WorldWideScience

Sample records for electrochemical hydrogenation behavior

  1. Electrochemical Hydrogen Compressor

    Energy Technology Data Exchange (ETDEWEB)

    Lipp, Ludwig [FuelCell Energy, Inc., Torrington, CT (United States)

    2016-01-21

    Conventional compressors have not been able to meet DOE targets for hydrogen refueling stations. They suffer from high capital cost, poor reliability and pose a risk of fuel contamination from lubricant oils. This project has significantly advanced the development of solid state hydrogen compressor technology for multiple applications. The project has achieved all of its major objectives. It has demonstrated capability of Electrochemical Hydrogen Compression (EHC) technology to potentially meet the DOE targets for small compressors for refueling sites. It has quantified EHC cell performance and durability, including single stage hydrogen compression from near-atmospheric pressure to 12,800 psi and operation of EHC for more than 22,000 hours. Capital cost of EHC was reduced by 60%, enabling a path to meeting the DOE cost targets for hydrogen compression, storage and delivery ($2.00-2.15/gge by 2020).

  2. Electrochemical hydrogen Storage Systems

    International Nuclear Information System (INIS)

    Macdonald, Digby

    2010-01-01

    As the global need for energy increases, scientists and engineers have found a possible solution by using hydrogen to power our world. Although hydrogen can be combusted as a fuel, it is considered an energy carrier for use in fuel cells wherein it is consumed (oxidized) without the production of greenhouse gases and produces electrical energy with high efficiency. Chemical storage of hydrogen involves release of hydrogen in a controlled manner from materials in which the hydrogen is covalently bound. Sodium borohydride and aminoborane are two materials given consideration as chemical hydrogen storage materials by the US Department of Energy. A very significant barrier to adoption of these materials as hydrogen carriers is their regeneration from 'spent fuel,' i.e., the material remaining after discharge of hydrogen. The U.S. Department of Energy (DOE) formed a Center of Excellence for Chemical Hydrogen Storage, and this work stems from that project. The DOE has identified boron hydrides as being the main compounds of interest as hydrogen storage materials. The various boron hydrides are then oxidized to release their hydrogen, thereby forming a 'spent fuel' in the form of a lower boron hydride or even a boron oxide. The ultimate goal of this project is to take the oxidized boron hydrides as the spent fuel and hydrogenate them back to their original form so they can be used again as a fuel. Thus this research is essentially a boron hydride recycling project. In this report, research directed at regeneration of sodium borohydride and aminoborane is described. For sodium borohydride, electrochemical reduction of boric acid and sodium metaborate (representing spent fuel) in alkaline, aqueous solution has been investigated. Similarly to literature reports (primarily patents), a variety of cathode materials were tried in these experiments. Additionally, approaches directed at overcoming electrostatic repulsion of borate anion from the cathode, not described in the

  3. Electrochemical hydrogen Storage Systems

    Energy Technology Data Exchange (ETDEWEB)

    Dr. Digby Macdonald

    2010-08-09

    As the global need for energy increases, scientists and engineers have found a possible solution by using hydrogen to power our world. Although hydrogen can be combusted as a fuel, it is considered an energy carrier for use in fuel cells wherein it is consumed (oxidized) without the production of greenhouse gases and produces electrical energy with high efficiency. Chemical storage of hydrogen involves release of hydrogen in a controlled manner from materials in which the hydrogen is covalently bound. Sodium borohydride and aminoborane are two materials given consideration as chemical hydrogen storage materials by the US Department of Energy. A very significant barrier to adoption of these materials as hydrogen carriers is their regeneration from 'spent fuel,' i.e., the material remaining after discharge of hydrogen. The U.S. Department of Energy (DOE) formed a Center of Excellence for Chemical Hydrogen Storage, and this work stems from that project. The DOE has identified boron hydrides as being the main compounds of interest as hydrogen storage materials. The various boron hydrides are then oxidized to release their hydrogen, thereby forming a 'spent fuel' in the form of a lower boron hydride or even a boron oxide. The ultimate goal of this project is to take the oxidized boron hydrides as the spent fuel and hydrogenate them back to their original form so they can be used again as a fuel. Thus this research is essentially a boron hydride recycling project. In this report, research directed at regeneration of sodium borohydride and aminoborane is described. For sodium borohydride, electrochemical reduction of boric acid and sodium metaborate (representing spent fuel) in alkaline, aqueous solution has been investigated. Similarly to literature reports (primarily patents), a variety of cathode materials were tried in these experiments. Additionally, approaches directed at overcoming electrostatic repulsion of borate anion from the cathode, not

  4. Electrochemical Hydrogen Evolution

    DEFF Research Database (Denmark)

    Laursen, A.B.; Varela Gasque, Ana Sofia; Dionigi, F.

    2012-01-01

    The electrochemical hydrogen evolution reaction (HER) is growing in significance as society begins to rely more on renewable energy sources such as wind and solar power. Thus, research on designing new, inexpensive, and abundant HER catalysts is important. Here, we describe how a simple experiment....... This exercise circumvents the complexity of traditional experiments while it still demonstrates the trends of the HER volcano known from literature....

  5. Electrochemical Hydrogen Peroxide Generator

    Science.gov (United States)

    Tennakoon, Charles L. K.; Singh, Waheguru; Anderson, Kelvin C.

    2010-01-01

    Two-electron reduction of oxygen to produce hydrogen peroxide is a much researched topic. Most of the work has been done in the production of hydrogen peroxide in basic media, in order to address the needs of the pulp and paper industry. However, peroxides under alkaline conditions show poor stabilities and are not useful in disinfection applications. There is a need to design electrocatalysts that are stable and provide good current and energy efficiencies to produce hydrogen peroxide under acidic conditions. The innovation focuses on the in situ generation of hydrogen peroxide using an electrochemical cell having a gas diffusion electrode as the cathode (electrode connected to the negative pole of the power supply) and a platinized titanium anode. The cathode and anode compartments are separated by a readily available cation-exchange membrane (Nafion 117). The anode compartment is fed with deionized water. Generation of oxygen is the anode reaction. Protons from the anode compartment are transferred across the cation-exchange membrane to the cathode compartment by electrostatic attraction towards the negatively charged electrode. The cathode compartment is fed with oxygen. Here, hydrogen peroxide is generated by the reduction of oxygen. Water may also be generated in the cathode. A small amount of water is also transported across the membrane along with hydrated protons transported across the membrane. Generally, each proton is hydrated with 3-5 molecules. The process is unique because hydrogen peroxide is formed as a high-purity aqueous solution. Since there are no hazardous chemicals or liquids used in the process, the disinfection product can be applied directly to water, before entering a water filtration unit to disinfect the incoming water and to prevent the build up of heterotrophic bacteria, for example, in carbon based filters. The competitive advantages of this process are: 1. No consumable chemicals are needed in the process. The only raw materials

  6. Electrochemical Hydrogen Compressor

    Energy Technology Data Exchange (ETDEWEB)

    David P. Bloomfield; Brian S. MacKenzie

    2006-05-01

    The Electrochemical Hydrogen Compressor EHC was evaluated against DOE applications for compressing hydrogen at automobile filling stations, in future hydrogen pipelines and as a commercial replacement for conventional diaphragm hydrogen compressors. It was also evaluated as a modular replacement for the compressors used in petrochemical refineries. If the EHC can be made inexpensive, reliable and long lived then it can satisfy all these applications save pipelines where the requirements for platinum catalyst exceeds the annual world production. The research performed did not completely investigate Molybdenum as a hydrogen anode or cathode, it did show that photoetched 316 stainless steel is inadequate for an EHC. It also showed that: molybdenum bipolar plates, photochemical etching processes, and Gortex Teflon seals are too costly for a commercial EHC. The use of carbon paper in combination with a perforated thin metal electrode demonstrated adequate anode support strength, but is suspect in promoting galvanic corrosion. The nature of the corrosion mechanisms are not well understood, but locally high potentials within the unit cell package are probably involved. The program produced a design with an extraordinary high cell pitch, and a very low part count. This is one of the promising aspects of the redesigned EHC. The development and successful demonstration of the hydraulic cathode is also important. The problem of corrosion resistant metal bipolar plates is vital to the development of an inexpensive, commercial PEM fuel cell. Our research suggests that there is more to the corrosion process in fuel cells and electrochemical compressors than simple, steady state, galvanic stability. It is an important area for scientific investigation. The experiments and analysis conducted lead to several recommended future research directions. First, we need a better understanding of the corrosion mechanisms involved. The diagnosis of experimental cells with titration to

  7. Electrochemical Hydrogen Refrigerator

    Data.gov (United States)

    National Aeronautics and Space Administration — The goal is to develop and test a 1 W at 20K Joule‐Thomson cryocooler using an electrochemical compressor. A Joule Thomson refrigerator based on electrochemical...

  8. Origin of the different behavior of some platinum decorated nanocarbons towards the electrochemical oxidation of hydrogen peroxide

    Energy Technology Data Exchange (ETDEWEB)

    Malara, A. [Dipartimento di Ingegneria dell' Informazione, delle Infrastrutture e dell' Energia Sostenibile (DIIES), Università “Mediterranea”, 89122 Reggio Calabria (Italy); Leonardi, S.G.; Bonavita, A. [Dipartimento di Ingegneria Elettronica, Chimica ed Ingegneria Industriale (DIECII), Università di Messina, 98166 Messina (Italy); Fazio, E. [Dipartimento di Scienze Matematiche e Informatiche, Scienze Fisiche e Scienze della Terra (MIFT), Università di Messina, 98166 Messina (Italy); Stelitano, S. [Dipartimento di Fisica (DF), Università della Calabria, 87036 Arcavacata di Rende (Italy); Neri, G. [Dipartimento di Ingegneria Elettronica, Chimica ed Ingegneria Industriale (DIECII), Università di Messina, 98166 Messina (Italy); Neri, F. [Dipartimento di Scienze Matematiche e Informatiche, Scienze Fisiche e Scienze della Terra (MIFT), Università di Messina, 98166 Messina (Italy); Santangelo, S., E-mail: saveria.santangelo@unirc.it [Dipartimento di Ingegneria Civile, dell' Energia, dell' Ambiente e dei Materiali (DICEAM), Università “Mediterranea”, 89122 Reggio Calabria (Italy)

    2016-12-01

    The electrochemical behavior of different platinum-decorated nanocarbons (Pt@C) towards the oxidation of hydrogen peroxide (H{sub 2}O{sub 2}) was investigated. Three different types of nanocarbons were considered: i) carbon black, ii) dahlia-like carbon nanohorns and iii) carbon nanotubes, which included both commercial (single-wall and multi-wall) and laboratory prepared (multi-wall) samples. Shape and size distribution of the platinum nanoparticles and morphology of the nanocarbons were analyzed by transmission electron microscopy. Their nanostructure was investigated by micro-Raman spectroscopy, while elemental composition of the samples and chemical bonding states were studied by X-ray photoelectron spectroscopy. Electrochemical behavior towards H{sub 2}O{sub 2} oxidation was evaluated by means of cyclic voltammetry modifying the working screen-printed carbon electrode surface with the prepared Pt@C nanocomposites. Data obtained suggest that the size and dispersion of the Pt nanoparticles play a key role in increasing the sensitivity towards H{sub 2}O{sub 2} detection. Thanks to the presence of smaller and more dispersed platinum particles and of a greater amount of platinum hydroxide, acting as intermediary in the H{sub 2}O{sub 2} oxidation process, Pt@dahlia-like carbon nanohorns result to be the most promising platform for the development of H{sub 2}O{sub 2} electrochemical sensors. - Highlights: • Different nanocarbons are decorated with Pt nanoparticles by wet impregnation method. • Pt@C-based hybrids are tested as active materials for sensing of hydrogen peroxide. • Sensor based on Pt@dahlia-like carbon nanohorns is the most performing device. • The origin of the different electrochemical behaviour is investigated. • Pt@C sensing performances are correlated with their structural and surface properties.

  9. Origin of the different behavior of some platinum decorated nanocarbons towards the electrochemical oxidation of hydrogen peroxide

    International Nuclear Information System (INIS)

    Malara, A.; Leonardi, S.G.; Bonavita, A.; Fazio, E.; Stelitano, S.; Neri, G.; Neri, F.; Santangelo, S.

    2016-01-01

    The electrochemical behavior of different platinum-decorated nanocarbons (Pt@C) towards the oxidation of hydrogen peroxide (H 2 O 2 ) was investigated. Three different types of nanocarbons were considered: i) carbon black, ii) dahlia-like carbon nanohorns and iii) carbon nanotubes, which included both commercial (single-wall and multi-wall) and laboratory prepared (multi-wall) samples. Shape and size distribution of the platinum nanoparticles and morphology of the nanocarbons were analyzed by transmission electron microscopy. Their nanostructure was investigated by micro-Raman spectroscopy, while elemental composition of the samples and chemical bonding states were studied by X-ray photoelectron spectroscopy. Electrochemical behavior towards H 2 O 2 oxidation was evaluated by means of cyclic voltammetry modifying the working screen-printed carbon electrode surface with the prepared Pt@C nanocomposites. Data obtained suggest that the size and dispersion of the Pt nanoparticles play a key role in increasing the sensitivity towards H 2 O 2 detection. Thanks to the presence of smaller and more dispersed platinum particles and of a greater amount of platinum hydroxide, acting as intermediary in the H 2 O 2 oxidation process, Pt@dahlia-like carbon nanohorns result to be the most promising platform for the development of H 2 O 2 electrochemical sensors. - Highlights: • Different nanocarbons are decorated with Pt nanoparticles by wet impregnation method. • Pt@C-based hybrids are tested as active materials for sensing of hydrogen peroxide. • Sensor based on Pt@dahlia-like carbon nanohorns is the most performing device. • The origin of the different electrochemical behaviour is investigated. • Pt@C sensing performances are correlated with their structural and surface properties.

  10. Electrochemical behavior of Azure A/gold nanoclusters modified electrode and its application as non-enzymatic hydrogen peroxide sensor.

    Science.gov (United States)

    Priya, C; Sivasankari, G; Narayanan, S Sriman

    2012-09-01

    A novel non-enzymatic hydrogen peroxide sensor was developed using Azure A/gold nanoclusters modified graphite electrode. The method of preparation of Azure A/gold nanoclusters was simple and it was characterized by UV-visible spectroscopy, field emission scanning electron microscopy (FESEM) and confocal Raman microscopy. The electrochemical properties of Azure A/gold nanoclusters modified graphite electrode was characterized by cyclic voltammetry. In 0.1M H(2)SO(4) the modified electrode showed redox peaks which correspond to the redox behavior of gold nanoparticle. In 0.1M PBS the modified electrode exhibited well defined redox peaks with the formal potential of -0.253 V which is analogous to the redox reaction of Azure A. The results have shown that the gold nanoclusters has reduced the formal potential of Azure A and enhanced the current due to the fast charge transfer kinetics. Also the modified electrode showed an enhanced electrocatalytic activity towards the reduction of H(2)O(2) in the concentration range of 3.26×10(-6)M to 3.2×10(-3)M with a detection limit of 1.08×10(-6)M (S/N=3). The proposed electrode exhibited good stability and reproducibility, and it has the potential application as a sensor for other biologically significant compounds. Copyright © 2012 Elsevier B.V. All rights reserved.

  11. Electrochemical behavior of NixW1−x materials as catalyst for hydrogen evolution reaction in alkaline media

    International Nuclear Information System (INIS)

    Oliver-Tolentino, Miguel A.; Arce-Estrada, Elsa M.; Cortés-Escobedo, Claudia A.; Bolarín-Miro, Ana M.; Sánchez-De Jesús, Félix; González-Huerta, Rosa de G.; Manzo-Robledo, Arturo

    2012-01-01

    Highlights: ► The electrochemical techniques used in this study elucidated the Ni–W surface state. ► The Ni–W materials were effective for the hydrogen evolution reaction. ► The prepared alloys exhibited higher catalytic activity than their precursors. ► The preparation method is relatively simple and effective procedure. - Abstract: In the present work, results of electrochemical evaluation, as well as morphological and structural characterization of Ni x W 1−x materials with x = 0.77, 0.64, 0.4, 0.19 and 0.07 processed by means of high energy ball milling from high purity powders are presented. Also, the electrocatalytic performance on the hydrogen evolution reaction (HER) of the Ni x W 1−x materials evaluated by linear polarization and cyclic voltammetry techniques in alkaline media at room temperature is discussed. The structural and morphological characterization of the as-prepared materials was carried out using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results indicated a small-particle clusters and solid solution formation. According to the kinetics parameters the best electrocatalytic activity was observed at Ni 64 W 36 .

  12. Study of the electrochemical behavior of the niobium in relation to the hydrogen cyclical charge and uncharge; Estudo do comportamento eletroquimico do niobio em relacao ao carregamento e descarregamento ciclicos de hidrogenio

    Energy Technology Data Exchange (ETDEWEB)

    Silva, A.G.S.G. da; Ponte, H.A.; Pashchuk, A. [Universidade Federal do Parana (UFPR), Curitiba, PR (Brazil). Centro Politecnico. Lab. de Eletroquimica de Superficie e Corrosao (LESK)], e-mail: aleksantos@hotmail.com

    2006-07-01

    One of the greatest problems found in the oil industry is the control of the deterioration at the steels structures of the units that compose the process petroleum refine. This deterioration is related the mechanisms involving processes of hydrogen embrittlement. The work had as objective to study the electrochemical behavior of the niobium (Nb) with relation to the charging and uncharging of hydrogen, to evaluate the potential to use of the Nb in the construction of electrochemical hydrogen probes. For this study techniques of cronopotenciometry and potential of open circuit (OCP) for the pure Nb submitted the different hydrogen charging conditions had been used. The gotten partial results indicate the viability to use of the niobium as hydrogen probe, however, it is necessary one better understanding of the mechanisms of hydrogen interaction with the niobium. (author)

  13. Electrochemical behavior of Ni{sub x}W{sub 1-x} materials as catalyst for hydrogen evolution reaction in alkaline media

    Energy Technology Data Exchange (ETDEWEB)

    Oliver-Tolentino, Miguel A. [UPIBI-IPN, Departamento de Ciencias Basicas, Av. Acueducto s/n, Barrio La Laguna, Col. Ticoman, Mexico D.F. 07340 (Mexico); Arce-Estrada, Elsa M. [ESIQIE-IPN Departamento de Ingenieria en Metalurgia y Materiales, UPALM, UPALM, Mexico D.F. 07738 (Mexico); Cortes-Escobedo, Claudia A. [Centro de Investigacion e Innovacion Tecnologica del IPN, Cda. Cecati s/n, Col. Sta. Catarina, CP 02250 Azcapotzalco D.F. (Mexico); Bolarin-Miro, Ana M.; Sanchez-De Jesus, Felix [Area Academica de Ciencias de la Tierra y Materiales, Universidad Autonoma del Estado de Hidalgo, CU, Carr. Pachuca-Tulancingo Km. 4.5, Mineral de la Reforma, CP 42184 Hidalgo (Mexico); Gonzalez-Huerta, Rosa de G. [ESIQIE-IPN, Departamento de Ingenieria Quimica - Laboratorio de Electroquimica y Corrosion, Edif. Z-5 3er piso, UPALM, Mexico D.F. 07738 (Mexico); Manzo-Robledo, Arturo, E-mail: amanzor@ipn.mx [ESIQIE-IPN, Departamento de Ingenieria Quimica - Laboratorio de Electroquimica y Corrosion, Edif. Z-5 3er piso, UPALM, Mexico D.F. 07738 (Mexico)

    2012-09-25

    Highlights: Black-Right-Pointing-Pointer The electrochemical techniques used in this study elucidated the Ni-W surface state. Black-Right-Pointing-Pointer The Ni-W materials were effective for the hydrogen evolution reaction. Black-Right-Pointing-Pointer The prepared alloys exhibited higher catalytic activity than their precursors. Black-Right-Pointing-Pointer The preparation method is relatively simple and effective procedure. - Abstract: In the present work, results of electrochemical evaluation, as well as morphological and structural characterization of Ni{sub x}W{sub 1-x} materials with x = 0.77, 0.64, 0.4, 0.19 and 0.07 processed by means of high energy ball milling from high purity powders are presented. Also, the electrocatalytic performance on the hydrogen evolution reaction (HER) of the Ni{sub x}W{sub 1-x} materials evaluated by linear polarization and cyclic voltammetry techniques in alkaline media at room temperature is discussed. The structural and morphological characterization of the as-prepared materials was carried out using X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results indicated a small-particle clusters and solid solution formation. According to the kinetics parameters the best electrocatalytic activity was observed at Ni{sub 64}W{sub 36}.

  14. Electrochemical hydrogen isotope sensor based on solid electrolytes

    International Nuclear Information System (INIS)

    Matsumoto, Hiroshige; Hayashi, Hiroyuki; Iwahara, Hiroyasu

    2002-01-01

    An electrochemical sensor of hydrogen isotopes based on solid electrolytes for determining the hydrogen isotope ratios and/or total hydrogen pressures in gases has been developed. This paper describes the methodology of the hydrogen isotope sensing together with experimental results. When hydrogen isotope gases are introduced to an electrochemical cell using a proton-conducting electrolyte (hydrogen isotope cell), the electromotive force (EMF) of the cell agrees with that theoretically estimated. The EMF signals can be used for the determination of the hydrogen isotope ratio in gases if the total hydrogen pressure is predetermined. By supplementary use of an oxide ion conductor cell, both the ratio and total pressure of the hydrogen isotopes can be simultaneously determined. (author)

  15. A kinetic study of the electrochemical hydrogenation of ethylene

    International Nuclear Information System (INIS)

    Sedighi, S.; Gardner, C.L.

    2010-01-01

    In this study, we have examined the kinetics of the electrochemical hydrogenation of ethylene in a PEM reactor. While in itself this reaction is of little industrial interest, this reaction can be looked upon as a model reaction for many of the important hydrogenation processes including the refining of heavy oils and the hydrogenation of vegetable oils. To study the electrochemical hydrogenation of ethylene, several experimental techniques have been used including polarization measurements, measurement of the composition of the exit gases and potential step, transient measurements. The results show that the hydrogenation reaction proceeds rapidly and essentially to completion. By fitting the experimental transient data to the results from a zero-dimensional mathematical model of the process, a set of kinetic parameters for the reactions has been obtained that give generally good agreement with the experimental results. It seems probable that similar experimental techniques could be used to study the electrochemical hydrogenation of other unsaturated organic molecules of more industrial significance.

  16. Efficient Electrochemical Hydrogen Peroxide Generation in Water, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — An electrochemical cell is proposed for the efficient generation of 3% hydrogen peroxide (H2O2) in pure water using only power, oxygen and water. H2O2 is an...

  17. Cathodic electrocatalyst layer for electrochemical generation of hydrogen peroxide

    Science.gov (United States)

    Rhodes, Christopher P. (Inventor); Tennakoon, Charles L. K. (Inventor); Singh, Waheguru Pal (Inventor); Anderson, Kelvin C. (Inventor)

    2011-01-01

    A cathodic gas diffusion electrode for the electrochemical production of aqueous hydrogen peroxide solutions. The cathodic gas diffusion electrode comprises an electrically conductive gas diffusion substrate and a cathodic electrocatalyst layer supported on the gas diffusion substrate. A novel cathodic electrocatalyst layer comprises a cathodic electrocatalyst, a substantially water-insoluble quaternary ammonium compound, a fluorocarbon polymer hydrophobic agent and binder, and a perfluoronated sulphonic acid polymer. An electrochemical cell using the novel cathodic electrocatalyst layer has been shown to produce an aqueous solution having between 8 and 14 weight percent hydrogen peroxide. Furthermore, such electrochemical cells have shown stable production of hydrogen peroxide solutions over 1000 hours of operation including numerous system shutdowns.

  18. Hydrogen-based electrochemical energy storage

    Science.gov (United States)

    Simpson, Lin Jay

    2013-08-06

    An energy storage device (100) providing high storage densities via hydrogen storage. The device (100) includes a counter electrode (110), a storage electrode (130), and an ion conducting membrane (120) positioned between the counter electrode (110) and the storage electrode (130). The counter electrode (110) is formed of one or more materials with an affinity for hydrogen and includes an exchange matrix for elements/materials selected from the non-noble materials that have an affinity for hydrogen. The storage electrode (130) is loaded with hydrogen such as atomic or mono-hydrogen that is adsorbed by a hydrogen storage material such that the hydrogen (132, 134) may be stored with low chemical bonding. The hydrogen storage material is typically formed of a lightweight material such as carbon or boron with a network of passage-ways or intercalants for storing and conducting mono-hydrogen, protons, or the like. The hydrogen storage material may store at least ten percent by weight hydrogen (132, 134) at ambient temperature and pressure.

  19. Electrochemical Hydrogen Storage in a Highly Ordered Mesoporous Carbon

    Directory of Open Access Journals (Sweden)

    Dan eLiu

    2014-10-01

    Full Text Available A highly order mesoporous carbon has been synthesized through a strongly acidic, aqueous cooperative assembly route. The structure and morphology of the carbon material were investigated using TEM, SEM and nitrogen adsorption-desorption isotherms. The carbon was proven to be meso-structural and consisted of graphitic micro-domain with larger interlayer space. AC impedance and electrochemical measurements reveal that the synthesized highly ordered mesoporous carbon exhibits a promoted electrochemical hydrogen insertion process and improved capacitance and hydrogen storage stability. The meso-structure and enlarged interlayer distance within the highly ordered mesoporous carbon are suggested as possible causes for the enhancement in hydrogen storage. Both hydrogen capacity in the carbon and mass diffusion within the matrix were improved.

  20. Electrochemical Hydrogen Evolution: Sabatier's Principle and the Volcano Plot

    Science.gov (United States)

    Laursen, Anders B.; Varela, Ana Sofia; Dionigi, Fabio; Fanchiu, Hank; Miller, Chandler; Trinhammer, Ole L.; Rossmeisl, Jan; Dahl, Soren

    2012-01-01

    The electrochemical hydrogen evolution reaction (HER) is growing in significance as society begins to rely more on renewable energy sources such as wind and solar power. Thus, research on designing new, inexpensive, and abundant HER catalysts is important. Here, we describe how a simple experiment combined with results from density functional…

  1. Applications of hydrogen peroxide in electrochemical technology

    Energy Technology Data Exchange (ETDEWEB)

    Alvarez Gallegos, Alberto Armando

    1998-12-01

    It is demonstrated that hydrogen peroxide can be produced with a current efficiency of 40-70% by the cathodic reduction of oxygen at a reticulated vitreous carbon electrode in a divided flow-cell using catholytes consisting of aqueous chloride or sulphate media, pH >>{sub 2}. The supporting electrolyte does not influence either the current efficiency for H{sub 2}O{sub 2} or its rate of production. The current efficiency for H{sub 2}O{sub 2} is not a strong function of the potential and this suggests that 2e- and 4e- reduction of oxygen occurs in parallel at different sites on the carbon surface. Voltammetry experiments showed that (a) the I-E response for oxygen reduction at pH >>{sub 2} is a function of the electrode surface and/or the supporting electrolyte; (b) both H{sub 2} evolution and oxygen reduction are retarded on carbon with increasing ionic strength; (c) the presence of ferrous ions lead to the homogeneous decomposition of H{sub 2}O{sub 2} away from the cathode surface but their effectiveness as a catalyst for this decomposition depends on their speciation in solution which changes during an electrolysis. The use of a three-dimensional electrode fabricated from reticulated vitreous carbon allows Fenton`s reagent to be electroproduced at a practical rate which makes possible the removal of organics in slightly acidic aqueous media. A wide range of highly toxic organic molecules (phenol, catechol, hydroquinone, p-benzoquinone, oxalic acid, aniline, cresol and amaranth) have been oxidised in mild conditions and a significant fraction of the organic carbon is evolved as CO{sub 2}. In all cases studied the initial chemical oxygen demand (COD) was depleted to levels higher than 85%, indicating a complete mineralisation of the organic pollutants. The life-time of the reticulated vitreous carbon cathode was demonstrated to be over 1000 hours during two and a half years of experiments. During this time the cathode performance was very good, leading to

  2. Electrochemical determination of hydrogen peroxide using o ...

    Indian Academy of Sciences (India)

    Unknown

    The proposed method was further applied to the determination of the content of H2O2 in fresh rainwater with satisfactory results. The catalytic reaction mechanism and the electrode reductive process of the re- action product were carefully studied. Keywords. Hemoglobin; hydrogen peroxide; o-dianisidine, polarography. 1.

  3. A study of the electrochemical hydrogenation of o-xylene in a PEM hydrogenation reactor

    International Nuclear Information System (INIS)

    Fonocho, R.; Gardner, C.L.; Ternan, M.

    2012-01-01

    In this study, we investigate the electrochemical hydrogenation of o-xylene in a proton exchange membrane hydrogenation reactor (PEMHR). The reactor was operated isothermally over the temperature range 20–68 °C and at a pressure of 1 atm in a semi-batch mode. Hydrogen was fed into the anode compartment and o-xylene into the cathode. The hydrogenation efficiency was investigated at different current densities and temperatures. Results obtained show that the hydrogenation efficiency increases with temperature but decreases with current density. At low current densities the hydrogenation efficiency approaches 100%. A zero dimensional model was used to fit the data and extract a rate constant for the hydrogenation reaction. The activation energy for this reaction was found to be 28 kJ/mole.

  4. Electrochemical measurement of tritium and hydrogen permeation through iron membranes

    International Nuclear Information System (INIS)

    Hagi, Hideki; Hayashi, Yasunori

    1988-01-01

    Permeation rates of tritium and hydrogen through iron were measured by the electrochemical method in which an aqueous solution containing 3.7 x 10 12 Bq/m 3 tritium was used as a cathodic electrolyte. Tritium and hydrogen were introduced from one side of a specimen by cathodic polarization with a constant current density, while at the other side of the specimen the permeated tritium and hydrogen were extracted by potentiostatical ionization. Nearly all of the potentiostatic current of the extraction side stands for the ionization of hydrogen, because the concentration of tritium in the cathodic electrolyte is very small. The amount of permeated hydrogen was obtained by integrating the anodic current, and that of tritium was determined by measuring the radioactivity of the electrolyte sampled from the extraction side. The separation factor for permeation obtained under steady state conditions (the ratio of permeation rates of hydrogen to tritium divided by the ratio of the concentration of hydrogen to tritium in the charging electrolyte) is 12 at 288 K. This value is independent of cathodic current density. Diffusion coefficients of tritium (D T ) and hydrogen (D H ) in iron were determined from the time lag of tritium and hydrogen permeation. For annealed specimens at 286 K, D T = 9 x 10 -10 m 2 /s and D H = 4 x 10 -9 m 2 /s, and for 9% cold-worked specimens at 284 K, D T = 3 x 10 -10 m 2 /s and D H = 4 x 10 -10 m 2 /s. (author)

  5. Electrochemical measurement of tritium and hydrogen permeation through iron membranes

    International Nuclear Information System (INIS)

    Hagi, Hideki; Hayashi, Yasunori

    1987-01-01

    Permeation rates of tritium and hydrogen through iron were measured by the electro-chemical method in which an aqueous solution containing 3.7 x 10 12 Bq/m 3 tritium was used as a cathodic electrolyte. Tritium and hydrogen were introduced from one side of a specimen by cathodic polarization with a constant current density, while at the other side of the specimen the permeated tritium and hydrogen were extracted by potentiostatical ionization. Nearly all of the potentiostatic current on the extraction side is produced by the ionization of hydrogen, because the concentration of tritium in the cathodic electrolyte is very small. The amount of permeated hydrogen was obtained by integrating the potentiostatic current, and that of permeated tritium was determined by measuring the radioactivity of the electrolyte sampled from the anodic side. The separation factor for permeation obtained under steady state conditions (the ratio of permeation rates of hydrogen to tritium divided by the ratio of the concentration of hydrogen to tritium in the cathodic electrolyte) is 12 at 288 K. This value is independent of cathodic current density. Diffusion coefficients of tritium (D T ) and hydrogen (D H ) in iron were determined from the tritium and hydrogen permeation by using time lag technique. For annealed iron at 286 K, D T = 9 x 10 -10 m 2 /s and D H = 4 x 10 -9 m 2 /s, and for 9 % cold-worked iron at 284 K, D T = 3 x 10 -10 m 2 /s and D H = 4 x 10 -10 m 2 /s. (author)

  6. Carbon catalysts for electrochemical hydrogen peroxide production in acidic media

    DEFF Research Database (Denmark)

    Čolić, Viktor; Yang, Sungeun; Révay, Zsolt

    2018-01-01

    Hydrogen peroxide is a commodity chemical, as it is an environmentally friendly oxidant. The electrochemical production of H2O2 from oxygen and water by the reduction of oxygen is of great interest, as it would allow the decentralized, on-site, production of pure H2O2. The ability to run the reac......Hydrogen peroxide is a commodity chemical, as it is an environmentally friendly oxidant. The electrochemical production of H2O2 from oxygen and water by the reduction of oxygen is of great interest, as it would allow the decentralized, on-site, production of pure H2O2. The ability to run...... the reaction in an acidic electrolyte with high performance is particularly important, as it would allow the use of polymer solid electrolytes and the production of pH-neutral hydrogen peroxide. Carbon catalysts, which are cheap, abundant, durable and can be highly selective show promise as potential catalysts...... to determine the cause of these differences, we employ prompt gamma ray/neutron activation analysis and XPS measurements to assess the contribution of heteroatoms and defects, as well as low temperature N2-adsorption and transmission electron microscopy to elucidate the particle size, shape, BET surface area...

  7. Renewable hydrogen production via thermochemical/electrochemical coupling

    Energy Technology Data Exchange (ETDEWEB)

    Ambrosini, Andrea [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Babiniec, Sean Michael [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Miller, James E. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2017-10-01

    A coupled electrochemical/thermochemical cycle was investigated to produce hydrogen from renewable resources. Like a conventional thermochemical cycle, this cycle leverages chemical energy stored in a thermochemical working material that is reduced thermally by solar energy. However, in this concept, the stored chemical energy only needs to be partially, but not fully, capable of splitting steam to produce hydrogen. To complete the process, a proton-conducting membrane is driven to separate hydrogen as it is produced, thus shifting the thermodynamics toward further hydrogen production. This novel coupled-cycle concept provides several benefits. First, the required oxidation enthalpy of the reversible thermochemical material is reduced, enabling the process to occur at lower temperatures. Second, removing the requirement for spontaneous steam-splitting widens the scope of materials compositions, allowing for less expensive/more abundant elements to be used. Lastly, thermodynamics calculations suggest that this concept can potentially reach higher efficiencies than photovoltaic-to-electrolysis hydrogen production methods. This Exploratory Express LDRD involved assessing the practical feasibility of the proposed coupled cycle. A test stand was designed and constructed and proton-conducting membranes were synthesized. While the full proof of concept was not achieved, the individual components of the experiment were validated and new capabilities that can be leveraged by a variety of programs were developed.

  8. Electrochemical Determination of Hydrogen Entry to HSLA Steel during Pickling

    Directory of Open Access Journals (Sweden)

    Jari Aromaa

    2018-01-01

    Full Text Available Pickling with hydrochloric acid is a standard method to clean steel surfaces before hot-dip galvanizing. When normal low strength steels are pickled, hydrogen formed in pickling reactions does not have any significant harmful effect on the mechanical properties of steel. However, in pickling of steels with higher strength, the penetration of hydrogen into the steel may cause severe damages. The effect of pickling of high-strength low-alloy (HSLA steels was investigated using a cell construction based on the Devanathan-Stachurski method with modified anodic surface treatment and hydrogen production using acid. The penetration and the permeability of hydrogen were measured using an electrochemical cell with hydrochloric acid on the one side of the steel sample and a solution of NaOH on the other side. No protective coating, for example, palladium on the anodic side of the sample, is needed. The penetration rate of hydrogen into the steel and exit rate from the steel were lower for higher strength steel.

  9. Electrochemical behavior of graphene/Nafion/Azure I/Au nanoparticles composites modified glass carbon electrode and its application as nonenzymatic hydrogen peroxide sensor

    International Nuclear Information System (INIS)

    Zhang, Yanli; Liu, Yanpei; He, Jiemei; Pang, Pengfei; Gao, Yuntao; Hu, Qiufen

    2013-01-01

    A novel nonenzymatic hydrogen peroxide sensor was developed using graphene/Nafion/azure I/Au nanoparticles composites modified glass carbon electrode (graphene/Nafion/AzI/AuNPs/GCE). The method of preparation of graphene/Nafion/AzI/AuNPs composite was simple and it was characterized by SEM. Cyclic voltammetry demonstrated that the direct electron transfer of redox molecule, Azure I, was realized, and the sensor had an excellent performance in terms of electrocatalytic reduction toward hydrogen peroxide (H 2 O 2 ). The sensor showed high sensitivity and fast response upon the addition of H 2 O 2 , under the conditions of pH 4.0, potential −0.2 V. The time to reach the stable-state current was less than 3 s, and the linear range to H 2 O 2 was from 30 μM to 5 mM with a detection limit of 10 μM (S/N = 3). Moreover, the sensor exhibited good reproducibility and long-term stability

  10. The electrochemical Peltier heat of the standard hydrogen electrode reaction

    International Nuclear Information System (INIS)

    Fang Zheng; Wang Shaofen; Zhang Zhenghua; Qiu Guanzhou

    2008-01-01

    A method for measuring the electrochemical Peltier heat (EPH) of a single electrode reaction has been developed and an absolute scale is suggested to obtain EPH of the standard hydrogen electrode. The scale is based on φ 0 * = 0 and ΔS 0 * = 0 for any electrode reaction at zero Kelvin, in accord with the third law of thermodynamics. The relationships between entropy, enthalpy and free energy changes on this scale and on the conventional scale are derived. Calorimetric experiments were made on the Fe(CN) 6 3- /Fe(CN) 6 4- system at five different concentrations at 298.15 K, and EPH for the standard hydrogen electrode reaction is obtained. EPHs and the entropy change on the absolute scale for the studied redox are linearly related to concentration of electrolyte. The reversible electric work is almost concentration independent in the range of concentration studied

  11. The behavior of electrochemical cell resistance

    International Nuclear Information System (INIS)

    Ritley, K.A.; Dull, P.M.; Weber, M.H.; Carroll, M.; Hurst, J.J.; Lynn, K.G.

    1990-01-01

    Knowledge of the basic electrochemical behavior found in typical cold fusion experiments is important to understanding and preventing experimental errors. For a Pd/LiOH(D)/Pt electrochemical cell, the applied cell voltage/current relationship (the effective cell resistance) does not obey Ohm's law directly, but instead exhibits a complicated response to the current, voltage, temperature, electrolyte conductance, and other factors. Failure to properly consider this response can possibly result in errors that could affect the heat balance in calorimetry and temperature measurement experiments. Measurements of this response under varying voltage, temperature, and electrolyte conductivity conditions are reported. A plausible scenario in which the temperature dependence of the effective cell resistance can either exaggerate or ameliorate novel exothermic processes is suggested

  12. An electrochemical hydrogen meter for measuring hydrogen in sodium using a ternary electrolyte mixture

    CERN Document Server

    Sridharan, R; Nagaraj, S; Gnanasekaran, T; Periaswami, G

    2003-01-01

    An electrochemical sensor for measuring hydrogen concentration in liquid sodium that is based on a ternary mixture of LiCl, CaCl sub 2 and CaHCl as the electrolyte has been developed. DSC experiments showed the eutectic temperature of this ternary system to be approx 725 K. Impedance spectroscopic analysis of the electrolyte indicated ionic conduction through a molten phase at approx 725 K. Two electrochemical hydrogen sensors were constructed using the ternary electrolyte of composition 70 mol% LiCl:16 mol% CaHCl:14 mol% CaCl sub 2 and tested at 723 K in a mini sodium loop and at hydrogen levels of 60-250 ppb in sodium. The sensors show linear response in this concentration range and are capable of detecting a change of 10 ppb hydrogen in sodium over a background level of 60 ppb. Identification of this electrolyte system and its use in a sensor for measuring hydrogen in sodium are described in this paper.

  13. Advanced Electrochemical Technologies for Hydrogen Production by Alternative Thermochemical Cycles

    Energy Technology Data Exchange (ETDEWEB)

    Lvov, Serguei; Chung, Mike; Fedkin, Mark; Lewis, Michele; Balashov, Victor; Chalkova, Elena; Akinfiev, Nikolay; Stork, Carol; Davis, Thomas; Gadala-Maria, Francis; Stanford, Thomas; Weidner, John; Law, Victor; Prindle, John

    2011-01-06

    Hydrogen fuel is a potentially major solution to the problem of climate change, as well as addressing urban air pollution issues. But a key future challenge for hydrogen as a clean energy carrier is a sustainable, low-cost method of producing it in large capacities. Most of the world's hydrogen is currently derived from fossil fuels through some type of reforming processes. Nuclear hydrogen production is an emerging and promising alternative to the reforming processes for carbon-free hydrogen production in the future. This report presents the main results of a research program carried out by a NERI Consortium, which consisted of Penn State University (PSU) (lead), University of South Carolina (USC), Tulane University (TU), and Argonne National Laboratory (ANL). Thermochemical water decomposition is an emerging technology for large-scale production of hydrogen. Typically using two or more intermediate compounds, a sequence of chemical and physical processes split water into hydrogen and oxygen, without releasing any pollutants externally to the atmosphere. These intermediate compounds are recycled internally within a closed loop. While previous studies have identified over 200 possible thermochemical cycles, only a few have progressed beyond theoretical calculations to working experimental demonstrations that establish scientific and practical feasibility of the thermochemical processes. The Cu-Cl cycle has a significant advantage over other cycles due to lower temperature requirements – around 530 °C and below. As a result, it can be eventually linked with the Generation IV thermal power stations. Advantages of the Cu-Cl cycle over others include lower operating temperatures, ability to utilize low-grade waste heat to improve energy efficiency, and potentially lower cost materials. Another significant advantage is a relatively low voltage required for the electrochemical step (thus low electricity input). Other advantages include common chemical agents and

  14. An electrochemical method for determining hydrogen concentrations in metals and some applications

    Science.gov (United States)

    Danford, M. D.

    1983-01-01

    An electrochemical method was developed for the determination of hydrogen in metals using the EG&G-PARC Model 350A Corrosion Measurement Console. The method was applied to hydrogen uptake, both during electrolysis and electroplating, and to studies of hydrogen elimination and the effect of heat treatment on elimination times. Results from these studies are presented.

  15. Hydrogen embrittlement, revisited by in situ electrochemical nanoindentation

    Energy Technology Data Exchange (ETDEWEB)

    Barnoush, Afrooz

    2007-07-01

    The fine scale mechanical probing capability of NI-AFM was used to examine hydrogen interaction with plasticity. To realize this, an electrochemical three electrode setup was incorporated into the NI-AFM. The developed ECNI-AFM is capable of performing nanoindentation as well as imaging surfaces inside electrolytes. The developed ECNI-AFM setup was used to examine the effect of cathodically charged hydrogen on dislocation nucleation in pure metals and alloys. It was shown that hydrogen reduces the pop-in load in all of the tested materials except Cu. The reduced pop-in load can be interpreted as the HELP mechanism. Classical dislocation theory was used to model the homogeneous dislocation nucleation and it was shown that H reduces the activation energy for dislocation nucleation in H sensitive metals which are not undergoing a phase transformation. The activation energy for dislocation nucleation is related to the material specific parameters; shear modulus {mu}, dislocation core radius {rho} and in the case of partial dislocation nucleation, stacking fault energy {gamma}. These material properties can be influenced by H resulting in a reduced activation energy for dislocation nucleation. The universality of cohesion in bulk metals relates the reduction of the shear modulus to the reduction of the cohesion, meaning HEDE mechanism. The increase in the core radius of a dislocation due to H is a direct evidence of decrease in dislocation line energy and H segregation on the dislocation line. In the case of partial dislocations, the H can segregate on to the stacking fault ribbon and decrease {gamma}. This inhibits the cross slip process and enhances the slip planarity. Thus, HELP and HEDE are the two sides of a coin resulting in H embrittlement. However depending on the experimental approach utilized to probe the H effect, either HELP or HEDE can be observed. In this study, however, by utilizing a proper experimental approach, it was possible to resolve the

  16. Electrochemical & Thermochemical Behavior of Cerium(IV) Oxide delta

    Science.gov (United States)

    Chueh, William C.

    The mixed-valent nature of nonstoichiometric ceria (CeO2-delta ) gives rise to a wide range of intriguing properties, such as mixed ionic and electronic conduction and oxygen storage. Surface and transport behavior in rare-earth (samaria) doped and undoped ceria were investigated, with particular emphasis on applications in electrochemical and thermochemical energy conversion processes such as fuel cells and solar fuel production. The electrochemical responses of bulk-processed ceria with porous Pt and Au electrodes were analyzed using 1-D and 2-D transport models to decouple surface reactions, near-surface transport and bulk transport. Combined experimental and numerical results indicate that hydrogen electro-oxidation and hydrolysis near open-circuit conditions occur preferentially over the ceria | gas interface rather than over the ceria | gas | metal interface, with the rate-limiting step likely to be either surface reaction or transport through the surface oxygen vacancy depletion layer. In addition, epitaxial thin films of ceria were grown on zirconia substrates using pulsed-laser deposition to examine electrocatalysis over well-defined microstructures. Physical models were derived to analyze the electrochemical impedance response. By varying the film thickness, interfacial and chemical capacitance were decoupled, with the latter shown to be proportional to the small polaron densities. The geometry of microfabricated metal current collectors (metal = Pt, Ni) was also systematically varied to investigate the relative activity of the ceria | gas and the ceria | metal | gas interfaces. The data suggests that the electrochemical activity of the metal-ceria composite is only weakly dependent on the metal due to the relatively high activity of the ceria | gas interface. In addition to electrochemical experiments, thermochemical reduction-oxidation studies were performed on ceria. It was shown that thermally-reduced ceria, upon exposure to H 2O and/or CO2, can be

  17. Scanning electrochemical microscopy determination of hydrogen flux at liquid|liquid interface with potentiometric probe

    OpenAIRE

    Jedraszko, Justyna; Nogala, Wojciech; Adamiak, Wojciech; Girault, Hubert H.; Opallo, Marcin

    2014-01-01

    Scanning electrochemical microscopy potentiometric determination of local hydrogen concentration and its flux next to the liquid|liquid interface was demonstrated. This method is based on the shift of open circuit potential of Pt-based reversible hydrogen electrode. The detection system was verified with a system generating hydrogen under galvanostatic conditions. Then, it was applied to aqueous|1,2-dichloroethane interface where hydrogen is produced with decamethylferrocene as electron donor.

  18. Electrochemical Separation, Pumping, and Storage of Hydrogen or Oxygen into Nanocapillaries Via High Pressure MEA Seals

    Science.gov (United States)

    2015-10-13

    412TW-PA-15560 Electrochemical Separation, Pumping, and Storage of Hydrogen or Oxygen into Nanocapillaries Via High Pressure MEA Seals ...TITLE AND SUBTITLE Electrochemical Separation, Pumping, and Storage of Hydrogen or Oxygen into Nanocapillaries Via High Pressure MEA Seals ...pumping of gas species into and out of the nanocapillaries. The MEA also serves as a high pressure seal . A theoretical discussion of the potential

  19. Electrochemically Synthesized Nanoporous Molybdenum Carbide as a Durable Electrocatalyst for Hydrogen Evolution Reaction.

    Science.gov (United States)

    Kang, Jin Soo; Kim, Jin; Lee, Myeong Jae; Son, Yoon Jun; Chung, Dong Young; Park, Subin; Jeong, Juwon; Yoo, Ji Mun; Shin, Heejong; Choe, Heeman; Park, Hyun S; Sung, Yung-Eun

    2018-01-01

    Demands for sustainable production of hydrogen are rapidly increasing because of environmental considerations for fossil fuel consumption and development of fuel cell technologies. Thus, the development of high-performance and economical catalysts has been extensively investigated. In this study, a nanoporous Mo carbide electrode is prepared using a top-down electrochemical process and it is applied as an electrocatalyst for the hydrogen evolution reaction (HER). Anodic oxidation of Mo foil followed by heat treatment in a carbon monoxide (CO) atmosphere forms a nanostructured Mo carbide with excellent interconnections, and these structural characteristics lead to high activity and durability when applied to the HER. Additionally, characteristic behavior of Mo is observed; metallic Mo nanosheets form during electrochemical anodization by exfoliation along the (110) planes. These nanosheets are viable for chemical modification, indicating their feasibility in various applications. Moreover, the role of carbon shells is investigated on the surface of the electrocatalysts, whereby it is suggested that carbon shells serve as a mechanical barrier against the oxidative degradation of catalysts that accompanies unavoidable volume expansion.

  20. Electrochemical Synthesis of Polypyrrole, Reduced Graphene Oxide, and Gold Nanoparticles Composite and Its Application to Hydrogen Peroxide Biosensor

    Directory of Open Access Journals (Sweden)

    Baoyan Wu

    2016-11-01

    Full Text Available Here we report a facile eco-friendly one-step electrochemical approach for the fabrication of a polypyrrole (PPy, reduced graphene oxide (RGO, and gold nanoparticles (nanoAu biocomposite on a glassy carbon electrode (GCE. The electrochemical behaviors of PPy–RGO–nanoAu and its application to electrochemical detection of hydrogen peroxide were investigated by cyclic voltammetry. Graphene oxide and pyrrole monomer were first mixed and casted on the surface of a cleaned GCE. After an electrochemical processing consisting of the electrooxidation of pyrrole monomer and simultaneous electroreduction of graphene oxide and auric ions (Au3+ in aqueous solution, a PPy–RGO–nanoAu biocomposite was synthesized on GCE. Each component of PPy–RGO–nanoAu is electroactive without non-electroactive substance. The obtained PPy–RGO–nanoAu/GCE exhibited high electrocatalytic activity toward hydrogen peroxide, which allows the detection of hydrogen peroxide at a negative potential of about −0.62 V vs. SCE. The amperometric responses of the biosensor displayed a sensitivity of 40 µA/mM, a linear range of 32 µM–2 mM, and a detection limit of 2.7 µM (signal-to-noise ratio = 3 with good stability and acceptable reproducibility and selectivity. The results clearly demonstrate the potential of the as-prepared PPy–RGO–nanoAu biocomposite for use as a highly electroactive matrix for an amperometric biosensor.

  1. 6 CFM Electrochemical Hydrogen Pump and Compressor, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — Hydrogen is an essential resource for space missions. NASA has a need for equipment to generate, handle and store hydrogen. In terms of handling hydrogen,...

  2. 6 CFM Electrochemical Hydrogen Pump and Compressor, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — Hydrogen is an essential resource for space missions. NASA has a need for equipment to generate, handle and store hydrogen. In terms of handling hydrogen,...

  3. Fabrication of Nickel Nanotube Using Anodic Oxidation and Electrochemical Deposition Technologies and Its Hydrogen Storage Property

    Directory of Open Access Journals (Sweden)

    Yan Lv

    2016-01-01

    Full Text Available Electrochemical deposition technique was utilized to fabricate nickel nanotubes with the assistance of AAO templates. The topography and element component of the nickel nanotubes were characterized by TEM and EDS. Furthermore, the nickel nanotube was made into microelectrode and its electrochemical hydrogen storage property was studied using cyclic voltammetry. The results showed that the diameter of nickel nanotubes fabricated was around 20–100 mm, and the length of the nanotube could reach micron grade. The nickel nanotubes had hydrogen storage property, and the hydrogen storage performance was higher than that of nickel powder.

  4. The electrochemical behavior and surface structure of titanium electrodes modified by ion beams

    International Nuclear Information System (INIS)

    Huang, G.F.; Xie, Z.; Huang, W.Q.; Yang, S.B.; Zhao, L.H.

    2004-01-01

    Industrial grade titanium modified by ion implantation and sputtering was used as electrodes. The effect of ion beam modification on the electrochemical behavior and surface structure of electrodes was investigated. Also discussed is the hydrogen evolution process of the electrode in acidic solution. Several ions such as Fe + , C + , W + , Ni + and others, were implanted into the electrode. The electrochemical tests were carried out in 1N H 2 SO 4 solution at 30±1 deg. C. The electrode potential was measured versus a saturate calomel electrode as a function of immersion time. The cathodic polarization curves were measured by the stable potential static method. The surface layer composition and the chemical state of the electrodes were also investigated by Auger electron spectrometer (AES) and X-ray photoelectron spectroscopy (XPS) technique. The results show that: (1) the stability of modified electrodes depends on the active elements introduced by ion implantation and sputtering deposition. (2) The hydrogen evolution activity of industrial grade titanium may be improved greatly by ion beam modification. (3) Ion beam modification changed the composition and the surface state of electrodes over a certain depth range and forms an activity layer having catalytic hydrogen evolution, which inhibited the absorption of hydrogen and formation of titanium hydride. Thus promoted hydrogen evolution and improved the hydrogen evolution catalytic activity in industrial grade titanium

  5. Electrocatalytic oxygen reduction and hydrogen evolution reactions on phthalocyanine modified electrodes: Electrochemical, in situ spectroelectrochemical, and in situ electrocolorimetric monitoring

    International Nuclear Information System (INIS)

    Koca, Atif; Kalkan, Ayfer; Bayir, Zehra Altuntas

    2011-01-01

    Highlights: → Electrochemical and in situ spectroelectrochemical characterizations of the metallophthalocyanines were performed. → The presence of O 2 influences both oxygen reduction reaction and the electrochemical behaviors of the complexes. → Homogeneous catalytic ORR process occurs via an 'inner sphere' chemical catalysis process. → CoPc and CuPc coated on a glassy carbon electrode decrease the overpotential of the working electrode for H + reduction. - Abstract: This study describes electrochemical, in situ spectroelectrochemical, and in situ electrocolorimetric monitoring of the electrocatalytic reduction of molecular oxygen and hydronium ion on the phthalocyanine-modified electrodes. For this purpose, electrochemical and in situ spectroelectrochemical characterizations of the metallophthalocyanines (MPc) bearing tetrakis-[4-((4'-trifluoromethyl)phenoxy)phenoxy] groups were performed. While CoPc gives both metal-based and ring-based redox processes, H 2 Pc, ZnPc and CuPc show only ring-based electron transfer processes. In situ electrocolorimetric method was applied to investigate the color of the electrogenerated anionic and cationic forms of the complexes. The presence of O 2 in the electrolyte system influences both oxygen reduction reaction and the electrochemical and spectral behaviors of the complexes, which indicate electrocatalytic activity of the complexes for the oxygen reduction reaction. Perchloric acid titrations monitored by voltammetry represent possible electrocatalytic activities of the complexes for hydrogen evolution reaction. CoPc and CuPc coated on a glassy carbon electrode decrease the overpotential of the working electrode for H + reduction. The nature of the metal center changes the electrocatalytic activities for hydrogen evolution reaction in aqueous solution. Although CuPc has an inactive metal center, its electrocatalytic activity is recorded more than CoPc for H + reduction in aqueous solution.

  6. Maximising biohydrogen yields via continuous electrochemical hydrogen removal and carbon dioxide scrubbing.

    Science.gov (United States)

    Massanet-Nicolau, Jaime; Jones, Rhys Jon; Guwy, Alan; Dinsdale, Richard; Premier, Giuliano; Mulder, Martijn J J

    2016-10-01

    The use of electrochemical hydrogen removal (EHR) together with carbon dioxide removal (CDR) was demonstrated for the first time using a continuous hydrogen producing fermenter. CDR alone was found to increase hydrogen yields from 0.07molH2molhexose to 0.72molH2molhexose. When CDR was combined with EHR, hydrogen yields increased further to 1.79molH2molhexose. The pattern of carbohydrate utilisation and volatile fatty acid (VFA) production are consistent with the hypothesis that increased yields are the result of relieving end product inhibition and inhibition of microbial hydrogen consumption. In situ removal of hydrogen and carbon dioxide as demonstrated here not only increase hydrogen yield but also produces a relatively pure product gas and unlike other approaches can be used to enhance conventional, mesophilic, CSTR type fermentation of low grade/high solids biomass. Crown Copyright © 2016. Published by Elsevier Ltd. All rights reserved.

  7. Standard practice for evaluation of hydrogen uptake, permeation, and transport in metals by an electrochemical technique

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    1997-01-01

    1.1 This practice gives a procedure for the evaluation of hydrogen uptake, permeation, and transport in metals using an electrochemical technique which was developed by Devanathan and Stachurski. While this practice is primarily intended for laboratory use, such measurements have been conducted in field or plant applications. Therefore, with proper adaptations, this practice can also be applied to such situations. 1.2 This practice describes calculation of an effective diffusivity of hydrogen atoms in a metal and for distinguishing reversible and irreversible trapping. 1.3 This practice specifies the method for evaluating hydrogen uptake in metals based on the steady-state hydrogen flux. 1.4 This practice gives guidance on preparation of specimens, control and monitoring of the environmental variables, test procedures, and possible analyses of results. 1.5 This practice can be applied in principle to all metals and alloys which have a high solubility for hydrogen, and for which the hydrogen permeation is ...

  8. Hydrogen from electrochemical reforming of C1–C3 alcohols using proton conducting membranes

    NARCIS (Netherlands)

    Sapountzi, F. M.; Tsampas, M. N.; Fredriksson, H. O. A.; Gracia, J. M.; Niemantsverdriet, J. W.

    2017-01-01

    This study investigates the production of hydrogen from the electrochemical reforming of short-chain alcohols (methanol, ethanol, iso-propanol) and their mixtures. High surface gas diffusion Pt/C electrodes were interfaced to a Nafion polymeric membrane. The assembly separated the two chambers of an

  9. A high-porosity carbon molybdenum sulphide composite with enhanced electrochemical hydrogen evolution and stability

    DEFF Research Database (Denmark)

    Laursen, Anders B.; Vesborg, Peter C. K.; Chorkendorff, Ib

    2013-01-01

    This work describes a highly active and stable acid activated carbon fibre and amorphous MoSx composite hydrogen evolution catalyst. The increased electrochemical-surface area is demonstrated to cause increased catalyst electrodeposition and activity. These composite electrodes also show...

  10. Assessing the Electrochemical Behavior of Microcontact-Printed Silver Nanogrids

    Science.gov (United States)

    Sanders, Wesley C.; Iles, Peter; Valcarce, Ron; Salisbury, Kyle; Johnson, Glen; Lines, Aubry; Meyers, John; Page, Cristofer; Vanweerd, Myles; Young, Davies

    2018-01-01

    This paper describes a laboratory exercise used to address the ongoing need for nanotechnology-related, hands-on laboratory experiences for undergraduate students. Determination of the electrochemical behavior of student-fabricated silver nanogrids is reported. Students successfully used cyclic voltammetry to analyze silver nanogrids printed using…

  11. The effect of hydrogen on the morphology of n-type silicon electrodes under electrochemical conditions

    DEFF Research Database (Denmark)

    Goldar, A.; Roser, S.J.; Caruana, D.

    2001-01-01

    We study the electrochemical roughening of a silicon electrode surface during the hydrogen evolution reaction in a fluoride electrolyte using neutron reflection. We demonstrate that as the roughening process modifies the morphology of the silicon surface we can follow the changes by observing...... the changes in the shape of the total reflection feature. We assume that the change in the morphology of the surface is due to the diffusion of hydrogen in the silicon electrode. This assumption allow us to model the changes in the reflected intensity at two different angles and find the diffusion exponent...... for the diffusion of hydrogen in the silicon lattice....

  12. Electrochemical Behavior of Biologically Important Indole Derivatives

    Directory of Open Access Journals (Sweden)

    Cigdem Karaaslan

    2011-01-01

    Full Text Available Voltammetric techniques are most suitable to investigate the redox properties of a new drug. Use of electrochemistry is an important approach in drug discovery and research as well as quality control, drug stability, and determination of physiological activity. The indole nucleus is an essential element of a number of natural and synthetic products with significant biological activity. Indole derivatives are the well-known electroactive compounds that are readily oxidized at carbon-based electrodes, and thus analytical procedures, such as electrochemical detection and voltammetry, have been developed for the determination of biologically important indoles. This paper explains some of the relevant and recent achievements in the electrochemistry processes and parameters mainly related to biologically important indole derivatives in view of drug discovery and analysis.

  13. Hydrogen behavior in ice condenser containments

    Energy Technology Data Exchange (ETDEWEB)

    Lundstroem, P.; Hongisto, O. [Power Plant Lab., Helsinki (Finland); Theofanous, T.G. [Univ. of California, Santa Barbara, CA (United States)] [and others

    1995-09-01

    A new hydrogen management strategy is being developed for the Loviisa ice condenser containment. The strategy relies on containment-wide natural circulations that develop, once the ice condenser doors are forced open, to effectively produce a well-mixed behavior, and a correspondingly slow rise in hydrogen concentration. Levels can then be kept low by a distributed catalytic recombiner system, and (perhaps) an igniter system as a backup, while the associated energy releases can be effectively dissipated in the ice bed. Verification and fine-tuning of the approach is carried out experimentally in the VICTORIA facility and by associated scaling/modelling studies. VICTORIA represents an 1/15th scale model of the Loviisa containment, hydrogen is simulated by helium, and local concentration measurements are obtained by a newly developed instrument specifically for this purpose, called SPARTA. This paper is focused on experimental results from several key experiments that provide a first delineation of key behaviors.

  14. Complex metal hydrides for hydrogen, thermal and electrochemical energy storage

    DEFF Research Database (Denmark)

    Møller, Kasper T.; Sheppard, Drew; Ravnsbæk, Dorthe B.

    2017-01-01

    Hydrogen has a very diverse chemistry and reacts with most other elements to form compounds, which have fascinating structures, compositions and properties. Complex metal hydrides are a rapidly expanding class of materials, approaching multi-functionality, in particular within the energy storage...... field. This review illustrates that complex metal hydrides may store hydrogen in the solid state, act as novel battery materials, both as electrolytes and electrode materials, or store solar heat in a more efficient manner as compared to traditional heat storage materials. Furthermore, it is highlighted...... inspiration to solve the great challenge of our time: efficient conversion and large-scale storage of renewable energy....

  15. Complex Metal Hydrides for Hydrogen, Thermal and Electrochemical Energy Storage

    DEFF Research Database (Denmark)

    Moller, Kasper T.; Sheppard, Drew; Ravnsbaek, Dorthe B.

    2017-01-01

    Hydrogen has a very diverse chemistry and reacts with most other elements to form compounds, which have fascinating structures, compositions and properties. Complex metal hydrides are a rapidly expanding class of materials, approaching multi-functionality, in particular within the energy storage...... field. This review illustrates that complex metal hydrides may store hydrogen in the solid state, act as novel battery materials, both as electrolytes and electrode materials, or store solar heat in a more efficient manner as compared to traditional heat storage materials. Furthermore, it is highlighted...... inspiration to solve the great challenge of our time: efficient conversion and large-scale storage of renewable energy....

  16. Corrosion behavior of construction materials for ionic liquid hydrogen compressor

    DEFF Research Database (Denmark)

    Arjomand Kermani, Nasrin; Petrushina, Irina; Nikiforov, Aleksey Valerievich

    2016-01-01

    The corrosion behavior of various commercially available stainless steels and nickel-based alloys as possible construction materials for components which are in direct contact with one of five different ionic liquids was evaluated. The ionic liquids, namely: 1-ethyl-3-methylimidazolium triflate, 1...... liquid hydrogen compressor. An electrochemical cell was specially designed, and steady-state cyclic voltammetry was used to measure the corrosion resistance of the alloys in the ionic liquids at 23 °C, under atmospheric pressure. The results showed a very high corrosion resistance and high stability...... for all the alloys tested. The two stainless steels, AISI 316L and AISI 347 showed higher corrosion resistance compared to AISI 321 in all the ionic liquids tested. It was observed that small addition of molybdenum, tantalum, and niobium to the alloys increased the corrosion stability in the ionic liquids...

  17. Electrochemical properties of undoped hydrogen terminated CVD diamond

    Czech Academy of Sciences Publication Activity Database

    Nebel, C.E.; Kato, H.; Rezek, Bohuslav; Shin, D.; Takeuchi, D.; Watanabe, H.; Yamamoto, T.

    2006-01-01

    Roč. 15, - (2006), s. 264-268 ISSN 0925-9635 Institutional research plan: CEZ:AV0Z10100521 Keywords : ion-sensitive field effect transistor * intrinsic CVD diamond * hydrogen termination, Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.935, year: 2006

  18. Combustion of hydrogen-oxygen mixture in electrochemically generated nanobubbles

    NARCIS (Netherlands)

    Svetovoy, Vitaly; Sanders, Remco G.P.; Lammerink, Theodorus S.J.; Elwenspoek, Michael Curt

    2011-01-01

    Ignition of exothermic chemical reactions in small volumes is considered as difficult or impossible due to the large surface-to-volume ratio. Here observation of the spontaneous reaction is reported between hydrogen and oxygen in bubbles whose diameter is smaller than a threshold value around 150

  19. Electrochemical titration of hydrogen adsorbed on supported platinum catalysts

    Czech Academy of Sciences Publication Activity Database

    Paseka, Ivo

    2007-01-01

    Roč. 329, - (2007), s. 161-163 ISSN 0926-860X R&D Projects: GA ČR GA104/03/0409 Institutional research plan: CEZ:AV0Z40320502 Keywords : platinum * hydrogen adsorption * specific surface area Subject RIV: CA - Inorganic Chemistry Impact factor: 3.166, year: 2007

  20. Complex Metal Hydrides for Hydrogen, Thermal and Electrochemical Energy Storage

    Directory of Open Access Journals (Sweden)

    Kasper T. Møller

    2017-10-01

    Full Text Available Hydrogen has a very diverse chemistry and reacts with most other elements to form compounds, which have fascinating structures, compositions and properties. Complex metal hydrides are a rapidly expanding class of materials, approaching multi-functionality, in particular within the energy storage field. This review illustrates that complex metal hydrides may store hydrogen in the solid state, act as novel battery materials, both as electrolytes and electrode materials, or store solar heat in a more efficient manner as compared to traditional heat storage materials. Furthermore, it is highlighted how complex metal hydrides may act in an integrated setup with a fuel cell. This review focuses on the unique properties of light element complex metal hydrides mainly based on boron, nitrogen and aluminum, e.g., metal borohydrides and metal alanates. Our hope is that this review can provide new inspiration to solve the great challenge of our time: efficient conversion and large-scale storage of renewable energy.

  1. A direct electrochemical route from ilmenite to hydrogen-storage ferrotitanium alloys.

    Science.gov (United States)

    Ma, Meng; Wang, Dihua; Hu, Xiaohong; Jin, Xianbo; Chen, George Z

    2006-06-23

    An unrecognised but predictable need for a hydrogen-supported society is tens or even hundreds of million tonnes of hydrogen-storage materials, and thus challenges existing technologies in terms of resource and economical realities. Ilmenite is an abundant mineral, and ferrotitanium alloys are among the earliest known hydrogen-storage materials. At present, industrial production of ferrotitanium alloys goes through separate extraction of individual metals, followed by a multistep arc-melting process. In particular, the extraction of titanium from ilmenite is highly energy intensive and tedious, accounting for titanium's high market price and restricted uses. This article reports the electrochemical synthesis of various ferrotitanium alloy powders directly from solid ilmenite in molten calcium chloride. More importantly, it demonstrates, for the first time, that such produced alloy powders can be used without further treatment for hydrogen storage and perform comparably with or better than similar products by means of other methods, but cost just a fraction.

  2. Flexible Thick-Film Electrochemical Sensors: Impact of Mechanical Bending and Stress on the Electrochemical Behavior

    Science.gov (United States)

    Cai, Jiaying; Cizek, Karel; Long, Brenton; McAferty, Kenyon; Campbell, Casey G.; Allee, David R.; Vogt, Bryan D.; La Belle, Jeff; Wang, Joseph

    2009-01-01

    The influence of the mechanical bending, rolling and crimping of flexible screen-printed electrodes upon their electrical properties and electrochemical behavior has been elucidated. Three different flexible plastic substrates, Mylar, polyethylene naphthalate (PEN), and Kapton, have been tested in connection to the printing of graphite ink working electrodes. Our data indicate that flexible printed electrodes can be bent to extremely small radii of curvature and still function well, despite a marginal increase the electrical resistance. Below critical radii of curvature of ~8 mm, full recovery of the electrical resistance occurs upon strain release. The electrochemical response is maintained for sub-mm bending radii and a 180° pinch of the electrode does not lead to device failure. The electrodes appear to be resistant to repeated bending. Such capabilities are demonstrated using model compounds, including ferrocyanide, trinitrotoluene (TNT) and nitronaphthalene (NN). These printed electrodes hold great promise for widespread applications requiring flexible, yet robust non-planar sensing devices. PMID:20160861

  3. Enhanced electrochemical reduction of hydrogen peroxide on silver paste electrodes modified with surfactant and salt

    OpenAIRE

    Gonzalez-Macia, L.; Smyth, M.; Morrin, A.; Killard, A.

    2011-01-01

    The modification of silver paste electrodes with a combination of dodecyl benzenesulphonic acid and KCl has been shown to lead to significant enhancements of the electrochemical reduction of hydrogen peroxide. The catalytic enhancement was shown to be dependent on the concentration of the surfactant/salt solution, which resulted in increases of some 80-fold in amperometric response to hydrogen peroxide at – 0.1 V vs. Ag/AgCl, pH 6.8 over unmodified silver paste. Physical analysis showed modif...

  4. Selective Electrochemical Generation of Hydrogen Peroxide from Water Oxidation

    DEFF Research Database (Denmark)

    Viswanathan, Venkatasubramanian; Hansen, Heine Anton; Nørskov, Jens K.

    2015-01-01

    Water is a life-giving source, fundamental to human existence, yet over a billion people lack access to clean drinking water. The present techniques for water treatment such as piped, treated water rely on time and resource intensive centralized solutions. In this work, we propose a decentralized...... evolution and form hydrogen peroxide. Using density functional theory calculations, we show that the free energy of adsorbed OH* can be used to determine selectivity trends between the 2e(-) water oxidation to H2O2 and the 4e(-) oxidation to O2. We show that materials which bind oxygen intermediates...

  5. Scalable and efficient separation of hydrogen isotopes using graphene-based electrochemical pumping

    OpenAIRE

    Lozada Hidalgo, Marcelo; Zhang, Sheng; Hu, Sheng; Esfandiar, Ali; Grigorieva, Irina; Geim, Andre

    2017-01-01

    Thousands of tons of isotopic mixtures are processed annually for heavy-water production and tritium decontamination. The existing technologies remain extremely energy intensive and require large capital investments. New approaches are needed to reduce the industry's footprint. Recently, micrometre-size crystals of graphene are shown to act as efficient sieves for hydrogen isotopes pumped through graphene electrochemically. Here we report a fully-scalable approach, using graphene obtained by ...

  6. Hydrogen evolution activity and electrochemical stability of selected transition metal carbides in concentrated phosphoric acid

    DEFF Research Database (Denmark)

    Tomás García, Antonio Luis; Jensen, Jens Oluf; Bjerrum, Niels J.

    2014-01-01

    Alternative catalysts based on carbides of Group 5 (niobium and tantalum) and 6 (chromium, molybdenum and tungsten) metals were prepared as films on the metallic substrates. The electrochemical activities of these carbide electrodes towards the hydrogen evolution reaction (HER) in concentrated......, attributable to the different electronic structures. Tungsten carbide among the studied electrode samples exhibited the highest HER activity. Upon anodic potential scans in the presence of oxygen, chromium, tantalum and tungsten carbides displayed passivation due to the formation of stable surface layers...

  7. Combustion of hydrogen-oxygen mixture in electrochemically generated nanobubbles.

    Science.gov (United States)

    Svetovoy, Vitaly B; Sanders, Remko G P; Lammerink, Theo S J; Elwenspoek, Miko C

    2011-09-01

    Ignition of exothermic chemical reactions in small volumes is considered as difficult or impossible due to the large surface-to-volume ratio. Here observation of the spontaneous reaction is reported between hydrogen and oxygen in bubbles whose diameter is smaller than a threshold value around 150 nm. The effect is attributed to high Laplace pressure and to fast dynamics in nanobubbles and is the first indication on combustion in the nanoscale. In this study the bubbles were produced by water electrolysis using successive generation of H(2) and O(2) above the same electrode with short voltage pulses in the microsecond range. The process was observed in a microsystem at current densities >1000 A/cm(2) and relative supersaturations >1000.

  8. Electrochemical behavior of labetalol at an ionic liquid modified carbon paste electrode and its electrochemical determination

    Directory of Open Access Journals (Sweden)

    Zhang Yan-Mei

    2013-01-01

    Full Text Available Electrochemical behavior of labetalol (LBT at carbon paste electrode (CPE and an ionic liquid1-benzyl-3-methylimidazolehexafluorophosphate([BnMIM]PF6modified carbon paste electrode([BnMIM]PF6/CPEin Britton-Robinson buffer solution (pH 2.0 was investigated by cyclic voltammetry (CV and square wave voltammetric (SWV. The experimental results showed that LBT at both the bare CPE and [BnMIM]PF6/CPEshowed an irreversible oxidation process, but at [BnMIM]PF6/CPE its oxidation peak current increased greatly and the oxidation peak potential shifted negatively. The electrode reaction process is a diffusion-controlled process involving one electron transferring accompanied by a participation of one proton at [BnMIM]PF6/CPE. At the same time, the electrochemical kinetic parameters were determined. Under the optimized electrochemical experimental conditions, the oxidation peak currents were proportional to LBT concentration in the range of 7.0 x 10-6-1.0 x 10-4 mol L-1 with the limit of detection(LOD, S/N=3 of 4.810 x 10-8 mol L-1and the limit of quantification(LOQ, S/N=10 of 1.60 x 10-7 mol L-1, respectively. The proposed method was successfully applied in the determination of LBT content in commercial tablet samples.

  9. On-site applicability of hydrogen peroxide producing microbial electrochemical cells (MECs) coupled with UV in wastewater disinfection study

    Science.gov (United States)

    Background: There is an increased interest in the application of microbial electrochemical cell (MEC) for the recovery of value-added products such as hydrogen gas and hydrogen peroxide (H2O2) from wastewater. H2O2 has strong oxidation capability and produces hydroxyl radicals wh...

  10. ON-SITE APPLICABILITY OF HYDROGEN PEROXIDE PRODUCING MICROBIAL ELECTROCHEMICAL CELLS COUPLED WITH UV IN WASTEWATER DISINFECTION STUDY

    Science.gov (United States)

    There is an increased interest in the application of microbial electrochemical cell (MEC) for the recovery of value-added products such as hydrogen gas and hydrogen peroxide (H2O2) from wastewater. H2O2 has strong oxidation capability and produces hydroxyl radicals when coupled w...

  11. An electrochemical study of the corrosion behavior of primer coated 2219-T87 aluminum

    Science.gov (United States)

    Danford, M. D.; Higgins, R. H.

    1985-01-01

    The corrosion behavior for 2219-T87 aluminum coated with various primers, including those used for the external tank and solid rocket boosters of the Space Shuttle Transportation System, were investigated using electrochemical techniques. Corrosion potential time, polarization resistance time, electrical resistance time, and corrosion rate time measurements were all investigated. It was found that electrical resistance time and corrosion rate time measurement were most useful for studying the corrosion behavior of painted aluminum. Electrical resistance time determination give useful information concerning the porosity of paint films, while corrosion rate time curves give important information concerning overall corrosion rates and corrosion mechanisms. In general, the corrosion rate time curves all exhibited at least one peak during the 30 day test period, which was attributed, according to the proposed mechanisms, to the onset of the hydrogen evolution reaction and the beginning of destruction of the protective properties of the paint film.

  12. In-situ electrochemical impedance spectroscopy measurements of zirconium alloy oxide conductivity: Relationship to hydrogen pickup

    International Nuclear Information System (INIS)

    Couet, Adrien; Motta, Arthur T.; Ambard, Antoine; Livigni, Didier

    2017-01-01

    Highlights: • In-situ electrochemistry on zirconium alloys in 360 °C pure water show oxide layer resistivity changes during corrosion. • A linear relationship is observed between oxide resistivity and instantaneous hydrogen pickup fraction. • The resistivity of the oxide layer formed on Zircaloy-4 (and thus its hydrogen pickup fraction) is higher than on Zr-2.5Nb. - Abstract: Hydrogen pickup during nuclear fuel cladding corrosion is a critical life-limiting degradation mechanism for nuclear fuel. Following a program dedicated to zirconium alloys, corrosion, it has been hypothesized that oxide electronic resistivity determines hydrogen pickup. In-situ electrochemical impedance spectroscopy experiments were performed on Zircaloy-4 and Zr-2.5Nb alloys in 360 °C water. The oxide resistivity was measured as function of time. The results show that as the oxide resistivity increases so does the hydrogen pickup fraction. The resistivity of the oxide layer formed on Zircaloy-4 is higher than on Zr-2.5Nb, resulting in a higher hydrogen pickup fraction of Zircaloy-4, compared to Zr-2.5Nb.

  13. Effect of hydrogen uptake on the electrochemical corrosion of N18 zircaloy under gamma irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Xin, Z.Y. [Lab of Advanced Materials, School of Materials Sciences and Engineering, Tsinghua University, Beijing 100084 (China); Ling, Y.H., E-mail: yhling@mail.tsinghua.edu.cn [Lab of Advanced Materials, School of Materials Sciences and Engineering, Tsinghua University, Beijing 100084 (China); Bai, Y.K.; Zeng, C.; Wang, S. [Lab of Advanced Materials, School of Materials Sciences and Engineering, Tsinghua University, Beijing 100084 (China); Clara, J.C. [Department of Chemistry, University of Western Ontario, London N6A 5B7, Ontario (Canada)

    2016-12-01

    Highlights: • Hydrogen permeation can promote the corrosion rate of N18 zircaloy. • Gamma irradiation can further accelerate the corrosion process. • A novel mechanism based on point defects was proposed to explain the relevant phenomena. - Abstract: It has been well recognized that dramatic hydrogen uptake occurred in zircaloy after kinetic transition and porous structure was observed subsequently due to phase transformation of tetragonal to monoclinic zirconia. Therefore, how hydrogen solute and gamma-induced capillary-embedded hydrolysis influence the corrosion of zircaloy is an intriguing issue. In this work, the effect of hydrogen uptake and gamma irradiation on corrosion of N18 zircaloy was studied. Raman spectra and atomic force microscopy (AFM) were employed to analyse phase structure and surface morphology. Potentiodynamic polarization and electrochemical impedance spectroscopy were utilized to qualitatively evaluate the electron transfer properties of the oxide film formed on the zircaloy surface after corrosion. The depth profile and surface chemical states of involving elements were analysed by auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS), respectively. It was found that hydrogen permeation can decline the integrity and impedance semicircle of the oxide films, the more the hydrogen uptake is; the smaller magnitude of impedance will be. In view of the gamma irradiation, it is demonstrated that it promotes the corrosion rate slightly. Based on the irradiation theory and existing phenomena, the underlying mechanism is proposed.

