 0.86 V for the oxygen reduction reaction (ORR) with well-defined kinetic and mass transfer regions and 2.5% H2O2 production. Pt*/ACCS-2 catalyst durability under 0.6-1.0 V potential cycling and support stability under 1.0-1.5 V potential cycling was evaluated. The results indicated excellent catalyst and support performance under simulated start-up/shut down operating conditions (1.0 – 1.5 V, 5000 cycles) which satisfy DOE 2017 catalyst and support durability and activity. The 30% Pt*/ACCS-2 catalyst showed high initial mass activity of 0.34 A/mgPGM at 0.9 ViR-free and loss of mass activity of 45% after 30,000 cycles (0.6-1.0 V). The catalyst performance under H2-air fuel cell operating conditions showed only 24 mV (iR-free) loss at 0.8 A/cm2 with an ECSA loss of 42% after 30,000 cycles (0.6-1.0 V). The support stability under 1.0-1.5 V potential cycling showed mass activity loss of 50% and potential loss of 8 mV (iR-free) at 1.5 A/cm2. The ECSA loss was 22% after 5,000 cycles. Furthermore, the Pt*/ACCS-2 catalyst showed an

  19. L-S mass transfer in G-L-S countercurrent magnetically stabilized bed with amorphous alloy SRNA-4 catalyst

    Institute of Scientific and Technical Information of China (English)

    Wei; Li; Baoning; Zong; Xiaofang; Li; Xiangkun; Meng; Jinli; Zhang

    2007-01-01

    Liquid-solid (L-S) mass transfer coefficients (Ks) were characterized in a gas-liquid-solid (G-L-S) three-phase countercurrent magnetically stabilized bed (MSB) using amorphous alloy SRNA-4 as the solid phase. Effects of superficial liquid velocity, superficial gas velocity, magnetic field strength, liquid viscosity and surface tension were investigated. Experimental results indicated that the external magnetic field increased Ks in three-phase MSB, as compared to those in conventional G-L-S fluidized beds; that Ks increased with magnetic field strength, superficial gas and liquid velocities and decreased with liquid viscosity and surface tension; and that Ks showed uniform axial and radial distributions except for small increases close to the wall. Dimensionless correlations were established to estimate Ks of the G-L-S countercurrent MSB using SRNA-4catalyst, with an average error of 3.6%.

  20. Hydrogenation of furfuryl alcohol to tetrahydrofurfuryl alcohol on NiB/SiO2 amorphous alloy catalyst

    Institute of Scientific and Technical Information of China (English)

    SONG Yun; LI Wei; ZHANG Minghui; TAO Keyi

    2007-01-01

    NiB/SiO2 amorphous alloy catalyst was prepared by power electroless plating method and characterized by induction coupled plasma (ICP),Brunauer-Emmett-Teller method (BET),transmission electron microscope (TEM)and X-ray diffraction (XRD) techniques.The catalytic performance of NiB/SiO2 was investigated for the hydrogenation of furfuryl alcohol (FA) to tetrahydrofurfuryl alcohol (THFA).The effects of operational conditions,such as reaction temperature,pressure,and stirring rate were carefully studied.The proper conditions were determined as the following:pressure 2.0 MPa,temperature 120℃ and stirring rate 550 r/min.A typical result with FA conversion of 99%and THFA selectivity of 100% was obtained under such conditions,which was close to that over Raney Ni.

  1. 石墨烯用作直接甲醇燃料电池阳极催化剂载体%Modified graphene as anode catalyst for direct methanol fuel cell

    Institute of Scientific and Technical Information of China (English)

    朱艳霞; 韩大量; 黄成德

    2015-01-01

    直接甲醇燃料电池(DMFC)阳极催化剂是决定电池性能、寿命和成本的关键材料之一。近年来人们主要从提高催化剂活性和降低催化剂成本两个方面出发进行了大量的研究,有力地推动了直接甲醇燃料电池的发展。石墨烯作为一种载体材料能够显著提高催化剂的催化活性和稳定性,引起了人们极大的兴趣。介绍了近几年石墨烯在直接甲醇燃料电池阳极催化剂载体的进展,并对其在未来的应用进行了展望。%Anode catalyst is one of the key materials determining the performance, longevity and cost of direct methanol fuel cell(DMFC). In recent years, extensive researches effectively promoting the development of DMFC are carried out, and these researches are mainly about two aspects:the activity improvement of catalyst and lowering the cost of catalyst. Graphene as a new carbon material can significantly improve the activity and stability of the catalyst. The research progress of modified graphene as anode catalyst of DMFC in recent years was reviewed and the application in the future was prospected.

  2. Synergistic effects of Ni 1- xCo x-YSZ and Ni 1- xCu x-YSZ alloyed cermet SOFC anodes for oxidation of hydrogen and methane fuels containing H 2S

    Science.gov (United States)

    Grgicak, Catherine M.; Pakulska, Malgosia M.; O'Brien, Julie S.; Giorgi, Javier B.

    Preparation and performance of bimetallic Ni (1- x)Co x-YSZ and Ni (1- x)Cu x-YSZ anodes were tested to overcome common deficiencies of carbon and sulfur poisoning in SOFCs. Ni 1- xCo xO-YSZ and Ni (1- x)Cu xO-YSZ precursors were synthesized via co-precipitation of their respective chlorides. Single cell solid oxide fuel cells of these bimetallic anodes were tested in H 2, CH 4, and H 2S/CH 4 fuel mixtures. Addition of Cu 2+ into the NiO lattice resulted in large metal particle sizes and decreased SOFC performance. Addition of Co 2+ into the NiO lattice to form Ni 0.92Co 0.08O-YSZ anode precursor produced a cermet with a large BET surface area and active metal surface area, thus increasing the rate of hydrogen oxidation for this sample. The performance of both bimetallics was found to quickly degrade in dry CH 4 due to carbon deposition and lifting of the anode from the electrolyte. However, Ni 0.69Co 0.31-YSZ showed superior activity in a 10% (v/v) H 2S/CH 4 fuel mixture, surpassing performance with H 2 fuel, thereby demonstrating the exciting prospect of using sulfidated Ni (1- x)Co x-YSZ as SOFC anodes in sulfur containing methane streams. The active anode becomes a sulfidated alloy (Ni-Co-S) under operating conditions. This anode showed enhanced performance, which surpassed those of sulfidated Ni and Co anodes, thereby suggesting a synergistic behaviour in the Ni-Co-S anode.

  3. Effect of magnesium on the aluminothermic reduction rate of zinc oxide obtained from spent alkaline battery anodes for the preparation of Al-Zn-Mg alloys

    Institute of Scientific and Technical Information of China (English)

    Rocio Ochoa; Alfredo Flores; Jesus Torres

    2016-01-01

    The aluminothermic reduction of zinc oxide (ZnO) from alkaline battery anodes using molten Al may be a good option for the elaboration of secondary 7000-series alloys. This process is affected by the initial content of Mg within molten Al, which decreases the sur-face tension of the molten metal and conversely increases the wettability of ZnO particles. The effect of initial Mg concentration on the alu-minothermic reduction rate of ZnO was analyzed at the following values:0.90wt%, 1.20wt%, 4.00t%, 4.25wt%, and 4.40wt%. The ZnO par-ticles were incorporated by mechanical agitation using a graphite paddle inside a bath of molten Al maintained at a constant temperature of 1123 K and at a constant agitation speed of 250 r/min, the treatment time was 240 min and the ZnO particle size was 450-500 mesh. The re-sults show an increase in Zn concentration in the prepared alloys up to 5.43wt%for the highest initial concentration of Mg. The reaction products obtained were characterized by scanning electron microscopy and X-ray diffraction, and the efficiency of the reaction was measured on the basis of the different concentrations of Mg studied.

  4. Post-annealing effects on the electrochemical performance of a Si/TiSi2 heteronanostructured anode material prepared by mechanical alloying

    Science.gov (United States)

    Shin, Min-Seon; Lee, Taeg-Woo; Park, Jung-Bae; Lim, Sung-Hwan; Lee, Sung-Man

    2017-03-01

    A change in the microstructure of Ti-Si alloys synthesized by high-energy mechanical milling through post-annealing significantly enhances their electrochemical performances as anode materials for lithium-ion batteries (LIBs). The microstructures of ball-milled and post-annealed powders are investigated using high-resolution transmission electron microscopy (HR-TEM). The Si phase is uniformly distributed on the silicide (TiSi2) matrix. The individual Si domains of the mechanical alloying (MA) sample consist of amorphous and crystalline regions with a diffuse interface between the two phases. When MA powder is annealed at 600 °C, the Si phase has a well-developed nanocrystalline microstructure: a multi-grain structure with random orientation of nanometric crystal domains. Annealing at 600 °C causes a significant improvement in electrochemical performance parameters like cycling stability and rate capability. However, when annealed at 800 °C, the electrochemical performances deteriorate due to an increase in the size of Si domains.

  5. Effect of magnesium on the aluminothermic reduction rate of zinc oxide obtained from spent alkaline battery anodes for the preparation of Al-Zn-Mg alloys

    Science.gov (United States)

    Ochoa, Rocio; Flores, Alfredo; Torres, Jesus

    2016-04-01

    The aluminothermic reduction of zinc oxide (ZnO) from alkaline battery anodes using molten Al may be a good option for the elaboration of secondary 7000-series alloys. This process is affected by the initial content of Mg within molten Al, which decreases the surface tension of the molten metal and conversely increases the wettability of ZnO particles. The effect of initial Mg concentration on the aluminothermic reduction rate of ZnO was analyzed at the following values: 0.90wt%, 1.20wt%, 4.00t%, 4.25wt%, and 4.40wt%. The ZnO particles were incorporated by mechanical agitation using a graphite paddle inside a bath of molten Al maintained at a constant temperature of 1123 K and at a constant agitation speed of 250 r/min, the treatment time was 240 min and the ZnO particle size was 450-500 mesh. The results show an increase in Zn concentration in the prepared alloys up to 5.43wt% for the highest initial concentration of Mg. The reaction products obtained were characterized by scanning electron microscopy and X-ray diffraction, and the efficiency of the reaction was measured on the basis of the different concentrations of Mg studied.

  6. Anodizing And Sealing Aluminum In Nonchromated Solutions

    Science.gov (United States)

    Emmons, John R.; Kallenborn, Kelli J.

    1995-01-01

    Improved process for anodizing and sealing aluminum involves use of 5 volume percent sulfuric acid in water as anodizing solution, and 1.5 to 2.0 volume percent nickel acetate in water as sealing solution. Replaces process in which sulfuric acid used at concentrations of 10 to 20 percent. Improved process yields thinner coats offering resistance to corrosion, fatigue life, and alloy-to-alloy consistency equal to or superior to those of anodized coats produced with chromated solutions.

  7. Catalytic activity of Pd-doped Cu nanoparticles for hydrogenation as a single-atom-alloy catalyst.

    Science.gov (United States)

    Cao, Xinrui; Fu, Qiang; Luo, Yi

    2014-05-14

    The single atom alloy of extended surfaces is known to provide remarkably enhanced catalytic performance toward heterogeneous hydrogenation. Here we demonstrate from first principles calculations that this approach can be extended to nanostructures, such as bimetallic nanoparticles. The catalytic properties of the single-Pd-doped Cu55 nanoparticles have been systemically examined for H2 dissociation as well as H atom adsorption and diffusion, following the concept of single atom alloy. It is found that doping a single Pd atom at the edge site of the Cu55 shell can considerably reduce the activation energy of H2 dissociation, while the single Pd atom doped at the top site or in the inner layers is much less effective. The H atom adsorption on Cu55 is slightly stronger than that on the Cu(111) surface; however, a larger nanoparticle that contains 147 atoms could effectively recover the weak binding of the H atoms. We have also investigated the H atom diffusion on the 55-atom nanoparticle and found that spillover of the produced H atoms could be a feasible process due to the low diffusion barriers. Our results have demonstrated that facile H2 dissociation and weak H atom adsorption could be combined at the nanoscale. Moreover, the effects of doping one more Pd atom on the H2 dissociation and H atom adsorption have also been investigated. We have found that both the doping Pd atoms in the most stable configuration could independently exhibit their catalytic activity, behaving as two single-atom-alloy catalysts.

  8. The effect of immersion time in a benzotriazole solution on anodic behaviour of AgCu50 alloy

    OpenAIRE

    Grekulović, Vesna; Rajčić-Vujasinović, Mirjana; Stević, Zoran; id_orcid 0000-0002-1867-9360

    2016-01-01

    Electrochemical behavior of silver ,copper and AgCu50 alloy after their immersion in 0.01 mol/dm3 benzotriazole solution for 30, 360, 720 i 1440 minutes, was investigated in 0.1 mol/dm3 NaOH using the cyclic voltammetry method. Currents on cyclic voltammograms for both, pure silver, pure copper and AgCu50 alloy recorded after imemersion in the benzotriazole solution are lower than the corresponding currents obtained without the contact of the metals with BTA. During the immersion of electrode...

  9. Effect of Anodic Current Density on Characteristics and Low Temperature IR Emissivity of Ceramic Coating on Aluminium 6061 Alloy Prepared by Microarc Oxidation

    Directory of Open Access Journals (Sweden)

    Mohannad M. S. Al Bosta

    2013-01-01

    Full Text Available High emitter MAO ceramic coatings were fabricated on the Al 6061 alloy, using different bipolar anodic current densities, in an alkali silicate electrolyte. We found that, as the current density increased from 10.94 A/dm2 to 43.75 A/dm2, the layer thickness was increased from 10.9 μm to 18.5 μm, the surface roughness was increased from 0.79 μm to 1.27 μm, the area ratio of volcano-like microstructure was increased from 55.6% to 59.6%, the volcano-like density was decreased from 2620 mm−2 to 1420 mm−2, and the γ-alumina phase was decreased from 66.6 wt.% to 26.2 wt.%, while the α-alumina phase was increased from 3.9 wt.% to 27.6 wt.%. The sillimanite and cristobalite phases were around 20 wt.% and 9 wt.%, respectively, for 10.94 A/dm2 and approximately constant around 40 wt.% and less than 5 wt.%, respectively, for the anodic current densities 14.58, 21.88, and 43.75 A/dm2. The ceramic surface roughness and thickness slightly enhanced the IR emissivity in the semitransparent region (4.0–7.8 μm, while the existing phases contributed together to raise the emissivity in the opaque region (8.6–16.0 μm to higher but approximately the same emissivities.

  10. Effect of Ni, Fe and Fe-Ni alloy catalysts on the synthesis of metal contained carbon nano-onions and studies of their electrochemical hydrogen storage properties

    Institute of Scientific and Technical Information of China (English)

    Chenguang Zhang; Jiajun Li; Chunsheng Shi; Chunnian He; Enzuo Liu; Naiqin Zhao

    2014-01-01

    Three types of carbon nano-onions (CNOs) including Ni@CNOs, Fe3C@CNOs and Fe0.64Ni0.36@CNOs nanoparticles have been synthesized by catalytic decomposition of methane at 850◦C using nickel, iron and iron-nickel alloy catalysts. Comparative and systematic studies have been carried out on the morphology, structural characteristics and graphitic crystallinity of these CNOs products. Furthermore, the electro-chemical hydrogen storage properties of three types of CNOs have been investigated. Measurements show that the Ni@CNOs have the highest discharge capacity of 387.2 mAh/g, corresponding to a hydrogen storage of 1.42%. This comparison study shows the advantages of each catalyst in the growth of CNOs, enabling the controllable synthesis and tuning the properties of CNOs by mediating different metals and their alloy for using in the fuel cell system.

  11. Nitrogen-doped graphene/CoNi alloy encased within bamboo-like carbon nanotube hybrids as cathode catalysts in microbial fuel cells

    Science.gov (United States)

    Hou, Yang; Yuan, Heyang; Wen, Zhenhai; Cui, Shumao; Guo, Xiaoru; He, Zhen; Chen, Junhong

    2016-03-01

    Cost-effective catalysts are of key importance to the successful deployment of microbial fuel cells (MFCs) for electricity generation from organic wastes. Herein, a novel catalyst prepared by one-step synthesis strategy is reported. The catalyst features N-doped bamboo-like carbon nanotube (BCNT) in which CoNi-alloy is encapsulated at the end and/or the middle section of the tube with many graphene layers inside inner cavities of BCNT (N-G@CoNi/BCNT). The prepared N-G@CoNi/BCNT exhibits a high oxygen reduction reaction (ORR) activity with an early onset potential of 0.06 V vs. Ag/AgCl and a comparable exchange current density to that of commercial Pt/C. The excellent catalytic activity is further evidenced by a high electron transfer number of 3.63. When being applied in MFCs, the N-G@CoNi/BCNT yields an average current density of 6.7 A m-2, slightly lower than that of Pt/C but with a less mass transfer potential loss. The cost of the N-G@CoNi/BCNT for constructing a 1-m2 cathode electrode is 200 times lower than that of Pt/C. With such a competitive price and excellent electrocatalytic-activity resulting from its unique morphology, CoNi-alloy/nitrogen dopants, considerable specific surface area, and carbon-coated alloy/graphene hybridization, the present catalyst is a promising candidate for ORR catalysts in MFCs for energy recovery from wastes.

  12. Influence of Metal Sulfides as Anode Catalysts on Performance of H2S SOFC%金属硫化物作为阳极材料对H2S固体氧化物燃料电池性能研究

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Two anode catalysts with Pt, MoS2 and composite metal sulfides (MoS2+NiS), are investigated forelectrochemical oxidation of hydrogen sulfide in solid oxide fuel cell (SOFC) at temperatures 750-850℃. Thecatalysts comprising MoS2 and MoS2+NiS exhibited good electrical conductivity and catalytic activity. MoS2 andcomposite catalysts were found to be more active than Pt, a widely used catalyst for high temperature H2S/O2fuel cell at 750-850℃. However, MoS2 itself sublimes above 450℃. In contrast, composite catalysts containingboth Mo and transition metal (Ni) are shown to be stable and effective in promoting the oxidation of H2S in SOFCup to 850℃. However, electric contact is poor between the platinum current collecting layer and the compositemetal sulfide layer, so that the cell performance becomes worse. This problem is overcome by adding conductiveAg powder into the anode layer (forming MoS2+NiS+Ag anode material) to increase anode electrical conductanceinstead of applying a thin layer of platinum on the top of anode.

  13. Combined high-pressure cell-ultrahigh vacuum system for fast testing of model metal alloy catalysts using scanning mass spectrometry

    DEFF Research Database (Denmark)

    Johansson, Martin; Jørgensen, Jan Hoffmann; Chorkendorff, Ib

    2004-01-01

    An apparatus for fabrication, surface analysis in ultrahigh vacuum, and testing of the catalytic activity of model metal alloy catalysts is described. Arrays of model catalysts are produced by electron-beam deposition of up to four metals simultaneously onto a substrate. The surface analysis...... techniques available are scanning electron microscopy, x-ray photoemission spectroscopy, ion scattering spectroscopy, Auger electron spectroscopy, sputter profiling, and temperature programmed desorption. The catalytic activity of the model catalysts is tested individually by scanning a combined gas delivery...... be studied on a substrate 10 mm in diameter. A high pressure cell with an all-metal sealed ultrahigh vacuum lock is also described as part of the work. ©2004 American Institute of Physics....

  14. A Platinum Monolayer Core-Shell Catalyst with a Ternary Alloy Nanoparticle Core and Enhanced Stability for the Oxygen Reduction Reaction

    Directory of Open Access Journals (Sweden)

    Haoxiong Nan

    2015-01-01

    Full Text Available We synthesize a platinum monolayer core-shell catalyst with a ternary alloy nanoparticle core of Pd, Ir, and Ni. A Pt monolayer is deposited on carbon-supported PdIrNi nanoparticles using an underpotential deposition method, in which a copper monolayer is applied to the ternary nanoparticles; this is followed by the galvanic displacement of Cu with Pt to generate a Pt monolayer on the surface of the core. The core-shell Pd1Ir1Ni2@Pt/C catalyst exhibits excellent oxygen reduction reaction activity, yielding a mass activity significantly higher than that of Pt monolayer catalysts containing PdIr or PdNi nanoparticles as cores and four times higher than that of a commercial Pt/C electrocatalyst. In 0.1 M HClO4, the half-wave potential reaches 0.91 V, about 30 mV higher than that of Pt/C. We verify the structure and composition of the carbon-supported PdIrNi nanoparticles using X-ray powder diffraction, X-ray photoelectron spectroscopy, thermogravimetry, transmission electron microscopy, and energy dispersive X-ray spectrometry, and we perform a stability test that confirms the excellent stability of our core-shell catalyst. We suggest that the porous structure resulting from the dissolution of Ni in the alloy nanoparticles may be the main reason for the catalyst’s enhanced performance.

  15. Influence of Temperature Gradient on the Performance of Hard Anodizing Film on Al Alloy%温度梯度降温对铝合金阳极氧化膜性能的影响

    Institute of Scientific and Technical Information of China (English)

    陈朝英; 魏晓伟; 王建; 魏德超

    2012-01-01

    The hard anodic oxidation film on 6061 aluminum alloy sheet surface was prepared by a self-made hard anodic oxidation device under the conditions of large temperature gradient along the direction of aluminum matrix.The oxide film morphology,hardness and thickness were observed and analyzed.The results showed that after hard anodizing the aluminium sheet the film quality was greatly improved,the thickness,hardness and uniformity of hard anodic oxide film prepared with temperature gradient method were far superior to that of the traditional hard anodic oxide film.%采用自制的硬质阳极氧化装置,在铝合金6061薄板表面沿着铝基体方向形成较大的温度梯度降温条件,对铝板进行硫酸硬质氧化试验。对氧化膜形貌、硬度、膜厚分别进行了观察和分析。结果表明,相同条件下,采用温度梯度法制备的硬质阳极氧化膜,其均匀性、膜的厚度和硬度都大大优于传统的硬质阳极氧化膜,膜的质量得到很大的提高。

  16. Formation and Characterization of Pd, Pt and Pd-Pt Alloy Films on Polyimide by Catalyst-Enhanced Chemical Vapor Deposition

    Institute of Scientific and Technical Information of China (English)

    ZHOU Jinlan; CHENG Yinhua; Yousuf Hamadan; YU Kaichao

    2007-01-01

    Platinum, palladium and their alloy films on polyimide were formed by catalyst-enhanced chemical vapor deposition (CVD) in the carrier gas (N2, O2) at 220-300 ℃ under reduced pressure and normal pressure. The deposition of palladium complexes [ Pd((η3-allyl)(hfac) and Pd(hfac)2 ] gives pure palladium film,while the deposition of platinum needs the enhancement of palladium complex by mixing precursor platinum complex Pt(COD)Me2 and palladium complex in the same chamber. The co-deposition of Pd and Pt metals was used for the deposition of alloy films. During the CVD of palladium-platinum alloy, the Pd/Pt atomic ratios vary under different co-deposition conditions. These metal films were characterized by XPS and SEM, and show a good adhesive property.

  17. Formic acid oxidation at platinum-bismuth catalysts

    Directory of Open Access Journals (Sweden)

    Popović Ksenija Đ.

    2015-01-01

    Full Text Available The field of heterogeneous catalysis, specifically catalysis on bimetallic surfaces, has seen many advances over the past few decades. Bimetallic catalysts, which often show electronic and chemical properties that are distinct from those of their parent metals, offer the opportunity to obtain new catalysts with enhanced selectivity, activity, and stability. The oxidation of formic acid is of permanent interest as a model reaction for the mechanistic understanding of the electrooxidation of small organic molecules and because of its technical relevance for fuel cell applications. Platinum is one of the most commonly used catalysts for this reaction, despite the fact that it shows a few significant disadvantages: high cost and extreme susceptibility to poisoning by CO. To solve this problem, several approaches have been used, but generally, they all consist in the modification of platinum with a second element. Especially, bismuth has received significant attention as Pt modifier. According to the results presented in this survey dealing with the effects influencing the formic acid oxidation it was found that two types of Pt-Bi bimetallic catalysts (bulk and low loading deposits on GC showed superior catalytic activity in terms of the lower onset potential and oxidation current density, as well as exceptional stability compared to Pt. The findings in this report are important for the understanding of mechanism of formic acid electrooxidation on a bulk alloy and decorated surface, for the development of advanced anode catalysts for direct formic acid fuel cells, as well as for the synthesis of novel low-loading bimetallic catalysts. The use of bimetallic compounds as the anode catalysts is an effective solution to overcoming the problems of the formic acid oxidation current stability for long term applications. In the future, the tolerance of both CO poisoning and electrochemical leaching should be considered as the key factors in the development

  18. Alternative alloys for catalysts and platinum jewelry? New structures in Pt-Hf and Pt-Mo

    Science.gov (United States)

    Gilmartin, Erin; Corbitt, Jacqueline; Hart, Gus

    2009-03-01

    The only known intermetallic structure with an 8:1 stoichiometry is that of Pt8Ti. It is intriguing that an ordered phase would occur at such low concentrations of the minority atom, but this structure occurs in about a dozen binary intermetallic systems. The formation of an ordered phase in an alloy can significantly enhance the performance of the material, particularly the hardness. We have taken a broad look at possible systems where this phase forms. Using first-principles, we calculated the stability of this structure relative to experimentally known phases for more than 80 Pt/Pd binary systems. We find the Pt8Ti structure is a possible ground state in more than 20 cases. Our experimental collaborators have verified our prediction in Pt-Mo and observed order-hardening in Pt-Hf. We discuss the discovery of new ground states that are likely to be verified experimentally and their impact on materials for Pt- and Pd-based catalysts and jewelry.

  19. Preparation and study of IrO2/SiC–Si supported anode catalyst for high temperature PEM steam electrolysers

    DEFF Research Database (Denmark)

    Nikiforov, Aleksey; Tomás García, Antonio Luis; Petrushina, Irina;

    2011-01-01

    of the IrO2 particles, affecting the IrO2 particle size. The prepared catalysts were electrochemically characterised by cyclic voltammetry experiments at 25,80,120 and 150 °C. In accordance with the observed variation in particle size, a support loading of up to 20% improved the activity of the catalyst...

  20. Self-Assembled Nanoporous Titania Layers on Ti Alloys by Anodic Oxidation%钛合金阳极氧化法制备自组装纳米多孔结构薄膜

    Institute of Scientific and Technical Information of China (English)

    张文彦; 李广忠; 奚正平; 张健; 汤慧萍; 汪强兵

    2012-01-01

    TiO2 nanotube arrays or nanoporous films fabricated by potentiostatic anodization of titanium (titanium alloy) in F-containing electrolytes constitute a material architecture that offers a large internal surface area and excellent electron percolation pathways for vectorial charge transfer between interfaces. The material architecture has proven to be of great interest for use in water photoelectrolysis, photocatalysis, heterojunction solar cells, and gas sensing. The parameters for TiO2 nanoporous film fabrication are found by changing the anodic oxidation voltage and phase composition of titanium alloys. When the anodization potential is below 30 V, TiO2 nanoporous film by anodizing TLM alloy aged at 550 °C for long time can be obtained%钛及钛合金在含有F-离子的电解液中阳极氧化,可自组装制备出有序TiO2纳米多孔或纳米管阵列薄膜,这类纳米阵列膜材料具有极大的内比表面积和优异的电子传输性能,可以用作纳米结构制备模板、高灵敏度传感器、染料敏化太阳能电池等.以TLM钛合金为阳极氧化的基片,通过改变阳极氧化电压、钛合金相结构,找到了制备纳米多孔阵列的参数,通过条件试验发现,在恒电压小于30 V时,经时效处理的TLM钛合金表面可以制备得到合金元素掺杂的TiO2纳米多孔结构薄膜.

  1. CuAu–ZnO–graphene nanocomposite: A novel graphene-based bimetallic alloy-semiconductor catalyst with its enhanced photocatalytic degradation performance

    Energy Technology Data Exchange (ETDEWEB)

    Xie, Hong [College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China); Ye, Xiaoliang [College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China); College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005 (China); Duan, Kaiyue; Xue, Muyin; Du, Yongling; Ye, Weichun [College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China); Wang, Chunming, E-mail: wangcm@lzu.edu.cn [College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000 (China)

    2015-07-05

    Graphical abstract: In this work, we have successfully synthesized a novel graphene-based bimetallic alloy-semiconductor catalyst: CuAu–ZnO–Gr nanocomposite, and which behaved an enhanced photocatalytic activity. - Highlights: • A bimetallic alloy-based catalyst: CuAu–ZnO–Gr is synthesized. • CuAu–ZnO–Gr behaves an enhanced photocatalytic activity. • The detailed explanation of photocatalytic mechanism of CuAu–ZnO–Gr. - Abstract: The bimetallic alloy CuAu nanoparticles (NPs) can produce more photogenerated electrons when compared with single metal Au NPs. Moreover, graphene (Gr) sheets can help the charge separation and slow down the recombination of the electron hole pairs of ZnO. Hence, a novel graphene-based bimetallic alloy-semiconductor catalyst: CuAu–ZnO–Gr nanocomposite is synthesized. Due to the synergistic effect among CuAu NPs, ZnO nanopyramids, and Gr sheets, CuAu–ZnO–Gr behaves an enhanced photocatalytic activity for the photocatalytic degradation of synthetic colorants methyl orange (MO), methylene blue (MB), indigotin (IN), sunset yellow (SY), and tartrazine (TT) under the simulated sunlight irradiation. Furthermore, the apparent rate constants (k{sub app}) of MO, MB, IN, SY, and TT degradation are estimated respectively. In addition, the as-prepared CuAu–ZnO–Gr nanocomposite is characterized by X-ray diffraction, UV–vis spectrum, transmission electron microscopy, energy dispersive X-ray analysis (EDX), and EDX mapping. As a result of the facile synthesis route and the enhanced photocatalytic activity, this new material CuAu–ZnO–Gr can be a promising photocatalyst for the degradation of dyes.

  2. Evaluating the role of Lead In A Novel Ternary Catalysts For DMFCs

    CERN Document Server

    Halder, Aditi; Trahan, Matthew; Mukerjee, Sanjeev

    2012-01-01

    The current density at lower potential is highly desirable in fuel cell technology and crucial center point for designing a new catalyst. By alloying platinum with various other metals, the improvisation of the fuel cell catalyst has achieved a lot of attention and interests. In this article, a novel porous ternary alloy PtPb@Ru as anode catalysts for direct methanol fuel cell had been synthesized by micro-emulsion technique. The catalysts had been characterized by various spectroscopic and microscopic techniques. The activity and durability of the catalysts had been tested by running cyclic voltammetry in 0.1 M HClO4 and 1M Methanol. To explain the many fold increase in current density of the PtPb@Ru catalysts in comparison to the commercial available PtRu catalysts, in situ X-ray absorption spectroscopy (XAS) measurements, at the PtL3 edge (XANES and EXAFS) were carried out on the PtPb@Ru catalysts in an electrochemical cell. The down-shift in the d-band center of platinum observed in the XAS study, might b...

  3. 铝基合金牺牲阳极在干湿交替环境中的耐腐蚀性能%Anti-corrosion Performance of Al-based Alloys for Sacrificial Anode in Wet-dry Cyclic Environment

    Institute of Scientific and Technical Information of China (English)

    方志刚; 刘斌; 王涛; 王洪仁

    2013-01-01

    Electrochemical impedance spectroscopy (EIS) was used to study the corrosion behavior of four Al-based alloys commonly used as sacrificial anode for submarine under wet-dry cyclic conditions with various drying periods. The EIS results showed that the failure of the sacrificial anodes was mainly attributed that the coverage effect of corrosion products on the surface of sacrificial anodes, leading to the decrease of the number of active sites on the anode surface. Thus, the further activation of the sacrificial anodes was prevented. After several wet-dry cycles, the severe accumulation of corrosion products on the anode surface resulted in enlargement at the capacitive loops, indicating significant decrease of the active dissolution of the anodes. The performance of the 4 Al-based alloys under wet-dry cyclic environment may be ranked as the following order: Zn-Al-Cd <Al-Zn-In-Cd <Al-Zn-In-Mg-Ti<Al-Zn-In-Mg-Ga-Mn.%测试潜艇常用的4种牺牲阳极在不同干湿交替周期的电化学阻抗谱,分析了它们的耐腐蚀性能.结果表明,干湿交替条件下阳极失效的主要原因是腐蚀产物覆盖致使阳极表面的活性溶解点减少,阻碍阳极的进一步活化.经过一定的干湿交替循环后有些阳极结壳严重,导致容抗弧增大,阳极的活化溶解能力大大降低.在干湿交替环境中,合金的使用性能从差到好的顺序为:Zn-Al-Cd<Al-Zn-In-Cd<Al-Zn-In-Mg-Ti<Al-Zn-In-Mg-Ga-Mn.

  4. A hexangular ring-core NiCo2O4 porous nanosheet/NiO nanoparticle composite as an advanced anode material for LIBs and catalyst for CO oxidation applications.

    Science.gov (United States)

    He, Yanyan; Xu, Liqiang; Zhai, Yanjun; Li, Aihua; Chen, Xiaoxia

    2015-10-11

    A porous hexangular ring-core NiCo2O4 nanosheet/NiO nanoparticle composite has been synthesized using a hydrothermal method followed by an annealing process in air. The as-obtained composite as an anode material exhibits a high initial discharge capacity of 1920.6 mA h g(-1) at a current density of 100 mA g(-1) and the capacity is retained at 1567.3 mA h g(-1) after 50 cycles. When it is utilized as a catalyst for CO oxidation, complete CO conversion is achieved at 115 °C and a catalytic life test demonstrates the good stability of the composite.

  5. Ultra-High Density Single Nanometer-Scale Anodic Alumina Nanofibers Fabricated by Pyrophosphoric Acid Anodizing

    Science.gov (United States)

    Kikuchi, Tatsuya; Nishinaga, Osamu; Nakajima, Daiki; Kawashima, Jun; Natsui, Shungo; Sakaguchi, Norihito; Suzuki, Ryosuke O.

    2014-12-01

    Anodic oxide fabricated by anodizing has been widely used for nanostructural engineering, but the nanomorphology is limited to only two oxides: anodic barrier and porous oxides. Therefore, the discovery of an additional anodic oxide with a unique nanofeature would expand the applicability of anodizing. Here we demonstrate the fabrication of a third-generation anodic oxide, specifically, anodic alumina nanofibers, by anodizing in a new electrolyte, pyrophosphoric acid. Ultra-high density single nanometer-scale anodic alumina nanofibers (1010 nanofibers/cm2) consisting of an amorphous, pure aluminum oxide were successfully fabricated via pyrophosphoric acid anodizing. The nanomorphologies of the anodic nanofibers can be controlled by the electrochemical conditions. Anodic tungsten oxide nanofibers can also be fabricated by pyrophosphoric acid anodizing. The aluminum surface covered by the anodic alumina nanofibers exhibited ultra-fast superhydrophilic behavior, with a contact angle of less than 1°, within 1 second. Such ultra-narrow nanofibers can be used for various nanoapplications including catalysts, wettability control, and electronic devices.

  6. Nano-molybdenum carbide/carbon nanotubes composite as bifunctional anode catalyst for high-performance Escherichia coli-based microbial fuel cell.