  14. A nanostructured Ni/graphene hybrid for enhanced electrochemical hydrogen storage

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Moon-Hyung; Min, Young-Je [Department of Chemistry and Green-Nano Materials Research Center, Kyungpook National University, Taegu 702-701 (Korea, Republic of); Gwak, Gyeong-Hyeon [Department of Chemistry and Medical Chemistry, College of Science and Technology, Yonsei University, Wonju, Gangwondo 220-710 (Korea, Republic of); Paek, Seung-Min, E-mail: smpaek@knu.ac.kr [Department of Chemistry and Green-Nano Materials Research Center, Kyungpook National University, Taegu 702-701 (Korea, Republic of); Oh, Jae-Min, E-mail: jaemin.oh@yonsei.ac.kr [Department of Chemistry and Medical Chemistry, College of Science and Technology, Yonsei University, Wonju, Gangwondo 220-710 (Korea, Republic of)

    2014-10-15

    Highlights: • Graphene oxide(GO) was hybridized with the Ni(OH){sub 2}. • The Ni(OH){sub 2}/GO was reduced to Ni/graphene. • XRD, TEM, and X-ray absorption spectroscopy were examined. • The hydrogen storage property of Ni/graphene was significantly enhanced. - Abstract: To fabricate electrochemical hydrogen storage materials with delaminated structure, the graphene oxide (GO) in the ethylene glycol solution was reassembled in the presence of the precursor of Ni nanoparticles, and then, the reassembled hybrid was reduced under hydrogen atmosphere to obtain Ni/graphene hybrid. X-ray diffraction patterns and X-ray absorption spectscopic (XAS) analysis clearly show that Ni nanoparticles in Ni/graphene hybrid maintain its nanosized nature even after hybridization with graphene nanosheet (GNS). According to the TEM analysis, the Ni nanoparticles with an average size of 5.2 nm are homogeneously distributed onto the GNS in such a way that the nanoporous structure with much amount of void spaces could be fabricated. The obtained Ni/GNS exhibits a hydrogen storage capacity of 160 mA h/g, while the specific capacity of the graphene nanosheet was only 21 mA h/g. A flexible delaminated structure of Ni/GNS nanocomposite could provide additional intercalation sites for accommodation of hydrogen, leading to the enhancement of hydrogen storage capacity.

  15. Nanoceria based electrochemical sensor for hydrogen peroxide detection.

    Science.gov (United States)

    Ujjain, Sanjeev Kumar; Das, Anubhav; Srivastava, Gaurav; Ahuja, Preety; Roy, Manas; Arya, Aditya; Bhargava, Kalpana; Sethy, Niroj; Singh, Sushil Kumar; Sharma, Raj Kishore; Das, Mainak

    2014-09-01

    Oxidative stress is a condition when the concentration of free radicals and reactive molecular species rise above certain level in living systems. This condition not only perturbs the normal physiology of the system but also has been implicated in many diseases in humans and other animals. Hydrogen peroxide (H2O2) is known to be involved in induction of oxidative stress and has also been linked to a variety of ailments such as inflammation, rheumatoid arthritis, diabetes, and cancer in humans. It is one of the more stable reactive molecular species present in living systems. Because of its stability and links with various diseases, sensing the level of H2O2 can be of great help in diagnosing these diseases, thereby easing disease management and amelioration. Nanoceria is a potent candidate in free radical scavenging as well as sensing because of its unique redox properties. These properties have been exploited, in the reported work, to sense and quantify peroxide levels. Nanoceria has been synthesized using different capping agents: Hexamethylene-tetra-amine (HMTA) and fructose. CeO2-HMTA show rhombohedral and cubic 6.4 nm particles whereas CeO2-fructose are found to be spherical with average particle diameter size 5.8 nm. CeO2-HMTA, due to the better exposure of the active (200) and (220) planes relative to (111) plane, exhibits superior electrocatalytic activity toward H2O2 reduction. Amperometric responses were measured by increasing H2O2 concentration. The authors observed a sensitivity of 21.13 and 9.6 μA cm(-2) mM(-1) for CeO2-HMTA and CeO2-fructose, respectively. The response time of 4.8 and 6.5 s was observed for CeO2-HMTA and CeO2-fructose, respectively. The limit of detection is as low as 0.6 and 2.0 μM at S/N ratio 3 for CeO2-HMTA and CeO2-fructose, respectively. Ceria-HMTA was further tested for its antioxidant activity in an animal cell line in vitro and the results confirmed its activity.

  16. An Integrated Device View on Photo-Electrochemical Solar-Hydrogen Generation.

    Science.gov (United States)

    Modestino, Miguel A; Haussener, Sophia

    2015-01-01

    Devices that directly capture and store solar energy have the potential to significantly increase the share of energy from intermittent renewable sources. Photo-electrochemical solar-hydrogen generators could become an important contributor, as these devices can convert solar energy into fuels that can be used throughout all sectors of energy. Rather than focusing on scientific achievement on the component level, this article reviews aspects of overall component integration in photo-electrochemical water-splitting devices that ultimately can lead to deployable devices. Throughout the article, three generalized categories of devices are considered with different levels of integration and spanning the range of complete integration by one-material photo-electrochemical approaches to complete decoupling by photovoltaics and electrolyzer devices. By using this generalized framework, we describe the physical aspects, device requirements, and practical implications involved with developing practical photo-electrochemical water-splitting devices. Aspects reviewed include macroscopic coupled multiphysics device models, physical device demonstrations, and economic and life cycle assessments, providing the grounds to draw conclusions on the overall technological outlook.

  17. Hydrogen Gas Recycling for Energy Efficient Ammonia Recovery in Electrochemical Systems.

    Science.gov (United States)

    Kuntke, Philipp; Rodríguez Arredondo, Mariana; Widyakristi, Laksminarastri; Ter Heijne, Annemiek; Sleutels, Tom H J A; Hamelers, Hubertus V M; Buisman, Cees J N

    2017-03-07

    Recycling of hydrogen gas (H 2 ) produced at the cathode to the anode in an electrochemical system allows for energy efficient TAN (Total Ammonia Nitrogen) recovery. Using a H 2 recycling electrochemical system (HRES) we achieved high TAN transport rates at low energy input. At a current density of 20 A m -2 , TAN removal rate from the influent was 151 g N m -2 d -1 at an energy demand of 26.1 kJ g N -1 . The maximum TAN transport rate of 335 g N m -2 d -1 was achieved at a current density of 50 A m -2 and an energy demand of 56.3 kJ g N -1 . High TAN removal efficiency (73-82%) and recovery (60-73%) were reached in all experiments. Therefore, our HRES is a promising alternative for electrochemical and bioelectrochemical TAN recovery. Advantages are the lower energy input and lower risk of chloride oxidation compared to electrochemical technologies and high rates and independence of organic matter compared to bioelectrochemical systems.

  18. Thermo-electrochemical production of compressed hydrogen from methane with near-zero energy loss

    Science.gov (United States)

    Malerød-Fjeld, Harald; Clark, Daniel; Yuste-Tirados, Irene; Zanón, Raquel; Catalán-Martinez, David; Beeaff, Dustin; Morejudo, Selene H.; Vestre, Per K.; Norby, Truls; Haugsrud, Reidar; Serra, José M.; Kjølseth, Christian

    2017-11-01

    Conventional production of hydrogen requires large industrial plants to minimize energy losses and capital costs associated with steam reforming, water-gas shift, product separation and compression. Here we present a protonic membrane reformer (PMR) that produces high-purity hydrogen from steam methane reforming in a single-stage process with near-zero energy loss. We use a BaZrO3-based proton-conducting electrolyte deposited as a dense film on a porous Ni composite electrode with dual function as a reforming catalyst. At 800 °C, we achieve full methane conversion by removing 99% of the formed hydrogen, which is simultaneously compressed electrochemically up to 50 bar. A thermally balanced operation regime is achieved by coupling several thermo-chemical processes. Modelling of a small-scale (10 kg H2 day-1) hydrogen plant reveals an overall energy efficiency of >87%. The results suggest that future declining electricity prices could make PMRs a competitive alternative for industrial-scale hydrogen plants integrating CO2 capture.

  19. Electrochemical behavior of some binary and polynary uranium alloys

    International Nuclear Information System (INIS)

    Levy, M.; Zabielski, C.V.

    1976-01-01

    The corrosion behavior of U-1.8Mo, U-3.75Mo, U-1.76Ti, U-3.41Ti, unalloyed uranium, uranium ''quad'', ''quint'', and U-3/4Ti (STA) has been studied by means of electrochemical measurements. Active-passive behavior was exhibited in sulfuric acid, sodium hydroxide, ammonium hydroxide, sodium sulfate, sodium niturate, sodium chromate, ammonium chromate, magnesium chromate and sodium molybdate solutions. Chloride additions as small as 0.005M destroyed passivity and caused pitting. Chromates, sulfates, nitrates, and molybdates behaved as inhibitors in solutions containing low concentrations of chlorides. The uranium-molybdenum alloys were resistant to corrosion in chloride solutions than the uranium-titanium alloys

  20. Hydrogen Production From Crude Bio-oil and Biomass Char by Electrochemical Catalytic Reforming

    Science.gov (United States)

    Li, Xing-long; Ning, Shen; Yuan, Li-xia; Li, Quan-xin

    2011-08-01

    We reports an efficient approach for production of hydrogen from crude bio-oil and biomass char in the dual fixed-bed system by using the electrochemical catalytic reforming method. The maximal absolute hydrogen yield reached 110.9 g H2/kg dry biomass. The product gas was a mixed gas containing 72%H2, 26%CO2, 1.9%CO, and a trace amount of CH4. It was observed that adding biomass char (a by-product of pyrolysis of biomass) could remarkably increase the absolute H2 yield (about 20%-50%). The higher reforming temperature could enhance the steam reforming reaction of organic compounds in crude bio-oil and the reaction of CO and H2O. In addition, the CuZn-Al2O3 catalyst in the water-gas shift bed could also increase the absolute H2 yield via shifting CO to CO2.

  1. Effects of current upon hydrogen production from electrochemical catalytic reforming of acetic acid

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Yaqiong; Yuan, Lixia; Ye, Tongqi; Qiu, Songbai; Zhu, Xifeng; Li, Quanxin [Department of Chemical Physics, Lab of Biomass Clean Energy, University of Science and Technology of China, 96 Jinzhai Road, Hefei, Anhui 230026 (China); Torimoto, Youshifumi [Oxy Japan Corporation, 7 Floor, Miya Building, 4-3-4, Kojimachi, Chiyoda-ku, Tokyo 102-0083 (Japan); Yamamoto, Mitsuo [College of Arts and Sciences, The University of Tokyo, 3-8-1 Komaba, Meguro-ku, Tokyo 153-8902 (Japan)

    2009-02-15

    Production of hydrogen from acetic acid (HAc) was performed by using a novel electrochemical catalytic reforming (ECR) approach over the 18%NiO/Al{sub 2}O{sub 3} catalyst. ECR was carried out in a fixed-bed continuous flow reactor, where an ac electric current was passed through the catalyst. A high yield of hydrogen (>90%) and carbon conversion (>90%) were obtained as the reforming temperature over 400 C via the ECR approach. The influences of the current on the HAc decomposition, its reforming, and the catalyst reduction in the ECR process have been investigated, which were compared with those in the common steam reforming (CSR) route. The mechanism of the HAc reforming in ECR was also discussed based on the present investigation. (author)

  2. The effect of hydrogen peroxide on the electrochemical behaviour of Ti-13Nb-13Zr alloy in Hanks' solution

    Directory of Open Access Journals (Sweden)

    Sérgio Luiz de Assis

    2006-12-01

    Full Text Available Titanium alloys are largely used for biomedical applications mainly due to their high corrosion resistance resulting from the protective oxide film formed on their surface. The literature, however, has pointed out discrepancies between in vitro tests and in vivo tests. These discrepancies have been ascribed to hydrogen peroxide (H2O2 generated by inflammatory reactions. In this investigation the electrochemical behaviour of a Ti-13Nb-13Zr alloy, which was developed as material for implants, has been evaluated in Hanks' solution, with and without H2O2. The evolution of the electrochemical behavior was monitored by electrochemical impedance spectroscopy (EIS and the results were fitted to an equivalent circuit that simulates an oxide film as a duplex layer structure composed of an inner barrier layer and an outer porous layer. In the solution without H2O2, the oxide film was very stable during the whole test period. On the other hand, in the solution with H2O2, the EIS results varied significantly, indicating a progressive decrease in the barrier layer resistance until 35 days which was followed by the restoration of the barrier layer protective characteristics against corrosion, either due to its growth or to its self-healing after partial consumption of the oxidant agent. The oxide film formed on the Ti alloy samples after 125 days of immersion in Hanks' solution, either with or without H2O2 was analyzed by XPS. The XPS results revealed the presence of TiO and TiO2 on the samples immersed in the two electrolytes, however, Ti2O3 was only found on the samples exposed to the H2O2 containing solution.

  3. Identification of intrinsic catalytic activity for electrochemical reduction of water molecules to generate hydrogen

    KAUST Repository

    Shinagawa, Tatsuya

    2015-01-01

    Insufficient hydronium ion activities at near-neutral pH and under unbuffered conditions induce diffusion-limited currents for hydrogen evolution, followed by a reaction with water molecules to generate hydrogen at elevated potentials. The observed constant current behaviors at near neutral pH reflect the intrinsic electrocatalytic reactivity of the metal electrodes for water reduction. This journal is © the Owner Societies.

  4. Hydrogen production aided solid oxide electrochemical reformer fed with octane: A theoretical analysis

    Energy Technology Data Exchange (ETDEWEB)

    Murashkina, A.A.; Demin, A.K.; Pikalova, E.Yu. [Institute of High Temperature Electrochemistry, 22 S. Kovalevskoy, 620219 Yekaterinburg (Russian Federation); Maragou, V.I.; Tsiakaras, P.E. [School of Engineering, Department of Mechanical Engineering, University of Thessaly, Pedion Areos, 383 34 Volos (Greece)

    2008-07-01

    In the present work the possibility of pure hydrogen production by a solid oxide electrochemical reformer (SOER) is examined. Initial reagents are water steam, flowing into the cathode channel and octane flowing into the anode channel. Three modes of reforming are considered: (i) steam reforming (SR-mode), (ii) preliminary octane partial oxidation (PO-mode) and (iii) preliminary octane reforming by exhaust anode gas recycling (EAGR-mode). A parametric analysis is carried out that can be easily applied for various hydrocarbons. It was found that the electromotive force (EMF) value depends mainly on the ratio of steam moles' number supplied to the cathode space to the number of hydrogen output moles (k-parameter). It was also found that EMF increases with k increase, while is weakly affected from the temperature and the heat losses amount. Moreover, the EMF average value under the PO-mode is lower than that under the SR-mode. Finally, it is shown that the SOER optimum characteristics can be reached under the EAGR-mode, since it provides the most favorable combination of the reforming efficiency and the rate of the electrochemical process. (author)

  5. Fatigue crack growth behavior in niobium-hydrogen alloys

    International Nuclear Information System (INIS)

    Lin, M.C.C.; Salama, K.

    1997-01-01

    Near-threshold fatigue crack growth behavior has been investigated in niobium-hydrogen alloys. Compact tension specimens (CTS) with three hydrogen conditions are used: hydrogen-free, hydrogen in solid solution, and hydride alloy. The specimens are fatigued at a temperature of 296 K and load ratios of 0.05, 0.4, and 0.75. The results at load ratios of 0.05 and 0.4 show that the threshold stress intensity range (ΔK th ) decreases as hydrogen is added to niobium. It reaches a minimum at the critical hydrogen concentration (C cr ), where maximum embrittlement occurs. The critical hydrogen concentration is approximately equal to the solubility limit of hydrogen in niobium. As the hydrogen concentration exceeds C cr , ΔK th increases slowly as more hydrogen is added to the specimen. At load ratio 0.75, ΔK th decreases continuously as the hydrogen concentration is increased. The results provide evidence that two mechanisms are responsible for fatigue crack growth behavior in niobium-hydrogen alloys. First, embrittlement is retarded by hydride transformation--induced and plasticity-induced crack closures. Second, embrittlement is enhanced by the presence of hydrogen and hydride

  6. The behavior of hydrogen in metals

    International Nuclear Information System (INIS)

    Hirabayashi, Makoto

    1975-01-01

    Explanation is made on the equilibrium diagrams of metal-hydrogen systems and the state of hydrogen in metals. Some metals perform exothermic reaction with hydrogen, and the others endothermic reaction. The former form stable hydrides and solid solutions over a wide range of composition. Hydrogen atoms in fcc and bcc metals are present at the interstitial positions of tetrahedron lattice and octahedron lattice. For example, hydrogen atoms in palladium are present at the intersititial positions of octahedron. When the ratio of the composition of hydrogen and palladium is 1:1, the structure becomes NaCl type. Hydrogen atoms in niobium and vanadium and present interstitially in tetrahedron lattice. Metal hydrides with high hydrogen concentration are becoming important recently as the containers of hydrogen. Hydrogen atoms diffuse in metals quite easily. The activation energy of the diffusion of hydrogen atoms in Nb and V is about 2-3 kcal/g.atom. The diffusion coefficient is about 10 -5 cm 2 /sec in alpha phase at room temperature. The number of jumps of a hydrogen atom between neighboring lattice sites is 10 11 --10 12 times per second. This datum is almost the same as that of liquid metals. Discussion is also made on the electronic state of hydrogen in metals. (Fukutomi, T.)

  7. [The effect of hydrogen peroxide on the electrochemical corrosion properties and metal ions release of nickel-chromium dental alloys].

    Science.gov (United States)

    Wang, Jue; Qiao, Guang-yan

    2013-04-01

    To investigate the effect of hydrogen peroxide on the electrochemical corrosion and metal ions release of nickel-chromium dental alloys. The corrosion resistance of nickel-chromium dental alloys was compared by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization curve (PD) methods in artificial saliva after immersed in different concentrations of hydrogen peroxide for 112 h. The metal ions released from nickel-chromium dental alloys to the artificial saliva were detected after electrochemical measurements using inductively coupled plasma mass spectrometry (ICP-MS). The data was statistically analyzed by analysis of variance (ANOVA) using SPSS 13.0 software package. The electrochemical experiment showed that the sequence of polarization resistance in equivalent circuit (Rct), corrosion potential (Ecorr), pitting breakdown potential (Eb), and the difference between Ecorr and Eb representing the "pseudo-passivation" (δE) of nickel-chromium alloys in artificial saliva was 30% alloys to the artificial saliva, and the order of the concentrations of metal ions was 0% corrosion resistance of nickel-chromium dental alloys decrease after immersed in different concentrations of hydrogen peroxide for 112 h. Nickel-chromium dental alloys are more prone to corrosion in the artificial saliva with the concentration of hydrogen peroxide increased, and more metal ions are released in the artificial saliva.

  8. Investigation of Physical Properties and Electrochemical Behavior of Nitrogen-Doped Diamond-Like Carbon Thin Films

    Directory of Open Access Journals (Sweden)

    Rattanakorn Saensak

    2014-03-01

    Full Text Available This work reports characterizations of diamond-like carbon (DLC films used as electrodes for electrochemical applications. DLC thin films are prepared on glass slides and silicon substrates by radio frequency plasma enhanced chemical vapor deposition (RF-PECVD using a gas mixture of methane and hydrogen. In addition, the DLC films are doped with nitrogen in order to reduce electrical resistivity. Compared to the undoped DLC films, the electrical resistivity of nitrogen-doped (N-doped DLC films is decreased by three orders of magnitude. Raman spectroscopy and UV/Vis spectroscopy analyses show the structural transformation in N-doped DLC films that causes the reduction of band gap energy. Contact angle measurement at N-doped DLC films indicates increased hydrophobicity. The results obtained from the cyclic voltammetry measurements with Fe(CN63-/Fe(CN64- redox species exhibit the correlation between the physical properties and electrochemical behavior of DLC films.

  9. Electrochemical Behaviour and Hydrogen Evolution Efficiency of Ni-30at.%Cu Electrode in Alkaline Medium

    International Nuclear Information System (INIS)

    Kibria, A.K.M. Fazle.

    2007-01-01

    The surface reaction characteristics, hydrogen evolution efficiency and hydrogen evolution reaction kinetics of Ni-30at.%Cu electrode have been investigated in 30wt.%KOH electrolyte at room temperature by cyclic voltammetric technique. The cyclic voltammogram of the electrode showed three couples of oxidation-reduction peaks in between the potential range -1.1 to + 0.4 V. It was realized that the peak couples originated from the electrochemical transformations of Ni(o)↔ Ni(OH) 2 , Cu(o) ↔ Cu(I) and Cu(I) ↔ Cu(OH) 2 , respectively. Cycling at progressively negative potentials starting from + 0.4 V and then prolonged cycling between -1.1 to + 0.4 V showed that the redox transformations are not enhancing the hydrogen adsorption and hydrogen evolution. An interference of the adsorped hydrogen over Cu surface on the transformation of Ni(OH) 2 → Ni(O) was observed. It can be eliminated by varying the anodic terminal potential from + 0.4 V to - 0.2 V. Hydrogen evolution current density (i) vs. overpotential(η) plot showed two well-defined Tafel regions. For the low η region, the exchange current density (i o ) and Tafel slope (b) values were found to be 8.71* 10 -3 mA/cm 2 and 85 mV/dec, respectively. In case of high η region, the obtained io and b values appeared to be 2.74 mA/cm 2 and 265 mV/dec, respectively. Experimental η values coincided with the calculated values at 100 mA/cm 2 and 10 mA/cm 2 indicating the experimental accuracy. The observed (i o ) value for the high η region is 1.3 and 2.2 times higher than those of pure Ni and Cu Electrodes, respectively. The b value for the lowη region showed almost equality to that of the pure Ni electrode. The results indicate that addition of Cu to Ni may increase the hydrogen evolution efficiency remarkably. Ni-30at.%Cu electrode showed better performance than the pure Ni and Cu electrodes when they employed separately.(author)

  10. Scalable and efficient separation of hydrogen isotopes using graphene-based electrochemical pumping

    Science.gov (United States)

    Lozada-Hidalgo, M.; Zhang, S.; Hu, S.; Esfandiar, A.; Grigorieva, I. V.; Geim, A. K.

    2017-05-01

    Thousands of tons of isotopic mixtures are processed annually for heavy-water production and tritium decontamination. The existing technologies remain extremely energy intensive and require large capital investments. New approaches are needed to reduce the industry's footprint. Recently, micrometre-size crystals of graphene are shown to act as efficient sieves for hydrogen isotopes pumped through graphene electrochemically. Here we report a fully-scalable approach, using graphene obtained by chemical vapour deposition, which allows a proton-deuteron separation factor of around 8, despite cracks and imperfections. The energy consumption is projected to be orders of magnitude smaller with respect to existing technologies. A membrane based on 30 m2 of graphene, a readily accessible amount, could provide a heavy-water output comparable to that of modern plants. Even higher efficiency is expected for tritium separation. With no fundamental obstacles for scaling up, the technology's simplicity, efficiency and green credentials call for consideration by the nuclear and related industries.

  11. Synthesis of Biokerosene through Electrochemical Hydrogenation of Terpene Hydrocarbons from Turpentine Oil

    Directory of Open Access Journals (Sweden)

    Tedi Hudaya

    2016-12-01

    Full Text Available Indonesia possesses great potential for developing renewable resources as alternative fuels. For example, turpentine oil obtained from Pinus merkusii, which contains mostly monoterpene hydrocarbons (C10H16. The oil is highly suitable to be processed for biokerosene or even jet biofuel. It consists of hydrocarbons within the range of C10 to C15. However, it contains insufficient H and thus needs to be upgraded. In the present work, electrochemical hydrogenation was used for upgrading. In the electrochemical cell, stainless steel, silver, and carbon were used alternately for the anode, while copper and silver Raschig rings were used for the cathode. An electrolyte solution of cuprous ammonium formate was utilized not only as a source of H but also to draw the unsaturated hydrocarbons into the aqueous phase. The electrolyte : oil ratio (up to 2:1, electrolyte concentration (between 0.4 and 2 M and reaction time were varied throughout the experiments. The bromine number (unsaturation level of the turpentine oil, which was initially 1,86 (mole Br2/mole, was lowered significantly to 0.69-0.90. Promising increase of smoke point values were observed from 11 mm to 16-24 mm, indicating a higher H content of the processed oil, thus making it suitable as a substitute for petroleum kerosene.

  12. Production of bioelectricity, bio-hydrogen, high value chemicals and bioinspired nanomaterials by electrochemically active biofilms.

    Science.gov (United States)

    Kalathil, Shafeer; Khan, Mohammad Mansoob; Lee, Jintae; Cho, Moo Hwan

    2013-11-01

    Microorganisms naturally form biofilms on solid surfaces for their mutual benefits including protection from environmental stresses caused by contaminants, nutritional depletion or imbalances. The biofilms are normally dangerous to human health due to their inherited robustness. On the other hand, a recent study suggested that electrochemically active biofilms (EABs) generated by electrically active microorganisms have properties that can be used to catalyze or control the electrochemical reactions in a range of fields, such as bioenergy production, bioremediation, chemical/biological synthesis, bio-corrosion mitigation and biosensor development. EABs have attracted considerable attraction in bioelectrochemical systems (BESs), such as microbial fuel cells and microbial electrolysis cells, where they act as living bioanode or biocathode catalysts. Recently, it was reported that EABs can be used to synthesize metal nanoparticles and metal nanocomposites. The EAB-mediated synthesis of metal and metal-semiconductor nanocomposites is expected to provide a new avenue for the greener synthesis of nanomaterials with high efficiency and speed than other synthetic methods. This review covers the general introduction of EABs, as well as the applications of EABs in BESs, and the production of bio-hydrogen, high value chemicals and bio-inspired nanomaterials. Copyright © 2013 Elsevier Inc. All rights reserved.

  13. A nanocomposite-based electrochemical sensor for non-enzymatic detection of hydrogen peroxide.

    Science.gov (United States)

    Du, Xin; Chen, Yuan; Dong, Wenhao; Han, Bingkai; Liu, Min; Chen, Qiang; Zhou, Jun

    2017-02-21

    Hydrogen peroxide (H2O2) plays important signaling roles in normal physiology and disease. However, analyzing the actions of H2O2 is often impeded by the difficulty in detecting this molecule. Herein, we report a novel nanocomposite-based electrochemical sensor for non-enzymatic detection of H2O2. Graphene oxide (GO) was selected as the dopant for the synthesis of polyaniline (PANI), leading to the successful fabrication of a water-soluble and stable GO-PANI composite. GO-PANI was subsequently subject to cyclic voltammetry to generate reduced GO-PANI (rGO-PANI), enhancing the conductivity of the material. Platinum nanoparticles (PtNPs) were then electrodeposited on the surface of the rGO-PANI-modified glassy carbon electrode (GCE) to form an electrochemical H2O2 sensor. Compared to previously reported sensors, the rGO-PANI-PtNP/GCE exhibited an expanded linear range, higher sensitivity, and lower detection limit in the quantification of H2O2. In addition, the sensor displayed outstanding reproducibility and selectivity in real-sample examination. Our study suggests that the rGO-PANI-PtNP/GCE may have broad utility in H2O2 detection under physiological and pathological conditions.

  14. Structure and electrochemical hydrogen storage properties of Ti2Ni alloy synthesized by ball milling

    International Nuclear Information System (INIS)

    Hosni, B.; Li, X.; Khaldi, C.; ElKedim, O.; Lamloumi, J.

    2014-01-01

    Highlights: • The Ti 2 Ni alloy activation requires only one cycle of charge and discharge, regardless of the temperature. • By increasing the temperature the capacity loss, undergoes an increase and it is more pronounced for the 60 °C. • A good correlation is found between the evolutions of the different electrochemical parameters according to the temperature. - Abstract: The structure and the electrochemical hydrogen storage properties of amorphous Ti 2 Ni alloy synthesized by ball milling and used as an anode in nickel–metal hydride batteries were studied. Nominal Ti 2 Ni was synthesized under argon atmosphere at room temperature using a planetary high-energy ball mill. The structural and morphological characterization of the amorphous Ti 2 Ni alloy is carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The electrochemical characterization of the Ti 2 Ni electrodes is carried out by the galvanostatic charging and discharging, the constant potential discharge, the open circuit potential and the potentiodynamic polarization techniques. The Ti 2 Ni alloy activation requires only one cycle of charge and discharge, regardless of the temperature. The electrochemical discharge capacity of the Ti 2 Ni alloy, during the first eight cycles, and at a temperature of 30 °C, remained practically unchanged and a good held cycling is observed. By increasing the temperature, the electrochemical discharge capacity loss after eight cycles undergoes an increase and it is more pronounced for the temperature 60 °C. At 30 °C, the anodic corrosion current density is 1 mA cm −2 and then it undergoes a rapid drop, remaining substantially constant (0.06 mA cm −2 ) in the range 40–60 °C, before undergoing a slight increase to 70 °C (0.3 mA cm −2 ). This variation is in good agreement with the maximum electrochemical discharge capacity values found for the different temperatures. By increasing the

  15. Nanoparticle-based electrochemical sensors for the detection of lactate and hydrogen peroxide

    Science.gov (United States)

    Uzunoglu, Aytekin

    In the present study, electrochemical sensors for the detection of lactate and hydrogen peroxide were constructed by exploiting the physicochemical properties of metal ad metal oxide nanoparticles. This study can be divided into two main sections. While chapter 2, 3, and 4 report on the construction of electrochemical lactate biosensors using CeO2 and CeO2-based mixed metal oxide nanoparticles, chapter 5 and 6 show the development of electrochemical hydrogen peroxide sensors by the decoration of the electrode surface with palladium-based nanoparticles. First generation oxidase enzyme-based sensors suffer from oxygen dependency which results in errors in the response current of the sensors in O2-lean environments. To address this challenge, the surface of the sensors must be modified with oxygen rich materials. In this regard, we developed a novel electrochemical lactate biosensor design by exploiting the oxygen storage capacity of CeO2 and CeO 2-CuO nanoparticles. By the introduction of CeO2 nanoparticles into the enzyme layer of the sensors, negative interference effect of ascorbate which resulted from the formation of oxygen-lean regions was eliminated successfully. When CeO2-based design was exposed to higher degree of O2 -depleted environments, however, the response current of the biosensors experienced an almost 21 % decrease, showing that the OSC of CeO2 was not high enough to sustain the enzymatic reactions. When CeO2-CuO nanoparticles, which have 5 times higher OSC than pristine CeO2, were used as an oxygen supply in the enzyme layer, the biosensors did not show any drop in the performance when moving from oxygen-rich to oxygen-lean conditions. In the second part of the study, PdCu/SPCE and PdAg/rGO-based electrochemical H2O2 sensors were designed and their performances were evaluated to determine their sensitivity, linear range, detection limit, and storage stability. In addition, practical applicability of the sensors was studied in human serum. The

  16. Effect of thermal treatment on the electrochemical hydrogen absorption of ZrCrNi alloy

    Energy Technology Data Exchange (ETDEWEB)

    Ruiz, F.C.; Peretti, H.A.; Corso, H.L [Centro Atomico Bariloche, Comision Nacional de Energia Atomica, Bariloche (Argentina); Visintin, A.; Real, S.G.; Castro, E.B.; Triaca, W.E. [Univ. Nacional de La Plata, La Plata (Argentina). Inst. de Investigaciones Fisiquimicas Teoricas y Aplicadas

    2006-07-01

    The catalytic effect of the secondary phases contained in a ZrCrNi alloy on its electrochemical properties was investigated. The purpose of the study was to improve the performance of Ni-MH battery electrodes. Four samples of the alloy were given annealing treatments at T=1250 K at variable times to obtain different concentrations of the secondary phases. Phase structure, morphology, and composition were studied using X-ray diffraction; radiation; scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) microanalysis. Results of the study were compatible with the presence of a major AB{sub 2} phase of C15 structure and the co-existence of C14 and C15 structures in both the as-melted and annealed alloys. The effect of the annealing in the ZrCrNi alloy resulted in a remarkable reduction of the discharge capacity and activation that was attributed to the dissolution of the secondary phases. The major catalytic effect was associated with the Zr{sub 8}Ni{sub 21} phase, by increasing the discharge capacity and favouring the activation. It was concluded that the presence of the catalytic phase in the alloy increased the hydrogen absorption capacity of the electrode due to an enhancement of the hydrogen production by electrolysis on the metal/catalytic phase and electrolyte interface. 6 refs., 1 fig.

  17. Hardness and electrochemical behavior of ceramic coatings on Inconel

    Directory of Open Access Journals (Sweden)

    C. SUJAYA

    2012-03-01

    Full Text Available Thin films of ceramic materials like alumina and silicon carbide are deposited on Inconel substrate by pulsed laser deposition technique using Q-switched Nd: YAG laser. Deposited films are characterized using UV-visible spectrophotometry and X-ray diffraction. Composite microhardness of ceramic coated Inconel system is measured using Knoop indenter and its film hardness is separated using a mathematical model based on area-law of mixture. It is then compared with values obtained using nanoindentation method. Film hardness of the ceramic coating is found to be high compared to the substrates. Corrosion behavior of substrates after ceramic coating is studied in 3.5% NaCl solution by potentiodynamic polarization and electrochemical impedance spectroscopy measurements. The Nyquist and the Bode plots obtained from the EIS data are fitted by appropriate equivalent circuits. The pore resistance, the charge transfer resistance, the coating capacitance and the double layer capacitance of the coatings are obtained from the equivalent circuit. Experimental results show an increase in corrosion resistance of Inconel after ceramic coating. Alumina coated Inconel showed higher corrosion resistance than silicon carbide coated Inconel. After the corrosion testing, the surface topography of the uncoated and the coated systems are examined by scanning electron microscopy.

  18. Effect of Hydrogen Charging on the Stress Corrosion Behavior of 2205 Duplex Stainless Steel Under 3.5 wt.% NaCl Thin Electrolyte Layer

    Science.gov (United States)

    Zhao, Tianliang; Liu, Zhiyong; Hu, Shanshan; Du, Cuiwei; Li, Xiaogang

    2017-05-01

    The effect of hydrogen charging on the stress corrosion cracking (SCC) behavior of 2205 duplex stainless steel (DSS) under 3.5 wt.% NaCl thin electrolyte layer was investigated on precharged samples through hydrogen determination, electrochemical measurement, and slow strain rate tensile test. Results show that hydrogen charging weakens the passive film without inducing any obvious trace of localized anodic dissolution. Therefore, hydrogen charging increases the SCC susceptibility of 2205 DSS mainly through mechanism of hydrogen embrittlement rather than mechanism of localized anodic dissolution. 2205 DSS shows a more susceptibility to hydrogen under the TEL when hydrogen charging current density (HCCD) is between 20 and 50 mA cm-2. The increasing trend is remarkable when hydrogen charging current density increases from 20 to 50 mA cm-2 and fades after 50 mA cm-2.

  19. Electrochemical behavior of uranyl in anhydrous polar organic media

    Energy Technology Data Exchange (ETDEWEB)

    Burn, Adam G.; Nash, Kenneth L. [Washington State Univ., Pullmann, WA (United States). Dept. of Chemistry

    2017-09-01

    Weak complexes between pentavalent and hexavalent actinyl cations have been reported to exist in acidic, non-complexing high ionic strength aqueous media. Such ''cation-cation complexes'' were first identified in the context of actinide-actinide redox reactions in acidic aqueous media relevant to solvent extraction-based separation systems, hence their characterization is of potential interest for advanced nuclear fuel reprocessing. This chemistry could be relevant to efforts to develop advanced actinide separations based on the upper oxidation states of americium, which are of current interest. In the present study, the chemical behavior of pentavalent uranyl was examined in non-aqueous, aprotic polar organic solvents (propylene carbonate and acetonitrile) to determine whether UO{sub 2}{sup +} cations generated at the reducing working electrode surface would interact with the UO{sub 2}{sup 2+} cations in the bulk phase to form cation-cation complexes in such media. In magnesium perchlorate media, the electrolyte adsorbed onto the working electrode surface and interfered with the uranyl reduction/diffusion process through an ECE (electron transfer/chemical reaction/electron transfer) mechanism. In parallel studies of uranyl redox behavior in tetrabutylammonium hexafluorophosphate solutions, an EC (electron transfer/chemical reaction) mechanism was observed in the cyclic voltammograms. Ultimately, no conclusive electrochemical evidence demonstrated uranyl cation-cation interactions in the non-aqueous, aprotic polar organic solvent solutions, though the results reported do not completely rule out the presence of UO{sub 2}{sup +}.UO{sub 2}{sup 2+} complexes.

  20. Photo-electrochemical Investigation of Radiation-Enhanced Galvanic Coupling and Hydrogen Permeation in TPBAR-related Materials

    Energy Technology Data Exchange (ETDEWEB)

    Larsen, G. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2017-10-02

    Research conducted in FY17 used photo-electrochemical methods to investigate the potential for radiationenhanced galvanic coupling in tritium-producing burnable absorber rod (TPBAR) materials. Specifically, a laboratory electrochemical cell was coupled with UV light in order to perform electrochemical opencircuit voltage and galvanic current measurements, techniques that have been used successfully in previous studies to replicate galvanic processes in reactor settings. UV irradiation can mimic reactor-like behavior because, similar to both directly and indirectly ionizing radiation, UV photons with energy greater than the band gap of the material will generate free charge carriers (electrons and holes) and can substantially alter the passivating effect of metal oxides.

  1. Studies on the permeation of hydrogen through steam generator tubes at high temperatures using an electrochemical method

    International Nuclear Information System (INIS)

    Giraudeau, F.; Yang, L.; Steward, F.R.; DeBouvier, O.

    1998-01-01

    The permeation of hydrogen through steam generator tubes at high temperatures (∼ 300 degrees C) has been studied using an electrochemical technique. With this technique, hydrogen is generated on one side of the tube and monitored on the other side. The time for the hydrogen to reach the other side is used to determine the diffusion coefficient of hydrogen in the tube. Boundary conditions at the entry and exit sides have been investigated separately. Preliminary studies were performed on Stainless Steel 316 and Nickel Alloy 800 to better understand the influence of the solution chemistry on the electrochemical evolution of hydrogen. The surface phenomena effect and the trapping effect are discussed to account for differences observed in the permeation response. The hydrogen permeation through oxides at the exit side has been studied. Two nickel alloys (Alloy 800 and Alloy 600), materials widely used for steam generator tubes, have been investigated. The tubes were prefilmed using two different treatments. The oxides were formed in dry air at high temperatures (300 degrees C to 600 degrees C), or in humid gas at 300 degrees C. The diffusion coefficients at 300 degrees C in Stainless Steel 316 and Alloy 800 were determined to be of the order of 10 -6 - 10 -7 cm 2 /s for the bare metal. This is in agreement with results obtained by gas phase permeation techniques in the literature. (author)

  2. Electrochemical preparation and characteristics of Ni-Co-LaNi5 composite coatings as electrode materials for hydrogen evolution

    International Nuclear Information System (INIS)

    Wu Gang; Li Ning; Dai Changsong; Zhou Derui

    2004-01-01

    Electrocatalytic activity for the hydrogen evolution reaction on Ni-Co-LaNi 5 composite electrodes prepared by electrochemical codeposition technique was evaluated. The relationship between the current density for hydrogen evolution reaction and the amount of LaNi 5 particles in Ni-Co baths is like the well-known 'volcano plot'. The Surface morphology and microstructure of Ni-Co-LaNi 5 coatings were determined by means of scanning electron microscopy (SEM) and X-ray diffraction (XRD). The kinetic parameters were determined from electrochemical steady-state Tafel polarization and electrochemical impedance spectroscopy technology in 1 M NaOH solution. The values obtained for the apparent energies of activation are 32.48, 46.29 and 57.03 kJ mol -1 for the Ni-Co-LaNi 5 , Ni-Co and Ni electrodes, respectively. The hydrogen evolution reaction on Ni-Co-LaNi 5 proceeds via Volmer-Tafel reaction route with the mixed rate determining characteristics. The composite coating Ni-Co-LaNi 5 is catalytically more active than Ni and Ni-Co electrodes due to the increase in its real surface areas and the decrease in the apparent free energy of activation caused by the electrocatalytic synergistic effect of the Ni-Co alloys and the hydrogen storage intermetallic particles on the electrode surface

  3. In-situ investigation of hydrogen evolution behavior in vanadium redox flow batteries

    International Nuclear Information System (INIS)

    Wei, L.; Zhao, T.S.; Xu, Q.; Zhou, X.L.; Zhang, Z.H.

    2017-01-01

    Highlights: • An in-situ method to investigate hydrogen evolution in VRFBs is developed. • The rate of hydrogen evolution during battery operation is quantified. • The gas evolution behaviors in the charge process of VRFBs are observed. - Abstract: In this work, we conceived and fabricated a three-electrode electrochemical cell and transparent vanadium redox flow battery to in-situ investigate the hydrogen evolution reaction during battery operation. Experimental results show that operating temperature has a strong influence on the HER rate. In particular, compared with V 3+ reduction reaction, HER is more sensitive to temperature variation. It is also found that, contrary to the conventional wisdom that side reactions occur at the late stage of the charge process, H 2 evolves at a relatively low SOC. About 0.26 and 1.94 mL H 2 were collected at an early (SOC lower than 20%) and end of the charge process, respectively, suggesting that attention to the hydrogen formation at the negative electrode in the early charge process should also be paid to during long-term battery operations. Moreover, the produced hydrogen gas at the negative side prefers to form macroscopically observable bubbles onto the electrode surface, covering the active sites for vanadium redox reactions, while oxygen evolution (including CO 2 production) at the positive side corrodes electrode surface and introduces certain oxygen-containing functional groups.

  4. Electrochemical behavior of synthesized Al{sub x}Sn{sub y} with mechanical grinding in hydrogen evolution reaction (HER); Comportamiento electroquimico del Al{sub x}Sn{sub y} sintetizado por molienda mecanica en la REH (Reaccion de Evolucion de Hidrogeno)

    Energy Technology Data Exchange (ETDEWEB)

    Olvera Vazquez, S. L.; Arce Estrada, E. M. [Instituto Politecnico Nacional, Mexico, D.F. (Mexico )]. E-mail: seydyliz@hotmail.com

    2009-09-15

    Currently, the best catalyst for HER is Pt, nevertheless because of its high costs, many studies have been performed with a variety of materials, including AI, which is a promising source of hydrogen. Therefore, this work studied the effect of tin on Al{sub x}Sn{sub y} alloys obtained by mechanical grinding. The materials obtained were characterized with electron sweep microscopy, x-ray diffraction and electrochemical techniques. It was determined that the synthesized materials have a micrometer size and present at least two phases. The electrochemical characterization for use as electrocatalysts for the hydrogen evolution reaction (HER) was performed in an NaCl 2 M solution using potentiodynamic polarization and chronoamperometry techniques, showing that the materials with low tin contents have better electrocatalytic activity for HER. [Spanish] Actualmente el mejor catalizador para la REH es el Pt, sin embargo debido a sus altos costos se han realizado numerosos estudios con diversos materiales entre los cuales se encuentra el Al, que es una promisoria fuente de hidrogeno. Por tal motivo en este trabajo se realizaron estudios del efecto que presenta el contenido de estano en aleaciones Al{sub x}Sn{sub y} obtenidas por molienda mecanica. Los materiales obtenidos se caracterizaron por microscopia electronica de barrido, difraccion de rayos X y tecnicas electroquimicas. Se determino que los materiales sintetizados son de tamano micrometrico y que al menos presentan dos fases. La caracterizacion electroquimica para su uso como electrocatalizadores para la reaccion de evolucion de hidrogeno, REH, se llevo a cabo en una solucion de NaCl 2 M, empleando las tecnicas de polarizacion potenciodinamica y cronoamperometria, observandose que los materiales con contenidos bajos de estano presentan una mejor actividad electrocatalitica para la REH.

  5. First Principles Calculations of Electrochemically Controlled Hydrogen Mobility and Uptake at the Ni(111)H2O Interface

    Energy Technology Data Exchange (ETDEWEB)

    C Taylor; R Kelly; M Neurock

    2005-11-14

    The binding of hydrogen on Ni(111) in the presence of an water is considered using both a bilayer and a saturated model of the solvent environment. The presence of a water bilayer did not change the binding energies or geometry of hydrogen on the Ni(111) compared to adsorption in ultra-high vacuum. Using the saturated model (four bilayers over the surface) we also monitored the change in hydrogen binding as a function of electrochemical potential. Binding energies for hydrogen at the hcp and octahedral sites shifted endothermically as the potential was made more anodic, indicating that reductive partial charge transfer occurs. Binding at the tetrahedral site was found to be partially oxidizing. Calculation of vibrational modes allowed the extrapolation of ab initio results to ambient and elevated temperatures. Surface Pourbaix diagrams were constructed illustrating the stability of various phases on the Ni(111) surface as a function of pH and potential.

  6. Surface science and electrochemical studies of metal-modified carbides for fuel cells and hydrogen production

    Science.gov (United States)

    Kelly, Thomas Glenn

    Carbides of the early transition metals have emerged as low-cost catalysts that are active for a wide range of reactions. The surface chemistry of carbides can be altered by modifying the surface with small amounts of admetals. These metal-modified carbides can be effective replacements for Pt-based bimetallic systems, which suffer from the drawbacks of high cost and low thermal stability. In this dissertation, metal-modified carbides were studied for reactions with applications to renewable energy technologies. It is demonstrated that metal-modified carbides possess high activity for alcohol reforming and electrochemical hydrogen production. First, the surface chemistry of carbides towards alcohol decomposition is studied using density functional theory (DFT) and surface science experiments. The Vienna Ab initio Simulation Package (VASP) was used to calculate the binding energies of alcohols and decomposition intermediates on metal-modified carbides. The calculated binding energies were then correlated to reforming activity determined experimentally using temperature programmed desorption (TPD). In the case of methanol decomposition, it was found that tungsten monocarbide (WC) selectively cleaved the C-O bond to produce methane. Upon modifying the surface with a single layer of metal such as Ni, Pt, or Rh, the selectivity shifted towards scission of the C-H bonds while leaving the C-O bond intact, producing carbon monoxide (CO) and H2. High resolution energy loss spectroscopy (HREELS) was used to examine the bond breaking sequence as a function of temperature. From HREELS, it was shown that the surfaces followed an activity trend of Rh > Ni > Pt. The Au-modified WC surface possessed too low of a methanol binding energy, and molecular desorption of methanol was the most favorable pathway on this surface. Next, the ability of Rh-modified WC to break the C-C bond of C2 and C3 alcohols was demonstrated. HREELS showed that ethanol decomposed through an acetaldehyde

  7. A novel enzymatic method for determination of homocysteine using electrochemical hydrogen sulfide sensor.

    Science.gov (United States)

    Zhao, Dong; Liu, Tsan-Zon; Chan, Err-Cheng; Fein, Harry; Zhang, Xueji

    2007-05-01

    Homocysteine is a sulfur-containing compound produced during metabolism process of methionine. Its uptake in human plasma is believed to be the cause of cardiovascular diseases and many other diseases. An electrochemical method was proposed for selective and quantitative measurement of homocysteine by employing hydrogen sulfide sensor coupled with methionine a, g-lyase. The principle of this method is to measure the evolved hydrogen sulfide from the enzymatic reaction between homocysteine and methionine a, g-lyase. The sensitivities of the measurements at different pH values of the tris buffer solutions and at room temperature peaked to 275 pA/mM at pH 6.5 with detection limit of 150 nM (based on 3 s cutoff). The linearity measurements at pH 6.5 were performed for the homocysteine concentrations range from 0.5 to 200 mM, which is wider than the human blood plasma total homocysteine level of 5 to 100 mM, and the regressive analysis of the experiments gave R2=0.9987. The enzyme also showed the fastest response to homocysteine in the tris buffer solution of pH 7.5 with the current approaching its maximum at 134 seconds. The interference tests against several common agents were carried out, and found that cysteine and methionine were the major two species to introduce measurement problem. The solution to this interference problem was explored and discussed thoroughly based on the preliminary tests. The sensitivities of the experiments against several enzyme concentrations were also performed.

  8. Synthesis of tantalum carbide and nitride nanoparticles using a reactive mesoporous template for electrochemical hydrogen evolution

    KAUST Repository

    Alhajri, Nawal Saad

    2013-01-01

    Tantalum carbide and nitride nanocrystals were prepared through the reaction of a tantalum precursor with mesoporous graphitic (mpg)-C 3N4. The effects of the reaction temperature, the ratio of the Ta precursor to the reactive template (mpg-C3N4), and the selection of the carrier gas (Ar, N2 and NH3) on the resultant crystal phases and structures were investigated. The produced samples were characterized using powder X-ray diffraction (XRD), CHN elemental analyses, thermogravimetric analyses (TGA), nitrogen sorption, a temperature-programmed reaction with mass spectroscopy (MS), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The results indicate that the different tantalum phases with cubic structure, TaN, Ta2CN, and TaC, can be formed under a flow of nitrogen when formed at different temperatures. The Ta3N5 phase with a Ta5+ oxidation state was solely obtained at 1023 K under a flow of ammonia, which gasified the C 3N4 template and was confirmed by detecting the decomposed gaseous products via MS. Significantly, the formation of TaC, Ta2CN, and TaN can be controlled by altering the weight ratio of the C 3N4 template relative to the Ta precursor at 1573 K under a flow of nitrogen. The high C3N4/Ta precursor ratio generally resulted in high carbide content rather than a nitride one, consistent with the role of mpg-C3N4 as a carbon source. Electrochemical measurements revealed that the synthesized nanomaterials were consistently able to produce hydrogen under acidic conditions (pH 1). The obtained Tafel slope indicates that the rate-determining step is the Volmer discharge step, which is consistent with adsorbed hydrogen being weakly bound to the surface during electrocatalysis. © 2013 The Royal Society of Chemistry.

  9. Molybdenum carbide-carbon nanocomposites synthesized from a reactive template for electrochemical hydrogen evolution

    KAUST Repository

    Alhajri, Nawal Saad

    2014-01-01

    Molybdenum carbide nanocrystals (Mo2C) with sizes ranging from 3 to 20 nm were synthesized within a carbon matrix starting from a mesoporous graphitic carbon nitride (mpg-C3N4) template with confined pores. A molybdenum carbide phase (Mo2C) with a hexagonal structure was formed using a novel synthetic method involving the reaction of a molybdenum precursor with the carbon residue originating from C3N4 under nitrogen at various temperatures. The synthesized nanocomposites were characterized using powder X-ray diffraction (XRD), temperature-programmed reaction with mass spectroscopy (MS), CHN elemental analyses, thermogravimetric analyses (TGA), nitrogen sorption, X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The results indicated that the synthesized samples have different surface structures and compositions, which are accordingly expected to exhibit different electrocatalytic activities toward the hydrogen evolution reaction (HER). Electrochemical measurements demonstrated that the sample synthesized at 1323 K exhibited the highest and most stable HER current in acidic media, with an onset potential of -100 mV vs. RHE, among the samples prepared in this study. This result is attributed to the sufficiently small particle size (∼8 nm on average) and accordingly high surface area (308 m2 g-1), with less oxidized surface entrapped within the graphitized carbon matrix. © 2014 the Partner Organisations.

  10. Deformation behavior of vanadium alloys containing hydrogen at constant stress

    International Nuclear Information System (INIS)

    Jiming Chen; Hui Cong; Yong Chen; Cong Li; Shaoyu Qiu

    2006-01-01

    Vanadium alloy, one of the candidates for next fusion reactors as structural materials, has the issue of mechanical property degradation by hydrogen absorption. In the present paper, V-4Cr-4Ti and an alternative V-6W-2.5Ti were studied for their tensile deformation behaviors at room temperature under constant load. The alloys contained 33-341 wppm H by a previous exposure in hydrogen gas at 500-800 o C for hours. Results showed hydrogen release during the tensile loading, which caused shrinkage of the specimens and the increase of elastic modulus and the decrease of tensile strength. Tensile holding the specimen at stress higher than yield strength led to a three-stage deformation behavior, similar to the traditional thermal creep but show stable deformation in the 3 rd stage. The steady deformation rate in this stage is much higher than that in the 2 nd one, and it increased with increasing hold stress and the increase of the hydrogen concentration. As the test temperature is fairly low, the deformation should be dislocation glide assisted and could be enhanced by hydrogen release. Hydrogen absorption and hydrogen release would bring about an issue of dimensional instability of structural components, which should be taken into account in the design. (author)

  11. Experimental studies of hydrogen behavior in ice condenser containments

    International Nuclear Information System (INIS)

    Lundstrom, P.; Tuomisto, H.; Lamberg, T.; Hongisto, O.

    1997-01-01

    A new hydrogen management scheme is being developed for the Loviisa ice condenser containment as a part of a comprehensive severe accident management (SAM) strategy. The scheme relies on containment-wide natural circulations that develop, once the ice condenser doors are forced open as a SAM measure, to produce effective mixing and a slow rise in hydrogen concentrations. Controlled removal of hydrogen from the containment atmosphere, and effective dissipation of the energy in the ice beds are also important elements of the hydrogen management scheme. The VICTORIA experiments in association with scaling and modelling studies are an important basis for the development of the hydrogen management scheme. VICTORIA represents an 1/15th scale model of the Loviisa containment. Numerous experiments have been carried out for studies of the convective flow behavior and hydrogen distribution. This paper focuses on experimental results on the important issues of containment upper compartment mixing behavior and containment behavior in a scenario with depleted ice condensers. (author)

  12. Study on the Carbonation Behavior of Cement Mortar by Electrochemical Impedance Spectroscopy

    Directory of Open Access Journals (Sweden)

    Biqin Dong

    2014-01-01

    Full Text Available A new electrochemical model has been carefully established to explain the carbonation behavior of cement mortar, and the model has been validated by the experimental results. In fact, it is shown by this study that the electrochemical impedance behavior of mortars varies in the process of carbonation. With the cement/sand ratio reduced, the carbonation rate reveals more remarkable. The carbonation process can be quantitatively accessed by a parameter, which can be obtained by means of the electrochemical impedance spectroscopy (EIS-based electrochemical model. It has been found that the parameter is a function of carbonation depth and of carbonation time. Thereby, prediction of carbonation depth can be achieved.

  13. Electrochemical Behavior of Quinoxalin-2-one Derivatives at Mercury Electrodes and Its Analytical Use

    OpenAIRE

    Zimpl, Milan; Skopalova, Jana; Jirovsky, David; Bartak, Petr; Navratil, Tomas; Sedonikova, Jana; Kotoucek, Milan

    2012-01-01

    Derivatives of quinoxalin-2-one are interesting compounds with potential pharmacological activity. From this point of view, understanding of their electrochemical behavior is of great importance. In the present paper, a mechanism of electrochemical reduction of quinoxalin-2-one derivatives at mercury dropping electrode was proposed. Pyrazine ring was found to be the main electroactive center undergoing a pH-dependent two-electron reduction process. The molecule protonization of nitrogen in th...

  14. Electrochemical behavior of parent and photodegradation products of some selected pesticides

    OpenAIRE

    Vaz, Carlos M. P.; Silva Jr., Paulo R. V.; Prado, Isis; Castanho, Giuliane M.; Simões, Fabio R.; Machado, Sérgio A. S.

    2008-01-01

    Electrochemical behavior of pesticides is extensively studied, but little attention has been given to the study of their degradation products (by-products) by electrochemical methods. However, the degradation products of pesticides can be even more toxic then the parent products and such studies should be encouraged. Therefore, the objective of this work was to evaluate the electroactivity of by-products of imazaquin, methylparathion, bentazon and atrazine, generated by UV irradiation and mea...

  15. Electrochemical hydrogen storage performance of Mg-Ti-Zr-Ni alloys

    Energy Technology Data Exchange (ETDEWEB)

    Anik, Mustafa; Akay, Isin; Oezdemir, Gizem; Baksan, Bedri [Department of Metallurgical and Materials Engineering Eskisehir Osmangazi University, 26480, Eskisehir (Turkey)

    2009-12-15

    Mg{sub 1.5}Ti{sub 0.5-x}Zr{sub x}Ni (x = 0, 0.1, 0.2, 0.3, 0.4), Mg{sub 1.5}Ti{sub 0.3}Zr{sub 0.1}Pd{sub 0.1}Ni and Mg{sub 1.5}Ti{sub 0.3}Zr{sub 0.1}Co{sub 0.1}Ni alloys were synthesized by mechanical alloying and their electrochemical hydrogen storage characteristics were investigated. X-ray diffraction studies showed that all the replacement elements (Ti, Zr, Pd and Co) perfectly dissolved in the amorphous phase and Zr facilitated the amorphization of the alloys. When the Zr/Ti ratio was kept at 1/4 (Mg{sub 1.5}Ti{sub 0.4}Zr{sub 0.1}Ni alloy), the initial discharge capacity of the alloy increased slightly at all the ball milling durations. The further increase in the Zr/Ti ratio resulted in reduction in the initial discharge capacity of the alloys. The presence of Zr in the Ti-including Mg-based alloys improved the cyclic stability of the alloys. This action of Zr was attributed to the less stable and more porous characteristics of the barrier hydroxide layer in the presence of Zr due to the selective dissolution of the disseminated Zr-oxides throughout the hydroxide layer on the alloy surface. Unlike Co, the addition of Pd into the Mg-Ti-Zr-Ni type alloy improved the alloy performance significantly. The positive contribution of Pd was assumed to arise from the facilitated hydrogen diffusion on the electrode surface in the presence of Pd. As the Zr/Ti atomic ratio increased, the charge transfer resistance of the alloy decreased at all the depths of discharges. Co and Pd were observed to increase the charge transfer resistance of the Mg-Ti-Zr-Ni alloys slightly. (author)

  16. Investigation on the Structure and Electrochemical Properties of La-Ce-Mg-Al-Ni Hydrogen Storage Alloy

    Directory of Open Access Journals (Sweden)

    Yuqing Qiao

    2013-01-01

    Full Text Available Structure and electrochemical characteristics of La0.96Ce0.04Mg0.15Al0.05Ni2.8 hydrogen storage alloy have been investigated. X-ray diffraction analyses reveal that the La0.96Ce0.04Mg0.15Al0.05Ni2.8 hydrogen storage alloy consisted of a (La, MgNi3 phase with the rhombohedral PuNi3-type structure and a LaNi5 phase with the hexagonal CaCu5-type structure. TEM shows that the alloy is multicrystal with a lattice space 0.187 nm. EDS analyse shows that the content of Mg is 3.48% (atom which coincide well with the designed composition of the electrode alloy. Electrochemical investigations show that the maximum discharge capacity of the alloy electrode is 325 mAh g−1. The alloy electrode has higher discharge capacity within the discharge current density span from 60 mA g−1 to 300 mA g−1. Electrochemical impedance spectroscopy measurements indicate that the charge transfer resistance RT on the alloy electrode surface and the calculated exchange current density I0 are 0.135 Ω and 1298 mA g−1, respectively; the better eletrochemical reaction kinetic of the alloy electrode may be responsible for the better high-rate dischargeability.

  17. Electrochemical Impedance Spectroscopy (bio)sensing through hydrogen evolution reaction induced by gold nanoparticles.

    Science.gov (United States)

    Mayorga-Martinez, Carmen C; Chamorro-Garcia, Alejandro; Merkoçi, Arben

    2015-05-15

    A new gold nanoparticle (AuNP) based detection strategy using Electrochemical Impedance Spectroscopy (EIS) through hydrogen evolution reaction (HER) is proposed. This EIS-HER method is used as an alternative to the conventional EIS based on [Fe(CN)6](3-/4-) or [Ru(NH3)6](3+/2+) indicators. The proposed method is based on the HER induced by AuNPs. EIS measurements for different amounts of AuNP are registered and the charge transfer resistance (Rct) was found to correlate and be useful for their quantification. Moreover the effect of AuNP size on electrical properties of AuNPs for HER using this sensitive technique has been investigated. Different EIS-HER signals generated in the presence of AuNPs of different sizes (2, 5, 10, 15, 20, and 50 nm) are observed, being the corresponding phenomena extendible to other nanoparticles and related catalytic reactions. This EIS-HER sensing technology is applied to a magneto-immunosandwich assay for the detection of a model protein (IgG) achieving improvements of the analytical performance in terms of a wide linear range (2-500 ng mL(-1)) with a good limit of detection (LOD) of 0.31 ng mL(-1) and high sensitivity. Moreover, with this methodology a reduction of one order of magnitude in the LOD for IgG detection, compared with a chroamperometric technique normally used was achieved. Copyright © 2014 Elsevier B.V. All rights reserved.

  18. Localized electrochemical deposition: the growth behavior of nickel microcolumns

    Science.gov (United States)

    Yeo, SweeHock; Choo, Jian H.; Yip, Kwan S.

    2000-08-01

    The development of MEMS has initiated the birth of various types of microfabrication processes. These processes in turn serve as a platform for the invention of newer improve3d processes with increasingly higher fabrication resolution. This paper reports on an investigative study on the growth characteristics of nickel micro-columns grown by localized electrochemical deposition - a new truly 3D micro-rapid prototyping and direct-fabrication process capable of producing extremely high aspect ratio microstructures. Nickel columns were electrochemically formed on copper cathodes form a nickel sulfamate plating solution using a non-soluble microelectrode as the anode. Initial experiments showed that zero, partial or complete growths of the columns were revealed, depending on the vertical traverse speed of the microelectrode away form the horizontal copper surface - the preferred traverse speed profile being a decreasing quadratic function that starts form a low traverse speed value followed by a constant function at a higher speed value with respect to time. Further work conducted based on this finding achieve da constant growth rate with an analog closed-loop feedback control of the process, which produced columns with more even dimensions. Understanding of the growth phenomena will allow increases in the rate of deposition and better dimensional control of 3D micro- components grown via localized electrochemical deposition.

  19. Oxide characterization and hydrogen behaviors of Zr-based alloys

    International Nuclear Information System (INIS)

    Kim, Y. S.; Kim, D. J.; Kwon, S. H.; Lee, H. S.; Oh, S. J.; Yim, B. J.; Son, S. B.; Yun, S. P.

    2006-03-01

    The work scope and contents of the research are as follows : basic properties of zirconium alloys, hydrogen pick-up mechanism of zirconium alloy, effects of hydride on the corrosion behaviors of zirconium alloys, estimation on stress of oxide layer in the zirconium alloy, microstructure and characteristic of oxide in pre-hydrided zirconium alloys

  20. Electrochemical behavior of alkali metal alcoholates (alcoxides) on mercury

    Czech Academy of Sciences Publication Activity Database

    Heyrovský, Michael

    2006-01-01

    Roč. 18, č. 2 (2006), s. 121-126 ISSN 1040-0397 R&D Projects: GA MPO 1H-PK/42 Institutional research plan: CEZ:AV0Z40400503 Keywords : methoxine ion * tert-butoxide * ethoxide * hydrogen catalysis * hydrolitic decomposition Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.444, year: 2006

  1. Electrochemical Behaviors of Binary Ti-Zr Alloys

    Energy Technology Data Exchange (ETDEWEB)

    Oh, M. Y.; Kim, W. G.; Choe, H. C.; Ko, Y. M. [Chosun University, Gwnagju (Korea, Republic of)

    2009-04-15

    Pure Ti as well as Ti-6Al-4V alloy exhibit excellent properties for dental implant applications. However, for a better biocompatibility it seems important to avoid in the composition the presence of V due to the toxic effects of V ion release. Thus Al and V free and composed of non-toxic element such as Nb, Zr alloys as biomaterials have been developed. Especially, Zr contains to same family in periodic table as Ti. The addition of Zr to Ti alloy has an excellent mechanical properties, good corrosion resistance, and biocompatibility. In this study, the electrochemical characteristics of Ti-Zr alloys for biomaterials have been investigated using by electrochemical methods. Methods: Ti-Zr(10, 20, 30 and 40 wt%) alloys were prepared by are melting and homogenized for 24 hr at 1000 .deg. C in argon atmosphere. Phase constitutions and microstructure of the specimens were characterized by XRD, OM and SEM. The corrosion properties of the specimens were examined through potentiodynamic test (potential range of - 1500 {approx} 2000 mV), potentiostatic test (const, potential of 300 mV) in artificial saliva solution by potentiostat (EG and G Co, PARSTAT 2273. USA)

  2. Electrochemical tuning of vertically aligned MoS2 nanofilms and its application in improving hydrogen evolution reaction.

    Science.gov (United States)

    Wang, Haotian; Lu, Zhiyi; Xu, Shicheng; Kong, Desheng; Cha, Judy J; Zheng, Guangyuan; Hsu, Po-Chun; Yan, Kai; Bradshaw, David; Prinz, Fritz B; Cui, Yi

    2013-12-03

    The ability to intercalate guest species into the van der Waals gap of 2D layered materials affords the opportunity to engineer the electronic structures for a variety of applications. Here we demonstrate the continuous tuning of layer vertically aligned MoS2 nanofilms through electrochemical intercalation of Li(+) ions. By scanning the Li intercalation potential from high to low, we have gained control of multiple important material properties in a continuous manner, including tuning the oxidation state of Mo, the transition of semiconducting 2H to metallic 1T phase, and expanding the van der Waals gap until exfoliation. Using such nanofilms after different degree of Li intercalation, we show the significant improvement of the hydrogen evolution reaction activity. A strong correlation between such tunable material properties and hydrogen evolution reaction activity is established. This work provides an intriguing and effective approach on tuning electronic structures for optimizing the catalytic activity.

  3. Electrochemical tuning of vertically aligned MoS2 nanofilms and its application in improving hydrogen evolution reaction

    Science.gov (United States)

    Wang, Haotian; Lu, Zhiyi; Xu, Shicheng; Kong, Desheng; Cha, Judy J.; Zheng, Guangyuan; Hsu, Po-Chun; Yan, Kai; Bradshaw, David; Prinz, Fritz B.; Cui, Yi

    2013-01-01

    The ability to intercalate guest species into the van der Waals gap of 2D layered materials affords the opportunity to engineer the electronic structures for a variety of applications. Here we demonstrate the continuous tuning of layer vertically aligned MoS2 nanofilms through electrochemical intercalation of Li+ ions. By scanning the Li intercalation potential from high to low, we have gained control of multiple important material properties in a continuous manner, including tuning the oxidation state of Mo, the transition of semiconducting 2H to metallic 1T phase, and expanding the van der Waals gap until exfoliation. Using such nanofilms after different degree of Li intercalation, we show the significant improvement of the hydrogen evolution reaction activity. A strong correlation between such tunable material properties and hydrogen evolution reaction activity is established. This work provides an intriguing and effective approach on tuning electronic structures for optimizing the catalytic activity. PMID:24248362

  4. Catalytic Hydrogenation Reaction of Naringin-Chalcone. Study of the Electrochemical Reaction

    Directory of Open Access Journals (Sweden)

    B. A. López de Mishima

    2000-03-01

    Full Text Available The electrocatalytic hydrogenation reaction of naringin derivated chalcone is studied. The reaction is carried out with different catalysts in order to compare with the classic catalytic hydrogenation.

  5. Enhanced Kinetics of Electrochemical Hydrogen Uptake and Release by Palladium Powders Modified by Electrochemical Atomic Layer Deposition.

    Science.gov (United States)

    Benson, David M; Tsang, Chu F; Sugar, Joshua D; Jagannathan, Kaushik; Robinson, David B; El Gabaly, Farid; Cappillino, Patrick J; Stickney, John L

    2017-05-31

    Electrochemical atomic layer deposition (E-ALD) is a method for the formation of nanofilms of materials, one atomic layer at a time. It uses the galvanic exchange of a less noble metal, deposited using underpotential deposition (UPD), to produce an atomic layer of a more noble element by reduction of its ions. This process is referred to as surface limited redox replacement and can be repeated in a cycle to grow thicker deposits. It was previously performed on nanoparticles and planar substrates. In the present report, E-ALD is applied for coating a submicron-sized powder substrate, making use of a new flow cell design. E-ALD is used to coat a Pd powder substrate with different thicknesses of Rh by exchanging it for Cu UPD. Cyclic voltammetry and X-ray photoelectron spectroscopy indicate an increasing Rh coverage with increasing numbers of deposition cycles performed, in a manner consistent with the atomic layer deposition (ALD) mechanism. Cyclic voltammetry also indicated increased kinetics of H sorption and desorption in and out of the Pd powder with Rh present, relative to unmodified Pd.

  6. Photo-Enhanced Hydrogen Transport Technology for Clean Renewable Electrochemical Energy Systems, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — Solid oxide fuel cells and electrolyzers are promising electrochemical devices for space and terrestrial applications due to their high power densities and clean...

  7. Corrosion-electrochemical behavior of metals in alkali solutions

    International Nuclear Information System (INIS)

    Levin, V.A.; Levina, E.Eh.

    1995-01-01

    Results of an investigation into corrosion-electrochemical behaviour of 12Kh18N10T, 10Kh17N13M2T, 08Kh21N6M2T and 15Kh25T steels, 06KhN28MDT and KhN78T alloys as well as NP-2 nickel in sodium, potassium and lithium hydroxide solutions at 95-180 deg C temperatures are considered. It is ascertained, that anode polarization curves of all metals irrespective of hydroxide nature, concentration, temperature, presence of chloride and chlorate additions, are of identic character. The movement of anode polarization curves in the direction of lower current of hydroxide type in NaOH-KOH-LiOH series, temperature and solution concentration reduction at other equal terms. 12 refs.; 6 figs

  8. Electrochemical behavior of bioactive coatings on cp-Ti surface for dental application.

    Science.gov (United States)

    Marques, Isabella da Silva Vieira; Barão, Valentim Adelino Ricardo; da Cruz, Nilson Cristino; Yuan, Judy Chia-Chun; Mesquita, Marcelo Ferraz; Ricomini-Filho, Antonio Pedro; Sukotjo, Cortino; Mathew, Mathew T

    2015-11-01

    The surface characteristics and electrochemical properties of bioactive coatings produced by plasma electrolytic oxidation (PEO) with calcium, phosphorous, silicon and silver on commercially pure titanium were evaluated. PEO treatment produced a porous oxide layer, which improved the surface topography, and enriched the surface chemistry with bioactive elements, responsible for mimicking bone surface. The surfaces with higher calcium concentration presented antibacterial and biocompability properties with better responses for corrosion and barrier properties, due to the presence of rutile crystalline structure. PEO may be a promising surface treatment option to improve the electrochemical behavior of dental implants mitigating treatment failures.

  9. Electrochemical behavior of parent and photodegradation products of some selected pesticides

    Directory of Open Access Journals (Sweden)

    Carlos M. P. Vaz

    2008-01-01

    Full Text Available Electrochemical behavior of pesticides is extensively studied, but little attention has been given to the study of their degradation products (by-products by electrochemical methods. However, the degradation products of pesticides can be even more toxic then the parent products and such studies should be encouraged. Therefore, the objective of this work was to evaluate the electroactivity of by-products of imazaquin, methylparathion, bentazon and atrazine, generated by UV irradiation and measured using cyclic and differential pulse voltammetry and UV-visible absorption spectrophotometry. Results have shown that several by-products exhibit electroactivity, allowing, in some cases, the simultaneous determination of both parent and degradation products.

  10. Controllable Electrochemical Activities by Oxidative Treatment toward Inner-Sphere Redox Systems at N-Doped Hydrogenated Amorphous Carbon Films

    Directory of Open Access Journals (Sweden)

    Yoriko Tanaka

    2012-01-01

    Full Text Available The electrochemical activity of the surface of Nitrogen-doped hydrogenated amorphous carbon thin films (a-CNH, N-doped DLC toward the inner sphere redox species is controllable by modifying the surface termination. At the oxygen plasma treated N-doped DLC surface (O-DLC, the surface functional groups containing carbon doubly bonded to oxygen (C=O, which improves adsorption of polar molecules, were generated. By oxidative treatment, the electron-transfer rate for dopamine (DA positively charged inner-sphere redox analyte could be improved at the N-doped DLC surface. For redox reaction of 2,4-dichlorophenol, which induces an inevitable fouling of the anode surface by forming passivating films, the DLC surfaces exhibited remarkably higher stability and reproducibility of the electrode performance. This is due to the electrochemical decomposition of the passive films without the interference of oxygen evolution by applying higher potential. The N-doped DLC film can offer benefits as the polarizable electrode surface with the higher reactivity and higher stability toward inner-sphere redox species. By making use of these controllable electrochemical reactivity at the O-DLC surface, the selective detection of DA in the mixed solution of DA and uric acid could be achieved.

  11. Structurally Deformed MoS2 for Electrochemically Stable, Thermally Resistant, and Highly Efficient Hydrogen Evolution Reaction.

    Science.gov (United States)

    Chen, Yen-Chang; Lu, Ang-Yu; Lu, Ping; Yang, Xiulin; Jiang, Chang-Ming; Mariano, Marina; Kaehr, Bryan; Lin, Oliver; Taylor, André; Sharp, Ian D; Li, Lain-Jong; Chou, Stanley S; Tung, Vincent

    2017-11-01

    The emerging molybdenum disulfide (MoS 2 ) offers intriguing possibilities for realizing a transformative new catalyst for driving the hydrogen evolution reaction (HER). However, the trade-off between catalytic activity and long-term stability represents a formidable challenge and has not been extensively addressed. This study reports that metastable and temperature-sensitive chemically exfoliated MoS 2 (ce-MoS 2 ) can be made into electrochemically stable (5000 cycles), and thermally robust (300 °C) while maintaining synthetic scalability and excellent catalytic activity through physical-transformation into 3D structurally deformed nanostructures. The dimensional transition enabled by a high throughput electrohydrodynamic process provides highly accessible, and electrochemically active surface area and facilitates efficient transport across various interfaces. Meanwhile, the hierarchically strained morphology is found to improve electronic coupling between active sites and current collecting substrates without the need for selective engineering the electronically heterogeneous interfaces. Specifically, the synergistic combination of high strain load stemmed from capillarity-induced-self-crumpling and sulfur (S) vacancies intrinsic to chemical exfoliation enables simultaneous modulation of active site density and intrinsic HER activity regardless of continuous operation or elevated temperature. These results provide new insights into how catalytic activity, electrochemical-, and thermal stability can be concurrently enhanced through the physical transformation that is reminiscent of nature, in which properties of biological materials emerge from evolved dimensional transitions. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Synthesis of novel ZnV₂O₄ hierarchical nanospheres and their applications as electrochemical supercapacitor and hydrogen storage material.

    Science.gov (United States)

    Butt, Faheem K; Tahir, Muhammad; Cao, Chuanbao; Idrees, Faryal; Ahmed, R; Khan, Waheed S; Ali, Zulfiqar; Mahmood, Nasir; Tanveer, M; Mahmood, Asif; Aslam, Imran

    2014-08-27

    Hierarchical nanostructures (Hs) have recently garnered enormous attention due to their remarkable performances in catalysis, electronic devices, energy storage and conversion. Considering the advantage of hierarchical nanostructures, we have formulated a facile and template free method to synthesize novel hierarchical nanospheres (NHNs) of ZnV2O4. Both zinc and vanadium are earth abundant, relatively economical and can offer several oxidation states, which can render a broad range of redox reactions favorable for electrochemical energy storage applications. Keeping these points in mind, we investigated for the first time the electrochemical supercapacitor performance of NHNs. The electrochemical measurements were performed in 2 M KOH solution. The measured specific capacitance of ZnV2O4 electrode is 360 F/g at 1 A/g with good stability and retention capacity of 89% after 1000 cycles. Moreover, the hydrogen storage properties of NHNs were measured at 473, 573, and 623 K with an absorption of 1.76, 2.03, and 2.49 wt %. respectively. These studies pave the way to consider ZnV2O4 as prospective material for energy storage applications.

  13. Structurally Deformed MoS2 for Electrochemically Stable, Thermally Resistant, and Highly Efficient Hydrogen Evolution Reaction

    KAUST Repository

    Chen, Yen-Chang

    2017-10-12

    The emerging molybdenum disulfide (MoS2) offers intriguing possibilities for realizing a transformative new catalyst for driving the hydrogen evolution reaction (HER). However, the trade-off between catalytic activity and long-term stability represents a formidable challenge and has not been extensively addressed. This study reports that metastable and temperature-sensitive chemically exfoliated MoS2 (ce-MoS2) can be made into electrochemically stable (5000 cycles), and thermally robust (300 °C) while maintaining synthetic scalability and excellent catalytic activity through physical-transformation into 3D structurally deformed nanostructures. The dimensional transition enabled by a high throughput electrohydrodynamic process provides highly accessible, and electrochemically active surface area and facilitates efficient transport across various interfaces. Meanwhile, the hierarchically strained morphology is found to improve electronic coupling between active sites and current collecting substrates without the need for selective engineering the electronically heterogeneous interfaces. Specifically, the synergistic combination of high strain load stemmed from capillarity-induced-self-crumpling and sulfur (S) vacancies intrinsic to chemical exfoliation enables simultaneous modulation of active site density and intrinsic HER activity regardless of continuous operation or elevated temperature. These results provide new insights into how catalytic activity, electrochemical-, and thermal stability can be concurrently enhanced through the physical transformation that is reminiscent of nature, in which properties of biological materials emerge from evolved dimensional transitions.

  14. Investigation of the Alkaline Electrochemical Interface and Development of Composite Metal/Metal-Oxides for Hydrogen and Oxygen Electrodes

    Science.gov (United States)

    Bates, Michael

    Understanding the fundamentals of electrochemical interfaces will undoubtedly reveal a path forward towards a society based on clean and renewable energy. In particular, it has been proposed that hydrogen can play a major role as an energy carrier of the future. To fully utilize the clean energy potential of a hydrogen economy, it is vital to produce hydrogen via water electrolysis, thus avoiding co-production of CO2 inherent to reformate hydrogen. While significant research efforts elsewhere are focused on photo-chemical hydrogen production from water, the inherent low efficiency of this method would require a massive land-use footprint to achieve sufficient hydrogen production rates to integrate hydrogen into energy markets. Thus, this research has primarily focused on the water splitting reactions on base-metal catalysts in the alkaline environment. Development of high-performance base-metal catalysts will help move alkaline water electrolysis to the forefront of hydrogen production methods, and when paired with solar and wind energy production, represents a clean and renewable energy economy. In addition to the water electrolysis reactions, research was conducted to understand the de-activation of reversible hydrogen electrodes in the corrosive environment of the hydrogen-bromine redox flow battery. Redox flow batteries represent a promising energy storage option to overcome the intermittency challenge of wind and solar energy production methods. Optimization of modular and scalable energy storage technology will allow higher penetration of renewable wind and solar energy into the grid. In Chapter 1, an overview of renewable energy production methods and energy storage options is presented. In addition, the fundamentals of electrochemical analysis and physical characterization of the catalysts are discussed. Chapter 2 reports the development of a Ni-Cr/C electrocatalyst with unprecedented mass-activity for the hydrogen evolution reaction (HER) in alkaline

  15. Microstructures and electrochemical behaviors of the friction stir welding dissimilar weld.

    Science.gov (United States)

    Shen, Changbin; Zhang, Jiayan; Ge, Jiping

    2011-06-01

    By using optical microscope, the microstructures of 5083/6082 friction stir welding (FSW) weld and parent materials were analyzed. Meanwhile, at ambient temperature and in 0.2 mol/L NaHS03 and 0.6 mol/L NaCl solutionby gravimetric test, potentiodynamic polarization curve test, electrochemical impedance spectra (EIS) and scanning electron microscope (SEM) observation, the electrochemical behavior of 5083/6082 friction stir welding weld and parent materials were comparatively investigated by gravimetric test, potentiodynamic polarization curve test, electrochemical impedance spectra (EIS) and scanning electron microscope (SEM) observation. The results indicated that at given processing parameters, the anti-corrosion property of the dissimilar weld was superior to those of the 5083 and 6082 parent materials. Copyright © 2011 The Research Centre for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

  16. Electrochemical characterization and redox behavior of Nb-doped SrTiO3

    DEFF Research Database (Denmark)

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

    2009-01-01

    Sr-vacancy compensated Nb-doped SrTiO3 with the nominal composition Sr0.94Ti0.9Nb0.1O3 has been evaluated as a solid oxide fuel cell (SOFC) anode material in terms of redox stability and electrochemical properties. Sr0.94Ti0.9Nb0.1O3 has been synthesized with a recently developed modified glycine......-nitrate process. The phase purity and redox behavior have been analyzed with XRD and TGA. The electrochemical properties of Sr0.94Ti0.9Nb0.1O3 and a composite electrode of Sr0.94Ti0.9Nb0.1O3/YSZ have been investigated by electrochemical impedance spectroscopy (EIS) on cone shaped electrodes and on electrodes...

  17. Electrochemical hydrogen storage properties of Mg100−xNix produced by hydriding combustion synthesis and mechanical milling

    Directory of Open Access Journals (Sweden)

    Delong Zhu

    2017-02-01

    Full Text Available In this work, Mg-based hydrogen storage composites with an initial 100-x: x (x=25, 32.3, 50, 66.7 of Mg:Ni molar ratio were prepared by HCS+MM and their phase compositions and electrochemical performances were investigated in detail. The results show that the composites with desirable constituents can be achieved by adjusting the molar ratio of the starting materials in the HCS process. Particularly, the HCS product of Mg67.7Ni32.3 consists of the principal phase Mg2NiH4 and minor phase Mg2NiH0.3. The dominate phase varies from Mg2NiH0.3 and MgH2 for the Mg enriched sample (x32.3. The MM modification not only brings about grain refinement of the alloys, but also leads to phase transformation of part Mg2NiH4 to Mg2NiH0.3 in the Mg67.7Ni32.3 sample. Electrochemical tests indicate that each sample can reach its maximum discharge capacity at the first cycle. Mg67.7Ni32.3 displays the highest discharge capacity as well as a superior electrochemical kinetics owing to its excellent H atom diffusion ability and lower charge-transfer resistance. The Mg67.7Ni32.3 provides the most optimized Mg/Ni atomic ratio considering the comprehensive electrochemical properties of all samples.

  18. Influence of boron introduction on structure and electrochemical hydrogen storage properties of Ti–V-based alloys

    International Nuclear Information System (INIS)

    Qiu, Shujun; Huang, Jianling; Chu, Hailiang; Zou, Yongjin; Xiang, Cuili; Zhang, Huanzhi; Xu, Fen; Sun, Lixian; Zhou, Huaiying

    2015-01-01

    In order to improve the properties of Ti–V-based alloys in the electrochemical system, Ti 0.17 Zr 0.08 V 0.35 Cr 0.1 Ni 0.3 B x (x = 0–0.04) alloys were prepared and their structural and electrochemical performances had been systematically investigated in this study. XRD patterns show that they are mainly comprised of a C14 Laves phase and a body centered cubic (BCC) solid solution phase. The introduction of boron has little effect on the structure, while it remarkably influences the electrochemical performances. The cycle life of each electrode made from the studied alloy is obviously improved. For instance, the cycle retention after 200 charge–discharge cycles is more than 90%. Furthermore, high rate dischargeability (HRD) is also enhanced after boron introduction. It is also found that the charge-transfer reaction resistance R ct , the limiting current density I L, and the hydrogen diffusion coefficient D are first decreased and then increased with the increase of boron amount. Taking into consideration various factors, the introduction of boron in the alloy has an optimal value of x = 0.01. - Graphical abstract: Trace amounts of B element was introduced into Ti 0.17 Zr 0.08 V 0.35 Cr 0.1 Ni 0.3 alloys. XRD patterns show that the introduction of B has little effect on the structure, while it remarkably influences the electrochemical performances. The cycle life and the high rate dischargeability (HRD) are obviously improved. - Highlights: • Trace amounts of B element was introduced into Ti–V-based alloys. • Ti 0.17 Zr 0.08 V 0.35 Cr 0.1 Ni 0.3 B 0.01 has an optimal property. • At x = 0.01, C 200 /C max is 89.4% and HRD 800 is 72.5%

  19. Halogen ions effect on cadmium electrochemical behavior in perchlorate solutions

    International Nuclear Information System (INIS)

    Zytner, Ya.D.

    1975-01-01

    Halide ions decrease the discharge potential of cadmium and zinc ions. To compare the electrochemical behaviour of cadmium and zinc measured under the equivalent conditions the cathodic deposition and anodic dissolution of Cd were studied in the following solutions: 0.1M Cd(ClO 4 ) 2 +xMNaHal+(2-x)MNaClO 4 (x=0.001, 0.01, 0.1, 1.0, 2.0). The cadmium equilibrium potential versus the log of sodium halide concentration are presented. Above 0.1M sodium halide concentrations the cadmium equilibrium potential shifts essentially to the negative side manifesting the formation of cadmium complex halides whose stabilities increase in the series Cl - - - . The cathodic and anodic potentials of cadmium electrode versus the log of sodium halide concentration were investigated at the current density 400 a/m 2 . The effect of halide ions versus the rate of discharge-cadmium ionization cannot be judged from the change in the electrode potential. For this purpose the potential value should be determined. Analysis of the dependence of anodic and cathodic potentials on the log of sodium halide concentration shows that the rates of anodic and cathodic processes increase with the halide ions concentration. The results obtained allow to conclude that the halide ions not only affect concentration of the discharging complex particles but also reduce the activation energy of discharge-ionization reaction of the metal

  20. Electrochemical behavior of ionically crosslinked polyampholytic gel electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Wanyu; Tang, Haitao; Ou, Ziwei; Wang, Hong; Yang, Yajiang [Department of Chemistry, Huazhong University of Science and Technology, Wuhan 430074 (China)

    2007-12-31

    An ionic complex of anionic and cationic monomers was obtained by protonation of (N,N-diethylamino)ethylmethacrylate (DEA) with acrylic acid (AAc). Free radical copolymerization of the ionic complex and acrylamide (AAm), yielded the ionically crosslinked polyampholytic gel electrolytes [poly(AAc-DEA-AAm), designated as PADA] using two types of organic solvents containing a lithium salt. The PADA gel electrolyte exhibited good thermal stability shown by the DSC thermogram. The impedance analysis at temperatures ranging from -30 to 75 C indicated that the ionic conductivities of the PADA gel electrolytes were rather close to those of liquid electrolytes. The temperature dependence of the ionic conductivities was found to be in accord with the Arrhenius equation. Moreover, the ionic conductivities of PADA gel electrolytes increased with an increase of the molar ratios of cationic/anionic monomers. The ionic conductivities of PADA gels prepared in solvent mixtures of propylene carbonate, ethyl methyl ether and dioxolane (3:1:1, v/v) were higher than those of PADA gels prepared in propylene carbonate only. Significantly, the ionic conductivities of two kinds of PADA gel electrolytes were in the range of 10{sup -3} and 10{sup -4} S cm{sup -1} even at -30 C. The electrochemical windows of PADA gel electrolytes measured by cyclic voltammetry were in the range from -1 V to 4.5 V. (author)

  1. Electrochemical behavior of ionically crosslinked polyampholytic gel electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Chen Wanyu; Tang Haitao; Ou Ziwei; Wang Hong [Department of Chemistry, Huazhong University of Science and Technology, Wuhan 430074 (China); Yang Yajiang [Department of Chemistry, Huazhong University of Science and Technology, Wuhan 430074 (China)], E-mail: yjyang@mail.hust.edu.cn

    2007-12-31

    An ionic complex of anionic and cationic monomers was obtained by protonation of (N,N-diethylamino)ethylmethacrylate (DEA) with acrylic acid (AAc). Free radical copolymerization of the ionic complex and acrylamide (AAm), yielded the ionically crosslinked polyampholytic gel electrolytes [poly(AAc-DEA-AAm), designated as PADA] using two types of organic solvents containing a lithium salt. The PADA gel electrolyte exhibited good thermal stability shown by the DSC thermogram. The impedance analysis at temperatures ranging from -30 to 75 deg. C indicated that the ionic conductivities of the PADA gel electrolytes were rather close to those of liquid electrolytes. The temperature dependence of the ionic conductivities was found to be in accord with the Arrhenius equation. Moreover, the ionic conductivities of PADA gel electrolytes increased with an increase of the molar ratios of cationic/anionic monomers. The ionic conductivities of PADA gels prepared in solvent mixtures of propylene carbonate, ethyl methyl ether and dioxolane (3:1:1, v/v) were higher than those of PADA gels prepared in propylene carbonate only. Significantly, the ionic conductivities of two kinds of PADA gel electrolytes were in the range of 10{sup -3} and 10{sup -4} S cm{sup -1} even at -30 deg. C. The electrochemical windows of PADA gel electrolytes measured by cyclic voltammetry were in the range from -1 V to 4.5 V.

  2. Hydrothermal synthesis and processing of hydrogen titanate nanotubes for nicotine electrochemical sensing

    Science.gov (United States)

    Mersal, Gaber A. M.; Mostafa, Nasser Y.; Omar, Abd-Elkader H.

    2017-08-01

    Hydrogen titanate nanotubes (HTNT) were prepared via acid washing of hydrothermally synthesized sodium titantate nanotube. HTNTs with diameters in the range 7-9 nm and length of several hundred nanometers were annealed at different temperatures and used to modify carbon paste electrode (CPE). Cyclic and square wave voltammetric techniques were used to investigate the behavior of nicotine at HTNT modified carbon paste electrode (HTNTCPE). The nicotine-oxidation reaction over HTNTCPE was irreversible and adsorption process is the rate determining step. HTNTs annealed at 500 °C showed the best response to nicotine. The nicotine concentration was determined at the ideal conditions by square wave voltammetry (SWV). The calibration was linear from 0.1 to 500.0 µmol l-1 with a correlation coefficient of 0.995. The detection limits were found to be 0.005 µmol l-1. The present HTNTCPE was used to the determination of nicotine in two cigarette brands and it showed outstanding performance with respect to detection limit and sensitivity.

  3. Electrochemical corrosion behavior of a Ti-35Nb alloy for medical prostheses

    International Nuclear Information System (INIS)

    Cremasco, Alessandra; Osorio, Wislei R.; Freire, Celia M.A.; Garcia, Amauri; Caram, Rubens

    2008-01-01

    Since the 1980s, the titanium alloys show attractive properties for biomedical applications where the most important factors are, firstly, biocompatibility, corrosion and mechanical resistances, low modulus of elasticity, very good strength to weight ratio, reasonable formability and osseointegration. The aim of this study was to investigate the effects of two different heat treatments; furnace cooling and water quenching, on the general electrochemical corrosion resistance of Ti-35 wt%Nb alloy samples immersed in a 0.9% NaCl (0.15 mol L -1 ) solution at 25 deg. C and neutral pH range. The samples were obtained using a non-consumable tungsten electrode furnace with a water-cooled copper hearth under argon atmosphere. The microstructural pattern was examined by scanning electron microscopy (SEM) and X-ray diffractometry (XRD). In order to evaluate the electrochemical corrosion behavior of such Ti-Nb alloy samples, corrosion tests were performed by using electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization curves. Analyses of an equivalent circuit have also been used to provide quantitative support for the discussions and understanding of the corrosion behavior. It was found that water quenching provides a microstructural pattern consisting of an alpha-martensite acicular phase which decreases the material electrochemical performance due to the stress-induced martensitic transformation

  4. Electrochemical corrosion behavior of a Ti-35Nb alloy for medical prostheses

    Energy Technology Data Exchange (ETDEWEB)

    Cremasco, Alessandra [Department of Materials Engineering, State University of Campinas, UNICAMP, P.O. Box 6122, 13083-970 Campinas, SP (Brazil); Osorio, Wislei R. [Department of Materials Engineering, State University of Campinas, UNICAMP, P.O. Box 6122, 13083-970 Campinas, SP (Brazil)], E-mail: wislei@fem.unicamp.br; Freire, Celia M.A.; Garcia, Amauri; Caram, Rubens [Department of Materials Engineering, State University of Campinas, UNICAMP, P.O. Box 6122, 13083-970 Campinas, SP (Brazil)

    2008-05-30

    Since the 1980s, the titanium alloys show attractive properties for biomedical applications where the most important factors are, firstly, biocompatibility, corrosion and mechanical resistances, low modulus of elasticity, very good strength to weight ratio, reasonable formability and osseointegration. The aim of this study was to investigate the effects of two different heat treatments; furnace cooling and water quenching, on the general electrochemical corrosion resistance of Ti-35 wt%Nb alloy samples immersed in a 0.9% NaCl (0.15 mol L{sup -1}) solution at 25 deg. C and neutral pH range. The samples were obtained using a non-consumable tungsten electrode furnace with a water-cooled copper hearth under argon atmosphere. The microstructural pattern was examined by scanning electron microscopy (SEM) and X-ray diffractometry (XRD). In order to evaluate the electrochemical corrosion behavior of such Ti-Nb alloy samples, corrosion tests were performed by using electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization curves. Analyses of an equivalent circuit have also been used to provide quantitative support for the discussions and understanding of the corrosion behavior. It was found that water quenching provides a microstructural pattern consisting of an alpha-martensite acicular phase which decreases the material electrochemical performance due to the stress-induced martensitic transformation.

  5. Nanosized Magnesium Electrochemically Deposited on a Carbon Nanotubes Suspension: Synthesis and Hydrogen Storage

    Directory of Open Access Journals (Sweden)

    Chaoqi Shen

    2017-10-01

    Full Text Available Herein, we report on a novel method for deposition of magnesium (Mg nanoparticles at the surface of carbon materials. Through the suspension of carbon nanotubes (CNTs in an electrolyte containing di-n-butylmagnesium as a precursor, Mg nanoparticles were effectively deposited at the surface of the CNTs as soon as these touched the working electrode. Through this process, CNTs supported Mg particles as small as 1 nm were synthesized and the distribution of the nanoparticles was found to be influenced by the concentration of the CNTs in the electrolyte. Hydrogenation of these nanoparticles at 100°C was found to lead to low temperature hydrogen release starting at 150°C, owing to shorter diffusion paths and higher hydrogen mobility in small Mg particles. However, these hydrogen properties drastically degraded as soon as the hydrogenation temperature exceeded 200°C and this may be related to the low melting temperature of ultrasmall Mg particles.

  6. Nanosized Magnesium Electrochemically Deposited on a Carbon Nanotubes Suspension: Synthesis and Hydrogen Storage

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Chaoqi; Aguey-Zinsou, Kondo-Francois, E-mail: f.aguey@unsw.edu.au [MERLin, School of Chemical Engineering, The University of New South Wales, Sydney, NSW (Australia)

    2017-10-17

    Herein, we report on a novel method for deposition of magnesium (Mg) nanoparticles at the surface of carbon materials. Through the suspension of carbon nanotubes (CNTs) in an electrolyte containing di-n-butylmagnesium as a precursor, Mg nanoparticles were effectively deposited at the surface of the CNTs as soon as these touched the working electrode. Through this process, CNTs supported Mg particles as small as 1 nm were synthesized and the distribution of the nanoparticles was found to be influenced by the concentration of the CNTs in the electrolyte. Hydrogenation of these nanoparticles at 100°C was found to lead to low temperature hydrogen release starting at 150°C, owing to shorter diffusion paths and higher hydrogen mobility in small Mg particles. However, these hydrogen properties drastically degraded as soon as the hydrogenation temperature exceeded 200°C and this may be related to the low melting temperature of ultrasmall Mg particles.

  7. Electrochemical Dealloying of PdCu3 Nanoparticles to Achieve Pt-like Activity for the Hydrogen Evolution Reaction.

    Science.gov (United States)

    Jana, Rajkumar; Bhim, Anupam; Bothra, Pallavi; Pati, Swapan K; Peter, Sebastian C

    2016-10-20

    Manipulating the d-band center of the metal surface and hence optimizing the free energy of hydrogen adsorption (ΔG H ) close to the optimal adsorption energy (ΔG H =0) for hydrogen evolution reaction (HER), is an efficient strategy to enhance the activity for HER. Herein, we report a oleylamine-mediated (acting as the solvent, stabilizer, and reducing agent) strategy to synthesize intermetallic PdCu 3 nanoparticles (NPs) without using any external reducing agent. Upon electrochemical cycling, PdCu 3 transforms into Pd-rich PdCu (ΔG H =0.05 eV), exhibiting remarkably enhanced activity (with a current density of 25 mA cm -2 at ∼69 mV overpotential) as an alternative to Pt for HER. The first-principle calculation suggests that formation of low coordination number Pd active sites alters the d-band center and hence optimal adsorption of hydrogen, leading to enhanced activity. This finding may provide guidelines towards the design and development of Pt-free highly active and robust electrocatalysts. © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. Electrochemical impedance spectroscopy of polycrystalline boron doped diamond layers with hydrogen and oxygen terminated surface

    Czech Academy of Sciences Publication Activity Database

    Vlčková Živcová, Zuzana; Petrák, Václav; Frank, Otakar; Kavan, Ladislav

    2015-01-01

    Roč. 55, MAY 2015 (2015), s. 70-76 ISSN 0925-9635 R&D Projects: GA ČR GA13-31783S Institutional support: RVO:61388955 ; RVO:68378271 Keywords : Boron doped diamond * Electrochemical impedance spectroscopy * Aqueous electrolyte solution Subject RIV: CG - Electrochemistry Impact factor: 2.125, year: 2015

  9. HYDROGENATION OF OLEFINS USING PALLADIUM NANOPARTICLES PREPARED WITH PULSE ELECTROCHEMICAL DEPOSITION

    Science.gov (United States)

    Electrochemistry has been used to synthesize nano-structured materials. In this project, we have conducted the application of electrochemistry for the synthesis of nano-palladium catalysts that may have application in the area of green chemistry. The electrochemical technique use...

  10. Electrochemical Corrosion Behavior of Near-Nano and Nanostructured WC-Co Cemented Carbides

    Directory of Open Access Journals (Sweden)

    Željko Alar

    2017-02-01

    Full Text Available In this paper, the electrochemical corrosion resistance of near-nano and nanostructured WC-Co cemented carbides was investigated. WC powders with an average grain size dBET in the range from 95 nm to 150 nm and with an addition of vanadium carbide (VC and chromium carbide Cr3C2 as grain growth inhibitors were used as starting powders. The mixtures with 6 wt. % and 9 wt. % Co were consolidated by two different processes; sintering in hydrogen atmosphere and the sinter-HIP process. WC-Co samples were researched by direct current and alternating current techniques in the solution of 3.5% NaCl at room temperature. Corrosion parameters such as corrosion potential (Ecorr, corrosion current density (jcorr and polarization resistance (Rp were determined by electrochemical techniques. From the conducted research, it was found that the consolidation processes and microstructural characteristics—grain growth inhibitors, grain size of the starting WC powders and η-phase—influenced the electrochemical corrosion resistance. η-phase enhanced the formation of a passive layer on the samples’ surfaces, thereby reducing the tendency of the sample dissolution and increasing the stability of oxides forming therewith a passive layer on the sample surface.

  11. Investigation of electrochemical synthesis of ferrate, Part I: Electrochemical behavior of iron and its several alloys in concentrated alkaline solutions

    Directory of Open Access Journals (Sweden)

    Čekerevac Milan I.

    2009-01-01

    cyclic voltammetry, galvanostatic and potentiostatic pulse method. Cyclic voltammetry gave useful data on potential regions where ferrate(VI formation is to be expected in the course of transpassive anodic oxidation of iron and some of its alloys, and its stability in the electrolytes of different composition. In addition, step-wise oxidation of iron in anodic oxidation is confirmed. Galvanostatic pulse experiments confirmed the character of successive anodic oxidation of iron, as the three-step process of ferrate(VI formation is clearly observed. In the cathodic pulse complex reduction of ferrate (VI, firstly to Fe(III species and then to mixed Fe(II and Fe(III compounds and finally to elementary iron is confirmed. The significant difference between the mechanisms of anodic oxidation of pure iron and low carbon steel at the one side and electrical ferrous-silicon steel at the other is observed. The influence of material chemical composition on the electrochemical behavior of electrode in course of anodic polarization in strong alkaline solutions is discussed in terms of composition of passivating layer formed on the electrode. On the base of the experimental data, efficient synthesis of ferrate(VI can be expected in the region of anodic potentials between + 0,55 and + 0,75 V against Hg|HgO reference electrode in the same solution, depending on the anode materials composition, in the alkaline electrolytes concentration between 10 and 15 M.

  12. Two-Dimensional MXenes as Catalysts for Electrochemical Hydrogen Evolution: A Computational Screening Study

    DEFF Research Database (Denmark)

    Pandey, Mohnish; Thygesen, Kristian Sommer

    2017-01-01

    is assessed via the calculated standard heat of formation. We find that most of the MXenes are metallic, and we investigate their performance as electrocatalysts for the hydrogen evolution reaction(HER) using the free energy of hydrogen adsorption at equilibrium coverage as an activity descriptor. For a given...... type of metal, we find that the hydrogen adsorption energy can vary by up to 0.5 eV depending on the number of metal layers in the structure, suggesting that the catalytic activity of MXenes can be tuned by controlling the layer thickness. On the basis of a combined stability and activity analysis...

  13. Effect of black clay soil moisture on the electrochemical behavior of API X70 pipeline steel

    Science.gov (United States)

    Hendi, R.; Saifi, H.; Belmokre, K.; Ouadah, M.; Smili, B.; Talhi, B.

    2018-03-01

    The effect of moisture content variation (20–100 wt.%) on the electrochemical behavior of API X70 pipeline steel buried in the soil of Skikda (East of Algeria) was studied using electrochemical techniques, scanning electron microscopy (SEM), X ray diffraction analysis (XRD) and weight loss measurement. The electrochemical measurements showed that the corrosion current Icorr is directly proportional to the moisture content up to 50 wt.%, beyond this content, this value becomes almost constant. The result were confirmed by electrochemical impedance spectroscopy; the capacitance of the double layer formed on the surface is the highest at 50 wt.%. A single time constant was detected by plotting the Bode diagrams. The steel surface degradation has been appreciated using the scanning electron microscopy observations. A few pitting corrosion at 20 wt.% moisture, followed by more degradation at 50 wt.% have been revealed. However, when the moisture amount exceeded 50 wt.%, the surface became entirely covered by a corrosion product. XRD analysis revealed the dominance of FeOOH and Fe3O4 phases on steel surface for a moisture content of 50 wt.%.

  14. Sensitive electrochemical immunoassay with signal enhancement based on nanogold-encapsulated poly(amidoamine) dendrimer-stimulated hydrogen evolution reaction.

    Science.gov (United States)

    Sun, Ai-Li

    2015-12-07

    A new electrochemical immunosensor with signal enhancement was designed for sensitive detection of disease-related protein (human carbohydrate antigen 19-9, CA 19-9 used in this case). The assay was carried out on a capture antibody-modified screen-printed carbon electrode with a sandwich-type mode by using detection antibody-functionalized nanogold-encapsulated poly(amidoamine) dendrimer (AuNP-PAAD). The AuNP-PAAD was first synthesized through the in situ reduction method and functionalized with the polyclonal rabbit anti-human CA 19-9 antibody. Upon target CA 19-9 introduction, a sandwiched immunocomplex could be formed between the capture antibody and detection antibody. Accompanying the AuNP-PAAD, the electrocatalytic activity of the carried gold nanoparticles toward the hydrogen evolution reaction (HER) allowed the rapid quantification of the target analyte on the electrode. The amplified electrochemical signal mainly derived from AuNP-catalyzed HER in an acidic medium. Under optimal conditions, the immuno-HER assay displayed a wide dynamic concentration range from 0.01 to 300 U mL(-1) toward target CA 19-9 with a detection limit (LOD) of 6.3 mU mL(-1). The reproducibility, precision, specificity and stability of our strategy were acceptable. Additionally, the system was further validated by assaying 13 human serum specimens, giving well matched results obtained from the commercialized enzyme-linked immunosorbent assay (ELISA) method.

  15. Electrical Characterization and Hydrogen Peroxide Sensing Properties of Gold/Nafion:Polypyrrole/MWCNTs Electrochemical Devices

    Directory of Open Access Journals (Sweden)

    Gaetano Saitta

    2013-03-01

    Full Text Available Electrochemical devices using as substrates copier grade transparency sheets are developed by using ion conducting Nafion:polypyrrole mixtures, deposited between gold bottom electrodes and upper electrodes based on Multi Walled Carbon Nanotubes (MWCNTs. The electrical properties of the Nafion:polypyrrole blends and of the gold/Nafion:polypyrrole/MWCNTs devices are investigated under dry conditions and in deionized water by means of frequency dependent impedance measurements and time domain electrical characterization. According to current-voltage measurements carried out in deionized water, the steady state current forms cycles characterized by redox peaks, the intensity and position of which reversibly change in response to H2O2, with a lower detection limit in the micromolar range. The sensitivity that is obtained is comparable with that of other electrochemical sensors that however, unlike our devices, require supporting electrolytes.

  16. Novel Electrochemical Synthesis of Polypyrrole/Ag Nanocomposite and Its Electrocatalytic Performance towards Hydrogen Peroxide Reduction

    OpenAIRE

    Ruma Gupta; Kavitha Jayachandran; J. S. Gamare; B. Rajeshwari; Santosh K. Gupta; J. V. Kamat

    2015-01-01

    A simple electrochemical method of synthesis of polypyrrole/silver (PPy/Ag) nanocomposite is presented. The method is based on potentiodynamic polymerization of pyrrole followed by electrodeposition of silver employing a single potentiostatic pulse. The synthesized PPy film has embedded Ag nanocubes. The morphology and structure of the resulting nanocomposite were characterized by field emission scanning electron microscopy and X-ray diffraction. Electron paramagnetic resonance studies showed...

  17. Structure and electrochemical hydrogen storage properties of Ti{sub 2}Ni alloy synthesized by ball milling

    Energy Technology Data Exchange (ETDEWEB)

    Hosni, B. [Equipe des Hydrures Métalliques, Laboratoire de Mécanique, Matériaux et Procédés, Ecole Nationale Supérieure d’Ingénieurs de Tunis, ENSIT Ex ESSTT, Université de Tunis, 5 Avenue Taha Hussein, 1008 Tunis (Tunisia); Li, X. [FEMTO-ST, MN2S, Université de Technologie de Belfort-Montbéliard, Site de Sévenans, 90010 Belfort cedex (France); Khaldi, C., E-mail: chokri.khaldi@esstt.rnu.tn [Equipe des Hydrures Métalliques, Laboratoire de Mécanique, Matériaux et Procédés, Ecole Nationale Supérieure d’Ingénieurs de Tunis, ENSIT Ex ESSTT, Université de Tunis, 5 Avenue Taha Hussein, 1008 Tunis (Tunisia); ElKedim, O. [FEMTO-ST, MN2S, Université de Technologie de Belfort-Montbéliard, Site de Sévenans, 90010 Belfort cedex (France); Lamloumi, J. [Equipe des Hydrures Métalliques, Laboratoire de Mécanique, Matériaux et Procédés, Ecole Nationale Supérieure d’Ingénieurs de Tunis, ENSIT Ex ESSTT, Université de Tunis, 5 Avenue Taha Hussein, 1008 Tunis (Tunisia)

    2014-12-05

    Highlights: • The Ti{sub 2}Ni alloy activation requires only one cycle of charge and discharge, regardless of the temperature. • By increasing the temperature the capacity loss, undergoes an increase and it is more pronounced for the 60 °C. • A good correlation is found between the evolutions of the different electrochemical parameters according to the temperature. - Abstract: The structure and the electrochemical hydrogen storage properties of amorphous Ti{sub 2}Ni alloy synthesized by ball milling and used as an anode in nickel–metal hydride batteries were studied. Nominal Ti{sub 2}Ni was synthesized under argon atmosphere at room temperature using a planetary high-energy ball mill. The structural and morphological characterization of the amorphous Ti{sub 2}Ni alloy is carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The electrochemical characterization of the Ti{sub 2}Ni electrodes is carried out by the galvanostatic charging and discharging, the constant potential discharge, the open circuit potential and the potentiodynamic polarization techniques. The Ti{sub 2}Ni alloy activation requires only one cycle of charge and discharge, regardless of the temperature. The electrochemical discharge capacity of the Ti{sub 2}Ni alloy, during the first eight cycles, and at a temperature of 30 °C, remained practically unchanged and a good held cycling is observed. By increasing the temperature, the electrochemical discharge capacity loss after eight cycles undergoes an increase and it is more pronounced for the temperature 60 °C. At 30 °C, the anodic corrosion current density is 1 mA cm{sup −2} and then it undergoes a rapid drop, remaining substantially constant (0.06 mA cm{sup −2}) in the range 40–60 °C, before undergoing a slight increase to 70 °C (0.3 mA cm{sup −2}). This variation is in good agreement with the maximum electrochemical discharge capacity values found for the

  18. Fabrication of a facile electrochemical biosensor for hydrogen peroxide using efficient catalysis of hemoglobin on the porous Pd@Fe3O4-MWCNT nanocomposite.

    Science.gov (United States)

    Baghayeri, Mehdi; Veisi, Hojat

    2015-12-15

    In this work, a sensitive amperometric biosensor for hydrogen peroxide based on synergetic catalysis of hemoglobin and porous Pd@Fe3O4-MWCNT nanocomposite has been constructed. With attention to the utilities of large surface area and outstanding catalytic performance, Pd@Fe3O4-MWCNT nanocomposite was employed as the nano-stabilizer for the immobilization of hemoglobin (Hb). The immobilized Hb on the surface of nanocomposite as an electrochemical biosensor efficiently catalyzed the reduction of hydrogen peroxide, amplified the electrochemical signal and enhanced the sensitivity. Results of voltammetry and electrochemical impedance examinations showed that the nanocomposite could enhance the electron conductivity and provide more sites for the immobilization of Hb. A linear response from 0.2-500 µM with detection limit of 0.063 µM for hydrogen peroxide was achieved. The apparent Michaelis-Menten constant Kapp(M) value was 21 µM. Thus, the nanocomposite could be applied for fabrication of a third generation biosensor for hydrogen peroxide with high sensitivity, selectivity and low detection limit. The excellent performance of the biosensor indicated its promising prospect as a valuable tool in simple and fast hydrogen peroxide detection in environmental and clinical applications. Copyright © 2015 Elsevier B.V. All rights reserved.

  19. Fabrication and electrochemical behavior of single-walled carbon nanotube/graphite-based electrode

    International Nuclear Information System (INIS)

    Moghaddam, Abdolmajid Bayandori; Ganjali, Mohammad Reza; Dinarvand, Rassoul; Razavi, Taherehsadat; Riahi, Siavash; Rezaei-Zarchi, Saeed; Norouzi, Parviz

    2009-01-01

    An electrochemical method for determining the dihydroxybenzene derivatives on glassy carbon (GC) has been developed. In this method, the performance of a single-walled carbon nanotube (SWCNT)/graphite-based electrode, prepared by mixing SWCNTs and graphite powder, was described. The resulting electrode shows an excellent behavior for redox of 3,4-dihydroxybenzoic acid (DBA). SWCNT/graphite-based electrode presents a significant decrease in the overvoltage for DBA oxidation as well as a dramatic improvement in the reversibility of DBA redox behavior in comparison with graphite-based and glassy carbon (GC) electrodes. In addition, scanning electron microscopy (SEM) and atomic force microscopy (AFM) procedures performed for used SWCNTs

  20. Electrodeposition of flower-like platinum on electrophoretically grown nitrogen-doped graphene as a highly sensitive electrochemical non-enzymatic biosensor for hydrogen peroxide detection

    Energy Technology Data Exchange (ETDEWEB)

    Tajabadi, M.T. [University Malaya Centre for Ionic Liquids, Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Sookhakian, M., E-mail: m.sokhakian@gmail.com [University Malaya Centre for Ionic Liquids, Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Department of Mechanical Convergence Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul, 133-791, Korea (Korea, Republic of); Zalnezhad, E., E-mail: erfan@hanyang.ac.kr [Department of Mechanical Convergence Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul, 133-791, Korea (Korea, Republic of); Yoon, G.H. [Department of Mechanical Convergence Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul, 133-791, Korea (Korea, Republic of); Hamouda, A.M.S. [Mechanical and Industrial Engineering Department, College of Engineering, Qatar University, 2713, Doha (Qatar); Azarang, Majid [Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Basirun, W.J. [Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Institute of Nanotechnology & Catalysis Research, Institute of Postgraduate Studies, University Malaya, 50603 Kuala Lumpur (Malaysia); Alias, Y., E-mail: yatimah70@um.edu.my [University Malaya Centre for Ionic Liquids, Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia); Department of Chemistry, Faculty of Science, University of Malaya, Kuala Lumpur 50603 (Malaysia)

    2016-11-15

    Highlights: • Nitrogen doped graphene with different thickness by electrophoretic deposition. • The conductivity of N-graphene layer depends on the tickness. • Support of platinum shows efficient electrocatalytic performance for biosensor. • CV curves and amperometric responses improved and optimized in the presence of N-graphene. - Abstract: An efficient non-enzymatic biosensor electrode consisting of nitrogen-doped graphene (N-graphene) and platinum nanoflower (Pt NF) with different N-graphene loadings were fabricated on indium tin oxide (ITO) glass using a simple layer-by-layer electrophoretic and electrochemical sequential deposition approach. N-graphene was synthesized by annealing graphene oxide with urea at 900 °C. The structure and morphology of the as-fabricated non-enzymatic biosensor electrodes were determined using X-ray diffraction, field emission electron microscopy, transmission electron microscopy, Raman and X-ray photoelectron spectra. The as-fabricated Pt NF-N-graphene-modified ITO electrodes with different N-graphene loadings were utilized as a non-enzymatic biosensor electrode for the detection of hydrogen peroxide (H{sub 2}O{sub 2}). The behaviors of the hybrid electrodes towards H{sub 2}O{sub 2} reduction were assessed using chronoamperometry, cyclic voltammetry and electrochemical impedance spectroscopy analysis. The Pt NF-N-graphene-modified ITO electrode with a 0.05 mg ml{sup −1} N-graphene loading exhibited the lowest detection limit, fastest amperometric sensing, a wide linear response range, excellent stability and reproducibility for the non-enzymatic H{sub 2}O{sub 2} detection, due to the synergistic effect between the electrocatalytic activity of the Pt NF and the high conductivity and large surface area of N-graphene.

  1. Electrodeposition of flower-like platinum on electrophoretically grown nitrogen-doped graphene as a highly sensitive electrochemical non-enzymatic biosensor for hydrogen peroxide detection

    International Nuclear Information System (INIS)

    Tajabadi, M.T.; Sookhakian, M.; Zalnezhad, E.; Yoon, G.H.; Hamouda, A.M.S.; Azarang, Majid; Basirun, W.J.; Alias, Y.

    2016-01-01

    Highlights: • Nitrogen doped graphene with different thickness by electrophoretic deposition. • The conductivity of N-graphene layer depends on the tickness. • Support of platinum shows efficient electrocatalytic performance for biosensor. • CV curves and amperometric responses improved and optimized in the presence of N-graphene. - Abstract: An efficient non-enzymatic biosensor electrode consisting of nitrogen-doped graphene (N-graphene) and platinum nanoflower (Pt NF) with different N-graphene loadings were fabricated on indium tin oxide (ITO) glass using a simple layer-by-layer electrophoretic and electrochemical sequential deposition approach. N-graphene was synthesized by annealing graphene oxide with urea at 900 °C. The structure and morphology of the as-fabricated non-enzymatic biosensor electrodes were determined using X-ray diffraction, field emission electron microscopy, transmission electron microscopy, Raman and X-ray photoelectron spectra. The as-fabricated Pt NF-N-graphene-modified ITO electrodes with different N-graphene loadings were utilized as a non-enzymatic biosensor electrode for the detection of hydrogen peroxide (H 2 O 2 ). The behaviors of the hybrid electrodes towards H 2 O 2 reduction were assessed using chronoamperometry, cyclic voltammetry and electrochemical impedance spectroscopy analysis. The Pt NF-N-graphene-modified ITO electrode with a 0.05 mg ml −1 N-graphene loading exhibited the lowest detection limit, fastest amperometric sensing, a wide linear response range, excellent stability and reproducibility for the non-enzymatic H 2 O 2 detection, due to the synergistic effect between the electrocatalytic activity of the Pt NF and the high conductivity and large surface area of N-graphene.

  2. Electrochemical behavior of some commercial dental amalgams in artificial saliva.

    Science.gov (United States)

    Cahoon, J R; Regalbuto, C

    1975-01-01

    Cathodic, linear anodic, and anodic polarization studies conducted on three commercial dental amalgams, Caulk Fine Cut Alloy, Spheralloy, and Dispersalloy, showed that all amalgams were in a passive state at the corrosion potential in synthetic saliva solution. The corrosion currents at the corrosion potential were therefore small for all the amalgams, in the range 0.08 to 0.30 muA/cm2. However, the Caulk Fine Cut Alloy and Spheralloy amalgams exhibited a breakdown of passivity and high anodic currents at potentials only approximately equal to 100 mV more noble than the corrosion potential whereas Dispersalloy amalgams maintained passivity at potentials up to 700 mV more noble than the corrosion potential. The breakdown of passivity in Caulk Alloy and Spheralloy amalgams is attributed to the presence of the gamma2 phase (Sn7-8Hg) whereas the passive behavior of Dispersalloy amalgam is attributed to the absence of the phase. It is concluded that none of the amalgams will exhibit severe general corrosion in use, but that both Caulk Alloy and Spheralloy amalgams will exhibit pitting corrosion whereas this type of corrosion should be minimal in Dispersalloy amalgams.

  3. Enhanced Photoelectrochemical Behavior of H-TiO2 Nanorods Hydrogenated by Controlled and Local Rapid Thermal Annealing

    Science.gov (United States)

    Wang, Xiaodan; Estradé, Sonia; Lin, Yuanjing; Yu, Feng; Lopez-Conesa, Lluis; Zhou, Hao; Gurram, Sanjeev Kumar; Peiró, Francesca; Fan, Zhiyong; Shen, Hao; Schaefer, Lothar; Braeuer, Guenter; Waag, Andreas

    2017-05-01

    Recently, colored H-doped TiO2 (H-TiO2) has demonstrated enhanced photoelectrochemical (PEC) performance due to its unique crystalline core—disordered shell nanostructures and consequent enhanced conduction behaviors between the core-shell homo-interfaces. Although various hydrogenation approaches to obtain H-TiO2 have been developed, such as high temperature hydrogen furnace tube annealing, high pressure hydrogen annealing, hydrogen-plasma assisted reaction, aluminum reduction and electrochemical reduction etc., there is still a lack of a hydrogenation approach in a controlled manner where all processing parameters (temperature, time and hydrogen flux) were precisely controlled in order to improve the PEC performance of H-TiO2 and understand the physical insight of enhanced PEC performance. Here, we report for the first time a controlled and local rapid thermal annealing (RTA) approach to prepare hydrogenated core-shell H-TiO2 nanorods grown on F:SnO2 (FTO) substrate in order to address the degradation issue of FTO in the typical TiO2 nanorods/FTO system observed in the conventional non-RTA treated approaches. Without the FTO degradation in the RTA approach, we systematically studied the intrinsic relationship between the annealing temperature, structural, optical, and photoelectrochemical properties in order to understand the role of the disordered shell on the improved photoelectrochemical behavior of H-TiO2 nanorods. Our investigation shows that the improvement of PEC performance could be attributed to (i) band gap narrowing from 3.0 to 2.9 eV; (ii) improved optical absorption in the visible range induced by the three-dimensional (3D) morphology and rough surface of the disordered shell; (iii) increased proper donor density; (iv) enhanced electron-hole separation and injection efficiency due to the formation of disordered shell after hydrogenation. The RTA approach developed here can be used as a suitable hydrogenation process for TiO2 nanorods/FTO system for

  4. Influence of boron introduction on structure and electrochemical hydrogen storage properties of Ti–V-based alloys

    Energy Technology Data Exchange (ETDEWEB)

    Qiu, Shujun; Huang, Jianling [Guangxi Key Laboratory of Information Materials, Guilin University of Electronic Technology, Guilin 541004 (China); School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin 541004 (China); Chu, Hailiang, E-mail: chuhailiang@guet.edu.cn [Guangxi Key Laboratory of Information Materials, Guilin University of Electronic Technology, Guilin 541004 (China); Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin 300071 (China); School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin 541004 (China); Zou, Yongjin; Xiang, Cuili; Zhang, Huanzhi; Xu, Fen [Guangxi Key Laboratory of Information Materials, Guilin University of Electronic Technology, Guilin 541004 (China); School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin 541004 (China); Sun, Lixian, E-mail: sunlx@guet.edu.cn [Guangxi Key Laboratory of Information Materials, Guilin University of Electronic Technology, Guilin 541004 (China); School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin 541004 (China); Zhou, Huaiying [Guangxi Key Laboratory of Information Materials, Guilin University of Electronic Technology, Guilin 541004 (China); School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin 541004 (China)

    2015-11-05

    In order to improve the properties of Ti–V-based alloys in the electrochemical system, Ti{sub 0.17}Zr{sub 0.08}V{sub 0.35}Cr{sub 0.1}Ni{sub 0.3}B{sub x} (x = 0–0.04) alloys were prepared and their structural and electrochemical performances had been systematically investigated in this study. XRD patterns show that they are mainly comprised of a C14 Laves phase and a body centered cubic (BCC) solid solution phase. The introduction of boron has little effect on the structure, while it remarkably influences the electrochemical performances. The cycle life of each electrode made from the studied alloy is obviously improved. For instance, the cycle retention after 200 charge–discharge cycles is more than 90%. Furthermore, high rate dischargeability (HRD) is also enhanced after boron introduction. It is also found that the charge-transfer reaction resistance R{sub ct}, the limiting current density I{sub L,} and the hydrogen diffusion coefficient D are first decreased and then increased with the increase of boron amount. Taking into consideration various factors, the introduction of boron in the alloy has an optimal value of x = 0.01. - Graphical abstract: Trace amounts of B element was introduced into Ti{sub 0.17}Zr{sub 0.08}V{sub 0.35}Cr{sub 0.1}Ni{sub 0.3} alloys. XRD patterns show that the introduction of B has little effect on the structure, while it remarkably influences the electrochemical performances. The cycle life and the high rate dischargeability (HRD) are obviously improved. - Highlights: • Trace amounts of B element was introduced into Ti–V-based alloys. • Ti{sub 0.17}Zr{sub 0.08}V{sub 0.35}Cr{sub 0.1}Ni{sub 0.3}B{sub 0.01} has an optimal property. • At x = 0.01, C{sub 200}/C{sub max} is 89.4% and HRD{sub 800} is 72.5%.

  5. Electrochemical corrosion behaviors of the X90 linepipe steel in NS4 solution

    Directory of Open Access Journals (Sweden)

    Jinheng Luo

    2016-10-01

    Full Text Available Oil and gas line pipes are laid underground and run through different areas in the laying process, so they will be subjected to different degrees of corrosion and even crack, leading to enormous casualties and economic losses. In order to guarantee the safe operation of line pipes, therefore, it is significant to investigate the electrochemical corrosion behaviors of pipe steel in a simulated soil environment. In this paper, the electrochemical corrosion behaviors of the base metals and welding materials of API 5L X90 steel longitudinally submerged arc welding pipes in near-neutral simulated soil solution (NS4 were studied by means of the electrochemical impedance spectroscopy (EIS and the potentiodynamic polarization testing technology. It is shown that the typical characteristic of anodic dissolution is presented but with no passivation phenomenon when X90 linepipe steel is put in NS4 solution. The base material is thermodynamically more stable than the seam weld material. The base material and seam weld samples were polarized under −850 mV polarization potential for different durations. It is demonstrated that with the proceeding of polarization, the polarization resistance and the corrosion resistance increase while the corrosion current density decreases. And the corrosion resistance of base material is better than that of seam weld material.

  6. Behavior of Dental/Implant Alloys in Commercial Mouthwash Solution Studied by Electrochemical Techniques

    Science.gov (United States)

    Mareci, Daniel; Strugaru, Sorin Iacob; Iacoban, Sorin; Bolat, Georgiana; Munteanu, Corneliu

    2013-03-01

    This study investigates the electrochemical behavior of the various dental materials: Paliag (Ag-Pd based), Wiron 99 (Ni-Cr based), Cp-Ti (commercial pure titanium), and experimental Ti12Mo5Ta alloy in commercial mouthwash solution with 500 ppm F- (Oral B®) and compares it with the behavior of the same dental materials in artificial saliva. Linear potentiodynamic polarization (LPP) and electrochemical impedance spectroscopy (EIS) are the electrochemical procedures of investigation. The passivation of all dental samples in artificial saliva and mouthwash solution occurred spontaneously at open circuit potential. The corrosion current density of all tested dental materials in mouthwash solution were low (1-2 μA/cm2). The results suggest a non-predominant fluoride effect on the passive layer formed on all samples at open circuit potential. No passivation could be established with Paliag alloy when polarized in mouthwash solution. The EIS results confirm that all dental sample exhibit passivity in mouthwash solution at open circuit potential (polarization resistance was around 5 × 105 Ω cm2). For Paliag alloy after LPP in mouthwash solution the protectiveness passive layer was no more present. The corrosion resistances of four dental materials in mouthwash solution are in the following order: Ti12Mo5Ta > Cp-Ti > Wiron 99 > Paliag.

  7. Modeling the Electrochemical Hydrogen Oxidation and Evolution Reactions on the Basis of Density Functional Theory Calculations

    DEFF Research Database (Denmark)

    Skulason, Egill; Tripkovic, Vladimir; Björketun, Mårten

    2010-01-01

    Density functional theory calculations have been performed for the three elementary steps―Tafel, Heyrovsky, and Volmer―involved in the hydrogen oxidation reaction (HOR) and its reverse, the hydrogen evolution reaction (HER). For the Pt(111) surface a detailed model consisting of a negatively...... charged Pt(111) slab and solvated protons in up to three water bilayers is considered and reaction energies and activation barriers are determined by using a newly developed computational scheme where the potential can be kept constant during a charge transfer reaction. We determine the rate limiting...

  8. Electrochemical reduction of disulfide-containing proteins for hydrogen/deuterium exchange monitored by mass spectrometry

    DEFF Research Database (Denmark)

    Mysling, Simon; Salbo, Rune; Ploug, Michael

    2014-01-01

    requires a high concentration (>200 mM) of the chemical reducing agent Tris(2-carboxyethyl)phosphine (TCEP) as the reduction rate constant is decreased at low pH and temperature. Serious adverse effects on chromatographic and mass spectrometric performances have been reported when using high concentrations......Characterization of disulfide bond-containing proteins by hydrogen/deuterium exchange monitored by mass spectrometry (HDX-MS) requires reduction of the disulfide bonds under acidic and cold conditions, where the amide hydrogen exchange reaction is quenched (pH 2.5, 0°C). The reduction typically...

  9. A Hydrogen-Evolving Hybrid-Electrolyte Battery with Electrochemical/Photoelectrochemical Charging from Water Oxidation.

    Science.gov (United States)

    Jin, Zhaoyu; Li, Panpan; Xiao, Dan

    2017-02-08

    Decoupled hydrogen and oxygen production were successfully embedded into an aqueous dual-electrolyte (acid-base) battery for simultaneous energy storage and conversion. A three-electrode configuration was adopted, involving an electrocatalytic hydrogen-evolving electrode as cathode, an alkaline battery-type or capacitor-type anode as shuttle, and a charging-assisting electrode for electro-/photoelectrochemically catalyzing water oxidation. The conceptual battery not only synergistically outputs electricity and chemical fuels with tremendous specific energy and power densities, but also supports various approaches to be charged by pure or solar-assisted electricity. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Electrochemical behavior of adrenaline at the carbon atom wire modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Xue Kuanhong [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China)], E-mail: khxue@njnu.edu.cn; Liu Jiamei [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China); Wei Ribing [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China); Chen Shaopeng [Chemistry Department, Nanjing Normal University, Jiangsu Engineering Research Center for Bio-medical Function Materials, 122 NingHai Road, Nanjing, JiangSu 210097 (China)

    2006-09-11

    Electrochemical behavior of adrenaline at an electrode modified by carbon atom wires (CAWs), a new material, was investigated by cyclic voltammetry combined with UV-vis spectrometry, and forced convection method. As to the electrochemical response of redox of adrenaline/adrenalinequinone couple in 0.50 M H{sub 2}SO{sub 4}, at a nitric acid treated CAW modified electrode, the anodic and cathodic peak potentials E {sub pa} and E {sub pc} shifted by 87 mV negatively and 139 mV in the positive direction, respectively, and standard heterogeneous rate constant k {sup 0} increased by 16 times compared to the corresponding bare electrode, indicating the extraordinary activity of CAWs in electrocatalysis for the process.

  11. Electrochemical behavior of adrenaline at the carbon atom wire modified electrode

    International Nuclear Information System (INIS)

    Xue Kuanhong; Liu Jiamei; Wei Ribing; Chen Shaopeng

    2006-01-01

    Electrochemical behavior of adrenaline at an electrode modified by carbon atom wires (CAWs), a new material, was investigated by cyclic voltammetry combined with UV-vis spectrometry, and forced convection method. As to the electrochemical response of redox of adrenaline/adrenalinequinone couple in 0.50 M H 2 SO 4 , at a nitric acid treated CAW modified electrode, the anodic and cathodic peak potentials E pa and E pc shifted by 87 mV negatively and 139 mV in the positive direction, respectively, and standard heterogeneous rate constant k 0 increased by 16 times compared to the corresponding bare electrode, indicating the extraordinary activity of CAWs in electrocatalysis for the process

  12. Electrochemical behavior of adrenaline at the carbon atom wire modified electrode

    Science.gov (United States)

    Xue, Kuan-Hong; Liu, Jia-Mei; Wei, Ri-Bing; Chen, Shao-Peng

    2006-09-01

    Electrochemical behavior of adrenaline at an electrode modified by carbon atom wires (CAWs), a new material, was investigated by cyclic voltammetry combined with UV-vis spectrometry, and forced convection method. As to the electrochemical response of redox of adrenaline/adrenalinequinone couple in 0.50 M H 2SO 4, at a nitric acid treated CAW modified electrode, the anodic and cathodic peak potentials Epa and Epc shifted by 87 mV negatively and 139 mV in the positive direction, respectively, and standard heterogeneous rate constant k0 increased by 16 times compared to the corresponding bare electrode, indicating the extraordinary activity of CAWs in electrocatalysis for the process.

  13. Comparative study between the electrochemical behavior of TiN, TiCxNy and CrN hard coatings by using microscopy and electrochemical techniques

    Directory of Open Access Journals (Sweden)

    L.F. Senna

    2001-01-01

    Full Text Available Hard thin TiN, TiCxNy and CrN films deposited by Physical Vapor Deposition (PVD techniques onto steel substrates were immersed in an aggressive environment and evaluated by Atomic Force Microscopy (AFM and Electrochemical Impedance Spectroscopy (EIS. The mechanical and electrochemical behavior, as well as the microstructure of TiCxNy depended directly on the contents of carbon and nitrogen in the coating. The best results were obtained with stoichiometric coatings that are presented in this work. Although a small amount of pinholes could be observed, the electrochemical performance of TiN film was poorer than the stoichiometric TiCxNy coating. However, the CrN films showed the highest initial and residual corrosion resistance values, probably due to their dense structure.

  14. Catalytic effect of additional metallic phases on the hydrogen absorption behavior of a Zr-Based alloy

    International Nuclear Information System (INIS)

    Ruiz, F; Peretti, H; Castro, E; Real, S; Visitin, A; Triaca, W

    2005-01-01

    The electrochemical hydrogen absorption of electrodes containing Zr 0 .9Ti 0 .1(Ni 0 .5Mn 0 .25Cr 0 .20V 0 .05) 2 is studied in alkaline media by monitoring the activation and discharge capacity along charge-discharge cycling.The considered alloy is tested in both as melted and annealed condition in order to investigate the catalytic effect of small amounts of micro segregated secondary phases of the Zr-Ni system. Since these catalytic phases are only present in the as melted alloys, tests are also carried out using a composite material elaborated from powders of the annealed alloy with the addition of 18 wt.% of the suspected catalytic phases, melted separately.The hydrogen absorption-desorption behavior for the different cases is discussed and correlated with the metallurgical characterization of the materials.The catalytic effects are studied employing cyclic voltammetry and electrochemical impedance techniques. The results are analyzed in terms of a developed physicochemical model

  15. In situ study of hydrogen silsesquioxane dissolution rate in salty and electrochemical developers

    NARCIS (Netherlands)

    Harry, K.J.; Strobel, S..; Yang, J.K.W.; Duan, H.; Berggren, K.K.

    2011-01-01

    In order to better characterize the development of the electron-beam resist hydrogen silsesquioxane (HSQ), the authors used a quartz crystal microbalance (QCM) to study its rate of dissolution in situ. The authors determined the effect of both salt concentration and applied electric potential on the

  16. Bonding titanium on multi-walled carbon nanotubes for hydrogen storage: An electrochemical approach

    Energy Technology Data Exchange (ETDEWEB)

    Brieno-Enriquez, K.M.; Ledesma-Garcia, J. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, S.C., Parque Tecnologico Queretaro-Sanfandila, Pedro Escobedo, Qro, C.P. 76703 (Mexico); Perez-Bueno, J.J., E-mail: jperez@cideteq.mx [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, S.C., Parque Tecnologico Queretaro-Sanfandila, Pedro Escobedo, Qro, C.P. 76703 (Mexico); Godinez, Luis A. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, S.C., Parque Tecnologico Queretaro-Sanfandila, Pedro Escobedo, Qro, C.P. 76703 (Mexico); Terrones, H. [Instituto Potosino de Investigacion Cientifica y Tecnologica, Division de Materiales Avanzados, Camino a la Presa San Jose 2055, Col. Lomas 4o Seccion C.P. 78216, San Luis Potosi (Mexico); Angeles-Chavez, C. [Instituto Mexicano del Petroleo, Programa de Ingenieria Molecular, Eje Central Lazaro Cardenas 152, A.P. 14-805, 07730 Mexico D.F. (Mexico)

    2009-06-15

    This work explores the use of some procedures, involving electrochemistry, in order to bond atomic Ti on the outer surface of multi-walled carbon nanotubes (MWNTs). It is assumed that each titanium atom has the potential of host up to four hydrogen molecules and relinquish them by heated. As a way to spread and stick nanotubes on an electrode, a tested route was drying a solution with nanotubes on a glassy carbon flat electrode. The MWNTs were treated by anodic polarization in organic media. Dichloromethane was selected as the medium and titanium tetrachloride as the precursor for attaching atomic Ti onto the nanotubes. The hydrogen adsorption, estimated from voltamperometry was five times higher on Ti-MWNTs that on bare nanotubes. The use of anodic polarization during the preparation of Ti-MWNTs may represent great significance in procedure, which was manifest during the voltamperometric evaluation of samples.

  17. Electrochemical Dynamics of a Single Platinum Nanoparticle Collision Event for the Hydrogen Evolution Reaction.

    Science.gov (United States)

    Xiang, Zhi-Peng; Deng, Hai-Qiang; Peljo, Pekka; Fu, Zhi-Yong; Wang, Su-Li; Mandler, Daniel; Sun, Gong-Quan; Liang, Zhen-Xing

    2018-03-19

    Chronoamperometry was used to study the dynamics of Pt nanoparticle (NP) collision with an inert ultramicroelectrode via electrocatalytic amplification (ECA) in the hydrogen evolution reaction. ECA and dynamic light scattering (DLS) results reveal that the NP colloid remains stable only at low proton concentrations (1.0 mm) under a helium (He) atmosphere, ensuring that the collision events occur at genuinely single NP level. Amperometry of single NP collisions under a He atmosphere shows that each discrete current profile of the collision event evolves from spike to staircase at more negative potentials, while a staircase response is observed at all of the applied potentials under hydrogen-containing atmospheres. The particle size distribution estimated from the diffusion-controlled current in He agrees well with electron microscopy and DLS observations. These results shed light on the interfacial dynamics of the single nanoparticle collision electrochemistry. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Characterization of electrochemically deposited films from aqueous and ionic liquid cobalt precursors toward hydrogen evolution reactions

    Energy Technology Data Exchange (ETDEWEB)

    Dushatinski, Thomas; Huff, Clay; Abdel-Fattah, Tarek M., E-mail: fattah@cnu.edu

    2016-11-01

    Highlights: • Co films deposition via aqueous and ionic liquid Precursors. • Hydrogen evolution produced from reactive surfaces. • Co deposited films characterized by SEM, AFM, EDX and XRD techniques. - Abstract: Electrodepositions of cobalt films were achieved using an aqueous or an ethylene glycol based non-aqueous solution containing choline chloride (vitamin B4) with cobalt chloride hexahydrate precursor toward hydrogen evolution reactions from sodium borohydride (NaBH{sub 4}) as solid hydrogen feedstock (SHF). The resulting cobalt films had reflectivity at 550 nm of 2.2% for aqueously deposited films (ACoF) and 1.3% for non-aqueously deposited films (NCoF). Surface morphology studied by scanning electron microscopy showed a positive correlation between particle size and thickness. The film thicknesses were tunable between >100 μm and <300 μm for each film. The roughness (Ra) value measurements by Dektak surface profiling showed that the NCoF (Ra = 165 nm) was smoother than the ACoF (Ra = 418 nm). The NCoFs and ACoFs contained only α phase (FCC) crystallites. The NCoFs were crystalline while the ACoFs were largely amorphous from X-ray diffraction analysis. The NCoF had an average Vickers hardness value of 84 MPa as compared to 176 MPa for ACoF. The aqueous precursor has a single absorption maximum at 510 nm and the non-aqueous precursor had three absorption maxima at 630, 670, and 695 nm. The hydrogen evolution reactions over a 1 cm{sup 2} catalytic surface with aqueous NaBH{sub 4} solutions generated rate constants (K) = equal to 4.9 × 10{sup −3} min{sup −1}, 4.6 × 10{sup −3} min{sup −1}, and 3.3 × 10{sup −3} min{sup −1} for ACoF, NCoF, and copper substrate respectively.

  19. Hollow Cobalt-Based Bimetallic Sulfide Polyhedra for Efficient All-pH-Value Electrochemical and Photocatalytic Hydrogen Evolution.

    Science.gov (United States)

    Huang, Zhen-Feng; Song, Jiajia; Li, Ke; Tahir, Muhammad; Wang, Yu-Tong; Pan, Lun; Wang, Li; Zhang, Xiangwen; Zou, Ji-Jun

    2016-02-03

    The development of highly active, universal, and stable inexpensive electrocatalysts/cocatalysts for hydrogen evolution reaction (HER) by morphology and structure modulations remains a great challenge. Herein, a simple self-template strategy was developed to synthesize hollow Co-based bimetallic sulfide (MxCo3-xS4, M = Zn, Ni, and Cu) polyhedra with superior HER activity and stability. Homogenous bimetallic metal-organic frameworks are transformed to hollow bimetallic sulfides by solvothermal sulfidation and thermal annealing. Electrochemical measurements and density functional theory computations show that the combination of hollow structure and homoincorporation of a second metal significantly enhances the HER activity of Co3S4. Specifically, the homogeneous doping in Co3S4 lattice optimizes the Gibbs free energy for H* adsorption and improves the electrical conductivity. Impressively, hollow Zn0.30Co2.70S4 exhibits electrocatalytic HER activity better than most of the reported nobel-metal-free electrocatalysts over a wide pH range, with overpotentials of 80, 90, and 85 mV at 10 mA cm(-2) and 129, 144, and 136 mV at 100 mA cm(-2) in 0.5 M H2SO4, 0.1 M phosphate buffer, and 1 M KOH, respectively. It also exhibits photocatalytic HER activity comparable to that of Pt cocatalyst when working with organic photosensitizer (Eosin Y) or semiconductors (TiO2 and C3N4). Furthermore, this catalyst shows excellent stability in the electrochemical and photocatalytic reactions. The strategy developed here, i.e., homogeneous doping and self-templated hollow structure, provides a way to synthesize transition metal sulfides for catalysis and energy conversion.

  20. Application of o-tolidine as substrate for the electrochemical determination of hemoglobin or hydrogen peroxide

    Directory of Open Access Journals (Sweden)

    Wei Sun

    2007-08-01

    Full Text Available In this paper hemoglobin (Hb was used to catalyze the oxidative reaction of ο-tolidine (OT with H2O2. The oxidative product of OT with H2O2 was an azo substrate, which was electroactive and had a sensitive linear sweep voltammetric reductive peak at -0.52 V (vs. SCE on hanging mercury drop working electrode (HMDE in pH 5.0 Britton-Robinson (B-R solution. The conditions of Hb catalytic reaction and voltammetric detection were optimized. Under the optimal conditions, the electrochemical behaviour of the oxidative product was carefully investigated and the electrode process of the product on mercury electrode was proposed. Based on the increase of the reductive peak current of the oxidative product with the concentration of the H2O2 or Hb, a new electrochemical method for the determination of trace amount of H2O2 or Hb was proposed. The calibration graph had a linear range of 6.0 x 10-8 to 4.0 x 10-5 M for H2O2 and 1.0 x 10-9 to 7.0 x 10-7 M for Hb with the detection limit of 1.0 x 10-8 M H2O2 and 5.0 x 10-10 M Hb (3σ, respectively. This new proposed method was further attempted to determine the content of H2O2 in fresh rainwater with satisfactory results.

  1. Electrochemical and passivation behavior investigation of ferritic stainless steel in simulated concrete pore media.

    Science.gov (United States)

    Luo, Hong; Su, Huaizhi; Dong, Chaofang; Xiao, Kui; Li, Xiaogang

    2015-12-01

    The applications of stainless steel are one of the most reliable solutions in concrete structures to reduce chloride-induced corrosion problems and increase the structures service life, however, due to high prices of nickel, especially in many civil engineering projects, the austenitic stainless steel is replaced by the ferritic stainless steels. Compared with austenite stainless steel, the ferritic stainless steel is known to be extremely resistant of stress corrosion cracking and other properties. The good corrosion resistance of the stainless steel is due to the formation of passive film. While, there is little literature about the electrochemical and passive behavior of ferritic stainless steel in the concrete environments. So, here, we present the several corrosion testing methods, such as the potentiodynamic measurements, EIS and Mott-Schottky approach, and the surface analysis methods like XPS and AES to display the passivation behavior of 430 ferritic stainless steel in alkaline solution with the presence of chloride ions. These research results illustrated a simple and facile approach for studying the electrochemical and passivation behavior of stainless steel in the concrete pore environments.

  2. Investigations on the Electrochemical Reduction Behaviors of Cu-Se Compound in Sulfuric Acid Solutions

    Science.gov (United States)

    Li, Yuan-yuan; Yang, Meng-qian; Yang, Wei-fang; Liu, Xiao-qing; Shen, Zheng-wu; Yi, Yun; Wang, Wei

    2017-05-01

    The electrochemical reduction behaviors of a Cu unitary system, Se unitary system and Cu-Se binary system were investigated by cyclic voltammetry, linear sweep voltammetry and electrochemical impedance spectroscopy in solutions containing H2SO4, K2SO4, CuSO4 (Cu unitary system) or H2SeO3 (Se unitary system) or both CuSO4 and H2SeO3 (Cu-Se binary system). The effects of CuSO4 concentration, H2SeO3 concentration, H2SO4 concentration and K2SO4 concentration were also considered. In the Cu unitary system, the electrochemical reduction of Cu2+ to Cu0 experiences a two-step reaction process. Cu2+ in the solutions was first reduced to Cu+ and then to Cu0 on the surface of the electrode. A four-step electrochemical reduction process takes place in the Se unitary system. Se4+ existing in the form of H2SeO3 is first reduced to Se2+ by a two-electron reaction step and then to Se0 at a more negative potential. With the potential moving negatively, the electrodeposited Se0 on the surface of the electrode is further reduced to Se2-. There is also a chemical reaction taking place between the reduced Se2- and H2SeO3 existing in the solution to form Se0. In the Cu-Se binary system, there are three major processes taking place which form CuSe, Cu3Se2 and Cu2Se. X-ray diffraction and energy-dispersive spectroscopy were used in combination to verify their formation.

  3. Effects of Nd-addition on the structural, hydrogen storage, and electrochemical properties of C14 metal hydride alloys

    Energy Technology Data Exchange (ETDEWEB)

    Wong, D.F. [BASF/Battery Materials-Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Department of Chemical Engineering, Wayne State University, Detroit, MI 48202 (United States); Young, K., E-mail: kwo.young@basf.com [BASF/Battery Materials-Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Department of Chemical Engineering, Wayne State University, Detroit, MI 48202 (United States); Nei, J.; Wang, L. [BASF/Battery Materials-Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Ng, K.Y.S. [Department of Chemical Engineering, Wayne State University, Detroit, MI 48202 (United States)

    2015-10-25

    Nd-addition to the AB{sub 2}-based alloy Ti{sub 12}Zr{sub 22.8−x}V{sub 10}Cr{sub 7.5}Mn{sub 8.1}Co{sub 7.0}Ni{sub 32.2}Al{sub 0.4}Nd{sub x} is studied for its effects on the structure, gaseous-phase hydrogen storage, and electrochemical properties. This study follows a series of Cu, Mo, Fe, Y, Si, and La doping studies in similar AB{sub 2}-based alloys. Limited solubility of Nd in the main Laves phase promotes the formation of secondary phases (AB and Zr{sub 7}Ni{sub 10}) to provide catalytic effects and synergies for improved capacity and high-rate dischargeability (HRD) performance. The main C14 storage phase has smaller lattice constants and cell volumes, and these effects reduce the storage capacity at higher Nd levels. Different hydrogen absorption mechanisms can occur in these multi-component, multi-phase alloys depending on the interfaces of the phases, and they have effects on the alloy properties. Higher Nd-levels improve the HRD performance despite having lower bulk diffusion and surface exchange current. Magnetic susceptibility measurements indicate large percentage of larger metallic nickel clusters are present in the surface oxide of alloys with higher Nd-content, and AC impedance studies show very low charge-transfer resistance with high catalytic capability in the alloys. The −40 °C charge-transfer resistance of 8.9 Ω g in this Nd-series of alloys is the lowest measured out of the studies investigating doped AB{sub 2}-based MH alloys for improved low-temperature characteristics. The improvement in HRD and low-temperature performance appears to be related to the proportion of the highly catalytic NdNi-phase at the surface, which must offset the increased bulk diffusion resistance in the alloy. - Graphical abstract: Schematics of hydrogen flow and corresponding PCT isotherms in funneling mode. - Highlights: • Structural and hydrogen storage properties of Nd-substituted AB{sub 2} metal hydride are reported. • Nd contributes to the lowest

  4. Highly efficient electrochemical hydrogen evolution based on nickel diselenide nanowall film

    Science.gov (United States)

    Tang, Chun; Xie, Lisi; Sun, Xuping; Asiri, Abdullah M.; He, Yuquan

    2016-05-01

    In this letter, we report on hydrothermal growth of nickel diselenide nanowall film on carbon cloth (NiSe2 NW/CC) through topotactic transformation from a Ni(OH)2 precursor based on anion exchange reactions. When tested as an integrated 3D hydrogen-evolving cathode in strongly acidic media, NiSe2 NW/CC exhibits outstanding catalytic activity superior to its powder counterpart and strong long-term durability. It displays 10 and 100 mA cm-2 at overpotentials of 145 and 183 mV, respectively, with its catalytic activity being retained for 40 h.

  5. The Surface Adsorption of Hydride Ions and Hydrogen Atoms on Zn Studied by Electrochemical Impedance Spectroscopy with a Non-Equilibrium Thermodynamic Formulation

    Science.gov (United States)

    Nakajima, Hironori; Nohira, Toshiyuki; Ito, Yasuhiko; Kjelstrup, Signe; Bedeaux, Dick

    2006-09-01

    We show that non-equilibrium thermodynamics theory for surfaces combined with electrochemical impedance spectroscopy can be used to derive the excess surface concentrations of reactants and products of an electrochemical reaction at an electrode. We predict the equivalent circuit for a postulated reaction using this theory, and derive expressions for the excess surface concentrations. The method is illustrated with experimental data for the following hydride reaction to hydrogen at a Zn anode in a molten eutectic mixture of LiCl and KCl at 673 K: The results support a two-step mechanism for hydrogen evolution via the hydrogen atom. We calculate the excess surface concentrations of the hydride ions and the hydrogen atoms at the metal surface, and find that the hydride ions cover a fraction of the surface while the hydrogen atoms are present in large excess. The excess surface concentration of the hydride ions varies largely with the polarized state of the surface, and so does its mean activity coefficient at the surface. The results contribute to a better understanding of the system in question. The method is general and is expected to give similar information for other electrodes.

  6. Electrochemical behavior of Ni-Mo electro catalyst for water electrolysis

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez V, S. M.; Ordonez R, E. [ININ, Departamento de Quimica, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico); Cabanas M, G. [IPN, Centro de Nanociencias y Micro y Nanotecnologias, A. P. 75-874, 07300 Mexico D. F. (Mexico); Solorza F, O., E-mail: suilma.fernandez@inin.gob.m [IPN, Centro de Investigacion y de Estudios Avanzados, Departamento de Quimica, A. P. 14-740, 07000 Mexico D. F. (Mexico)

    2010-07-01

    Nickel-molybdenum based electrocatalysts were synthesized in organic media for the hydrogen evolution reaction and oxygen evolution reaction in alkaline media. The structure, morphology and chemical composition of the catalysts were evaluated by X-ray diffraction, scanning electron microscopy and Aas. Results revealed nanocrystalline powder materials with Ni{sub 0.006}Mo, Ni{sub 0.1}Mo and Ni Mo compositions. The best performance for hydrogen evolution reaction, was obtained on Ni{sub 0.1}Mo electrode, whereas Ni Mo was for the oxygen evolution reaction. Results suggest that the material with 1:1 stoichiometric ratio could be considered as a promising electro catalyst for oxygen evolution reaction. This nanocrystalline powder is formed by Ni{sub 2}Mo{sub 3}O{sub 8} and a crystalline structure attributed to the possible formation of a Ni Mo cluster, becomes NiMoO{sub 4} after thermal treatment at 1073 K in air. The Ni Mo 1:1 cluster catalyst presented electrochemical stability during the oxygen evolution reaction. (Author)

  7. Electrochemical behavior of Ni-Mo electro catalyst for water electrolysis

    International Nuclear Information System (INIS)

    Fernandez V, S. M.; Ordonez R, E.; Cabanas M, G.; Solorza F, O.

    2010-01-01

    Nickel-molybdenum based electrocatalysts were synthesized in organic media for the hydrogen evolution reaction and oxygen evolution reaction in alkaline media. The structure, morphology and chemical composition of the catalysts were evaluated by X-ray diffraction, scanning electron microscopy and Aas. Results revealed nanocrystalline powder materials with Ni 0.006 Mo, Ni 0.1 Mo and Ni Mo compositions. The best performance for hydrogen evolution reaction, was obtained on Ni 0.1 Mo electrode, whereas Ni Mo was for the oxygen evolution reaction. Results suggest that the material with 1:1 stoichiometric ratio could be considered as a promising electro catalyst for oxygen evolution reaction. This nanocrystalline powder is formed by Ni 2 Mo 3 O 8 and a crystalline structure attributed to the possible formation of a Ni Mo cluster, becomes NiMoO 4 after thermal treatment at 1073 K in air. The Ni Mo 1:1 cluster catalyst presented electrochemical stability during the oxygen evolution reaction. (Author)

  8. Single step synthesis of gold-amino acid composite, with the evidence of the catalytic hydrogen atom transfer (HAT) reaction, for the electrochemical recognition of Serotonin

    Science.gov (United States)

    Choudhary, Meenakshi; Siwal, Samarjeet; Nandi, Debkumar; Mallick, Kaushik

    2016-03-01

    A composite architecture of amino acid and gold nanoparticles has been synthesized using a generic route of 'in-situ polymerization and composite formation (IPCF)' [1,2]. The formation mechanism of the composite has been supported by a model hydrogen atom (H•≡H++e-) transfer (HAT) type of reaction which belongs to the proton coupled electron transfer (PCET) mechanism. The 'gold-amino acid composite' was used as a catalyst for the electrochemical recognition of Serotonin.

  9. Cationic Vacancy Defects in Iron Phosphide: A Promising Route toward Efficient and Stable Hydrogen Evolution by Electrochemical Water Splitting.

    Science.gov (United States)

    Kwong, Wai Ling; Gracia-Espino, Eduardo; Lee, Cheng Choo; Sandström, Robin; Wågberg, Thomas; Messinger, Johannes

    2017-11-23

    Engineering the electronic properties of transition metal phosphides has shown great effectiveness in improving their intrinsic catalytic activity for the hydrogen evolution reaction (HER) in water splitting applications. Herein, we report for the first time, the creation of Fe vacancies as an approach to modulate the electronic structure of iron phosphide (FeP). The Fe vacancies were produced by chemical leaching of Mg that was introduced into FeP as "sacrificial dopant". The obtained Fevacancy-rich FeP nanoparticulate films, which were deposited on Ti foil, show excellent HER activity compared to pristine FeP and Mg-doped FeP, achieving a current density of 10 mA cm -2 at overpotentials of 108 mV in 1 m KOH and 65 mV in 0.5 m H 2 SO 4 , with a near-100 % Faradaic efficiency. Our theoretical and experimental analyses reveal that the improved HER activity originates from the presence of Fe vacancies, which lead to a synergistic modulation of the structural and electronic properties that result in a near-optimal hydrogen adsorption free energy and enhanced proton trapping. The success in catalytic improvement through the introduction of cationic vacancy defects has not only demonstrated the potential of Fe-vacancy-rich FeP as highly efficient, earth abundant HER catalyst, but also opens up an exciting pathway for activating other promising catalysts for electrochemical water splitting. © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

  10. Electrochemical performances and capacity fading behaviors of activated carbon/hard carbon lithium ion capacitor

    International Nuclear Information System (INIS)

    Sun, Xianzhong; Zhang, Xiong; Liu, Wenjie; Wang, Kai; Li, Chen; Li, Zhao; Ma, Yanwei

    2017-01-01

    Highlights: • Three-electrode pouch cell is used to investigate the capacity fading of AC/HC LIC. • the electrode potential swing is critical for the cycleability of a LIC cell. • Different capacity fading behaviors are discussed. • A large-capacity LIC pouch cell has been assembled with a specific energy of 18.1 Wh kg −1 based on the total weight. - Abstract: Lithium ion capacitor (LIC) is one of the most promising electrochemical energy storage devices, which offers rapid charging-discharging capability and long cycle life. We have fabricated LIC pouch cells using an electrochemically-driven lithium pre-doping method through a three-electrode pouch cell structure. The active materials of cathode and anode of LIC cell are activated carbon and pre-lithiated hard carbon, respectively. The electrochemical performances and the capacity fading behaviors of LICs in the voltage range of 2.0 − 4.0 V have been studied. The specific energy and specific power reach 73.6 Wh kg −1 and 11.9 kW kg −1 based on the weight of the active materials in both cathode and anode, respectively. Since the cycling performance is actually determined by hard carbon anode, the anode potential swings are emphasized. The capacity fading of LIC upon cycling is proposed to be caused by the increases of internal resistance and the consumption of lithium stored in anode. Finally, a large-capacity LIC pouch cell has been assembled with a maximum specific energy of 18.1 Wh kg −1 and a maximum specific power of 3.7 kW kg −1 based on the weight of the whole cell.

  11. Electrochemical behavior of antimony and electrodeposition of Mg-Li-Sb alloys from chloride melts

    International Nuclear Information System (INIS)

    Wei Shuquan; Zhang Milin; Han Wei; Yan Yongde; Xue Yun; Zhang Meng; Zhang Bin

    2011-01-01

    Research highlights: → The electrochemical behavior of Sb(III) ions was investigated in LiCl-KCl molten salt at 673 K. → The electrochemical reduction of Sb(III) in LiCl-KCl melts occurred in a reaction step with an exchange of three electrons. → AlSb alloys were prepared in LiCl-KCl-SbCl 3 melts at 742 K by potentiostatic electrolysis at an Al electrode. → The activity of Sb and the Gibbs energy of AlSb formation was calculated. - Abstract: The electrochemical behavior of Sb(III) ions was investigated in LiCl-KCl molten salt at 673 K. The reaction mechanism and transport parameters of electroactive species were determined by transient electrochemical techniques (such as cyclic voltammetry, square wave voltammetry, chronopotentiometry and chronoamperometry) at a molybdenum electrode. The results showed that electrochemical reduction of Sb(III) in LiCl-KCl melts occurred in a reaction step with an exchange of three electrons. A voltammogram with a different scan rate in LiCl-KCl containing 1.45 x 10 -4 mol cm -3 SbCl 3 showed that the deposition/dissolution reaction of Sb(III) ions was not completely reversible. The diffusion coefficient of Sb(III) ions was 1.65(±0.01) x 10 -5 cm -2 s -1 at 673 K. The electroreduction of Sb(III) ions at an Al electrode was also studied by cyclic voltammetry and open circuit chronopotentiometry in the temperature range of 668-742 K. The redox potential of Sb(III)/Sb at an Al electrode was observed at the more positive potentials values than those at an inert electrode. This potential shift due to the formation of intermetallic compound with Al electrode. AlSb alloys were prepared in LiCl-KCl-SbCl 3 melts at 742 K by potentiostatic electrolysis at an Al electrode. The activity of Sb and the Gibbs energy of AlSb formation were also calculated. Mg-Li-Sb alloys were obtained by galvanostatic electrolysis at 673 K and the electrochemical codeposition of Mg, Li and Sb was investigated on a molybdenum electrode in Li

  12. Electrochemical behavior and voltammetric determination of acetaminophen based on glassy carbon electrodes modified with poly(4-aminobenzoic acid)/electrochemically reduced graphene oxide composite films.