    Science.gov (United States)

    Wang, Yaqiong; Li, Bin; Cui, Dan; Xiang, Xingde; Li, Weishan

    2014-01-15

    A novel electrode, carbon felt-supported nano-molybdenum carbide (Mo2C)/carbon nanotubes (CNTs) composite, was developed as platinum-free anode of high performance microbial fuel cell (MFC). The Mo2C/CNTs composite was synthesized by using the microwave-assisted method with Mo(CO)6 as a single source precursor and characterized by using X-ray diffraction and transmission electron microscopy. The activity of the composite as anode electrocatalyst of MFC based on Escherichia coli (E. coli) was investigated with cyclic voltammetry, chronoamperometry, and cell discharge test. It is found that the carbon felt electrode with 16.7 wt% Mo Mo2C/CNTs composite exhibits a comparable electrocatalytic activity to that with 20 wt% platinum as anode electrocatalyst. The superior performance of the developed platinum-free electrode can be ascribed to the bifunctional electrocatalysis of Mo2C/CNTs for the conversion of organic substrates into electricity through bacteria. The composite facilitates the formation of biofilm, which is necessary for the electron transfer via c-type cytochrome and nanowires. On the other hand, the composite exhibits the electrocatalytic activity towards the oxidation of hydrogen, which is the common metabolite of E. coli.

  7. Optimizing Misch-Metal Compositions In Metal Hydride Anodes

    Science.gov (United States)

    Bugga, Ratnakumar V.; Halpert, Gerald

    1995-01-01

    Electrochemical cells based on metal hydride anodes investigated experimentally in effort to find anode compositions maximizing charge/discharge-cycle performances. Experimental anodes contained misch metal alloyed with various proportions of Ni, Co, Mn, and Al, and experiments directed toward optimization of composition of misch metal.

  8. Noble metals on anodic TiO2 nanotubes mouths: Thermal dewetting of minimal Pt co-catalyst loading leads to significantly enhanced photocatalytic H2 generation

    CERN Document Server

    Nguyen, Nhat Truong; Yoo, JeongEun; Taccardi, Nicola; Schmuki, Patrik

    2016-01-01

    The least is the best. We introduce a technique to strongly reduce Pt use for photocatalytic hydrogen generation from TiO2 nanotubes. By site-selectively depositing thin layers of Pt only at the mouth of the nanotubes and by a subsequent thermal dewetting step, we achieve an outstanding photocatalytic improvement with minimal amounts of co-catalyst.

  9. Evaluation of nanostructured Pt-Ru catalyst for application in DMFC

    Energy Technology Data Exchange (ETDEWEB)

    Ocampo, A.L.; Gamboa, S.A. [Centro de Investigacion en Energia-UNAM, Morelos (Mexico); Sebastien, P.J. [Centro de Investigacion en Energia-UNAM, Morelos (Mexico)]|[Chiapas Politecnica Univ., Chiapas (Mexico); Morgado, J.; Montoya, J.A. [IMP, Eje Central Lazaro Cardenas, (Mexico); Savadogo, O. [Ecole Polytechnique, Montreal, PQ (Canada). Laboratoire d' electrochimie et de materiaux energetiques

    2006-07-01

    Slow methanol oxidation kinetics and the poisoning of the anode catalyst are the major factors that limit the performance of the direct methanol fuel cell (DMFC). Catalysts with higher catalytic activity are needed in order to overcome these challenges. Although platinum (Pt) is a good catalyst for methanol oxidation, it can be highly affected by carbon monoxide (CO) reaction intermediates. Superior catalytic activity occurs in Pt based alloys, such as platinum ruthenium (Pt-Ru), platinum molybdenum (Pt-Mo), platinum tin (Pt-Sn), and platinum osmium (Pt-Os). This is due to the bifunctional mechanism and/or by the electronic effect, which indicates a promotional effect of the alloyed metal on Pt. The most studied binary system is the Pt-Ru (ruthenium), which has shown the best catalytic activity. There are many factors that influence the physical properties and the electrochemical performance of the Pt-Ru catalyst. These include the preparation method; the atomic ratio between platinum and ruthenium; the nature of the catalyst support; and, an optional heat treatment. Other important factors such as the particle size, the morphology, the electrochemically active area, and the crystalline phase influence the physical properties. In this study, nanostructured Pt-Ru catalysts were fabricated and evaluated physicochemically and electrochemically for its use in direct methanol fuel cell (DMFC). The catalysts were synthesized from the carbonyl compounds of Pt and Ru via a pyrolysis-condensation reaction. The high resolution results showed a homogenous distribution of the nanostructured catalysts on Vulcan support. The catalyst was evaluated by XRD, HRTEM, electrochemical impedance spectroscopy and the methanol oxidation on the catalyst was studied using volt-amperometry. The performance of the catalyst was found to be similar or better than the commercial one. It was concluded that it is possible to synthesize Pt-Ru/C with good morphological characteristics and improve it

  10. Final technical report. Bimetallic complexes as methanol oxidation catalysts

    Energy Technology Data Exchange (ETDEWEB)

    McElwee-White, Lisa

    2002-01-21

    Our work on the electrocatalyzed oxidation of methanol was initially motivated by the interest in methanol as an anodic reactant in fuel cells. The literature on electrochemical oxidation of alcohols can be roughly grouped into two sets: fuel cell studies and inorganic chemistry studies. Work on fuel cells primarily focuses on surface-catalyzed oxidation at bulk metal anodes, usually Pt or Pt/Ru alloys. In the surface science/electrochemistry approach to these studies, single molecule catalysts are generally not considered. In contrast, the inorganic community investigates the electrooxidation of alcohols in homogeneous systems. Ruthenium complexes have been the most common catalysts in these studies. The alcohol substrates are typically either secondary alcohols (e.g., isopropanol) such that the reaction stops after 2 e{sup -} oxidation to the aldehyde and 4 e{sup -} oxidation to the carboxylic acid can be observed. Methanol, which can also undergo 6 e{sup -} oxidation to CO{sub 2}, rarely appears in the homogeneous catalysis studies. Surface studies have shown that two types of metal centers with different functions result in more effective catalysts than a single metal; however, application of this concept to homogeneous systems has not been demonstrated. The major thrust of the work is to apply this insight from the surface studies to homogeneous catalysis. Even though homogeneous systems would not be appropriate models for active sites on Pt/Ru anodes, it is possible that heterobimetallic catalysts could also utilize two metal centers for different roles. Starting from that perspective, this work involves the preparation and investigation of heterobinuclear catalysts for the electrochemical oxidation of methanol.

  11. 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

  12. Process of black sealing with inorganic salts for aluminum alloy after anodic oxidation%铝合金阳极氧化后无机盐黑色封闭工艺

    Institute of Scientific and Technical Information of China (English)

    杨改航

    2012-01-01

    Considering the disadvantages of black sealing with organic dyes for anodic oxidation film on aluminum alloy, black sealing with inorganic salts based on the principle of A-B blackening process was carried out for anodized aluminum alloy products. Three kinds of inorganic salt black sealing processes were introduced, including Co(CH3COOH)r-Na2S, FeSO4-(NH4)2S, and NiSO4-(NH4)2S. The anodic oxidation films treated by black sealing were examined by heat and moisture test, salt spray test, high temperature test, and solar radiation test according to related standards. It is proved that the three kinds of anodized aluminum alloy samples after black sealing treatment meet the requirement of standard. The inorganic salt black sealing processes eliminate the defects of easily dissolving in organic solvents as well as fall-off and discoloration, and easy discoloration under strong illumination after sealing by using traditional organic dyes.%针对铝合金阳极氧化有机染料染黑封闭的缺点,采用无机盐A-B染黑工艺对铝合金阳极氧化产品进行黑色封闭处理.介绍了Co(CH3COOH)2-Na2S、FeSO4-(NH4)2S、NiSO4-(NH4)2S等3种无机盐黑色封闭处理工艺,根据相关标准对经黑色封闭处理后的铝合金阳极氧化膜进行了湿热、盐雾、高温及太阳辐射试验.结果表明,3种铝合金阳极氧化黑色封闭处理试样均符合标准要求.无机盐黑色封闭工艺消除了传统有机染料封闭后易溶于有机溶剂而脱落变色以及在强光照射下易变色的缺陷.

  13. Anode materials for lithium-ion batteries

    Science.gov (United States)

    Sunkara, Mahendra Kumar; Meduri, Praveen; Sumanasekera, Gamini

    2014-12-30

    An anode material for lithium-ion batteries is provided that comprises an elongated core structure capable of forming an alloy with lithium; and a plurality of nanostructures placed on a surface of the core structure, with each nanostructure being capable of forming an alloy with lithium and spaced at a predetermined distance from adjacent nanostructures.

  14. A new application of photocatalysts: synthesis of nano-sized metal and alloy catalysts by a photo-assisted deposition method.

    Science.gov (United States)

    Mori, Kohsuke; Araki, Takashi; Takasaki, Tomoya; Shironita, Sayoko; Yamashita, Hiromi

    2009-05-01

    Supported Pd catalysts were synthesized using various semiconductor materials by a photo-assisted deposition method under UV-light irradiation. The Pd precursor was deposited and partially reduced by the direct interaction with the photo-excited state of the semiconductor materials, and subsequently transformed into metal particles by H(2) reduction. CO adsorption and Pd K-edge XAFS measurements demonstrated that the mean diameter of the deposited Pd particles can be controlled by the type of employed semiconductor materials. The catalytic activities in the direct synthesis of hydrogen peroxide (H(2)O(2)) using H(2) and O(2) gases under atmospheric pressure were strongly dependent on the type of supports. Here, the use of TiO(2) comprising a mixed phase of anatase and rutile was the most efficient based on the amount of Pd. The photo-assisted deposition also provides a simple and straightforward method to synthesize PdAu alloy nanoparticles. For the structural model of PdAu nanoparticles, we suggest that most of the Au atoms are preferentially located in the core region, whereas the Pd atoms are preferentially located in the shell region. The PdAu/TiO(2) catalysts prepared by the photo-assisted deposition method were shown to perform significantly better than the pure Pd/TiO(2) catalysts.

  15. Alloy

    Science.gov (United States)

    Cabeza, Sandra; Garcés, Gerardo; Pérez, Pablo; Adeva, Paloma

    2014-07-01

    The Mg98.5Gd1Zn0.5 alloy produced by a powder metallurgy route was studied and compared with the same alloy produced by extrusion of ingots. Atomized powders were cold compacted and extruded at 623 K and 673 K (350 °C and 400 °C). The microstructure of extruded materials was characterized by α-Mg grains, and Mg3Gd and 14H-LPSO particles located at grain boundaries. Grain size decreased from 6.8 μm in the extruded ingot, down to 1.6 μm for powders extruded at 623 K (350 °C). Grain refinement resulted in an increase in mechanical properties at room and high temperatures. Moreover, at high temperatures the PM alloy showed superplasticity at high strain rates, with elongations to failure up to 700 pct.

  16. Quantification of zinc atoms in a surface alloy on copper in an industrial-type methanol synthesis catalyst

    DEFF Research Database (Denmark)

    Kuld, Sebastian; Moses, Poul Georg; Sehested, Jens;

    2014-01-01

    Methanol has recently attracted renewed interest because of its potential importance as a solar fuel.1 Methanol is also an important bulk chemical that is most efficiently formed over the industrial Cu/ZnO/Al2O3 catalyst. The identity of the active site and, in particular, the role of ZnO...... as a promoter for this type of catalyst is still under intense debate.2 Structural changes that are strongly dependent on the pretreatment method have now been observed for an industrial-type methanol synthesis catalyst. A combination of chemisorption, reaction, and spectroscopic techniques provides...

  17. Quantification of zinc atoms in a surface alloy on copper in an industrial-type methanol synthesis catalyst

    DEFF Research Database (Denmark)

    Kuld, Sebastian; Moses, Poul Georg; Sehested, Jens;

    2014-01-01

    Methanol has recently attracted renewed interest because of its potential importance as a solar fuel. Methanol is also an important bulk chemical that is most efficiently formed over the industrial Cu/ZnO/Al2O3 catalyst. The identity of the active site and, in particular, the role of ZnO...... as a promoter for this type of catalyst is still under intense debate. Structural changes that are strongly dependent on the pretreatment method have now been observed for an industrial-type methanol synthesis catalyst. A combination of chemisorption, reaction, and spectroscopic techniques provides a consistent...

  18. Preparation and characterization of nano-sized Pt-Ru/C catalysts and their superior catalytic activities for methanol and ethanol oxidation.

    Science.gov (United States)

    Şen, Selda; Şen, Fatih; Gökağaç, Gülsün

    2011-04-21

    Carbon-supported PtRu nanoparticles (Ru/Pt: 0.25) were prepared by three different methods; simultaneous reduction of PtCl(4) and RuCl(3) (catalyst I) and changing the reduction order of PtCl(4) and RuCl(3) (catalysts II and III) to enhance the performance of the anodic catalysts for methanol and ethanol oxidation. Structure, microstructure and surface characterizations of all the catalysts were carried out by X-ray diffraction (XRD), transmission electron microscopy (TEM) coupled with energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). The results of the XRD analysis showed that all catalysts had a face-centered cubic (fcc) structure with different and smaller lattice parameters than that of pure platinum, showing that the Ru incorporates into the Pt fcc structure by different ratios in all the catalysts. The typical particle sizes of all catalysts were in the range of 2-3 nm. The most active and stable catalyst for methanol and ethanol oxidation is catalyst III, in which a large amount (more than 90%) of PtRu alloy formation was observed. It has been found that this catalyst is about 8.0 and 33.4 times more active at ∼0.60 V towards the methanol and ethanol oxidation reactions, respectively, compared to the commercial Pt catalyst.

  19. Investigation of nano Pt and Pt-based alloys electrocatalysts for direct methanol fuel cells and their properties

    Directory of Open Access Journals (Sweden)

    Chunguang Suo

    2014-03-01

    Full Text Available The electrocatalysts used in micro direct methanol fuel cell (μDMFC, such as Pt/C and Pt alloy/C, prepared by liquid-phase NaBH4 reduction method have been investigated. XC-72 (Cobalt corp. Company, U.S.A is chosen as the activated carrier for the electrocatalysts to keep the catalysts powder in the range of several nanometers. The XRD, SEM, EDX analyses indicated that the catalysts had small particle size in several nanometers, in excellent dispersed phase and the molar ratio of the precious metals was found to be optimal. The performances of the DMFCs using cathodic catalyst with Pt percentage of 30wt% and different anodic catalysts (Pt-Ru, Pt-Ru-Mo were tested. The polarization curves and power density curves of the cells were measured to determine the optimal alloy composition and condition for the electrocatalysts. The results showed that the micro direct methanol fuel cell with 30wt% Pt/C as the cathodic catalyst and n(Pt:n(Ru:n(Mo = 3:2:2 PtRuMo/C as the anodic catalyst at room temperature using 2.0mol/L methanol solution has the best performances.

  20. Sodium citrate assisted facile synthesis of AuPd alloy networks for ethanol electrooxidation with high activity and durability

    Science.gov (United States)

    Zhai, Yanling; Zhu, Zhijun; Lu, Xiaolin; Zhou, H. Susan

    2016-10-01

    The direct ethanol fuel cell is an emerging energy conversion device for which palladium is considered as the one of the most effective components for anode catalyst, however, its widespread application has been still limited by the activity and durability of the anode catalyst. In this work, AuPd alloy networks (NWs) are synthesized using H2PdCl4 and HAuCl4 as precursors reduced by NaBH4 in the presence of sodium citrate (SC). The results reveal that SC plays significant role in network structure, resulting in the enhanced electrocatalytic activity of the catalyst. This self-supported AuPd NWs catalyst exhibits much higher electrochemical catalytic activity than commercial Pd/C catalyst toward ethanol electrooxidation in alkaline solution. Significantly, AuPd NWs catalyst shows extremely high durability at the beginning of the chronoamperometry test, and as high as 49% of the mass current density (1.41 A/mgPd) remains after 4000 s current-time test at -0.3 V (vs. Ag/AgCl) in N2-saturated KOH-ethanol solution. This strategy provides a facile method for the preparation of alloy networks with high electrochemical activity, and can be potentially expanded to a variety of electrochemical applications.

  1. Performance and life-time behaviour of NiCu-CGO anodes for the direct electro-oxidation of methane in IT-SOFCs

    Science.gov (United States)

    Sin, A.; Kopnin, E.; Dubitsky, Y.; Zaopo, A.; Aricò, A. S.; La Rosa, D.; Gullo, L. R.; Antonucci, V.

    An anodic cermet of NiCu alloy and gadolinia doped ceria has been investigated for CH 4 electro-oxidation in IT-SOFCs. Polarization curves have been recorded in the temperature range from 650 to 800 °C. A maximum power density of 320 mW cm -2 at 800 °C has been obtained in the presence of dry methane in an electrolyte-supported cell. The electrochemical behaviour during 1300 h operation in dry methane and in the presence of redox-cycles has been investigated at 750 °C; variation of the electrochemical properties during these experiments have been interpreted in terms of anode morphology modifications. The methane cracking process at the anode catalyst has been investigated by analysing the oxidative stripping of deposited carbon species.

  2. Performance and life-time behaviour of NiCu-CGO anodes for the direct electro-oxidation of methane in IT-SOFCs

    Energy Technology Data Exchange (ETDEWEB)

    Sin, A.; Kopnin, E.; Dubitsky, Y.; Zaopo, A. [Pirelli Labs S.p.A., Viale Sarca 222, I-20126 Milan (Italy); Arico, A.S.; La Rosa, D.; Gullo, L.R.; Antonucci, V. [CNR-ITAE, Via Salita Santa Lucia Sopra Contesse 5, I-98125 Messina (Italy)

    2007-01-10

    An anodic cermet of NiCu alloy and gadolinia doped ceria has been investigated for CH{sub 4} electro-oxidation in IT-SOFCs. Polarization curves have been recorded in the temperature range from 650 to 800{sup o}C. A maximum power density of 320mWcm{sup -2} at 800{sup o}C has been obtained in the presence of dry methane in an electrolyte-supported cell. The electrochemical behaviour during 1300h operation in dry methane and in the presence of redox-cycles has been investigated at 750{sup o}C; variation of the electrochemical properties during these experiments have been interpreted in terms of anode morphology modifications. The methane cracking process at the anode catalyst has been investigated by analysing the oxidative stripping of deposited carbon species. (author)

  3. Anodization and Optical Appearance of Sputter Deposited Al-Zr Coatings

    DEFF Research Database (Denmark)

    Gudla, Visweswara Chakravarthy; Canulescu, Stela; Shabadi, Rajashekhara

    2014-01-01

    Anodized Al alloy components are extensively used in various applications like architectural, decorative and automobiles for corrosion protection and/or decorative optical appearance. However, tailoring the anodized layer for specific optical appearance is limited due to variation in composition...

  4. LC4铝合金表面硬质阳极氧化膜制备及表征%Preparation and Characterization of Hard Anodic Oxidation Film on LC4 Aluminum Alloy Surface

    Institute of Scientific and Technical Information of China (English)

    王英才; 陈岁元; 刘平平

    2014-01-01

    目的:在 LC4铝合金表面制备硬质阳极氧化膜,讨论工艺参数对膜层厚度和硬度的影响。方法对阳极氧化的时间、温度、电流密度及正负脉冲电流时间比等参数进行优化实验,通过 OM,SEM,XRD 及显微硬度计等对制备的氧化膜层的厚度、硬度、形貌等进行研究。结果工艺优化后的参数为:温度-2~0℃,正脉冲电流密度4 A/ dm2,负脉冲电流密度1 A/ dm2,正负脉冲电流时间比6:1,氧化时间50 min。得到由一系列直径约为50 nm 的管状单元结构组成的氧化膜,其厚度为36μm,硬度为420HV。结论制备的阳极氧化膜具有致密的组织结构和高的硬度值。%Objective The hard anodic oxidation films were prepared on the surface of the LC4 aluminum alloy and the effects of different parameters on the thickness and hardness of the films were discussed. Methods By optimizing parameters of the anodic ox-idation time, temperature, current density and the positive and negative pulse time ratio, the thickness, hardness and microstruc-ture of the films were studied by means of OM, SEM, XRD, and hardness tester. Results The optimized parameters were: a tem-perature of -2 ~ 0 ℃ , a positive pulse current density of 4 A/ dm2 , a negative pulse current density of 1 A/ dm2 , a positive and negative pulse current time ratio of 6 : 1, and an oxidation time of 50 min. The structure of the oxide film on LC4 aluminum alloy was composed of a series of tubular cells with a diameter of 50 nm, the thickness of anodic oxidation film was 36 μm, and the hard-ness was 420HV. Conclusion The anodic oxidation film had fine structure and high hardness.

  5. Widely tunable alloy composition and crystal structure in catalyst-free InGaAs nanowire arrays grown by selective area molecular beam epitaxy

    Energy Technology Data Exchange (ETDEWEB)

    Treu, J., E-mail: Julian.Treu@wsi.tum.de, E-mail: Gregor.Koblmueller@wsi.tum.de; Speckbacher, M.; Saller, K.; Morkötter, S.; Xu, X.; Riedl, H.; Abstreiter, G.; Finley, J. J.; Koblmüller, G., E-mail: Julian.Treu@wsi.tum.de, E-mail: Gregor.Koblmueller@wsi.tum.de [Walter Schottky Institut, Physik Department, Center of Nanotechnology and Nanomaterials, Technische Universität München, Am Coulombwall 4, Garching 85748 (Germany); Döblinger, M. [Department of Chemistry, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, Munich 81377 (Germany)

    2016-02-01

    We delineate the optimized growth parameter space for high-uniformity catalyst-free InGaAs nanowire (NW) arrays on Si over nearly the entire alloy compositional range using selective area molecular beam epitaxy. Under the required high group-V fluxes and V/III ratios, the respective growth windows shift to higher growth temperatures as the Ga-content x(Ga) is tuned from In-rich to Ga-rich InGaAs NWs. Using correlated x-ray diffraction, transmission electron microscopy, and micro-photoluminescence spectroscopy, we identify structural defects to govern luminescence linewidths in In-rich (x(Ga) < 0.4) and Ga-rich (x(Ga) > 0.6) NWs, whereas limitations at intermediate Ga-content (0.4 < x(Ga) < 0.6) are mainly due to compositional inhomogeneities. Most remarkably, the catalyst-free InGaAs NWs exhibit a characteristic transition in crystal structure from wurtzite to zincblende (ZB) dominated phase near x(Ga) ∼ 0.4 that is further reflected in a cross-over from blue-shifted to red-shifted photoluminescence emission relative to the band edge emission of the bulk ZB InGaAs phase.

  6. 可溶性阳极电刷镀纳米晶Ni-Fe合金镀层的退火再强化%Annealing hardening of nanocrystalline Ni-Fe alloy coatings synthesized by brush plating using soluble anode

    Institute of Scientific and Technical Information of China (English)

    戴品强; 陈晓文; 项忠楠; 许伟长

    2009-01-01

    Nanocrystalline Ni-Fe alloy coatings were synthesized by brush plating using soluble anode. Microhardness test and techniques of XRD, SEM and TEM were applied to characterize the microstructures and mechanical properties of Ni-Fe alloy coatings. The results show that the microhardness of Ni-Fe alloy coatings increases with increasing annealing temperature and reaches a peak value at 200 ℃, showing a significant hardening during annealing. With further increasing annealing temperature, the microhardness decreases gradually, but the microhardness of the coating after being annealed at 400 ℃ is still as high as that of the as-deposited sample. The abnormal grain growth is not observed during annealing of Ni-Fe alloy coatings, which indicates a better thermal stability.%采用可溶性Ni阳极电刷镀方法制备纳米晶Ni-Fe合金镀层,利用XRD、SEM、TEM、显微硬度计等测试方法分析低温退火对镀层结构和性能的影响.结果表明:纳米晶Ni-Fe合金镀层的硬度随退火温度的升高而提高,在200 ℃时达到最大值,存在明显的退火再强化;继续提高退火温度导致镀层硬度降低;400 ℃退火后的镀层硬度与镀态的接近;纳米晶Ni-Fe合金镀层退火过程没有出现晶粒异常长大,表现出比纯Ni镀层更高的热稳定性.

  7. 镁合金阳极氧化膜腐蚀特性的红外显微成像分析%Studies on Corrosion Property of the Anodic Coating on the Mg Alloy by Micro-FTIR Mapping

    Institute of Scientific and Technical Information of China (English)

    李美超; 易景苗; 卢金金; 李静; 赵卫娟

    2014-01-01

    采用显微红外成像技术对镁合金阳极氧化膜表面的腐蚀特性进行了研究。镁合金在7.3 Wt%Na2 SO4溶液中浸泡后,表面氧化层中的部分M gO逐渐转化为M g (O H )2,进而发生溶解和脱落,使得镁合金失去保护作用。当浸泡时间达到2 h时,显微红外成像结果表明阳极氧化膜中Mg(OH)2的红外吸收信号最强,Mg(OH)2的含量最多。而4 h后Mg(OH)2的红外吸收信号开始减弱,Mg(OH)2开始减少,镁合金不断被腐蚀。氧化膜中另一成分Al2 O3随浸泡时间的显微红外成像信息与Mg(OH)2的变化规律相同。采用电化学阻抗谱技术对阳极氧化膜的阻抗进行测试,其阻抗随时间的变化特点基本符合氧化膜腐蚀规律。本研究对于镁合金阳极氧化膜的表征具有很好的指导作用和推广应用价值。%Micro-FTIR mapping technology was used to monitor the amount and distribution of Mg (OH)2 on the anodic coating of magnesium alloy which was immersed in the 7 .3 Wt% Na2 SO4 solution for different time .In the solution ,part of the MgO on the surface of the Mg alloy could gradually transform into Mg (OH)2 which could be detached from the Mg alloy surface and dis-solved into the solution .With immersion time of 2 h in 7 .3 Wt% Na2 SO4 solution 2h ,FTIR mapping results showed that FTIR absorption signal of Mg(OH)2 was strongest and Mg(OH)2 was most on the surface of the anodic coating .After 4 hours ,the content of Mg(OH)2 began to decrease ,and the Mg alloy was etched gradually .The FTIR mapping results of another compo-nent Al2O3 with immersion time were almost similar to those of Mg(OH)2 .The impedance of the oxide film was also analyzed using electrochemical impedance spectroscopy .It showed that the impedance changed with the immersion time and conformed to the corrosion law of the oxide coating .This research has a good guidance and application value for characterization of the anodic coating on

  8. Correlation between diffusion barriers and alloying energy in binary alloys

    DEFF Research Database (Denmark)

    Vej-Hansen, Ulrik Grønbjerg; Rossmeisl, Jan; Stephens, Ifan;

    2016-01-01

    In this paper, we explore the notion that a negative alloying energy may act as a descriptor for long term stability of Pt-alloys as cathode catalysts in low temperature fuel cells.......In this paper, we explore the notion that a negative alloying energy may act as a descriptor for long term stability of Pt-alloys as cathode catalysts in low temperature fuel cells....

  9. Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions

    Directory of Open Access Journals (Sweden)

    Webster TJ

    2013-01-01

    Full Text Available Alexandra P Ross, Thomas J WebsterSchool of Engineering and Department of Orthopedics, Brown University, Providence, RI, USAAbstract: Current titanium-based implants are often anodized in sulfuric acid (H2SO4 for color coding purposes. However, a crucial parameter in selecting the material for an orthopedic implant is the degree to which it will integrate into the surrounding bone. Loosening at the bone–implant interface can cause catastrophic failure when motion occurs between the implant and the surrounding bone. Recently, a different anodization process using hydrofluoric acid has been shown to increase bone growth on commercially pure titanium and titanium alloys through the creation of nanotubes. The objective of this study was to compare, for the first time, the influence of anodizing a titanium alloy medical device in sulfuric acid for color coding purposes, as is done in the orthopedic implant industry, followed by anodizing the device in hydrofluoric acid to implement nanotubes. Specifically, Ti6Al4V model implant samples were anodized first with sulfuric acid to create color-coding features, and then with hydrofluoric acid to implement surface features to enhance osteoblast functions. The material surfaces were characterized by visual inspection, scanning electron microscopy, contact angle measurements, and energy dispersive spectroscopy. Human osteoblasts were seeded onto the samples for a series of time points and were measured for adhesion and proliferation. After 1 and 2 weeks, the levels of alkaline phosphatase activity and calcium deposition were measured to assess the long-term differentiation of osteoblasts into the calcium depositing cells. The results showed that anodizing in hydrofluoric acid after anodizing in sulfuric acid partially retains color coding and creates unique surface features to increase osteoblast adhesion, proliferation, alkaline phosphatase activity, and calcium deposition. In this manner, this study

  10. Effects of cerium on performance of Al-Zn-Sn sacrificial anode alloy%Ce对Al-Zn-Sn牺牲阳极合金性能的影响

    Institute of Scientific and Technical Information of China (English)

    贺俊光; 文九巴; 孙乐民; 高军伟; 李登辉

    2015-01-01

    采用扫描电镜(SEM)、X射线衍射(XRD)、动电位极化、电化学阻抗等方法研究了Ce含量对Al-7Zn-0.1Sn(质量分数,%)合金显微组织和电化学性能的影响。结果表明:Ce可明显细化晶粒,使Al-7Zn-0.1Sn合金从粗大枝状晶向细小等轴晶转变;适量的Ce可有效改善Al-7Zn-0.1Sn合金的电化学性能;随着Ce含量增加,合金电位负移、电流效率逐步提高;当 Ce 含量(质量分数)为0.5%时,合金具有最好的电化学性能,其电流效率相比Al-7Zn-0.1Sn 合金的提高10%。%The effects of cerium content on the microstructure and electrochemical performance of Al-7Zn-0.1Sn (mass fraction, %) alloy were investigated by scanning electron microscopy (SEM), X-ray diffractometry (XRD), potentiodynamic polarization and electrochemical impedance spectra measurements. The results show that cerium can refine the crystalline structure and make the microstructure of Al-7Zn-0.1Sn alloy transform from bulky dendrite grain to fine equiaxed grain. Proper cerium addition is effective on improving the electrochemical properties of Al-7Zn-0.1Sn alloy. The corrosion potential shifts negatively and the current efficiency increases with increasing the cerium content. The optimal electrochemical performance can be obtained when the Ce content in the alloy is 0.5%. The current efficiency of the Al-7Zn-0.1Sn-0.5Ce alloy increases by 10% than that of Al-7Zn-0.1Sn alloy.

  11. The effect of zinc on the aluminum anode of the aluminum-air battery

    Science.gov (United States)

    Tang, Yougen; Lu, Lingbin; Roesky, Herbert W.; Wang, Laiwen; Huang, Baiyun

    Aluminum is an ideal material for batteries, due to its excellent electrochemical performance. Herein, the effect of zinc on the aluminum anode of the aluminum-air battery, as an additive for aluminum alloy and electrolytes, has been studied. The results show that zinc can decrease the anodic polarization, restrain the hydrogen evolution and increase the anodic utilization rate.

  12. Anodizing color coded anodized Ti6Al4V medical devices for increasing bone cell functions.

    Science.gov (United States)

    Ross, Alexandra P; Webster, Thomas J

    2013-01-01

    Current titanium-based implants are often anodized in sulfuric acid (H(2)SO(4)) for color coding purposes. However, a crucial parameter in selecting the material for an orthopedic implant is the degree to which it will integrate into the surrounding bone. Loosening at the bone-implant interface can cause catastrophic failure when motion occurs between the implant and the surrounding bone. Recently, a different anodization process using hydrofluoric acid has been shown to increase bone growth on commercially pure titanium and titanium alloys through the creation of nanotubes. The objective of this study was to compare, for the first time, the influence of anodizing a titanium alloy medical device in sulfuric acid for color coding purposes, as is done in the orthopedic implant industry, followed by anodizing the device in hydrofluoric acid to implement nanotubes. Specifically, Ti6Al4V model implant samples were anodized first with sulfuric acid to create color-coding features, and then with hydrofluoric acid to implement surface features to enhance osteoblast functions. The material surfaces were characterized by visual inspection, scanning electron microscopy, contact angle measurements, and energy dispersive spectroscopy. Human osteoblasts were seeded onto the samples for a series of time points and were measured for adhesion and proliferation. After 1 and 2 weeks, the levels of alkaline phosphatase activity and calcium deposition were measured to assess the long-term differentiation of osteoblasts into the calcium depositing cells. The results showed that anodizing in hydrofluoric acid after anodizing in sulfuric acid partially retains color coding and creates unique surface features to increase osteoblast adhesion, proliferation, alkaline phosphatase activity, and calcium deposition. In this manner, this study provides a viable method to anodize an already color coded, anodized titanium alloy to potentially increase bone growth for numerous implant applications.

  13. Failure Mechanisms of Nickel/Metal Hydride Batteries with Cobalt-Substituted Superlattice Hydrogen-Absorbing Alloy Anodes at 50 °C

    Directory of Open Access Journals (Sweden)

    Tiejun Meng

    2016-06-01

    Full Text Available The incorporation of a small amount of Co in the A2B7 superlattice hydrogen absorbing alloy (HAA can benefit its electrochemical cycle life performance at both room temperature (RT and 50 °C. The electrochemical properties of the Co-substituted A2B7 and the failure mechanisms of cells using such alloys cycled at RT have been reported previously. In this paper, the failure mechanisms of the same alloys cycled at 50 °C are reported. Compared to that at RT, the trend of the cycle life at 50 °C versus the Co content in the Co-substituted A2B7 HAAs is similar, but the cycle life is significantly shorter. Failure analysis of the cells at 50 °C was performed using X-ray diffraction (XRD, scanning electron microscopy (SEM, X-ray energy dispersive spectroscopy (EDS, and inductively coupled plasma (ICP analysis. It was found that the elevated temperature accelerates electrolyte dry-out and the deterioration (both pulverization and oxidation of the A2B7 negative electrode, which are major causes of cell failure when cycling at 50 °C. Cells from HAA with higher Co-content also showed micro-shortage in the separator from the debris of the corrosion of the negative electrode.

  14. Bifunctional Pt-Si Alloys for Small Organic Molecule Electro-oxidation

    DEFF Research Database (Denmark)

    Permyakova, Anastasia Aleksandrovna; Suntivich, Jin; Han, Binghong

    Designing highly active catalysts for electro-oxidation of small organic molecules can help to reduce the anodic overpotential for more efficient utilization of hydrocarbon fuels. The challenge in developing more active electrocatalysts for electro-oxidation reactions is to satisfy the stringent...... bifunctional requirement, which demands both adsorption and water oxidation sites. In this contribution, we explore the possibility of using Pt-Si alloys to fulfill this bifunctional requirement. Silicon, a highly oxophillic element, is alloyed into Pt as a site for water oxidation, while Pt serves as a CO...... adsorption site. We will discuss the enhanced activity of Pt-Si alloys for small organic molecule oxidation, which can be attributed to the improved CO electro-oxidation kinetics on Pt-Si....

  15. Anodizing of High Electrically Stressed Components

    Energy Technology Data Exchange (ETDEWEB)

    Flores, P. [NSTec; Henderson, D. J. [NSTec; Good, D. E. [NSTec; Hogge, K. [NSTec; Mitton, C. V. [NSTec; Molina, I. [NSTec; Naffziger, C. [NSTec; Codova, S. R. [SNL; Ormond, E. U. [SNL

    2013-06-01

    Anodizing creates an aluminum oxide coating that penetrates into the surface as well as builds above the surface of aluminum creating a very hard ceramic-type coating with good dielectric properties. Over time and use, the electrical carrying components (or spools in this case) experience electrical breakdown, yielding undesirable x-ray dosages or failure. The spool is located in the high vacuum region of a rod pinch diode section of an x-ray producing machine. Machine operators have recorded decreases in x-ray dosages over numerous shots using the reusable spool component, and re-anodizing the interior surface of the spool does not provide the expected improvement. A machine operation subject matter expert coated the anodized surface with diffusion pump oil to eliminate electrical breakdown as a temporary fix. It is known that an anodized surface is very porous, and it is because of this porosity that the surface may trap air that becomes a catalyst for electrical breakdown. In this paper we present a solution of mitigating electrical breakdown by oiling. We will also present results of surface anodizing improvements achieved by surface finish preparation and surface sealing. We conclude that oiling the anodized surface and using anodized hot dip sealing processes will have similar results.