    Science.gov (United States)

    Zhu, Wencai; Huang, Hui; Gao, Xiaochun; Ma, Houyi

    2014-12-01

    Poly(4-aminobenzoic acid)/electrochemically reduced graphene oxide composite film modified glassy carbon electrodes (4-ABA/ERGO/GCEs) were fabricated by a two-step electrochemical method. The electrochemical behavior of acetaminophen at the modified electrode was investigated by means of cyclic voltammetry. The results indicated that 4-ABA/ERGO composite films possessed excellent electrocatalytic activity towards the oxidation of acetaminophen. The electrochemical reaction of acetaminophen at 4-ABA/ERGO/GCE is proved to be a surface-controlled process involving the same number of protons and electrons. The voltammetric determination of acetaminophen performed with the 4-ABA/ERGO modified electrode presents a good linearity in the range of 0.1-65 μM with a low detection limit of 0.01 μM (S/N=3). In the case of using the 4-ABA/ERGO/GCE, acetaminophen and dopamine can be simultaneously determined without mutual interference. Furthermore, the 4-ABA/ERGO/GCE has good reproducibility and stability, and can be used to determine acetaminophen in tablets. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. Electrochemical hydrogen storage in ZrCrNiPd{sub x} alloys

    Energy Technology Data Exchange (ETDEWEB)

    Ruiz, F.C. [Centro Atomico Bariloche (CAB), Comision Nacional de Energia Atomica (CNEA), C. P. 8400, S. C. de Bariloche (RN) (Argentina); CONICET Consejo Nacional de Investigaciones Cientificas y Tecnicas, Av. Rivadavia 1917, C1033AAJ, Ciudad de Buenos Aires (Argentina); Peretti, H.A. [Centro Atomico Bariloche (CAB), Comision Nacional de Energia Atomica (CNEA), C. P. 8400, S. C. de Bariloche (RN) (Argentina); Instituto Balseiro, Universidad Nacional de Cuyo, C. P. 8400, S. C. de Bariloche (RN) (Argentina); Visintin, A. [CONICET Consejo Nacional de Investigaciones Cientificas y Tecnicas, Av. Rivadavia 1917, C1033AAJ, Ciudad de Buenos Aires (Argentina); Instituto de Investigaciones Fisicoquimicas, Teoricas y Aplicadas, Universidad Nacional de La Plata, Suc. 4, C.C.: 16/Comision de Investigaciones Cientificas Provincia de Buenos Aires (C.I.C.), CP: 1900, La Plata (Argentina)

    2010-06-15

    The consumption of rechargeable batteries at worldwide level has increased constantly in the last years, mainly due to the use of portable devices such as cellular phones, digital cameras, computers, music and video reproducers, etc. Nickel Metal Hydride (NiMH) is a rechargeable battery system widely used in these devices, also including the most of electrical and hybrid vehicles (EV and HEV). The study of hydride forming alloys is fundamental for its use as negative electrode component in NiMH batteries. In previous works, the electrocatalytic effect of Pd element addition to the electrode, in powder form and by means of electroless technique, has been studied. In this work, AB{sub 2}-type alloys are studied, in which Pd is incorporated to the structure by re-melting inside an arc furnace. The base alloy composition is ZrCrNi, and the composition of the elaborated compounds is ZrCrNiPd{sub x} (x = 0.095 and 0.19). The effect of the composition modification on these materials on properties such as electrochemical discharge capacity, activation and high rate dischargeability (HRD) is analyzed. (author)

  14. Construction of CuS/Au Heterostructure through a Simple Photoreduction Route for Enhanced Electrochemical Hydrogen Evolution and Photocatalysis

    Science.gov (United States)

    Basu, Mrinmoyee; Nazir, Roshan; Fageria, Pragati; Pande, Surojit

    2016-01-01

    An efficient Hydrogen evolution catalyst has been developed by decorating Au nanoparticle on the surface of CuS nanostructure following a green and environmental friendly approach. CuS nanostructure is synthesized through a simple wet-chemical route. CuS being a visible light photocatalyst is introduced to function as an efficient reducing agent. Photogenerated electron is used to reduce Au(III) on the surface of CuS to prepare CuS/Au heterostructure. The as-obtained heterostructure shows excellent performance in electrochemical H2 evolution reaction with promising durability in acidic condition, which could work as an efficient alternative for novel metals. The most efficient CuS-Au heterostructure can generate 10 mA/cm2 current density upon application of 0.179 V vs. RHE. CuS-Au heterostructure can also perform as an efficient photocatalyst for the degradation of organic pollutant. This dual nature of CuS and CuS/Au both in electrocatalysis and photocatalysis has been unveiled in this study. PMID:27703212

  15. Degradation of pentachlorophenol by hydroxyl radicals and sulfate radicals using electrochemical activation of peroxomonosulfate, peroxodisulfate and hydrogen peroxide.

    Science.gov (United States)

    Govindan, Kadarkarai; Raja, Mohan; Noel, Michael; James, E J

    2014-05-15

    The present study is to investigate the reactivity of free radicals (SO4(-) and HO) generated from common oxidants (peroxomonosulfate (PMS), peroxodisulfate (PDS) and hydrogen peroxide (HP)) activated by electrochemically generated Fe(2+)/Fe(3+) ions which furthermore are evaluated to destroy pentachlorophenol (PCP) in aqueous solution. The effect of solution pH and amount of oxidants (PMS, PDS and HP) in electrocoagulation (EC) on PCP degradation is analyzed in detail. The experimental results reveal that, optimum initial solution pH is 4.5 and PMS is more efficient oxidant addition in EC. 75% PCP degradation is achieved at 60min electrolysis time from PMS assisted EC. According to the first order rate constant, faster PCP degradation rate is obtained by PMS assisted EC. The PCP degradation rate by oxidant assisted EC is observed in the following order: EC/PMS>EC/PDS>EC/HP>EC. Further to identify the influences of experimental factors involved in PCP degradation by oxidant assisted EC, an experimental design based on an orthogonal array (OA) L9 (3(3)) is proposed using Taguchi method. The factors that most significantly affect the process robustness are identified as A (oxidant) and B (pH) which together account for nearly 86% of the variance. Copyright © 2014 Elsevier B.V. All rights reserved.

  16. Effects of pH and elevated glucose levels on the electrochemical behavior of dental implants.

    Science.gov (United States)

    Tamam, Evsen; Turkyilmaz, Ilser

    2014-04-01

    Implant failure is more likely to occur in persons with medically compromising systemic conditions, such as diabetes related to high blood glucose levels and inflammatory diseases related to pH levels lower than those in healthy people. The aim of this study was to investigate the effects of lower pH level and simulated- hyperglycemia on implant corrosion as these effects are critical to biocompatibility and osseointegration. The electrochemical corrosion properties of titanium implants were studied in four different solutions: Ringer's physiological solution at pH = 7.0 and pH = 5.5 and Ringer's physiological solution containing 15 mM dextrose at pH = 7 and pH = 5.5. Corrosion behaviors of dental implants were determined by cyclic polarization test and electrochemical impedance spectroscopy. Surface alterations were studied using a scanning electron microscope. All test electrolytes led to apparent differences in corrosion behavior of the implants. The implants under conditions of test exhibited statistically significant increases in I(corr) from 0.2372 to 1.007 μAcm(-2), corrosion rates from 1.904 to 8.085 mpy, and a decrease in polarization resistances from 304 to 74 Ω. Implants in dextrose-containing solutions were more prone to corrosion than those in Ringer's solutions alone. Increasing the acidity also yielded greater corrosion rates for the dextrose-containing solutions and the solutions without dextrose.

  17. Electrochemical corrosion behavior of AZ91D alloy in ethylene glycol

    Energy Technology Data Exchange (ETDEWEB)

    Fekry, A.M. [Chemistry Department, Faculty of Science, Cairo University, Giza 12613 (Egypt)], E-mail: hham4@hotmail.com; Fatayerji, M.Z. [Chemistry Department, Faculty of Science, Cairo University, Giza 12613 (Egypt)

    2009-11-01

    The effect of concentration on the corrosion behavior of Mg-based alloy AZ91D was investigated in ethylene glycol-water solutions using electrochemical techniques i.e. potentiodynamic polarization, electrochemical impedance measurements (EIS) and surface examination via scanning electron microscope (SEM) technique. This can provide a basis for developing new coolants for magnesium alloy engine blocks. Corrosion behavior of AZ91D alloy by coolant is important in the automotive industry. It was found that the corrosion rate of AZ91D alloy decreased with increasing concentration of ethylene glycol. For AZ91D alloy in chloride >0.05 M or fluoride <0.05 M containing 30% ethylene glycol solution, they are more corrosive than the blank (30% ethylene glycol-70% water). However, at concentrations <0.05 for chloride or >0.05 M for fluoride containing ethylene glycol solution, some inhibition effect has been observed. The corrosion of AZ91D alloy in the blank can be effectively inhibited by addition of 0.05 mM paracetamol that reacts with AZ91D alloy and forms a protective film on the surface at this concentration as confirmed by surface examination.

  18. A coupled model between hydrogen diffusion and mechanical behavior of superelastic NiTi alloys

    Science.gov (United States)

    Elkhal Letaief, W.; Hassine, T.; Gamaoun, F.

    2017-07-01

    The undesirable effects of hydrogen show significant alterations to the thermomechanical behavior of superelastic NiTi shape memory alloys. Through experimental results, the presence of hydrogen induces a delay of forward transformation. Added to that, hydrogen-induced expansion is clearly noticed. We also remark a loss of superelasticity. These effects occur according to the hydrogen absorption by the NiTi alloy. The aim of this paper is to develop a coupled diffusion-mechanical model of shape memory alloys, which regards the aforesaid effects of hydrogen on the thermomechanical behavior and the transformation mechanism of NiTi alloys. The model is derived from the relationship between the chemical potential of hydrogen and the thermodynamics laws. Furthermore, we introduce a special transformation hardening function that predicts stress-strain behavior well during the transformation plateau. The model is implemented in ABAQUS finite element analysis software through the UMAT and UMATHT subroutines. The simulation results present good concordance with the experiments.

  19. Influence of microstructure and mechanical stress on behavior of hydrogen in 500 nm Pd films

    Energy Technology Data Exchange (ETDEWEB)

    Vlček, Marián, E-mail: Marian.Vlcek@gmail.com [Faculty of Mathematics and Physics, Charles University in Prague, V Holešovičkách 2, CZ-18000 Praha 8 (Czech Republic); Lukáč, František; Vlach, Martin [Faculty of Mathematics and Physics, Charles University in Prague, V Holešovičkách 2, CZ-18000 Praha 8 (Czech Republic); Wagner, Stefan; Uchida, Helmut [Institute of Materials Physics, University of Göttingen, Friedrich-Hund-Platz 1, D-37077 Göttingen (Germany); Baehtz, Carsten; Shalimov, Artem [Institute of Ion Beam Physics and Materials Research, Helmholtz-Zentrum Dresden-Rossendorf, D-01314 Dresden (Germany); Pundt, Astrid [Institute of Materials Physics, University of Göttingen, Friedrich-Hund-Platz 1, D-37077 Göttingen (Germany); Čížek, Jakub [Faculty of Mathematics and Physics, Charles University in Prague, V Holešovičkách 2, CZ-18000 Praha 8 (Czech Republic)

    2015-10-05

    Highlights: • Influence of nano-structure and stresses on hydrogenation of Pd films was studied. • Nanocrystalline Pd films deposited on hard and soft substrates were compared. • It was found that nanocrystalline structure leads to narrowing of the miscibility gap. • Compressive in-plane stress suppresses the hydride formation. • The lattice constants for α-phase and the hydride phase are closer than in bulk Pd. - Abstract: Pd films can be used as a model system to examine the influence of microstructure and stress on the hydrogen absorption. In this work we study 500 nm Pd films deposited on different substrates with different binding strengths. The films were electrochemically loaded with hydrogen up to hydride concentration. Development of lattice constant during hydrogen loading of Pd films was investigated by in situ X-ray diffraction using synchrotron radiation. The influence of microstructure and mechanical stress in the films on the phase transition from Pd to Pd hydride was examined.

  20. Effect of hydrogen on the corrosion behavior of the Mg–xZn alloys

    Directory of Open Access Journals (Sweden)

    Yingwei Song

    2014-09-01

    Full Text Available Hydrogen evolution reaction is inevitable during the corrosion of Mg alloys. The effect of hydrogen on the corrosion behavior of the Mg–2Zn and Mg–5Zn alloys is investigated by charging hydrogen treatment. The surface morphologies of the samples after charging hydrogen were observed using a scanning electron microscopy (SEM and the corrosion resistance was evaluated by polarization curves. It is found that there are oxide films formed on the surface of the charged hydrogen samples. The low hydrogen evolution rate is helpful to improve the corrosion resistance of Mg alloys, while the high hydrogen evolution rate can increases the defects in the films and further deteriorates their protection ability. Also, the charging hydrogen effect is greatly associated with the microstructure of Mg substrate.

  1. Fabrication of a novel electrochemical sensor for determination of hydrogen peroxide in different fruit juice samples

    OpenAIRE

    Nasirizadeh, Navid; Shekari, Zahra; Nazari, Ali; Tabatabaee, Masoumeh

    2016-01-01

    A new hydrogen peroxide (H2O2) sensor is fabricated based on a multiwalled carbon nanotube-modified glassy carbon electrode (MWCNT-GCE) and reactive blue 19 (RB). The charge transfer coefficient, α, and the charge transfer rate constant, ks, of RB adsorbed on MWCNT-GCE were calculated and found to be 0.44 ± 0.01 Hz and 1.9 ± 0.05 Hz, respectively. The catalysis of the electroreduction of H2O2 by RB-MWCNT-GCE is described. The RB-MWCNT-GCE shows a dramatic increase in the peak current and a de...

  2. Electrochemical behavior and corrosion resistance of Ti-15Mo alloy in naturally-aerated solutions, containing chloride and fluoride ions.

    Science.gov (United States)

    Rodrigues, A V; Oliveira, N T C; dos Santos, M L; Guastaldi, A C

    2015-01-01

    The electrochemical behavior and corrosion resistance of Ti-15Mo alloy to applications as biomaterials in solutions 0.15 mol L(-1) Ringer, 0.15 mol L(-1) Ringer plus 0.036 mol L(-1) NaF and 0.036 mol L(-1) NaF (containing 1,500 ppm of fluoride ions, F(-)) were investigated using open-circuit potential, cyclic voltammetry, and electrochemical impedance spectroscopy techniques, X-ray photoelectron spectroscopy and scanning electron microscope. Corrosion resistance and electrochemical stability of the Ti-15Mo alloy decreased in solutions containing F(-) ions. In all cases, there were formation and growth of TiO2 and MoO3 (a protector film), not being observed pitting corrosion, which might enable Ti-15Mo alloys to be used as biomedical implant, at least in the studied conditions, since the electrochemical stability and corrosion resistance of the passive films formed are necessary conditions for osseointegration.

  3. Degradation of the fluoroquinolone enrofloxacin by electrochemical advanced oxidation processes based on hydrogen peroxide electrogeneration

    Energy Technology Data Exchange (ETDEWEB)

    Guinea, Elena; Garrido, Jose Antonio; Rodriguez, Rosa Maria; Cabot, Pere-Lluis; Arias, Conchita; Centellas, Francesc [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain); Brillas, Enric, E-mail: brillas@ub.ed [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Facultat de Quimica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)

    2010-02-15

    Solutions of the veterinary fluoroquinolone antibiotic enrofloxacin in 0.05 M Na{sub 2}SO{sub 4} of pH 3.0 have been comparatively degraded by electrochemical advanced oxidation processes such as anodic oxidation with electrogenerated H{sub 2}O{sub 2} (AO-H{sub 2}O{sub 2}), electro-Fenton (EF), photoelectro-Fenton (PEF) and solar photoelectro-Fenton (SPEF) at constant current density. The study has been performed using an undivided stirred tank reactor of 100 ml and a batch recirculation flow plant of 2.5 l with an undivided filter-press cell coupled to a solar photoreactor, both equipped with a Pt or boron-doped diamond (BDD) anode and a carbon-polytetrafluoroethylene gas diffusion cathode to generate H{sub 2}O{sub 2} from O{sub 2} reduction. In EF, PEF and SPEF, hydroxyl radical (centre dotOH) is formed from Fenton's reaction between added catalytic Fe{sup 2+} and generated H{sub 2}O{sub 2}. Almost total decontamination of enrofloxacin solutions is achieved in the stirred tank reactor by SPEF with BDD. The use of the batch recirculation flow plant showed that this process is the most efficient and can be viable for industrial application, becoming more economic and yielding higher mineralization degree with raising antibiotic content. This is feasible because organics are quickly oxidized with centre dotOH formed from Fenton's reaction and at BDD from water oxidation, combined with the fast photolysis of complexes of Fe(III) with generated carboxylic acids under solar irradiation. The lower intensity of UVA irradiation used in PEF with BDD causes a slower degradation. EF with BDD is less efficient since centre dotOH cannot destroy the most persistent Fe(III)-oxalate and Fe(III)-oxamate complexes. AO-H{sub 2}O{sub 2} with BDD yields the poorest mineralization because pollutants are only removed with centre dotOH generated at BDD. All procedures are less potent using Pt as anode due to the lower production of centre dotOH at its surface. Enrofloxacin

  4. Exploiting differential electrochemical stripping behaviors of Fe3O4 nanocrystals toward heavy metal ions by crystal cutting.

    Science.gov (United States)

    Yao, Xian-Zhi; Guo, Zheng; Yuan, Qing-Hong; Liu, Zhong-Gang; Liu, Jin-Huai; Huang, Xing-Jiu

    2014-08-13

    This study attempts to understand the intrinsic impact of different morphologies of nanocrystals on their electrochemical stripping behaviors toward heavy metal ions. Two differently shaped Fe3O4 nanocrystals, i.e., (100)-bound cubic and (111)-bound octahedral, have been synthesized for the experiments. Electrochemical results indicate that Fe3O4 nanocrystals with different shapes show different stripping behaviors toward heavy metal ions. Octahedral Fe3O4 nanocrystals show better electrochemical sensing performances toward the investigated heavy metal ions such as Zn(II), Cd(II), Pb(II), Cu(II), and Hg(II), in comparison with cubic ones. Specifically, Pb(II) is found to have the best stripping performance on both the (100) and (111) facets. To clarify these phenomena, adsorption abilities of as-prepared Fe3O4 nanocrystals have been investigated toward heavy metal ions. Most importantly, combined with theoretical calculations, their different electrochemical stripping behaviors in view of facet effects have been further studied and enclosed at the level of molecular/atom. Finally, as a trial to find a disposable platform completely free from noble metals, the potential application of the Fe3O4 nanocrystals for electrochemical detection of As(III) in drinking water is demonstrated.

  5. On the Electrochemical Behavior of PVD Ti-Coated AISI 304 Stainless Steel in Borate Buffer Solution

    Science.gov (United States)

    Fattah-alhosseini, Arash; Elmkhah, Hassan; Attarzadeh, Farid Reza

    2017-04-01

    This work aims at studying the electrochemical behavior of annealed pure titanium (Ti) and nano-structured (NS) Ti coating in borate buffer solutions. Cathodic arc evaporation was successfully applied to deposit NS Ti coating. Samples were characterized by means of scanning electron microscope and x-ray diffraction. Potentiodynamic polarization tests, electrochemical impedance spectroscopy, and Mott-Schottky analysis were employed to discuss the electrochemical behavior of samples thoroughly. Electrochemical measurements showed that the deposited NS Ti coating offers a superior passivity in borate buffer solutions of pH 9.0 and 9.5. Mott-Schottky analysis revealed that all passive films are of n-type semiconducting nature in these alkaline solutions and the deposition process did not alter the semiconducting type of passive films formed on samples. Additionally, this analysis showed that the NS Ti coating possessed lower levels of donor densities. Finally, all electrochemical tests showed that passive behavior of the NS Ti samples was superior, mainly due to the formation of thicker and less defective passive films.

  6. Fabrication of a novel electrochemical sensor for determination of hydrogen peroxide in different fruit juice samples

    Directory of Open Access Journals (Sweden)

    Navid Nasirizadeh

    2016-01-01

    Full Text Available A new hydrogen peroxide (H2O2 sensor is fabricated based on a multiwalled carbon nanotube-modified glassy carbon electrode (MWCNT-GCE and reactive blue 19 (RB. The charge transfer coefficient, α, and the charge transfer rate constant, ks, of RB adsorbed on MWCNT-GCE were calculated and found to be 0.44 ± 0.01 Hz and 1.9 ± 0.05 Hz, respectively. The catalysis of the electroreduction of H2O2 by RB-MWCNT-GCE is described. The RB-MWCNT-GCE shows a dramatic increase in the peak current and a decrease in the overvoltage of H2O2 electroreduction in comparison with that seen at an RB modified GCE, MWCNT modified GCE, and activated GCE. The kinetic parameters such as α and the heterogeneous rate constant, k', for the reduction of H2O2 at RB-MWCNT-GCE surface were determined using cyclic voltammetry. The detection limit of 0.27μM and three linear calibration ranges were obtained for H2O2 determination at the RB-MWCNT-GCE surface using an amperometry method. In addition, using the newly developed sensor, H2O2 was determined in real samples with satisfactory results.

  7. Facile fabrication of nanoporous PdFe alloy for nonenzymatic electrochemical sensing of hydrogen peroxide and glucose

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jinping [Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China); Wang, Zhihong [School of Basic Medical Sciences, Shandong University of Traditional Chinese Medicine, Jinan 250355 (China); Zhao, Dianyun [Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China); Xu, Caixia, E-mail: chm_xucx@ujn.edu.cn [Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China)

    2014-06-01

    Graphical abstract: Nanoporous PdFe alloy, characterized by open three-dimensional bicontinuous nanospongy architecture, was easily fabricated by selectively dealloying PdFeAl source alloys, which exhibits greatly enhanced sensing performance and structure stability towards H{sub 2}O{sub 2} and glucose compared with NP-Pd and Pd/C catalysts. - Highlights: • NP-PdFe alloy is fabricated by a simple dealloying method. • NP-PdFe possesses open three-dimensional bicontinuous spongy morphology. • NP-PdFe shows high electrochemical sensing activities towards H{sub 2}O{sub 2} and glucose. • NP-PdFe shows good long-term stability for H{sub 2}O{sub 2} and glucose detection. • NP-PdFe shows good reproducibility for H{sub 2}O{sub 2} and glucose detection. - Abstract: Nanoporous (NP) PdFe alloy is easily fabricated through one step mild dealloying of PdFeAl ternary source alloy in NaOH solution. Electron microscopy characterization demonstrates that selectively dissolving Al from PdFeAl alloy generates three-dimensional bicontinuous nanospongy architecture with the typical ligament size around 5 nm. Electrochemical measurements show that the NP-PdFe alloy exhibits the superior electrocatalytic activity and durability towards hydrogen peroxide (H{sub 2}O{sub 2}) detection compared with NP-Pd and commercial Pd/C catalysts. In addition, NP-PdFe performs high sensing performance towards H{sub 2}O{sub 2} in a wide linear range from 0.5 to 6 mM with a low detection limit of 2.1 μM. This nanoporous structure also can sensitively detect glucose over a wide concentration range (1–32 mM) with a low detection limit of 1.6 μM and high resistance against chloride ions. Along with these attractive features, the as-made NP-PdFe alloy also has a good anti-interference towards ascorbic acid, uric acid, and dopamine.

  8. Anomalous melting behavior of solid hydrogen at high pressures

    OpenAIRE

    Liu, Hanyu; Hernández, Eduardo R.; Yan, Jun; Ma, Yanming

    2013-01-01

    Hydrogen is the most abundant element in the universe, and its properties under conditions of high temperature and pressure are crucial to understand the interior of of large gaseous planets and other astrophysical bodies. At ultra high pressures solid hydrogen has been predicted to transform into a quantum fluid, because of its high zero point motion. Here we report first principles two phase coexistence and Z method determinations of the melting line of solid hydrogen in a pressure range sp...

  9. Novel electrochemical behavior of zinc anodes in zinc/air batteries in the presence of additives

    Science.gov (United States)

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

    In our continued efforts to find an electrically rechargeable zn/air secondary battery, we report the unique behavior of a zinc oxide anode in the presence of additives such as phosphoric acid, tartaric acid, succinic acid and citric acid. These additives were added to the electrolyte, which is an 8.5 M KOH solution containing 25 g of ZnO and 3000 ppm of polyethylene glycol in 1 l of water. In zn/air systems there are two main problems namely the hydrogen overpotential and dendrite formation during recharging. Investigations have studied in detail both of the problems in order to overcome them. The results obtained in presence of additives are compared with the behavior of the electrolyte 8.5 M KOH in the absence of additives. It has been concluded that the hydrogen overpotential is raised enormously while dendrite formation is reduced to some extent. Out of the four acids studied, the order of increase in hydrogen overpotential is: tartaric acid > succinic acid > phosphoric acid > citric acid. The prevention of dendrite formation follows the order: citric acid > succinic acid > tartaric acid > phosphoric acid.

  10. Electrochemical behavior of quinoxalin-2-one derivatives at mercury electrodes and its analytical use.

    Science.gov (United States)

    Zimpl, Milan; Skopalova, Jana; Jirovsky, David; Bartak, Petr; Navratil, Tomas; Sedonikova, Jana; Kotoucek, Milan

    2012-01-01

    Derivatives of quinoxalin-2-one are interesting compounds with potential pharmacological activity. From this point of view, understanding of their electrochemical behavior is of great importance. In the present paper, a mechanism of electrochemical reduction of quinoxalin-2-one derivatives at mercury dropping electrode was proposed. Pyrazine ring was found to be the main electroactive center undergoing a pH-dependent two-electron reduction process. The molecule protonization of nitrogen in the position 4 precedes the electron acceptance forming a semiquinone radical intermediate which is relatively stable in acidic solutions. Its further reduction is manifested by separated current signal. A positive mesomeric effect of the nonprotonized amino group in the position 7 of the derivative III accelerates the semiquinone reduction yielding a single current wave. The suggested reaction mechanism was verified by means of direct current polarography, differential pulse, cyclic and elimination voltammetry, and coulometry with subsequent GC/MS analysis. The understanding of the mechanism was applied in developing of analytical method for the determination of the studied compounds.

  11. Electrochemical Behavior of Quinoxalin-2-one Derivatives at Mercury Electrodes and Its Analytical Use

    Directory of Open Access Journals (Sweden)

    Milan Zimpl

    2012-01-01

    Full Text Available Derivatives of quinoxalin-2-one are interesting compounds with potential pharmacological activity. From this point of view, understanding of their electrochemical behavior is of great importance. In the present paper, a mechanism of electrochemical reduction of quinoxalin-2-one derivatives at mercury dropping electrode was proposed. Pyrazine ring was found to be the main electroactive center undergoing a pH-dependent two-electron reduction process. The molecule protonization of nitrogen in the position 4 precedes the electron acceptance forming a semiquinone radical intermediate which is relatively stable in acidic solutions. Its further reduction is manifested by separated current signal. A positive mesomeric effect of the nonprotonized amino group in the position 7 of the derivative III accelerates the semiquinone reduction yielding a single current wave. The suggested reaction mechanism was verified by means of direct current polarography, differential pulse, cyclic and elimination voltammetry, and coulometry with subsequent GC/MS analysis. The understanding of the mechanism was applied in developing of analytical method for the determination of the studied compounds.

  12. Electrochemical Behavior of Biomedical Titanium Alloys Coated with Diamond Carbon in Hanks' Solution

    Science.gov (United States)

    Gnanavel, S.; Ponnusamy, S.; Mohan, L.; Radhika, R.; Muthamizhchelvan, C.; Ramasubramanian, K.

    2018-03-01

    Biomedical implants in the knee and hip are frequent failures because of corrosion and stress on the joints. To solve this important problem, metal implants can be coated with diamond carbon, and this coating plays a critical role in providing an increased resistance to implants toward corrosion. In this study, we have employed diamond carbon coating over Ti-6Al-4V and Ti-13Nb-13Zr alloys using hot filament chemical vapor deposition method which is well-established coating process that significantly improves the resistance toward corrosion, wears and hardness. The diamond carbon-coated Ti-13Nb-13Zr alloy showed an increased microhardness in the range of 850 HV. Electrochemical impedance spectroscopy and polarization studies in SBF solution (simulated body fluid solution) were carried out to understand the in vitro behavior of uncoated as well as coated titanium alloys. The experimental results showed that the corrosion resistance of Ti-13Nb-13Zr alloy is relatively higher when compared with diamond carbon-coated Ti-6Al-4V alloys due to the presence of β phase in the Ti-13Nb-13Zr alloy. Electrochemical impedance results showed that the diamond carbon-coated alloys behave as an ideal capacitor in the body fluid solution. Moreover, the stability in mechanical properties during the corrosion process was maintained for diamond carbon-coated titanium alloys.

  13. Passivation and electrochemical behavior of 316L stainless steel in chlorinated simulated concrete pore solution

    International Nuclear Information System (INIS)

    Luo, Hong; Su, Huaizhi; Dong, Chaofang; Li, Xiaogang

    2017-01-01

    Highlights: • The pH value play an important role on passive mechanism of stainless steel. • The relationship between Cr/Fe ratio within the passive film and pH is non-linear. • Better corrosion resistance due to high Cr/Fe ratio and molybdates ions. - Abstract: In this paper, the passivation and electrochemical behavior of 316L stainless steel in chlorinated simulated concrete pore solutions at different pH was evaluated by potentiodynamic measurements, electrochemical impedance spectroscopy. The composition of the passive film and surface morphology were investigated by X-ray photoelectron spectroscopy (XPS), secondary ion mass spectrometry (SIMS), and scanning electron microscopy, respectively. The results reveal that metastable pitting susceptibility, stable pitting corrosion, and composition of the passive film are influenced by pH value. After long time immersion, a bilayer structure passive film can be formed in this environment. The appearance of molybdates on the outermost surface layer, further enhancing the stability of the passive film. Moreover, the good pitting corrosion resistance of 316L stainless steel in simulated concrete pore solution without carbonated is mainly due to the presence of high Cr/Fe ratio and molybdates ions within the passive film.

  14. Electrochemical Corrosion Behavior of Oxidation Layer on Fe30Mn5Al Alloy

    Directory of Open Access Journals (Sweden)

    ZHU Xue-mei

    2017-08-01

    Full Text Available The Fe30Mn5Al alloy was oxidized at 800℃ in air for 160h, the oxidation-induced layer about 15μm thick near the scale-metal interface was induced to transform to ferrite and become enriched in Fe and depletion in Mn. The effect of the oxidation-induced Mn depletion layer on the electrochemical corrosion behavior of Fe30Mn5Al alloy was evaluated. The results show that in 1mol·L-1 Na2SO4 solution, the anodic polarization curve of the Mn depletion layer exhibits self-passivation, compared with Fe30Mn5Al austenitic alloy, and the corrosion potential Evs SCE is increased to -130mV from -750mV and the passive current density ip is decreased to 29μA/cm2 from 310μA/cm2. The electrochemical impedance spectroscopy(EIS of the Mn depletion layer has the larger diameter of capacitive arc, the higher impedance modulus|Z|, and the wider phase degree range, and the fitted polarization resistant Rt is increased to 9.9kΩ·cm2 from 2.7kΩ·cm2 by using an equivalent electric circuit of Rs-(Rt//CPE. The high insulation of the Mn depletion layer leads to an improved corrosion resistance of Fe30Mn5Al austenitic alloy.

  15. Experimental characterization of electrochemically polymerized polycarbazole film and study of its behavior with different metals contacts

    Science.gov (United States)

    Srivastava, Aditi; Chakrabarti, P.

    2017-12-01

    In this paper, we present the method of fabrication, experimental characterization, and comparison of electrical parameters of semiconducting polycarbazole film with different rectifying metals contacts. Electrochemical polymerization and deposition of organic semiconductor, i.e., polycarbazole on ITO-coated glass substrate, were performed using an electrochemical workstation. Experimental characterization of the prepared polymer film was done in respect of morphology, absorption, bandgap, and thickness. The stability and electro-activity of polycarbazole film were verified by the cyclic voltammetric method. Study of the behavior of prepared polycarbazole film with the different metals contacts such as Aluminum, Copper, Tungsten, and Tin has been done using semiconductor device analyzer. Various electrical parameters such as barrier height, ideality factor, and reverse saturation current have been extracted with different metal contacts, and the values were compared and contrasted. The nature of I- V characteristic of polycarbazole film in non-contact mode has also been analyzed using scanning tunneling microscope. The rectifying I- V characteristics obtained with different metals contacts have also been validated by the simulation on Deckbuild platform of the of ATLAS® software tool from Silvaco Inc.

  16. Electrochemical hydrogen pumping from high temperature plasma-chemical reactor involving H{sub 2}O/SO{sub 2} gas mixture

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Myoung Seok; Koo, Il Gyo; Kim, Jong Hoon; Lee, Woong Moo [Department of Chemistry and Division of Energy Systems Research, Ajou University, Suwon 443-749 (Korea)

    2009-01-15

    We demonstrate that the energy efficiency of hydrogen production by electrochemical hydrogen pumping out of a plasma-energized mixture of water vapor and sulfur dioxide (SO{sub 2}) can be greatly enhanced by raising the rector temperature above 800 C. The critical elements for this reactor design include the use of a microporous ceramic configuration for the discharge region, a bipolar electrode connecting the plasma reactor with the hydrogen pump, and a solid oxide membrane as the electrolyte of the pump. The amount of hydrogen produced per 100 joules of electrical energy consumed to operate the reactor at 850 C is 16 mL, which is more than twice the volume produced from the same reactor, operating at 100 C. The energy efficiency is almost 75% of that for the electrolysis of an H{sub 2}O/SO{sub 2} mixture. This type of plasma-assisted hydrogen pump opens up the possibility of producing hydrogen gas from water using the thermal energy from a nuclear reactor. (author)

  17. Hydrogen behavior at a subcomparment in the containment building

    Energy Technology Data Exchange (ETDEWEB)

    Lee, U. J.; Park, G. C. [Seoul National University, Seoul (Korea, Republic of)

    1997-12-31

    For hydrogen management in severe accidents with degraded nuclear core of PWR`s, several experiments have been performed in the SNU hydrogen mixing facility. The objectives are understanding the extent of hydrogen mixing and analyzing the effects of factors which dominate uniform or non-uniform mixing at compartments in the containment building. The facility represents on a 1/11th linearly scaled model of the YGN unit 3 and 4, hydrogen was simulated by helium. Because there are the gaps between safety injection tank and compartment layers in the containment, the test facility was constructed in three dimensional mode for analyzing of mixture behaviour through the gaps. >From the experimental results we could conclude that overall hydrogen concentration distributed uniformly in the free volume of the test compartment, but fluctuated in the gaps. This paper is focused on experimental result from several experiments. 5 refs., 4 figs. (Author)

  18. Study of inclusion complex of β-cyclodextrin and diphenylamine: photophysical and electrochemical behaviors.

    Science.gov (United States)

    Srinivasan, K; Kayalvizhi, K; Sivakumar, K; Stalin, T

    2011-06-01

    The photophysical, electrochemical and photoprototropic behaviors of diphenylamine (DPA) in aqueous β-cyclodextrin (β-CD) solution have been investigated using absorption spectroscopy and cyclic voltammetric techniques. Absorption of the neutral and cationic form of DPA is enhanced due to the formation of a 1:1 complex with β-CD. The formation of this complex has been confirmed by Benesi-Hildebrand plot and docking studies by RasMol tool methods. The solid complex of β-CD with DPA is investigated by FT-IR, XRD and AFM methods. The thermodynamic parameters (ΔG, ΔH and ΔS) of inclusion process are also determined. The pK(a) values of neutral-monocation equilibria have been determined with absorption (conjugate acid-base) titrations. A mechanism is proposed to explain the inclusion process. Copyright © 2011 Elsevier B.V. All rights reserved.

  19. Comparison of the Electrochemical Behavior of Ti and Nanostructured Ti-Coated AISI 304 Stainless Steel in Strongly Acidic Solutions

    Science.gov (United States)

    Attarzadeh, Farid Reza; Elmkhah, Hassan; Fattah-Alhosseini, Arash

    2017-02-01

    In this study, the electrochemical behaviors of pure titanium (Ti) and nanostructured (NS) Ti-coated AISI 304 stainless steel (SS) in strongly acidic solutions of H2SO4 were investigated and compared. A type of physical vapor deposition method, cathodic arc evaporation, was applied to deposit NS Ti on 304 SS. Scanning electron microscope and X-ray diffraction were used to characterize surface coating morphology. Potentiodynamic polarization, electrochemical impedance spectroscopy, and Mott-Schottky (M-S) analysis were used to evaluate the passive behavior of the samples. Electrochemical measurements revealed that the passive behavior of NS Ti coating was better than that of pure Ti in 0.1 and 0.01 M H2SO4 solutions. M-S analysis indicated that the passive films behaved as n-type semiconductors in H2SO4 solutions and the deposition method did not affect the semiconducting type of passive films formed on the coated samples. In addition, this analysis showed that the NS Ti coating had lower donor densities. Finally, all electrochemical tests showed that the passive behavior of the Ti-coated samples was superior, mainly due to the formation of thicker, yet less defective passive films.

  20. A facile approach to prepare crumpled CoTMPyP/electrochemically reduced graphene oxide nanohybrid as an efficient electrocatalyst for hydrogen evolution reaction

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Juanjuan, E-mail: majj0518@hotmail.com [Department of Chemical Engineering, Huaihai Institute of Technology, Lianyungang 222005 (China); School of Materials Science and Engineering, Nanyang Technological University, 639798, Singapore (Singapore); Liu, Lin; Chen, Qian; Yang, Min [Department of Chemical Engineering, Huaihai Institute of Technology, Lianyungang 222005 (China); Wang, Danping [School of Materials Science and Engineering, Nanyang Technological University, 639798, Singapore (Singapore); Tong, Zhiwei [Department of Chemical Engineering, Huaihai Institute of Technology, Lianyungang 222005 (China); Chen, Zhong, E-mail: aszchen@ntu.edu.sg [School of Materials Science and Engineering, Nanyang Technological University, 639798, Singapore (Singapore)

    2017-03-31

    Highlights: • Crumpled CoTMPyP/ERGO hybrid was successfully prepared by a facile two-step process. • CoTMPyP nanoaggregates are homogeneously distributed over the graphene surface. • CoTMPyP/ERGO hybrid film shows good electrocatalytic activity and stability for HER. - Abstract: Elaborate design and synthesis of efficient and stable non-Pt electrocatalysts for some renewable energy related conversion/storage processes are one of the major goals of sustainable chemistry. Herein, we report a facile method to fabricate Co porphyrin functionalized electrochemically reduced graphene oxide (CoTMPyP/ERGO) thin film by direct assembly of oppositely charged tetrakis(N-methylpyridyl) porphyrinato cobalt (CoTMPyP) and GO nanosheets under mild conditions followed by an electrochemical reduction procedure. STEM analysis confirms that CoTMPyP nanoaggregates are homogeneously distributed over the graphene surface. The electrochemical properties of CoTMPyP/ERGO were investigated by cyclic voltammetry, linear sweep voltammetry and electrochemical impedance spectroscopy. The results demonstrate that CoTMPyP/ERGO nanohybrid film can serve as excellent electrocatalyst for hydrogen evolution in alkaline solution with high activity and stability. The intimate contact and efficient electron transfer between CoTMPyP and ERGO, as well as the crumpled structure, contribute to the improvement of the electrocatalytic performance.

  1. An extensive study of electrochemical behavior of brimonidine and its determination at glassy carbon electrode

    International Nuclear Information System (INIS)

    Aleksić, Mara M.; Radulović, Valentina; Agbaba, Danica; Kapetanović, Vera

    2013-01-01

    Highlights: • The electrochemical behavior of BRIM was investigated by CV, DPV and SWV at GCE. • The effects of pH, scan rate and BRIM concentriation was studied. • The nature of the electrode process, and the mechanism scheme was proposed. • DPV method was developed for the estimation of BRIM in the Alphagan eye drops. -- Abstract: The electrochemical behavior of brimonidine (BRIM), an antiglaucoma agent applied in therapy for lowering high intraocular pressure, was investigated by cyclic voltammetry, differential pulse voltammetry and square wave voltammetry using a glassy carbon electrode (GCE). The reduction of BRIM occurs as one-step quasi-reversible reaction in acid and neutral medium, reaching the full reversibility in alkaline solutions. Reduction process involves the transfer of two electrons and two protons at the pyrazine ring of quinoxaline moiety, forming a dihydro-derivative. In acid and neutral solutions, brimonidine reduction product is partly oxidized to its hydroxy-derivative. BRIM is also oxidized irreversibly with the transfer of one electron and one proton at secondary amine moiety. The effects of pH of the electrolyte solution, scan rate and BRIM concentration were monitored. The nature of the electrode process was found to be controlled by the adsorption at pH > 6 and the total surface concentration of brimonidine adsorbed onto the GCE surface at pH 7, Γ BRIM = 1.35 × 10 −10 mol cm −2 was obtained. Based on this study, differential pulse voltammetric method was developed, validated and suggested for rapid electroanalytical determination of the low concentration of brimonidine. The linearity was achieved within the concentration range from 5 × 10 −7 to 5 × 10 −6 M with LOD = 1.6 × 10 −7 M and LOQ = 5.3 × 10 −7 M. The method was applied for brimonidine determination in pharmaceutical dosage form, eye drops

  2. Electrochemical behavior of platinum nanoparticles on a carbon xerogel support modified with a [(trifluoromethyl)-benzenesulfonyl]imide electrolyte.

    Science.gov (United States)

    Liu, Bing; Mei, Hua; DesMarteau, Darryl; Creager, Stephen E

    2014-12-11

    A monoprotic [(trifluoromethyl)benzenesulfonyl]imide (SI) superacid electrolyte was used to covalently modify a mesoporous carbon xerogel (CX) support via reaction of the corresponding trifluoromethyl aryl sulfonimide diazonium zwitterion with the carbon surface. Electrolyte attachment was demonstrated by elemental analysis, acid-base titration, and thermogravimetric analysis. The ion-exchange capacity of the fluoroalkyl-aryl-sulfonimide-grafted carbon xerogel (SI-CX) was ∼0.18 mequiv g(-1), as indicated by acid-base titration. Platinum nanoparticles were deposited onto the SI-grafted carbon xerogel samples by the impregnation and reduction method, and these materials were employed to fabricate polyelectrolyte membrane fuel-cell (PEMFC) electrodes by the decal transfer method. The SI-grafted carbon-xerogel-supported platinum (Pt/SI-CX) was characterized by X-ray diffraction and transmission electron microscopy to determine platinum nanoparticle size and distribution, and the findings are compared with CX-supported platinum catalyst without the grafted SI electrolyte (Pt/CX). Platinum nanoparticle sizes are consistently larger on Pt/SI-CX than on Pt/CX. The electrochemically active surface area (ESA) of platinum catalyst on the Pt/SI-CX and Pt/CX samples was measured with ex situ cyclic voltammetry (CV) using both hydrogen adsorption/desorption and carbon monoxide stripping methods and by in situ CV within membrane electrode assemblies (MEAs). The ESA values for Pt/SI-CX are consistently lower than those for Pt/CX. Some possible reasons for the behavior of samples with and without grafted SI layers and implications for the possible use of SI-grafted carbon layers in PEMFC devices are discussed.

  3. Electrochemical hydrogen storage of Ti-V-based body-centered-cubic phase alloy surface-modified with AB5 nanoparticles

    International Nuclear Information System (INIS)

    Yu, X.B.; Walker, G.S.; Grant, D.M.; Wu, Z.; Xia, B.J.; Shen, J.

    2005-01-01

    A composite of Ti-V-based bcc phase alloy surface-modified with AB 5 nanoparticles was prepared by ball milling. The composite showed significantly improved electrochemical hydrogen release capacities. For example, the 30 min ball milled Ti-30V-15Mn-15Cr+10 wt %AB 5 showed a discharge capacity in the first cycle, at 353 K, of 886 mA h g -1 , corresponding to 3.38 wt % of hydrogen, with a 45 mA g -1 discharge current. It is thought that this high capacity is due to the enhanced electrochemical-catalytic activity from the alloy surface covered with AB 5 nanoparticles, which not only have better charge-discharge capacity themselves, acting as both an electrocatalyst and a microcurrent collector, but also result in the greatly enhanced hydrogen atomic diffusivities in the nanocrystalline relative to their conventional coarse-grained counterparts. These results provide new insight for use of Ti-V-based bcc phase alloy for high-energy batteries

  4. Effect of Systematic Hydrogenation on the Phase Behavior and Nanostructural Dimensions of Block Copolymers.

    Science.gov (United States)

    Ashraf, Arman R; Ryan, Justin J; Satkowski, Michael M; Smith, Steven D; Spontak, Richard J

    2018-01-31

    Unsaturated polydienes are frequently hydrogenated to yield polyolefins that are more chemically stable. Here, the effects of partial hydrogenation on the phase behavior and nanostructure of polyisoprene-containing block copolymers are investigated. To ensure access to the order-disorder transition temperature (T ODT ) over a wide temperature range, we examine copolymers with at least one random block. Dynamic rheological and scattering measurements indicate that T ODT increases linearly with increasing hydrogenation. Small-angle scattering reveals that the temperature-dependence of the Flory-Huggins parameter changes and the microdomain period increases, while the interfacial thickness decreases. The influence of hydrogenation becomes less pronounced in more constrained multiblock copolymers.

  5. Research on the surface chemical behavior of uranium metal in hydrogen atmosphere by XPS

    International Nuclear Information System (INIS)

    Fu Xiaoguo; Wang Xiaolin; Yu Yong; Zhao Zhengping

    2001-01-01

    The surface chemical behavior clean uranium metal in hydrogen atmosphere at 100 and 200 degree C is studied by X-ray photoelectron spectroscopy (XPS), respectively. It leads to hydriding reaction when the hydrogen exposure is 12.0 Pa·s, and the U4f 7/2 binding energy of UH 3 is found to be 378.7 eV. The higher temperature (200 degree C) is beneficial to UH 3 formation at the same hydrogen exposures. XPS elemental depth profiles indicate that the distribution of uranium surface layer is UO 2 , UH 3 and U after exposure to 174.2 Pa·s hydrogen

  6. Electrochemical behavior of Mg in H3PO4 and phosphating solution

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Daobing [R & D Center of Wuhan Iron and Steel Co., Wuhan (China); Huazhong University of Science and Technology, Hubei Key Laboratory of Materials Chemistry and Service Failure, Wuhan (China); Tu, Yuanqiang [R & D Center of Wuhan Iron and Steel Co., Wuhan (China); Hu, Ting [WuHan QingJiang Chemical CO. LTD., Wuhan (China); Song, GuangLing [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Materials Science & Technology Division; Guo, Xingpeng [Huazhong University of Science and Technology,

    2014-12-01

    The electrochemical behavior of pure Mg in H3PO4 acid (0.42 M) and phosphating solution (0.42 M H3PO4+0.34 M ZnO) was investigated through electrochemical impedance spectroscopy (EIS), potentiodynamic polarization curve and XRD measurements. In conclusion, the results show that Mg has higher corrosion resistance in the phosphating solution than that in the H3PO4 acid which may be due to the relative protective phosphating film on the surface.

  7. A study on the modelling and simulation of the hydrogen behavior

    International Nuclear Information System (INIS)

    Park, Jae Hong

    1993-02-01

    The severe accident hydrogen control regulation of 10CFR50.34 (f) requires that the plant design shall include a hydrogen control system which can safely accommodate the hydrogen resulting from a 100% metal-water reaction, and limit its concentration in the containment to no greater than 10%. This regulation is applied to UCN 3 and 4 design for the first time in Korea. However, the severe accident hydrogen control system such as hydrogen igniters is not designed to be installed at UCN 3 and 4 containment. Further, UCN 3 and 4 do not have the safety-grade containment fan cooler system that will influence on the hydrogen transport and combustion. This study is focussed on the modelling and simulation of the hydrogen behavior by CONTAIN computer code to identify quantitatively how the containment ESFs such as containment fan system, hydrogen igniters and containment spray system have influence on the hydrogen mixing and burning in the severe accident conditions in order to determine whether the hydrogen control system such as igniters is needed for large dry containment and suggest the severe accident mitigation scheme for the hydrogen combustion. However, the direct containment heating (DCH) effects and corium-coolant-concrete interactions including steam explosion in the reactor cavity are not analyzed in this study, the following conclusions are effective only in the severe accident sequences without these phenomena. About 1 hour after RPV breach, high turbulent flow is predicted to prevail in the lower containment compartments. During this period, the irreversible flow loss coefficients govern the hydrogen mixing in the lower compartments. However, after this period, it is estimated that the containment fan system do not have a significant influence on the hydrogen transport in the containment. A more detailed investigation for the estimation of relevant flow loss coefficients for the lumped-parameter code such as CONTAIN should be carried out. After completion of

  8. Numerical Study on Hydrogen Flow Behavior in Two Compartments with Different Connecting Pipes

    Directory of Open Access Journals (Sweden)

    HanChen Liu

    2017-01-01

    Full Text Available Hydrogen accumulation in the containment compartments under severe accidents would result in high concentration, which could lead to hydrogen deflagration or detonation. Therefore, getting detailed hydrogen flow and distribution is a key issue to arrange hydrogen removal equipment in the containment compartments. In this study, hydrogen flow behavior in local compartments has been investigated in two horizontal compartments. The analysis model is built by 3-dimensional CFD code in Cartesian coordinates based on the connection structure of the Advanced Pressurized Water Reactor (PWR compartments. It consists of two cylindrical vessels, representing the Steam Generator compartment (SG and Core Makeup Tank compartment (CMT. With standard k-ε turbulence model, the effects of the connecting pipe size and location on hydrogen concentration distribution are investigated. Results show that increasing the diameter of connection pipe (IP which is located at 800 mm from 150 mm to 300 mm facilitates hydrogen flow between compartments. Decreasing the length of IP which is located at 800 mm from 1000 mm to 500 mm can also facilitate hydrogen flow between compartments. Lower IP is in favor of hydrogen mixing with air in non-source compartment. Higher IP is helpful for hydrogen flow to the non-source term compartment from source term compartment.

  9. The influence of the pyrolysis temperature on the electrochemical behavior of carbon-rich SiCN polymer-derived ceramics as anode materials in lithium-ion batteries

    Science.gov (United States)

    Reinold, Lukas Mirko; Yamada, Yuto; Graczyk-Zajac, Magdalena; Munakata, Hirokazu; Kanamura, Kiyoshi; Riedel, Ralf

    2015-05-01

    Within this study we report on the impact of the pyrolysis temperature on the structural and electrochemical properties of the poly(phenylvinylsilylcarbodiimide) derived silicon carbonitride (SiCN) ceramic. Materials pyrolysed at 800 °C and 1300 °C, SiCN 800 and SiCN 1300, are found amorphous. Raman spectroscopy measurements indicate the increase in ordering of the free carbon phase with increasing pyrolysis temperature which leads to lower capacity recovered by SiCN 1300. Significant hysteresis is found for materials pyrolysed at 800 °C during electrochemical lithium insertion/extraction. This feature is attributed to much higher hydrogen content in SiCN 800 sample. An aging of SiCN 800 reflected by a change of elemental composition upon contact to air and a strong film formation are attenuated at a higher pyrolysis temperature. Single particle microelectrode investigation on SiCN 800 and SiCN 1300 clarify different electrochemical behavior of the materials. Much lower charge transfer resistance of SiCN 1300 in comparison to SiCN 800 explains better high currents electrochemical performance. Lithium ions diffusion coefficient Dmin ranges from 3.2 10-9 cm2s-1 to 6.4 10-11 cm2s-1 and is independent on the potential.

  10. Electrochemical behavior of tube-fin assembly for an aluminum automotive condenser with improved corrosion resistance

    Directory of Open Access Journals (Sweden)

    M.A. Pech-Canul

    Full Text Available An aluminum automotive condenser was designed to exhibit high corrosion resistance in the seawater acetic acid test (SWAAT combining zinc coated microchannel tubes and fins made with AA4343/AA3003(Zn/AA4343 brazing sheet. Electrochemical measurements in SWAAT solution were carried out under laboratory conditions using tube-fin assembly and individual fin and tube samples withdrawn from the condenser core. The aim was to gain information on the protective role of the zinc sacrificial layer and about changes in corrosion behavior as a function of immersion time. External corrosion of the tube-fin system was simulated by immersion of mini-core samples under open circuit conditions. The corrosion rate increased rapidly during the first 6 h and slowly afterwards. The short time behavior was related to the dissolution of the oxide film and fast dissolution of the outermost part of the zinc diffusion layer. With the aid of cross-sectional depth corrosion potential profiles, it was shown that as the sacrificial layer gets dissolved, the surface concentration of zinc decreases and the potential shifts to less negative values. The results of galvanic coupling of tube and fins in a mini-cell showed that the tube became the anode while the fins exhibited cathodic behavior. An evolution in the galvanic interaction was observed, due to the progressive dissolution of the sacrificial zinc layer. The difference of uncoupled potentials between tube and fins decreased from 71 mV to 32 mV after 84 h of galvanic coupling. At the end of such period there was still a part of the zinc sacrificial layer remaining which would serve for protection of the tube material for even longer periods and there were indications of slight corrosion in the fins. Keywords: Aluminum, Automotive, Corrosion, Galvanic, Zn coating

  11. Release Behavior of Hydrogen Isotopes from JT-60U Graphite Tiles

    International Nuclear Information System (INIS)

    Katayama, K.; Takeishi, T.; Nagase, H.; Manabe, Y.; Nishikawa, M.; Miya, N.; Masaki, K.

    2005-01-01

    Release behavior of hydrogen isotopes from the graphite tiles used in JT-60U was observed using the thermal desorption method where temperature was stepwise elevated to 300, 600 and 1000 deg. C. When first wall tile was left under helium atmosphere at 600 deg. C for 8 hours, about 40 % of total amount of hydrogen and deuterium retained in the tile was released, although only a small amount of hydrogen isotopes was released at 300 deg. C, which is the base temperature of inner wall of JT-60U. This indicates that a higher temperature of inner wall causes hydrogen retention to reduce considerably. When the graphite tiles were exposed to hydrogen at 1000 deg. C, the release of deuterium and tritium was enhanced. It is considered that the deuterium and tritium left in the graphite tile was released by the isotope exchange reaction. In order to remove almost all deuterium or tritium from the graphite tile without combustion of graphite, isotope exchange method at high temperature is effective. It was found that the amount of hydrogen retained in the graphite tile was much larger than that of deuterium. This indicates that a large amount of deuterium trapped in the tiles during deuterium discharge experiments was replaced with hydrogen during hydrogen discharge experiments. Additionally, depth profiles of hydrogen isotope are discussed from the obtained release curves

  12. Electrochemically deposited Cu{sub 2}O cubic particles on boron doped diamond substrate as efficient photocathode for solar hydrogen generation

    Energy Technology Data Exchange (ETDEWEB)

    Mavrokefalos, Christos K. [Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, England (United Kingdom); Hasan, Maksudul, E-mail: maksudul.hasan@chem.ox.ac.uk [Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, England (United Kingdom); Tyndall National Institute, University College Cork, Lee Maltings, Cork (Ireland); Rohan, James F. [Tyndall National Institute, University College Cork, Lee Maltings, Cork (Ireland); Compton, Richard G. [Department of Chemistry, Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QZ, England (United Kingdom); Foord, John S., E-mail: john.foord@chem.ox.ac.uk [Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, England (United Kingdom)

    2017-06-30

    Highlights: • Fabrication of low-cost photocathode by electrochemical method is described. • Boron-doped diamond is presented as catalyst support. • NiO nanoparticles on Cu{sub 2}O surface enhances photocurrent and electrode stability. • Synergy of metallic interaction between Cu and Ni leads to high efficiency. - Abstract: Herein, we report a novel photocathode for the water splitting reaction. The electrochemical deposition of Cu{sub 2}O particles on boron doped diamond (BDD) electrodes and the subsequent decoration with NiO nanoparticles by a dip coating method to act as co-catalyst for hydrogen evolution reaction is described. The morphology analysis by scanning electron microscope (SEM) revealed that Cu{sub 2}O particles are cubic and decorated sporadically with NiO nanoparticles. X-ray photoelectron spectroscopy (XPS) confirmed the electronic interaction at the interface between Cu{sub 2}O and NiO through a binding energy shift of the main Cu 2p peak. The photoelectrochemical (PEC) performance of NiO-Cu{sub 2}O/BDD showed a much higher current density (−0.33 mA/cm{sup 2}) and photoconversion efficiency (0.28%) compared to the unmodified Cu{sub 2}O/BDD electrode, which are only −0.12 mA/cm{sup 2} and 0.06%, respectively. The enhancement in PEC performance is attributable to the synergy of NiO as an electron conduction mediator leading to the enhanced charge separation and transfer to the reaction interface for hydrogen evolution as evidenced by electrochemical impedance spectroscopy (EIS) and charge carrier density calculation. Stability tests showed that the NiO nanoparticles loading content on Cu{sub 2}O surface is a crucial parameter in this regard.

  13. Electrochemical behavior of heavily cycled nickel electrodes in Ni/H2 cells containing electrolytes of various KOH concentrations

    Science.gov (United States)

    Lim, H. S.; Verzwyvelt, S. A.

    1989-01-01

    A study has been made of charge and discharge voltage changes with cycling of Ni/H2 cells containing electrolytes of various KOH concentrations. A study has also been made of electrochemical behavior of the nickel electrodes from the cycled Ni/H2 cells as a function of overcharge amounts. Discharge voltages depressed gradually with cycling for cells having high KOH concentrations (31 to 36 percent), but the voltages increased for those having low KOH concentrations (21 to 26 percent). To determine if there was a crystallographic change of the active material due to cycling, electrochemical behavior of nickel electrodes was studied in an electrolyte flooded cell containing either 31 or 26 percent KOH electrolyte as a function of the amount of overcharge. The changes in discharge voltage appear to indicate crystal structure changes of active material from gamma-phase to beta-phase in low KOH concentrations, and vice versa in high KOH concentration.

  14. Electrochemical behavior of zinc particles with silica based coatings as anode material for zinc air batteries with improved discharge capacity

    Science.gov (United States)

    Schmid, M.; Willert-Porada, M.

    2017-05-01

    Silica coatings on zinc particles as anode material for alkaline zinc air batteries are expected to reduce early formation of irreversible ZnO passivation layers during discharge by controlling zinc dissolution and precipitation of supersaturated zincates, Zn(OH)42-. Zinc particles were coated with SiO2 (thickness: 15 nm) by chemical solution deposition and with Zn2SiO4 (thickness: 20 nm) by chemical vapor deposition. These coatings formed a Si(OH)4 gel in aqueous KOH and retarded hydrogen evolution by 40%. By treatment in aqueous KOH and drying afterwards, the silica coatings were changed into ZnO-K2O·SiO2 layers. In this work, the electrochemical performance of such coated zinc particles is investigated by different electrochemical methods in order to gain a deeper understanding of the mechanisms of the coatings, which reduce zinc passivation. In particular, zinc utilization and changes in internal resistance are investigated. Moreover, methods for determination of diffusion coefficients, charge carrier numbers and activation energies for electrochemical oxidation are determined. SiO2-coated zinc particles show improved discharge capacity (CVD-coated zinc: 69% zinc utilization, CSD-coated zinc: 62% zinc utilization) as compared to as-received zinc (57% zinc utilization) at C/20 rate, by reducing supersaturation of zincates. Additionally, KOH-modified SiO2-coated zinc particles enhance rechargeability after 100% depth-of-discharge.

  15. Buoyant Unstable Behavior of Initially Spherical Lean Hydrogen-Air Premixed Flames

    Directory of Open Access Journals (Sweden)

    Zuo-Yu Sun

    2014-07-01

    Full Text Available Buoyant unstable behavior in initially spherical lean hydrogen-air premixed flames within a center-ignited combustion vessel have been studied experimentally under a wide range of pressures (including reduced, normal, and elevated pressures. The experimental observations show that the flame front of lean hydrogen-air premixed flames will not give rise to the phenomenon of cellular instability when the equivalence ratio has been reduced to a certain value, which is totally different from the traditional understanding of the instability characteristics of lean hydrogen premixed flames. Accompanied by the smoothened flame front, the propagation mode of lean hydrogen premixed flames transitions from initially spherical outwardly towards upwardly when the flames expand to certain sizes. To quantitatively investigate such buoyant instability behaviors, two parameters, “float rate (ψ” and “critical flame radius (Rcr”, have been proposed in the present article. The quantitative results demonstrate that the influences of initial pressure (Pint on buoyant unstable behaviors are different. Based on the effects of variation of density difference and stretch rate on the flame front, the mechanism of such buoyant unstable behaviors has been explained by the competition between the stretch force and the results of gravity and buoyancy, and lean hydrogen premixed flames will display buoyant unstable behavior when the stretch effects on the flame front are weaker than the effects of gravity and buoyancy.

  16. Electrochemical behavior of LiCoO2 as aqueous lithium-ion battery electrodes

    KAUST Repository

    Ruffo, Riccardo

    2009-02-01

    Despite the large number of studies on the behavior of LiCoO2 in organic electrolytes and its recent application as a positive electrode in rechargeable water battery prototypes, a little information is available about the lithium intercalation reaction in this layered compound in aqueous electrolytes. This work shows that LiCoO2 electrodes can be reversibly cycled in LiNO3 aqueous electrolytes for tens of cycles at remarkably high rates with impressive values specific capacity higher than 100 mAh/g, and with a coulomb efficiency greater than 99.7%. Stable and reproducible cycling measurements have been made using a simple cell design that can be easily applied to the study of other intercalation materials, assuming that they are stable in water and that their intercalation potential range matches the electrochemical stability window of the aqueous electrolyte. The experimental arrangement uses a three-electrode flooded cell in which another insertion compound acts as a reversible source and sink of lithium ions, i.e., as the counter electrode. A commercial reference electrode is also present. Both the working and the counter electrodes have been prepared as thin layers on a metallic substrate using the procedures typical for the study of electrodes for lithium-ion batteries in organic solvent electrolytes. © 2008 Elsevier B.V. All rights reserved.

  17. Electrochemical behavior of H3PW12O40/ acid-activated bentonite powders

    Directory of Open Access Journals (Sweden)

    Mojović Zorica

    2012-01-01

    Full Text Available Electrochemical behavior of 12-tungstophosphoric acid (HPW/acid-activated bentonite (AAB powders with various loadings of HPW was investigated. The physicochemical properties of the prepared powders were examined by X-ray powder diffraction, nitrogen adsorption-desorption isotherms, atomic force microscopy and cyclic voltammetry measurements. The results indicated that the prepared powders are composed mainly of oriented domains of large rock blocks, probably resulting from a preferable deposition of bentonite particles having a face-to-face interaction. The particles had a mainly disordered mesoporous structure with a pore volume that varied according to the pore size in the range of 2-50 nm. In addition, the particles had crystallite size between 4.9 and 9.0 nm. The electrocatalytic activities of prepared HPW/Aelectrodes were studied in the oxidation of NO2-ions and the results revealed that the electrodes possessed relatively higher nitrite oxidation currents than Aelectrode. The best electroactivity was observed for HPW3/Aelectrode (AAB+20 wt. % HPW and the limit of detection (3σ was determined as 8 μM.

  18. Effects of chitosan inhibitor on the electrochemical corrosion behavior of 2205 duplex stainless steel

    Science.gov (United States)

    Yang, Se-fei; Wen, Ying; Yi, Pan; Xiao, Kui; Dong, Chao-fang

    2017-11-01

    The effects of chitosan inhibitor on the corrosion behavior of 2205 duplex stainless steel were studied by electrochemical measurements, immersion tests, and stereology microscopy. The influences of immersion time, temperature, and chitosan concentration on the corrosion inhibition performance of chitosan were investigated. The optimum parameters of water-soluble chitosan on the corrosion inhibition performance of 2205 duplex stainless steel were also determined. The water-soluble chitosan showed excellent corrosion inhibition performance on the 2205 duplex stainless steel. Polarization curves demonstrated that chitosan acted as a mixed-type inhibitor. When the stainless steel specimen was immersed in the 0.2 g/L chitosan solution for 4 h, a dense and uniform adsorption film covered the sample surface and the inhibition efficiency (IE) reached its maximum value. Moreover, temperature was found to strongly influence the corrosion inhibition of chitosan; the inhibition efficiency gradually decreased with increasing temperature. The 2205 duplex stainless steel specimen immersed in 0.4 g/L water-soluble chitosan at 30°C displayed the best corrosion inhibition among the investigated specimens. Moreover, chitosan decreased the corrosion rate of the 2205 duplex stainless steel in an FeCl3 solution.

  19. Morphology and electrochemical behavior of Ag-Cu nanoparticle-doped amalgams.

    Science.gov (United States)

    Chung, Kwok-Hung; Hsiao, Li-Yin; Lin, Yu-Sheng; Duh, Jenq-Gong

    2008-05-01

    The aim of this study was to introduce Ag-Cu phase nanopowder as an additive to improve the corrosion behavior of dental amalgams. A novel Ag-Cu nanopowder was synthesized by the precipitation method. An amalgam alloy powder (World-Cap) was added and mixed with 5 wt.% and 10 wt.% of Ag-Cu nanopowders, respectively, to form experimental amalgam alloy powders. The original alloy powder was used as a control. Alloy powders were examined using X-ray diffraction, transmission electron microscopy (TEM), scanning electron microscopy and electron probe microanalysis. Amalgam disk specimens of metallurgically prepared were tested in 0.9% NaCl solution using electrochemical methods. The changes in the corrosion potential and anodic polarization characteristics were determined. Corrosion potential data were analyzed statistically (n=3, analysis of variance, Tukey's test, pamalgams. The Ag-Cu nanoparticle-doped amalgams exhibited zero current potentials more positive than the control (pamalgam could be improved by Ag-Cu nanoparticle-doping.

  20. High loading MnO2 nanowires on graphene paper: facile electrochemical synthesis and use as flexible electrode for tracking hydrogen peroxide secretion in live cells.

    Science.gov (United States)

    Dong, Shuang; Xi, Jiangbo; Wu, Yanan; Liu, Hongwei; Fu, Chaoyang; Liu, Hongfang; Xiao, Fei

    2015-01-01

    Recent progress in flexible and lightweight electrochemical sensor systems requires the development of paper-like electrode materials. Here, we report a facile and green synthesis of a new type of MnO2 nanowires-graphene nanohybrid paper by one-step electrochemical method. This strategy demonstrates a collection of unique features including the effective electrochemical reduction of graphene oxide (GO) paper and the high loading of MnO2 nanowires on electrochemical reduced GO (ERGO) paper. When used as flexible electrode for nonenzymatic detection of hydrogen peroxide (H2O2), MnO2-ERGO paper exhibits high electrocatalytic activity toward the redox of H2O2 as well as excellent stability, selectivity and reproducibility. The amperometric responses are linearly proportional to H2O2 concentration in the range 0.1-45.4 mM, with a detection limit of 10 μM (S/N=3) and detection sensitivity of 59.0 μA cm(-2) mM(-1). These outstanding sensing performances enable the practical application of MnO2-ERGO paper electrode for the real-time tracking H2O2 secretion by live cells macrophages. Therefore, the proposed graphene-based nanohybrid paper electrode with intrinsic flexibility, tailorable shapes and adjustable properties can contribute to the full realization of high-performance flexible electrode material used in point-of-care testing devices and portable instruments for in-vivo clinical diagnostics and on-site environmental monitoring. Copyright © 2014 Elsevier B.V. All rights reserved.

  1. Electrochemical Behavior of Molten V2O5-K2S2O7-KHSO4 Systems

    DEFF Research Database (Denmark)

    Petrushina, Irina; Bjerrum, Niels; Berg, Rolf W.

    1997-01-01

    The electrochemical behavior of K2S2O7-KHSO4-V2O5, K2S2O7-V2O4 and K2S2O7-KHSO4-V2O4 melts was studied in argon and SO2/air atmospheres using a gold electrode. In order to identify the voltammetric waves due to KHSO4, molten KHSO4 and mixtures of K2S2O7-KHSO4 were investigated by voltammetry...

  2. The annealing behavior of hydrogen implanted into Al-Si alloy

    Energy Technology Data Exchange (ETDEWEB)

    Ogura, Masahiko; Yamaji, Norisuke; Imai, Makoto; Itoh, Akio; Imanishi, Nobutsugu [Kyoto Univ. (Japan). Faculty of Engineering

    1997-03-01

    We have studied effects of not only defects but also an added elements on trap-sites of hydrogen in metals. For the purpose, we observed depth profiles and thermal behaviors of hydrogen implanted into Al-1.5at.%Si alloy samples in an implantation-temperature range of liquid nitrogen temperature (LNT) to 373K at different doses. The results were compared with those for pure aluminum samples. It was found that hydrogen is trapped as molecules in grain boundaries of Al/Si. (author)

  3. Correlations between preparation methods, structural features and electrochemical Li-storage behavior of reduced graphene oxide.

    Science.gov (United States)

    Sonia, Farjana J; Kalita, Hemen; Aslam, M; Mukhopadhyay, Amartya

    2017-08-10

    Wide differences in the structural features of graphenic carbon, especially in the case of reduced graphene oxides (rGO), are expected to have considerable impacts on the properties, thus leading to significant scatter and poor understanding/prediction of their performances for various applications, including as electrode materials for electrochemical Li-storage. In this context, the present work develops a comprehensive understanding (via thorough experimentation, including in situ X-ray diffraction studies, and analysis) on the effects of graphene oxide (GO) reduction methods/conditions on the structural features (mainly 'graphenic' ordering) and concomitant influences of the same on electrochemical Li-storage behavior. 'Moderately oxidized' GO (O/C ∼0.41) was reduced via three different methods, viz., (i) using hydrazine hydrate vapor at room temperature (rGO-H; O/C ∼0.23), (ii) thermal reduction by annealing at just 500 °C (rGO-A; O/C ∼0.20) and (iii) hydrazine treatment, followed by the same annealing treatment (rGO-HA; O/C ∼0.17). Raman spectroscopy, in situ X-ray diffraction recorded during annealing and high resolution TEM imaging indicate that while GO and rGO-H had considerable defect contents [I(D)/I(G) ∼1.4 for rGO-H], including a very non-uniform interlayer spacing (varying between 3.1 and 3.6 Å), the 500 °C annealed rGO-A and rGO-HA had significantly reduced defect contents [I(D)/I(G) ∼0.6] and near-perfect 'graphenic' ordering with a uniform interlayer spacing of ∼3.35 Å. Despite the nanoscaled dimensions, defect structures, especially the non-uniform interlayer spacing, resulted in relatively poor reversible Li-capacity and rate capability for the non-annealed rGO-H, even in comparison to the bulk graphitic carbon. By contrast, the annealed rGOs, especially the rGO-HA, not only possessed a superior reversible Li-capacity of ∼450 mA h g -1 (at C/20), but also exhibited a significantly improved rate capability (even compared to

  4. Microstructure and electrochemical behavior of cerium conversion coating modified with silane agent on magnesium substrates

    Energy Technology Data Exchange (ETDEWEB)

    Lei, Li; Shi, Jing, E-mail: shijing@ouc.edu.cn; Wang, Xin, E-mail: wangxin.hd@163.com; Liu, Dan; Xu, Haigang

    2016-07-15

    Graphical abstract: The unmodified coating shows averaged static water contact angles of a little more than 50º, which is clearly hydrophilic for water solutions. With the silane concentration increases, the water contact angles show an increase tendency. Especially, when the silane addition is increased to 25 ml L-1, the coating surface presents a hydrophobic feature, with static water contact angle of more than 110º. - Highlights: • BTESPT modification can effectively improve the uniformity, hydrophobic performance, chemical stability and corrosion inhibition capability of traditional cerium conversion coating. • Si-O-Si linkage builds a robust structure to increase of the coating density. Si−O−Mg bonds strengthen the adhesion between the coating/substrate. • The system modified with 25 ml L{sup −1} BTESPT displays the optimum corrosion protection performance. - Abstract: The cerium conversion coating with and without different concentrations of silane agent bis-(γ-triethoxysilylpropyl)-tetrasulfide (BTESPT) modification is obtained on magnesium alloys. Detailed properties of the coatings and the role of BTESPT as an additive are studied and followed with careful discussion. The coating morphology, wettability, chemical composition and corrosion resistance are characterized by scanning electronic microscope (SEM), water contact-angle, X-ray photoelectron spectroscopy (XPS), potentiodynamic measurements and electrochemical impedance spectroscopy (EIS). The electrochemical behavior of the coatings is investigated using EIS. The results indicate that the coating morphology and composition can be controlled by changing silane concentration. The combination of cerium ions and silane molecules could promote the formation of more homogenous and higher hydrophobic coating. The coating turns to be more compact and the adhesive strength between the coating and the magnesium substrate are strongly improved with the formation of Si−O−Si and Si

  5. The pipeline fracture behavior and pressure assessment under HIC (Hydrogen induced cracking) environment

    Energy Technology Data Exchange (ETDEWEB)

    Shaohua, Dong [China National Petroleum Corporation (CNPC), Beijing (China); Lianwei, Wang [University of Science and Technology Beijing (USTB), Beijing (China)

    2009-07-01

    As Hydrogen's transmit and diffuse, after gestating for a while, the density of hydrogen around crack tip of pipeline will get to the critical density, and the pipeline material will descend, make critical stress factor, the reason of pipeline Hydrogen Induced Cracking is Hydrogen's transmit and diffuse. The stress factor of Hydrogen Induced Cracking under surroundings-condition of stress is the key that estimate material's rupture behavior. The paper study the relationship among hydrogen concentrate, crack tip stress, stain field, hydrogen diffusion and inner pressure for crack tip process zone, then determined the length of HIC (hydrogen induced cracking) process zone. Based on the theory of propagation which reason micro-crack making core, dislocation model is produced for fracture criteria of HIC, the influence between material and environments under the HIC is analyzed, step by step pipeline maximum load pressure and threshold of J-integrity ( J{sub ISCC} ) is calculated, which is very significant for pipeline safety operation. (author)

  6. Hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Pier, M.

    1943-02-19

    A transcript is presented of a speech on the history of the development of hydrogenation of coal and tar. Apparently the talk had been accompanied by the showing of photographic slides, but none of the pictures were included with the report. In giving the history, Dr. Pier mentioned the dependence of much of the development of hydrogenation upon previous development in the related areas of ammonia and methanol syntheses, but he also pointed out several ways in which equipment appropriate for hydrogenation differed considerably from that used for ammonia and methanol. Dr. Pier discussed the difficulties encountered with residue processing, design of the reaction ovens, manufacture of ovens and preheaters, heating of reaction mixtures, development of steels, and development of compressor pumps. He described in some detail his own involvement in the development of the process. In addition, he discussed the development of methods of testing gasolines and other fuels. Also he listed some important byproducts of hydrogenation, such as phenols and polycyclic aromatics, and he discussed the formation of iso-octane fuel from the butanes arising from hydrogenation. In connection with several kinds of equipment used in hydrogenation (whose pictures were being shown), Dr. Pier gave some of the design and operating data.

  7. Coupling of Mechanical Behavior of Lithium Ion Cells to Electrochemical-Thermal (ECT) Models for Battery Crush

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Chao; Santhanagopalan, Shriram; Pesaran, Ahmad; Sahraei, Elham; Wierzbicki, Tom

    2016-06-14

    Vehicle crashes can lead to crushing of the battery, damaging lithium ion battery cells and causing local shorts, heat generation, and thermal runaway. Simulating all the physics and geometries at the same time is challenging and takes a lot of effort; thus, simplifications are needed. We developed a material model for simultaneously modeling the mechanical-electrochemical-thermal behavior, which predicted the electrical short, voltage drop, and thermal runaway behaviors followed by a mechanical abuse-induced short. The effect of short resistance on the battery cell performance was studied.

  8. Electrochemical catalytic reforming of oxygenated-organic compounds: a highly efficient method for production of hydrogen from bio-oil.

    Science.gov (United States)

    Yuan, Lixia; Chen, Yaqiong; Song, Chongfu; Ye, Tongqi; Guo, Qingxiang; Zhu, Qingshi; Torimoto, Youshifumi; Li, Quanxin

    2008-11-07

    A novel approach to produce hydrogen from bio-oil was obtained with high carbon conversion (>90%) and hydrogen yield (>90%) at Tcatalytic reforming of oxygenated-organic compounds over 18%NiO/Al(2)O(3) reforming catalyst; thermal electrons play important promoting roles in the decomposition and reforming of the oxygenated-organic compounds in the bio-oil.

  9. Hydrogen sorption and desorption properties of Pd-alloys and steels investigated by electrochemical methods and mass spectrometry

    NARCIS (Netherlands)

    Uluc, A.V.

    2015-01-01

    Although it has been more than a century since the first known hydrogen embrittlement case was reported, the fundamental question regarding its mechanism is still open to debate. Understanding the hydrogen-metal interactions is of great importance in tailoring microstructures that will have

  10. Mechanical behavior of NiTi arc wires under pseudoelastic cycling and cathodically hydrogen charging

    Science.gov (United States)

    Sarraj, R.; Hassine, T.; Gamaoun, F.

    2018-01-01

    NiTi wires are mainly used to design orthodontic devices. However, they may be susceptible to a delayed fracture while they are submitted to cyclic loading with the presence of hydrogen in the oral cavity. Hydrogen may cause the embrittlement of the structure, leading to lower ductility and to a change in transformation behavior. The aim of the present study is to predict the NiTi behavior under cyclic loading with hydrogen charging. One the one hand, samples are submitted to superelastic cyclic loading, which results in investigating their performance degradations. On the other hand, after hydrogen charging, cyclic tensile aging tests are carried out on NiTi orthodontic wires at room temperature in the air. During cyclic loading, we notice that the critical stress for the martensite transformation evolves, the residual strain is accumulated in the structure and the hysteresis loop changes. Thus, via this work, we can assume that the embrittlement is due to the diffusion of hydrogen and the generation of dislocations after aging. The evolution of mechanical properties of specimens becomes more significant with hydrogen charging rather than without it.

  11. Electrochemical behavior of hydroxyapatite/TiN multi-layer coatings on Ti alloys

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Eun-Ju [Department of Dental Materials, Research Center of Nano-Interface Activation for Biomaterials, School of Dentistry, Chosun University (Korea, Republic of); Jeong, Yong-Hoon [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, Research Center of Nano-Interface Activation for Biomaterials, School of Dentistry, Chosun University (Korea, Republic of); Brantley, William A. [Division of Restorative Science and Prosthodontics, College of Dentistry, The Ohio State University, Columbus, OH (United States)

    2014-12-01

    The electrochemical behavior of hydroxyapatite (HA) and titanium nitride (TiN) multi-layer coatings on Ti–Nb–Zr alloys was investigated by a variety of surface analytical methods. The HA/TiN layers were deposited using a magnetron sputtering system. The HA target was made of human tooth-ash sintered at 1300 °C for 1 h and had an average Ca/P ratio of 1.9. From X-ray diffraction patterns, the Ti–29Nb–5Zr alloy was composed entirely of equiaxed β-phase exhibiting the principal (110) reflection, and the coating exhibited the (111) and (200) reflections for TiN and the (112) and (202) reflections for HA. At the coating surface the HA films consisted of granular particles, and the surface roughness was 4.22 nm. The thickness of the coating layers increased in the order of HA/TiN (lowest), TiN, and HA (highest). Potentiodynamic polarization measurements revealed that the corrosion current density was the lowest, and the corrosion potential and polarization resistance the highest, when the Ti–29Nb–5Zr surface was covered by the HA/TiN film, compared to solely HA or TiN films. - Highlights: • HA/TiN films were deposited by magnetron sputtering on a Ti–29Nb–5Zr biomedical alloy. • The corrosion current density for the HA/TiN films was lower than that of the non-coated alloy. • The polarization resistance of the HA/TiN films was higher than that of the non-coated alloy.

  12. The corrosion rate and the hydrogen absorption behavior of titanium under anaerobic condition

    International Nuclear Information System (INIS)

    Suzuki, Hiroyuki; Taniguchi, Naoki

    2006-01-01

    Titanium is one of the candidate materials for overpacks as a high corrosion resistance metal. Hydrogen embrittlement is a main cause of the damage of long term integrity of titanium overpack. It is not well known about the corrosion resistance and hydrogen absorption behavior of titanium under anaerobic condition. In this study, the completely sealed ampoule test and the immersion test of titanium was carried out in aqueous solution and bentonite in order to obtain reliable data about the hydrogen generation rate and the ratio of hydrogen absorption in titanium. As the results of the tests with changing the environmental factors, obvious higher corrosion rates were observed at high carbonate (1 M) and high pH (pH 13) conditions due to the increase in the anodic reaction rate. In other condition, corrosion rate of titanium were estimated to be in the order of 10 -3 - 10 -2 μm/y. Almost all (<98%) of the hydrogen generated by corrosion was absorbed into titanium. Assuming that the time evolution of the hydrogen content in titanium follows linear law to make conservative assessment, the absorbed hydrogen content was estimated to be of 400-500 ppm in 1000 years. (author)

  13. Complex electrochemical investigation of ordered mesoporous carbon synthesized by soft-templating method: charge storage and electrocatalytical or Pt-electrocatalyst supporting behavior

    International Nuclear Information System (INIS)

    Momčilović, Milan; Stojmenović, Marija; Gavrilov, Nemanja; Pašti, Igor; Mentus, Slavko; Babić, Biljana

    2014-01-01

    Ordered mesoporous carbon (OMC) was synthesized by an evaporation induced self-assembly method, under acidic conditions, with resorcinol as the carbon precursor and Pluronic F127 triblock copolymer (EO 106 PO 70 EO 106 ) as a structure directing agent. The obtained OMC product was characterized by N 2 sorptometry, X-ray diffractometry and Raman spectroscopy. The mean pore radius of 2 nm and specific surface area of 712 m 2 g −1 were found. The OMC sample was subjected to a complex electrochemical testing in order to check for its applicability in various energy conversion processes. For pure OMC, the charge storage properties and kinetics of oxygen reduction reaction (ORR) in alkaline solution were measured. The OMC sample delivered specific capacitance of 232 F g −1 at 5 mV s −1 with 83.6% capacitance retained at 100 mV s −1 . Effective ORR electrocatalysis by OMC in alkaline media was evidenced, with onset potential amounting to −0.10 V vs. saturated calomel electrode. A part of the OMC sample was used as a support of Pt nanoparticles, and examined as electrocatalyst for hydrogen evolution reaction (HOR) and ORR in acidic media. Reversible HOR kinetics was observed, while ORR performances were found to be competitive to the ones on other carbon-supported Pt electrocatalysts reported so far. A superb electrochemical behavior was correlated to physico-chemical properties of OMC. Described OMC stands out as a highly versatile material, which can be used to replace carbon materials developed for specific purposes, allowing rationalization of carbon-based technologies aimed for energy conversion purposes

  14. A study on electrochemical redox behavior of nitric acid by using a glassy carbon fiber column electrode system

    International Nuclear Information System (INIS)

    Kim, K. W.; Song, K. C.; Lee, I. H.; Choi, I. K.; You, J. H.

    1999-01-01

    Electrochemical redox behaviors of nitric acid were studied by using a glassy carbon fiber column electrode system, and its reaction mechanism was analyzed in several ways. The electrochemical reaction in less than 2.0 M nitric acid was not observed, but in more than 2.0 M nitric acid, the reduction rate of nitric acid to produce nitrous acid was slow so that the nitric acid solution had to be contacted with electrode enough in order for a apparent reduction current of nitric acid to nitrous acid be to observed. The nitrous acid generated in more than 2.0 M nitric acid was rapidly and easily reduced to NOx through an autocatalytic reaction. Sulfamic acid was confirmed to be effective to destroy the nitrous acid. The sulfamic acid of at least 0.05M was necessary to remove the nitrous acid generated in 3.5 M nitric acid

  15. Hydrogen.

    Science.gov (United States)

    Bockris, John O'M

    2011-11-30

    The idea of a "Hydrogen Economy" is that carbon containing fuels should be replaced by hydrogen, thus eliminating air pollution and growth of CO₂ in the atmosphere. However, storage of a gas, its transport and reconversion to electricity doubles the cost of H₂ from the electrolyzer. Methanol made with CO₂ from the atmosphere is a zero carbon fuel created from inexhaustible components from the atmosphere. Extensive work on the splitting of water by bacteria shows that if wastes are used as the origin of feed for certain bacteria, the cost for hydrogen becomes lower than any yet known. The first creation of hydrogen and electricity from light was carried out in 1976 by Ohashi et al. at Flinders University in Australia. Improvements in knowledge of the structure of the semiconductor-solution system used in a solar breakdown of water has led to the discovery of surface states which take part in giving rise to hydrogen (Khan). Photoelectrocatalysis made a ten times increase in the efficiency of the photo production of hydrogen from water. The use of two electrode cells; p and n semiconductors respectively, was first introduced by Uosaki in 1978. Most photoanodes decompose during the photoelectrolysis. To avoid this, it has been necessary to create a transparent shield between the semiconductor and its electronic properties and the solution. In this way, 8.5% at 25 °C and 9.5% at 50 °C has been reached in the photo dissociation of water (GaP and InAs) by Kainthla and Barbara Zeleney in 1989. A large consortium has been funded by the US government at the California Institute of Technology under the direction of Nathan Lewis. The decomposition of water by light is the main aim of this group. Whether light will be the origin of the post fossil fuel supply of energy may be questionable, but the maximum program in this direction is likely to come from Cal. Tech.

  16. Enhanced activity of CaFeMg layered double hydroxides-supported gold nanodendrites for the electrochemical evolution of oxygen and hydrogen in alkaline media

    Science.gov (United States)

    Havakeshian, Elaheh; Salavati, Hossein; Taei, Masoumeh; Hasheminasab, Fatemeh; Seddighi, Mohadeseh

    2018-02-01

    In this study, Au was electrodeposited on a support of CaFeMg layered double hydroxide and then, its catalytic activity was investigated for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Field emission scanning electron microscopy images showed that a uniform porous film of aggregated nano-particles of the LDH has been decorated with Au nanodendrite-like structures (AuNDs@LDH). The results obtained from polarization curves, Tafel plots and electrochemical impedance spectroscopy showed that the AuNDs@LDH exhibits lower overpotential, higher current density, faster kinetics and enhanced stability for both of the OER and HER, in comparison with the single AuNPs and LDH catalysts.

  17. MOF-derived Cu-Pd/nanoporous carbon composite as an efficient catalyst for hydrogen evolution reaction: A comparison between hydrothermal and electrochemical synthesis

    Science.gov (United States)

    Mandegarzad, Sakineh; Raoof, Jahan Bakhsh; Hosseini, Sayed Reza; Ojani, Reza

    2018-04-01

    In this study, a novel catalyst based on Cu-Pd bimetallic nanoparticles supported on nanoporous carbon composite (NPCC) is successfully fabricated through three-step process and used as an electrocatalyst towards hydrogen evolution reaction (HER). At the first step, MOF-199 is synthesized via two distinct strategies; (1) hydrothermal (HT) and (2) electrochemical (EC). Next, the synthesized MOF-199 is used as a template in order to prepare Cu/NPCC by direct carbonization under N2 atmosphere followed by galvanic replacement reaction of Cu metals by PdII ions. All the prepared materials are characterized by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), and nitrogen adsorption/desorption measurements. The effect of synthesis method of MOF-199 on the electrocatalytic activity of the final product towards HER is investigated. The electrochemical measurements indicate that Cu-Pd/NPCC derived from the MOF prepared by EC method (Cu-Pd/NPCC/EC) exhibits an enhanced catalytic activity towards HER in H2SO4 solution than the Cu-Pd/NPCC/HT. This improvement may be attributed to using of supporting electrolyte in the preparation of Cu-Pd/NPCC/EC.

  18. WC-CoCr coatings sprayed by high velocity oxygen-fuel (HVOF flame on AA7050 aluminum alloy: electrochemical behavior in 3.5% NaCl solution

    Directory of Open Access Journals (Sweden)

    Marina Magnani

    2007-12-01

    Full Text Available In the present work, the electrochemical behavior of WC-CoCr coatings with 10 (W10, 15 (W15 and 20 (W20 torch passes sprayed by High Velocity Oxygen-Fuel (HVOF flame on AA7050 aluminum alloy substrate, evaluated in 3.5% NaCl solution, were compared using open-circuit potential (E OC measurements, electrochemical impedance spectroscopy (EIS and polarization curves. The coating surfaces and their cross sections were characterized by X ray diffraction and the Rockwell-C hardness test, and also by optical (OM and scanning electron microscopy (SEM before and after the corrosion tests. The electrochemical data showed that sample W10 presented higher corrosion resistance than the others in chloride solutions. In some tests, aluminum salts on the coating surface were identified by EDS, indicating the corrosion of the substrate. And using aluminon, aluminum ions were detected and analyzing the surface via stereomicroscopy, hydrogen bubbles were observed, both showing that the electrolyte reached the substrate and galvanic corrosion possibly occurred. The physical characterization showed that sample W10 presented a lower number of cracks and pores, justifying its higher corrosion resistance.

  19. Effects of hydrogen on the behavior of metals. III. Mechanicals behavior of the TD12ZrE titanium alloy in presence of hydrogen; influence of heat treatments and oxygen content

    International Nuclear Information System (INIS)

    Criqui, Bernard.

    1976-04-01

    The influence of heat treatments, hydrogen state and concentration are studied. Tensile tests on specimens STA at 510 deg C show opposite behavior according to the hydrogen loading mode, either cathodic (embrittlement increases with small hydrogen content) or during aging (embrittlement begins at about 4500ppm). As aging and hydrogen loading temperatures increase, hydrogen-induced β stabilization decreases. Previous cold-work or oxygen loading favor α phase nucleation. More severe biaxial disk pressure tests, conducted on the alloy aged and loaded at 510 deg C, reveal various embrittlement caused by dissolved hydrogen, one due to hydrogen dragging by dislocations at medium epsilon and beginning at 1500ppm, one at high epsilon due to the Kolachev effect. Disk pressure testing of hydrogen gas embrittlement shows the competitition between film rupture and repassivation phenomena together with the influence of heat treatments, surface conditions and trace impurities [fr

  20. Hydrogen-rich saline attenuates anxiety-like behaviors in morphine-withdrawn mice.

    Science.gov (United States)

    Wen, Di; Zhao, Peng; Hui, Rongji; Wang, Jian; Shen, Qianchao; Gong, Miao; Guo, Hongyan; Cong, Bin; Ma, Chunling

    2017-05-15

    Hydrogen therapy is a new medical approach for a wide range of diseases. The effects of hydrogen on central nervous system-related diseases have recently become increasingly appreciated, but little is known about whether hydrogen affects the morphine withdrawal process. This study aims to investigate the potential effects of hydrogen-rich saline (HRS) administration on naloxone-precipitated withdrawal symptoms and morphine withdrawal-induced anxiety-like behaviors. Mice received gradually increasing doses (25-100 mg/kg, i.p.) of morphine over 3 days. In the naloxone-precipitated withdrawal procedure, the mice were treated with three HRS (20 μg/kg, i.p.) injections, and naloxone (1 mg/kg, i.p.) was given 30 min after HRS administration. Body weight, jumping behavior and wet-dog shakes were immediately assessed. In the spontaneous withdrawal procedure, the mice were treated with HRS (20 μg/kg, i.p.) every 8-h. Mice underwent naloxone-precipitated or spontaneous withdrawal were tested for anxiety-like behaviors in the elevated plus-maze (EPM) and light/dark box (L/D box) paradigm, respectively. In addition, the levels of plasma corticosterone were measured. We found that HRS administration significantly reduced body weight loss, jumping behavior and wet-dog shakes in mice underwent naloxone-precipitated withdrawal, and attenuated anxiety-like behaviors in the EPM and L/D box tests after naloxone-precipitated withdrawal or a 2-day spontaneous withdrawal period. Hypo-activity or motor impairment after HRS administration was not observed in the locomotion tests. Furthermore, HRS administration significantly decreased the levels of corticosterone in morphine-withdrawn mice. These are the first findings to indicate that hydrogen might ameliorate withdrawal symptoms and exert an anxiolytic-like effect in morphine-withdrawal mice. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Electrochemical oxidation behavior of some hazardous phenolic compounds in acidic solution

    Directory of Open Access Journals (Sweden)

    H. Nady

    2017-09-01

    Full Text Available The electrochemical oxidation of phenol, resorcinol and pyrogallol was investigated in sulfuric acid solution. Cyclic voltammetry and electrochemical impedance spectroscopy, EIS, were used. The mechanism of the electrochemical oxidation process was proposed and discussed. The process includes a selective oxidation and PtOx formation. EIS measurements were carried out to further examine the reaction kinetics involved in the phenolic compounds electro-oxidation. The EIS responses were found to be strongly dependent on electrode potentials. The result showed the presence of an oxidation peak in the region around 1 V vs SCE to all conditions evaluated. In cyclic voltammetric experiments a gradual decrease of the oxidation peak with the number of cycles was observed. This suggests the deactivation or blockage of the electrode surface by the adsorption of substances and/or phenoxy radical polymerization.

  2. Promising and Reversible Electrolyte with Thermal Switching Behavior for Safer Electrochemical Storage Devices.

    Science.gov (United States)

    Shi, Yunhui; Zhang, Qian; Zhang, Yan; Jia, Limin; Xu, Xinhua

    2018-02-28

    A major stumbling block in large-scale adoption of high-energy-density electrochemical devices has been safety issues. Methods to control thermal runaway are limited by providing a one-time thermal protection. Herein, we developed a simple and reversible thermoresponsive electrolyte system that is efficient to shutdown the current flow according to temperature changes. The thermal management is ascribed to the thermally activated sol-gel transition of methyl cellulose solution, associated with the concentration of ions that can move between isolated chains freely or be restricted by entangled molecular chains. We studied the effect of cellulose concentration, substituent types, and operating temperature on the electrochemical performance, demonstrating an obvious capacity loss up to 90% approximately of its initial value. Moreover, this is a cost-effective approach that has the potential for use in practical electrochemical storage devices.

  3. Simulation of electrochemical behavior in Lithium ion battery during discharge process

    Science.gov (United States)

    Chen, Yong; Lin, Muyi; Zhao, Li

    2018-01-01

    An electrochemical Lithium ion battery model was built taking into account the electrochemical reactions. The polarization was divided into parts which were related to the solid phase and the electrolyte mass transport of species, and the electrochemical reactions. The influence factors on battery polarization were studied, including the active material particle radius and the electrolyte salt concentration. The results showed that diffusion polarization exist in the positive and negative electrodes, and diffusion polarization increase with the conducting of the discharge process. The physicochemical parameters of the Lithium ion battery had the huge effect on cell voltage via polarization. The simulation data show that the polarization voltage has close relationship with active material particle size, discharging rate and ambient temperature. PMID:29293535

  4. The electrochemical behavior of poly 1-pyrenemethyl methacrylate binder and its effect on the interfacial chemistry of a silicon electrode

    Science.gov (United States)

    Haregewoin, Atetegeb Meazah; Terborg, Lydia; Zhang, Liang; Jurng, Sunhyung; Lucht, Brett L.; Guo, Jinghua; Ross, Philip N.; Kostecki, Robert

    2018-02-01

    The physico-chemical properties of poly (1-pyrenemethyl methacrylate) (PPy) are presented with respect to its use as a binder in a Si composite anode for Li-ion batteries. PPy thin-films on Si(100) wafer and Cu model electrodes are shown to exhibit superior adhesion as compared to conventional polyvinylidene difluoride (PVdF) binder. Electrochemical testing of the model bi-layer PPy/Si(100) electrodes in a standard organic carbonate electrolyte reveal higher electrolyte reduction current and an overall irreversible cathodic charge consumption during initial cycling versus the uncoated Si electrode. The PPy thin-film is also shown to impede lithiation of the underlying Si. XAS, AFM, TGA and ATR-FTIR analysis indicated that PPy binder is both chemically and electrochemically stable in the cycling potential range however significant swelling is observed due to a selective uptake of diethyl carbonate (DEC) from the electrolyte. The increased concentration of DEC and depletion of ethylene carbonate (EC) at the Si/PPy interface leads to continuous decomposition of the electrolyte and results in non-passivating behavior of the Si(100)/PPy electrode as compared to pristine silicon. Consequently, PPy binder improves the mechanical integrity of composite Si anodes but it influences mass transport at the Si(100)/PPy interface and alters electrochemical response of silicon during cycling in an adverse manner.

  5. Study on transient hydrogen behavior and effect on passive containment cooling system of the advanced PWR

    International Nuclear Information System (INIS)

    Wang Yan

    2014-01-01

    A certain amount of hydrogen will be generated due to zirconium-steam reaction or molten corium concrete interaction during severe accidents in the pressurized water reactor (PWR). The generated hydrogen releases into the containment, and the formed flammable mixture might cause deflagration or detonation to produce high thermal and pressure loads on the containment, which may threaten the integrity of the containment. The non-condensable hydrogen in containment may also reduce the steam condensation on the containment surface to affect the performance of the passive containment cooling system (PCCS). To study the transient hydrogen behavior in containment with the PCCS performance during the accidents is significant for the further study on the PCCS design and the hydrogen risk mitigation. In this paper, a new developed PCCS analysis code with self-reliance intellectual property rights, which had been validated by comparison on the transients in the containment during the design basis accidents with other developed PCCS analysis code, is brief introduced and used for the transient simulation in the containment under a postulated small break LOCA of cold-leg. The results show that the hydrogen will flow upwards with the coolant released from the break and spread in the containment by convection and diffusion, and it results in the increase of the pressure in the containment due to reducing the heat removal capacity of the PCCS. (author)

  6. Effect of C/Si Ratio on the Electrochemical Behavior of a-SiCx:H Coatings on SS301 Substrate Deposited by PECVD

    Directory of Open Access Journals (Sweden)

    D. Li

    2014-01-01

    Full Text Available Amorphous hydrogenated silicon carbide (a-SiCx:H coatings were deposited on stainless steel 301 (SS301 using plasma enhanced chemical vapor deposition with the methane gas flow ranging from 30 to 90 sccm. XRD spectra confirmed the amorphous structure of these coatings. The as-deposited coatings all exhibited homogenous dense feature, and no porosities were observed in SEM and AFM analysis. The a-SiCx:H coatings remarkably increased the corrosion resistance of the SS301 substrate. With the increase of the C concentration, the a-SiCx:H coatings exhibited significantly enhanced electrochemical behavior. The a-SiCx:H coating with the highest carbon concentration acted as an excellent barrier to charge transfer, with a corrosion current of 3.5×10-12 A/cm2 and a breakdown voltage of 1.36 V, compared to 2.5×10-8 A/cm2 and 0.34 V for the SS301 substrate.

  7. Hydrogen

    Directory of Open Access Journals (Sweden)

    John O’M. Bockris

    2011-11-01

    Full Text Available The idea of a “Hydrogen Economy” is that carbon containing fuels should be replaced by hydrogen, thus eliminating air pollution and growth of CO2 in the atmosphere. However, storage of a gas, its transport and reconversion to electricity doubles the cost of H2 from the electrolyzer. Methanol made with CO2 from the atmosphere is a zero carbon fuel created from inexhaustible components from the atmosphere. Extensive work on the splitting of water by bacteria shows that if wastes are used as the origin of feed for certain bacteria, the cost for hydrogen becomes lower than any yet known. The first creation of hydrogen and electricity from light was carried out in 1976 by Ohashi et al. at Flinders University in Australia. Improvements in knowledge of the structure of the semiconductor-solution system used in a solar breakdown of water has led to the discovery of surface states which take part in giving rise to hydrogen (Khan. Photoelectrocatalysis made a ten times increase in the efficiency of the photo production of hydrogen from water. The use of two electrode cells; p and n semiconductors respectively, was first introduced by Uosaki in 1978. Most photoanodes decompose during the photoelectrolysis. To avoid this, it has been necessary to create a transparent shield between the semiconductor and its electronic properties and the solution. In this way, 8.5% at 25 °C and 9.5% at 50 °C has been reached in the photo dissociation of water (GaP and InAs by Kainthla and Barbara Zeleney in 1989. A large consortium has been funded by the US government at the California Institute of Technology under the direction of Nathan Lewis. The decomposition of water by light is the main aim of this group. Whether light will be the origin of the post fossil fuel supply of energy may be questionable, but the maximum program in this direction is likely to come from Cal. Tech.

  8. Electrochemical Behavior of Bilayer Thermal-Spray Coatings in Low-Temperature Corrosion Protection

    Directory of Open Access Journals (Sweden)

    Esmaeil Sadeghimeresht

    2017-09-01

    Full Text Available Cr3C2-NiCr coatings are greatly used to protect critical components in corrosive environments and to extend their lifetime and/or improve functional performance. However, the pores formed during spraying restrict the coating’s applicability area for many corrosion protection applications. To overcome this technical challenge, bilayer coatings have been developed, in which an additional layer (the so-called “intermediate layer” is deposited on the substrate before spraying the Cr3C2-NiCr coating (the so-called “top layer”. The corrosion behavior of the bilayer coating depends on the composition and microstructure of each layer. In the present work, different single-layer coatings (i.e., Cr3C2-NiCr, Fe- and Ni-based coatings were initially sprayed by a high-velocity air fuel (HVAF process. Microstructure analysis, as well as electrochemical tests, for example, open-circuit potential (OCP and polarization tests, were performed. The potential difference (ΔE had a great influence on galvanic corrosion between the top and intermediate layers, and thus, the coatings were ranked based on the OCP values (from high to low as follows: NiCoCrAlY > NiCr > Cr3C2-NiCr > NiAl > Fe-based coatings (alloyed with Cr > pure Ni. The Ni-based coatings were chosen to be further used as intermediate layers with the Cr3C2-NiCr top layer due to their capabilities to show high OCP. The corrosion resistance (Rp of the bilayer coatings was ranked (from high to low as follows: NiCoCrAlY/Cr3C2-NiCr > NiCr/Cr3C2-NiCr > NiAl/Cr3C2-NiCr > Ni/Cr3C2-NiCr. It was shown that splat boundaries and interconnected pores are detrimental for corrosion resistance, however, a sufficient reservoir of protective scale-forming elements (such as Cr or/and Al in the intermediate layer can significantly improve the corrosion resistance.

  9. Effect of Different Welding Processes on Electrochemical and Corrosion Behavior of Pure Nickel in 1 M NaCl Solution

    Directory of Open Access Journals (Sweden)

    Xijing Wang

    2017-11-01

    Full Text Available A plasma arc welding (PAW-tungsten inert gas (TIG hybrid welding process is proposed to weld pure nickel. In PAW-TIG welding, the arc of the PAW was first to be ignited, then TIG was ignited, while in PAW welding, only the PAW arc was launched. This paper investigated the effect of different welding processes on electrochemical and corrosion performance of between a pure nickel joint and a base metal in an aerated 1 M NaCl solution, respectively. The average grain size of the joint fabricated by PAW welding (denoted as JP joint is 463.57 μm, the joint fabricated by PAW-TIG welding(denoted as JP-T joint is 547.32 μm, and the base metal (BM is 47.32 μm. In this work, the passivity behaviors of samples were characterized for two welding processes by electrochemical impedance spectroscopy (EIS, open circuit potential versus immersion time (OCP-t, and the potentiodynamic polarization plots. EIS spectra, attained with different immersion times, were analyzed and fitted by an equivalent electrical circuit. Photomicrographs of BM, JP, and JP-T were also taken with a scanning electron microscope (SEM to reveal the morphological structure of the pit surfaces. Electrochemical tests show that the sequence of the corrosion resistance is BM > JP > JP-T. The size and quantity of the hemispherical corrosion pits of all samples are different. The corrosion morphology observations found a consistency with the consequence of the electrochemical measurements. The results show that an increase of the grain dimensions due to different heat treatments decreased the pure nickel stability to pitting corrosion.

  10. Electrochemical Behavior Of Bioactive Coatings On Cp-ti Surface For Dental Application.

    OpenAIRE

    Marques, Isabella da Silva Vieira; Barão, Valentim Adelino Ricardo; da Cruz, Nilson Cristino; Yuan, Judy Chia-Chun; Mesquita, Marcelo Ferraz; Ricomini-Filho, Antonio Pedro; Sukotjo, Cortino; Mathew, Mathew T

    2016-01-01

    The surface characteristics and electrochemical properties of bioactive coatings produced by plasma electrolytic oxidation (PEO) with calcium, phosphorous, silicon and silver on commercially pure titanium were evaluated. PEO treatment produced a porous oxide layer, which improved the surface topography, and enriched the surface chemistry with bioactive elements, responsible for mimicking bone surface. The surfaces with higher calcium concentration presented antibacterial and biocompatibility ...

  11. Electrochemical behavior of an anticancer drug 5-fluorouracil at methylene blue modified carbon paste electrode

    International Nuclear Information System (INIS)

    Bukkitgar, Shikandar D.; Shetti, Nagaraj P.

    2016-01-01

    A novel sensor for the determination of 5-fluorouracil was constructed by electrochemical deposition of methylene blue on surface of carbon paste electrode. The electrode surface morphology was studied using Atomic force microscopy and XRD. The electrochemical activity of modified electrode was characterized using cyclic voltammetry and differential pulse method. The developed sensor shows impressive enlargement in sensitivity of 5-fluorouracil determination. The peak currents obtained from differential pulse voltammetry was linear with concentration of 5-fluorouracil in the range 4 × 10 −5 –1 × 10 −7 M and detection limit and quantification limit were calculated to be 2.04 nM and 6.18 nM respectively. Further, the sensor was successfully applied in pharmaceutical and biological fluid sample analysis. - Highlights: • Electrochemical oxidation of 5-fluorouracil has been investigated for first time at methylene blue modified carbon paste electrode • The electrode process was irreversible and diffusion controlled • Probable electrochemical mechanism was proposed which involved two proton and two electron transfer reaction • The LOD and LOQ values were calculated to be 2.04 nM and 6.18 nM, respectively, with good selectivity and sensitivity. • Proposed method was applied to 5-Fluorouracil determination in pharmaceutical and spiked human urine samples

  12. Electrochemical behavior of an anticancer drug 5-fluorouracil at methylene blue modified carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Bukkitgar, Shikandar D.; Shetti, Nagaraj P., E-mail: dr.npshetti@gmail.com

    2016-08-01

    A novel sensor for the determination of 5-fluorouracil was constructed by electrochemical deposition of methylene blue on surface of carbon paste electrode. The electrode surface morphology was studied using Atomic force microscopy and XRD. The electrochemical activity of modified electrode was characterized using cyclic voltammetry and differential pulse method. The developed sensor shows impressive enlargement in sensitivity of 5-fluorouracil determination. The peak currents obtained from differential pulse voltammetry was linear with concentration of 5-fluorouracil in the range 4 × 10{sup −5}–1 × 10{sup −7} M and detection limit and quantification limit were calculated to be 2.04 nM and 6.18 nM respectively. Further, the sensor was successfully applied in pharmaceutical and biological fluid sample analysis. - Highlights: • Electrochemical oxidation of 5-fluorouracil has been investigated for first time at methylene blue modified carbon paste electrode • The electrode process was irreversible and diffusion controlled • Probable electrochemical mechanism was proposed which involved two proton and two electron transfer reaction • The LOD and LOQ values were calculated to be 2.04 nM and 6.18 nM, respectively, with good selectivity and sensitivity. • Proposed method was applied to 5-Fluorouracil determination in pharmaceutical and spiked human urine samples.

  13. Facile fabrication and electrochemical behaviors of Mn:ZnS nanocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Xie, Ruishi [Analytical and Testing Center, Southwest University of Science and Technology, Mianyang, 621010 (China); Li, Yuanli, E-mail: yuanlyl@foxmail.com [Department of Materials, Southwest University of Science and Technology, Mianyang, 621010 (China); Liu, Haifeng; Guo, Baogang [Analytical and Testing Center, Southwest University of Science and Technology, Mianyang, 621010 (China)

    2016-07-05

    Here, we demonstrate the rational design and synthesis of Mn:ZnS nanocrystals with adjustable doping concentrations utilizing a facile, cost effective, and environmentally benign chemical protocol. These nanostructures were investigated as electrode materials for lithium-ion batteries. Compared with pristine ZnS nanocrystals, the Mn:ZnS nanocrystals exhibit significantly improved electrochemical performances in terms of specific capacity and cycling performance. The Mn:ZnS nanocrystal sample with doping concentration of 1 at% displays second discharge capacity of 789.9 mA h g{sup −1} at a current density of 24 mA g{sup −1}, about 2.39 times higher than that of the pure ZnS nanocrystal. Furthermore, the Mn:ZnS nanocrystal electrodes represent much better capacity retention than that of the undoped one. The greatly improved electrochemical performances of the Mn:ZnS nanocrystal samples could be attributed to the following factors. The large specific surface area can significantly enhance structural integrity by acting as mechanical buffer, effectively alleviating the volume changes generated during the lithiation/delithiation process. The incorporation of Mn into the lattice of ZnS improves charge transfer kinetics and results in a faster Li{sup +} diffusion rate during the charge–discharge process. It is of great significance to incorporate guest metal ions into nanostructured materials to display especial electrochemical characteristics triggering an effective approach to improve the electrochemical properties.

  14. Zircaloy oxidation and hydrogen generation behavior during severe accidents

    International Nuclear Information System (INIS)

    Cronenberg, A.W.; Miller, R.W.; Osetek, D.J.

    1987-01-01

    Zircaloy oxidation and H 2 generation data are presented for recent in-pile severe fuel damage tests. The principal questions investigated concern zircaloy melting and bundle reconfiguration effects on oxidation behavior. A comparison of H 2 generation and cladding temperature data indicate that significant oxidation occurred after the onset of fuel liquefaction. Posttest metallographic observations of the test debris also indicate a high degree of oxidation of once-molten zircaloy. Analysis of bundle reconfiguration effects indicate that essentially complete flow area blockage (>98%) would be required to retard steam flow through the degraded bundle so as to diminish H 2 production. Such extreme blockage conditions are not supported by posttest bundle examination

  15. Electrochemical Hydrogen Oxidation in Toluene/LiCB11Me12: H2 as a Surrogate for Lithium Metal?

    Czech Academy of Sciences Publication Activity Database

    Pospíšil, Lubomír; Kaleta, Jiří; Michl, Josef

    2016-01-01

    Roč. 3, č. 2 (2016), s. 332-336 ISSN 2196-0216 R&D Projects: GA ČR GA13-19213S Institutional support: RVO:61388955 ; RVO:61388963 Keywords : electrochemistry * hydrogen * lithium Subject RIV: CG - Electrochemistry; CF - Physical ; Theoretical Chemistry (UOCHB-X) Impact factor: 4.136, year: 2016

  16. Electrochemical and anticorrosion behaviors of hybrid functionalized graphite nano-platelets/tripolyphosphate in epoxy-coated carbon steel

    Energy Technology Data Exchange (ETDEWEB)

    Mohammadi, Somayeh, E-mail: somaye.mohammadi32@aut.ac.ir [Department of Chemistry, Amirkabir University of Technology, Tehran (Iran, Islamic Republic of); Shariatpanahi, Homeira [Corrosion Department, Research Institute of Petroleum Industry (RIPI), P.O. Box 18745-4163, Tehran (Iran, Islamic Republic of); Taromi, Faramarz Afshar [Department of Polymer Engineering, Amirkabir University of Technology, Tehran (Iran, Islamic Republic of); Neshati, Jaber [Corrosion Department, Research Institute of Petroleum Industry (RIPI), P.O. Box 18745-4163, Tehran (Iran, Islamic Republic of)

    2016-08-15

    Highlights: • FGNP was combined with TPP to obtain a hybrid nano-particle. • TEM image showed uniform distribution of the hybrid nanoparticles in epoxy coating. • FGNP is a substrate for linking of TPP anions by hydrogen bonding. • FGNP as an accelerator, provides rapid iron phosphate passive film formation. • The hybrid nano-particle can provide long-term corrosion protection. - Abstract: Functionalized graphite nano-platelets (FGNP) were combined with tripolyphosphate (TPP) to gain a hybrid nano-particle (FGNP-TPP) with homogenous dispersion in epoxy, resulting in an excellent anti-corrosion coating for carbon steel substrate. Characterization analyses of the hybrid nano-particle were performed by FT-IR, SEM, XRD and TEM. TPP was linked to FGNP nano-particles by hydrogen bondings. Different epoxy coatings formulated with 1 wt.% of FGNP, FGNP-TPP and TPP were evaluated. Electrochemical investigations, salt spray and pull-off tests showed that the hybrid nano-particle can provide long-term corrosion protection compared to FGNP and TPP due to synergistic effect between FGNP as an accelerator and TPP as a corrosion inhibitor to produce a uniform and stable iron-phosphate passive film with high surface coverage.

  17. Hydrogen isotope storage behavior of Zr1-xTixCo alloys

    International Nuclear Information System (INIS)

    Jat, Ram Avtar; Pati, Subhasis; Parida, S.C.; Agarwal, Renu; Mukerjee, S.K.

    2016-01-01

    Tritium storage properties similar to uranium make ZrCo as a suitable candidate material for storage, supply and recovery of hydrogen isotopes in various tritium facilities. Beside non-radioactive, nonpyrophoric at room temperature and higher storage capacity (H/f.u. up to 3, f.u. = ZrCo), it has been reported that upon repeated hydriding-dehydriding cycles, ZrCo undergoes dis-proportionation as per the reaction; ZrCo + H 2 ↔ ZrH 2 + ZrCo 2 . The present study is aimed to investigate the effect of Ti content on the hydrogen storage behavior of Zr 1-x Ti x Co alloys and the hydrogen isotope effect

  18. Modulating the spin transport behaviors in ZBNCNRs by edge hydrogenation and position of BN chain

    Directory of Open Access Journals (Sweden)

    Jun Ouyang

    2016-03-01

    Full Text Available Using the density functional theory and the nonequilibrium Green’s function method, we study the spin transport behaviors in zigzag boron-nitrogen-carbon nanoribbons (ZBNCNRs by modulating the edge hydrogenation and the position of B-N nanoribbons (BNNRs chain. The different edge hydrogenations of the ZBNCNRs and the different position relationships of the BNNRs have been considered systematically. Our results show that the metallic, semimetallic and semiconductive properties of the ZBNCNRs can be modulated by the different edge hydrogenations and different position relationships of BN chains. And our proposaled ZBNCNRs devices act as perfect spin-filters with nearly 100% spin polarization. These effects would have potential applications for boron-nitrogen-carbon-based nanomaterials in spintronics nano-devices.

  19. Electrochemical behavior of gold (III) in cyanide-free bath with 5,5′-dimethylhydantoin as complexing agent

    International Nuclear Information System (INIS)

    Yang Xiaowei; An Maozhong; Zhang Yunwang; Zhang Lin

    2011-01-01

    Highlights: ► The DMH gold plating electrolyte with good stability studied in this paper is cyanide-free and the influence of novel additive (pyridyl-compound) on the nucleation and growth of gold is also investigated. ► The electrochemical behavior of gold electrodeposition in DMH bath is firstly analyzed using cyclic voltammograms and chronoamperometry techniques. - Abstract: Gold electrodeposits are prepared in a cyanide-free bath with 5,5′-dimethylhydantoin (DMH) as complexing agent. The electrochemical behavior of the electrodeposition is then investigated together with the influence of additive A (pyridyl-compound) as an additive on the nucleation and growth of gold using electrochemical techniques on gold working electrode at different temperatures. Cyclic voltammogram consists of a single cathodic reduction wave at −0.62 V which corresponds to the reduction of Au(III) to Au without anodic oxidation wave observed. The diffusion coefficient of Au(III) in the bath is found to be ∼10 −6 cm 2 /s and the energy of activation (43 kJ/mol) is deduced from the cyclic voltammograms at different temperatures. The nucleation and growth of gold on gold working electrode is investigated by chronoamperometry. The progressive nucleation mechanism is found for gold deposition using Scharifker–Hills’ model with three-dimensional (3D) diffusion-controlled growth nucleation. The introduction of the additive A does not influence this mechanism. The gold electrodeposits are characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and cathodic polarization measurements. Experimental results indicate that additive A increases the cathodic polarization of bath, refines the grains of electrodeposit and changes the preferred orientation of electrodeposit from [1 1 1] direction to [2 0 0] direction.

  20. Influence of enzymatic reactions on the electrochemical behavior of EN X2CrNiMo17-11-2 (AISI 316L) stainless steel in bio-corrosion: role of interfacial processes on the modification of the passive layer

    International Nuclear Information System (INIS)

    Landoulsi, J.

    2008-01-01

    The outstanding corrosion behavior of stainless steels (SS) results from the presence of thin oxide layer (some nanometers). In non sterile aqueous media, stainless steels may exhibit a non stable behavior resulting from interactions between microbial species and passive film. In fact, microorganisms can be deeply involved in the corrosion processes usually reported as Microbial Influenced Corrosion (MIC). They can induce the initiation or the acceleration of this phenomenon and they do so when organized in bio-films. From the electrochemical point of view, stainless steels showed an increase of the free corrosion potential (Ecorr) attributed to the bio-film settlement. The Eco' ennoblement was broadly reported in seawater and seems to be confirmed in fresh water according to recent findings. A considerable progress in the comprehension of MIC processes was related to the role of extracellular species, essentially enzymes. Many enzymatic reactions occurring in bio-films consist on using oxygen as electron acceptor to generate hydrogen peroxide and related species. The aim of this work is to understand the mechanisms involved in the electrochemical behavior of stainless steel according to an enzymatic approach in medium simulating fresh water. To this end, glucose oxidase was chosen to globalize aerobic activities of bio-films. Electrochemical measurements in situ and surface analysis allow the comprehension of the role and the nature of interfacial processes. Surface characterization was performed with the help of a new quantitative utilization of XPS analysis and AFM. Results show a significant evolution in term of morphology (surface organization), (ii) chemical composition (passive layer, adsorbed organic species) and (iii) chemical reaction (oxidation, dissolution, effect of enzyme). Finally, a new enzymatic system is proposed to mimic specific physicochemical conditions at the SS / bio-film interface, in particular enzymatic generation of oxidant species in

  1. Influence of Oxidation Treatments and Surface Finishing on the Electrochemical Behavior of Ni-20Cr HVOF Coatings

    Science.gov (United States)

    Ruiz-Luna, H.; Porcayo-Calderon, J.; Alvarado-Orozco, J. M.; Mora-García, A. G.; Martinez-Gomez, L.; Trápaga-Martínez, L. G.; Muñoz-Saldaña, J.

    2017-12-01

    The low-temperature electrochemical behavior of HVOF Ni-20Cr coatings was assessed. The coatings were evaluated in different conditions including as-sprayed, as-ground, and heat-treated in air and argon atmospheres. A detailed analysis of the coatings was carried out by means of XRD, SEM, and EPMA, prior and after the corrosion test. The corrosion rate was analyzed in a NaCl solution saturated with CO2. Results demonstrate that the use of a low-oxygen partial pressure favors the formation of a Cr2O3 layer on the surface of the coatings. According to the electrochemical results, the lower corrosion rates were obtained for the heat-treated coatings irrespective of the surface finishing, being the ground and argon heat-treated condition that shows the best corrosion performance. This behavior is due to the synergistic effect of the low-pressure heat treatment and the grinding processes. The grinding promotes a more homogeneous reaction area without surface heterogeneities such as voids, and the pre-oxidation treatment decreases the porosity content of the coating and also allows the growing of a Cr-rich oxide scale which acts as a barrier against the ions of the aqueous solution.

  2. Numerical Methods for an Analysis of Hydrogen Behaviors Coupled with Thermal Hydraulics in a NPP Containment

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jongtae; Park, Rae-Joon; Hong, Seong-Wan; Kim, Gun-Hong [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2016-10-15

    In a containment safety analysis, multi-dimensional characteristics in thermal hydraulics are very important because the flow paths are not confined in a large free volume of the containment. The analysis is difficult because of a difference in length scales between a characteristic length of the flow and representative length of the containment. In order to simulate hydrogen and steam behaviors in a containment during postulated severe accidents, the GASFLOW code as a multi-dimensional analysis tool for NPP containment has been used for years because of its computational efficiency. Though GASFLOW is well developed for a real NPP containment analysis, there exist shortcomings in nodalization, two-phase and turbulence models. It is based on a Cartesian or cylindrical coordinate mesh, so it is impractical to refine a mesh locally in a region with a physical or geometrical complication. In this paper, the importance of the hydrogen safety in an NPP containment and requirements of the analysis tool was described. And physical models necessary for the hydrogen safety analysis code were listed. As a member of international collaborative project HYMERES for containment thermal hydraulics, KAERI is actively participating in an analytic working group. As an analysis tool for blind benchmarkes, the analysis code described in this paper was used. From the blind benchmark analyses, it was found that the code is very promising for hydrogen safety analysis. Currently, it is proposed to develop the code collaboratively in a hydrogen safety community based on an open-source strategy.

  3. Revisiting the Hydrogen Storage Behavior of the Na-O-H System

    Directory of Open Access Journals (Sweden)

    Jianfeng Mao

    2015-04-01

    Full Text Available Solid-state reactions between sodium hydride and sodium hydroxide are unusual among hydride-hydroxide systems since hydrogen can be stored reversibly. In order to understand the relationship between hydrogen uptake/release properties and phase/structure evolution, the dehydrogenation and hydrogenation behavior of the Na-O-H system has been investigated in detail both ex- and in-situ. Simultaneous thermogravimetric-differential thermal analysis coupled to mass spectrometry (TG-DTA-MS experiments of NaH-NaOH composites reveal two principal features: Firstly, an H2 desorption event occurring between 240 and 380 °C and secondly an additional endothermic process at around 170 °C with no associated weight change. In-situ high-resolution synchrotron powder X-ray diffraction showed that NaOH appears to form a solid solution with NaH yielding a new cubic complex hydride phase below 200 °C. The Na-H-OH phase persists up to the maximum temperature of the in-situ diffraction experiment shortly before dehydrogenation occurs. The present work suggests that not only is the inter-phase synergic interaction of protic hydrogen (in NaOH and hydridic hydrogen (in NaH important in the dehydrogenation mechanism, but that also an intra-phase Hδ+… Hδ– interaction may be a crucial step in the desorption process.

  4. Enhancement of Hydrogen Storage Behavior of Complex Hydrides via Bimetallic Nanocatalysts Doping

    Directory of Open Access Journals (Sweden)

    Prakash C. Sharma

    2012-10-01

    Full Text Available Pristine complex quaternary hydride (LiBH4/2LiNH2 and its destabilized counterpart (LiBH4/2LiNH2/nanoMgH2 have recently shown promising reversible hydrogen storage capacity under moderate operating conditions. The destabilization of complex hydride via nanocrystalline MgH2 apparently lowers the thermodynamic heat values and thus enhances the reversible hydrogen storage behavior at moderate temperatures. However, the kinetics of these materials is rather low and needs to be improved for on-board vehicular applications. Nanocatalyst additives such as nano Ni, nano Fe, nano Co, nano Mn and nano Cu at low concentrations on the complex hydride host structures have demonstrated a reduction in the decomposition temperature and overall increase in the hydrogen desorption reaction rates. Bi-metallic nanocatalysts such as the combination of nano Fe and nano Ni have shown further pronounced kinetics enhancement in comparison to their individual counterparts. Additionally, the vital advantage of using bi-metallic nanocatalysts is to enable the synergistic effects and characteristics of the two transitional nanometal species on the host hydride matrix for the optimized hydrogen storage behavior.

  5. Electrochemical sensor for monitoring electrochemical potentials of fuel cell components

    Science.gov (United States)

    Kunz, Harold R.; Breault, Richard D.

    1993-01-01

    An electrochemical sensor comprised of wires, a sheath, and a conduit can be utilized to monitor fuel cell component electric potentials during fuel cell shut down or steady state. The electrochemical sensor contacts an electrolyte reservoir plate such that the conduit wicks electrolyte through capillary action to the wires to provide water necessary for the electrolysis reaction which occurs thereon. A voltage is applied across the wires of the electrochemical sensor until hydrogen evolution occurs at the surface of one of the wires, thereby forming a hydrogen reference electrode. The voltage of the fuel cell component is then determined with relation to the hydrogen reference electrode.

  6. Evaluation of Electrochemical Behavior of Nopal Extract (Opuntia Ficus- Indica as Possible Corrosion Inhibitor

    Directory of Open Access Journals (Sweden)

    Araceli Mandujano-Ruíz

    2017-11-01

    Full Text Available Corrosion is one of the main problems of degradation in components, tooling, equipment and even in structural applications, examples of this are the carbon steels. In the present work, the capacity of corrosion inhibition of a biodegradable organic extract from the Nopal plant (Opuntia ficus-indica, for the protection of carbon steel type AISI 1018 was studied adding 50% v/v of the Nopal extract (EN in a solution of H2SO4 (0.6 mol.l-1. Polarization Resistance (LPR and Electrochemical Impedance Spectroscopy (EIS techniques were used for the electrochemical evaluation at room temperature for 24 h in order to obtain corrosion rates (Vcorr and inhibition efficiency (IE. Metallographic examination was also carried out to register the surface damage by corrosion. The results showed a reduction of the Vcorr with a maximum IE value of about 84% by adding the organic- liquid extracted from Nopal.

  7. Corrosion-electrochemical behavior of zirconium in molten alkali metal carbonates

    Science.gov (United States)

    Nikitina, E. V.

    2016-08-01

    The corrosion and electrochemical characteristics of zirconium during its interaction with molten lithium, sodium, and potassium carbonates containing from 1 to 5 wt % additives to the salt phase are studied in a temperature range of 500-800°C using gravimetry, corrosion potential measurement, and anodic polarization. The substances decreasing the corrosion losses due to the strengthening and thickening of an oxide film (lithium, sodium, potassium hydroxides) are used as passivators. Sodium chloride, fluoride, and sulfate serve as corrosion stimulators (activators).

  8. Synthesis of Some Novel Pyrimidine Derivatives and Investigation of their Electrochemical Behavior

    Energy Technology Data Exchange (ETDEWEB)

    Akbas, Esvet; Gumus, Selcuk; Sumer, Mehmet Rauf; Akyaz, Inci [Yuzuncu Yil University, Van (Turkmenistan); Levent, Abdulkadir [Batman University, Batman (Turkmenistan)

    2010-12-15

    2-Iminopyrimidines (1a-e) and 2-thioxopyrimidine (2) were synthesized using the Biginelli three component cyclocondensation reaction of an appropriate β-diketone, arylaldehyde, and guanidine (for 1a-e) or thiourea (for 2). The electrochemical properties of the novel systems were investigated by CV and DPV. Moreover, B3LYP/6-31G(d,p) method was applied to the present structures in order to gather some structural and physicochemical data.

  9. Study of caffeine as corrosion inhibitors of carbon steel in chloride solution containing hydrogen sulfide using electrochemical impedance spectroscopy (EIS)

    Science.gov (United States)

    Solehudin, Agus; Berman, Ega Taqwali; Nurdin, Isdiriayani

    2015-09-01

    The corrosion behaviour of steel surface in the absence and presence of caffeine in 3.5% NaCl solution containing dissolved H2S gas is studied using electrochemical impedance spectroscopy (EIS). The experimental results of carbon steel corrosion in 3.5% NaCl solution containing 500 mg/l H2S at different caffeine concentrations showed that corrosion rate of carbon steel decreases with increasing of caffeine concentrations from 0 to 0,1 mmol/l. Whereas, the corrosion rate increase with increasing of caffeine concentrations from 1 to 10 mmol/l. It is clear that no inhibition efficiency increases with increasing inhibitor concentration. The optimum value of inhibition efficiency was 90% at a caffeine concentration of 0.1 mmol/l. This suggests that caffeine's performance as a corrosion inhibitor is more effective at a concentration of 0.1 mmol/l.

  10. Numerical Simulation of Tensile Behavior of Corroded Aluminum Alloy 2024 T3 Considering the Hydrogen Embrittlement

    Directory of Open Access Journals (Sweden)

    Marina C. Vasco

    2018-01-01

    Full Text Available A multi-scale modeling approach for simulating the tensile behavior of the corroded aluminum alloy 2024 T3 was developed, accounting for both the geometrical features of corrosion damage and the effect of corrosion-induced hydrogen embrittlement (HE. The approach combines two Finite Element (FE models: a model of a three-dimensional Representative Unit Cell (RUC, representing an exfoliated area and its correspondent hydrogen embrittled zone (HEZ, and a model of the tensile specimen. The models lie at the micro- and macro-scales, respectively. The characteristics of the HEZ are determined from measurements of nanoindentation hardness, conducted on pre-corroded specimens. Using the model of the RUC, the local homogenized mechanical behavior of the corroded material is simulated. Then, the behavior of the exfoliated areas is assigned into different areas (elements of the tensile specimen and final analyses are performed to simulate the tensile behavior of the corroded material. The approach was applied to model specimens after 8, 16 and 24 h exposure periods of the Exfoliation Corrosion (EXCO test. For validation of the approach, tensile tests were used. The numerical results show that this approach is suitable for accurately simulating the tensile behavior of pre-corroded experimental specimens, accounting for both geometrical features of corrosion damage and corrosion-induced HE.

  11. Carbonate anion controlled growth of LiCoPO4/C nanorods and its improved electrochemical behavior

    International Nuclear Information System (INIS)

    Gangulibabu; Nallathamby, Kalaiselvi; Meyrick, Danielle; Minakshi, Manickam

    2013-01-01

    Highlights: ► Carbonate anion controlled growth of LiCoPO 4 nanorods has been prepared. ► Mixture of H 2 CO 3 + (NH 4 ) 2 CO 3 increases the CO 3 2− concentration and acts as an effective growth inhibitor. ► Heating the carbonate rich precursor in an inert atmosphere produces a Co 2 P phase that is conductive. ► Addition of super P carbon resulted in an amorphous carbon coating on LiCoPO 4 particles. ► LiCoPO 4 /C nanorods with a co-existence of Co 2 P exhibit excellent discharge capacity with retention on multiple cycling. -- Abstract: LiCoPO 4 /C nanocomposite with growth controlled by carbonate anions was synthesized via a unique solid-state fusion method. Carbonate anions in the form of H 2 CO 3 or a mixture of H 2 CO 3 + (NH 4 ) 2 CO 3 have been used as a growth inhibiting modifier to produce morphology controlled lithium cobalt phosphate. The presence of cobalt phosphide (Co 2 P) as a second phase improved the conductivity and electrochemical properties of the parent LiCoPO 4. The formation of Co 2 P is found to be achievable only in an inert atmosphere. Super P ® carbon (10 wt.%) provided an adherent carbon coating on pristine LiCoPO 4 resulting in the LiCoPO 4 /C composite cathode. This electrode exhibited enhanced electrochemical properties: capacity of 123 mAh g −1 with excellent capacity retention of 89% after 30 cycles, and reasonable rate capability of up to 5 C rate. The synergistic effect of carbonate anions and formation of Co 2 P under inert atmosphere has influenced the electrochemical behavior of LiCoPO 4 /C cathode through controlling the morphology and increasing the conductivity

  12. Electrochemical behavior of nanostructured MnO2/C (Vulcan® composite in aqueous electrolyte LiNO3

    Directory of Open Access Journals (Sweden)

    Vujković Milica

    2011-01-01

    Full Text Available The electrolytic solutions of contemporary Li-ion batteries are made exclusively with the organic solvents since anodic materials of these batteries have potentials with greater negativity than the potential of the water reduction, thus the organic electrolytes can withstand the voltages of 3-5 V that are characteristic for these batteries. Ever since it was discovered that some materials can electrochemically intercalate and deintercalate Li+ ions in aqueous solutions, numerous studies have been conducted with the aim of extending operational time of the aqueous Li-ion batteries. Manganese oxide has been studied as the electrode material in rechargeable lithium-ion batteries with organic electrolytes. In this paper its electrochemical behavior as an anode material in aqueous electrolyte solutions was examined. MnO2 as a component of nanodispersed MnO2/C (Vulcan® composite was successfully synthesized hydrothermally. Electrochemical properties of this material were investigated in aqueous saturated LiNO3 solution by both cyclic voltammetry and galvanostatic charging/discharging (LiMn2O4 as cathode material techniques. The obtained composite shows a relatively good initial discharge capacity of 96.5 mAh/g which, after 50th charging/discharging cycles, drops to the value of 57mAh/g. MnO2/C (Vulcan® composite, in combination with LiMn2O4 as a cathode material, shows better discharge capacity compared to other anodic materials used in aqueous Li-ion batteries according to certain studies that have been conducted. Its good reversibility and cyclability, and the fact that hydrothermal method is simple and effective, makes MnO2/C(Vulcan® composite a promising anodic material for aqueous Li-ion batteries.

  13. Microstructure, Surface Characterization, and Electrochemical Behavior of New Ti-Zr-Ta-Ag Alloy in Simulated Human Electrolyte

    Science.gov (United States)

    Vasilescu, Cora; Drob, Silviu Iulian; Osiceanu, Petre; Moreno, Jose Maria Calderon; Prodana, Mariana; Ionita, Daniela; Demetrescu, Ioana; Marcu, Maria; Popovici, Ion Alexandru; Vasilescu, Ecaterina

    2017-01-01

    A new Ti-20Zr-5Ta-2Ag alloy was elaborated and characterized regarding its microstructure, its native passive film composition and thickness, its surface wettability, its electrochemical behavior in Ringer solution of different pH values, and its ion release. The new alloy has a bi-phase, α + β, acicular, homogeneous microstructure (scanning electron microscopy (SEM)). Its native passive film (12-nm thicknesses) consists of the protective TiO2, ZrO2, and Ta2O5 oxides, Ti and Ta suboxides, and metallic Ag (X-ray photoelectron spectroscopy (XPS) data). The alloy possesses high hydrophilic properties. The main electrochemical parameters of the new alloy are superior to those of Ti as a result of the beneficial influence of Zr, Ta, and Ag alloying elements, which reinforce its native passive film. Electrochemical impedance spectroscopy (EIS) spectra in Ringer solutions for the new alloy displayed better values of impedances and phase angles, proving a more insulate passive film than that on the Ti surface. The main corrosion parameters for the new Ti-20Zr-5Ta-2Ag alloy are more favorable by about 25 to 38 times than those of Ti, confirming extremely resistant passive film. The new Ti-20Zr-5Ta-2Ag alloy releases into Ringer solution low quantities of Ti4+, Zr4+ metallic ions (inductively coupled plasma-mass spectroscopy (ICP-MS)). The Ag+ ions are released in low quantity, conferring to this alloy's low antibacterial activity. All experimental results show that the new Ti-20Zr-5Ta-2Ag alloy fulfills the requirements for biocompatibility, corrosion resistance, and antibacterial protection.

  14. Effects of Ce, La and Ba addition on the electrochemical behavior of super duplex stainless steels

    International Nuclear Information System (INIS)

    Yoo, Yun-Ha; Choi, Yoon-Seok; Kim, Jung-Gu; Park, Yong-Soo

    2010-01-01

    The effects of rare earth metal (REM: Ce, La) and Ba addition on aqueous corrosion properties of super duplex stainless steels (SDSS) were investigated by electrochemical tests and surface analyses. The results of potentiodynamic test indicated that the passive range increased by the addition of Ce, La, and Ba, indicating increased relative resistance to localized corrosion. The EIS measurements showed that the Ce-La-Ba-bearing alloys exhibited higher R ct and R p values than the Ce-La-Ba-free alloy at the passive and breakdown states. Furthermore, the additions of REMs and Ba together promoted the formation of dense chromium-enriched passive film.

  15. Research on Electrochemical Behavior of Ti-Ir-Ru Anode Coating in Electrolytic Antifouling of Flowing Brine

    Science.gov (United States)

    Liang, Chenghao; Huang, Naibao

    2009-11-01

    By electrochemical techniques, the electrochemical behavior of Ti-Ir-Ru anode coating was studied in electrolytic antifouling of flowing brine. The effect of the brine’s flow rate and the anode/cathode interval on electrolysis was also considered. The results indicated that the brine’s flow rate had remarkable effect on the characteristic of the Ti-Ir-Ru anode. The electrolytic voltage and the evolved active chlorine concentration of Ti-Ir-Ru anode increased with increasing flow rate. Its energy consumption displayed the same variable rule as the electrolytic voltage. But the current density reduced with increasing flow rate. Increasing flow rate favored attenuation of the thickness of mass-transfer control layer and expediting the oxygen’s mass transfer, which accelerated the cathode polarization and the oxygen absorption reaction. The maximal current efficiency for Ti-Ir-Ru anode was obtained at the anode/cathode interval of 5 cm with the current density of 60 mA/cm2. At this point, Ti-Ir-Ru anode also had relatively low electrolytic voltage. The above operating procedure was ideal for electrolyzing flowing brine using Ti-Ir-Ru anode coating.

  16. Corrosion Behavior of Surface-Treated Implant Ti-6Al-4V by Electrochemical Polarization and Impedance Studies

    Science.gov (United States)

    Paul, Subir; Yadav, Kasturi

    2011-04-01

    Implant materials for orthopedic and heart surgical services demand a better corrosion resistance material than the presently used titanium alloys, where protective oxide layer breaks down on a prolonged stay in aqueous physiological human body, giving rise to localized corrosion of pitting, crevice, and fretting corrosion. A few surface treatments on Ti alloy, in the form of anodization, passivation, and thermal oxidation, followed by soaking in Hank solution have been found to be very effective in bringing down the corrosion rate as well as producing high corrosion resistance surface film as reflected from electrochemical polarization, cyclic polarization, and Electrochemical Impedance Spectroscopy (EIS) studies. The XRD study revealed the presence of various types of oxides along with anatase and rutile on the surface, giving rise to high corrosion resistance film. While surface treatment of passivation and thermal oxidation could reduce the corrosion rate by 1/5th, anodization in 0.3 M phosphoric acid at 16 V versus stainless steel cathode drastically brought down the corrosion rate by less than ten times. The mechanism of corrosion behavior and formation of different surface films is better understood from the determination of EIS parameters derived from the best-fit equivalent circuit.

  17. Electrochemical oxidation behavior of hydrochlorothiazide on a glassy carbon electrode and its voltammetric determination in pharmaceutical formulations and biological fluids

    Directory of Open Access Journals (Sweden)

    Ali F. Alghamdi

    2014-09-01

    Full Text Available The electrochemical oxidation behavior of hydrochlorothiazide (HCT on a glassy carbon as a working electrode was investigated in Britton–Robinson (B–R buffer pH 3, by using anodic stripping voltammetry (ASV and cyclic voltammetry (CV. This drug gave a well-defined voltammetric oxidation peak at + 1200 mV versus an Ag/AgCl reference electrode. The electrochemical oxidation process was shown to be irreversible and diffusion controlled, with adsorption characterized over the entire pH range. The optimized conditions, such as accumulation time and potential, scan rate, frequency, pulse amplitude, varying of working electrodes, and instrumental parameters were studied. The calibration graph for HCT was obtained from 4 × 10−6 to 4 × 10−5 M (correlation coefficient = 0.997 using the developed electroanalytical method (ASV. The detection limit of this drug was 4.3 × 10−9 M. ASV and CV techniques with adequate precision and accuracy have been developed and applied for direct determination of HCT in commercial tablets without separation or extraction procedures and biological fluids such as urine and plasma.

  18. Electrochemical behavior and biological response of Mesenchymal Stem Cells on cp-Ti after N-ions implantation

    Science.gov (United States)

    Rizwan, M.; Ahmad, A.; Deen, K. M.; Haider, W.

    2014-11-01

    Titanium and its alloys are most widely used as implant materials due to their excellent biocompatibility, mechanical properties and chemical stability. In this study Nitrogen ions of known dosage were implanted over cp-Ti by Pelletron accelerator with beam energy of 0.25 MeV.The atomic force microscopy of bare and nitrogen implanted specimens confirmed increase in surface roughness with increase in nitrogen ions concentration. X-ray diffraction patterns of ions implanted surfaces validated the formation of TiN0.3 and Ti3N2-xnitride phases. The tendency to form passive film and electrochemical behavior of these surfaces in ringer lactate (RL) solution was evaluated by Potentiodynamic polarization and electrochemical impedance spectroscopy respectively. It is proved that nitrogen ions implantation was beneficial to reduce corrosion rate and stabilizing passive film by increasing charge transfer resistance in RL. It was concluded that morphology and proliferation of Mesenchymal Stem Cells on nitrogen ions implanted surfaces strongly depends on surface roughness and nitride phases.

  19. Role of polymeric binders on mechanical behavior and cracking resistance of silicon composite electrodes during electrochemical cycling

    Science.gov (United States)

    Li, Dawei; Wang, Yikai; Hu, Jiazhi; Lu, Bo; Dang, Dingying; Zhang, Junqian; Cheng, Yang-Tse

    2018-05-01

    This work focuses on understanding the role of various binders, including sodium alginate (SA), Nafion, and polyvinylidene fluoride (PVDF), on the mechanical behavior and cracking resistance of silicon composite electrodes during electrochemical cycling. In situ curvature measurement of bilayer electrodes, consisting of a silicon-binder-carbon black composite layer on a copper foil, is used to determine the effects of binders on bending deformation, elastic modulus, and stress on the composite electrodes. It is found that the lithiation induced curvature and the modulus of the silicon/SA electrodes are larger than those of electrodes with Nafion and PVDF as binders. Although the modulus of Nafion is smaller than that of PVDF, the curvature and the modulus of silicon/Nafion composite are larger than those of silicon/PVDF electrodes. The moduli of all three composites decrease not only during lithiation but also during delithiation. Based on the measured stress and scanning electron microscopy observations of cracking in the composite electrodes, we conclude that the stress required to crack the composite electrodes with SA and Nafion binders is considerably higher than that of the silicon/PVDF electrode during electrochemical cycling. Thus, the cracking resistance of silicon/SA and silicon/Nafion composite electrodes is higher than that of silicon/PVDF electrodes.

  20. Effects of Ni-5%RExOy Composite Additives on Electrochemical Hydrogen Storage Performances of Mg2Ni

    Directory of Open Access Journals (Sweden)

    ZHANG Guo-fang

    2017-11-01

    Full Text Available The Ni-5%RExOy (CeO2, La2O3, Eu2O3 as composite additives, Mg2Ni-Ni-5%RExOy composites were prepared by the ball milling method. The effects of different additives on the structure, morphology, electrochemistry and kinetic properties of Mg2Ni alloy were studied systematically. The results show that composite additives can improve the proportion of amorphous and nanocrystalline structure of Mg2Ni alloy. The particle size is homogeneous but the agglomeration is observed in the sample with Ni-5%CeO2 additives. The composites with additives show higher maximum discharge capacity and better cycle stabilities. All of these three kinds of composite additives can improve the kinetic properties of the composites effectively, including optimizing the charge-transfer ability, the reversibility of the electrochemical reaction on the alloy surface, and enhancing the diffusion coefficients of H atoms in the bulk of alloy. Among these three kinds of additives, Ni-5%CeO2 additive shows the best catalysis effect on promoting the kinetic properties of the composites.

  1. Thermodynamic and structural study of the Zr-Ni-Cr ternary system (Zr<50 at%) and of its equilibria with hydrogen: electrochemical application; Etude thermodynamique et structurale du systeme ternaire Zr-Ni-Cr (Zr<50at%) et de ses equilibres avec l`hydrogene: application electrochimique

    Energy Technology Data Exchange (ETDEWEB)

    Joubert, J.M.

    1995-07-12

    In the frame of the research on intermetallic compounds for nickel-hydride battery application, attention is focused on AB{sub 2} alloys so called Laves phases. ZrCr{sub 2}, for example, exhibits a large hydrogen capacity but a too low hydride formation equilibrium pressure for practical application. Moreover, the electrolyte (concentrated potassium hydroxide) involves surface passivation through blocking electrochemical mechanisms. First, the study is devoted to the adjustment of the hydride thermodynamic properties regarded to electrochemical application. This was achieved on ZrCr{sub 2} by substitution of chromium by nickel. In a second part surface properties are modified by the precipitation of secondary phases in equilibrium with the Laves phase. The Zr-Ni-Cr phase diagram has been determined at 1000 deg C in the ZrCr{sub 2}-ZrNi-Ni-Cr region and has revealed large solubility of nickel in C14 and C15 Laves phases as well as equilibrium of these phases with three Zr-Ni intermetallic compounds. The knowledge of this diagram has allowed the synthesis of biphasic alloys where the Laves phase of constant composition is in equilibrium with a secondary phase at variable rate. The study of hydrogenation properties of Laves phases has shown the possibility of adjusting the equilibrium pressure of its hydrides to electrochemical application keeping high hydrogen capacity. The hydrogenation properties of secondary phases were also characterized. Finally, it appeared that secondary phases precipitation with increasing rate in the Laves phase matrix produces a spectacular increase of electrochemical capacities. Such an effect of hydrogen by the modification of the surface in contact with electrolyte and by the diffusion of hydrogen from electrolyte to the Laves through the secondary phase when present. (author)

  2. Peroxide induced volatile and non-volatile switching behavior in ZnO-based electrochemical metallization memory cell.

    Science.gov (United States)

    Simanjuntak, Firman Mangasa; Chandrasekaran, Sridhar; Pattanayak, Bhaskar; Lin, Chun-Chieh; Tseng, Tseung-Yuen

    2017-09-20

    We explore the use of cubic-zinc peroxide (ZnO 2 ) as a switching material for electrochemical metallization memory (ECM) cell. The ZnO 2 was synthesized with a simple peroxide surface treatment. Devices made without surface treatment exhibits a high leakage current due to the self-doped nature of the hexagonal-ZnO material. Thus, its switching behavior can only be observed when a very high current compliance is employed. The synthetic ZnO 2 layer provides a sufficient resistivity to the Cu/ZnO 2 /ZnO/ITO devices. The high resistivity of ZnO 2 encourages the formation of a conducting bridge to activate the switching behavior at a lower operation current. Volatile and non-volatile switching behaviors with sufficient endurance and an adequate memory window are observed in the surface-treated devices. The room temperature retention of more than 10 4 s confirms the non-volatility behavior of the devices. In addition, our proposed device structure is able to work at a lower operation current among other reported ZnO-based ECM cells.

  3. Influence of hydrogen on metals behavior. 1 - Mechanical behavior of Ti 6 pc Al 6 pc V 2 pc Sn titanium alloy versus hydrogen: influence of heat treatment and of oxygen content

    International Nuclear Information System (INIS)

    Schaller, Bernard

    1972-01-01

    The mechanical behavior of Ti 6 pc Al 6 pc V Sn alloy during dynamic testing has been investigated versus hydrogen and oxygen content. The hydrogen susceptibility depends only slightly on its microstructure, acicular or equi-axed: it depends much more on conditions of hydrogen contamination and on the thermal history afterward. When the alloy has been stabilized by annealing in α - β and provided hydrogen absorption does not induce phase transformations, hydrogen sensitivity is relatively low: brittleness occurs suddenly but at a high concentration threshold (2000 ppm H), which coincides with hydrogen saturation of β phase. When the alloy includes unstabilized phases, its response to hydrogen changes whether it has been finally annealed or not, in the 300 - 500 C temperature area, prone to ω phase formation. In the absence of such an annealing, a reduction in ductility only occurs at high concentrations (> 1500 ppm H). In the other and, after annealing at 400 C, alloy hardening and a ductility decrease start even at the lowest hydrogen amounts: then hydrogen susceptibility is very high. Low oxygen concentration (up to 2000 ppm) do not sensibly affect the good hydrogen tolerance of this alloy. Beyond 2500 ppm, oxygen, while improving tensile strength, yet severely decreases ductility. [fr

  4. Influence of Pore Characteristics on Electrochemical and Biological Behavior of Ti Foams

    Science.gov (United States)

    Salehi, Akram; Barzegar, Faezeh; Amini Mashhadi, Hossein; Nokhasteh, Samira; Abravi, Mohammad Sadegh

    2017-08-01

    This study reports on titanium (Ti) foams produced using the powder metallurgy technique. During the investigation, the cross-sectional area and perimeter distributions of the pores within the foam were measured. Metallographic image processing analysis software combined with scanning electron microscopic images demonstrated that the pore size and circularity were affected by varying the volume percentage of the space-holder material. The corrosion resistance was investigated using electrochemical impedance spectroscopy and cyclic polarization tests. MG-63 osteoblast-like cells were used to study the biocompatibility and to evaluate the cell attachment, viability, and alkaline phosphatase activity. Analytical results indicated that 50 and 60 vol.% samples were suitable for biomedical applications. Because of the high degree of interconnectivity in the 60 and 70% porosity samples, the electrochemical parameters produced similar results. The corrosion rate of the porous samples showed that the amount of dissolved Ti was at an acceptable level that can be ejected by the body. Applying a fluoridated hydroxyapatite coating significantly increased the osteoblast cell functions on the porous surface.

  5. Mass transfer behavior of rotating square cylinder electrochemical reactor in relation to wastewater treatment

    International Nuclear Information System (INIS)

    Abdel-Aziz, M.S.M.; El-Shazly, A.H.; Farag, H.A.; Sedahmed, G.H.

    2011-01-01

    Highlights: → The work explores a new electrochemical reactor by using square rotating cylinders. → The results show that it is superior to the traditional circular rotating cylinder. → A dimensionless design equation for the new reactor was correlated. → The oxalic acid removal by the new reactor was succeeded and found promising. → The energy consumption per kg oxalic acid removed by the unit was calculated. - Abstract: Rates of mass transfer at a rotating square cylinder were measured by an electrochemical technique which involved measuring the limiting current of the cathodic reduction of K 3 Fe(CN) 6 in a large excess of NaOH solution. Variables studied were: cylinder rotation speed, physical properties of the solution and cylinder equivalent diameter. The data for the condition 1577 0.33 Re 0.45 For a given set of conditions the rate of mass transfer at the square rotating cylinder was found to be higher than that at the traditional circular rotating cylinder by an amount ranging from 47% to 200% depending on Re. The use of the square rotating cylinder electrode in removing oxalic acid from wastewater by anodic oxidation on Pb/PbO anode was examined and found to be promising.

  6. Synthesis and characterization of nanocrystalline vanadium oxide thin films: electrochemical behavior by annealing in different atmosphere

    Science.gov (United States)

    Asiabar, M. Amiri; Mohaghegh, Z.; Ghodsi, F. E.

    2018-01-01

    Nanocrystalline vanadium oxide thin films were prepared using sol-gel dip-coating technique. The effect of heat treatment in different environment including air, N2, Ar, and O2 gas on the structural, optical, electrical, and electrochemical properties of nanocrystalline vanadium oxide thin films were investigated. The results indicated that the calculated average crystallite size was reduced by annealing in Ar environment. Scanning electron microscopy (SEM) images showed layered morphology on the surface of the film annealed in air atmosphere, whereas the film annealed under Ar and N2 ambient revealed granular and wrinkle morphology, respectively. This morphology altered to rather smooth surface by annealing in O2 environment. The optical bandgap of the films were found to be 1.75, 1.84, 2.08, and 2.10 eV annealed in air, O2, N2, and Ar environment, respectively. It was observed that the films annealed under Ar and N2 ambient had low resistivity ( 0.2 Ω cm) and high carrier concentration, while the film annealed in nitrogen environment showed higher mobility of charge carrier. The electrochemical measurements showed that annealing under N2 ambient improved the intercalation of Li ions, leading a higher interfacial capacitance of 19.18 mF Cm-2, and decreased the charge transfer resistance due to surface defects created by heat treatment in nitrogen environment.

  7. Adherence and electrochemical behavior of calcium titanate coatings onto 304 stainless steel substrate

    Energy Technology Data Exchange (ETDEWEB)

    Esguerra A, J.; Aguilar, Y. [Universidad del Valle, Escuela de Ingenieria de Materiales, TPMR, Calle 13 No. 100-00, A. A. 25360 Cali (Colombia); Aperador, W. [Escuela Colombiana de Ingenieria Julio Garavito, Escuela de Ingenieria Mecanica, AK 45 No. 205-59 (Autopista Norte), A. A. 14520 Bogota (Colombia); Alba de Sanchez, N. [Universidad Autonoma de Occidente, Grupo de Investigacion en Ciencia e Ingenieria de Materiales, Calle 25 No. 115-85, A. A. 2790 Cali (Colombia); Bolanos P, G.; Rincon, C., E-mail: johanna.esguerra@univalle.edu.co [Universidad del Cauca, Departamento de Fisica, Laboratorio de Fisica de Bajas Temperaturas, Calle 5 No. 4-70, A. A. 996 Popayan (Colombia)

    2014-07-01

    Calcium titanate has been proposed as a coating for biomedical applications but it has not been reported characterization of adhesion failure mechanisms or electrochemical properties in time. In this work have been studied these properties of a calcium titanate coating growth onto AISI 304 steel deposited by r.f. magnetron sputtering. It was found that the coating has a critical adhesive load of 6.53 ± 0.14 N. With respect to its electrochemical properties potentiodynamic polarization curves show that the calcium titanate coating provides protection to AISI 304 steel. However. EIS indicates that even though metal dissolution occur through the pores in the coating, this leads to the precipitation of salts that block pores; this precipitates layer acts like and additional barrier to the metal dissolution in the system. The coatings deposition was carried out via magnetron sputtering during 4 hours at 500 grades C. The crystal structure of the films was determined by using glancing incident X-ray diffraction. The chemical composition of deposited films was performed by impedance dispersive X-ray spectroscopy (EDX) in the scanning electron microscopy (Jeol JSM-649 OLV Sem), and the grain size and the roughness was obtained using an atomic force microscopy from Asylum Research MFP-3D using a cantilever silicon tip in non-contact mode and calculated by scanning probe image processor. (Author)

  8. Experimental and analytical analysis of polarization and water transport behaviors of hydrogen alkaline membrane fuel cell

    Science.gov (United States)

    Huo, Sen; Zhou, Jiaxun; Wang, Tianyou; Chen, Rui; Jiao, Kui

    2018-04-01

    Experimental test and analytical modeling are conducted to investigate the operating behavior of an alkaline electrolyte membrane (AEM) fuel cell fed by H2/air (or O2) and explore the effect of various operating pressures on the water transfer mechanism. According to the experimental test, the cell performance is greatly improved through increasing the operating pressure gradient from anode to cathode which leads to significant liquid water permeation through the membrane. The high frequency resistance of the A901 alkaline membrane is observed to be relatively stable as the operating pressure varies based on the electrochemical impedance spectroscopy (EIS) method. Correspondingly, based on the modeling prediction, the averaged water content in the membrane electrode assembly (MEA) does not change too much which leads to the weak variation of membrane ohmic resistance. This reveals that the performance enhancement should give the credit to better electro-chemical reaction kinetics for both the anode and cathode, also prone by the EIS results. The reversion of water back diffusion direction across the membrane is also observed through analytical solution.

  9. Effect of hydrogen on transformation characteristics and deformation behavior in a Ti-Ni shape memory alloy

    International Nuclear Information System (INIS)

    Hoshiya, Taiji; Ando, Hiroei; Den, Shoji; Katsuta, Hiroshi.

    1992-01-01

    Transformation characteristics and deformation behavior of hydrogenated Ti-50.5 at% Ni alloys, which were occluded in a low pressure range of hydrogen between 1.1 and 78.5 kPa, have been studied by electrical resistivity measurement, tensile test, X-ray diffraction analysis and microstructural observation. M S temperature of the Ti-Ni alloys decreased with an increase in hydrogen content. This corresponds to the stabilization of the parent phase during cooling, which was confirmed by X-ray diffraction: The suppression effect of hydrogen takes place on the martensitic transformation. Critical stress for slip deformation of hydrogenated Ti-Ni alloys changed with hydrogen content and thus hydrogen had a major influence on deformation behavior of those alloys. With hydrogen contents above 0.032 mol%, hardening was distinguished from softening which was pronounced in the contents from 0 to 0.032 mol% H. Hydrides were formed in hydrogen contents over 1.9 mol%. The hydride formation results in the reorientation in variants of the R phase and increase in the lattice strains of the parent phase. (author)

  10. Effect of incorporation of fly ash and granulated blast furnace in the electrochemical behavior of concretes of commercial cement

    International Nuclear Information System (INIS)

    Gutierrez-Junco, O. J.; Pineda-Triana, Y.; Vera-Lopez, E.