  16. Excitation of anodized alumina films with a light source

    DEFF Research Database (Denmark)

    Aggerbeck, Martin; Canulescu, Stela; Rechendorff, K.;

    . The UV-VIS reflectance of Ti-doped anodized aluminium films was measured over the wavelength range of 200 nm to 900 nm. Titanium doped-anodized aluminium films with 5-15 wt% Ti were characterized. Changes in the diffuse light scattering of doped anodized aluminium films, and thus optical appearance......Optical properties of anodized aluminium alloys were determined by optical diffuse reflectance spectroscopy of such films. Samples with different concentrations of dopants were excited with a white-light source combined with an integrating sphere for fast determination of diffuse reflectance...

  17. Recovery of plutonium from electrorefining anode heels at Savannah River

    Energy Technology Data Exchange (ETDEWEB)

    Gray, J H; Gray, L W; Karraker, D G

    1987-03-01

    In a joint effort, the Savannah River Laboratory (SRL), Savannah River Plant (SRP), and the Rocky Flats Plant (RFP) have developed two processes to recover plutonium from electrorefining anode heel residues. Aqueous dissolution of anode heel metal was demonstrated at SRL on a laboratory scale and on a larger pilot scale using either sulfamic acid or nitric acid-hydrazine-fluoride solutions. This direct anode heel metal dissolution requires the use of a geometrically favorable dissolver. The second process developed involves first diluting the plutonium in the anode heel residues by alloying with aluminum. The alloyed anode heel plutonium can then be dissolved using a nitric acid-fluoride-mercury(II) solution in large non-geometrically favorable equipment where nuclear safety is ensured by concentration control.

  18. La0.6Sr0.4Co0.2Fe0.8O3 Perovskite: A Stable Anode Catalyst for Direct Methane Solid Oxide Fuel Cells

    Directory of Open Access Journals (Sweden)

    Jelvehnaz Mirzababaei

    2014-05-01

    Full Text Available Direct methane solid oxide fuel cells, operated by supplying methane to a Ni/YSZ anode, suffer from degradation via accumulation of carbon deposits on the Ni surface. Coating a 40 µm thin film of La0.6Sr0.4Co0.2Fe0.8O3 (LSCF perovskite on the Ni/YSZ anode surface decreased the amount of carbon deposits, slowing down the degradation rate. The improvement in anode durability could be related to the oxidation activity of LSCF which facilitates oxidation of CH4 and carbon deposits. Analysis of the crystalline structure of LSCF revealed that LSCF was stable in the reducing anode environment under H2 and CH4 flow at 750 °C and retained its perovskite structure throughout the 475 h long-term stability test.

  19. 5052铝合金硬质阳极氧化工艺研究%Study of Hard Anodizing of 5052 Aluminum Alloy

    Institute of Scientific and Technical Information of China (English)

    陈梁; 廖重重; 刘晨岑; 熊雄; 王茜

    2016-01-01

    以硫酸为基础电解液,同时混合加入草酸与添加剂,优化了电源参数及添加剂浓度配比,优化得出最佳工艺参数:10 g/L草酸和44 g/L添加剂,电流密度为3 A/dm2,氧化时间为40 min ,占空比为80%。在该条件下得到的氧化膜厚度为40μm ,硬度为490 HV ,氧化膜表面纳米孔结构均匀致密。%The base electricity of experiment is sulfuric acid. Oxalate and additive are added into elec-trolyte. Optimizing power parameter and the concentration of additive to reach the best parameter that 10 g/L oxalate, 44 g/L additive, current density was 3 A/dm2 , time of anodizing was 40 min, duty ratio was 80%. The thickness of oxidization film was 40 μm. The hardness of oxidization film was 490 HV. The structure of nano-hole was very uniform and dense.

  20. Palladium-Based Catalysts as Electrodes for Direct Methanol Fuel Cells: A Last Ten Years Review

    Directory of Open Access Journals (Sweden)

    Juan Carlos Calderón Gómez

    2016-08-01

    Full Text Available Platinum-based materials are accepted as the suitable electrocatalysts for anodes and cathodes in direct methanol fuel cells (DMFCs. Nonetheless, the increased demand and scarce world reserves of Pt, as well as some technical problems associated with its use, have motivated a wide research focused to design Pd-based catalysts, considering the similar properties between this metal and Pt. In this review, we present the most recent advancements about Pd-based catalysts, considering Pd, Pd alloys with different transition metals and non-carbon supported nanoparticles, as possible electrodes in DMFCs. In the case of the anode, different reported works have highlighted the capacity of these new materials for overcoming the CO poisoning and promote the oxidation of other intermediates generated during the methanol oxidation. Regarding the cathode, the studies have showed more positive onset potentials, as fundamental parameter for determining the mechanism of the oxygen reduction reaction (ORR and thus, making them able for achieving high efficiencies, with less production of hydrogen peroxide as collateral product. This revision suggests that it is possible to replace the conventional Pt catalysts by Pd-based materials, although several efforts must be made in order to improve their performance in DMFCs.

  1. Effects of Additives on Corrosion Resistance of Anodic Film for AZ 31 Magnesium Alloy%添加剂对AZ31镁合金阳极氧化膜耐蚀性能的影响

    Institute of Scientific and Technical Information of China (English)

    王桂香; 穆俊宏; 李云虎

    2011-01-01

    The effects of several additives on the anodization of Mg alloy AZ 31 were investigated with an electrolyte based on 50.0 g/L NaOH + 10. 0 g/L H3BO3+ 20. 0 g/L Na2B,O7 ·10H2O and by constant potential mode. The morphology and corrosion resistance of the anodic oxide films were tested by scanning electron microscopy, spot test and polarization curves respectively. The results show that the optimal mass concentrations for sodium silicate, sodium citrate and sodium oxalate are 10 g/L, 7. 5 g/L, 0. 8 g/L respectively. Spark discharge is enhanced by sodium silicate and weakened by sodium citrate in electrolysis, and when sodium oxalate is added, spark discharge will disappear.%以50.0 g/L NaOH+10.0 g/L H3BO3+20.0 g/L Na2B4O7· 10 H2O为基础电解液,采用恒电位模式,研究了几种添加剂对AZ 31镁合金阳极氧化膜性能的影响.采用扫描电镜、点滴实验和极化曲线分别对阳极氧化膜的表面形貌和耐蚀性能进行测试.结果表明:硅酸钠的最佳质量浓度为10.0 g/L,柠檬酸钠的最佳质量浓度为7.5 g/L,草酸钠的最佳质量浓度为0.2 g/L.硅酸钠增强了火花放电的剧烈程度,柠檬酸钠减缓了火花放电,而添加草酸钠后为无火花放电.

  2. Oxidation catalyst

    Science.gov (United States)

    Ceyer, Sylvia T.; Lahr, David L.

    2010-11-09

    The present invention generally relates to catalyst systems and methods for oxidation of carbon monoxide. The invention involves catalyst compositions which may be advantageously altered by, for example, modification of the catalyst surface to enhance catalyst performance. Catalyst systems of the present invention may be capable of performing the oxidation of carbon monoxide at relatively lower temperatures (e.g., 200 K and below) and at relatively higher reaction rates than known catalysts. Additionally, catalyst systems disclosed herein may be substantially lower in cost than current commercial catalysts. Such catalyst systems may be useful in, for example, catalytic converters, fuel cells, sensors, and the like.

  3. 铈盐对铝合金硼酸-硫酸阳极氧化膜的封闭效应%Sealing effect of cerium salt on boric-sulfuric acid anodic film of aluminum alloy

    Institute of Scientific and Technical Information of China (English)

    王帅星; 赵晴; 杜楠; 邵志松; 舒伟发; 陈庆龙

    2012-01-01

    The boric-sulfuric acid anodic (BSAA) film on aluminum alloy was sealed by cerium salt conversion solution. The effects of sealing parameters on the corrosion resistance of BSAA film were researched through electrochemical impedance spectroscopy (EIS), while the corrosion resistance of anodic films sealed by different methods was studied. It is found that the resistance of porous layer increases significantly, the corrosion resistance is improved greatly and the corrosion current density is reduced by about 1 order of magnitude when the BSAA film was immersed in the cerium conversion solution (5 g/L Ce(NO3)3+0.5% H2O2) at 30 ℃ for 30 min. Besides, the corrosion resistance of BSAA film sealed by this method is much better than that by boiling water sealing, and also slightly superior to that of the dilute CrO3 solution sealing. Combined with EDS analysis results, it is indicated that a intact, compact cerium conversion film forms on the outside surface of BSAA film, and the porous layer is also filled with sealing products when the BSAA film is sealed by cerium salt conversion solution. The synergism of the two actions almost completely sealed the pores of BSAA film, thereby effectively improving the corrosion resistance of anodic film.%将铝合金硼酸-硫酸阳极氧化膜浸入铈盐转化液中进行封闭.采用交流阻抗谱技术研究各封闭参数对氧化膜耐蚀性的影响,比较了不同方法封闭的氧化膜的耐蚀性差异.结果表明:将硼酸-硫酸阳极氧化试样浸入30℃的铈盐转化液(5 g/L Ce(NO3)3+0.5% H2O2)中处理30min后,多孔层电阻Rp大幅增加,且腐蚀电流密度降低1个数量级,耐蚀性明显优于沸水封闭氧化膜的,也稍优于稀铬酸封闭氧化膜的耐蚀性.结合EDS分析表明:铈盐转化封闭后硼酸-硫酸阳极氧化膜的外表面形成了一层完整致密的铈盐转化膜,多孔层内也充满了铈的封闭产物,二者的协同作用几乎完全封住了硼酸-硫酸阳极氧

  4. 化学镀制备锡-锌-镍合金锂离子电池阳极材料%Electroless Deposition of Sn-Zn-Ni Alloy Film for Anodic Materials of Lithium Ion Batteries

    Institute of Scientific and Technical Information of China (English)

    李峰; 张世超

    2012-01-01

    Sn-Zn-Ni ternary alloy film was prepared on copper foil and foam copper respectively by a modified electroless plating process* which used both of sodium borohydride and sodium hypophosphite as reducing agents and was combined with alkaline tin disproportionating reaction. X-ray diffraction (XRD) . Scanning electron microscopy (SEM) , and energy dispersive X-ray spectrometry (EDS) were used to characterize the phases, morphology and composition of the films respectively on both copper foil and copper foam. The EDS results show that the elements,such as Sn, Zn and Ni can be found in the coating. By optimizing, the mass fraction of zinc in the coating can reach 25 %. A three-dimensional porous foam copper used as substrate to deposit Sn-Zn-Ni ternary alloy film, and then the film is coated with glucose-derived carbon-rich polysaccharide by a hydrothermal approach. When it is used as anode materials in lithium ion batteries, the reversible lithium storage capacity of more than 400 mA ? H " g"1 can be after 10 cycles.%应用经过改进的化学镀工艺,即:采用硼氢化钠、次磷酸钠同时作为还原剂,结合锡的碱性歧化反应,分别在铜箔及泡沫铜上制备Sn-Zn-Ni三元合金镀层.用X射线衍射仪(XRD)、扫描电子显微镜(SEM)、X射线能量衍射谱(EDS)分析镀层的结构与组成.结果表明:镀层中含有锡、锌、镍三种元素;优化沉积条件,镀层中锌的质量分数可达25%.采用三维多孔泡沫铜为基体,制备化学镀层并对其进行水热葡萄糖碳包覆处理.作为锂离子电池阳极材料,充放电循环10周,放电容量仍可保持在400mA·h·g-1以上.

  5. Distribution of soluble and precipitated iron and chromium products generated by anodic dissolution of 316L stainless steel and alloy C-22: final report

    Energy Technology Data Exchange (ETDEWEB)

    Estill, J; Farmer, J; Gordon, S; King, K; Logotetta, L; Silberman, D

    1999-08-11

    At near neutral pH and at applied potentials above the threshold potential for localized breakdown of the passive film, virtually all of the dissolved chromium appeared to be in the hexavalent oxidation state (Cr(VI)). In acidic environments, such as crevice solutions formed during the crevice corrosion of 316L and C-22 samples in 4 M NaCl, virtually all of the dissolved chromium appeared to be in the trivalent oxidation state (Cr(III)). These general observations appear to be consistent with the Pourbaix diagram for chromium (Pourbaix 1974), pp. 307-321. At high pH and high anodic polarization (pH {approximately} 8 and 800 mV vs. SHE), the predominate species is believed to be the soluble chromate anion (CrO{sub 4}{sup 2{minus}}). At the same pH, but lower polarization (pH {approximately} 8 and 0 mV vs. SHE), the predominate species are believed to be precipitates such as trivalent Cr(OH){sub 3} {center_dot} n(H{sub 2}O) and hexavalent Cr{sub 2}O{sub 3}. In acidified environments such as those found in crevices (pH < 3), soluble Cr{sup 3+} is expected to form over a wide range of potential extending from 400 mV vs. SHE to approximately 1200 mV vs. SHE. Again, this is consistent with the observations from the creviced samples. In earlier studies by the principal investigator, it has been found that low-level chromium contamination in ground water is usually in the hexavalent oxidation state (Farmer et al. 1996). In general, dissolved iron measured during the crevice experiments appears to be Fe(II) in acidic media and Fe(III) in near-neutral and alkaline solutions (table 3). In the case of cyclic polarization measurements, the dissolved iron measured at the end of some cyclic polarization measurements with C-22 appeared to be in the Fe(III) state. This is probably due to the high electrochemical potential at which these species were generated during the potential scan. Note that the reversal potential was approximately 1200 mV vs. Ag/AgCl during these scans. These

  6. Engineering Platinum Alloy Electrocatalysts in Nanoscale for PEMFC Application

    Energy Technology Data Exchange (ETDEWEB)

    He, Ting [Idaho National Laboratory

    2016-03-01

    Fuel cells are expected to be a key next-generation energy source used for vehicles and homes, offering high energy conversion efficiency and minimal pollutant emissions. However, due to large overpotentials on anode and cathode, the efficiency is still much lower than theoretically predicted. During the past decades, considerable efforts have been made to investigate synergy effect of platinum alloyed with base metals. But, engineering the alloy particles in nanoscale has been a challenge. Most important challenges in developing nanostructured materials are the abilities to control size, monodispersity, microcomposition, and even morphology or self-assembly capability, so called Nanomaterials-by-Design, which requires interdisciplinary collaborations among computational modeling, chemical synthesis, nanoscale characterization as well as manufacturing processing. Electrocatalysts, particularly fuel cell catalysts, are dramatically different from heterogeneous catalysts because the surface area in micropores cannot be electrochemically controlled on the same time scale as more transport accessible surfaces. Therefore, electrocatalytic architectures need minimal microporous surface area while maximizing surfaces accessible through mesopores or macropores, and to "pin" the most active, highest performance physicochemical state of the materials even when exposed to thermodynamic forces, which would otherwise drive restructuring, crystallization, or densification of the nanoscale materials. In this presentation, results of engineering nanoscale platinum alloy particles down to 2 ~ 4 nm will be discussed. Based on nature of alloyed base metals, various synthesis technologies have been studied and developed to achieve capabilities of controlling particle size and particle microcomposition, namely, core-shell synthesis, microemulsion technique, thermal decomposition process, surface organometallic chemical method, etc. The results show that by careful engineering the

  7. 通过Au修饰提高质子交换膜燃料电池PtCo合金催化剂稳定性%Improved Stability of PtCo Alloy Catalysts for Proton Exchange Membrane Fuel Cells by Gold Decoration

    Institute of Scientific and Technical Information of China (English)

    陈磊; 齐意; 木士春

    2015-01-01

    目的:解决质子交换膜燃料电池贵金属催化剂利用率低、电化学稳定性差的问题,从而堆动其产业化进程。方法通过湿化学共沉积法获得低Pt特征的PtCo合金催化剂,采用欠电位沉积方法制备Au修饰的PtCo合金催化剂,应用原子吸收光谱和电化学循环伏安加速测试技术研究Au修饰PtCo合金催化剂的电化学稳定性。结果成功制备了Au修饰的PtCo合金催化剂。 Au修饰后,PtCo合金催化剂的氧还原反应性能几乎没有改变,但Co的溶蚀率得到降低,而且电化学稳定性也得到提高。结论通过采用Au等具有高电化学腐蚀电位的金属修饰Pt合金催化剂,以提高催化剂电化学稳定性的研究思路是可行的。%ABSTRACT:Objective To facilitate the commercialization of proton exchange membrane fuel cells by revolving the key issues in-cluding low utilization and deteriorated stability of noble metal catalysts. Methods After preparation of PtCo alloy catalysts with low Pt loading by a chemical co-deposition method, the gold decorated PtCo alloy catalyst was prepared in terms of an under-potential-deposition method, and then the electrochemical stability of the gold-decorated PtCo alloy catalyst was characterized by atomic ab-sorption spectroscopy and electrochemical accelerated test technique. Results Au-decorated PtCo alloy catalyst was successfully prepared. After decoration of gold, the oxygen reduction reaction activity of PtCo alloy catalysts remained unchanged, and the ero-sion rate of Co element for PtCo alloy catalysts in electrolyte solutions decreased with an improved electrochemical stability. Con-clusion It was feasible to improve the stability of PtCo alloy catalysts by decoration with metals possessing a high corrosion potential such as Au.

  8. Modeling of the anode side of a direct methanol fuel cell with analytical solutions

    CERN Document Server

    Mosquera, Martín A

    2010-01-01

    In this work, analytical solutions were derived (for any methanol oxidation reaction order) for the profiles of methanol concentration and proton current density by assuming diffusion mass transport mechanism, Tafel kinetics, and fast proton transport in the anodic catalyst layer of a direct methanol fuel cell. An expression for the Thiele modulus that allows to express the anodic overpotential as a function of the cell current, and kinetic and mass transfer parameters was obtained. For high cell current densities, it was found that the Thiele modulus ($\\phi^2$) varies quadratically with cell current density; yielding a simple correlation between anodic overpotential and cell current density. Analytical solutions were derived for the profiles of both local methanol concentration in the catalyst layer and local anodic current density in the catalyst layer. Under the assumptions of the model presented here, in general, the local methanol concentration in the catalyst layer cannot be expressed as an explicit fun...

  9. The mechanism of stress-corrosion cracking in 7075 aluminum alloy

    Science.gov (United States)

    Jacobs, A. J.

    1970-01-01

    Various aspects of stress-corrosion cracking in 7075 aluminum alloy are discussed. A model is proposed in which the continuous anodic path along which the metal is preferentially attacked consists of two phases which alternate as anodes.

  10. Effect of Solid Solution Treatment on Hard Anodic Quality Oxidation Film on Aluminum Alloy 6061%固溶工艺对6061铝合金硬质阳极氧化膜层质量的影响

    Institute of Scientific and Technical Information of China (English)

    江涛; 沈健; 闫晓东; 李俊鹏; 杨银

    2011-01-01

    The influence of solid solution treatment on the thickness, hardness, uniformity and densification of hard anodic oxidation film for aluminum alloy 6061 was investigated by hardneS8 tests, optical microscopy and electron microscopy.The results ahowed that the hardness of oxide films increased from the 8urface to the substrate, because electrolyte corrosion between the intemal and external surfacea was different.The change of heal treatment had no obvious effect on the unifonnity of thickness, which was detected by the composition structure of the films.The films which had a good compatibility with aubstrate, no pinhole and loose defect, and no any pitting on surface was grained on condition that the sample was treated at 530℃ for 3h, then quenched with water.Although the strengthening phase M92Si and the second particle could dissolve totally after improving solution temperature, the grain size was uneven extremely because of the coarae grain.Then it caused that the growth rate of oxide film was inconsi8tent in the anodic oxidation process.The microcracks deformed from intemal stress which existed in the place between the fast-growing oxide film and the stow-growing oxide film, made the quality and hardness of the oxidation film decrease.%采用显微硬度测试、金相和扫描电子显微分析,研究了固溶工艺对6061硬质阳极氧化膜层厚度、硬度、均匀性、致密度的影响.结果表明:阳极氧化膜因内外表面受到电解液的腐蚀程度不同而表现为氧化膜的硬度自膜层表面到基体逐渐升高.固溶工艺的改变对阳极氧化膜的厚度均匀性无显著影响,氧化膜自身的成分结构决定了其膜层厚度的均匀性.试样在530℃x3 h下采用水冷的方式所获得的硬质氧化膜与基体结合平整,不存在针孔、疏松等缺陷,表面无孔残蚀现象.提高固溶温度,虽然能使强化相Mg2Si、第二相质点等全部回溶到基体里,但因形成粗晶组织,使晶粒度极为不

  11. Inert Anode Life in Low Temperature Reduction Process

    Energy Technology Data Exchange (ETDEWEB)

    Bradford, Donald R.

    2005-06-30

    The production of aluminum metal by low temperature electrolysis utilizing metal non-consumable anodes and ceramic cathodes was extensively investigated. Tests were performed with traditional sodium fluoride--aluminum fluoride composition electrolytes, potassium fluoride-- aluminum fluoride electrolytes, and potassium fluoride--sodium fluoride--aluminum fluoride electrolytes. All of the Essential First-Tier Requirements of the joint DOE-Aluminum Industry Inert Anode Road Map were achieved and those items yet to be resolved for commercialization of this technology were identified. Methods for the fabrication and welding of metal alloy anodes were developed and tested. The potential savings of energy and energy costs were determined and potential environmental benefits verified.

  12. Disordered anodes for Ni-metal rechargeable battery

    Energy Technology Data Exchange (ETDEWEB)

    Young, Kwo-hsiung; Wang, Lixin; Mays, William C.

    2016-11-22

    An electrochemical cell is provided that includes a structurally and compositionally disordered electrochemically active alloy material as an anode active material with unexpected capacity against a nickel hydroxide based cathode active material. The disordered metal hydroxide alloy includes three or more transition metal elements and is formed in such a way so as to produce the necessary disorder in the overall system. When an anode active material includes nickel as a predominant, the resulting cells represent the first demonstration of a functional Ni/Ni cell.

  13. Releasing metal catalysts via phase transition: (NiO)0.05-(SrTi0.8Nb0.2O3)0.95 as a redox stable anode material for solid oxide fuel cells.

    Science.gov (United States)

    Xiao, Guoliang; Wang, Siwei; Lin, Ye; Zhang, Yanxiang; An, Ke; Chen, Fanglin

    2014-11-26

    Donor-doped perovskite-type SrTiO3 experiences stoichiometric changes at high temperatures in different Po2 involving the formation of Sr or Ti-rich impurities. NiO is incorporated into the stoichiometric strontium titanate, SrTi0.8Nb0.2O3-δ (STN), to form an A-site deficient perovskite material, (NiO)0.05-(SrTi0.8Nb0.2O3)0.95 (Ni-STN), for balancing the phase transition. Metallic Ni nanoparticles can be released upon reduction instead of forming undesired secondary phases. This material design introduces a simple catalytic modification method with good compositional control of the ceramic backbones, by which transport property and durability of solid oxide fuel cell anodes are largely determined. Using Ni-STN as anodes for solid oxide fuel cells, enhanced catalytic activity and remarkable stability in redox cycling have been achieved. Electrolyte-supported cells with the cell configuration of Ni-STN-SDC anode, La0.8Sr0.2Ga0.87Mg0.13O3 (LSGM) electrolyte, and La0.6Sr0.4Co0.2Fe0.8O3 (LSCF) cathode produce peak power densities of 612, 794, and 922 mW cm(-2) at 800, 850, and 900 °C, respectively, using H2 as the fuel and air as the oxidant. Minor degradation in fuel cell performance resulted from redox cycling can be recovered upon operating the fuel cells in H2. Such property makes Ni-STN a promising regenerative anode candidate for solid oxide fuel cells.

  14. Effect of heat treatment on the activity and stability of carbon supported PtMo alloy electrocatalysts for hydrogen oxidation in proton exchange membrane fuel cells

    Science.gov (United States)

    Hassan, Ayaz; Carreras, Alejo; Trincavelli, Jorge; Ticianelli, Edson Antonio

    2014-02-01

    The effect of heat treatment on the activity, stability and CO tolerance of PtMo/C catalysts was studied, due to their applicability in the anode of proton exchange membrane fuel cells (PEMFCs). To this purpose, a carbon supported PtMo (60:40) alloy electrocatalyst was synthesized by the formic acid reduction method, and samples of this catalyst were heat-treated at various temperatures ranging between 400 and 700 °C. The samples were characterized by temperature programmed reduction (TPR), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), Transmission electron microscopy (TEM), X-ray absorption spectroscopy (XAS), cyclic voltammetry (CV), scanning electron microscopy (SEM) and wavelength dispersive X-ray spectroscopy (WDS). Cyclic voltammetry was used to study the stability, and polarization curves were used to investigate the performance of all materials as CO tolerant anode on a PEM single cell text fixture. The catalyst treated at 600 °C, for which the average crystallite size was 16.7 nm, showed the highest hydrogen oxidation activity in the presence of CO, giving an overpotential induced by CO contamination of 100 mV at 1 Acm-2. This catalyst also showed a better stability up to 5000 potential cycles of cyclic voltammetry, as compared to the untreated catalyst. CV, SEM and WDS results indicated that a partial dissolution of Mo and its migration/diffusion from the anode to the cathode occurs during the single cell cycling. Polarization results showed that the catalytic activity and the stability can be improved by a heat treatment, in spite of a growth of the catalyst particles.

  15. New High-Energy Nanofiber Anode Materials

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Xiangwu; Fedkiw, Peter; Khan, Saad; Huang, Alex; Fan, Jiang

    2013-11-15

    The overall goal of the proposed work was to use electrospinning technology to integrate dissimilar materials (lithium alloy and carbon) into novel composite nanofiber anodes, which simultaneously had high energy density, reduced cost, and improved abuse tolerance. The nanofiber structure allowed the anodes to withstand repeated cycles of expansion and contraction. These composite nanofibers were electrospun into nonwoven fabrics with thickness of 50 μm or more, and then directly used as anodes in a lithium-ion battery. This eliminated the presence of non-active materials (e.g., conducting carbon black and polymer binder) and resulted in high energy and power densities. The nonwoven anode structure also provided a large electrode-electrolyte interface and, hence, high rate capacity and good lowtemperature performance capability. Following are detailed objectives for three proposed project periods. • During the first six months: Obtain anodes capable of initial specific capacities of 650 mAh/g and achieve ~50 full charge/discharge cycles in small laboratory scale cells (50 to 100 mAh) at the 1C rate with less than 20 percent capacity fade; • In the middle of project period: Assemble, cycle, and evaluate 18650 cells using proposed anode materials, and demonstrate practical and useful cycle life (750 cycles of ~70% state of charge swing with less than 20% capacity fade) in 18650 cells with at least twice improvement in the specific capacity than that of conventional graphite electrodes; • At the end of project period: Deliver 18650 cells containing proposed anode materials, and achieve specific capacities greater than 1200 mAh/g and cycle life longer than 5000 cycles of ~70% state of charge swing with less than 20% capacity fade.

  16. Nanoshell Encapsulated Li-ion Battery Anodes for Long Cycle Life Project

    Data.gov (United States)

    National Aeronautics and Space Administration — A new high capacity rechargeable Li battery anode based on Li metal alloys protected by carbon nanoshells will be developed. A reversible Li-ion capacity exceeding...

  17. Nano-Engineered Catalysts for Direct Methanol Fuel Cells

    Science.gov (United States)

    Myung, Nosang; Narayanan, Sekharipuram; Wiberg, Dean

    2008-01-01

    Nano-engineered catalysts, and a method of fabricating them, have been developed in a continuing effort to improve the performances of direct methanol fuel cells as candidate power sources to supplant primary and secondary batteries in a variety of portable electronic products. In order to realize the potential for high energy densities (as much as 1.5 W h/g) of direct methanol fuel cells, it will be necessary to optimize the chemical compositions and geometric configurations of catalyst layers and electrode structures. High performance can be achieved when catalyst particles and electrode structures have the necessary small feature sizes (typically of the order of nanometers), large surface areas, optimal metal compositions, high porosity, and hydrophobicity. The present method involves electrodeposition of one or more catalytic metal(s) or a catalytic-metal/polytetrafluoroethylene nanocomposite on an alumina nanotemplate. The alumina nanotemplate is then dissolved, leaving the desired metal or metal/polytetrafluoroethylene-composite catalyst layer. Unlike some prior methods of making fine metal catalysts, this method does not involve processing at elevated temperature; all processing can be done at room temperature. In addition, this method involves fewer steps and is more amenable to scaling up for mass production. Alumina nanotemplates are porous alumina membranes that have been fabricated, variously, by anodizing either pure aluminum or aluminum that has been deposited on silicon by electronbeam evaporation. The diameters of the pores (7 to 300 nm), areal densities of pores (as much as 7 x 10(exp 10)sq cm), and lengths of pores (up to about 100 nm) can be tailored by selection of fabrication conditions. In a given case, the catalytic metal, catalytic metal alloy, or catalytic metal/ polytetrafluoroethylene composite is electrodeposited in the pores of the alumina nanotemplate. The dimensions of the pores, together with the electrodeposition conditions

  18. Effects of anodizing parameters and heat treatment on nanotopographical features, bioactivity, and cell culture response of additively manufactured porous titanium.

    Science.gov (United States)

    Amin Yavari, S; Chai, Y C; Böttger, A J; Wauthle, R; Schrooten, J; Weinans, H; Zadpoor, A A

    2015-06-01

    Anodizing could be used for bio-functionalization of the surfaces of titanium alloys. In this study, we use anodizing for creating nanotubes on the surface of porous titanium alloy bone substitutes manufactured using selective laser melting. Different sets of anodizing parameters (voltage: 10 or 20V anodizing time: 30min to 3h) are used for anodizing porous titanium structures that were later heat treated at 500°C. The nanotopographical features are examined using electron microscopy while the bioactivity of anodized surfaces is measured using immersion tests in the simulated body fluid (SBF). Moreover, the effects of anodizing and heat treatment on the performance of one representative anodized porous titanium structures are evaluated using in vitro cell culture assays using human periosteum-derived cells (hPDCs). It has been shown that while anodizing with different anodizing parameters results in very different nanotopographical features, i.e. nanotubes in the range of 20 to 55nm, anodized surfaces have limited apatite-forming ability regardless of the applied anodizing parameters. The results of in vitro cell culture show that both anodizing, and thus generation of regular nanotopographical feature, and heat treatment improve the cell culture response of porous titanium. In particular, cell proliferation measured using metabolic activity and DNA content was improved for anodized and heat treated as well as for anodized but not heat-treated specimens. Heat treatment additionally improved the cell attachment of porous titanium surfaces and upregulated expression of osteogenic markers. Anodized but not heat-treated specimens showed some limited signs of upregulated expression of osteogenic markers. In conclusion, while varying the anodizing parameters creates different nanotube structure, it does not improve apatite-forming ability of porous titanium. However, both anodizing and heat treatment at 500°C improve the cell culture response of porous titanium.

  19. Anodized aluminum on LDEF

    Science.gov (United States)

    Golden, Johnny L.

    1993-01-01

    A compilation of reported analyses and results obtained for anodized aluminum flown on the Long Duration Exposure Facility (LDEF) was prepared. Chromic acid, sulfuric acid, and dyed sulfuric acid anodized surfaces were exposed to the space environment. The vast majority of the anodized surface on LDEF was chromic acid anodize because of its selection as a thermal control coating for use on the spacecraft primary structure, trays, tray clamps, and space end thermal covers. Reports indicate that the chromic acid anodize was stable in solar absorptance and thermal emittance, but that contamination effects caused increases in absorptance on surfaces exposed to low atomic oxygen fluences. There were some discrepancies, however, in that some chromic acid anodized specimens exhibited significant increases in absorptance. Sulfuric acid anodized surfaces also appeared stable, although very little surface area was available for evaluation. One type of dyed sulfuric acid anodize was assessed as an optical baffle coating and was observed to have improved infrared absorptance characteristics with exposure on LDEF.

  20. Anodizing Aluminum with Frills.

    Science.gov (United States)

    Doeltz, Anne E.; And Others

    1983-01-01

    "Anodizing Aluminum" (previously reported in this journal) describes a vivid/relevant laboratory experience for general chemistry students explaining the anodizing of aluminum in sulfuric acid and constrasting it to electroplating. Additions to this procedure and the experiment in which they are used are discussed. Reactions involved are…

  1. Determination of reaction rate constants for phenol oxidation using SnO2/Ti anodes coupled with activated carbon adsorption in the presence of TiO2 as catalyst.

    Science.gov (United States)

    Zhao, Yuemin; Ding, Yi; Wang, Lizhang; Wang, Xiao

    2011-01-01

    Series of experiments for phenol degradation with assistance of TiO2 catalyst at pH of 6.5 and temperature of 25 degrees C were conducted using a lab-scale electrochemical reactor constructed in our laboratory. According to the results, at the presence of the TiO2 catalyst the removal of phenol was increased and first-order kinetics could describe the evolution of phenol concentration. For inspecting the relationship between rate constants and dosage of TiO2, two possible kinetics were proposed in this study. Contrasted to the abundant experimental data, a reasonable kinetics was obtained for the estimation of phenol concentration effluent during continuous flow of raw wastewater, especially when the TiO2 dosage was less than 0.5g L(-1). The model obtained from these experiments could employed for the calculation of rate constants at different TiO2 dosage and the necessary dosage of catalyst when a discharge standard was designed.

  2. Pt-Ni and Pt-Co Catalyst Synthesis Route for Fuel Cell Applications

    Science.gov (United States)

    Firdosy, Samad A.; Ravi, Vilupanur A.; Valdez, Thomas I.; Kisor, Adam; Narayan, Sri R.

    2013-01-01

    Oxygen reduction reactions (ORRs) at the cathode are the rate-limiting step in fuel cell performance. The ORR is 100 times slower than the corresponding hydrogen oxidation at the anode. Speeding up the reaction at the cathode will improve fuel cell efficiency. The cathode material is generally Pt powder painted onto a substrate (e.g., graphite paper). Recent efforts in the fuel cell area have focused on replacing Pt with Pt-X alloys (where X = Co, Ni, Zr, etc.) in order to (a) reduce cost, and (b) increase ORR rates. One of these strategies is to increase ORR rates by reducing the powder size, which would result in an increase in the surface area, thereby facilitating faster reaction rates. In this work, a process has been developed that creates Pt-Ni or Pt-Co alloys that are finely divided (on the nano scale) and provide equivalent performance at lower Pt loadings. Lower Pt loadings will translate to lower cost. Precursor salts of the metals are dissolved in water and mixed. Next, the salt mixtures are dried on a hot plate. Finally, the dried salt mixture is heattreated in a furnace under flowing reducing gas. The catalyst powder is then used to fabricate a membrane electrode assembly (MEA) for electrochemical performance testing. The Pt- Co catalyst-based MEA showed comparable performance to an MEA fabri cated using a standard Pt black fuel cell catalyst. The main objective of this program has been to increase the overall efficiencies of fuel cell systems to support power for manned lunar bases. This work may also have an impact on terrestrial programs, possibly to support the effort to develop a carbon-free energy source. This catalyst can be used to fabricate high-efficiency fuel cell units that can be used in space as regenerative fuel cell systems, and terrestrially as primary fuel cells. Terrestrially, this technology will become increasingly important when transition to a hydrogen economy occurs.