    2015-01-01

    This paper presents the findings of the research properties evaluation pastes of commercial cement (CPC), mixed with fly ash (FA) and granulated blast furnace slag (GBFS). Initially, the sample of 30 combinations were evaluated in terms of compressive strength to establish the optimal proportions from raw material. After that, four optimized blends were characterized during the setting and hardening process. Electrochemical tests were performed on concrete cylinders samples prepared with cementitious materials and a structural steel rod placed in the center of the specimen. With the objective to evaluate the performance before corrosion, thermodynamic and kinetic aspects were taken into consideration. The findings showed that commercial cements blended with fly ash and blast furnace slag as the ones used in this research presents a decreased behavior in mechanical and corrosion strength regarding to CPC. (Author)

  11. The Electrochemical Behavior of Mo-Ta Alloy in Phosphoric Acid Solution for TFT-LCD Application.

    Science.gov (United States)

    Lee, Sang-Hyuk; Kim, Byoung O; Seo, Jong Hyun

    2015-10-01

    Molybdenum-tantalum alloy thin film is a suitable material for the higher corrosion resistance and low resistivity for gate and data metal lines. In this study, Mo-Ta alloy thin films were prepared by using a DC magnetron co-sputtering system on a glass substrate. An abrupt increase in the etching rates of low Mo-Ta alloys was observed. From the observed impedance analysis, the defect densities in the MoTa oxide films increased from 5.4 x 10(21) (cm(-3)) to 8.02 x 10(21) (cm(-3)) up to the 6 at% of tantalum level; and above the 6 at% of tantalum level, the defect densities decreased. This electrochemical behavior is explained by the mechanical instability of the MoTa oxide film.

  12. Study of the behavior of explosimeters in an atmosphere of air and hydrogen

    International Nuclear Information System (INIS)

    Perilhon, Pierre; Garnier, Gilbert.

    1976-04-01

    A study of some types of explosion-meters in the presence of air-hydrogen mixtures is described. The behavior of the instruments was studied under various environmental conditions: high and low temperatures, air current, presence of poisons in the gas, concentration well above the LIE. A technical notice was established for each instrument. A chapter is devoted to a reliability study on the instruments tested under actual working conditions (reproduction of a laboratory cell with ventilation, false ceiling and simulation of hydrogen leaks). Another chapter deals with the explosion-meter network set up on the Grenoble Centre. Some accidents avoided by this equipment are mentioned in conclusion, illustrating the validity of such a set-up [fr

  13. Electrochemical reduction behavior of U3O8 powder in a LiCl molten salt

    International Nuclear Information System (INIS)

    Jeong, Sang Mun; Shin, Ho-Sup; Hong, Sun-Seok; Hur, Jin-Mok; Do, Jae Bum; Lee, Han Soo

    2010-01-01

    The reduction path of the U 3 O 8 powder vol-oxidized at 1200 deg. C has been determined by a series of electrochemical experiments in a 1 wt.% Li 2 O/LiCl molten salt. Various reaction intermediates are observed by during electrolysis of U 3 O 8 . The formation of the metallic uranium is caused from two different reduction paths, a direct reduction of uranium oxide and an electro-lithiothermic reduction. As the uranium oxide is converted to the metallic uranium, the lithium metal is more actively formed in the cathode basket. The reducibility of the rare earth oxides with the U 3 O 8 powder has been tested by constant voltage electrolysis. The results suggest the advanced vol-oxidation could lead to the enhancement in the reducibility of the rare earth fission products.

  14. Electrochemical behavior of boron in LiF-NaF-KF- melts

    DEFF Research Database (Denmark)

    Polyakova, L.P.; Bukatova, G.A.; Polyakova, E.G.

    1996-01-01

    The electrochemical reduction of B(III) to B(0) in KBF4-LiF-NaF-KF melts has been studied by voltammetric and chronopotentiometric methods, Glassy carbon, Pt, and Ag were used as working electrode materials. Only in the case of Ag was the reduction not complicated by interaction between boron...... and the electrode material. On a silver electrode B(III) was reduced to B(0) in a single irreversible step in the KBF4 concentration range up to 5.7 x 10(-2) mole percent (m/o). The cathodic half-wave potential was -1.34 V us, an Ag/AgCl reference electrode at 700 degrees C. The diffusion coefficient of BF4- at 700...

  15. Effect of zinc crystals size on galvanized steel deformation and electrochemical behavior

    Directory of Open Access Journals (Sweden)

    José Daniel Culcasi

    2009-09-01

    Full Text Available Hot-dip galvanized steel sheets with different spangle sizes were deformed by means of rolling and tension. The change of preferential crystallographic orientation and of superficial characteristics due to the deformation was analyzed by means of both X-rays diffraction and optical and scanning electronic microscopy. A correlation between such changes and the involving deformation modes was intended to be done and the spangle size influence on these modes was studied. Coating reactivity change due to the deformation was investigated by means of quasi-steady DC electrochemical tests. The results allow to infer that, in great spangle samples, the main deformation mechanism is twinning whereas in small spangle ones, pyramidal slip systems happen as well. The increase of the reactivity with the deformation is greater in tension than in rolling and it is more important in small than in great spangle samples.

  16. Hydrogen evolution behavior in the corrosion of carbon steel in contact with magnetite

    International Nuclear Information System (INIS)

    Taniguchi, Naoki; Kawakami, Susumu; Tateishi, Tsuyoshi; Fukudome, Kazuyuki; Nishimura, Tsutomu

    2005-07-01

    It has been reported that the corrosion of carbon steel is accelerated by a contact with magnetite, which is a representative corrosion product in low oxygen environment. It is important to clarify the corrosion mechanism in the presence of magnetite for long term prediction of overpack corrosion. There are two possible cathodic reactions in the presence of magnetite coupled with anodic reaction. One is reduction of Fe(III) in magnetite, and the other is hydrogen evolution reaction. If the former dominates the cathodic reaction, corrosion acceleration will stop with the consumption of Fe(III). While, if the latter is the main cathodic reaction, corrosion acceleration is possible to continue for a long time. In this study, corrosion rate and hydrogen evolution behavior were investigated by the immersion test of carbon steel in contact with dummy corrosion product to contribute to understanding the corrosion mechanism. The immersion tests of carbon steel were carried out in sealed glass ampoule in the presence of dummy corrosion product with changing the Fe(III)/Fe(II) ratio. The corrosion rates increased with increase in Fe(III)/Fe(II) ratio, and rapid acceleration was observed when Fe(III)/Fe(II) ratio over stoichiometrical value of magnetite(=2). The hydrogen evolution reaction was not influenced by Fe(III)/Fe(II) although its rate was larger that without dummy corrosion product. According to the results, the cause of severe corrosion acceleration due to magnetite is inferred to be the oxidation by excessive Fe(III) in the magnetite. It was also indicated that corrosion acceleration by a factor of several times is possible to occur when Fe(III)/Fe(II) ratio in magnetite is 2 or less, and the hydrogen evolution reaction dominates the cathodic reaction. The hydrogen evolution rate and its change with time of carbon steel in contact with high purity magnetite without excessive Fe(III) were measured. As a result, the hydrogen evolution reaction was accelerated up to

  17. Electrochemical behavior and biological response of Mesenchymal Stem Cells on cp-Ti after N-ions implantation

    Energy Technology Data Exchange (ETDEWEB)

    Rizwan, M.; Ahmad, A. [Department of Metallurgical and Materials Engineering, University of Engineering and Technology, 54890 Lahore (Pakistan); Deen, K.M. [Corrosion Control Research Cell, Department of Metallurgy and Materials Engineering, CEET, University of the Punjab, 54590 Lahore (Pakistan); Haider, W., E-mail: haiderw@utpa.edu [Mechanical Engineering Department, University of Texas Pan American, Edinburg, TX 78539 (United States)

    2014-11-30

    Highlights: • Nitrogen ions of known dosage were implanted on cp-Ti. • Increase in surface roughness with increase in ions dose was confirmed by AFM. • TiN{sub 0.3} and Ti{sub 3}N{sub 2−x} nitride phases were formed and validated by XRD. • The ions implantation reduced the corrosion rate and stabilized the passive film. • Surface roughness greatly affected the morphology and growth of Mesenchymal Stem Cells. - Abstract: Titanium and its alloys are most widely used as implant materials due to their excellent biocompatibility, mechanical properties and chemical stability. In this study Nitrogen ions of known dosage were implanted over cp-Ti by Pelletron accelerator with beam energy of 0.25 MeV.The atomic force microscopy of bare and nitrogen implanted specimens confirmed increase in surface roughness with increase in nitrogen ions concentration. X-ray diffraction patterns of ions implanted surfaces validated the formation of TiN{sub 0.3} and Ti{sub 3}N{sub 2-x}nitride phases. The tendency to form passive film and electrochemical behavior of these surfaces in ringer lactate (RL) solution was evaluated by Potentiodynamic polarization and electrochemical impedance spectroscopy respectively. It is proved that nitrogen ions implantation was beneficial to reduce corrosion rate and stabilizing passive film by increasing charge transfer resistance in RL. It was concluded that morphology and proliferation of Mesenchymal Stem Cells on nitrogen ions implanted surfaces strongly depends on surface roughness and nitride phases.

  18. ELECTROCHEMICAL BEHAVIOUR AND VOLTAMMETRIC ...

    African Journals Online (AJOL)

    The electrochemical behaviour of Geshoidin was investigated at a glassy carbon electrode in mixtures of citric acid and di-sodium hydrogen orthophosphate aqueous buffer system over a wide pH range (pH 2-11) using cyclic voltammetry. Chemically irreversible single oxidation and reduction peaks were obtained in the ...

  19. The influence of hydrogen on the deformation behavior of zircaloy 4

    International Nuclear Information System (INIS)

    Flanagan, M. E.; Koss, D. A.; Motta, A. T.

    2008-01-01

    The deformation behavior of Zr based cladding forms a basis for fuel behavior codes and affects failure criteria; as such, it is critical to reactor safety. The present study examines the influence of hydrogen on the uniaxial deformation behavior of hydrided cold worked and stress relieved Zircaloy 4 plate material. Specimens of various orientations (i.e., stress axis aligned with the rolling direction, the transverse direction, or normal to the plate surface direction) were tested in compression at a range of temperatures (25 .deg. , 300 .deg. , and 400 .deg. C), and strain rates (from 10-4/s to 10-1/s). Contrasting the deformation behavior of the material containing ∼45 wt ppm H with that of the material containing ∼420 wt. ppm H shows that increasing H content (a) causes a small decrease in the 0.2% yield stress that is eliminated at 1.0% flow stress, (b) increases the strain hardening in the rolling direction but not in the other orientations, (c) has no effect on the temperature dependence of the strain hardening, and (d) does not affect the strain rate hardening behavior. Increasing H content also has no observable effect on the high degree of plastic anisotropy of this plate material which is manifested in difficult through thickness deformation, resulting in high flow stresses for specimens oriented in the normal to plate surface direction

  20. Effects of Anion Mobility on Electrochemical Behaviors of Lithium–Sulfur Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Han, Kee Sung; Chen, Junzheng; Cao, Ruiguo; Rajput, Nav Nidhi; Murugesan, Vijayakumar; Shi, Lili; Pan, Huilin; Zhang, Jiguang; Liu, Jun; Persson, Kristin A.; Mueller, Karl T.

    2017-10-27

    The electrolyte is a crucial component of lithium-sulfur (Li-S) batteries, as it controls polysulfide dissolution, charge shuttling processes, and solid-electrolyte interphase (SEI) layer formation. Experimentally, the overall performance of Li-S batteries varies with choice of solvent system and Li-salt used in the electrolyte, and a lack of predictive understanding about the effects of individual electrolyte components inhibits the rational design of electrolytes for Li-S batteries. Here we analyze the role of the counter anions of common Li salts (such as TfO-, FSI-, TFSI-, and TDI-) when dissolved in DOL/DME (1:1 vol.) for use in Li-S batteries. The evolution of ion-ion and ion-solvent interactions due to vari-ous anions was analyzed using 17O NMR and pulsed-field gradient (PFG) NMR and then correlated with electrochemi-cal performance in Li-S cells. These data reveal that the for-mation of the passivation layer on the anode and the loss of active materials from the cathode (evidenced by polysulfide dissolution) are related to anion mobility and affinity with lithium polysulfide, respectively. For future electrolyte de-sign, anions with lower mobility and weaker interactions with lithium polysulfides may be superior candidates for increasing the long-term stability of Li-S batteries.

  1. Stability, electrochemical behaviors and electronic structures of iron hydroxyl-phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Wang Zhongli; Sun Shaorui; Li Fan; Chen Ge [College of Environmental and Energy Engineering, Beijing University of Technology, Pingleyuan 100, Chaoyang District, Beijing 100022 (China); Xia Dingguo, E-mail: dgxia@bjut.edu.cn [College of Environmental and Energy Engineering, Beijing University of Technology, Pingleyuan 100, Chaoyang District, Beijing 100022 (China); Zhao Ting; Chu Wangsheng [Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); University of Science and Technology of China, Hefei 230026 (China); Wu Ziyu, E-mail: wuzy@ihep.ac.cn [Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); University of Science and Technology of China, Hefei 230026 (China)

    2010-09-01

    Iron hydroxyl-phosphate with a uniform spherical particle size of around 1 {mu}m, a compound of the type Fe{sub 2-y}{open_square}{sub y}(PO{sub 4})(OH){sub 3-3y}(H{sub 2}O){sub 3y-2} (where {open_square} represents a vacancy), has been synthesized by hydrothermal methods. The particles are composed of spheres of diameter <100 nm. The compound exhibits good electrochemical performance, with reversible capacities of around 150 mAh g{sup -1} and 120 mAh g{sup -1} at current densities of 170 mA g{sup -1} and 680 mA g{sup -1}, respectively. The stability of crystal structure of this material was studied by TGA and XRD which show that the material remains stable at least up to the temperature 200 deg. C. Investigation of the electronic structure of the iron hydroxyl-phosphate by GGA + U calculation has indicated that it has a better electronic conductivity than LiFePO{sub 4}.

  2. The electrochemical behavior of steel in concrete and how to evaluate the corrosion rate

    Energy Technology Data Exchange (ETDEWEB)

    Videm, K. [Univ. of Oslo (Norway). Centre for Materials Research; Myrdal, R. [Rescon AS, Sagstua (Norway)

    1996-11-01

    Various electrochemical methods for evaluation of corrosion of steel reinforcement in concrete have been studied and reviewed regarding applicability in the field. Laboratory experiments have been carried out with steel in synthetic pore water and in concrete blocks with chloride additions. The field measurements were performed at a large concrete bridge on the coast. The methods examined are manual potential mapping, automatic measurements of the corrosion potential with embedded reference electrodes, potentiokinetic linear polarization resistance (LPR) measurements with cut reinforcement bars, analysis of the shape of galvanostatic charging curves, and LPR measurements of the reinforcement with a commercial instrument containing a guard ring. The corrosion rates determined with the guard electrode instrument were not in good agreement with estimates based on potential mapping and with result of visual inspection. Due to the high interfacial capacitance of the steel in concrete, potentiokinetic LPR measurements were found to be little suited for determination of the corrosion rate. Good experience was obtained by computer modelling of the galvanostatic charging curve with calculation of the polarization resistance from this type of data. The important advantage of this method is that it is little influenced by the electrical resistance in the concrete and that unreliable measurements can be sorted out when the curves do not follow the theoretical pattern.

  3. Electrochemical behavior of steel in concrete and evaluation of the corrosion rate

    Energy Technology Data Exchange (ETDEWEB)

    Videm, K. [Univ. of Oslo (Norway). Centre for Materials Science; Myrdal, R. [Rescon AS, Sagstua (Norway)

    1997-09-01

    Various electrochemical methods for evaluation of corrosion of steel reinforcement in concrete were studied regarding their applicability in the field. Laboratory experiments were carried out with steel in synthetic pore water and in concrete blocks with chloride (Cl{sup {minus}}) additions. Field measurements were performed at a large, coastal concrete bridge. Methods examined included manual potential mapping, automatic measurements of corrosion potential (E{sub corr}) with embedded reference electrodes (RE), potentiokinetic linear polarization resistance (LPR) measurements with cut reinforcement bars, analysis of the shape of galvanostatic charging curves, and LPR measurements of the reinforcement with a commercial instrument containing a guard ring. Corrosion rates determined with the guard electrode (GE) instrument were not in good agreement with estimates based upon potential mapping or visual inspection. Because of the high interfacial capacitance (C) of the steel in concrete, potentiokinetic LPR measurements will ill-suited for determination of corrosion rates. Goo experience was obtained by computer modeling of the galvanostatic charging curve with calculation of the polarization resistance (R{sub p}) from this type of data. Advantages of this method were that it was influenced little by electrical resistance in the concrete and that unreliable measurements could be sorted out when curves did not follow the theoretical pattern.

  4. Electrochemical behavior of polypyrrole/chitosan composite coating on Ti metal for biomedical applications.

    Science.gov (United States)

    Rikhari, Bhavana; Pugal Mani, S; Rajendran, N

    2018-06-01

    In the present work, the corrosion resistance performance and biocompatibility of polypyrrole/chitosan (PPy/CHI) composite coated Ti was studied. The deposition of composite coating was carried out by electropolymerization method. The deposited PPy/CHI composite coatings were different in morphology, structural, surface roughness and wettability compared PPy coated Ti. The presence of composite coating was confirmed by solid 13 C NMR. The PPy/CHI composite coating showed enhanced microhardness and adhesion strength compared to the PPy coating. The corrosion protection ability of PPy/CHI composite coatings at various applied potentials was analyzed by dynamic electrochemical impedance spectroscopy (DEIS), exhibited higher impedance in all the potentials compared to uncoated and PPy coated Ti. The lower corrosion current density obtained for PPy/CHI-2 composite coating from polarization studies revealed increased corrosion protection ability in SBF solution. The stability of composite coating was confirmed by immersion studies. PPy/CHI-2 composite coating immersed in SBF solution enhances hydroxyapatite (HAp) formation. Copyright © 2018 Elsevier Ltd. All rights reserved.

  5. Dimeric Self-assembling via Hydrogen Bonding and Emissive Behavior of a New Copper (I Complex

    Directory of Open Access Journals (Sweden)

    Juciely M. dos Reis

    2017-04-01

    Full Text Available This work describes the synthesis, structural characterization and emissive behavior of a new copper (I complex based on 1-thiocarbamoyl-5-(4-methoxiphenyl-3-phenyl-4,5-dihydro-1H-pyrazole ligand. A dimeric self-assembling via hydrogen bonding was determined by analyzing the short contacts present in the solid-state structure by means of X-ray crystallography. The spectroscopic properties were determined using UV-Vis and fluorescence experiments and an interesting behavior as bluish luminescence was assigned mainly to the mixed (MLCT + IL electronic transitions of the Cu(Id10 ® (S=C–Nligand type. The complete characterization of the new copper (I complex also included elemental analyses and IR spectroscopy. DOI: http://dx.doi.org/10.17807/orbital.v9i1.952

  6. Electrochemical behavior of Ti and Ti6Al4V in aqueous solutions of citric acid containing halides

    Directory of Open Access Journals (Sweden)

    Anelise Marlene Schmidt

    2006-12-01

    Full Text Available This paper reports on an investigation of the electrochemical behavior of Ti grade 2 and Ti6Al4V alloy in aqueous citric acid solutions with pH 2.0 containing halide ions. Voltammetric studies of Ti and the alloy in citric acid, with and without chloride ions, indicate that the Ti and Ti alloy presented a passive behavior in the test solutions used. Pitting was observed at 3.0 and 2.5 V/SCE for Ti and Ti6Al4V, respectively, when bromide ions were added to the solution. In solutions containing fluoride ions, dissolution of the film occurred at potentials close to - 1.0 V/SCE in both electrodes. The iodide ions oxidized on the passive oxide film at potentials close to 1.0 V/SCE. EIS results of the materials in citric acid solutions containing chloride ions revealed that the film's resistance increased as the applied potential rose from 0 to 1.0 V. In bromide-containing solutions, breakdown of the film was confirmed at potentials above 2.0 V/SCE in both electrodes. These results suggest film reformation for Ti and the alloy in solutions containing fluoride at potentials within the passive region.

  7. Electrochemical and surface behavior of hydyroxyapatite/Ti film on nanotubular Ti-35Nb-xZr alloys

    International Nuclear Information System (INIS)

    Jeong, Yong-Hoon; Choe, Han-Cheol; Brantley, William A.

    2012-01-01

    In this paper, we investigated the electrochemical and surface behavior of hydroxyapatite (HA)/Ti films on the nanotubular Ti-35Nb-xZr alloy. The Ti-35Nb-xZr ternary alloys with 3-10 wt.% Zr content were made by an arc melting method. The nanotubular oxide layers were developed on the Ti-35Nb-xZr alloys by an anodic oxidation method in 1 M H 3 PO 4 electrolyte containing 0.8 wt% NaF at room temperature. The HA/Ti composite films on the nanotubular oxide surfaces were deposited by a magnetron sputtering method. Their surface characteristics were analyzed by field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS) and an X-ray diffractometer (XRD). The corrosion behavior of the specimens was examined through potentiodynamic and AC impedance tests in 0.9% NaCl solution. From the results, the Ti-35Nb-xZr alloys showed a solely β phase microstructure that resulted from the addition of Zr. The nanotubular structure formed with a diameter of about 200 nm, and the HA/Ti thin film was deposited on the nanotubular structure. The HA/Ti thin film-coated nanotubular Ti-35Nb-xZr alloys showed good corrosion resistance in 0.9% NaCl solution.

  8. Defect effect on tribological behavior of diamond-like carbon films deposited with hydrogen diluted benzene gas in aqueous environment

    Science.gov (United States)

    Yi, Jin Woo; Park, Se Jun; Moon, Myoung-Woon; Lee, Kwang-Ryeol; Kim, Seock-Sam

    2009-05-01

    This study examined the friction and wear behavior of diamond-like carbon (DLC) films deposited from a radio frequency glow discharge using a hydrogen diluted benzene gas mixture. The DLC films were deposited on Si (1 0 0) and polished stainless steel substrates by radio frequency plasma-assisted chemical vapor deposition (r.f.-PACVD) at hydrogen to benzene ratios, or the hydrogen dilution ratio, ranging from 0 to 2.0. The wear test was carried out in both ambient and aqueous environments using a homemade ball-on-disk type wear rig. The stability of the DLC coating in an aqueous environment was improved by diluting the benzene precursor gas with hydrogen, suggesting that hydrogen dilution during the deposition of DLC films suppressed the initiation of defects in the film and improved the adhesion of the coating to the interface.

  9. One-pot synthesis of MoS2/In2S3 ultrathin nanoflakes with mesh-shaped structure on indium tin oxide as photocathode for enhanced photo-and electrochemical hydrogen evolution reaction

    Science.gov (United States)

    Sun, Baoliang; Shan, Fei; Jiang, Xinxin; Ji, Jing; Wang, Feng

    2018-03-01

    A bifunctional MoS2/In2S3 hybrid composite that has both photo- and electrocatalytic activity toward hydrogen evolution reaction (HER) is prepared by a facile one pot hydrothermal method. The characterizations by scanning electron microscope (SEM), high resolution transmission electron microscope (HRTEM) and Photoluminescence (PL) shows that the MoS2/In2S3 hybrid exhibits ultrathin nanoflakes with mesh-shaped structure on transparent conductive substrates, and the as prepared catalyst composite obviously improves the separation of electro-hole pairs. The as prepared hybrid nanosheets with Mo:In of 1/2 integrate In-doped MoS2 to reduce the stacking and increase the active surface area. The novel mesh-shaped nanostructure with a moderate degree of disorder provides not only simultaneously intrinsic conductivity and defects but also higher electrochemically active surface area (ECSA). By electrochemical measurements, such as linear sweep voltammetry (LSV), electrochemical impedance spectroscope (EIS) and cyclic voltammetry (CV), we find that the MoS2/In2S3 hybrid possesses much better photo/electrochemical activity than pristine MoS2 or In2S3. MoS2/In2S3 ultrathin nanoflaks are anticipated to be a superior photoelectrocatalyst for PEC cells, and the rational use of the MoS2/In2S3 cathode offers a new avenue toward achieving effective photo-assistant electrocatalytic activity.

  10. An electrochemical study of the effect of Li on the corrosion behavior of Ni3Al intermetallic alloy in molten (Li + K) carbonate

    International Nuclear Information System (INIS)

    Gonzalez-Rodriguez, J.G.; Mejia, E.; Lucio-Garcia, M.A.; Salinas-Bravo, V.M.; Porcayo-Calderon, J.; Martinez-Villafane, A.

    2009-01-01

    A study of the effect of lithium content (1, 3 and 5 wt.%) and heat treatment (400 deg. C during 144 h) on the corrosion behavior of Ni 3 Al alloy has been carried out in a 62 mol.%Li 2 CO 3 -38 mol.%K 2 CO 3 mixture at 650 deg. C using electrochemical techniques. Employed electrochemical techniques included potentiodynamic polarization curves, linear polarization resistance, LPR, electrochemical impedance spectroscopy, EIS, and electrochemical noise, measurements EN. Results have shown that the alloys exhibited an active-passive behavior regardless of the heat treatment. For alloys without heat treatment, the most corrosion resistant was the Ni 3 Al base alloy, but when they were heat treated, the most corrosion resistant was the alloy containing 3%Li. EIS results showed that for short immersion tests, the corrosion process was under diffusion control, but for longer exposure times, the presence of a protective scale was evident. All the alloys were highly susceptible to a localized type of corrosion according to EN measurements and supported by SEM micrographs.

  11. An electrochemical study of the effect of Li on the corrosion behavior of Ni{sub 3}Al intermetallic alloy in molten (Li + K) carbonate

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez-Rodriguez, J.G. [Universidad Autonoma del Estado de Morelos, CIICAp, Av. Universidad 1001, Col. Chamilpa, 62209 Cuernavaca, Mor. (Mexico); Centro de Investigacion en Materiales Avanzados. S.C. Miguel de Cervantes 120, Complejo Industrial Chihuahua, Chih. (Mexico)], E-mail: ggonzalez@uaem.mx; Mejia, E. [Universidad Autonoma del Estado de Morelos, CIICAp, Av. Universidad 1001, Col. Chamilpa, 62209 Cuernavaca, Mor. (Mexico); Lucio-Garcia, M.A. [Centro de Investigacion en Materiales Avanzados. S.C. Miguel de Cervantes 120, Complejo Industrial Chihuahua, Chih. (Mexico); Salinas-Bravo, V.M.; Porcayo-Calderon, J. [Instituto de Inv. Electricas, Gerencia de Procesos Termicos, Reforma 108, Temixco, Mor. (Mexico); Martinez-Villafane, A. [Centro de Investigacion en Materiales Avanzados. S.C. Miguel de Cervantes 120, Complejo Industrial Chihuahua, Chih. (Mexico)

    2009-08-15

    A study of the effect of lithium content (1, 3 and 5 wt.%) and heat treatment (400 deg. C during 144 h) on the corrosion behavior of Ni{sub 3}Al alloy has been carried out in a 62 mol.%Li{sub 2}CO{sub 3}-38 mol.%K{sub 2}CO{sub 3} mixture at 650 deg. C using electrochemical techniques. Employed electrochemical techniques included potentiodynamic polarization curves, linear polarization resistance, LPR, electrochemical impedance spectroscopy, EIS, and electrochemical noise, measurements EN. Results have shown that the alloys exhibited an active-passive behavior regardless of the heat treatment. For alloys without heat treatment, the most corrosion resistant was the Ni{sub 3}Al base alloy, but when they were heat treated, the most corrosion resistant was the alloy containing 3%Li. EIS results showed that for short immersion tests, the corrosion process was under diffusion control, but for longer exposure times, the presence of a protective scale was evident. All the alloys were highly susceptible to a localized type of corrosion according to EN measurements and supported by SEM micrographs.

  12. Hydrogen electrosorption on TiHg alloy in acidic solution

    International Nuclear Information System (INIS)

    Jafarian, M.; Azizi, O.; Gobal, F.; Mahjani, M.G.

    2007-01-01

    Hydrogen evolution and electrosorption on/in TiHg alloy have been investigated in acidic solution using cyclic voltammetry, open circuit potential transient, steady-state polarization, chronopotentiometry and electrochemical impedance measurements. Comparison has been made with pure Ti. Cyclic voltammetry and open circuit potential measurements show that hydrogen absorption into the electrode material occurs during proton discharge. The steady-state polarization curves in the course of positive and negative potential scans illustrate that the formation of absorbed hydrogen slightly improves the electrocatalytic properties of the electrode. The hydrogen diffusion coefficient into the bulk of TiHg alloy was estimated as 1.24 x 10 -13 cm 2 s -1 from a chronoamperometry measurement and was compared with other materials. Finally, the electrochemical impedance spectroscopy was used to further characterize this electrode. The results show that this electrode displays porous behavior and may be well described by a serial combination of two parallel R-CPE circuit

  13. Hydrogen-Based Energy Conservation System, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — Sustainable Innovations is developing a technology for efficient separation and compression of hydrogen gas. The electrochemical hydrogen separator and compressor...

  14. Surface treatment influences electrochemical stability of cpTi exposed to mouthwashes

    Energy Technology Data Exchange (ETDEWEB)

    Beline, Thamara [Department of Prosthodontics and Periodontology, Piracicaba Dental School, University of Campinas (UNICAMP), Av Limeira, 901, Piracicaba, São Paulo 13414-903 (Brazil); IBTN/Br — Institute of Biomaterials, Tribocorrosion and Nanomedicine, Brazilian Branch (Brazil); Garcia, Camila S. [Department of Prosthodontics and Periodontology, Piracicaba Dental School, University of Campinas (UNICAMP), Av Limeira, 901, Piracicaba, São Paulo 13414-903 (Brazil); Ogawa, Erika S. [Department of Prosthodontics and Periodontology, Piracicaba Dental School, University of Campinas (UNICAMP), Av Limeira, 901, Piracicaba, São Paulo 13414-903 (Brazil); IBTN/Br — Institute of Biomaterials, Tribocorrosion and Nanomedicine, Brazilian Branch (Brazil); Marques, Isabella S.V. [Department of Prosthodontics and Periodontology, Piracicaba Dental School, University of Campinas (UNICAMP), Av Limeira, 901, Piracicaba, São Paulo 13414-903 (Brazil); Matos, Adaias O. [Department of Prosthodontics and Periodontology, Piracicaba Dental School, University of Campinas (UNICAMP), Av Limeira, 901, Piracicaba, São Paulo 13414-903 (Brazil); IBTN/Br — Institute of Biomaterials, Tribocorrosion and Nanomedicine, Brazilian Branch (Brazil); Sukotjo, Cortino [Department of Restorative Dentistry, University of Illinois at Chicago, College of Dentistry, 801 S Paulina, Chicago, IL 60612 (United States); IBTN — Institute of Biomaterials, Tribocorrosion and Nanomedicine (United States); Mathew, Mathew T. [IBTN — Institute of Biomaterials, Tribocorrosion and Nanomedicine (United States); Department of Orthopedic Surgery, Rush University Medical Center, 1611 W Harrison, Chicago, IL 60612 (United States); and others

    2016-02-01

    The role of surface treatment on the electrochemical behavior of commercially pure titanium (cpTi) exposed to mouthwashes was tested. Seventy-five disks were divided into 15 groups according to surface treatment (machined, sandblasted with Al{sub 2}O{sub 3}, and acid etched) and electrolyte solution (artificial saliva — control, 0.12% chlorhexidine digluconate, 0.05% cetylpyridinium chloride, 0.2% sodium fluoride, and 1.5% hydrogen peroxide) (n = 5). Open-circuit-potential and electrochemical impedance spectroscopy were conducted at baseline and after 7 and 14 days of immersion in each solution. Potentiodynamic test and total weight loss of disks were performed after 14 days of immersion. Scanning electron microscopy, energy dispersive spectroscopy, white light interferometry and profilometry were conducted for surface characterization before and after the electrochemical tests. Sandblasting promoted the lowest polarization resistance (R{sub p}) (P < .0001) and the highest capacitance (CPE) (P < .006), corrosion current density (I{sub corr}) and corrosion rate (P < .0001). In contrast, acid etching increased R{sub p} and reduced CPE, independent to the mouthwash; while hydrogen peroxide reduced R{sub p} (P < .008) and increased I{sub corr} and corrosion rate (P < .0001). The highest CPE values were found for hydrogen peroxide and 0.2% sodium fluoride. Immersion for longer period improved the electrochemical stability of cpTi (P < .05). In conclusion, acid etching enhanced the electrochemical stability of cpTi. Hydrogen peroxide and sodium fluoride reduced the resistance to corrosion of cpTi, independent to the surface treatment. Chlorhexidine gluconate and cetylpyridinium chloride did not alter the corrosive behavior of cpTi. - Highlights: • Acid etching enhanced the electrochemical stability of cpTi. • Hydrogen peroxide and sodium fluoride reduced the corrosion resistance of cpTi. • Chlorhexidine gluconate and cetylpyridinium chloride can be safely used.

  15. Surface treatment influences electrochemical stability of cpTi exposed to mouthwashes

    International Nuclear Information System (INIS)

    Beline, Thamara; Garcia, Camila S.; Ogawa, Erika S.; Marques, Isabella S.V.; Matos, Adaias O.; Sukotjo, Cortino; Mathew, Mathew T.

    2016-01-01

    The role of surface treatment on the electrochemical behavior of commercially pure titanium (cpTi) exposed to mouthwashes was tested. Seventy-five disks were divided into 15 groups according to surface treatment (machined, sandblasted with Al 2 O 3 , and acid etched) and electrolyte solution (artificial saliva — control, 0.12% chlorhexidine digluconate, 0.05% cetylpyridinium chloride, 0.2% sodium fluoride, and 1.5% hydrogen peroxide) (n = 5). Open-circuit-potential and electrochemical impedance spectroscopy were conducted at baseline and after 7 and 14 days of immersion in each solution. Potentiodynamic test and total weight loss of disks were performed after 14 days of immersion. Scanning electron microscopy, energy dispersive spectroscopy, white light interferometry and profilometry were conducted for surface characterization before and after the electrochemical tests. Sandblasting promoted the lowest polarization resistance (R p ) (P < .0001) and the highest capacitance (CPE) (P < .006), corrosion current density (I corr ) and corrosion rate (P < .0001). In contrast, acid etching increased R p and reduced CPE, independent to the mouthwash; while hydrogen peroxide reduced R p (P < .008) and increased I corr and corrosion rate (P < .0001). The highest CPE values were found for hydrogen peroxide and 0.2% sodium fluoride. Immersion for longer period improved the electrochemical stability of cpTi (P < .05). In conclusion, acid etching enhanced the electrochemical stability of cpTi. Hydrogen peroxide and sodium fluoride reduced the resistance to corrosion of cpTi, independent to the surface treatment. Chlorhexidine gluconate and cetylpyridinium chloride did not alter the corrosive behavior of cpTi. - Highlights: • Acid etching enhanced the electrochemical stability of cpTi. • Hydrogen peroxide and sodium fluoride reduced the corrosion resistance of cpTi. • Chlorhexidine gluconate and cetylpyridinium chloride can be safely used.

  16. 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.

  17. ELECTROCHEMICAL PROPERTIES AND ELECTROCHEMICAL ...

    African Journals Online (AJOL)

    Rct is about five times higher in acetonitrile relative to water. All these EIS results of the different types of PPy suggest a relation with the wettability of the polymer. KEY WORDS: Conducting polymers, Polypyrrole, Electrochemical impedance spectroscopy, Equivalent- electrical circuit, Micellar media. INTRODUCTION.

  18. Electrochemical and corrosion behavior of two chromium dental alloys in artificial bioenvironments

    Directory of Open Access Journals (Sweden)

    Banu Alexandra

    2017-01-01

    Full Text Available The purpose of this study is to compare the corrosion and tarnish behavior of NiCrMo and CoCrMo cast dental alloys in artificial bio environments. The cobalt chromium alloys are known and used in dentistry for many years, but its difficult machinability because of the strength and hardness, is an argument for scientists to study alternative materials with comparable biocompatibility. On the other hand, for dentistry devices beside corrosion behavior is important the aesthetic so, the used alloys have to preserve their shining and do not stain. The corrosion resistance has been evaluated using the Atomic mass spectroscopy method for ion release determination, the anodic polarization curves and the open circuit potential – time monitoring for corrosion behavior evaluation and optical microscopy for the structure analysis. The tarnish tendency of alloys was estimated using the method of cyclic immersion with frequency of 10 seconds for each minute during 72 hours in Na2S containing solution. The most important conclusion is that the alloys are comparable from corrosion and tarnish point of view, but we recommend to use the nickel base alloy only for orthodontic devices implanted for short periods of time, because of higher quantity of released ions.

  19. MRI-compatible Nb-60Ta-2Zr alloy for vascular stents: Electrochemical corrosion behavior in simulated plasma solution.

    Science.gov (United States)

    Li, Hui-Zhe; Zhao, Xu; Xu, Jian

    2015-11-01

    Using revised simulated body fluid (r-SBF), the electrochemical corrosion behavior of an Nb-60Ta-2Zr alloy for MRI compatible vascular stents was characterized in vitro. As indicated by XPS analysis, the surface passive oxide film of approximately 1.3nm thickness was identified as a mixture of Nb2O5, Ta2O5 and ZrO2 after immersion in the r-SBF. The Nb-60Ta-2Zr alloy manifests a low corrosion rate and high polarization resistance similar to pure Nb and Ta, as shown by the potentiodynamic polarization curves and EIS. Unlike 316L stainless steel and the L605 Co-Cr alloy, no localized corrosion has been detected. Semiconducting property of passive film on the Nb-60Ta-2Zr alloy was identified as the n-type, with growth mechanism of high-field controlled growth. The excellent corrosion resistance in simulated human blood enviroment renders the Nb-60Ta-2Zr alloy promising as stent candidate material. Copyright © 2015 Elsevier B.V. All rights reserved.

  20. Functional behavior of bio-electrochemical treatment system with increasing azo dye concentrations: Synergistic interactions of biocatalyst and electrode assembly.

    Science.gov (United States)

    Sreelatha, S; Velvizhi, G; Naresh Kumar, A; Venkata Mohan, S

    2016-08-01

    Treatment of dye bearing wastewater through biological machinery is particularly challenging due to its recalcitrant and inhibitory nature. In this study, functional behavior and treatment efficiency of bio-electrochemical treatment (BET) system was evaluated with increasing azo dye concentrations (100, 200, 300 and 500mg dye/l). Maximum dye removal was observed at 300mg dye/l (75%) followed by 200mg dye/l (65%), 100mg dye/l (62%) and 500mg dye/l (58%). Concurrent increment in dye load resulted in enhanced azo reductase and dehydrogenase activities respectively (300mg dye/l: 39.6U; 4.96μg/ml). Derivatives of cyclic voltammograms also supported the involvement of various membrane bound redox shuttlers, viz., cytochrome-c, cytochrome-bc1 and flavoproteins during the electron transfer. Bacterial respiration during BET operation utilized various electron acceptors such as electrodes and dye intermediates with simultaneous bioelectricity generation. This study illustrates the synergistic interaction of biocatalyst with electrode assembly for efficient treatment of azo dye wastewater. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Novel thiourea derivative and its complexes: Synthesis, characterization, DFT computations, thermal and electrochemical behavior, antioxidant and antitumor activities

    Science.gov (United States)

    Yeşilkaynak, Tuncay; Muslu, Harun; Özpınar, Celal; Emen, Fatih Mehmet; Demirdöğen, Ruken Esra; Külcü, Nevzat

    2017-08-01

    A novel thiourea derivative, N-((2-chloropyridin-3-yl)carbamothioyl) thiophene-2-carboxamide,C11H8ClN3OS2 (HL) and its Co(II), Ni(II) and Cu(II) complexes (ML2 type) were prepared and characterized by elemental analysis, FT-IR,1H NMR and HR-MS methods. The crystal structure of HL was also investigated by single crystal X-ray diffraction study. The HL crystallizes in the orthorhombic crystal system with P 21 21 21 space group, Z = 4, a = 3.8875(3) Å, b = 14.6442(13) Å, c = 21.8950(19) Å. The [ML2] complex structures were optimized by using B97D/TZVP level. Molecular orbitals of HL ligand were calculated at the same level. Thermal and electrochemical behaviors of the complexes were investigated. Anticancer and antioxidant activities of the complexes were also investigated. Antioxidant activities were determined by using DPPH (2,2-diphenyl-1-picrylhydrazyl) and ABTS (2,2‧-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) assays. Anticancer activities were studied via MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay in MCF-7 (Michigan Cancer Foundation-7) breast cancer cells.

  2. Large-field behavior of the LoSurdo-Stark resonances in atomic hydrogen

    Energy Technology Data Exchange (ETDEWEB)

    Alvarez, G. (Departamento de Fisica Teorica, Facultad de Ciencias Fisicas, Universidad Complutense, 28040 Madrid (Spain)); Silverstone, H.J. (Department of Chemistry, The Johns Hopkins University, Baltimore, Maryland 21218 (United States))

    1994-12-01

    The Schroedinger equation for atomic hydrogen in a large electric field [ital F] is solved by separation in parabolic coordinates. As [ital F][r arrow][infinity], the scaled field [ital f] that enters the separated equations tends to 0. Thus the large-[ital F] asymptotics depend on the small-[ital f] behavior of the separated equations, each of which in turn is equivalent to a quarticly perturbed two-dimensional anharmonic oscillator. The Bender-Wu branch cuts of the oscillator play a major role in the hydrogen asymptotics. A simple iterative algorithm permits the calculation of the branch points at which two eigenvalues coincide. We have found numerically that, as [ital F][r arrow][infinity], the separation constant [beta][sub 1] returns to the smaller of the unperturbed values [beta][sub 1][sup (0)] or [beta][sub 2][sup (0)]. At the same time, [beta][sub 2] tends to the negative of the smaller value. As the real electric field [ital F] increases from 0 to [infinity], in each case that [beta][sub 1][sup (0)] and [beta][sub 2][sup (0)] are not equal, the trajectory of either [ital f] or [ital e][sup [minus][ital i][pi

  3. Electrical properties and degradation behavior of hydrogenated amorphous Si alloys for solar cells

    Science.gov (United States)

    Krühler, W.; Kusian, W.; Karg, F.; Pfleiderer, H.

    1986-12-01

    The electrical properties and the degradation behavior of hydrogenated amorphous silicon alloys (a-Si1- x A x : H, with A=C, Ge, B, P) in designs of pin, pip, nin, and MOS structures are investigated by measuring the dark and light I(V) characteristics and the spectral response as well as the space-charge-limited current (SCLC), the time of flight (TOF) of carriers and the field effect (FE). These investigations give an overview of our recent work combined with new results emphasizing the physics of the a-Si:H pin solar cells. We discuss the stabilizing influence on the degradation behavior achieved by profiling the i layers of the pin solar cells with P and B. Two kinds of pin solar cells, namely glass/SnO2/p(C)in/metal and glass/metal/pin/ITO, are investigated and an explanation of their different spectral response behavior is given. SCLC measurements lead to the conclusion that trapping is also involved in the degradation mechanism, as is recombination. TOF experiments on a-Si1- x Ge x : H pin diodes indicate that the incorporation of Ge widens the tail-state distribution below the conduction band. FE measurements showed densities of gap states of about 5×l016cm-3eV-1.

  4. Electrochemical Characteristics of Layered Transition Metal Oxide Cathode Materials for Lithium Ion Batteries: Surface, Bulk Behavior, and Thermal Properties.

    Science.gov (United States)

    Tian, Chixia; Lin, Feng; Doeff, Marca M

    2018-01-16

    Layered lithium transition metal oxides, in particular, NMCs (LiNi x Co y Mn z O 2 ) represent a family of prominent lithium ion battery cathode materials with the potential to increase energy densities and lifetime, reduce costs, and improve safety for electric vehicles and grid storage. Our work has focused on various strategies to improve performance and to understand the limitations to these strategies, which include altering compositions, utilizing cation substitutions, and charging to higher than usual potentials in cells. Understanding the effects of these strategies on surface and bulk behavior and correlating structure-performance relationships advance our understanding of NMC materials. This also provides information relevant to the efficacy of various approaches toward ensuring reliable operation of these materials in batteries intended for demanding traction and grid storage applications. In this Account, we start by comparing NMCs to the isostructural LiCoO 2 cathode, which is widely used in consumer batteries. Effects of changing the metal content (Ni, Mn, Co) upon structure and performance of NMCs are briefly discussed. Our early work on the effects of partial substitution of Al, Fe, and Ti for Co on the electrochemical and bulk structural properties is then covered. The original aim of this work was to reduce the Co content (and thus the raw materials cost) and to determine the effect of the substitutions on the electrochemical and bulk structural properties. More recently, we have turned to the application of synchrotron and advanced microscopy techniques to understand both bulk and surface characteristics of the NMCs. Via nanoscale-to-macroscale spectroscopy and atomically resolved imaging techniques, we were able to determine that the surfaces of NMC undergo heterogeneous reconstruction from a layered structure to rock salt under a variety of conditions. Interestingly, formation of rock salt also occurs under abuse conditions. The surface

  5. A study on the hydrogen behavior and its mitigation in the APR1400 containment during a severe accident

    International Nuclear Information System (INIS)

    Kim, Jong Tae; Hong, Seong Wan; Park, Rae Joon; Kim, Sang Baik

    2005-02-01

    During a hypothetical severe accident in a nuclear power plant (NPP), hydrogen is generated by the active reaction of fuel-cladding and steam in the reactor pressure vessel and released with steam into the containment. In this study, the analysis of the hydrogen and steam behavior during selected severe accidents in the APR1400 containment has been conducted by using the GASFLOW code. For the SBLOCA, hydrogen was accumulated in the containment dome region quickly when only PARSs were used. When the igniters were turned on, a standing flame was formed around a coolant pump and burnt most of the hydrogen blown-out. For the TLOFW accident, the flap-type pressure damper installed at the IRWST vents strongly affected the flow structure of the hydrogen. And by the steam-rich and oxygen starvation conditions in the IRWST, DDT is not likely to occur. For the SBO accident, dry hydrogen was release in the IRWST by the assumption of full condensation of the released steam in the IRWST water. In this case, the possibility of flame acceleration is high in the IRWST and annular compartment. In this study two design modifications were proposed in view of the hydrogen mitigation strategy and their effectiveness was evaluated by the GASFLOW analysis

  6. Reversible swelling-shrinking behavior of hydrogen-bonded free-standing thin film stabilized by catechol reaction.

    Science.gov (United States)

    Sun, Jiaxing; Su, Chao; Zhang, Xuejian; Yin, Wenjing; Xu, Jian; Yang, Shuguang

    2015-05-12

    Dopamine-modified poly(acrylic acid) (PAA-dopa) and poly(vinylpyrrolidone) (PVPON) was layer-by-layer (LbL) assembled to prepare thin film based on hydrogen bonding. The carboxylic group of acrylic acid and the phenolic hydroxyl group of dopamine can both act as hydrogen bond donors. The critical assembly and the critical disintegration pH values of PVPON/PAA-dopa film are enhanced compared with PVPON/PAA film. The hydrogen-bonded PVPON/PAA-dopa thin film can be cross-linked via catechol chemistry of dopamine. After cross-linking, the film can be exfoliated from the substrate in alkaline solution to get a free-standing film. Moreover, by tuning the pH value, deprotonation and protonation of PAA will make the hydrogen bond in the film break and reconstruct, which induces that the free-standing film has a reversible swelling-shrinking behavior.

  7. Effects of molybdenum dithiocarbamate and zinc dialkyl dithiophosphate additives on tribological behaviors of hydrogenated diamond-like carbon coatings

    International Nuclear Information System (INIS)

    Yue, Wen; Liu, Chunyue; Fu, Zhiqiang; Wang, Chengbiao; Huang, Haipeng; Liu, Jiajun

    2014-01-01

    Highlights: • For MoDTC, DLC coating showed better anti-friction and worse anti-wear behaviors. • The improved anti-friction property was due to graphitization and MoS 2 . • Formation of MoO x resulted in a high wear volume. • For ZDDP, DLC coating showed the best anti-wear and the worst anti-friction behaviors. • Absence of friction reducing product and graphitized layer resulted in a higher friction. - Abstract: The tribological behaviors of hydrogenated diamond-like carbon (DLC) coatings under varied load conditions lubricated with polyalpha olefin (PAO), molybdenum dithiocarbamate (MoDTC) and zinc dialkyl dithiophosphate (ZDDP) additives were investigated in this paper. Hydrogenated DLC coatings were synthesized through the decomposition of acetylene by the ion source. The tribological performances were measured on a SRV tribometer. The morphologies and chemical structures of the DLC coatings were investigated by the scanning electron microscope (SEM), Raman spectrometer (Raman) and X-ray photoelectron spectroscope (XPS). It was shown that the low friction and high wear were achieved on the hydrogenated DLC coating under MoDTC lubrication, while low wear was found on the hydrogenated DLC coating lubricated by ZDDP. The primary reason was attributed to different tribofilms formed on the contact area and the formation of graphitic layer. Both factors working together leaded to quite different tribological behaviors

  8. Investigations on Microstructure and Corrosion behavior of Superalloy 686 weldments by Electrochemical Corrosion Technique

    Science.gov (United States)

    Arulmurugan, B.; Manikandan, M.

    2018-02-01

    In the present study, microstructure and the corrosion behavior of Nickel based superalloy 686 and its weld joints has been investigated by synthetic sea water environment. The weldments were fabricated by Gas Tungsten Arc Welding (GTAW) and Pulsed Current Gas Tungsten Arc Welding (PCGTAW) techniques with autogenous mode and three different filler wires (ERNiCrMo-4, ERNiCrMo-10 and ERNiCrMo-14). Microstructure and Scanning electron microscope examination was carried out to evaluate the structural changes in the fusion zones of different weldments. Energy Dispersive X-ray Spectroscopy (EDS) analysis was carried out to evaluate the microsegregation of alloying elements in the different weld joints. Potentiodynamic polarization study was experimented on the base metal and weld joints in the synthetic sea water environment to evaluate the corrosion rate. Tafel’s interpolation technique was used to obtain the corrosion rate. The microstructure examination revealed that the fine equiaxed dendrites were observed in the pulsed current mode. EDS analysis shows the absence of microsegregation in the current pulsing technique. The corrosion rates of weldments are compared with the base metal. The results show that the fine microstructure with the absence of microsegregation in the PCGTA weldments shows improved corrosion resistance compared to the GTAW. Autogenous PCGTAW shows higher corrosion resistance irrespective of all weldments employed in the present study.

  9. Electrochemical behavior of meso-substituted iron porphyrins in alkaline aqueous media

    Science.gov (United States)

    Berezina, N. M.; Bazanov, M. I.; Maksimova, A. A.; Semeikin, A. S.

    2017-12-01

    The effect meso-substitution in iron porphyrin complexes has on their redox behavior in alkaline aqueous solutions is studied via cyclic voltammetry. The voltammetric features of the reduction of iron pyridylporphyrins suggest that the sites of electron transfer lie at the ligand, the metal ion, and the pyridyl moieties. The electron transfer reactions between the different forms of these compounds, including the oxygen reduction reaction they mediate, are outlined to show the sequence and potential ranges in which they occur in alkaline aqueous media. Under our experimental conditions, the iron porphyrins exist as μ-oxo dimmers whose activity for the electrocatalytic reduction of oxygen displays a considerable dependence on the nature of the substitutents and nitrogen isomerization (for pyridylporphyrins) and grows in the order (Fe( ms-Ph)4P)2O, (Fe[ ms-(Py-3)Ph3]P)2O, (Fe[ ms-(Py-4)4]P)2O, and (Fe[ ms-(Py-3)4]P)2O.

  10. Effect of fluorination treatment on electrochemical properties of M1Ni{sub 3.5}Co{sub 0.6}Mn{sub 0.4}Al{sub 0.5} hydrogen storage alloy

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Hongxia, E-mail: hhxhunan@yahoo.com.cn [College of Chemistry and Bioengineering, Guilin University of Technology, Guilin (China); Huang, Kelong [College of Chemistry and Chemical Engineering, Central South University (China)

    2012-05-15

    The influence of surface treatment by solutions of NH{sub 4}F, LiF and LiF containing KBH{sub 4} on the structure and electrochemical properties of the M1Ni{sub 3.5}Co{sub 0.6}Mn{sub 0.4}Al{sub 0.5} hydrogen storage alloy (in which M1 denotes mischmetal) is investigated. The fluorination treatment improves the electrochemical performances of the M1Ni{sub 3.5}Co{sub 0.6}Mn{sub 0.4}Al{sub 0.5} alloy. The maximum discharge capacity (C{sub max}) increases from 314.8 to 325.7 (NH{sub 4}F), 326.5 (LiF) and 316.4 mAh g{sup -1} (LiF+KBH{sub 4}). After 60 cycles, the capacity retention rate increases from 83.5 to 84.8% (NH{sub 4}F), 89.5% (LiF) and 93.9% (LiF+KBH{sub 4}). The results of the linear polarization and anodic polarization reveal that the exchange current density (I{sub 0}) and the limiting current density (I{sub L}) increase after fluorination treatment, indicating an improvement of the kinetics of the hydrogen absorption/desorption. (author)

  11. Electrochemical behavior and localized corrosion of X65 steel in high salt concentration brines with CO2 saturated

    Science.gov (United States)

    Sun, Jianbo; Yang, Liying; Liu, Wei; Lu, Minxu

    2018-02-01

    The electrochemical characteristics and localized corrosion of X65 steel were investigated in CO2-saturated brines as a function of salt concentration employing electrochemical techniques and immersion tests. The results show that, as salt concentration increases, the corrosion mechanism changes from electrochemical steps control to the mixed control of mass transfer and electrochemical steps. The higher the salt concentration is, the more obvious the mass transfer control will be. The corrosion rate firstly increases and then decreases with salt content. There is a maximum corrosion rate somewhere between 60 and 120 g l‑1 salt content. The salting-out effect may play a crucial role in steel corrosion in CO2-bearing systems with higher salt concentrations. Chloride ions account for the decrease of the surface layer thickness and make them non-adherent, thereby promoting the initiation and development of localized corrosion at salt concentration above 120 g l‑1.

  12. Effect of surface modification by nitrogen ion implantation on the electrochemical and cellular behaviors of super-elastic NiTi shape memory alloy.

    Science.gov (United States)

    Maleki-Ghaleh, H; Khalil-Allafi, J; Sadeghpour-Motlagh, M; Shakeri, M S; Masoudfar, S; Farrokhi, A; Beygi Khosrowshahi, Y; Nadernezhad, A; Siadati, M H; Javidi, M; Shakiba, M; Aghaie, E

    2014-12-01

    The aim of this investigation was to enhance the biological behavior of NiTi shape memory alloy while preserving its super-elastic behavior in order to facilitate its compatibility for application in human body. The surfaces of NiTi samples were bombarded by three different nitrogen doses. Small-angle X-ray diffraction was employed for evaluating the generated phases on the bombarded surfaces. The electrochemical behaviors of the bare and surface-modified NiTi samples were studied in simulated body fluid (SBF) using electrochemical impedance and potentio-dynamic polarization tests. Ni ion release during a 2-month period of service in the SBF environment was evaluated using atomic absorption spectrometry. The cellular behavior of nitrogen-modified samples was studied using fibroblast cells. Furthermore, the effect of surface modification on super-elasticity was investigated by tensile test. The results showed the improvement of both corrosion and biological behaviors of the modified NiTi samples. However, no significant change in the super-elasticity was observed. Samples modified at 1.4E18 ion cm(-2) showed the highest corrosion resistance and the lowest Ni ion release.

  13. On the behavior of reduced graphene oxide based electrodes coated with dispersed platinum by alternate current methods in the electrochemical degradation of reactive dyes.

    Science.gov (United States)

    Del Río, A I; García, C; Molina, J; Fernández, J; Bonastre, J; Cases, F

    2017-09-01

    The electrochemical behavior of different carbon-based electrodes with and without nanoparticles of platinum electrochemically dispersed on their surface has been studied. Among others, reduced graphene oxide based electrodes was used to determine the best conditions for the decolorization/degradation of the reactive dye C.I. Reactive Orange 4 in sulfuric medium. Firstly, the electrochemical behavior was evaluated by cyclic voltammetry. Secondly, different electrolyses were performed using two cell configurations: cell with anodic and cathodic compartments separated (divided configuration) and without any separation (undivided configuration). The best results were obtained when reduced graphene oxide based anodes were used. The degree of decolorization was monitored by spectroscopic methods and high performance liquid chromatography. It was found that all of them followed pseudo-first order kinetics. When reduced graphene oxide-based electrodes coated with dispersed platinum by alternate current methods electrodes were used, the lowest energy consumption and the higher decolorization kinetics rate were obtained. Scanning Electronic Microscopy was used to observe the morphological surface differences. Copyright © 2017 Elsevier Ltd. All rights reserved.

  14. Properties and electrochemical behaviors of AuPt alloys prepared by direct-current electrodeposition for lithium air batteries

    International Nuclear Information System (INIS)

    Zhang, Jinqiu; Li, Da; Zhu, Yiming; Chen, Miaomiao; An, Maozhong; Yang, Peixia; Wang, Peng

    2015-01-01

    AuPt catalyst has a prospective application in a lithium air battery because of its bi-function on catalyzing Oxygen Reduction Reaction (ORR) and Oxygen Evolution Reaction (OER). Electrodeposition is an in-situ convenient technology for catalyst preparation without chemical residue. In an acid electrolyte, AuPt alloy catalysts were electrodeposited on carbon paper. The effect of main salt concentration, electrodeposition time and current density were studied by deposit micromorphology observation, structure analyses and composition testing. Catalytic abilities of AuPt alloys were measured by cyclic voltammetry (CV) in an ionic liquid of EMI-TFSI/Li-TFSI [1- Ethyl - 3- methylimidazolium–bis (trifluoromethanesulphonyl) imide/lithium–bis (trifluoromethanesulphonyl) imide]. The electrochemical behaviors of Au, Pt and AuPt deposits were also measured. An optimized direct-current electrodeposition process of getting high active AuPt catalyst is concluded, which is an aqueous solution containing 6.7∼10 mmol · L −1 HAuCl 4 , 10∼13.3 mmol · L −1 H 2 PtCl 6 and 0.5 mol · L −1 H 2 SO 4 as the electrolyte, current density of 20mA · cm −2 and electrodeposition time of 8∼34 s. The co-deposition of AuPt alloy is an irregular co-deposition controlled by diffusion, while gold atoms enter the platinum’s crystal lattice in the structure of AuPt alloy. The increase of the concentration of H 2 PtCl 6 in the electrolyte, the extension of the electrodeposition time or the raise of the current density can improve the content of Pt in the deposit. The clusters’ diameters of AuPt catalysts decrease to 150∼250 nm by adjusting current densities during electrodeposition

  15. A study of hydrogen environment effects on microstructure property behavior of NASA-23 alloy and related alloy systems

    International Nuclear Information System (INIS)

    Diwan, R.M.

    1990-01-01

    The influence of hydrogen on the tensile properties and ductility behavior of NASA-23 alloy were analyzed. NASA-23 and other referenced alloys in cast and hipped conditions were solution treated and aged under selected conditions and characterized using optical metallography, scanning electron microscopy, and electron microprobe analysis techniques. The yield strength of NASA-23 is not affected much by hydrogen under tensile tests carried at 5000 psig conditions; however, the ultimate strength and ductility properties are degraded. This implies that the physical mechanisms operating would be related to the plastic deformation process. The fracture surfaces characteristics of NASA-23 specimens tensile tested in hydrogen, helium, and air were also analyzed. These revealed surface cracks around specimen periphery with the fracture surface showing a combination of intergranular and transgranular modes of fracture. It is seen that the specimens charged in hydrogen seem to favor a more brittle fracture mode in comparison to air and helium charged specimens. The AMCC casting characterization program is to be analyzed for their hydrogen behavior. As a result of this program, the basic microstructural factors and fracture characteristics in some cases were analyzed

  16. A study of hydrogen environment effects on microstructure property behavior of NASA-23 alloy and related alloy systems

    Science.gov (United States)

    Diwan, Ravinder M.

    1990-01-01

    This work is part of the overall advanced main combustion chamber (AMCC) casting characterization program of the Materials and Processes Laboratory of the Marshall Space Flight Center. The influence of hydrogen on the tensile properties and ductility behavior of NASA-23 alloy were analyzed. NASA-23 and other referenced alloys in cast and hipped conditions were solution treated and aged under selected conditions and characterized using optical metallography, scanning electron microscopy, and electron microprobe analysis techniques. The yield strength of NASA-23 is not affected much by hydrogen under tensile tests carried at 5000 psig conditions; however, the ultimate strength and ductility properties are degraded. This implies that the physical mechanisms operating would be related to the plastic deformation process. The fracture surfaces characteristics of NASA-23 specimens tensile tested in hydrogen, helium, and air were also analyzed. These revealed surface cracks around specimen periphery with the fracture surface showing a combination of intergranular and transgranular modes of fracture. It is seen that the specimens charged in hydrogen seem to favor a more brittle fracture mode in comparison to air and helium charged specimens. The AMCC casting characterization program is to be analyzed for their hydrogen behavior. As a result of this program, the basic microstructural factors and fracture characteristics in some cases were analyzed.

  17. The effects to the structure and electrochemical behavior of zinc phosphate conversion coatings with ethanolamine on magnesium alloy AZ91D

    Energy Technology Data Exchange (ETDEWEB)

    Li Qing, E-mail: liqingswu@yeah.ne [School of Chemistry and Chemical Engineering, Southwest University, 1 Tiansheng Road, Beibei, Chongqing 400715 (China); Xu Shuqiang; Hu Junying; Zhang Shiyan; Zhong Xiankang [School of Chemistry and Chemical Engineering, Southwest University, 1 Tiansheng Road, Beibei, Chongqing 400715 (China); Yang Xiaokui [School of Materials Science and Engineering, Southwest University, Chongqing 400715 (China)

    2010-01-01

    This paper discussed a zinc phosphate conversion coating formed on magnesium alloy AZ91D from the phosphating bath with varying amounts of ethanolamine (MEA). The effects of MEA on the form, structure, phase composition and electrochemical behavior of the phosphate coatings were examined using an scanning electron microscopy (SEM), X-ray diffraction (XRD) potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS) measurements. Interpretations of the electrical elements of the equivalent circuit were obtained from the SEM structure of the coatings, assumed to be formed of two layers: an outer porous crystal layer and an inner flat amorphous layer. The result showed that adding MEA refined the microstructure of the crystal layer and that the phosphate coating, derived at the optimal content of 1.2 g/L, with the most uniform and compact outer crystal layer provided the best corrosion protection.

  18. Effect of pH Value on the Electrochemical and Stress Corrosion Cracking Behavior of X70 Pipeline Steel in the Dilute Bicarbonate Solutions

    Science.gov (United States)

    Cui, Z. Y.; Liu, Z. Y.; Wang, L. W.; Ma, H. C.; Du, C. W.; Li, X. G.; Wang, X.

    2015-11-01

    In this work, effects of pH value on the electrochemical and stress corrosion cracking (SCC) behavior of X70 pipeline steel in the dilute bicarbonate solutions were investigated using electrochemical measurements, slow strain rate tensile tests and surface analysis techniques. Decrease of the solution pH from 6.8 to 6.0 promotes the anodic dissolution and cathodic reduction simultaneously. Further decrease of the pH value mainly accelerates the cathodic reduction of X70 pipeline steel. As a result, when the solution pH decreases form 6.8 to 5.5, SCC susceptibility decreases because of the enhancement of the anodic dissolution. When the solution pH decreases from 5.5 to 4.0, SCC susceptibility increases gradually because of the acceleration of cathodic reactions.

  19. The electrochemical behavior of Co(TPTZ)2 complex on different carbon based electrodes modified with TiO2 nanoparticles

    International Nuclear Information System (INIS)

    Ortaboy, Sinem; Atun, Gülten

    2015-01-01

    Electrochemical behavior of cobalt (II) complex with the N-donor ligand 2,2′-bipyridyl-1,3,5-tripyridyl-s-triazine (TPTZ) was investigated to elucidate the electron-proton transfer mechanisms. The electrochemical response of the complex was studied using square-wave voltammetry (SWV) and electrochemical impedance spectroscopy (EIS) techniques. A conventional three-electrode system, consisting of glassy carbon (GCE), TiO 2 modified glassy carbon (T/GCE), carbon paste (CPE) and TiO 2 modified carbon paste (T/CPE) working electrodes were employed. The ligand/metal ratio and stability constant of the complex as well as the mechanisms of the electrode processes were elucidated by examining the effects of pH, ligand concentration and frequency on the voltammograms. The EIS results indicated that the samples modified with TiO 2 had the higher charge transfer resistance than that of the bare electrodes and also suggested that the electroactivity of the electrode surfaces increased in the following order, T/CPE > CPE > T/GCE > GCE. The surface morphology of the working electrodes was also characterized by atomic force microscopy (AFM). The values of surface roughness parameters were found to be consistent with the results obtained by EIS experiments. - Graphical abstract: Schematic illustration of the experimental process. - Highlights: • Electrochemical behavior of Co(TPTZ) 2 complex studied by SWV and EIS techniques. • GCE, CPE T/GCE and T/CPE were used as working electrodes for comparative studies. • The surface morphologies of the electrodes were characterized by AFM. • Mechanisms were proposed from the effects of pH, ligand concentration and frequency. • EIS and morphologic relationships of the surfaces were established successfully

  20. A study of hydrogen effects on fracture behavior of radioactive waste storage tanks. Final report, October 1992-September 1994

    International Nuclear Information System (INIS)

    Murty, K.L.; Elleman, T.S.

    1994-01-01

    The processing of high-level radioactive wastes now stored at Hanford and Savannah River Laboratories will continue over many years and it will be necessary for some of the liquids to remain in the tanks until well into the next century. Continued tank integrity is therefore an issue of prime importance and it will be necessary to understand any processes which could lead to tank failure. Hydrogen embrittlement resulting from absorption of radiolytic hydrogen could alter tank fracture behavior and be an issue in evaluating the effect of stresses on the tanks from rapid chemical oxidation-reduction reactions. The intense radiation fields in some of the tanks could be a factor in increasing the hydrogen permeation rates through protective oxide films on the alloy surface and be an additional factor in contributing to embrittlement. The project was initiated in October 1992 for a two year period to evaluate hydrogen uptake in low carbon steels that are representative of storage tanks. Steel specimens were exposed to high gamma radiation fields to generate radiolytic hydrogen and to potentially alter the protective surface films to increase hydrogen uptake. Direct measurements of hydrogen uptake were made using tritium as a tracer and fracture studies were undertaken to determine any alloy embrittlement. The rates of hydrogen uptake were noted to be extremely low in the experimental steels. Gamma radiation did not reveal any significant changes in the mechanical and fracture characteristics following exposures as long as a month. It is highly desirable to investigate further the tritium diffusion under stress in a cracked body where stress-assisted diffusion is expected to enhance these rates. More importantly, since welds are the weakest locations in the steel structures, the mechanical and fracture tests should be performed on welds exposed to tritium with and without stressed crack-fronts

  1. Electrochemical properties and lithium ion solvation behavior of sulfone-ester mixed electrolytes for high-voltage rechargeable lithium cells

    Science.gov (United States)

    Watanabe, Yuu; Kinoshita, Shin-ichi; Wada, Satoshi; Hoshino, Keiji; Morimoto, Hideyuki; Tobishima, Shin-ichi

    2008-05-01

    Sulfone-ester mixed solvent electrolytes were examined for 5 V-class high-voltage rechargeable lithium cells. As the base-electrolyte, sulfolane (SL)-ethyl acetate (EA) (1:1 mixing volume ratio) containing 1 M LiBF4 solute was investigated. Electrolyte conductivity, electrochemical stability, Li+ ion solvation behavior and cycleability of lithium electrode were evaluated. 13C NMR measurement results suggest that Li+ ions are solvated with both SL and EA. Charge-discharge cycling efficiency of lithium anode in SL-EA electrolytes was poor, being due to its poor tolerance for reduction. To improve lithium charge-discharge cycling efficiency in SL-EA electrolytes, following three trials were carried out: (i) improvement of the cathodic stability of electrolyte solutions by change in polarization through modification of solvent structure; isopropyl methyl sulfone and methyl isobutyrate were investigated as alternative SL and EA, respectively, (ii) suppression of the reaction between lithium and electrolyte solutions by addition of low reactivity surfactants of cycloalkanes (decalin and adamantane) or triethylene glycol derivatives (triglyme, 1,8-bis(tert-butyldimethylsilyloxy)-3,6-dioxaoctane and triethylene glycol di(methanesulfonate)) into SL-EA electrolytes, and (iii) change in surface film by addition of surface film formation agent of vinylene carbonate (VC) into SL-EA electrolytes. These trials made lithium cycling behavior better. Lithium cycling efficiency tended to increase with a decrease in overpotential. VC addition was most effective for improvement of lithium cycling efficiency among these additives. Stable surface film is formed on lithium anode by adding VC and the resistance between anode/electrolyte interfaces showed a constant value with an increase in cycle number. When the electrolyte solutions without VC, the interfacial resistance increased with an increase in cycle number. VC addition to SL-EA was effective not only for Li/LiCoO2 cell with charge

  2. Electrochemical properties and electrochemical impedance ...

    African Journals Online (AJOL)

    Polypyrrole (PPy) films of different thickness were characterized by electrochemical impedance spectroscopy (EIS) measurements in acetonitrile and aqueous solutions, containing 0.1 M NaClO4 or sodium dodecylsulfate as the dopant. The PPy films were electrochemically deposited on Pt, and their electrochemical ...

  3. Hydrogen isotope effect on storage behavior of U{sub 2}Ti and UZr{sub 2.3}

    Energy Technology Data Exchange (ETDEWEB)

    Jat, Ram Avtar; Sawant, S.G.; Rajan, M.B.; Dhanuskar, J.R. [Product Development Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Kaity, Santu [Radiometallurgy Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India); Parida, S.C., E-mail: sureshp@barc.gov.in [Product Development Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085 (India)

    2013-11-15

    U{sub 2}Ti and UZr{sub 2.3} alloys were prepared by arc melting method, vacuum annealed and characterized by XRD, SEM and EDX methods. Hydrogen isotope effect on the storage behavior of these alloys were studied by measuring the hydrogen/deuterium desorption pressure–composition–temperature (PCT) profiles in the temperature range of 573–678 K using a Sievert’s type volumetric apparatus. It was observed that, in the temperature and pressure range of investigation, all the isotherms show a single desorption plateau. The PCT data reveals that both U{sub 2}Ti and UZr{sub 2.3} alloys had normal isotope effects on hydrogen/deuterium desorption at all experimental temperatures. Thermodynamic parameters for dehydrogenation and dedeuteration reactions of the corresponding hydrides and deuterides of the above alloys were deduced from the PCT data.

  4. Widely available active sites on Ni2P for electrochemical hydrogen evolution - insights from first principles calculations

    DEFF Research Database (Denmark)

    Hansen, Martin Hangaard; Stern, Lucas-Alexandre; Feng, Ligang

    2015-01-01

    We present insights into the mechanism and the active site for hydrogen evolution on nickel phosphide (Ni2P). Ni2P was recently discovered to be a very active non-precious hydrogen evolution catalyst. Current literature attributes the activity of Ni2P to a particular site on the (0001) facet. In ...

  5. Phase Behavior and Magnetic Alignment of Hydrogen Bonded Side Chain Liquid Crystalline Block Copolymers

    Science.gov (United States)

    Gopinadhan, Manesh; Majewski, Pawel; Beach, Evan; Anastas, Paul; Osuji, Chinedum

    2010-03-01

    Hydrogen bonding between a poly(styrene-b-acrylic acid) backbone and an imidazole terminated biphenyl mesogen results in the formation of a side-group liquid crystalline block copolymer (LC BCP).We use a combination of FTIR, X-ray scattering and DSC to characterize the phase behavior of the PAA-LC system, which is largely dominated by the sub-stoichiometric saturation of the binding capacity of the chain. In the melt, the self assembled materials exhibited composition and temperature dependent smectic LC phases along with characteristic birefringence and multiple thermal transitions associated with LC polymers. The diblock copolymers (LC BCP) microphase separated into lamellar microdomains with homeotropic anchoring at the IMDS. Alignment of a hierarchically ordered lamellar BCP was performed using a 5 T magnetic field at elevated temperature in the melt state and characterized by SAXS. The system exhibits a tilted smectic structure, which on alignment by the field displays scattering patterns akin to those observed in bookshelf or chevron-type structures. These results demonstrate that simple non-covalent interactions can be used to generate LC order and thus provide a convenient handle for subsequent alignment of BCP structures by magnetic fields.

  6. The Electrochemical Behavior of Carbon Fiber Microelectrodes Modified with Carbon Nanotubes Using a Two-Step Electroless Plating/Chemical Vapor Deposition Process

    Directory of Open Access Journals (Sweden)

    Longsheng Lu

    2017-03-01

    Full Text Available Carbon fiber microelectrode (CFME has been extensively applied in the biosensor and chemical sensor domains. In order to improve the electrochemical activity and sensitivity of the CFME, a new CFME modified with carbon nanotubes (CNTs, denoted as CNTs/CFME, was fabricated and investigated. First, carbon fiber (CF monofilaments grafted with CNTs (simplified as CNTs/CFs were fabricated in two key steps: (i nickel electroless plating, followed by (ii chemical vapor deposition (CVD. Second, a single CNTs/CF monofilament was selected and encapsulated into a CNTs/CFME with a simple packaging method. The morphologies of as-prepared CNTs/CFs were characterized by scanning electron microscopy. The electrochemical properties of CNTs/CFMEs were measured in potassium ferrocyanide solution (K4Fe(CN6, by using a cyclic voltammetry (CV and a chronoamperometry method. Compared with a bare CFME, a CNTs/CFME showed better CV curves with a higher distinguishable redox peak and response current; the higher the CNT content was, the better the CV curves were. Because the as-grown CNTs significantly enhanced the effective electrode area of CNTs/CFME, the contact area between the electrode and reactant was enlarged, further increasing the electrocatalytic active site density. Furthermore, the modified microelectrode displayed almost the same electrochemical behavior after 104 days, exhibiting remarkable stability and outstanding reproducibility.

  7. Electrochemical energy storage behavior of Sn/SnO2 double phase nanocomposite anodes produced on the multiwalled carbon nanotube buckypapers for lithium-ion batteries

    Science.gov (United States)

    Alaf, Mirac; Akbulut, Hatem

    2014-02-01

    Recent development of electrode materials for Li-ion batteries is driven mainly by hybrid nanocomposite structures consisting of Li storage compounds and CNTs. In this study, tin/tinoxide (Sn/SnO2) films and tin/tinoxide/multi walled carbon nanotube (Sn/SnO2/MWCNT) nanocomposites are produced by a two steps process; thermal evaporation and subsequent plasma oxidation as anode materials for Li-ion batteries. The physical, structural, and electrochemical behaviors of the nanocomposite electrodes containing MWCNTs are discussed. The ratio between metallic tin (Sn) and tinoxide (SnO2) is controlled with plasma oxidation time and effects of the ratio are investigated on the structural and electrochemical properties. The greatly enhanced electrochemical performance is mainly due to the morphological stability and reduced diffusion resistance, which are induced by MWCNT core and deposited Sn/SnO2 double phase shell. The outstanding long-term cycling stability is a result of the two layers Sn and SnO2 phases on MWCNTs. The nanoscale Sn/SnO2/MWCNT network provides good electrical conductivity, and the creation of open spaces that buffer a large volume change during the Li-alloying/de-alloying reaction.

  8. Electrochemical and wear behavior of niobium-vanadium carbide coatings produced on AISI H13 tool steel through thermo-reactive deposition/diffusion

    International Nuclear Information System (INIS)

    Castillejo Nieto, Fabio Enrique; Olaya Flores, Jhon Jairo; Alfonso Orjuela, Jose Edgar

    2016-01-01

    We deposited of niobium-vanadium carbide coatings on tool steel AISI H13 using the thermo-reactive substrates deposition/diffusion (TRD) technique. The carbides were obtained using salt baths composed of molten borax, ferroniobium, vanadium and aluminum, by heating this mixture at 1020°C for 4 hours. The coatings were characterized morphologically via electron microscopy scanning (SEM), the chemical surface composition was determined through X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray spectroscopy (EDX); the crystal structure was analyzed using x-ray diffraction (XRD), the mechanical properties of the coatings were evaluated using nano-indentation, The tribological properties of the coatings obtained were determined using a Pin-on-disk tribometer and the electrochemical behavior was studied through potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS). The results showed that the hardness of the coated steel increased four times with respect to uncoated steel, and the electrochemical test established that the corrosion current is lower by one order of magnitude for coated steel

  9. Electrochemical detection of DNA binding by tumor suppressor p53 protein using osmium-labeled oligonucleotide probes and catalytic hydrogen evolution at the mercury electrode

    Czech Academy of Sciences Publication Activity Database

    Němcová, Kateřina; Šebest, Peter; Havran, Luděk; Orság, Petr; Fojta, Miroslav; Pivoňková, Hana

    2014-01-01

    Roč. 406, č. 24 (2014), s. 5843-5852 ISSN 1618-2642 R&D Projects: GA ČR(CZ) GAP301/11/2076; GA AV ČR(CZ) IAA400040901 Institutional support: RVO:68081707 Keywords : Electrochemical analysis * Labeled probes * Osmium complex Subject RIV: BO - Biophysics Impact factor: 3.436, year: 2014

  10. The corrosion rate and the hydrogen absorption behavior of titanium under reducing condition-III. Research document

    International Nuclear Information System (INIS)

    Suzuki, H.; Taniguchi, N.; Kawakami, S.

    2005-03-01

    Titanium is one of the candidate materials for overpacks as a high corrosion resistance metal. At the initial stage of repository, oxidizing condition will be given around the overpack because oxygen will be brought from the ground. The oxygen will be consumed by the reaction with impurities in buffer material or corrosion of overpack, and reducing condition will be achieved around the overpack. With the changing of redox condition, the water reduction becomes to dominate the cathodic reaction accompanying hydrogen generation. Crevice corrosion and hydrogen embrittlement are main causes of the damage of long term integrity of titanium overpack. However, it is not known about the corrosion resistance and hydrogen absorption behavior of titanium under reduction condition. In this study, the completely sealed ampoule test and the immersion test of titanium in aqueous solution and bentonite was carried out. In order to obtain reliable data about the hydrogen generation rate and the ratio of hydrogen absorption in titanium. From the result of 3 years immersion tests, corrosion rate of titanium were estimated to be in the order of 10 -2 ∼10 -1 μm/y in the aqueous solution, and 10 -3 ∼10 -2 μm/y in bentonite. This value is almost the same as the last report. Almost all the hydrogen generated by corrosion was absorbed in titanium in the immersion tests in completely sealed ampoule. In the examination that changed each parameter, it was suggested that the amount of the hydrogen absorption become 2∼3 times in 1M HCO 3- and pH13. (author)

  11. Electrochemical corrosion behavior and elasticity properties of Ti-6Al-xFe alloys for biomedical applications.

    Science.gov (United States)

    Lu, Jinwen; Zhao, Yongqing; Niu, Hongzhi; Zhang, Yusheng; Du, Yuzhou; Zhang, Wei; Huo, Wangtu

    2016-05-01

    The present study is to investigate the microstructural characteristics, electrochemical corrosion behavior and elasticity properties of Ti-6Al-xFe alloys with Fe addition for biomedical application, and Ti-6Al-4V alloy with two-phase (α+β) microstructure is also studied as a comparison. Microstructural characterization reveals that the phase and crystal structure are sensitive to the Fe content. Ti-6Al alloy displays feather-like hexagonal α phase, and Ti-6Al-1Fe exhibits coarse lath structure of hexagonal α phase and a small amount of β phase. Ti-6Al-2Fe and Ti-6Al-4Fe alloys are dominated by elongated, equiaxed α phase and retained β phase, but the size of α phase particle in Ti-6Al-4Fe alloy is much smaller than that in Ti-6Al-2Fe alloy. The corrosion resistance of these alloys is determined in SBF solution at 37 °C. It is found that the alloys spontaneously form a passive oxide film on their surface after immersion for 500 s, and then they are stable for polarizations up to 0 VSCE. In comparison with Ti-6Al and Ti-6Al-4V alloys, Ti-6Al-xFe alloys exhibit better corrosion resistance with lower anodic current densities, larger polarization resistances and higher open-circuit potentials. The passive layers show stable characteristics, and the wide frequency ranges displaying capacitive characteristics occur for high iron contents. Elasticity experiments are performed to evaluate the elasticity property at room temperature. Ti-6Al-4Fe alloy has the lowest Young's modulus (112 GPa) and exhibits the highest strength/modulus ratios as large as 8.6, which is similar to that of c.p. Ti (8.5). These characteristics of Ti-6Al-xFe alloys form the basis of a great potential to be used as biomedical implantation materials. Copyright © 2016 Elsevier B.V. All rights reserved.

  12. Force spectroscopy of hyaluronan by atomic force microscopy: from hydrogen-bonded networks toward single-chain behavior.

    Science.gov (United States)

    Giannotti, Marina I; Rinaudo, Marguerite; Vancso, G Julius

    2007-09-01

    The conformational behavior of hyaluronan (HA) polysaccharide chains in aqueous NaCl solution was characterized directly at the single-molecule level. This communication reports on one of the first single-chain atomic force microscopy (AFM) experiments performed at variable temperatures, investigating the influence of the temperature on the stability of the HA single-chain conformation. Through AFM single-molecule force spectroscopy, the temperature destabilization of a local structure was proven. This structure involved a hydrogen-bonded network along the polymeric chain, with hydrogen bonds between the polar groups of HA and possibly water, and a change from a nonrandom coil to a random coil behavior was observed when increasing the temperature from 29 +/- 1 to 46 +/- 1 degrees C. As a result of the applied force, this superstructure was found to break progressively at room temperature. The use of a hydrogen-bonding breaker solvent demonstrated the hydrogen-bonded water-bridged nature of the network structure of HA single chains in aqueous NaCl solution.

  13. Electrochemical synthesis of alkyl nitroaromatic compounds.

    Science.gov (United States)

    Gallardo, Iluminada; Guirado, Gonzalo; Marquet, Jordi

    2003-01-24

    Alkyl nitroaromatic compounds were readily prepared via nucleophilic aromatic substitution for hydrogen or a heteroatom by electrochemical oxidation of the sigma-complex. Butyllithium and butylmagnesium chloride were used as nucleophiles, and several nitrocompounds were tested to explore the possibilities of the NASH and NASX reactions promoted electrochemically.

  14. Study for electrochemical behavior of uranium oxide in a molten LiCl-Li2O system

    International Nuclear Information System (INIS)

    Park, Sung Bin; Park, Byung Heung; Seo, Chung Seok; Jung, Ki Jung; Park, Seong Won

    2005-01-01

    Interest in the electrolytic reduction of uranium oxide is increasing in the treatment of spent fuel oxides. With complicated and expensive procedures many reactive metals can be prepared in a pure metal form, the electrochemical reduction of a metal oxide has been recently proposed in metallurgy. The electrochemical reduction process is simple and rapid when compared to the conventional processes. The process can reduce the production costs and be applicable to a wide range of metal oxides. Chen et al. proposed the direct electrochemical reduction of titanium dioxide to titanium in a molten calcium chloride. Argonne National Laboratory (ANL) has reported the experimental results of an electrochemical reduction of the uranium oxide fuel in a bench-scale apparatus with a cyclic voltammetry, and has designed high-capacity reduction (HCR) cells and conducted three kg-scale UO 2 reduction runs. Gourishankar et al. classified the mechanisms of the electrolytic reduction of the metal oxides in a LiCl-Li 2 O molten salt system into two types; the simultaneous reduction and the direct electrochemical reduction. The uranium oxide in LiCl-Li 2 O molten salt was converted to uranium metal according to two mechanisms. Korea Atomic Energy Research Institute (KAERI) has developed the Advanced Spent Fuel Conditioning Process (ACP) to be an innovative technology in handling the PWR spent fuel. As part of ACP, the electrolytic reduction process (ER process) is the electrochemical reduction process of uranium oxide to uranium metal in molten salt. The ER process has advantages in a technical stability, an economic potential and a good proliferation resistance. KAERI has reported on the good experimental results of an electrochemical reduction of the uranium oxide in a 20 kg HM/batch lab-scale. In this work, cyclic voltammograms for a LiCl-3 wt% Li 2 O system and an U 3 O 8 -LiCl-3 wt% Li 2 O system with the integrated cathode assembly have been obtained. From the cyclic

  15. Hydrogen fuel. Uses

    International Nuclear Information System (INIS)

    Darkrim-Lamari, F.; Malbrunot, P.

    2006-01-01

    Hydrogen is a very energetic fuel which can be used in combustion to generate heat and mechanical energy or which can be used to generate electricity and heat through an electrochemical reaction with oxygen. This article deals with the energy conversion, the availability and safety problems linked with the use of hydrogen, and with the socio-economical consequences of a generalized use of hydrogen: 1 - hydrogen energy conversion: hydrogen engines, aerospace applications, fuel cells (principle, different types, domains of application); 2 - hydrogen energy availability: transport and storage (gas pipelines, liquid hydrogen, adsorbed and absorbed hydrogen in solid materials), service stations; 3 - hazards and safety: flammability, explosibility, storage and transport safety, standards and regulations; 4 - hydrogen economy; 5 - conclusion. (J.S.)

  16. Electrochemical hydrogen peroxide sensor based on a glassy carbon electrode modified with nanosheets of copper-doped copper(II) oxide

    International Nuclear Information System (INIS)

    Song, Haiyan; Ma, Chaohong; You, Liyan; Cheng, Zhenyu; Zhang, Xinhui; Yin, Baishuang; Zhang, Keqin; Ni, Yongnian

    2015-01-01

    A new electrochemical sensor for H 2 O 2 was constructed by depositing copper doped CuO nanosheets on a glassy carbon electrode (GCE). The morphology and composition of the modified electrode were characterized via scanning electron microscopy, energy dispersive X-ray spectroscopy and X-ray diffraction. The electrochemical properties of the electrode were studied using cyclic voltammetry and electrochemical impedance spectroscopy. The catalytic performance of the sensor was studied in 100 mM NaOH solution via differential pulse voltammetry and revealed the sensor to display significantly improved electrocatalytic activity with respect to the analysis of the H 2 O 2 in comparison to a plain GCE or a GCE modified with copper only. The response to H 2 O 2 at a working voltage of −0.46 V (vs. Ag/AgCl) is linear in the 0.003 – 8 mM concentration range, and the detection limit is 0.21 mM (at an S/N ratio of 3). Satisfactory results were obtained in the analysis of tap, rain and river waters spiked with H 2 O 2 . The analytical performance of this electrode compares favorably to the results obtained with other commonly used techniques for analysis of H 2 O 2 . (author)

  17. Surface treatment influences electrochemical stability of cpTi exposed to mouthwashes.

    Science.gov (United States)

    Beline, Thamara; Garcia, Camila S; Ogawa, Erika S; Marques, Isabella S V; Matos, Adaias O; Sukotjo, Cortino; Mathew, Mathew T; Mesquita, Marcelo F; Consani, Rafael X; Barão, Valentim A R

    2016-02-01

    The role of surface treatment on the electrochemical behavior of commercially pure titanium (cpTi) exposed to mouthwashes was tested. Seventy-five disks were divided into 15 groups according to surface treatment (machined, sand blasted with Al2O3, and acid etched) and electrolyte solution (artificial saliva — control, 0.12% chlorhexidine digluconate, 0.05% cetylpyridinium chloride, 0.2% sodium fluoride, and 1.5% hydrogen peroxide) (n = 5). Open-circuit-potential and electrochemical impedance spectroscopy were conducted at baseline and after 7 and 14 days of immersion in each solution. Potentiodynamic test and total weight loss of disks were performed after 14 days of immersion. Scanning electron microscopy, energy dispersive spectroscopy, white light interferometry and profilometry were conducted for surface characterization before and after the electrochemical tests. Sandblasting promoted the lowest polarization resistance (Rp) (P b .0001) and the highest capacitance (CPE) (P b .006), corrosion current density (Icorr) and corrosion rate (P b .0001). In contrast, acid etching increased Rp and reduced CPE, independent to the mouthwash; while hydrogen peroxide reduced Rp (P b .008) and increased Icorr and corrosion rate (P b .0001). The highest CPE values were found for hydrogen peroxide and 0.2% sodium fluoride. Immersion for longer period improved the electrochemical stability of cpTi (P b .05). In conclusion, acid etching enhanced the electrochemical stability of cpTi. Hydrogen peroxide and sodium fluoride reduced the resistance to corrosion of cpTi, independent to the surface treatment. Chlorhexidine gluconate and cetylpyridinium chloride did not alter the corrosive behavior of cpTi.

  18. Nuclear hydrogen production: re-examining the fusion option

    International Nuclear Information System (INIS)

    Baindur, S.

    2007-01-01

    This paper describes a scheme for nuclear hydrogen production by fusion. The basic idea is to use nuclear energy of the fuel (hydrogen plasma) to produce molecular hydrogen fro carbon-free hydrogen compounds. The hydrogen is then stored and utilized electrochemically in fuel cells or chemically as molecular hydrogen in internal combustion engines

  19. Electrochemical biosensors

    CERN Document Server

    Cosnier, Serge

    2015-01-01

    "This is an excellent book on modern electrochemical biosensors, edited by Professor Cosnier and written by leading international experts. It covers state-of-the-art topics of this important field in a clear and timely manner."-Prof. Joseph Wang, UC San Diego, USA  "This book covers, in 13 well-illustrated chapters, the potential of electrochemical methods intimately combined with a biological component for the assay of various analytes of biological and environmental interest. Particular attention is devoted to the description of electrochemical microtools in close contact with a biological cell for exocytosis monitoring and to the use of nanomaterials in the electrochemical biosensor architecture for signal improvement. Interestingly, one chapter describes the concept and design of self-powered biosensors derived from biofuel cells. Each topic is reviewed by experts very active in the field. This timely book is well suited for providing a good overview of current research trends devoted to electrochemical...

  20. Research Update: Nanoscale electrochemical transistors in correlated oxides

    Directory of Open Access Journals (Sweden)

    Teruo Kanki

    2017-04-01

    Full Text Available Large reversible changes of the electronic transport properties of solid-state oxide materials induced by electrochemical fields have received much attention as a new research avenue in iontronics. In this research update, dramatic transport changes in vanadium dioxide (VO2 nanowires were demonstrated by electric field-induced hydrogenation at room temperature through the nanogaps separated by humid air in a field-effect transistor structure with planar-type gates. This unique structure allowed us to investigate hydrogen intercalation and diffusion behavior in VO2 channels with respect to both time and space. Our results will contribute to further strategic researches to examine fundamental chemical and physical properties of devices and develop iontronic applications, as well as offering new directions to explore emerging functions for sensing, energy, and neuromorphologic devices combining ionic and electronic behaviors in solid-state materials.

  1. The Influence of Charged Species on the Phase Behavior, Self-Assembly, and Electrochemical Performance of Block Copolymer Electrolytes

    OpenAIRE

    Thelen, Jacob Lloyd

    2016-01-01

    One of the major barriers to expanding the capacity of large-scale electrochemical energy storage within batteries is the threat of a catastrophic failure. Catastrophic battery pack failure can be initiated by a defect within a single battery cell. If the failure of a defective battery cell is not contained, the damage can spread and subsequently compromise the integrity of the entire battery back, as well as the safety of those in its surroundings. Replacing the volatile, flammable liquid el...

  2. Microstructure and electrochemical corrosion behavior of a Pb-1 wt%Sn alloy for lead-acid battery components

    Energy Technology Data Exchange (ETDEWEB)

    Peixoto, Leandro C.; Osorio, Wislei R.; Garcia, Amauri [Department of Materials Engineering, University of Campinas - UNICAMP, PO Box 612, 13083-970, Campinas - SP (Brazil)

    2009-07-15

    The aim of this study was to evaluate the effect of solidification cooling rates on the as-cast microstructural morphologies of a Pb-1 wt%Sn alloy, and to correlate the resulting microstructure with the corresponding electrochemical corrosion resistance in a 0.5 M H{sub 2}SO{sub 4} solution at 25 C. Cylindrical low-carbon steel and insulating molds were employed permitting the two extremes of a significant range of solidification cooling rates to be experimentally examined. Electrochemical impedance spectroscopy (EIS) diagrams, potentiodynamic polarization curves and an equivalent circuit analysis were used to evaluate the electrochemical corrosion response of Pb-1 wt%Sn alloy samples. It was found that lower cooling rates are associated with coarse cellular arrays which result in better corrosion resistance than fine cells which are related to high cooling rates. The experimental results have shown that that the pre-programming of microstructure cell size of Pb-Sn alloys can be used as an alternative way to produce as-cast components of lead-acid batteries with higher corrosion resistance. (author)

  3. On the Stress Corrosion Cracking and Hydrogen Embrittlement Behavior of Austenitic Stainless Steels in Boiling Saturated Magnesium Chloride Solutions

    Directory of Open Access Journals (Sweden)

    Osama M. Alyousif

    2012-01-01

    Full Text Available The stress corrosion cracking (SCC and hydrogen embrittlement (HE behaviors for types 304, 310, and 316 austenitic stainless steels were investigated in boiling saturated magnesium chloride solutions using a constant load method under different conditions including test temperature, applied stress, and sensitization. Both of type 304 and type 316 stainless steels showed quite similar behavior characteristics, whereas type 310 stainless steel showed a different behavior. The time to failure (tf parameter was used among other parameters to characterize the materials behavior in the test solution and to develop a mathematical model for predicting the time to failure in the chloride solution. The combination of corrosion curve parameters and fracture surface micrographs gave some explanation for the cracking modes as well as an indication for the cracking mechanisms. On the basis of the results obtained, it was estimated that intergranular cracking was resulted from hydrogen embrittlement due to strain-induced formation of martensite along the grain boundaries, while transgranular cracking took place by propagating cracks nucleated at slip steps by dissolution.

  4. Thermomechanical behavior modeling and experimental validation of polymer-wound composite multi-layers. Hydrogen storage application

    International Nuclear Information System (INIS)

    Gentilleau, Benoit

    2012-01-01

    The purpose of this research is to study the thermomechanical behavior of the constituent materials of a type IV hydrogen storage tank: a composite, ensuring the strength, is wound around the polyurethane liner that ensures sealing of the tank and thermal insulation; at the extremities, stainless steel parts are used to allow the process connection. In this type of tank, during filling, there is a significant increase in hydrogen temperature, resulting in a gradual heating of the structure and the presence of temperature gradients. The purpose of this study is primarily to characterize the behavior of such a structure when subjects to complex thermomechanical loading. Initially, mechanical and thermal characterization tests have been made over the service life range of temperature of the tank to obtain the necessary data for the realization of a thermomechanical numerical model. Then, a behavior law of the composite, easily transferable to a complex structure such as the whole tank and taking into account the non-linearity, the matrix damage, the progressive loss of shear modulus, and the thermo-dependence of the materials parameters, is developed. The tests on technological representative specimens have been performed to better understand the mechanisms that can appear in the tank and to validate the model. Finally, a numerical study of a tank was performed. The coupled influence of temperature and damage matrix on the behavior of this structure is analyzed. (author)

  5. Hydrogen generation behaviors of NaBH4-NH3BH3 composite by hydrolysis

    Science.gov (United States)

    Xu, Yanmin; Wu, Chaoling; Chen, Yungui; Huang, Zhifen; Luo, Linshan; Wu, Haiwen; Liu, Peipei

    2014-09-01

    In this work, NH3BH3 (AB) is used to induce hydrogen generation during NaBH4 (SB) hydrolysis in order to reduce the use of catalysts, simplify the preparation process, reduce the cost and improve desorption kinetics and hydrogen capacity as well. xNaBH4-yNH3BH3 composites are prepared by ball-milling in different proportions (from x:y = 1:1 to 8:1). The experimental results demonstrate that all composites can release more than 90% of hydrogen at 70 °C within 1 h, and their hydrogen yields can reach 9 wt% (taking reacted water into account). Among them, the composites in the proportion of 4:1 and 5:1, whose hydrogen yields reach no less than 10 wt%, show the best hydrogen generation properties. This is due to the impact of the following aspects: AB additive improves the dispersibility of SB particles, makes the composite more porous, hampers the generated metaborate from adhering to the surface of SB, and decreases the pH value of the composite during hydrolysis. The main solid byproduct of this hydrolysis system is NaBO2·2H2O. By hydrolytic kinetic simulation of the composites, the fitted activation energies of the complexes are between 37.2 and 45.6 kJ mol-1, which are comparable to the catalytic system with some precious metals and alloys.

  6. Performance and Electrochemical Characterisation of Thin Electrolyte SOFCs

    DEFF Research Database (Denmark)

    Ramos, Tania; Hjelm, Johan; Wandel, Marie Emilie

    2008-01-01

    The performance and electrochemical behavior of two anode-supported thin electrolyte cells, with different manufacturing parameters, is determined by polarization measurements and electrochemical impedance spectroscopy (EIS). In addition to characterization, a previously suggested equivalent......-depth electrochemical characterization can provide valuable guidelines for production/performance optimization. © 2008 ECS - The Electrochemical Society...

  7. Noble metal nanoparticle-functionalized ZnO nanoflowers for photocatalytic degradation of RhB dye and electrochemical sensing of hydrogen peroxide

    DEFF Research Database (Denmark)

    Hussain, Muhammad; Sun, Hongyu; Karim, Shafqat

    2016-01-01

    due to increase in defects. Moreover, the presence of Au NPs on ZnO surface remarkably enhances photocatalytic activity as compared to Ag–ZnO and pure ZnO due to the higher catalytic activity and stability of Au NPs. On the other hand, Ag–ZnO-modified glassy carbon electrode shows good amperometric......Flower-like hierarchical Zinc oxide nanostructures synthesized by co-precipitation method have been hydrothermally functionalized with 8 nm Au NPs and 15 nm Ag nanoparticles. The photocatalytic and electrochemical performance of these structures are investigated. XPS studies show that the composite...

  8. Low-crystallinity molybdenum sulfide nanosheets assembled on carbon nanotubes for long-life lithium storage: Unusual electrochemical behaviors and ascending capacities

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xiaodan, E-mail: xiaodan_li@yeah.net [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China ElectricPower University, Beijing, 102206 (China); Wu, Gaoxiang, E-mail: wgxjimmy@126.com [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China ElectricPower University, Beijing, 102206 (China); Chen, Jiewei, E-mail: kzscjw@126.com [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China ElectricPower University, Beijing, 102206 (China); Li, Meicheng, E-mail: mcli@ncepu.edu.cn [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China ElectricPower University, Beijing, 102206 (China); Chongqing Materials Research Institute, Chongqing 400707 (China); Li, Wei, E-mail: wei.li@inl.int [International Iberian Nanotechnology Laboratory (INL), Braga 4715-330 (Portugal); Wang, Tianyue, E-mail: 1355796015@qq.com [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China ElectricPower University, Beijing, 102206 (China); Jiang, Bing, E-mail: BingJiang@ncepu.edu.cn [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China ElectricPower University, Beijing, 102206 (China); He, Yue, E-mail: 947667748@qq.com [State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China ElectricPower University, Beijing, 102206 (China); Mai, Liqiang, E-mail: mlq518@whut.edu.cn [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China)

    2017-01-15

    Highlights: • Low-crystallinity molybdenum sulfide coated on carbon nanotubes were synthesized. • This anode material has unusual electrochemical behaviors compared to typical MoS{sub 2}. • It exhibits noticable ascending trends in capacity and superior rate performance. • The ascending performance can effectively extend the circulation life of batteries. - Abstract: Low-crystallinity molybdenum sulfide (LCMS, Mo:S = 1:2.75) nanosheets synthesized by a facile and low temperature solvothermal method is now reported. The as-prepared LCMS anode material is composited of MoS{sub 2} layers mixed with amorphous MoS{sub 3}, which leads to an unusual electrochemical process for lithium storage compared to typical MoS{sub 2} anode. The existence of MoS{sub 3} and Mo (VI) provide strong adsorption and binding sites for polar polysulphides, which compels abundant sulfur to turn into new-formed MoS{sub 3} rather than diffuse into electrolyte. To fully utilize this novel electrochemical process, LCMS is decorated on carbon nanotubes, obtaining well-dispersed CNTs@LCMS. As electrode material for lithium storage, CNTs@LCMS exhibits a noticable ascending trend in capacity from 820 mA h g{sup −1} to 1350 mA h g{sup −1} at 100 mA g{sup −1} during 130 cycles. The persistent ascending capacity is ascribed to the increasing lithium storage caused by new-formed MoS{sub 3}, combined with the reduced volume change benifiting from well-dispersed CNTs@LCMS. Furthermore, the ascending performance is proved to be able to effectively extend the circulation life (up to 200%) for lithium-ion batteries by mathematical modeling and calculation. Accordingly, the CNTs@LCMS composite is a promising anode material for long-life lithium-ion batteries.

  9. Creep-rupture behavior of candidate Stirling engine iron supperalloys in high-pressure hydrogen. Volume 2: Hydrogen creep-rupture behavior

    Science.gov (United States)

    Bhattacharyya, S.; Peterman, W.; Hales, C.

    1984-01-01

    The creep rupture behavior of nine iron base and one cobalt base candidate Stirling engine alloys is evaluated. Rupture life, minimum creep rate, and time to 1% strain data are analyzed. The 3500 h rupture life stress and stress to obtain 1% strain in 3500 h are also estimated.

  10. Behaviors of hydrogen in C-SiC films with IR and SIMS analyses

    CERN Document Server

    Huang, N K; Xiong, Q; Liu, Y G; Wang, D Z; Lei, J R

    2002-01-01

    C-SiC films with different content of SiC were prepared with magnetron sputtering deposition followed by Ar sup + ion bombardment. Secondary ion mass spectroscopy depth profiles of hydrogen for the samples of C-SiC coated stainless steel and stainless steel substrate after H sup + ion implantation and thermal annealing show different hydrogen concentrations in C-SiC coatings and stainless steel. Infrared (IR) transmission measurement was selected to study the mechanism of hydrogen retention by C-SiC films. The vibrational spectra in the range between 400 and 3200 cm sup - sup 1 in IR transmission spectra show the Si-CH sub 3 , Si-CH sub 2 , Si-H, CH sub 2 , CH sub 3 etc. bonds, which are responsible for retaining hydrogen. Apart from the mode above, there also exist bonds related to carbon and silicon such as Si-C, C=C. The contamination of oxygen entered the film to form C=O and SiO sub 2 configurations and hydrogen contamination also formed Si-CH sub 2 mode in the films.

  11. Electrochemical Processes

    DEFF Research Database (Denmark)

    Bech-Nielsen, Gregers

    1997-01-01

    The notes describe in detail primary and secondary galvanic cells, fuel cells, electrochemical synthesis and electroplating processes, corrosion: measurments, inhibitors, cathodic and anodic protection, details of metal dissolution reactions, Pourbaix diagrams and purification of waste water from...... galvanic industries....

  12. Effect of Ca(OH)2, NaCl, and Na2SO4 on the corrosion and electrochemical behavior of rebar

    Science.gov (United States)

    Jin, Zuquan; Zhao, Xia; Zhao, Tiejun; Hou, Baorong; Liu, Ying

    2017-05-01

    The corrosion of rebar in reinforced concrete in marine environments causes significant damage to structures built in ocean environments. Studies on the process and mechanism of corrosion of rebar in the presence of multiple ions may help to control damage and predict the service life of reinforced concrete structures in such environments. The effect of interactions between sulfate and chloride ions and calcium hydroxide on the electrochemical behavior of rebar are also important for evaluation of structure durability. In this work, electrochemical impedance spectroscopy (EIS) plots of rebar in Ca(OH)2 solution and cement grout, including NaCl and Na2SO4 as aggressive salts, were measured for diff erent immersion times. The results show that corrosion of rebar was controlled by the rate of charge transfer as the rebar was exposed to chloride solution. In the presence of high concentrations of sulfate ions in the electrolyte, generation and dissolution of the passive film proceeded simultaneously and corrosion was mainly controlled by the diff usion rate. When Na2SO4 and NaCl were added to Ca(OH)2 solution, the instantaneous corrosion rate decreased by a factor of 10 to 20 as a result of the higher pH of the corroding solution.

  13. Electrochemical Migration Behavior of Copper-Clad Laminate and Electroless Nickel/Immersion Gold Printed Circuit Boards under Thin Electrolyte Layers

    Directory of Open Access Journals (Sweden)

    Pan Yi

    2017-02-01

    Full Text Available The electrochemical migration (ECM behavior of copper-clad laminate (PCB-Cu and electroless nickel/immersion gold printed circuit boards (PCB-ENIG under thin electrolyte layers of different thicknesses containing 0.1 M Na2SO4 was studied. Results showed that, under the bias voltage of 12 V, the reverse migration of ions occurred. For PCB-Cu, both copper dendrites and sulfate precipitates were found on the surface of FR-4 (board material between two plates. Moreover, the Cu dendrite was produced between the two plates and migrated toward cathode. Compared to PCB-Cu, PCB-ENIG exhibited a higher tendency of ECM failure and suffered from seriously short circuit failure under high relative humidity (RH environment. SKP results demonstrated that surface potentials of the anode plates were greater than those of the cathode plates, and those potentials of the two plates exhibited a descending trend as the RH increased. At the end of the paper, an electrochemical migration corrosion failure model of PCB was proposed.

  14. Coupling of Mechanical Behavior of Lithium Ion Cells to Electrochemical-Thermal Models for Battery Crush; NREL (National Renewable Energy Laboratory)

    Energy Technology Data Exchange (ETDEWEB)

    Pesaran, Ahmad; Zhang, Chao; Santhanagopalan, Shriram; Sahraei, Elham; Wierzbiki, Tom

    2015-06-15

    Propagation of failure in lithium-ion batteries during field events or under abuse is a strong function of the mechanical response of the different components in the battery. Whereas thermal and electrochemical models that capture the abuse response of batteries have been developed and matured over the years, the interaction between the mechanical behavior and the thermal response of these batteries is not very well understood. With support from the Department of Energy, NREL has made progress in coupling mechanical, thermal, and electrochemical lithium-ion models to predict the initiation and propagation of short circuits under external crush in a cell. The challenge with a cell crush simulation is to estimate the magnitude and location of the short. To address this, the model includes an explicit representation of each individual component such as the active material, current collector, separator, etc., and predicts their mechanical deformation under different crush scenarios. Initial results show reasonable agreement with experiments. In this presentation, the versatility of the approach for use with different design factors, cell formats and chemistries is explored using examples.

  15. In-situ preparation and unique electrochemical behavior of pore-embedding CoO/Co3O4 intermixed composite for Li+ rechargeable battery electrodes

    Science.gov (United States)

    Kim, Jin Kyu; Ju, Ji Young; Choi, Seul Ki; Unithrattil, Sanjith; Lee, Sun Sook; Kang, Yongku; Kim, Yongseon; Im, Won Bin; Choi, Sungho

    2018-02-01

    Electrochemically active CoO/Co3O4 co-existing microspheres with morphology-inherited porous particles is successfully synthesized via a simple solvothermal method. The as-prepared intermixed composite undergoes a monoxide CoO-preferred conversion reaction with an extremely enhanced capacity retention, ∼905 mA h g-1 after 250 cycles for discharge state, which is 1.6 times higher than the conventional CoOx-based anodes. Moreover, stable catalytic behavior of the electrocatalysts in Li-air cathodes of the given composites is also demonstrated. We believe that the extraordinarily enhanced electrode performance might be due to the novel pore-tempered microspheres packed with double electrochemically active centers of the CoO/Co3O4 composite effectively confine the detrimental volume exchange during the reversible cyclic reactions as well as the preserved multiple reactive sites for a reversible Li+ ⇄ LiOx reaction, which is advantageous for advanced Li rechargeable battery.

  16. Nickel foam/polyaniline-based carbon/palladium composite electrodes for hydrogen storage

    International Nuclear Information System (INIS)

    Skowronski, Jan M.; Urbaniak, Jan

    2008-01-01

    The sandwich-like nickel/palladium/carbon electrodes exhibiting ability to absorb hydrogen in alkaline solution are presented. Electrodes were prepared by successive deposition of palladium and polyaniline layers on nickel foam substrate followed by heat treatment to give Ni/Pd/C electrode. It was shown that thermal conversion of polymer into carbon layer and subsequent thermal activation of carbon component bring about the modification of the mechanism of reversible hydrogen sorption. It was proven that carbon layer, interacting with Pd catalyst, plays a considerable role in the process of hydrogen storage. In the other series of experiments, Pd particles were dispersed electrochemically on carbon coating leading to Ni/C/Pd system. The adding of the next carbon layer resulted in Ni/C/Pd/C electrodes. Electrochemical properties of the electrodes depend on both the sequence of Pd and C layers and the preparation/activation of carbon coating. Electrochemical behavior of sandwich-like electrodes in the reaction of hydrogen sorption/desorption was characterized in 6 M KOH using the cyclic voltammetry method and the results obtained were compared to those for Ni/Pd electrode. The anodic desorption of hydrogen from electrodes free and containing carbon layer was considered after the potentiodynamic as well as potentiostatic sorption of hydrogen. The influence of the sorption potential and the time of rest of electrodes at a cut-off circuit on the kinetics of hydrogen recovery were examined. The results obtained for Ni/Pd/C electrodes indicate that the displacement of hydrogen between C and Pd phase takes place during the rest at a cut-off circuit. Electrodes containing carbon layer require longer time for hydrogen electrosorption. On the other hand, the presence of carbon layer in electrodes is advantageous because a considerable longer retention of hydrogen is possible, as compared to Pd/Ni electrode. Hydrogen stored in sandwich-like electrodes can instantly be

  17. The electrochemical impedance of metal hydride electrodes

    DEFF Research Database (Denmark)

    Valøen, Lars Ole; Lasia, Andrzej; Jensen, Jens Oluf

    2002-01-01

    , explaining the experimental impedances in a wide frequency range for electrodes of hydride forming materials mixed with copper powder, were obtained. Both charge transfer and spherical diffusion of hydrogen in the particles are important sub processes that govern the total rate of the electrochemical...... hydrogen absorption/desorption reaction. To approximate the experimental data, equations describing the current distribution in porous electrodes were needed. Indications of one or more parallel reduction/oxidation processes competing with the electrochemical hydrogen absorption/desorption reaction were...

  18. Electrochemical studies of a reconstituted photosynthetic electron-transfer chain or towards a biomimetic photoproduction of hydrogen; Etudes electrochimiques de chaines de transfert d'electrons photosynthetiques ou vers une photoproduction biomimetique d'hydrogene

    Energy Technology Data Exchange (ETDEWEB)

    Fourmond, V

    2007-04-15

    The aim of this work is to find an efficient process to convert solar energy into hydrogen. The electrons transfers in reconstituted photosynthetic chains have been particularly studied with the aims 1)in one hand, to better understand the interactions of the different molecules of the photosynthetic chain in order to optimize the changes of the entire organisms for hydrogen production 2)in another hand, to insert the hydrogenases in a photosynthetic chain and then to photo reduce them in order to obtain kinetic data to better understand how it works. (O.M.)

  19. Acoustic emission monitoring of activation behavior of LaNi5 hydrogen storage alloy

    Directory of Open Access Journals (Sweden)

    Igor Maria De Rosa, Alessandro Dell'Era, Mauro Pasquali, Carlo Santulli and Fabrizio Sarasini

    2011-01-01

    Full Text Available The acoustic emission technique is proposed for assessing the irreversible phenomena occurring during hydrogen absorption/desorption cycling in LaNi5. In particular, we have studied, through a parametric analysis of in situ detected signals, the correlation between acoustic emission (AE parameters and the processes occurring during the activation of an intermetallic compound. Decreases in the number and amplitude of AE signals suggest that pulverization due to hydrogen loading involves progressively smaller volumes of material as the number of cycles increases. This conclusion is confirmed by electron microscopy observations and particle size distribution measurements.

  20. Methanol oxidation reaction on core-shell structured Ruthenium-Palladium nanoparticles: Relationship between structure and electrochemical behavior

    Science.gov (United States)

    Kübler, Markus; Jurzinsky, Tilman; Ziegenbalg, Dirk; Cremers, Carsten

    2018-01-01

    In this work the relationship between structural composition and electrochemical characteristics of Palladium(Pd)-Ruthenium(Ru) nanoparticles during alkaline methanol oxidation reaction is investigated. The comparative study of a standard alloyed and a precisely Ru-core-Pd-shell structured catalyst allows for a distinct investigation of the electronic effect and the bifunctional mechanism. Core-shell catalysts benefit from a strong electronic effect and an efficient Pd utilization. It is found that core-shell nanoparticles are highly active towards methanol oxidation reaction for potentials ≥0.6 V, whereas alloyed catalysts show higher current outputs in the lower potential range. However, differential electrochemical mass spectrometry (DEMS) experiments reveal that the methanol oxidation reaction on core-shell structured catalysts proceeds via the incomplete oxidation pathway yielding formaldehyde, formic acid or methyl formate. Contrary, the alloyed catalyst benefits from the Ru atoms at its surface. Those are found to be responsible for high methanol oxidation activity at lower potentials as well as for complete oxidation of CH3OH to CO2 via the bifunctional mechanism. Based on these findings a new Ru-core-Pd-shell-Ru-terrace catalyst was synthesized, which combines the advantages of the core-shell structure and the alloy. This novel catalyst shows high methanol electrooxidation activity as well as excellent selectivity for the complete oxidation pathway.

  1. Hydrogenation behavior of Ti-implanted Zr-1Nb alloy with TiN films deposited using filtered vacuum arc and magnetron sputtering

    Science.gov (United States)

    Kashkarov, E. B.; Nikitenkov, N. N.; Sutygina, A. N.; Bezmaternykh, A. O.; Kudiiarov, V. N.; Syrtanov, M. S.; Pryamushko, T. S.

    2018-02-01

    More than 60 years of operation of water-cooled reactors have shown that local or general critical hydrogen concentration is one of the basic limiting criteria of zirconium-based fuel element claddings. During the coolant radiolysis, released hydrogen penetrates and accumulates in zirconium alloys. Hydrogenation of zirconium alloys leads to degradation of their mechanical properties, hydride cracking and stress corrosion cracking. In this research the effect of titanium nitride (TiN) deposition on hydrogenation behavior of Ti-implanted Zr-1Nb alloy was described. Ti-implanted interlayer was fabricated by plasma immersion ion implantation (PIII) at the pulsed bias voltage of 1500 V to improve the adhesion of TiN and reduce hydrogen penetration into Zr-1Nb alloy. We conducted the comparative analysis on hydrogenation behavior of the Ti-implanted alloy with sputtered and evaporated TiN films by reactive dc magnetron sputtering (dcMS) and filtered cathodic vacuum arc deposition (FVAD), respectively. The crystalline structure and surface morphology were investigated using X-ray diffraction (XRD) and scanning electron microscopy (SEM). The elemental distribution was analyzed using glow-discharge optical emission spectroscopy (GD-OES). Hydrogenation was performed from gas atmosphere at 350 °C and 2 atm hydrogen pressure. The results revealed that TiN films as well as Ti implantation significantly reduce hydrogen absorption rate of Zr-1Nb alloy. The best performance to reduce the rate of hydrogen absorption is Ti-implanted layer with evaporated TiN film. Morphology of the films impacted hydrogen permeation through TiN films: the denser film the lower hydrogen permeation. The Ti-implanted interface plays an important role of hydrogen accumulation layer for trapping the penetrated hydrogen. No deterioration of adhesive properties of TiN films on Zr-1Nb alloy with Ti-implanted interface occurs under high-temperature hydrogen exposure. Thus, the fabrication of Ti

  2. Electrochemical sensing platforms based on the different carbon derivative incorporated interface.

    Science.gov (United States)

    Dervisevic, Muamer; Çevik, Emre; Durmuş, Zehra; Şenel, Mehmet

    2016-01-01

    their effects on the properties of these biosensors. Biosensors were prepared by Horseradish peroxidase (HRP) immobilization on the composite electrodes composed of carbon black, carbon nanofiber (CNF), extended graphite, multiwalled carbon nanotube (MWCNT), reduced graphene oxide (REGO) and poly(glycidyl methacrylateco-vinylferrocene) (P(GMA-co-VFc)) as mediator, covalent linker, and host matrix for carbon derivatives. The modified pencil graphite electrode (PGE) was used for the detection of hydrogen peroxide and to follow electrochemical behavior of different carbon derivatives which were recorded. The electrochemical characterization was investigated by cyclic voltammetry and electrochemical impedance spectroscopy methods. Amperometric measurements showed that the REGO and MWCNT modified electrodes have excellent performance in comparison with other carbon derivatives studied.

  3. Microscopic observation of shear-mode fatigue crack growth behavior under the condition of continuous hydrogen-charging

    Science.gov (United States)

    Akaki, Y.; Matsuo, T.; Nishimura, Y.; Miyakawa, S.; Endo, M.

    2017-05-01

    Rolling bearings facilitate the smooth motion of moving mechanical transmission devices substantially reducing the energy loss. However, flaking failure caused in bearings by rolling contact fatigue can crucially deteriorate the integrity of an overall mechanical system composed using bearings. It is understood nowadays that this phenomenon is intimately associated with shear-mode (Mode II and III) fatigue crack growth caused by cyclic shear stress in the presence of large compression. Further, a problem has become of importance that the premature flaking in ball bearings could be caused by the assistance of the penetration of hydrogen into material during the operation. In this study, torsional fatigue test of a bearing steel (JIS SUJ2) was performed by using a newly-developed method of continuous hydrogen-charging. Based on the microscopic observation, it was found that continuous hydrogen-charging had an influence on the shear-mode fatigue crack growth behavior in the high-cycle fatigue regime and reduced the threshold level.

  4. Facile polyol synthesis of CoFe2O4 nanosphere clusters and investigation of their electrochemical behavior in different aqueous electrolytes

    Science.gov (United States)

    Malaie, K.; Ganjali, M. R.; Alizadeh, T.; Norouzi, P.

    2018-04-01

    CoFe2O4 nanosphere clusters (CFNCs) with good crystallinity were synthesized through a facile polyol process without using any surfactant or template. FESEM images show cobalt ferrite clusters with a diameter of 200-400 nm with nanospheres grown on the surface. The electrochemical behavior of the CFNCs was investigated in different electrolytes of KOH, K2SO4, and Na2SO3 in the negative potential window of - 0.3 to - 1.3 V for possible application in supercapacitor electrodes. CFNCs exhibited best performance in KOH electrolyte with a specific capacitance of 151 F g-1 in 5 mV s-1 and a cycling stability of 87% over 1000 voltammetric cycles. These studies indicate the potential application of the as-obtained CFNCs as negative electrodes in alkaline supercapacitors.

  5. Contribution to the Study of the Relation between Microstructure and Electrochemical Behavior of Iron-Based FeCoC Ternary Alloys

    Directory of Open Access Journals (Sweden)

    Farida Benhalla-Haddad

    2012-01-01

    Full Text Available This work deals with the relation between microstructure and electrochemical behavior of four iron-based FeCoC ternary alloys. First, the arc-melted studied alloys were characterized using differential thermal analyses and scanning electron microscopy. The established solidification sequences of these alloys show the presence of two primary crystallization phases (δ(Fe and graphite as well as two univariante lines : peritectic L+(Fe↔(Fe and eutectic L↔(Fe+Cgraphite. The ternary alloys were thereafter studied in nondeaerated solution of 10−3 M NaHCO3 + 10−3 M Na2SO4, at 25°C, by means of the potentiodynamic technique. The results indicate that the corrosion resistance of the FeCoC alloys depends on the carbon amount and the morphology of the phases present in the studied alloys.

  6. Investigation of hydrogen-deformation interactions in β-21S titanium alloy using thermal desorption spectroscopy

    International Nuclear Information System (INIS)

    Tal-Gutelmacher, E.; Eliezer, D.; Boellinghaus, Th.

    2007-01-01

    The focus of this paper is the investigation of the combined influence of hydrogen and pre-plastic deformation on hydrogen's absorption/desorption behavior, the microstructure and microhardness of a single-phased β-21S alloy. In this study, thermal desorption analyses (TDS) evaluation of various desorption and trapping parameters provide further insight on the relationships between hydrogen absorption/desorption processes and deformation, and their mutual influence on the microstructure and the microhardness of β-21S alloy. TDS spectra were supported by other experimental techniques, such as X-ray diffraction, scanning and transmission electron microscopy, hydrogen quantity analyses and microhardness tests. Pre-plastic deformation, performed before the electrochemical hydrogenation of the alloy, increased significantly the hydrogen absorption capacity. Its influence was also evident on the notably expanded lattice parameter of β-21S alloy after hydrogenation. However, no hydride precipitation was observed. An interesting softening effect of the pre-deformed hydrogenated alloy was revealed by microhardness tests. TDS demonstrated the significant effect of pre-plastic deformation on the hydrogen evolution process. Hydrogen desorption temperature and the activation energy for hydrogen release increased, additional trap states were observed and the amount of desorbed hydrogen decreased

  7. Electrochemical behavior and stability of a commercial activated carbon in various organic electrolyte combinations containing Li-salts

    International Nuclear Information System (INIS)

    Zhang, Tong; Fuchs, Bettina; Secchiaroli, Marco; Wohlfahrt-Mehrens, Margret; Dsoke, Sonia

    2016-01-01

    Highlights: • 1 M LiPF 6 in PC displays the widest electrochemical stability window among others couples electrolyte/activated carbon. • Electrolytes based on EC-DMC show lower impedance than electrolytes containing PC. • 1 M LiPF 6 in PC has the highest cycling stability with 75% of capacitance retention after 20 000 cycles. - Abstract: The fast development of Li-ion capacitor (LIC) technologies requires the use of low resistance and stable electrolytes. An electrolyte for a LIC not only has to provide Li for the intercalation/deintercalation of the battery-type materials, but it also needs to be compatible with the supercapacitor material. Before designing a hybrid Li-ion capacitor device containing Li-insertion and double layer-type materials, it is necessary to understand and separate the contribution of each electrode material to the resistance, capacity and stability in the chosen electrolyte. Due to the intensive research on Li-ion batteries, the interactions of Li-salt containing electrolytes combined with Li insertion materials have been extensively investigated, and a lot of literature is available on this field. In contrast, there is only little knowledge about the exclusive interaction and compatibility of Li containing electrolytes with supercapacitor-type electrode materials (in absence of battery materials). With this purpose, this paper explores the electrochemical performance of electrodes based on commercial activated carbon (AC) in various lithium salt-containing electrolytes. A standard electrolyte for Li-ion batteries (1 M LiPF 6 in EC:DMC, 1:1) is evaluated and compared with an electrolyte prepared with the same salt dissolved in propylene carbonate (1 M LiPF 6 in PC) which is a solvent typically used in commercial supercapacitors. Furthermore, two new electrolyte solutions are proposed, based on a blend of salts 0.8 M LiPF 6 + 0.2 M NEt 4 BF 4 in EC:DMC (1:1) as well as in pure PC. The effect of the electrolyte composition is evaluated

  8. Synthesis of IV-VI Transition Metal Carbide and Nitride Nanoparticles Using a Reactive Mesoporous Template for Electrochemical Hydrogen Evolution Reaction

    KAUST Repository

    Alhajri, Nawal Saad

    2016-01-01

    Interstitial carbides and nitrides of early transition metals in Groups IV-VI exhibit platinum-like behavior which makes them a promising candidate to replace noble metals in a wide variety of reactions. Most synthetic methods used to prepare these materials lead to bulk or micron size powder which limits their use in reactions in particular in catalytic applications. Attempts toward the production of transition metal carbide and nitride nanoparticles in a sustainable, simple and cheap manner have been rapidly increasing. In this thesis, a new approach was presented to prepare nano-scale transition metal carbides and nitrides of group IV-VI with a size as small as 3 nm through the reaction of transition metal precursor with mesoporous graphitic carbon nitride (mpg-C3N4) that not only provides confined spaces for nanoparticles formation but also acts as a chemical source of nitrogen and carbon. The produced nanoparticles were characterized by powder X-ray diffraction (XRD), temperature-programmed reaction with mass spectroscopy (MS), CHN elemental analyses, thermogravimetric analyses (TGA), nitrogen sorption, X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The effects of the reaction temperature, the ratio of the transition metal precursor to the reactive template (mpg-C3N4), and the selection of the carrier gas (Ar, N2, and NH3) on the resultant crystal phases and structures were investigated. The results indicated that different tantalum phases with cubic structure, TaN, Ta2CN, and TaC, can be formed under a flow of nitrogen by changing the reaction temperatures. Two forms of tantalum nitride, namely TaN and Ta3N5, were selectively formed under N2 and NH3 flow, respectively. Significantly, the formation of TaC, Ta2CN, and TaN can be controlled by altering the weight ratio of the C3N4 template relative to the Ta precursor at 1573 K under a flow of nitrogen where high C3N4/Ta precursor ratio generally resulted in high carbide

  9. Mechanistic and kinetic study of pyrite (FeS2)-hydrogen (H2) interaction at 25°C using electrochemical techniques

    OpenAIRE

    Betelu, Stéphanie; Lerouge, Catherine; Berger, Gilles; Giffaut, Eric; Ignatiadis, Ioannis

    2012-01-01

    After the closure of the underground nuclear waste repository, aqueous corrosion of the steel canister and, to a lesser extent, radiolysis of water would produce significant amounts of H2. This H2 can interact with materials from the repository and with the surrounding clay host formation. The COx formation contains pyrite (FeS2), which has been demonstrated to react with Hydrogen gas (H2) (Truche et al. 2010) at temperature ranging from 90°C to 180°C. This work aims at understanding these in...

  10. Metal alloys for the new generation of compressors at hydrogen stations: Parametric study of corrosion behavior

    DEFF Research Database (Denmark)

    Arjomand Kermani, Nasrin; Petrushina, Irina; Nikiforov, Aleksey Valerievich

    2017-01-01

    the corrosion rate. However, even at 80 °C, the very low corrosion current densities proved that all of the tested alloys are safe to use as construction materials. AISI 347 showed very high corrosion resistance in all of the ionic liquids. The highest corrosion resistance among all of the tested alloys......, consequently, significantly reduce the final cost of hydrogen production. The correct choice of ionic liquid and construction materials is critical for avoiding significant corrosion problems. Hence, the objective of this study is to evaluate the compatibility of various austenitic stainless steels and nickel......-based alloys as construction materials in contact with 80 °C ionic liquids in an ionic liquid hydrogen compressor, considering the role of parameters such as the temperature, viscosity, ionic liquid cation and anion, and water absorption. The results show that temperature contributes to increasing...

  11. Self-Ignition Behavior of Propane-Air Mixtures with Hydrogen Addition in Catalytic Micro-Channels Coupling Reduced-Order Kinetic Model and Heat Transfer

    OpenAIRE

    Junjie Chen

    2016-01-01

    Hydrogen-assisted self-ignition of propane-air mixtures under ambient condition were carried out in platinum-coated micro-channels, using a two-dimensional model with reduced-order reaction schemes, heat conduction in the solid walls, convection and surface radiation heat transfer. The self-ignition behavior of the hydrogen-propane mixed fuel is compared for the case of heated feed is analyzed. Simulations indicate that hydrogen can successfully cause self-ignition of propane-air mixtures in ...

  12. Ruthenium Ion-Complexed Graphitic Carbon Nitride Nanosheets Supported on Reduced Graphene Oxide as High-Performance Catalysts for Electrochemical Hydrogen Evolution.

    Science.gov (United States)

    Peng, Yi; Pan, Wanzhang; Wang, Nan; Lu, Jia-En; Chen, Shaowei

    2018-01-10

    Carbon-based materials are promising, low-cost electrocatalysts toward hydrogen evolution reaction (HER), although the catalytic performance needs to be further improved before commercialization. In this study, ruthenium ions are incorporated into graphitic carbon nitride/reduced graphene oxide (rGO) hybrids to form Ru-C 3 N 4 /rGO composites through Ru-N coordination bonds. The incorporation of Ru ions, at a loading of 1.93 at. %, leads to electron redistribution within the materials and dramatically enhances the HER performance over those of C 3 N 4 , C 3 N 4 /rGO, and Ru-C 3 N 4 , with an overpotential of only -80 mV to reach a current density of 10 mA cm -2 , a Tafel slope of 55 mV dec -1 , and an exchange current density of 0.462 mA cm -2 . This performance is comparable to that of Pt/C, and ascribed to the positive shift of the conduction band of the composite, where the charge carrier density increases by a factor of about 250 over that of C 3 N 4 , leading to a lower energy barrier for hydrogen evolution. The results suggest a new strategy in the design and engineering of functional nanocomposites for effective HER electrocatalysis by embedding select metal ions into carbon-based molecular skeletons. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Tuning the activity of nanoplatelet MoS{sub 2}-based catalyst for efficient hydrogen evolution via electrochemical decoration with Pt nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Jagminas, Arunas, E-mail: jagmin@ktl.mii.lt [State Research Institute Centre for Physical Sciences and Technology, Savanoriu 231, LT-02300 Vilnius (Lithuania); Naujokaitis, Arnas [State Research Institute Centre for Physical Sciences and Technology, Savanoriu 231, LT-02300 Vilnius (Lithuania); Vilnius University, Faculty of Physics, Sauletekio av. 9, LT-10222 Vilnius (Lithuania); Žalnėravičius, Rokas; Jasulaitiene, Vitalija [State Research Institute Centre for Physical Sciences and Technology, Savanoriu 231, LT-02300 Vilnius (Lithuania); Valušis, Gintaras [State Research Institute Centre for Physical Sciences and Technology, Savanoriu 231, LT-02300 Vilnius (Lithuania); Vilnius University, Faculty of Physics, Sauletekio av. 9, LT-10222 Vilnius (Lithuania)

    2016-11-01

    Highlights: • MoS{sub 2}-based nanoplatelet films on Mo substrate by hydrothermal treatment. • Electrochemical decoration of MoS{sub 2} nanoplatelets with Pt nanoparticles. • Ultra-high efficiency of HER at heterostructured electrode surface. - Abstract: This study establishes a novel methodology for increasing the HER activity of the molybdenum substrate covered with amorphous molybdenum sulfide-oxide nano-structured film up to ultra-high level. We show that utilization of such nanoplatelet/nanoflowered film as electrocatalyst for HER in the sulfuric acidic solution cell with Pt anode and Ag/AgCl,KCl reference leads to obvious structural transformations and nice decoration of nanoplatelet edges with few-nm sized Pt nanoparticles. By this way, a surprising HER efficiency attaining ∼160 mA cm{sup −2} current density at −200 mV and ∼260 mA cm{sup −2} at −300 mV vs RHE overpotentials with the onset of reaction close to the one carried out at the bulk Pt electrode was obtained. To the best of our knowledge, these HER characteristics are among the best reported to date for hybrid MoS{sub 2}-based HER electrocatalysts. The results obtained were confirmed by SEM, XPS, XRD, conductive mode AFM and cyclic voltammetry. It is worth noticing that to achieve this synergetic effect only about 0.5 μg cm{sup −2} of Pt is required.

  14. Electrochemical and chemical corrosion of chromium

    International Nuclear Information System (INIS)

    Drazic, Dragutin M.; Popic, Jovan P.

    2004-01-01

    It was shown that chromium in deaerated sulfuric acid of pH 1 exhibits two stable corrosion potentials, depending whether the metal had previously been in contact with air or subjected to activation by cathodic evolving hydrogen. Electrochemical polarization measurements, as well as the measurements of the actual metal dissolution rate at the corrosion potential, anodic or cathodic polarization, using the analytical determination of Cr ions in the solution, or volumes of hydrogen evolved, showed that hydrogen can evolve on chromium by three different reaction mechanisms. The first one is the electrochemical hydrogen evolution reaction from H + ions at the bare chromium surface obtained by cathodic activation. This reaction and the active anodic dissolution of chromium determine one stable corrosion potential. The second reaction is the reaction of H + ions on the oxidized chromium surface which, coupled with the anodic dissolution of passivated chromium determines the other stable corrosion potential. The third one is the 'anomalous' or chemical reaction of chromium with water molecules and hydrogen ions whereby hydrogen is liberated. This is a potential independent reaction, occurring on the bare metal surface, and which is at pH 1 several times faster at the corrosion potential than the electrochemical hydrogen evolution reaction. The consequence is that the overall corrosion rate is several times faster than that determined by the usual electrochemical methods. The measurements were performed in the temperature interval 20 - 65 o C and apparent energies of activation for anodic, cathodic and anomalous dissolution reactions were estimated as 63.1, 19.5 and 66.9 kJ mol -1 , respectively. This implies that the anomalous dissolution rate increases more with the increase of temperature than the electrochemical corrosion rate. The applicability of the different methods of measuring electrochemical corrosion rates is discussed. (Author)

  15. Characterization of the electrochemical behavior of coating by steel welding 308l and in presence of noble metals deposits

    International Nuclear Information System (INIS)

    Piedras, P.; Arganis J, C. R.

    2014-10-01

    In this work the oxide deposits and noble metals deposit were characterized (Ag and Pt) on a coating of stainless steel 308l that were deposited by the shield metal arc welding (SMAW) on steel A36 by means of scanning electron microscopy, energy-dispersive X-ray spectroscopy and X-ray diffraction. The extrapolation of Tafel technique was also used to obtain the corrosion potential (Ec) for the pre-rusty steel and for the samples with deposits of Pt and Ag under conditions of hydrogen water chemistry (HWC), demonstrating that this parameter diminishes with the presence of this deposits. (Author)

  16. Preparation of three-dimensional nitrogen-doped graphene layers by gas foaming method and its electrochemical capactive behavior

    International Nuclear Information System (INIS)

    Hao, Junnan; Shu, Dong; Guo, Songtao; Gao, Aimei; He, Chun; Zhong, Yayun; Liao, Yuqing; Huang, Yulan; Zhong, Jie

    2016-01-01

    Highlights: • A three-dimensional porous graphene layers was prepared via a gas foaming method. • Melamine was the nitrogen source to synthesize the N-doped 3D graphene layers. • The specific surface area of 3D N-doped graphene material is as high as 1196 m 2 g −1 . • The 3D N-doped graphene specific capacitance is 335 F g −1 in three-electrode system. • The energy density of 3D N-doped graphene reaches 58.1 Wh kg −1 in a symmetric cell. - Abstract: A porous graphene layers with a three-dimensional structure (3DG) was prepared via a gas foaming method based on a polymeric predecessor. This intimately interconnected 3DG structure not only significantly increases the specific surface area but also provides more channels to facilitate electron transport. In addition, 3D N-doped (3DNG) layers materials were synthesized using melamine as a nitrogen source. The nitrogen content in the 3DNG layers significantly influenced the electrochemical performance. The sample denoted as 3DNG-2 exhibited a specific capacitance of 335.2 F g −1 at a current density of 1 A g −1 in a three-electrode system. Additionally, 3DNG-2 exhibited excellent electrochemical performance in aqueous and organic electrolytes using a two-electrode symmetric cell. An energy density of 58.1 Wh kg −1 at a power density of 2500 W kg −1 was achieved, which is approximately 3 times that (19.6 Wh kg −1 ) in an aqueous electrolyte in a two-electrode system. After 1000 cycles, the capacity retention in aqueous electrolyte was more than 99.0%, and this retention in organic electrolytes was more than 89.4%, which demonstrated its excellent cycle stability. This performance makes 3DNG-2 a promising candidate as an electrode material in high-power and high-energy supercapacitor applications.

  17. (Nd/Pr)2NiO4+δ: Reaction Intermediates and Redox Behavior Explored by in Situ Neutron Powder Diffraction during Electrochemical Oxygen Intercalation.

    Science.gov (United States)

    Ceretti, Monica; Wahyudi, Olivia; André, Gilles; Meven, Martin; Villesuzanne, Antoine; Paulus, Werner

    2018-04-16

    Oxygen intercalation/deintercalation in Pr 2 NiO 4+δ and Nd 2 NiO 4+δ was followed by in situ neutron powder diffraction during electrochemical oxidation/reduction, in a dedicated reaction cell at room temperature. For both systems three phases, all showing the same line width, were identified. The starting phases Pr 2 NiO 4.23 and Nd 2 NiO 4.24 , considered with an average orthorhombic Fmmm symmetry, although both show a slight monoclinic distortion, get reduced in a two-phase reaction step to tetragonal intermediate phases with 0.07 ≤ δ ≤ 0.10 and P4 2 / ncm space group, which on further reduction transform, again in a two-phase reaction step, toward the respective stoichiometric (Pr/Nd) 2 NiO 4.0 phases, with Bmab space group. Electrochemical oxidation does, however, not proceed fully reversibly for both cases: while the reoxidation of Nd 2 NiO 4+δ is limited to the tetragonal intermediate phase with δ = 0.10, the homologous Pr 2 NiO 4+δ can be reoxidized up to δ = 0.17, showing orthorhombic symmetry. For the intermediate tetragonal phase, we were able to establish for Pr 2 NiO 4.09 a complex anharmonic displacement behavior of the apical oxygen atoms, as analyzed by single-crystal neutron diffraction and maximum entropy analysis, in agreement with a low- T diffusion pathway for oxygen ions, activated by lattice dynamics.

  18. Electrochemical studies of materials for cathodes in hydrogen-producing systems; Estudios electroquimicos de materiales para catodos em sistemas productores de hidrogeno

    Energy Technology Data Exchange (ETDEWEB)

    Goni Capurro, M.J.; Gaisch, A.M.; Kessler, T. [Universidad Nacional del Centro de la Provincia de Buenos Aires, Tandil (Argentina). Facultad de Ingenieria; Triaca, W.E. [INIFTA, La Plata (Argentina)

    1997-12-31

    Hydrogen gas has been proposed as an alternative fuel considering the problem of environmental contamination due to the combustion of fossil fuels. In the search of new electrode material for industrial water electrolysis systems, commercially available amorphous alloys present interesting physicochemical properties and mechanical stability when used in different aqueous solutions. The most frequently materials used as electrodes are steel and nickel. In this work, the electrocatalytic behaviour of the following amorphous alloys, Fe{sub 76} Si{sub 1 }B{sub 12} and Ni{sub 78} Si{sub 8} B{sub 14} are presented. The results are compared to the polycrystalline metals. (author) 13 refs., 2 figs., 2 tabs.; e-mail: postmaster at unceni.edu.ar

  19. Electrochemical Cell

    DEFF Research Database (Denmark)

    1999-01-01

    The invention relates to a rechargeable electrochemical cell comprising a negative electrode, an electrolyte and a positive electrode in which the positive electrode structure comprises a lithium cobalt manganese oxide of the composition Li¿2?Co¿y?Mn¿2-y?O¿4? where 0 ... for capacity losses in lithium ion cells and lithium-alloy cells....

  20. Electrochemical capacitor

    Science.gov (United States)

    Anderson, Marc A.; Liu, Kuo -Chuan; Mohr, Charles M.

    1999-10-05

    An inexpensive porous metal oxide material having high surface area, good conductivity and high specific capacitance is advantageously used in an electrochemical capacitor. The materials are formed in a sol-gel process which affords control over the properties of the resultant metal oxide materials.

  1. Metallic glassy Zr70Ni20Pd10 powders for improving the hydrogenation/dehydrogenation behavior of MgH2

    Science.gov (United States)

    El-Eskandarany, M. Sherif

    2016-01-01

    Because of its low density, storage of hydrogen in the gaseous and liquids states possess technical and economic challenges. One practical solution for utilizing hydrogen in vehicles with proton-exchange fuel cells membranes is storing hydrogen in metal hydrides. Magnesium hydride (MgH2) remains the best hydrogen storage material due to its high hydrogen capacity and low cost of production. Due to its high activation energy and poor hydrogen sorption/desorption kinetics at moderate temperatures, the pure form of MgH2 is usually mechanically treated by high-energy ball mills and catalyzed with different types of catalysts. These steps are necessary for destabilizing MgH2 to enhance its kinetics behaviors. In the present work, we used a small mole fractions (5 wt.%) of metallic glassy of Zr70Ni20Pd10 powders as a new enhancement agent to improve its hydrogenation/dehydrogenation behaviors of MgH2. This short-range ordered material led to lower the decomposition temperature of MgH2 and its activation energy by about 121 °C and 51 kJ/mol, respectively. Complete hydrogenation/dehydrogenation processes were successfully achieved to charge/discharge about 6 wt.%H2 at 100 °C/200 °C within 1.18 min/3.8 min, respectively. In addition, this new nanocomposite system shows high performance of achieving continuous 100 hydrogen charging/discharging cycles without degradation. PMID:27220994

  2. Comment on "Uncovering the Complex Behavior of Hydrogen in Cu2O"

    OpenAIRE

    Biswas, K.; Du, M. -H.; -Thienprasert, J. T.; Limpijumnong, S.; Singh, D. J.

    2011-01-01

    In a recent Letter Scanlon and Watson reported their first principles results on hydrogen in Cu2O. Their main conclusions are: (1) an interstitial H in Cu2O prefers to occupy the tetrahedral site, which is coordinated with four Cu cations, in all three charge states (+1, neutral, and -1); (2) H will bind with a Cu vacancy and form an electrically active H-VCu defect complex, which is amphoteric with (+/0) and (0/-)transition levels at Ev + 0.1 and Ev + 1.1 eV, respectively. However, these two...

  3. Comparative electrochemical sodium insertion/extraction behavior in layered NaxVS2 and NaxTiS2

    International Nuclear Information System (INIS)

    Lee, Eungje; Sahgong, SunHye; Johnson, Christopher S.; Kim, Youngsik

    2014-01-01

    This study investigates the electrochemical sodium insertion/extraction of Na x VS 2 , and Na x TiS 2 in the voltage range where either intercalation (0.2 ≤ x ≤ 1) or displacement-conversion reaction (x > 1) occurs. Both Na x VS 2 and Na x TiS 2 showed good reversible capacities, as high as ∼160 mAh/g at an average voltage of ∼1.9 V vs. Na in the region for the intercalation reaction (0.2 ≤ x ≤ 1). When sodium (Na) insertion was forced further to the x > 1 composition, Na x VS 2 exhibited the direct displacement-conversion reaction at 0.3 V vs. Na without further Na intercalation, which contrasted with the wider lithium intercalation range of 0 < x ≤ 2 for Li x VS 2 . The displacement-conversion reaction for Na x VS 2 (x > 1) was reversible with a specific capacity of above 200 mAh/g up to 15 cycles, but the displacement reaction for Na x TiS 2 (x > 1) was not observed

  4. Preparation, electrochemical behavior and electrocatalytic activity of chlorogenic acid multi-wall carbon nanotubes as a hydroxylamine sensor

    Energy Technology Data Exchange (ETDEWEB)

    Zare, Hamid R., E-mail: hrzare@yazduni.ac.ir; Nasirizadeh, Navid; Ajamain, Hamideh; Sahragard, Ali

    2011-07-20

    Electrochemical characteristics of an electrodeposited chlorogenic acid film on multi-wall carbon nanotubes glassy carbon electrode (CGA-MWCNT-GCE) and its role as a sensor for electrocatalytic oxidation of hydroxylamine are described. Cyclic voltammograms of the CGA-MWCNT-GCE indicate a pair of well-defined and nearly reversible redox couple with the surface confined characteristics at a wide pH range of 2.0-12.0. The charge transfer coefficient, {alpha}, and the charge transfer rate constant, k{sub s}, of CGA adsorbed on MWCNT were calculated 0.48 and 44 {+-} 2 s{sup -1} respectively. The CGA-MWCNT-GCE shows a dramatic increase in the peak current and/or a decrease in the overvoltage of hydroxylamine electrooxidation in comparison with that seen at a CGA modified GCE, MWCNT modified GCE and activated GCE. The kinetic parameters of electron transfer coefficient, {alpha}, the heterogeneous electron transfer rate constant, k', and exchange current, i{sub 0}, for oxidation of hydroxylamine at the modified electrode surface were determined using cyclic voltammetry. Four linear calibration ranges and high repeatability with relative standard deviation of 4.6%, for a series of four successive measurements in 17.7 {mu}M hydroxylamine, are obtained at the CGA-MWCNT-GCE using an amperometric method. Finally, the modified electrode was successfully used for determination of spiked hydroxylamine in two water samples.

  5. Electrochemical Behavior and Determination of Chlorogenic Acid Based on Multi-Walled Carbon Nanotubes Modified Screen-Printed Electrode

    Directory of Open Access Journals (Sweden)

    Xiaoyan Ma

    2016-10-01

    Full Text Available In this paper, the multi-walled carbon nanotubes modified screen-printed electrode (MWCNTs/SPE was prepared and the MWCNTs/SPE was employed for the electrochemical determination of the antioxidant substance chlorogenic acids (CGAs. A pair of well-defined redox peaks of CGA was observed at the MWCNTs/SPE in 0.10 mol/L acetic acid-sodium acetate buffer (pH 6.2 and the electrode process was adsorption-controlled. Cyclic voltammetry (CV and differential pulse voltammetry (DPV methods for the determination of CGA were proposed based on the MWCNTs/SPE. Under the optimal conditions, the proposed method exhibited linear ranges from 0.17 to 15.8 µg/mL, and the linear regression equation was Ipa (µA = 4.1993 C (×10−5 mol/L + 1.1039 (r = 0.9976 and the detection limit for CGA could reach 0.12 µg/mL. The recovery of matrine was 94.74%–106.65% (RSD = 2.92% in coffee beans. The proposed method is quick, sensitive, reliable, and can be used for the determination of CGA.

  6. Effect of rigidity of porous structure on electrochemical behavior of pristine Li4Ti5O12 microspheres

    International Nuclear Information System (INIS)

    Jia, Zhenyong; Zhou, Qun; Li, Xiaowei; Fu, Yu; Ming, Hai; Zheng, Junwei

    2015-01-01

    Highlights: • Rigid porous framework of Li 4 Ti 5 O 12 microspheres can be fabricated by mutual molten growth of primary particles. • Well-confined nanosized tortuous channels are formed inside Li 4 Ti 5 O 12 microspheres. • Li 4 Ti 5 O 12 microspheres with rigid porous structures exhibit greatly enhanced electrochemical performance. - Abstract: Highly controllable porous architecture is desirable to tailor the physical and chemical properties of functional materials in advanced lithium ion batteries. Here, porous microspheres of spinel lithium titanate (Li 4 Ti 5 O 12 ), a promising alternative anode material for lithium ion batteries, are fabricated by mutual molten growth method in a controllable manner. The key role of the rigidity of the porous structure on the performance of the electrode materials in lithium ion batteries is demonstrated. Rigid framework of the materials is formed by second growth of the primary particles that fused together to generate an interconnected nanopore system inside the spheres, leading to better electrolyte diffusion and lower interparticle contact resistance, relative to the non-porous counterpart. The pristine Li 4 Ti 5 O 12 microspheres with uniform pore distribution and continuous framework exhibit high tap density, remarkable reversible capacity and rate capability, as well as excellent cycling stability. The present method is scalable and may provide a new approach to fabricate other candidate electrode materials for applications that require both high power and high volumetric energy density

  7. Preparation, electrochemical behavior and electrocatalytic activity of chlorogenic acid multi-wall carbon nanotubes as a hydroxylamine sensor

    International Nuclear Information System (INIS)

    Zare, Hamid R.; Nasirizadeh, Navid; Ajamain, Hamideh; Sahragard, Ali

    2011-01-01

    Electrochemical characteristics of an electrodeposited chlorogenic acid film on multi-wall carbon nanotubes glassy carbon electrode (CGA-MWCNT-GCE) and its role as a sensor for electrocatalytic oxidation of hydroxylamine are described. Cyclic voltammograms of the CGA-MWCNT-GCE indicate a pair of well-defined and nearly reversible redox couple with the surface confined characteristics at a wide pH range of 2.0-12.0. The charge transfer coefficient, α, and the charge transfer rate constant, k s , of CGA adsorbed on MWCNT were calculated 0.48 and 44 ± 2 s -1 respectively. The CGA-MWCNT-GCE shows a dramatic increase in the peak current and/or a decrease in the overvoltage of hydroxylamine electrooxidation in comparison with that seen at a CGA modified GCE, MWCNT modified GCE and activated GCE. The kinetic parameters of electron transfer coefficient, α, the heterogeneous electron transfer rate constant, k', and exchange current, i 0 , for oxidation of hydroxylamine at the modified electrode surface were determined using cyclic voltammetry. Four linear calibration ranges and high repeatability with relative standard deviation of 4.6%, for a series of four successive measurements in 17.7 μM hydroxylamine, are obtained at the CGA-MWCNT-GCE using an amperometric method. Finally, the modified electrode was successfully used for determination of spiked hydroxylamine in two water samples.

  8. Electrochemical behavior of ruthenium-hexacyanoferrate modified glassy carbon electrode and catalytic activity towards ethanol electro oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Costa, Wendell M.; Marques, Aldalea L.B., E-mail: aldalea.ufma@hotmail.com [Universidade Federal do Maranhao (UFMA), Sao Luis, MA (Brazil). Departamento de Quimica Tecnologica; Cardoso, William S.; Marques, Edmar P.; Bezerra, Cicero W.B. [Universidade Federal do Maranhao (UFMA), Sao Luis, MA (Brazil). Departamento de Qumica; Ferreira, Antonio Ap. P. [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), Araraquara, SP (Brazil). Instituto de Quimica; Song, Chaojie; Zhang, Jiujun [Energy, Mining and Environment Portfolio, National Research Council of Canada, Vancouver, BC (Canada)

    2013-04-15

    Ruthenium-based hexacyanoferrate (RuHCF) thin film modified glassy carbon electrode was prepared by drop evaporation method. The RuHCF modified electrode exhibited four redox couples in strong acidic solution (pH 1.5) attributed to Fe(CN){sub 6}{sup 3-} ion and three ruthenium forms (Ru(II), Ru(III) and Ru(IV)), characteristic of ruthenium oxide compounds. The modified electrode displayed excellent electrocatalytic activity towards ethanol oxidation in the potential region where electrochemical processes Ru(III)-O-Ru(IV) and Ru(IV)-O-Ru(VI) occur. Impedance spectroscopy data indicated that the charge transfer resistance decreased with the increase of the applied potential and ethanol concentration, indicating the use of the RuHCF modified electrode as an ethanol sensor. Under optimized conditions, the sensor responded linearly and rapidly to ethanol concentration between 0.03 and 0.4 mol L{sup -1} with a limit of detection of 0.76 mmol L{sup -1}, suggesting an adequate sensitivity in ethanol analyses. (author)

  9. An electrochemical investigation of the corrosion behavior of Al-Si-Cu hypereutectic alloys in alcoholic environments

    International Nuclear Information System (INIS)

    Traldi, S. M.; Rossi, J. L.; Costa, I.

    2003-01-01

    Al-Si-Cu hypereutectic alloys produced by spray forming are mostly used in the automotive industry, especially for cylinder liners. they the advantage of low weight associated with low coefficient of thermal expansion and excellent mechanical properties- mainly wear resistance at high temperatures. The corrosion s resistance of these alloys in fuels, particularly alcoholic media, however is not yet known. In this investigation, electrochemical impedance spectroscopy (EIS) and potentiodynamic polarisation hove been used to evaluate the corrosion resistance of a hyper eutectic Al-Si-Cu alloy in alcoholic environments. the EIS tests carried out in pure ethanol, and ethanol with small additions (1 mM) of acid an chloride to investigate the effect of these contaminants on corrosion resistance. The corrosion resistance of a grey cast iron has also been evaluated in pure ethanol for comparison. The Al-Si-Cu alloy showed high corrosion resistance in pure ethanol, far superior to that of grey cast iron in the same medium. (Author) 13 refs

  10. Improvement of the electrochemical and electrocatalytic behavior of Prussian blue/carbon nanotubes composite via ionic liquid treatment

    International Nuclear Information System (INIS)

    Keihan, A.H.; Sajjadi, S.

    2013-01-01

    This paper reports the greatly improved electrochemical properties of Prussian blue/carbon nanotubes (PB/CNTs) modified glassy carbon electrode via a room temperature ionic liquid (RTIL) treatment. Firstly, the GC electrodes were modified with nanocomposites of RTIL/CNTs. Then, the PB nanoparticles were electrodeposited onto the modified electrode surface. Compared with the PB/CNTs/GC, the PB/RTIL/CNTs/GC electrodes showed higher PB surface concentration value of 2.42 × 10 −9 mol cm −2 , indicating that PB deposition efficiency was improved by 1.8 fold. The apparent diffusion coefficient for K + displayed value of 5.77 × 10 −11 cm 2 s −1 , which was one order of magnitude higher than that in the absence of RTIL. PB/RTIL/CNTs/GC modified electrodes showed higher electron transfer rate of 2.44 s −1 (2.35 times as much as that of PB/CNTs/GC electrodes). RTIL modified electrodes also displayed high sensitivity toward H 2 O 2 reduction (185.90 μA mM −1 cm −2 ) with low detection limit of 0.49 μM. The RTIL modified electrodes stored dry at room temperature preserved almost 100% of their initial currents over a period of 1 month, a useful property for commercial applications

  11. Electrochemical Behavior of PEDOT/Lignin in Ionic Liquid Electrolytes: Suitable Cathode/Electrolyte System for Sodium Batteries.

    Science.gov (United States)

    Casado, Nerea; Hilder, Matthias; Pozo-Gonzalo, Cristina; Forsyth, Maria; Mecerreyes, David

    2017-04-22

    Biomass-derived polymers, such as lignin, contain quinone/ hydroquinone redox moieties that can be used to store charge. Composites based on the biopolymer lignin and several conjugated polymers have shown good charge-storage properties. However, their performance has been only studied in acidic aqueous media limiting their applications mainly to supercapacitors. Here, we show that PEDOT/lignin (PEDOT: poly(3,4-ethylenedioxythiophene)) biopolymers are electroactive in aprotic ionic liquids (ILs) and we move a step further by assembling sodium full cell batteries using PEDOT/lignin as electrode material and IL electrolytes. Thus, the electrochemical activity and cycling of PEDOT/lignin electrodes was investigated in 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide (BMPyrTFSI), 1-butyl-1-methylpyrrolidinium bis(fluorosulfonyl)imide (BMPyrFSI), 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMImTFSI) and 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide (EMImFSI) IL electrolytes. The effects of water and sodium salt addition to the ILs were investigated to obtain optimum electrolyte systems for sodium batteries. Finally, sodium batteries based on PEDOT/lignin cathode with imidazolium-based IL electrolyte showed higher capacity values than pyrrolidinium ones, reaching 70 mAhg -1 . Our results demonstrate that PEDOT/lignin composites can serve as low cost and sustainable cathode materials for sodium batteries. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Electrochemical Corrosion Behavior of Carbon Steel and Hot Dip Galvanized Steel in Simulated Concrete Solution with Different pH Values

    Directory of Open Access Journals (Sweden)

    Wanchen XIE

    2017-08-01

    Full Text Available Hot dip galvanizing technology is now widely used as a method of protection for steel rebars. The corrosion behaviors of Q235 carbon steel and hot galvanized steel in a Ca(OH2 solution with a pH from 10 to 13 was investigated by electrode potential and polarization curves testing. The results indicated that carbon steel and hot galvanized steel were all passivated in a strong alkaline solution. The electrode potential of hot dip galvanized steel was lower than that of carbon steel; thus, hot dip galvanized steel can provide very good anodic protection for carbon steel. However, when the pH value reached 12.5, a polarity reversal occurred under the condition of a certain potential. Hot dip galvanized coating became a cathode, and the corrosion of carbon steel accelerated. The electrochemical behaviors and passivation abilities of hot dip galvanized steel and carbon steel were affected by pH. The higher the pH value was, the more easily they were passivated.DOI: http://dx.doi.org/10.5755/j01.ms.23.3.16675

  13. An electrochemical investigation of the corrosion behavior of aluminum alloys in chloride containing solutions; Investigacao eletroquimica da corrosao de ligas de aluminio em solucoes contendo cloretos

    Energy Technology Data Exchange (ETDEWEB)

    Campos Filho, Jorge Eustaquio de [Minas Gerais Univ., Belo Horizonte, MG (Brazil). Escola de Engenharia. Dept. de Engenharia Quimica]. E-mail: jorgecamposfilho@yahoo.com.br; Neves, Celia de Figueiredo Cordeiro; Campos, Wagner Reis da Costa; Moreira, Marcilio Soares [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Belo Horizonte, MG (Brazil)]. E-mail: caf@cdtn.br; wrcc@cdtn.br; msm@cdtn.br

    2005-07-01

    Aluminum alloys have been used as cladding materials for nuclear fuel in research reactors due to its corrosion resistance. Aluminum owes its good corrosion resistance to a protective barrier oxide film formed and strongly bonded to its surface. In pool type TRIGA IPR-R1 reactor, located at Centro de Desenvolvimento da Tecnologia Nuclear in Belo Horizonte, previous immersion coupon tests revealed that aluminum alloys suffer from pitting corrosion, in spite of high quality of water control. Corrosion attack is initiated by breaking the protective oxide film on aluminum alloy surface. Chloride ions can break this oxide film and stimulate metal dissolution. In this study the aluminum alloys 1050, 5052 and 6061 were used to evaluate their corrosion behavior in chloride containing solutions. The electrochemical techniques used were potentiodynamic anodic polarization and cyclic polarization. Results showed that aluminum alloys 5052 and 6061 present similar corrosion resistance in low chloride solutions (0,1 ppm NaCl) and in reactor water but both alloys are less resistant in high chloride solution (1 ppm NaCl). Aluminum alloy 1050 presented similar behavior in the three electrolytes used, regarding to pitting corrosion, indicating that the concentration of the chloride ions was not the only variable to influence its corrosion susceptibility. (author)

  14. Multiferroic behavior associated with an order-disorder hydrogen bonding transition in metal-organic frameworks (MOFs) with the perovskite ABX3 architecture.