  3. New Construction and Catalyst Support Materials for Water Electrolysis at Elevated Temperatures

    DEFF Research Database (Denmark)

    Nikiforov, Aleksey

    4 reports results of testing dierent types of commercially available stainless steels, Ni-based alloys as well as titanium and tantalum as possible metallic bipolar plates and construction materials for HTPEMEC. The corrosion resistance was measured under simulated conditions of high temperature PEM...... steam electrolyzer. Steady-state voltammetry was used in combination with scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX) to evaluate the stability of the mentioned materials. It was found that stainless steels were the least resistant to corrosion under strong anodic...... stainless steel showed outstanding resistance to corrosion in selected media, while passivation of titanium was weak, and the highest rate of corrosion among all tested materials was observed for titanium at 120 °C. Today, there is a high interest in the eld towards investigation of new catalyst materials...

  4. Supported bimetallic nano-alloys as highly active catalysts for the one-pot tandem synthesis of imines and secondary amines from nitrobenzene and alcohols

    NARCIS (Netherlands)

    Meenakshisundaram, Sankar; He, Qian; Dawson, Simon; Nowicka, Ewa; Lu, Li; Bruijnincx, Pieter C. A.; Beale, Andrew M.; Kiely, Christopher J.; Weckhuysen, Bert M.

    2016-01-01

    The synthesis and functionalization of imines and amines are key steps in the preparation of many fine chemicals and for pharmaceuticals in particular. Traditionally, metal complexes are used as homogeneous catalysts for these organic transformations. Here we report gold-palladium and ruthenium-pall

  5. A multiscale physical model for the transient analysis of PEM water electrolyzer anodes.

    Science.gov (United States)

    Oliveira, Luiz Fernando L; Laref, Slimane; Mayousse, Eric; Jallut, Christian; Franco, Alejandro A

    2012-08-07

    Polymer electrolyte membrane water electrolyzers (PEMWEs) are electrochemical devices that can be used for the production of hydrogen. In a PEMWE the anode is the most complex electrode to study due to the high overpotential of the oxygen evolution reaction (OER), not widely understood. A physical bottom-up multi-scale transient model describing the operation of a PEMWE anode is proposed here. This model includes a detailed description of the elementary OER kinetics in the anode, a description of the non-equilibrium behavior of the nanoscale catalyst-electrolyte interface, and a microstructural-resolved description of the transport of charges and O(2) at the micro and mesoscales along the whole anode. The impact of different catalyst materials on the performance of the PEMWE anode, and a study of sensitivity to the operation conditions are evaluated from numerical simulations and the results are discussed in comparison with experimental data.

  6. In situ anodization of aluminum surfaces studied by x-ray reflectivity and electrochemical impedance spectroscopy

    Science.gov (United States)

    Bertram, F.; Zhang, F.; Evertsson, J.; Carlà, F.; Pan, J.; Messing, M. E.; Mikkelsen, A.; Nilsson, J.-O.; Lundgren, E.

    2014-07-01

    We present results from the anodization of an aluminum single crystal [Al(111)] and an aluminum alloy [Al 6060] studied by in situ x-ray reflectivity, in situ electrochemical impedance spectroscopy and ex situ scanning electron microscopy. For both samples, a linear increase of oxide film thickness with increasing anodization voltage was found. However, the slope is much higher in the single crystal case, and the break-up of the oxide film grown on the alloy occurs at a lower anodization potential than on the single crystal. The reasons for these observations are discussed as are the measured differences observed for x-ray reflectivity and electrochemical impedance spectroscopy.

  7. In situ anodization of aluminum surfaces studied by x-ray reflectivity and electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Bertram, F., E-mail: florian.bertram@sljus.lu.se; Evertsson, J.; Messing, M. E.; Mikkelsen, A.; Lundgren, E. [Division of Synchrotron Radiation Research, Lund University, Box 118, 221 00 Lund (Sweden); Zhang, F.; Pan, J. [KTH Royal Institute of Technology, School of Chemical Science and Engineering, Department of Chemistry, Division of Surface and Corrosion Science, Drottning Kristinas väg 51, 10044 Stockholm (Sweden); Carlà, F. [ESRF, B. P. 220, 38043 Grenoble (France); Nilsson, J.-O. [Sapa Technology, Kanalgatan 1, 612 31 Finspång (Sweden)

    2014-07-21

    We present results from the anodization of an aluminum single crystal [Al(111)] and an aluminum alloy [Al 6060] studied by in situ x-ray reflectivity, in situ electrochemical impedance spectroscopy and ex situ scanning electron microscopy. For both samples, a linear increase of oxide film thickness with increasing anodization voltage was found. However, the slope is much higher in the single crystal case, and the break-up of the oxide film grown on the alloy occurs at a lower anodization potential than on the single crystal. The reasons for these observations are discussed as are the measured differences observed for x-ray reflectivity and electrochemical impedance spectroscopy.

  8. Anodic aluminium oxide membranes used for the growth of carbon nanotubes.

    Science.gov (United States)

    López, Vicente; Morant, Carmen; Márquez, Francisco; Zamora, Félix; Elizalde, Eduardo

    2009-11-01

    The suitability of anodic aluminum oxide (AAO) membranes as template supported on Si substrates for obtaining organized iron catalyst for carbon nanotube (CNT) growth has been investigated. The iron catalyst was confined in the holes of the AAO membrane. CVD synthesis with ethylene as carbon source led to a variety of carbon structures (nanotubes, helices, bamboo-like, etc). In absence of AAO membrane the catalyst was homogeneously distributed on the Si surface producing a high density of micron-length CNTs.

  9. CO methanation over supported bimetallic Ni-Fe catalysts: From computational studies towards catalyst optimization

    DEFF Research Database (Denmark)

    Kustov, Arkadii; Frey, Anne Mette; Larsen, Kasper Emil

    2007-01-01

    DFT calculations combined with a computational screening method have previously shown that bimetallic Ni-Fe alloys should be more active than the traditional Ni-based catalyst for CO methanation. That was confirmed experimentally for a number of bimetallic Ni-Fe catalysts supported on MgAl2O4. He...

  10. Electroplating Zn-Al Alloy Technology

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The method of controlling separating anode and separating power source was used to perform orthogonal optimization for the parameters in electroplating Zn-Al alloy.The electroplating Zn-Al alloy technology was decided, in which the content of Al is about 12%-15%.

  11. 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...

  12. Direct borohydride fuel cell using Ni-based composite anodes

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Jia; Sahai, Yogeshwar; Buchheit, Rudolph G. [Department of Materials Science and Engineering, The Ohio State University, 2041 College Rd., Columbus, OH 43210 (United States)

    2010-08-01

    In this study, nickel-based composite anode catalysts consisting of Ni with either Pd on carbon or Pt on carbon (the ratio of Ni:Pd or Ni:Pt being 25:1) were prepared for use in direct borohydride fuel cells (DBFCs). Cathode catalysts used were 1 mg cm{sup -2} Pt/C or Pd electrodeposited on activated carbon cloth. The oxidants were oxygen, oxygen in air, or acidified hydrogen peroxide. Alkaline solution of sodium borohydride was used as fuel in the cell. High power performance has been achieved by DBFC using non-precious metal, Ni-based composite anodes with relatively low anodic loading (e.g., 270 mW cm{sup -2} for NaBH{sub 4}/O{sub 2} fuel cell at 60 C, 665 mW cm{sup -2} for NaBH{sub 4}/H{sub 2}O{sub 2} fuel cell at 60 C). Effects of temperature, oxidant, and anode catalyst loading on the DBFC performance were investigated. The cell was operated for about 100 h and its performance stability was recorded. (author)

  13. Catalyst and electrode research for phosphoric acid fuel cells

    Science.gov (United States)

    Antoine, A. C.; King, R. B.

    1987-01-01

    An account is given of the development status of phosphoric acid fuel cells' high performance catalyst and electrode materials. Binary alloys have been identified which outperform the baseline platinum catalyst; it has also become apparent that pressurized operation is required to reach the desired efficiencies, calling in turn for the use of graphitized carbon blacks in the role of catalyst supports. Efforts to improve cell performance and reduce catalyst costs have led to the investigation of a class of organometallic cathode catalysts represented by the tetraazaannulenes, and a mixed catalyst which is a mixture of carbons catalyzed with an organometallic and a noble metal.

  14. Nanoporosity formation in silver-gold alloys

    Science.gov (United States)

    Dursun, Aziz

    Selective dissolution also known as dealloying is a corrosion process in which one component of a binary alloy system is selectively removed through an electrochemically controlled process which leads to the formation of a porous metal "sponge" with a porosity that is completely interconnected and random in direction. Nanoporous metals are desirable since they have larger surface areas than an equal volume of non-porous material. Because of their enormous surface area per volume, these highly porous metal electrodes are superior materials for high surface area applications such as in biomedical devices, microfilters and catalysts. Understanding the kinetic processes governing the development of porosity during dealloying and having ability to change the electrochemical conditions will allow us to better control over the average ligament size and distribution in porosity. The basic kinetic processes involved in the formation of these structures are related to such issues as environmental effects and electrochemical conditions on diffusion, microscopic coarsening phenomenon at room temperature and elevated temperatures, alloy passivation, and Gibbs-Thomson effects. The average pore size and distribution was found to depend on the electrolyte composition, dealloying rate, applied potential and time. The porosity was found to significantly coarsen at room temperature during the dealloying process and this coarsening was highly dependent on the applied potential. It is showed that the commonly accepted measurement of the critical potential for alloy dissolution calculated based on extrapolation of anodic polarization data results in an overestimation of this quantity. A series of constant applied potential experiments prove to be a more accurate method for critical potential determination.

  15. Homogeneous catalysts

    CERN Document Server

    Chadwick, John C; Freixa, Zoraida; van Leeuwen, Piet W N M

    2011-01-01

    This first book to illuminate this important aspect of chemical synthesis improves the lifetime of catalysts, thus reducing material and saving energy, costs and waste.The international panel of expert authors describes the studies that have been conducted concerning the way homogeneous catalysts decompose, and the differences between homogeneous and heterogeneous catalysts. The result is a ready reference for organic, catalytic, polymer and complex chemists, as well as those working in industry and with/on organometallics.

  16. Effects of anodizing parameters and heat treatment on nanotopographical features, bioactivity, and cell culture response of additively manufactured porous titanium

    Energy Technology Data Exchange (ETDEWEB)

    Amin Yavari, S., E-mail: s.aminyavari@tudelft.nl [Faculty of Mechanical, Maritime, and Materials Engineering, Delft University of Technology (TU Delft), Mekelweg 2, 2628 CD Delft (Netherlands); Chai, Y.C. [Prometheus, Division of Skeletal Tissue Engineering, Bus 813, O& N1, Herestraat 49, KU Leuven, 3000 Leuven (Belgium); Tissue Engineering Laboratory, Skeletal Biology and Engineering Research Center, Bus 813, O& N1, Herestraat 49, KU Leuven, 3000 Leuven (Belgium); Department of Biomedical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur (Malaysia); Böttger, A.J. [Faculty of Mechanical, Maritime, and Materials Engineering, Delft University of Technology (TU Delft), Mekelweg 2, 2628 CD Delft (Netherlands); Wauthle, R. [KU Leuven, Department of Mechanical Engineering, Section Production Engineering, Machine Design and Automation (PMA), Celestijnenlaan 300B, 3001 Leuven (Belgium); 3D Systems — LayerWise NV, Grauwmeer 14, 3001 Leuven (Belgium); Schrooten, J. [Department of Metallurgy and Materials Engineering, KU Leuven, Kasteelpark Arenberg 44 — PB2450, B-3001 Heverlee (Belgium); Weinans, H. [Faculty of Mechanical, Maritime, and Materials Engineering, Delft University of Technology (TU Delft), Mekelweg 2, 2628 CD Delft (Netherlands); Department of Orthopedics and Dept. Rheumatology, UMC Utrecht, Heidelberglaan100, 3584CX Utrecht (Netherlands); Zadpoor, A.A. [Faculty of Mechanical, Maritime, and Materials Engineering, Delft University of Technology (TU Delft), Mekelweg 2, 2628 CD Delft (Netherlands)

    2015-06-01

    Anodizing could be used for bio-functionalization of the surfaces of titanium alloys. In this study, we use anodizing for creating nanotubes on the surface of porous titanium alloy bone substitutes manufactured using selective laser melting. Different sets of anodizing parameters (voltage: 10 or 20 V anodizing time: 30 min to 3 h) are used for anodizing porous titanium structures that were later heat treated at 500 °C. The nanotopographical features are examined using electron microscopy while the bioactivity of anodized surfaces is measured using immersion tests in the simulated body fluid (SBF). Moreover, the effects of anodizing and heat treatment on the performance of one representative anodized porous titanium structures are evaluated using in vitro cell culture assays using human periosteum-derived cells (hPDCs). It has been shown that while anodizing with different anodizing parameters results in very different nanotopographical features, i.e. nanotubes in the range of 20 to 55 nm, anodized surfaces have limited apatite-forming ability regardless of the applied anodizing parameters. The results of in vitro cell culture show that both anodizing, and thus generation of regular nanotopographical feature, and heat treatment improve the cell culture response of porous titanium. In particular, cell proliferation measured using metabolic activity and DNA content was improved for anodized and heat treated as well as for anodized but not heat-treated specimens. Heat treatment additionally improved the cell attachment of porous titanium surfaces and upregulated expression of osteogenic markers. Anodized but not heat-treated specimens showed some limited signs of upregulated expression of osteogenic markers. In conclusion, while varying the anodizing parameters creates different nanotube structure, it does not improve apatite-forming ability of porous titanium. However, both anodizing and heat treatment at 500 °C improve the cell culture response of porous titanium

  17. Evaluation of anode (electro)catalytic materials for the direct borohydride fuel cell: Methods and benchmarks

    Science.gov (United States)

    Olu, Pierre-Yves; Job, Nathalie; Chatenet, Marian

    2016-09-01

    In this paper, different methods are discussed for the evaluation of the potential of a given catalyst, in view of an application as a direct borohydride fuel cell DBFC anode material. Characterizations results in DBFC configuration are notably analyzed at the light of important experimental variables which influence the performances of the DBFC. However, in many practical DBFC-oriented studies, these various experimental variables prevent one to isolate the influence of the anode catalyst on the cell performances. Thus, the electrochemical three-electrode cell is a widely-employed and useful tool to isolate the DBFC anode catalyst and to investigate its electrocatalytic activity towards the borohydride oxidation reaction (BOR) in the absence of other limitations. This article reviews selected results for different types of catalysts in electrochemical cell containing a sodium borohydride alkaline electrolyte. In particular, propositions of common experimental conditions and benchmarks are given for practical evaluation of the electrocatalytic activity towards the BOR in three-electrode cell configuration. The major issue of gaseous hydrogen generation and escape upon DBFC operation is also addressed through a comprehensive review of various results depending on the anode composition. At last, preliminary concerns are raised about the stability of potential anode catalysts upon DBFC operation.

  18. An Analysis of Mechanical Properties of Anodized Aluminum Film at High Stress

    Science.gov (United States)

    Zhao, Xixi; Wei, Guoying; Yu, Yundan; Guo, Yuemei; Zhang, Ao

    2015-10-01

    In this paper, a new environmental-friendly electrolyte containing sulfuric acid and tartaric acid has been used as the substitute of chromic acid for anodization. The work discussed the influence of anodizing voltages on the fatigue life of anodized Al 2024-T3 by performing fatigue tests with 0.1 stress ratio (R) at 320 MPa. Meanwhile the fatigue cycles to failure, yield strength, tensile strength and fracture surface of anodic films at different conditions were investigated. The results showed that the fatigue life of anodized and sealed specimens reduced a lot compared to aluminum alloy, which can be attributed to the crack sites initiated at the oxide layer. The fracture surface analyses also revealed that the number of crack initiation sites enlarged with the increase of anodizing voltage.

  19. Internal reforming over nickel/zirconia anodes in SOFCS operating on methane: influence of anode formulation, pre-treatment and operating conditions

    Energy Technology Data Exchange (ETDEWEB)

    Finnerty, C.M.; Ormerod, R.M. [Birchall Centre of Inorganic Chemistry and Materials Science, Department of Chemistry, Keele Univ. (United Kingdom)

    2000-03-01

    Internal methane reforming over nickel/zirconia cermet anodes has been studied in detail using a thin-walled extruded zirconia tubular SOFC reactor. The influence of anode formulation, anode pre-treatment, operating temperature and methane/steam ratio on the reforming characteristics, resistance to carbon deposition and durability of the anode have been investigated under actual operating conditions. Post-reaction TPO has been used to determine the amount of carbon deposition and its strength of interaction with the anode. A 90-vol.% nickel/zirconia anode shows higher activity than a 50-vol.% Ni anode at higher reforming temperatures, and shows very good durability. Pre-reducing the anodes in H{sub 2} at 1173 K leads to a more active reforming catalyst. Carbon is removed from the anodes in two processes during TPO, suggesting two types of carbon species. As the reforming temperature increases both carbon types are removed at higher temperature, and there is an increase in the relative population of the more strongly bound form of carbon. (orig.)

  20. Tin-phosphate glass anode for sodium ion batteries

    Directory of Open Access Journals (Sweden)

    Tsuyoshi Honma

    2013-11-01

    Full Text Available The electrochemical property of tin-phosphate (designate as GSPO glass anode for the sodium ion battery was studied. During the first charge process, sodium ion diffused into GSPO glass matrix and due to the reduction of Sn2+ to Sn0 state sodiated tin metal nano-size particles are formed in oxide glass matrix. After the second cycle, we confirmed the steady reversible reaction ∼320 mAh/g at 0–1 V cutoff voltage condition by alloying process in NaxSn4. The tin-phosphate glass is a promising candidate of new anode active material that realizes high energy density sodium ion batteries.

  1. Na-Ion Battery Anodes: Materials and Electrochemistry.

    Science.gov (United States)

    Luo, Wei; Shen, Fei; Bommier, Clement; Zhu, Hongli; Ji, Xiulei; Hu, Liangbing

    2016-02-16

    The intermittent nature of renewable energy sources, such as solar and wind, calls for sustainable electrical energy storage (EES) technologies for stationary applications. Li will be simply too rare for Li-ion batteries (LIBs) to be used for large-scale storage purposes. In contrast, Na-ion batteries (NIBs) are highly promising to meet the demand of grid-level storage because Na is truly earth abundant and ubiquitous around the globe. Furthermore, NIBs share a similar rocking-chair operation mechanism with LIBs, which potentially provides high reversibility and long cycling life. It would be most efficient to transfer knowledge learned on LIBs during the last three decades to the development of NIBs. Following this logic, rapid progress has been made in NIB cathode materials, where layered metal oxides and polyanionic compounds exhibit encouraging results. On the anode side, pure graphite as the standard anode for LIBs can only form NaC64 in NIBs if solvent co-intercalation does not occur due to the unfavorable thermodynamics. In fact, it was the utilization of a carbon anode in LIBs that enabled the commercial successes. Anodes of metal-ion batteries determine key characteristics, such as safety and cycling life; thus, it is indispensable to identify suitable anode materials for NIBs. In this Account, we review recent development on anode materials for NIBs. Due to the limited space, we will mainly discuss carbon-based and alloy-based anodes and highlight progress made in our groups in this field. We first present what is known about the failure mechanism of graphite anode in NIBs. We then go on to discuss studies on hard carbon anodes, alloy-type anodes, and organic anodes. Especially, the multiple functions of natural cellulose that is used as a low-cost carbon precursor for mass production and as a soft substrate for tin anodes are highlighted. The strategies of minimizing the surface area of carbon anodes for improving the first-cycle Coulombic efficiency are

  2. Real time measurement of Al anode degradation in thin film batteries

    Science.gov (United States)

    Leite, Marina; Ruzmetov, Dmitry; Li, Zhipeng; Bendersky, Leonid; Talin, A. Alec

    2013-03-01

    Li-ion battery (LIB) anodes that alloy with Li, including Si, Ge, Sn, and Al have specific capacities that significantly exceed that of carbon-based intercalation anodes. However, the large volume expansion and contraction that accompany charging and discharging processes lead to large mechanical stresses that ultimately lead to loss of capacity and failure of the anodes. To better understand the failure mechanism, we cycle a thin film LIB with an Al anode in a scanning electron microscope to measure in real time the nucleation and growth of a highly strained (-44%) Al-Li alloy. We use galvanostatic charging and discharging to control the rate of Li diffusion into the Al anode, and by collecting a series of SEM images in small time intervals we are able to directly correlate the nucleation events of Li-Al with specific peaks in the measured voltage. Based on these observations and ex situ transmission electron microscopy we develop a semi-quantitative description for the mechanism of Al anode degradation that could be extended to other alloy anode materials.

  3. Deactivation and poisoning of fuel cell catalysts

    Science.gov (United States)

    Ross, P. N., Jr.

    1985-06-01

    The deactivation and poisoning phenomena reviewed are: the poisoning of anode (fuel electrode) catalyst by carbon monoxide and hydrogen sulfide; the deactivation of the cathode (air electrode) catalyst by sintering; and the deactivation of the cathode by corrosion of the support. The anode catalyst is Pt supported on a conductive, high area carbon black, usually at a loading of 10 w/o. This catalyst is tolerant to some level of carbon monoxide or hydrogen sulfide or both in combination, the level depending on temperature and pressure. Much less is known about hydrogen sulfide poisoning. Typical tolerance levels are 2% CO, and 10 ppM H2S. The cathode catalyst is typically Pt supported on a raphitic carbon black, usually a furnace black heat-treated to 2700 C. The Pt loading is typically 10 w/o, and the dispersion (or percent exposed) as-prepared is typically 30%. The loss of dispersion in use depends on the operational parameters, most especially the cathode potential history, i.e., higher potentials cause more rapid decrease in dispersion. The mechanism of loss of dispersion is not well known. The graphitic carbon support corrodes at a finite rate that is also potential dependent. Support corrosion causes thickening of the electrolyte film between the gas pores and the catalyst particles, which in turn causes increased diffusional resistance and performance loss.

  4. Manufacture of Catalyst Systems for Ammonia Conversion

    Institute of Scientific and Technical Information of China (English)

    GAKH S.V.; SAVENKOV D.A.

    2012-01-01

    Platinum catalyst gauzes have been in use since the moment of development of the process of catalyst oxidation of ammonia for production of nitric acid or hydrocyanic acid.Catalyst gauzes are usually made of platinum or its alloys with rhodium and palladium.These precious metals have remarkable properties that make them ideal catalysts for acceleration of the ammonia/oxygen reaction.In 2008,OJSC "SIC ‘Supermetal’" and Umicore AG&Co.KG launched a production line for Pt-alloy-based catalyst systems to be used for ammonia oxidation in the production of weak nitric acid.Catalyst systems consist of a pack of catalyst gauzes and a pack of catchment gauzes,which are made using flat-bed knitting machines and wire-cloth looms.Today,up-to-date catalyst systems MKSpreciseTM are being manufactured,the basic advantages of which are an individual structure of gauzes and composition of the material,which allows to define precisely the position of each gauze in the catalyst pack,a high activity of the catalyst pack,direct catching of platinum and rhodium in the catalyst system,and a reasonable combination of single- and multilayer types of gauzes.This makes it possible to vary the configuration of the catalyst and select an optimum composition of the system to ensure the maximum efficiency of the ammonia oxidation process.We also produce the catchment systems that allow to find the best decision from the economic point view for each individual case.

  5. Alternative Anodes for the Electrolytic Reduction of Uranium Dioxide

    Science.gov (United States)

    Merwin, Augustus

    Reprocessing of spent nuclear fuel is an essential step in closing the nuclear fuel cycle. In order to consume current stockpiles, ceramic uranium dioxide spent nuclear fuel will be subjected to an electrolytic reduction process. The current reduction process employs a platinum anode and a stainless steel alloy 316 cathode in a molten salt bath consisting of LiCl-2wt% Li 2O and occurs at 700°C. A major shortcoming of the existing process is the degradation of the platinum anode under the severely oxidizing conditions encountered during electrolytic reduction. This work investigates alternative anode materials for the electrolytic reduction of uranium oxide. The high temperature and extreme oxidizing conditions encountered in these studies necessitated a unique set of design constraints on the system. Thus, a customized experimental apparatus was designed and constructed. The electrochemical experiments were performed in an electrochemical reactor placed inside a furnace. This entire setup was housed inside a glove box, in order to maintain an inert atmosphere. This study investigates alternative anode materials through accelerated corrosion testing. Surface morphology was studied using scanning electron microscopy. Surface chemistry was characterized using energy dispersive spectroscopy and Raman spectroscopy. Electrochemical behavior of candidate materials was evaluated using potentiodynamic polarization characteristics. After narrowing the number of candidate electrode materials, ferrous stainless steel alloy 316, nickel based Inconel 718 and elemental tungsten were chosen for further investigation. Of these materials only tungsten was found to be sufficiently stable at the anodic potential required for electrolysis of uranium dioxide in molten salt. The tungsten anode and stainless steel alloy 316 cathode electrode system was studied at the required reduction potential for UO2 with varying lithium oxide concentrations. Electrochemical impedance spectroscopy

  6. Lithium batteries, anodes, and methods of anode fabrication

    KAUST Repository

    Li, Lain-Jong

    2016-12-29

    Prelithiation of a battery anode carried out using controlled lithium metal vapor deposition. Lithium metal can be avoided in the final battery. This prelithiated electrode is used as potential anode for Li- ion or high energy Li-S battery. The prelithiation of lithium metal onto or into the anode reduces hazardous risk, is cost effective, and improves the overall capacity. The battery containing such an anode exhibits remarkably high specific capacity and a long cycle life with excellent reversibility.

  7. Effect of Sn on Microstructure and Electrochemistry Properties of Rolled Mg-Al-Sn-Zn Magnesium Alloys Anode Materials%Sn 对轧制 Mg-Al-Sn-Zn 系海水电池用镁阳极材料组织及电性能的影响

    Institute of Scientific and Technical Information of China (English)

    李晓航; 吴永兴; 杨志玲; 李鸿雁

    2015-01-01

    针对合金元素 Sn 对轧制态镁基阳极材料显微组织及电性能的影响,探讨其提高海水电池用镁阳极材料电化学性能的途径。采用金相显微镜、X 射线衍射、扫描电镜,结合能谱分析了 Sn 含量对轧制态镁阳极材料显微组织、相结构、表面形貌及成分分布的影响;通过恒电流法、动电位极化法、排水集气法等研究了该镁合金的腐蚀行为和电性能。研究结果表明:随着Sn 含量的增加,合金晶粒愈加细小,且球形颗粒相 Mg2 Sn 析出逐渐增多。轧制处理使大部分β-Mg17 Al12相溶解,残留 Mg2 Sn 未溶相;Sn 的加入可以提高镁合金放电电压和电流效率,降低析氢率。由于镁合金的“负差数效应”使得析氢率随电流密度的增大而增大;腐蚀产物主要成分为 MgO 和 Al2 O3,且疏松,易脱落,使镁合金阳极的工作电极电位负而且稳定,可促进电池反应深入进行。%According to the effect of elements Sn on the micro structure and electrical properties of rolled anode material- magnesium-based alloy,the ways are explored to improve electrochemical properties of magnesium anode materials for marine battery.The effect of elements Sn on the micro structure,phase structure,morphology and the composition distribution of the rolled magnesium-based alloy is investigated by metallographic microscopy,X-ray diffraction (XRD ),scanning electron microscope (SEM)and energy dispersive spectroscopy (EDS)respectively.Its corrosion behavior and electrochemical properties are also tested by constant current method,potentiodynamic polarization,air collection in drainage process,etc.The results show:With the increase of Sn content,magnesium alloys present fine grain size,and spherical particle phase of Mg2 Sn precipitation gradually increases.After rolling treatment,most of β-Mg17 Al12 phase is dissolved,while most of Mg2 Sn is not dissolved.Sn improves the discharge potential and

  8. Effects of HF and anodic oxidation treated Ti-6Al-7Nb alloy on rat bone marrow mesenchymal stem cells%Ti-6Al-7Nb合金表面经HF酸蚀+阳极氧化处理后对骨髓间充质干细胞特性影响的研究

    Institute of Scientific and Technical Information of China (English)

    张述寅; 胡开进; 莫静珍; 李永锋; 沈舒宁; 高麒; 孔亮

    2013-01-01

    目的:观察HF酸蚀+阳极氧化处理后Ti-6Al-7Nb表面形貌、化学成分以及对骨髓间充质干细胞(BMSCs)生物学特性的影响.方法:纯钛和Ti-6Al-7Nb样本各30个,碳化硅砂纸打磨抛光表面后,各随分对照组(n=15),对照组不作处理;处理组进行HF酸蚀+阳极氧化.分别用扫描电镜(SEM)、原子力学显微镜(AFM)和X线能谱仪(XPS)观察4组样本表面形貌,分析表面化学成分.将体外培养的第4代SD大鼠BMSCs接种于各组合金表面,SEM观察细胞形貌;MTT方法检测细胞在材料表面的粘附和增殖;ALP试剂盒检测细胞ALP活性.结果:纯钛和Ti-6Al-7Nb经HF酸蚀+阳极氧化处理后表面有均匀分布的纳米管状结构,表面凹凸不平;XPS检测发现表面出现氟(F)化物,铝(Al)元素主要以Al2O3的稳定形式存在.BMSCs在两处理组表面粘附、增殖及ALP活性均显著高于其相应对照组(P<0.05);两材料间相比,Ti-6Al-7Nb处理组ALP活性显著高于纯钛处理组(P<0.05).结论:Ti-6Al-7Nb经HF酸蚀+阳极氧化处理后,可以促进BMSCs的粘附、增殖和ALP活性.%AIM: To investigate the surface morphology and chemical composition of HF acid etch and a- nodic oxidation modified Ti-6A1-7Nb alloy and to observe the effects of surface modification on the biological characteristics of rat bone marrow mesenchymal stem cells (BMSCs). METHODS: 30 Ti samples and 30 Ti-6Al-7Nb samples were used. 15 pure Ti and 15 Ti-6A1-7Nb samples were treated by HF acid etch and anodic oxidation, another 15 of each brand were untreated as the controls. The morphology of the samples was observed by SEM and atomic force microscope (AFM). The chemical composition was examined by X-ray photoelectron spectroscopy (XPS). Rat BMSCs were cultured on the samples and the cell morphology was observed by SEM. Cell adhesion and proliferation rate were tested by MTT assay. Alkaline phosphatase (ALP) activity of BMSCs was determined by ALP kit. RESULTS: The treated

  9. Superhydrophobicity of Bionic Alumina Surfaces Fabricated by Hard Anodizing

    Institute of Scientific and Technical Information of China (English)

    Jing Li; Feng Du; Xianli Liu; Zhonghao Jiang; Luquan Ren

    2011-01-01

    Bionic alumina samples were fabricated on convex dome type aluminum alloy substrate using hard anodizing technique.The convex domes on the bionic sample were fabricated by compression molding under a compressive stress of 92.5 MPa.The water contact angles of the as-anodized bionic samples were measured using a contact angle meter (JC2000A) with the 3 μL water drop at room temperature.The measurement of the wetting property showed that the water contact angle of the unmodified as-anodized bionic alumina samples increases from 90° to 137° with the anodizing time.The increase in water contract angle with anodizing time arises from the gradual formation of hierarchical structure or composite structure.The structure is composed of the micro-scaled alumina columns and pores.The height of columns and the depth of pores depend on the anodizing time.The water contact angle increases significantly from 96° to 152° when the samples were modified with self-assembled monolayer of octadecanethiol (ODT),showing a change in the wettability from hydrophobicity to super-hydrophobicity.This improvement in the wetting property is attributed to the decrease in the surface energy caused by the chemical modification.

  10. Catalysts, Protection Layers, and Semiconductors

    DEFF Research Database (Denmark)

    Chorkendorff, Ib

    2015-01-01

    Hydrogen is the simplest solar fuel to produce and in this presentation we shall give a short overview of the pros and cons of various tandem devices [1]. The large band gap semiconductor needs to be in front, but apart from that we can chose to have either the anode in front or back using either...... acid or alkaline conditions. Since most relevant semiconductors are very prone to corrosion the advantage of using buried junctions and using protection layers offering shall be discussed [2-4]. Next we shall discuss the availability of various catalysts for being coupled to these protections layers...... and how their stability may be evaluated [5, 6]. Examples of half-cell reaction using protection layers for both cathode and anode will be discussed though some of recent examples under both alkaline and acidic conditions. Si is a very good low band gap semiconductor and by using TiO2 as a protection...

  11. Electrochemical Evaluation of Thin-Film Li-Si Anodes Prepared by Plasma Spraying

    Energy Technology Data Exchange (ETDEWEB)

    GUIDOTTI,RONALD A.; REINHARDT,FREDERICK W.; SCHARRER,GREGORY L.

    1999-09-08

    Thin-film electrodes of a plasma-sprayed Li-Si alloy were evaluated for use as anodes in high-temperature thermally activated (thermal) batteries. These anodes were prepared using 44% Li/56% Si (w/w) material as feed material in a special plasma-spray apparatus under helium or hydrogen, to protect this air- and moisture-sensitive material during deposition. Anodes were tested in single cells using conventional pressed-powder separators and lithiated pyrite cathodes at temperatures of 400 to 550 C at several different current densities. A limited number of 5-cell battery tests were also conducted. The data for the plasma-sprayed anodes was compared to that for conventional pressed-powder anodes. The performance of the plasma-sprayed anodes was inferior to that of conventional pressed-powder anodes, in that the cell emfs were lower (due to the lack of formation of the desired alloy phases) and the small porosity of these materials severely limited their rate capability. Consequently, plasma-sprayed Li-Si anodes would not be practical for use in thermal batteries.

  12. 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...

  13. Application of Anodization Process for Cast Aluminium Surface Properties Enhancement

    Directory of Open Access Journals (Sweden)

    Włodarczyk-Fligier A.

    2016-09-01

    Full Text Available An huge interest is observed in last years in metal matrix composite, mostly light metal based, which have found their applications in many industry branches, among others in the aircraft industry, automotive-, and armaments ones, as well as in electrical engineering and electronics, where one of the most important issue is related to the corrosion resistance, especially on the surface layer of the used aluminium alloys. This elaboration presents the influence of ceramic phase on the corrosion resistance, quality of the surface layer its thickness and structure of an anodic layer formed on aluminium alloys. As test materials it was applied the aluminium alloys Al-Si-Cu and Al-Cu-Mg, for which heat treatment processes and corrosion tests were carried out. It was presented herein grindability test results and metallographic examination, as well. Hardness of the treated alloys with those ones subjected to corrosion process were compared.

  14. Anodes for alkaline electrolysis

    Science.gov (United States)

    Soloveichik, Grigorii Lev

    2011-02-01

    A method of making an anode for alkaline electrolysis cells includes adsorption of precursor material on a carbonaceous material, conversion of the precursor material to hydroxide form and conversion of precursor material from hydroxide form to oxy-hydroxide form within the alkaline electrolysis cell.

  15. Inert Anode Report

    Energy Technology Data Exchange (ETDEWEB)

    none,

    1999-07-01

    This ASME report provides a broad assessment of open literature and patents that exist in the area of inert anodes and their related cathode systems and cell designs, technologies that are relevant for the advanced smelting of aluminum. The report also discusses the opportunities, barriers, and issues associated with these technologies from a technical, environmental, and economic viewpoint.

  16. Movable anode x-ray source with enhanced anode cooling

    Science.gov (United States)

    Bird, C.R.; Rockett, P.D.

    1987-08-04

    An x-ray source is disclosed having a cathode and a disc-shaped anode with a peripheral surface at constant radius from the anode axis opposed to the cathode. The anode has stub axle sections rotatably carried in heat conducting bearing plates which are mounted by thermoelectric coolers to bellows which normally bias the bearing plates to a retracted position spaced from opposing anode side faces. The bellows cooperate with the x-ray source mounting structure for forming closed passages for heat transport fluid. Flow of such fluid under pressure expands the bellows and brings the bearing plates into heat conducting contact with the anode side faces. A worm gear is mounted on a shaft and engages serrations in the anode periphery for rotating the anode when flow of coolant is terminated between x-ray emission events. 5 figs.

  17. Catalyst mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Masel, Richard I.; Rosen, Brian A.

    2017-02-14

    Catalysts that include at least one catalytically active element and one helper catalyst can be used to increase the rate or lower the overpotential of chemical reactions. The helper catalyst can simultaneously act as a director molecule, suppressing undesired reactions and thus increasing selectivity toward the desired reaction. These catalysts can be useful for a variety of chemical reactions including, in particular, the electrochemical conversion of CO.sub.2 or formic acid. The catalysts can also suppress H.sub.2 evolution, permitting electrochemical cell operation at potentials below RHE. Chemical processes and devices using the catalysts are also disclosed, including processes to produce CO, OH.sup.-, HCO.sup.-, H.sub.2CO, (HCO.sub.2).sup.-, H.sub.2CO.sub.2, CH.sub.3OH, CH.sub.4, C.sub.2H.sub.4, CH.sub.3CH.sub.2OH, CH.sub.3COO.sup.-, CH.sub.3COOH, C.sub.2H.sub.6, O.sub.2, H.sub.2, (COOH).sub.2, or (COO.sup.-).sub.2, and a specific device, namely, a CO.sub.2 sensor.

  18. Photo-oxidation catalysts

    Science.gov (United States)

    Pitts, J. Roland; Liu, Ping; Smith, R. Davis

    2009-07-14

    Photo-oxidation catalysts and methods for cleaning a metal-based catalyst are disclosed. An exemplary catalyst system implementing a photo-oxidation catalyst may comprise a metal-based catalyst, and a photo-oxidation catalyst for cleaning the metal-based catalyst in the presence of light. The exposure to light enables the photo-oxidation catalyst to substantially oxidize absorbed contaminants and reduce accumulation of the contaminants on the metal-based catalyst. Applications are also disclosed.

  19. X-ray absorption spectroscopy for characterisation of catalysts for PEM fuel cells; Roentgenabsorptionsspektroskopie zur Charakterisierung von Katalysatoren fuer die PEM-Brennstoffzelle

    Energy Technology Data Exchange (ETDEWEB)

    Koehl, G.

    2001-10-01

    The investigation of bimetallic nanoparticles is of great interest for the development of powerful anode catalysts in PEM fuel cells. The determination of their electronic and geometric structure is crucial for the optimization of the activity and selectivity in the fuel cell. Especially carbon supported PtRu particles have shown superior activity as anode catalysts due to their high CO tolerance. To state the reason on an atomic level, X-ray absorption spectroscopy (XAS) with synchrotron radiation has been used to examine several Pt and PtRu nanoparticle systems. They were either prepared on the basis of preformed PtRu alloy colloids stabilized by different surfactants or by chemical reduction of precursors, Na{sub 6}Pt(SO{sub 3}){sub 4} and Na{sub 6}Ru(SO{sub 3}){sub 4}. Although a PtRu interaction was observed in all systems, a nonstatistical distribution of Pt and Ru atoms in the nanoparticles could be verified. In additional investigations the reaction mechanism during the synthesis of an organometallic stabilized Pt colloid was examined. In-situ measurements revealed the formation of an hitherto unknown Pt complex as intermediate state prior to the nucleation of the particles. (orig)

  20. Structure of anodized Al–Zr sputter deposited coatings and effect on optical appearance

    Energy Technology Data Exchange (ETDEWEB)

    Gudla, Visweswara Chakravarthy [Department of Mechanical Engineering, Technical University of Denmark, DK-2800 Kgs. Lyngby (Denmark); Canulescu, Stela [Department of Photonics Engineering, Technical University of Denmark, DK-4000 Roskilde (Denmark); Shabadi, Rajashekhara [Unité Matériaux et Transformations, Université Lille1, 59655 Villeneuve ‘Ascq (France); Rechendorff, Kristian [Tribology Centre, Danish Technological Institute, DK-8000 Århus C (Denmark); Dirscherl, Kai [Danish Fundamental Metrology, DK-2800 Kgs., Lyngby (Denmark); Ambat, Rajan, E-mail: ram@mek.dtu.dk [Department of Mechanical Engineering, Technical University of Denmark, DK-2800 Kgs. Lyngby (Denmark)

    2014-10-30

    Highlights: • Microstructure of magnetron sputtered Al–Zr coatings on AA6060 under as coated and heat treated condition. • Effect of heat treatment and precipitation of Al–Zr–Si (τ{sub 1}) phase on optical appearance of anodized layer. • Partial oxidation of τ{sub 1} precipitates after anodizing and relation to darkening of the anodized layer. • Oxidized region of τ{sub 1} precipitates was amorphous while unoxidized region retained crystallinity. • Unoxidized metallic τ{sub 1} in amorphous anodic alumina acts as light absorption centres and causes darkening after anodizing. - Abstract: The mechanism of interaction of light with the microstructure of anodized layer giving specific optical appearance is investigated using Al–Zr sputter deposited coating as a model system on an AA6060 substrate. Differences in the oxidative nature of various microstructural components result in the evolution of typical features in the anodized layer, which are investigated as a function of microstructure and correlated with its optical appearance. The Zr concentration in the coating was varied from 6 wt.% to 23 wt.%. Heat treatment of the coated samples was carried out at 550 °C for 4 h in order to evolve Al–Zr based second phase precipitates in the microstructure. Anodizing was performed using 20 wt.% sulphuric acid at 18 °C with an intention to study the effect of anodizing on the Al–Zr based precipitates in the coating. Detailed microstructural characterization of the coating and anodized layer was carried out using high resolution scanning and transmission electron microscopy, grazing incidence X-ray diffraction analysis, glow discharge optical emission spectroscopy, and optical appearance using spectrophotometry. The evolution of microstructure in the anodized layer as a function of anodizing parameters and their influence on the interaction of light is investigated and the results in general are applicable to discolouration of anodized layer on

  1. Enhancing hybrid direct carbon fuel cell anode performance using Ag2O

    DEFF Research Database (Denmark)

    Deleebeeck, Lisa; Ippolito, Davide; Kammer Hansen, Kent

    2015-01-01

    A hybrid-direct carbon fuel cell (HDCFC), consisting of a molten slurry of solid carbon black and (Li-K)2CO3 added to the anode chamber of a solid oxide fuel cell, was characterized using current-potential-power density curves, electrochemical impedance spectroscopy, and cyclic voltammetry. Two...... types of experimental setups were employed in this study, an anode-supported full cell configuration (two electrodes, two atmospheres setup) and a 3-electrode electrolyte-supported half-cell setup (single atmosphere). Anode processes with and without catalysts were investigated as a function...

  2. Phenol-degrading anode biofilm with high coulombic efficiency in graphite electrodes microbial fuel cell.

    Science.gov (United States)

    Zhang, Dongdong; Li, Zhiling; Zhang, Chunfang; Zhou, Xue; Xiao, Zhixing; Awata, Takanori; Katayama, Arata

    2017-03-01

    A microbial fuel cell (MFC), with graphite electrodes as both the anode and cathode, was operated with a soil-free anaerobic consortium for phenol degradation. This phenol-degrading MFC showed high efficiency with a current density of 120 mA/m(2) and a coulombic efficiency of 22.7%, despite the lack of a platinum catalyst cathode and inoculation of sediment/soil. Removal of planktonic bacteria by renewing the anaerobic medium did not decrease the performance, suggesting that the phenol-degrading MFC was not maintained by the planktonic bacteria but by the microorganisms in the anode biofilm. Cyclic voltammetry analysis of the anode biofilm showed distinct oxidation and reduction peaks. Analysis of the microbial community structure of the anode biofilm and the planktonic bacteria based on 16S rRNA gene sequences suggested that Geobacter sp. was the phenol degrader in the anode biofilm and was responsible for current generation.

  3. SnSe2 2D Anodes for Advanced Sodium Ion Batteries

    KAUST Repository

    Zhang, Fan

    2016-08-22

    A simple synthesis method to prepare pure SnSe2 nanosheet anodes for Na ion batteries is reported. The SnSe2 2D sheets achieve a stable and reversible specific capacity of 515 mA h g-1 after 100 cycles, with excellent rate performance. The sodiation and desodiation process in this anode material is shown to occur via a combination of conversion and alloying reactions.

  4. Processing of copper anodic-slimes for extraction of valuable metals.

    Science.gov (United States)

    Amer, A M

    2003-01-01

    This work focuses on processing of anodic slimes obtained from an Egyptian copper electrorefining plant. The anodic slimes are characterized by high concentrations of copper, lead, tin and silver. The proposed hydrometallurgical process consists of two leaching stages for the extraction of copper (H(2)SO(4)-O(2)) and silver (thiourea-Fe3+), and pyrometallurgical treatment of the remaining slimes for production of Pb-Sn soldering alloy. Factors affecting both the leaching and smelting stages were studied.

  5. Discovery of technical methanation catalysts based on computational screening

    DEFF Research Database (Denmark)

    Sehested, Jens; Larsen, Kasper Emil; Kustov, Arkadii

    2007-01-01

    Methanation is a classical reaction in heterogeneous catalysis and significant effort has been put into improving the industrially preferred nickel-based catalysts. Recently, a computational screening study showed that nickel-iron alloys should be more active than the pure nickel catalyst...

  6. Fabrication of Corrosion Resistance Micro-Nanostructured Superhydrophobic Anodized Aluminum in a One-Step Electrodeposition Process

    Directory of Open Access Journals (Sweden)

    Ying Huang

    2016-02-01

    Full Text Available The formation of low surface energy hybrid organic-inorganic micro-nanostructured zinc stearate electrodeposit transformed the anodic aluminum oxide (AAO surface to superhydrophobic, having a water contact angle of 160°. The corrosion current densities of the anodized and aluminum alloy surfaces are found to be 200 and 400 nA/cm2, respectively. In comparison, superhydrophobic anodic aluminum oxide (SHAAO shows a much lower value of 88 nA/cm2. Similarly, the charge transfer resistance, Rct, measured by electrochemical impedance spectroscopy shows that the SHAAO substrate was found to be 200-times larger than the as-received aluminum alloy substrate. These results proved that the superhydrophobic surfaces created on the anodized surface significantly improved the corrosion resistance property of the aluminum alloy.

  7. CO-Tolerant Pt–BeO as a Novel Anode Electrocatalyst in Proton Exchange Membrane Fuel Cells

    Directory of Open Access Journals (Sweden)

    Kyungjung Kwon

    2016-05-01

    Full Text Available Commercialization of proton exchange membrane fuel cells (PEMFCs requires less expensive catalysts and higher operating voltage. Substantial anodic overvoltage with the usage of reformed hydrogen fuel can be minimized by using CO-tolerant anode catalysts. Carbon-supported Pt–BeO is manufactured so that Pt particles with an average diameter of 4 nm are distributed on a carbon support. XPS analysis shows that a peak value of the binding energy of Be matches that of BeO, and oxygen is bound with Be or carbon. The hydrogen oxidation current of the Pt–BeO catalyst is slightly higher than that of a Pt catalyst. CO stripping voltammetry shows that CO oxidation current peaks at ~0.85 V at Pt, whereas CO is oxidized around 0.75 V at Pt–BeO, which confirms that the desorption of CO is easier in the presence of BeO. Although the state-of-the-art PtRu anode catalyst is dominant as a CO-tolerant hydrogen oxidation catalyst, this study of Be-based CO-tolerant material can widen the choice of PEMFC anode catalyst.

  8. Catalysts for Efficient Production of Carbon Nanotubes

    Science.gov (United States)

    Sun, Ted X.; Dong, Yi

    2009-01-01

    Several metal alloys have shown promise as improved catalysts for catalytic thermal decomposition of hydrocarbon gases to produce carbon nanotubes (CNTs). Heretofore almost every experiment on the production of carbon nanotubes by this method has involved the use of iron, nickel, or cobalt as the catalyst. However, the catalytic-conversion efficiencies of these metals have been observed to be limited. The identification of better catalysts is part of a continuing program to develop means of mass production of high-quality carbon nanotubes at costs lower than those achieved thus far (as much as $100/g for purified multi-wall CNTs or $1,000/g for single-wall CNTs in year 2002). The main effort thus far in this program has been the design and implementation of a process tailored specifically for high-throughput screening of alloys for catalyzing the growth of CNTs. The process includes an integral combination of (1) formulation of libraries of catalysts, (2) synthesis of CNTs from decomposition of ethylene on powders of the alloys in a pyrolytic chemical-vapor-decomposition reactor, and (3) scanning- electron-microscope screening of the CNTs thus synthesized to evaluate the catalytic efficiencies of the alloys. Information gained in this process is put into a database and analyzed to identify promising alloy compositions, which are to be subjected to further evaluation in a subsequent round of testing. Some of these alloys have been found to catalyze the formation of carbon nano tubes from ethylene at temperatures as low as 350 to 400 C. In contrast, the temperatures typically required for prior catalysts range from 550 to 750 C.

  9. Anodization Mechanism on SiC Nanoparticle Reinforced Al Matrix Composites Produced by Power Metallurgy

    Directory of Open Access Journals (Sweden)

    Sonia C. Ferreira

    2014-12-01

    Full Text Available Specimens of aluminum-based composites reinforced by silicon carbide nanoparticles (Al/SiCnp produced by powder metallurgy (PM were anodized under voltage control in tartaric-sulfuric acid (TSA. In this work, the influence of the amount of SiCnp on the film growth during anodizing was investigated. The current density versus time response and the morphology of the porous alumina film formed at the composite surface are compared to those concerning a commercial aluminum alloy (AA1050 anodized under the same conditions. The processing method of the aluminum alloys influences the efficiency of the anodizing process, leading to a lower thicknesses for the unreinforced Al-PM alloy regarding the AA1050. The current density versus time response is strongly dependent on the amount of SiCnp. The current peaks and the steady-state current density recorded at each voltage step increases with the SiCnp volume fraction due to the oxidation of the SiCnp. The formation mechanism of the anodic film on Al/SiCnp composites is different from that occurring in AA1050, partly due the heterogeneous distribution of the reinforcement particles in the metallic matrix, but also to the entrapment of SiCnp in the anodic film.

  10. Ideal anodization of silicon

    Energy Technology Data Exchange (ETDEWEB)

    Yamani, Z.; Thompson, W.H.; AbuHassan, L.; Nayfeh, M.H. [Department of Physics, University of Illinois at Urbana-Champaign, 1110 W. Green Street, Urbana, Illinois 61801 (United States)

    1997-06-01

    Silicon has been anodized such that the porous layer is passivated with a homogeneous stretching phase by incorporating H{sub 2}O{sub 2} in the anodization mixture. Fourier transform infrared spectroscopy measurements show that the Si{endash}H stretching mode oriented perpendicular to the surface at {approximately}2100cm{sup {minus}1} dominates the spectrum with negligible contribution from the bending modes in the 600{endash}900cm{sup {minus}1} region. Material analysis using Auger electron spectroscopy shows that the samples have very little impurities, and that the luminescent layer is very thin (5{endash}10 nm). Scanning electron microscopy shows that the surface is smoother with features smaller than those of conventional samples. {copyright} {ital 1997 American Institute of Physics.}

  11. Electrochemical behaviors of anodic alumina sealed by Ce-Mo in NaCl solutions

    Institute of Scientific and Technical Information of China (English)

    TIAN Lian-peng; ZHAO Xu-hui; ZHAO Jing-mao; ZHANG Xiao-feng; ZUO Yu

    2006-01-01

    The elimination of toxic materials in sealing methods for anodic films on 1070 aluminum alloy was studied. The new process uses chemical treatments in cerium solution and an electrochemical treatment in a molybdate solution. Potentiodynamic polarization and electrochemical impedance spectroscopy(EIS) were used to study the influences of sealing methods on the corrosion behavior of anodic films in NaCl solutions. The results show that the Ce-Mo sealing makes the surface structure and morphology of anodic films uniform and compact. Ce and Mo produce a cooperative effect to improve the corrosion resistance of anodic films. Anodic films sealed by Ce-Mo provide high corrosion resistance both in acidic and basic solutions.

  12. 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...... dark to greyish white. This is attributed to the localized microstructural and morphological differences around the metal oxide particles incorporated into the anodic alumina matrix. The metal oxide particles in the FSP zone electrochemically shadowed the underlying Al matrix and modified the local...

  13. Si-Based Anode Materials for Li-Ion Batteries:A Mini Review

    Institute of Scientific and Technical Information of China (English)

    Delong Ma; Zhanyi Cao; Anming Hu

    2014-01-01

    Si has been considered as one of the most attractive anode materials for Li-ion batteries (LIBs) because of its high gravimetric and volumetric capacity. Importantly, it is also abundant, cheap, and environmentally benign. In this review, we summarized the recent progress in developments of Si anode materials. First, the electrochemical reaction and failure are outlined, and then, we summarized various methods for improving the battery performance, including those of nanostructuring, alloying, forming hierarchic structures, and using suitable binders. We hope that this review can be of benefit to more intensive investigation of Si-based anode materials.

  14. Fuel cell development for transportation: Catalyst development

    Energy Technology Data Exchange (ETDEWEB)

    Doddapaneni, N. [Sandia National Lab., Albuquerque, NM (United States)

    1996-04-01

    Fuel cells are being considered as alternate power sources for transportation and stationary applications. With proton exchange membrane (PEM) fuel cells the fuel crossover to cathodes causes severe thermal management and cell voltage drop due to oxidation of fuel at the platinized cathodes. The main goal of this project was to design, synthesize, and evaluate stable and inexpensive transition metal macrocyclic catalysts for the reduction of oxygen and be electrochemically inert towards anode fuels such as hydrogen and methanol.

  15. Highly dispersed metal catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Xin; West, William L.; Rhodes, William D.

    2016-11-08

    A supported catalyst having an atomic level single atom structure is provided such that substantially all the catalyst is available for catalytic function. A process of forming a single atom catalyst unto a porous catalyst support is also provided.

  16. Friction coefficient and microhardness of anodized aluminum alloys under different elaboration conditions%不同加工条件下阳极化铝合金的摩擦因数和显微硬度

    Institute of Scientific and Technical Information of China (English)

    M GUEZMIL; W BENSALAH; A KHALLADI; K ELLEUCH; M DEPETRIS-WERY; HF AYEDI

    2015-01-01

    研究电解液、电流密度和温度等阳极化条件对在Al 5745和Al 1050A基质上形成的氧化膜层摩擦因数和维氏硬度的影响。采用DELTALAB HVS−1000维氏硬度计和旋转销盘摩擦试验机测量样品的硬度和摩擦性能。结果表明:当草酸浓度为10 g/L、电流密度为3 A/dm2及温度为5°C时,样品获得最高的维氏硬度(>HV 400)和最低的摩擦因数(HV 400) and the lowest friction coefficient (<0.4) were obtained with the oxalic acid addition of 10 g/L at high current density of 3 A/dm2 and low temperature of 5 °C. The presence of oxidized Mg through the anodic oxide layer formed on Al 5754 was examined using glow-discharge optical emission spectroscopy (GDOES). The MgO was found to act negatively on the mechanical property of the layer. Finally, the scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and atomic force microscopy (AFM) were used to characterize the anodic layer before and after friction tests. It is found that the wear mechanism is related to many aspects of the initial morphology, chemical composition of the layer (C, S and Mg), porosity and internal stress.

  17. Studies on black anodic coatings for spacecraft thermal control applications

    Energy Technology Data Exchange (ETDEWEB)

    Uma Rani, R.; Subba Rao, Y.; Sharma, A.K. [ISRO Satellite Centre, Bangalore (India). Thermal Systems Group

    2011-10-15

    An inorganic black colouring process using nickel sulphate and sodium sulphide was investigated on anodized aluminium alloy 6061 to provide a flat absorber black coating for spacecraft thermal control applications. Influence of colouring process parameters (concentration, pH) on the physico-optical properties of black anodic film was investigated. The nature of black anodic film was evaluated by the measurement of film thickness, micro hardness and scanning electron microscopy (SEM). Energy dispersive X-ray spectroscopy studies confirmed the presence of nickel and sulphur in the black anodic coating. Electrochemical impedance spectroscopy (EIS) was used to evaluate the corrosion resistance of the coating. The environmental tests, namely, humidity, corrosion resistance, thermal cycling and thermo vacuum performance tests were used to evaluate the space worthiness of the coating. Optical properties of the film were measured before and after each environmental test to ascertain its stability in harsh space environment. The black anodic films provide higher thermal emittance ({proportional_to} 0.90) and solar absorptance ({proportional_to} 0.96) and their high stability during the environmental tests indicated their suitability for space and allied applications. (orig.)

  18. 用于质子交换膜燃料电池的高活性、高稳定性PtIrFe/C三元合金催化剂∗%Remarkably Active and Durable PtIrFe/C Ternary Alloy Catalysts with Potential Application to Proton Exchange Membrane Fuel Cells

    Institute of Scientific and Technical Information of China (English)

    杜鑫鑫; 王晓霞; 贺阳; 王健农

    2016-01-01

    采用催化裂解法制备了多孔碳,将其作为催化剂载体,利用液相还原和真空热处理工艺制备出PtIrFe/C三元合金催化剂。采用 X射线衍射、透射电子显微镜等手段对样品的结构形貌进行表征。使用电化学测试手段研究了不同热处理温度对其催化性能的影响。实验结果表明,热处理带来的合金化作用使催化剂的催化活性和耐久性得到了极大的提高。经过700℃热处理的样品,其面积比活性和质量比活性分别是传统商业 Pt/C 催化剂的3~4倍。%Using a mesoporous carbon (prepared via catalyzed pyrolysis)as a support material,PtIrFe/C alloy catalysts were synthesized by a liquid reduction and heat treatment method,and characterized by transmission electron microscopy and powder X-ray diffraction to explore and study the morphologies and crystallization properties.The an-nealing of the as prepared catalysts was performed at different temperatures,tested by electrochemical measurements, and proved to be of great importance for the improvement of the catalyst′s activity and durability due to the alloying effect.The catalysts annealed at 700 ℃ exhibited the highest area-specific activity and mass-specific activity which were 3-4 times higher than those of a commercial Pt/C catalyst.

  19. Preparation of Pt-Re/Vulcan carbon nanocomposites using a single-source molecular precursor and relative performance as a direct methanol fuel cell electrooxidation catalyst.

    Science.gov (United States)

    Anderson, Angela D; Deluga, Gregg A; Moore, Joshua T; Vergne, Matthew J; Hercules, David M; Kenik, Edward A; Lukehart, C M

    2004-09-01

    Pt-Re/Vulcan carbon powder nanocomposites have been prepared with total metal loadings of 18 wt.% and 40 wt.% using a new non-cluster (1:1)-PtRe bimetallic precursor as the source of metal. Pt-Re nanoparticles having an average diameter of ca. 6 nm and atomic stoichiometry near 1:1 are formed. TEM, on-particle HR-EDS, and powder XRD data are consistent with the formation of Pt-Re alloy nanoparticles having a hexagonal unit cell with cell constants of a = 2.77 A and c = 4.47 A. A nanocomposite prepared at higher total metal loading under more rigorous thermal treatment also contains Pt-Re alloy nanoparticles having a fcc unit cell structure (a = 3.95 A). The precise dependence of Pt-Re nanocrystal structure on the thermal history of the nanocomposite specimen has not been investigated in detail. While these Pt-Re/carbon nanocomposites are active as anode catalysts in operating direct methanol fuel cells, the measured performance is less than that of commercial Pt-Ru/carbon catalysts and has marginal practical importance.

  20. SISGR: Theoretically relating the surface composition of Pt alloys to their performance as the electrocatalysts of low-temperature fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Guofeng

    2010-12-31

    The main goal of this project is to gain fundamental knowledge about the relation between surface composition and catalytic performance of Pt alloy catalysts for oxygen reduction reaction (ORR). Specific objectives are: to develop and improve a first-principles based multiscale computation approach to simulating surface segregation phenomena in Pt alloy surfaces; to evaluate the surface electronic structure and catalytic activity of Pt alloy catalysts and; to relate the surface composition to the catalytic performance of Pt alloy catalysts.

  1. Effect of hydrogen on aluminium and aluminium alloys: A review

    DEFF Research Database (Denmark)

    Ambat, Rajan; Dwarakadasa, E.S.

    1996-01-01

    in aluminium and its alloys and its effect on mechanical properties. The importance of hydrogen embrittlement over anodic dissolution to explain the stress corrosion cracking mechanism of these alloys is also examined in considerable detail. The various experimental findings concerning the link between...

  2. Corrosion protection of aluminum alloys in contact with other metals

    Science.gov (United States)

    Kuster, C. A.

    1969-01-01

    Study establishes the quality of chemical and galvanized protection afforded by anodized and aldozided coatings applied to test panels of various aluminum alloys. The test panels, placed in firm contact with panels of titanium alloys, were subjected to salt spray tests and visually examined for corrosion effect.

  3. Examining the surfaces in used platinum catalysts

    Directory of Open Access Journals (Sweden)

    Trumić B.

    2009-01-01

    Full Text Available For the purpose of finding more advanced platinum catalyst manufacturing technologies and achieving a higher degree of ammonia oxidation, metallographic characterization has been done on the surface of catalyst gauzes and catalyst gripper gauzes made from platinum and palladium alloys. For the examined samples of gauzes as well as the cross section of the wires, a chemical analysis was provided. The purpose of this paper is the metallographic characterization of examined alloys carried out by way of electronic microscopic scanning, X-rays as well as chemical assays which contributed greatly to a better understanding of the surface deactivation, in other words a better consideration of structural changes occurring on the wire surface.

  4. Heterogeneous Catalysts

    NARCIS (Netherlands)

    Dakka, J.; Sheldon, R.A.; Sanderson, W.A.

    1997-01-01

    Abstract of GB 2309655 (A) Heterogeneous catalysts comprising one or more metal compounds selected from the group consisting of tin, molybdenum, tungsten, zirconium and selenium compounds deposited on the surface of a silicalite are provided. Preferably Sn(IV) and/or Mo(VI) are employed. The cat

  5. Assembly of a Cost-Effective Anode Using Palladium Nanoparticles for Alkaline Fuel Cell Applications

    Science.gov (United States)

    Feliciano-Ramos, Ileana; Casan~as-Montes, Barbara; García-Maldonado, María M.; Menendez, Christian L.; Mayol, Ana R.; Díaz-Vazquez, Liz M.; Cabrera, Carlos R.

    2015-01-01

    Nanotechnology allows the synthesis of nanoscale catalysts, which offer an efficient alternative for fuel cell applications. In this laboratory experiment, the student selects a cost-effective anode for fuel cells by comparing three different working electrodes. These are commercially available palladium (Pd) and glassy carbon (GC) electrodes, and…

  6. Thin flexible intercalation anodes

    Energy Technology Data Exchange (ETDEWEB)

    Levy, S.C.; Cieslak, W.R.; Klassen, S.E.; Lagasse, R.R.

    1994-10-01

    Poly(acrylonitrile) fibers have been pyrolyzed under various conditions to form flexible carbon yarns capable of intercalating lithium ions. These fibers have also been formed into both woven and non woven cloths. Potentiostatic, potentiodynamic and galvanostatic tests have been conducted with these materials in several electrolytes. In some tests, a potential hold was used after each constant current charge and discharge. These tests have shown some of these flexible materials to reversibly intercalate lithium ions to levels that are suitable for use as a practical battery anode.

  7. 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

    Heterogeneous catalysis studies were conducted on two crushed solid oxide fuel cell (SOFC) anodes in fixed-bed reactors. The baseline anode was Ni/ScYSZ (Ni/scandia and yttria stabilized zirconia), the other was Ni/ScYSZ modified with Pd/doped ceria (Ni/ScYSZ/Pd-CGO). Three main types...... 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....... Deactivation of reforming activity by sulfur was much more severe under steam reforming conditions than dry reforming; a result of greater sulfur retention on the catalyst surface during steam reforming....

  8. CdS{sub x}Se{sub 1−x} alloyed quantum dots-sensitized solar cells based on different architectures of anodic oxidation TiO{sub 2} film

    Energy Technology Data Exchange (ETDEWEB)

    Li, Zhen; Yu, Libo; Liu, Yingbo; Sun, Shuqing, E-mail: sunshuqing@tju.edu.cn [Tianjin University, Department of Chemistry (China)

    2014-12-15

    Nanostructured TiO{sub 2} translucent films with different architectures including TiO{sub 2} nanotube (NT), TiO{sub 2} nanowire (NW), and TiO{sub 2} nanowire/nanotube (NW/NT) have been produced by second electrochemical oxidization of TiO{sub 2} NT with diameter around 90–110 nm via modulation of applied voltage. These TiO{sub 2} architectures are sensitized with CdS{sub x}Se{sub 1−x} alloyed quantum dots (QDs) in sizes of around 3–5 nm aiming to tune the response of the photoelectrochemical properties in the visible region. One-step hydrothermal method facilitates the deposition of CdS{sub x}Se{sub 1−x} QDs onto TiO{sub 2} films. These CdS{sub x}Se{sub 1−x} QDs exhibit a tunable range of light absorption with changing the feed molar ratio of S:Se in precursor solution, and inject electrons into TiO{sub 2} films upon excitation with visible light, enabling their application as photosensitizers in sensitized solar cells. Power conversion efficiency (PCE) of 2.00, 1.72, and 1.06 % are achieved with CdS{sub x}Se{sub 1−x} (obtained with S:Se = 0:4) alloyed QDs sensitized solar cells based on TiO{sub 2} NW/NT, TiO{sub 2} NW, and TiO{sub 2} NT architectures, respectively. The significant enhancement of power conversion efficiency obtained with the CdS{sub x}Se{sub 1−x}/TiO{sub 2} NW/NT solar cell can be attributed to the extended absorption of light region tuned by CdS{sub x}Se{sub 1−x} alloyed QDs and enlarged deposition of QDs and efficient electrons transport provided by TiO{sub 2} NW/NT architecture.

  9. Nanosegregated bimetallic oxide anode catalyst for proton exchange membrane electrolyzer

    Science.gov (United States)

    Danilovic, Nemanja; Kang, Yijin; Markovic, Nenad; Stamenkovic, Vojislav; Myers, Deborah J.; Subbaraman, Ram

    2016-08-23

    A surface segregated bimetallic composition of the formula Ru.sub.1-xIr.sub.x wherein 0.1.ltoreq.x.ltoreq.0.75, wherein a surface of the material has an Ir concentration that is greater than an Ir concentration of the material as a whole is provided. The surface segregated material may be produced by a method including heating a bimetallic composition of the formula Ru.sub.1-xIr.sub.x, wherein 0.1.ltoreq.x.ltoreq.0.75, at a first temperature in a reducing environment, and heating the composition at a second temperature in an oxidizing environment. The surface segregated material may be utilized in electrochemical devices.

  10. CO2 emission free co-generation of energy and ethylene in hydrocarbon SOFC reactors with a dehydrogenation anode.

    Science.gov (United States)

    Fu, Xian-Zhu; Lin, Jie-Yuan; Xu, Shihong; Luo, Jing-Li; Chuang, Karl T; Sanger, Alan R; Krzywicki, Andrzej

    2011-11-21

    A dehydrogenation anode is reported for hydrocarbon proton conducting solid oxide fuel cells (SOFCs). A Cu-Cr(2)O(3) nanocomposite is obtained from CuCrO(2) nanoparticles as an inexpensive, efficient, carbon deposition and sintering tolerant anode catalyst. A SOFC reactor is fabricated using a Cu-Cr(2)O(3) composite as a dehydrogenation anode and a doped barium cerate as a proton conducting electrolyte. The protonic membrane SOFC reactor can selectively convert ethane to valuable ethylene, and electricity is simultaneously generated in the electrochemical oxidative dehydrogenation process. While there are no CO(2) emissions, traces of CO are present in the anode exhaust when the SOFC reactor is operated at over 700 °C. A mechanism is proposed for ethane electro-catalytic dehydrogenation over the Cu-Cr(2)O(3) catalyst. The SOFC reactor also has good stability for co-generation of electricity and ethylene at 700 °C.

  11. The Technological Improvements of Aluminum Alloy Coloring by Electrolysis

    Institute of Scientific and Technical Information of China (English)

    LI Nai-jun

    2004-01-01

    The technological process of coloring golden-tawny on aluminum alloy by electrolysis was improved in this paper. The optimum composition of electrolyte was found, the conditions of deposition and anodic oxidation by electrolysis were studied. The oxidative membrane on aluminum alloy was satisfying, the colored aluminum alloy by electrolysis is uniformity,bright and beautiful, and the coloring by electrolysis is convenient and no pollution.

  12. Biocorrosion study of titanium-nickel alloys.

    Science.gov (United States)

    Chern Lin, J H; Lo, S J; Ju, C P

    1996-02-01

    The present study provides results of the corrosion behaviour in Hank's physiological solution and some other properties of three Ti-Ni alloys with 18, 25 and 28.4 wt% Ni, respectively. Results indicate that alpha-titanium and Ti2Ni were the two major phases in all three Ti-Ni alloys. The relative amount of the Ti2Ni phase increased with additional Ni content. Hardness of the Ti-Ni alloys also increased with added nickel content, ranging from 310 to 390 VHN, similar to the hardness of enamel. Melting temperatures of the Ti-Ni alloys were all lower than that of pure titanium by least 600 degrees C. The three Ti-Ni alloys behaved almost identically when potentiodynamically polarized in Hank's solution at 37 degrees C. The critical anodic current densities of the alloys were nearly 30 microA/cm2 and the breakdown potentials were all above 1100 mV (SCE).

  13. Synthesis and Electrocatalytic Performance of Multi-Component Nanoporous PtRuCuW Alloy for Direct Methanol Fuel Cells

    Directory of Open Access Journals (Sweden)

    Xiaoting Chen

    2015-06-01

    Full Text Available We have prepared a multi-component nanoporous PtRuCuW (np-PtRuCuW electrocatalyst via a combined chemical dealloying and mechanical alloying process. The X-ray diffraction (XRD, transmission electron microscopy (TEM and electrochemical measurements have been applied to characterize the microstructure and electrocatalytic activities of the np-PtRuCuW. The np-PtRuCuW catalyst has a unique three-dimensional bi-continuous ligament structure and the length scale is 2.0 ± 0.3 nm. The np-PtRuCuW catalyst shows a relatively high level of activity normalized to mass (467.1 mA mgPt−1 and electrochemically active surface area (1.8 mA cm−2 compared to the state-of-the-art commercial PtC and PtRu catalyst at anode. Although the CO stripping peak of np-PtRuCuW 0.47 V (vs. saturated calomel electrode, SCE is more positive than PtRu, there is a 200 mV negative shift compared to PtC (0.67 V vs. SCE. In addition, the half-wave potential and specific activity towards oxygen reduction of np-PtRuCuW are 0.877 V (vs. reversible hydrogen electrode, RHE and 0.26 mA cm−2, indicating a great enhancement towards oxygen reduction than the commercial PtC.