    Science.gov (United States)

    Jain, Prashant; Ramachandran, Vasanth; Clark, Ronald J; Zhou, Hai Dong; Toby, Brian H; Dalal, Naresh S; Kroto, Harold W; Cheetham, Anthony K

    2009-09-30

    Multiferroic behavior in perovskite-related metal-organic frameworks of general formula [(CH(3))(2)NH(2)]M(HCOO)(3), where M = Mn, Fe, Co, and Ni, is reported. All four compounds exhibit paraelectric-antiferroelectric phase transition behavior in the temperature range 160-185 K (Mn: 185 K, Fe: 160 K; Co: 165 K; Ni: 180 K); this is associated with an order-disorder transition involving the hydrogen bonded dimethylammonium cations. On further cooling, the compounds become canted weak ferromagnets below 40 K. This research opens up a new class of multiferroics in which the electrical ordering is achieved by means of hydrogen bonding.

  15. Nuclear hydrogen power stations

    International Nuclear Information System (INIS)

    Eroshov, M.E.

    1976-01-01

    Short information about investigations on hydrogen energetics being carried out in the USSR as well as a review of the world literature on this subject are given. Combined cycles of thermochemical and electrochemical reactions applied for hydrogen and oxygen production from water are shown to be of interest, as a number of reactions in a cycle may be reduced to two, and the temperature of processes may be decreased to the temperature range specific to modern reactors. Construction features of nuclear-hydrogen power stations producing hydrogen through the use of thermo-electrochemical cycles are considered. It is shown that at this stage it is possible to reduce time and expenses needed for realization of hydrogen production on a wide scale as compared to other reaction cycles requiring high temperatures and consequently, construction of high-temperature reactors. The conditions of energy and water transport at great distances by using hydrogen lines and the possibilities of development of desert and arid lands by using this mode of operation are considered. Possible ecological effect of hydrogen energetics development on the environment is pointed out, in particular, when power complexes are concentrated on a limited area. It is shown that it is reasonable to locate nuclear-hydrogen stations on shores

  16. Specific equilibrium behavior of hydrogen isotopes adsorbed onto synthetic zeolite A-type governed by lithium cations

    Energy Technology Data Exchange (ETDEWEB)

    Takashima, Shoji [Graduate School of Engineering, Kyushu University, Moto-oka 744, Nishi-ku, Fukuoka 819-0395 (Japan); Kotoh, Kenji, E-mail: kotoh@nucl.kyushu-u.ac.jp [Graduate School of Engineering, Kyushu University, Moto-oka 744, Nishi-ku, Fukuoka 819-0395 (Japan); Faculty of Engineering, Kyushu University, Moto-oka 744, Nishi-ku, Fukuoka 819-0395 (Japan)

    2013-10-15

    Highlights: • Isotherms for H{sub 2} and D{sub 2} adsorbed onto SZ-LiA at 77.4 K are shown. • The adsorption isotherms exhibit specific deviation in the range lower than 10 Pa. • SZ-LiA indicates the power of several 100-times at 0.1 Pa, compared with SZ-NaA. • Experimental isotherms are described empirically by a dual-site Langmuir equation. • The isotope effect on adsorption isotherms appears in the Langmuir constants. -- Abstract: Since synthetic zeolites (SZs) are powerfully adsorptive for hydrogen isotopes at cryogenic temperatures such as liquefied nitrogen, adsorption processes using these have been considered applicable to such as recovery of tritium from the lithium blanket of DT fusion reactor system. Onto these zeolites the adsorptions isotherms for hydrogen isotopes onto SZ-NaA, SZ-CaA and SZ-NaX at 77.4 K were already clarified experimentally and analytically. These isotherms exhibit similar profiles of Langmuir type. In this work, adsorption isotherms were examined for H{sub 2} and D{sub 2} on SZ-LiA at 77.4 K. SZ-LiA was made from SZ-NaA by exchanging its sodium ions for lithium ones, provided by TOSOH Corp. The experimental results demonstrate the specific equilibrium behavior of hydrogen isotopes adsorbed on SZ-LiA, deviating from isothermal profiles on SZ-CaA and SZ-NaX. SZ-LiA show the isothermal profiles of adsorption for H{sub 2} and D{sub 2} similar to on the conventional zeolites in the range from around 1 kPa to the atmospheric pressure, but exhibit a plateau around 1 mol/kg between 0.1 Pa and 100 Pa, while other zeolites show linearly profiling isotherms. This deviation indicates the adsorptive power of SZ-LiA remarkably greater than that of the others.

  17. Specific equilibrium behavior of hydrogen isotopes adsorbed onto synthetic zeolite A-type governed by lithium cations

    International Nuclear Information System (INIS)

    Takashima, Shoji; Kotoh, Kenji

    2013-01-01

    Highlights: • Isotherms for H 2 and D 2 adsorbed onto SZ-LiA at 77.4 K are shown. • The adsorption isotherms exhibit specific deviation in the range lower than 10 Pa. • SZ-LiA indicates the power of several 100-times at 0.1 Pa, compared with SZ-NaA. • Experimental isotherms are described empirically by a dual-site Langmuir equation. • The isotope effect on adsorption isotherms appears in the Langmuir constants. -- Abstract: Since synthetic zeolites (SZs) are powerfully adsorptive for hydrogen isotopes at cryogenic temperatures such as liquefied nitrogen, adsorption processes using these have been considered applicable to such as recovery of tritium from the lithium blanket of DT fusion reactor system. Onto these zeolites the adsorptions isotherms for hydrogen isotopes onto SZ-NaA, SZ-CaA and SZ-NaX at 77.4 K were already clarified experimentally and analytically. These isotherms exhibit similar profiles of Langmuir type. In this work, adsorption isotherms were examined for H 2 and D 2 on SZ-LiA at 77.4 K. SZ-LiA was made from SZ-NaA by exchanging its sodium ions for lithium ones, provided by TOSOH Corp. The experimental results demonstrate the specific equilibrium behavior of hydrogen isotopes adsorbed on SZ-LiA, deviating from isothermal profiles on SZ-CaA and SZ-NaX. SZ-LiA show the isothermal profiles of adsorption for H 2 and D 2 similar to on the conventional zeolites in the range from around 1 kPa to the atmospheric pressure, but exhibit a plateau around 1 mol/kg between 0.1 Pa and 100 Pa, while other zeolites show linearly profiling isotherms. This deviation indicates the adsorptive power of SZ-LiA remarkably greater than that of the others

  18. Influence of external extrusion on stability of hydrogen molecule and its chaotic behavior

    Science.gov (United States)

    Jarosik, M. W.; SzczÈ©śniak, R.; Durajski, A. P.; Kalaga, J. K.; Leoński, W.

    2018-01-01

    We have determined the stability conditions of the hydrogen molecule under the influence of an external force of harmonic-type explicitly dependent on the amplitude (A) and frequency (Ω). The ground state of the molecule has been determined in the framework of the Born-Oppenheimer approximation, whereas the energy of the electronic subsystem has been calculated using the Hubbard model including all two-site electron interactions. The diagram of RT0(A ,Ω) , where RT0 denotes the distance between protons after the fixed initial time T0, allowed us to visualize the area of the instability with the complicated structure. We have shown that the vibrations of the hydrogen molecule have a chaotic nature for some points of the instability region. In addition to the amplitude and frequency of the extrusion, the control parameter of the stability of the molecule is the external force associated with pressure. The increase in its value causes the disappearance of the area of the instability and chaotic vibrations.

  19. Kinetic Studies on State of the Art Solid Oxide Cells – A Comparison between Hydrogen/Steam and Reformate Fuels

    DEFF Research Database (Denmark)

    Njodzefon, Jean-Claude; Graves, Christopher R.; Mogensen, Mogens Bjerg

    2015-01-01

    Electrochemical reaction kinetics at the electrodes of Solid Oxide Cells (SOCs) were investigated at 700 °C for two cells with different fuel electrode microstructures as well as on a third cell with a reduced active electrode area. Three fuel mixtures were investigated – hydrogen....../steam and reformate fuels hydrogen/carbon-dioxide and hydrogen/methane/steam. It was found that the kinetics at the fuel electrode were exactly the same in both reformates. The hydrogen/steam fuel displayed slightly faster kinetics than the reformate fuels. Furthermore the gas conversion impedance in the hydrogen....../steam fuel split into two processes with opposing temperature behavior in the reformate fuels. An 87.5% reduction in active electrode area diminishes the gas conversion impedance in the hydrogen/steam fuel at high fuel flow rates. In both reformates, the second and third lowest frequency processes merged...

  20. Effects of modified surfaces produced at plasma-facing surface on hydrogen release behavior in the LHD

    Directory of Open Access Journals (Sweden)

    Y. Nobuta

    2017-08-01

    Full Text Available In the present study, an additional deuterium (D ion irradiation was performed against long-term samples mounted on the helical coil can and in the outer private region in the LHD during the 17th experimental campaign. Based on the release behavior of the D and hydrogen (H retained during the experimental campaign, the difference of release behavior at the top surface and in bulk of modified surfaces is discussed. Almost all samples on the helical coil can were erosion-dominant and some samples were covered with boron or carbon, while a very thick carbon films were formed in the outer private region. In the erosion-dominant area, the D desorbed at much lower temperatures compared to that of H retained during the LHD plasma operation. For the samples covered with boron, the D tended to desorb at lower temperatures compared to H. For the carbon deposition samples, the D desorbed at much higher temperatures compared to no deposition and boron-covered samples, which was very similar to that of H. The D retention capabilities at the top surface of carbon and boron films were 2–3 times higher than no deposition area. The results indicate that the retention and release behavior at the top surface of the modified layer can be different from that of bulk substrate material.

  1. Antibacterial effects, biocompatibility and electrochemical behavior of zinc incorporated niobium oxide coating on 316L SS for biomedical applications

    Science.gov (United States)

    Pradeep PremKumar, K.; Duraipandy, N.; Manikantan Syamala, Kiran; Rajendran, N.

    2018-01-01

    In the present study, Nb2O5 (NZ0) composite coatings with various concentrations of zinc (NZ2, NZ4 & NZ6) are produced on 316L SS by sol-gel method with the aim of improving its antibacterial activity, bone formability and corrosion resistance properties. This work studied the surface characterization of NZ0, NZ2, NZ4 & NZ6 coated 316L SS by ATR-FTIR, XRD, HR-SEM with EDAX. The synthesized coatings were different in the morphological aspects, NZ0 shows mesoporous morphology whereas irregular cluster like morphology was observed for the zinc incorporated coatings. The chemical composition of the NZ0 and NZ4 composite coatings were studied by XPS and the results revealed that the zinc exist as ZnO and Nb as Nb2O5 in the coatings. The increase in the concentration of zinc in Nb2O5 increases the hydrophilic nature identified by water contact angle studies. The potentiodynamic polarization studies in simulated body fluid reveals the increase in polarization resistance with decrease in current density (icorr) and electrochemical impedance spectroscopic studies with increase in charge transfer resistance (Rct) and double layer capacitance (Qdl) were observed for NZ4 coated 316L SS. The inhibition of Staphylococcus aureus and Escherichia coli bacteria were identified for NZ4 coated 316L SS by bacterial viability studies. The NZ4 coated 316L SS showed better Osseo-integration by spreading the MG 63 osteoblast cells. The study results imply that zinc incorporated Nb2O5 (NZ4) composite coating exhibits antibacterial activity and also enhance the corrosion resistance and biocompatibility of the 316L SS.

  2. Hydrogen-bonding behavior of various conformations of the HNO3…(CH3OH)2 ternary system.

    Science.gov (United States)

    Özsoy, Hasan; Uras-Aytemiz, Nevin; Balcı, F Mine

    2017-12-21

    Nine minima were found on the intermolecular potential energy surface for the ternary system HNO 3 (CH 3 OH) 2 at the MP2/aug-cc-pVDZ level of theory. The cooperative effect, which is a measure of the hydrogen-bonding strength, was probed in these nine conformations of HNO 3 …(CH 3 OH) 2 . The results are discussed here in terms of structures, energetics, infrared vibrational frequencies, and topological parameters. The cooperative effect was observed to be an important contributor to the total interaction energies of the cyclic conformers of HNO 3 …(CH 3 OH) 2 , meaning that it cannot be neglected in simulations in which the pair-additive potential is applied. Graphical abstract The H-bonding behavior of various conformations of the HNO 3 (CH 3 OH) 2 trimer was investigated.

  3. Synthesis and evaluation of MoWCoS/G and MoWCuS/G as new transition metal dichalcogenide nanocatalysts for electrochemical hydrogen evolution reaction

    Science.gov (United States)

    Askari, Mohammad Bagher; Beheshti-Marnani, Amirkhosro; Banizi, Zoha Tavakoli; Seifi, Majid; Ramezan zadeh, Mohammad Hassan

    2018-01-01

    New nanocomposites based on transition metal dichalcogenides, MoWCoS and MoWCuS, were synthesized through one step hydrothermal method. X-ray diffraction (XRD) and energy dispersive X-ray (EDX) techniques as well as field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) images confirmed the synthesis of nanocomposites. For investigation of hydrogen evolution reaction (HER) properties of new nanocomposites, linear sweep voltammetry (LSV) was applied for this purpose. According to the results of similar previous works, the prepared nanocomposites showed promising HER properties as low overpotential equal to 41.4 mV/dec for MoWCoS hybridized with reduced graphene (G) and a little higher one equal to 49 mV/dec for MoWCuS hybridized with reduced graphene. Based on obtained Tafel slopes 38 and 53 mV/dec for MoWCoS/G and MoWCuS/G, respectively, the "Heyrovsky-Volmer" mechanism was suggested for the new HER three component nanocatalysts as the first effort to this purpose.

  4. Facile fabrication of 3D layer-by-layer graphene-gold nanorod hybrid architecture for hydrogen peroxide based electrochemical biosensor

    Directory of Open Access Journals (Sweden)

    Chenming Xue

    2015-03-01

    Full Text Available Three-dimensional (3D layer-by-layer graphene-gold nanorod (GNR architecture has been constructed. The resulting hybrid nanomaterials’ architecture has been tested for detecting hydrogen peroxide (H2O2 through the electrocatalytic reaction on a three electrode disposable biosensor platform. Cyclic voltammetry and amperometry were used to characterize and assess the performance of the biosensor. The 3D layer-by-layer modified electrode exhibited the highest sensitivity compared to the active carbon, graphene-oxide, cysteine-graphene oxide and GNR coated electrodes. This research explored the feasibility of using the 3D hybrid graphene-GNR as a template for biosensor. The 3D hybrid structure exhibited higher sensitivity than GNRs alone. SEM showed the explanation that GNRs had self-aggregates reducing the contact surface area when coated on the active carbon electrode, while there were no such aggregates in the 3D structure, and TEM illustrated that GNRs dispersed well in the 3D structure. This research demonstrated a better way to prepare well-separated metal nanoparticles by using the 3D layer-by-layer structure. Consequently, other single and bi-metallic metal nanoparticles could be incorporated into such structure. As a practical example, 3D layer-by-layer nanomaterials modified active carbon electrode was used for detecting glucose showing very good sensitivity and minimum interference by ascorbic acid and uric acid in test solution, which indicated a good selectivity of the biosensor as well.

  5. Process for electrochemically gasifying coal using electromagnetism

    Science.gov (United States)

    Botts, Thomas E.; Powell, James R.

    1987-01-01

    A process for electrochemically gasifying coal by establishing a flowing stream of coal particulate slurry, electrolyte and electrode members through a transverse magnetic field that has sufficient strength to polarize the electrode members, thereby causing them to operate in combination with the electrolyte to electrochemically reduce the coal particulate in the slurry. Such electrochemical reduction of the coal produces hydrogen and carbon dioxide at opposite ends of the polarized electrode members. Gas collection means are operated in conjunction with the process to collect the evolved gases as they rise from the slurry and electrolyte solution.

  6. Electrochemical ammonia production on molybdenum nitride nanoclusters

    DEFF Research Database (Denmark)

    Howalt, Jakob Geelmuyden; Vegge, Tejs

    2013-01-01

    Theoretical investigations of electrochemical production of ammonia at ambient temperature and pressure on nitrogen covered molybdenum nanoparticles are presented. Density functional theory calculations are used in combination with the computational hydrogen electrode approach to calculate the free...... energy profile for electrochemical protonation of N2 and N adatoms on cuboctahedral Mo13 nanoparticles. Pathways for electrochemical ammonia production via direct protonation of N adatoms and N2 admolecules with an onset potential as low as -0.5 V and generally lower than -0.8 V on both a nitrogen...

  7. Study of the hydrogen behavior in amorphous hydrogenated materials of type a - C:H and a - SiC:H facing fusion reactor plasma

    International Nuclear Information System (INIS)

    Barbier, G.

    1997-01-01

    Plasma facing components of controlled fusion test devices (tokamaks) are submitted to several constraints (irradiation, high temperatures). The erosion (physical sputtering and chemical erosion) and the hydrogen recycling (retention and desorption) of these materials influence many plasma parameters and thus affect drastically the tokamak running. First, we will describe the different plasma-material interactions. It will be pointed out, how erosion and hydrogen recycling are strongly related to both chemical and physical properties of the material. In order to reduce these interactions, we have selected two amorphous hydrogenated materials (a-C:H and a-SiC:H), which are known for their good thermal and chemical qualities. Some samples have been then implanted with lithium ions at different fluences. Our materials have been then irradiated with deuterium ions at low energy. From our results, it is shown that both the lithium implantation and the use of an a - SiC:H substrate can be beneficial in enhancing the hydrogen retention. These results were completed with thermal desorption studies of these materials. It was evidenced that the hydrogen fixation was more efficient in a-SiC:H than in a-C:H substrate. Results in good agreement with those described above have been obtained by exposing a - C:H and a - SiC:H samples to the scrape off layer of the tokamak of Varennes (TdeV, Canada). A modelling of hydrogen diffusion under irradiation has been also proposed. (author)

  8. An electrochemical investigation of the corrosion behavior of Al-Si-Cu hypereutectic alloys in alcoholic environments

    Directory of Open Access Journals (Sweden)

    Traldi, S. M.

    2003-12-01

    Full Text Available Al-Si-Cu hypereutetic alloys produced by spray forming are mostly used in the automotive industry, especially for cylinder liners. They have the advantage of low weight associated with low coefficient of thermal expansion and excellent mechanical properties - mainly wear resistance at high temperatures. The corrosion resistance of these alloys in fuels, particularly alcoholic media, however is not yet known. In this investigation, electrochemical impedance spectroscopy (EIS and potentiodynamic polarisation have been used to evaluate the corrosion resistance of a hypereutectic Al-Si-Cu alloy in alcoholic environments. The EIS tests were carried out in pure ethanol, and ethanol with small additions (1 mM of acid and chloride, to investigate the effect of these contaminants on corrosion resistance. The corrosion resistance of a grey cast iron has also been evaluated in pure ethanol for comparison. The Al-Si-Cu alloy showed high corrosion resistance in pure ethanol, far superior to that of grey cast iron in the same medium.

    Aleaciones hipereutécticas producidas por conformación por spray son muy empleadas en la industria automovilística, especialmente en los revestimientos de los cilindros. Tienen la ventaja de añadir menos peso con bajo coeficiente de expansión térmica y excelentes propiedades mecánicas, sobre todo resistencia al desgaste en altas temperaturas. Todavía, la resistencia a la corrosión de estas aleaciones en combustibles no es conocida. En este estudio fueron utilizadas las técnicas de espectroscopia de impedancia electroquímica y polarización potenciodinámica, para evaluar la resistencia a la corrosión de una aleación hipereutéctica Al-Si-Cu en medio alcohólico. Las pruebas fueron conducidas en etanol puro y etanol con pequeñas adiciones (1 mM de ácido y cloruro, con la finalidad de investigar el efecto de estos contaminantes en la resistencia a la corrosión. Hierro fundido gris, también fue

  9. Facile synthesis of silver nanostructures by using various deposition potential and time: A nonenzymetic sensor for hydrogen peroxide

    Energy Technology Data Exchange (ETDEWEB)

    Amiri, Mandana, E-mail: mandanaamiri@uma.ac.ir [Department of Chemistry, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of); Nouhi, Sima [Department of Chemistry, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of); Azizian-Kalandaragh, Yashar [Department of Physics, University of Mohaghegh Ardabili, Ardabil (Iran, Islamic Republic of)

    2015-04-01

    Silver nanostructures have been successfully fabricated by using electrodeposition method onto indiumtinoxide (ITO) substrate. Scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS) and ultraviolet–visible spectroscopy (UV–Vis) techniques were employed for characterization of silver nanostructures. The results show nanostructures with different morphology and electrochemical properties can be obtained by various deposition potentials and times. Electrochemical behavior of the nanostructures has been studied by using cyclic voltammetry. Silver nanostructures exhibits good electrocatalytic activity towards the reduction of H{sub 2}O{sub 2}. The presented electrode can be employed as sensing element for hydrogen peroxide. - Highlights: • Silver nanostructures (AgNS) have been fabricated using electrodeposition ITO. • AgNS with different morphology and electrochemical properties obtained. • AgNS exhibits good electrocatalytic activity for reduction of H{sub 2}O{sub 2}.

  10. Electrochemical cell

    Science.gov (United States)

    Redey, L.I.; Myles, K.M.; Vissers, D.R.; Prakash, J.

    1996-07-02

    An electrochemical cell is described with a positive electrode having an electrochemically active layer of at least one transition metal chloride. A negative electrode of an alkali metal and a compatible electrolyte including an alkali metal salt molten at cell operating temperature is included in the cell. The electrolyte is present at least partially as a corrugated {beta}{double_prime} alumina tube surrounding the negative electrode interior to the positive electrode. The ratio of the volume of liquid electrolyte to the volume of the positive electrode is in the range of from about 0.1 to about 3. A plurality of stacked electrochemical cells is disclosed each having a positive electrode, a negative electrode of an alkali metal molten at cell operating temperature, and a compatible electrolyte. The electrolyte is at least partially present as a corrugated {beta}{double_prime} alumina sheet separating the negative electrode and interior to the positive electrodes. The alkali metal is retained in a porous electrically conductive ceramic, and seals for sealing the junctures of the electrolyte and the adjacent electrodes at the peripheries thereof. 8 figs.

  11. The Influence of Charged Species on the Phase Behavior, Self-Assembly, and Electrochemical Performance of Block Copolymer Electrolytes

    Science.gov (United States)

    Thelen, Jacob Lloyd

    One of the major barriers to expanding the capacity of large-scale electrochemical energy storage within batteries is the threat of a catastrophic failure. Catastrophic battery pack failure can be initiated by a defect within a single battery cell. If the failure of a defective battery cell is not contained, the damage can spread and subsequently compromise the integrity of the entire battery back, as well as the safety of those in its surroundings. Replacing the volatile, flammable liquid electrolyte components found in most current lithium ion batteries with a solid polymer electrolyte (SPE) would significantly improve the cell-level safety of batteries; however, poor ionic conductivity and restricted operating temperatures compared to liquid electrolytes have plagued the practical application of SPEs. Rather than competing with the performance of liquid electrolytes directly, our approach to developing SPEs relies on increasing electrolyte functionality through the use of block copolymer architectures. Block copolymers, wherein two or more chemically dissimilar polymer chains are covalently bound, have a propensity to microphase separate into nanoscale domains that have physical properties similar to those of each of the different polymer chains. For instance, the block copolymer, polystyrene-b-poly(ethylene oxide) (SEO), has often been employed as a solid polymer electrolyte because the nanoscale domains of polystyrene (PS) can provide mechanical reinforcement, while the poly(ethylene oxide) microphases can solvate and conduct lithium ions. Block copolymer electrolytes (BCEs) formed from SEO/salt mixtures result in a material with the bulk mechanical properties of a solid, but with the ion conducting properties of a viscoelastic fluid. The efficacy SEO-based BCEs has been demonstrated; the enhanced mechanical functionality provided by the PS domains resist the propagation of dendritic lithium structures during battery operation, thus enabling the use of a

  12. Interfacial stability and electrochemical behavior of Li/LiFePO4 batteries using novel soft and weakly adhesive photo-ionogel electrolytes

    Science.gov (United States)

    Aidoud, D.; Etiemble, A.; Guy-Bouyssou, D.; Maire, E.; Le Bideau, J.; Guyomard, D.; Lestriez, B.

    2016-10-01

    We have developed flexible polymer-gel electrolytes based on a polyacrylate cross-linked matrix that confines an ionic liquid doped with a lithium salt. Free-standing solid electrolyte membrane is obtained after UV photo-polymerization of acrylic monomers dissolved inside the ionic liquid/lithium salt mixture. The liquid precursor of the photo-ionogel may also be directly deposited onto porous composite electrode, which results in all-solid state electrode/electrolyte stacking after UV illumination. Minor variations in the polymer component of the electrolyte formulation significantly affect the electrochemical behavior in LiFePO4/lithium and lithium/lithium cells. The rate performance increases with an increase of the ionic conductivity, which decreases with the polymer content and decreases with increasing oxygen content in the polyacrylate matrix. Their fairly low modulus endow them weak and beneficial pressure-sensitive-adhesive character. X-Rays Tomography shows that the solid-state photo-ionogel electrolytes keep their integrity upon cycling and that their surface remains smooth. The coulombic efficiency of LiFePO4/lithium cells increases with an increase of the adhesive strength of the photo-ionogel, suggesting a relationship between the contact intimacy at the lithium/photo-ionogel interface and the efficiency of the lithium striping/plating. In lithium/lithium cells, only the photo-ionogels with the higher adhesion strength are able to allow the reversible striping/plating of lithium.

  13. Comparative investigation on electrochemical behavior of hydroquinone at carbon ionic liquid electrode, ionic liquid modified carbon paste electrode and carbon paste electrode

    International Nuclear Information System (INIS)

    Zhang, Ya; Zheng, Jian Bin

    2007-01-01

    Ionic liquid, 1-heptyl-3-methylimidazolium hexafluorophosphate (HMIMPF 6 ), has been used to fabricate two new electrodes, carbon ionic liquid electrode (CILE) and ionic liquid modified carbon paste electrode (IL/CPE), using graphite powder mixed with HMIMPF 6 or the mixture of HMIMPF 6 /paraffin liquid as the binder, respectively. The electrochemical behaviors of hydroquinone at the CILE, the IL/CPE and the CPE were investigated in phosphate buffer solution. At all these electrodes, hydroquinone showed a pair of redox peaks. The order of the current response and the standard rate constant of hydroquinone at these electrodes were as follows: CILE > IL/CPE > CPE, while the peak-to-peak potential separation was in an opposite sequence: CILE < IL/CPE < CPE. The results show the superiority of CILE to IL/CPE and CPE, and IL/CPE to CPE in terms of promoting electron transfer, improving reversibility and enhancing sensitivity. The CILE was chosen as working electrode to determine hydroquinone by differential pulse voltammetry, which can be used for sensitive, simple and rapid determination of hydroquinone in medicated skin cosmetic cream

  14. Differences in the electrochemical behavior of ruthenium and iridium oxide in electrocatalytic coatings of activated titanium anodes prepared by the sol–gel procedure

    Directory of Open Access Journals (Sweden)

    VLADIMIR V. PANIĆ

    2010-10-01

    Full Text Available The electrochemical characteristics of Ti0.6Ir0.4O2/Ti and Ti0.6Ru0.4O2/Ti anodes prepared by the sol–gel procedure from the corresponding oxide sols, obtained by force hydrolysis of the corresponding metal chlorides, were compared. The voltammetric properties in H2SO4 solution indicate that Ti0.6Ir0.4O2/Ti has more pronounced pseudocapacitive characteristics, caused by proton-assisted, solid state surface redox transitions of the oxide. At potentials negative to 0.0 VSCE, this electrode is of poor conductivity and activity, while the voltammetric behavior of the Ti0.6Ru0.4O2/Ti electrode is governed by proton injection/ejection into the oxide structure. The Ti0.6Ir0.4O2/Ti electrode had a higher electrocatalytical activity for oxygen evolution, while the investigated anodes were of similar activity for chlorine evolution. The potential dependence of the impedance characteristics showed that the Ti0.6Ru0.4O2/Ti electrode behaved like a capacitor over a wider potential range than the Ti0.6Ir0.4O2/Ti electrode, with fully-developed pseudocapacitive properties at potentials positive to 0.60 VSCE. However, the impedance characteristics of the Ti0.6Ir0.4O2/Ti electrode changed with increasing potential from resistor-like to capacitor-like behavior.

  15. Modifying the photoelectric behavior of bacteriorhodopsin by site-directed mutagenesis: electrochemical and genetic engineering approaches to molecular devices

    Science.gov (United States)

    Hong, F. T.; Hong, F. H.; Needleman, R. B.; Ni, B.; Chang, M.

    1992-07-01

    Bacteriorhodopsins (bR's) modified by substitution of the chromophore with synthetic vitamin A analogues or by spontaneous mutation have been reported as successful examples of using biomaterials to construct molecular optoelectronic devices. The operation of these devices depends on desirable optical properties derived from molecular engineering. This report examines the effect of site-directed mutagenesis on the photoelectric behavior of bR thin films with an emphasis on their application to the construction of molecular devices based on their unique photoelectric behavior. We examine the photoelectric signals induced by a microsecond light pulse in thin films which contain reconstituted oriented purple membrane sheets isolated from several mutant strains of Halobacterium halobium. A recently developed expression system is used to synthesize mutant bR's in their natural host, H. halobium. We then use a unique analytical method (tunable voltage clamp method) to investigate the effect of pH on the relaxation of two components of the photoelectric signals, B1 and B2. We found that for the four mutant bR's examined, the pH dependence of the B2 component varies significantly. Our results suggest that genetic engineering approaches can produce mutant bR's with altered photoelectric characteristics that can be exploited in the construction of devices.

  16. Antioxidant activity and electrochemical elucidation of the enigmatic redox behavior of curcumin and its structurally modified analogues

    International Nuclear Information System (INIS)

    Jha, Niki S.; Mishra, Satyendra; Jha, Shailendra K.; Surolia, Avadhesha

    2015-01-01

    Highlights: • Structural analogues of curcumin have been synthesized. • Confirmation of redox behaviour emanates from H- shift from central methylene group in curcumin. • Mechanism of curcumin oxidation has been proposed. • Correlation between redox behavior and antioxidant activity has been established. - Abstract: Here, we report studies on the antioxidant activity and redox behavior of curcumin and its structurally modified synthetic analogues. We have synthesized a number of analogues of curcumin which abrogate its keto-enol tautomerism or substitute the methylene group at the centre of its heptadione moiety implicated in the hydride transfer and studied their redox property. From cyclic voltammetric studies, it is demonstrated that H- atom transfer from CH 2 group at the center of the heptadione link also plays an important role in the antioxidant properties of curcumin along with that of its phenolic –OH group. In addition, we also show that the conversion of 1, 3- dicarbonyl moiety of curcumin to an isosteric heterocycle as in pyrazole curcumin, which decreases its rotational freedom, leads to an improvement of its redox properties as well as its antioxidant activity

  17. Effect of hydrogen on the behavior of metals II - Hydrogen embrittlement of titanium alloy TV13CA - effect of oxygen - comparison with non-alloyed titanium

    International Nuclear Information System (INIS)

    Arditty, Jean-Pierre

    1973-01-01

    The effect of oxygen on the hydrogen embrittlement of non-alloyed titanium and the metastable β titanium alloy, TV13 CA, was studied during dynamic mechanical tests, the concentrations considered varying from 1000 to 5000 ppm (oxygen) and from 0 to 5000 ppm (hydrogen) respectively. TV13 CA alloy has a very high solubility for hydrogen. The establishment of a temperature range and a rate of deformation region in which the embrittlement of the alloy is maximum leads to the conclusion that an embrittlement mechanism occurs involving the dragging and accumulation of hydrogen by dislocations. This is the case for all annealings effected in the medium temperature range, which, by favoring the re-establishment of the stable two-phase α + β state of the alloy, produce hardening. The same is true for oxygen which, in addition to hardening the alloy by the solid solution effect, tends to increase its instability and, in consequence, favors the decomposition of the β phase. Nevertheless oxygen concentrations of up to 1500 ppm contribute to increasing the mechanical resistance without catastrophically reducing the deformation capacity. In the case of non-alloyed titanium, the hardening effect also leads to an increase in E 0.2p c and R, and to a reduction in the deformation capacity. Nevertheless, hydrogen is only very slightly soluble at room temperature and a distribution of the hydride phase linked to the thermal history of the sample predominates. Thus a fine acicular structure obtained from the β phase by quenching, enables an alloy having a good mechanical resistance to be conserved even when large quantities of hydrogen are present; the deformation capacity remains small. On the other hand, when the hydride phase separates the metallic phase into large grains, a very small elongation leads to a breakdown in mechanical resistance. (author) [fr

  18. Electrochemical cell

    Science.gov (United States)

    Kaun, T.D.

    An improved secondary electrochemical cell is disclosed having a negative electrode of lithium aluminum, a positive electrode of iron sulfide, a molten electrolyte of lithium chloride and potassium chloride, and the combination that the fully charged theoretical capacity of the negative electrode is in the range of 0.5 to 1.0 that of the positive electrode. The cell thus is negative electrode limiting during discharge cycling. Preferably, the negative electrode contains therein, in the approximate range of 1 to 10 volume % of the electrode, an additive from the materials of graphitized carbon, aluminum-iron alloy, and/or magnesium oxide.

  19. Behavior of Electrochemically Prepared CuInSe2 as Photovoltaic Absorber in thin Film Solar Cells

    International Nuclear Information System (INIS)

    Guillen, C; Martinez, M.A.; Dona, J. M.; Herrero, J; Gutierrez, M. T.

    2000-01-01

    Two different objectives have been pursued in the present investigation: 1) optimization of the CuInSe, preparation parameters from electrodeposited precursors, and 2) evaluation of their photovoltaic behavior by preparing and enhancing Mo/CuInSe,/CdS/TCO devices. When Cu-In-Se precursors are directly electrodeposited, the applied potential fit is essential to improve the photovoltaic performance. Suitable absorbers have been also obtained by evaporating an In layer onto electrodeposited Cu-Se precursors. In this case, the substrate temperature during evaporation determines the CuInSe, quality. Similar results have been reached by substituting typical Mo-coated glass substrates by flexible Mo foils. Different TCO tested (ZnO and ITO) have been found equivalent as front electrical contact in the devices. Solar cell performance can be improved by annealing in air at 200 degree centigree. (Author) 46 refs

  20. Unique crystallization behavior of sodium manganese pyrophosphate Na2MnP2O7 glass and its electrochemical properties

    Directory of Open Access Journals (Sweden)

    Morito Tanabe

    2017-06-01

    Full Text Available Crystallization behavior of Na2MnP2O7 precursor glass was examined. Layered type Na2MnP2O7 was formed at 461 °C for 3 h in N2 filled electric furnace. Irreversible phase change was confirmed from layered Na2MnP2O7 to β-Na2MnP2O7 over 600 °C. At 650 °C crystallized phase was completely changed to β-phase. By means of charge and discharge testing it is found that layered Na2MnP2O7 is also active as cathode in sodium ion batteries. We found glass-ceramics technology is one of the suitable process for the synthesis of layered Na2MnP2O7 cathode without any complicate process.

  1. Hydrogen assisted cracking and CO2 corrosion behaviors of low-alloy steel with high strength used for armor layer of flexible pipe

    Science.gov (United States)

    Liu, Zhenguang; Gao, Xiuhua; Du, Linxiu; Li, Jianping; Zhou, Xiaowei; Wang, Xiaonan; Wang, Yuxin; Liu, Chuan; Xu, Guoxiang; Misra, R. D. K.

    2018-05-01

    In this study, hydrogen induced cracking (HIC), sulfide stress corrosion cracking (SSCC) and hydrogen embrittlement (HE) were carried out to study hydrogen assisted cracking behavior (HIC, SSCC and HE) of high strength pipeline steel used for armor layer of flexible pipe in ocean. The CO2 corrosion behavior of designed steel with high strength was studied by using immersion experiment. The experimental results demonstrate that the corrosion resistance of designed steel with tempered martensite to HIC, SSCC and HE is excellent according to specific standards, which contributes to the low concentration of dislocation and vacancies previously formed in cold rolling process. The corrosion mechanism of hydrogen induced cracking of designed steel, which involves in producing process, microstructure and cracking behavior, is proposed. The designed steel with tempered martensite shows excellent corrosion resistance to CO2 corrosion. Cr-rich compound was first formed on the coupon surface exposed to CO2-saturated brine condition and chlorine, one of the corrosion ions in solution, was rich in the inner layer of corrosion products.

  2. Electrochemical behavior of folic acid at calixarene based chemically modified electrodes and its determination by adsorptive stripping voltammetry

    International Nuclear Information System (INIS)

    Vaze, Vishwanath D.; Srivastava, Ashwini K.

    2007-01-01

    Voltammetric behavior of folic acid at plain carbon paste electrode and electrode modified with calixarenes has been studied. Two peaks for irreversible oxidation were observed. Out of the three calixarenes chosen for modification of the electrodes, p-tert-butyl-calix[6]arene modified electrode (CME-6) was found to have better sensitivity for folic acid. Chronocoulometric and differential pulse voltammetric studies reveal that folic acid can assemble at CME-6 to form a monolayer whose electron transfer rate is 0.00273 s -1 with 2-electron/2-proton transfer for the peak at +0.71 V against SCE. An adsorption equilibrium constant of 5 x 10 3 l/mol for maximum surface coverage of 2.89 x 10 -10 mol/cm 2 was obtained. The current is found to be rectilinear with concentration by differential pulse voltammetry. However, linearity in the lower range of concentration 8.79 x 10 -12 M to 1.93 x 10 -9 M with correlation coefficient of 0.9920 was achieved by adsorptive stripping voltammetry. The limit of detection obtained was found to be 1.24 x 10 -12 M. This method was used for the determination of folic acid in a variety of samples, viz. serum, asparagus, spinach, oranges and multivitamin preparations

  3. Electrochemical behavior of folic acid at calixarene based chemically modified electrodes and its determination by adsorptive stripping voltammetry

    Energy Technology Data Exchange (ETDEWEB)

    Vaze, Vishwanath D. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India); Srivastava, Ashwini K. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India)], E-mail: aksrivastava@chem.mu.ac.in

    2007-12-31

    Voltammetric behavior of folic acid at plain carbon paste electrode and electrode modified with calixarenes has been studied. Two peaks for irreversible oxidation were observed. Out of the three calixarenes chosen for modification of the electrodes, p-tert-butyl-calix[6]arene modified electrode (CME-6) was found to have better sensitivity for folic acid. Chronocoulometric and differential pulse voltammetric studies reveal that folic acid can assemble at CME-6 to form a monolayer whose electron transfer rate is 0.00273 s{sup -1} with 2-electron/2-proton transfer for the peak at +0.71 V against SCE. An adsorption equilibrium constant of 5 x 10{sup 3} l/mol for maximum surface coverage of 2.89 x 10{sup -10} mol/cm{sup 2} was obtained. The current is found to be rectilinear with concentration by differential pulse voltammetry. However, linearity in the lower range of concentration 8.79 x 10{sup -12} M to 1.93 x 10{sup -9} M with correlation coefficient of 0.9920 was achieved by adsorptive stripping voltammetry. The limit of detection obtained was found to be 1.24 x 10{sup -12} M. This method was used for the determination of folic acid in a variety of samples, viz. serum, asparagus, spinach, oranges and multivitamin preparations.

  4. Microstructural characterization of hydrogen induced cracking in TRIP-assisted steel by EBSD

    International Nuclear Information System (INIS)

    Laureys, A.; Depover, T.; Petrov, R.; Verbeken, K.

    2016-01-01

    The present work evaluates hydrogen induced cracking by performing an elaborate EBSD (Electron BackScatter Diffraction) study in a steel with transformation induced plasticity (TRIP-assisted steel). This type of steel exhibits a multiphase microstructure which undergoes a deformation induced phase transformation. Additionally, each microstructural constituent displays a different behavior in the presence of hydrogen. The aim of this study is to obtain a better understanding on the mechanisms governing hydrogen induced crack initiation and propagation in the hydrogen saturated multiphase structure. Tensile tests on notched samples combined with in-situ electrochemical hydrogen charging were conducted. The tests were interrupted at stresses just after reaching the tensile strength, i.e. before macroscopic failure of the material. This allowed to study hydrogen induced crack initiation and propagation by SEM (Scanning Electron Microscopy) and EBSD. A correlation was found between the presence of martensite, which is known to be very susceptible to hydrogen embrittlement, and the initiation of hydrogen induced cracks. Initiation seems to occur mostly by martensite decohesion. High strain regions surrounding the hydrogen induced crack tips indicate that further crack propagation may have occurred by the HELP (hydrogen-enhanced localized plasticity) mechanism. Small hydrogen induced cracks located nearby the notch are typically S-shaped and crack propagation was dominantly transgranularly. The second stage of crack propagation consists of stepwise cracking by coalescence of small hydrogen induced cracks. - Highlights: • Hydrogen induced cracking in TRIP-assisted steel is evaluated by EBSD. • Tensile tests were conducted on notched hydrogen saturated samples. • Crack initiation occurs by a H-Enhanced Interface DEcohesion (HEIDE) mechanism. • Crack propagation involves growth and coalescence of small cracks. • Propagation is governed by the characteristics of

  5. Electrochemical behavior of 45S5 bioactive ceramic coating on Ti6Al4V alloy for dental applications

    Science.gov (United States)

    Machado López, M. M.; Espitia Cabrera, M. I.; Faure, J.; Contreras García, M. E.

    2016-04-01

    Titanium and its alloys are widely used as implant materials because of their mechanical properties and non-toxic behavior. Unfortunately, they are not bioinert, which means that they can release ions and can only fix the bone by mechanical anchorage, this can lead to the encapsulation of dense fibrous tissue in the body. The bone fixation is required in clinical conditions treated by orthopedic and dental medicine. The proposal is to coat metallic implants with bioactive materials to establish good interfacial bonds between the metal substrate and bone by increasing bioactivity. Bioactive glasses, ceramics specifically 45 S5 Bioglass, have drawn attention as a serious functional biomaterial because osseointegration capacity. The EPD method of bioglass gel precursor was proposed in the present work as a new method to obtain 45S5/Ti6A14V for dental applications. The coatings, were thermally treated at 700 and 800°C and presented the 45 S5 bioglass characteristic phases showing morphology and uniformity with no defects, quantification percentages by EDS of Si, Ca, Na, P and O elements in the coating scratched powders, showed a good proportional relationship demonstrating the obtention of the 45S5 bioglass. The corrosion tests were carried out in Hank's solution. By Tafel extrapolation, Ti6Al4V alloy showed good corrosion resistance in Hank's solution media, by the formation of a passivation layer on the metal surface, however, in the system 45S5/Ti6Al4V there was an increase in the corrosion resistance; icon-, Ecorr and corrosion rate decreased, the mass loss and the rate of release of ions, were lower in this system than in the titanium alloy without coating.

  6. Electrochemical Behavior of Catechol and Hydroquinone at Copper Doped Poly (Methyl Red Coated Hydroxyl Multiwalled Carbon Nanotube Film and Their Simultaneous Determination in Water Samples

    Directory of Open Access Journals (Sweden)

    Ying Zhang

    2014-09-01

    Full Text Available A glassy carbon electrode modified with copper doped poly (methyl red coated hydroxyl multiwalled carbon nanotube film (Cu-PMR/MWCNTs, was developed to serve as a sensor for simultaneous determination of Hydroquinone (HQ and catechol (CC in this paper. The fabricated electrode showed excellent electrocatalytic behaviors towards the oxidation of HQ and CC with the enhancement of the redox peak current and the decrease of the peak-to-peak separation. Under the optimized condition, the individual determination of HQ or CT in their mixtures was performed, the response peak currents of the modified electrodes were linear over ranges of 8.0´10-7~4.0´10-4 M (R2=0.999 for CT and 5.0´10-7~2.0´10-4 M (R2=0.993 for HQ. The sensor also exhibited good sensitivity with the detection limit of 1.0´10-8 mol/L and 5.0´10-8 mol/L for HQ and CT, respectively. The simultaneous determination of HQ and CC was demonstrated by simultaneously changing their concentrations. The reduction peak currents of HQ and CC increased linearly with the concentration of their own in the range of 8´10-7 and 2.0´10-4 M for HQ and CC, with correlation coefficients of 0.994 and 0.995 (S/N=3, respectively. This study provides a new kind of composite modified electrode for electrochemical sensors with good selectivity and strong anti-interference. It has been applied to simultaneous determination of HQ and CT in water sample with high selectivity.

  7. Solution behavior of hydrogen isotopes and other non-metallic elements in liquid lithium

    International Nuclear Information System (INIS)

    Maroni, V.A.; Calaway, W.F.; Veleckis, E.; Yonco, R.M.

    1976-01-01

    Results of experimental studies to measure selected thermodynamic properties for systems of lithium with non-metallic elements are reported. Investigations of the Li-H, Li-D, and Li-T systems have led to the elucidation of the dilute solution behavior and the H/D/T isotope effects. In the case of the Li-H and Li-D systems, the principal features of the respective phase diagrams have been delineated. The solubility of Li-D in liquid lithium has been measured down to 200 0 C. The solubility of Li 3 N in liquid lithium and the thermal decomposition of Li 3 N have also been studied. From these data, the free energy of formation of Li 3 N and the Sieverts' constant for dissolution of nitrogen in lithium have been determined. Based on studies of the distribution of non-metallic elements between liquid lithium and selected molten salts, it appears that molten salt extraction offers promise as a means of removing these impurity elements (e.g., H, D, T, O, N, C) from liquid lithium

  8. Hydrogen bonding as the origin of the switching behavior in dithiolated phenylene-vinylene oligomers

    KAUST Repository

    Obodo, Tobechukwu Joshua

    2013-08-29

    We investigate theoretically the switching behavior of a dithiolated phenylene-vinylene oligomer sandwiched between Au(111) electrodes using self-interaction corrected density-functional theory combined with the nonequilibrium Green\\'s-function method for quantum transport. The molecule presents a configurational bistability, which can be exploited in constructing molecular memories, switches, and sensors. We find that protonation of the terminating thiol groups is at the origin of the change in conductance. H bonding at the thiol group weakens the S-Au bond and reduces by about one order of magnitude the transmission coefficient at the Fermi level, and thus the linear response conductance. Furthermore, protonation downshifts in energy the position of the highest occupied molecular orbital, so that the current of the protonated species is lower than that of the unprotonated one along the entire bias range investigated, from −1.5 to 1.5 V. A second protonation at the opposite thiol group has only minor effects and no further drastic reduction in transmission takes place. Our results allow us to re-interpret the experimental data originally attributing the conductance reduction to H dissociation.

  9. Influence of hydrogen on the corrosion behavior of stainless steels in lithium

    Science.gov (United States)

    Shulga, A. V.

    2008-02-01

    Corrosion behavior of several stainless steels in lithium and lithium with 0.05%H has been examined. Corrosion tests were performed under static conditions at 600 and 700 °C in the austenitic stainless steel of the type AISI 304 containers. Intensive formation of σ-phase of the composition Fe 50Cr 43Mo 3Ni 4 on the surface of austenitic stainless steels of the type AISI 316 at 700 °C for 1000 h was established as a result of isothermal mass transfer. Addition of 0.05%H in the form of LiH to lithium resulted in an increase in the quantity of the σ-phase. After corrosion tests of ferritic/martensitic steel in lithium at 700 °C for 1000 h the formation of the γ-phase was observed. In Li + 0.05%H besides the γ-phase was also formed the σ-phase. The features of decarburization of investigated stainless steels were examined using the direct method of activation autoradiography on carbon. Addition of 0.05%H in lithium significantly decreased the carbon content in the decarburization zone of austenitic stainless steel Fe-18Cr-15Ni-0.15C-0.23B without a noticeable change in the thickness of the decarburization zone. Decarburization of ferritic/martensitic stainless steel was less than of austenitic stainless steel using the same corrosion tests.

  10. Impact of hydrogenated starch hydrolysate on glass transition, hygroscopic behavior and crystallization of isomalt-based systems

    Directory of Open Access Journals (Sweden)

    Kanitha Tananuwong

    2017-02-01

    Full Text Available Glass transition behavior, adsorption isotherm and crystallization of isomalt-hydrogenated starch hydrolysate (HSH mixtures (0-20% HSH and pure HSH were investigated. At similar solid content, Tg decreased as HSH concentration increased. Tg data at different solid contents were well-fitted with Gordon-Taylor equation (gR2≥0.97. Adsorption isotherm showed that systems with greater HSH concentration became more hygroscopic. Accelerated storage test (30°C, 84% RH of modeled hard candy containing 10% HSH and pure isomalt formula was done. HSH enhanced water uptake and crystallization of polyols in hard candy during aging without packaging; however, those effects were lessen for the samples aged in polyethylene terephthalate/cast polypropylene (PET/CPP pouches, and were negligible after the application of superior moisture barrier, oriented polypropylene/metalized cast polypropylene (OPP/MCPP film. Although HSH adversely affected storage stability of sugarless hard candies, it could be add into the formulation together with the application of packaging having a good moisture barrier.

  11. Hydrogenated amorphous carbon films on steel balls and Si substrates: Nanostructural evolutions and their trigging tribological behaviors

    Science.gov (United States)

    Wang, Yongfu; Wang, Yan; Zhang, Xingkai; Shi, Jing; Gao, Kaixiong; Zhang, Bin; Zhang, Junyan

    2017-10-01

    In this study, we prepared hydrogenated amorphous carbon films on steel balls and Si substrates (steel ball- and Si substrate-films) with different deposition time, and discussed their carbon nanostructural evolutions and tribological behaviors. The steel ball-film structure started to be graphite-like structure and then gradually transformed into fullerene-like (FL) structure. The Si substrate-film structure began in FL structure and kept it through the thickness. The difference may be result from the competition between high starting substrate temperature after additional nitriding applied on the steel balls (its supply power is higher than that in the film deposition), and relaxation of compressive stress from energized ion bombardment in film deposition process. The FL structural film friction couples could achieve ultra-low friction in open air. In particular, the Si substrate-film with 3 h, against the steel ball-film with 2 h and 3 h, exhibited super-low friction (∼0.009) and superlong wear life (∼5.5 × 105 cycles). Our result could widen the superlubricity scope from previously high load and velocity, to middle load and velocity.

  12. Insight to the Thermal Decomposition and Hydrogen Desorption Behaviors of NaNH2-NaBH4Hydrogen Storage Composite.

    Science.gov (United States)

    Pei, Ziwei; Bai, Ying; Wang, Yue; Wu, Feng; Wu, Chuan

    2017-09-20

    The lightweight compound material NaNH 2 -NaBH 4 is regarded as a promising hydrogen storage composite due to the high hydrogen density. Mechanical ball milling was employed to synthesize the composite NaNH 2 -NaBH 4 (2/1 molar ratio), and the samples were investigated utilizing thermogravimetric-differential thermal analysis-mass spectroscopy (TG-DTA-MS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) analyses. The full-spectrum test (range of the ratio of mass to charge: 0-200) shows that the released gaseous species contain H 2 , NH 3 , B 2 H 6 , and N 2 in the heating process from room temperature to 400 °C, and possibly the impurity gas B 6 H 12 also exists. The TG/DTA analyses show that the composite NaNH 2 -NaBH 4 (2/1 molar ratio) is conductive to generate hydrogen so that the dehydrogenation process can be finished before 400 °C. Moreover, the thermal decomposition process from 200 to 400 °C involves two-step dehydrogenation reactions: (1) Na 3 (NH 2 ) 2 BH 4 hydride decomposes into Na 3 BN 2 and H 2 (200-350 °C); (2) remaining Na 3 (NH 2 ) 2 BH 4 reacts with NaBH 4 and Na 3 BN 2 , generating Na, BN, NH 3 , N 2 , and H 2 (350-400 °C). The better mechanism understanding of the thermal decomposition pathway lays a foundation for tailoring the hydrogen storage performance of the composite complex hydrides system.

  13. Behavior of hydrogen atoms in boron films during H{sub 2} and He glow discharge and thermal desorption

    Energy Technology Data Exchange (ETDEWEB)

    Tsuzuki, K.; Natsir, M.; Inoue, N. [and others

    1995-09-01

    Hydrogen absorption and desorption characteristics in boron films deposited on a graphite liner have been studied. Number of hydrogen atoms absorbed in the films is estimated from a decrease in hydrogen pressure during a hydrogen glow discharge. It was 1.9 x 10{sup 17} atoms/cm{sup 2} in the 1 hour discharge after an evacuation of H atoms contained in the original boron films by thermal desorption. Hydrogen atoms were absorbed continuously without saturation for 3 hours during the discharge. Number of H atoms absorbed reached to 2.6 x 10{sup 17} atoms/cm{sup 2} at 3 hour. A discharge in helium was carried out to investigate H desorption characteristics from hydrogen implanted boron films. It was verified that reactivity for hydrogen absorption was recovered after the He discharge. Hydrogen atoms were accumulated in the films by repetition of alternate He and H{sub 2} discharge. Thermal desorption experiments have been carried out by raising the liner temperature up to 500degC for films after 1 hour, 3 hours hydrogen discharge and 6 times repetition of H{sub 2}/He discharges. Most of H atoms in the films were desorbed for all these cases. The slow absorption process was confirmed through the thermal desorption experiments. (author).

  14. Nuclear hydrogen power stations

    International Nuclear Information System (INIS)

    Eroshov, M.E.

    1976-01-01

    Short information about investigations on hydrogen energetics being carried out in the USSR as well as a review of the world literature on this subject are given. Combined cycles of thermochemical and electrochemical reactions applied for hydrogen and oxigen production from water are shown to be of interest, as a number of reactions in a cycle may be reduced to two, and the temperature of processes may be decreased to the temperature range specific to modern reactors. Construction features of nuclear-hydrogen power stations producing hydrogen through the use of thermo-electro-chemical cycles are considered. It is shown that at this stage it is possible to reduce time and expenses needed for realization of hydrogen production on a wide scale as compared to other reaction cycles requiring high temperatures and consequently, construction of high-temperature reactors. The conditions of energy and water transport at great distances by using hydrogen lines and the possibilities of development of desert and arid lands by using this mode of operation are considered. Possible ecological effect of hydrogen energetics development on the environment is pointed out, in particular, when power complexes are concentrated on a limited area. It is shown that it is reasonable to locate nuclear-hydrogen stations on shores

  15. Electrochemical impedance spectroscopy of oxidized porous silicon

    Energy Technology Data Exchange (ETDEWEB)

    Mula, Guido, E-mail: guido.mula@unica.it [Dipartimento di Fisica, Università degli Studi di Cagliari, Cittadella Universitaria di Monserrato, S.P. 8 km 0.700, 09042 Cagliari (Italy); Tiddia, Maria V. [Dipartimento di Fisica, Università degli Studi di Cagliari, Cittadella Universitaria di Monserrato, S.P. 8 km 0.700, 09042 Cagliari (Italy); Ruffilli, Roberta [Nanochemistry, Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy); Falqui, Andrea [Nanochemistry, Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy); Dipartimento di Scienze Chimiche e Geologiche, Università degli Studi di Cagliari, Cittadella Universitaria di Monserrato, S.P. 8 km 0.700, 09042 Cagliari (Italy); Palmas, Simonetta; Mascia, Michele [Dipartimento di Ingegneria Meccanica Chimica e dei Materiali, Università degli Studi di Cagliari, Piazza d' Armi, 09126 Cagliari (Italy)

    2014-04-01

    We present a study of the electrochemical oxidation process of porous silicon. We analyze the effect of the layer thickness (1.25–22 μm) and of the applied current density (1.1–11.1 mA/cm{sup 2}, values calculated with reference to the external samples surface) on the oxidation process by comparing the galvanostatic electrochemical impedance spectroscopy (EIS) measurements and the optical specular reflectivity of the samples. The results of EIS were interpreted using an equivalent circuit to separate the contribution of different sample parts. A different behavior of the electrochemical oxidation process has been found for thin and thick samples: whereas for thin samples the oxidation process is univocally related to current density and thickness, for thicker samples this is no more true. Measurements by Energy Dispersive Spectroscopy using a Scanning Electron Microscopy confirmed that the inhomogeneity of the electrochemical oxidation process is increased by higher thicknesses and higher currents. A possible explanation is proposed to justify the different behavior of thin and thick samples during the electrochemical process. - Highlights: • A multidisciplinary approach on porous Si electrochemical oxidation is proposed. • Electrochemical, optical, and structural characterizations are used. • Layer thickness and oxidation current effects are shown. • An explanation of the observed behavior is proposed.

  16. Electrochemical determination of hydrogen peroxide using o ...

    Indian Academy of Sciences (India)

    Unknown

    ip"(nA). -E(V). 4. Figure 2. The linear sweep second order derivative po- larogram of Hb-H2O2-ODA catalytic system. (1) 0⋅05 mol/l KH2PO4–Na2HPO4 buffer solution (pH 6⋅6); (2) (1). +1⋅0 × 10–3 mol/l ODA + 1⋅0 × 10–7 mol/l Hb; (3) (1). +1⋅0 × 10–3 mol/l ODA + 1⋅5 × 10–5mol/l H2O2; (4) (2) +. 1⋅5 × 10–5 mol/l ...

  17. Electrochemical determination of hydrogen peroxide using ...

    Indian Academy of Sciences (India)

    This method can also be used to the determination of Hb content in the range of 2.0 × 10-9 ∼ 3.0 × 10-7 mol/l with a detection limit of 1.0 × 10-9 mol/l. The proposed method was further applied to the determination of the content of H2O2 in fresh rainwater with satisfactory results. The catalytic reaction mechanism and the ...

  18. Hydrogen energy

    International Nuclear Information System (INIS)

    2005-03-01

    This book consists of seven chapters, which deals with hydrogen energy with discover and using of hydrogen, Korean plan for hydrogen economy and background, manufacturing technique on hydrogen like classification and hydrogen manufacture by water splitting, hydrogen storage technique with need and method, hydrogen using technique like fuel cell, hydrogen engine, international trend on involving hydrogen economy, technical current for infrastructure such as hydrogen station and price, regulation, standard, prospect and education for hydrogen safety and system. It has an appendix on related organization with hydrogen and fuel cell.

  19. Effect of residual stress relaxation by means of local rapid induction heating on stress corrosion cracking behavior and electrochemical characterization of welded Ti-6Al-4V alloy under slow strain rate test

    Science.gov (United States)

    Liu, Yan; Tang, Shawei; Liu, Guangyi; Sun, Yue; Hu, Jin

    2017-05-01

    In this study, a welded Ti-6Al-4V alloy was treated by means of local rapid induction heating in order to relax the residual stress existed in the weldment. The welded samples were heat treated at the different temperatures. The stress corrosion cracking behavior and electrochemical characterization of the as-welded samples before and after the post weld heat treatment as a function of residual stress were investigated. Electrochemical impedance spectroscopy measurements of the samples under slow strain rate test were performed in a LiCl-methanol solution. The results demonstrated that the residual stress in the as-welded sample was dramatically reduced after the post weld heat treatment, and the residual stress decreased with the increase in the heat treatment temperature. The stress corrosion cracking susceptibility and electrochemical activity of the as-welded sample were significantly reduced after the heat treatment due to the relaxation of the residual stress, which gradually decreased with the decreasing value of the residual stress distributed in the heat treated samples.

  20. Behavior of the monophosphate tungsten bronzes (PO2)4(WO3)2m (m = 7 and 8) in the course of electrochemical lithium insertion

    International Nuclear Information System (INIS)

    Martinez-de la Cruz, A.; Longoria Rodriguez, F.E.; Gonzalez, Lucy T.; Torres-Martinez, Leticia M.

    2007-01-01

    The electrochemical lithium insertion process has been studied in the family of monophosphate tungsten bronzes (PO 2 ) 4 (WO 3 ) 2m , where m = 7 and 8. Structural changes in the pristine oxides were followed as lithium insertion proceeded. Through potentiostatic intermittent technique the different processes which take place in the cathode during the discharge of the cell were analyzed. The nature of the bronzes Li x (PO 2 ) 4 (WO 3 ) 2m formed was determined by in situ X-ray diffraction experiments. These results have allowed establishing a correlation with the reversible/irreversible processes detected during the electrochemical lithium insertion

  1. Dynamic behavior of hydrogen in silicon nitride and oxynitride films made by low-pressure chemical vapor deposition

    Science.gov (United States)

    Arnoldbik, W. M.; Marée, C. H. M.; Maas, A. J. H.; van den Boogaard, M. J.; Habraken, F. H. P. M.; Kuiper, A. E. T.

    1993-08-01

    The diffusion and reactivity of hydrogen, incorporated in silicon oxynitride films during low-pressure chemical vapor deposition (LPCVD) at 800 °C, has been studied using elastic recoil detection and infrared spectroscopy for temperatures ranging from 700 to 1000 °C. The experiments are based on the determination of the hydrogen and deuterium depth profiles in layer structures in which H and D have been incorporated in different layers. This was achieved in two ways. Double layers have been produced directly during deposition or through exchange of incorporated hydrogen with gas-phase deuterium. The diffusion coefficient of hydrogen (or deuterium) is in the range between 3×1018 and 1×10-13 cm2/s, at temperatures between 700 and 1000 °C, and is characterized by a single activation energy of 3 eV, for [O]/([O]+[N]) values up to 0.45. The diffusion coefficient and hence the rate of the exchange of incorporated hydrogen and gas-phase deuterium increases with [O]/([O]+[N]) in the oxynitrides for [O]/([O]+[N]) >0.3. As a result we propose a model in which the rate-limiting step in the process of the diffusion of hydrogen in the LPCVD oxynitrides is the breaking of N-H bonds. Subsequent to the bond breaking, the hydrogen atom becomes trapped in a nitrogen-related trapping site or exchanges with a nitrogen-bonded hydrogen (deuterium) atom. If the bond breaking occurs within a distance of about 10 nm from the immediate surface, the hydrogen atom is able to desorb into the gas phase. A SiO2 capping layer is not able to prevent the desorption.

  2. Effect of N{sub 2} flow rate on the microstructure and electrochemical behavior of TaN{sub x} films deposited by modulated pulsed power magnetron sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Mendizabal, L., E-mail: lucia.mendizabal@tekniker.es [IK4-TEKNIKER, Department of Surface Physics and Technology, Iñaki Goenaga 5, 20600 Eibar (Spain); Bayón, R. [IK4-TEKNIKER, Department of Tribology, Iñaki Goenaga 5, 20600 Eibar (Spain); G-Berasategui, E.; Barriga, J. [IK4-TEKNIKER, Department of Surface Physics and Technology, Iñaki Goenaga 5, 20600 Eibar (Spain); Gonzalez, J.J. [ETSIB University of Basque Country, Department of Material Science, Alameda de Urquijo s/n, 48013 Bilbao (Spain)

    2016-07-01

    Modulated pulsed power magnetron sputtering (MPPMS) technology offers the possibility to grow high performance coatings compared to the ones developed by conventional dc magnetron sputtering. The high degree of ionization of sputtered particles developed during MPPMS can be usefully utilized to precisely tailor the properties of the growing films. One of the main advantages of such a high metal ion flux is related to the densification of the coatings due to enhance ion bombardment towards the growing film. The development of extremely dense and low-defect microstructure coatings can have a positive effect on the corrosion resistance of tantalum nitride (TaN{sub x}) films. In this study, TaN{sub x} thin films have been deposited by MPPMS in a closed field unbalanced magnetron sputtering system. Structure, surface morphology, hardness and corrosion resistance of the developed coatings have been analyzed as a function of different N{sub 2}-to-Ar ratios (0, 0.25, 0.625, 1). X-ray diffraction and scanning electron microscopy analysis reveal high dependence of the grown crystal phases and the microstructure on N{sub 2}-to-Ar ratio. The hardness of the TaN{sub x} coatings increases when increasing N{sub 2}-to-Ar ratio up to a maximum value of 25 GPa (N{sub 2}-to-Ar ratio of 0.625). The corrosion behavior was investigated using electrochemical impedance spectroscopy (EIS) and linear sweep voltammetry. EIS measurements registered at different immersion times show high impedance values (in the order of 10 MΩ cm{sup 2}) and corrosion resistance enhancement with time, indicating the formation of a passive protective oxide layer on the top of their surfaces. TaN{sub x} film grown at 0.25 N{sub 2}-to-Ar ratio exhibits the highest corrosion resistance of 103.53 MΩ cm{sup 2} and low porosity of 1.63 × 10{sup −3} and is characterized by columnar-free microstructure. - Highlights: • TaN{sub X} coatings deposited by MPPMS at different N{sub 2}-to-Ar ratios have been

  3. Modeling the vapor-liquid equilibria of polymer-solvent mixtures: Systems with complex hydrogen bonding behavior

    DEFF Research Database (Denmark)

    Tsivintzelis, Ioannis; Kontogeorgis, Georgios

    2009-01-01

    The vapor–liquid equilibria of binary polymer–solvent systems was modeled using the Non-Random Hydrogen Bonding (NRHB) model. Mixtures of poly(ethylene glycol), poly(propylene glycol), poly(vinyl alcohol) and poly(vinyl acetate) with various solvents were investigated, while emphasis was put...... on hydrogen bonding systems, in which functional groups of the polymer chain can self-associate or cross-associate with the solvent molecules. Effort has been made to explicitly account for all hydrogen bonding interactions. The results reveal that the NRHB model offers a flexible approach to account...

  4. Electrochemical behavior of lanthanum and yttrium ions in two molten chlorides with different oxoacidic properties: The eutectic LiCl-KCl and the equimolar mixture CaCl2-NaCl

    Directory of Open Access Journals (Sweden)

    Castrillejo Y.

    2003-01-01

    Full Text Available The electrochemical behavior of LaCl3 and YCl3 was studied in two molten chloride mixtures with different oxoacidic properties, the eutectic LiCl-KCl and the equimolar CaCl2-NaCl melt at different temperatures. The stable oxidation states of both elements have been found to be (III and (0 in both melts, and it was found that both La(III and Y(III cations were less solvated by the chloride ions in the calcium-based melt, which was explained by the stability of CaCl4 2- ions in that melt. Transient electrochemical techniques, such as cyclic voltammetry, chronopotentiometry and chronoamperometry were used in order to study the reaction mechanism and the transport parameters of electro active species at a tungsten electrode. The results showed that in the eutectic LiCl-KCl, the electro crystallization of lanthanum and yttrium seems to be the controlling electrochemical step while in CaCl2-NaCl this phenomenon has not been observed. That was explained in terms of the differences in the physicochemical properties of the systems, especially interfacial tensions. In the eutectic LiCl-KCl chronoamperometric studies indicated instantaneous and three dimensional nucleation and crystal growth of lanthanum and yttrium whatever the applied over potential of the rare earth metal is, whereas in the equimolar mixture CaCl2-NaCl, the corresponding electrochemical exchanges were found to be quasi-reversible, and the values of the kinetic parameters, K0 and α,were obtained for both reactions. Mass transport towards the electrode is a simple diffusion process, and the diffusion coefficients have been calculated. The validity of the Arrhenius law was also verified by plotting the variation of the logarithm of the diffusion coefficient versus 1/T.

  5. Electrochemical Chloride extraction using external electrodes?

    DEFF Research Database (Denmark)

    Ottosen, Lisbeth M.; Pedersen, Anne Juul

    2006-01-01

    Electrochemical methods for the removal of chloride from concrete have been developed and the methods are primarily designed for situations where corrosion has started due to an increased chloride concentration in the vicinity of the reinforcement. In these methods the reinforcement is used as th......, it is possible to use external electrodes and not use of the reinforcement as cathode thus avoiding side effects....... as the cathode. However, some unwanted side effects can occur, including alkali-silica reaction and in some cases hydrogen embrittlement. It is also suggested also to use electrochemical chloride extraction in a preventive way in constructions where chloride induced corrosion is likely to be a problem after...

  6. Comparison of hydrogenated vegetable shortening and nutritionally complete high fat diet on limited access-binge behavior in rats

    OpenAIRE

    Davis, Jon F.; Melhorn, Susan J.; Heiman, Justin U.; Tschöp, Matthias H.; Clegg, Deborah J.; Benoit, Stephen C.

    2007-01-01

    Previous studies have suggested that intermittent exposure to hydrogenated vegetable shortening yields a binge/compensate pattern of feeding in rats. The present study was designed to assess whether rats would exhibit similar patterns of intake when given intermittent access to a nutritionally complete high-fat diet. Four groups of rats received varying exposure to either hydrogenated vegetable shortening or high-fat diet for 8 consecutive weeks. Animals were given daily and intermittent acce...

  7. Investigation of the gas-phase hydrogen/deuterium exchange behavior of aromatic dicarboxylic acids in a quadrupole ion trap

    Science.gov (United States)

    Chipuk, Joseph E.; Brodbelt, Jennifer S.

    2007-11-01

    Gas-phase hydrogen/deuterium (H/D) exchange reactions of four deprotonated aromatic dicarboxylic acids (phthalic acid, isophthalic acid, terephthalic acid and 2,6-naphthalic acid) with D2O were performed in a quadrupole ion trap mass spectrometer. Experimental results showed significant differences in the rate and extent of exchange when the relative position of the carboxylic acid groups varied. Spontaneous and near complete exchange of one aromatic hydrogen atom occurred when the carboxylic acid groups were in the meta-position, whereas no additional exchange was observed for either the ortho- or para-isomers or for the structurally similar naphthalic acid. Computational investigations support the participation of several possible exchange mechanisms with the contribution of each relying heavily on the relative orientation of the acid moieties. A relay mechanism that bridges the deprotonation site and the labile hydrogen site appears to be responsible for the H/D exchange of not only the labile hydrogen atom of isophthalic acid, but also for the formation of a stable carbanion and corresponding subsequent exchange of one aromatic hydrogen atom. The impact of hydrogen bonding on the relay mechanism is demonstrated by the reaction of phthalic acid as the extent and rate of reaction are greatly retarded by the favorable interaction of the two carboxylic acid groups. Finally, a flip-flop mechanism is likely responsible for the exchange of both terephthalic acid and 2,6-naphthalic acid where the reactive sites are too remote for exchange via relay.

  8. Anodes for Lithium-Ion Batteries Based on Type I Silicon Clathrate Ba8Al16Si30- Role of Processing on Surface Properties and Electrochemical Behavior.

    Science.gov (United States)

    Zhao, Ran; Bobev, Svilen; Krishna, Lakshmi; Yang, Ting; Weller, J Mark; Jing, Hangkun; Chan, Candace K

    2017-11-29

    Type I silicon clathrates based on Ba 8 Al y Si 46-y (8 lithium-ion batteries and display electrochemical properties that are distinct from those found in conventional silicon anodes. Processing steps such as ball-milling (typically used to reduce the particle size) and acid/base treatment (used to remove nonclathrate impurities) may modify the clathrate surface structure or introduce defects, which could affect the observed electrochemical properties. In this work, we perform a systematic investigation of Ba 8 Al y Si 46-y clathrates with y ≈ 16, i.e, having a composition near Ba 8 Al 16 Si 30 , which perfectly satisfies the Zintl condition. The roles of ball-milling and acid/base treatment were investigated using electrochemical, X-ray diffraction, electron microscopy, X-ray photoelectron and Raman spectroscopy analysis. The results showed that acid/base treatment removed impurities from the synthesis, but also led to formation of a surface oxide layer that inhibited lithiation. Ball-milling could remove the surface oxide and result in the formation of an amorphous surface layer, with the observed charge storage capacity correlated with the thickness of this amorphous layer. According to the XRD and electrochemical analysis, all lithiation/delithiation processes are proposed to occur in single phase reactions at the surface with no discernible changes to the crystal structure in the bulk. Electrochemical impedance spectroscopy results suggest that the mechanism of lithiation is through surface-dominated, Faradaic processes. This suggests that for off-stoichiometric clathrates, as we studied in our previous work, Li + insertion at defects or vacancies on the framework may be the origin of reversible Li cycling. However, for clathrates Ba 8 Al y Si 46-y with y ≈ 16, Li insertion in the structure is unfavorable and low capacities are observed unless amorphous surface layers are introduced by ball-milling.

  9. ELECTROCHEMICAL BEHAVIOUR OF ENVIRONMENTALLY ...

    African Journals Online (AJOL)

    dell

    ABSTRACT. Electrochemical behaviour of Aloe secundiflora on carbon steel corrosion control in neutral and aerated soft water solutions have been investigated using electrochemical impedance spectroscopy and Tafel polarization techniques. The investigation was performed at different inhibitor concentrations under ...

  10. Separators for electrochemical cells

    Energy Technology Data Exchange (ETDEWEB)

    Carlson, Steven Allen; Anakor, Ifenna Kingsley; Farrell, Greg Robert

    2018-01-16

    Provided are separators for use in an electrochemical cell comprising (a) an inorganic oxide and (b) an organic polymer, wherein the inorganic oxide comprises organic substituents. Also provided are electrochemical cells comprising such separators.

  11. DIRAC: A new version of computer algebra tools for studying the properties and behavior of hydrogen-like ions

    Science.gov (United States)

    McConnell, Sean; Fritzsche, Stephan; Surzhykov, Andrey

    2010-03-01

    During recent years, the DIRAC package has proved to be an efficient tool for studying the structural properties and dynamic behavior of hydrogen-like ions. Originally designed as a set of MAPLE procedures, this package provides interactive access to the wave and Green's functions in the non-relativistic and relativistic frameworks and supports analytical evaluation of a large number of radial integrals that are required for the construction of transition amplitudes and interaction cross sections. We provide here a new version of the DIRAC program which is developed within the framework of MATHEMATICA (version 6.0). This new version aims to cater to a wider community of researchers that use the MATHEMATICA platform and to take advantage of the generally faster processing times therein. Moreover, the addition of new procedures, a more convenient and detailed help system, as well as source code revisions to overcome identified shortcomings should ensure expanded use of the new DIRAC program over its predecessor. New version program summaryProgram title: DIRAC Catalogue identifier: ADUQ_v2_0 Program summary URL:http://cpc.cs.qub.ac.uk/summaries/ADUQ_v2_0.html Program obtainable from: CPC Program Library, Queen's University, Belfast, N. Ireland Licensing provisions: Standard CPC license, http://cpc.cs.qub.ac.uk/licence/licence.html No. of lines in distributed program, including test data, etc.: 45 073 No. of bytes in distributed program, including test data, etc.: 285 828 Distribution format: tar.gz Programming language: Mathematica 6.0 or higher Computer: All computers with a license for the computer algebra package Mathematica (version 6.0 or higher) Operating system: Mathematica is O/S independent Classification: 2.1 Catalogue identifier of previous version: ADUQ_v1_0 Journal reference of previous version: Comput. Phys. Comm. 165 (2005) 139 Does the new version supersede the previous version?: Yes Nature of problem: Since the early days of quantum mechanics, the

  12. Study on the hydrogen storage and electrochemical properties of Mm{sub 0.75}Mg{sub 0.25}Ni{sub 3.5}Co{sub 0.2}Al{sub x} (x = 0.0–0.4) alloys

    Energy Technology Data Exchange (ETDEWEB)

    Zhiqiang, Lan; Wenqi, Peng; Shuying, Fu; Wenlou, Wei; Ningyan, Wei; Jin, Guo, E-mail: guojin@gxu.edu.cn

    2015-02-25

    Highlights: • Al doping improves the hydrogen desorption property of the Re–Mg–Ni hydrides. • Al doping improves the electrochemical property of the Re–Mg–Ni electrodes. • The high discharge rate of the electrodes depended on the hydrogen atom diffusion. - Abstract: Mm{sub 0.75}Mg{sub 0.25}Ni{sub 3.5}Co{sub 0.2}Al{sub x} (x = 0.0–0.4) alloys were prepared by the magnetic induction melting method. The influence of Al content on the hydrogen storage and electrochemical properties of the alloy was investigated. The results show that the hydrogen storage capacity is gradually reduced as the Al content increases. The (La,Pr,Nd)Ni{sub 5} cell volume and the change of enthalpy also decrease as Al is added. Although the discharge capacity decreases with increasing Al content, the addition of Al can reduce the stability of Mm{sub 0.75}Mg{sub 0.25}Ni{sub 3.5}Co{sub 0.2}Al{sub x} (x = 0.0–0.4) hydride and improve the performance of hydrogen desorption thermodynamics. For the alloy electrode without Al, the maximum discharge capacity (C{sub max}) and retention discharge capacity after 100 charge–discharge cycles (C{sub 100}) is 385 mA h g{sup −1} and 202 mA h g{sup −1}, respectively. For the alloy electrode with x = 0.4, while C{sub max} is only 323 mA h g{sup −1}, C100 is 273 mA h g{sup −1}, which is much higher than that of the alloy without Al. The addition of Al can improve the charge–discharge cycle lifetime effectively and can increase t