  14. Fundamental investigations of catalyst nanoparticles

    DEFF Research Database (Denmark)

    Elkjær, Christian Fink

    area Cu=ZnO=Al2O3 structure that is difficult to study by TEM. We therefore created size-selected CuZn alloy nanoparticles that were transformed by oxidation and reduction into Cu nanoparticles decorated with ZnO. This represents a simplified model system for the high surface area catalyst...... been unknown. We used nanoreactor technology which allows for simultaneous TEM imaging and activity measurement, also referred to as an Operando experiment. With this we revealed that the shape of the Pt nanoparticles changed in phase with changes in global reaction rate. By the use of reactor modeling...... fundamental understanding of catalytic processes and our ability to make use of that understanding. This thesis presents fundamental studies of catalyst nanoparticles with particular focus on dynamic processes. Such studies often require atomic-scale characterization, because the catalytic conversion takes...

  15. Unifying the templating effects of porous anodic alumina on metallic nanoparticles for carbon nanotube synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Haase, Mark R., E-mail: Mark.R.Haase@gmail.com, E-mail: haasemr@mail.uc.edu; Alvarez, Noe T.; Malik, Rachit; Schulz, Mark; Shanov, Vesselin [580 Engineering Research Center, Department of Biomedical, Chemical and Environmental Engineering (United States)

    2015-09-15

    Carbon nanotubes (CNTs) are a promising material for many applications, due to their extraordinary properties. Some of these properties vary in relation to the diameter of the nanotubes; thus, precise control of CNT diameter can be critical. Porous anodic alumina (PAA) membranes have been successfully used to template electrodeposited catalyst. However, the catalysts used in CNT synthesis are frequently deposited with more precise techniques, such as electron beam deposition. We test the efficacy of PAA as a template for electron beam-deposited catalyst by studying the diameter distribution of CNTs grown catalyst of various thicknesses supported by PAA. These are then compared by ANOVA to the diameter distributions of CNTs grown on metal catalyst supported by a conventional alumina film. These results also allow a unified description of two templating effects, the more common particles-in-pores model, and the recently described particles-between-pores.

  16. Anode protection system for shutdown of solid oxide fuel cell system

    Energy Technology Data Exchange (ETDEWEB)

    Li, Bob X; Grieves, Malcolm J; Kelly, Sean M

    2014-12-30

    An Anode Protection Systems for a SOFC system, having a Reductant Supply and safety subsystem, a SOFC anode protection subsystem, and a Post Combustion and slip stream control subsystem. The Reductant Supply and safety subsystem includes means for generating a reducing gas or vapor to prevent re-oxidation of the Ni in the anode layer during the course of shut down of the SOFC stack. The underlying ammonia or hydrogen based material used to generate a reducing gas or vapor to prevent the re-oxidation of the Ni can be in either a solid or liquid stored inside a portable container. The SOFC anode protection subsystem provides an internal pressure of 0.2 to 10 kPa to prevent air from entering into the SOFC system. The Post Combustion and slip stream control subsystem provides a catalyst converter configured to treat any residual reducing gas in the slip stream gas exiting from SOFC stack.

  17. Reduced Graphene Oxide/Tin-Antimony Nanocomposites as Anode Materials for Advanced Sodium-Ion Batteries.

    Science.gov (United States)

    Ji, Liwen; Zhou, Weidong; Chabot, Victor; Yu, Aiping; Xiao, Xingcheng

    2015-11-11

    Reduced graphene oxides loaded with tin-antimony alloy (RGO-SnSb) nanocomposites were synthesized through a hydrothermal reaction and the subsequent thermal reduction treatments. Transmission electron microscope images confirm that SnSb nanoparticles with an average size of about 20-30 nm are uniformly dispersed on the RGO surfaces. When they were used as anodes for rechargeable sodium (Na)-ion batteries, these as-synthesized RGO-SnSb nanocomposite anodes delivered a high initial reversible capacity of 407 mAh g(-1), stable cyclic retention for more than 80 cycles and excellent cycle stability at ultra high charge/discharge rates up to 30C. The significantly improved performance of the synthesized RGO-SnSb nanocomposites as Na-ion battery anodes can be attributed to the synergetic effects of RGO-based flexible framework and the nanoscale dimension of the SnSb alloy particles (batteries.

  18. Etching Behavior of Aluminum Alloy Extrusions

    Science.gov (United States)

    Zhu, Hanliang

    2014-11-01

    The etching treatment is an important process step in influencing the surface quality of anodized aluminum alloy extrusions. The aim of etching is to produce a homogeneously matte surface. However, in the etching process, further surface imperfections can be generated on the extrusion surface due to uneven materials loss from different microstructural components. These surface imperfections formed prior to anodizing can significantly influence the surface quality of the final anodized extrusion products. In this article, various factors that influence the materials loss during alkaline etching of aluminum alloy extrusions are investigated. The influencing variables considered include etching process parameters, Fe-rich particles, Mg-Si precipitates, and extrusion profiles. This study provides a basis for improving the surface quality in industrial extrusion products by optimizing various process parameters.

  19. Environmental friendly plasma electrolytic oxidation of AM60 magnesium alloy and its corrosion resistance

    Institute of Scientific and Technical Information of China (English)

    CAO Fa-he; LIN Long-yong; ZHANG Zhao; ZHANG Jian-qing; CAO Chu-nan

    2008-01-01

    Plasma electrolytic oxidation of Mg-based AM60 alloys was investigated using 50 Hz AC anodizing technique in an alkaline borate solution, which contained a new kind of organic. The anodic film is relatively smooth with some micro pores and cracks, while the anodic film consists of MgO, MgAl2O4 and MgSiO3. The electrochemical behavior of anodic film was studied by electrochemical impedance spectroscopy and potentiodynamic polarization. Polarization results indicate the PEO treatment can decrease corrosion current by 3-4 magnitude compared with blank AM60 alloy. The anodic film presents a good level of corrosion protection for AM60 magnesium alloy, over 272 h of the salt spray test based on ASTM B117. The effect of micro-structure and composition on corrosion protection efficiency was also investigated.

  20. Alternate Anodes for the Electrolytic Reduction of UO2

    Science.gov (United States)

    Merwin, Augustus; Chidambaram, Dev

    2015-01-01

    The electrolytic reduction process of UO2 employs a platinum anode and a stainless steel cathode in molten LiCl-LiO2 maintained at 973 K (700 °C). The degradation of platinum under the severely oxidizing conditions encountered during the process is an issue of concern. In this study, Inconel 600 and 718, stainless steel alloy 316, tungsten, nickel, molybdenum, and titanium, were investigated though electrochemical polarization techniques, electron microscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy to serve as potential anode materials. Of the various materials investigated, only tungsten exhibited sufficient stability at the required potential in the molten electrolyte. Tungsten anodes were further studied in molten LiCl-LiO2 electrolyte containing 2, 4, and 6 wt pct of Li2O. In LiCl-2 wt pct Li2O tungsten was found to be sufficiently stable to both oxidation and microstructural changes and the stability is attributed to the formation of a lithium-intercalated tungsten oxide surface film. Increase in the concentration of Li2O was found to lead to accelerated corrosion of the anode, in conjunction with the formation of a peroxotungstate oxide film.

  1. Electrochemical behaviour of passive zirconium alloys

    Energy Technology Data Exchange (ETDEWEB)

    Patrito, E.M.; Torresi, R.M.; Leiva, E.P.M.; Macagno, V.A. (Universidad Nacional de Cordoba (Argentina). Inst. de Investigaciones en Fisicoquimica de Cordoba)

    1991-02-01

    The potentiodynamic oxidation of zirconium, zircaloy-2 (Zry-2) and zircaloy-4 (Zry-4) was studied in the O V{<=}V{<=}8 V potential range. Side reactions take place during the oxidation of Zry-2 and Zry-4 in phosphate electrolytes. With Zry-2, oxygen evolution occurs at high anodic potentials. The oxidation of the alloys in nitric acid shows dissolution of their minor alloying elements but no oxygen evolution at high potentials. The role played by the alloying elements in connection with the appearance of side reactions is discussed. The oxide film were characterized by impedance measurements, X-ray photoelectron spectroscopy and Auger spectroscopy. (author).

  2. Catalyst Architecture

    DEFF Research Database (Denmark)

    Kiib, Hans; Marling, Gitte; Hansen, Peter Mandal

    2014-01-01

    of programs, have a role in mediating positive social and/or cultural development. In this sense, we talk about architecture as a catalyst for: sustainable adaptation of the city’s infrastructure appropriate renovation of dilapidated urban districts strengthening of social cohesiveness in the city development...... meaningful for everyone. The exhibited works are designed by SANAA, Diller Scofidio + Renfro, James Corner Field Operation, JBMC Arquitetura e Urbanismo, Atelier Bow-Wow, Ateliers Jean Nouvel, COBE, Transform, BIG, Topotek1, Superflex, and by visual artist Jane Maria Petersen....

  3. Multi-anode ionization chamber

    Energy Technology Data Exchange (ETDEWEB)

    Bolotnikov, Aleksey E. (South Setauket, NY); Smith, Graham (Port Jefferson, NY); Mahler, George J. (Rocky Point, NY); Vanier, Peter E. (Setauket, NY)

    2010-12-28

    The present invention includes a high-energy detector having a cathode chamber, a support member, and anode segments. The cathode chamber extends along a longitudinal axis. The support member is fixed within the cathode chamber and extends from the first end of the cathode chamber to the second end of the cathode chamber. The anode segments are supported by the support member and are spaced along the longitudinal surface of the support member. The anode segments are configured to generate at least a first electrical signal in response to electrons impinging thereon.

  4. 通过阳极氧化TiFe合金的新方法制备Fe掺杂TiO2纳米管阵列%A Novel Way to Fabricate Fe Doped TiO2 Nanotubes by Anodization of TiFe Alloys

    Institute of Scientific and Technical Information of China (English)

    李广忠; 张文彦; 张健; 李亚宁; 康新婷; 汤慧萍

    2011-01-01

    研究在乙二醇和NH4F混合电解液中通过阳极氧化Ti-xFe合金制备自组装、高度有序的Ti-Fe-O纳米管阵列薄膜,以及该薄膜的Uv-Vis (200-1000 nm)光响应性能.薄膜形貌的关键影响因素为Fe含量.随着Fe含量的增加,纳米管阵列的表面越平整,而纳米管的底部越无序.GAXRD和光响应测试表明,Fe成功地掺杂在纳米管层中,并导致纳米管具有明显的可见光响应.利用该工艺在Ti-12Fe合金表面制备的样品在可见光谱范围内具有大的光响应能力.%We reported the fabrication of self-organized,vertically oriented Ti-Fe-O nanotube array films grown by anodization of Ti-xFe alloys in an ethylene glycol and NH4F mixed electrolyte and their Uv-Vis spectrum (200-1000 nm) photoresponse properties.The key factor affecting the morphology is the Fe content.The higher the Fe content is,the flatter the nanotubes surface is,and the more disorder the bottom surface appears.XRD and photorespense measurements demonstrate the realizable iron doping of the nanotube layers,which leads to a significant visible photoresponse.The Ti- 12Fe sample prepared has a high photoresponse in visible range of the spectrum.

  5. Galvanic corrosion of selected dental alloys.

    Science.gov (United States)

    Karov, J; Hinberg, I

    2001-03-01

    Samples prepared from three different amalgam brands were coupled to two gold alloys and orthodontic brackets. In the resulting galvanic cells, the amalgam coupled to gold were anodic, exhibiting galvanic current densities about one order of magnitude higher than the uncoupled corrosion current densities of 0.2-0.5 microA. Coupling amalgams to orthodontic brackets resulted in galvanic current densities of the same magnitude as the uncoupled samples. Corrosion current densities at the anode were found to be up to six times higher than the measured galvanic current densities. Brushing caused transient increases in galvanic current densities that decayed within 100 s to the previous steady state levels. Brushing of amalgam/bracket couples, caused an anodic peak followed by brief polarization reversal during which the brackets were anodic.

  6. PROPERTIES OF POLYMER SUPPORTED Ni-Cu BIMETALLIC CATALYSTS PREPARED BY SOLVATED METAL ATOM IMPREGNATION

    Institute of Scientific and Technical Information of China (English)

    WU Shihua; ZHU Changying; HUANG Wenqiang

    1996-01-01

    D-72 resin supported nickel-copper catalysts prepared by solvated metal atom impregnation (SMAI) were studied by magnetic measurements and X-ray photoelectron spectroscopy (XPS). The Ni particles on the catalysts are very highly dispersed and display superparamagnetic behaviour. Ni-Cu alloy clusters were found to be formed. The surface compositions are different from the bulk concentrations. In contrast with the surface enrichment in copper generally observed on conventional Ni-Cu catalysts, the surfaces of these catalysts are enriched in nickel. The nickel is in both zero and valent states, while copper is mainly in metallic state. Catalytic data show that the formation of Ni-Cu alloy clusters has a profound effect on the catalytic activities of the catalysts in the hydrogenation of furfural. The activity of the Ni:Cu ratio of one bimetallic catalysts is much higher than that of the Ni or Cu monometallic catalyst.

  7. Solvent effects on Pt-Ru/C catalyst for methanol electro-oxidation

    Institute of Scientific and Technical Information of China (English)

    Jinwei Chen; Chunping Jiang; Hui Lu; Lan Feng; Xin Yang; Liangqiong Li; Ruilin Wang

    2009-01-01

    Alloying degree,particle size and the level of dispersion are the key structural parameters of Pt-Ru/C catalyst in fuel cells. Solvent(s) used in the preparation process can affect the particle size and alloying degree of the object substance,which lead to a great positive impact on its properties. In this work,three types of solvents and their mixtures were used in preparation of the Pt-Ru/C catalysts by chemical reduction of metal precursors with sodium borohydride at room temperature. The structure of the catalysts was characterized by X-ray diffraction (XRD) and Transmission electron microscopy (TEM). The catalytic activity and stability for methanol electro-oxidation were studied by Cyclic Voltammetry (CV) and Chronoamperometry (CA). Pt-Ru/C catalyst prepared in H_2O or binary solvents of H_2O and isopropanol had large particle size and low alloying degree leading to low catalytic activity and less stability in methanol electro-oxidation. When tetrahydrofuran was added to the above solvent systems,Pt-Ru/C catalyst prepared had smaller particle size and higher alloying degree which resulted in better catalytic activity,lower onset and peak potentials,compared with the above catalysts. Moreover,the catalyst prepared in ternary solvents of isopropanol,water and tetrahydrofuran had the smallest particle size,and the high alloying degree and the dispersion kept unchanged. Therefore,this kind of catalyst showed the highest catalytic activity and good stability for methanol electro-oxidation.

  8. Effect of CrO3 Sealing Time on Anodized A12024-T3

    Science.gov (United States)

    Korda, Akhmad A.; Hidayat, R. Z.

    2016-08-01

    The effect of CrO3 sealing time on anodized aluminum alloy has been investigated. A1 2024-T3 were used as substrate. Anodizing was carried out using chromic acid. CrO3 sealing was conducted in CrO3 solution for 30, 60, 90, 120 and 150 minutes. As comparison, other specimens were also prepared as anodized and boiled water sealing. Thickness of the coating was observed by optical microscope. Anodized and sealing layer was analyzed by X- ray diffraction. The hardness of as anodized, boiled water sealing and CrO3 sealing were compared. The highest hardness is achieved by CrO3 sealed specimen and followed by boiled water sealing and as anodized specimens. The longer the processes of CrO3 sealing the higher layer thickness and therefore the higher hardness of the oxide layer. The best resistance to electrolyte penetration is achieved by the CrO3 sealed specimen followed by boiled water sealed and as anodized specimens. The higher thickness of oxide layer, the higher the resistance against electrolyte penetration.

  9. Anodic-Cathodic Electrocatalytic Degradation of Phenol with Oxygen Sparged in the Presence of Iron(Ⅱ)

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Under oxygen sparged, the synergetic effects of both anodic-cathodic electrocatalysis(ACE) and ferrous ion catalyzed anodic-cathodic electrocatalysis(FeACE) on phenol degradation were observed in an undivided cell composed of a β-PbO2 anode modified with fluorine resin and a nickel-chromium-titanium alloy net cathode. Oxygen sparging rate, ferrous concentration, and current significantly affect phenol destruction. The phenol was removed by 10%-13% increasingly under FeACE vs. ACE, and by 12%-15% under ACE vs. anodic electrocatalysis(AE). The phenol destruction was due to the formation of hydroxyl oxidant on the surface of lead oxide at the anode and the reduction of oxygen at the cathode.

  10. Electrically Conductive Anodized Aluminum Surfaces

    Science.gov (United States)

    Nguyen, Trung Hung

    2006-01-01

    Anodized aluminum components can be treated to make them sufficiently electrically conductive to suppress discharges of static electricity. The treatment was conceived as a means of preventing static electric discharges on exterior satin-anodized aluminum (SAA) surfaces of spacecraft without adversely affecting the thermal-control/optical properties of the SAA and without need to apply electrically conductive paints, which eventually peel off in the harsh environment of outer space. The treatment can also be used to impart electrical conductivity to anodized housings of computers, medical electronic instruments, telephoneexchange equipment, and other terrestrial electronic equipment vulnerable to electrostatic discharge. The electrical resistivity of a typical anodized aluminum surface layer lies between 10(exp 11) and 10(exp 13) Omega-cm. To suppress electrostatic discharge, it is necessary to reduce the electrical resistivity significantly - preferably to anodized surface becomes covered and the pores in the surface filled with a transparent, electrically conductive metal oxide nanocomposite. Filling the pores with the nanocomposite reduces the transverse electrical resistivity and, in the original intended outer-space application, the exterior covering portion of the nanocomposite would afford the requisite electrical contact with the outer-space plasma. The electrical resistivity of the nanocomposite can be tailored to a value between 10(exp 7) and 10(exp 12) Omega-cm. Unlike electrically conductive paint, the nanocomposite becomes an integral part of the anodized aluminum substrate, without need for adhesive bonding material and without risk of subsequent peeling. The electrodeposition process is compatible with commercial anodizing production lines. At present, the electronics industry uses expensive, exotic, electrostaticdischarge- suppressing finishes: examples include silver impregnated anodized, black electroless nickel, black chrome, and black copper. In

  11. Effect of Anodization on the Graphitization of PANbased Carbon Fibers of PAN-based Carbon Fibers

    Institute of Scientific and Technical Information of China (English)

    HE Dongmei; YAO Yinghua; XU Shihai; CAI Qingyun

    2011-01-01

    One-step pretreatment,anodization,is used to activate the polyacrylonitrile (PAN)-based carbon fibers instead of the routine two-step pretreatment,sensitization with SnCl2 and activation with PdCl2 The effect of the anodization pretreatment on the graphitization of PAN-based carbon fibers is investigated as a function of Ni-P catalyst.The PAN-based carbon fibers are anodized in H3PO4 electrolyte resulting in the formation of active sites,which thereby facilitates the following electroless Ni-P coating.Carbon fibers in the presence and absence of Ni-P coatings are heat treated and the structural changes are characterized by X-ray diffraction and Raman spectroscopy,both of which indicate that the graphitization of PAN-based carbon fibers are accelerated by both the anodization treatment and the catalysts Ni-E Using the anodized carbon fibers,the routine two-step pretreatment,sensitization and activation,is not needed.

  12. High capacity anode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Lopez, Herman A.; Anguchamy, Yogesh Kumar; Deng, Haixia; Han, Yongbon; Masarapu, Charan; Venkatachalam, Subramanian; Kumar, Suject

    2015-11-19

    High capacity silicon based anode active materials are described for lithium ion batteries. These materials are shown to be effective in combination with high capacity lithium rich cathode active materials. Supplemental lithium is shown to improve the cycling performance and reduce irreversible capacity loss for at least certain silicon based active materials. In particular silicon based active materials can be formed in composites with electrically conductive coatings, such as pyrolytic carbon coatings or metal coatings, and composites can also be formed with other electrically conductive carbon components, such as carbon nanofibers and carbon nanoparticles. Additional alloys with silicon are explored.

  13. ANALYSIS AND DEVELOPMENT OF COPPER RECYCLING OF DEAD COPPER-CONTAINING CATALYSTS

    OpenAIRE

    O. S. Komarov; I. V. Provorova; V. I. Volosatikov; D. O. Komarov; N. I. Urbanovich

    2009-01-01

    The technology of processing of copper-bearing dead catalysts, which includes leaching and deposition of copper by means of electrolysis and also their application in composition of the mixture for alloy doping is offered.

  14. ANALYSIS AND DEVELOPMENT OF COPPER RECYCLING OF DEAD COPPER-CONTAINING CATALYSTS

    Directory of Open Access Journals (Sweden)

    O. S. Komarov

    2009-01-01

    Full Text Available The technology of processing of copper-bearing dead catalysts, which includes leaching and deposition of copper by means of electrolysis and also their application in composition of the mixture for alloy doping is offered.

  15. Study of localized corrosion in aluminum alloys by the scanning reference electrode technique

    Science.gov (United States)

    Danford, M. D.

    1995-01-01

    Localized corrosion in 2219-T87 aluminum (Al) alloy, 2195 aluminum-lithium (Al-Li) alloy, and welded 2195 Al-Li alloy (4043 filler) have been investigated using the relatively new scanning reference electrode technique (SRET). Anodic sites are more frequent and of greater strength in the 2195 Al-Li alloy than in the 2219-T87 Al alloy, indicating a greater tendency toward pitting for the latter. However, the overall corrosion rates are about the same for these two alloys, as determined using the polarization resistance technique. In the welded 2195 Al-Li alloy, the weld bean is entirely cathodic, with rather strongly anodic heat affected zones (HAZ) bordering both sides, indicating a high probability of corrosion in the HAZ parallel to the weld bead.

  16. Research Update: Nickel filling in nanofeatures using supercritical fluid and its application to fabricating a novel catalyst structure for continuous growth of nanocarbon fibers

    Directory of Open Access Journals (Sweden)

    Mitsuhiro Watanabe

    2014-10-01

    Full Text Available A novel catalyst structure for continuous growth of nanocarbon fibers is proposed. In this structure, catalyst nanofibers are embedded in a membrane that separates the growth ambient into carbon-supplying and carbon-precipitating environments. The catalyst nanofibers pierce through the membrane so that carbon source gas is supplied only to one end of the catalyst fibers and nanocarbon fibers grow continuously at the other end. To realize this structure, self-supporting anodized alumina was used as a membrane, and its nano-through-holes were filled with catalyst Ni in supercritical CO2 fluid. Direct carbon growth from the Ni nanofibers was confirmed using this catalyst structure.

  17. Effect of the layer of anodized 7075-T6 aluminium corrosion properties

    Science.gov (United States)

    Montoya Z, R. D.; L, E. Vera; Pineda T, Y.; Cedeño, M. L.

    2017-01-01

    Aluminium alloys are widely used in various sectors of industry. The 7075-T6 alloy corresponding to an Al-Zn T6, is mostly used as structural component in the aviation industry, due to the good relationship between weight and mechanical properties. However, the negative point of this alloys is the resistance to corrosion, which is why they need to be coated with an anodic film. Different surface treatments, such as anodizing, are used to improve corrosion resistance. Anodizing is an electrolytic process by which a protective layer on aluminium known as “alumina” is formed, this is formed by the passage of an electric current in an acidic electrolyte. This investigation presents a study of the effect of the thickness of layers of alumina deposited by anodized method, in the corrosion resistance of 7075-T6 aluminium. This study was performed by using in a solution of tartaric acid - sulfuric acid and an inorganic salt. To evaluate the influence alumina layer thickness on the corrosion properties some tests were carried out by using the electrochemical spectroscopy impedances (EIS) technique and Tafel polarization curves. It was found that the grown of the thickness of film favourably influences in the corrosion resistance.

  18. TiO2 nanostructured surfaces for biomedical applications developed by electrochemical anodization

    Science.gov (United States)

    Strnad, G.; Petrovan, C.; Russu, O.; Jakab-Farkas, L.

    2016-11-01

    Present research demonstrates the formation of self-ordered nanostructured oxide layer on the surface of two phase Ti6Al4V alloy by using electrochemical anodization in H3PO4/HF electrolytes. Our results show that the ordered oxide nanotubes grow on large areas on the samples surface, on both phases of (α+β) Ti6Al4V titanium alloy. We developed nanotubes of 70 nm (internal diameter) using 0.3 wt% HF and of 80 nm using 0.5 wt% HF additions to 1M H3PO4, at an anodization potential of 20 V, and an anodization time of 2 hours. We show that anodization potential has a strong influence on nanostructures morphology. Our results show that nanotubes’ internal diameter is ∼30 nm at 10 V potential, ∼40 nm at 15 V potential, and ∼70-80 nm at 20 V potential in anodization process performed in 1M H3PO4 + 0.5 wt% HF, 2 hours. The thickness of the developed nanostructured oxide layer is in 200-250 nm range.

  19. A new anode material for oxygen evolution in molten oxide electrolysis.

    Science.gov (United States)

    Allanore, Antoine; Yin, Lan; Sadoway, Donald R

    2013-05-16

    Molten oxide electrolysis (MOE) is an electrometallurgical technique that enables the direct production of metal in the liquid state from oxide feedstock, and compared with traditional methods of extractive metallurgy offers both a substantial simplification of the process and a significant reduction in energy consumption. MOE is also considered a promising route for mitigation of CO2 emissions in steelmaking, production of metals free of carbon, and generation of oxygen for extra-terrestrial exploration. Until now, MOE has been demonstrated using anode materials that are consumable (graphite for use with ferro-alloys and titanium) or unaffordable for terrestrial applications (iridium for use with iron). To enable metal production without process carbon, MOE requires an anode material that resists depletion while sustaining oxygen evolution. The challenges for iron production are threefold. First, the process temperature is in excess of 1,538 degrees Celsius (ref. 10). Second, under anodic polarization most metals inevitably corrode in such conditions. Third, iron oxide undergoes spontaneous reduction on contact with most refractory metals and even carbon. Here we show that anodes comprising chromium-based alloys exhibit limited consumption during iron extraction and oxygen evolution by MOE. The anode stability is due to the formation of an electronically conductive solid solution of chromium(iii) and aluminium oxides in the corundum structure. These findings make practicable larger-scale evaluation of MOE for the production of steel, and potentially provide a key material component enabling mitigation of greenhouse-gas emissions while producing metal of superior metallurgical quality.

  20. Electrochemical catalyst recovery method

    Science.gov (United States)

    Silva, Laura J.; Bray, Lane A.

    1995-01-01

    A method of recovering catalyst material from latent catalyst material solids includes: a) combining latent catalyst material solids with a liquid acid anolyte solution and a redox material which is soluble in the acid anolyte solution to form a mixture; b) electrochemically oxidizing the redox material within the mixture into a dissolved oxidant, the oxidant having a potential for oxidation which is effectively higher than that of the latent catalyst material; c) reacting the oxidant with the latent catalyst material to oxidize the latent catalyst material into at least one oxidized catalyst species which is soluble within the mixture and to reduce the oxidant back into dissolved redox material; and d) recovering catalyst material from the oxidized catalyst species of the mixture. The invention is expected to be particularly useful in recovering spent catalyst material from petroleum hydroprocessing reaction waste products having adhered sulfides, carbon, hydrocarbons, and undesired metals, and as well as in other industrial applications.

  1. Electronic-Structure-Based Design of Ordered Alloys

    DEFF Research Database (Denmark)

    Bligaard, Thomas; Andersson, M.P.; Jacobsen, Karsten Wedel

    2006-01-01

    We describe some recent advances in the methodology of using electronic structure calculations for materials design. The methods have been developed for the design of ordered metallic alloys and metal alloy catalysts, but the considerations we present are relevant for the atomic-scale computation...

  2. The study of aluminium anodes for high power density Al/air batteries with brine electrolytes

    Science.gov (United States)

    Nestoridi, Maria; Pletcher, Derek; Wood, Robert J. K.; Wang, Shuncai; Jones, Richard L.; Stokes, Keith R.; Wilcock, Ian

    Aluminium alloys containing small additions of both tin (∼0.1 wt%) and gallium (∼0.05 wt%) are shown to dissolve anodically at high rates in sodium chloride media at room temperatures; current densities >0.2 A cm -2 can be obtained at potentials close to the open circuit potential, ∼-1500 mV versus SCE. The tin exists in the alloys as a second phase, typically as ∼1 μm inclusions (precipitates) distributed throughout the aluminium structure, and anodic dissolution occurs to form pits around the tin inclusions. Although the distribution of the gallium in the alloy could not be established, it is also shown to be critical in the formation of these pits as well as maintaining their activity. The stability of the alloys to open circuit corrosion and the overpotential for high rate dissolution, both critical to battery performance, are shown to depend on factors in addition to elemental composition; both heat treatment and mechanical working influence the performance of the alloy. The correlation between alloy performance and their microstructure has been investigated.

  3. The study of aluminium anodes for high power density Al/air batteries with brine electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Nestoridi, Maria; Pletcher, Derek [School of Chemistry, The University, Southampton SO19 1BJ (United Kingdom); Wood, Robert J.K.; Wang, Shuncai [School of Engineering Sciences, The University, Southampton SO19 1BJ (United Kingdom); Jones, Richard L.; Stokes, Keith R.; Wilcock, Ian [dstl, Physical Sciences Department, Porton Down, Salisbury, Wilts SP4 0JQ (United Kingdom)

    2008-03-15

    Aluminium alloys containing small additions of both tin ({proportional_to}0.1 wt%) and gallium ({proportional_to}0.05 wt%) are shown to dissolve anodically at high rates in sodium chloride media at room temperatures; current densities >0.2 A cm{sup -2} can be obtained at potentials close to the open circuit potential, {proportional_to}-1500 mV versus SCE. The tin exists in the alloys as a second phase, typically as {proportional_to}1 {mu}m inclusions (precipitates) distributed throughout the aluminium structure, and anodic dissolution occurs to form pits around the tin inclusions. Although the distribution of the gallium in the alloy could not be established, it is also shown to be critical in the formation of these pits as well as maintaining their activity. The stability of the alloys to open circuit corrosion and the overpotential for high rate dissolution, both critical to battery performance, are shown to depend on factors in addition to elemental composition; both heat treatment and mechanical working influence the performance of the alloy. The correlation between alloy performance and their microstructure has been investigated. (author)

  4. Metal-air batteries: from oxygen reduction electrochemistry to cathode catalysts.

    Science.gov (United States)

    Cheng, Fangyi; Chen, Jun

    2012-03-21

    Because of the remarkably high theoretical energy output, metal-air batteries represent one class of promising power sources for applications in next-generation electronics, electrified transportation and energy storage of smart grids. The most prominent feature of a metal-air battery is the combination of a metal anode with high energy density and an air electrode with open structure to draw cathode active materials (i.e., oxygen) from air. In this critical review, we present the fundamentals and recent advances related to the fields of metal-air batteries, with a focus on the electrochemistry and materials chemistry of air electrodes. The battery electrochemistry and catalytic mechanism of oxygen reduction reactions are discussed on the basis of aqueous and organic electrolytes. Four groups of extensively studied catalysts for the cathode oxygen reduction/evolution are selectively surveyed from materials chemistry to electrode properties and battery application: Pt and Pt-based alloys (e.g., PtAu nanoparticles), carbonaceous materials (e.g., graphene nanosheets), transition-metal oxides (e.g., Mn-based spinels and perovskites), and inorganic-organic composites (e.g., metal macrocycle derivatives). The design and optimization of air-electrode structure are also outlined. Furthermore, remarks on the challenges and perspectives of research directions are proposed for further development of metal-air batteries (219 references).

  5. Cathodic catalysts in bioelectrochemical systems for energy recovery from wastewater.

    Science.gov (United States)

    Liu, Xian-Wei; Li, Wen-Wei; Yu, Han-Qing

    2014-11-21

    Bioelectrochemical systems (BESs), in which microorganisms are utilized as a self-regenerable catalyst at the anode of an electrochemical cell to directly extract electrical energy from organic matter, have been widely recognized as a promising technology for energy-efficient wastewater treatment or even for net energy generation. However, currently BES performance is constrained by poor cathode reaction kinetics. Thus, there is a strong impetus to improve the cathodic catalysis performance through proper selection and design of catalysts. This review introduces the fundamentals and current development status of various cathodic catalysts (including electrocatalysts, photoelectrocatalysts and bioelectrocatalysts) in BES, identifies their limitations and influential factors, compares their catalytic performances in terms of catalytic efficiency, stability, selectivity, etc., and discusses the possible optimization strategies and future research directions. Special focus is given on the analysis of how the catalytic performance of different catalysts can be improved by fine tuning their physicochemical or physiological properties.

  6. 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.

  7. Effect of Oxide Inclusions on Electrochemical Properties of Aluminium Sacrificial Anodes

    Institute of Scientific and Technical Information of China (English)

    M. Emamy; A. Keyvani; M. Mahta; J. Campbell

    2009-01-01

    Oxide films are incorporated into melts by an entrainment process, and are expected to be present in most metals, but particularly cast Al alloys. The oxides are necessarily present as folded-over double films (bifilms) that are effectively cracks. Their effect on the electrochemical behaviour of cast Al-5Zn-0.02ln sacrificial anodes was studied in 3 wt pct sodium chloride solution using the NACE efficiency evaluation. Three methods were employed to entrain progressive amounts of oxide in the alloy, including the addition of Al-Zn-ln maching chips to the charge, increasing the pouring height, and agitating the melt. The introduction of oxide bifilms in the cast alloy resulted in the deterioration of the electrochemical properties of the sacrificial anodes, such as current capacity and anode efficiency, and introduced increasing variability in these properties. The results suggest that corrosion behaviour is strongly related to the presence of bifilms suspended in the liquid alloy because bifilms provide crack paths allowing the corrodant to penetrate deeply into the metal matrix, and simultaneously provide localized galvanic cells because of the precipitation of Fe rich intermetallic compounds on their outer surfaces.

  8. Studying Cu Alloy Corrosion Products in Cooling Liquid

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The effect of cooiing liquid used for heat exchangers on the Cu alloy corrosion products has been examined using potential-time measurements under applied current condition (anodizing), potentiodynamic polarization, X-ray diffraction (XRD) and infrared spectroscopy (IR). The corrosion products formed on the Cu alloy surface during anodizing, are Cu2O, Cu2(OH)3CI, and Cu2S. NaCI is detected in the corrosion products. The film formation depends on the applied current and the shift of potential to nobler direction indicates its formation progress.

  9. Effect of Surface Pretreatment on Adhesive Properties of Aluminum Alloys

    Institute of Scientific and Technical Information of China (English)

    Jinsheng ZHANG; Xuhui ZHAO; Yu ZUO; Jinping XIONG; Xiaofeng ZHANG

    2008-01-01

    The lap-shear strength and durability of adhesive bonded AI alloy joints with different pretreatments were studied by the lap-shear test and wedge test. The results indicate that the maximum lap-shear strength and durability of the bonding joints pretreated by different processes are influenced by the grade of abrasive papers and can be obviously improved by phosphoric acid anodizing. Alkali etching can obviously improve the durability of bonding joints although it slightly influences the maximum lap-shear strength. The process which is composed of grit-finishing, acetone degreasing, alkali etching and phosphoric acid anodizing, provides a better adhesive bonding property of AI alloy.

  10. Platinum and Palladium Alloys Suitable as Fuel Cell Electrodes

    DEFF Research Database (Denmark)

    2011-01-01

    and innovative catalyst compositions in fuel cell electrodes. The novel electrode catalysts of the invention comprise a noble metal selected from Pt, Pd and mixtures thereof alloyed with a further element selected from Sc, Y and La as well as any mixtures thereof, wherein said alloy is supported on a conductive......The present invention concerns electrode catalysts used in fuel cells, such as proton exchange membrane (PEM) fuel cells. The invention is related to the reduction of the noble metal content and the improvement of the catalytic efficiency by low level substitution of the noble metal to provide new...

  11. Preparation and evaluation of advanced catalysts for phosphoric acid fuel cells

    Science.gov (United States)

    Stonehart, P.; Baris, J.; Hockmuth, J.; Pagliaro, P.

    1984-01-01

    The platinum electrocatalysts were characterized for their crystallite sizes and the degree of dispersion on the carbon supports. One application of these electrocatalysts was for anodic oxidation of hydrogen in hot phosphoric acid fuel cells, coupled with the influence of low concentrations of carbon monoxide in the fuel gas stream. In a similar way, these platinum on carbon electrocatalysts were evaluated for oxygen reduction in hot phosphoric acid. Binary noble metal alloys were prepared for anodic oxidation of hydrogen and noble metal-refractory metal mixtures were prepared for oxygen reduction. An exemplar alloy of platinum and palladium (50/50 atom %) was discovered for anodic oxidation of hydrogen in the presence of carbon monoxide, and patent disclosures were submitted. For the cathode, platinum-vanadium alloys were prepared showing improved performance over pure platinum. Preliminary experiments on electrocatalyst utilization in electrode structures showed low utilization of the noble metal when the electrocatalyst loading exceeded one weight percent on the carbon.

  12. Growth and corrosion behaviors of thin anodic alumina membrane on AA5083 Al-Mg alloy in incalescent medium%非恒温电解液中AA5083 Al-Mg合金阳极氧化膜的制备及其耐蚀性

    Institute of Scientific and Technical Information of China (English)

    王加余; 李澄; 郑顺丽; 尹成勇; 王艳慧

    2014-01-01

    采用硼酸-硫酸-草酸电解液在铝合金表面制备有序多孔层,研究阳极氧化过程中电流随时间的变化,分析界面反应并计算膜层的生长效率。采用扫描电子显微镜、交流阻抗和动电位极化曲线研究膜层的微结构及其在不同温度环境下的耐蚀性。结果表明:在氧化层界面双离子层浓度的增大有利于提高膜层的生长效率。所制备的阳极氧化膜厚度为8~9μm,孔径为10~14 nm,膜层的微观形貌受金属基体组织结构的影响较大。在沸水封闭后膜层为分层结构,表面呈细片状。氧化膜层封闭后能够明显降低试样的自腐蚀电流密度,且耐蚀性随着环境温度的升高而具有更好的稳定性。%A self-ordered porous film was fabricated on aluminum alloy in a ternary boric-sulfuric-oxalic acid electrolyte system. By means of voltage-time response, the oxidation process as well as the growth efficiency was studied. Field emission scanning electron microscopy (FE-SEM) was adopted to reveal the morphological and microstructural features of as-fabricated oxide layers. The corrosion protection properties of the films were investigated by electrochemical impedance spectroscopy and potentiodynamic polarization measurements. The results showed that increasing the concentration of the double ionic layer located at the oxide interface could accelerate the film growth rate. The anodic oxidative layer with thickness of 8-9μm and pore diameter of 10-14 nm maintains the pattern and topography of workpieces, compared with the overall closed film with hierarchical structure. Both samples exhibited much lower corrosion current density after boil water sealing. Meanwhile, a superior stability could be achieved through raising the ambient temperature.

  13. Steam reforming of methanol over copper loaded anodized aluminum oxide (AAO) prepared through electrodeposition

    Science.gov (United States)

    Linga Reddy, E.; Karuppiah, J.; Lee, Hyun Chan; Kim, Dong Hyun

    2014-12-01

    In order to study the steam reforming of methanol (SRM) to produce hydrogen for fuel cells, porous γ-alumina support is developed on Al substrate using anodic oxidation process and copper catalyst particles are deposited homogeneously over anodic aluminum oxide (AAO) surface by electrodeposition method. We investigated the effect of electrodeposition time and hot water treatment (HWT) on the activity of catalysts for SRM reaction in the temperature range between 160 and 360 °C. The experimental results indicate that the SRM activity, CO2 and dimethyl ether (DME) selectivity's over Cu catalysts increased as the electrodeposition time increased from 30 to 120 s, further increment in deposition time of Cu have no significant effect on it. The rates of SRM conversion are found to be higher for the catalysts made from the supports obtained after HWT, which may be due to the enhancement in the surface area of AAO support. It is found that the SRM activity and CO2 selectivity strongly depended upon the free exposed copper sites available for methanol adsorption and reaction, and DME in products is mainly observed in the reaction temperature range between 300 and 350 °C and it is higher for the catalysts with low Cu content.

  14. Electrochemical coating of dental implants with anodic porous titania for enhanced osteointegration

    Directory of Open Access Journals (Sweden)

    Amirreza Shayganpour

    2015-11-01

    Full Text Available Clinical long-term osteointegration of titanium-based biomedical devices is the main goal for both dental and orthopedical implants. Both the surface morphology and the possible functionalization of the implant surface are important points. In the last decade, following the success of nanostructured anodic porous alumina, anodic porous titania has also attracted the interest of academic researchers. This material, investigated mainly for its photocatalytic properties and for applications in solar cells, is usually obtained from the anodization of ultrapure titanium. We anodized dental implants made of commercial grade titanium under different experimental conditions and characterized the resulting surface morphology with scanning electron microscopy equipped with an energy dispersive spectrometer. The appearance of nanopores on these implants confirm that anodic porous titania can be obtained not only on ultrapure and flat titanium but also as a conformal coating on curved surfaces of real objects made of industrial titanium alloys. Raman spectroscopy showed that the titania phase obtained is anatase. Furthermore, it was demonstrated that by carrying out the anodization in the presence of electrolyte additives such as magnesium, these can be incorporated into the porous coating. The proposed method for the surface nanostructuring of biomedical implants should allow for integration of conventional microscale treatments such as sandblasting with additive nanoscale patterning. Additional advantages are provided by this material when considering the possible loading of bioactive drugs in the porous cavities.

  15. DIRECT METHANOL FUEL CELLS AT REDUCED CATALYST LOADINGS

    Energy Technology Data Exchange (ETDEWEB)

    P. ZELENAY; F. GUYON; SM. GOTTESFELD

    2001-05-01

    We focus in this paper on the reduction of catalyst loading in direct methanol fuel cells currently under development at Los Alamos National Laboratory. Based on single-cell DMFC testing, we discuss performance vs. catalyst loading trade-offs and demonstrate optimization of the anode performance. We also show test data for a short five-cell DMFC stack with the average total platinum loading of 0.53 mg cm{sup {minus}2} and compare performance of this stack with the performance of a single direct methanol fuel cell using similar total amount of precious metal.

  16. Direct methanol fuel cells at reduced catalyst loadings

    Energy Technology Data Exchange (ETDEWEB)

    Zelenay, P. (Piotr); Guyon, F. (Francois); Gottesfeld, Shimshon

    2001-01-01

    We focus in this paper on the reduction of catalyst loading in direct methanol fuel cells currently under development at Los Alamos National Laboratory. Based on single-cell DMFC testing, we discuss performance vs. catalyst loading trade-offs and demonstrate optimization of the anode performance. We also show test data for a short five-cell DMFC stack with the average total platinum loading of 0.53 mg cm{sup -2} and compare performance of this stack with the performance of a single direct methanol fuel cell using similar total amount of precious metal.

  17. Downscaled anodic oxidation process for aluminium in oxalic acid

    Science.gov (United States)

    Sieber, M.; Morgenstern, R.; Kuhn, D.; Hackert-Oschätzchen, M.; Schubert, A.; Lampke, T.

    2017-03-01

    The increasing multi-functionality of parts and assemblies in several fields of engineering demands, amongst others, highly functionalised surfaces. For the different applications, on the one hand, there is a need to scale up surface modification processes originating in the nano- and micro-scale. On the other hand, conventional macro-scale surface refinement methods offer a huge potential for application in the said nano- and micro-scale. The anodic oxidation process, which is established especially for aluminium and its alloys, allows the formation of oxide ceramic layers on the surface. The build-up of an oxide ceramic coating comes along with altered chemical, tribological and electrical surface properties. As a basis for further investigations regarding the use of the anodic oxidation process for micro-scale-manufacturing, the scale effects of oxalic acid anodising on commercially pure aluminium as well as on the AlZn5.5MgCu alloy are addressed in the present work. The focus is on the amount of oxide formed during a potentiostatic process in relation to the exchanged amount of charge. Further, the hardness of the coating as an integral measure to assess the porous oxide structure is approached by nano-indentation technique.

  18. Design criteria for stable Pt/C fuel cell catalysts

    Directory of Open Access Journals (Sweden)

    Josef C. Meier

    2014-01-01

    Full Text Available Platinum and Pt alloy nanoparticles supported on carbon are the state of the art electrocatalysts in proton exchange membrane fuel cells. To develop a better understanding on how material design can influence the degradation processes on the nanoscale, three specific Pt/C catalysts with different structural characteristics were investigated in depth: a conventional Pt/Vulcan catalyst with a particle size of 3–4 nm and two Pt@HGS catalysts with different particle size, 1–2 nm and 3–4 nm. Specifically, Pt@HGS corresponds to platinum nanoparticles incorporated and confined within the pore structure of the nanostructured carbon support, i.e., hollow graphitic spheres (HGS. All three materials are characterized by the same platinum loading, so that the differences in their performance can be correlated to the structural characteristics of each material. The comparison of the activity and stability behavior of the three catalysts, as obtained from thin film rotating disk electrode measurements and identical location electron microscopy, is also extended to commercial materials and used as a basis for a discussion of general fuel cell catalyst design principles. Namely, the effects of particle size, inter-particle distance, certain support characteristics and thermal treatment on the catalyst performance and in particular the catalyst stability are evaluated. Based on our results, a set of design criteria for more stable and active Pt/C and Pt-alloy/C materials is suggested.

  19. Design criteria for stable Pt/C fuel cell catalysts.

    Science.gov (United States)

    Meier, Josef C; Galeano, Carolina; Katsounaros, Ioannis; Witte, Jonathon; Bongard, Hans J; Topalov, Angel A; Baldizzone, Claudio; Mezzavilla, Stefano; Schüth, Ferdi; Mayrhofer, Karl J J

    2014-01-01

    Platinum and Pt alloy nanoparticles supported on carbon are the state of the art electrocatalysts in proton exchange membrane fuel cells. To develop a better understanding on how material design can influence the degradation processes on the nanoscale, three specific Pt/C catalysts with different structural characteristics were investigated in depth: a conventional Pt/Vulcan catalyst with a particle size of 3-4 nm and two Pt@HGS catalysts with different particle size, 1-2 nm and 3-4 nm. Specifically, Pt@HGS corresponds to platinum nanoparticles incorporated and confined within the pore structure of the nanostructured carbon support, i.e., hollow graphitic spheres (HGS). All three materials are characterized by the same platinum loading, so that the differences in their performance can be correlated to the structural characteristics of each material. The comparison of the activity and stability behavior of the three catalysts, as obtained from thin film rotating disk electrode measurements and identical location electron microscopy, is also extended to commercial materials and used as a basis for a discussion of general fuel cell catalyst design principles. Namely, the effects of particle size, inter-particle distance, certain support characteristics and thermal treatment on the catalyst performance and in particular the catalyst stability are evaluated. Based on our results, a set of design criteria for more stable and active Pt/C and Pt-alloy/C materials is suggested.

  20. STUDY OF ANODIC OVERVOLTAGE IN NEODYMIUM ELECTROLYSIS

    Institute of Scientific and Technical Information of China (English)

    K.R. Liu; J.S. Chen; Q. Han; X.J. Wei

    2003-01-01

    The anodic overvoltage of neodymium electrolysis was determined by slow scanning oscillogram. The effects of some factors, i.e. the temperature, the anodic current density, the concentration of Nd2O3 and the components of the electrolyte were investigated and the approaches to decrease the anodic overvoltage were also discussed. The results show that the anodic overvoltage increases with the anodic current density and decreases with the increasing temperature. The linear relation between the anodic overvoltage and the current density corresponding to Tafel equation is determined to some extent. The anodic overvoltage decreases with the increasing concentrations of LiF and NdF3. It also decreases by controlling the anodic current density properly, increasing the temperature or the concentrations of LiF and NdF3 and the reducing polar distance.

  1. DEVELOPMENT OF TECHNOLOGY FOR ANODE BALL PRODUCTION

    Directory of Open Access Journals (Sweden)

    G. V. Kozhevnikova

    2015-01-01

    Full Text Available Technology of copper anode balls manufacturing by means of cross-wedge rolling method is developed. The technology satisfies the requirements towards anode balls’ crystalline structure, form and geometrical dimensions accuracy.

  2. Flow-through 3D biofuel cell anode for NAD{sup +}-dependent enzymes

    Energy Technology Data Exchange (ETDEWEB)

    Rincon, Rosalba A.; Lau, Carolin; Garcia, Kristen E. [Department of Chemical and Nuclear Engineering, Center for Emerging Energy Technologies, University of New Mexico, Albuquerque, NM 87131 (United States); Atanassov, Plamen, E-mail: plamen@unm.ed [Department of Chemical and Nuclear Engineering, Center for Emerging Energy Technologies, University of New Mexico, Albuquerque, NM 87131 (United States)

    2011-02-01

    NAD{sup +}-dependent enzymes require the presence of catalysts for cofactor regeneration in order to be employed in enzymatic biofuel cells. Poly-(methylene green) catalysts have proven to help the oxidation reaction of NADH allowing for the use of such enzymes in electrocatalytic oxidation reactions. In this paper we present the development of 3D anode based on NAD{sup +}-dependent malate dehydrogenase. The 3D material chosen was reticulated vitreous carbon (RVC) which was modified with poly-(MG) for NADH oxidation and it also accommodated the porous immobilization matrix for MDH consisting of MWCNTs embedded in chitosan; allowing for mass transport of the substrate to the electrode. Scanning electron microscopy was used in order to characterize the poly-(MG)-modified RVC, and electrochemical evaluation of the anode was performed.

  3. Foundation Flash Catalyst

    CERN Document Server

    Goralski, Greg

    2010-01-01

    This book offers an introduction to Flash Catalyst for designers with intermediate to advanced skills. It discusses where Catalyst sits within the production process and how it communicates with other programs. It covers all of the features of the Flash Catalyst workspace, teaching you how to create designs from scratch, how to build application designs and add functionality, and how to master the Catalyst/Flex workflow. * Introduces Flash Catalyst * Focuses on production process * Covers the interrelation between Flash Catalyst and Photoshop/Illustrator/Flex/Flash What you'll learn Starting f

  4. Lithium based alloy-thionyl chloride cells for applications at temperatures to 200 C

    Science.gov (United States)

    Kane, P.; Marincic, N.; Epstein, J.; Lindsey, A.

    A long-life lithium battery for industrial applications at temperatures up to 200 C was developed by combining Li-based alloy anodes with oxyhalide electrolytes. Cathodes were fabricated by rolling the blend of polycarbonomonofluoride, a conductive carbon additive, and a binder, while anodes were fabricated as those used in oxyhalide cells, incorporating a modified anode current collector designed to prevent the formation of 'lithium islands' at the end of discharge; nonwoven glass fiber separators were pretreated to remove excessive binders and lubricants. Various active electrode surface areas were combined with a corresponding thickness of electrodes and separators, matched in capacity. Tests of the high-rate electrode structure, using Li-Mg alloy anode in conjunction with thionyl chloride electrolyte, have demonstrated that the battery with this anode can be used under abusive conditions such as short circuit and external heating (at 175 C). Raising the operating temperature to 200 C did require some modifications of regular cell hardware.

  5. Preparation and Hydrodesulfurization Performance of Ni-B Amorphous Alloy Catalyst Supported by APTS Modified SBA-15%APTS改性SBA-15负载Ni-B非晶态合金催化剂的制备及加氢脱硫性能

    Institute of Scientific and Technical Information of China (English)

    谌伟庆; 黄勇; 石秋杰

    2012-01-01

    SBA-15 was modified by APTS with covalent grafting method,and then Ni-B amorphous alloy catalysts were prepared by using APTS modified SBA-15 and unmodified SBA-15 as supports.The catalytic activities of both catalysts were characterized,and thiophene hydrodesulfurization was selected as probe reaction.The results show that thiophene conversation of Ni-B/SBA-15-APTS is 50.8%,which is higher than the one of Ni-B/SBA-15.The complexation between NH2 and Ni2+ would be benefit for dispersion of Ni-B alloy particles and reduction of Ni2+.According to ICP results,Ni-B/SBA-15-APTS show bigger quantity of Ni in support and higher content of Ni in Ni-B amorphous alloy than Ni-B/SBA-15,resulting in the higher activity.%采用共价接枝法制备APTS改性介孔分子筛SBA-15,将氨基官能团接枝到SBA-15表面.并采用化学还原法制备了Ni-B/SBA-15-APTS非晶态合金催化剂,以噻吩加氢脱硫为探针反应,研究了其催化加氢脱硫性能.结果表明,240℃时,APTS改性SBA-15所负载的Ni-B催化剂噻吩转化率达到50.8%,较未改性SBA-15所负载的催化剂噻吩转化率有显著地提高.由于氨基与Ni2+的配合作用,有助于Ni在催化剂中的分散,因而更容易被还原.ICP结果表明,在相同的制备条件下,相比未改性的SBA-15,APTS改性SBA-15使其催化剂中Ni的负载量增加,并且非晶态合金组成中Ni的含量也增大,B的含量降低,有利于提高催化剂的活性.

  6. Nano-gold Catalyst for Direct Alcohol Fuel Cells

    Institute of Scientific and Technical Information of China (English)

    Z.Ogumi; K.Miyazaki; Y.Iriyama; T.Abe

    2007-01-01

    1 Results Direct alcohol fuel cells have been regarded as attractive power sources for portable electric devices. One of the major roadblocks to the implementation of direct alcohol fuel cells is the exploration of the anode catalyst that can electrochemically oxidize alcohols at lower potentials. Carbon-monoxide (CO) produced through alcohol oxidation deteriorates catalytic activity of Pt, and therefore, the high tolerance for CO poisoning is an important issue to attain high voltage from direct alcoho...

  7. Microfabrication of an anodic oxide film by anodizing laser-textured aluminium

    OpenAIRE

    2007-01-01

    A simple method for the fabrication of microstructures of an aluminium anodic oxide film (anodic alumina) by anodizing laser-textured aluminium is demonstrated. In the process, the aluminium substrate was first textured by a low power laser beam, and then the textured aluminium was subjected to anodizing, to develop a continuous, thick porous layer on the textured surface. Microstructures with a depth of a few to several tens of micrometres were fabricated successfully on the anodic oxide fil...

  8. In silico search for novel methane steam reforming catalysts

    DEFF Research Database (Denmark)

    Xu, Yue; Lausche, Adam C; Wang, Shengguang

    2013-01-01

    This paper demonstrates a method for screening transition metal and metal alloy catalysts based on their predicted rates and stabilities for a given catalytic reaction. This method involves combining reaction and activation energies (available to the public via a web-based application ‘CatApp’) w...

  9. Ellipsometry of anodic film growth

    Energy Technology Data Exchange (ETDEWEB)

    Smith, C.G.

    1978-08-01

    An automated computer interpretation of ellisometer measurements of anodic film growth was developed. Continuous mass and charge balances were used to utilize more fully the time dependence of the ellipsometer data and the current and potential measurements. A multiple-film model was used to characterize the growth of films which proceeds via a dissolution--precipitation mechanism; the model also applies to film growth by adsorption and nucleation mechanisms. The characteristic parameters for film growth describe homogeneous and heterogeneous crystallization rates, film porosities and degree of hydration, and the supersaturation of ionic species in the electrolyte. Additional descriptions which may be chosen are patchwise film formation, nonstoichiometry of the anodic film, and statistical variations in the size and orientation of secondary crystals. Theories were developed to describe the optical effects of these processes. An automatic, self-compensating ellipsometer was used to study the growth in alkaline solution of anodic films on silver, cadmium, and zinc. Mass-transport conditions included stagnant electrolyte and forced convection in a flow channel. Multiple films were needed to characterize the optical properties of these films. Anodic films grew from an electrolyte supersatuated in the solution-phase dissolution product. The degree of supersaturation depended on transport conditions and had a major effect on the structure of the film. Anodic reaction rates were limited by the transport of charge carriers through a primary surface layer. The primary layers on silver, zinc, and cadmium all appeared to be nonstoichiometric, containing excess metal. Diffusion coefficients, transference numbers, and the free energy of adsorption of zinc oxide were derived from ellipsometer measurements. 97 figures, 13 tables, 198 references.

  10. Effect of Process Variables on the Formation of Streak Defects on Anodized Aluminum Extrusions: An Overview

    Science.gov (United States)

    Zhu, Hanliang; Couper, Malcolm J.; Dahle, Arne K.

    2012-04-01

    Streak defects are often present on anodized extrusions of 6xxx series aluminum alloys, increasing the fabrication cost of these products. Moreover, streaking often only becomes visible after etching and anodizing treatments, rather than in the as-extruded condition, making it difficult to identify the original causes and influencing factors of these defects. In this paper, various process variables that influence the formation of streak defects on anodized aluminium extrusions are reviewed on the basis of a literature review, industrial practice and experimental results. The influencing factors involved in various processing steps such as billet quality, extrusion process, die design and etching process are considered. Effective measures for preventing the formation of streak defects in industrial extrusion products are discussed.

  11. Pd Close Coupled Catalyst

    Institute of Scientific and Technical Information of China (English)

    Zhong Hua SHI; Mao Chu GONG; Yao Qiang CHEN

    2006-01-01

    A catalyst comprised novel high surface area alumina support was prepared to control emission of automobiles. The results showed that prepared catalyst could satisfy the requirements of a high performance close coupled catalyst for its good catalytic activity at low temperature and good stability at high temperature.

  12. [Vernier Anode Design and Image Simulation].

    Science.gov (United States)

    Zhao, Ai-rong; Ni, Qi-liang; Song, Ke-fei

    2015-12-01

    Based-MCP position-sensitive anode photon-counting imaging detector is good at detecting extremely faint light, which includes micro-channel plate (MCP), position-sensitive anode and readout, and the performances of these detectors are mainly decided by the position-sensitive anode. As a charge division anode, Vernier anode using cyclically varying electrode areas which replaces the linearly varying electrodes of wedge-strip anode can get better resolution and greater electrode dynamic range. Simulation and design of the Vernier anode based on Vernier's decode principle are given here. Firstly, we introduce the decode and design principle of Vernier anode with nine electrodes in vector way, and get the design parameters which are the pitch, amplitude and the coarse wavelength of electrode. Secondly, we analyze the effect of every design parameters to the imaging of the detector. We simulate the electron cloud, the Vernier anode and the detector imaging using Labview software and get the relationship between the pitch and the coarse wavelength of the anode. Simultaneously, we get the corresponding electron cloud for the designing parameters. Based on the result of the simulation and the practical machining demand, a nine electrodes Vernier anode was designed and fabricated which has a pitch of 891 µm, insulation width of 25 µm, amplitude of 50 µm, coarse pixel numbers of 5.

  13. Electrocatalysis of carbon anode in aluminium electrolysis

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The anodic overvoltage of the carbon anode in aluminum electrolysis isof the order of 0.6 V at normal current densities. However, it can be reduced somewhat by doping the anode carbon with various inorganic compounds. A new apparatus was designed to improve the precision of overvoltage measurements. Anodes were doped with MgAl2O4 and AlF3 both by impregnation of the coke and by adding powder, and the measured overvoltage was compared with that of undoped samples. For prebake type anodes baked at around 1150 oC, the anodic overvoltage was reduced by 40-60 mV, and for Soderberg type anodes, baked at 950 oC, by 60-80 mV.

  14. Carbon Materials Metal/Metal Oxide Nanoparticle Composite and Battery Anode Composed of the Same

    Science.gov (United States)

    Hung, Ching-Cheh (Inventor)

    2006-01-01

    A method of forming a composite material for use as an anode for a lithium-ion battery is disclosed. The steps include selecting a carbon material as a constituent part of the composite, chemically treating the selected carbon material to receive nanoparticles, incorporating nanoparticles into the chemically treated carbon material and removing surface nanoparticles from an outside surface of the carbon material with incorporated nanoparticles. A material making up the nanoparticles alloys with lithium.

  15. Structure and Stability of Pt-Y Alloy Particles for Oxygen Reduction Studied by Electron Microscopy

    DEFF Research Database (Denmark)

    Deiana, Davide; Wagner, Jakob Birkedal; Hansen, Thomas Willum

    2015-01-01

    Platinum-yttrium alloy nanoparticles show both a high activity and stability for the oxygen reduction reaction. The catalysts were prepared by magnetron sputter aggregation and mass filtration providing a model catalyst system with a narrow size distribution. The structure and stability...... of nanostructured Pt-Y alloy catalysts were studied using transmission electron microscopy techniques. Using elemental X-ray mapping and high-resolution electron microscopy, the specific compositional structure and distribution of the individual nanoparticles was unraveled and the stability assessed. Studying...... the catalyst after reaction and after aging tests shows the development of a core-shell type structure after being exposed to reaction conditions....

  16. Corrosion of Aluminum Alloys by IRFNA

    Science.gov (United States)

    1990-02-24

    and electropolishing and anodising, have been studied. aNeither had a significant long term effect on the corrosion rate of 2014 alumninium alloy in... steel spatula. (iv) The cell was assembled and raw eghed, the charge of galled Acid being determined by difference. Two additional bottom-working...The anodiuing solution was 1swt% sulphuric acid And the conditions were 25oC, 1 Mwm, 12V. The anodic oxide film waS scaled in delonised water (30

  17. Effects of Anode Wettability and Slots on Anodic Bubble Behavior Using Transparent Aluminium Electrolytic Cells

    Science.gov (United States)

    Zhao, Zhibin; Gao, Bingliang; Feng, Yuqing; Huang, Yipeng; Wang, Zhaowen; Shi, Zhongning; Hu, Xianwei

    2017-02-01

    Transparent aluminum electrolytic cells were used to study the effects of anode wettability and slots on bubble behavior in a similar environment to that used in industrial cells. Observations were conducted using two types of transparent cells, one with side-observation and the other with a bottom-observation cell design. Anodic bubbles rising process in the side channel is strongly affected by the wettability of the anode. After rising a short distance, the bubbles detach from the anode vertical surface at good-wetting anode cases, while the bubbles still attach to the vertical surface at poor-wetting anode cases. Anode slots of width of 4 mm are able to prevent smaller bubbles from coalescing into larger bubbles and thus decrease the bubble size and gas coverage on the anode. Anode slots also make a contribution in slightly reducing bubble thickness. With the presence of slots, the bubble-induced cell voltage oscillation decreases as well.

  18. Fabrication and anodic polarization behavior of lead-based porous anodes in zinc electrowinning

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A new type of lead-based porous anode in zinc electrowinning was prepared by negative pressure infiltration.The anodie polarization potential and corrosion rate were studied and compared with those of traditional fiat anodes (Pb-0.8%Ag) used in industry.The anode eorrosion rate was determined by anode actual current density and microstructure.The results show that the anodic oxygen evolution potential decreases first and then increases with the decrease of pore diameter.The anodic potential decreases to the lowest value of 1.729 V at the pore diameter of 1.25-1.60 mm.The porous anode can decrease its actual current density and thus decrease the anodic corrosion rate.When the pore diameter is 1.60-2.00 mm,the anodic relative corrosion rate reaches the lowest value of 52.1%.

  19. Vapor phase hydrogenation of furfural over nickel mixed metal oxide catalysts derived from layered double hydroxides

    Energy Technology Data Exchange (ETDEWEB)

    Sulmonetti, Taylor P.; Pang, Simon H.; Claure, Micaela Taborga; Lee, Sungsik; Cullen, David A.; Agrawal, Pradeep K.; Jones, Christopher W.

    2016-05-01

    The hydrogenation of furfural is investigated over various reduced nickel mixed metal oxides derived from layered double hydroxides (LDHs) containing Ni-Mg-Al and Ni-Co-Al. Upon reduction, relatively large Ni(0) domains develop in the Ni-Mg-Al catalysts, whereas in the Ni-Co-Al catalysts smaller metal particles of Ni(0) and Co(0), potentially as alloys, are formed, as evidenced by XAS, XPS, STEM and EELS. All the reduced Ni catalysts display similar selectivities towards major hydrogenation products (furfuryl alcohol and tetrahydrofurfuryl alcohol), though the side products varied with the catalyst composition. The 1.1Ni-0.8Co-Al catalyst showed the greatest activity per titrated site when compared to the other catalysts, with promising activity compared to related catalysts in the literature. The use of base metal catalysts for hydrogenation of furanic compounds may be a promising alternative to the well-studied precious metal catalysts for making biomass-derived chemicals if catalyst selectivity can be improved in future work by alloying or tuning metal-oxide support interactions.

  20. Interfacial phenomena in electric field-assisted anodic bonding of Kovar/Al film-glass

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Anodic bonding of glass to Kovar alloy coated with Al film (Glass-Al film/Kovar) was performed in the temperature range of 513~713?K under the static electric voltage of 500?V in order to investigate the interfacial phenomena of Al-glass joint. The results reveal that Na and K ions within the glass are displaced by the applied field from the anode-side surface of the glass to form depletion layers of them. The K ion depletion layer is narrow and followed by a K pile-up layer, and both the two layers are formed within the Na depletion layer. The width of the Na and K depletion layers is increased with increasing bonding temperature and time. The activation energies for the growth of both depletion layers were close to that for Na diffusion in the glass. TEM observations reveal that Al film coated at the surface of Kovar alloy is oxidized to amorphous Al2O3 containing a few of Fe, Ni and Co by oxygen ions from the glass drifted by high electric field during bonding. The amount of Fe ions diffusing into the glass adjacent to the anode is significantly low due to the presence of Al film between Kovar alloy and the glass. As a result, the amorphous reaction layer of Fe-Si-O in the glass near the interface is avoided which is formed in Kovar-glass joints.

  1. Effect of surface treatments on anodic oxide film growth and electrochemical properties of tantalum used for biomedical applications.

    Science.gov (United States)

    Silva, R A; Silva, I P; Rondot, B

    2006-07-01

    Self-expandable nitinol (nickel-titanium) alloys and 316L stainless steel are the most commonly used materials in the production of coronary stents. However, tantalum (Ta) has already been used to make stents for endovascular surgery and may constitute an alternative to other materials because of its better electrochemical performance, namely its higher corrosion resistance, as well as its radio-opacity. The characterization of wet polished, chemically polished, wet polished anodized, and chemically polished anodized Ta electrodes has been performed in a 0.15 M NaCl solution (simulated body fluid) using Ucorr = f(t) measurements, anodic polarizations, capacity measurements, anodic oxidations, and atomic force microscopy (AFM) imaging. Anodic polarization curves have shown that the abnormal current density peak with a maximum value around 1.65 V (critical applied potential, Uc) disappeared for the anodized electrodes indicating a probable relationship between the surface states and the film growth. These results are confirmed by capacity measurements. The behavior of wet polished and chemically polished electrodes during anodic oxidations seemingly indicated that for these particular treatments the film growth is different. The AFM images and roughness measurements have shown that chemical polishing produced smoother electrodes, a fact probably related to the differences in film growth.

  2. Ceramic Lithium Ion Conductor to Solve the Anode Coking Problem of Practical Solid Oxide Fuel Cells.

    Science.gov (United States)

    Wang, Wei; Wang, Feng; Chen, Yubo; Qu, Jifa; Tadé, Moses O; Shao, Zongping

    2015-09-07

    For practical solid oxide fuel cells (SOFCs) operated on hydrocarbon fuels, the facile coke formation over Ni-based anodes has become a key factor that limits their widespread application. Modification of the anodes with basic elements may effectively improve their coking resistance in the short term; however, the easy loss of basic elements by thermal evaporation at high temperatures is a new emerging problem. Herein, we propose a new design to develop coking-resistant and stable SOFCs using Li(+) -conducting Li0.33 La0.56 TiO3 (LLTO) as an anode component. In the Ni/LLTO composite, any loss of surface lithium can be efficiently compensated by lithium diffused from the LLTO bulk under operation. Therefore, the SOFC with the Ni/LLTO anode catalyst layer yields excellent power outputs and operational stability. Our results suggest that the simple adoption of a Li(+) conductor as a modifier for Ni-based anodes is a practical and easy way to solve the coking problem of SOFCs that operate on hydrocarbons.

  3. Discovering Inexpensive, Effective Catalysts for Solar Energy Conversion: An Authentic Research Laboratory Experience

    Science.gov (United States)

    Shaner, Sarah E.; Hooker, Paul D.; Nickel, Anne-Marie; Leichtfuss, Amanda R.; Adams, Carissa S.; de la Cerda, Dionisia; She, Yuqi; Gerken, James B.; Pokhrel, Ravi; Ambrose, Nicholas J.; Khaliqi, David; Stahl, Shannon S.; Schuttlefield Christus, Jennifer D.

    2016-01-01

    Electrochemical water oxidation is a major focus of solar energy conversion efforts. A new laboratory experiment has been developed that utilizes real-time, hands-on research to discover catalysts for solar energy conversion. The HARPOON, or Heterogeneous Anodes Rapidly Perused for Oxygen Overpotential Neutralization, experiment allows an array of…

  4. Electrochemical oxidation of carbon monoxide: from platinum single crystals to low temperature fuel catalysts. Part II: Electrooxidation of H2, CO and H2/CO mixtures on well characterized PtMo alloy

    Directory of Open Access Journals (Sweden)

    PHILIP N. ROSS JR.

    2003-03-01

    Full Text Available The oxidation of hydrogen and hydrogen–carbon monoxide mixture has been investigated on well-characterized metallurgically prepared platinum–molybdenum (PtMo alloys. It was concluded that the optimum surface concentration of molybdenum is near 23 mol.%. Based on experimentally determined parameters and simulations, the mechanism of the oxidation of CO/H2 mixtures is discussed.

  5. Metalloporphyrin catalysts for oxygen reduction developed using computer-aided molecular design

    Energy Technology Data Exchange (ETDEWEB)

    Ryba, G.N.; Hobbs, J.D.; Shelnutt, J.A. [and others

    1996-04-01

    The objective of this project is the development of a new class of metalloporphyrin materials used as catalsyts for use in fuel cell applications. The metalloporphyrins are excellent candidates for use as catalysts at both the anode and cathode. The catalysts reduce oxygen in 1 M potassium hydroxide, as well as in 2 M sulfuric acid. Covalent attachment to carbon supports is being investigated. The computer-aided molecular design is an iterative process, in which experimental results feed back into the design of future catalysts.

  6. Reactions on carbon anodes in aluminium electrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Eidet, Trygve

    1997-12-31

    The consumption of carbon anodes and energy in aluminium electrolysis is higher than what is required theoretically. This thesis studies the most important of the reactions that consume anode materials. These reactions are the electrochemical anode reaction and the airburn and carboxy reactions. The first part of the thesis deals with the kinetics and mechanism of the electrochemical anode reaction using electrochemical impedance spectroscopy. The second part deals with air and carboxy reactivity of carbon anodes and studies the effects of inorganic impurities on the reactivity of carbon anodes in the aluminium industry. Special attention is given to sulphur since its effect on the carbon gasification is not well understood. Sulphur is always present in anodes, and it is expected that the sulphur content of available anode cokes will increase in the future. It has also been suggested that sulphur poisons catalyzing impurities in the anodes. Other impurities that were investigated are iron, nickel and vanadium, which are common impurities in anodes which have been reported to catalyze carbon gasification. 88 refs., 92 figs., 24 tabs.

  7. Anodization of Ti-based materials for biomedical applications: A review

    Directory of Open Access Journals (Sweden)

    Dragana R. Barjaktarević

    2016-09-01

    Full Text Available Commercially pure titanium (cpTi and titanium alloys are the most commonly used metallic biomaterials. Biomedical requirements for the successful usage of metallic implant materials include their high mechanical strength, low elastic modulus, excellent biocompatibility and high corrosion resistance. It is evident that the response of a biomaterial implanted into the human body depends entirely on its biocompatibility and surface properties. Therefore, in order to improve the performance of biomaterials in biological systems modification of their surface is necessary. One of most commonly used method of implant materials surface modification is electrochemical anodization and this method is reviewed in the present work.Aim of the presented review article is to explain the electrochemical anodization process and the way in which the nanotubes are formed by anodization on the metallic material surface. Influence of anodizing parameters on the nanotubes characteristics, such as nanotube diameter, length and nanotubular layer thickness, are described, as well as the anodized nanotubes influence on the material surface properties, corrosion resistance and biocompatibility.

  8. Self-ordered nanopore arrays through hard anodization assisted by anode temperature ramp

    Science.gov (United States)

    Mohammadniaei, M.; Maleki, K.; Kashi, M. Almasi; Ramezani, A.; Mayamei, Y.

    2016-10-01

    In the present work, hard anodization assisted by anode temperature ramp was employed to fabricate self-ordered nanoporous alumina in the wide range of interpore distances (259-405 nm) in pure oxalic acid and mixture of oxalic and phosphoric acid solutions. Anode temperature ramp technique was employed to adjust the anodization current density to optimize the self-ordering of the nanopore arrays in the interpore range in which no ordered self-assembled hard anodized anodic aluminum oxide has reported. It is found that the certain ratios of oxalic and phosphoric acid solutions in this anodization technique increased self-ordering of the nanopores especially for anodization voltages over the 170 V by increasing alumina's viscous flow which could lead to decrease the overall current density of anodization, yet leveled up by anode temperature ramp. However, below 150 V anodization voltage, the ratio of interpore distance to the anodization voltage of the both anodization techniques was the same (~2 nm/V), while above this voltage, it increased to about 2.2 nm/V.

  9. Improvement of low-humidity performance of PEMFC by addition of hydrophilic SiO 2 particles to catalyst layer

    Science.gov (United States)

    Jung, Un Ho; Park, Ki Tae; Park, Eun Hee; Kim, Sung Hyun

    Hydrophilic SiO 2 particles are added to the catalyst layer of a fuel cell membrane-electrode assembly (MEA) to improve wettability and performance at low-humidity conditions. The SiO 2 added MEAs are prepared by spraying technique and the contact angle is measured by the sessile drop method. The effects of SiO 2 additions of 0, 20, 40 and 60 wt.% (based on Pt/C) are investigated for various relative humidity levels in the anode and the cathode. The increased wettability of the cathode catalyst layer exerts an adverse effect on cell performance by causing flooding; this result demonstrates the hydrophilicity of SiO 2. With 40 wt.% addition of SiO 2 to the anode catalyst layer, the current density at 0.6 V and 0% relative humidity of the anode is 93% of that at 100% relative humidity. By comparison, the performance of a cell using a MEA with no added SiO 2 is only 85% of that at 0% relative humidity. A MEA with SiO 2 addition in the anode gives a higher performance at 60% relative humidity of the cathode than one with an undoped MEA. Increased wettability of the anode catalyst layer caused by SiO 2 addition renders it easy to absorb water from back diffusion.

  10. 石墨烯制备及其在低温燃料电池阳极催化中的应用进展%The preparation of Graphenes and their application progress in anode catalyst of low temperature fuel cell

    Institute of Scientific and Technical Information of China (English)

    田春贵; 付宏刚

    2011-01-01

    Graphene, an new star in the material science, has attracted intensive attention in electronics, energy, environment and catalysis. For application in electro-catalysis, the special structure of graphene are favorable to dispersion and stability of noble metal catalyst, thus to enhance largely catalytic activity of metal catalyst. In this paper, the preparation methods of graphene are introduced, and the design of noble metal/graphene electro - catalysts is also be reviewed.%石墨烯是材料科学领域的新星,在电子、能源、环境、生物医学及催化领域的应用备受关注.在电催化领域,石墨烯特殊的结构有利于贵金属催化剂的分散和稳定,可大幅度提高贵金属的催化活性,是理想的载体材料.本文对石墨烯的制备方法及贵金属/石墨烯电催化剂的设计合成的研究进展进行评述.

  11. Fabrication and evaluation of nickel cobalt alloy electrocatalysts for alkaline water splitting

    Energy Technology Data Exchange (ETDEWEB)

    Hong, Sung Hoon [School of Integrative Engineering, Chung-Ang University, Heukseokno 84, Dongjak-gu, Seoul 156-756 (Korea, Republic of); Ahn, Sang Hyun; Choi, Insoo [Fuel Cell Research Center, Korea Institute of Science and Technology, Hwarangno 14-gil 5, Seongbuk-gu, Seoul 136-791 (Korea, Republic of); Pyo, Sung Gyu [School of Integrative Engineering, Chung-Ang University, Heukseokno 84, Dongjak-gu, Seoul 156-756 (Korea, Republic of); Kim, Hyoung-Juhn; Jang, Jong Hyun [Fuel Cell Research Center, Korea Institute of Science and Technology, Hwarangno 14-gil 5, Seongbuk-gu, Seoul 136-791 (Korea, Republic of); Kim, Soo-Kil, E-mail: sookilkim@cau.ac.kr [School of Integrative Engineering, Chung-Ang University, Heukseokno 84, Dongjak-gu, Seoul 156-756 (Korea, Republic of)

    2014-07-01

    As a catalyst for the hydrogen evolution reaction (HER) in alkaline water splitting, NiCo alloys of various compositions were prepared through electrodeposition onto Cu substrates. The composition of each alloy catalyst was varied by controlling the molar ratio of Co{sup 2+} ions in the electrolyte. With an increase in the Co content, the morphologies of the NiCo alloys were progressively changed from a round to polygonal shape. The NiCo alloys all exhibited a Ni rich surface, as confirmed by the bulk-to-surface compositional ratio and degree of alloying. The catalytic activities of the NiCo alloys toward the HER of water splitting were electrochemically tested in a KOH electrolyte, and the specific activities were characterized by considering the electrochemical surface areas of Ni and Co. The effect of alloying was demonstrated to be a significant enhancement of HER activity, resulting from a change in the electronic structures of Ni and Co.

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

    Science.gov (United States)

    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/dm2 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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Dongya; Dong, Guangneng, E-mail: donggn@mail.xjtu.edu.cn; Chen, Yinjuan; Zeng, Qunfeng

    2014-01-30

    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{sup 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.

  14. Robust CoAl Alloy: Highly Active, Reusable and Green Catalyst in the Hydrogenolysis of Glycerol%Robust CoAl Alloy: Highly Active, Reusable and Green Catalyst in the Hydrogenolysis of Glycerol

    Institute of Scientific and Technical Information of China (English)

    郭晓洋; 尹安远; 郭晓东; 郭秀英; 戴维林; 范康年

    2011-01-01

    CoAl alloy catalyst is found, for the first time, to be highly active, selective and reusable for the synthesis of diols via the hydrogenolysis of glycerol under mild conditions. The products and the catalyst could be self-separated from the reaction system through a simple reactor.

  15. Structural engineering of nanoporous anodic aluminium oxide by pulse anodization of aluminium.

    Science.gov (United States)

    Lee, Woo; Schwirn, Kathrin; Steinhart, Martin; Pippel, Eckhard; Scholz, Roland; Gösele, Ulrich

    2008-04-01

    Nanoporous anodic aluminium oxide has traditionally been made in one of two ways: mild anodization or hard anodization. The first method produces self-ordered pore structures, but it is slow and only works for a narrow range of processing conditions; the second method, which is widely used in the aluminium industry, is faster, but it produces films with disordered pore structures. Here we report a novel approach termed "pulse anodization" that combines the advantages of the mild and hard anodization processes. By designing the pulse sequences it is possible to control both the composition and pore structure of the anodic aluminium oxide films while maintaining high throughput. We use pulse anodization to delaminate a single as-prepared anodic film into a stack of well-defined nanoporous alumina membrane sheets, and also to fabricate novel three-dimensional nanostructures.

  16. Synthesis and characterization of hybrid micro/nano-structured NiTi surfaces by a combination of etching and anodizing.

    Science.gov (United States)

    Huan, Z; Fratila-Apachitei, L E; Apachitei, I; Duszczyk, J

    2014-02-07

    The purpose of this study was to generate hybrid micro/nano-structures on biomedical nickel-titanium alloy (NiTi). To achieve this, NiTi surfaces were firstly electrochemically etched and then anodized in fluoride-containing electrolyte. With the etching process, the NiTi surface was micro-roughened through the formation of micropits uniformly distributed over the entire surface. Following the subsequent anodizing process, self-organized nanotube structures enriched in TiO2 could be superimposed on the etched surface under specific conditions. Furthermore, the anodizing treatment significantly reduced water contact angles and increased the surface free energy compared to the surfaces prior to anodizing. The results of this study show for the first time that it is possible to create hybrid micro/nano-structures on biomedical NiTi alloys by combining electrochemical etching and anodizing under controlled conditions. These novel structures are expected to significantly enhance the surface biofunctionality of the material when compared to conventional implant devices with either micro- or nano-structured surfaces.

  17. Synthesis and characterization of hybrid micro/nano-structured NiTi surfaces by a combination of etching and anodizing

    Science.gov (United States)

    Huan, Z.; Fratila-Apachitei, L. E.; Apachitei, I.; Duszczyk, J.

    2014-02-01

    The purpose of this study was to generate hybrid micro/nano-structures on biomedical nickel-titanium alloy (NiTi). To achieve this, NiTi surfaces were firstly electrochemically etched and then anodized in fluoride-containing electrolyte. With the etching process, the NiTi surface was micro-roughened through the formation of micropits uniformly distributed over the entire surface. Following the subsequent anodizing process, self-organized nanotube structures enriched in TiO2 could be superimposed on the etched surface under specific conditions. Furthermore, the anodizing treatment significantly reduced water contact angles and increased the surface free energy compared to the surfaces prior to anodizing. The results of this study show for the first time that it is possible to create hybrid micro/nano-structures on biomedical NiTi alloys by combining electrochemical etching and anodizing under controlled conditions. These novel structures are expected to significantly enhance the surface biofunctionality of the material when compared to conventional implant devices with either micro- or nano-structured surfaces.

  18. Electrochemical behavior of cast Ti-Ag alloys.

    Science.gov (United States)

    Takahashi, Masatoshi; Kikuchi, Masafumi; Takadai, Yukyo; Okabe, Toru; Okuno, Osamu

    2006-09-01

    Anodic polarization tests were performed in 0.9% NaCl and 1% lactic acid solutions to characterize the relationship between the corrosion behavior and the microstructures of cast Ti-Ag (5-40% Ag) alloys. The anodic polarization curves for the Ti-Ag alloys up to 17.5% Ag were similar to those for pure titanium in both solutions. On the other hand, an abrupt increase in the current density was observed for the alloys with more than 20% Ag in the NaCl solution and with more than 27.5% Ag in the lactic acid solution. The microstructures of the corroded alloy surfaces indicated the deterioration of precipitated intermetallic compounds along the grain boundaries. The Ti-Ag alloys up to 17.5% Ag had excellent corrosion resistance similar to that of pure titanium. The alloys with 20-25% Ag may be also used as dental alloys, since they passivated again immediately after preferential dissolution in the NaCl solution.

  19. Alternative anode materials for solid oxide fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Goodenough, John B.; Huang, Yun-Hui [Texas Materials Institute, ETC 9.102, 1 University Station, C2200, The University of Texas at Austin, Austin, TX 78712 (United States)

    2007-11-08

    The electrolyte of a solid oxide fuel cell (SOFC) is an O{sup 2-}-ion conductor. The anode must oxidize the fuel with O{sup 2-} ions received from the electrolyte and it must deliver electrons of the fuel chemisorption reaction to a current collector. Cells operating on H{sub 2} and CO generally use a porous Ni/electrolyte cermet that supports a thin, dense electrolyte. Ni acts as both the electronic conductor and the catalyst for splitting the H{sub 2} bond; the oxidation of H{sub 2} to H{sub 2}O occurs at the Ni/electrolyte/H{sub 2} triple-phase boundary (TPB). The CO is oxidized at the oxide component of the cermet, which may be the electrolyte, yttria-stabilized zirconia, or a mixed oxide-ion/electron conductor (MIEC). The MIEC is commonly a Gd-doped ceria. The design and fabrication of these anodes are evaluated. Use of natural gas as the fuel requires another strategy, and MIECs are being explored for this application. The several constraints on these MIECs are outlined, and preliminary results of this on-going investigation are reviewed. (author)

  20. Anodic Materials for Electrocatalytic Ozone Generation

    Directory of Open Access Journals (Sweden)

    Yun-Hai Wang

    2013-01-01

    Full Text Available Ozone has wide applications in various fields. Electrocatalytic ozone generation technology as an alternative method to produce ozone is attractive. Anodic materials have significant effect on the ozone generation efficiency. The research progress on anodic materials for electrocatalytic ozone generation including the cell configuration and mechanism is addressed in this review. The lead dioxide and nickel-antimony-doped tin dioxide anode materials are introduced in detail, including their structure, property, and preparation. Advantages and disadvantages of different anode materials are also discussed.

  1. Resin Catalyst Hybrids

    Institute of Scientific and Technical Information of China (English)

    S. Asaoka

    2005-01-01

    @@ 1Introduction: What are resin catalyst hybrids? There are typically two types of resin catalyst. One is acidic resin which representative is polystyrene sulfonic acid. The other is basic resin which is availed as metal complex support. The objective items of this study on resin catalyst are consisting of pellet hybrid, equilibrium hybrid and function hybrid of acid and base,as shown in Fig. 1[1-5].

  2. Towards the Rational Design of Nanoparticle Catalysts

    Science.gov (United States)

    Dash, Priyabrat

    stabilization in BMIMPF6 IL is described, and have shown that nanoparticle stability and catalytic activity of nanoparticles is dependent on the overall stability of the nanoparticles towards aggregation (manuscript submitted). The second major project is focused on synthesizing structurally well-defined supported catalysts by incorporating the nanoparticle precursors (both alloy and core shell) into oxide frameworks (TiO2 and Al2O 3), and examining their structure-property relationships and catalytic activity. a full article has been published on this project (Journal of Physical Chemistry C, 2009, 113, 12719) in which a route to rationally design supported catalysts from structured nanoparticle precursors with precise control over size, composition, and internal structure of the nanoparticles has been shown. In a continuation of this methodology for the synthesis of heterogeneous catalysts, efforts were carried out to apply the same methodology in imidazolium-based ILs as a one-pot media for the synthesis of supported-nanoparticle heterogeneous catalysts via the trapping of pre-synthesized nanoparticles into porous inorganic oxide materials. Nanoparticle catalysts in highly porous titania supports were synthesized using this methodology (manuscript to be submitted).

  3. Bimetallic Nickel/Ruthenium Catalysts Synthesized by Atomic Layer Deposition for Low-Temperature Direct Methanol Solid Oxide Fuel Cells.

    Science.gov (United States)

    Jeong, Heonjae; Kim, Jun Woo; Park, Joonsuk; An, Jihwan; Lee, Tonghun; Prinz, Fritz B; Shim, Joon Hyung

    2016-11-09

    Nickel and ruthenium bimetallic catalysts were heterogeneously synthesized via atomic layer deposition (ALD) for use as the anode of direct methanol solid oxide fuel cells (DMSOFCs) operating in a low-temperature range. The presence of highly dispersed ALD Ru islands over a porous Ni mesh was confirmed, and the Ni/ALD Ru anode microstructure was observed. Fuel cell tests were conducted using Ni-only and Ni/ALD Ru anodes with approximately 350 μm thick gadolinium-doped ceria electrolytes and platinum cathodes. The performance of fuel cells was assessed using pure methanol at operating temperatures of 300-400 °C. Micromorphological changes of the anode after cell operation were investigated, and the content of adsorbed carbon on the anode side of the operated samples was measured. The difference in the maximum power density between samples utilizing Ni/ALD Ru and Pt/ALD Ru, the latter being the best catalyst for direct methanol fuel cells, was observed to be less than 7% at 300 °C and 30% at 350 °C. The improved electrochemical activity of the Ni/ALD Ru anode compared to that of the Ni-only anode, along with the reduction of the number of catalytically active sites due to agglomeration of Ni and carbon formation on the Ni surface as compared to Pt, explains this decent performance.

  4. Synergetic effects leading to coke-resistant NiCo bimetallic catalysts for dry reforming of methane

    KAUST Repository

    Li, Lidong

    2015-01-08

    A new dry reforming of methane catalyst comprised of NiCo bimetallic nanoparticles and a Mgx(Al)O support that exhibits high coke resistance and long-term on-stream stability is reported. The structural characterization by XRD, TEM, temperature-programmed reduction, and BET analysis demonstrates that the excellent performance of this catalyst is ascribed to the synergy of various parameters, including metal-nanoparticle size, metal-support interaction, catalyst structure, ensemble size, and alloy effects.

  5. Facile Synthesis of Nanoporous Pt-Y alloy with Enhanced Electrocatalytic Activity and Durability

    Science.gov (United States)

    Cui, Rongjing; Mei, Ling; Han, Guangjie; Chen, Jiyun; Zhang, Genhua; Quan, Ying; Gu, Ning; Zhang, Lei; Fang, Yong; Qian, Bin; Jiang, Xuefan; Han, Zhida

    2017-02-01

    Recently, Pt-Y alloy has displayed an excellent electrocatalytic activity for oxygen reduction reaction (ORR), and is regarded as a promising cathode catalyst for fuel cells. However, the bulk production of nanoscaled Pt-Y alloy with outstanding catalytic performance remains a great challenge. Here, we address the challenge through a simple dealloying method to synthesize nanoporous Pt-Y alloy (NP-PtY) with a typical ligament size of ~5 nm. By combining the intrinsic superior electrocatalytic activity of Pt-Y alloy with the special nanoporous structure, the NP-PtY bimetallic catalyst presents higher activity for ORR and ethanol oxidation reaction, and better electrocatalytic stability than the commercial Pt/C catalyst and nanoporous Pt alloy. The as-made NP-PtY holds great application potential as a promising electrocatalyst in proton exchange membrane fuel cells due to the advantages of facile preparation and excellent catalytic performance.

  6. Manufacture of Raney Ni catalyst with metastable Ni2Al3 by high-energy milling

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    The Ni-Al alloy containing Cr, Fe additives were prepared as Raney Ni catalyst by high energy milling. The size and surface state of Ni-Al alloy powder were studied by particle size analyzer and sanning electron microscopy, the structure was analyzed by XRD and Mossbauer methods. The results showed that after a high-energy milling (HEM), the Ni-Al alloy transforms to a nano-scale NiAl structure with rich Al. Byannealing the alloy, a metastable Ni2Al3 phase can be obtained.

  7. Manufacture of Raney Ni catalyst with metastable Ni2Al3 by high—energy milling

    Institute of Scientific and Technical Information of China (English)

    滕荣厚; 马如璋; 等

    1999-01-01

    The Ni-Al alloy containing Cr,Fe additives were prepared as Raney Ni Catalyst by high energy milling.The size and surface state of Ni-Al alloy powder were studied by particle size analyzer and sanning electron microscopy.the Structure was analyzed by XRD and Moessbauer methods.The results showed that after a high-energy milling(HEM).the Ni-Al alloy transforms to a nano-scale NiAl structure with rich Al.By annealing the alloy,a metastable Ni2Al3 phase can be obtained.

  8. Ternary alloy nanocatalysts for hydrogen evolution reaction

    Indian Academy of Sciences (India)

    SOUMEN SAHA; SONALIKA VAIDYA; KANDALAM V RAMANUJACHARY; SAMUEL E LOFLAND; ASHOK K GANGULI

    2016-04-01

    Cu–Fe–Ni ternary alloys (size ∼55–80 nm) with varying compositions viz. CuFeNi (A1), CuFe2Ni (A2) and CuFeNi2 (A3) were successfully synthesized using microemulsion. It is to be noted that synthesis of nanocrystallineternary alloys with precise composition is a big challenge which can be overcome by choosing an appropriate microemulsion system. High electrocatalytic activity towards HER in alkaline medium was achieved by the formation of alloys of metals with low and high binding energies. A high value of current density (228 mA cm$^2$) at an overpotential of 545 mV was obtained for CuFeNi (A1), which is significantly high as compared to the previously reported Ni$_{59}$Cu$_{41}$ alloy catalyst.

  9. Effect of the synthesis method of SnSb anode materials on their electrochemical properties

    Institute of Scientific and Technical Information of China (English)

    Chaoli Yin; Hailei Zhao; Hong Guo; Xianliang Huang; Weihua Qiu

    2007-01-01

    SnSb alloy powders for the anode of Li-ion batteries were synthesized by two kinds of reduction precipitation methods:solution titration and rapid mixing. Two kinds of SnSb alloy powders showed different phase compositions and particle morphologies although the same starting materials were used. The SnSb alloy electrode synthesized by titration exhibits high reversible specific capacity and good cycling stability, whereas the rapid-mixing sample shows high irreversible capacity and fast capacity fade. The broad particle size distribution of SnSb powders synthesized by titration is considered to be responsible for the improvement of cycling stability. The initial charge-discharge efficiency exceeding 80% has been obtained for the titration sample. The electrochemical reaction process of two kinds of synthesized SnSb composite electrodes was characterized by cyclic voltammetry and AC impedance techniques.

  10. Study on hemocompatibility and corrosion behavior of ion implanted TiNi shape memory alloy and Co-based alloys.

    Science.gov (United States)

    Liang, Chenghao; Huang, Naibao

    2007-10-01

    Biomedical TiNi shape memory alloy and Co-based alloys were ion implanted, and corrosion resistance and hemocompatibility of these had been investigated with electrochemical method, dynamic clotting time, and hemolysis rate tests. The results indicated that the electrochemical stability and anodic polarization behavior of the materials were improved significantly after ion implantation. When TiNi, Co-based alloys were implanted Mo + C and Ti + C, respectively, the corrosion potentials were enhanced more than 200 mV, passive current densities decreased, and passive ranges were broadened. Dynamic clotting time of the ion implanted substances was prolonged and hemolysis rate decreased. All the results pointed out that corrosion resistance and hemocompatibility of the alloys were improved by ion implantation, and effects of dual implantation was better than that of C single implantation. X-ray diffraction analysis of the alloys after dual implantation revealed that TiC, Mo(2)C, Mo(9)Ti(4), and Mo appeared on the surface of TiNi alloy, and CoC(x), Co(3)Ti, TiC, and TiO on the surface of Co-based alloys. These phases dispersing on the alloy surface formed amorphous film, prevented dissolving of alloy elements and improved the corrosion resistance and hemocompatibility of the alloys.

  11. [Hardened anodized aluminum as a replacement material for bracket manufacture].

    Science.gov (United States)

    Fischer-Brandies, H; Bönhoff, M

    1994-12-01

    Attention has been repeatedly drawn to the problem of corrosion and the risk of allergic reaction to nickel resulting from the use of stainless steel brackets. In the search for a suitable alternative, manufacturers have turned to thin coating technology using hardened anodized aluminium. Applying resistance to corrosion and abrasion as the criteria to be met, they have selected aluminium alloy type 6082 as the material of choice. Purpose of this study is to examine the physical suitability of this material. Using the above noted alloy, 60 prototype brackets were made with a hardened anodized surface. They were then subjected to the following 3 stress tests: first an abrasion test using a tooth polishing machine, second, a deformation test using a device designed to simulate torque movement, and, third, a corrosion test. The effects on the brackets resulting from the three types of stress were evaluated by light microscopy. A quantitative analysis of the corrosion test was performed by ICP spectrometry. The control group consisted of conventional stainless steel brackets. The light microscopic analysis revealed no evidence of surface damage or signs of deformation in the prototype brackets. The steel brackets, on the other hand, showed clear signs of wear and corrosion. The quantitative analysis of the corrosion solution revealed metallic ion wear of 1.75 ng x mm-2 x h-1 for the prototypes subjected to abrasion. The steel brackets showed at a factor of around 104.6 metallic ion wear of 183 ng x mm-2 x h-1. In addition to this, no Ni ions were found in the corrosion solution of the prototype brackets.(ABSTRACT TRUNCATED AT 250 WORDS)

  12. 以非晶态合金催化剂SRNA-4为固相的气液固磁稳定床的界面传质研究%Interphase Mass Transfer in G-L-S Magnetically Stabilized Bed with Amorphous Alloy SRNA-4 Catalyst

    Institute of Scientific and Technical Information of China (English)

    李(韦华); 宗保守; 李晓芳; 孟祥坤; 张金利

    2006-01-01

    Gas-liquid (G-L) and liquid-solid (L-S) mass transfer coefficients were characterized in a gas-liquid-solid(G-L-S) three-phase magnetically stabilized bed (MSB) using amorphous alloy SRNA-4 as the solid phase. Effects such as superficial liquid velocity, superficial gas velocity, magnetic strength, liquid viscosity, and particle size were investigated. Experimental results indicated that the G-L volumetric mass transfer coefficients (KLa) increased along with the magnetic strength, superficial gas and liquid velocities. Proper increase of liquid viscosity promoted KLa only in the range of lower liquid viscosity. The external magnetic field made L-S mass transfer coefficients (Ks)in the G-L-S MSB lower than those of conventional fluidized beds. Ks in the MSB almost kept constant as the superficial liquid velocity and superficial gas velocity increased and decreased with the liquid viscosity and surface tension, while increased with the particle size Ks showed uniform axial and radial distributions except of small decreases close to the wall. Dimensionless correlations were established to estimate KLa and Ks of the MSB with SRNA-4 catalysts, which showed the average error of 5.4% and 2.5% respectively.

  13. Quantum Mechanics Studies of Fuel Cell Catalysts and Proton Conducting Ceramics with Validation by Experiment

    Science.gov (United States)

    Tsai, Ho-Cheng

    We carried out quantum mechanics (QM) studies aimed at improving the performance of hydrogen fuel cells. In part I, The challenge was to find a replacement for the Pt cathode that would lead to improved performance for the Oxygen Reduction Reaction (ORR) while remaining stable under operational conditions and decreasing cost. Our design strategy was to find an alloy with composition Pt3M that would lead to surface segregation such that the top layer would be pure Pt, with the second and subsequent layers richer in M. Under operating conditions we expect the surface to have significant O and/or OH chemisorbed on the surface; we searched for M that would remain segregated under these conditions. Using QM we examined surface segregation for 28 Pt3M alloys, where M is a transition metal. We found that only Pt3Os and Pt3Ir showed significant surface segregation when O and OH are chemisorbed on the catalyst surfaces. This result indicates that Pt3Os and Pt 3Ir favor formation of a Pt-skin surface layer structure that would resist the acidic electrolyte corrosion during fuel cell operation environments. We chose to focus on Os because the phase diagram for Pt-Ir indicated that Pt-Ir could not form a homogeneous alloy at lower temperature. To determine the performance for ORR, we used QM to examine intermediates, reaction pathways, and reaction barriers involved in the processes for which protons from the anode reactions react with O2 to form H2O. These QM calculations used our Poisson-Boltzmann implicit solvation model include the effects of the solvent (water with dielectric constant 78 with pH 7 at 298K). We also carried out similar QM studies followed by experimental validation for the Os/Pt core-shell catalyst fabricated by the underpotential deposition (UPD) method. The QM results indicated that the RDS for ORR is a compromise between the OOH formation step (0.37 eV for Pt, 0.23 eV for Pt2ML/Os core-shell) and H2O formation steps (0.32 eV for Pt, 0.22 eV for Pt2ML

  14. Aluminum alloy

    Science.gov (United States)

    Blackburn, Linda B. (Inventor); Starke, Edgar A., Jr. (Inventor)

    1989-01-01

    This invention relates to aluminum alloys, particularly to aluminum-copper-lithium alloys containing at least about 0.1 percent by weight of indium as an essential component, which are suitable for applications in aircraft and aerospace vehicles. At least about 0.1 percent by weight of indium is added as an essential component to an alloy which precipitates a T1 phase (Al2CuLi). This addition enhances the nucleation of the precipitate T1 phase, producing a microstructure which provides excellent strength as indicated by Rockwell hardness values and confirmed by standard tensile tests.

  15. Anodization process produces opaque, reflective coatings on aluminum

    Science.gov (United States)

    1965-01-01

    Opaque, reflective coatings are produced on aluminum articles by an anodizing process wherein the anodizing bath contains an aqueous dispersion of finely divided insoluble inorganic compounds. These particles appear as uniformly distributed occlusions in the anodic deposit on the aluminum.

  16. Nickel-based anodic electrocatalysts for fuel cells and water splitting

    Science.gov (United States)

    Chen, Dayi

    Our world is facing an energy crisis, so people are trying to harvest and utilize energy more efficiently. One of the promising ways to harvest energy is via solar water splitting to convert solar energy to chemical energy stored in hydrogen. Another of the options to utilize energy more efficiently is to use fuel cells as power sources instead of combustion engines. Catalysts are needed to reduce the energy barriers of the reactions happening at the electrode surfaces of the water-splitting cells and fuel cells. Nickel-based catalysts happen to be important nonprecious electrocatalysts for both of the anodic reactions in alkaline media. In alcohol fuel cells, nickel-based catalysts catalyze alcohol oxidation. In water splitting cells, they catalyze water oxidation, i.e., oxygen evolution. The two reactions occur in a similar potential range when catalyzed by nickel-based catalysts. Higher output current density, lower oxidation potential, and complete substrate oxidation are preferred for the anode in the applications. In this dissertation, the catalytic properties of nickel-based electrocatalysts in alkaline medium for fuel oxidation and oxygen evolution are explored. By changing the nickel precursor solubility, nickel complex nanoparticles with tunable sizes on electrode surfaces were synthesized. Higher methanol oxidation current density is achieved with smaller nickel complex nanoparticles. DNA aggregates were used as a polymer scaffold to load nickel ion centers and thus can oxidize methanol completely at a potential about 0.1 V lower than simple nickel electrodes, and the methanol oxidation pathway is changed. Nickel-based catalysts also have electrocatalytic activity towards a wide range of substrates. Experiments show that methanol, ethanol, glycerol and glucose can be deeply oxidized and carbon-carbon bonds can be broken during the oxidation. However, when comparing methanol oxidation reaction to oxygen evolution reaction catalyzed by current nickel

  17. One pot aqueous synthesis of nanoporous Au85Pt15 material with surface bound Pt islands: an efficient methanol tolerant ORR catalyst

    Science.gov (United States)

    Anandha Ganesh, P.; Jeyakumar, D.

    2014-10-01

    For the first time, we are reporting the synthesis of Au100-xPtx nanoporous materials in the size range of 7-10 nm through the galvanic replacement of Ag by Pt from Au100-xAg2x spherical nano-alloys (x = 20, 15, 10 and 5) in an aqueous medium. The galvanic replacement reaction follows the `Volmer-Weber' growth mode, resulting in the formation of surface bound platinum islands on a nanoporous gold surface. The high angle annular dark field image and low angle X-ray diffraction studies confirm the presence of nanoporous Au100-xPtx NPs. The electrochemical studies using the Au85Pt15/C catalyst show excellent methanol tolerance behaviour and better performance towards oxygen reduction reaction (ORR) in terms of high mass activity, mass-specific activity and figure of merit (FOM) when compared to HiSPEC Pt/C commercial catalyst. Preliminary studies on a full cell using nanoporous Au85Pt15/C (loading 1.0 mg cm-2) as the cathode material and Pt-Ru/C (loading: 0.5 mg cm-2) as the anode material performed better (38 mW cm-2) than the HiSPEC Pt/C cathode material (16 mW cm-2).For the first time, we are reporting the synthesis of Au100-xPtx nanoporous materials in the size range of 7-10 nm through the galvanic replacement of Ag by Pt from Au100-xAg2x spherical nano-alloys (x = 20, 15, 10 and 5) in an aqueous medium. The galvanic replacement reaction follows the `Volmer-Weber' growth mode, resulting in the formation of surface bound platinum islands on a nanoporous gold surface. The high angle annular dark field image and low angle X-ray diffraction studies confirm the presence of nanoporous Au100-xPtx NPs. The electrochemical studies using the Au85Pt15/C catalyst show excellent methanol tolerance behaviour and better performance towards oxygen reduction reaction (ORR) in terms of high mass activity, mass-specific activity and figure of merit (FOM) when compared to HiSPEC Pt/C commercial catalyst. Preliminary studies on a full cell using nanoporous Au85Pt15/C (loading 1.0 mg

  18. Iridium-Doped Ruthenium Oxide Catalyst for Oxygen Evolution

    Science.gov (United States)

    Valdez, Thomas I.; Narayan, Sri R.; Billings, Keith J.

    2011-01-01

    NASA requires a durable and efficient catalyst for the electrolysis of water in a polymer-electrolyte-membrane (PEM) cell. Ruthenium oxide in a slightly reduced form is known to be a very efficient catalyst for the anodic oxidation of water to oxygen, but it degrades rapidly, reducing efficiency. To combat this tendency of ruthenium oxide to change oxidation states, it is combined with iridium, which has a tendency to stabilize ruthenium oxide at oxygen evolution potentials. The novel oxygen evolution catalyst was fabricated under flowing argon in order to allow the iridium to preferentially react with oxygen from the ruthenium oxide, and not oxygen from the environment. Nanoparticulate iridium black and anhydrous ruthenium oxide are weighed out and mixed to 5 18 atomic percent. They are then heat treated at 300 C under flowing argon (in order to create an inert environment) for a minimum of 14 hours. This temperature was chosen because it is approximately the creep temperature of ruthenium oxide, and is below the sintering temperature of both materials. In general, the temperature should always be below the sintering temperature of both materials. The iridium- doped ruthenium oxide catalyst is then fabricated into a PEM-based membrane- electrode assembly (MEA), and then mounted into test cells. The result is an electrolyzer system that can sustain electrolysis at twice the current density, and at the same efficiency as commercial catalysts in the range of 100-200 mA/sq cm. At 200 mA/sq cm, this new system operates at an efficiency of 85 percent, which is 2 percent greater than commercially available catalysts. Testing has shown that this material is as stable as commercially available oxygen evolution catalysts. This means that this new catalyst can be used to regenerate fuel cell systems in space, and as a hydrogen generator on Earth.

  19. Titania Supported Pt and Pt/Pd Nano-particle Catalysts for the Oxidation of Sulfur Dioxide

    DEFF Research Database (Denmark)

    Koutsopoulos, Sotiris; Johannessen, Tue; Eriksen, Kim Michael

    2006-01-01

    Several types of titania (anatase) were used as supports for pure platinum and Pt–Pd bimetallic alloy catalysts. The preparation methods, normal wet impregnation technique and flame aerosol synthesis, obtained metal loadings of 2% by weight. The prepared catalysts were tested for SO2 oxidation...... activity at atmospheric pressure in the temperature range 250–600 °C. The SO2 to SO3 conversion efficiency of the Pt–Pd alloy was significantly higher than that of the individual metals. The effects of the preparation method and the titania type used on the properties and activity of the resulting catalyst...

  20. Catalyst for Ammonia Oxidation

    DEFF Research Database (Denmark)

    2015-01-01

    The present invention relates to a bimetallic catalyst for ammonia oxidation, a method for producing a bimetallic catalyst for ammonia oxidation and a method for tuning the catalytic activity of a transition metal. By depositing an overlayer of less catalytic active metal onto a more catalytic...